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1 BAB 22 EL 3004 Material Biomedika Bab POLYMERS [Adopsi dari: Zbigniew D Jastrzebski, The Nature And Properties of Engineering Materials, John Wiley & Sons, ISBN , 1987, CHAPTER 10.] Polymers A large group of engineering materials of steadily increasing importance in industrial applications is composed of natural and synthetic organic polymers. Natural polymers such as starch and cellulose are the basic constituents of all plants, while proteins form the basis for all animal life. Advances in our understanding of the relation between the molecular structure of polymers and their chemical and physical properties make it possible to design and produce various polymeric materials of required characteristics for specific engineering applications. Three main types of commercial products are considered: plastics. rubbers, and fibers. FORMATION OF POLYMERS High polymers are formed by polymerization reactions that occur by two main mechanisms: addition polymerization and condensation polymerization.the name polymer is formed by adding the prefix poly to the monomer generic name, for example, polyethylene. When the monomer has a substituted parent name or a multiword name, the parentheses are used after the prefix poly. Thus we can write poly(vinyl chloride), poly(propylene oxide), and poly(chlorotrifluoroethylene). The parentheses are purposely omitted in common usage ADDITION POLYMERIZATION Addition polymerization is defined as the reaction that yields a product that is an exact multiple of the original monomeric molecule. Such a monomeric molecule usually contains one or more double bonds that, by intermolecular rearrangement, may make the molecule bifunctional. Addition polymerization reactions usually proceed by a chain mechanism involving either free radicals or ionic catalysis. The reaction involves three steps: initiation, chain propagation, and termination (Equation 10-lb, 10-1c, and 10-1d). Initiation involves the dissociation of an initiator or catalyst into two free radicals (R) and addition to a monomer molecule M to form an active radical, R M*. Propagation or growth of the polymer chain results from successive addition of other monomers to the active group. Propagation Termination may occur because of collision between the active ends of two growing chains resulting either in their combination (coupling) or chain transfer mechanism, or by addition of terminator such as a free radical or another molecular species present in the system. Termination Examples are given by polymerization of ethylene, styrene, and vinyl chloride. 265

2 In all these reactions only bifunctional monomeric molecules are formed by the intermolecular rearrangement of the double bond present in the original molecule. This can result only in the formation of long chains. Another kind of addition polymerization is copolymerization. Copolymerization is the simultaneous polymerization of two or more chemically different monomers that react to form a polymer containing both monomers linked in one chain. For example. GRS rubber is the product of copolymerization of butadiene and styrene. In this long-chain polymer double bonds are still present that, on activation, are able to form crosslinks between the chains in further polymerization reactions CONDENSATION POLYMERIZATION Condensation polymerization can be defined as the reactions between functional molecules that lead to the formation of a polymer with elimination of some small molecules, usually water. Condensation polymerization reactions proceed by a stepwise intermolecular mechanism. The following reactions between dicarboxylic acid and dihydroxy alcohol, resulting in polyesters, illustrate this process. The resultant molecule reacts again in the same way with the dihydroxy alcohol molecule; the process repeats itself until linear chains of indefinite length are formed. R and R stand for organic groups such as CH 2, (CH 2 ) n, and others. The resulting polymer is a linear polymer that, depending on the degree of polymerization, may range from viscous liquids to rigid solids. Because of its relatively symmetrical structure and the presence of numerous polar groups, the polymer is a good fiber-forming material and can be converted into commercial fibers such as Dacron and Terylene. 266 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

3 Another reaction of polycondensation, which results in the formation of long linear chains, is used in the manufacture of nylon. The resultant molecule can subsequently react with other molecules or either adipic acid or hexamethylenediamine, yielding a linear polyamide, characterized by the linkage NH CO. These reactions also show that a compound having two functional groups at the end can only produce long linear molecules. Still another type of polycondensation reaction can be illustrated by the formation of a linear polycarbonate polymer. Here, the HCl molecule is evolved as the result of condensation and the carbonate linkage is formed. Phenol is an aromatic compound consisting of six-membered carbon ring of the benzene type in which one hydrogen atom is replaced by the hydroxyl group. The accepted schematic designation of the benzene ring is shown here. 267

4 10-3 CONFIGURATION OF POLYMER CHAIN During addition polymerization of a monomer A, the resultant polymer can be either a straight chain Furthermore, the monomer molecules can react in one or more of the following ways: head-to-head, head-to-tail, and tail-to-tail. This is illustrated by the formation of vinyl polymers, which are obtained from vinyl monomers with the general formula where X may stand for any atom or group, such as H, Cl. F, CH 3, etc. The mechanism of polymerization involves adding a free radical R to the monomer in two possible ways: Form I would lead to the formation of a head-to-tail arrangement in which the substituents occur on the alternate carbon atoms as shown by A combination of forms I and II may lead to the tail-to-tail or head-to-head arrangement: The possibility of obtaining only a regular head-to-head or tail-to-tail arrangement is relatively remote. Usually a mixture of all these arrangements occurs. In the case of copolymerization, where two different monomers A and B are added together, or polycondensation reactions, where two different monomers react with the evolution of a small molecule, there is a greater variety of structural forms and, 268 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

5 correspondingly, greater differences in polymer properties may result. Depending on the reactivities of monomers A and B on their relative proportions, different copolymers are formed. 1f the two monomer units alternate in random statistical distribution in the polymer chain random polymers result: Alternating copolymers are formed when the A and B units are placed alternately along the polymer chain: Another possibility is the formation of a graft copolymer, which is essentially a branched-chain structure having side chains composed of one type of the monomer unit attached to the backbone chain from another monomer unit: Such a graft copolymer can be produced either by prepolymerizing monomer B and grafting it onto the main backbone chain consisting of the monomer A. or by polymerizing in situ where a molecule first attaches to the backbone chain A and forms a grafted-on section: Stereoregular Polymers. Using special stereospecifïc catalysts, like Ziegler-Natta, it is possible to control the stereoregularity of the polymer chain by varying the type of initiator and the polymerization conditions. For example, a polymer chain of the composition contains asymmetric carbon atoms (C*) holding bulky R groups. The R group may stand for CH 3, C 2 H 5, C 6 H 5, and the like. If the R groups are all located on the same side of the plane, above or below, the arrangement is called isotactic; if the groups are alternate regularly from one side of the plane to another a syndiotactic 269

6 polymer is obtained (Fig. 10-1). Finally, if the groups are oriented at random then the polymer has an atactic arrangement and it is amorphous. Both isotactic and syndiotactic arrangements produce crystalline polymers (Fig. 10-1). FIGURE 10-1 Stereoisomers of a polymer chain having a bulky group R along the backbone chain. The bonds between the repeat units of a polymer chain are relatively flexible to permit rotation of the groups about the bond. This may result in various helical conformations of the chain to attain their close packing. The distinct rotational states of the groups that stabilize the helical conformation are the trans position and the two gauche positions. The trans and two gauche forms are alternately located along the backbone polymer chain to relieve any steric hindrance that might arise because of the bulky group. For two gauche positions left or right, either a left-hand helix or right-hand helix is formed (Fig. 10-2). A polymer helix is usually characterized by the identity period, I.P., and by the number of monomeric or repeat units in this period. For example, the propylene helix has an identity period of 650 pm and the number of repeat units per turn is 3. If the side groups are very bulky more space is required and the resultant helix may contain more than three repeat units per turn, forming much looser helices MOLECULAR WEIGHT DISTRIBUTION In straight-chain and branched-chain polymers, the individual chains are held together by intermolecular forces of attraction that increase with molecular weight or chain length of the polymer. Such polymers exhibit mechanical strength only when macromolecules have a chain length greater than about 150 to 200 atoms in line. Shorter chains produce oils or crystalline solids, such as paraffin. The lower molecular weight polymers are quite soft and gummy resins, but they are brittle to impact at fairly low temperatures. The higher molecular weight resins are tougher and more heat resistant. Thus, by controlling the molecular weight or chain length of individual macromolecules, it is possible to vary the properties of the polymer from soft and flexible up to hard, hornlike products. 270 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

7 FIGURE 10.2 Helical conformation of an isotactic vinyl polymer. IP is the identity period of the repeat distance of the helix containing three repeat units. Hydrogen atoms are not shown. As the molecular weight of the polymer is related to its chain length or to the degree of polymerization, it can be defined as where M m is the molecular weight of the monomer and DP denotes the degree of polymerization. During the course of the polymerization reactions, the polymer chains grow to different lengths, giving a product consisting of a mixture of macromolecules of wide molecular weight range. This is because the rates governing the growth and termination of polymer chains are subject to the hazards of random encounter of reacting molecules. Thus the resulting distribution of molecular weight of the polymer can, in most cases, be estimated from statistical analysis of kinetics of polymerization reactions. To characterize the polymer, we have to use certain average values of molecular weight. These averages can be obtained by several different methods and are defined below. 271

8 Number-average molecular weight, M n, is the weight of a polymer sample divided directly by the number of molecules in this sample. Mathematically this is expressed as Number-average molecular weights are obtained from such measurements as osmotic pressure, boiling point elevation, and freezing point depression. In all these methods the number of molecules for each fraction is counted in a known mass of the polymer and, through Avogadro s number, the number-average molecular weight is estimated. Weight-average molecular weight, M w, is defined as the weight fraction of w i of the polymer chains times their corresponding molecular weight M i divided by the total weight of the polymer sample investigated. This can be represented by the relation where w i is the weight of fraction i having mean molecular weight M i, and n i is defined as before. The weight-average molecular weight is usually determined by light scattering, which depends on the size and the mass of the molecule. Number-average and weight-average molecular weights are most frequently used in characterization of the molecular weight and the molecular weight distribution of the polymer. Another two averages occasionally used are z-average molecular weight, obtained by sedimentation in an ultracentrifuge and defined as and viscosity-average molecular weight, defined by where K and a are constants to be determined experimentally. The term [η] is specific viscosity of a polymer solution, which is determined from The curve representing the number and weight fraction of the molecular-weight distribution is given in Fig. 10-3, which shows the number- and weight average molecular weights. For a polymer with all chains of the same length all four averages will be the same: Frequently, the ratio of the weight-average molecular weight to the number average molecular weight, M w / M n is used to determine the spread of the molecular weight distribution of the polymer. For a narrow molecular weight distribution the ratio M w / M n is close to one but, for a broad molecular weight distribution, it may be as high as 3 to Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

9 Illustrative Problem 10.1 Solution: 273

10 FIGURE 10-3 Differential molecular weight distribution. Illustrative problem Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

11 LINEAR POLYMERS Linear polymers form the largest group of plastics covering a great variety of diversified products used in different forms and applications. Linear polymers can be obtained by either addition polymerization or condensation polymerization of bifunctional monomers. Being thermoplastic, they can be easily worked into required forms and shapes at elevated temperatures. The structure and properties of linear polymers depend on the chemical nature of the monomer, the geometry of the polymer chain, and the magnitude of the intermolecular forces between the chains. These intermolecular forces depend on the molecular weight or the chain length, the presence of polar groups and their spacing and regular distribution along the backbone chain, the possibility of formation of the hydrogen bond, and the distance between chains. The structural regularity of the chain determines the degree of packing of the chains and its state, either amorphous, crystalline, or semicrystalline DEGREE OF CRYSTALLINITY Polymers crystallized from melt on cooling of different degrees of perfection consist of individual single crystal lamellae connected to each other through tie molecules, which may meander randomly through the disordered regions before participating in the formation of another chain-folded crystal (Fig. 10-4). We can therefore consider such a crystalline polymer as a two-phase system consisting of an amorphous phase and an ordered crystalline phase that differ in their density and other physical characteristics. Crystallization causes a denser packing of molecules, increasing the intermolecular forces. The degree of crystallinity may range from 0% for noncrystallizable polymers through intermediate crystallinities such as 20% for poly(vinyl chloride), 50% for branched polyethylene, and up to 95% for polytetrafluoroethylene (TFE) and a linear polyethylene. FIGURE 10.4 Schematic representation of the typical crystalline polymer showing randomly arranged crystalline and amorphous regions. A polymer chain may go through several crystalline and amorphous regions. Crystallinity in polymers crystallized from the melt develops through spherulitic growth (see Fig. 5-15). Spherulites have different sizes and degrees of perfection, and they completely fill the volume of all well-crystallized polymers. They play a role similar to that of the grain structures in polycrystalline metals. The crystalline phase has a higher and sharper softening point, a greater tensile strength, and a greater density than the amorphous phase of the same chemical nature and molecular weight. For example, the isotactic crystalline polystyrene has a melting point of 230 C (446 F), whereas the 275

12 normal amorphous polystyrene of similar molecular weight has a softening point of only 90 C (190 F). Similarly, branched-chain polyethylene, which is only up to 60% crystalline, has a density of 910 to 930 kg/m 3 ( g/cm) and a melting point of 115 C (240 F). whereas linear polyethylene, considered to be 90 to 95% crystalline, has a density of 940 to 965 kg/rn3 and a melting point of 135 C (275 F). The density of perfectly crystalline material can be obtained from X-ray measurement, while that of the amorphous material can be easily determined above its melting point and extrapolated to room temperature. Thus the percentage crystallinity can be calculated from the relation The degree of crystallinity and the amount of amorphous region can be controlled by copolymerization, which lowers the structural symmetry of the polymer chain, thereby decreasing the crystallization tendency. For example, vinylidene chloride is usually copolymenzed with about 10% to 15% vinyl chloride to produce a material of greater flexibility than the pure vinylidene polymer. A copolymerization is a normal procedure in producing rubberlike polymers. A crystalline or amorphous polymer can be made more flexible by adding plasticizers. Crystallinity of a polymer is also controlled by its cooling rate. At fast cooling rates, even a strongly crystalline polymer will not be able to crystallize and will form an amorphous structure. Many polymers that crystallize more slowly can be quenched to a glassy amorphous solid and, if their T g is sufficiently high, as in the case of a polyamide (nylon 66) or isotactic polystyrene and poly(ethylene terephthalate), they may remain amorphous at room temperature for an indefinite period of time. On the other hand the rate of crystallization in polyethylene and Teflon is so high that crystallization cannot be prevented by quenching the melt, even in liquid nitrogen EFFECT OF POLAR GROUPS The presence of a polar group in the monomer increases the intermolecular forces between the chains, resulting in a higher softening point and a greater stiffness and rigidity of polymer, as exemplified by poly(vinyl chloride) compared with polyethylene. A normal poly(vinyl chloride), although much less crystalline than polyethylene because of the introduction of a chlorine atom, which lowers the symmetry of the chain, is stronger than polyethylene: However, when polar groups are spaced regularly and symmetrically along the backbone, polymer chain crystallization is enhanced, as exemplified by linear polyesters (Dacron), polyamides (nylons), polyvinylidene chloride, and others. Such 276 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

13 structures produce polymers of high melting points, high rigidity, and tenacity. The polyamides and polyterephthalates have a molecular weight only around 20,000. This value is an order of magnitude lower than that of other plastics, such as polystyrene. poly(methyl methacrylate), poly(vinylchloride), and polyethylene, which would have very low strength with such a low molecular weight. This shows clearly that the excellent strength of polyamides is due to the strong secondary valences caused by the presence of the regularly ordered polar groups. Thus, in nylon 66, the frequency of the polar groups CO NH- - and the formation of 0... H N hydrogen bonds between the chains leads to maximum interaction between the chains, which accounts for a high degree of crystallization and a strong, rigid material with a melting point of 260 C (500 F). Another example of the effect of the numerous polar groups and hydrogen bonding between the chains is given by natural polymer of cellulose. Cellulose, a main substance of all plants, is composed of anhydroglucose groups linked together to form a long chain having from 3000 to 4000 glucose unit: The structure shows three hydroxyl groups on each glucose unit. The hydrogenbonded structure of cellulose and its molecular weight account for the very strong intermolecular forces between the chains. These give high rigidity and crystallinity to the polymer, preventing it from melting and dissolving below its decomposition temperature. To make the cellulose more amenable for manufacturing operations, it is necessary to decrease these intermolecular forces by reducing the molecular weight or by neutralizing the polar character of the hydroxyl groups. Regenerated cellulose is essentially the same chemical compound as natural cellulose, but it has a much lower molecular weight, containing only from 300 to 500 glucose units. This lower molecular weight decreases greatly the intermolecular forces between the individual chains, making it possible to obtain cellulose in a solution form. This reduction of the molecular weight is accomplished by special chemical treatments with sodium hydroxide and subsequent treatment with carbon disulfide to produce a heavy viscous solution, known as viscose. The viscose can be spun to give fibers or extruded through a die for film. Then the cellulose is regenerated from this viscous solution by precipitating it in an acid batch as fibers (viscose rayon) or as film (cellophane), If the hydroxyl groups are replaced by acetate groups in the natural cellulose as the result of an esterification reaction with acetic anhydride and glacial acetic acid so that about 2 to 2.5 acetyl groups per glucose residue remain, cellulose acetate is produced. Cellulose acetate is no longer soluble in sodium hydroxide, but it is soluble in acetone. Complete substitution of three acetyl groups per glucose unit, however, makes the polymer insoluble in acetone. Cellulose acetate can be spun from viscous solution in acetone as flbers or used with plasticizers to form various plastic products and films. Other industrially important cellulosic polymers that are obtained from natural cellulose by modifying its molecular weight and the polarity of the side groups are cellulose nitrate, cellulose acetate butyrate, cellulose propionate, ethyl and methyl cellulose, and hydroxy- and sodium carboxymethyl cellulose. 277

14 The requirements of high tensile strength and high melting point (usually above 200 C (400 F)) require a high cohesion energy associated with a high degree of crystallinity. Thus the characteristic feature of a linear polymer to be a good fibermaking material is a high geometrical symmetry of the polymer chain and high intermolecular forces between the chains. Branching is not desirable because it disrupts the crystalline lattice and lowers the crystallinity. The crystallization of a polymer can be enhanced by its exposure to a shear gradient, as in stretching or drawing the solution or the melt of the polymer during or after cooling. This is used in the production of synthetic fibers and films. The melt or solution is first squeezed through a thin spinneret or a die, and the resulting fiber or film is stretched while being cooled or the solvent from viscous solution is evaporated TRANSITION TEMPERATURES Since crystalline polymers are never completely crystalline and contain both ordered (crystalline) regions and unordered amorphous regions, depending on the structure and thermal history of the polymer, they usually exhibit two characteristic temperatures: the melting point, T m, defined as the temperature at which crystalline aggregates disappear, and the glass transition temperature, T g. The glassy state of polymers is a rigid and brittle noncrystalline state. However, the brittle characteristics vary widely from polymer to polymer and with temperature. The glass transition temperature arises because of hindered relaxation of the chain molecules as the volume decreases with the temperature. Although the translational movement of the chain segment can be frozen and the rotation of the bulky groups may be stopped, some degree of vibration and local motion of the atoms may occur. Thus many polymers have other secondary or tertiary transitions in addition to the main glass transition. For example, crystalline polytetrafluoroethylene (TFE) shows four different transitions below its melting point of 327 C the main glass transition at C and the other three glass transitions at , and 97 C. Polycarbonate has a glass transition of 150 C but it is a strong, rigid polymer having exceptional impact resistance at temperatures much below T g. This appears to be due to the local motion within the carbonate linkage which persists up to 110 C and is capable of absorbing energy upon impact loading. Another example can be provided by nylon 66, which has a main glass transition at about 50 C, but retains a crankshaft motion of its methyl groups within the chain up to a temperature of 120 C. Polymers may also exhibit the decomposition temperature, T d, at which the molecular structure breaks down and the material decomposes. These three 278 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

15 temperatures (T m, T g, and T d ) define the range of applicability of the polymers in practice. Rubbers are used between T g and T d, whereas amorphous polymers are used below their glass transition temperature, but they must be formed and shaped between T g and T d, where they are already soft and rubbery. Crystalline polymers can be used up to their T m ; they are hot formed and shaped between T m and T d and cold formed between T g and T m. Because of the complex structure of crystalline polymers and the many defects in the crystalline regions, their melting temperature is usually within a few degrees of the thermodynamic melting temperature, T = H / S. The heat capacity, coefficient of expansion, diffusion coefficient, and elastic moduli undergo rapid changes in going through the glass transition. The mechanical damping of low-frequency oscillations exhibits a sharp peak in the region of T g. The glass transition temperature increases with the increase in intermolecular forces, molecular weight, crosslinking, and bulky and side group substituents that restrict rotation. For crystalline polymers the glass transition temperature is related to the melting point: m f f For symmetric polymers T g /T m 0.5, whereas for unsymmetrical polymers such as poly(trifluorochloroethylefle) or propylene, the ratio T g /T m is about The glass transition temperature is lowered with the addition of plasticizers. Below T g, the segments of an amorphous polymer undergo vibratory motions around fixed positions, while above T g, the segments exhibit translational and diffusional motions. Above T g. linear amorphous polymers exhibit time-dependent behavior. At a small constant stress, they show an elastic response, a retarded recoverable response, and finally, a non-newtonian flow. Amorphous linear (thermoplastic) polymers show the glass transition temperature which may vary from 40 to 150 C ( F) and sometimes higher, depending on the type and the structure of the polymer. For high molecular weight polymers, the solid is glassy below T g but, as the temperature gradually increases, it becomes leathery, rubbery and, finally, liquid. For low molecular weight polymer, the polymer changes from glassy below T g to liquid above T g. The major factor determining the value of T g is the flexibility of the polymer chain. Steric hindrance and bulkiness of the side groups attached to the backbone chain usually cause an increase in T g. The viscoelastic behavior of a polymer as a function of temperature is illustrated in Fig. 10-5, which shows the changes in modulus elasticity versus temperature for different structural arrangements. There are five regions of viscoelastic behavior of the amorphous polymer. The glassy state below T g characterized by a steady value of the modulus of elasticity, the glass transition region T g where the modulus drops rapidly, the rubbery plateau region with a steady value of the modulus, and the rubbery flow and liquid flow regions where the modulus again sharply drops. For a crosslinked polymer (curve D) a plateau is reached and the polymer is infusible. This depends on the degree of crosslinking, and the curve moves up with increasing density of crosslinks of the polymer. For such a highly crosslinked polymer the glass transition temperature does not have any physical meaning. 279

16 FlGUR 10-5 Changes of the modulus elasticity with temperature at constant time of 10 s for different structural arrangements. E r (10) is the relaxation tensile modulus during 10 s at a particular temperature. Curve A represents an amorphous polymer of low molecular weight, B is an amorphous polymer of high molecular weight, C is the crystalline polymer, and D is a crosslinked polymer. (After A. V. Tobolsky, Propemes and Structure of Polymers, John Wiley & Sons, Inc.. New York, 1960.) CROSSLINKING IN POLYMERS Crosslinking usually involves the introduction of a covalent type of link between polymer chains or their segments. An initially small amount of cross-linking causes formation of some branched molecules that still are soluble but, on further reaction, gelation sets in. This stage is characterized by the presence of insoluble gel and the soluble sol, which can be extracted from the gel. On further crosslinking a giant three-dimensional network is formed that imparts rigidity, infusibility, insolubility, and improved heat resistance to the polymer. If the crosslinks are short and densely located, hard and strong polymers are obtained that exhibit little elongation and high moduli. Crosslinking may occur through (1) functional groups, (2) addition at the double bond of the polymer or to the reactive groups located along the polymer chain, (3) radical formation, and (4) secondary valences, such as vander Waals forces, dipole-dipole interaction, hydrogen bond, and ionic bonding CROSSLINKING THROUGH FUNCTIONAL GROUPS This mechanism of crosslinking involves a condensation reaction that follows exactly the same path as that of the original polycondensation reactions during the formation of the polymer macromolecule. For this reason the term thermoset is applied to such crosslinked polymers, since their final curing after application is carried out under a pressure adequate to prevent the evolution of water molecules formed during crosslinking from the system. Phenol-Formaldehyde (Phenolic) Resins. Phenol-formaldehyde resins, simply called phenolic resins, are formed by polycondensation reactions between phenol and formaldehyde in the presence of suitable catalysts by a one- or two-stage process. The initial reaction results in the formation of mono-, di-, and trimethylol phenols, depending on the ratio of phenol to formaldehyde (P/F), the kind of 280 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

17 catalyst, the temperature, and the time of reaction. Two quite separate phenolic resins are produced: With two or three molecules of formaldehyde we obtain The reaction between methylol phenols and phenol may occur either (1) between the methylol hydroxyl group and the hydrogen in the benzene ring, or (2) between the two methylol hydroxyl groups. In both cases the water molecule is split off: Further heating produces a linear polymer of varying length: A bond through the radical CH2 in Reaction is called the methylene linkage; the bond through the radical CH2 O CH2 in Reaction is called the ether linkage. In the one-stage process, phenol is reacted in the presence of alkaline catalysts with an excess of formaldehyde, so that the phenol-toformaldehyde ratio (P/F) is less than one. The reaction is stopped when the product is still soluble and fusible, producing either A-stage or B-stage resin. The A-stage resin, called resol, is a relatively short, low molecular weight, linear polymer, which is completely soluble in the alkaline solution present in the reaction vessel. The B stage, called resitol, is a rather long, linear polymer with a slight amount of crosslinking between chains; it is insoluble in alkaline so lutions but readily soluble inorganic solvents and it is fusible. Resin A or B, or the combination of both, is used for adhesives, casting, plastics, and laminates. In the two-stage process only a part of formaldehyde is introduced so that the P/F ratio is greater than one. The reaction is carried out in the presence of acid catalysts. and it results in a hard, brittle product, called Novolac resin which, still being a linear chain, is fusible and soluble. Novolac resin is then ground to a powder and mixed 281

18 with proper ingredients such as fillers, stabilizers. lubricants, and dies. A crosslinking agent (hexamethylenetetramine) is added to provide the source of CH 2 links for subsequent crosslinking reactions. Final curing of either A- or B- stage resin or Novolac, which is carried out after the application of material, gives a three-dimensional network of densely spaced but relatively short crosslinks, designated as C-stage resin: Phenolic resins find numerous and varied industrial applications as adhesives, casting, coatings, laminates, and structural products with various fillers and fibers where high rigidity, corrosion resistance, and heat resistance are required. Amino ResIns. Similar mechanisms of reactions occur during polycondensation of urea-formaldehyde and melamine-formaldehyde, producing various amino resins known as urea and melamine resins: 10-9 CROSSLINKING THROUGH ADDITION Crosslinking through addition may involve reaction of an unsaturated compound between two polymer chains containing a polymerizable double bond, as in unsaturated polyesters or some rubbers. Another addition reaction may occur between a compound (catalyst) and the active end group of prepolymer chains, as exemplified by curing epoxy and polyurethane resins. In the first case the covalent crosslink is formed through the rearrangement of double bonds in the crosslinking agent as well as in the polymer. In the second case the crosslink results from the rearrangement of atoms in the end groups so that a simple addition of the catalyst molecule to both chains becomes possible. In both cases no molecule is evolved as the result of crosslinking reactions. This makes possible easy casting of the prepolymer resin with the catalyst (crosslinking agents) and various additives such as reinforcing agents under normal atmospheric pressure. Unsaturated Polyesters. Linear, or saturated, polyesters as mentioned before, are typical thermoplastic polymers, and they are not subject to crosslinking. However, unsaturated polyesters and alkyd resins offer another possibility of introducing crosslinks to produce a network polymer. The unsaturated polyesters are obtained by introducing unsaturated dibasic acids such as maleic and fumaric or dibasic unsaturated alcohols. The resulting polymers are usually crosslinked by monomeric compounds such as styrene, resulting in a thermosetting resin, as illustrated by the following reactions: 282 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

19 A vinyl-type compound of general formula is used for crosslinking of the linear chains, as shown below. The reaction occurs by simple addition. The extent of crosslinking can be controlled by varying the amount of unsaturation in the polyester and the amount and kind of crosslinking agent. For example, an unsaturated polyester crosslinked with styrene is harder and tougher than that crosslinked with methyl methacrylate. Unsaturated polyester resins are widely used as glass-fiber reinforced materials for various structural applications. Epoxy Resins. Epoxy resins are the combination of bisphenol A and epichlorohydrin. Which leads to the formation of a relatively short chain linear polymer containing two reactive groups, epoxide and hydroxyl: The reactive epoxide and hydroxyl groups are the points of reaction with catalysts, also called curing agents or hardeners, to form a three-dimensional network. Such catalysts, as various polyamines, react only with an epoxide group, whereas aliphatic and aromatic anhydrides react with both hydroxyl and terminal epoxy groups. Thus the density of the resultant crosslinks in a cured resin is much greater with anhydrides and catalysts, especially with dianhydrides instead of with amines. The example of crosslinking between the epoxide groups of the linear epoxy resin is given here using ethylenediamine as a catalyst. Note that no elimination of a small molecule takes place during crosslinking. 283

20 It is also possible to carry out a wide range of crosslinking reactions with other polymeric resins such as amines, phenolics, polyamides, cellulose, and vegetable oil fatty acids, producing a great variety of products of specifically modified properties. Because the ether linkage is a very stable one, epoxy resins have high chemical resistance to water, various solvents, acids and alkalies, and other chemicals. The reactive groups are comparatively widely spaced, resulting in high flexibility, but, at the same time, the presence of crosslinks accounts for the toughness and heat resistance of the cured polymer. Furthermore, the polar nature of such groups as epoxide and hydroxyl contributes to good adhesion. Epoxy resins are most frequently used as coatings, adhesives, and glass-fiber reinforced plastics CROSSLINKING BY FREE RADICALS This crosslinking may be accomplished by using free radicals that being a very active species, can attach themselves between the polymer chains, forming covalent links. Such free radicals can be formed as the result of intensive irradiation or by chemical action on the prepolymer, creating active centers along the backbone chains, or by using highly reactive compounds as organic peroxides and azo compounds. On heating, the latter decompose, giving free radicals. Crosslinking by Irradiation. Radiation-induced crosslinking occurs as the result of the impact of high-energy radiation on the polymer chains, which causes knocking out of hydrogen atoms and produces secondary free radicals on the polymer chain. This makes possible the formation of covalent links between the polymer chains. Crosslinking is generally found to occur more readily in the amorphous regions between polar crystallites. High-energy irradiation results in either crosslinking or chain scission, depending on the chemical structure of the polymer, and on the dose of radiation. Polymers that crosslink are polymethylene, polyethylene, polypropylene, polystyrene, polyvinyl chloride, polyamides, polyethylene siloxane, and others. Polymers that disintegrate are polybutylene, polytetratluorethylene, poly(methylmethacrylate), cellulose derivatives, and others. High-energy radiation is also used to initiate polymerization in grafting polymer on another polymer as polystyrene and rubber. Crosslinking by Organic Peroxide. Organic peroxides are frequently used in the curing of many polymeric products such as unsaturated polyesters and various saturated backbone rubbers. On heating, these peroxides decompose. giving free radicals that, in turn, activate the double bonds of the monomer, effecting polymerization. In the case of saturated backbone polymers such as polyethylene, fluororubber, silicone rubbers, and ethylene propylene rubbers, crosslinking requires hydrogen abstraction as shown by crosslinking silicone rubber with peroxides: 284 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

21 Free radicals abstract hydrogen atoms from methyl groups of the two polymer chains forming a crosslink between them. where R* stands for C 6 H 5 COO* or C 6 H 5 * CROSSLINKING THROUGH SECONDARY VALENCES We can extend the concept of crosslinking through secondary valence forces, especially groups such as COOH and CONH 2 which, because of hydrogen bond formation, are especially tight together. Such secondary valence cross-linking does not always have to be caused by hydrogen bonds. In principle all groups with high molar cohesion are capable of secondary valence cross-linking, especially polar groups such as COOH and SO 3 H. Secondary valence crosslinking differs from covalent crosslinking in that it disappears on heating. This makes the polymer thermoplastic in nature and accounts for its easy processability as compared to completely crosslinked covalent materials. This secondary crosslinking can also be removed by treatment with suitable polar solvents such as dimethylformamide. After removal of the solvent during wet spinning, the resulting threads behave as vulcanized rubber. Secondary valence crosslinking plays a highly important and decisive role in nature; all proteins are reversibly crosslinked through the CONH groups. A similar type of crosslinking can be found in polyelectrolytes, also called ionomers. lonomers are copolymers derived from ethylene and methacrylic acid in which the ionized carboxylic groups form ionic crosslinks in the intermolecular structure: The ionized groups are neutralized by zinc or sodium ion ELASTOMERS Elastomers are an important group of polymeric materials that are subject to many crosslinking processes to impart desired properties to the rubber. Any linear polymer can be made a good rubber if it meets the following characteristics. 1. The polymer chain should be very long and geometrically irregular so that thermal agitation will result in a strongly entangled and coiled-type arrangement. 2. The intermolecular forces between the polymer chains should be such that at room temperatures thermal energy is sufficient to maintain them in a state of constant mobility. This is comparable to the statement that the glass transition temperature should be below the working range of the temperature for a rubber. 3. There must be a possibility for introducing crosslinks between the chains so that the required degree of rigidity can be obtained. To achieve these desired characteristics, synthetic rubbers are usually produced by copolymerization processes, which have a tendency to lower the symmetry and 285

22 regularity of the chain and give a long chain of relatively weak intermolecular attraction. The presence of polar groups is usually avoided unless special characteristics such as oil resistance and improved heat resistance are required at the expense of flexibility of the polymer chain. Vulcanization. Vulcanization is the term used in the rubber industry to refer to the variety of crosslinking processes used. Natural and synthetic rubbers such as styrene butadiene (SBR), polybutadiene, acrylonitrile, and others contain a double bond capable of crosslinking (see Appendix A7). The mechanism of such crosslinking is essentially identical with crosslinking through addition polymerization, as illustrated by the curing of unsaturated polyesters. However, in a typical rubber, there is only about one crosslink to every few hundred chain atoms. FIGURE 10-6 Vulcanization of natural rubber. (a) Mechanism of crosslinking of isoprene molecules by means of sulfur atoms between two carbon atoms with double bonds (b) Schematic representation of transition from the randomly crosslinked coiled snarls to the oriented state on stretching. The presence of crosslinks causes the chain molecules to return to their previously coiled conformation on relaxation of stress, thereby preventing the permanent set. Vulcanization can be accomplished by heating raw rubber with sulfur or some sulfur compounds and accelerating agents. The snarls of the rubber are fastened at certain points by the covalent bonds between sulfur and two carbon atoms associated with the double bond (Fig. 10-6a). The more numerous the points of linkage are, the greater restriction of molecular slip exists and the lower the extensibility is until, finally, in hard rubber (ebonite) the structure becomes similar to that of a completely crosslinked thermosetting resin such as Bakelite (phenol formaldehyde resin). In the unstretched state the snarls are in a random arrangement, thereby accounting for the amorphous state of the polymer. On stretching, the snarls begin to disentangle and straighten out and the 286 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

23 chains become oriented (Fig. 10-6b). This orientation results in crystallization that increases the attraction forces between the chains, causing the material to stiffen. When the force is released, strained bonds are allowed to return to the original random snarl arrangement of the molecules. Such changes in the molecular configuration account for characteristic elongation of rubbers on stretching and their contraction (unloading) on the release of force (see also Fig. 7-9). Some rubbers, especially the natural rubber, crystallize easily on stretching. considerably improving their tensile strength. On the other hand, synthetic rubbers such as styrene butadiene rubbers do not crystallize readily when stretched. They show poor tensile strength unless reinforced with fillers such as carbon black. Speciality Rubbers. The presence of the double bond in the polymer chain results in the rather poor oxidation resistance of the rubber. To improve that, new synthetic rub bers such as chiorosulfonated polyethylene, silicones, polyurethanes, and fluororubbers have been developed that have a completely saturated backbone chain. For crosslinking, special reactive groups are provided at certain intervals along the main chain, or specially active compounds such as peroxides, producing free radicals on heating, are used. For example, chlorosulfonated polyethylene, known as Hypalon, is produced by reacting polyethylene with chlorine and sulfur dioxide. This results in the introduction of chlorine atoms and a small number of chlorosulfonyl groups. SO 2 Cl, into the polyethylene chain. A random spacing of chlorine atoms in the chain reduces the crystallinity of the polyethylene, and chemically active chlorosulfonyl groups form crosslinks with vulcanizing agents such as PbO or MgO. The reaction proceeds as follows: R stands for the chain repeat unit of Hypalon. and crosslinking can be schematically shown by Since the rubber has no unsaturated bonds, it shows high oxidation resistance and high chemical resistance. Still another example is polyurethane elastomers, which can be made by reacting a prepared prepolymer chain B with an aromatic diisocyanate to produce a very long, 287

24 irregular chain possessing active isocyanate groups for crosslinking. This can be accomplished using glycols, producing the isocyanate linkage: Water can also be used producing the urea linkage in two steps with the elimination of CO 2 : Reactions 10-55a and 10-55b are used to produce various polyurethane foams with water. The final structure of the polyurethane can be represented schematically by where B designates the prepolymer, which can be a polyester, or a polyether, or a polyester polyamide. Polyurethanes are highly resistant to oxidation because of their saturated character; they also show good resistance to many organic solvents, but they are attacked by acids and alkalies, especially hot or concentrated, similarly to polyamides. Isocyanates are also used to produce fibers as well as other resins, which are characterized by strong adhesion to many material surfaces THERMOPLASTIC ELASTOMERS Thermoplastic elastomers are the block copolymers which exhibit the elastic properties of elastomers at the use temperature but can be processed as thermoplastics at elevated temperatures. Usually. thermoplastic elastomers are two-phase block copolymers containing both hard and soft polymer segments. The hard segments form domains which, at service temperature. prevent the flow of the soft elastomeric segments but, at elevated temperatures. soften and plasticize the rubber segments so that the material can be processed as a conventional thermoplastic. There are two main types of thermoplastic elastomers: modified thermoplastic elastomers and thermoplastic elastomers by polymer blending. Modified Thermoplastic Elastomers. The modified thermoplastic elastomers are blends of homogeneous polymers having various types of temporary crosslinkings such as glassy block polymers of polystyrene (PS) in styrene butadiene styrene (SBS) copolymers or the crystalline hard phase of tetramethylene terephthalate in a thermoplastic copolyester/polyether (Fig. 10-7). In SBS thermoplastic elastomers the polybutadiene functions as a soft ciastomeric phase while the polystyrene phase acts as a hard crosslinking component. The latter can be modified with another polymer such as a poly(phenylene oxide) to increase its glass transition temperature. SBS block copolymers are frequently blended with other polymers such as polystyrene (PS), polyethylene (PE), and polypropylene (PP) together with oils and fillers. Generally blends of this type can be modified by the addition of rubbery materials to improve their impact resistance and flexibility. 288 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

25 FIGURE 10-7 Schematic diagram of a thermoplastic elastomer morphology. Hard crystalline or glassy domains function as crosslinks for soft amorphous rubbery phase. Thermoplastic polyester elastomers (TPE) and thermoplastic polyurethane elastomers (TPU) are alternating block copolymers having segments of a hard. highly polar or crystallizable material linked by segments of amorphous (soft) rubber-like material at normal service temperature. in TPE the crystalline block consists of dimethyl terephthalate segments and the amorphous soft rubbery phase is poly(tetramethylene ether) glycol terephthalate segments randomly distributed along the polymer chain. Crystalline regions are about 10 nm (100 Å) wide and several hundreds nanometers long. The melting point of these domains is around 200 C (400 F). In TPU the hard, highly polar blocks of 4.4-phenylmethane diisocyanate or 2,4 2,6- toluene diisocyante extended with 1,4-butane diol form hydrogen-bonded crystalline or glassy domains and the soft elastomeric phase consisting of polyol segments. TPU and TPE are polar materials and the choice of polymers for blending is limited to polar polymers such as PVC, ABS. and polyesters. Such blending improves abrasion resistance and flexibility and gives a product that is less expensive than pure thermoplastic elastomers. Because of their crystalline blocks both TPU and TPE materials show good resistance to fuels, oils, and similar products. TPU are characterized by exceptionally high tensile strength up to 50 MPa (7 ksi), large hysteresis, and stress softening. Thermoplastic Elostomers by Polymer Blending. The most useful thermoplastic elastomers under this group are polyolefin blends of a crystalline polyolefin such as isotactic propylene or less frequently polyethylene (HDPE) with a polyolefin rubber such as an ethylene propylene copolymer (EDR) or ethylene propylenediene terpolymer (EPDM). The rubbery phase is slightly crosslinked during mixing to enhance elastic recovery. At higher temperatures, the crystalline phase melts and flow of the mixture becomes possible. Upon cooling, the crystalline phase rehardens and the original properties return. Other examples of this class of thermoplastic elastomers are butyl rubber polyethylene blends and silicone polyethylene blends INTERPENETRATING POLYMER NETWORK An interpenetrating polymer network is defined as a material which consists of a pair of networks, one of which at least has been synthesized and/or crosslinked in the presence of the other. interpenetrating polymer networks (IPN) are more or less intimate mixtures of two or more distinct crosslinked polymer networks that cannot be physically separated. IPN can be considered as another technique, very much like graft or block copolymerization, for inducing polymer blend compatibility through polymer structure modification. For example, styrene plus divinyl benzene polymerizes by free radical 289

26 initiation in the presence of a polyurethane network. The possibility of combining various chemical types of polymeric networks has produced IPN compositions that exhibit synergistic behavior. If one polymer is elastomeric in nature and another is glassy, then a reinforced rubber is obtained if the elastomer phase predominates, and an impact-resistant plastic results if the glassy phase predominates. There are a few categories of interpenetrating networks. When only one polymer is crosslinked and the other is linear the product is called a semi IPN. Semi-1-IPN or semi- 2-IPN exists when, respectively, polymer 1 or polymer 2 is the crosslinked component. Furthermore, in addition to IPN the general term for interpenetrating polymer network we can distinguish the simultaneous interpenetrating network (SIN), where both polymers are synthesized simultaneously, by either addition or condensation polymerization reactions, and the interpenetrating elastomeric network (IEN). The latter refers to those materials that are made by mixing and coagulating two different polymer latexes and crosslinking the coagulum to form a three-dimensional structure. If the latex coagulum is not crosslinked, the resulting product is called a latex polyblend. GENERAL PROPERTIES HIGH-TEMPERATURE RESISTANCE AND THERMAL STABILITY A serious drawback of polymers as engineering materials is their relatively poor heat resistance and low thermal stability. A considerable research effort has been made in developing new polymers of improved thermal stability and heat resistance. The progress has been achieved along two main directions: developing aromatic polymers and developing inorganic polymeric materials. Aromatic Polymers. Polymers having more cyclic rings in their chains are stiffer and more resistant to deformation because segmental rotation of the chain segments becomes more difficult. Hence the melting points and the glass transition temperatures increase, and the solubility and the deformation-under-load at elevated temperatures decrease. The presence of aromatic rings improves the thermal stability of a polymer still more, since aromatic rings are thermally very stable by nature. The application of these principles in creating new polymers has brought remarkable improvement in heat resistance and oxidation resistance of some specific polymeric materials. Examples of this are polybenzimidazole and polyimides, which show heat resistance for a short time up to a temperature of about 600 C (1112 F). (10-57) The other way to provide good heat resistance is to use the inorganic material, as exemplified by silicone polymers. as a backbone chain. Silicone polymers are based on an inorganic silicon oxygen structure that has organic radicals attached to silicon atoms. Because of the presence of silicon oxygen links, they exhibit outstanding heat resistance, but their chemical resistance is generally lower than that of other plastics. Two or more functional groups can be attached to the tetravalent silicon atom that, on polycondensation, may lead to chain or crosslinked polymers (Table 10-1). The low molecular weight silicone polymers with linear structure, where x is a small number of about 10, are oily liquids. These may be compounded with silica aerogel and lithium stearate to produce lubricating greases. When x is a very large number, silicone rubbers 290 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

27 result. Finally, when the ratio R/Si is lower than 2, combinations of ABC units, crosslinked polymers, are obtained. The type of organic radical in silicone polymers greatly affects the properties of the resultant products. For example, the methyl silicone polymers with a high R/Si ratio are oily liquids, but the corresponding phenyl silicones of the same chain length are hard, brittle resins, If the methyl group is replaced by an ethyl group a softer, more soluble, and slower-curing product results. Silicones show satisfactory heat resistance at 250 C (482 F); however, at higher temperatures [350 C (662 F)] they undergo extensive degradation and decomposition to low molecular weight products. Replacement of oxygen with nitrogen in a siloxane leads to the so-called silazanes which are sensitive to water, decomposing with NH3 evolution. In the search for higher thermal stability numerous polymetallosiloxanes such as silicon-oxygen-aluminum and silicon-oxygen-titanium have been developed: These materials, however, are very brittle and of very little practical use CHEMICAL RESISTANCE The chemical resistance of polymers depends on the chemical nature and molecular arrangement of monomeric units. The chemical attack on polymers is most often internal, involving softening, swelling, and loss of strength of the material. A general rule stating that like materials attract and unlike materials repel is helpful in predicting the chemical resistance of many polymers. Thus a polymer is more soluble in a solvent of similar chemical structure. Polymers having polar groups such as hydroxyl (OH) and carboxyl (COOH) are usually swollen or even dissolved by polar liquids such as water or alcohols, hut they are resistant to nonpolar solvents such as gasoline, henzene, and carbon tetrachloride. 291

28 Polymers with nonpolar groups such as methyl (CH 3 ) and phenyl (C 6 H 5 ) are resistant to polar solvents such as water and ethyl alcohol, but they are usually swollen or dissolved by nonpolar solvents such as gasoline, benzene, and carbon tetrachloride. Furthermore, polymers of more aromatic character are more soluble in aromatic solvents, whereas those of aliphatic character are more soluble in aliphatic solvents. Polymers may be affected by solvents in several ways: dissolution, swelling, permeability, environmental stress cracking, and crazing. The solution process occurs very slowly in two stages: diffusion to produce swelling and then solution. As the molecular weight of the polymer increases, its solubility or tendency to swell in a particular solvent decreases. Polymers of high molecular weight usually yield solutions of high viscosities. The symmetry of the molecular structure of the polymer also affects the resistance of polymers toward solvents. More crystalline polymers exhibit higher chemical resistance than do less crystalline polymers having the same chemical character. The higher resistance is due to a denser packing of the chain molecules, which makes the penetration of a solvent or other chemical substance in the material more difficult. The degree of crosslinking greatly affects the solubility of polymers, so that even a slight crosslinking insufficient to cause infusibility may make a polymer insoluble. Less effective is the influence of branching, which usually decreases the rate of dissolution, but it does not render a material completely insoluble. The behavior of a heavily branched polymer is similar to that of a slightly crosslinked one, and lis usually very difficult to distinguish between these two types. Crosslinked polymers do not dissolve but only swell if interaction with solvents occurs at all. Polymers generally have better resistance to attacks by acids and alkalies than metals do; however, they may contain certain vulnerable polar groups that may make them susceptible to attack. Thus alkalies, especially at higher concentrations or higher temperatures, may saponify the ester groupings in cellulose acetate, polyesters, polyvinyl acetate, and similar polymers. Non-oxidizing acids may also hydrolyze these materials in a similar manner. Polyamides (nylons) and polyurethanes having the linkages NH CO and NH COO, respectively, are also susceptible to attack by strong acids and alkalies. The relative resistance depends on the chain length of the polymethylene groups between the linkages. All polyolefins, PVC, ABS polymers, fluorocarbons, polystyrene, and others have excellent resistance to all acids and alkalies OXIDATION RESISTANCE Many commercially important polymers are susceptible to oxidation when exposed to atmospheric oxygen either during manufacturing processes or during the use. Oxidation is a chain reaction initiated and propagated by free radicals which, in the air, readily combine with molecular oxygen to form a polymer peroxy radical (POO ). Most polymers are prone to oxidation and photoinitiated degradation. Molecular weight is changed by chain scission or by crosslinking, causing deterioration of physical properties such as softening or brittleness. The greater the amount of unsaturation (carbon-to-carbon double bond) the more susceptible is the material to oxidation and subsequent degradation. Among saturated polymers those containing a tertiary carbon hydrogen bond such as polypropylene (PP) are more easily oxidized than polymers that do not show such bonding. In PP, oxidation causes scission of the main polymer chain, attacking the carbon carbon bond. In certain high-density polyethylenes (HDPE) the crosslinking reaction predominates. In polyvinyl chloride (PVC) breakdown occurs by dehydrochiorination with evolution of a hydrogen chloride molecule (HCl). Polyesters, polyurethanes, polyamides and polycarbonates usually discolor under oxidation with little change in physical properties. However, at higher temperatures or under prolonged exposure to UV radiation, the physical properties may deteriorate. Polymers also differ in the effects of oxidation on their properties. Depending on the polymer and the type of reactions that take place during polymer breakdown, changes may occur that adversely 292 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

29 affect melt flow, or elongation, impact strength, electrical properties, surface crazing. and gloss and clarity. Certain rubbers, especially those that contain a double bond, like natural rubber, styrene butadiene, neoprene, and acrylonitrile rubber, are very sensitive to oxidation. The attack is enhanced by the presence of ozone in the atmosphere which under normal conditions may range from 0 to 20 parts per 100 million. Ozone (O 3 ), unlike molecular oxygen (O 2 ), adds directly to a double bond, forming ozonides which further decompose to peroxides and ketones. In an unstressed rubber a silvery film is formed on the surface especially in a humid atmosphere. When rubber is under stress, cracks appear perpendicular to the direction of stress which may lead to failure of the material. Light, especially UV radiation, enhances the action of oxygen, causing deterioration of the physical strength and the phenomenon of crazing, and alligatoring at the surface occurs. When the film is washed away filler particles are exposed which are easily rubbed off. To prevent or to reduce oxidation effects on polymers a number of antioxidants and antiozonants are mixed with the polymer during processing operations. Antioxidants are compounds that inhibit or retard atmospheric oxidation and the effects on a polymer system. There are three main classes of antioxidants used: (1) secondary amine bodies R 2 NH, which react with chain-propagating radicals that intercept either R or RO 2, (2) phenolic bodies R(OH) x, and (3) phosphites (RO 3 )P that decompose peroxide into nonradical and stable products PERMEABILITY Closely related to the chemical resistance of polymers is their permeability toward gases and liquids. The passage of gas may take place by simple diffusion through very fine channels between rigid molecular units, as in the case of crystalline, glassy, or highly crosslinked polymers, or by diffusion through viscous materials, as in the case of a rubbery polymer. Diffusion can be enhanced by a solution of gases or liquids in some component of the polymer structure, such as plasticizers. A higher degree of crystallinity, which results in a higher density and also a higher degree of crosslinking, lowers the rates of diffusion of both gases and liquids through the polymer, thereby also improving their chemical resistance. It appears that CO 2 has a rate of permeability through most polymers considerably greater than that of oxygen and still greater than that of nitrogen. This is perhaps due to its ability to be absorbed by materials that permit high rates of water transfer. The average ratio rates between N 2 : O 2 : CO 2 is 1:4:14. The absorption of water and its passage through polymer follow general principles: polymers having polar groups show much a higher permeation or absorption rate than nonpolar polymers. Water itself may act as a plasticizer, contributing to the swelling of the polymer and the loosening of its network. The permeability of other solvent molecules under conditions of insolubility of the polymer resembles the mechanism for the permeability of gases, with the added complication of polar effects, as in the case of water transfer. Permeation or permeability rate is the product of the diffusion term and the solubility constant of the gas-liquid in the polymer network, Permeability rate is a function of many parameters, but the gas permeability coefficient is a basic property of a material independent of specimen geometry. There are certain molecular structures that lead to good barrier properties in polymers. A high-barrier polymer exhibits a high resistance to molecular flow of a permeating agent through the polymer matrix. This includes resistance to gas flow, resistance to liquid, and resistance to absorption and diffusion of organic vapors through the polymer. Frequently 293

30 the low permeability of a polymer toward oxygen or carbon dioxide P CO 2, can make the material highly permeable toward water and water vapor. For example, polyvinyl alcohol has excellent resistance to gas flow (permeation) but it is a very poor water barrier. In addition, it becomes a poor gas barrier when plasticized with water which causes swelling of the polymer, thereby loosening its structure. Conversely, polyethylene has very good water barrier properties but it is a poor gas barrier. To be a truly good barrier polymer toward the gases the material must have some degree of polarity as provided by nitrile, ester, chlorine, fluorine, or acrylic groups, it should have high chain stiffness, close chain-to-chain packing, crystallinity, and orientation. Note that polyethylene and polypropylene are poor gas barriers but excellent water barriers, whereas polyacrylonitrile is an excellent gas barrier but a poor water barrier. Dimethyl silicone rubber because of its open structure shows extremely high permeability to gases and water. It is used as a membrane oxygenator because of good biocompatibility; however, it is very weak (Table 10-2). The permeability of polymers plays an important part in applications of polymers as films in the packaging industry, for plastic containers, for corrosion-resistant coatings and sheets, for electrical applications, and as membranes in industrial, biological, and waste treatment processes. Permeability of organic coatings to water and oxygen has been extensively studied because of its importance in controlling the corrosion protection of the coating. The presence of particles (fillers and pigments) may affect the permeability of water in a very specific way dependent on the type of particles and pathway mechanisms. The rate of oxygen diffusion through the film was always found to decrease markedly with increasing particle concentration in the film. The rate of transmission of liquid water through glass/polyester laminates and polyester resin castings is a function of resin structure and it always increases with temperature. The effect is a reduction in tensile stress, in flexural strength, and in modulus of elasticity with time when exposed to water for a long time. An additional requirement of high-barrier polymers used in food packaging and beverages is that the taste and odor of the pack aging cannot be affected in any way by interaction with the polymer wall FLAMMABILITY Polymer combustion occurs in a continuous cycle. Heat released from combustion is transferred back to the surface of the polymer. This results in generation of volatile fragments which diffuse into the flame zone and undergo there rapid chain reactions producing heat, and the cycle is continued. Polymers vary greatly in their inherent flammability behavior, it is convenient to divide them into three classes according to their behavior before compounding with additional flame retardants: 294 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

31 Class I forming relatively flame-retardant structures contains either halogen or aromatic groups; all these polymers form char on burning and/or show high thermal stability. High thermal stability is one prerequisite for materials of high fire resistance and low smoke generation. Such materials will yield volatile fuels only under very severe conditions. High aromatic polymers will play an important part in the future of flame-resistant materials because they have very low flammability, generate little smoke during a fire, and do not contain halogens thereby reducing the risk of secondary damage to corrosive gases which may be liberated in afire. No flame-retardant material is required that may adversely affect processing and end-use properties. Class II compounds do not show much tendency to crosslink or char; but they have a sufficiently close fire-retardant structure so that the addition of flame retardants such as halogen, halogen-antimony, or phosphorus either enhances char formation or inhibits flame generation. Class III represents polymers which are highly flammable and do not char but easily decompose, producing a high proportion of volatile, combustible fragments. Class III polymers require the addition of flame retardants which are physically compounded with various plastics to meet the specific requirements of flammability. The most important flame retardants are halogenated compounds. phosphorous compounds, metallic oxides, nitrogen compounds, alumina hydrates, and various metallic salts. Flame retardants function as free radicals interrupting melting of the solid polymer and preventing or inhibiting burning of the gases. Triaryl phosphates function very well in the vapor phase while highly chlorinated paraffins can be used to reduce flammability and smoke. Alumina trihydrate is an ideal retardant to be used with fiber-rein forced polymer (FRP) composites. It undergoes endothermic decomposition at C ( F) well above molding temperature, to quench a flame and reduce smoke under burning conditions as well as to provide a good arc track resistance in service. Another adverse aspect of the exposure of polymers to fire is the danger of decomposition associated with the emission of toxic fumes and corrosive gases. Even the Class I inflammable polymers such as highly halogenated and highly aromatic polymers may decompose on prolonged exposure to fire, producing highly toxic and corrosive gases. POLYMER PROCESSING Polymer processing consists of a series of operations carried Out on polymeric materials to increase their utility. Most polymers are seldom used as pure organic resins, but they are modified and compounded with various additives to obtain desirable properties for particular uses. The process of selection of such additives and their incorporation into a polymer is called compounding. After compounding, (he resultant mix is subjected to a variety of forming and finishing Operations to provide the desired shape, form, and appearance COMPOUNDING Modification of the polymer properties is accomplished by mixing it with various ingredients such as polymeric resins, plasticizers, fillers and reinforcing agents, various 295

32 stabilizers, lubricants, coloring agents, flame retardants, and crosslinking agents, when needed. Blending of Polymers. Blending is a process of mixing or reacting two or more polymer resins to obtain a product with improved properties. espcially impact resistance. Blend ing can be accomplished by physical blending, interpolymerization, and graft polymerization. Physical blending is achieved by milling together two incompatible polymers and heating them to above their softening points. On cooling, a two-phase system is formed that consists of a continuous matrix in which the particles of the other constituent are dispersed as spheres, cylinders, rods, or lamellae of varying dimensions. The microstructure and morphology of such a system greatly affect the toughness of the final product. A variety of microstructures are possible, and the dispersed particles may range from 1 to 20 µm, but better properties result with particles from 1 to 5 µm. An example of such a system is the so-called toughened polystyrene (TPS), also called highimpact polystyrene. which consists of a polystyrene matrix with a dispersed rubber phase such as potybutadiene or styrene butadiene rubber. Interpolymerization involves the polymerization of a styrene solution of rubber using organic peroxides or azo compounds as catalysts. With increasing polymerization a continuous matrix of polystyrene is formed in which rubber droplets form the dispersed phase. Another two-phase polymer mixture, acrylonitrile-butadiene-styrene, is produced by graft polymerization of butadiene acrylonitrile or polybutadiene as the rubbery component and styrene-acrylonitrile as the hard, glassy component. High impact strength is achieved by grafting the matrix glassy polymer to the rubber backbone. The dispersed rubber particles are from 0.1 to 0.5 µm. Plasticizers. Plasticizers are materials that are added to polymeric materials to increase their plasticity and flexibility. Plasticizers range from solvents with high boiling points to nonvolatile oils and resinous materials. There are three general types of materials used as plasticizers: (1) vegetable oils (nondrying type): (2) monomeric chemicals of high boiling points: and (3) polymeric resinous materials of low molecular weight. The action of plasticizers is considered to be the weakening of the intermolecular forces between macromolecules. This results in greater freedom of movement of the polymeric macromolecules, increasing the flexibility and plasticity of the material but, at the same time reducing its tensile strength and chemical resistance. The effect of plasticizers is to lower the T g of amorphous polymers and to decrease the degree of crystallinity of crystalline polymers. The amount of plasticizer added controls the final properties of plastics. For example. PVC is produced as rigid nonplasticized, rigid partially plasticized, and flexible rubbery-type polymer. The most widely used plasticizers are various phthalates. Fillers and Reinforcing Agents. In order to counteract the weakening effect of the plasticizer, fillers and various reinforcing agents are added. Fillers improve the strength, impact resistance, heat resistance, dimensional stability, and other similar properties of the polymers. The quantitative aspect of the reinforcement effects of various fillers and fibers is discussed in Chapter 14. Stabilizers and Other Additives. Stabilizers are added to prevent decomposition or deterioration of the polymer under the action of light, atmosphere, and other possible external environ mental factors. For example. the addition of carbon black, which is also a very effective filler, to polyethylene resin prevents photochemical degradation of the material by excluding light. Antioxidants are a special kind of stabilizer that prevent or inhibit the oxidation of the polymeric resin. Other additives used are antistats, blowing agents, colorants, organic peroxides, flame retardants, lubricants, crosslinking agents, and various processing aids. 296 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

33 10-21 FORMING OPERATIONS In most forming operations the polymer is subjected to intensive shearing and stressing, usually at molten or nearly molten states. This results in the deformation and orientation of the polymer chains, imparting to the polymer a specific molecular configuration and morphology of the final product. This is particularly strongly marked during spinning, drawing, blowing, and rolling processes, which produce fibers and films. Most forming operations, especially molding, extrusion, and casting, involve the melting or softening of the polymer by heating it to a temperature at which it will flow usually through a narrow nozzle under pressure to fill the cavity of the mold. Under such conditions, most polymeric resins are highly viscous materials having viscosities between 10 4 and 10 8 Pa.s (10 4 and 10 9 P), depending on the temperature and pressure. Furthermore, the presence of fillers and other additives may considerably affect the rheological characteristics of the polymer melts. Usually, polymer melts behave as pseudoplastic materials whose viscosity de creases rapidly with increasing shearing rate. Furthermore, they exhibit viscoelastic behavior that becomes more and more pronounced on gradual cooling of the polymer during molding or extrusion operations. During the polymer flow, the whole polymer chains cannot slide over one another completely, but movement occurs by segmental motion. The movement of the entire chain length is restricted because of numerous entanglements between the chains. Molding. Molding is our most widely used forming operation; it involves injection molding, blow molding, compression molding, and transfer molding (see Fig.10-8). Many of the problems that arise during molding, especially injection molding. are caused by rapid changes in the volume and the density of the polymer with pressure and temperature. The increase in density with decreasing temperatures at constant pressure results in considerable shrinkage of the polymer which, in some cases. may result in cracks and imperfections in the molded article. Furthermore, this also gives rise to strains within the body that will adversely affect the mechanical properties and heat resistance of the polymer. To counteract the natural thermal shrinkage occurring on cooling of the polymer from its melt temperature to room temperature, injection molding is usually carried out at as high a pressure as practically feasible. This is because the density of the polymer increases with pressure. FIGURE 10-8 Diagram of a conventional plunger injection-molding machine. (From Textbook of Polymer Science, 2nd edition, F. W. Billmeyer. Jr., p Fig Copyright by John Wiley & Sons, Inc., New York, Reprinted by permission.) When the molding pressure is released, the polymer will tend to expand according to the relation 297

34 For all substances the volume decreases with increasing pressure; hence the compressibility factor is always a positive quantity. However, the effect of molding pressure on reducing thermal shrinkage is much less in crystalline polymers than in amorphous polymers. This is because crystallization occurring on cooling from the molten state results in much denser material than the amorphous one, causing considerable volume changes. Thus even very high injection pressure cannot prevent excessive shrinkage of the crystalline polymers. The increasing pressure increases the packing density of the polymer chains and favors crystallization at temperatures higher than those for lower molding pressures (Fig. 10-9). FIGURE 10-9 Diagram of a compression-molding press and mold. (From Textbook of Polymer Science, 2nd edition, F. W. Billmeyer, Jr., p. 492, Fig Copyright O by John Wiley & Sons, Inc., New York, Reprinted by permission.) Another cause of strains in the molded article is the orientation of the polymer molecules during its flow into the mold and through the orifice. On cooling in the cold mold this orientation of the chains becomes frozen; furthermore, a nonuniform cooling of the polymer within the mold also contributes to frozen strains. For example, in thick molding, a stiff outer skin may be formed, while the interior is still fluid. Since the polymer in the interior will subsequently solidify, it will set up stresses in the outer skin. The presence of frozen strains frequently results in the development of a multitude of very small, almost infinitesimal platelike cracks on the surface of the plastic. This phenomenon is called crazing; it may also occur as the result of tensile load acting on the plastic for a long time. Another effect of the presence of frozen strains is a lowering of the distortion temperature of the plastic. Extrusion. in the extrusion process, the polymer is continuously forced along a screw through a region of high temperature and pressure where it is melted and compacted and then forced through a die, shaped to give the final article (see Fig ). At the entry to the die the polymer melt is subjected to rapidly changing deformation rates. The energy imparted to the material during the deformation is not only used up to cause the polymer to flow, but some part of it is stored as the elastic energy. This causes normal stresses in the material, which will subsequently relax during the flow of the polymer through a die. When this relaxation occurs after the material has left the die, the swelling of the extrudate occurs and surface irregularities result. This phenomenon, known as Tordello s effect or melt fracture, is due to the recovery of the elastic shear strain in the exit region. To avoid this swelling, the relaxation time of the extruded polymer should be less than its residence time during the flow in the die. This can be controlled by decreacing the rate of flow through a die, increasing the length of a die, or increasing the polymer temperature in the die. 298 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

35 Rolling and Drawing. During drawing or rolling operations, the resultant deformation consists of (1) the instantaneous elastic deformation caused by the distortions of the bond angle and bond stretching; (2) the molecular alignment, which involves mobilization of whole chains or their segments or plastic deformation in the crystallites: and (3) the nonrecoverable viscous flow. The orientation can be predominantly uniaxial or biaxial but, in general, the orientation appears to be a combination of the two. In uniaxial orientation a polymer is stretched in one direction. For example, during the drawing of fibers, the polymer chains align in the direction of stretching. Orientation can be accomplished by cold drawing and hot drawing. Cold drawing of the polymers is carried out below its annealing temperature. Cold drawing, as compared to hot drawing, requires considerable expenditure of energy to produce the desired deformation; it results in residual or internal stresses, which may be subsequently removed by annealing. Some fiber-forming polymers can be cold drawn in the form of ribbons or fibers to many times their original length. The process is quite similar to stretching the rubber (with nylon a 400% extension is possible before breaking occurs). In a molecular sense, drawing is a flow process, similar to rubber-elastic stretching, in which a parallel orientation of the polymer chains and the chain segments occurs until the chains are so interlocked (because of crystallization) that a further gliding past each other becomes impossible. However, even before drawing, there is some crystallization. Hot drawing refers to the deformation of crystalline or semicrystalline polymers at temperatures between the annealing temperature and the melting point as, for example, in polyethylene, at around 80 C. However, hot drawing, which involves both simultaneous annealing and hardening rates, does not produce significant residual stresses. Hot drawing imparts to the polymer a high degree of crystal orientation, and it is a preferred method for producing commercial fibers and films because high deformation rates could be obtained. Rolling through compression rollers is similar in some respects to the hot and cold drawing operations. If the polymer is rolled below its annealing range or if it is deformed very rapidly, residual stresses will be present. Orientation of the amorphous polymer is carried out above its glass transition temperatures where polymer chains have sufficient mobility to disentangle and align themselves in a preferred direction. Below T g in its glass state, the polymer fractures in a brittle manner during orientation. Strengthening Effect. The strengthening of the polymer through the predeformation is phenomenologically identical to the strain hardening observed and utilized in metals. The strain at which hardening sets in depends on the actual polymer. This occurs only 299

36 when a substantial amount of orientation hardening has taken place and. consequently, at characteristic necking strains. This indicates that such differences are due to some structural features of the polymer. For example, necking strains are 0.4 to 1.5 for PVC, 2.24 for polycarbonate, 3.5 for polystyrene, 2.8 to 3.5 for nylon, and 5 to 10 for polyethylene MOLECULAR ORIENTATION AND MORPHOLOGY Deformation of a polycrystalline film results in an orientation of both crystalline and noncrystalline (amorphous) regions with respect to the deformation direction. As the polymer is deformed, spherulites change from a spherical to a spheroidal shape. When the spherulites are deformed, the substructures of crystalline and noncrystalline regions reorient. As the deformation continues, crystal reorganization proceeds by the process of lamellar slip, orientation, and separation, until the crystal lamellae in all regions of the spherulite become aligned with their helix axis direction nearly parallel to the deformation direction. Further extension of the polymer results in a new deformation mechanism, crystal cleavage. The substructure is no longer spherulitic but has evolved into a fibrillar structure. It has been a well-established fact that orientation of the polymer enhances its tendency for crystallization as, for example, crystallization of natural rubbers. Thus, on stretching, the stiffness and the strength of the polymer in the stretch direction are increased about 25 times of the original value. However, in the direction perpendicular to the stretch direction, the oriented polymer is weak and tends to split. This behavior is of little importance in fibers where stress is usually applied in one direction but, in films, more uniform properties are required. This is achieved by stretching the film in two directions at right angles to each other so as to orient the molecules randomly within the plane. Films. The rate of cooling and the degree of stretching determine the structure and final properties of the produced film. Rapid cooling results in very fine spherulites or amorphous regions, depending on the nature of the polymer. This gives a hazy appearance to the film. The film then may undergo further crystallization and increase the size of spherulites, which may make it opaque. The phenomenon of the retractive force caused by stretching of the polymers is used in the production of shrinkable films. The films are biaxially stretched and then used for packages. Then, on application of heat, the retractive forces relax, causing shrinkage of the film that will tightly fit the package material. Such films may exhibit shrinkage up to 20%. Much greater shrinkage and stronger films for packaging can be obtained by irradiation. The film is irradiated so that a certain degree of crosslinking is produced. The film is heated and stretched biaxially, cooled, and rolled up. Then such a film is used for the packaging and, after wrapping. it is again reheated. This causes relaxation of stresses and return to its original dimensions at the time of irradiation. The shrinkage may be as high as 70% but, usually, films of average shrinkage from 30 to 50% are produced. Fibers. A fiber is defined as a unit of matter having a length at least 100 times greater than its width or diameter. A filament, on the other hand, is an individual strand of continuous length. In order to impart to the polymer fibers desirable mechanical characteristics, drawing is peformed after spinning. A draw ratio (or drawing conditions) is selected according to the properties of the polymer and desired properties of the fiber. 1f fiber that was essentially unoriented is drawn to different tensions at 80 C (176 F), two processes occur: (1) the noncrystalline chains become oriented, and (2) crystallization occurs. The noncrystalline chains seem to decrease in orientation with increasing temperature by an amount of shrinkage. At high temperatures, a high draw ratio can be obtained because the crystallites fracture under the combined action of heat and stress. Actually, spherulites also fracture during cold drawing but, at this temperature. they do not have a chance to align themselves. An increase in temperature results in an increased crystallinity of the fiber. The natural draw ratio is not affected by 300 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

37 strain rate. Young s modulus is determined more by molecular orientation than by the number of interlamellar ties. The modulus increases with the draw ratio. For high tensile strength, high draw ratios (about 6 to 10) are used. After drawing, cold drawn fibers are usually annealed in order to increase their crystallinity and to remove the residual stresses within the fiber ANNEALING In all forming processes polymers are subjected to many conditions that cause internal stresses and frozen strains. This adversely affects the physical properties, heat resistance, and thermal stability of polymers. To eliminate or reduce these defects, polymeric materials are subjected to annealing. At present amorphous thermoplastic polymers undergo commercial annealing only if high quality, such as dimensional stability, optimum strength, and heat resistance, is required. Thermosetting polymers are usually not annealed. Annealing is carried out by heating the plastic object to a temperature just below its glass transition temperature, soaking it for a suitable time, and subsequently slowly cooling to room temperature. During annealing, the chain mobility increases so much that the highly strained macromolecules can relax almost completely and the relaxation of internal stresses and frozen strains occurs according to the Maxwell relation (see Equation 7-55) Figure illustrates the changes in the specific volume of an amorphous polymer with temperature for different cooling rates. FIGURE Specific volume-temperature curves for an amorphous polymer. Curve Q results from quenching, curve S from slow (equilibrium) cooling. T g and T g are the glass transition temperatures of the polymer on quenching and slow cooling, respectively. DE represents the volume change on annealing the quenched polymer at the annealing temperature T a, which is only slightly below the glass transition temperature T g. Points B and C represent the specific volumes at room temperature, T r, or quenching and slow cooling, respectively. (From Annealing by Z. D. Jastrzebski, Encyclopedia of Polymer Science and Technology, Vol. 2, p. 140, edited by H. Mark, John Wiley & Sons, Inc., New York, 1966.) 301

38 We can see that for a polymer the T is lower and the specific volume is greater after rapid quenching than after equilibrium cooling. Thus the quenched polymer will show heat distortion at lower temperatures and considerable changes in dimensions that are highly undesirable for the product. Annealing will eliminate these discrepancies and, as path DEC of Fig indicates, the annealed material will be much denser and will show higher distortion temperatures. Quantitatively, the time for annealing at a particular temperature can be evaluated, provided that the curves relating specific volume versus temperature for different cooling rates and the rate constant k for isothermal volume changes are given Crystalline polymers are frequently annealed for research purposes only. Generally, annealing slightly improves the impact strength of crystalline polymers by lowering their brittleness temperature. This is due to relaxation of internal stresses instead of to the morphological changes of the polymer structure. On the other hand, annealing may increase the size of spherulites so that the crystalline polymer may become susceptible to environmental stress cracking. Perhaps the most evident practical benefit of annealing crystalline polymers is the reduction of the possible future shrinkage. The annealing of semicrystalline polymers is a useful method of increasing their strengths. This method is applied frequently in the manufacture of fibers and films. Annealing has three effects: it increases the initial modulus, increases the ultimate tensile stress, and reduces the ultimate elongation. 302 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

39 Polymeric Biomaterials BAB 23 POLYMERIC BIOMATERIALS [Adopsi dari: Joseph D. Bronzino, Biomedical Engineering Fundamentals, CRC Press, third edition, 2006, Section V, CHAPTER 40, by Hae Bang Lee, Gilson Kang, Jin Ho Lee INTRODUCTION Synthetic polymeric materials have been widely used in medical disposable supply, prosthetic materials, dental materials, implants, dressings, extracorporeal devices, encapsulants, polymeric drug delivery systems, tissue engineered products, and orthodoses as that of metal and ceramics substituents [Lee, 1989]. The main advantages of the polymeric biomaterials compared to metal or ceramic materials are ease of manufacturability to produce various shapes (latex, film, sheet, fibers, etc.), ease of secondary processability, reasonable cost, and availability with desired mechanical and physical properties. The required properties of polymeric biomaterials are similar to other biomaterials, that is, biocompatibility, sterilizability, adequate mechanical and physical properties, and manuflicturability as given in Table TABLE 40.1 Requirements for Biomedical Polymers The objectives of this chapter are (1) the review of basic chemical and physical properties of the synthetic polymers, (2) the sterilization of the polymeric biomaterials, (3) the importance of the surface treatment for improving biocompatability, and (4) the application of the chemogradient surface for the study on cell to polymer interactions POLYMERIZATION AND BASIC STRUCTURE Polymerization In order to link the small molecules one has to force them to lose their electrons by the chemical processes of condensation and addition. By controlling the reaction temperature, pressure, and time in the presence of catalyst(s), the degree to which repeating units are put together into chains can be manipulated Condensation or Step Reaction Polymerization. During condensation polymerization a small molecule such as water will be condensed out by the chemical reaction. For example This particular process is used to make polyamides (Nylons). Nylon was the first commercial polymer, made in the 1930s. Some typical condensation polymers and their interunit linkages are given in Table One major drawback of condensation polymerization is the tendency for the reaction to cease before the chains grow to a sufficient length. This is due to the decreased mobility of the chains and reactant chemical species as polymerization progresses. This results in 303

40 Polymeric Biomaterials short chains. However, in the case of Nylon the chains are polymerized to a sufficiently large extent before this occurs and the physical properties of the polymer are preserved. Natural polymers, such as polysaccharides and proteins are also made by condensation polymerization. The condensing molecule is always water (H 2 O). TABLE 40.2 Typical Condensation Polymers Addition or Free Radical Polymerization. Addition polymerization can be achieved by rearranging the bonds within each monomer. Since each mer has to share at least two covalent electrons with other mers the monomer should have at least one double bond. For example, in the case of ethylene: The breaking of a double bond can be made with an initiator. This is usually a free radical such as benzoyl peroxide (H 5 C 6 COO OOCC 6 H 5 ). The initiation can be activated by heat, ultraviolet light, and other chemicals. The free radicals (initiators) can react with monomers and this free radical can react with another monomer and the process can continue on. This process is called propagation. The propagation process can be terminated by combining two free radicals, by transfer, or by disproportionate processes. Some of the free radical polymers are given in Table There are three more types of initiating species for addition polymerization beside free-radicals; cations, anions, and coordination (stereospecific) catalysts. Some monomers can use two or more of the initiation processes but others can use only one process as given in Table Basic Structure Polymers have very long chain molecules which are formed by covalent bonding along the backbone chain. The long chains are held together either by secondary bonding forces such as van der Waals and hydrogen bonds or primary covalent bonding forces through crosslinks between chains. The long chains are very flexible and can be tangled easily. In addition, each chain can have side groups, branches and copolymeric chains or blocks which can also interfere with the long-range ordering of chains. For example, paraffin wax has the same chemical formula as polyethylene (PE) [(CH 2 CH 2 ) n ], but will crystallize almost completely because of its much shorter chain lengths. However, when the chains become extremely long {from 40 to 50 repeating units [ CH2CH2 ] to several thousands as in linear PE} they cannot be crystallized completely (up to 80 to 90% crystallization is possible). Also, branched PE in which side chains are attached to the main backbone chain at positions normally occupied by a hydrogen atom, will not crystallize easily due to the steric hindrance of side chains resulting in a more noncrystalline structure. The partially crystallized structure is called semicrystalline which is the most commonly occurring structure for linear polymers. The semicrystalline 304 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

41 Polymeric Biomaterials structure is represented by disordered noncrystalline (amorphous) regions and ordereð crystalline regions which may contain folded chains as shown in Figure TABLE 40.3 Monomers for Addition Polymerization and Suitable Process FIGURE 40.1 Fringed-micelle model of a linear polymer with semi-crystalline structure. The degree of polymerization (DP) is defined as an average number of mers, or repeating units, per molecule, that is, chain. Each chain may have a different number of mers depending on the condition of polymerization. Also, the length of each chain may be different. Therefore, it is assumed there is an average degree of polymerization or average molecular weight (MW). The relationship between molecular weight and degree of polymerization can be expressed as: 305

42 Polymeric Biomaterials The two average molecular weights most commonly used are defined in terms of the numbers of molecules, N i, having molecular weight, M i ; or wi, the weight of species with molecular weights M i as follows: An absolute method of measuring the molecular weight is one that depends on theoretical considerations, counting molecules and their weight directly. The relative methods require calibration based on an absolute method and include intrinsic viscosity and gel permeation chromatography (GPC). Absolute methods of determining the number-average molecular weight (Mn) include osmometry and other colhgative methods, and end group analysis. Light-scattering yields an absolute weight-average molecularweight (Mw). As the molecular chains become longer by the progress of polymerizations their relative mobility decreases. The chain mobility is also related to the physical properties of the final polymer. Generally, the higher the molecular weight, the less the mobility of chains which results in higher strength and greater thermal stability. The polymer chains can be arranged in three ways; linear, branched, and a cross-linked (or three-dimensional) network as shown in Figure Linear polymers such as polyvinyls, polyamides and polyesters are much easier to crystallize than the cross-linked or branched polymers. However, they cannot be crystallized 100% as with metals. Instead they become semicrystalline polymers. The arrangement of chains in crystalline regions is believed to be a combination of folded and extended chains. The chain folds, which are seemingly more difficult to form, are necessary to explain observed single crystal structures in which the crystal thickness is too small to accommodate the length of the chain as determined by electron and x-ray diffraction studies. The classical fringed-micelle model in which the amorphous and crystalline regions coexist has been modified to include chain folds in the crystalline regions. The cross-linked or three-dimensional network polymers such as polyphenolformaldellyde cannot be crystallized at all and they become noncrystalline, amorphous polymers. Vinyl polymers have a repeating unit CH2 CHX where X is some monovalent side group. There are three possible arrangements of side groups (X) (1) atactic, (2) isotactic, and (3) syndiotactic. In atactic arrangements the side groups are randomly distributed while in syndiotactic and isotactic arrange ments they are either in alternating positions or on one side of the main chain. If side groups are small like polyethylene (X = H) and the chains are linear, the polymer crystallizes easily. However, if the side groups are large as in polyvinyl chloride (X = Cl) and polystyrene (X = C 6 H 5, benzene ring) and are randomly distributed along the chains (atactic), then a noncrystalline structure will be formed. The isotactic and syndiotactic polymers usually crystallize even when the side groups are large. Copolymerization, in which two or more homopolymers (one type of repeating unit throughout its structure) are chemically combined, always disrupts the regularity of polymer chains thus promoting the formation of a noncrystalline structure. Possible arrangement of the different copolymerization is shown in Figure The addition of plasticizers to prevent crystallization by keeping the chains separated from one another 306 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

43 Polymeric Biomaterials will result in more flexible polymers, a noncrystalline version of a polymer which normally crystallizes. An example is celluloid which is normally made of crystalline nitrocellulose plasticized with camphor. Plasticizers are also used to make rigid noncrystalline polymers like polyvinylchloride (PVC) into a more flexible solid (a good example is Tygon tubing). FIGURE 40.2 Arrangement of polymer chains into linear, branched, and network structure depending on the functionality of the repeating units. FIGURE 40.3 Possible arrangements of copolymers. 307

44 Polymeric Biomaterials Elastomers, or rubbers, are polymers which exhibit large stretchability at room temperature and can snap back to their original dimensions when the load is released. The elastomers are non-crystalline polymers which have an intermediate structure consisting of long chain molecules in three-dimensional net-works (see next section for more details). The chains also have kinks or bends in them which straighten when a load is applied. For example, the chains of cis-polyisoprene (natural rubber) are bent at the double bond due to the methyl group interfering with the neighboring hydrogen in the repeating unit [ CH 2 C(CH 3 )=CH CH 2 ]. If the methyl group is on the opposite side of the hydrogen then it becomes trans-polyisoprene which will crystallize due to the absence of the steric hindrance present in the cis form. The resulting polymer is a very rigid solid called gutta percha which is not an elastomer. Below the glass transition temperature (T g : second-order transition temperature between viscous liquid and solid) natural rubber loses its compliance and becomes a glass-like material. Therefore, to be flexible, all elastomers should have T g well below room temperature. What makes the elastomers not behave like liquids above T g is in fact due to the crosslinks between chains which act as pinning points. Without cross-links the polymer would deform permanently. An example is latex which behaves as a viscous liquid. Latex can be cross-linked with sulfur (vulcanization) by breaking double bonds (C=C) and forming C-S-S-C bonds between the chains. The more cross-links are introduced the more rigid the structure becomes. If all the chains are cross-linked together, the material will become a three-dimensional rigid polymer Effect of Structural Modification on Properties The physical properties of polymers can be affected in many ways. In particular, the chemical composition and arrangement of chains will have a great effect on the final properties. By such means the polymers can be tailored to meet the end use Effect of Molecular Weight and Composition. The molecular weight and its distribution have a great effect on the properties of a polymer since its rigidity is primarily due to the immobilization or entanglement of the chains. This is because the chains are arranged like cooked spaghetti strands in a bowl. By increasing the molecular weight the polymer chains become longer and less mobile and a more rigid material results as shown in Figure Equally important is that all chains should be equal in length since if there are short chains they will act as plasticizers. Another obvious way of changing properties is to change the chemical composition of the backbone or side chains. Substituting the backbone carbon of a polyethylene with divalent oxygen or sulfur will decrease the melting and glass transition temperatures since the chain becomes more flexible due to the increased rotational freedom. On the other hand if the backbone chains can be made more rigid then a stiffer polymer will result. FIGURE 40.4 Approximate relations among molecular weight, T g, T m, and polymer properties. 308 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

45 Polymeric Biomaterials Effect of Side Chain Substitution, Cross-Linking, and Branching. Increasing the size of side groups in linear polymers such as polyethylene will decrease the melting temperature dueto the lesser perfection of molecular packing. that is, decreased crystallinity. This effect is seen until the side group itself becomes large enough to hinder the movement of the main chain as shown in Table Very long side groups can be thought of as being branches. Cross-linking of the main chains is in effect similar to the side-chain substitution with a small molecule, that is, it lowers the melting temperature. This is due to the interference of the cross-linking which causes TABLE 40.4 Effect of Side Chain Substitution on Melting Temperature in Polyethylene FIGURE 40.5 Change of volume vs. temperature of solid. The glass transition temperature (T g ) depends on the rate of cooling and below (T g ) the material behaves as a solid like a window glass. decreased mobility of the chains resulting in further retardation of the crystallization rate. In fact, A large degree of cross-linking can prevent crystallization completely. However, when the cross-linking density increases for a rubber, the material becomes harder and the glass transition temperature also increases Effect of Temperature on Properties. Amorphous polymers undergo a substantial change in their properties as a function of temperature. The glass transition temperature, T g, is a boundary between the glassy region of behavior in which the polymer is relatively stiff and the rubbery region in which it is very compliant. T g can also be defined as the temperature at which the slope of volume change versus temperature has a discontinuity n slope as shown in Figure Since polymers are non- 309

46 Polymeric Biomaterials crystalline or at most semicrystalline, the value obtained in this measurement depends on how fast it is taken. TABLE 40.5 Biomedical Application of Polymeric Biomaterials 40.3 POLYMERS USED AS BIOMATERIALS Although hundreds of polymers are easily synthesized and could be used as biomaterials only ten to twenty polymers are mainly used in medical device fabrications from disposable to long-term implants as given in Table In this section, the general information of the characteristics, properties, and applications of the most commonly used polymers will be discussed [Billmeyer, 1984; Park, 1984; Leininger and Bigg. 1986; Shalaby, 1988; Brandrup and Immergul, 1989; Sharma and Szycher. 1991; Park and Lakes, 1992; Dumitriu, 1993; Lee and Lee, 1995; Ratner et al., 1996] Polyvinylchloride (PVC) The PVC is an amorphous. rigid polymer due to the large side group (Cl, chloride) with a T g of 75 to 105 C. It has a high melt viscosity hence it is difficult to process. To prevent the thermal degradation of the polymer (HCl could be released), thermal stabilizers such as metallic soaps or salts are incorporated. Lubricants are formulated on PVC compounds to prevent adhesion to metal surfaces and facilitate the melt flow during processing. Plasticizers are used in the range of 10 to 100 parts per 100 parts of PVC resin to make it flexible. Di-2-ethylhexylphthalate (DEHP or DOP) is used in medical PVC formulation. However, the plasticizers of trioctyltrimellitate (TOTM), polyester, azelate, and phosphate ester are also used to prevent extraction by blood, aqueous solution, and hot water during autoclaving sterilization. PVC sheets and films are used in blood and solution storage bags and surgical packaging. PVC tubing is commonly used in intravenous (IV) administration, dialysis devices, catheters, and cannulae Polyethylene (PE) PE is available commercially in five major grades: (I) high density (HDPE), (2) low density (LDPE), (3) linear low density (LLDPE). (4) very low density (VLDPE), and (5) ultra high molecular weight (UHMWPE). HDPE is polymerized in a low temperature (60-80 C), and at a low pressure ( 40 kg/cm2) using metal catalysts. A highly crystalline, linear polymer with a density ranging from 0.94 to g/cm3 is obtained. LDPE is derived from a high temperature ( C) and pressures ( kg/cm2) using free radical initiators. A highly branched polymer with lower crystallinity and densities ranging from to g/cm3 is obtained. LLDPE (density g/cm3) and VLDPE (density: g/cm 3 ), which are linear polymers, are polymerized under low pressures and temperatures using metal catalysts with 310 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

47 Polymeric Biomaterials comonomers such as 1-butene, 1-hexene, or 1-octene to obtain the desired physical properties and density ranges. HDPE is used in pharmaceutical bottles, nonwoven fabrics, and caps. LDPE is found in flexible container applications, nonwoven-disposable and laminated (or coextruded with paper) foil, and polymers for packaging. LLDPE is frequently employed in pouches and bags due to its excellent puncture resistance and VLDPE is used in extruded tubes. UHMWPE (MW>2x10 6 g/mol) has been used for orthopedic implant fabrications, especially for load-bearing applications such as an acetabular cup of total hip and the tibial plateau and patellar surfaces of knee joints. Biocompatability tests for PE are given by ASTM standards in F981, F639, and F Polypropylene (PP) PP can be polymerized by a Ziegler-Natta stereospecific catalyst which controls the isotactic position of the methyl group. Thermal (T g : 12 C, T m : C and density: g/cm3) and physical properties of PP are similar to PE. The average molecular weight of commercial PP ranges from 2.2 to 7.0 x l0 5 g/mol and has a wide molecular weight distribution (polydispersity) which is from 2.6 to 12. Additives for PP such as antioxidants, light stabilizer, nucleating agents, lubricants, mold release agents. antiblock, and slip agents are formulated to improve the physical properties and processability. PP has an exceptionally high flex life and excellent environment stresscracking resistance, hence it had been tried for finger joint prostheses with an integrally molded hinge design [Park, 1984]. The gas and water vapor permeability of PP are inbetween those of LDPE and HDPE. PP is used to make disposable hypothermic syringes, blood oxygenator membrane, packaging for devices, solutions, and drugs, suture, artificial vascular grafts, nonwoven fabrics, etc Polymethylmetacrylate (PMMA) Commercial PMMA is an amorphous (T g : 105 C and density: 1.15 to g/cm 3 ) material with good resistance to dilute alkalis and other inorganic solutions. PMMA is best known for its exceptional light transparency (92% transmission), high refractive index (1.49), good weathering properties, and as one of the most biocompatible polymers. PMMA can be easily machined with conventional tools, molded, surface coated, and plasma etched with glow or corona discharge. PMMA is used broadly in medical applications such as a blood pump and reservoir, an IV system, membranes for blood dialyzer, and in in vitro diagnostics. It is also found in contact lenses and implantable ocular lenses due to excellent optical properties, dentures, and maxillofacial prostheses due to good physical and coloring properties, and bone cement for joint prostheses fixation (ASTM standard F451). Another acrylic polymer such as polymethylacrylate (PMA), polyhydroxyethylmethacrylate (PHEMA), and polyacrylamide (PAAm) are also used in medical applications. PHEMA and PAAm are hydrogels, lightly cross-linked by ethyleneglycoldimethylacrylate (EGDM) to increase their mechanical strength. The extended wear soft contact lenses are synthesized from PMMA and N-vinylpyrollidone or PHEMA which have high water content (above 70%) and a high oxygen permeability Polystyrene (PS) and Its Copolymers The PS is polymerized by free radical polymerization and is usually atactic. Three grades are available; unmodified general purpose PS (GPPS, T: 100 C), high impact PS (HIPS), and PS foam. GPPS has good transparency. lack of color, ease of fabrication, thermal stability, low specific gravity ( g/cm 3 ), and relatively high modulus. HIPS contains a rubbery modifier which forms chemical bonding with the growing PS chains. Hence the ductility and impact strength are increased and the resistance to environmental 311

48 Polymeric Biomaterials stress-cracking is also improved. PS is mainly processed by injection molding at C. To improve processability additives such as stabilizers, lubricants, and mold releasing agents are formulated. GPPS is commonly used in tissue culture flasks, roller bottles, vacuum canisters, and filterware. Acrylonitrile-butadiene-styrene (ABS) copolymers are produced by three monomers; acrylonitrile, butadiene, and styrene. The desired physical and chemical properties of ABS polymers with a wide range of functional characteristics can be controlled by changing the ratio of these monomers. They are resistant to the common inorganic solutions, have good surface properties, and dimensional stability. ABS is used for IV sets, clamps, blood dialyzers, diagnostic test kits, and so on Polyesters Polyesters such as polyethyleneterephthalate (PET) are frequently found in medical applications due to their unique chemical and physical properties. PET is so far the most important of this group of polymers in terms of biomedical applications such as artificial vascular graft, sutures, and meshes. It is highly crystalline with a high melting temperature (T m : 265 C), hydrophobic and resistant to hydrolysis in dilute acids. In addition, PET can be converted by conventional techniques into molded articles such as luer filters, check valves, and catheter housings. Polycaprolactofle is crystalline and has a low melting temperature (T m : 64 C). Its use as a soft matrix or coating for conventional polyester fibers was proposed by recent investigation [Leininger and Bigg, 1980] Polyamides (Nylons) Polyamides are known as nylons and are designated by the number of carbon atoms in the repeating units. Nylons can be polymerized by step-reaction (or condensation) and ring-scission polymerization. They have excellent fiber-forming ability due to interchain hydrogen bonding and a high degree of crystallinity, which increases strength in the fiber direction. The presence of CONH groups in polyamides attracts the chains strongly toward one another by hydrogen bonding. Since the hydrogen bond plays a major role in determining properties, the number and distribution of CONH groups are important factors. For example, T g can be decreased by decreasing the number of CONH groups. On the other hand, an increase in the number of CONH groups improves physical properties such as strength as one can see that Nylon 66 is stronger than Nylon 610 and Nylon 6 is stronger than Nylon 11. In addition to the higher Nylons (610 and 11) there are aromatic polyamides named aramids. One of them is poly (p-phenylene terephthalate) commonly known as Kevlar, made by DuPont. This material can be made into fibers. The specific strength of such fibers is five times that of steel, therefore, it is most suitable for making composites. Nylons are hygroscopic and lose their strength in vivo when implanted. The water molecules serve as plasticizers which attack the amorphous region. Proteolytic enzymes also aid in hydrolyzing by attacking the amide group. This is probably due to the fact that the proteins also contain the amide group along their molecular chains which the proteolytic enzymes could attack Fluorocarbon Polymers The best known fluorocarbon polymer is polytetrafluoroethylene (PTFE), commonly known as Teflon (DuPont). Other polymers containing fluorine are polytrifluorochloroethylete (PTFCE), polyvinylfluoride (PVF), and fluorinated ethylene propylene (FEP). Only PTFE will be discussed here since the others have rather inferior chemical and physical properties and are rarely used for implant fabrication. 312 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

49 Polymeric Biomaterials PTFE is made from tetrafluoroethylene under pressure with a peroxide catalyst in the presence of excess water for removal of heat. The polymer is highly crystalline (over 94% crystallinity) with an average molecular weight of x 10 6 g/mol. This polymer has a very high density ( g/cm 3 ), low modulus of elasticity (0.5 GPa) and tensile strength (14 MPa). It also has a very low surface tension (18.5 erg/cm 2 ) and friction coefficient (0.1). Standard specifications for the implantable PTFE are given by ASTM F754. PTFE also has an unusual property of being able to expand on a microscopic scale into a microporous material which is an excellent thermal insulator. PTFE cannot be injection molded or melt extruded because of its very high melt viscosity and it cannot be plasticized. Usually the powders are sintered to above 327 C under pressure to produce implants Rubbers Silicone, natural, and synthetic rubbers have been used for the fabrication of implants. Natural rubber is made mostly from the latex of the Hevea brasiliensis tree and the chemical formula is the same as that of cis-1.4 polyisoprene. Natural rubber was found to be compatible with blood in its pure form. Also, cross-linking by x-ray and ofpnic peroxides produces rubber with superior blood compatibility compared with rubbers made by the conventional sulfur vulcanization. Synthetic rubbers were developed to substitute for natural rubber. The Ziegler-Natta types of stereospecific polymerization techniques have made this variety possible. The synthetic rubbers have rarely been used to make implants. The physical properties vary widely due to the wide variations in preparation recipes of these rubbers. Silicone rubber, developed by Dow Corning company, is one of the few polymers developed for medical use. The repeating unit is dimethyl siloxane which is polymerized by a condensation polymerization. Low molecular weight polymers have low viscosity and can be cross-linked to make a higher molecular weight, rubber-like material. Medical grade silicone rubbers contain stannous octate as a catalyst and can be mixed with a base polymer at the time of implant fabrication Polyurethanes Polyurethanes are usually thermosetting polymers: they are widely used to coat implants. Polyurethane rubbers are produced by reacting a prepared prepolymer chain with an aromatic di-isocyanate to make very long chains possessing active isocyanae groups for cross-linking. The polyurethane rubber is quite strong and has good resistance to oil and chemicals Polyacetal, Polysulfone, and Polycarbonate These polymers have excellent mechanical, thermal, and chemical properties due to their stiffened main backbone chains. Polyacetals and polysulfones are being tested as implant materials, while polycarbonates have found their applications in the heart/lung assist devices, food packaging, etc. Polyacetals are produced by reacting formaldehyde. These are also sometimes called polyoxymethylene (POM) and known widely as Delrin (DuPont). These polymers have a reasonably high molecular weight (>2x10 4 g/mol) and have excellent mechanical properties. More importantly, they display an excellent resistance to most chemicals and to water over wide temperature ranges. Polysulfones were developed by Union Carbide in the 1960s. These polymers have a high thermal stability due to the bulky side groups (therefore, they are amorphous) and rigid main backbone chains. They are also highly stable to most chemicals but are not so 313

50 Polymeric Biomaterials stable in the presence of polar organic solvents such as ketones and chlorinated hydrocarbons. Polycarbonates are tough, amorphous, and transparent polymers made by reacting bisphenol A and diphenyl carbonate. It is noted for its excellent mechanical and thermal properties (high T g : 150 C), hydrophobicity, and antioxidative properties Biodegradable Polymers Recently, several biodegradable polymers such as polylactide (PLA), polyglycolide (PGA), poly(glycolide co-lactide) (PLGA), poly(dioxanone), poly(trimethylene carbonate), poly(carbonate), and so on are extensively used or tested on a wide range of medical applications due to their good biocompatibility, controllable biodegradability, and relatively good processability [Khang et al., 1997]. PLA, PGA, and PLGA are bioresorbable polyester, belonging to the group of poly α-hydroxy acids. These polymers degrade by nonspecific hydrolytic scission of their ester bonds. The hydrolysis of PLA yields lactic acid which is a normal byproduct of anaerobic metabolism in the human body and is incorporated in the tricarboxylic acid (TCA) cycle to be finally excreted by the body as carbon dioxide and water. PGA biodegrades by a combination of hydrolytic scission and enzymatic (esterase) action producing glycolic acid which can either enter the TCA cycle or is excreted in urine and can be eliminated as carbon dioxide and water. The degradation time of PLGA can be controlled from weeks to over a year by varying the ratio of monomers and the processing conditions. It might be a suitable biomaterial for use in tissue engineered repair systems in which cells are implanted within PLGA films or scaffolds and in drug delivery systems in which drugs are loaded within PLGA microspheres. PGA (T m : C T g : C) can be melt spun into fibers which can be converted into bioresorbable sutures, meshes, and surgical products. PLA (T m : C T g : C) exhibit high tensile strength and low elongation resulting in a high modulus suitable for load-bearing applications such as in bone fracture fixation. Poly-p-dioxanone (T m : C T g : I0 C) is a bioabsorbable polymer which can be fabricated into flexible monofilament surgical sutures STERILIZATION Sterilizability of biomedical polymers is an important aspect of the properties because polymers have lower thermal and chemical stability than other materials such as ceramics and metals, consequently, they are also more difficult to sterilize using conventional techniques. Commonly used sterilization techniques are dry heat, autoclaving, radiation, and ethylene oxide gas [Block, 1977]. In dry heat sterilization, the temperature varies between 160 and 190 C. This is above the melting and softening temperatures of many linear polymers like polyethylene and PMMA. in the case of polyamide (Nylon), oxidation will occur at the dry sterilization temperature although this is below its melting temperature. The only polymers which can safely be dry sterilized are PTFE and silicone rubber. Steam sterilization (autoclaving) is performed under high steam pressure at relatively low temperature ( C). However, if the polymer is subjected to attack by water vapor, this method cannot be employed. PVC, polyacetals, PE (low-density variety), and polyamides belong to this category. Chemical agents such as ethylene and propylene oxide gases [Glaser, 1979], and phenolic and hypochloride solutions are widely used for sterilizing polymers since they can be used at low temperatures. Chemical agents sometimes cause polymer deterioration even when sterilization takes place at room temperature. However, the time of exposure is relatively short (overnight), and most polymeric implants can be sterilized with this method. 314 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

51 Polymeric Biomaterials Radiation sterilization [Sato, 1983] using the isotopic 60 Co can also deteriorate polymers since at high dosage the polymer chains can be dissociated or cross-linked according to the characteristics of the chemical structures, as shown in Table In the case of PE, at high dosage (above 10 6 Gy) it becomes a brittle and hard material. This is due to a combination of random chain scission cross-linking. PP articles will often discolor during irradiation giving the product an undesirable color tint but the more severe problem is the embrittlement resulting in flange breakage, luer cracking, and tip breakage. The physical properties continue to deteriorate with time, following irradiation. These problems of coloration and changing physical properties are best resolved by avoiding the use of any additives which discolor at the sterilizing dose of radiation [Khang, 1996] SURFACE MODIFICATIONS FOR IMPROVING BIOCOMPATABILITY Prevention of thrombus formation is important in clinical applications where blood is in contact such as hemodialysis membranes and tubes, artificial heart and heart lung machines, prosthetic valves, and artificial vascular grafts. In spite of the use of anticoagulants, considerable platelet deposition and thrombus formation take place on the artificial surfaces [Branger, 1990]. Heparin one of the complex carbohydrates known as mucopolysaccharides or glycosaminoglycan is currently used to prevent formation of clots. In general, heparin is well tolerated and devoid of serious consequences. However, it allows platelet adhesion to foreign surfaces and may cause hemorrhagic complications such as subdural hematoma, retroperitoneal hematoma, gastrointestinal bleeding, hemorrhage into joints, ocular and retinal bleeding, and bleeding at surgical sites [Lazarus, 1980]. These difficulties give rise to an interest in developing new methods of hemocompatible materials. TABLE 40.6 Effect of Gamma Irradiation on Polymers Which Could be Cross-Linked or Degraded Many different groups have studied immobilization of heparin [Kim and Feijen, 1985; Park et al., 1988] on the polymeric surfaces, heparin analogues and heparinprostaglandin or heparin-fibrinolytic enzyme conjugates [Jozefowicz and Jozcfowicz, 1985]. The major drawback of these surfaces is that they are not stable in the blood environment. It has not been firmly established that a slow leakage of heparin is needed for it to be effective as an immobilized antithrombogenic agent, if not its effectiveness could be hindered by being coated over with an adsorbed layer of more common proteins such as albumin and fibrinogen. Fibrinolytic enzymes, urokinase, and various 315

52 Polymeric Biomaterials prostaglandins have also been immobilized by themselves in order to take advantage of their unique fibrin dissolution or antiplatelet aggregation actions [Ohshiro, 1983]. Albumin-coated surfaces have been studied because surfaces that resisted platelet adhesion in vitro were noted to adsorb albumin preferentially [Keogh et al., 1992]. Fibronectin coatings have been used in in vitro endothelial cell seeding to prepare a surface similar to the natural blood vessel lumen [Lee et al., 1989]. Also, algin-coated surfaces have been studied due to their good biocompatibility and biodegradability [Lee et al., 1990b; 1997b]. Recently, plasma gas discharge [Khang et al., l997a] and corona treatment [Khang et al., 1996d] with reactive groups introduced on the polymeric surfaces have emerged as other ways to modify biomaterial surfaces [Lee et al., 1991; 1992]. Hydrophobic coatings composed of silicon- and fluorine-containing polymeric materials as well as polyurethanes have been studied because of the relatively good clinical performances of Silastic, Teflon, and polyurethane polymers in cardiovascular implants and devices. Polymeric fluorocarbon coatings deposited from a tetrafluoroethylene gas discharge have been found to greatly enhance resistance to both acute thrombotic occlusion and embolization in small diameter Dacron grafts. Hydrophilic coatings have also been popular because of their low interfacial tension in biological environments [Hoffman, Hydrogels as well as various combinations of hydrophilic and hydrophobic monomers have been studied on the premise that there will be an optimum polar-dispersion force ratio which could be matched on the surfaces of the most passivating proteins. The passive surface may induce less clot formation. Polyethylene oxide coated surfaces have been found to resist protein adsorption and cell adhesion and have therefore been proposed as potential blood compatible coatings [Lee et al., 1990a]. General physical and chemical methods to modify the surfaces of polymeric biomaterials are listed in Table 40.7 [Ratner et al., 1996]. TABLE 40.7 Physical and Chemical Surface Modification Methods for Polymeric Biomaterials 316 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

53 Polymeric Biomaterials Another way of making antithrombogenic surfaces is the saline perfusion method, which is designed to prevent direct contacts between blood and the surface of biomaerials by means of perfusing saline solution through the porous wall which is in contact with blood [Park and Kim, 1993; Khang et al., l996a,b]. It has been demonstrated that the adhesion of the blood cells could be prevented by the saline perfusion through PE, alumina, sulfonated/nonsulfonated PS/SBR, eptfe (expanded polyletrafluoroethylene), and polysulfone porous tubes CHEMOGRADIENT SURFACES FOR CELL AND PROTEIN INTERACTION The behavior of the adsorption and desorption of blood proteins or adhesion and proliferation of different types of mammalian cells on polymeric materials depends on the surface characteristics such as wettability. hydrophilicity/hydrophobicity ratio, bulk chemistry, surface charge and charge distribution, surface roughness, and rigidity. Many research groups have studied the effect of the surface wettability on the interactions of biological species with polymeric materials. Some have studied the interactions of different types of cultured cells or blood proteins with various polymers with different wettabilities to correlate the surface wettability and blood- or tissue-compatibility [Baier et al., 1984]. One problem encountered from the study using different kinds of polymers is that the surfaces are heterogeneous, both chemically and physically (different surface chemistry, roughness, rigidity. crystallinity, etc.), which caused widely varying results. Some others have studied the interactions of different types of cells or proteins with a range of methacrylate copolymers with different wettabilities and have the same kind of chemistry but are still physically heterogeneous [van Wachem et al, 1987]. Another methodological problem is that such studies are often tedious, laborious, and timeconsuming because a large number of samples must be prepared to characterize the complete range of the desired surface properties. FIGURE 40.6 Schematic diagram showing corona discharge apparatus for the preparation of wettability chemo gradient surfaces. Many studies have been focused on the preparation of surfaces whose properties are changed gradually along the material length. Such chemogradient surfaces are of particular interest in basic studies of the interactions between biological species and synthetic materials surfaces since the affect of a selected property can be examined in a single experiment on one surface preparation. A chemogradient of methyl groups was formed by diffusion of dimethyldichiorosilane through xylene on flat hydrophilic silicone-dioxide surfaces [Eiwing et al ]. The wettability chemogradient surfaces were made to investigate hydrophilicity-induced changes of adsorbed proteins. Recently, a method for preparing wettabilitychemogradients on various polymer surfaces was developed [Lee et al., 1989, 1990; Khang et al b]. The wettability chemogradients were produced via radio frequency (RF) and plasma discharge treatment by exposing the polymer sheets continuously to the plasma [Lee et al., 1991]. The polymer surfaces oxidized gradually along the sample length with increasing plasma exposure time and thus the wettability chemogradient was created. Another method for preparing a wettability chemogradients on polymer surfaces using corona discharge 317

54 Polymeric Biomaterials treatment has been developed as shown in Figure 40.6 [Lee et al., 1992]. The wettability chemogradient was produced by treating the polymer sheets with corona from a knifetype electrode whose power was gradually changed along the sample length. The polymer surface gradually oxidized with the increasing power and the wettability chemogradient was created. Chemogradient surfaces with different functional groups such as COOH, CH 2 OH, CONH 2, and CH 2 NH 2 were produced on PE surfaces by the above corona treatment followed by vinyl monomer grafting and substitution reactions [Kim et al., 1993; Lee et al., 1994a, b]. We have also prepared chargeable functional groups [Lee et al., 1997c, d, 1998a], comb-like polyethyleneoxide (PEO) [Jeong et al., 1996; Lee et al., 1997a] and phospholipid polymer chemogradient surfaces [Iwasaki et al., 1997] by the corona discharge treatment, followed by the graft copolymerization with subsequent substitution reaction of functional vinyl monomers as acrylic acid, sodium p-sulfonic styrene and N, N-dimethyl aminopropyl acrylamide, poly(ethyleneglycol) mono-methacrylate, and ω-methacryloyloxyalkyl phosphoryicholine (MAPC), respectively. The water contact angles of the corona-treated PE surfaces gradually decrease along the sample length with increasing corona power (from about 950 to about 450) as shown in Figure The decrease in contact angles, that is, the increase in wettability along the sample length was due to the oxygen-based polar functionalities incorporated on the surface by the corona treatment. It was also confirmed also by fourier-transform infrared spectroscopy in the attenuated total reflectance mode and electron spectroscopy for chemical analysis (ESCA). FIGURE 40.7 Changes in water contact angle of corona-treated PE surface along the sample length. Sample numbers, n = 3. In order to investigate the interaction of different types of cells in terms of the surface hydrophilicity/hydrophobicity of polymeric materials, Chinese hamster ovaries (CHO), fibroblasts, and bovine aortic endothelial cells (EC) were cultured for 1 and 2 days on the PE wettability chemogradient surfaces. The maximum adhesion and growth of the cells appeared around a water contact angle of 50 to 55 o, as shown in Figure The observation of scanning electron microscopy (SEM) also verified that the cells are more adhered, spread, and grown onto the sections with moderate hydrophilicity as shown in Figure To determine the cell proliferation rates, the migration of fibroblasts on PE wettability chemogradient surfaces were observed [Khang et al., 1998b]. After the change of culture media at 24 h, cell growth morphology was recorded for 1 or 2 h intervals at the position of 0.5, 1.5, 2.5, and 4.5cm for the counting of grown cells and the observation of cell morphology with a video tape recorder. The proliferation rates of fibroblast cells were calculated from the slopes of Figure as given in Table The proliferation rates on the PE surfaces with wettability chemogradient showed that as the surface wettability increased, it increased and then decreased. The maximum proliferation rate of the cells as 1111 cells/h.cm 2 appeared at around the position 2.5 cm. 318 Sudaryatno Sudirham, Catatan Kuliah EL3004 Material Biomedika

55 Polymeric Biomaterials FIGURE 40.8 CHO, fibroblast, and endothelial cell growth on wettabihty chemogradient PE surfaces after 2 days culture (number of seeded cells, 4 x 104/cm2). n = 3. FIGURE 40.9 SIM rnicrophotograph of CHO, fibroblas, and endothelial cells grown on PE wettability chemogradient surface along the sample length after 2 days culture (original magnification; x400). FIGURE Fibroblast cell proliferation rates on wettability chemogradient PE surfaces (24 to 60 h culture). 319

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