Optimizing GPC Separations

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Optimizing GPC Separations

Criteria for Solvent Selection True sample solubility (Polarity and Time dependant) Compatibility with columns Avoid non-size exclusion effects (eg adsorption by reverse phase interaction) Permit adequate detection (eg refractive index, UV cut off) Safety (eg toxicity, elevated temperature, etc)

Sample Concentration The viscosity of the polymer solution is dependant on both the molecular weight and the concentration A high viscosity in the separation zone leads to reduced mass transfer and band broadening This results in decreased resolution and in extreme cases peak splitting

Effect of Concentration on Peak Shape and Resolution 0.05% 0.10% Column: PLgel 10µm MIXED-B 300x7.5mm Eluent: THF Flow Rate: 1.0ml/min Detector: UV 0.15% 0.20% Polystyrene standards 1. 8,500,000 4. 34,500 2. 1,130,000 5. 5,100 3. 170,000 6. 580

Effects of Column Loading Analytical column Narrow bore column

Adding Columns Adds Pore Volume and Yields Higher Resolution And Yields Greater Reproducibility

Sample Loading for GPC, General Guidelines viscosity = MW * concentration For high MW samples use lower concentration and if detector response requires it, increase injection volume For low MW samples use higher concentrations and avoid larger injection volumes to maintain high resolution MW Conc (%) Inj vol (ul) <50,000 0.20-0.50 20-50 50,000-500,000 0.10-0.20 50-200 >500,000.01-0.10 50-200

Effect of Temperature on Specific Resolution Column: Eluent: Flow Rate: PLgel 5µm MIXED-D 300x7.5mm Toluene 1.0ml/min Test Probes: Polystyrene standards Resolution increases with temperature, more obvious for the higher MW probes

Effect of Temperature on Separations in Polar Solvents Column : PLgel 5µm MIXED-C 300x7.5mm Eluent : DMF Flow rate : 1.0ml/min Increased temperature : Reduced operating pressure Improved resolution, particularly at high MW PEO/PEG standards 990,000 252,000 86,000 18,000 4,800 200

Effect of Flow Rate on Column Efficiency (2) Eluent: Column: THF PLgel 10µm MIXED-B For high MW samples, high flow rate should be avoided, reduced flow rate may be required to improve resolution

Determination of Column Performance t R = retention time W ½ = peak width at 50% peak height W 5s = peak width at 4.4% peak height L = column length in meters Efficiency (½ height) N=5.54(t R /W) 2 L Plate count efficiency (5s) N=25(t R /W 5s ) 2 L Symmetry =W 1 /W 2

Effect of Particle Size on Resolution

Effects of Band Broadening Modern high performance GPC columns have minimised the effect of band broadening in the separation. However poor system design with large amounts of dead volume can still cause loss of resolution. System dead volume should be minimised, especially when using very high efficiency columns.

Eluent Modification in GPC Required to: minimise non-size exclusion interactions between the sample and the column stabilise the solution of the polymer (ionic aggregation) Possibilities: addition of more polar solvent to organic eluent (eg methanol or water added to THF or chloroform) addition of ionic compound to solvent (eg lithium salts in polar organic solvents, triethanolamine or acetic acid to THF)

Adsorption of Polystyrene Standards in DMF PS/DVB columns are excellent in many solvents, but remember that although the column may be used in certain solvents this does not mean SEC will occur - the example here is polystyrene standards running in DMF Column : PLgel 5um 500Å 300x7.5mm

Polystyrene Sulfonates - ANIONIC and HYDROPHOBIC Column: Eluent: Flow Rate: Detector: 2xPL aquagel-oh MIXED 8µm, 300x7.5mm 70% 0.2M NaNO 3, 0.01M NaH 2 PO 4, ph9 30% methanol 1.0ml/min DRI Mp values 1. 400,000 2. 35,000 3. 4,600

Starch Analysis Column: 4xPLgel 20µm MIXED-A 300x7.5mm Eluent: DMSO + 5mM NaNO 3 Flow Rate: 1.0 ml/min Temp: 80 C Detector : DRI Addition of salt is often required for polar organic solvents to suppress ionic interaction effects

Eluent Modification in Organic GPC Hostavin N30 Polymeric UV stabiliser containing secondary amine groups Column: 2xPLgel 3µm MIXED-E Flow Rate: 1.0ml/min Detector: PL-ELS 1000

Analysis of Natural Rubber, RI Limitations Columns 3 x PLgel 10µm MIXED-B 300x7.5mm Eluent Toluene Loading ~0.2%, 200µl Detectors DRI at 1V FSD

Refractive Index Values for Common Solvents Solvent: Refractive Index (@ 25 o C) Acetic Acid 1.37 Acetone 1.35 Acetonitrile 1.34 Chloroform (amylene) 1.44 Chloroform 1.44 Cyclohexane 1.42 0-Dichlorobenzene 1.55 Ether (Anhydrous) 1.35 Ethyl Acetate 1.37 n-heptane 1.38 Hexanes 1.37 Isobutyl Alcohol 1.38 Methanol 1.32 Methyl tert-butyl Ether 1.36 Methylene Chloride 1.42 Methyl Ethyl Ketone 1.37 Pentane 1.35 2-Propanol 1.38 Pyridine 1.5 THF (BHT) 1.4 THF 1.4 Toluene 1.49 Trichlorobenzene 1.57 Trimethylpentane 1.38 Water 1.33

Advantages of the Varian 380 and 385 Evaporative Light Scattering Detectors Ability to Detect Semi-Volatile and Volatile Compounds Novel Three Stage Addition of Gas Makes Detection Possible Post Nebulization Gas Reduces Relative Humidity Inside Evaporator Tube Which Allows for Low Temperature Evaporation of Solvents

Sensitivity of DRI Versus ELS Columns 2 x PLgel 5µm MIXED-C 300x7.5mm Eluent THF Flow rate 1.0ml/min Loading 0.1%, 20µl Mp values 1. 7,500,000 2. 841,700 3. 148,000 4. 28,500 5. 2,930 ELS is essentially independent of dn/dc, improvement in sensitivity will depend on a number of solute parameters

PVP/PVA Copolymer (Kollidon VA64) Column: Eluent: Flow Rate: Detector: 2xPL aquagel-oh MIXED 8µm, 300x7.5mm 1. 70% 0.2M NaNO 3, 0.01M NaH 2 PO 4, ph7, 30% methanol 2. 70% 0.1M ammonium formate, 30% methanol 1.0ml/min 1. DRI 2. PL-ELS 1000 5 Retention time (min) 22

Effects of Non-Linearity With ELSD Detection Non-linearity results in loss of response for low concentration peak tails Distribution narrower than that calculated by DRI, polydispersity low

Molecular Weight Sensitive These are GPC detectors that give a response directly related to the molecular weight of the material eluting from the GPC column By using molecular weight sensitive detectors, you can get information that is not available from conventional GPC Molecular weights that aren t dependent on the chemistry of your standards and samples The determination of structural information about the polymer in solution

A Concentration Detector is Needed Can be any type that gives a response proportional to concentration Typically a differential refractive index detector is used DRI detector response proportional to concentration only Operation identical to conventional GPC, determines the concentration of material eluting from a GPC column RI signal = K RI (dn/dc) C

Viscosity Detectors Detector response proportional to the intrinsic viscosity [ ] of the polymer Generate molecular weight values for a variety of polymer types via Universal Calibration approach Permits determination of branching in polymers Light Scattering Detectors Detector response directly proportional to weight average molecular weight (Mw) of the polymer No column calibration required Scattered light intensity measured at more than one angle permits determination of radius of gyration

Conventional GPC Column separates on basis of molecular size NOT molecular weight Two different polymers will interact differently with solvent At any molecular weight, the two polymers will have different sizes in solution Molecular weights from conventional GPC are dependent on a comparison in size between the standards and the sample

Conventional and Universal Calibration

However, if a calibration of size versus retention time could be generated then one true calibration would hold for all sample types Hydrodynamic volume = [ ] M A Universal Calibration plot of log[ ]M versus RT holds true for all polymer types Can use measured intrinsic viscosity and retention time to get accurate molecular weights Universal Calibration

Simplified Schematic of PL-BV 400 Differential Viscometer

The Mark-Houwink Plot A Mark-Houwink plot of log IV versus log M should give a straight line as long as the Universal Calibration is obeyed (i.e no interactions occur) K and alpha vary between different solvents and polymers Alpha is a measure of the shape of the polymer in solution

Structural Information Branching

Using Viscometry and Light Scattering to Determine Branching Linear versus branched polymers Compared to a linear polymer the hydrodynamic volume of the branched molecule is smaller and so Rg will be smaller. Also, with the same mass of polymer enclosed the density will be higher producing a lower Intrinsic viscosity

Mark Houwink and Conformation Plots For Branched Polyethylene NIST 1476

Light Scattering of Polymers In static light scattering, coherent incident radiation (usually a laser) interacts with components of the polymer backbone in a small scattering volume Excitation of the polymer chain results in re-emission of the radiation at the same wavelength and frequency but at variable intensity Measurement of the intensity of the scattered radiation allows the calculation of molecular weight and the chain dimensions

Effect of Polymer Size on Light Scattering Can use the difference in intensity of light scattered at two or more angles to determine Rg, the radius of gyration, by the Dissymmetry method

Static Light Scattering Equation 2

The Light Scattering/Refractive Index Combination LSsig = R (q) = C M (dn/dc) 2 P (q) K (q) RI signal = K RI (dn/dc) C Light Scattering equation Refractive Index equation Calculate dn/dc for sample LS = K (q) M (dn/dc) P (q) RI signal K RI LS ~ M LS / RI Combination RI signal Directly Proportional to Mass In addition radius of gyration (Rg) can be measured using combination of 15 and 90 detectors

Case Study - Analysis of Polyolefins Polyolefins are important hightonnage engineering polymers Crystalline materials, only soluble at >120 C Structures can contain branching morphologies depending on the method of synthesis Long chain branching (over 6 carbons in length) can serious effect viscosity, density and processability Multi detector GPC is an ideal means of probing the structure of polyolefins

Polyethylene Triple Detection Data

PE Samples by GPC/Viscometry The four samples had very similar molecular weight distributions but the Mark Houwink plots showed that there were some branching differences.

Summary of GPC Detector Capabilities