Accurately Densities, Dielectric Constants and Volumes of Mixed Formamide (FA) Water at K

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AASCIT Communications Volume 2, Issue 3 May 10, 2015 online ISSN: 2375-3803 Accurately Densities, Dielectric Constants and Volumes of Mixed Formamide (FA) Water at 298.15K Esam A. Gomaa Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt Mohamed A. Tahoon Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt Nermeen A. Muharam Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt Keywords Densities, Dielectric Constant, Molar Volume, Van der Waals Volume, Electrostriction Volume, Crystal Volume, Formamide Water Mixtures T he densities and dielectric constants for mixed formamide water solvents at 298.15K were accurately measured using densimeter DMA-58 and decameter DK-300 respectively. Different volumes (molar volume V M, Van der Waals volume V W, electrostriction volume V e and crystal volume ( V C ) for mixed FA H 2 O solvents were evaluated from density measurements. Accurately values of densities and dielectric constants are needed for further thermodynamic parameters evaluation. Introduction The mixing of different solvents results in the formation of a solution that is different from ideal. The thermodynamic properties of multi component liquid mixtures and their analysis in terms of interpretative models constitute a very interesting subject. The practical need for thermodynamic data for teaching and research aswell as for design and set up of industrial processes continue to drive research in the study of multi component systems. The characterization of mixtures through their thermodynamic and transport properties is important from the fundamental viewpoint of understand their mixing behavior. A thorough knowledge of transport properties of non-aqueous solutions is essential in many chemical and industrial applications.densities and dielectric constants are necessary parameters for solution thermodynamic and statistical thermodynamics and their accurate determination is the target of this work. Studies on density and dielectric constant of binary mixtures along with other thermodynamic properties are being increasingly used as a tool for investigation of the properties of pure components and the nature of intermolecular interaction between liquid mixtures constituents. [1,2] Also volumes, excess volumes and heat capacities give good information about solvent solvent interactions [3], also these studies find direct applications in chemical and biochemical industry [4]. Density and viscosity are important properties for characterizing liquid flow through a channel, as well as heat and mass transfer in many food processing processes.[5]

ISSN: 2375-3803 89 Experimental Materials Formamide (FA) of the highest purity available and was purchased from Merck Company. Mixture Preparation Binary mixtures were prepared by weighing appropriate amounts of formamide and water on an electronic balance. An AE Adam balance (Adam Equipment Inc. USA) model PW124 with a maximum capacity of 120 g, a readability range 0.0001 g and repeatability (S.D.) of 0.00015 g, linearity 0.0002 g, operating temperature +10 o C to 40 o C was used in all measurements. Density and Dielectric Constant Measurements Densimeter DMA-58 and decameter DK-300 were used for measuring both density and dielectric constant respectively. The temperature was maintained constant using a thermostat (INSREF-India make) with an accuracy of ±0.1K.The dielectric constants were measured experimentally by the use of Decameter of the type DK 300(WTW). Results and Discussion The densities of mixed FA- H 2 O at 298.15K were evaluated from the measured oscillation parameter (T) and β parameter as given in equations (1-3). = (1) = (2) = Where (T) is the oscillation period measured by densimeter, d H 2 O is the density of water and dl is the density of air. The densities are increased with increase FA mole fractions (Fig.1).The densities of mixed FA H 2 O are given in Table (1) with calculated molecular weights for used mixtures from equation (4). =. +... (4) The molar volumes (V M ) were obtained from density measurements. The V M as calculated by dividing the molecular weight by exact solution densities. The packing density (ρ) as explained in literature [6-8] the relation between Van der Waals volumes (V W ) and the molar volumes (V M ) for relatively large molecules was found to be constant [9-20] and equal to 0.661. ρ = V W / V M = 0.661 ± 0.017 (5) The electrostriction volumes (V e ) [20-27] which is the volume compressed by the solvent can be calculated by using equation (6) as follows: V e = V W V M (6) The solvated radii of the organic aqueous mixtures (FA-H 2 O) were calculated using equation (7) by considering the spherical form of the solvated molecules. 1 3 V = πn σ (7) 6 Where V is the molar volume calculated from the densities as described before and σ is the solvated diameter. All different volumes evaluated are tabulated in Table 2 with increase in their values with decrease in FA percentages in the mixture. (3)

90 2015; 2(3): 88-92 The dielectric constants (є) are measured exactly by using the above mentioned dekameter and their values are listed in Table with decrease in them by decrease formamide mole fraction in the mixture. The dipole moments and diameters (σ) for mixed FA-H 2 O were estimated by the sum of the dipole moments (ref.7) for each solvent multiplied by their mole fractions. The estimated dipole moments together with the ratio µ s / σ 2 are also cited in Table 3. All different values in Table 3 are decreased with decrease of FA mole fractions indicating less solvation. Table 1. Oscillation period (T) and density (D) values for (FA-H 2O) mixtures at 298.15K. vol. % X S(FA) T D (g/cm 3 ) M.Wt 100 1 4.0179 1.1282 45.04 95 0.8958 4.0128 1.1227 42.22 90 0.8628 4.0071 1.1167 38.63 85 0.7194 4.0018 1.1110 37.45 80 0.6441 3.9963 1.1052 35.42 75 0.5758 3.9908 1.0994 33.57 70 0.5136 3.9853 1.0935 31.89 65 0.4566 3.9799 1.0878 30.35 60 0.4043 3.9746 1.0822 28.94 55 0.3566 3.9677 1.0749 27.65 50 0.3115 3.9622 1.0691 26.43 Fig 1. Relation between mole fraction of formamide (X S) and density at 298.15K. Table 2. Different volumes of mixed (FA H 2O) solvents at 298.15K. X S(FA) V M(cm 3 /mole) V W(cm 3 /mole) V e(cm 3 /mole) V C(cm 3 /mole) 1 39.92 26.38-13.54 40.69 0.8958 40.11 26.51-13.60 40.89 0.8628 40.33 26.65-13.68 41.11 0.7194 40.53 26.79-13.74 41.32 0.6441 40.75 26.93-13.82 41.54 0.5758 40.96 27.07-13.89 41.76 0.5136 41.18 27.21-13.91 41.97 0.4566 41.40 27.36-14.04 42.20 0.4043 41.61 27.50-14.11 42.42 0.3566 41.90 27.69-14.21 42.71 0.3115 42.12 27.84-14.28 42.94

ISSN: 2375-3803 91 Table 3. Diameter (σ), dipole moment(µ s), (µ s/σ 2 ) and dielectric constant (є) of mixed (FA H 2O) solvents at 298.15K. X S(FA) σ (A 0 ) µ s (10 18 esu) µ s/ σ 2 є 1 2.120 3.410 0.75 109.7 0.8958 2.120 3.240 0.72 106.448 0.8628 2.121 3.190 0.70 103.549 0.7194 2.130 2.910 0.65 100.947 0.6441 2.134 2.850 0.62 98.598 0.5758 2.138 2.150 0.60 96.465 0.5136 2.140 2.650 0.57 94.524 0.4566 2.146 2.560 0.55 92.748 0.4043 2.149 2.520 0.52 91.116 0.3566 2.150 2.410 0.51 89.627 0.3115 2.158 2.340 0.50 88.221 Conclusion The density of aqueous formamide solutions have been accurately measured experimentally at 298.15K. The different volumes (molar volume, Van der Waals volume, electrostriction volume, crystal volume) are determined. Also the dielectric constrants for mixed FA-H 2 O solvents were experimentally measured. References Prof. Dr. Esam A. Gomaa Prof. of Physical Chemistry, Faculty of Science, Mansoura University. Email Address: Esam1947@yahoo.com Special area,chemical Thermodynamics and Solution Chemistry. Dr.Rer.Nat..from Muich Technical University, Germany on 1982.Got Prof.degree on 1994.Has more than 140 published paper in international journals in Chemistry, Physics and Environment. Participates in more than 20 international conferences. Has scientific school consists of about twenty scientists. [1] A. F. Hollemanm, E. Wiberg, Inorganic Chemistry. San Diego:Academic Press. ISBN 0-12-352651-5, (2001). [2] David A. Wright and Pamela Welbourn, Environmenaltoxicology, Cambridge University Press, UK (2002). [3] Lide, David R., ed. (2006). CRC Handbook of Chemistry and Physics (87th ed.). Boca Raton, FL: CRC Press. ISBN 0-8493-0487-3. [4] A. A. El-Khouly, E. A. Gomaa, and S. Abou-El-Leef, Bull. Electrochem 19, 153 (2003). [5] Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry ofthe Elements (2nd ed.). Butterworth-Heinemann.ISBN0080379419. [6] S. Budavari (Ed.), The Merck Index: An Encyclopedia of Chemicals, Drugs and Biologicals, 12th ed.,merckco.inc.,whitehouse Station, NJ, 1996. [7] EsamA.Gomaa. Eur. Chem. Bull., 1(2013 ) 259-261.J.I.Kim,Z.Phys.Chem.,N.Folge,113(1978)129. [8] EsamA.Gomaa, Elsayed Abou Elleef and E.A.Mahmoud, Eur. Chem. Bull, 2(2013),732-735. [9] Esam A Gomaa and Elsayed M.Abou Elleef, American Chemical Science Journal, 3(2013), 489-499. [10] Esam A. Gomaa, Elsayed M.Abou Elleef, Science and Technology, 3(2013)118-122. [11] Esam A Gomaa and M.G.Abdel Razek, International Research Journal of Pure and Applied Chemistry,3(2013)320-329 [12] Esam A.Gomaa, International Journal of Theoretical and Mathematical Physcics,3(2013)151-154. [13] Esam A.Gomaa and B.A.AlJahadali, Education., 2(3),(2012)37-40. [14] Esam A Gomaa, American Journal of Biochemistry, 2(3), 92012),25-28. [15] Esam A. Gomaa, Food and Public Health, 2(3),2012, 65-68. [16] Esam A.Gomaa, Global Advanced Research Journal of Chemistry and Material Science, 1(2012) 35-38.

92 2015; 2(3): 88-92 [17] Esam A.Gomaa, Frontiers in Science, 2(2012)24-27. [18] Esam A Gomaa, Elsayed M.Abou Elleef, E.T.Helmy and Sh.M. Defrawy, Southern Journal of Chemistry, 21 (2013) 1-10. [19] Esam A Gomaa,Elsayed M.Abou Elleef,Elsayed T. Helmy, Research and reviews Journal of Chemistry, 3 (2014) 22-27. [20] Esam A. Gomaa,Science and Technology,3 (2013) 123-126. [21] E.A.Gomaa, Research and Reviews:Journal of Chemistry, 62 (1989) 4753(2014),28-37. [22] Esam A.Gomaa,Thermochimica Acta,142(1989) 19. [23] Esam A. Gomaa,Croatica Chimica Acta,. 62 (1989) 475 [24] J.I. Kim, A. Cecal, H.J. Born, and E.A. Gomaa, Z. Physik Chemic, Neue Folge 110, 209 (1978). [25] J.I.Kim and E.A.Gomaa,Bull. Soci. Chim. Belg., 90(1981)391. [26] EsamA.Gomaa,Thermochimica Acta,140( 1989)7. [27] EsamA.Gomaa, Bull.Soc.Chim.Fr. 5 (1989) 620.