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Indian Journal of Chemical Technology Vol. 11, September 2004, pp. 714-718 Evaluation of apparent and partial molar volume of potassium ferro- and ferricyanides in aqueous alcohol solutions at different temperatures U N Dash a , G S Roy b * & S Mohanty c a Department of Chemistry, Utkal University, Bhubaneswar 751 004, India b Department of Physics, Rajadhani College, Bhubaneswar, India c Department of Physics, S V M College, Jagatsinghpur 754 103, India Received 19 September 2003; revised received 20 May 2004; accepted 16 June 2004 Apparent and partial molar volume of potassium ferro- and ferricyanides in aqueous alcohol solutions have been determined at four different temperatures 298.15, 303.15, 308.15 and 313.15K with the objective of studying ion-solvent interaction in these systems. The transfer of volumes for the transfer of these salts from aqueous alcohol solution to water has been evaluated. Negative transfer of volume was observed and the results have been explained on the basis of electrostriction. IPC Code: G01 N 9/00, C01 C 3/12 Keywords: Apparent molar volume, partial molar volume, potassium ferrocyanide, apparent molar expansibility, aqueous alcohol. Evaluation of partial molar quantities are of importance as they give a lot of informations regarding ion-solvent interaction in various complex compounds. But since these quantities are not directly experimentally determined it is difficult to throw light on molecular interaction in ternary mixtures. Further, these quantities are related to the corresponding apparent molar quantities which are directly experimentally determined and can be used for studying ion-solvent interaction in solution. The partial and apparent molar properties of potassium ferro and ferricyanides in water and water+acetone mixtures have been reported earlier 1 . The same properties of these salts in water + methanol, water + ethanol and water + n-propanol mixtures (5, 10 and 20 wt% in each case) at four different temperatures: 298.15, 303.15, 308.15 and 313.15 K are reported here. Further, the transfer of volumes for the transfer of these salts from aqueous alcohol solution to water have also been determined. The contributions of change in temperature, change in composition and increase of chain length have been discussed in the light of electrostriction. Theory The apparent molar volume Φ V and apparent molar expansibility Φ E are computed by the following relations 2 , Φ V = 1000 (d 0 c -1 ) (d 0 - d ) + M 2 d 0 -1 … (1) and Φ Ε = α 0 Φ V + (α − α 0 ) 1000 c -1 … (2) where c is the molar concentration, d 0 and d are the densities of solvent and solution respectively, M 2 is the molecular weight of the solute, α 0 and α are the co-efficients of thermal expansion of solvent and solution respectively. The Φ V and Φ Ε data are fitted to Masson equation 2 by least squares method, Φ V = Φ V 0 +S V c 1/2 … (3) and Φ Ε = Φ Ε 0 + S Ε c 1/2 … (4) to obtain Φ V 0 , the limiting apparent molar volume, S V the experimental slope of Eq.(3), Φ Ε 0 , the limiting apparent molar expansibility and S Ε , the experimental slope of Eq.(4). The partial molar volume and partial molar expansibility have been calculated from the relations 3 , 2 V = Φ V + (1000 - cΦ V ) (2000 + S V c 3/2 ) -1 S V c 1/2 … (5) and 2 E =Φ Ε + (1000 - cΦ Ε ) (2000 + S Ε c 3/2 ) -1 S Ε c 1/2 … (6) __________ *For correspondence.

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  • Indian Journal of Chemical Technology Vol. 11, September 2004, pp. 714-718

    Evaluation of apparent and partial molar volume of potassium ferro- and ferricyanides in aqueous alcohol solutions at different temperatures

    U N Dasha, G S Royb* & S Mohantyc aDepartment of Chemistry, Utkal University, Bhubaneswar 751 004, India

    bDepartment of Physics, Rajadhani College, Bhubaneswar, India cDepartment of Physics, S V M College, Jagatsinghpur 754 103, India

    Received 19 September 2003; revised received 20 May 2004; accepted 16 June 2004

    Apparent and partial molar volume of potassium ferro- and ferricyanides in aqueous alcohol solutions have been determined at four different temperatures 298.15, 303.15, 308.15 and 313.15K with the objective of studying ion-solvent interaction in these systems. The transfer of volumes for the transfer of these salts from aqueous alcohol solution to water has been evaluated. Negative transfer of volume was observed and the results have been explained on the basis of electrostriction.

    IPC Code: G01 N 9/00, C01 C 3/12

    Keywords: Apparent molar volume, partial molar volume, potassium ferrocyanide, apparent molar expansibility, aqueous alcohol.

    Evaluation of partial molar quantities are of importance as they give a lot of informations regarding ion-solvent interaction in various complex compounds. But since these quantities are not directly experimentally determined it is difficult to throw light on molecular interaction in ternary mixtures. Further, these quantities are related to the corresponding apparent molar quantities which are directly experimentally determined and can be used for studying ion-solvent interaction in solution. The partial and apparent molar properties of potassium ferro and ferricyanides in water and water+acetone mixtures have been reported earlier1. The same properties of these salts in water + methanol, water + ethanol and water + n-propanol mixtures (5, 10 and 20 wt% in each case) at four different temperatures: 298.15, 303.15, 308.15 and 313.15 K are reported here. Further, the transfer of volumes for the transfer of these salts from aqueous alcohol solution to water have also been determined. The contributions of change in temperature, change in composition and increase of chain length have been discussed in the light of electrostriction. Theory The apparent molar volume V and apparent molar

    expansibility E are computed by the following relations2,

    V= 1000 (d0 c-1) (d0- d ) + M2 d0-1 (1) and = 0 V + ( 0) 1000 c-1 (2) where c is the molar concentration, d0 and d are the densities of solvent and solution respectively, M2 is the molecular weight of the solute, 0 and are the co-efficients of thermal expansion of solvent and solution respectively. The V and data are fitted to Masson equation2 by least squares method, V = V 0+S V c1/2 (3) and = 0 + S c1/2 (4) to obtain V 0, the limiting apparent molar volume, SV the experimental slope of Eq.(3), 0, the limiting apparent molar expansibility and S, the experimental slope of Eq.(4). The partial molar volume and partial molar expansibility have been calculated from the relations3,

    2V = V + (1000 - c V) (2000 + S V c3/2)-1 S V c1/2 (5) and 2E = + (1000 - c) (2000 + S c3/2)-1 S c1/2

    (6) __________ *For correspondence.

  • DASH et al.: EVALUATION OF MOLAR VOLUME OF POTASSIUM FERRO AND FERRICYANIDES

    715

    The apparent molar volume at infinite dilution, also called the limiting apparent molar volume is equal to the partial molar volume at infinite dilution 2V

    0. The partial molar volume of transfer of the above mentioned salts from aqueous alcohol solution to water are calculated from the relation,

    V0(tr) = V0 (aqueous alcohol) - V0 (water) (7)

    Experimental Procedure Potassium ferrocyanide and potassium ferricyanide (BDH, Anal Rs) were kept over anhydrous calcium chloride in vacuum desiccator until required. Methanol, ethanol and n-propanol (BDH, Anal Rs.) were dried over 4A molecular sieve and distilled. Conductivity water (sp.cand.~10-6S cm-1) was used for preparing water + alcohol mixtures. The alcohol content in the mixed solvents was accurate to within 0.01% . The solutions were prepared on molal basis and conversion of molarity was done by using standard expression4. The densities were measured pychnometrically (uncertainty 110-2 kg m-3). Temperature was maintained by a thermostat with a precision of 0.05 K.

    Results and Discussion A perusal of Table 1 and Fig. 1 shows that, V0 values of ferrocyanide salt are positive in water and increases with temperature in all the solvents. With increase of alcohol concentration, the value decreases and becomes negative at certain composition. Negative value of V0 provides evidence of electrostriction5. Again, since V0 is a measure of ion-solvent interaction, the negative value indicates weaker ion-solvent interaction. The result indicates, that, the ion-solvent interaction increases with temperature, decreases with alcohol concentration and number of -CH2- groups in alcohol (i.e. chain length). The lowering of V0 values is probably due to the increased steric hindrance of the bulkier solvent molecules to the ion-solvent interaction. The presence of ion-solvent interaction between the molecules promotes the structure making effect of the salts in water + alcohol mixtures. In case of ferricyanide salt (Table 2, Fig. 2), V0 values are positive in all the solvents and at all the four temperatures. Ion-solvent interaction of ferricyanide salt is greater than that of ferrocyanide salt which implies that ferrocyanide salt shows more structure making effect than ferricyanide salt.

    As observed, SV values are high and positive at every temperature and decrease with temperature for both the salts. Since, SV is a measure of ion-ion interaction, the result indicates the presence of ion-ion interaction in the system at every temperature and both the salts ionize to a greater extent with increase in temperature. Ion-ion interaction increases with increase of alcohol content in the solution. This suggests that more and more solute molecules are accommodated within the void spaces left in the packing of the large associated solvent molecules and as such enhance the structure of the solvent.

    Fig. 1V ~ c1/2 for potassium ferrocyanide in 5wt% methanol at (1) 298.15 K, (2) 303.15 K, (3) 308.15 K, (4) 313.15 K and in (5) 10 wt% methanol and (6) 20 wt% methanol at 298.15 K.

    Fig. 2E ~ c1/2 for potassium ferricyanide in (1) 5 wt% methanol, (2) 10 wt% methanol, (3) 20 wt% methanol, (4) 20 wt% ethanol and (5) 20 wt% n-propanol at 298.15 K.

  • INDIAN J. CHEM. TECHNOL., SEPTEMBER 2004

    716

    It is observed that the partial molar volume 2V increases with concentration and temperature in all the solvents whereas decreases with increase of alcohol content in the mixed solvent. Increase of 2V with concentration is owing to the structure breaking of the solvent molecules in concentrated solutions of high charge density ions like potassium characterized by very strong interaction forces with the solvent

    molecules and this interaction increases with temperature and decreases with alcohol concentration.

    The values of V0 (tr) are negative for both the salts. The measured partial molar volume can be considered to be a sum of the geometric volume of the solute and changes in the solvent due to its interaction with solvent. This simple approach has been widely used in many models6 to interpret partial molar

    Table 1Values of V0 (m3mol-1), SV (m9/2 mol-3/2), V0(tr) (m3mol-1), E0 (m3mol-1K-1) and SE (m9/2 mol-3/2K-1) for potassium ferrocyanide in water and water+alcohol system at different temperatures

    wt. % alcohol Temp (K) 106 V

    0 109 SV

    105 V

    0(tr) 106 E

    0 -109 SE

    0.0 298.15 43.6 380.59 - 7.72 18.52 303.15 101.8 205.36 - 7.75 18.59 308.15 133.8 150.84 - 7.79 18.69 313.15 158.9 119.38 - 7.81 18.71

    5 (methanol) 298.15 56.6 87.33 1.30 1.54 4.83 303.15 67.3 48.90 -3.45 1.57 4.99 308.15 73.4 31.85 -6.04 1.58 4.99 313.15 80.3 14.96 -7.86 1.59 5.01

    10 (methanol) 298.15 15.1 167.02 -2.85 2.53 6.26 303.15 32.3 120.87 -6.95 2.55 6.36 308.15 47.8 79.03 -8.60 2.56 6.32 313.15 52.6 76.11 -10.63 2.58 6.40

    20 (methanol) 298.15 -14.3 358.48 -5.79 2.02 6.29 303.15 -7.4 338.48 -10.92 2.04 6.43 308.15 2.5 311.37 -13.13 2.05 6.36 313.15 16.7 261.62 -14.22 2.06 6.41

    5 (ethanol) 298.15 47.5 111.85 0.39 1.27 4.70 303.15 54.4 87.91 -4.74 1.26 4.57 308.15 60.8 64.42 -7.30 1.26 4.57 313.15 67.0 38.49 -9.19 1.28 4.64

    10 (ethanol) 298.15 31.9 150.20 -1.17 1.50 5.79 303.15 39.2 126.10 -6.26 1.52 5.85 308.15 46.3 97.50 -8.75 1.54 5.94 313.15 55.2 60.30 -10.37 1.56 6.01

    20 (ethanol) 298.15 -39.6 481.44 -8.32 5.86 24.50 303.15 -14.6 391.74 -11.64 5.89 24.60 308.15 18.1 246.84 -11.57 5.95 24.90 313.15 48.5 114.48 -11.04 6.04 25.40

    5 (n-propanol) 298.15 17.1 267.49 -2.65 1.97 3.31 303.15 24.9 261.62 -7.69 1.99 3.36 308.15 34.6 250.06 -9.92 2.02 3.46 313.15 47.9 213.88 -11.10 2.05 3.54

    10 (n-propanol) 298.15 4.6 275.16 -3.90 2.08 3.49 303.15 12.3 271.01 -8.95 2.09 3.49 308.15 25.6 252.65 -10.82 2.12 3.56 313.15 35.1 226.87 -12.38 2.13 3.56

    20 (n-propanol) 298.15 -46.5 434.54 -9.01 4.85 1.37 303.15 -25.6 386.28 -12.74 4.87 1.38 308.15 -0.2 304.79 -13.40 4.92 1.40 313.15 27.3 228.51 -13.16 4.98 1.41

  • DASH et al.: EVALUATION OF MOLAR VOLUME OF POTASSIUM FERRO AND FERRICYANIDES

    717

    volume data for a broad range of solutes. When two charged centres are not separated by the distance 3-4 A, then their hydration co-spheres overlap which results in the decrease in the electrostriction. The overlap of co-spheres of two ionic species shows an increase in volume whereas overlap of hydrophobic-hydrophobic and ion-hydrophobic groups results in decrease in volume. In the present case there is

    increase of electrostrictive solvation as well as hydrophobic solvation. Hydrophobic solvation increases as the number of -CH2- group increases in the alcohols. As expected, the partial molar expansibility E2 decreases with concentration and increases with temperature. The value of 0 increases with temperature indicating the presence of caging or

    Table 2Values of V0 (m3mol-1), Sv(m9/2 mol-3/2), V0(tr) (m3mol-1), E0(m3mol-1K-1) and SE (m9/2 mol-3/2K-1) for potassium ferricyanide in water and water+alcohol system at different temperatures.

    wt. % alcohol Temp (K) 106 V0 109 SV 105 V0(tr) 106 E0 -109 SE 0.0 298.15 104.1 23.58 - 4.21 7.81 303.15 131.9 148.11 - 4.24 7.91 308.15 151.7 131.64 - 4.27 7.95 313.15 168.6 107.06 - 4.28 7.98

    5 (methanol) 298.15 99.2 178.27 -0.49 2.07 7.26 303.15 104.7 158.92 -2.72 2.10 7.51 308.15 119.9 103.26 -3.18 2.13 7.53 313.15 129.2 73.63 -3.94 2.13 7.49

    10 (methanol) 298.15 83.5 182.69 -2.06 2.14 6.32 303.15 90.3 169.32 -4.16 2.16 6.52 308.15 103.0 125.21 -4.87 2.16 6.37 313.15 114.9 94.68 -5.37 2.17 6.40

    20 (methanol) 298.15 71.5 190.83 -3.26 2.60 7.10 303.15 75.7 188.21 -5.62 2.64 7.39 308.15 95.0 129.56 -5.67 2.65 7.24 313.15 107.8 98.26 -6.08 2.67 7.28

    5 (ethanol) 298.15 80.3 252.67 -2.38 3.45 12.94 303.15 110.8 134.01 -2.11 3.48 13.05 308.15 125.1 77.81 -2.66 3.52 13.23 313.15 133.9 51.37 -3.47 3.54 13.31

    10 (ethanol) 298.15 73.4 241.68 -3.07 3.09 11.72 303.15 93.9 157.87 -3.80 3.13 11.89 308.15 107.5 108.55 -4.42 3.17 12.09 313.15 121.3 59.14 -4.73 3.25 12.50

    20 (ethanol) 298.15 51.9 292.23 -5.22 2.79 11.20 303.15 71.9 209.08 -6.00 2.81 11.33 308.15 85.4 151.55 -6.63 2.83 11.40 313.15 94.9 121.07 -7.37 2.87 11.59

    5 (n-propanol) 298.15 89.7 88.22 -1.44 1.81 2.89 303.15 95.7 88.10 -3.62 1.83 2.94 308.15 107.7 59.53 -4.40 1.83 2.88 313.15 116.5 46.20 -5.21 1.86 2.97

    10 (n-propanol) 298.15 78.1 128.29 -2.60 2.40 5.33 303.15 92.4 94.69 -3.95 2.41 5.34 308.15 104.6 62.69 -4.71 2.45 5.47 313.15 114.1 50.97 -5.45 2.49 5.45

    20 (n-propanol) 298.15 32.6 353.16 -7.15 3.68 8.54 303.15 49.7 318.98 -8.22 3.69 8.53 308.15 69.9 270.41 -8.18 3.73 8.64 313.15 87.9 227.95 -8.07 3.77 8.76

  • INDIAN J. CHEM. TECHNOL., SEPTEMBER 2004

    718

    packing effect8. As is seen, the 0 values increase with increase of alcohol content in the mixed solvent. This suggests that the structure making effect of the electrolytes studied is favoured in aqueous alcohol medium as compared to aqueous medium.

    References 1 Dash U N, Roy G S & Mohanty S, J T R Chem, 9(1) (2002)

    55. 2 Harned H S & Owen B B, The Physical Chemistry of

    Electrolytic Solutions, 3rd Edn (Reinhold Publishing Corporation, New York), 1958, 358.

    3 Dash U N & Nayak S K, Thermochim Acta, 32 (1979) 331; 34 (1979) 165.

    4 Robinson R A & Stokes R H, Electrolyte Solutions (Butter Worths Scientific Publications, London), 1955, 30.

    5 Davis C W, Ion Association (Butter Worths Scientific Publication, London), 1962, 154.

    6 Rohankar P G & Aswar A S, Indian J Chem, 41A (2002) 312.

    7 Chalikian T V, Sarvzyam A P & Breslauer K J, J Phys Chem, 97 (1993) 13017

    8 Millero F J, Structure and Transport Processes in Water and Aqueous Solutions, Ch.15 edited by Horne R A (Wiley Interscience, New York), 1971.