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Research Article Ultrasonic Investigations of Molecular Interaction in Binary Mixtures of Benzyl Benzoate with Isomers of Butanol Sk Md Nayeem a and *D.Krishna Rao b a. Department of Physics, KRK Govt. Degree College, Addanki-523 21, A.P., India. b. Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar 522 51, A.P., India ABSTRACT The density and speed of sound have been measured for the systems (Benzyl Benzoate + n-butanol, secbutanol, tert-butanol) at different molefraction and at different temperatures 38.15K, 313.15K respectively. From these experimental data the excess/ deviation acoustic parameters such as deviation in isentropic compressibility, excess intermolecular free length, excess acoustic impedance and deviation in ultrasonic velocity have been calculated for the binary systems at 38.15 K and 313.15 K tempera tures. The calculated excess / deviation functions have been fitted to Redlich-Kister polynomial using multi parametric non- linear regression analysis to estimate the coefficients and standard errors. The variation of these properties with composition and temperature of the binary mixtures have been studied in terms of molecular interactions between unlike mol ecules of the mixtures. Further, the results are supported by FTIR spectra. Keywords: Benzyl Benzoate, n-butanol, sec-butanol, tert-butanol, ul trasonic v elocity, density, excess / deviation parameters, Redlich-Kister polynomial, intermolecular interaction, FTIR spectra. Received 25 Sept 213 Received in revised form 11 Oct 213 Accepted 14 Oct 213 *Address for correspondence: Prof. D.Krishna Rao Department of Physics, Acharya Nagarjuna University, Nagarjuna Nagar 52251, India. Email : krdhanekula @ yahoo.co.in INTRODUCTION The work on medicinally used chemical compounds requires the attention of the society in all aspects including ultrasonic behavior. Practically, ultrasonic studies are of immense use to study the molecular interactions when these compounds are in binary mixture form with some other liquids - protic /aprotic /polar /non-pol ar etc. Benzyl Benzoate (bb) is a carboxylate ester, which is used as an insect repellent, a medicine for scabies and also used in oily injections. Behavior of benzyl benzoate in many liquids such as aliphatic alkanes, aromatic alkenes, aliphatic alcohols, substituted benzenes, acetates, ketones and DMSO (super solvent) [1-4] has been thoroughly studied ultrasonically. Alcohols are self-associated organic liquids, used for the synthesis of other organic compounds. They are also widely used as coupling and dispersing agents in the chemical, pharmaceutical and household industries and as carrier and extraction solvents for natural Products. Branching of alkyl group attached to the hydroxyl group results in abnormal behavior of alcohols. The interaction of alcohol [s] with organic liquids is interesting due to its acidic nature. The O -H bonds in alcohols are polar and allow the release of the hydrogen atom as proton (H+). The order of acidity in alcohols is: 1 -alcohol> 2 - alcohol > 3 -alcohol. This order is due to +I effect [5]. While the interacting ability of alcohols is well established, no such opinion is suggested from literature with regards to Benzyl Benzoate. Keeping this in view; three binary liquid mixtures n-butanol, sec-butaol and tert-butaol with Benzyl Benzoate were selected to study their molecular interactions through their acoustical behavior at two temperatures Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 65

38.15 K and 313.15 K respectively. The measurement of ultrasonic speed enabl es us to the accurate measurement of some useful acoustic and thermodynamic parameters and their excess values [6-9]. These excess values of free length, acoustic impedance, deviations in isentropic compressibility and ul trasonic velocity in binary liquid mixture are useful in understanding the solute-solvent interactions. MATERIALS AND METHODS The chemicals Benzyl Benzoate (>99%) and n- butanol, sec-butanol and tert-butanol (all of AR grade, 99.5%) are acquired from s.d. fine chemicals. The chemicals Benzyl Benzoate and alkanols are purified by employing the standard methods mentio-ned in literature [1,11] respectively. The purity of the chemicals is assessed by comparing their measured densities (ρ) and ultrasonic velocities (u) which are in good agreement with literature [12-15] values as can be seen in Table 1. Table 1: comparison of experimental values of density (ρ) and ultrasonic speed(u) of pure liquids with the corresponding literature values at 33.15 K and 313.15 K. Pure Temperature Density Ultrasonic velocity Liquid (K) (Kg.m 3 ) (m. s ¹) Expt Litt Expt Litt Benzyl Benzoate 38.15 1114.54 -- 1493.3 -- 313.15 119.77 119.7 a 1471.44 1471.4 a n-butanol 38.15 796.15 796.2 d 129.3 129.3 b 313.15 792.3 792.3 c 1181.5 1181.5 c sec-butanol 38.15 793.22 793.2 d 1177.1 1177.1 c 318.15 791.1 791.1 c 1159.1 1159.1 c tert-butanol 38.15 771.1 771.1 c 186.7 186.7 c 313.15 766.91 766.9 c 165.61 165.6 c a ->Reference(12), b->reference(13), c->reference(14), d->reference(15) Job s method of continuous variation is used to prepare the mixtures of required proportions. The prepared mixtures are pres erved in wellstoppard conical flasks. After mixing the liquids thoroughly, the flasks are left undisturbed to allow them to attain thermal equilibrium. The ultrasonic velocity (u) in liquid and liquids mixtures have been measured using an ultrasonic interferometer (Mittal ty pe, Model F- 81) working at 2 MHz fixed frequency with an accuracy of ±.1 ms ¹. An electronically digital operated constant temperature water bath has been used to circulate water through the double walled measuring cell made up of steel containing the experimental solution at the desire temperature. The density (ρ) of pure liquids and liquid mixtures are determined using pycknometer by rel ative measurement method with an accuracy of ±.1Kgm 3.The temperature around the pycknometer is maintained within ±.1K in an electronically operated constant temperature water bath. All the precautions are taken to minimize the possible experimental errors. THEORY The ultrasonic velocity (u) and density (ρ) in pure liquids and liquid mixture of various concentrations have been measured at 38.15K and 313.15K respectively. Thermodynamic and acoustical parameters such as isentropic compressibility (ks), inter molecular free length (Lf), acoustic impedance (z), are determined using the observed values of velocity and density and the deviation/excess values of isentropic compressibility(δks), free length(l E f), acoustic impedance (z E ) and ultrasonic velocity ( u) are evaluated using the following equations Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 66

Isentropic compressibility (ks ): The speed of sound (u) and the density of the medium (ρ) using Newton and Laplace equations ks = (1/ ρ u 2 ) (1) Intermolecular free length ( Lf) The free length (Lf) is the distance between the surfaces of the neighbouring molecules and is given by the equation Lf = KT ks 1/2 (2) Where KT is the temperature dependent constant. Acoustic Impedance (z) The acoustic impedance is the product of the velocity of ultrasound in a medium (u) and its density (ρ ) which can be calculated by the relation. z = u ρ (3) where u and are velocity and density of the liquid respectively. Excess / deviation values (Y E ): In order to understand the nature of the molecular interactions between the components of the liquid mixtures, it is of interest to discuss the same in terms of excess parameters rather than actual values. Non-ideal liquid mixtures show considerable deviation from linearity in their concentrations, and this has been interpreted to arise from the presence of strong or weak interactions. The difference between the parameters of the real mixtures (Yreal) and those corresponding to an ideal mixture( Y ideal x Y ) values, namely excess parameters (Y E ) such as free length ( E L f ), acoustic impedance (z E ), and deviations in ultrasonic velocity ( u), isentropic compressibility ( ks), are computed by the relation E Y Yreal xiyi (4) Where Y E = L, z E and u; xi is the mole E f fraction and Yi is the value of the parameter of the i th component liquid of mixture. The deviations in isentropic compressibility has been calculated from the equation ks = ks (ɸ1 ks1 + ɸ2 ks2) (5) Since ks is not additive on mole fraction (xi) but is additive on volume fraction. Hence, such values are calculated using i i volume fraction ɸi = xi Vi (6) xivi The excess/deviation properties (Y E ) have been fitted to Redlich-Kister type polynomial equation [16] using j Y E = x(1-x) A (1-2x) i i (7) i= Where Y E = L, z E, u and ks ; x is the mole E f fraction of the solute, Ai are the adjustable parameters of the function; and are determined using the least square method. In the present investigation i values taken from to 4. The corresponding standard deviations σ (Y E ) were calculated using the expression. 1/2 E E 2 ΣYexp -Y E cal σ(y )= (8) m-n Where m is the total number of experimental points and n is the number of coefficients in equation (6). The calculated values of the coefficients Ai along with the standard deviations (σ) for the systems 38.15 K and 313.15 K are given in Table 4 (A) and 4 (B) respectively. RESULTS AND DISCUSSION Ultrasonic velocity (u), density (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance(z) and other related excess/deviation thermodynamic parameters Δks, L E f, z E and u are evaluated for the binary mixture Benzyl Benzoate in n-, sec-, tert-butanols over the whole concentration range at two temperatures 38.15K and 313.15K are presented in Tables 2 (A, B, C) and Tables 3 (A,B,C)respectively. The R-K coefficients and standard deviation σ(yᴱ) values for the systems at 38.15 K and 313.15 K are represented in Tables 4(A, B). The excess / deviation values of isentropic compressibility, free length, acoustic impedance and ultrasonic velocity for all the systems at 38.15 K and 313.15 K are plotted in the Figures 1 to 8. Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 67

Table 2 (A): Ultrasonic velocity (u), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f,z E and deviations in ks, u as a function of mole fraction (x) of Benzyl Benzoate in n-butanol (A) at 38.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) Δks(x1 ¹⁰) L E f(x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 1114.54 1493.26 4.238.421.1664.....9234 11. 1475.5 4.1782.4281.1623 -.1867 -.68.13 3.54.8854 193.26 147.31 4.2312.438.167 -.367 -.115.23 9.59.7631 17.76 145.98 4.4359.4411.1554 -.6631 -.249.56 24.99.6688 151.13 1433.15 4.6319.457.156 -.8999 -.336.74 33.93.5914 133.61 1416.33 4.823.4599.1464-1.645 -.393.86 39.9.4753 14.38 1385.87 5.1839.4768.1392-1.2382 -.449.96 41.6.327 959.39 1343.28 5.7766.534.1289-1.3267 -.471.97 41.12.2768 941.29 1327.51 6.284.5142.125-1.345 -.46.93 39.6.14 881.16 1278.8 6.9475.552.1126-1.68 -.347.65 29.2. 796.1 129.3 8.5894.6138.963.... Table2 (B): Ultrasonic velocity (u ), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f,z E and deviations in ks, u as a function of mole fraction (x) of Benzyl Benzoate in sec-butanol (B) at 38.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) ks(x1 ¹⁰) L E f (x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 1114.54 1493.26 4.238.421.1664.....9243 11. 1474.46 4.1816.4283.1622 -.2167 -.78.13 5.13.8868 192.95 1469.1 4.2393.4312.166 -.3473 -.129.25 11.62.7361 163.83 144.11 4.5325.4459.1532 -.824 -.3.61 3.28.6787 153.54 1428.48 4.6516.4517.155-1.8 -.364.76 36.8.596 132.5 147.84 4.8866.463.1454-1.2129 -.437.89 44.1.4689 12.73 1373.85 5.2837.4814.1378-1.442 -.511.12 48.5.3293 959.12 1328.91 5.939.589.1275-1.5323 -.531.11 47.69.2797 939.97 1311.6 6.1842.528.1233-1.517 -.517.95 46.7.144 88.32 1256.31 7.1972.5619.116-1.1941 -.41.7 34.82. 793.21 1177.1 9.988.6317.934.... Table2 (C): Ultrasonic velocity (u), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f, z E and deviations in k s, u as a function of mole fraction (x) of Benzyl Benzoate in tert-butanol (C) at 38.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) Δks(x1 ¹⁰) L E f (x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 1114.54 1493.26 4.238.421.1664.....9231 198.84 1469.63 4.2136.4299.1615 -.3334 -.113.15 7.63.8896 194.43 146.24 4.2851.4335.1598 -.569 -.168.25 11.86 Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 68

.7356 158.74 1426.53 4.6414.4512.151-1.268 -.413.64 4.76.6815 149.7 1414.3 4.7655.4572.1484-1.4737 -.51.83 5.52.5997 128.44 1387.82 5.484.476.1427-1.762 -.591.94 57.3.4619 991.41 1334.96 5.6599.4982.1323-2.125 -.693.13 6.46.3312 949.79 1278.79 6.4383.5314.1215-2.2591 -.719.13 57.43.2795 928.73 1254.43 6.8425.5478.1165-2.2119 -.696.96 54.9.1433 871.31 1181.6 8.223.65.13-1.781 -.543.74 36.64. 771.1 186.7 1.9817.694.838.... Table3 (A): Ultrasonic velocity (u), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f,z E and deviations in ks, u as a function of mole fraction (x) of Benzyl Benzoate in n-butanol (A) at 313.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) ks(x1 ¹⁰) L E f (x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 119.77 1471.44 4.1618.4311.1633.....9234 191.35 1454.95 4.3285.4396.1588 -.1812 -.71.8 5.71.8854 182.94 1449.67 4.394.4429.157 -.2943 -.116.17 11.45.7631 166.8 1426.74 4.681.4536.1521 -.729 -.259.53 23.98.6688 146.11 149.67 4.815.4635.1475 -.9616 -.353.73 34.25.5914 128.88 1396.44 4.9841.4717.1437-1.1696 -.429.89 43.46.4753 1.28 137.59 5.3219.4875.1371-1.447 -.58.14 51.28.327 951.57 1326.66 5.979.5163.1262-1.477 -.523.98 5.34.2768 931.4 139.36 6.2625.5288.122-1.4284 -.5.91 47.6.14 87.88 1256.4 7.2742.5699.194-1.837 -.369.6 34.3. 792.3 1181.5 9.416.6354.936.... Table3 (B): Ultrasonic velocity (u ), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f,z E and deviations in ks, u as a function of mole fraction (x) of Benzyl Benzoate in sec-butanol (B) at 313.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) ks(x1 ¹⁰) L E f (x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 119.77 1471.44 4.1618.4311.1633.....9243 192.72 1455.92 4.3173.4391.1591 -.2196 -.84.12 8.12.8868 185.29 1448.46 4.3918.4428.1572 -.3382 -.129.2 12.37.7361 163.37 1421.19 4.656.456.1511 -.8941 -.324.67 32.17.6787 152.7 1411.25 4.7725.4616.1485-1.824 -.392.82 4.16.596 132.93 1394. 4.982.4716.144-1.3394 -.483.1 5.43.4689 997.51 1361.68 5.467.4913.1358-1.5448 -.55.15 56.12.3293 95.79 1317.46 6.596.522.1253-1.6212 -.564.1 55.5.2797 931.65 1299.78 6.3534.5326.1211-1.5871 -.548.94 53.31.144 866.92 1243. 7.4658.5774.178-1.23 -.42.6 4.4. 791.1 1159.1 9.486.6481.917.... Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 69

Table3 (C): Ultrasonic velocity (u), densities (ρ), isentropic compressibility(ks), intermolecular free length(lf), acoustic impedance (z), their excess thermodynamic parameters L E f,z E and deviations in ks, u as a function of mole fraction (x) of Benzyl Benzoate in tert-butanol (C) at 313.15K x ρ u ks(x1 ¹⁰) Lf(x1 ¹⁰) z(x1⁶) Δks(x1 ¹⁰) L E f ( x1 ¹⁰) z E (x1⁶) u (Kg.m -3 ) ( m.s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( P.a -1 ) (m) (Kg.m².s -1 ) ( m.s -1 ) 1. 119.77 1471.44 4.1618.4311.1633.....9231 195.99 145.64 4.3358.44.159 -.3876 -.13.2 1.4.8896 19.5 1442.35 4.497.4437.1572 -.5619 -.189.29 15.71.7356 161.68 142.42 4.7891.4624.1489-1.335 -.441.72 38.28.6815 15.65 1391.57 4.9151.4685.1462-1.672 -.534.89 49.39.5997 132.33 137.27 5.159.4799.1415-1.971 -.653.19 61.28.4619 994.73 1322.66 5.7464.565.1316-2.3947 -.78.122 69.6.3312 947.12 1265.53 6.5925.5425.1199-2.4924 -.792.112 65.51.2795 927.14 1239.9 7.159.5597.115-2.4453 -.767.15 6.86.1433 858.96 1167.22 8.5452.6177.13-1.8972 -.576.69 43.46. 766.9 165.6 11.4835.7161.817.... Table 4 (A): R-K coefficients (Ai) and standard deviation σ(yi) for the systems at 38.15 K property system A A₁ A₂ A₃ A₄ σ(yi) -4.8254-2.5767-1.7982-1.725.1412.65 ks(x1 1 ) -5.5567-3.1832-1.737-1.3815 -.742.288 ( P.a -1 ) -8.146-4.4556-2.5529-3.1175-1.658.194-1.759 -.8369 -.5966 -.643.226.49 L E f (x1-1 ) -1.9861-1.211 -.4793 -.455.563.451 (m).413.16.183.222 -.117 1.3589.377.1356.1181.136 -.23.829 z E (x1 6 ).3961.161.321.227 -.1418.39 (Kg.m².s -1 ).413.16.183.222 -.117.24 1.6554.3429.5425 1.1144 -.94.57 u 1.9119.5589.2118 1.368 -.1854.85 ( m.s -1 ) 2.4399.89 -.1 2.665.5219.284 Table 4 (B): R-K coefficients (Ai) and standard deviation σ(yi) for the systems at 313.15 K property system A A₁ A₂ A₃ A₄ σ(yi) -5.433-3.4261-1.1432.2532 1.514.444 ks(x1 1 ) -6.118-3.751-1.3-2.9192-2.1137.196 ( P.a -1 ) -9.654-5.294-1.2822-3.1258-3.6439.72-1.9733-1.1512 -.231.2692.5695.845 L E f (x1-1 ) -2.1596 -.9316 -.1187-1.1685 -.885.19 (m) -3.25-1.4786.688-1.66-1.538.69.424.1985 -.32 -.265 -.4349.83 z E (x1 6 ).4249.58 -.189.3983.211.54 (Kg. m².s -1 ).6623-3.45 3.516 1.637 -.735.2526 1.9986 1.119 -.5458 -.2652.2269.2 u 2.2278.737 -.6489 1.878 2.2139.183 ( m.s -1 ) 2.774.751-1.736 1.711 3.2789.188 Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 7

L E f (1-1 m) Δk s (1-1 P. a -1 ) Δk s (1-1 P. a -1 ) International Journal of Pharma Research & Review, Feb 214; 3(2):65-78 ISSN: 2278-674 Fig(1). with deviation in isentropic compressibility at 38.15K -.5.2.4.6.8 1-1 -1.5-2 -2.5 -.5 Fig (2). with deviation in isentropic compressibility at 313.15 K.2.4.6.8 1-1 -1.5-2 -2.5 Fig (3). with excess free length at 38.15 K -.1 -.2 -.3 -.4 -.5 -.6 -.7 -.8.2.4.6.8 1 Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 71

zᴱ (1 6 Kg. m². s ¹) zᴱ (1 6 Kg.m². s ¹) L E f (1-1 m) International Journal of Pharma Research & Review, Feb 214; 3(2):65-78 ISSN: 2278-674 Fig (4). with excess free length at 313.15 K -.1.2.4.6.8 1 -.2 -.3 -.4 -.5 -.6 -.7 -.8.12 Fig (5). with excess acoustic impedence at 38.15 K.1.8.6.4.2.2.4.6.8 1.14.12.1 Fig (6). with excess acoustic impedence at 313.15 K.8.6.4.2.2.4.6.8 1 Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 72

Δu (m. s ¹) u ( m s -1 ) International Journal of Pharma Research & Review, Feb 214; 3(2):65-78 ISSN: 2278-674 7 6 5 Fig(7). with deviation in ultrasonic velocity at 38.15 K 4 3 2 1.2.4.6.8 1 x Fig (8). with deviation in ultrasonic velocity at 313.15 K 7 6 5 4 3 2 1.2.4.6.8 1 Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 73

Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 74

Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 75

The non-linear variation of excess/deviation properties with mole fraction of Benzyl Benzoate is responsible for non-ideality in the systems of binary liquid mixture [ 17]. The factors responsible for such departure from ideality may either be due to the presence of intermolecular forces between the constituents in the mixture, or to compound formation between solute and solvent, or as a result of association of either to form complex molecules [18]. These excess/ deviation parameters throw light upon the strength of interaction, and their variation with mole fraction finds application in characterizing the physico-chemical behaviour of liquid mixtures [19]. From the Tables 2(A, B, C) and 3(A, B, C), the deviation in isentropic compressibility (Δks) and excess free l ength (L E f) are negative. The curves highlighted in Figures 1 to 4 shows that both Δks and L E f curves are negative for all the systems under investigation. The nature of Δks and L E f play vital role in assessing the compactness due to molecular rearrangement. The extent of molecular interactions in liquid mixtures may be due to charge transfer, dipoleinduced-dipole, dipole-dipole interactions and interstitial accommodation, leading to more compact structure giving Δks and Lf E negative. The values of the excess/ deviation functions Δks, L E f depend upon several physical and/or chemical contributions. The physical contribution consists of dispersion forces or weak dipole-dipole interaction that leads to positive values Δks and L E f. Another factor, which involves a physical contribution, is the geometrical effect allowing the fitting of molecules of two different sizes into each other s structure resulting in negative Δks and L E f values. The strength of the interactions increases with temperatures as observed from more negative values of the excess parameters. They are negative throughout and become more negative at all concentrations as the temperature is increased. In hetero-molecular interaction between the component molecul es of the mixtures, Fort and Moore [2] found that the negative value of deviation in isentropic compressibility indicates greater interaction between the components of the mixtures due to the formation of hydrogen bond. Thus the negative Δks values for binary mixtures indicate strong interactions between Benzyl Benzoate and the three isomers of butanols. It is also evident from the tables that the negative values of Δks are in the increasing order for all the existing systems which implies that the i nteractions are in the order: bb+tertbutanol>>. According to Ramamoorthy and Alwan [21], negative values of excess intermol ecular free length L E f indicates that sound waves cover longer distances due to decrease in intermolecular free length ascribing the dominant nature of hydrogen bond interaction between unlike molecules. Fort and Moore[2] indicated that the positive values of excess free length should be attributed to the dispersive forces, and negative excess values should be due to hydrogen bond formation between solute and solvent. In the present study the negative contribution in all the systems prevail to the existence of greater interactions. Spencer, Jeffery and Robert [22] have also reported a similar observation on the basis of excess values of free l ength. It is also evident from the tables that negative values of L E f are in the increasing order which implies that these interactions are in the order: bb + tert-butanol > >. From the Tables 2 (A, B, C) and 3(A, B, C), the excess values of z E are found to be positive and the curves highlighted in Figures (5, 6) show the same for all the systems under investigation. In another words, the curve of z E in Figures shows the opposite trends as observed in Figures (1, 2, 3, and 4) for Δks and L E f. According to Ali, Hyder and Nain [23], the nature of the positive values of z E is attributed to specific interaction between the heteromolecules. This further supports our earlier finding. From the Figures (7) and (8), it is observed that the deviation in ultrasonic velocity u for all the three binary liquid mixtures is positive over the whole range of mole fraction at all temperatures. According to Ali et al. [24], positive deviations in u from linear dependence suggest the presence of strong interaction and more positive values means much more strong interactions between the component Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 76

of molecules. Therefore basing on the above reference for the present scenario, interactions are found to be in the order: bb+tertbutanol>>, this again reinforces our view regarding the interaction between bb and n-butanol, secbutanol, tert-butanol mole-cules. Similar trends in u have also been reported for dimethylsulphoxide+n, Ndimethylformamide/N,N dimethylacet-amide binary mixtures [25]. Generally in an IR spectrum of absorption, the change in the intensity is related to the interaction between solute and solvent. According to Rajendran [26], large changes in absorption show strong interaction in the system. As per the FTIR figures (a - g), the present mixtures show large variations in their intensity and hence it supports the fact that strong interactions take place in the liquid mixture of Benzyl Benzoate +n-butanol, sec-butanol, tert-butanol. CONCLUSION From the present study, it may be concluded that the v ariation in the acoustic parameters, the sign and extent of deviation of the excess function derived from the ultrasonic velocity and density suggest the presence of molecular interaction between the components of molecules in the binary liquid mixtures. The negative values of Δks, L E f and the positive values of Z E, u in all the systems at all temperatures reveal the presence of strong interactions between the component molecules in the mixtures. The interaction tends to be stronger with rise in temperature. The existence of strong molecular interaction in the mixture is in the order: >bb+secbutanol>. It is also supported by the IR spectra. The conclusions highlight the importance of ultrasonic method in detecting strong molecular interaction between the component molecules of the mixtures. REFERENCES 1. Geetalakshmi M. Molecular interaction in the binary liquid mixtures-an ultrasonic Study. Phil dissertation. Sri Venkateswara University. Tirupati (India). 26. 2. Geetalakshmi M, Naidu P S and Ravindra Prasad K. J Pure Applied Ul trasonics 28:3(1):18-23. 3. Sivasankar J, Geetalakshmi M, Naidu P S and Ravindra Prasad K. J Pure & Applied Ultrasonics 27:29(2-3): 82-88. 4. Ramesh P. Ultrasonic study of the binary liquid mixtures (Benzyl Benzoate + Substituted Benzenes), M. Phil, dissertation submitted to Sri Venkateswara Univeristy, Tirupati 28, India. 5. Bahl and Arun Bahl. Text book of organic chemistry 25:17: 292 6. Jacobson B. Acta chemistry 1985: 6: 148. 7. Bhatti S S and Singh D P. Indian J Pure &Applied Physics 1983:21: 56. 8. Sheshadri A T and subramanyam B. J Physics and condensed matter199: 2: 7353. 9 Manohar Murthi N, Shivkumar K V, Rajgopal E, subramanyam S V.Acoustica 1981: 48:341. 1. Furniss B S, Hannaford A J, Rogers V S, Smith P W G and Tachell A R.Vogel s TextBook of Practical Organic chemistry. 4th ed. Longmann; 198. 11. Riddick J A, Bunger W B and Sakano T K. Techniquesin chemistry. Organic Solvents.4th ed. John Wiley(New York);7: 1986. 12. Jaya madhuri N. Ultrasonic Investigations of Molecular Interaction in Binary Mixtures of Benzyl Benzoate with Acetonitrile and Benzonitrile. E-Journal of Chemistry211: 8(1):457-469. 13. Palani R and Geetha A. Physico-Chemical behaviour of binary liquid mixtures of some monohydroxy alcohols with DMSO as common solvent. Rasayan J. Chemistry 28:1(3):481-488. 14. Santhi N and Sabarathinam P L. Ultrasonic study of molecular interaction in binary liquid mixtures of n-hexane with alcohols. International Letters of Chemistry, Physics and Astronomy 212:5: 59-71. 15. Ranjith B. Densities, viscosities and speed of sound of binary mixtures of phenyl acetonitrile with some aliphatic alcohols at 38.15 K. Indian Journal of Chemistry 28July:47(A):126-131. 16. Redlich O and Kister AT. Algebric representation of thermodynamic properties and the classification solutions. Ind. Eng. Chem. 1948;4: 345 8. 17. Jacobson B. Intermolecular Free Lengths in the Liquid State. I. Isentropic an Isothermal Compressibilities. Acta Chemica Scandinavia 1952:6:1485-1498. 18. Glasstone S. Text Book of Physical Chemistry. 2nd ed. The Macmillan (India);1995. 19. Vijayakumar R, Vishwanathan S and Anand Rao M. Excess Volumes, Speeds Of Sound and Isentropic Compressibilities of 2- Propyn-1-ol+1,2-Dichloroethane, +1,1,1- Trichloroethane,+1,1,2,2- Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 77

Tetrachloroethane, and +Trichloroethylene at 33.15K. Journal of Chemical and Engineering Data 1996: 41b:755-757. 2. Fort R J and Moore W R. Isentropic compressibilities of binary mixtures. Trans Faraday Society 1965: 61:212-2111. 21. Ramamoorthy K and Alwan S. Current Science 1978: 47: 334. 22. Spencer J N, Jeffery E and C. Robert. J of Physical Chemistry 1979: 83: 1249. 23. Ali A, Hyder, Nain. Indian J Physics 22:76 B(5): 661 24. Ali A, Pandey J D, Soni N K, Nain A K, Lal B, Chand D. Chin. J. Chemistry 25:23:1. 25. Ali A, Hyder S, Nain A K. Acoustic Letters 2:23: 2183. 26. Rajedran V. Volumetric, Viscosmetric and Ultrasonic behavior of n-heptane with Isomeric alcohols at 298.15 K. Indian J Pure and Applied Physics 1996:34:52-56. Shaik Mahammad Nayeem et.al, IJPRR 214; 3(2) 78