Partial molar heat capacities and volumes of some mono-, di- and tri-saccharides in water at 298.15, 308.15 and 318.15 K

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P. K. Banipal, T. S. Banipal, B. S. Lark and J. C. Ahluwalia


Abstract

Partial molar heat capacities ([C with combining macron]p,20) and partial molar volumes ([V with combining macron]20) of seven monosaccharides [D(−)-ribose, D(−)-arabinose, D(+)-xylose, D(+)-glucose, D(+)-mannose, D(+)-galactose and D(−)-fructose], seven disaccharides [sucrose, D(+)-cellobiose, lactulose, D(+)-melibiose hemihydrate, D(+)-maltose monohydrate, D(+)-lactose monohydrate, D(+)-trehalose dihydrate] and one trisaccharide [D(+)-raffinose pentahydrate] have been determined at 298.15, 308.15 and 318.15 K using a Picker flow microcalorimeter and a vibrating-tube densimeter respectively. From these data partial molar expansion coefficients (∂[V with combining macron]20/∂T)P, isothermal compressibilities (KT,20), excess partial molecular volumes ([v with combining macron]20,ex) and partial molar heat capacity coefficients (∂[C with combining macron]p,20/∂T )p of the various sugars have been calculated. The [C with combining macron]p,20 and [V with combining macron]20 values were found to be highly positive and increased with increase in temperature. High positive values of [C with combining macron]p,20 showed that the dissolution of the sugars was accompanied by the enhancement of the structural order in water. The results have been rationalized in terms of the specific hydration model.


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