Affiliation:
1. RNC Arts, JDB Commerce and NSC Science College
2. Sandip Institute of Engineering and Management
Abstract
Densities of sodium cyclamate (Na-cycl) in water and (0.1, 0.3, and 0.5) m (glucose/sucrose) have been measured at (298.15, 303.15, 308.15, and 313.15) K. From density values, partial molar volumes (V0Φ), expansion coefficient (E∞), Hepler’s constant (δ2V0Φ/δT2)p, apparent specific volumes (ASV), partial molar volumes of transfer (∆trsV0Φ), doublet (VAB) and triplet (VABB) interaction coefficients have been calculated. An increase in the values of V0Φ and ∆trsV0Φ was observed with increase in the concentration of glucose/sucrose. The positive values of E∞ and V0Φ are due to the strong solute-solvent interactions. The positive values of (δ2V0Φ/δT2)p suggest structure making behaviour of sodium cyclamate in water and in presence of glucose and sucrose. The positive values of (∆trsV0Φ) and VAB may be due to the interactions between hydrophilic group (–OH, C=O, and –O–) of glucose/sucrose and sodium ion of sodium cyclamate. All solutions studied exhibit sweet taste because ASV of all solutions ranges from (0.569 × 10-6) m3×kg-1 to (0.626 × 10-6) m3×kg-1.
Publisher
AOA Academic Open Access Ltd.
Subject
Psychiatry and Mental health,Neuropsychology and Physiological Psychology
Reference42 articles.
1. T.H. Grenby, K.J. Parker, M. G. Lindley (Eds. ), Developments in sweeteners, 2. Appl. Sci. Publ., London und New York, (1983).
2. T.H. Grenby, Prospects for sugar substitutes, Chem. Br. 27 (1991) 342-345.
3. L. Mathlouthi, Laser-Raman spectra of D-glucose and D-sucrose in aqueous solutions, Carbohydr. Res. 81 (1980) 203-213.
4. M. Mathalouthi, A.M. Suevre, G.G. Birch, Relation between the structure and properties of carbohydrates in aqueous solutions: sweetness of chlorinated sugars, Carbohydr. Res. 152 (1986) 47-61.
5. G.G. Birch, S. Shamil, Structure-activity relationship in sweetness, Food Chem. 21(4) (1986) 245-258.