Enthalpies of solution for (fumaric acid + water) have been measured at the temperatures (298.15, 313.15, and 333.15) K over the composition range of homogeneous solutions by using a SETARAM C80 D mixing calorimeter. The concentration and temperature dependence of the molar enthalpies of solutions a
Novel Phenomena of Crystallization and Emulsification of Hydrophobic Solute in Aqueous Solution
β Scribed by Kouji Maeda; Yasuki Aoyama; Keisuke Fukui; Shouji Hirota
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 207 KB
- Volume
- 234
- Category
- Article
- ISSN
- 0021-9797
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β¦ Synopsis
Emulsification of lauric acid in an aqueous ethanol solution including lauric acid solute has been observed during cooling before crystallization of lauric acid occurs. The nature of two different solubility curves was explained for the system of lauric acid and aqueous ethanol solution. The mutual solubility of the two liquid phases controls emulsification; the solid solubility of lauric acid controls crystallization. The mutual solubility curve appears at relatively high temperature, and the solid solubility curve at relatively low temperature. Crystallization essentially generates a solid metastable zone under the solid solubility curve. A supersaturated solution can be obtained in the metastable zone. However, no nucleation occurs in the metastable zone. The metastable zone, therefore, still caused emulsification at low temperature before crystallization of lauric acid occurred. The hypothetical mutual solubility curve for the aqueous solution including hydrophobic solutes appeared invariably even at low temperature in the metastable zone under the solid solubility. Copyright 2001 Academic Press.
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Veszprem, Hungary Β΄Ε½ . Enthalpies of solution for L-ascorbic acid q water have been measured in a SETARAM C80 D mixing calorimeter over the composition range of homogeneous solutions at temperatures of 298.15 K and 323.15 K. The results are reported in terms of excess molar ΓΕ½ Ε½ . 4 enthalpies for x
The hydrophobic interaction between the surfaces hydrophobized by the adsorption of STAC in a STAC solution (system I) and the interaction between the surfaces hydrophobized by the reaction with OTS in water (system II) were investigated using an atomic force microscope, and their difference was com