Journal
JOURNAL OF CHEMICAL THERMODYNAMICS
Volume 70, Issue -, Pages 227-232Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jct.2013.11.011
Keywords
Uranium(VI) complex; Dicarboxylic acid; Stability constant; Enthalpy; Calorimetry
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Funding
- Japanese Ministry of Education, Culture, Sports, Science and Technology (MEXT)
- Grants-in-Aid for Scientific Research [24760713] Funding Source: KAKEN
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The thermodynamic quantities (Delta G, Delta H, Delta S) of complex formation of U(VI) with three aliphatic di-carboxylic acids, i.e. oxydiacetic acid (ODA), thiodiacetic acid (TDA), iminodiacetic acid (IDA), and three aromatic di-carboxylic acids, i.e. 2,5-furandicarboxylic acid (FDA), 2,5-thiophenedicarboxylic acid (TDCA) and dipicolinic acid (DPA) were determined by potentiometric titration and micro-calorimetric titration. The obtained thermodynamic quantities are compared with each other for the discussion of the effect of structural difference, i.e. aliphatic-and aromatic structure and types of central atom in the ligands on the complex formation thermodynamics. A clear tendency is observed in the complexation data between aliphatic-and aromatic ligands. The complexation of those aliphatic ligands are completely entropy driven, on the contrary, the enthalpy change is a certain driving force in the complexation of those aromatic ligands while entropy change also contributes to progress of the reaction. The Delta G, Delta H and Delta S of 1: 1 IDA complex show remarkable difference from those of glutaric acid (GA) complex, while those of ODA and TDA complex are almost equal to those of GA complex, which seems to be attributed to the difference of the coordination mode. (C) 2013 Elsevier Ltd. All rights reserved.
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