Surfactant binding by humic acids in the presence of divalent metal salts

被引:18
作者
Matsuda, Miyuki [1 ]
Kaminaga, Akiko [1 ]
Hayakawa, Katumitu [1 ]
Takisawa, Noboru [2 ]
Miyajima, Tohru [2 ]
机构
[1] Kagoshima Univ, Fac Sci, Dept Chem & Biosci, Kagoshima 8900065, Japan
[2] Saga Univ, Fac Sci & Engn, Dept Chem & Appl Chem, Saga 8408502, Japan
关键词
Alkyltrimethylammonium ion; Binding; Gibbs energy; Humic acid; Metal ion; ION-BINDING; MINERAL PARTICLES; CATION-BINDING; ADSORPTION; ASSOCIATION; SUBSTANCES; COMPLEXES; BEHAVIOR; SYSTEM; MODEL;
D O I
10.1016/j.colsurfa.2008.11.037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The binding of metal ions and surfactant to humic substances plays an important role in the distribution of toxic metal ions and toxic organic contaminants in the environment. We measured the binding of dodecyl-(C12TA(+)) and decyltrimethylammonium (C10TA(+)) surfactants to humic acid in the presence of heavy metal salts (Cu(II), Cd(II), Zn(II), Pb(II), and Ca(II)) at pH 8 using a surfactant ion-selective electrode. The binding curves of the surfactant cation were analyzed using the Langmuir equation to determine the binding constant K and capacity m. From the dependence of K on ionic strength, the hydrophobic interaction term is inferred to have Gibbs energy of -28 kJ/mol for the binding of C12TA(+) ion to HA, and the dependence of K on the surfactant chain length revealed a 4 kJ/mol difference in Gibbs energy between C12TA(+) and C10TA(+) ion binding. In the presence of 0.5 mM divalent metal salts, K decreased significantly, partly because of territorial binding and partly because of the irreversible binding of metal ions. Aldrich humic acid had a smaller binding constant and capacity. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 49
页数:5
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