Electrochemical study of the interfacial behavior of cationic polyelectrolytes and their complexation with monovalent anionic surfactants

被引:10
|
作者
Riva, Julieta S. [1 ,2 ]
Bierbrauer, Karina [2 ,3 ]
Beltramo, Dante M. [2 ,3 ]
Yudi, Lidia M. [1 ,2 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Fis Quim, Inst Invest Fisicoquim Cordoba INFIQC, RA-5000 Cordoba, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Ministerio Ciencia & Tecnol Cordoba, Ctr Excelencia Prod & Proc Cordoba CEPROCOR, RA-5164 Cordoba, Argentina
关键词
Liquid/liquid interfaces; Hydroxyethylcellulose; Perfluorate acids; Polyelectrolites; Cooperative binding; FACILITATED ION TRANSFER; IMMISCIBLE ELECTROLYTE-SOLUTIONS; WATER-NITROBENZENE INTERFACE; LIQUID; VOLTAMMETRY; ADSORPTION; CELLULOSE; BINDING; CHLORIDE; SULFATE;
D O I
10.1016/j.electacta.2012.08.049
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The complexation of two hydroxyethylcellulose, of different molecular weights, SC230 and SC240, with the anionic surfactants perfluorodecanoic acid, PFDA, and perfluorooctanoic acid, PFOA, has been studied. For this purpose, the anions transfer current across a water/1,2-dichloroethane interface was employed to quantify PFDA and PFOA concentration in the absence or in the presence of the polyelectrolyte. When polymers were added in increasing amounts to solutions containing PFDA or PFOA, a gradual decrease in current values was observed, evincing the binding of the anions to the polymer. Peak Current values for the transfer, were used for the drawing up the binding isotherms, which were fitted by Satake and Yang theory. Cooperative binding was observed, but all fluorinated acids gave a similar cooperativity parameter, and it was found that both the overall constant as well as the cooperative binding process, increases with the molecular weight of the polymer. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:659 / 664
页数:6
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