Dynamic surface tension studies on poly(N-vinylcaprolactam/N-vinylpyrrolidone/N,N-dimethylaminoethyl methacrylate) at the air-liquid interface

被引:24
|
作者
Rojas, Yenny V. [1 ]
Phan, Chi M. [1 ]
Lou, Xia [1 ]
机构
[1] Curtin Univ Technol, Dept Chem Engn, Bentley, WA 6102, Australia
关键词
Dynamic surface tension; Air-liquid interface; Gaffix (R) VC-713; HYDRATE FORMATION; AIR/WATER INTERFACE; WATER INTERFACE; ADSORPTION; METHANE; KINETICS; DROP; SDS;
D O I
10.1016/j.colsurfa.2009.11.038
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 adsorption of poly(N-vinylcaprolactam/N-vinylpyrrolidone/N,N-dimethylaminoethyl methacrylate), a commercial product with the trade name of Gaffix (R) VC-713 and currently used as a kinetic inhibitor for natural gas hydrates, has been experimentally studied at the air-liquid interface using surface tension measurements. The influence of polymer concentration and temperature on the adsorption of the polymer was analysed. The equilibrium experimental data obtained at both 293 K and 278 K has been fitted using the analogous Surface equation of state for the Langmuir isotherm. Dynamic adsorption has been modelled using both diffusion-con trolled and asymptotic models. The values of the surface tension and the Surface excess at saturation showed that the polymer was very active at the air-liquid interface. Equilibrium Surface tension indicated that temperature has a weak influence on the number of moles of Gaffix (R) VC-713 adsorbed on the interface. The dynamic adsorption was controlled by diffusion process initially, in which a rapid reduction in surface tension was observed. It was then followed by a slow polymer reorganization process. A strong dependence of the dynamic adsorption on both the temperature and the polymer concentrations was well demonstrated. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:99 / 103
页数:5
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