Kinetics of adsorption of disperse dyes by polyepicholorohydrin-dimethylamine cationic polymer/bentonite

被引:51
|
作者
Yue, Qin-Yan [1 ]
Li, Qian [1 ]
Gao, Bao-Yu [1 ]
Wang, Yan [1 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Jinan 250100, Peoples R China
关键词
EPI-DMA/bentonite; disperse dyes; adsorption kinetics; rate constants; thermodynamic parameters;
D O I
10.1016/j.seppur.2006.10.024
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The characterization of polyepicholorohydrin-dimethylaminelbentonite and the kinetics of adsorption of four disperse dyes, namely, Disperse Yellow Brown S-2RFL (DYB S-2RFL), Disperse Red S-R (DR S-R), Disperse Blue SBL (DB SBL) and Disperse Yellow (DY SE-6GFL) onto organophilic bentonite (polyepicholorohydrin-dimethylamineibentonite) have been studied at various solution concentrations and temperatures. The adsorption kinetics was studied in terms of a two-step first-order kinetic rate equation and intra-particle diffusion model. The adsorption process has been found to follow with two different rate constants (k(1) and k(2)) for two-step first-order kinetic rate equation and also two different intra-particle diffusion rate constants (k(int1) and k(int2)) for intra-particle diffusion model. For both the kinetic steps, the energies of activation of adsorption (E-a1 and E-a2) and other thermodynamic parameters (Delta H-1* and Delta H-2*, Delta S-1* and Delta S-2*, Delta G(1)* and Delta G(2)*) have been calculated using Arrhenius's and Eyring's equation, respectively. It has been found that or both the adsorption kinetic steps, E-a1 and E-a2 are corresponding to the values of k(1) and k(2) and Delta H-1* < -T-av Delta S-1*, Delta H-2* < -T-av Delta S-2* and Delta G* > 0, which means that the influence of entropy is more remarkable than enthalpy in activation reaction and the adsorption process is not spontaneous. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:279 / 290
页数:12
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