Simple method for preparation of chitosan/poly(acrylic acid) blending hydrogel beads and adsorption of copper(II) from aqueous solutions

被引:197
作者
Dai, Jie [1 ]
Yan, Han [1 ]
Yang, Hu [1 ]
Cheng, Rongshi [1 ,2 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, Dept Polymer Sci & Technol, Key Lab Mesoscop Chem MOE, Nanjing 210093, Peoples R China
[2] S China Univ Technol, Coll Mat Sci & Engn, Guangzhou 510641, Peoples R China
关键词
CS/PAA GLA beads; CS GLA beads; Adsorption of copper(II); Adsorption mechanisms; CARBOXYMETHYL-CHITOSAN RESIN; HUMIC-ACID; CROSS-LINKING; CU(II) IONS; GLA BEADS; EQUILIBRIUM; KINETICS; SORPTION; REMOVAL; LEAD;
D O I
10.1016/j.cej.2010.09.024
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
In this paper poly(acrylic acid) blended chitosan (CS/PAA) hydrogel beads have been prepared by one-step method simply It was found that glutaraldehyde (GLA) cross-linked CS/PAA beads had better stability in lower pH solutions and higher mechanical strength than CS-GLA beads without PAA Results from removal of Copper(Cu) ions from aqueous solutions showed that the adsorption capacity of CS/PAA-GLA beads was greater than that of CS-GLA beads Moreover the adsorption capacity for two types of beads both showed temperature independent Furthermore the adsorption isotherms of various beads at different temperatures were both better fitted for Langmuir equation while the adsorption kinetics was both better described by the pseudo-second order equation Furthermore Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy have been employed to investigate the adsorption mechanisms from molecular levels It indicated that the efficient effects of CS/PAA-GLA beads on removal of Cu(II) resulted from the fact that carboxyl groups were facile to form bidentate carboxylates with metal ions In addition Cu( II) ions could be desorbed efficiently from both aforementioned beads at pH below 40 and the adsorption capacity of the regenerated beads had no loss until six cycles (C) 2010 Elsevier B V All rights reserved
引用
收藏
页码:240 / 249
页数:10
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