Efficient multicyclic sorption and desorption of lead ions on facilely prepared poly(m-phenylenediamine) particles with extremely strong chemoresistance

被引:69
作者
Huang, Mei-Rong [1 ]
Lu, Hong-Jie [1 ]
Li, Xin-Gui [1 ]
机构
[1] Tongji Univ, Coll Mat Sci & Engn, Inst Mat Chem, Key Lab Adv Civil Engn Mat, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
polyphenylenediamine; microparticle; lead ion; successive multicyclic sorption and desorption; chemoresistant sorbent; desorbent; water purification;
D O I
10.1016/j.jcis.2007.04.024
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
Nitric acid, hydrochloric acid and EDTA were carefully chosen as desorbent to systematically evaluate the adsorption/desorption performance of the Pb2+-adsorbing fine microparticles of poly (m-phenylenediamine). The sorption/desorption efficiency was maximized by optimizing desorption condition including the desorbent concentration, contact time, and desorption mode. The variation of the solution pH with Pb2+ desorption was recorded to speculate the desorption mechanism. The practical reusability of the microparticles was elaborated through the sorption-desorption cycle experiments in an optimum condition. It was found that the desorption was very rapid with an equilibrium time of several minutes. A strong dependence of the desorbability on the species and concentration of the desorbents was observed. When 20 mM EDTA was chosen as the desorbent, the highest desorptivity was up to 94.2% that was much higher than those using nitric and hydrochloric acids. A successive sorption-desorption study employing nitric acid indicated that the microparticles could be simply regenerated and reutilized for more than 5 cycles together with Pb2+ re-adsorption efficiency of about 50% and accumulative Pb2+ adsorption capacity of up to 720.4 mg L-1. Facilely prepared, extremely chemoresistant and cost-effective PmPD microparticles would be potentially used for multicyclic sorption of lead ions from aqueous solution. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:72 / 79
页数:8
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