Application of 'waste' metal hydroxide sludge for adsorption of azo reactive dyes

被引:196
作者
Netpradit, S
Thiravetyan, P
Towprayoon, S
机构
[1] King Mongkuts Univ Technol Thonburi, Sch Bioresources & Technol, Div Biotechnol, Bangkok 10140, Thailand
[2] King Mongkuts Univ TEchnol Thonburi, Joint Grad Sch Energy & Environm, Bangkok 10140, Thailand
关键词
adsorption; desorption; ion exchange; metal hydroxides; reactive dyes;
D O I
10.1016/S0043-1354(02)00375-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The capacity and mechanism of metal hydroxide sludge in removing azo reactive dyes from aqueous solution was investigated with different parameters, such as charge amount of dyes, system pH, adsorbent particle size, and adsorbent dosage. The three anionic dyes used were CI Reactive Red 2, CI Reactive Red 120, and CI Reactive Red 141, increasing in number of sulfonic groups, respectively. Only 0.2%` (w/v) of powdered sludge (< 75 mum) achieved color removal from 30 mg l(-1) reactive dye solutions within 5min without pH adjustment. The larger the charge amount of the dyes, the greater the adsorption (> 90%) on the metal hydroxide sludge. The system pH played a significant role in the adsorption on metal hydroxides and formation of dye-metal complexes. The optimum system pH for dye adsorption was 8-9 which was close to the pH(zpc) of the sludge while the precipitation of dye-metal complexes occurred at system pH 2. The maximum adsorption capacity (Qdegrees) of the sludge for the reactive dyes was 48-62 mg dye g(-1) adsorbent. The Langmuir and Freundlich models showed that the higher charged dyes had a higher affinity of adsorption. The smaller particle size and the greater amount of adsorbent showed the faster process, due to an increase in surface area of adsorbent. Desorption studies elucidated that metal hydroxide sludge had a tendency for ion exchange adsorption of sulfonated azo reactive dyes. Leaching data showed that the treated water was nontoxic at a system pH above 5 or a solution pH above 2. (C) 2002 Elsevier science Ltd. All rights reserved.
引用
收藏
页码:763 / 772
页数:10
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