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理解负载砷酸盐的氢氧化铁基吸附剂的再生

Understanding Regeneration of Arsenate-Loaded Ferric Hydroxide-Based Adsorbents.

作者信息

Chaudhary Binod Kumar, Farrell James

机构信息

Department of Chemical and Environmental Engineering, University of Arizona , Tucson, Arizona.

出版信息

Environ Eng Sci. 2015 Apr 1;32(4):353-360. doi: 10.1089/ees.2014.0453.

DOI:10.1089/ees.2014.0453
PMID:25873779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4378614/
Abstract

Adsorbents comprising ferric hydroxide loaded on a variety of support materials are commonly used to remove arsenic from potable water. Although several studies have investigated the effects of support properties on arsenic adsorption, there have been no investigations of their effects on adsorbent regeneration. Furthermore, the effect of regenerant solution composition and the kinetics of regeneration have not been investigated. This research investigated the effects of adsorbent and regenerant solution properties on the kinetics and efficiency of regeneration of arsenate-loaded ferric hydroxide-based adsorbents. Solutions containing only 0.10-5.0 M NaOH or 0.10-1.0 M NaCl, as well as solutions containing both compounds, were used as regenerants. On all media, >99% of arsenate was adsorbed through complexation with ferric hydroxide. Arsenate recovery was controlled by both equilibrium and kinetic limitations. Adsorbents containing support material with weak base anion-exchange functionality or no anion-exchange functionality could be regenerated with NaOH solutions alone. Regeneration of media containing strong base anion (SBA)-exchange functionality was greatly enhanced by addition of 0.10 M NaCl to the NaOH regenerant solutions. Adsorbed silica had a significant effect on NaOH regeneration of media containing type I SBA-exchange functionality, but on other media, adsorbed silica had little impact on regeneration. On all media, 5-25% of arsenate was resistant to desorption in 1.0 M NaOH solutions. However, the use of 2.5-5.0 M NaOH solutions significantly reduced the desorption-resistant fraction.

摘要

负载在多种载体材料上的氢氧化铁吸附剂常用于去除饮用水中的砷。尽管已有多项研究探讨了载体性质对砷吸附的影响,但尚未有关于其对吸附剂再生影响的研究。此外,再生剂溶液组成的影响以及再生动力学也未得到研究。本研究考察了吸附剂和再生剂溶液性质对负载砷酸根的氢氧化铁基吸附剂再生动力学和效率的影响。仅含0.1-5.0 M NaOH或0.1-1.0 M NaCl的溶液,以及同时含有这两种化合物的溶液被用作再生剂。在所有介质上,>99%的砷酸根通过与氢氧化铁络合而被吸附。砷酸根的回收受平衡和动力学限制的控制。含有弱碱阴离子交换功能或无阴离子交换功能载体材料的吸附剂可以仅用NaOH溶液再生。向NaOH再生剂溶液中添加0.10 M NaCl可大大增强含有强碱阴离子(SBA)交换功能介质的再生效果。吸附的二氧化硅对含有I型SBA交换功能介质的NaOH再生有显著影响,但在其他介质上,吸附的二氧化硅对再生影响很小。在所有介质上,5-25%的砷酸根在1.0 M NaOH溶液中抗解吸。然而,使用2.5-5.0 M NaOH溶液可显著降低抗解吸部分。

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本文引用的文献

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