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EDTA对Pd/Fe体系还原脱氯2,4-D的影响
摘要点击 2315  全文点击 1014  投稿时间:2015-06-06  修订日期:2015-09-10
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中文关键词  Pd/Fe  脱氯  EDTA  2,4-D  苯氧乙酸
英文关键词  Pd/Fe  dechlorination  EDTA  2,4-D  phenoxyacetic acid
作者单位E-mail
周红艺 浙江工业大学环境学院, 杭州 310014 zhouhy@zjut.edu.cn 
聂亚中 浙江工业大学环境学院, 杭州 310014  
陈勇 浙江工业大学环境学院, 杭州 310014  
雷双健 浙江工业大学环境学院, 杭州 310014  
中文摘要
      针对 Pd/Fe体系对含氯有机物催化还原脱氯过程中,零价铁易腐蚀并在颗粒表面形成钝化层,阻碍目标污染物的进一步脱氯去除,本研究利用乙二胺四乙酸(EDTA)与Fe2+和Fe3+的络合作用,消除Pd/Fe颗粒表面的钝化层,使还原脱氯过程得到持续进行. 实验考察了EDTA的投加方式和投加量、 pH、 钯负载率、 温度等因素对2,4-二氯苯氧乙酸(2,4-D)还原脱氯的影响. 结果表明:①EDTA浓度为25.0 mmol ·L-1、 投加速率为20 mL ·h-1时,苯氧乙酸(PA)生成率在20 min达到了90.7%. 而未加EDTA的反应体系,反应210 min后,PA的生成率仅为74.5%; ②EDTA可以络合Pd/Fe体系在催化脱氯过程中生成的Fe2+和Fe3+,防止或减缓了Pd/Fe颗粒表面钝化层的形成,提高了反应活性; ③适宜的2,4-D催化脱氯条件为:浓度25.0 mmol ·L-1的EDTA溶液,投加速率20 mL ·h-1、 初始pH为4.2、 钯负载率0.050%、 温度30.0℃、 搅拌速率200 r ·min-1,反应210 min,20.0 mg ·L-1的2,4-D几乎可完全转化为PA; ④2,4-D催化脱氯的中间产物主要是2-氯苯氧乙酸及微量的4-氯苯氧乙酸,最终产物为苯氧乙酸.
英文摘要
      In Pd/Fe system, zero-valent iron (ZVI) passivation layer is easily formed on the particle surface during the catalytic reductive dechlorination of chlorinated organics, hindering further dechlorination of target contaminants. In this paper, the passivation layer on the Pd/Fe particle surfaces could be eliminated by the chelation of disodium edetate (EDTA) with Fe2+, Fe3+, making the reductive dechlorination continue. The experiment investigated the effects of EDTA addition manner and dosage, pH, Pd loading and temperature on dechlorination of 2,4-dichlorophenoxyacetic acid (2,4-D) by Pd/Fe. The conclusions can be summarized as follows: ① Phenoxyacetic acid (PA) generation ratio reached 90.7% within 20 min with EDTA concentration of 25.0 mmol ·L-1 and flow rate of 20 mL ·h-1, while it was only 74.5% after 210 min in the system without EDTA. ② The EDTA could chelate the Fe2+ and Fe3+ generated from the process of 2,4-D dechlorination by Pd/Fe, preventing or slowing down the formation of passivation layer, and accelerating the reduction efficiency. ③ The appropriate experimental parameters for 2,4-D removal were as follows: EDTA flow rate of 20 mL ·h-1, cEDTA of 25.0 mmol ·L-1, Pd loading of 0.050%, 200 r ·min-1, pH 4.2 and 30.0℃. The removal percentage of 20.0 mg ·L-1 2,4-D reached nearly up to 100% within 210 min under these conditions. ④ The intermediates of 2,4-D catalytic dechlorination included 2-chlorophenoxyacetic acid (2-CPA) and trace 4-chlorophenoxyacetic acid (4-CPA), and the end product was PA.

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