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应用纳米零价铁处理模拟含Cr(Ⅵ)无氧地下水
摘要点击 3580  全文点击 2211  投稿时间:2009-05-14  修订日期:2009-08-14
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中文关键词  纳米零价铁  Cr(Ⅵ)  地下水  动力学  机制
英文关键词  nanoscale zero-valent iron(Fe)  Cr(Ⅵ)  ground water  kinetics  mechanism
作者单位
武甲 北京交通大学市政与环境工程系北京100044 
田秀君 北京交通大学市政与环境工程系北京100044 
王锦 北京交通大学市政与环境工程系北京100044 
景传勇 中国科学院生态环境研究中心北京100085 
中文摘要
      研究了实验室自制的纳米零价铁处理模拟含Cr(Ⅵ)无氧地下水的影响因素、吸附动力学,并结合体系中Fe2+浓度、氧化还原电位、Zeta电位和理论计算得到的pe-pH图对纳米零价铁去除Cr(Ⅵ)的机制进行了探讨.实验结果表明,纳米零价铁对Cr(Ⅵ)的去除率随着初始Cr(Ⅵ)/Fe质量比的升高而降低.当溶液的pH为7.0,初始Cr(Ⅵ)/Fe质量比为0.025、0.050、0.075和0.100时,相应地Cr(Ⅵ)的去除率分别为100.0%、85.6%、72.7%和39.6%.酸性条件更有利于纳米零价铁对Cr(Ⅵ)的去除,当初始Cr(Ⅵ)/Fe质量比为0.100,溶液的pH为3.0、5.0、7.0、9.0和11.0时,体系中Cr(Ⅵ)的去除率分别为73.4%、57.6%、39.6%、44.1%和41.2%.纳米零价铁去除Cr(Ⅵ)的过程符合拟二级动力学方程.当溶液的pH为7.0,初始Cr(Ⅵ)/Fe质量比为0.025时,吸附速率常数(k)最大,为9.76×10-3g·(mg·min)-1.Cr2O2-7 吸附到纳米零价铁表面后被迅速地还原为Cr3+,生成的Cr3+ 与纳米零价铁表面的FeOOH结合生成Cr-Fe膜.而Cr-Fe膜将阻断电子在纳米零价铁与Cr2O2-7之间的传输,Cr(Ⅵ)得不到还原,从而纳米零价铁对Cr2O2-7的去除以吸附为主.
英文摘要
      Laboratory experiments and theoretical modeling studies were performed to investigate the mechanisms of Cr(Ⅵ) removal from deoxygenated simulated groundwater using nanoscale zero-valent iron,and to evaluate influencing factors and kinetics based on zeta potential,redox potential,ferrous concentrations,and the pe-pH diagram of Fe-Cr-H2O system. Experimental results demonstrate that the removal efficiency of Cr(Ⅵ) decreases with the increasing Cr(Ⅵ)/Fe mass ratio. When the Cr(Ⅵ)/Fe mass ratios are 0.025,0.050,0.075,and 0.100,the corresponding Cr(Ⅵ) removal rates are 100.0%,85.6%,72.7% and 39.6%,respectively. The Cr(Ⅵ) removal is favorable at acidic pH with fixed Cr(Ⅵ)/Fe mass ratio of 0.100. When pH are 3.0,5.0,7.0,9.0 and 11.0,the Cr(Ⅵ) removal rates are 73.4%,57.6%,39.6%,44.1%,and 41.2%,accordingly. The Cr(Ⅵ) removal follows the pseudo second-order kinetics. When pH is 7.0 and Cr(Ⅵ)/nZVI mass ratio is 0.025,the rate of Cr(Ⅵ) removal is the highest with rate constant at 9.76×10-3g·(mg·min)-1. The conversion from Cr2O2-7 to Cr3+ should be instantaneous when Cr2O2-7 is absorbed on the surface of Fe. The Cr(Ⅵ) was reduced to Cr(Ⅲ),which was subsequently incorporated into the FeOOH shell and formed a Cr-Fe film. The film once formed could further inhibit the electron transfer between Cr2O2-7 and Fe. Then Cr(V) removal was primary controlled by the adsorption process.

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