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在腐殖酸存在下,影响镍铁纳米颗粒对2,4-二氯苯酚脱氯的因素。

Factors influencing the dechlorination of 2,4-dichlorophenol by Ni-Fe nanoparticles in the presence of humic acid.

作者信息

Zhang Zhen, Cissoko Naman, Wo Jingjing, Xu Xinhua

机构信息

Department of Environmental Engineering, Zhejiang University, Hangzhou, People's Republic of China.

出版信息

J Hazard Mater. 2009 Jun 15;165(1-3):78-86. doi: 10.1016/j.jhazmat.2008.09.080. Epub 2008 Sep 27.

Abstract

The dechlorination of 2,4-dichlorophenol (2,4-DCP) by Ni-Fe nanoparticles in the presence of humic acid (HA) was investigated to understand the feasibility of using Ni-Fe for the in situ remediation of contaminated groundwater. 2,4-DCP was first adsorbed by Ni-Fe nanoparticles, then quickly reduced to o-chlorophenol (o-CP), p-chlorophenol (p-CP), and finally to phenol (P). However, the introduction of HA decreased the removal percentage of 2,4-DCP, as a result, the phenol production rates dropped from 86% (in the absence of HA) to 29% within 2h. Our data suggested that the dechlorination rate was dependent on a number of factors including Ni-Fe availability, Ni loading percentage over Fe, temperature, pH, and HA concentration. In particular, the removal percentage of 2,4-DCP was determined to be 100, 99, 95, 84 and 69%, for HA concentrations of 0, 5, 10, 30 and 40 mg L(-1), respectively. The kinetic calculations for the dechlorination of 2,4-DCP indicated that k values for 2,4-DCP dechlorination dropped from 0.14, 0.051, 0.039, 0.021 to 0.011 min(-1) with increasing concentrations of HA from 0, 5, 10, 30 to 40 mg L(-1).

摘要

研究了在腐殖酸(HA)存在下,镍铁纳米颗粒对2,4-二氯苯酚(2,4-DCP)的脱氯作用,以了解使用镍铁原位修复受污染地下水的可行性。2,4-DCP首先被镍铁纳米颗粒吸附,然后迅速还原为邻氯苯酚(o-CP)、对氯苯酚(p-CP),最终还原为苯酚(P)。然而,HA的引入降低了2,4-DCP的去除率,结果,苯酚生成率在2小时内从86%(无HA时)降至29%。我们的数据表明,脱氯速率取决于许多因素,包括镍铁的有效性、镍在铁上的负载百分比、温度、pH值和HA浓度。特别是,对于HA浓度分别为0、5、10、30和40 mg L(-1)的情况,2,4-DCP的去除率分别确定为100%、99%、95%、84%和69%。2,4-DCP脱氯的动力学计算表明,随着HA浓度从0、5、10、30增加到40 mg L(-1),2,4-DCP脱氯的k值从0.14、0.051、0.039、0.021降至0.011 min(-1)。

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