Degradation of PCE, TCE and 1,1,1-TCA by nanosized FePd bimetallic particles under various experimental conditions

被引：57

作者：

Cho, Yunchul ^{[1
]}

Choi, Sang-Il ^{[1
]}

机构：

[1] Kwangwoon Univ, Dept Environm Engn, Seoul 139701, South Korea

来源：

CHEMOSPHERE | 2010年 / 81卷 / 07期

关键词：

FePd bimetallic nanoparticles; Chlorinated organic compounds; Groundwater remediation; Zero valent iron; ZERO-VALENT IRON; PD NANOPARTICLES; KINETICS; DECHLORINATION; WATER; ULTRASOUND; REDUCTION; MECHANISM; PATHWAYS; AQUIFER;

D O I：

10.1016/j.chemosphere.2010.07.054

中图分类号：

X [环境科学、安全科学];

学科分类号：

08 ; 0830 ;

摘要：

The degradation of chlorinated organic compounds such as PCE (tetrachloroethene) TCE (trichloroethene) and 1 1 1-TCA (1 1 1-trichloroethane) was conducted using nanosized FePd bimetallic particles In order to enhance the reactivity of ZVI (zero valent iron) nanoparticles surface modification of ZVI nano particles was performed using Pd and CMC (carboxymethyl cellulose) The surface modification was found to form CMC-stabilized FePd bimetallic nanoparticles (CMC-FePd) The average TCE removal efficiency by the CMC-FePd was significantly Increased by similar to 85% compared to employing conventional ZVI nanoparticles (similar to 15%) This increase in the TCE removal efficiency was most likely due to the increased amount of atomic hydrogen produced by the formation of CMC-FePd For PCE and 1 1 1-TCA the removal efficiencies by CMC-FePd were approximately 80% and 56% respectively For all three chlorinated organic compounds the amount of Cl(-) ions in the aqueous phase during the degradation increased with increasing reaction time This result suggests that the main degradation mechanism of the chlorinated compounds by CMC-FePd was reductive dechlormation (C) 2010 Elsevier Ltd All rights reserved

引用

页码：940 / 945

页数：6

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