Simultaneous Adsorption and Electrochemical Reduction of N-Nitrosodimethylamine Using Carbon-Ti4O7 Composite Reactive Electrochemical Membranes

被引:65
|
作者
Almassi, Soroush [1 ]
Li, Zhao [2 ]
Xu, Wenqing [2 ]
Pu, Changcheng [3 ]
Zeng, Teng [3 ]
Chaplin, Brian P. [1 ]
机构
[1] Univ Illinois, Dept Chem Engn, 810 S Clinton St, Chicago, IL 60607 USA
[2] Villanova Univ, Dept Civil & Environm Engn, 800 E Lancaster Ave, Villanova, PA 19085 USA
[3] Syracuse Univ, Dept Civil & Environm Engn, 151 Link Hall, Syracuse, NY 13244 USA
基金
美国国家科学基金会;
关键词
NICKEL-ENHANCED IRON; REVERSE-OSMOSIS; CATALYZED REDUCTION; UV/H2O2; TREATMENT; GRANULAR IRON; NDMA; WATER; KINETICS; ENERGY; DIMETHYLNITROSAMINE;
D O I
10.1021/acs.est.8b05933
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study focused on synthesis and characterization of Ti4O7 reactive electrochemical membranes (REMs) amended with powder-activated carbon (PAC) or multiwalled carbon nanotubes (MWCNTs). These composite REMs were evaluated for simultaneous adsorption and electrochemical reduction of N-nitrosodimethylamine (NDMA). The carbon-Ti4O7 composite REMs had high electrical conductivities (1832 to 2991 S m(-1)), where carbon and Ti4O7 were in direct electrical contact. Addition of carbonaceous materials increased the residence times of NDMA in the REMs by a factor of 3.8 to 5.4 and therefore allowed for significant electrochemical NDMA reduction. The treatment of synthetic solutions containing 10 mu M NDMA achieved >4-log NDMA removal in a single pass (liquid residence time of 11 to 22 s) through the PAC-REM and MWCNT-REM with the application of a -1.1 V/SHE cathodic potential, with permeate concentrations between 18 and 80 ng L-1. The treatment of a 6.7 nM NDMA-spiked surface water sample, under similar operating conditions (liquid residence time of 22 s), achieved 92 to 97% removal with permeate concentrations between 16 and 40 ng L-1. Density functional theory calculations determined a probable reaction mechanism for NDMA reduction, where the rate-limiting step was a direct electron transfer reaction.
引用
收藏
页码:928 / 937
页数:10
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