Decomposition of N-nitrosamines formed in CO2 capture systems through electrochemically-mediated reduction on carbon xerogel electrode

被引:7
|
作者
Thompson, Jesse G. [1 ,2 ]
Gao, Xin [1 ]
Toma, Shino [1 ]
Abad, Keemia [1 ]
Bhatnagar, Saloni [1 ]
Landon, James [1 ]
Liu, Kunlei [1 ,3 ]
机构
[1] Univ Kentucky, Ctr Appl Energy Res, 3572 Iron Works Pike, Lexington, KY 40511 USA
[2] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[3] Univ Kentucky, Dept Mech Engn, Lexington, KY 40506 USA
关键词
CO2; capture; N-nitrosamine; Electrochemical reduction; Carbon xerogel electrode; Amine CCS waterwash; DISINFECTION BY-PRODUCTS; WATER TREATMENT PLANTS; WASTE-WATER; CAPACITIVE DEIONIZATION; DIOXIDE CAPTURE; RISK-ASSESSMENT; PILOT-SCALE; NITRAMINES; DEGRADATION; AMINES;
D O I
10.1016/j.ijggc.2019.02.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
N-nitrosamines, as a class of compounds, have been reported to be mutagenic, cytotoxic, genotoxic and carcinogenic. N-nitrosamine formation and emission are a major concern for amine-based CO2 capture systems. A process using a stationary carbon electrode inside an electrochemical cell was developed and tested in this study to adsorb and decompose two N-nitrosamines, N-nitrosopyrrolidine and N-nitrosodiethylamine, from an aqueous amine solution. The carbon xerogel electrode material has a high N-nitrosamine adsorption capacity and can initiate an electrochemically-mediated reduction of N-nitrosamines to a secondary amine. A greater than 80% reduction of N-nitrosodiethylamine and 90% of N-nitrosopyrrolidine was observed from a simulated amine-based waterwash solution using an applied current up to 300 mA. N-nitrosamine decomposition was effective in solutions with relatively high amine or salt concentrations.
引用
收藏
页码:83 / 90
页数:8
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