Carbon Nanotube Membrane Stack for Flow-through Sequential Regenerative Electro-Fenton

被引:219
|
作者
Gao, Guandao [1 ,2 ]
Zhang, Qiaoying [2 ]
Hao, Zhenwei [1 ]
Vecitis, Chad D. [2 ]
机构
[1] Nankai Univ, Coll Environm Sci & Engn, Tianjin Key Lab Environm Remediat & Pollut Contro, Key Lab Pollut Proc & Environm Criteria,Minist Ed, Tianjin 300071, Peoples R China
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
基金
芬兰科学院;
关键词
SOLAR PHOTOELECTRO-FENTON; RESPONSE-SURFACE METHODOLOGY; ADVANCED OXIDATION PROCESSES; OXYGEN REDUCTION REACTION; WASTE-WATER TREATMENT; HYDROGEN-PEROXIDE; AQUEOUS-MEDIUM; ACTIVE-SITES; FELT CATHODE; DEGRADATION;
D O I
10.1021/es505679e
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electro-Fenton is a promising advanced oxidation process for water treatment consisting a series redox reactions. Here, we design and examine an electrochemical filter for sequential electro-Fenton reactions to optimize the treatment process. The carbon nanotube (CNT) membrane stack (thickness similar to 200 mu m) used here consisted of 1) a CNT network cathode for O-2 reduction to H2O2, 2) a CNT-COOFe2+ cathode to chemical reduction H2O2 to OH and HO and to regenerate Fe2+ in situ, 3) a porous PVDF or PTFE insulating separator, and 4) a CNT filter anode for remaining intermediate oxidation intermediates. The sequential electro-Fenton was compared to individual electrochemical and Fenton process using oxalate, a persistent organic, as a target molecule. Synergism is observed during the sequential electro-Fenton process. For example, when [DO](in) = 38 +/- 1 mg L-1, J = 1.6 mL min(-1), neutral pH, and E-cell = 2.89 V, the sequential electro-Fenton oxidation rate was 206.8 +/- 6.3 mgC m(-2) h(-1), which is 4-fold greater than the sum of the individual electrochemistry (16.4 +/- 3.2 mgC m(-2) h(-1)) and Fenton (33.3 +/- 1.3 mgC m(-2) h(-1)) reaction fluxes, and the energy consumption was 45.8 kWh kgTOC(-)1. The sequential electro-Fenton was also challenged with the refractory trifluoroacetic acid (TFA) and trichloroacetic acid (TCA), and they can be transferred at a removal rate of 11.3 +/- 1.2 and 21.8 +/- 1.9 mmol m(-2) h(-1), respectively, with different transformation mechanisms.
引用
收藏
页码:2375 / 2383
页数:9
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