Insights into electrochemical decomposition mechanism of lipopolysaccharide using TiO2 nanotubes arrays electrode

被引:17
作者
Wang, Kaixuan [1 ,2 ]
Li, Yang [2 ]
Huang, Junxiong [2 ]
Xu, Lei [1 ]
Yin, Lifeng [2 ]
Ji, Yangyuan [2 ]
Wang, Chong [2 ]
Xu, Zesheng [3 ]
Niu, Junfeng [1 ]
机构
[1] Dongguan Univ Technol, Res Ctr Ecoenvironm Engn, Dongguan 523808, Guangdong, Peoples R China
[2] Beijing Normal Univ, Sch Environm, Key Lab Water & Sediment Sci, State Key Lab Water Environm Simulat,Minist Educ, Beijing 100875, Peoples R China
[3] Chinese Acad Environm Planning, Beijing 100012, Peoples R China
基金
中国国家自然科学基金;
关键词
Lipopolysaccharide; TiO2; nanotubes arrays electrode; Toxicity; (OH)-O-center dot oxidation; Direct electron transfer; ENDOTOXIN EXPOSURE; ANODIC-OXIDATION; WATER TREATMENT; OUTER-MEMBRANE; DEGRADATION; REMOVAL; MINERALIZATION; TOXICITY; KINETICS; PHENOL;
D O I
10.1016/j.jhazmat.2020.122259
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Electrochemical decomposition of lipopolysaccharide (LPS) was firstly investigated over titania nanotubes (TNTs) arrays electrode. The TNTs layer of this electrode consisted of numerous tubular structures which arranged tightly, and the average diameter of each nanotube is 100 +/- 5 nm. The degradation of LPS and poly-saccharides followed pseudo-first-order kinetics. The optimal LPS removal ratio was nearly 800/0. The endotoxin toxicity of LPS steadily decreased during the electrolysis process. The acute toxicity of the intermediates increased suddenly at the beginning of electrochemical degradation process ( < 5 min), then maintained high inhibition ratio ( > 95 %) for about 150 min, and decreased significantly ( < 10 %) after electrolysis for 240 min. After 20 min of electrolysis, LPS with molecular weight of 116,854 Da was transformed into small molecular compounds with molecular weights of 59,312 - 12,209 Da. Possible degradation and detoxification mechanisms of LPS including electric-field-force-driving accumulation, adsorption and direct electron transfer on TNTs arrays electrode, and center dot OH oxidation were proposed. This study underscores that electrochemical technique can be applied to eliminate and decrease the toxicity of LPS from contaminated water.
引用
收藏
页数:10
相关论文
共 77 条
[1]   Endotoxin inactivation in water by using medium-pressure [J].
Anderson, WB ;
Huck, PM ;
Dixon, DG ;
Mayfield, CL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2003, 69 (05) :3002-3004
[2]   Endotoxin removal by affinity sorbents [J].
Anspach, FB .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2001, 49 (1-3) :665-681
[3]   Electrocatalytic degradation of phenol on Pt- and Ru-doped Ti/SnO2-Sb anodes in an alkaline medium [J].
Berenguer, R. ;
Sieben, J. M. ;
Quijada, C. ;
Morallon, E. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2016, 199 :394-404
[4]   DETECTION OF ENDOTOXINS IN RECLAIMED AND CONVENTIONALLY TREATED DRINKING-WATER [J].
BURGER, JS ;
GRABOW, WOK ;
KFIR, R .
WATER RESEARCH, 1989, 23 (06) :733-738
[5]   Structure of bacterial lipopolysaccharides [J].
Caroff, M ;
Karibian, D .
CARBOHYDRATE RESEARCH, 2003, 338 (23) :2431-2447
[6]   Oxidative destruction of perfluorooctane sulfonate using boron-doped diamond film electrodes [J].
Carter, Kimberly E. ;
Farrell, James .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2008, 42 (16) :6111-6115
[7]   Electrocatalytic Enhancement of Salicylic Acid Oxidation at Electrochemically Reduced TiO2 Nanotubes [J].
Chang, Xin ;
Thind, Sapanbir S. ;
Chen, Aicheng .
ACS CATALYSIS, 2014, 4 (08) :2616-2622
[8]   Electrochemical oxidation of model compounds and olive mill wastewater over DSA electrodes: 1. The case of Ti/IrO2 anode [J].
Chatzisymeon, E. ;
Dimou, A. ;
Mantzavinos, D. ;
Katsaounis, A. .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 167 (1-3) :268-274
[9]   Formate, an active intermediate for direct oxidation of methanol on Pt electrode [J].
Chen, YX ;
Miki, A ;
Ye, S ;
Sakai, H ;
Osawa, M .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (13) :3680-3681
[10]   ANODIC-OXIDATION OF PHENOL FOR WASTE-WATER TREATMENT [J].
COMNINELLIS, C ;
PULGARIN, C .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 1991, 21 (08) :703-708