Excellent performance of cobalt-impregnated activated carbon in peroxymonosulfate activation for acid orange 7 oxidation

被引:0
作者
Tianyin Huang
Jiabin Chen
Zhongming Wang
Xin Guo
John C. Crittenden
机构
[1] Suzhou University of Science and Technology,School of Environmental Science and Engineering
[2] Georgia Institute of Technology,Brook Byers Institute for Sustainable Systems and the School of Civil and Environmental Engineering
来源
Environmental Science and Pollution Research | 2017年 / 24卷
关键词
Peroxymonosulfate; Orange acid 7; Activated carbon; Cobalt; Chloride;
D O I
暂无
中图分类号
学科分类号
摘要
Cobalt-impregnated activated carbon (GAC/Co) was used to produce sulfate radical (SO4·−) from peroxymonosulfate (PMS) in aqueous solution (hereafter called PMS activation). We evaluated its effectiveness by examining the degradation of orange acid 7 (AO7). GAC/Co exhibited high activity to activate PMS to degrade AO7. The degradation efficiency of AO7 increased with increasing dosage of GAC/Co or PMS and elevated temperatures. pH 8 was most favorable for the degradation of AO7 by GAC/Co-activated PMS. The radical quenching experiments indicated that the reactions most likely took place both in the bulk solution and on the surface of GAC/Co. We found that SO4·− played a dominant role in AO7 degradation. Sodium chloride (NaCl) which presents in most dye wastewater had a significant impact on AO7 degradation. Low dosages (<0.4 M) of NaCl showed a slight inhibitory effect, whereas high dosages (0.8 M) increased the reaction rate. HOCl was confirmed as the main contributor for accelerating AO7 degradation with high concentration of NaCl. In a continuous-flow reaction with an empty-bed contact time of 1.35 min, AO7 was not detected in the effluent for 0 to 18.72 L of treated influent volume (156 h) and 85% removal efficiency was still observed after 40.32 L of treated volume (336 h). Finally, the azo bond and the naphthalene structure in AO7 were destroyed and the degradation pathway was proposed.
引用
收藏
页码:9651 / 9661
页数:10
相关论文
共 271 条
[1]  
Ahn YY(2016)Activation of peroxymonosulfate by surface-loaded noble metal nanoparticles for oxidative degradation of organic compounds Environ Sci Technol 50 10187-10197
[2]  
Yun ET(2004)Radical generation by the interaction of transition metals with common oxidants Environ Sci Technol 38 3705-3712
[3]  
Seo JW(2006)Cobalt-mediated activation of peroxymonosulfate and sulfate radical attack on phenolic compounds. Implications of chloride ions Environ Sci Technol 40 1000-1007
[4]  
Lee C(2010)Degradation of microcystin-LR using sulfate radicals generated through photolysis, thermolysis and e Appl Catal B Environ 96 290-298
[5]  
Kim SH(2006) transfer mechanisms J Hazard Mater 133 167-171
[6]  
Kim JH(2013)Effects of gap size and UV dosage on decolorization of C.I. Acid Orange 7 by UV/H2O2 process Water Res 47 6234-6243
[7]  
Lee J(2001)Electro-peroxone treatment of Orange II dye wastewater J Photoch Photobio A 140 87-92
[8]  
Anipsitakis GP(2015)Photooxidation of an azo dye induced by visible light incident on the surface of TiO2 Appl Catal B Environ 166 603-643
[9]  
Dioniou DD(2014)Decontamination of wastewaters containing synthetic organic dyes by electrochemical methods. An updated review J Environ Sci 26 1267-1273
[10]  
Anipsitakis GP(2014)Ultrasound enhanced heterogeneous activation of peroxydisulfate by bimetallic Fe-Co/GAC catalyst for the degradation of acid Orange 7 in water Water Res 66 473-485