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紫外/过硫酸盐降解水中对氨基苯甲酸的研究 被引量:2

Degradation of p-Aminobenzoic Acid in Water by UV/Persulfate Process
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摘要 采用紫外/过硫酸盐催化氧化工艺去除水中污染物对氨基苯甲酸(PABA),分析了过硫酸盐(PDS)投加量、溶液中不同阴离子、腐植酸(HA)投加量、不同pH以及不同真实水样等多种因素对该工艺的影响。结果表明,紫外/过硫酸盐工艺能有效去除PABA,去除率可达到99%。实验条件下,PABA去除率随着PDS投加量的增加而增大;反应过程中SO_4^-·对目标污染物的去除起主要作用,溶液pH和不同离子对PABA去除效果影响不大,而HA对PABA降解具有抑制作用。并且,紫外/过硫酸盐工艺对于真实PABA水样的处理也有很好的去除效果。 The UV/persulfate process was used to remove para-aminobenzoic acid(PABA).The effects of several factors such as dosage of persulfate(PDS),different anions in the solution,dosage of humic acid,different pH and different real water samples on PABA removal were investigated.The results show that the PABA removal efficiency could be significantly improved through the combination of the UV process and the PDS process.Under the experimental conditions,the removal rate of PABA increased with the increase of PDS dosage;pH and different ions had little effect on the final removal rate of PABA,while HA had inhibitory effect on PABA removal.Free radical quenching experiments shows that SO4^-·plays a major role in the removal of the target contaminants during the reaction.Moreover,the UV/persulfate process is also very practical for the treatment of real PABA water samples.
作者 吴强 陈建挺 郭黎 施德剑 林驰浩 翟志才 Wu Qiang;Chen Jian-ting;Guo Li;Shi De-jian;Lin Chi-hao;Zhai Zhi-cai(College of Biological,Chemical Sciences and Engineering,Jiaxing University,Zhejiang Jiaxing 314001;Jiaxing Environmental Protection Monitoring Station,Zhejiang Jiaxing 314001)
出处 《生物化工》 2019年第1期83-86,共4页 Biological Chemical Engineering
基金 国家自然科学基金资助项目(21607058) 浙江省教育厅一般科研项目(Y201840526) 嘉兴市皮革和纺织品染整清洁生产创新团队开放基金项目(JXLD2016-08) 嘉兴学院2018年度校级重点SRT计划项目(85178433)
关键词 对氨基苯甲酸 紫外 过硫酸盐 去除效率 Para-aminobenzoic acid (PABA) Ultraviolet Persulfate (PDS) Removal efficiency
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  • 1Hirsch R, Temes T, Habereer K, et al. Occurrence of antibiotics in the aquatic environment [J]. Science of the Total Environment, 1999,225( 1/2): 109-118.
  • 2Sallustio B, Harkin L, Mann M, et al. Genotoxicity of acyl glueurodine metabolites formed from clofibrie acid and gemfibrozil: a novel role for phase II-mediated bioactivation in the hepatocarcinogenicity of the parent aglyeones [J]. Toxicology and Applied Pharmacology, 1997,147(2):459-464.
  • 3Liang C, Lee I L, Hsu I Y, et al. Persulfate oxidation of triehloroethylene with and without iron activation in porous media [J]. Chemosphere, 2008,70(3):426-435.
  • 4Liang C J, Bruell C, Marley M C, et al. Thermally activated persulfate oxidation of trichloroethylene (TCE) and 1, 1, 1-trichloroethane (TCA) in aqueous systems and soil slurries [J]. Soil & Sediment Contamination, 2003,12(2):207-228.
  • 5Tan C Q, Gao N Y, Deng Y, et al. Heat-activated persulfate oxidation of diuron in water [J]. Chemical Engineering Journal, 2012,203 (5):294-300.
  • 6Gu X, Lu S, Qiu Z, et al. Photodegradation performance of 1, I, 1-triehloroethane in aqueous solution: In the presence and absence of persulfate [J]. Chemical Engineering Journal, 2013,215-216(3):29-35.
  • 7Gao Y, Gao N, Deng Y, et al. Ultraviolet (UV) light-activated persulfate oxidation of sulfamethazine in water [J]. Chemical Engineering Journal, 2012,195-196:248-253.
  • 8Tan C Q, Gao N Y, Deng Y, et al. Comparison of antipyrine degradation by UV, UV/H202 and UV/Persulfate [J]. Journal of Hazardous Materials, 2013,260:1008-1016.
  • 9Hori H, Yamamoto A, Hayakawa E, et al. Efficient decomposition of environmentally persistent perfluorocarboxylic acids by use of persulfate as a photochemical oxidant [J]. Environmental Science & Technololgy, 2005,39(7):2383-2388.
  • 10Furman O S, Teel A L, Watts R J. Mechanism of base activation of persulfate [J]. Environment Science & Technology, 2010, 44(16):6423-6428.

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