期刊文献+

二氧化氯和臭氧对吉非贝齐的降解机制 被引量:1

Degradation mechanism of gemfibrozil by chlorine dioxide and ozone
下载PDF
导出
摘要 吉非贝齐(GFRZ)为常见的脂质调节剂,广泛应用于高血脂病患的治疗.GFRZ对水生生物存在内分泌干扰活性,由其造成的潜在生态环境风险备受关注.本文研究了二氧化氯(ClO2)和臭氧(O3)体系中GFRZ的降解机制及影响因素.结果表明,ClO2及O3均可有效去除水中的GFRZ,氧化剂浓度、温度、pH值及腐殖酸均影响GFRZ的降解过程;增加ClO2投加量可显著提高GFRZ的去除率(P<0.01);提高温度可促进ClO2体系中GFRZ的降解,而O3体系中,温度升高使O3的浓度降低,GFRZ的去除率降低;酸性及中性条件下GFRZ在ClO2体系中的降解效果优于碱性条件,而在O3体系中,随着pH值升高(pH=3—11),GFRZ的去除率呈先增加后减小的趋势;反应体系中的腐殖酸与GFRZ竞争氧化性基团,从而抑制GFRZ的降解过程(P<0.05).在ClO2及O3体系中,在氧化性基团的作用下,GFRZ分子的支链首先断开,继而被进一步氧化,发生开环及断键,生成小分子有机酸. Gemfibrozil(GFRZ),a common lipid regulator,is widely used in the treatment of hyperlipidemia.The potential ecological risk caused by GFRZ has attracted much attention because of its endocrine disruptive activity to aquatic organisms.The degradation mechanism and influencing factors of GFRZ in chlorine dioxide(ClO2)and ozone(O3)systems were studied.The results showed that GFRZ was removed effectively by ClO2 and O3 from water.The degradation process of GFRZ was affected by factors such as oxidant concentration,temperature,pH value and humic acid.The removal rate of GFRZ was significantly increased by increasing ClO2 dosage(P<0.01).In ClO2 system,the degradation of GFRZ was promoted by temperature increasing,while in O3 system,the concentration of O3 decreased with temperature increasing,which reduced the removal of GFRZ.Under acidic and neutral conditions,the degradation effect of GFRZ in ClO2 system was better than that in alkaline condition.While in O3 system,the removal rate of GFRZ increased first and then decreased when pH value increased from 3 to 11.And humic acid in the reaction system competed with GFRZ for oxidizing groups,which inhibited the degradation of GFRZ(P<0.05).In ClO2 and O3 systems,the branched chain of GFRZ molecule was first broken by oxidizing groups,and then further oxidized to open and break bonds,resulting in the formation of small molecular organic acids.
作者 乔子杰 曹飞 吴道琦 袁守军 王伟 胡真虎 QIAO Zijie;CAO Fei;WU Daoqi;YUAN Shoujun;WANG Wei;HU Zhenhu(School of Civil Engineering,Hefei University of Technology,Hefei,230009,China;State Grid Bengbu Electric Power Supply Company,Bengbu,233000,China)
出处 《环境化学》 CAS CSCD 北大核心 2020年第9期2551-2558,共8页 Environmental Chemistry
基金 国家自然科学基金(51578205) 中国科学院大学生创新实践训练计划(20194000134)资助
关键词 吉非贝齐 二氧化氯 臭氧 影响因素 降解机制 gemfibrozil chlorine dioxide ozone influencing factor degradation mechanism
  • 相关文献

参考文献4

二级参考文献52

  • 1黄超云,程江,文秀芳,戴松林.停流光谱法测定臭氧化快速反应动力学参数[J].仪器仪表学报,2003,24(z2):60-61. 被引量:3
  • 2LIU Jinquan1, HUANG Junli1, SU Liqiang2, CAO Xiangyu1 & JI Ying1 1. School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin 150090, China,2. School of Chemistry and Chemical Engineering, Qiqihar University, Qiqihar 161006, China.Degradation of anthracene, pyrene and benzo[a]-anthracene in aqueous solution by chlorine dioxide[J].Science China Chemistry,2006,49(6):565-572. 被引量:7
  • 3黄翔峰,吴志超,王荣生.硫代硫酸钠脱氯特性及其动力学分析[J].中国给水排水,2006,22(1):36-40. 被引量:8
  • 4季颖,赵吉娜,黄君礼,苏立强,崔崇威,付娇.ClO_2对微囊藻毒素(LR)的去除效果和反应特征[J].哈尔滨工业大学学报,2006,38(10):1806-1808. 被引量:4
  • 5Acero J L, Stemmler K, Von Gunten U. 2000. Degradation kinetics of atrazine and its degradation products with ozone and OH radicals: a predictive tool for drinking water treatment [ J ]. Environmental Science & Technology, 34 (4): 591-597.
  • 6Anipsitakis G P, Dionysiou D D. 2004. Radical generation by the interaction of transition metals with common oxidants [ J ]. Environmental Science & Technology, 38 (13): 3705-3712.
  • 7Antoniou M G, Armah A, Dionysiou D D. 2010. Degradation of microcystin-LR using sulfate radicals generated through photolysis, thermolysis and e- transfer mechanisms [ J ]. Applied Catalysis B : Environmental, 96 (3): 290-298.
  • 8Araujo L, Villa N, Camargo N, et al. 2011. Persistence of gemfibrozil, naproxen and mefenamic acid in natural waters [ J ]. Environmental Chemistry Letters, 9 (1) : 13-18.
  • 9Bendz D, Paxeus N A, Ginn T R, et al. 2005. Occurrence and fate of pharmaceutically active compounds in the environment, a case study: H6je River in Sweden [ J ]. Journal of Hazardous Materials, 122 (3) : 195-204.
  • 10Bennedsen L R, Muff J, Sogaard E G.2012. Influence of chloride and carbonates on the reactivity of activated persulfate [ J ]. Chemosphere, 86(11) : 1092-1097.

共引文献19

同被引文献15

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部