期刊文献+

水溶液中异喹啉与羟基的作用机理 被引量:1

The Reaction Mechanism Studies on Isoquinoline with Hydroxyl Radical in Aqueous Solution
原文传递
导出
摘要 利用脉冲辐解技术对异喹啉水溶液与羟基的作用机理进行了详细研究,对其瞬态吸收峰进行了归属,初步考察了这些瞬态粒子的生成和衰减行为.研究表明,.OH与异喹啉在中性和碱性条件下反应生成羟基加合物,生成速率常数分别为3.4×109和6.6×109mol-1.dm3.s-1.在酸性条件下异喹啉先被质子化,再与羟基发生加成反应,反应速率常数为3.9×109mol-1.dm3.s-1,这为异喹啉的氧化降解提供了理论基础. The reaction mechanism between isoquinoline and()~·OH radical in aqueous dilute solutions under different conditions was studied by pulse radiolysis.The main characteristic peaks in these transient absorption spectra were attributed and the growth-decay trends of several transient species were investigated.Under neutral or alkaline conditions,the reaction of()~·OH radical and isoquinoline produces OH-adducts with respective rate constant of 3.4×10~9 and 6.6×10~9 mol^(-1)·dm^3·s^(-1) while under acidic condi...
出处 《复旦学报(自然科学版)》 CAS CSCD 北大核心 2006年第6期774-778,共5页 Journal of Fudan University:Natural Science
基金 国家自然科学基金资助项目(50572074)
关键词 异喹啉 脉冲辐解 瞬态吸收光谱 羟基 isoquinoline pulse radiolysis transient absorption spectra hydroxyl radical
  • 相关文献

参考文献18

  • 1[1]Hirao K,Shinohara Y,Tsuda H,et al.Hyperprolactinemia and steroid metabolism by rat mammary adenocarcinomas[J].Cancer Res,1976,36:329-335.
  • 2[2]Nagao M,Yahagi T,Seino Y,et al.Mutagenicities of quinoline and its derivatives[J].Mutat.Res,1977,42:335-342.
  • 3[3]Willems M I,Dubois G,Boyd D R,et al.Comparison of the mutagenicity of quinoline and all monohydroxyquinolines with a series of arene oxide,trans-dihydrodiol,diol epoxide,N-oxide and arene hydrate derivatives of quinoline in the Ames/Salmonella microsome test[J].Mutat Res,1992,278:227-236.
  • 4[4]Warshawsky D.Environmental sources,carcinogenicity,mutagenicity,metabolism and DNA binding of nitrogen and sulfur heterocyclic aromatics[J].Environ Carcinog Ecotoxicol Rev,1992,10:1-71.
  • 5[5]Hecht S S.Tobacco smoke carcinogens and breast cancer[J].Environ Mol Mutagen,2002,39:119-126.
  • 6[6]Asakura S,Sawada S,Sughihara T.Quinoline-induced chromosome aberrations and sister chromatid exchanges in rat liver[J].Environ Mol Mutagen,1997,30:459-467.
  • 7[7]Capel P D,Larson S J.Effect of Scale on the Behavior of Atrazine in Surface Waters[J].Environ Sci Technol,2001,35:648-657.
  • 8[8]Kolpin D W,Thurman E M,Linhart S M.Occurrence of cyanazine compounds in groundwater:degradates more prevalent than the parent compound[J].Environ Sci Technol,2001,35:1217-1222.
  • 9[9]Johansen S S,Hansen A B,Mosbaek H,et al.Identification of heteroaromatic and other organic compounds in ground water at creosote-contaminated sites in Denmark[J].Groundwater Monit Rem,1997,17:106-115.
  • 10[10]Li Yongmei,Gu Guowei,Zhao Jianfu,et al.Anoxic degradation of nitrogenous heterocyclic compounds by acclimated activated sludge[J].Process Biochemistry,2001,37:81-86.

二级参考文献21

  • 1李咏梅,顾国维,赵建夫.厌氧酸化-缺氧-好氧生物膜法处理焦化废水的研究[J].上海环境科学,2000,19(z1):63-66. 被引量:13
  • 2[1]Sims G K, Sommers L E, Konopka A. Degradation of pyridine by Micrococcus lutens isolated from soil. Appl Enviro Microbiol, 1986, 51(5): 963~968.
  • 3[3]Aislabie J, Bej A, Hurst H, et al. Microbial degradtionof quinoline and methylquinolines. Appl Environ Microb, 1990, 56: 345~351.
  • 4Foth H, Walther U I, Kahl G F. Taxicology and Applied Pharmacology, 1990, 105: 382.
  • 5SvenssonCK. Clin Pharmacokinet, 1987, 12: 30.
  • 6Palmer K J. Drugs, 1992, 44: 498.
  • 7Sherwood N. Psychopharmacology , 1992, 108: 432.
  • 8Pritchard W S. Psychophysiology, 1995, 32 : 19.
  • 9Benowim N L. J pharmacol Exp. Ther., 1982, 221: 368.
  • 10Benowltz N L. Clin Pharmacol Ther., 1984, 36: 74.

共引文献57

同被引文献16

  • 1ZhangRan(张冉).Heterogeneous catalytic ozonation process tbradvanced treatment of coal chemical wastewater [D]. Harbin: Harbin Institute of Technology, 2011.
  • 2Rameshraja D, Srivastava V C, Kushwaha J P, Mall I N. Quinoline adsorption onto granular activated carbon and bagasse fly ash [J]. Chemical Engineering Journal, 2012, 181/182:343-351.
  • 3Tuo Banhua, Yan Jiabao, Fan Ban'an, Yang Zhongbua, Liu Jianzhong. Biodegradation characteristics and bioaugmentation potential of a novel quinoline-degrading strain of Bacillus sp. isolated from petroleum-eontaminated soil [J]. Bioresource Technology, 2012, 107: 55-60.
  • 4Thomsen A B, Laturnus F, Hazard M. The influence of different soil constituents on the reaction kinetics of wet oxidation on of creosote compound quinoline [J]. Journal of Hazardous Materials, 2001, 81 (1/2): 193-203.
  • 5Jing Jieying, Li Wenying, Boyd A, Zhang Yu, Colvin V L, Yu W W. Photocatalytic degradation of quinoline in aqueous TiO2 suspension [J]. Journal of Hazardous Materials, 2012, 237/238:247-255.
  • 6Subbaramaiah V, Srivastav V C, Mall I D. Catalytic wet peroxidation of pyridine bearing wastewater by cerium supported SBA-15 [J]. Journal of Hazardous Materials, 2013, 247/248:355-363.
  • 7Munoza M, Pedro Z M, Menendez N, et al. A ferromagnetic 7-alumina-supported iron catalyst for CWPO application to chlorophenols [J]. Applied Catalysis B: Environmental, 2013, 136/137 218-224.
  • 8Inchaurrondo N S, Massa P, Fenoglio R, et aL Efficient catalytic wet peroxide oxidation of phenol at moderate temperature using a high-load supported copper catalyst [J]. Chemical Engineering Journal, 2012: 198/199:426-434.
  • 9Suranjana V Mayani, Vishal J Mayani, Sang Wook Kim. Catalytic oxidation of phenol analogues in aqueous medium over Fe/SBA-15 [J]. Chem. Soc., 2012, 33 (9): 3009-3016.
  • 10Kondru A K, Kumar P, Chand S. Catalytic wet peroxide oxidation of azo dye (Congo red) using modified Y zeolite as catalyst [J]. Journal of Hazardous Materials, 2009, 166:342-347.

引证文献1

二级引证文献11

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