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利用瞬态吸收光谱技术研究水体中苯与亚硝酸的交叉反应机理 被引量:12

Study on the Cross-Reaction Mechanism of Aqueous Benzene with Nitrous Acid in Dilute Solutions by Transient Absorption Spectrum Technique
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摘要 利用瞬态吸收光谱技术进行了有氧、无氧条件下苯与亚硝酸水溶液复相体系的交叉反应机理研究 ,初步考察了这些瞬态物种的生长与衰减等行为 ;并对其光解产物进行了GC/MS分析 .研究表明 ,HNO2 在 3 5 5nm紫外光的照射下可产生·OH和NO+ ,·OH自由基和苯反应生成C6H6 OHadduct ,反应速率常数为 8 9× 10 9L·mol-1·s-1,在有氧条件下C6H6 OHadduct进一步氧化为C6H6 OHO2 ,反应速率常数 3 3× 10 8L·mol-1·s-1;NO+ 自由基和苯作用形成C6H6 NO+ πcomplex 。 The cross-reaction microscopic mechanism of aqueous benzene with nitrous acid in the presence of O-2 or absence of O-2 in dilute solutions was studied by laser flash photolysis. The main characteristic peaks in these transient absorption spectra were attributed and the build-up/decay trends of several transient species were investigated. (.) OH radical and nitrosonium. cation (NO+) can be produced in aqueous solution of nitrous acid exposed to 355 nm laser beam. NO+ reacts with benzene to produce C6H6-NO+ pi complex. The rate constant of the reaction between (.) OH radical and benzene was measured to be 8.9 x 10(9) L (.) mol(-1) (.) s(-1). The transient product C6H6-OH adduct reacts with O-2 to form C6H6-OHO2 with the rate constant of 3.3 x 10(8) L (.) mol(-1) (.) s(-1). The final photolysis products were analyzed by using GUMS method and the possible reaction pathways were also discussed.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2004年第12期1115-1122,MJ02,共9页 Acta Chimica Sinica
基金 上海市科技发展基金 (No.0 2 2 31 2 1 1 6)资助项目
关键词 瞬态吸收光谱技术 水体污染 亚硝酸 交叉反应机理 反应速率常数 激光闪光光解 laser flash photolysis benzene nitrous acid transient absorption spectrum free radical
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  • 1[4]Michael, B. D.; Hart, E. J. J. Phys. Chem. 1970, 98(15), 2878.
  • 2[5]Treinin, A.; Hayon, E. A. J. Am. Chem. Soc. 1970, 92(20), 821.
  • 3[6]Cox, R. A. J. Photochemistry. 1974, 3, 175.
  • 4[7]Gordon, S.; Schmidt, K. H.; Hart, E. J. J. Phys. Chem. 1977, 81(2), 104.
  • 5[8]Marketons, D. G. Radiolysis J. Phys. Chem. 1974, 78(20), 1987.
  • 6[9]Mantake, A.; Marketons, D. G.; Stein, G. J. Phys. Chem. 1971, 75(25), 3886.
  • 7[10]Ashton, L.; Buxton, G. V.; Stuart, C. R. J. Chem. Soc., Faraday Trans. 1995, 91, 1631.
  • 8[11]Kochany, J.; Bolton, J. R. Environ. Sci. Technol. 1992, 26, 262.
  • 9[12]Bansal, K. M.; Patterson, L. K.; Fendler, E. J.; Fendler, J. H. Int. J. Radiat. Phys. Chem. 1971, 3, 321.
  • 10[13]Ashton, L.; Buxton, G. V.; Stuart, C. R. J. Chem. Soc., Faraday Trans. 1995, 91, 1631.

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