Photochemical oxidation of styrene in acetonitrile solution in presence of H2O2, TiO2/H2O2 and ZnO/H2O2

被引:18
作者
Lachheb, Hinda [1 ]
Guillar, Chantal [2 ]
Lassoued, Hayfa [1 ]
Haddaji, Marwa [1 ]
Rajah, Mariem [1 ]
Houas, Ammar [3 ]
机构
[1] Univ Gabes, Fac Sci GABES, Unite Rech Catalyse & Mat Environm & Proc URCMEP, Campus Univ Cite Erriadh, Gabes 6072, Tunisia
[2] Univ Claude Bernard Lyon 1, Univ Lyon, Inst Rech Catalyse & Environm LYON IRCELYON, CNRS,UMR 5256, 2 Ave Albert Einstein, F-69626 Villeurbanne, France
[3] Al IMAM Mohamed Ibn Saud Islamic Univ IMSIU, Coll Sci, Dept Chem, Riyadh 11623, Saudi Arabia
关键词
Photocatalytic synthesis; TiO2; ZnO; H2O2; Oxidation pathways; HYDROGEN-PEROXIDE; SELECTIVE EPOXIDATION; CATALYTIC-PROPERTIES; MECHANISM; OLEFINS;
D O I
10.1016/j.jphotochem.2017.06.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photochemical oxidation of styrene under UV-A irradiation in acetonitrile solution containing H2O2 was investigated in absence or in presence of TiO2 or ZnO. The effects of the molar ratio H2O2/styrene and of the pH on the disappearance rate and on the selectivity into benzaldehyde and benzene oxide were investigated. Under H202/UV, a conversion of about 6% and a total selectivity into benzaldehyde was observed. In presence of TiO2 the conversion is multiply by 2 and styrene oxide was detected. However, its selectivity is only 10%. At basic pH, in presence of TiO2 or ZnO, the conversion of styrene are 47% and 60% respectively. A similar selectivity of styrene oxide (50%) was found for the both catalysts. However, in presence of TiO2 benzoic acid is formed with a selectivity of 20% whereas only benzaldehyde was found on ZnO. The impact of the nature of the catalyst and of the active species generated under irradiation were suggested for explaining the difference of reactivity observed. A mechanism of the formation of benzaldehyde and styrene oxide in absence or presence of photocatalyst and of NaOH was proposed. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:462 / 469
页数:8
相关论文
共 42 条
[1]   THE PHOTOLYSIS OF HYDROGEN PEROXIDE AT HIGH LIGHT INTENSITIES [J].
BAXENDALE, JH ;
WILSON, JA .
TRANSACTIONS OF THE FARADAY SOCIETY, 1957, 53 (03) :344-356
[2]  
Bernas A., 1984, J PHYS CHEM C, V68, P8
[3]   ADSORPTION OF HYDROGEN-PEROXIDE ON SURFACE OF TITANIUM-DIOXIDE [J].
BOONSTRA, AH ;
MUTSAERS, CAHA .
JOURNAL OF PHYSICAL CHEMISTRY, 1975, 79 (18) :1940-1943
[4]   CRITICAL-REVIEW OF RATE CONSTANTS FOR REACTIONS OF HYDRATED ELECTRONS, HYDROGEN-ATOMS AND HYDROXYL RADICALS (.OH/.O-) IN AQUEOUS-SOLUTION [J].
BUXTON, GV ;
GREENSTOCK, CL ;
HELMAN, WP ;
ROSS, AB .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1988, 17 (02) :513-886
[5]   Selective epoxidation of cyclohexene to cyclohexene oxide catalyzed by Keggin-type heteropoly compounds using anhydrous urea-hydrogen peroxide as oxidizing reagent and acetonitrile as the solvent [J].
Ding, Y ;
Gao, Q ;
Li, GX ;
Zhang, HP ;
Wang, JM ;
Yan, L ;
Suo, JS .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 218 (02) :161-170
[6]   Synthesis and catalytic properties of a new titanosilicate molecular sieve with the structure analogous to MWW-type lamellar precursor [J].
Fan, Weibin ;
Wu, Peng ;
Namba, Seitaro ;
Tatsumi, Takashi .
JOURNAL OF CATALYSIS, 2006, 243 (01) :183-191
[7]  
FORMENTI M, 1970, CR ACAD SCI C CHIM, V270, P138
[8]   HETEROGENEOUS PHOTOCATALYSIS [J].
FOX, MA ;
DULAY, MT .
CHEMICAL REVIEWS, 1993, 93 (01) :341-357
[9]   MECHANISTIC FEATURES OF THE SEMICONDUCTOR PHOTOCATALYZED OLEFIN-TO-CARBONYL OXIDATIVE CLEAVAGE [J].
FOX, MA ;
CHEN, CC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1981, 103 (22) :6757-6759
[10]   Tunable catalytic properties of multi-metal-organic frameworks for aerobic styrene oxidation [J].
Fu, Yanghe ;
Xu, Lai ;
Shen, Huanmei ;
Yang, Huan ;
Zhang, Fumin ;
Zhu, Weidong ;
Fan, Maohong .
CHEMICAL ENGINEERING JOURNAL, 2016, 299 :135-141