Activities for phenol formation using Cu catalysts supported on Al2O3 in the liquid-phase oxidation of benzene in aqueous solvent with high acetic acid concentration

被引:55
作者
Kanzaki, H
Kitamura, T
Hamada, R
Nishiyama, S
Tsuruya, S [1 ]
机构
[1] Kobe Univ, Fac Engn, Dept Sci & Chem Engn, Kobe, Hyogo 6578501, Japan
[2] Kobe Univ, Grad Sch Sci & Technol, Div Mol Sci, Kobe, Hyogo 6578501, Japan
关键词
copper catalyst supported on Al2O3; oxidation; benzene; phenol; oxygen; ascorbic acid; acetic acid;
D O I
10.1016/S1381-1169(03)00516-8
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 liquid-phase oxidation of benzene to phenol using a Cu catalyst supported on Al2O3 was studied at 303 K in an aqueous solvent with a variety of concentrations of acetic acid. Gaseous O-2 and ascorbic acid were utilized as an oxidant and a reducing reagent, respectively. An aqueous solvent with more than around 70-80 vol.% acetic acid concentration was confirmed to cause a sharp apparent decrease in the Cu leaching from a Cu catalyst (Cu/Al2O3) impregnated on Al2O3, as well as a CuO-Al2O3 catalyst prepared by a co-precipitation method reported previously, during the benzene oxidation, keeping the yield of phenol comparatively high. The apparent Cu leaching was largely inhibited in an aqueous solvent with high acetic acid concentration in comparison with a solvent of low acetic acid concentration, irrespective of the presence of benzene and/or ascorbic acid. The influences of both the Cu amount supported on the Cu/Al2O3 catalyst and the amount of ascorbic acid on the yield of phenol were investigated in the aqueous solvents with acetic acid concentrations of both 5.7 and 80 vol. %. The Cu/Al2O3 catalyst in the aqueous acetic acid solvent was deactivated in the comparatively initial stage of the oxidation of benzene. The catalytic activity of the used Cu supported catalyst for phenol formation was almost completely recovered by calcining the catalyst at 773 K. The amount of the deactivated Cu species based on a XRD peak at 2theta = 23degrees in the used Cu/Al2O3 catalyst was found to have a correlation with the yield of phenol. (C) 2003 Published by Elsevier B.V.
引用
收藏
页码:203 / 211
页数:9
相关论文
共 27 条
[1]   Oxidation of aromatic hydrocarbons with hydrogen peroxide over Zn,Cu,Al-layered double hydroxides [J].
Bahranowski, K ;
Dula, R ;
Gasior, M ;
Labanowska, M ;
Michalik, A ;
Vartikian, LA ;
Serwicka, EM .
APPLIED CLAY SCIENCE, 2001, 18 (1-2) :93-101
[2]   SOME INNOVATIVE ASPECTS IN THE PRODUCTION OF MONOMERS VIA CATALYZED OXIDATION PROCESSES [J].
CAVANI, F ;
TRIFIRO, F .
APPLIED CATALYSIS A-GENERAL, 1992, 88 (02) :115-135
[3]  
Centi G., 2001, Selective Oxidation by Heterogeneous Catalysis
[4]   ELECTRON SPIN RESONANCE STUDIES OF OXIDATION .4. SOME BENZENOID COMPOUNDS [J].
DIXON, WT ;
NORMAN, ROC .
JOURNAL OF THE CHEMICAL SOCIETY, 1964, (DEC) :4857-&
[5]  
FLESZAR B, 1976, ROCZ CHEM, V50, P271
[6]   Liquid-phase oxidation of 2,6-di-tert-butylphenol with Cu-impregnated MCM-41 catalysts in the presence of alkali metals [J].
Fujiyama, H ;
Kohara, I ;
Iwai, K ;
Nishiyama, S ;
Tsuruya, S ;
Masai, M .
JOURNAL OF CATALYSIS, 1999, 188 (02) :417-425
[7]  
HAMADA M, 1995, Patent No. 05004935
[8]   HYDROXYLATION OF AROMATIC COMPOUNDS BY HYDROGEN PEROXIDE IN PRESENCE OF CATALYTIC AMOUNTS OF FERRIC ION AND CATECHOL . PRODUCT STUDIES MECHANISM AND RELATION TO SOME ENZYMIC REACTION [J].
HAMILTON, GA ;
HANIFIN, JW ;
FRIEDMAN, JP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1966, 88 (22) :5269-&
[9]   Liquid-phase oxygenation of benzene over supported vanadium catalysts [J].
Ishida, MA ;
Masumoto, Y ;
Hamada, R ;
Nishiyama, S ;
Tsuruya, S ;
Masai, M .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1999, (04) :847-853
[10]  
ITHO S, 1983, J ORG SYNTH CHEM, V41, P839