One-step gas-phase catalytic oxidation of benzene to phenol with molecular oxygen over Cu-supported ZSM-5 zeolites

被引:52
作者
Hamada, R
Shibata, Y
Nishiyama, S
Tsuruya, S [1 ]
机构
[1] Kobe Univ, Fac Engn, Dept Sci & Chem Engn, Nada Ku, Kobe, Hyogo 6578501, Japan
[2] Kobe Univ, Grad Sch Sci & Technol, Dept Mol Sci, Nada Ku, Kobe, Hyogo 6578501, Japan
关键词
D O I
10.1039/b209706k
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 gas-phase catalytic oxidation of benzene was carried out using molecular oxygen as an oxidant over Cu-supported catalysts. Phenol was formed only when using Cu-supported high-silica-type zeolites as catalysts. The Cu-supported H-ZSM-5 zeolite (CuH-ZSM-5) was the most active among those tested. Deep oxidation products (CO and CO2) were also produced together with phenol and they were suggested to form either via phenol or directly from benzene, based on the activity test experiments by varying the contact time. The yield and selectivity of phenol had a maximum with respect to the Cu contents in the CuH-ZSM-5, and were optimized with ca. a 0.77 wt.% Cu loading ( phenol yield similar to4.9%). The calcination of the CuH-ZSM-5 at the higher temperature of around 1123 K was found to be effective for the phenol formation. The H-ZSM-5 with lower Si/Al atomic ratios was an effective support for the phenol formation. The EPR study revealed that the increase in the square-pyramidal Cu2+ species was brought about when the CuH-ZSM-5 was calcined at higher temperatures or when HZSM-5 with lower Si/Al atomic ratios was used as a support. The isolated square-pyramidal Cu2+ species was suggested to be the active species for the phenol formation.
引用
收藏
页码:956 / 965
页数:10
相关论文
共 48 条
[1]  
ABREU CT, 1997, APPL CATAL B-ENVIRON, V12, P262
[2]  
ARGAUER RJ, 1988, Patent No. 3702886
[3]   Redox chemistry of Cu/ZSM-5 [J].
Beutel, T ;
Sarkany, J ;
Lei, GD ;
Yan, JY ;
Sachtler, WMH .
JOURNAL OF PHYSICAL CHEMISTRY, 1996, 100 (02) :845-851
[4]   INVESTIGATION OF ZEOLITE CATALYSTS FOR THE DIRECT PARTIAL OXIDATION OF BENZENE TO PHENOL [J].
BURCH, R ;
HOWITT, C .
APPLIED CATALYSIS A-GENERAL, 1993, 103 (01) :135-162
[5]   The effect of hydrogen superoxide on unsaturated hydrocarbons [J].
Cross, CF ;
Bevan, EJ ;
Heiberg, T .
BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT, 1900, 33 :2015-2018
[6]   OXIDATION BY MOLECULAR OXYGEN .I. REACTIONS OF POSSIBLE MODEL SYSTEM FOR MIXED-FUNCTION OXIDASES [J].
HAMILTON, GA ;
WOO, L ;
WORKMAN, RJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1964, 86 (16) :3390-&
[7]   DIRECT CONVERSION OF BENZENE TO HYDROQUINONE - COOPERATIVE ACTION OF CU(I) ION AND DIOXYGEN [J].
ITO, S ;
KUNAI, A ;
OKADA, H ;
SASAKI, K .
JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (02) :296-300
[8]   EVIDENCE FOR HYDROXYL RADICALS AS AN ACTIVE SPECIES GENERATED FROM UDENFRIENDS REAGENT [J].
ITO, S ;
UENO, K ;
MITARAI, A ;
SASAKI, K .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1993, (02) :255-259
[9]   OXIDATION OF BENZENE TO PHENOLS WITH MOLECULAR-OXYGEN PROMOTED BY COPPER(I) CHLORIDE [J].
ITO, S ;
YAMASAKI, T ;
OKADA, H ;
OKINO, S ;
SASAKI, K .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1988, (03) :285-293
[10]   CATALYTIC-OXIDATION BY OXIDE RADICAL IONS .1. ONE-STEP HYDROXYLATION OF BENZENE TO PHENOL OVER GROUP-5 AND GROUP-6 OXIDES SUPPORTED ON SILICA-GEL [J].
IWAMOTO, M ;
HIRATA, J ;
MATSUKAMI, K ;
KAGAWA, S .
JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (06) :903-905