Methanol decomposition over copper particles incorporated in the interlayer regions of zinc aluminum silicate hydroxide

被引:9
作者
Hashimot, K [1 ]
Toukai, N [1 ]
机构
[1] Osaka Municipal Tech Res Inst, Joto Ku, Osaka 5368553, Japan
关键词
methanol decomposition; mica; copper oxide; fine particles;
D O I
10.1016/S1381-1169(01)00416-2
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 decomposition of methanol over copper particles incorporated in the interlayer regions of zinc aluminum silicate hydroxide, reduced CuO/Zn-mica and Cu2+/Zn-mica, was studied. CuO/Zn-mica reduced with H, is high active for the decomposition, compared with reduced Cu2+/Zn-mica. Methanol is selectively converted at 200 degreesC to H-2 and CO in reduced CuO/Zn-mica, whereas the methanol decomposition over reduced Cu2+/Zn-mica forms formaldehyde as a by-product. IR data support that the decomposition over reduced CuO/Zn-mica proceeds via copper methoxide and/or copper formate as an intermediate. An adsorption of NH3 shows that the amount of the adsorption on reduced CuO/Zn-mica is about six times as large as that on reduced Cu2+/Zn-mica. The results indicate the difficulty of the reduction of copper ion in Cu2+/Zn-mica, compared with CuO/Zn-mica. These results support that the active site for methanol decomposition on reduced CuO/Zn-mica is metallic Cu in the interlayer regions of Zn-mica. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:79 / 88
页数:10
相关论文
共 64 条
[1]   AN INFRARED SPECTROSCOPIC STUDY ON THE MECHANISM OF METHANOL FORMATION FROM CO AND H-2 OVER ZIRCONIA [J].
ABE, H ;
MARUYA, K ;
DOMEN, K ;
ONISHI, T .
CHEMISTRY LETTERS, 1984, (11) :1875-1878
[2]   INFRARED STUDY OF METHANOL ADSORPTION ON AEROSIL .I. CHEMISORPTION AT ROOM TEMPERATURE [J].
BORELLO, E ;
ZECCHINA, A ;
MORTERRA, C .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (09) :2938-&
[3]   An IR study of methanol adsorption on Pt/CeO2-SiO2 and Pt/CeO2-Al2O3 catalysts [J].
Brogan, MS ;
Cairns, JA ;
Dines, TJ ;
Rochester, CH .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 1997, 53 (07) :943-950
[4]   THE ROLE OF COPPER AND ZINC-OXIDE IN METHANOL SYNTHESIS CATALYSTS [J].
BURCH, R ;
GOLUNSKI, SE ;
SPENCER, MS .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1990, 86 (15) :2683-2691
[5]   SYNERGY BETWEEN COPPER AND ZINC-OXIDE DURING METHANOL SYNTHESIS - TRANSFER OF ACTIVATING SPECIES [J].
BURCH, R ;
CHAPPELL, RJ ;
GOLUNSKI, SE .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1989, 85 :3569-3578
[6]   THE ROLE OF HYDROGEN IN METHANOL SYNTHESIS OVER COPPER-CATALYSTS [J].
BURCH, R ;
GOLUNSKI, SE ;
SPENCER, MS .
CATALYSIS LETTERS, 1990, 5 (01) :55-60
[7]   Variable-temperature electron paramagnetic resonance studies of copper-exchanged zeolites [J].
Carl, PJ ;
Larsen, SC .
JOURNAL OF CATALYSIS, 1999, 182 (01) :208-218
[8]   ALCOHOL DECOMPOSITION BY REVERSE SPILLOVER [J].
CHEN, BS ;
FALCONER, JL .
JOURNAL OF CATALYSIS, 1993, 144 (01) :214-226
[9]   Competition between C-O bond scission and retention in methanol reaction on Co-covered Mo(110) [J].
Chen, DA ;
Friend, CM .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (29) :5712-5716
[10]   Promotion of Cu/Cr/Mn catalyst by alkali additives in methanol decomposition [J].
Cheng, WH ;
Shiau, CY ;
Liu, TH ;
Tung, HL ;
Lu, JF ;
Hsu, CC .
APPLIED CATALYSIS A-GENERAL, 1998, 170 (02) :215-224