Chemical deposition of foreign metals on a Pd sheet and its application to continuous hydrogenation of 4-methylstyrene

被引:14
作者
Yoshida, Y
Ogata, S
Nakamatsu, S
Shimamune, T
Inoue, H
Iwakura, C [1 ]
机构
[1] Univ Osaka Prefecture, Coll Engn, Dept Appl Chem, Sakai, Osaka 5998531, Japan
[2] Permelec Electrode Ltd, Fujisawa, Kanagawa 2520816, Japan
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1998年 / 444卷 / 02期
关键词
chemical metal deposition; continuous hydrogenation system; Pd sheet electrode; 4-methylstyrene;
D O I
10.1016/S0022-0728(97)00577-9
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chemical deposition of foreign metals such as Pt, Au, Cu and Zn on a Pd sheet was carried out by using hydrogen atoms passing through the Pd sheet (thickness, 50 mu m) which served as a working electrode for water electrolysis to produce H atoms, a separator between the electrochemical and chemical reaction compartments, a selectively permeable membrane of H atoms and a chemical reaction field for hydrogenation. The amounts of Pt and Au were found to increase linearly with electrolysis time in the 6 M KOH side of a two-compartment cell, whereas Cu and Zn were scarcely deposited (less than 0.2 mg cm(-2)). This result can be explained in terms of the dissociative adsorbability of hydrogen on these metals. Its application to the hydrogenation of 4-methylstyrene was also investigated by using the same electrochemical cell. It became clear that the deposition of noble metals such as Pt and Au on a Pd sheet greatly improves the hydrogenation rate of 4-methylstyrene as compared with a bare Pd sheet, while no hydrogenation products were detected in the case of the Pd sheet on which Cu or Zn had been deposited. This is because, in contrast to Pd, Pt and Au, both Cu and Zn have only very weak catalytic activity for hydrogenation, and they rather suppress the hydrogen diffusion through the Pd sheet, as proved by measurements of H permeation. (C) 1998 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:203 / 207
页数:5
相关论文
共 15 条
[1]   SORPTION BEHAVIOR OF THE OVERPOTENTIAL-DEPOSITED H-SPECIES IN THE CATHODIC H-2 EVOLUTION REACTION AT PD AND PT-PD ELECTROPLATED COMPOSITE ELECTRODES [J].
ELAM, M ;
CONWAY, BE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1988, 135 (07) :1678-1685
[2]   REDUCTION OF ORGANIC-COMPOUNDS WITH RARE-EARTH INTERMETALLICS CONTAINING ABSORBED HYDROGEN [J].
IMAMOTO, T ;
MITA, T ;
YOKOYAMA, M .
JOURNAL OF ORGANIC CHEMISTRY, 1987, 52 (26) :5695-5699
[3]   Successive hydrogenation of styrene at a palladium sheet electrode combined with electrochemical supply of hydrogen [J].
Inoue, H ;
Abe, T ;
Iwakura, C .
CHEMICAL COMMUNICATIONS, 1996, (01) :55-56
[4]   A new hydrogenation system of 4-methylstyrene using a palladinized palladium sheet electrode [J].
Iwakura, C ;
Yoshida, Y ;
Inoue, H .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1997, 431 (01) :43-45
[5]  
IWAKURA C, 1985, DENKI KAGAKU, V53, P722
[6]   A new successive system for hydrogenation of styrene using a two-compartment cell separated by a Pd sheet electrode [J].
Iwakura, C ;
Abe, T ;
Inoue, H .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (04) :L71-L72
[7]   A novel plating process for microencapsulating metal hydrides [J].
Law, HH ;
Vyas, B ;
Zahurak, SM ;
Kammlott, GW .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1996, 143 (08) :2596-2601
[8]  
NAGASAWA S, 1994, CHEM LETT, P431
[9]   Hydrogenation of biphenyl using a hydrogen storage alloy as a hydrogenation reagent [J].
Nakagawa, S ;
Murata, S ;
Nomura, M ;
Sakai, T .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1996, 69 (06) :1599-1603
[10]   ELECTROCHEMICAL REDUCTION OF CARBON-DIOXIDE ON HYDROGEN-STORING MATERIALS .3. THE EFFECT OF THE ABSORPTION OF HYDROGEN ON THE PALLADIUM ELECTRODES MODIFIED WITH COPPER [J].
OHKAWA, K ;
NOGUCHI, Y ;
NAKAYAMA, S ;
HASHIMOTO, K ;
FUJISHIMA, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1994, 367 (1-2) :165-173