SOLID-STATE H-1 MAS NMR-STUDY ON THE HIGHLY-ACTIVE PROTONS IN PARTIALLY REDUCED AG3PW12O40

被引:12
作者
BABA, T
NOMURA, M
ONO, Y
OHNO, Y
机构
[1] COSMO RES INST GONGENDO,CTR RES & DEV,SATTE,SAITAMA 34001,JAPAN
[2] TOKYO INST TECHNOL,DEPT CHEM ENGN,MEGURO KU,TOKYO 152,JAPAN
关键词
D O I
10.1021/j100151a042
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 physicochemical nature of protons generated by the partial reduction of Ag+ cations in Ag3PW12O40 with hydrogen was investigated by means of H-1 MAS NMR. When Ag3PW12O40 was partially reduced with hydrogen, the IH MAS NMR spectrum demonstrated the generation of two kinds of acidic protons, which are observed at 6.4 and 9.3 ppm. The protons at 6.4 ppm exist only in the presence of hydrogen in the gas phase. The amount of these protons reversibly changes with the hydrogen pressure. In contrast, the amount of protons at 9.3 ppm is independent of the hydrogen pressure. The amount of protons at 6.4 and 9.3 ppm depended on the degree of the reduction of Ag+ cations in Ag3PW12O40. When the degree of the reduction of Ag+ was 13%, the protons at 6.4 ppm were mainly observed and the protons at 9.3 ppm were only slightly observed. The amount of protons at 6.4 ppm increased by increasing the degree of the reduction of Ag+ cations from 13% to 32%. These protons were scarcely observed when the degree of reduction of Ag+ cations reached 67%. In contrast, the amount of protons at 9.3 ppm increased by increasing the degree of reduction of Ag+ cations from 13% to 67%. The acid strength of the protons observed at 6.4 ppm is higher than that of the protons at 9.3 ppm. The catalytic activity of partially reduced Ag3PW12O40 for the isomerization of 3,3-dimethylbut-1-ene and hexane reversibly changes with hydrogen pressure.
引用
收藏
页码:12888 / 12893
页数:6
相关论文
共 18 条
  • [1] GENERATION OF ACIDIC SITES IN METAL-SALTS OF HETEROPOLYACIDS
    BABA, T
    WATANABE, H
    ONO, Y
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1983, 87 (13) : 2406 - 2411
  • [2] ENHANCING EFFECT OF HYDROGEN ON THE CATALYTIC ACTIVITY OF TRISILVER DODECATUNGSTOPHOSPHATE FOR THE ISOMERIZATION OF 1-BUTENE
    BABA, T
    ONO, Y
    [J]. APPLIED CATALYSIS, 1989, 55 (02): : 301 - 313
  • [3] REVERSIBILITY IN THE TRANSFORMATION BETWEEN CATIONIC AND METALLIC SILVER AND THE GENERATION OF BRONSTED-ACID SITES IN THE SILVER SALT OF DODECATUNGSTOPHOSPHORIC ACID
    BABA, T
    NOMURA, M
    ONO, Y
    KANSAKI, Y
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1992, 88 (01): : 71 - 76
  • [4] HYDROGEN INDUCED CATALYSIS BY SILVER-EXCHANGED ZEOLITES - TRANSFORMATION OF ETHYLBENZENE OVER AGY ZEOLITE
    BABA, T
    ONO, Y
    [J]. ZEOLITES, 1987, 7 (04): : 292 - 294
  • [5] CORRELATIONS BETWEEN PROTON CHEMICAL-SHIFT TENSORS, DEUTERIUM QUADRUPOLE COUPLINGS, AND BOND DISTANCES FOR HYDROGEN-BONDS IN SOLIDS
    BERGLUND, B
    VAUGHAN, RW
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1980, 73 (05) : 2037 - 2043
  • [6] REDOX BEHAVIOR OF TRANSITION-METAL IONS IN ZEOLITES .2. KINETIC STUDY OF REDUCTION AND REOXIDATION OF SILVER-Y ZEOLITES
    BEYER, H
    JACOBS, PA
    UYTTERHOEVEN, JB
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1976, 72 : 674 - 685
  • [7] CARPENTER TA, 1986, J MAGN RESON, V68, P561, DOI 10.1016/0022-2364(86)90347-1
  • [8] ENGELHARDT G, 1987, HIGH RESOLUTION SOLI, P169
  • [9] FREUDE D, 1986, CHEM PHYS LETT, V128, P62, DOI 10.1016/0009-2614(86)80146-4
  • [10] REDOX BEHAVIOR OF TRANSITION-METAL IONS IN ZEOLITES .1. STUDY OF REVERSIBILITY OF HYDROGEN REDUCTION OF COPPER Y ZEOLITES
    HERMAN, RG
    LUNSFORD, JH
    BEYER, H
    JACOBS, PA
    UYTTERHOEVEN, JB
    [J]. JOURNAL OF PHYSICAL CHEMISTRY, 1975, 79 (22) : 2388 - 2394