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Journal of the Research Institute for Catalysis, Hokkaido University最新文献

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N M R Chemical Shifts and Reactivity of Solid Surfaces 固体表面的化学位移和反应性
Pub Date : 1980-01-01 DOI: 10.1007/978-94-009-9079-1_16
J. Fraissard
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引用次数: 0
INTERMEDIATES OF HYDROGEN EVOLUTION REACTION ON NICKEL IN AQUEOUS SODIUM HYDROXIDE 氢氧化钠水溶液中镍的析氢反应中间体
Pub Date : 1978-10-17 DOI: 10.1002/CHIN.197842028
T. Ohmori, A. Matsuda
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引用次数: 3
INFLUENCE OF PRODUCTS AND PRETREATMENTS ON THE KETONISATION OF ACETIC ACID OVER IRON OXIDE 产物及预处理对乙酸在氧化铁上酮化的影响
Pub Date : 1977-05-24 DOI: 10.1002/CHIN.197721142
S. S. Jewur, J. Kuriacose
'With a view to understand the mechanistic details of the ketonisation of acetic acid on iron oxide the influence of products on the rate of the reaction was studied at different temperatures. Inhibition of the ketonisation due to water is greater than that due to carbon dioxide and acetone at all temperatures. The extent of catalytic dehydration and dehydrogenation of alcohols and the ketonisation of acetic acid was also studied on catalysts reduced to different degrees. The results suggest the necessity of dehydrogenation as well as dehydration activities of the catalyst for the ketonisation reaction.
为了了解醋酸在氧化铁上酮化的机理细节,研究了不同温度下产物对反应速率的影响。在任何温度下,水对酮化的抑制作用都大于二氧化碳和丙酮。研究了不同还原程度的催化剂对醇类脱水脱氢和乙酸酮化反应的催化程度。结果表明,酮化反应需要脱氢反应以及催化剂的脱水活性。
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引用次数: 4
PERIODIC VARIATION OF EXCHANGE CURRENT DENSITY OF HYDROGEN ELECTRODE REACTION WITH ATOMIC NUMBER 氢电极反应交换电流密度随原子序数的周期性变化
Pub Date : 1966-11-01 DOI: 10.1149/1.2423772
H. Kita
The works on hydrogen electrode reaction have been increasingly accumulated during the last decade. These works are much more reliable than earlier ones, in­ asmuch as the special precaution has been taken against contaminations of solution and electrode surface. Survey of the results shows that the activity of metals for the reaction in terms of the exchange current density, io (Acm -2), varies in a wide range, namely from log io = -1.2 on Pd to -12.9 on Pb and even on the same metal, from -3.15 to -7.04 on Au (ef Table 1). Such variations in the activity may be caused by several factors such as bulk property of electrode material, surface state of the electrode and solution. The present note is concerned with the relation of the exchange current density of various metals to their position in the Periodic Table and with the decision of the determining factor of the activity.
近十年来,关于氢电极反应的研究工作逐渐积累起来。由于对溶液和电极表面的污染采取了特别的预防措施,这些工作比以前的工作可靠得多。对结果的调查表明,金属在交换电流密度io (Acm -2)方面的反应活性变化范围很广,即Pd上的log io = -1.2到Pb上的-12.9,甚至在同一种金属上,Au上的log io = -3.15到-7.04(见表1)。这种活性变化可能是由电极材料的体积性质、电极的表面状态和溶液等多种因素引起的。本附注讨论各种金属的交换电流密度与其在元素周期表中的位置的关系,以及确定其活度的决定因素。
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引用次数: 209
ISOTOPIC SEPARATION FACTOR OF SLOW DISCHARGE MECHANISM OF HYDROGEN ELECTRODE REACTION. II 氢电极反应慢放电机理的同位素分离因子研究。2
Pub Date : 1959-09-01 DOI: 10.1016/0022-0728(60)85498-8
T. Kodera
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引用次数: 0
STUDIES OF THE HYDROGEN ELECTRODE PROCESS ON LEAD CATHODE AT VERY HIGH ELECTRODE POTENTIALS 高电极电位下铅阴极上氢电极过程的研究
Pub Date : 1959-09-01 DOI: 10.1016/0022-0728(60)85553-2
Atusi Mituya, T. Yamazaki
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引用次数: 0
期刊
Journal of the Research Institute for Catalysis, Hokkaido University
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