低温还原Pt/TiO2的丙烯加氢反应。TiO2相和H2处理对催化活性的影响

Q4 Chemical Engineering 分子催化 Pub Date : 1994-12-15 DOI:10.1016/0304-5102(94)00130-8
G. Cocco , R. Campostrini , M.A. Cabras , G. Carturan
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引用次数: 17

摘要

将四正丁醇钛水解得到的TiO2凝胶在不同温度下加热,得到结晶不良的TiO2、无序的锐钛矿和结晶良好的锐钛矿-金红石混合物。在278 K下,用H2还原铂烯丙基,得到了铂在TiO2载体上的分散体。用这些催化剂和Pt/ sio2 -凝胶样品在不同温度和H2/丙烯分子比下进行丙烯加氢。用x射线衍射分析了新催化剂和运行催化剂的存在相,并测定了铂颗粒的平均尺寸。在所有情况下,制备的催化剂或在493 K下H2处理后的催化剂的结果表明,普通的加氢机制保持不变,但根据H2处理和载体的性质,观察到比催化活性的重要变化。TiO2的形态被认为是导致Pt在金红石-锐钛矿混合物上的比活性下降的原因,也是铂在锐钛矿上的相反作用的原因。
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Propene hydrogenation on low-temperature reduced Pt/TiO2. Effects of TiO2 phases and H2 treatment on specific catalytic activity

TiO2 gel obtained by hydrolysis of titanium tetra-n-butoxide was heated at various temperatures, providing poorly crystallized TiO2, disordered anatase and a well crystallized anatase—rutile mixture. Platinum dispersion was obtained on these TiO2 supports by the reduction of platinum—allyl species with H2 at 278 K. These catalysts and a Pt/SiO2-gel sample were used for propene hydrogenation at various temperatures and H2/propene molecular ratios. Fresh and run catalysts were subjected to X-ray diffraction analysis for the study of extant phases and determination of average size of platinum particles. In all cases, results obtained for catalysts as prepared or after H2 treatment at 493 K indicated that the ordinary hydrogenation mechanism was maintained but that important changes of specific catalytic activity were observed, depending on H2 treatment and nature of the support. TiO2 morphology was assumed to be responsible for the specific activity decrease in Pt on the rutile—anatase mixture and for the opposite effect found for platinum on anatase.

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来源期刊
分子催化
分子催化 Chemical Engineering-Catalysis
CiteScore
1.50
自引率
0.00%
发文量
2959
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Author index Subject index Hydrolysis of sucrose by dealuminated Y-zeolites Synthesis and application of organophilic polystyrene-montmorillonite supported onium salts in organic reactions Effect of the reduction temperature on the selectivity of the high temperature reaction of acetone and hydrogen over alumina and titania supported nickel and cobalt catalysts
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