Catalytic conversion of oxygen containing cyclic compounds. Part II. Cyclohexanone conversion on HZSM-5 zeolites

Q4 Chemical Engineering 分子催化 Pub Date : 1994-11-27 DOI:10.1016/S0304-5102(94)87046-2
Libor Brabec, Jana Nováková, Ludmila Kubelková
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引用次数: 5

Abstract

Low-pressure on-stream conversion of cyclohexanone (CHN) was studied over HZSM-5 zeolites with various Si/ Al ratios (different number of strong acid sites). Each conversion run was followed by thermal decomposition of surface species which also were investigated using FTIR spectroscopy. It was found that, below 300°C, surface complexes consisting predominantly of CHN were held in the zeolites. The release of products, consisting of dehydrated CHN (C6H8), substituted aromatics and olefins, began above 250°C. The latter two compounds were formed via intermediates most probably of the aldol type (however, the dimerized methylcyclopentadiene intermediate cannot be excluded). The CHN dehydration to C6H8 predominated at 480°C. The yield of all products increased with the increasing number of zeolite strong acid sites. Ammonia, co-fed or preadsorbed, reacted with CHN to surface imines which hindered all other CHN reactions. The imine was strongly held in zeolites and decomposed at about 450°C to gaseous C6H8 and ammonia. Methanol partially methylated the reaction products but did not affect the main reaction routes, monomolecular dehydration and secondary intermolecular reactions.

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含氧环化合物的催化转化。第二部分。环己酮在HZSM-5分子筛上的转化
在不同Si/ Al比(不同强酸位数)的HZSM-5沸石上研究了环己酮(CHN)的低压流态转化。每次转化后都进行了表面物质的热分解,并利用红外光谱对其进行了研究。结果表明,在300℃以下,沸石中的表面络合物主要由CHN组成。由脱水CHN (C6H8)、取代芳烃和烯烃组成的产物在250℃以上开始释放。后两个化合物是通过中间体形成的,最有可能是醛醇型(然而,二聚甲基环戊二烯中间体也不能排除)。在480℃时,CHN主要脱水为C6H8。随着沸石强酸位点数量的增加,各产物的收率均有所提高。氨,共投或预吸附,与CHN反应生成表面亚胺,这阻碍了所有其他CHN反应。亚胺在沸石中被强力吸附,在450℃左右分解成气态C6H8和氨。甲醇使反应产物部分甲基化,但不影响主要反应途径、单分子脱水和二次分子间反应。
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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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