非促进ZnCrO: 1-丙醇流动微反应器合成高级醇的机理研究

Q4 Chemical Engineering 分子催化 Pub Date : 1994-12-15 DOI:10.1016/0304-5102(94)00157-X
Luca Lietti, Enrico Tronconi
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引用次数: 2

摘要

通过1-丙醇的流动微反应器实验,研究了ZnCrO样品上高级醇合成(HAS)的机理。结果表明,该催化剂能促进加氢/脱氢、“正”和“逆”醇型缩合、酮化、α加成、脱水等一系列化学功能。通过与k -促进样品的数据比较,发现碱掺杂剂对ZnCrO的加氢/脱氢和正常醛缩反应活性没有影响,但对逆转醛缩反应和α加成反应至关重要,有利于酮化反应,并从根本上抑制脱水功能。因此,碱促进剂除了在C1→C2步骤中发挥关键作用外,还显著影响了C2+氧合物的链生长机制,并有效地保留了氧合物分子,使其通过脱水产生不需要的碳氢化合物。
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Mechanistic aspects of the higher alcohol synthesis over unpromoted ZnCrO: 1-Propanol flow microreactor study

Mechanistic aspects of the higher alcohol synthesis (HAS) over a ZnCrO sample are investigated by flow-microreactor experiments of 1-propanol. Results indicate that the catalyst can promote a number of chemical functions including hydrogenation/dehydrogenation, ‘normal’ and ‘reversal’ aldolic-type condensation, ketonization, α-addition, dehydration. On comparing the data with those obtained over a K-promoted sample it appears that the alkali dopant does not affect the reactivity of ZnCrO towards hydrogenation/dehydrogenation and ‘normal’ aldolic-type condensation, is essential for ‘reversal’ aldolic-type condensation and α-addition, favors ketonization and essentially suppresses the dehydration function. Thus the alkali promoter, besides playing a crucial role in the C1→C2 step, significantly affects the chain growth mechanisms involving C2+ oxygenates and effectively preserves oxygenate molecules towards the production of undesired hydrocarbons by dehydration.

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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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