首页> 外文期刊>Journal of Catalysis >High-pressure vapor-phase hydrodeoxygenation of lignin-derived oxygenates to hydrocarbons by a PtMo bimetallic catalyst: Product selectivity, reaction pathway, and structural characterization
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High-pressure vapor-phase hydrodeoxygenation of lignin-derived oxygenates to hydrocarbons by a PtMo bimetallic catalyst: Product selectivity, reaction pathway, and structural characterization

机译:PtMo双金属催化剂将木质素衍生的含氧化合物进行高压气相加氢脱氢成烃:产品选择性,反应途径和结构表征

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摘要

High-pressure, vapor-phase, hydrodeoxygenation (HDO) reactions of dihydroeugenol (2-methoxy-4-propylphenol), as well as other phenolic, lignin-derived compounds, were investigated over a bimetallic platinum and molybdenum catalyst supported on multi-walled carbon nanotubes (5%Pt2.5%Mo/MWCNT). Hydrocarbons were obtained in 100% yield from dihydroeugenol, including 98% yield of the hydrocarbon propylcyclohexane. The final hydrocarbon distribution was shown to be a strong function of hydrogen partial pressure. Kinetic analysis showed three main dihydroeugenol reaction pathways: HDO, hydrogenation, and alkylation. The major pathway occurred via Pt catalyzed hydrogenation of the aromatic ring and methoxy group cleavage to form 4-propylcyclohexanol, then Mo catalyzed removal of the hydroxyl group by dehydration to form propylcyclohexene, followed by hydrogenation of propylcyclohexene on either the Pt or Mo to form the propylcyclohexane. Transalkylation by the methoxy group occurred as a minor side reaction. Catalyst characterization techniques including chemisorption, scanning transmission electron microscopy, X-ray absorption spectroscopy, and X-ray photoelectron spectroscopy were employed to characterize the catalyst structure. Catalyst component's identified were Pt particles, bimetallic PtMo particles, a Mo carbide-like phase, and Mo oxide phases. (C) 2016 Elsevier Inc. All rights reserved.
机译:在多壁负载的双金属铂和钼催化剂上研究了二氢丁香酚(2-甲氧基-4-丙基苯酚)以及其他酚类,木质素衍生化合物的高压气相加氢脱氧(HDO)反应碳纳米管(5%Pt2.5%Mo / MWCNT)。由二氢丁香酚以100%的产率获得烃,包括98%的烃丙基环己烷。最终的碳氢化合物分布被证明是氢分压的强函数。动力学分析显示了三种主要的二氢丁香酚反应途径:HDO,氢化和烷基化。主要途径是通过Pt催化芳香环的加氢和甲氧基裂解形成4-丙基环己醇,然后Mo催化通过脱水脱除羟基而形成丙基环己烯,然后在Pt或Mo上丙基环己烯加氢以形成羟基。丙基环己烷。通过甲氧基的烷基转移是次要的副反应。使用包括化学吸附,扫描透射电子显微镜,X射线吸收光谱和X射线光电子光谱在内的催化剂表征技术来表征催化剂结构。鉴定出的催化剂组分是Pt颗粒,双金属PtMo颗粒,类碳化钼相和氧化钼相。 (C)2016 Elsevier Inc.保留所有权利。

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