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Heterogeneous Catalytic Transfer Hydrogenation as an Effective Pathway in Biomass Upgrading

机译:非均相催化转移加氢是生物质提升的有效途径

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Reducing oxygen content in biomass-derived feedstocks via hydrodeoxygenation (HDO) is a key step in their upgrading to fuels and valuable chemicals. Organic molecules, e.g., alcohols and formic acid, can donate hydrogen to reduce the substrate in a process called catalytic transfer hydrogenation (CTH). Although it is practiced far less frequently than molecular hydrogen-based HDO processes, CTH has been proven to be an efficient and selective strategy in biomass upgrading in the last two decades. In this paper, we present a selective review of recent progress made in the upgrade of biomass-derived feedstocks through heterogeneous CTH, with a focus on the mechanistic interpretation. Hydrogenation and cleavage of C=O and C-O bonds, respectively, are the two main categories of reactions discussed, owing to their importance in the HDO of biomass-derived feedstocks. On acid base catalysts, Lewis acid base pair sites, rather than a single acid or base site, mediate hydrogenation of carbonyl groups with alcohols as the hydrogen donor. While acid base catalysts typically only catalyze the hydrogenation of carbonyl groups with alcohols as the hydrogen donor, metal-based catalysts are able to mediate both hydrogenation and hydrogenolysis reactions with either alcohols or formic acid. Several model reactions involving platform chemicals in biomass upgrading, e.g., 5-hydroxymethylfurfural, levulinic acid, and glycerol, are used in the discussion to illustrate general trends. Because alcohols are typically both the hydrogen donor and the solvent, the donor and solvent effects are intertwined. Therefore, solvent effects are discussed primarily in the context of sugar isomerization and reactions with formic acid as the hydrogen donor, in which the solvent and hydrogen donor are two separate species. Current challenges and opportunities of future research to develop CTH into a competitive and complementary strategy of the conventional molecular-hydrogen-based processes are also discussed.
机译:通过加氢脱氧(HDO)降低生物质原料中的氧含量是将其升级为燃料和有价值的化学物质的关键步骤。有机分子(例如醇和甲酸)可以在称为催化转移氢化(CTH)的过程中提供氢以还原底物。尽管CTH的实施频率远低于基于分子氢的HDO工艺,但在过去的二十年中,CTH已被证明是生物质升级的有效且选择性的策略。在本文中,我们对通过异质CTH升级生物质衍生原料的最新进展进行了选择性回顾,重点是机理解释。 C = O和C-O键的氢化和裂解分别是讨论的两个主要类别的反应,因为它们在生物质原料的HDO中很重要。在酸碱催化剂上,路易斯酸碱对位点而不是单个酸或碱位点介导以醇为氢供体的羰基的氢化。虽然酸碱催化剂通常仅以醇作为氢供体来催化羰基的氢化,但是金属基催化剂能够介导与醇或甲酸的氢化和氢解反应。讨论中使用了几种涉及平台化学物质进行生物质升级的模型反应,例如5-羟甲基糠醛,乙酰丙酸和甘油,以说明总体趋势。因为醇通常既是氢供体又是溶剂,所以供体和溶剂的影响相互交织。因此,主要在糖异构化和与甲酸作为氢供体的反应的背景下讨论溶剂的作用,其中溶剂和氢供体是两个独立的物种。还讨论了将CTH发展为常规分子氢基工艺的竞争性和互补性策略的当前挑战和未来研究的机会。

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