首页> 外文期刊>American Chemical Society, Division of Fuel Chemistry, Preprints >CATALYTIC HYDRO-LIQUEFACTION OF SAWDUST INTO HIGH-VALUE SMALL-MOLECULAR CHEMICALS OVER A NOVEL MAGNETIC SOLID SUPER-BASE CATALYST
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CATALYTIC HYDRO-LIQUEFACTION OF SAWDUST INTO HIGH-VALUE SMALL-MOLECULAR CHEMICALS OVER A NOVEL MAGNETIC SOLID SUPER-BASE CATALYST

机译:新型磁性固体超碱催化剂将木屑催化液化为高价小分子化学品

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Selective hydrogenolysis of aromatic carbon-oxygen(C-O)nbonds is challenging because of the strength and stability of thesenlinkages (4, 5). The cleavage of bridged bonds (BBs), especially C-Onbridged bonds, in coals and biomass is one of the most importantnreactions for the hydrogenation liquefaction and efficient utilizationn(6,7). However, most processes to recover energy from coal or tonconvert it to higher valued products depend on the major chemicalnchanges that occur when coal is heated above 350-400 oC (8). Thesenhigher temperatures leading to severe increase in the yields of bothngases and heavy products with huge energy consumption (9,10). Biooilsnhave been identified as renewable liquid fuel that can benproduced from lignocellulosic biomass (11-13). Pyrolysis of biomassnhas been shown to be cheaper than biomass conversion technologiesnbased on gasification or fermentation processes (14). But, bio-oils arenlow-quality fuels that cannot be used in conventional gasoline orndiesel fuel engines because they are immiscible with petroleumderivednfuels, on account of their high oxygen, acid, and waterncontent (11, 15). Brown coal’s polymeric network contains aromaticnC-O bonds inherited from biomass (16), yet, selective cleavage of COnbond is important for the conversion of coal or biomass tondeoxygenated fuels and commercial chemicals (17-19).nConsequently, selective cleavage of C-O bond at a lower temperaturenin the presence of a proper catalyst is the key of hydrogenationnliquefaction and model reactions.
机译:芳香族碳-氧(C-O)n键的选择性氢解是具有挑战性的,因为其强度和稳定性高(4,5)。煤和生物质中桥键(BBs)尤其是C-桥键的裂解是加氢液化和有效利用的最重要反应之一(6,7)。但是,大多数从煤中回收能量或将其吨化为更高价值产品的过程都取决于将煤加热到350-400 oC以上时发生的主要化学变化(8)。较高的温度导致双糖酶和重产品产量的急剧增加,同时消耗大量能源(9,10)。生物油已被鉴定为可从木质纤维素生物质中生产的可再生液体燃料(11-13)。研究表明,生物质的热解比基于气化或发酵过程的生物质转化技术便宜(14)。但是,生物油是低质量的燃料,由于其高的氧,酸和水含量,它们不能与石油衍生的燃料混溶,因此不能用于常规的汽油或柴油燃料发动机(11、15)。褐煤的聚合物网络包含从生物质继承的芳烃C-O键(16),然而,COnbond的选择性裂解对于煤炭或生物质的脱氧氧燃料和商业化学品的转化很重要(17-19)。在适当的催化剂存在下,较低的温度是加氢液化和模型反应的关键。

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    Key Laboratory of Coal Processing and Efficient UtilizationChina University of Mining TechnologyXuzhou 221116 China;

    Key Laboratory of Coal Processing and Efficient UtilizationChina University of Mining TechnologyXuzhou 221116 China;

    Key Laboratory of Coal Processing and Efficient UtilizationChina University of Mining TechnologyXuzhou 221116 China;

    Key Laboratory of Coal Processing and Efficient UtilizationChina University of Mining TechnologyXuzhou 221116 China;

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