文献类型：期刊文献

英文题名：Directional liquefaction of biomass for phenolic compounds and in situ hydrodeoxygenation upgrading of phenolics using bifunctional catalysts

作者：Feng, Junfeng[1,2] Hse, Chung-yun[2] Wang, Kui[1] Yang, Zhongzhi[1] Jiang, Jianchun[1] Xu, Junming[3]

第一作者：Feng, Junfeng

通信作者：Jiang, Jianchun|[a0005af0d5390473d5077]蒋剑春;

机构：[1] Institute of Chemical Industry of Forest Products, Chinese Academy of Forestry, National Engineering Lab. for Biomass Chemical Utilization, Key and Open Lab. on Forest Chemical Engineering, SFA, Key Lab. of Biomass Energy and Material, Nanjing, 210042, China; [2] United States Department of Agriculture [USDA] Forest Service, Southern Research Station, Pineville, LA, 71360, United States; [3] Research Institute of Forestry New Technology, Chinese Academy of Forestry, Beijing, 100091, China

年份：2017

卷号：135

起止页码：1-13

外文期刊名：Energy

收录：EI(收录号：20172603813731);Scopus(收录号：2-s2.0-85021138525)

语种：英文

外文关键词：Catalyst selectivity - Hydrocarbons - Fuel additives - Biofuels - Liquefaction - Hydrogenation - Catalysis - Phenols

摘要：Phenolic compounds derived from biomass are important feedstocks for the sustainable production of hydrocarbon biofuels. Hydrodeoxygenation is an effective process to remove oxygen-containing functionalities in phenolic compounds. This paper reported a simple method for producing hydrocarbons by liquefying biomass and upgrading liquefied products. Three phenolic compounds fractions (1#, 2#, and 3#) were separated from liquefied biomass with stepwise precipitation and extraction. Based on HSQC NMR analysis, three phenolic compounds fractions were mainly comprised of aromatic and phenolic derivatives. Three phenolic compounds fractions were hydrogenated and deoxygenated to cyclohexanes using bifunctional catalysts via in situ hydrodeoxygenation. During the in situ hydrodeoxygenation, we introduced bifunctional catalysts combined of Raney Ni with HZSM-5. The bifunctional catalysts showed high selectivity for removing oxygen-containing groups in biomass-derived phenolic compounds. And the hydrogen was supplied by aqueous phase reforming of methanol without external H2. Additionally, the mechanism based on our investigation of in situ hydrodeoxygenation of phenolic compounds was proposed. During the in situ hydrodeoxygenation, the metal-catalyzed hydrogenation and acid-catalyzed hydrolysis/dehydration were supposed to couple together. Current results demonstrated that in situ hydrodeoxygenation using bifunctional catalysts is a promising and efficient route for converting biomass-derived phenolic compounds into fuel additives and liquid hydrocarbon biofuels. ? 2017 Elsevier Ltd