Production of phenols from lignin-derived slurry liquid using iron oxide catalyst

被引:77
|
作者
Yoshikawa, Takuya [1 ,3 ]
Shinohara, Satoshi [1 ]
Yagi, Taichi [1 ]
Ryumon, Naonori [2 ]
Nakasaka, Yuta [1 ]
Tago, Teruoki [1 ]
Masuda, Takao [1 ]
机构
[1] Hokkaido Univ, Fac Engn, Div Chem Proc Engn, Res Grp Chem Engn,Kita Ku, Sapporo, Hokkaido 0608628, Japan
[2] Idemitsu Kosan Co Ltd, Adv Technol Res Labs, Chiba 2990293, Japan
[3] Japan Soc Promot Sci, Tokyo, Japan
基金
日本科学技术振兴机构;
关键词
Biomass utilization; Lignin conversion; Phenols; Iron oxide catalyst; High pressure flow reactor; PETROLEUM RESIDUAL OIL; USEFUL HYDROCARBONS; BIOMASS CONVERSION; OXIDATIVE CRACKING; MODEL COMPOUNDS; LIGHTER FUELS; STEAM; ACID; RECOVERY; HYDRODEOXYGENATION;
D O I
10.1016/j.apcatb.2013.03.010
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A two-step process consisting of depolymerization and catalytic cracking without hydrogen addition was carried out to produce phenols from lignin. In the first step, lignin was depolymerized using a silica-alumina catalyst in a water/1 -butanol solution at 623 K for 2 h. After the reaction, lignin-derived slurry liquid was obtained in 67 C-mol% yield. From the model studies, it was considered that lignin was mainly depolymerized via hydrolysis of aryl ether bonds between lignin units. For the second step, the catalytic reaction of the 1-butanol phase of the slurry liquid was carried out over an iron oxide catalyst using a high pressure fixed-bed flow reactor at 673 K. The catalytic reaction under high pressure steam conditions was effective for the suppression of the formation of solid products. In addition, the recovery fraction of phenols increased as the F-H2O/F value (the flow rate ratio of steam to the slurry liquid) increased, resulting in 17% of phenols at F-H2O/F = 5 for 2-4h. From the model studies and our previous results, catechol and methoxyphenol in the slurry liquid were considered to be converted into phenols, cresols and other alkyl phenols over the iron oxide catalyst. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 297
页数:9
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