加氢脱氧
愈创木酚
催化作用
化学
儿茶酚
选择性
苯酚
钼
苯
无机化学
对苯二酚
有机化学
核化学
作者
Jie Chang,Tanate Danuthai,Silvia Dewiyanti,Chuan Wang,Armando Borgna
出处
期刊:Chemcatchem
[Wiley]
日期:2013-07-02
卷期号:5 (10): 3041-3049
被引量:168
标识
DOI:10.1002/cctc.201300096
摘要
Abstract Catalytic bio‐oil upgrading to produce renewable fuels has attracted increasing attention in response to the decreasing oil reserves and the increased fuel demand worldwide. Herein, the catalytic hydrodeoxygenation (HDO) of guaiacol with carbon‐supported non‐sulfided metal catalysts was investigated. Catalytic tests were performed at 4.0 MPa and temperatures ranging from 623 to 673 K. Both Ru/C and Mo/C catalysts showed promising catalytic performance in HDO. The selectivity to benzene was 69.5 and 83.5 % at 653 K over Ru/C and 10Mo/C catalysts, respectively. Phenol, with a selectivity as high as 76.5 %, was observed mainly on 1Mo/C. However, the reaction pathway over both catalysts is different. Over the Ru/C catalyst, the OCH 3 bond was cleaved to form the primary intermediate catechol, whereas only traces of catechol were detected over Mo/C catalysts. In addition, two types of active sites were detected over Mo samples after reduction in H 2 at 973 K. Catalytic studies showed that the demethoxylation of guaiacol is performed over residual MoO x sites with high selectivity to phenol whereas the consecutive HDO of phenol is performed over molybdenum carbide species, which is widely available only on the 10Mo/C sample. Different deactivation patterns were also observed over Ru/C and Mo/C catalysts.
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