Highly Selective Nonoxidative Coupling of Methane over Pt-Bi Bimetallic Catalysts

被引:92
|
作者
Xiao, Yang [1 ]
Varma, Arvind [1 ]
机构
[1] Purdue Univ, Davidson Sch Chem Engn, W Lafayette, IN 47907 USA
来源
ACS CATALYSIS | 2018年 / 8卷 / 04期
基金
美国国家科学基金会;
关键词
shale and natural gas utilization; nonoxidative coupling of methane (NOCM); Pt-Bi bimetallic catalysts; high selectivity toward C-2 species; Bi promoter effect on C-2 species formation; 2-STEP REACTION SEQUENCE; HIGHER HYDROCARBONS; ETHANE DEHYDROGENATION; AROMATIZATION REACTION; CONVERSION; PLATINUM; HYDROGEN; METAL; MO/ZSM-5; PT(111);
D O I
10.1021/acscatal.8b00156
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
There is widespread interest in converting methane, primary component of natural gas and shale gas, into valuable chemicals. As an important direct methane transformation technique, despite extensive research conducted for decades, oxidative coupling of methane (OCM) remains industrially uneconomical owing to low selectivity toward valuable target products (C-2 species, ethane/ethylene). In the present work, we describe that ZSM-5 zeolite supported bimetallic Pt-Bi catalysts stably and selectively convert methane to C-2 species with high carbon selectivity (> 90%) at relatively moderate temperatures (600-700 degrees C). On the basis of experimental observations, it is proposed that the surface Pt in the catalysts functions as the active site for methane activation, while Bi addition as promoter plays an important role in C-2 species formation and catalyst stability.
引用
收藏
页码:2735 / 2740
页数:11
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