CH4 conversion to value added products: Potential, limitations and extensions of a single step heterogeneous catalysis

被引:211
作者
Taifan, William [1 ]
Baltrusaitis, Jonas [1 ]
机构
[1] Lehigh Univ, Dept Chem & Biomol Engn, B336 Iacocca Hall,111 Res Dr, Bethlehem, PA 18015 USA
关键词
Methane; Heterogeneous; Catalysis; Direct; In situ; TEMPERATURE NONOXIDATIVE ACTIVATION; ALKALI-PROMOTED MGO; DEEP-UV PHOTOLYSIS; OXIDATIVE METHYLATION; ACETIC-ACID; HCN SYNTHESIS; PHOTOCATALYTIC CONVERSION; METHANE CONVERSION; ZEOLITE CATALYSTS; LIGHT OLEFINS;
D O I
10.1016/j.apcatb.2016.05.081
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
Natural gas is envisioned as a primary source of energy and hydrocarbons in the foreseeable future. Though shale gas has recently become abundant, it has two main concerns: its environmental impact and sustainable utilization. The former is the result of recent reports of natural gas emissions and flares into the environment, where it acts as a powerful greenhouse gas, whereas the latter is dictated by the need for efficient hydrocarbon utilization. Modern natural gas processing units that yield clean fuels and feedstock from methane, CH4, require extremely large capital investments and are not economical in remote natural gas extraction sites. Single step (direct), non-syngas based catalytic routes of CH4 conversion to value added products have not been competitive economically and need to be reevaluated in the light of shale gas availability. This perspective discusses general considerations for the desired hydrocarbon products, the thermodynamic limitations involved in a single step conversion of CH4 and heterogeneous catalytic routes based on high temperatures and oxide based catalysts. We then discuss other catalysts and methods of CH4 activation that have recently emerged and are conceptually different from metal oxide catalyst based routes, such as those using sulfur or halogens. Lastly, we discuss a possible route of CH4 monetization beyond the first reactive product (such as ethylene oligomerization into fuels), as well as currently explored photo(electro)chemical routes of CH4 activation. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:525 / 547
页数:23
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