CO2 capture by activated and impregnated anthracites

被引:251
作者
Maroto-Valer, MM
Tang, Z
Zhang, YZ
机构
[1] Penn State Univ, Energy Inst, State Coll, PA 16802 USA
[2] Penn State Univ, Dept Energy & GeoEnvironm Engn, State Coll, PA 16802 USA
关键词
anthracite; activation; CO2; adsorption; surface treatment; pore structure; functional group;
D O I
10.1016/j.fuproc.2005.01.003
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Porous materials are being proposed as suitable candidates for CO2 capture due to their highly developed porous structure. Although anthracites are known to produce high surface area activated carbons, there are very limited studies on the application of activated anthracites. Accordingly, in this work, high surface area activated anthracites were prepared by steam activation and their CO2 capacities were investigated. The activated anthracites are mainly microporous. The increase in activation time results in a continuous steady rise of the mesopore area and volume, while the micropore and total pore area and volume reach a maximum at 3 h. The surface areas go through a maximum with increasing solid yields. The adsorption capacity of the activated anthracites decreases rapidly with increasing adsorption temperature, probably due to the adsorption being a physisorption process. The anthracite with the highest CO2 adsorption capacity is the sample activated at 800 degrees C for 2 h, whose surface area was only 540 m(2)/g, and the adsorbed amount Of CO2 was 65.7 mg-CO2/ g-adsorbent, This is probably due to a relationship between microporosity and CO2 physisorption processes. Several surface treatment methods, including NH3 heat treatment and polyethylenimine (PEI) impregnation, were used to modify the surface properties of the activated anthracites in an attempt to increase their CO2 capture capacity at higher temperatures. The surface treatment methods investigated change the porous structure and surface chemistry of the anthracites, and therefore, affect their CO2 capacities. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:1487 / 1502
页数:16
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