Ammonia modification of activated carbon to enhance carbon dioxide adsorption: Effect of pre-oxidation

被引:268
|
作者
Shafeeyan, Mohammad Saleh [1 ]
Daud, Wan Mohd Ashri Wan [1 ]
Houshmand, Amirhossein [1 ]
Arami-Niya, Arash [1 ]
机构
[1] Univ Malaya, Dept Chem Engn, Fac Engn, Kuala Lumpur 50603, Malaysia
关键词
Activated carbon; Ammonia treatment; Oxidation; Heat treatment; Surface characterization; Carbon dioxide adsorption; SURFACE FUNCTIONAL-GROUPS; CO2; CAPTURE; OXIDATION REACTIONS; NITRIC-ACID; FLUE-GAS; FT-IR; FIBERS; SORBENTS; OXYGEN; ADSORBENTS;
D O I
10.1016/j.apsusc.2010.11.127
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 commercial granular activated carbon (GAC) was subjected to thermal treatment with ammonia for obtaining an efficient carbon dioxide (CO2) adsorbent. In general, CO2 adsorption capacity of activated carbon can be increased by introduction of basic nitrogen functionalities onto the carbon surface. In this work, the effect of oxygen surface groups before introduction of basic nitrogen functionalities to the carbon surface on CO2 adsorption capacity was investigated. For this purpose two different approaches of ammonia treatment without preliminary oxidation and amination of oxidized samples were studied. Modified carbons were characterized by elemental analysis and Fourier Transform Infrared spectroscopy (FT-IR) to study the impact of changes in surface chemistry and formation of specific surface groups on adsorption properties. The texture of the samples was characterized by conducting N-2 adsorption/desorption at -196 degrees C. CO2 capture performance of the samples was investigated using a thermogravimetric analysis (TGA). It was found that in both modification techniques, the presence of nitrogen functionalities on carbon surface generally increased the CO2 adsorption capacity. The results indicated that oxidation followed by high temperature ammonia treatment (800 degrees C) considerably enhanced the CO2 uptake at higher temperatures. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:3936 / 3942
页数:7
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