Further investigations of CO2 capture using triamine-grafted pore-expanded mesoporous silica

被引:154
作者
Serna-Guerrero, Rodrigo [2 ]
Belmabkhout, Youssef [1 ]
Sayari, Abdelhamid [1 ,2 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Dept Chem & Biol Engn, Ottawa, ON K1N 6N5, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CO2; capture; Aminosilane grafting; Adsorption capacity; Adsorption selectivity; Adsorbent regeneration; CARBON-DIOXIDE; AMBIENT-TEMPERATURE; MCM-41; SILICA; DRY GASES; ADSORPTION; AMINE; SIZE; NITROGEN; EQUILIBRIUM; SEPARATION;
D O I
10.1016/j.cej.2010.01.041
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A promising adsorbent for acid gas removal, referred to as TRI-PE-MCM-41, was produced by grafting a triamine-containing silane on an MCM-41-type mesoporous silica whose pores have been enlarged by post-synthesis hydrothermal treatment in the presence of a pore-expander. The CO2 adsorption capacity was determined gravimetrically, and via column breakthrough measurements. The tolerance of TRI-PE-MCM-41 to moisture in the feed was substantiated by measurements under both equilibrium and dynamic conditions. Using a combination of mass spectrometry and thermogravimetry, it was corroborated that the presence of moisture enhances the CO2 uptake at equilibrium. Adsorption measurements using fixed bed columns showed that moisture does not affect negatively the CO2 working adsorption capacity compared to dry streams. Furthermore, since the material hardly adsorbed any N-2 or O-2, the selectivity for CO2 over N-2 and O-2 was practically infinitely high. Cyclic measurements of pure CO2 and CO2 :N-2 = 10:90 mixture using different regeneration modes shed light on the stability of the material and the influence of adsorption/desorption operating conditions on its performance. It was found that the temperature swing regeneration mode is suitable for desorption above 120 degrees C. while regeneration under temperature-vacuum swing may be attractive at lower desorption temperatures. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:513 / 519
页数:7
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