Amine-functionalized monodispersed porous silica microspheres with enhanced CO2 adsorption performance and good cyclic stability

被引:70
作者
Le, Yao [1 ]
Guo, Daipeng [1 ]
Cheng, Bei [1 ]
Yu, Jiaguo [1 ]
机构
[1] Wuhan Univ Technol, State Key Lab Adv Technol Mat Synth & Proc, Wuhan 430070, Peoples R China
关键词
Monodispersed porous silica microspheres; Amine functionalization; Tetraethylenepentamine; Carbon dioxide; Adsorption; CARBON-DIOXIDE CAPTURE; MESOPOROUS SILICA; PHOTOCATALYTIC ACTIVITY; HYDROTHERMAL SYNTHESIS; ASSISTED SYNTHESIS; EFFICIENT REMOVAL; SIO2; MICROSPHERES; HIGH-CAPACITY; SURFACE-AREA; SORBENT;
D O I
10.1016/j.jcis.2013.07.014
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
Carbon dioxide capture using solid adsorbent has caused more and more attention in the world. Herein, amine-functionalized monodispersed porous silica microspheres (MPSM) were prepared by the hydrolysis and condensation of tetraethoxysilane (TEOS) in a water-ethanol-dodecylamine mixed solution, then calcined at 600 degrees C, and finally functionalized with tetraethylenepentamine (TEA). The CO2 adsorption performance of the prepared samples was measured using a Chemisorb 2720 pulse chemisorption system (Micromeritics, USA). The results showed that the specific surface area and pore volume of the 600 degrees C-calcined SiO2 microspheres reached 921 m(2)/g and 0.48 cm(3)/g, respectively. All the TEA-functionalized samples exhibited good CO2 adsorption performance, which were related to the amount of loaded TEA, adsorption temperatures, and the specific surface areas of the prepared samples. An optimal TEA loading amount (34 wt%) and adsorption temperature (75 degrees C) were determined. The maximum CO2 adsorption amount (4.27 mmol g(-1) adsorbent) was achieved on the 600 degrees C-calcined SiO2 microsphere sample with TEA loading of 34 wt%. Repeated adsorption/desorption cycle experiments revealed that the TEA-functionalized SiO2 microspheres were good CO2 adsorbents exhibiting excellent cyclic stability. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:173 / 180
页数:8
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