DOI: 10.1016/j.jcou.2014.11.005
Scopus记录号: 2-s2.0-84918772347
论文题名: Porous sulfur-doped titanate as the support of tetraethylenepentamine for CO2 capture
作者: Song F. ; Zhong Q. ; Chen Q. ; Rong X. ; Wang B.
刊名: Journal of CO2 Utilization
ISSN: 22129820
出版年: 2015
卷: 9 起始页码: 23
结束页码: 28
语种: 英语
英文关键词: CO2 adsorption
; Sulfur-doped
; Tetraethylenepentamine
; Titanate
Scopus关键词: Adsorption
; Chemical reactors
; Experiments
; Infrared spectroscopy
; Scanning electron microscopy
; Sulfur
; Temperature
; Temperature programmed desorption
; Titanium compounds
; X ray diffraction
; Adsorption and desorptions
; Adsorption capacities
; Adsorption desorption
; Fixed bed reactor system
; Hydrothermal methods
; Physicochemical property
; Tetraethylenepentamine
; Titanate
; Carbon dioxide
英文摘要: Porous sulfur-doped titanate was synthesized by hydrothermal method as the support of amine for CO2 capture. Tetraethylenepentamine (TEPA) was selected as the modifier to enhance CO2 adsorption capacity and selectivity by the introduction of chemisorptions. The physicochemical properties of raw and TEPA modified sulfur-doped titanate were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), infrared spectroscopy (IR), as well as low temperature N2 adsorption. CO2 adsorption and desorption were investigated by a fixed bed reactor system and temperature programmed desorption (TPD), respectively. With the maximum TEPA loading of 45 wt%, the maximum CO2 adsorption capacity reached 3.58 mmol/g at 70 °C. The adsorption capacity for CO2 remained almost the same after cyclic regeneration experiments. Ultimately, the results of characterization and experiments were summarized to understand the CO2 adsorption-desorption mechanism. © 2014 Elsevier Ltd. All rights reserved.
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资源类型: 期刊论文
标识符: http://119.78.100.158/handle/2HF3EXSE/52985
Appears in Collections: 影响、适应和脆弱性
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Recommended Citation:
Song F.,Zhong Q.,Chen Q.,et al. Porous sulfur-doped titanate as the support of tetraethylenepentamine for CO2 capture[J]. Journal of CO2 Utilization,2015-01-01,9