中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Oxidation mechanisms of H2S by oxygen and oxygen-containing functional groups on activated carbon

文献类型:期刊论文

作者Li, Yuran1; Lin, Yuting1,2; Xu, Zhicheng1,2; Wang, Bin1; Zhu, Tingyu1,3
刊名FUEL PROCESSING TECHNOLOGY
出版日期2019-06-15
卷号189页码:110-119
关键词Activated carbon Hydrogen sulfide Elemental sulfur Sulfate Sulfite
ISSN号0378-3820
DOI10.1016/j.fuproc.2019.03.006
英文摘要Activated carbon (AC) has the advantage of multi-pollutant control with a high removal efficiency for flue gas purification. It is necessary to determine the oxidation mechanism and oxidation products of hydrogen sulfide (H2S) on AC to simultaneously capture H2S and SO2. A fixed-bed reactor was coupled with a mass spectrometer (MS) to detect the gaseous components and X-ray photoelectron spectroscopy (XPS) was used to distinguish the sulfur-containing species in the oxidation products on AC and thermally treated AC to investigate the actions of the oxygen-containing functional groups. The results revealed that H2S was adsorbed on the AC surface and combined with oxygen-containing functional groups to form sulfate (SO42-) in the absence of O-2. In the presence of O-2, H2S and O-2 in the atmosphere were adsorbed on the AC active sites, and the catalytic reaction produced elemental sulfur. Elemental sulfur further reacted with O-2 to produce gaseous SO2. According to the detection results of XPS and the in situ diffuse reflectance infrared Fourier transform (in situ DRIFT) spectra, an oxidation mechanism of H2S by O-2 and oxygen-containing functional groups was described. The C=C and C = O bonds were broken by H2S, and then, C-S and S-O bonds of the intermediate products were generated. The C-S bond tended to form elemental sulfur, while the S-O bond likely formed a sulfate or gaseous SO2. Porosity analysis showed that the AC specific surface area decreased after H2S adsorption and that sulfate reduced the specific surface area much more than elemental sulfur.
WOS关键词SELECTIVE CATALYTIC-REDUCTION ; HYDROGEN-SULFIDE ; NO ; ADSORPTION ; SULFUR ; SO2 ; NH3 ; REACTIVITY ; NH3-SCR ; MERCURY
资助项目National Key R&D Program of China[2017YFC0210600] ; National Natural Science Foundation of China[21477131] ; Industry-School-Research Institution Program of HBIS Group Tangsteel Company
WOS研究方向Chemistry ; Energy & Fuels ; Engineering
语种英语
WOS记录号WOS:000464486300011
出版者ELSEVIER SCIENCE BV
资助机构National Key R&D Program of China ; National Natural Science Foundation of China ; Industry-School-Research Institution Program of HBIS Group Tangsteel Company
源URL[http://ir.ipe.ac.cn/handle/122111/28156]  
专题中国科学院过程工程研究所
通讯作者Li, Yuran; Zhu, Tingyu
作者单位1.Chinese Acad Sci, Beijing Engn Res Ctr Proc Pollut Control, Natl Engn Lab Hydromet Cleaner Prod Technol, Inst Proc Engn, Beijing 100190, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Inst Urban Environm, Ctr Excellence Reg Atmospher Environm, Xiamen 361021, Peoples R China
推荐引用方式
GB/T 7714
Li, Yuran,Lin, Yuting,Xu, Zhicheng,et al. Oxidation mechanisms of H2S by oxygen and oxygen-containing functional groups on activated carbon[J]. FUEL PROCESSING TECHNOLOGY,2019,189:110-119.
APA Li, Yuran,Lin, Yuting,Xu, Zhicheng,Wang, Bin,&Zhu, Tingyu.(2019).Oxidation mechanisms of H2S by oxygen and oxygen-containing functional groups on activated carbon.FUEL PROCESSING TECHNOLOGY,189,110-119.
MLA Li, Yuran,et al."Oxidation mechanisms of H2S by oxygen and oxygen-containing functional groups on activated carbon".FUEL PROCESSING TECHNOLOGY 189(2019):110-119.

入库方式: OAI收割

来源:过程工程研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。