Back to Search Start Over

Fe–Ti bimetal oxide adsorbent for removing low concentration H2S at room temperature.

Authors :
Guo, Zhuangzhuang
Zhang, Zhihong
Cao, Xiaoyan
Feng, Dongfang
Source :
Environmental Technology; Oct2022, Vol. 43 Issue 24, p3693-3705, 13p
Publication Year :
2022

Abstract

Herein, a series of Fe–Ti bimetal oxide adsorbents were prepared by reduction–co-precipitation method, and their performance in removing low concentration H<subscript>2</subscript>S at room temperature was investigated. The adsorbents were characterized by X-Ray diffraction (XRD), Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), Ultraviolet Visible diffuse reflectance spectroscopy (UV–Vis-DRS), X-Ray photoelectron spectroscopy (XPS) and N<subscript>2</subscript> adsorption–desorption. The results showed that the addition of Ti increased the specific surface area, pore volume and small oligomeric Fe<subscript>2</subscript>O<subscript>3</subscript> of ferrihydrite. When the Fe/Ti molar ratio was 8:1, Fe–Ti bimetal oxide formed a large amount of oligomeric Fe<subscript>2</subscript>O<subscript>3</subscript>, and its specific surface area and pore volume reached 344.99 m<superscript>2</superscript>/g and 0.34 cm<superscript>3</superscript>/g, respectively. At this time, Fe–Ti bimetal oxide exhibited the highest breakthrough sulfur capacity of 222.8 mg/g. High temperature calcination caused Fe–Ti bimetal oxide to form small specific surface area and pore volume, and produced crystalline α-Fe<subscript>2</subscript>O<subscript>3</subscript>. And the breakthrough sulfur capacity of Fe–Ti bimetal oxide decreased with the increasing calcination temperature. In addition, the desulfurization process conformed to the unreacted shrinking nucleus model. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09593330
Volume :
43
Issue :
24
Database :
Complementary Index
Journal :
Environmental Technology
Publication Type :
Academic Journal
Accession number :
159503644
Full Text :
https://doi.org/10.1080/09593330.2021.1931472