Issue 15, 2023

A study on the catalytic performance of the ZrO2@γ-Al2O3 hollow sphere catalyst for COS hydrolysis

Abstract

In order to achieve the catalytic removal of COS gas from blast furnace gas by hydrolysis, it is necessary to obtain a hydrolysis catalyst with excellent performance. A hollow sphere hydrolysis catalyst with low catalytic energy consumption, long catalytic life and high conversion COS efficiency was prepared by using carbon spheres as a template and urea as a precipitant to increase the alkalinity of the impregnating solution to overcome the shortcomings of limited adsorption of a carbon sphere template. The structural characteristics of the prepared Al2O3 hollow sphere hydrolysis catalyst were first analyzed; then different proportions of zirconium nitrate were loaded onto the surface of the Al2O3 hollow spheres to investigate the effect of the formed ZrO2@γ-Al2O3 hollow sphere hydrolysis catalyst on the catalytic performance of COS hydrolysis. The results showed that the average pore size, total pore volume and specific surface area of the ZrO2@γ-Al2O3 hollow sphere hydrolysis catalyst roasted at 500 °C reached the maximum, with 12.921 nm, 0.177 cm3 g−1 and 52.969 m2 g−1, respectively. The hydrolytic catalytic efficiency of COS was highest when the roasting temperature was 500 °C. After 70 min of reaction, the hydrolytic conversion efficiency of COS remained at about 82% with a conversion of 158 mg m−3. The key problems of low catalytic activity and short catalytic life of hydrolysis catalysts can be effectively solved when using hydrolysis catalysis for the removal of COS.

Graphical abstract: A study on the catalytic performance of the ZrO2@γ-Al2O3 hollow sphere catalyst for COS hydrolysis

Article information

Article type
Paper
Submitted
10 Oct 2022
Accepted
15 Feb 2023
First published
22 Mar 2023

New J. Chem., 2023,47, 7070-7083

A study on the catalytic performance of the ZrO2@γ-Al2O3 hollow sphere catalyst for COS hydrolysis

Z. Lei, W. Hengliang, L. Zhang, J. Yang and W. Qi, New J. Chem., 2023, 47, 7070 DOI: 10.1039/D2NJ04970H

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