首页 | 本学科首页   官方微博 | 高级检索  
     


Hydrogen sulfide removal by catalytic oxidative absorption method using rotating packed bed reactor
Authors:Liangliang Zhang  Shuying Wu  Zuozhong Liang  Hong Zhao  Haikui Zou  Guangwen Chu
Affiliation:1.Research Center of the Ministry of Education for High Gravity Engineering and Technology, Beijing University of Chemical Technology, Beijing 100029, China;2.Suzhou Research Institute of Beijing University of Chemical Technology, Suzhou 215100, China
Abstract:Using catalytic oxidative absorption for H2S removal is of great interest due to its distinct advantages. However, traditional scrubbing process faces a great limitation in the confined space. Therefore, there is an urgent demand to develop high-efficiency process intensification technology for such a system. In this article, H2S absorption ex-perimental research was conducted in a rotating packed bed (RPB) reactor with ferric chelate absorbent and a mixture of N2 and H2S, which was used to simulate natural gas. The effects of absorbent pH value, gas–liquid ratio, gravity level of RPB, absorption temperature and character of the packing on the desulfurization efficiency were investigated. The results showed that H2S removal efficiency could reach above 99.6%under the most of the experimental condition and above 99.9%under the optimal condition. A long-time continuous experiment was conducted to investigate the stability of the whole process combining absorption and regeneration. The result showed that the process could well realize simultaneous desulfurization and absorbent regeneration, and the H2S removal efficiency kept relatively stable in the whole duration of 72 h. It can be clearly seen that high gravity technology desulfurization process, which is simple, high-efficiency, and space intensive, has a good prospect for industrial application of H2S removal in confined space.
Keywords:Confined space  RPB  Desulfurization  Catalytic oxidative  Absorption
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《中国化学工程学报》浏览原始摘要信息
点击此处可从《中国化学工程学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号