氧化物
X射线光电子能谱
催化作用
分解
吸附
化学工程
基质(水族馆)
热分解
纳米颗粒
介孔材料
原位
材料科学
化学
无机化学
纳米技术
有机化学
海洋学
工程类
地质学
作者
Byeong Jun,Ji Yoon Choi,Yujing Ji,Shufang Zhao,Soong Yeon Kim,Soo Hyun Kim,Young Dok Kim
标识
DOI:10.1016/j.cej.2022.136459
摘要
Fe-oxide nanoparticles (less than 2 nm) were evenly dispersed onto mesoporous Al2O3 beads, and the structure was used as an adsorbent and catalyst for removing H2S. The Fe-oxide enhanced the removal efficiency of H2S molecules at room temperature and suppressed SO2 emission into the gas phase upon thermal treatment of the H2S-covered substrate. Compelling evidence is provided by in-situ DRIFTS and XPS that Fe-oxide not only catalyzes the conversion of H2S to S8, as previously suggested, but also facilitates the formation of SO42− species on the surface of Fe-oxide/Al2O3. A spill-over process of SO42− from Fe-oxide to Al2O3 at their interfacial site was proposed. The removal efficiency of the SO42−-poisoned surfaces could be recovered by water cleaning. This study clearly provides molecular level information about the problems one can face when supported Fe-oxide catalysts are used as H2S-removing agents in field applications, and details regarding how one can avoid such problems.
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