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可再生 Fe-Mn-ZnO/SiO2 吸附剂用于室温下脱除燃料重整物中的 H2S:性能、活性位、原位研究。

Regenerable Fe-Mn-ZnO/SiO2 sorbents for room temperature removal of H2S from fuel reformates: performance, active sites, Operando studies.

机构信息

Department of Chemical Engineering, Auburn University, Auburn, AL 36849, USA.

出版信息

Phys Chem Chem Phys. 2011 Feb 14;13(6):2179-87. doi: 10.1039/c0cp01355b. Epub 2010 Dec 6.

Abstract

Fe- and Mn-promoted H(2)S sorbents Fe(x)-Mn(y)-Zn(1-x-y)O/SiO(2) (x, y = 0, 0.025) for desulfurization of model fuel reformates at room temperature were prepared, tested and characterized. Sulfur uptake capacity at 25 °C significantly exceeds that of both commercial unsupported ZnO sorbents and un-promoted supported ZnO/SiO(2) sorbents. Sulfur capacity and breakthrough characteristics remain satisfactory after multiple (∼10) cycles of adsorption/regeneration, with regeneration performed by a simple and robust heating in air. XRD shows that both "calcined" and "spent" sorbents contain nano-dispersed ZnO, and XPS confirms conversion of ZnO to ZnS. "Calcined" sorbent contains Fe(3+) and Mn(3+) that are reduced to Mn(2+) upon reaction with H(2)S, but not with H(2). Operando ESR is used for the first time to study dynamics of reduction of Mn(3+) promoter sites simultaneously with measuring sulfidation dynamics of the Fe(x)-Mn(y)-Zn(1-x-y)O/SiO(2) sorbent. Fe cations are believed to occupy the surface of supported ZnO nanocrystallites, while Mn cations are distributed within ZnO.

摘要

用于室温下模型燃料重整物脱硫的 Fe(x)-Mn(y)-Zn(1-x-y)O/SiO(2) (x, y = 0, 0.025) 负载型 H(2)S 吸附剂 Fe 和 Mn 促进剂被制备、测试和表征。在 25°C 时,硫吸收容量显著超过商业无载体 ZnO 吸附剂和未促进的负载型 ZnO/SiO(2)吸附剂。经过多次(约 10 次)吸附/再生循环后,硫容量和穿透特性仍保持满意,再生采用简单而稳健的空气加热法。XRD 表明“煅烧”和“用过”的吸附剂均含有纳米分散的 ZnO,XPS 证实 ZnO 转化为 ZnS。“煅烧”吸附剂含有 Fe(3+)和 Mn(3+),它们在与 H(2)S 反应时被还原为 Mn(2+),但不与 H(2)反应。ESR 是首次用于同时研究 Mn(3+)促进剂位还原动力学和 Fe(x)-Mn(y)-Zn(1-x-y)O/SiO(2)吸附剂硫化动力学的操作模式。认为 Fe 阳离子占据负载型 ZnO 纳米晶的表面,而 Mn 阳离子分布在 ZnO 中。

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