Mercury selective adsorption characteristics and SO2 poison performance on CaO

被引:0
|
作者
Li C. [1 ]
Duan Y. [1 ]
Tang H. [1 ]
Zhu C. [1 ]
Zheng Y. [1 ]
Wei H. [1 ]
机构
[1] Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, 210096, Jiangsu
来源
Huagong Xuebao/CIESC Journal | 2017年 / 68卷 / 09期
基金
中国国家自然科学基金;
关键词
CaO adsorbents; Elemental mercury; Mercuric chloride; Selective adsorption; Sulfur poisoning;
D O I
10.11949/j.issn.0438-1157.20170343
中图分类号
学科分类号
摘要
Using Ca(NO3)2 as a precursor and SiO2 as carrier, a supported CaO adsorbent was prepared. The selective adsorption performances of elemental mercury (Hg0) and mercuric chloride (HgCl2) of the sorbent were conducted in a fixed bed, and the effects of SO2 on CaO mercury adsorption process were also investigated. At the same time, combined with the program temperature desorption (TPD) and in situ diffuse reflectance infrared spectroscopy (in-situ DRIFT) characterization technology, the selective adsorption mechanism of CaO and the mechanism of SO2 poisoning were deeply investigated. The mercury adsorption results showed that CaO maintained a breakthrough of nearly 100% for Hg0 in pure N2 atmosphere and doped SO2 atmosphere, while HgCl2 manifested 66.0% and 60.3% adsorption efficiency in two atmospheres, respectively, indicating that there was a competitive adsorption relationship between SO2 and HgCl2 on CaO surface. The characterized results of CaO before and after adsorption suggested that as compared with Hg0, HgCl2 was able to form monodentate, bidentate and other adsorption structure with the basic sites on the CaO surface. SO2 and HgCl2 formed a competitive adsorption relationship in the active sites where the bridged bidentate was easily formed, resulting in the reduction of adsorption efficiency of HgCl2 on CaO. © All Right Reserved.
引用
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页码:3565 / 3572
页数:7
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