Ce-doping CuO/HZSM-5 as a regenerable sorbent for Adsorption-Oxidation removal of PH3 at low temperature

被引:23
作者
Feng, Jiayu [1 ]
Wang, Fei [1 ]
Wang, Chi [3 ]
Li, Kai [1 ]
Ning, Ping [1 ,2 ]
Sun, Xin [1 ]
Jia, Lijuan [4 ]
机构
[1] Kunming Univ Sci & Technol, Fac Environm Sci & Engn, Kunming 650500, Yunnan, Peoples R China
[2] Kunming Univ Sci & Technol, Natl Reg Engn Ctr Recovery Waste Gases Met & Chem, Kunming 650500, Yunnan, Peoples R China
[3] Kunming Univ Sci & Technol, Fac Chem Engn, Kunming 650500, Yunnan, Peoples R China
[4] Yunnan Minzu Univ, Sch Chem & Environm, Kunming 650504, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
PH3; Adsorption-oxidation; Ce-doping CuO/HZSM-5; CATALYTIC-ACTIVITY; HYDROGEN-SULFIDE; CO OXIDATION; H2S; PHOSPHORUS; ZEOLITE; SBA-15; IDENTIFICATION; ADSORBENTS; CONVERSION;
D O I
10.1016/j.seppur.2021.119420
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A series CemCunOx/HZSM-5 sorbents were introduced to remove PH3 in low-temperature and low-oxygen en-vironments. The effects of copper loading and cerium doping on the adsorption-oxidation performance of the sorbents were investigated. Experimental results showed that doping with 1 wt% of cerium (Ce1Cu30OX/HZSM-5) could significantly improve the performance of the sorbent. The PH3 breakthrough capacity was identified as 114.36 mg(PH3).g(sorbent)(-1). In addition, after three thermal regeneration cycles, the sorbent still has ideal per-formance. X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS) analyses exhibited that CuO was the main active species, and Ce-doping can increase the chemisorption oxygen on the surface of the sorbent. BET results demonstrated that the introduction of cerium could improve the specific surface area and pore volume of sorbent. Hydrogen temperature-programmed reduction (H-2-TPR) and scanning electron microscope (SEM-EDS) indicated that cerium species played an important role in uniformly dispersing copper species on the HZSM-5 surface and improving the oxidation performance of sorbent. Moreover, the reaction products and mechanisms were also investigated by XRD, XPS, and in-situ FTIR spectra. The results indicated that the consumption of CuO and the accumulation of phosphorus species (e.g., P, P2O5, and Cu3P) on the surface and inner pores of the sorbent were the primary reasons for the deactivation of the sorbent.
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页数:10
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