4.7 Article

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

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出版社

ELSEVIER
DOI: 10.1016/j.seppur.2021.119420

关键词

PH3; Adsorption-oxidation; Ce-doping CuO/HZSM-5

资金

  1. National Natural Science Foundation of China [51968034, 41807373, 22006058]
  2. Science and Technology Program of Yunnan province [2019FB069]
  3. Analysis and Testing Foundation of Kunming University of Science and Technology [2020P20181107015]

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The introduction of cerium was found to significantly improve the performance and regeneration ability of the sorbent for PH3 removal. Analytical techniques such as XRD, XPS, and BET showed that cerium doping not only increased the specific surface area and pore volume of the sorbent, but also enhanced the chemisorption oxygen on the surface. SEM-EDS and H-2-TPR analyses demonstrated that cerium species played a crucial role in dispersing copper species and improving the oxidation performance.
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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