Logo BSU

Please use this identifier to cite or link to this item: https://elib.bsu.by/handle/123456789/288315
Title: Adsorption and Decomposition of NOx on Heteropolyacids: An Evaluation of the Adsorption Performance
Authors: Zhu, H.
Yu, M.
Tao, M.
Rui, W.
Korchak, V.
Korchak, V.N.
Matulis, V.E.
Keywords: ЭБ БГУ::ЕСТЕСТВЕННЫЕ И ТОЧНЫЕ НАУКИ::Химия
Issue Date: 2021
Publisher: AAGR Aerosol and Air Quality Research
Citation: Aerosol Air Qual Res 2021;21(12)
Abstract: In order to develop an efficient method by which to eliminate NOx pollution, several new catalyst systems including different heteropolyacids (HPAs) and supported phosphotungstic acids (HPWs) (HPW/SiO2, HPW/SnO2, HPW/USY and HPW/ZSM-5) for adsorption-decomposition of NOx were prepared and studied. The obtained catalysts were characterized using Brunauer-Emmett-Teller (BET) measurement and Fourier transform infrared (FT-IR) analysis. The results showed that W-containing HPAs were superior to Mo-containing HPAs. Among the selected catalysts, HPW/SnO2 with a 50% HPW loading had the highest NOx adsorption rate of 77.3%, for which the amount of saturated NOx adsorption (85.4 mg g–1) was much higher than that of HPW (50.5 mg g–1). The NOx adsorption performance of the catalyst was mainly determined by the interaction between the support and the HPW, which was also affected by the specific surface area of the catalyst. FTIR characterization revealed that the adsorbed NOx mainly existed in the HPW bulk phase in the form of NOH+. A gas chromatograph-mass spectrometer (GC-MS) was used to confirm the effectiveness of NOx decomposition into N2.
URI: https://elib.bsu.by/handle/123456789/288315
DOI: 10.4209/AAQR.210251
Scopus: 85123047028
Sponsorship: This work was supported by the National Natural Science Foundation of China [No. 20776080, 20911120088] and the Scientific Innovation program of Shenzhen city, China, under basic research program (JCYJ20170818102915033).
Licence: info:eu-repo/semantics/openAccess
Appears in Collections:Статьи сотрудников НИИ ФХП

Files in This Item:
File Description SizeFormat 
aaqr-21-09-oa-0251.pdf1,14 MBAdobe PDFView/Open
Show full item record Google Scholar



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.