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Investigation of the Role of Copper Species-Modified Active Carbon by Low-Temperature Roasting on the Improvement of Arsine Adsorption

[Image: see text] Traditional adsorbents undershot the expectations for arsine (AsH(3)) removal under low-temperature operation conditions in the industry. In this study, the copper (Cu) precursor was used to modify activated carbon and yield novel adsorbents by low-temperature roasting for high-eff...

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Detalles Bibliográficos
Autores principales: Chen, Xiaoyu, Feng, Xuan, Xie, Yibing, Wang, Langlang, Chen, Lu, Wang, Xueqian, Ma, Yixing, Ning, Ping, Pu, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9134391/
https://www.ncbi.nlm.nih.gov/pubmed/35647465
http://dx.doi.org/10.1021/acsomega.2c01355
Descripción
Sumario:[Image: see text] Traditional adsorbents undershot the expectations for arsine (AsH(3)) removal under low-temperature operation conditions in the industry. In this study, the copper (Cu) precursor was used to modify activated carbon and yield novel adsorbents by low-temperature roasting for high-efficiency removal of AsH(3). The best conditions were determined as impregnation with 2 mol/L Cu(NO(3))(2) adsorbent and roasting at 180 °C. At a reaction temperature of 40 °C and an oxygen content of 1%, the AsH(3) removal efficiency reached over 90% and lasted for 40 h and the best capacity of 369.6 mg/g was obtained with the Cu/Ac adsorbent. The characterization results showed the decomposition of Cu(NO(3))(2) during the low-temperature roasting process to form surface functional groups. The formation of the important intermediate Cu(2)(NO(3))(OH)(3) in the decomposition of Cu(NO(3))(2) into CuO plays a role in the good regeneration performance of the Cu/Ac adsorbent using water washing and the gas regeneration method. The results of in situ diffuse reflectance infrared Fourier transform spectroscopy combined with X-ray photoelectron spectroscopy demonstrated that the interaction of trace oxygen with Lewis (L) acid sites increased chemisorbed oxygen by 17.34%, significantly promoting the spontaneity of AsH(3) oxidation reaction. These results provide a friendly economic method with industrial processes practical for AsH(3) removal.