Cu+-Doped PVA-Derived Mesoporous CarbonDiatomite Adsorbent for Selective Adsorption Desulfurization

Herein, we successfully constructed a Cu+-doped PVA-derived mesoporous carbondiatomite (DE) composite by virtue of N2-suffered carbonization and self-reduction at a high temperature. The structure and composition of C/Cu@DE composite adsorbents were determined by a series of characterizations. The r...

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Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1992. - 39(2023), 41 vom: 17. Okt., Seite 14595-14604
1. Verfasser: Xiang, Yang (VerfasserIn)
Weitere Verfasser: Liu, Zan, Cheng, Zhilin
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
Beschreibung
Zusammenfassung:Herein, we successfully constructed a Cu+-doped PVA-derived mesoporous carbondiatomite (DE) composite by virtue of N2-suffered carbonization and self-reduction at a high temperature. The structure and composition of C/Cu@DE composite adsorbents were determined by a series of characterizations. The results affirmed that Cu+ species are highly scattered in PVA-derived mesoporous carbon, which covered the DE surface. The effect of carbonization temperature on the structure and composition of the C/Cu@DE composite adsorbents were intensively investigated, indicating that the C/Cu@DE composite at an 800 °C carbonization temperature (C/Cu@DE-800 °C) showed the formation of many Cu+ species and preferable hierarchical pore properties. The adsorption experiments of benzothiophene (BT) indicated that C/Cu@DE-800 °C possessed a better adsorption capacity. The adsorption behavior of BT onto C/Cu@DE-800 °C was investigated by a variety of adsorption times, initial concentrations, and recycle times, of which the largest adsorption capacity for BT attained 34.2 mg/g. Furthermore, the adsorption kinetics, intraparticle diffusion, adsorption isotherms, and adsorption thermodynamics of BT onto C/Cu@DE-800 °C was deeply studied, which contributed to the proposed adsorption mechanism
Beschreibung:Date Revised 31.10.2023
published: Print-Electronic
Citation Status PubMed-not-MEDLINE
ISSN:1520-5827
DOI:10.1021/acs.langmuir.3c01839