Study on the lifetime of photocatalyst by photocatalytic membrane reactors (PMR)

The continuously photocatalytic degradation of methyl orange (MO) was carried out using a photocatalytic membrane reactor (PMR). The lifetime, cause of deactivation, and regeneration of Degussa P25 titanium dioxide (TiO2) were investigated. The photocatalyst was deactivated when the concentration of...

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Veröffentlicht in:Water science and technology : a journal of the International Association on Water Pollution Research. - 1986. - 81(2020), 1 vom: 21. Jan., Seite 131-137
1. Verfasser: Yan, Xiaoju (VerfasserIn)
Weitere Verfasser: Li, Junyu, Ma, Cong, Tang, Yu, Kong, Xiangji, Lu, Jinfeng
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2020
Zugriff auf das übergeordnete Werk:Water science and technology : a journal of the International Association on Water Pollution Research
Schlagworte:Journal Article Oxidants Hydrogen Peroxide BBX060AN9V Titanium D1JT611TNE
Beschreibung
Zusammenfassung:The continuously photocatalytic degradation of methyl orange (MO) was carried out using a photocatalytic membrane reactor (PMR). The lifetime, cause of deactivation, and regeneration of Degussa P25 titanium dioxide (TiO2) were investigated. The photocatalyst was deactivated when the concentration of MO in the effluent of the PMR was stable. To characterize the lifetime of the photocatalyst, we applied g MO/g TiO2. The lifetime of the photocatalyst during the photocatalytic degradation of 10 mg/L MO was 3.71 times that of 5 mg/L MO. Changing the hydraulic retention time of the PMR from 0.75 to 3 h prolonged the lifetime of the photocatalyst. Deactivation of the photocatalyst was not due to pore blocking by the reactant (MO) or intermediate products. The surface adsorption of MO and the reaction intermediates deactivated the catalyst. The spent catalysts were regenerated after washing with methanol and hydrogen peroxide (H2O2) and then treated with heat. H2O2 treatment generated the highest regeneration rate, because H2O2 is a strong oxidizing agent that oxidized the deposited species on the surface of the photocatalyst
Beschreibung:Date Completed 17.04.2020
Date Revised 15.12.2020
published: Print
Citation Status MEDLINE
ISSN:0273-1223
DOI:10.2166/wst.2020.091