Photocatalytic degradation of dye (Reactive Red 198) and pharmaceutical (tetracycline) using MIL-53(Fe) and MIL-100(Fe): catalyst synthesis and pollutant degradation

被引:16
作者
Ahmadi, Shahin [1 ,2 ]
Mahmoodi, Bahaaddin [1 ]
Kazemini, Mohammad [2 ]
Mahmoodi, Niyaz Mohammad [1 ]
机构
[1] Inst Color Sci & Technol, Dept Environm Res, Tehran, Iran
[2] Sharif Univ Technol, Dept Chem & Petr Engn, Tehran, Iran
关键词
Dye; Pharmaceutical; Photocatalysis; MIL-53(Fe); MIL-100(Fe); NONIONIC CO-SURFACTANTS; METAL-ORGANIC FRAMEWORK; RHODAMINE-B; WASTE-WATER; REMOVAL; ISOTHERM; SINGLE;
D O I
10.1108/PRT-05-2022-0067
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Purpose Environmental issues and lack of drinking water have forced researchers to find some alternatives to wastewater treatment. Because dyes are used in a variety of industrial applications such as textile and pharmaceutical, wastewater of these factories leads to several environmental problems. Using catalysis under ultraviolet-irradiation (photocatalysis) is one of the cases that is used in wastewater treatment. The purpose of this work is the photocatalytic degradation of dye (Reactive Red 198) and pharmaceutical (tetracycline) using MIL-53(Fe) and MIL-100(Fe). Design/methodology/approach In this work, Reactive Red 198 (RR198), an anionic dye and tetracycline as a pharmaceutical are tested with two catalysts, MIL-53(Fe) and MIL-100(Fe). Catalyst synthesis method and characterization were discussed by X-ray diffraction, scanning electron microscopy and Fourier Transform Infrared analyses, and their results are described in detail. Findings Dye concentration varies among 15, 20, 30 and 40 mg/L for MIL-100(Fe) for which the removal percent is 97%, 94%, 89% and 58% and for MIL-53(Fe), dye concentration increases from 20 to 40, 60 and 80 mg/L, the removal percent of which is 98%, 88%, 75% and 50%. Pharmaceutical degradation by MIL-53(Fe) and MIL-100(Fe) was 75% and 80%, respectively. Originality/value Photocatalytic degradation of RR198 and tetracycline using MIL-53(Fe) and MIL-100(Fe) was not studied in detail.
引用
收藏
页码:357 / 368
页数:12
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