Photocatalytic degradation of VOCs from air stream using Mo:TiO2/GAC nanocomposites

Modification of TiO _2 is one of the techniques used to enhance its photodegradation efficiency and to make it visible-light-active. In this study, Mo-doped TiO _2 nanoparticles were synthesized using a fast sol-gel technique and then coated on granular activated carbon (GAC) as both substrate and a...

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Detalhes bibliográficos
Main Authors: Kamaladdin Abedi, Behzad Shahmoradi, Ebrahim Mohammadi, Kitirote Wantala, Afshin Maleki, Yahya Zandsalimi, Sonya Salimi, Shadi Kohzadi
Formato: Artigo
Idioma:English
Publicado em: IOP Publishing 2022-01-01
Colecção:Materials Research Express
Assuntos:
Acesso em linha:https://doi.org/10.1088/2053-1591/ac4aa3
Descrição
Resumo:Modification of TiO _2 is one of the techniques used to enhance its photodegradation efficiency and to make it visible-light-active. In this study, Mo-doped TiO _2 nanoparticles were synthesized using a fast sol-gel technique and then coated on granular activated carbon (GAC) as both substrate and adsorbent to obtain Mo:TiO _2 /GAC composite. The fabricated composite was characterized by many techniques such as powder XRD, SEM, EDX, FTIR, and N _2 adsorption-desorption analysis. Then, the composite was applied to photodegrade volatile organic compounds (VOCs) under both UV and visible light irradiations. The characterization results showed high crystallinity and purity. Mo:TiO _2 /GAC composite gave a higher photodegradation efficiency compared with bare TiO _2 and bare GAC. Moreover, studying operational parameters showed that the optimum condition for photodegradation efficiency of VOCs was at a flowrate of 1 L min ^−1 , VOCs concentration of 20 ppm, and light intensity of 400 and 600 W m ^−2 for UV and visible light, respectively. The results suggest that Mo:TiO _2 /GAC is a visible-light-active composite and can be acceptably used to decompose VOCs under visible light with adequate efficiency and without the generation of harmful by-products such as O _3 as compared with UV.
ISSN:2053-1591