UV and visible activation of Cr(III)-doped TiO2 catalyst prepared by a microwave-assisted sol–gel method during MCPA degradation
Photocatalytic degradation of 4-chloro-2-methylphenoxyacetic acid (MCPA) in aqueous solution using Cr(III)-doped TiO 2 under UV and visible light was investigated. The semiconductor material was synthesized by a microwave-assisted sol–gel method with Cr(III) doping contents of 0.02, 0.04, and 0.06 w...
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Published in | Environmental science and pollution research international Vol. 24; no. 14; pp. 12673 - 12682 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.05.2017
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Photocatalytic degradation of 4-chloro-2-methylphenoxyacetic acid (MCPA) in aqueous solution using Cr(III)-doped TiO
2
under UV and visible light was investigated. The semiconductor material was synthesized by a microwave-assisted sol–gel method with Cr(III) doping contents of 0.02, 0.04, and 0.06 wt%. The catalyst was characterized using X-ray powder diffraction (XRD), scanning electron microscopy (SEM), nitrogen physisorption, UV–Vis diffuse reflectance spectroscopy (DRS), and atomic absorption spectroscopy (AAS). The photocatalytic activity for the photodegradation of MCPA was followed by reversed-phase high-performance liquid chromatography (HPLC) and total organic carbon (TOC) analysis. The intermediates formed during degradation were identified using gas chromatography–mass spectrometry (GC–MS). Chloride ion evolution was measured by ion chromatography. Characterization results showed that Cr(III)-doped TiO
2
materials possessed a small crystalline size, high surface area, and mesoporous structure. UV–Vis DRS showed enhanced absorption in the visible region as a function of the Cr(III) concentration. The Cr(III)-doped TiO
2
catalyst with 0.04 wt% of Cr(III) was more active than bare TiO
2
for the degradation of MCPA under both UV and visible light. The intermediates identified during MCPA degradation were 4-chloro-2-methylphenol (CMP), 2-(4-hydroxy-2-methylphenoxy) acetic acid (HMPA), and 2-hydroxybuta-1,3-diene-1,4-diyl-bis (oxy)dimethanol (HBDM); the formation of these intermediates depended on the radiation source. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0944-1344 1614-7499 |
DOI: | 10.1007/s11356-016-8034-x |