Photocatalytic degradation of chlorophenols using star block copolymers: Removal efficiency, by-products and toxicity of catalyst
- Authors
- Chung, Seung-Gun; Chang, Yoon-Seok; Choi, Jae-Woo; Baek, Kyung-Youl; Hong, Seok-Won; Yun, Seong-Taek; Lee, Sang-Hyup
- Issue Date
- 15-1월-2013
- Publisher
- ELSEVIER SCIENCE SA
- Keywords
- Chlorophenols; Photocatalytic degradation; Star block copolymer; Porphyrin; Hydrophobicity; Toxicity
- Citation
- CHEMICAL ENGINEERING JOURNAL, v.215, pp.921 - 928
- Indexed
- SCIE
SCOPUS
- Journal Title
- CHEMICAL ENGINEERING JOURNAL
- Volume
- 215
- Start Page
- 921
- End Page
- 928
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/104195
- DOI
- 10.1016/j.cej.2012.11.070
- ISSN
- 1385-8947
- Abstract
- This study investigated the photocatalytic degradation of chlorophenols using two different types of porphyrin core star block copolymers (P-PSD and P-PD) with irradiation using visible light. Both P-PSD and P-PD catalysts show similar tendencies in the degradation of chlorophenols. Pentachlorophenol degraded faster than other chlorinated phenols (pentachlorophenol > 2,4,6-trichlorophenol > 2,4-dichlorophenol). The removal rate of chlorophenols using P-PSD was higher than the removal rate using P-PD, a difference which could be attributed to the hydrophobicity of P-PSD. The degradation intermediates and by-products of the chlorophenols were also identified. The analysis results revealed that the degradation of highly-chlorinated phenols was more rapid than the degradation of the less-chlorinated phenols, as confirmed by residual chlorinated compound and chloride ions that were released. The newly synthesized P-PSD catalyst is non-toxic to bacteria. For these reasons, the process of photocatalytic degradation using porphyrin core star block copolymers has potential advantages for the degradation of dissolved chlorophenol pollutants in water. (C) 2012 Elsevier B.V. All rights reserved.
- Files in This Item
- There are no files associated with this item.
- Appears in
Collections - College of Science > Department of Earth and Environmental Sciences > 1. Journal Articles
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.