Photocatalytic degradation of methylparaben by TiO2: Multivariable experimental design and mechanism

被引:140
作者
Lin, Yixin [1 ,2 ]
Ferronato, Corinne [1 ]
Deng, Nansheng [2 ]
Wu, Feng [2 ]
Chovelon, Jean-Marc [1 ]
机构
[1] Univ Lyon 1, CNRS, UMR 5256, Inst Rech Catalyse & Environm Lyon, F-69626 Villeurbanne, France
[2] Wuhan Univ, Sch Resources & Environm Sci, Wuhan 430079, Peoples R China
关键词
Methylparaben; Photocatalysis; Multivariate experimental design; Mechanism; ENDOCRINE-DISRUPTING CHEMICALS; HETEROGENEOUS PHOTOCATALYSIS; COSMETIC PRODUCTS; TITANIUM-DIOXIDE; AZO-DYES; WATER; PARABENS; ACID; PATHWAYS; PHENOL;
D O I
10.1016/j.apcatb.2008.09.026
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Methylparaben is widely used as a bactericide and as an antimicrobial agent in the formulation of personal care products (PCPs) such as tooth pastes, deodorants, beauty creams, solar filters, and bath gels. Owing to a certain estrogenic activity, a possible relationship with breast cancer has been proved by many researchers. Photocatalytic degradation of methylparaben was carried out in an aqueous suspension of TiO2 irradiated by ultraviolet light. A multivariable center composite design based on response surface methodology was applied to estimate the individual and interaction factors including pH, TiO2 loading, oxygen concentration and light flux. An acceptable semi-empirical expression (R-2 = 0.9896) was obtained via data analysis to predict the response of 50% methylparaben removal time, and optimal experimental conditions were also achieved thanks to the experimental design (pH 9, TiO2 loading 2.5 g L-1, dissolved oxygen concentration 18 mg L-1 and light flux 5.8 x 10(15) photophotons s(-1) cm(-2)). Under these conditions, after 6 h of irradiation, 80% of methylparaben mineralization evaluated through total organic carbon measurement was obtained and 10 photocatalytic intermediates were identified by GC-MS. In addition, a tentative reaction pathway was proposed. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 41
页数:10
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