Photocatalytic decomposition of humic acids on TiO2 Part I:: Discussion of adsorption and mechanism

被引:117
|
作者
Wiszniowski, J
Robert, D
Surmacz-Gorska, J
Miksch, K
Weber, JV
机构
[1] Univ Metz, Lab Chim & Applicat EA 3471, F-57500 St Avold, France
[2] Silesian Tech Univ, Environm Biotechnol Dept, PL-44100 Gliwice, Poland
关键词
photocatalysis; titanium dioxide; humic acids; TOC; BOD5; adsorption;
D O I
10.1016/S1010-6030(02)00022-9
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
In this paper we present the results of the photocatalytic degradation of humic acids (HAs) in aqueous solution. Bench scale experiments were carried out using titanium oxide as photocatalyst. We studied the adsorption of HAs on TiO2 surface and we describe the kinetics of their photocatalytic degradation. The adsorption study of HA at three pH solution (1.9/7 5/11) by FT-IR DRIFT technique indicated that at acidic pH, HA are adsorbed on TiO2 mainly by carboxylate groups. We determined the isotherms of HA and it was shown that Langmuir model cannot be applied in this case. However, if the asymptotic values of the isotherms were assumed for these analytical methods the close values were obtained. The kinetics of degradation was followed with TOC and pH. There are no important pH evolutions. It was obtained 88% of TOC removal after 6 h of irradiation with optimum TiO2 loading 1 0 g/l. We observed the presence of two domains of HA degradation kinetics. In the first step, slight TOC decreased possibly due to the photodepolymerization of adsorbed HA on TiO2. In the second one, the photodegradation followed pseudo-first-order kinetics. Organic intermediates were determined by high performance liquid chromatography (HPLC) (PDA-detector) analysis as well as biological oxygen demand (BOD5). It was shown that photocatalysis process improved the biodegradability of HA nevertheless mineralization process mainly occurred and there was no large amount of easy biodegradable species present in the reaction solution. (C) 2002 Elsevier Science B.V All rights reserved.
引用
收藏
页码:267 / 273
页数:7
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