Degradation of short-chain alkyl- and alkanolamines by TiO2- and Pt/TiO2-assisted photocatalysis

被引:113
作者
Klare, M
Scheen, J
Vogelsang, K
Jacobs, H
Broekaert, JAC
机构
[1] Univ Leipzig, Inst Analyt Chem, D-04103 Leipzig, Germany
[2] Univ Dortmund, Inst Umweltforsch, D-44221 Dortmund, Germany
[3] Univ Dortmund, Fachbereich Chem, D-44221 Dortmund, Germany
关键词
photocatalytic degradation; alkylamines; alkanolamines; advanced oxidation process; photooxidation;
D O I
10.1016/S0045-6535(99)00447-6
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photooxidation of C2H5NH2, (C2H5)(2)NH, HOC2H4NH2, (HOC2H4)(2)NH and (HOC2H4)(3)N using TiO2 and Pt/ TiO2 as photocatalysts has been investigated. A laboratory set up was designed and a study on the influence of the concentration of the photocatalyst, the pH-value and the structure of the amine performed. The photocatalytic process was optimized with respect to the concentrations of the model substances during degradation. The decrease of the amine concentrations was found to be maximum at a pH of 10. The time-dependence of the formation of cationic breakdown products, such as NH3/NH4+ and short-chain alkyl- and alkanolamines was studied by analyses with single column ion chromatography. The experimental data show that the photodegradation follows a Langmuir-Hinshelwood kinetic. The mineralization of the model substances also was monitored by measurements of the decrease of the TOC and of the formation of NO2- and NO3-. The different mineralization efficiencies for the model substances studied are discussed with regard to their structure and adsorption behaviour on the photocatalyst, A possible breakdown mechanism involving the electrophilic attack of the hydroxyl radical is given. The applicability of the TiO2-assisted photocatalytic degradation of C2H5NH2 and (C2H5)(2)NH was tested at the pilot plant-scale with real solar radiation. The degradation rates and products obtained were similar to those found in the laboratory experiments. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:353 / 362
页数:10
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