Photocatalytic intrinsic reaction kinetics I:: Mineralization of dichloroacetic acid

被引:50
作者
Zalazar, CS
Romero, RL
Martín, CA
Cassano, AE
机构
[1] Univ Nacl Litoral, INTEC, RA-3000 Santa Fe, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-3000 Santa Fe, Argentina
关键词
photocatalysis; dichloroacetic acid; environments; kinetics; chemical reactors; modelling;
D O I
10.1016/j.ces.2005.04.050
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The intfinsic reaction kinetics of the photocatalytic decomposition of dichloroacetic acid (DCA) at different, but constant oxygen concentrations was studied. Other significant variables were initial DCA concentration, catalyst (titanium dioxide) concentration and light intensities. The results of the kinetic measurements were analyzed using a complete mathematical model of the experimental device that was used for the laboratory operation (a differential reactor inside a recycle). In this way it was expected to obtain intrinsic kinetic parameters. The kinetic model, that was developed from a proposed complete reaction sequence, has only two lumped specific kinetic constants and represents the dependence of the reaction rate with oxygen, DCA and catalyst concentrations as well as the local volumetric rate of photon absorption. Simulation results are in good agreement with experiments and, at the same time, permit a detailed description of the existing radiation field in the experimental reactor. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5240 / 5254
页数:15
相关论文
共 32 条
[1]   SCATTERING EFFECTS PRODUCED BY INERT PARTICLES IN PHOTOCHEMICAL REACTORS .1. MODEL AND EXPERIMENTAL-VERIFICATION [J].
ALFANO, OM ;
NEGRO, AC ;
CABRERA, MI ;
CASSANO, AE .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1995, 34 (02) :488-499
[2]   A mechanistic approach to modeling the effect of dissolved oxygen in photo-oxidation reactions on titanium dioxide in aqueous systems [J].
Almquist, CB ;
Biswas, P .
CHEMICAL ENGINEERING SCIENCE, 2001, 56 (11) :3421-3430
[3]   MECHANISTIC STUDIES OF WATER DETOXIFICATION IN ILLUMINATED TIO2 SUSPENSIONS [J].
BAHNEMANN, D ;
BOCKELMANN, D ;
GOSLICH, R .
SOLAR ENERGY MATERIALS, 1991, 24 (1-4) :564-583
[4]  
Bahnemann D., 1999, ACS Division of Environmental Chemistry, Preprints, V41, P285, DOI DOI 10.1007/978-3-540-69044-3_11
[5]   Charge carrier dynamics at TiO2 particles: Reactivity of free and trapped holes [J].
Bahnemann, DW ;
Hilgendorff, M ;
Memming, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (21) :4265-4275
[6]  
BLANCO J, 2001, ELIMINACION CONTAMIN, P51
[7]   Modeling of radiation absorption in a flat plate photocatalytic reactor [J].
Brandi, RJ ;
Alfano, OM ;
Cassano, AE .
CHEMICAL ENGINEERING SCIENCE, 1996, 51 (11) :3169-3174
[8]   Rigorous model and experimental verification of the radiation field in a flat-plate solar collector simulator employed for photocatalytic reactions [J].
Brandi, RJ ;
Alfano, OM ;
Cassano, AE .
CHEMICAL ENGINEERING SCIENCE, 1999, 54 (13-14) :2817-2827
[9]   Photocatalytic reactors - Reaction kinetics in a flat plate solar simulator [J].
Brandi, RJ ;
Rintoul, G ;
Alfano, OM ;
Cassano, AE .
CATALYSIS TODAY, 2002, 76 (2-4) :161-175
[10]   Photocatalytic reactions involving hydroxyl radical attack - II. Kinetics of the decomposition of trichloroethylene using titanium dioxide [J].
Cabrera, MI ;
Negro, AC ;
Alfano, OM ;
Cassano, AE .
JOURNAL OF CATALYSIS, 1997, 172 (02) :380-390