Developing a Langmuir-type excitation equilibrium equation to describe the effect of light intensity on the kinetics of the photocatalytic oxidation

被引:36
作者
Deng, Yanxi [1 ]
机构
[1] China Univ Geosci, Beijing Key Lab Mat Utilizat Nonmetall Minerals &, Natl Lab Mineral Mat, Sch Mat Sci & Technol, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
Light intensity; Photocatalytic oxidation; The electron-hole pair; The excitation equilibrium equation; GAS-PHASE; MECHANISTIC ANALYSIS; HYDROGEN-PRODUCTION; TIO2; PHOTOCATALYST; AIR PURIFICATION; TITANIUM-DIOXIDE; UV/TIO2; PROCESS; DEGRADATION; MODEL; FORMALDEHYDE;
D O I
10.1016/j.cej.2017.12.059
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The electron-hole pair is a higher energy state of catalyst atoms due to the absorption of photons and thus is viewed to be a single species in photocatalytic reactions. The excitation rate of the electron-hole pair is assumed to depend on light intensity and the unexcited coverage. The destruction rate of the electron-hole pair is proportional to the excited coverage of the electron-hole pair. A Langmuir-type excitation equilibrium equation of the electron-hole pair is derived. The adsorption, desorption and reaction of pollutants on the surface of catalyst are considered simultaneously in the conservation equation of pollutant coverage. A Langmuir-Hinshelwood type kinetics is derived that is valid for all light intensity values and reproduce the three typical dependences of reaction rate on light intensity. The present reaction rate equation is validated against the experimental data in literature. Good agreements have been obtained for light intensity regimes in literature.
引用
收藏
页码:220 / 227
页数:8
相关论文
共 56 条
[1]  
Atkins PW., 2014, PHYS CHEM THERMODYNA
[2]   Modelling and experimental study of the NOx photocatalytic degradation employing concrete pavement with titanium dioxide [J].
Ballari, M. M. ;
Hunger, M. ;
Husken, G. ;
Brouwers, H. J. H. .
CATALYSIS TODAY, 2010, 151 (1-2) :71-76
[3]   Gas phase photocatalysis and liquid phase photocatalysis: Interdependence and influence of substrate concentration and photon flow on degradation reaction kinetics [J].
Brosillon, Stephan ;
Lhomme, Ludovic ;
Vallet, Cedric ;
Bouzaza, Abdelkrim ;
Wolbert, Dominique .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2008, 78 (3-4) :232-241
[4]   Comprehensive multiphysics modeling of photocatalytic processes by computational fluid dynamics based on intrinsic kinetic parameters determined in a differential photoreactor [J].
Casado, Cintia ;
Marugan, Javier ;
Timmers, Ruud ;
Munoz, Marcos ;
van Grieken, Rafael .
CHEMICAL ENGINEERING JOURNAL, 2017, 310 :368-380
[5]   Kinetic analysis and CFD simulations of the photocatalytic production of hydrogen in silicone microreactors from water-ethanol mixtures [J].
Castedo, Alejandra ;
Uriz, Irantzu ;
Soler, Lluis ;
Gandia, Luis M. ;
Llorca, Jordi .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2017, 203 :210-217
[6]   Photocatalytic Hydrogen Production: A Rift into the Future Energy Supply [J].
Christoforidis, Konstantinos C. ;
Fornasiero, Paolo .
CHEMCATCHEM, 2017, 9 (09) :1523-1544
[7]  
D'Ollveral J. C., 1990, ENV SCI TECHNOL, V24
[8]   Kinetic study on visible-light photocatalytic removal of formaldehyde from air over plasmonic Au/TiO2 [J].
Deng, Xiao-Qing ;
Liu, Jing-Lin ;
Li, Xiao-Song ;
Zhu, Bin ;
Zhu, Xiaobing ;
Zhu, Ai-Min .
CATALYSIS TODAY, 2017, 281 :630-635
[9]   Influence of inlet concentration and light intensity on the photocatalytic oxidation of nitrogen(II) oxide at the surface of Aeroxide® TiO2 P25 [J].
Dillert, Ralf ;
Stoetzner, Julia ;
Engel, Astrid ;
Bahnemann, Detlef W. .
JOURNAL OF HAZARDOUS MATERIALS, 2012, 211 :240-246
[10]   Photocatalytic degradation of dimethyl phthalate in aqueous TiO2 suspension: a modified Langmuir-Hinshelwood model [J].
Du, Erdeng ;
Zhang, Yu Xian ;
Zheng, Lu .
REACTION KINETICS AND CATALYSIS LETTERS, 2009, 97 (01) :83-90