The fate of organic nitrogen in photocatalysis: an overview

被引:87
作者
Calza, P [1 ]
Pelizzetti, E [1 ]
Minero, C [1 ]
机构
[1] Univ Turin, Dipartimento Chim Analit, I-10125 Turin, Italy
关键词
photocatalysis; titanium dioxide; organic nitrogen; nitrate; ammonium;
D O I
10.1007/s10800-005-1626-7
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Photocatalytic processes taking place on TiO2 have been widely employed and investigated. However, nitrogen-containing substances have not received the same attention as other substrates. Mineralization of such compounds is expected to lead to the formation of N-2 gas, ammonium and/or nitrate ions through photooxidative and/or photoreductive pathways. Herein, we will focus the attention on how the chemical structure may influence both the ratio and the extent of formation of the inorganic nitrogen. This review will consider heteroaromatic compounds, containing two or three-nitrogen in the ring, and small molecules, that could be formed as intermediate during the degradation of more complex substrates (i.e. pesticides), such as amino-alcohols, and molecules containing amide groups and nitriles. The fate final of the nitrogen in all these structures has been rationalized on the basis of the nature of N-N and C-N bonds in which the organic nitrogen is involved.
引用
收藏
页码:665 / 673
页数:9
相关论文
共 43 条
[1]   Photocatalytic oxidation of cyanide in aqueous TiO2 suspensions irradiated by sunlight in mild and strong oxidant conditions [J].
Augugliaro, V ;
Gálvez, JB ;
Vázquez, JC ;
López, EG ;
Loddo, V ;
Muñoz, MJL ;
Rodríguez, SM ;
Marcì, G ;
Palmisano, L ;
Schiavello, M ;
Ruiz, JS .
CATALYSIS TODAY, 1999, 54 (2-3) :245-253
[2]   Photocatalytic oxidation of acetonitrile in aqueous suspension of titanium dioxide irradiated by sunlight [J].
Augugliaro, V ;
Prevot, AB ;
Vázquez, JC ;
García-López, E ;
Irico, A ;
Loddo, V ;
Rodríguez, SM ;
Marcì, G ;
Palmisano, L ;
Pramauro, E .
ADVANCES IN ENVIRONMENTAL RESEARCH, 2004, 8 (3-4) :329-335
[3]  
BAHNEMANN D, 1993, SURFACE AQUATIC PHOT, P261
[4]   The photocatalytic process as a tool to identify metabolitic products formed from dopant substances: the case of buspirone [J].
Calza, P ;
Pazzi, M ;
Medana, C ;
Baiocchi, C ;
Pelizzetti, E .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2004, 35 (01) :9-19
[5]   Ion trap tandem mass spectrometry study of dexamethasone transformation products on light activated TiO2 surface [J].
Calza, P ;
Pelizzetti, E ;
Brussino, M ;
Baiocchi, C .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2001, 12 (12) :1286-1295
[6]   Photocatalytically assisted hydrolysis of chlorinated methanes under anaerobic conditions [J].
Calza, P ;
Minero, C ;
Pelizzetti, E .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1997, 31 (08) :2198-2203
[7]  
CALZA P, IN PRESS APPL CATA B
[8]   Probing the TiO2 photocatalytic mechanisms in water purification by use of quinoline, photo-fenton generated OH. radicals and superoxide dismutase [J].
Cermenati, L ;
Pichat, P ;
Guillard, C ;
Albini, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (14) :2650-2658
[9]   TiO2 photocatalytic degradation of haloquinolines in water:: Aromatic products GM-MS identification.: Role of electron transfer and superoxide [J].
Cermenati, L ;
Albini, A ;
Pichat, P ;
Guillard, C .
RESEARCH ON CHEMICAL INTERMEDIATES, 2000, 26 (03) :221-234
[10]   HETEROGENEOUS PHOTOCATALYSIS [J].
FOX, MA ;
DULAY, MT .
CHEMICAL REVIEWS, 1993, 93 (01) :341-357