Adsorption and photocatalytic degradation of acetonitrile:: FT-IR investigation

被引:38
作者
Davit, P
Martra, G
Coluccia, S
Augugliaro, V
López, EG
Loddo, V
Marcì, G
Palmisano, L
Schiavello, M
机构
[1] Univ Turin, Dipartimento Chim IFM, I-10125 Turin, Italy
[2] Univ Palermo, Dipartimento ICPM, I-90128 Palermo, Italy
关键词
TiO2; acetonitrile; adsorption; photocatalysis; FF-IR investigation;
D O I
10.1016/S1381-1169(03)00354-6
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
The photocatalytic degradation of acetonitrile was carried out in liquid-solid regime in a batch reactor by using two types of commercial TiO2 powders (Merck and Degussa P25) as photocatalysts. The concentration of acetonitrile and non-purgeable organic carbon (NPOC) were monitored. The initial rate of acetonitrile conversion was found higher on TiO2 Merck than on TiO2 P25. FT-IR spectroscopy was used to investigate the molecular features of the adsorption and photo-oxidation of acetonitrile on the two TiO2 powders in a fully surface hydrated form. Acetonitrile was found adsorbed on Ti4+ surface ions and hydroxyl groups for both types of TiO2. This interaction appeared fully reversible in the case of the Merck photocatalyst, whereas acetonitrile was more strongly stabilized on Ti4+ ions of TiO2 P25. Furthermore, the adsorption of CD3CN...Ti4+ on this type of photocatalyst resulted in the formation of acetamide-like species, because of the presence of nucleophilic surface O2- and hydroxyl groups. The formation of these species, strongly bound to the TiO2 surface and recalcitrant to the photo-oxidation, could result in the poisoning of a part of the photocatalytic sites of TiO2 P25, accounting for its lower initial acetonitrile conversion rate. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:693 / 701
页数:9
相关论文
共 23 条
[1]   IR STUDY OF ACETONITRILE ADSORPTION ON HYDROXYLATED ZIRCONIUM DIOXIDE - MECHANISM OF ACETONITRILE HYDROLYSIS [J].
ABOULAYT, A ;
BINET, C ;
LAVALLEY, JC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1995, 91 (17) :2913-2920
[2]   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
[3]   Photocatalytic oxidation of cyanides in aqueous titanium dioxide suspensions [J].
Augugliaro, V ;
Loddo, V ;
Marci, G ;
Palmisano, L ;
LopezMunoz, MJ .
JOURNAL OF CATALYSIS, 1997, 166 (02) :272-283
[4]  
AUGUGLIARO V, 1999, ADV ENVIRON RES, V3, P179
[5]  
AUGUGLIARO V, IN PRESS ADV ENV RES
[6]   A theoretical study of the molecular structure and vibrational spectra of methyl cyanate and its sulfur and selenium analogues [J].
Babinec, P ;
Leszczynski, J .
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM, 2000, 501 :277-284
[7]   ADSORPTION OF ACETONITRILE ON CERIUM OXIDE - AN INFRARED SPECTROSCOPIC STUDY ACCORDING TO THE REDUCTION STATE OF THE OXIDE [J].
BINET, C ;
JADI, A ;
LAVALLEY, JC .
JOURNAL DE CHIMIE PHYSIQUE ET DE PHYSICO-CHIMIE BIOLOGIQUE, 1992, 89 (01) :31-45
[8]   FT-IR CHARACTERIZATION OF THE SURFACE-ACIDITY OF DIFFERENT TITANIUM-DIOXIDE ANATASE PREPARATIONS [J].
BUSCA, G ;
SAUSSEY, H ;
SAUR, O ;
LAVALLEY, JC ;
LORENZELLI, V .
APPLIED CATALYSIS, 1985, 14 (1-3) :245-260
[9]   Formation of isocyanate on Cu(100) from the oxidation of cyanogen and from the decomposition of isocyanic acid [J].
Celio, H ;
Mudalige, K ;
Mills, P ;
Trenary, M .
SURFACE SCIENCE, 1997, 394 (1-3) :L168-L173
[10]   STRUCTURAL AND MORPHOLOGICAL MODIFICATIONS OF SINTERING MICROCRYSTALLINE TIO2 - AN XRD, HRTEM AND FTIR STUDY [J].
CERRATO, G ;
MARCHESE, L ;
MORTERRA, C .
APPLIED SURFACE SCIENCE, 1993, 70-1 (1 -4 pt A) :200-205