Effect of rutile phase on the photocatalytic properties of nanocrystalline titania during the degradation of p-coumaric acid

被引:338
作者
Bacsa, RR [1 ]
Kiwi, J [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Chem Phys, CH-1015 Lausanne, Switzerland
关键词
photocatalysis; coumaric acid; titania; anatase; rutile;
D O I
10.1016/S0926-3373(97)00058-1
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
Nanocrystalline titania catalysts with high surface area (68-100 m(2)/g) with varying amounts of anatase and rutile phases were tested during the photocatalyzed degradation of p-coumaric acid. This is a pollutant found in agricultural waste waters originating from the wine and olive oil industry. The catalysts were prepared by the same route namely, the hydrolysis of alkoxides followed by densification under hydrothermal conditions (1500-4000 kPa). Hydrolysis of Ti-butoxide gives rise to predominantly anatase containing titania whereas the Ti-ethoxide hydrolysis leads to mixtures of anatase and rutile. Compared to pure anatase or rutile, titania containing both phases shows a significantly higher catalytic activity during the degradation of p-coumaric acid. After preliminary optimization experiments, the degradation of 0.1 mM p-coumaric acid was achieved in 45 min under light irradiation in the presence of H(2)O(2) The most efficient catalyst is TiO(2) containing 30% rutile and 70% anatase and is prepared by the hydrolysis of tetraisopropyl-orthotitanate. Pore size distribution measurements indicate the presence of mesopores of radii in the range 6-25 Angstrom which were responsible for the effective adsorption of the pollutant on the catalyst. Electrophoretic mobility measurements show the isoelectric point for the most efficient catalyst at pH 5.5. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:19 / 29
页数:11
相关论文
共 20 条
[1]   Rutile formation in hydrothermally crystallized nanosized titania [J].
Bacsa, RR ;
Gratzel, M .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1996, 79 (08) :2185-2188
[2]   THE DETERMINATION OF PORE VOLUME AND AREA DISTRIBUTIONS IN POROUS SUBSTANCES .1. COMPUTATIONS FROM NITROGEN ISOTHERMS [J].
BARRETT, EP ;
JOYNER, LG ;
HALENDA, PP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1951, 73 (01) :373-380
[3]   A STRUCTURAL INVESTIGATION OF TITANIUM-DIOXIDE PHOTOCATALYSTS [J].
BICKLEY, RI ;
GONZALEZCARRENO, T ;
LEES, JS ;
PALMISANO, L ;
TILLEY, RJD .
JOURNAL OF SOLID STATE CHEMISTRY, 1991, 92 (01) :178-190
[4]   Photocatalytic degradation of hydroxylated biphenyl compounds [J].
BouquetSomrani, C ;
Finiels, A ;
Graffin, P ;
Olive, JL .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1996, 8 (01) :101-106
[5]   Study of the room temperature ageing effect on structural evolution of gel-derived nanocrystalline titania powders [J].
Ding, XZ ;
He, YZ .
JOURNAL OF MATERIALS SCIENCE LETTERS, 1996, 15 (04) :320-322
[6]  
HENRY M, 1992, STRUCT BOND, V77, P155
[7]   ENVIRONMENTAL APPLICATIONS OF SEMICONDUCTOR PHOTOCATALYSIS [J].
HOFFMANN, MR ;
MARTIN, ST ;
CHOI, WY ;
BAHNEMANN, DW .
CHEMICAL REVIEWS, 1995, 95 (01) :69-96
[8]   TiO2 coating photocatalysts with nanostructure and preferred orientation showing excellent activity for decomposition of aqueous acetic acid [J].
Kato, K ;
Torii, Y ;
Taoda, H ;
Kato, T ;
Butsugan, Y ;
Niihara, K .
JOURNAL OF MATERIALS SCIENCE LETTERS, 1996, 15 (10) :913-915
[9]  
KIWI J, 1997, J PHYS CHEM-US, V91, P670
[10]   STABILIZATION OF THE POROUS TEXTURE OF NANOSTRUCTURED TITANIA BY AVOIDING A PHASE-TRANSFORMATION [J].
KUMAR, KNP ;
KEIZER, K ;
BURGGRAAF, AJ .
JOURNAL OF MATERIALS SCIENCE LETTERS, 1994, 13 (01) :59-61