Sulfate ions in titania polymorphs

被引:42
作者
Bokhimi, X
Morales, A
Ortíz, E
López, T
Gómez, R
Navarrete, J
机构
[1] Univ Autonoma Metropolitana Iztapalapa, Dept Chem, Mexico City 9340, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Inst Phys, Mexico City 01000, DF, Mexico
[3] Inst Mexicano Petr, Programa Ingn Mol, Mexico City 07730, DF, Mexico
关键词
sulfated titania; brookite atomic bond lengths; anatase atomic bond lengths; brookite transformation; anatase stabilization; rutile crystallite growing;
D O I
10.1023/B:JSST.0000016135.02238.0e
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Sol-gel titania was sulfated by using sulfuric acid as hydrolysis catalyst, or by impregnating with ammonium sulfate fresh samples prepared with nitric acid or ammonium hydroxide as hydrolysis catalyst. Samples were characterized with X-ray powder diffraction, infrared spectroscopy, thermogravimetry and atomic absorption spectroscopy. Sulfate ions were found anchored to brookite and anatase phases, because they have short O-O atomic bond lengths slightly larger than the largest O-O bond length of sulfate ion. Since the shortest O-O atomic bond in anatase is smaller than the one in brookite, the sulfate ions are then less deformed when they are anchored to anatase, and consequently more stable. Therefore when the sample temperature is raised, the brookite with sulfate ions was transformed mainly to anatase and not into rutile, which is the most probably transformation when these ions are not involved. Sulfate ions also hindered anatase and brookite crystallite growing and stabilized the crystalline structure of anatase. When the sulfate ions are lost the crystalline anatase phase is transformed into rutile, leaving a large number of vacancies that favored atom diffusion and consequently the growing of rutile crystallites. The crystalline evolution of the samples as a function of the annealing temperature is almost independent of the sulfating method.
引用
收藏
页码:31 / 40
页数:10
相关论文
共 53 条
[1]  
ARATA K, 1979, SHOKUBAI, V21, P217
[2]  
Arata K., 1990, ADV CATAL, V37, P165
[3]   Local order in titania polymorphs [J].
Bokhimi, X ;
Morales, A ;
Aguilar, M ;
Toledo-Antonio, JA ;
Pedraza, F .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2001, 26 (12) :1279-1287
[4]  
BOKHIMI X, 2002, UNPUB J SOLID STATE
[5]   ORDERED ASO4 AND SO4 TETRAHEDRA IN DIAMMONIUM TRIHYDROGENARSENATE SULFATE [J].
BOUBIA, M ;
AVERBUCHPOUCHOT, MT ;
DURIF, A .
ACTA CRYSTALLOGRAPHICA SECTION C-CRYSTAL STRUCTURE COMMUNICATIONS, 1985, 41 (NOV) :1562-1564
[6]   MODIFICATION OF THE CATALYTIC PROPERTIES OF SULFATED ZIRCONIA BY ADDITION OF METAL PROMOTERS [J].
COELHO, MA ;
RESASCO, DE ;
SIKABWE, EC ;
WHITE, RL .
CATALYSIS LETTERS, 1995, 32 (3-4) :253-262
[7]   A COMPARATIVE-STUDY OF O-4(2-)/ZRO2 AND ZEOLITE-BETA AS CATALYSTS FOR THE ISOMERIZATION OF N-BUTANE AND THE ALKYLATION OF ISOBUTANE WITH 2-BUTENE [J].
CORMA, A ;
JUANRAJADELL, MI ;
LOPEZNIETO, JM ;
MARTINEZ, A ;
MARTINEZ, C .
APPLIED CATALYSIS A-GENERAL, 1994, 111 (02) :175-189
[8]   INORGANIC SOLID ACIDS AND THEIR USE IN ACID-CATALYZED HYDROCARBON REACTIONS [J].
CORMA, A .
CHEMICAL REVIEWS, 1995, 95 (03) :559-614
[9]   ISOBUTANE 2-BUTENE ALKYLATION ON MCM-22 CATALYST - INFLUENCE OF ZEOLITE STRUCTURE AND ACIDITY ON ACTIVITY AND SELECTIVITY [J].
CORMA, A ;
MARTINEZ, A ;
MARTINEZ, C .
CATALYSIS LETTERS, 1994, 28 (2-4) :187-201
[10]   Solid solutions of WO3 into zirconia in WO3-ZrO2 catalysts [J].
Cortés-Jácome, MA ;
Toledo-Antonio, JA ;
Armendáriz, H ;
Hernández, I ;
Bokhimi, X .
JOURNAL OF SOLID STATE CHEMISTRY, 2002, 164 (02) :339-344