Synthesis of pure tetragonal zirconium oxide with high surface area

被引:42
作者
Rezaei, M. [1 ]
Alavi, S. M.
Sahebdelfar, S.
Yan, Zi-Feng
Teunissen, H.
Jacobsen, J. H.
Sehested, J.
机构
[1] China Univ Petr, CNPC, Key Lab Catalysis, State Key Lab Heavy Oil Proc, Dongying, Peoples R China
[2] Iran Univ Sci & Technol, Chem Engn Dept, Tehran, Iran
[3] NPC RT, Tehran, Iran
[4] Haldor Tropsoe AS, DK-2800 Lyngby, Denmark
关键词
D O I
10.1007/s10853-006-0079-7
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Zirconium oxide (ZrO2) with high surface area and high content of the tetragonal polymorph was prepared by precipitation from aqueous solutions under basic conditions in the presence of hexadecyltrimethylammonium bromide as surfactant. The surfactant to zirconium molar ratio, pH of precipitation, aging time and zirconium concentration in aqueous solution were optimized by the Taguchi method. The sample, prepared under optimized conditions had a high surface area of 168 m(2) g(-1) after calcination at 600 degrees C for 10 h. Pellets, prepared by pressing this sample and after calcination at 800 degrees C for 0.5 h had a surface area of 105 m(2) g(-1). X-ray diffraction analyses showed that both heat treatments gave pure tetragonal zirconium oxide.
引用
收藏
页码:1228 / 1237
页数:10
相关论文
共 37 条
[1]   A study of the crystallization of ZrO2 in the sol-gel system:: ZrO2-SiO2 [J].
Aguilar, DH ;
Torres-Gonzalez, LC ;
Torres-Martinez, LM ;
Lopez, T ;
Quintana, P .
JOURNAL OF SOLID STATE CHEMISTRY, 2001, 158 (02) :349-357
[2]   Characterization of high-surface-area zirconia aerogel synthesized from combined alcohothermal and supercritical fluid drying techniques [J].
Cao, Y ;
Hu, JC ;
Hong, ZS ;
Deng, JF ;
Fan, KN .
CATALYSIS LETTERS, 2002, 81 (1-2) :107-112
[3]   Catalytic behavior and nature of active sites in copper-on-zirconia catalysts for the decomposition of N2O [J].
Centi, G ;
Cerrato, G ;
DAngelo, S ;
Finardi, U ;
Giamello, E ;
Morterra, C ;
Perathoner, S .
CATALYSIS TODAY, 1996, 27 (1-2) :265-270
[4]   On the size-dependent phase transformation in nanoparticulate zirconia [J].
Chraska, T ;
King, AH ;
Berndt, CC .
MATERIALS SCIENCE AND ENGINEERING A-STRUCTURAL MATERIALS PROPERTIES MICROSTRUCTURE AND PROCESSING, 2000, 286 (01) :169-178
[5]   The influence of preparation conditions on the surface area of zirconia [J].
Chuah, GK ;
Jaenicke, S ;
Cheong, SA ;
Chan, KS .
APPLIED CATALYSIS A-GENERAL, 1996, 145 (1-2) :267-284
[6]  
DAWSON EA, 1992, APPL CATAL A-GEN, V90, P217
[7]   STABILIZATION OF TETRAGONAL STRUCTURE IN ZIRCONIA MICROCRYSTALS [J].
GARVIE, RC .
JOURNAL OF PHYSICAL CHEMISTRY, 1978, 82 (02) :218-224
[8]   INTRINSIC SIZE DEPENDENCE OF THE PHASE-TRANSFORMATION TEMPERATURE IN ZIRCONIA MICROCRYSTALS [J].
GARVIE, RC ;
GOSS, MF .
JOURNAL OF MATERIALS SCIENCE, 1986, 21 (04) :1253-1257
[9]   OCCURRENCE OF METASTABLE TETRAGONAL ZIRCONIA AS A CRYSTALLITE SIZE EFFECT [J].
GARVIE, RC .
JOURNAL OF PHYSICAL CHEMISTRY, 1965, 69 (04) :1238-&
[10]   Preparation and characterisation of mesoporous, high-surface-area zirconium(IV) oxide [J].
Hudson, MJ ;
Knowles, JA .
JOURNAL OF MATERIALS CHEMISTRY, 1996, 6 (01) :89-95