Alumina dissolution promoted by CuSO4 precipitation

被引:12
作者
Balint, I
Miyazaki, A
Aika, K
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Technol, Dept Environm Chem & Engn, Midori Ku, Yokohama, Kanagawa 226, Japan
[2] Romanian Acad, Inst Phys Chem, Bucharest 77208, Romania
关键词
D O I
10.1021/cm9806026
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 impregnation of gamma-Al2O3 with CuSO4 at 50 degrees C was investigated at pH 9 and 7 using a dialysis membrane reactor. It was observed that alumina is not inert at pH values close to its isoelectric point when impregnated with CuSO4. Although the alumina was kept in a membrane bag, the presence of aluminum ions in the copper precipitate, which was formed outside of the membrane bag at pH 9 and 7, was detected by ICP, XRD, XRF, and SEM-EDAX. The molar ratios of Cu to Al in the precipitate formed at pH 9 and 7 were 80.8 and 222, respectively. The total amounts of alumina dissolved at pH 9 (after 240 h) and 7 (after 336 h) were 2.21 mg and 0.51 mg,respectively. It was observed that aluminum ions deriving from the support prefer to accumulate in the copper basic sulfate phase rather than in the CuO (Cu(OH)(2)) phase. The dialysis and XANES experiments proved that Cu(OH)(2) is mainly responsible for the alumina dissolution at pH 9. On the other hand, copper basic sulfate, which is the main compound formed at pH 7, was found to be less active in alumina dissolution, It was suggested that the presence of aluminum ions in the copper compound phase may influence the active sites formation of the catalyst by inducing the formation of lattice defects.
引用
收藏
页码:378 / 383
页数:6
相关论文
共 13 条
[1]   COPPER-CATALYSTS FOR THE STEAM REFORMING OF METHANOL - ANALYSIS OF THE PREPARATION VARIABLES [J].
AGARAS, H ;
CERRELLA, G ;
LABORDE, MA .
APPLIED CATALYSIS, 1988, 45 (01) :53-60
[2]   Defect chemistry of lithium-doped magnesium oxide [J].
Balint, I ;
Aika, K .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1997, 93 (09) :1797-1801
[3]  
Caillerie J. B. E., 1995, J AM CHEM SOC, V117, P11471
[4]   PREPARATION AND CHARACTERIZATION OF NICKEL ALUMINUM MIXED OXIDES OBTAINED BY THERMAL-DECOMPOSITION OF HYDROTALCITE-TYPE PRECURSORS [J].
CLAUSE, O ;
REBOURS, B ;
MERLEN, E ;
TRIFIRO, F ;
VACCARI, A .
JOURNAL OF CATALYSIS, 1992, 133 (01) :231-246
[5]  
COTTON FA, 1980, ADV INORG CHEM, P334
[6]  
Dumas J., 1989, J APPL CATAL, V47, pL9
[7]  
Foger K., 1984, CATALYSIS SCI TECHNO, V6, P228
[8]  
Katheuser B., 1991, IND ENG CHEM RES, V30, P2105
[9]   SURFACE COPRECIPITATION OF CO(II), NI(II), OR ZN(II) WITH AL(III) IONS DURING IMPREGNATION OF GAMMA-ALUMINA AT NEUTRAL PH [J].
PAULHIAC, JL ;
CLAUSE, O .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (24) :11602-11603
[10]  
STERFIELD CN, 1991, HETEROGENEOUS CATALY