Studies of the roles of Sn or Fe on γ-Al2O3-supported Pt catalysts by CO adsorption microcalorimetry and dehydrogenation reaction of C4 alkanes

被引:10
作者
Jia, JF
Lin, LW [1 ]
Shen, JY
Xu, ZS
Zhang, T
Liang, DB
Chen, Y
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Nanjing Univ, Dept Chem, Nanjing 210093, Peoples R China
来源
SCIENCE IN CHINA SERIES B-CHEMISTRY | 1998年 / 41卷 / 06期
基金
中国国家自然科学基金;
关键词
CO; gamma-Al2O3; Pt; Sn; Fe; differential heat; dehydrogenation of C-4 alkanes;
D O I
10.1007/BF02883022
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CO adsorption microcalorimetry was employed in the study of gamma-Al2O3-supported Pt, Pt-Sn and Pt-Fe catalysts. The results indicated that the initial differential heat of CO adsorption of the Pt/gamma-Al2O3 catalyst was 125 kJ/mol. As CO coverage increased, the differential heat of adsorption decreased. At higher coverages, the differential heat of adsorption decreased significantly. 60% of the differential heat of CO adsorption on the Pt/gamma-Al2O3 catalyst was higher than 100 kJ/mol. No significant effect on the initial differential heat was found after adding Sn and Fe to the Pt/gamma-Al2O3 catalyst. The amount of strong CO adsorption sites decreased, while the portion of CO adsorption sites with differential heat of 60-110 kJ/mol increased after increasing the Sn or Fe content. This indicates that the surface adsorption energy was changed by adding Sn or Fe to Pt/gamma-Al2O3. The distribution of differential heat of CO adsorption on the PI-Sn(C)/gamma-Al2O3 catalyst was broad and homogeneous. Comparison of the dehydrogenation performance of C-4 alkanes with the number of CO adsorption sites with differential heat of 60-110 kJ/mol showed a good correlation. These results indicate that the surface Pt centers with differential heats of 60-110 kJ/mol for CO adsorption possess superior activity for the dehydrogenation of alkanes.
引用
收藏
页码:606 / 615
页数:10
相关论文
共 14 条
[1]   Propane dehydrogenation over supported Pt and Pt-Sn catalysts: Catalyst preparation, characterization, and activity measurements [J].
Barias, OA ;
Holmen, A ;
Blekkan, EA .
JOURNAL OF CATALYSIS, 1996, 158 (01) :1-12
[2]   APPLICATIONS OF ADSORPTION MICROCALORIMETRY TO THE STUDY OF HETEROGENEOUS CATALYSIS [J].
CARDONAMARTINEZ, N ;
DUMESIC, JA .
ADVANCES IN CATALYSIS, 1992, 38 :149-244
[3]   MICROCALORIMETRIC STUDIES OF ZEOLITE ACIDITY [J].
CHEN, DT ;
SHARMA, SB ;
FILIMONOV, I ;
DUMESIC, JA .
CATALYSIS LETTERS, 1992, 12 (1-3) :201-212
[4]   CALORIMETRIC HEAT OF ADSORPTION MEASUREMENTS ON PALLADIUM .2. INFLUENCE OF CRYSTALLITE SIZE AND SUPPORT ON CO ADSORPTION [J].
CHOU, P ;
VANNICE, MA .
JOURNAL OF CATALYSIS, 1987, 104 (01) :17-30
[5]   CALORIMETRIC HEAT OF ADSORPTION MEASUREMENTS ON PALLADIUM .1. INFLUENCE OF CRYSTALLITE SIZE AND SUPPORT ON HYDROGEN ADSORPTION [J].
CHOU, P ;
VANNICE, MA .
JOURNAL OF CATALYSIS, 1987, 104 (01) :1-16
[6]   Effects of potassium on silica-supported Pt and Pt/Sn catalysts for isobutane dehydrogenation [J].
Cortright, RD ;
Dumesic, JA .
JOURNAL OF CATALYSIS, 1995, 157 (02) :576-583
[7]   MICROCALORIMETRIC, SPECTROSCOPIC, AND KINETIC-STUDIES OF SILICA-SUPPORTED PT AND PT/SN CATALYSTS FOR ISOBUTANE DEHYDROGENATION [J].
CORTRIGHT, RD ;
DUMESIC, JA .
JOURNAL OF CATALYSIS, 1994, 148 (02) :771-778
[8]   MICROCALORIMETRIC, IR SPECTROSCOPIC AND THERMODESORPTION STUDIES OF CO INTERACTION WITH GAMMA-AL2O3-SUPPORTED RH, PD, IR AND PT [J].
EFREMOV, AA ;
BAKHMUTOVA, NI ;
PANKRATIEV, YD ;
KUZNETSOV, BN .
REACTION KINETICS AND CATALYSIS LETTERS, 1985, 28 (01) :103-110
[9]   CALORIMETRIC STUDY OF THE COADSORPTION OF HYDROGEN AND CARBON-MONOXIDE OVER RUTHENIUM GRAPHITIZED CARBON-BLACK CATALYSTS [J].
GUERRERORUIZ, A .
APPLIED CATALYSIS, 1989, 55 (01) :21-31
[10]  
JIA J, 1997, CHINESE J CATAL, V2, P97