Interactions between Ni and La2O3 in Ni/La2O3 catalysts prepared using different Ni precursors

被引:86
作者
Ruckenstein, E [1 ]
Hu, YH [1 ]
机构
[1] XIAMEN UNIV,DEPT CHEM,XIAMEN 361005,PEOPLES R CHINA
关键词
D O I
10.1006/jcat.1996.0161
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 role of the anion (NO3- or Cl-), used in the preparation via impregnation of unreduced Ni/La2O3 catalysts, in the interactions between Ni and La2O3 was investigated using XRD, TPR, and ESCA experiments. The following results have been obtained: In the 20 wt% Ni/La2O3 prepared using Ni(NO3)(2) as precursor, LaNiO3 and La(OH)(3) were the only compounds identified by XRD in the sample calcined in O-2, and La2NiO4 and La(OH)(3) were the only compounds identified in the sample calcined in He. At lower Ni contents, the L(2)O(3) phase was additionally identified. For the 20 wt% Ni/La2O3 prepared using Ni chloride as precursor, LaOCl was the only compound detected by XRD; no phase containing Ni was identified by XRD in the samples calcined in O-2 or He. At lower Ni chloride contents, LaNiO3 was additionally detected in the sample calcined in O-2 and La2NiO4 in that calcined in He. A comparison between the XRD spectra and the TPR curves suggested the presence of amorphous NiO in the samples based on Ni chloride. It is also shown that the Ni precursor employed in the preparation of the catalyst plays a role in the CO2 reforming of CH4. During the CO2 reforming of methane, the unreduced Ni/La2O3 catalysts, based on Ni nitrate, had a high initial CO yield but a low time stability; in contrast, the unreduced Ni/La2O3 catalysts, based on chloride, had a high stability. A possible explanation of this behavior, based on ESCA analysis and on the reaction between CH4 and catalysts, is provided. (C) 1996 Academic Press, Inc.
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页码:55 / 61
页数:7
相关论文
共 22 条
[1]  
CASTRO E, 1995, APPL OPTICS, V34, P2317
[2]   REDUCED FORMS OF LANIO3 PEROVSKITE .1. EVIDENCE FOR NEW PHASES - LA2NI2O5 AND LANIO2 [J].
CRESPIN, M ;
LEVITZ, P ;
GATINEAU, L .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1983, 79 :1181-1194
[3]   STABILIZATION OF PLATINUM ON SILICA PROMOTED WITH LANTHANUM OXIDE AND ZIRCONIUM-OXIDE [J].
DEEBA, M ;
FARRAUTO, RJ ;
LUI, YK .
APPLIED CATALYSIS A-GENERAL, 1995, 124 (02) :339-344
[4]   PREPARATION, STRUCTURE, AND SELECTED CATALYTIC PROPERTIES OF SYSTEM LAMN1-XCUXO3-Y [J].
GALLAGHER, PK ;
JOHNSON, DW ;
VOGEL, EM .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1977, 60 (1-2) :28-31
[5]   REACTION BETWEEN CALCIUM-DOPED LANTHANUM CHROMITE AND SILICA [J].
HORITA, T ;
CHOI, JM ;
LEE, YK ;
SAKAI, N ;
KAWADA, T ;
YOKOKAWA, H ;
DOKIYA, M .
JOURNAL OF THE AMERICAN CERAMIC SOCIETY, 1995, 78 (07) :1729-1736
[6]   An optimum NiO content in the CO2 reforming of CH4 with NiO/MgO solid solution catalysts [J].
Hu, YH ;
Ruckenstein, E .
CATALYSIS LETTERS, 1996, 36 (3-4) :145-149
[7]   PULSE-MS STUDY OF THE PARTIAL OXIDATION OF METHANE OVER NI/LA2O3 CATALYST [J].
HU, YH ;
RUCKENSTEIN, E .
CATALYSIS LETTERS, 1995, 34 (1-2) :41-50
[8]   Transient kinetic studies of partial oxidation of CH4 [J].
Hu, YH ;
Ruckenstein, E .
JOURNAL OF CATALYSIS, 1996, 158 (01) :260-266
[9]  
LEVITZ P, 1993, J CHEM SOC FARADAY T, V2, P1195
[10]   PROMISING CATALYST FOR AUTO EXHAUST [J].
LIBBY, WF .
SCIENCE, 1971, 171 (3970) :499-&