Phase relations in the system Ta-Rh-O and thermodynamic properties of TaRhO4

被引:11
作者
Jacob, K. T. [1 ]
Shekhar, Chander [1 ]
Waseda, Y. [2 ]
机构
[1] Indian Inst Sci, Dept Mat Engn, Bangalore 560012, Karnataka, India
[2] Tohoku Univ, IMRAM, Sendai, Miyagi 9808577, Japan
关键词
TaRhO4; Gibbs free energy; Enthalpy; Entropy; Oxygen potential; System Ta-Rh-O; Phase diagram; SUPPORTED RHODIUM CATALYSTS; SYNTHESIS GAS; PARTIAL OXIDATION; GIBBS ENERGIES; PLUS OXYGEN; METHANE; OXIDES; NO; REDUCTION; DIAGRAM;
D O I
10.1016/j.matchemphys.2009.03.030
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Phase relations in the system Ta-Rh-O were determined by analysis of quenched samples corresponding to thirteen compositions inside the ternary triangle after equilibration at 1273 K. All the Ta-Rh alloys were found to be in equilibrium with Ta2O5. Only one ternary oxide TaRhO4 was detected. Based on phase relations in the ternary system, a solid-state electrochemical cell, incorporating calcia-stabilized zirconia as the electrolyte, was designed to measure the standard Gibbs energy of formation (Delta G degrees, J mol(-1)) of TaRhO4 in the temperature range from 900 to 1300 K. For the reaction, 1/2 beta-Ta2O5 + 1/2 Rh2O3(ortho) -> TaRhO4 Delta G degrees = -42993 + 5.676T (+/- 85) The calculated decomposition temperatures of TaRhO4 are 1644 +/- 5K in pure O-2 and 1543 +/- 5K in air at a total pressure p(o) = 0.1 MPa. Thermodynamic properties of TaRhO4 at 298.15K have been evaluated from the results. The limited experimental thermodynamic data for Rh-rich alloys available in the literature are in fair accord with Miedema's model. The Gibbs energies of formation of the different phases in the binary system Ta-Rh were estimated based on these inputs, consistent with the binary phase diagram. Based on the thermodynamic information on the stability of various phases, an oxygen potential diagram for the system Ta-Rh-O at 1273K was constructed. Also presented are temperature-composition diagrams for the ternary system at constant oxygen partial pressures (po(2)/p(o) = 0.212 and 10(-6)) calculated form the basic data. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:289 / 293
页数:5
相关论文
共 24 条
[1]   Catalytic decomposition of N2O over monolithic supported noble metal-transition metal oxides [J].
Boissel, Viviane ;
Tahir, Saad ;
Koh, Carolyn Ann .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2006, 64 (3-4) :234-242
[2]   THE DISSOCIATION KINETICS OF NO ON RH(III) AS STUDIED BY TEMPERATURE-PROGRAMMED STATIC SECONDARY-ION MASS-SPECTROMETRY AND DESORPTION [J].
BORG, HJ ;
REIJERSE, JFCJM ;
VANSANTEN, RA ;
NIEMANTSVERDRIET, JW .
JOURNAL OF CHEMICAL PHYSICS, 1994, 101 (11) :10052-10063
[3]  
CHAO CY, 1977, THESIS U WISCONSIN M
[4]  
de Boer F.R., 1988, COHESION METALS TRAN, P544
[5]  
GIESSEN BC, 1964, T METALL SOC AIME, V230, P113
[6]   Catalytic performance of rhodium supported on ceria-zirconia mixed oxides for reduction of NO by propene [J].
Haneda, Masaaki ;
Shinoda, Kiyoshi ;
Nagane, Akira ;
Houshito, Ohki ;
Takagi, Hiromitsu ;
Nakahara, Yuunosuke ;
Hiroe, Kazumi ;
Fujitani, Tadahiro ;
Hamada, Hideaki .
JOURNAL OF CATALYSIS, 2008, 259 (02) :223-231
[7]   ADSORPTION OF NO ON RH(100) [J].
HO, P ;
WHITE, JM .
SURFACE SCIENCE, 1984, 137 (01) :103-116
[8]   An update on the thermodynamics of Ta2O5 [J].
Jacob, K. T. ;
Shekhar, Chander ;
Waseda, Y. .
JOURNAL OF CHEMICAL THERMODYNAMICS, 2009, 41 (06) :748-753
[9]   Phase relations in the system (chromium plus rhodium plus oxygen) and thermodynamic properties of CrRhO3 [J].
Jacob, K. T. ;
Shekhar, Chander ;
Waseda, Y. .
JOURNAL OF CHEMICAL THERMODYNAMICS, 2009, 41 (01) :56-61
[10]  
Jacob KT, 2000, J CHEM THERMODYN, V32, P1399