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Vaporization and thermodynamics of La1-xCaxCrO3-delta investigated by Knudsen effusion mass spectrometry

机译:Knudsen渗流质谱研究La1-xCaxCrO3-δ的汽化和热力学

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Vaporization of the La1-xCaxCrO3-delta perovskite phase, x = 0.047-0.21, was investigated by the use of Knudsen effusion mass spectrometry in the temperature range of 1950-2050 K. Ion intensities were assigned to the neutral precursors by the isothermal evaporation method in addition to literature data. The partial pressures of Cr(g), CrO(g), CrO,(g), CaO(g), and LaO(g) were determined for all the samples investigated. The partial pressure of O-2(g) was evaluated from the gaseous equilibria. The experimental data were interpreted using the phase equilibria in the CaO-Cr2O3-La2O3 system under low oxygen pressure we previously studied. The ion intensities were used to calculate the thermodynamic activities of the system components at 2000 K. The Gibbs energy of formation of La0.79Ca0.21CrO3 at 2000 K was estimated from the thermodynamic activities as -81.5 kJ mol(-1). The results were compared with thermodynamic data of the undoped LaCrO3(s). Implications of the present data for the potential use of the material in SOFC technology were discussed as well. (C) 2001 Elsevier Science B.V. All rights reserved. [References: 24]
机译:在1950-2050 K的温度范围内,使用Knudsen渗流质谱法研究了La1-xCaxCrO3-δ钙钛矿相的汽化x = 0.047-0.21。通过等温蒸发法将离子强度分配给中性前体除了文献数据。确定了所有研究样品的Cr(g),CrO(g),CrO,(g),CaO(g)和LaO(g)的分压。从气态平衡评估O-2(g)的分压。我们先前研究的低氧气压力下,使用CaO-Cr2O3-La2O3系统中的相平衡来解释实验数据。离子强度用于计算系统组分在2000 K时的热力学活性。从2000 K的La0.79Ca0.21CrO3形成热的吉布斯能量估计为-81.5 kJ mol(-1)。将结果与未掺杂的LaCrO3的热力学数据进行了比较。还讨论了本数据对材料在SOFC技术中的潜在用途的影响。 (C)2001 Elsevier Science B.V.保留所有权利。 [参考:24]

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