sic的吉布斯形成能:对改性的热力学稳定性的贡献

Heiko Kleykamp
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引用次数: 21

摘要

采用原电池Si, SiO2|Th(Y)O2|SiO2, α-SiC, C,在1200 ~ 1300 K范围内测定了六方α-SiC的吉布斯生成能ΔfGo,得到(K中的T): ΔfGo (α-SiC) =-94770+24.24·T J/mol。在298 K时,第三定律生成焓为ΔfHo298 (α-SiC)=-74.4 kJ/mol。为了更仔细地考察α-SiC和立方β-SiC的相对稳定性,用相同的方法在1100 ~ 1300 K之间用β-SiC, C, SiO2|Th(Y)O2|SiO2, C, α-SiC进行了Gibbs转化能ΔtrG的测量。测量了亚稳定电池运行5小时的电动势,电动势约为20 mV。这表明α-SiC是在所研究的温度范围内更稳定的改性,在1200 K时的产率为ΔtrG (βα-SiC)≈︁−8 kJ/mol。
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Gibbs energy of formation of sic: A contribution to the thermodynamic stability of the modifications

The Gibbs energy of formation ΔfGo of hexagonal α-SiC was determined by electromotive force (emf) measurements between 1200 and 1300 K using the galvanic cell Si, SiO2|Th(Y)O2|SiO2, α-SiC, C which gives (T in K): ΔfGo (α-SiC) =-94770+24.24·T J/mol. The third-law enthalpy of formation was calculated as ΔfHo298 (α-SiC)=-74.4 kJ/mol at 298 K. In order to examine more closely the relative stability of α-SiC and cubic β-SiC, Gibbs energy of transformation ΔtrG measurements were made by the same method between 1100 and 1300 K using the cell β-SiC, C, SiO2|Th(Y)O2|SiO2, C, α-SiC. An emf of about 20 mV of the meta-stable cell was measured up to 5 h cell operation. This observation implies that α-SiC is the more stable modification in the investigated temperature range yielding ΔtrG (βα-SiC) ≈︁ −8 kJ/mol at 1200 K.

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