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Mineral reaction buffering of Venus' atmosphere: A thermochemical constraint and implications for Venus-like planets
被引:14
|作者:
Treiman, Allan H.
[1
]
Bullock, Mark A.
[2
]
机构:
[1] Lunar & Planetary Inst, Houston, TX 77058 USA
[2] SW Res Inst, Dept Space Studies, Boulder, CO 80302 USA
来源:
基金:
美国国家科学基金会;
关键词:
Venus;
Atmosphere;
Surface;
Atmospheres;
Chemistry;
Extrasolar planets;
SUPER-EARTH;
CLIMATE;
SURFACE;
EVOLUTION;
DIOXIDE;
PHASES;
MASS;
D O I:
10.1016/j.icarus.2011.08.019
中图分类号:
P1 [天文学];
学科分类号:
0704 ;
摘要:
The equilibrium suggested as a buffer for CO2 in the Venus atmosphere, CaCO3 + SiO2 = CaSiO3 + CO2, cannot act as a buffer at the Venus surface/troposphere - the pressure-temperature slope of the equilibrium and that of the atmosphere (dry adiabat with significant greenhouse heating) do not provide buffering capacity (if indeed CaCO3 were present). Instead, perturbations to T or P(CO2) can produce catastrophic expansion or collapse of the atmosphere. This instability can be generalized to all devolatilization reactions that produce a radiatively active gas in a planetary atmosphere dominated by such gases, and gives a simple thermochemical criterion for whether a reaction could buffer such an atmosphere. Simple decarbonation reactions fail this criterion, suggesting that the abundance of CO2 in a CO2-dominated atmosphere cannot be buffered by chemical reactions with the surface; a similar conclusion holds for the abundance of H2O in an H2O-dominated (steam) atmosphere. Buffering of minor gases is more likely; a mineral buffer equilibrium for SO2 proposed for Venus, FeS2 + CO2 = Fe3O4 + SO2 + CO, passes the thermochemical criterion, as does a reaction involving Ca sulfate. These inferences can be generalized to atmospheres in 'moist' adiabatic equilibria, and to extrasolar Venus-like planets, and will help in interpreting the compositions of their atmospheres. (C) 2011 Elsevier Inc. All rights reserved.
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页码:534 / 541
页数:8
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