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• W2076468218 abstract "The heat capacities of two different molecule-containing melanophlogites of approximate composition 46SiO2·1.80CH4·3.54N2·1.02CO2 from Mt. Hamilton, California, and 46SiO2·3.59CH4·3.10N2·1.31CO2 from Racalmuto, Sicily, along with a heat-treated (molecule-free) sample of composition SiO2, were studied between 5 and 300 K using heat-pulse microcalorimetry. The molecule-free sample was obtained by heating natural Racalmuto crystals at 1173 K for 24 h. The standard third-law entropy of the molecule-free sample is S° = 2216.3 ± 6.6 J/(mol·K) for 46SiO2 and the natural Mt. Hamilton and Racalmuto samples give S° = 2805.7 ± 8.4 J/(mol·K) and S° = 2956.8 ± 8.9 J/(mol·K), respectively. The entropy and Gibbs free energy for molecule-free melanophlogite relative to quartz at 298 K are ΔStrans = 6.7 J/(mol·K) and ΔGtrans = 7.5 kJ/mol, respectively and, thus, it does not have a thermodynamic field of stability in the SiO2 system. The difference in CP values between molecule-containing and molecule-free melanophlogite is characterized by an increase in CP from 0 to ~70 K, and it then reaches a roughly constant value at 70 K < T < 250 K. The ΔSrxn at 298 K for 46SiO2(melan.) + xCH4(gas) + yCO2(gas) + zN2(gas) = 46SiO2·(xCH4)12·(yCO2, zN2)14 is estimated to be about -642 and -802 J/(mol·K) for the Mt. Hamilton and Racalmuto samples, respectively. The thermodynamic data, as well as published results on the occurrence of natural molecule-containing samples suggest that melanophlogite crystallizes metastabily. The occurrence of melanophlogite and the lack of other porosils in nature are probably due to the essential role of molecular structure-directing agents. For melanophlogite they can be CO2, N2, and CH4, whereas the crystallization of other porosils requires more chemically and structurally complex molecules that are not naturally abundant." @default.
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• W2076468218 date "2008-07-01" @default.
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• W2076468218 title "Heat capacity and entropy of melanophlogite: Molecule-containing porosils in nature" @default.
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• W2076468218 doi "https://doi.org/10.2138/am.2008.2969" @default.
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