<?xml version='1.0' encoding='utf-8'?>
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:contributor>S. H. Kirby</dc:contributor>
  <dc:contributor>L.A. Stern</dc:contributor>
  <dc:creator>S. Circone</dc:creator>
  <dc:date>2006</dc:date>
  <dc:description>Using the Gibbs function of reaction, equilibrium pressure, temperature conditions for the formation of methane clathrate hydrate have been calculated from the thermodynamic properties of phases in the system CH4-H 2O. The thermodynamic model accurately reproduces the published phase-equilibria data to within ??2 K of the observed equilibrium boundaries in the range 0.08-117 MPa and 190-307 K. The model also provides an estimate of the third-law entropy of methane hydrate at 273.15 K, 0.1 MPa of 56.2 J mol-1 K-1 for 1/n CH4??H 2O, where n is the hydrate number. Agreement between the calculated and published phase-equilibria data is optimized when the hydrate composition is fixed and independent of the pressure and temperature for the conditions modeled. ?? 2006 American Chemical Society.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>10.1021/jp055422f</dc:identifier>
  <dc:language>en</dc:language>
  <dc:title>Thermodynamic calculations in the system CH4-H2O and methane hydrate phase equilibria</dc:title>
  <dc:type>article</dc:type>
</oai_dc:dc>