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Passing gas through the hydrate stability zone at southern Hydrate Ridge, offshore Oregon: Earth and Planetary
- Science Letters
, 2006
"... We present an equilibrium model of methane venting through the hydrate stability zone at southern Hydrate Ridge, offshore Oregon. Free gas supplied from below forms hydrate, depletes water, and elevates salinity until pore water is too saline for further hydrate formation. This system self-generates ..."
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Cited by 8 (2 self)
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We present an equilibrium model of methane venting through the hydrate stability zone at southern Hydrate Ridge, offshore Oregon. Free gas supplied from below forms hydrate, depletes water, and elevates salinity until pore water is too saline for further hydrate formation. This system self-generates local three-phase equilibrium and allows free gas migration to the seafloor. Log and core data from Ocean Drilling Program (ODP) Site 1249 show that from the seafloor to 50 m below seafloor (mbsf), pore water salinity is elevated to the point where liquid water, hydrate and free gas coexist. The elevated pore water salinity provides a mechanism for vertical migration of free gas through the regional hydrate stability zone (RHSZ). This process may drive gas venting through hydrate stability zones around the world. Significant amount of gaseous methane can bypass the RHSZ by shifting local thermodynamic conditions.
Uncorking the bottle: What triggered the Paleocene/Eocene thermal maximum methane release?
"... Abstract. The Paleocene/Eocene thermal maximum (PETM) was a time of rapid global warming in both marine and continental realms that has been attributed to a massive methane (CH4) release from marine gas hydrate reservoirs. Previously proposed mechanisms for this methane release rely on a change in d ..."
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Cited by 1 (0 self)
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Abstract. The Paleocene/Eocene thermal maximum (PETM) was a time of rapid global warming in both marine and continental realms that has been attributed to a massive methane (CH4) release from marine gas hydrate reservoirs. Previously proposed mechanisms for this methane release rely on a change in deepwater source region(s) to increase water temperatures rapidly enough to trigger the massive thermal dissociation of gas hydrate reservoirs beneath the seafloor. To establish constraints on thermal dissociation, we model heat flow through the sediment column and show the effect of the temperature change on the gas hydrate stability zone through time. In addition, we provide seismic evidence tied to borehole data for methane release along portions of the U.S. continental slope; the release sites are proximal to a buried Mesozoic reef front. Our model results, release site locations, published isotopic records, and ocean circulation models neither confirm nor refute thermal dissociation as the trigger for the PETM methane release. In the absence of definitive evidence to confirm thermal dissociation, we investigate an alternative hypothesis in which continental slope failure resulted in a catastrophic methane release. Seismic and isotopic evidence indicates that Antarctic source deepwater circulation and seafloor erosion caused slope retreat along the western margins of the North Atlantic in the late Paleocene. Continued erosion or seismic activity along the oversteepened continental margin may have allowed methane to escape from gas reservoirs trapped between the frozen hydrate-bearing sediments and the underlying buried Mesozoic reef front, precipitating the Paleocene/Eocene boundary methane release. An important implication of this scenario is that the methane release caused (rather than resulted from) the
Oil & Natural Gas Technology Detection and Production of Methane Hydrate Semi-annual Progress Report Reporting Period: November-March, 2010 Submitted by:
, 2010
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Phase Behavior of CO2 and CH4 Hydrate in Porous Media
"... Abstract—Hydrate phase equilibria for the binary CO2+water and CH 4+water mixtures in silica gel pore of nominal diameters 6, 30, and 100 nm were measured and compared with the calculated results based on van der Waals and Platteeuw model. At a specific temperature, three-phase hydrate-water-vapor ( ..."
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Abstract—Hydrate phase equilibria for the binary CO2+water and CH 4+water mixtures in silica gel pore of nominal diameters 6, 30, and 100 nm were measured and compared with the calculated results based on van der Waals and Platteeuw model. At a specific temperature, three-phase hydrate-water-vapor (HLV) equilibrium curves for pore hydrates were shifted to the higher-pressure condition depending on pore sizes when compared with those of bulk hydrates. Notably, hydrate phase equilibria for the case of 100 nominal nm pore size were nearly identical with those of bulk hydrates. The activities of water in porous silica gels were modified to account for capillary effect, and the calculation results were generally in good agreement with the experimental data. The structural characteristics of gas hydrates in silica gel pores were investigated through NMR spectroscopy. Keywords—CO 2, CH 4, gas hydrate, equilibria. I.

