National Library of Energy BETA

Sample records for nitrous oxide methane

  1. Closing the Gaps in the Budgets of Methane and Nitrous Oxide

    SciTech Connect (OSTI)

    Khalil, Aslam; Rice, Andrew; Rasmussen, Reinhold

    2013-11-22

    Together methane and nitrous oxide contribute almost 40% of the estimated increase in radiative forcing caused by the buildup of greenhouse gases during the last 250 years (IPCC, 2007). These increases are attributed to human activities. Since the emissions of these gases are from biogenic sources and closely associated with living things in the major terrestrial ecosystems of the world, climate change is expected to cause feedbacks that may further increase emissions even from systems normally classified as natural. Our results support the idea that while past increases of methane were driven by direct emissions from human activities, some of these have reached their limits and that the future of methane changes may be determined by feedbacks from warming temperatures. The greatly increased current focus on the arctic and the fate of the carbon frozen in its permafrost is an example of such a feedback that could exceed the direct increases caused by future human activities (Zimov et al. 2006). Our research was aimed at three broad areas to address open questions about the global budgets of methane and nitrous oxide. These areas of inquiry were: The processes by which methane and nitrous oxide are emitted, new sources such as trees and plants, and integration of results to refine the global budgets both at present and of the past decades. For the process studies the main research was to quantify the effect of changes in the ambient temperature on the emissions of methane and nitrous oxide from rice agriculture. Additionally, the emissions of methane and nitrous oxide under present conditions were estimated using the experimental data on how fertilizer applications and water management affect emissions. Rice was chosen for detailed study because it is a prototype system of the wider terrestrial source, its role in methane emissions is well established, it is easy to cultivate and it represents a major anthropogenic source. Here we will discuss the highlights of the

  2. Nitrous oxide and methane emissions and nitrous oxide isotopic composition from waste incineration in Switzerland

    SciTech Connect (OSTI)

    Harris, Eliza; Zeyer, Kerstin; Kegel, Rainer; Müller, Beat; Emmenegger, Lukas; Mohn, Joachim

    2015-01-15

    plants with SNCR, which had considerable N{sub 2}O emissions, was measured using quantum cascade laser spectroscopy. The isotopic site preference of N{sub 2}O – the enrichment of {sup 14}N{sup 15}NO relative to {sup 15}N{sup 14}NO – was found to be 17.6 ± 0.8‰, with no significant difference between the two plants. Comparison to previous studies suggests SP of 17–19‰ may be characteristic for N{sub 2}O produced from SNCR. Methane emissions were found to be insignificant, with a maximum emission factor of 2.5 ± 5.6 g CH{sub 4} t{sup −1} (0.2 ± 0.5 g CH{sub 4} GJ{sup −1}), which is expected due to high incinerator temperatures and efficient combustion.

  3. Global methane and nitrous oxide emissions from terrestrial ecosystems due to multiple environmental changes

    DOE PAGES-Beta [OSTI]

    Tian, Hanqin; Chen, Guangsheng; Lu, Chaoqun; Xu, Xiaofeng; Ren, Wei; Zhang, Bowen; Banger, Kamaljit; Tao, Bo; Pan, Shufen; Chu, Mingliang; et al

    2015-03-16

    Greenhouse gas (GHG)-induced climate change is among the most pressing sustainability challenges facing humanity today, posing serious risks for ecosystem health. Methane (CH4) and nitrous oxide (N2O) are the two most important GHGs after carbon dioxide (CO2), but their regional and global budgets are not well known. In this paper, we applied a process-based coupled biogeochemical model to concurrently estimate the magnitude and spatial and temporal patterns of CH4 and N2O fluxes as driven by multiple environmental changes, including climate variability, rising atmospheric CO2, increasing nitrogen deposition, tropospheric ozone pollution, land use change, and nitrogen fertilizer use.

  4. Nitrous oxide production and methane oxidation by different ammonia-oxidizing bacteria

    SciTech Connect (OSTI)

    Jiang, Q.Q.; Bakken, L.R.

    1999-06-01

    Ammonia-oxidizing bacteria (AOB) are thought to contribute significantly to N{sub 2}O production and methane oxidation in soils. Most knowledge derives from experiments with Nitrosomonas europaea, which appears to be of minor importance in most soils compared to Nitrosospira spp. The authors have conducted a comparative study of levels of aerobic N{sub 2}O production in six phylogenetically different Nitrosospira strains newly isolated from soils and in two N. europaea and Nitrosospira multiformis type strains. The fraction of oxidized ammonium released as N{sub 2}O during aerobic growth was remarkably constant for all the Nitrosospira strains, irrespective of the substrate supply (urea versus ammonium), the pH, or substrate limitation. N. europaea and Nitrosospira multiformis released similar fractions of N{sub 2}O when they were supplied with ample amounts of substrates, but the fractions rose sharply when they were restricted by a low pH or substrate limitation. Phosphate buffer doubled the N{sub 2}O release for all types of AOB. No detectable oxidation of atmospheric methane was detected. Calculations based on detection limits as well as data in the literature on CH{sub 4} oxidation by AOB bacteria prove that none of the tested strains contribute significantly to the oxidation of atmospheric CH{sub 4} in soils.

  5. Global methane and nitrous oxide emissions from terrestrial ecosystems due to multiple environmental changes

    SciTech Connect (OSTI)

    Tian, Hanqin; Chen, Guangsheng; Lu, Chaoqun; Xu, Xiaofeng; Ren, Wei; Zhang, Bowen; Banger, Kamaljit; Tao, Bo; Pan, Shufen; Chu, Mingliang; Zhang, Chi; Bruhwiler, Lori; Wofsy, Steven

    2015-03-16

    Greenhouse gas (GHG)-induced climate change is among the most pressing sustainability challenges facing humanity today, posing serious risks for ecosystem health. Methane (CH4) and nitrous oxide (N2O) are the two most important GHGs after carbon dioxide (CO2), but their regional and global budgets are not well known. In this paper, we applied a process-based coupled biogeochemical model to concurrently estimate the magnitude and spatial and temporal patterns of CH4 and N2O fluxes as driven by multiple environmental changes, including climate variability, rising atmospheric CO2, increasing nitrogen deposition, tropospheric ozone pollution, land use change, and nitrogen fertilizer use.

  6. EIA - Greenhouse Gas Emissions - Nitrous Oxide Emissions

    Gasoline and Diesel Fuel Update

    4. Nitrous Oxide Emissions 4.1 Total emissions U.S. nitrous oxide emissions in 2009 were 4 MMTCO2e (1.7 percent) below their 2008 total (Table 22). Sources of U.S. nitrous oxide emissions include agriculture, energy use, industrial processes, and waste management (Figure 22). The largest source is agriculture (73 percent), and the majority of agricultural emissions result from nitrogen fertilization of agricultural soils (87 percent of the agriculture total) and management of animal waste (13

  7. Measuring and modeling the lifetime of nitrous oxide including...

    Office of Scientific and Technical Information (OSTI)

    Published Article: Measuring and modeling the lifetime of nitrous oxide including its variability: NITROUS OXIDE AND ITS CHANGING LIFETIME Prev Next Title: Measuring and ...

  8. Spatial variability of nitrous oxide and methane emissions from an MBT landfill in operation: Strong N{sub 2}O hotspots at the working face

    SciTech Connect (OSTI)

    Harborth, Peter; Fu, Roland; Mnnich, Kai; Flessa, Heinz; Fricke, Klaus

    2013-10-15

    Highlights: ? First measurements of N{sub 2}O and CH{sub 4} emissions from an MBT landfill. ? High N{sub 2}O emissions from recently deposited material. ? N{sub 2}O emissions associated with aeration and the occurrence of nitrite and nitrate. ? Strong negative correlation between CH{sub 4} and N{sub 2}O production activity. - Abstract: Mechanical biological treatment (MBT) is an effective technique, which removes organic carbon from municipal solid waste (MSW) prior to deposition. Thereby, methane (CH{sub 4}) production in the landfill is strongly mitigated. However, direct measurements of greenhouse gas emissions from full-scale MBT landfills have not been conducted so far. Thus, CH{sub 4} and nitrous oxide (N{sub 2}O) emissions from a German MBT landfill in operation as well as their concentrations in the landfill gas (LFG) were measured. High N{sub 2}O emissions of 20200 g CO{sub 2} eq. m{sup ?2} h{sup ?1} magnitude (up to 428 mg N m{sup ?2} h{sup ?1}) were observed within 20 m of the working face. CH{sub 4} emissions were highest at the landfill zone located at a distance of 3040 m from the working face, where they reached about 10 g CO{sub 2} eq. m{sup ?2} h{sup ?1}. The MBT material in this area has been deposited several weeks earlier. Maximum LFG concentration for N{sub 2}O was 24.000 ppmv in material below the emission hotspot. At a depth of 50 cm from the landfill surface a strong negative correlation between N{sub 2}O and CH{sub 4} concentrations was observed. From this and from the distribution pattern of extractable ammonium, nitrite, and nitrate it has been concluded that strong N{sub 2}O production is associated with nitrification activity and the occurrence of nitrite and nitrate, which is initiated by oxygen input during waste deposition. Therefore, CH{sub 4} mitigation measures, which often employ aeration, could result in a net increase of GHG emissions due to increased N{sub 2}O emissions, especially at MBT landfills.

  9. Enzymatic Oxidation of Methane

    SciTech Connect (OSTI)

    Sirajuddin, S; Rosenzweig, AC

    2015-04-14

    Methane monooxygenases (MMOs) are enzymes that catalyze the oxidation of methane to methanol in methanotrophic bacteria. As potential targets for new gas-to-liquid methane bioconversion processes, MMOs have attracted intense attention in recent years. There are two distinct types of MMO, a soluble, cytoplasmic MMO (sMMO) and a membrane-bound, particulate MMO (pMMO). Both oxidize methane at metal centers within a complex, multisubunit scaffold, but the structures, active sites, and chemical mechanisms are completely different. This Current Topic review article focuses on the overall architectures, active site structures, substrate reactivities, proteinprotein interactions, and chemical mechanisms of both MMOs, with an emphasis on fundamental aspects. In addition, recent advances, including new details of interactions between the sMMO components, characterization of sMMO intermediates, and progress toward understanding the pMMO metal centers are highlighted. The work summarized here provides a guide for those interested in exploiting MMOs for biotechnological applications.

  10. On-Board Measurement of Ammonia and Nitrous Oxide Using Feedback...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Laser Spectroscopy Combined with Amplified Resonance and Low Pressure Sampling On-Board Measurement of Ammonia and Nitrous Oxide Using Feedback Absorption Laser ...

  11. Benzene/nitrous oxide flammability in the precipitate hydrolysis process

    SciTech Connect (OSTI)

    Jacobs, R A

    1989-09-18

    The HAN (hydroxylamine nitrate) process for destruction of nitrite in precipitate hydrolysis produces nitrous oxide (N2O) gas as one of the products. N2O can form flammable mixtures with benzene which is also present due to radiolysis and hydrolysis of tetraphenylborate. Extensive flame modeling and explosion testing was undertaken to define the minimum oxidant for combustion of N2O/benzene using both nitrogen and carbon dioxide as diluents. The attached memorandum interprets and documents the results of the studies.

  12. Laboratory flammability studies of mixtures of hydrogen, nitrous oxide, and air

    SciTech Connect (OSTI)

    Cashdollar, K L; Hertzberg, M; Zlochower, I A; Lucci, C E; Green, G M; Thomas, R A

    1992-06-26

    At the request of the Department of Energy and the Westinghouse Hanford Company, the Bureau of Mines has investigated the flammability of mixtures of hydrogen, nitrous oxide, and air. This work is relevant to the possible hazards of flammable gas generation from nuclear waste tanks at Hanford, WA. The tests were performed in a 120-L spherical chamber under both quiescent and turbulent conditions using both electric spark and pyrotechnic ignition sources. The data reported here for binary mixtures of hydrogen in air generally confirm the data of previous investigators, but they are more comprehensive than those reported previously. The results clarify to a greater extent the complications associated with buoyancy, turbulence, and selective diffusion. The data reported here for ternary mixtures of hydrogen and nitrous oxide in air indicate that small additions of nitrous oxide (relative to the amount of air) have little effect, but that higher concentrations of nitrous oxide (relative to air) significantly increase the explosion hazard.

  13. Final Report for DOE grant no. DE-FG02-04ER63883: Can soil genomics predict the impact of precipitation on nitrous oxide flux from soil

    SciTech Connect (OSTI)

    Egbert Schwartz

    2008-12-15

    Nitrous oxide is a potent greenhouse gas that is released by microorganisms in soil. However, the production of nitrous oxide in soil is highly variable and difficult to predict. Future climate change may have large impacts on nitrous oxide release through alteration of precipitation patterns. We analyzed DNA extracted from soil in order to uncover relationships between microbial processes, abundance of particular DNA sequences and net nitrous oxide fluxes from soil. Denitrification, a microbial process in which nitrate is used as an electron acceptor, correlated with nitrous oxide flux from soil. The abundance of ammonia oxidizing archaea correlated positively, but weakly, with nitrous oxide production in soil. The abundance of bacterial genes in soil was negatively correlated with gross nitrogen mineralization rates and nitrous oxide release from soil. We suggest that the most important control over nitrous oxide production in soil is the growth and death of microorganisms. When organisms are growing nitrogen is incorporated into their biomass and nitrous oxide flux is low. In contrast, when microorganisms die, due to predation or infection by viruses, inorganic nitrogen is released into the soil resulting in nitrous oxide release. Higher rates of precipitation increase access to microorganisms by predators or viruses through filling large soil pores with water and therefore can lead to large releases of nitrous oxide from soil. We developed a new technique, stable isotope probing with 18O-water, to study growth and mortality of microorganisms in soil.

  14. Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions

    SciTech Connect (OSTI)

    Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E.; Meisel, D.

    1992-07-01

    Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

  15. Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions

    SciTech Connect (OSTI)

    Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. ); Meisel, D. )

    1992-01-01

    Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

  16. Surface water and atmospheric carbon dioxide and nitrous oxide observations by shipboard automated gas chromatography: Results from expeditions between 1977 and 1990

    SciTech Connect (OSTI)

    Weiss, R.F.; Van Woy, F.A.; Salameh, P.K.; Sepanski, R.J.

    1992-12-01

    This document presents the results of surface water and atmospheric carbon dioxide (CO{sub 2}) and nitrous oxide (N{sub 2}O) measurements carried out by shipboard gas chromatography over the period 1977--1990. These data include results from 11 different oceanic surveys for a total of 41 expedition legs. Collectively, they represent a globally distributed sampling that includes locations in the Atlantic, Pacific, Indian, and Southern Oceans, as well as the Mediterranean and Red Seas. The measurements were made by an automated high-precision shipboard gas chromatographic system developed during the late 1970s and used extensively over the intervening years. This instrument measures CO{sub 2} by flame ionization after quantitative reaction to methane in a stream of hydrogen. Nitrous oxide is measured by a separate electron capture detector. The chromatographic system measures 196 dry-gas samples a day, divided equally among the atmosphere, gas equilibrated with surface water, a low-range gas standard, and a high-range gas standard.

  17. Surface water and atmospheric carbon dioxide and nitrous oxide observations by shipboard automated gas chromatography: Results from expeditions between 1977 and 1990

    SciTech Connect (OSTI)

    Weiss, R.F.; Van Woy, F.A.; Salameh, P.K. ); Sepanski, R.J. . Energy, Environment and Resources Center)

    1992-12-01

    This document presents the results of surface water and atmospheric carbon dioxide (CO[sub 2]) and nitrous oxide (N[sub 2]O) measurements carried out by shipboard gas chromatography over the period 1977--1990. These data include results from 11 different oceanic surveys for a total of 41 expedition legs. Collectively, they represent a globally distributed sampling that includes locations in the Atlantic, Pacific, Indian, and Southern Oceans, as well as the Mediterranean and Red Seas. The measurements were made by an automated high-precision shipboard gas chromatographic system developed during the late 1970s and used extensively over the intervening years. This instrument measures CO[sub 2] by flame ionization after quantitative reaction to methane in a stream of hydrogen. Nitrous oxide is measured by a separate electron capture detector. The chromatographic system measures 196 dry-gas samples a day, divided equally among the atmosphere, gas equilibrated with surface water, a low-range gas standard, and a high-range gas standard.

  18. Design and Testing of a Liquid Nitrous Oxide and Ethanol Fueled Rocket Engine

    SciTech Connect (OSTI)

    Youngblood, Stewart

    2015-08-01

    A small-scale, bi-propellant, liquid fueled rocket engine and supporting test infrastructure were designed and constructed at the Energetic Materials Research and Testing Center (EMRTC). This facility was used to evaluate liquid nitrous oxide and ethanol as potential rocket propellants. Thrust and pressure measurements along with high-speed digital imaging of the rocket exhaust plume were made. This experimental data was used for validation of a computational model developed of the rocket engine tested. The developed computational model was utilized to analyze rocket engine performance across a range of operating pressures, fuel-oxidizer mixture ratios, and outlet nozzle configurations. A comparative study of the modeling of a liquid rocket engine was performed using NASA CEA and Cantera, an opensource equilibrium code capable of being interfaced with MATLAB. One goal of this modeling was to demonstrate the ability of Cantera to accurately model the basic chemical equilibrium, thermodynamics, and transport properties for varied fuel and oxidizer operating conditions. Once validated for basic equilibrium, an expanded MATLAB code, referencing Cantera, was advanced beyond CEAs capabilities to predict rocket engine performance as a function of supplied propellant flow rate and rocket engine nozzle dimensions. Cantera was found to comparable favorably to CEA for making equilibrium calculations, supporting its use as an alternative to CEA. The developed rocket engine performs as predicted, demonstrating the developedMATLAB rocket engine model was successful in predicting real world rocket engine performance. Finally, nitrous oxide and ethanol were shown to perform well as rocket propellants, with specific impulses experimentally recorded in the range of 250 to 260 seconds.

  19. Silicon oxynitride films deposited by reactive high power impulse magnetron sputtering using nitrous oxide as a single-source precursor

    SciTech Connect (OSTI)

    Hänninen, Tuomas Schmidt, Susann; Jensen, Jens; Hultman, Lars; Högberg, Hans

    2015-09-15

    Silicon oxynitride thin films were synthesized by reactive high power impulse magnetron sputtering of silicon in argon/nitrous oxide plasmas. Nitrous oxide was employed as a single-source precursor supplying oxygen and nitrogen for the film growth. The films were characterized by elastic recoil detection analysis, x-ray photoelectron spectroscopy, x-ray diffraction, x-ray reflectivity, scanning electron microscopy, and spectroscopic ellipsometry. Results show that the films are silicon rich, amorphous, and exhibit a random chemical bonding structure. The optical properties with the refractive index and the extinction coefficient correlate with the film elemental composition, showing decreasing values with increasing film oxygen and nitrogen content. The total percentage of oxygen and nitrogen in the films is controlled by adjusting the gas flow ratio in the deposition processes. Furthermore, it is shown that the film oxygen-to-nitrogen ratio can be tailored by the high power impulse magnetron sputtering-specific parameters pulse frequency and energy per pulse.

  20. OXIDATIVE COUPLING OF METHANE USING INORGANIC MEMBRANE REACTORS

    SciTech Connect (OSTI)

    Dr. Y.H. Ma; Dr. W.R. Moser; Dr. A.G. Dixon; Dr. A.M. Ramachandra; Dr. Y. Lu; C. Binkerd

    1998-04-01

    The objective of this research is to study the oxidative coupling of methane in catalytic inorganic membrane reactors. A specific target is to achieve conversion of methane to C{sub 2} hydrocarbons at very high selectivity and higher yields than in conventional non-porous, co-feed, fixed bed reactors by controlling the oxygen supply through the membrane. A membrane reactor has the advantage of precisely controlling the rate of delivery of oxygen to the catalyst. This facility permits balancing the rate of oxidation and reduction of the catalyst. In addition, membrane reactors minimize the concentration of gas phase oxygen thus reducing non selective gas phase reactions, which are believed to be a main route for the formation of CO{sub x} products. Such gas phase reactions are a cause of decreased selectivity in the oxidative coupling of methane in conventional flow reactors. Membrane reactors could also produce higher product yields by providing better distribution of the reactant gases over the catalyst than the conventional plug flow reactors. Membrane reactor technology also offers the potential for modifying the membranes both to improve catalytic properties as well as to regulate the rate of the permeation/diffusion of reactants through the membrane to minimize by-product generation. Other benefits also exist with membrane reactors, such as the mitigation of thermal hot-spots for highly exothermic reactions such as the oxidative coupling of methane. The application of catalytically active inorganic membranes has potential for drastically increasing the yield of reactions which are currently limited by either thermodynamic equilibria, product inhibition, or kinetic selectivity.

  1. Understanding complete oxidation of methane on spinel oxides at a molecular level

    DOE PAGES-Beta [OSTI]

    Tao, Franklin Feng; Shan, Jun-jun; Nguyen, Luan; Wang, Ziyun; Zhang, Shiran; Zhang, Li; Wu, Zili; Huang, Weixin; Zeng, Shibi; Hu, P.

    2015-08-04

    It is crucial to develop a catalyst made of earth-abundant elements highly active for a complete oxidation of methane at a relatively low temperature. NiCo2O4 consisting of earth-abundant elements which can completely oxidize methane in the temperature range of 350-550 °C. Being a cost-effective catalyst, NiCo2O4 exhibits activity higher than precious-metal-based catalysts. Here we report that the higher catalytic activity at the relatively low temperature results from the integration of nickel cations, cobalt cations and surface lattice oxygen atoms/oxygen vacancies at the atomic scale. Finally, in situ studies of complete oxidation of methane on NiCo2O4 and theoretical simulations show thatmore » methane dissociates to methyl on nickel cations and then couple with surface lattice oxygen atoms to form -CH3O with a following dehydrogenation to -CH2O; a following oxidative dehydrogenation forms CHO; CHO is transformed to product molecules through two different sub-pathways including dehydrogenation of OCHO and CO oxidation.« less

  2. Assessment of the methane oxidation capacity of compacted soils intended for use as landfill cover materials

    SciTech Connect (OSTI)

    Rachor, Ingke; Gebert, Julia; Groengroeft, Alexander; Pfeiffer, Eva-Maria

    2011-05-15

    The microbial oxidation of methane in engineered cover soils is considered a potent option for the mitigation of emissions from old landfills or sites containing wastes of low methane generation rates. A laboratory column study was conducted in order to derive design criteria that enable construction of an effective methane oxidising cover from the range of soils that are available to the landfill operator. Therefore, the methane oxidation capacity of different soils was assessed under simulated landfill conditions. Five sandy potential landfill top cover materials with varying contents of silt and clay were investigated with respect to methane oxidation and corresponding soil gas composition over a period of four months. The soils were compacted to 95% of their specific proctor density, resulting in bulk densities of 1.4-1.7 g cm{sup -3}, reflecting considerably unfavourable conditions for methane oxidation due to reduced air-filled porosity. The soil water content was adjusted to field capacity, resulting in water contents ranging from 16.2 to 48.5 vol.%. The investigated inlet fluxes ranged from 25 to about 100 g CH{sub 4} m{sup -2} d{sup -1}, covering the methane load proposed to allow for complete oxidation in landfill covers under Western European climate conditions and hence being suggested as a criterion for release from aftercare. The vertical distribution of gas concentrations, methane flux balances as well as stable carbon isotope studies allowed for clear process identifications. Higher inlet fluxes led to a reduction of the aerated zone, an increase in the absolute methane oxidation rate and a decline of the relative proportion of oxidized methane. For each material, a specific maximum oxidation rate was determined, which varied between 20 and 95 g CH{sub 4} m{sup -2} d{sup -1} and which was positively correlated to the air-filled porosity of the soil. Methane oxidation efficiencies and gas profile data imply a strong link between oxidation capacity

  3. Methane and methanol oxidation in supercritical water: Chemical kinetics and hydrothermal flame studies

    SciTech Connect (OSTI)

    Steeper, R.R.

    1996-01-01

    Supercritical water oxidation (SCWO) is an emerging technology for the treatment of wastes in the presence of a large concentration of water at conditions above water`s thermodynamic critical point. A high-pressure, optically accessible reaction cell was constructed to investigate the oxidation of methane and methanol in this environment. Experiments were conducted to examine both flame and non-flame oxidation regimes. Optical access enabled the use of normal and shadowgraphy video systems for visualization, and Raman spectroscopy for in situ measurement of species concentrations. Flame experiments were performed by steadily injecting pure oxygen into supercritical mixtures of water and methane or methanol at 270 bar and at temperatures from 390 to 510{degrees}C. The experiments mapped conditions leading to the spontaneous ignition of diffusion flames in supercritical water. Above 470{degrees}C, flames spontaneously ignite in mixtures containing only 6 mole% methane or methanol. This data is relevant to the design and operation of commercial SCWO processes that may be susceptible to inadvertent flame formation. Non-flame oxidation kinetics experiments measured rates of methane oxidation in supercritical water at 270 bar and at temperatures from 390 to 442{degrees}C. The initial methane concentration was nominally 0.15 gmol/L, a level representative of commercial SCWO processes. The observed methane concentration histories were fit to a one-step reaction rate expression indicating a reaction order close to two for methane and zero for oxygen. Experiments were also conducted with varying water concentrations (0 to 8 gmol/L) while temperature and initial reactant concentrations were held constant. The rate of methane oxidation rises steadily with water concentration up to about 5 gmol/L and then abruptly falls off at higher concentrations.

  4. Effect of Co/Ni ratios in cobalt nickel mixed oxide catalysts on methane combustion

    SciTech Connect (OSTI)

    Lim, Tae Hwan; Cho, Sung June; Yang, Hee Sung; Engelhard, Mark H.; Kim, Do Heui

    2015-07-31

    A series of cobalt nickel mixed oxide catalysts with the varying ratios of Co to Ni, prepared by co-precipitation method, were applied to methane combustion. Among the various ratios, cobalt nickel mixed oxides having the ratios of Co to Ni of (50:50) and (67:33) demonstrate the highest activity for methane combustion. Structural analysis obtained from X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) evidently demonstrates that CoNi (50:50) and (67:33) samples consist of NiCo2O4and NiO phase and, more importantly, NiCo2O4spinel structure is largely distorted, which is attributed to the insertion of Ni2+ions into octahedral sites in Co3O4spinel structure. Such structural dis-order results in the enhanced portion of surface oxygen species, thus leading to the improved reducibility of the catalysts in the low temperature region as evidenced by temperature programmed reduction by hydrogen (H2TPR) and X-ray photoelectron spectroscopy (XPS) O 1s results. They prove that structural disorder in cobalt nickel mixed oxides enhances the catalytic performance for methane combustion. Thus, it is concluded that a strong relationship between structural property and activity in cobalt nickel mixed oxide for methane combustion exists and, more importantly, distorted NiCo2O4spinel structure is found to be an active site for methane combustion.

  5. Thermal and combined thermal and radiolytic reactions involving nitrous oxide, hydrogen, nitrogen, and ammonia in contact with tank 241-SY-101 simulated waste

    SciTech Connect (OSTI)

    Bryan, S.A.; Pederson, L.R.

    1996-02-01

    Work described in this report was conducted at Pacific Northwest National Laboratory (PNNL) for the Flammable Gas Safety Project, the purpose of which is to develop information needed to support Westinghouse Hanford Company (WHC) in their efforts to ensure the safe interim storage of wastes at the Hanford Site. Described in this report are the results of tests to evaluate the rates of thermal and combined thermal and radiolytic reactions involving flammable gases in the presence of Tank 241-SY-101 simulated waste. Flammable gases generated by the radiolysis of water and by the thermal and radiolytic decomposition of organic waste constituents may themselves participate in further reactions. Examples include the decomposition of nitrous oxide to yield nitrogen and oxygen, the reaction of nitrous oxide and hydrogen to produce nitrogen and water, and the reaction of nitrogen and hydrogen to produce ammonia. The composition of the gases trapped in bubbles in the wastes might therefore change continuously as a function of the time that the gas bubbles are retained.

  6. Non-covalent interactions of nitrous oxide with aromatic compounds: Spectroscopic and computational evidence for the formation of 1:1 complexes

    SciTech Connect (OSTI)

    Cao, Qian; School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275 ; Gor, Gennady Y.; Krogh-Jespersen, Karsten; Khriachtchev, Leonid

    2014-04-14

    We present the first study of intermolecular interactions between nitrous oxide (N{sub 2}O) and three representative aromatic compounds (ACs): phenol, cresol, and toluene. The infrared spectroscopic experiments were performed in a Ne matrix and were supported by high-level quantum chemical calculations. Comparisons of the calculated and experimental vibrational spectra provide direct identification and characterization of the 1:1 N{sub 2}O-AC complexes. Our results show that N{sub 2}O is capable of forming non-covalently bonded complexes with ACs. Complex formation is dominated by dispersion forces, and the interaction energies are relatively low (about ?3 kcal mol{sup ?1}); however, the complexes are clearly detected by frequency shifts of the characteristic bands. These results suggest that N{sub 2}O can be bound to the amino-acid residues tyrosine or phenylalanine in the form of ? complexes.

  7. Low-Energy, Low Cost Production of Ethylene by Low Temperature Oxidative Coupling of Methane

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Guido Radaelli, Divya Jonnavittula, David Zaziski, Jarod McCormick Siluria Technologies U.S. DOE Advanced Manufacturing Office Program Review Meeting Washington, D.C. June 14-15, 2016 This presentation does not contain any proprietary, confidential, or otherwise restricted information. Project Objective  Overall Objective: To develop a new catalytic process for distributed production of ethylene via low-temperature oxidative coupling of methane using the advanced OCM catalyst developed by

  8. Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly report, July - September 1996

    SciTech Connect (OSTI)

    McCormick, R.L.; Alptekin, G.O.

    1996-12-01

    This document covers the period July-September, 1996. Activities included studies of the oxidation of dimethyl ether over vanadyl pyrophosphate and synthesis of all previously acquired kinetic data. This synthesis revealed the need for additional data on methane and methanol oxidation and these experiments were performed. A further series of methanol oxidation/dehydration experiments was conducted on samples with varying surface acidity that have been described in earlier reports. Oxidation of methane over Cr- promoted VPO was also reinvestigated. The kinetic studies performed to date allow us to determine optimum conditions for methanol and formaldehyde production from methane using VPO catalysts, and in particular determine the effect of lean conditions (excess oxygen), oxygen deficient conditions (used in most other methane oxidation studies), and the potential of using the catalyst as a stoichiometric oxidant or oxygen carrier. However, unpromoted VPO yields only CO as the primary oxidation product. Studies of promoters have shown improvements in the formaldehyde selectivity but no methanol has been observed. The best promoters tested have been Fe and Cr (results for Cr are described in this report). We have also examined the use of iron phosphate for the methane conversion reaction. FePO{sub 4}is a more selectivity catalyst than the promoted VPO materials. Support of this iron phosphate on silica results in further improvements in selectivity. Current work is directed at understanding the improved selectivity for promoted VPO and at obtaining a knowledge of the optimum conditions for methane conversion of iron phosphate. 15 refs., 2 figs., 1 tab.

  9. Methyl Chloride from Direct Methane Partial Oxidation: A High-Temperature Shilov-Like Catalytic System

    SciTech Connect (OSTI)

    Yongchun Tang; John Ma

    2012-03-23

    The intention of this study is to demonstrate and evaluate the scientific and economic feasibility of using special solvents to improve the thermal stability of Pt-catalyst in the Shilov system, such that a high reaction temperature could be achieved. The higher conversion rate (near 100%) of methyl chloride from partial oxidation of methane under the high temperature ({approx} 200 C) without significant Pt0 precipitation has been achieved. High concentration of the Cl- ion has been identified as the key for the stabilization of the Pt-catalysts. H/D exchange measurements indicated that the over oxidation will occur at the elevated temperature, developments of the effective product separation processes will be necessary in order to rationalize the industry-visible CH4 to CH3Cl conversion.

  10. Plasma-produced phase-pure cuprous oxide nanowires for methane gas sensing

    SciTech Connect (OSTI)

    Cheng, Qijin Zhang, Fengyan; Yan, Wei; Randeniya, Lakshman; Ostrikov, Kostya

    2014-03-28

    Phase-selective synthesis of copper oxide nanowires is warranted by several applications, yet it remains challenging because of the narrow windows of the suitable temperature and precursor gas composition in thermal processes. Here, we report on the room-temperature synthesis of small-diameter, large-area, uniform, and phase-pure Cu{sub 2}O nanowires by exposing copper films to a custom-designed low-pressure, thermally non-equilibrium, high-density (typically, the electron number density is in the range of 10{sup 11}10{sup 13}?cm{sup ?3}) inductively coupled plasmas. The mechanism of the plasma-enabled phase selectivity is proposed. The gas sensors based on the synthesized Cu{sub 2}O nanowires feature fast response and recovery for the low-temperature (?140?C) detection of methane gas in comparison with polycrystalline Cu{sub 2}O thin film-based gas sensors. Specifically, at a methane concentration of 4%, the response and the recovery times of the Cu{sub 2}O nanowire-based gas sensors are 125 and 147?s, respectively. The Cu{sub 2}O nanowire-based gas sensors have a potential for applications in the environmental monitoring, chemical industry, mining industry, and several other emerging areas.

  11. Development of a hydrogen generator for fuel cells based on the partial oxidation of methane

    SciTech Connect (OSTI)

    Recupero, V.; Torre, T.; Saija, G.; Fiordano, N.

    1996-12-31

    As well known, the most acknowledged process for generation of hydrogen for fuel cells is based upon the steam reforming of methane or natural gas (SRM). The reaction is endothermic ({Delta}H{sub 298}= 206 kJ/mole) and high H{sub 2}O/CH{sub 4} ratios are required in order to limit coke formation at T higher than 1000 K. Moreover, it is a common practice that the process`s fuel economy is highly sensitive to proper heat fluxes and reactor design (tubular type) and to operational conditions. Efficient heat recovery can be accomplished only on large scale units (> 40,000 Nm{sup 3}/h), far from the range of interest of {open_quotes}on-site{close_quotes} fuel cells. Even if, to fit the needs of the fuel cell technology, medium sized external reforming units (50-200 Nm{sup 3} H{sub 2}/h) have been developed and/or planned for integration with both the first and the second generation fuel cells, amelioration in their heat recovery and efficiency is at the expense of an increased sophistication and therefore at higher per unit costs. In all cases, SRM requires an extra {open_quotes}fuel{close_quotes} supply (to substain the endothermicity of the reaction) in addition to stoichiometric requirements ({open_quotes}feed{close_quotes} gas). A valid alternative could be a process based on catalytic partial oxidation of CH{sub 4} (CSPOM), since the process is mildly exothermic ({Delta}H{sub 298}= -35.6 kJ/mole) and therefore not energy intensive. Consequently, great interest is expected from conversion of methane into syngas, if an autothermal, low energy intensive, compact and reliable process could be developed.

  12. Nitrogen Oxides in the Nocturnal Boundary Layer: Chemistry of Nitrous Acid (HONO) and the Nitrate Radical (N03)

    SciTech Connect (OSTI)

    Jochen Stutz

    2005-05-24

    Summary Chemical processes occurring at night in the lowest part of the urban atmosphere, the so called nocturnal boundary layer (NBL), can influence the composition of the atmosphere during the night as well as the following day. They may impact the budgets of some of the most important pollutants, such as ozone and nitrogen oxides, as well as influence size and composition of particular matter. Few studies have thus far concentrated on the nocturnal chemistry of the urban NBL, most likely due to the strong influence of vertical transport and mixing, which requires the measurement of trace gas profiles instead of simple point observations. Motivated by our lack of observations and understanding of nocturnal chemistry, the focus of this project was the study of the vertical distribution of trace gases and the altitude dependence of nocturnal chemistry under polluted conditions through field observations and modeling studies. The analysis of three field experiments (TEXAQS, Houston, 2000; Phoenix Sunrise Ozone Experiment, 2001; NAPOX, Boston, 2002), two of which were performed in this project, showed that ozone concentrations typically increase with height in the lowest 150m, while NO2 typically decreases. NO3, the dominant nocturnal radical species, showed much higher concentrations in the upper part of the NBL, and was often not present at the ground. With the help of a one-dimensional chemical transport model, developed in this project, we found that the interaction of ground emissions of NOx and hydrocarbons, together with their vertical transport, is responsible for the vertical profiles. The dominant chemical reactions influencing ozone, NO2 and NO3 are the reaction of ozone and NO3 with freshly emitted NO. Sensitivity studies with our model showed that the magnitude of the trace gas gradients depend both on the emission rates and the vertical stability of the NBL. Observations and model analysis clearly show that nocturnal chemistry in urban areas is altitude

  13. Geochemical, metagenomic and metaproteomic insights into trace metal utilization by methane-oxidizing microbial consortia in sulfidic marine sediments

    SciTech Connect (OSTI)

    Glass, DR. Jennifer; Yu, DR. Hang; Steele, Joshua; Dawson, Katherine; Sun, S; Chourey, Karuna; Hettich, Robert {Bob} L; Orphan, V

    2014-01-01

    Microbes have obligate requirements for trace metals in metalloenzymes that catalyze important biogeochemical reactions. In anoxic methane- and sulfide-rich environments, microbes may have unique adaptations for metal acquisition and utilization due to decreased bioavailability as a result of metal sulfide precipitation. However, micronutrient cycling is largely unexplored in cold ( 10 C) and sulfidic (>1 mM H2S) deep-sea methane seep ecosystems. We investigated trace metal geochemistry and microbial metal utilization in methane seeps offshore Oregon and California, USA, and report dissolved concentrations of nickel (0.5-270 nM), cobalt (0.5-6 nM), molybdenum (10-5,600 nM) and tungsten (0.3-8 nM) in Hydrate Ridge sediment porewaters. Despite low levels of cobalt and tungsten, metagenomic and metaproteomic data suggest that microbial consortia catalyzing anaerobic oxidation of methane utilize both scarce micronutrients in addition to nickel and molybdenum. Genetic machinery for cobalt-containing vitamin B12 biosynthesis was present in both anaerobic methanotrophic archaea (ANME) and sulfate-reducing bacteria (SRB). Proteins affiliated with the tungsten-containing form of formylmethanofuran dehydrogenase were expressed in ANME from two seep ecosystems, the first evidence for expression of a tungstoenzyme in psychrotolerant microorganisms. Finally, our data suggest that chemical speciation of metals in highly sulfidic porewaters may exert a stronger influence on microbial bioavailability than total concentration

  14. Geochemical, metagenomic and metaproteomic insights into trace metal utilization by methane-oxidizing microbial consortia in sulphidic marine sediments

    SciTech Connect (OSTI)

    Glass, DR. Jennifer; Yu, DR. Hang; Steele, Joshua; Dawson, Katherine; Sun, S; Chourey, Karuna; Pan, Chongle; Hettich, Robert {Bob} L; Orphan, V

    2013-01-01

    Microbes have obligate requirements for trace metals in metalloenzymes that catalyse important biogeochemical reactions. In anoxic methane- and sulphiderich environments, microbes may have unique adaptations for metal acquisition and utilization because of decreased bioavailability as a result of metal sulphide precipitation. However, micronutrient cycling is largely unexplored in cold ( 10 C) and sulphidic (> 1 mM H2S) deep-sea methane seep ecosystems. We investigated trace metal geochemistry and microbial metal utilization in methane seeps offshore Oregon and California, USA, and report dissolved concentrations of nickel (0.5 270 nM), cobalt (0.5 6 nM), molybdenum (10 5600 nM) and tungsten (0.3 8 nM) in Hydrate Ridge sediment porewaters. Despite low levels of cobalt and tungsten, metagenomic and metaproteomic data suggest that microbial consortia catalysing anaerobic oxidation of methane (AOM) utilize both scarce micronutrients in addition to nickel and molybdenum. Genetic machinery for cobalt-containing vitamin B12 biosynthesis was present in both anaerobic methanotrophic archaea (ANME) and sulphate-reducing bacteria. Proteins affiliated with the tungsten-containing form of formylmethanofuran dehydrogenase were expressed in ANME from two seep ecosystems, the first evidence for expression of a tungstoenzyme in psychrophilic microorganisms. Overall, our data suggest that AOM consortia use specialized biochemical strategies to overcome the challenges of metal availability in sulphidic environments.

  15. Promotional Effects of In on Non-Oxidative Methane Transformation Over Mo-ZSM-5

    DOE PAGES-Beta [OSTI]

    Zhang, Yang; Kidder, Michelle; Ruther, Rose E.; Nanda, Jagjit; Foo, Guo Shiou; Wu, Zili; Narula, Chaitanya K.

    2016-08-16

    In this paper, we present a new class of catalysts, InMo-ZSM-5, which can be prepared by indium impregnation of Mo-ZSM-5. The incorporation of indium dramatically decreases coke formation during methane dehydroaromatization. The benzene and C2 hydrocarbons selectivity among total hydrocarbons over InMo-ZSM-5 remains comparable to that of Mo-ZSM-5 despite reduced methane conversion due to decreased coke formation. We found 1 wt% indium to be optimal loading for reducing coke selectivity to half that of Mo-ZSM-5. Characterization methods were not helpful in discerning the interaction of In with Mo but experiments with bimetallic 1In2Mo-ZSM-5 and mechanical mixture 1In+2Mo-ZSM-5 suggest that Inmore » and Mo need to be in close proximity to suppress coke formation. Finally, this is supported by temperature programmed reduction experiments which show that In incorporation leads to lower Mo reduction temperature in In2Mo-ZMS-5.« less

  16. Electrochemical methane sensor

    DOE Patents [OSTI]

    Zaromb, S.; Otagawa, T.; Stetter, J.R.

    1984-08-27

    A method and instrument including an electrochemical cell for the detection and measurement of methane in a gas by the oxidation of methane electrochemically at a working electrode in a nonaqueous electrolyte at a voltage about 1.4 volts vs R.H.E. (the reversible hydrogen electrode potential in the same electrolyte), and the measurement of the electrical signal resulting from the electrochemical oxidation.

  17. Ni modified ceramic anodes for direct-methane solid oxide fuel cells

    DOE Patents [OSTI]

    Xiao, Guoliang; Chen, Fanglin

    2016-01-19

    In accordance with certain embodiments of the present disclosure, a method for fabricating a solid oxide fuel cell is described. The method includes synthesizing a composition having a perovskite present therein. The method further includes applying the composition on an electrolyte support to form an anode and applying Ni to the composition on the anode.

  18. In situ studies of surface of NiFe2O4 catalyst during complete oxidation of methane

    DOE PAGES-Beta [OSTI]

    Zhang, Shiran; Shan, Junjun; Nie, Longhui; Nguyen, Luan; Wu, Zili; Tao, Franklin

    2015-12-21

    Here, NiFe2O4 with an inverse spinel structure exhibits high activity for a complete oxidation of methane at 400 °C–425 °C and a higher temperature. The surface of the catalyst and its adsorbates were well characterized with ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and in situ infrared spectroscopy (IR). In situ studies of the surface of NiFe2O4 using AP-XPS suggest the formation of methoxy-like and formate-like intermediates at a temperature lower than 200 °C, supported by the observed vibrational signatures in in situ IR studies. Evolutions of C1s photoemission features and the nominal atomic ratios of C/(Ni + Fe) of themore » catalyst surface suggest that the formate-like intermediate is transformed to product molecules CO2 and H2O in the temperature range of 250–300 °C. In situ studies suggest the formation of a spectator, – Olattice – CH2 – Olattice –. It strongly bonds to surface through C–O bonds and cannot be activated even at 400 °C.« less

  19. Characterization of Methane Degradation and Methane-Degrading Microbes in Alaska Coastal Water

    SciTech Connect (OSTI)

    Kirchman, David L.

    2012-03-29

    The net flux of methane from methane hydrates and other sources to the atmosphere depends on methane degradation as well as methane production and release from geological sources. The goal of this project was to examine methane-degrading archaea and organic carbon oxidizing bacteria in methane-rich and methane-poor sediments of the Beaufort Sea, Alaska. The Beaufort Sea system was sampled as part of a multi-disciplinary expedition (Methane in the Arctic Shelf or MIDAS) in September 2009. Microbial communities were examined by quantitative PCR analyses of 16S rRNA genes and key methane degradation genes (pmoA and mcrA involved in aerobic and anaerobic methane degradation, respectively), tag pyrosequencing of 16S rRNA genes to determine the taxonomic make up of microbes in these sediments, and sequencing of all microbial genes (metagenomes ). The taxonomic and functional make-up of the microbial communities varied with methane concentrations, with some data suggesting higher abundances of potential methane-oxidizing archaea in methane-rich sediments. Sequence analysis of PCR amplicons revealed that most of the mcrA genes were from the ANME-2 group of methane oxidizers. According to metagenomic data, genes involved in methane degradation and other degradation pathways changed with sediment depth along with sulfate and methane concentrations. Most importantly, sulfate reduction genes decreased with depth while the anaerobic methane degradation gene (mcrA) increased along with methane concentrations. The number of potential methane degradation genes (mcrA) was low and inconsistent with other data indicating the large impact of methane on these sediments. The data can be reconciled if a small number of potential methane-oxidizing archaea mediates a large flux of carbon in these sediments. Our study is the first to report metagenomic data from sediments dominated by ANME-2 archaea and is one of the few to examine the entire microbial assemblage potentially involved in

  20. Performance of Ni-Fe/gadolinium-doped CeO{sub2} anode supported tubular solid oxide fuel cells using steam reforming of methane

    SciTech Connect (OSTI)

    Liang, B.; Suzuki, T.; Hamamoto, K.; Yamaguchi, T.; Sumi, H.; Fujishiro, Y.; Ingram, B. J.; Carter, J. D.

    2012-03-15

    Iron nanoparticles (Fe{sub 2}O{sub 3}) were added to NiO/gadolinium-doped CeO{sub 2} (GDC) anode supported solid oxide fuel cell (SOFC) for the direct methane-water fuel operation. The cell was co-sintered at 1400 C, and the anode porosity is 31.8%. The main size corresponding to peak volume is around 1.5 {mu}m. When steam and methane directly fed to the cell, the power density is about 0.57 W cm{sup -2} at 650 C. It is the familiar performance for H{sub 2} operation (4 times of flow rate) with same fuel utilization. Compare with the testing temperature of 600 and 650 C, there is almost no carbon fiber deposition at 700 C with steam/methane (S/C) of 5. At the same time, fuel operation of high value of S/C (=3.3) resulted in fiber-like deposition and degradation of power performance based on loading test results.

  1. Syntrophic interactions and mechanisms underpinning anaerobic methane oxidation: targeted metaproteogenomics, single-cell protein detection and quantitative isotope imaging of microbial consortia

    SciTech Connect (OSTI)

    Orphan, Victoria Jeanne

    2014-11-26

    Syntrophy and mutualism play a central role in carbon and nutrient cycling by microorganisms. Yet, our ability to effectively study symbionts in culture has been hindered by the inherent interdependence of syntrophic associations, their dynamic behavior, and their frequent existence at thermodynamic limits. Now solutions to these challenges are emerging in the form of new methodologies. Developing strategies that establish links between the identity of microorganisms and their metabolic potential, as well as techniques that can probe metabolic networks on a scale that captures individual molecule exchange and processing, is at the forefront of microbial ecology. Understanding the interactions between microorganisms on this level, at a resolution previously intractable, will lead to our greater understanding of carbon turnover and microbial community resilience to environmental perturbations. In this project, we studied an enigmatic syntrophic association between uncultured methane-oxidizing archaea and sulfate-reducing bacteria. This environmental archaeal-bacterial partnership represents a globally important sink for methane in anoxic environments. The specific goals of this project were organized into 3 major tasks designed to address questions relating to the ecophysiology of these syntrophic organisms under changing environmental conditions (e.g. different electron acceptors and nutrients), primarily through the development of microanalytical imaging methods which enable the visualization of the spatial distribution of the partners within aggregates, consumption and exchange of isotopically labeled substrates, and expression of targeted proteins identified via metaproteomics. The advanced tool set developed here to collect, correlate, and analyze these high resolution image and isotope-based datasets from methane-oxidizing consortia has the potential to be widely applicable for studying and modeling patterns of activity and interactions across a broad range of

  2. Methane Hydrates

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Special Report: Frozen Heat: A Global Outlook on Methane Hydrates The United Nations Environmental Programme released this new, two-volume report in March 2015. Frozen Heat: A ...

  3. Effect of metallo-organic precursors on the synthesis of Sm-Sn pyrochlore catalysts: Application to the oxidative coupling of methane

    SciTech Connect (OSTI)

    Roger, A.C.; Petit, C.; Kiennemann, A.

    1997-04-15

    Synthesis of a series of Sm{sub 2}Sn{sub 2}O{sub 7} pyrochlore catalysts by a sol-gel-like method has been developed. The preparation from the oxides gives stoichiometric pyrochlore, unlike the result obtained when starting from chlorinated salts (SmCl{sub 3} or SnCl{sub 2}), which form tin-deficient pyrochlores. A spectroscopic study of the behavior of the starting oxides or chlorides in propionic acid, to generate a series of precursors, has been carried out, particular attention being focused on the precursors generated by SnCl{sub 2} in propionic acid using {sup 119}Sn NMR and FTIR spectroscopy. The formation of SnCl{sub 2}(C{sub 2}H{sub 5}COO){sub 2} as the main precursor is responsible for the tin deficiency observed in the pyrochlore structure. The catalytic performance in oxidative coupling of methane is directly correlated with the tin deficiency in the bulk of the pyrochlore. The work highlights the importance of controlling precisely the synthesis of the catalysts. 42 refs., 10 figs., 5 tabs.

  4. ARM - Methane Background Information

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    WarmingMethane Background Information Outreach Home Room News Publications Traditional Knowledge Kiosks Barrow, Alaska Tropical Western Pacific Site Tours Contacts Students Study Hall About ARM Global Warming FAQ Just for Fun Meet our Friends Cool Sites Teachers Teachers' Toolbox Lesson Plans Methane Background Information What is Methane? Why Do We Use Methane? How is Methane Made? Where Do We Find Methane? Can Methane Be Dangerous? Does Methane Contribute to Climate Change? What is Methane?

  5. Methane emissions from MBT landfills

    SciTech Connect (OSTI)

    Heyer, K.-U. Hupe, K.; Stegmann, R.

    2013-09-15

    Highlights: • Compilation of methane generation potential of mechanical biological treated (MBT) municipal solid waste. • Impacts and kinetics of landfill gas production of MBT landfills, approach with differentiated half-lives. • Methane oxidation in the waste itself and in soil covers. • Estimation of methane emissions from MBT landfills in Germany. - Abstract: Within the scope of an investigation for the German Federal Environment Agency (“Umweltbundesamt”), the basics for the estimation of the methane emissions from the landfilling of mechanically and biologically treated waste (MBT) were developed. For this purpose, topical research including monitoring results regarding the gas balance at MBT landfills was evaluated. For waste treated to the required German standards, a methane formation potential of approximately 18–24 m{sup 3} CH{sub 4}/t of total dry solids may be expected. Monitoring results from MBT landfills show that a three-phase model with differentiated half-lives describes the degradation kinetics in the best way. This is due to the fact that during the first years of disposal, the anaerobic degradation processes still proceed relatively intensively. In addition in the long term (decades), a residual gas production at a low level is still to be expected. Most of the soils used in recultivation layer systems at German landfills show a relatively high methane oxidation capacity up to 5 l CH{sub 4}/(m{sup 2} h). However, measurements at MBT disposal sites indicate that the majority of the landfill gas (in particular at non-covered areas), leaves the landfill body via preferred gas emission zones (hot spots) without significant methane oxidation. Therefore, rather low methane oxidation factors are recommended for open and temporarily covered MBT landfills. Higher methane oxidation rates can be achieved when the soil/recultivation layer is adequately designed and operated. Based on the elaborated default values, the First Order Decay (FOD

  6. Methane conversion to methanol

    SciTech Connect (OSTI)

    Noble, R.D.; Falconer, J.L.

    1992-06-01

    The objective of this research study is to demonstrate the effectiveness of a catalytic membrane reactor for the partial oxidation of methane. The specific goals are to demonstrate that we can improve product yield, demonstrate the optimal conditions for membrane reactor operation, determine the transport properties of the membrane, and provide demonstration of the process at the pilot plant scale. The last goal will be performed by Unocal, Inc., our industrial partner, upon successful completion of this study.

  7. Methane conversion to methanol

    SciTech Connect (OSTI)

    Noble, R.D.; Falconer, J.L.

    1992-01-01

    The objective of this research study is to demonstrate the effectiveness of a catalytic membrane reactor for the partial oxidation of methane. The specific goals are to demonstrate that we can improve product yield, demonstrate the optimal conditions for membrane reactor operation, determine the transport properties of the membrane, and provide demonstration of the process at the pilot plant scale. The last goal will be performed by Unocal, Inc., our industrial partner, upon successful completion of this study.

  8. Modeling of Pressurized Electrochemistry and Steam-Methane Reforming in Solid Oxide Fuel Cells and the Effects on Thermal and Electrical Stack Performance

    SciTech Connect (OSTI)

    Recknagle, Kurtis P.; Khaleel, Mohammad A.

    2009-03-01

    Summarizes work done to extend the electrochemical performance and methane reforming submodels to include the effects of pressurization and to demonstrate this new modeling capability by simulating large stacks operating on methane-rich fuel under pressurized and non-pressurized conditions. Pressurized operation boosts electrochemical performance, alters the kinetics of methane reforming, and effects the equilibrium composition of methane fuels. This work developed constitutive submodels that couple the electrochemistry, reforming, and pressurization to yield an increased capability of the modeling tool for prediction of SOFC stack performance.

  9. In situ studies of surface of NiFe2O4 catalyst during complete oxidation of methane

    SciTech Connect (OSTI)

    Zhang, Shiran; Shan, Junjun; Nie, Longhui; Nguyen, Luan; Wu, Zili; Tao, Franklin

    2015-12-21

    Here, NiFe2O4 with an inverse spinel structure exhibits high activity for a complete oxidation of methane at 400 °C–425 °C and a higher temperature. The surface of the catalyst and its adsorbates were well characterized with ambient pressure X-ray photoelectron spectroscopy (AP-XPS) and in situ infrared spectroscopy (IR). In situ studies of the surface of NiFe2O4 using AP-XPS suggest the formation of methoxy-like and formate-like intermediates at a temperature lower than 200 °C, supported by the observed vibrational signatures in in situ IR studies. Evolutions of C1s photoemission features and the nominal atomic ratios of C/(Ni + Fe) of the catalyst surface suggest that the formate-like intermediate is transformed to product molecules CO2 and H2O in the temperature range of 250–300 °C. In situ studies suggest the formation of a spectator, – Olattice – CH2 – Olattice –. It strongly bonds to surface through C–O bonds and cannot be activated even at 400 °C.

  10. Synthesis of murdochite-type Ni{sub 6}MnO{sub 8} with variable specific surface areas and the application in methane oxidation

    SciTech Connect (OSTI)

    Taguchi, Hideki; Tahara, Shohei; Okumura, Mikoto; Hirota, Ken

    2014-07-01

    To synthesize a murdochite-type Ni{sub 6}MnO{sub 8} with variable specific surface areas, an oxalate precursor was calcined at 350500 C in flowing argon, and the calcined sample was heated to 600 C in air. The lattice constant of the Ni{sub 6}MnO{sub 8} did not depend on the calcination temperature of the precursor, while the specific surface area decreased from 8.4 m{sup 2}/g to 2.6 m{sup 2}/g when increasing the calcination temperature of the precursor. The methane (CH{sub 4}) oxidation data indicated that the temperature corresponding to the 50% conversion (T{sub 50%}) of Ni{sub 6}MnO{sub 8} calcined at 350 C or 400 C was lower than that of all other Ni{sub 6}MnO{sub 8} specimens. However, the intrinsic conversion of Ni{sub 6}MnO{sub 8} calcined at 350 C, which is defined as conversion per specific surface area, was half of that of all other Ni{sub 6}MnO{sub 8} specimens. The degree of crystallinity and catalytic performance of the Ni{sub 6}MnO{sub 8} calcined at 400 C were high. - Graphical abstract: The conversion of CH{sub 4} into CO{sub 2} and H{sub 2}O on Ni{sub 6}MnO{sub 8}, which was heated at 600 C in air after the calcination of the precursor at 350 C, 400 C, 450 C, or 500 C in flowing argon, was measured. Since the specific surface area was strongly affected by the calcination temperature of the precursor, intrinsic conversion (IC) was defined as conversion per the specific surface area. For comparison, the IC value on Ni{sub 6}MnO{sub 8} synthesized by the direct calcination of the precursor at 600 C in air is plotted. - Highlights: The oxalate precursor was calcined at 350500 C in flowing argon. Murdochite-type Ni{sub 6}MnO{sub 8} was obtained by heating the calcined sample in air. The specific surface area of Ni{sub 6}MnO{sub 8} varied with the calcination temperature. The degree of crystallinity and catalysis of Ni{sub 6}MnO{sub 8} calcined at 400 C were high.

  11. Shift conversion and methanation in coal gasification: bench-scale evaluation of a sulfur-resistant catalyst. Final report. [Iridium-promoted nickel catalysts supported or aluminium oxide

    SciTech Connect (OSTI)

    Wood, B. J.; McCarty, J. G.; Sheridan, D.; Ablow, C. M.; Wise, H.

    1980-10-24

    The results of this study demonstrate that the Ir-promoted Ni/Al/sub 2/O/sub 3/ catalyst possesses several valuable and superior characteristics when used for catalytic methanation under typical industrial conditions. These properties include: higher activity by a factor of > 2 than that of the unpromoted Ni/Al/sub 2/O/sub 3/ catalyst; enhanced resistance to deactivation by hydrogen sulfide during exposure to contaminated feedstock, as manifested by the prolonged high methanation activity and extended service lifetime; and high resistance to carbon fouling.

  12. Methane Credit | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    Methane Credit Jump to: navigation, search Name: Methane Credit Place: Charlotte, North Carolina Zip: 28273 Product: Specialises in utilising methane produced on municipal landfill...

  13. Assessing methane oxidation under landfill covers and its contribution to the above atmospheric CO{sub 2} levels: The added value of the isotope ({delta}{sup 13}C and {delta}{sup 18}O CO{sub 2}; {delta}{sup 13}C and {delta}D CH{sub 4}) approach

    SciTech Connect (OSTI)

    Widory, D.; Proust, E.; Bellenfant, G.; Bour, O.

    2012-09-15

    Highlights: Black-Right-Pointing-Pointer Comparison of the isotope and mass balance approaches to evaluate the level of methane oxidation within a landfill. Black-Right-Pointing-Pointer The level of methane oxidation is not homogenous under the landfill cover and is strongly correlated to the methane flux. Black-Right-Pointing-Pointer Isotope tracking of the contribution of the methane oxidation to the CO{sub 2} concentrations in the ambient air. - Abstract: We are presenting here a multi-isotope approach ({delta}{sup 13}C and {delta}{sup 18}O of CO{sub 2}; {delta}{sup 13}C and {delta}D of CH{sub 4}) to assess (i) the level(s) of methane oxidation during waste biodegradation and its migration through a landfill cover in Sonzay (France), and (ii) its contribution to the atmospheric CO{sub 2} levels above the surface. The isotope approach is compared to the more conventional mass balance approach. Results from the two techniques are comparable and show that the CH{sub 4} oxidation under the landfill cover is heterogenous, with low oxidation percentages in samples showing high biogas fluxes, which was expected in clay covers presenting fissures, through which CH{sub 4} is rapidly transported. At shallow depth, more immobile biogas pockets show a higher level of CH{sub 4} oxidation by the methanotrophic bacteria. {delta}{sup 13}C of CO{sub 2} samples taken at different heights (from below the cover up to 8 m above the ground level) were also used to identify and assess the relative contributions of its main sources both under the landfill cover and in the surrounding atmosphere.

  14. New manganese catalyst for light alkane oxidation

    DOE Patents [OSTI]

    Durante, Vincent A.; Lyons, James E.; Walker, Darrell W.; Marcus, Bonita K.

    1994-01-01

    Aluminophosphates containing manganese in the structural framework are employed for the oxidation of alkanes, for example the vapor phase oxidation of methane to methanol.

  15. ARM - Methane Gas

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Methane Gas Outreach Home Room News Publications Traditional Knowledge Kiosks Barrow, Alaska Tropical Western Pacific Site Tours Contacts Students Study Hall About ARM Global Warming FAQ Just for Fun Meet our Friends Cool Sites Teachers Teachers' Toolbox Lesson Plans Methane Gas Methane gas is another naturally occurring greenhouse gas. It is produced as a result of microbial activity in the absence of oxygen. Pre-industrial concentrations of methane were about 700 ppb and in 1994 they were up

  16. Methane Hydrate Program

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    FY 2011 Methane Hydrate Program Report to Congress July 2012 United States Department of Energy Washington, DC 20585 Department of Energy | July 2012 FY 2011 Methane Hydrate Program Report to Congress | Page ii Message from the Secretary Section 968 of the Energy Policy Act of 2005 requires the Department of Energy to submit to Congress an annual report on the results of methane hydrate research. I am pleased to submit the enclosed report entitled U.S. Department of Energy FY 2011 Methane

  17. Heat pipe methanator

    DOE Patents [OSTI]

    Ranken, William A.; Kemme, Joseph E.

    1976-07-27

    A heat pipe methanator for converting coal gas to methane. Gravity return heat pipes are employed to remove the heat of reaction from the methanation promoting catalyst, transmitting a portion of this heat to an incoming gas pre-heat section and delivering the remainder to a steam generating heat exchanger.

  18. Methane Hydrate | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Methane Hydrate Methane Hydrate Types of Methane Hydrate Deposits Types of Methane Hydrate Deposits Methane hydrate is a cage-like lattice of ice inside of which are trapped molecules of methane, the chief constituent of natural gas. If methane hydrate is either warmed or depressurized, it will revert back to water and natural gas. When brought to the earth's surface, one cubic meter of gas hydrate releases 164 cubic meters of natural gas. Hydrate deposits may be several hundred meters thick and

  19. Method of determining methane and electrochemical sensor therefor

    DOE Patents [OSTI]

    Zaromb, Solomon; Otagawa, Takaaki; Stetter, Joseph R.

    1986-01-01

    A method and instrument including an electrochemical cell for the detection and measurement of methane in a gas by the oxidation of methane electrochemically at a working electrode in a nonaqueous electrolyte at a voltage about about 1.4 volts versus R.H.E. (the reversible hydrogen electrode potential in the same electrolyte), and the measurement of the electrical signal resulting from the electrochemical oxidation.

  20. Kyoto Protocol | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    The goal is to lower overall emissions from six greenhouse gases - carbon dioxide, methane, nitrous oxide, sulfur hexafluoride, HFCs, and PFCs - calculated as an average over...

  1. The Greenhouse Gas Protocol Initiative: GHG Emissions from Purchased...

    Open Energy Information (Open El) [EERE & EIA]

    Outputs include: The tool outputs greenhouse gas emissions (carbon dioxide, methane, nitrous oxide, and carbon dioxide equivalent) for each facility as well as total...

  2. The Greenhouse Gas Protocol Initiative: GHG Emissions from Transport...

    Open Energy Information (Open El) [EERE & EIA]

    Outputs include: The tool outputs greenhouse gas emissions (including carbon dioxide, methane, nitrous oxide, carbon dioxide equivalent, and biogenic carbon dioxide) for each...

  3. Research Highlight

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    that contributed to the Intergovernmental Panel on Climate Change Fourth Assessment Report ... in which methane and nitrous oxide were increased from zero to their 1860 concentration. ...

  4. Word Pro - S12

    Gasoline and Diesel Fuel Update

    Note 1. Emissions of Carbon Dioxide and Other Green- house Gases. Greenhouse gases are those gases-such as water vapor, carbon dioxide (CO 2 ), methane, nitrous oxide, ...

  5. Deep oxidation of methane on particles derived from YSZ-supported Pd-Pt-(O) coatings synthesized by pulsed filtered cathodic arc

    SciTech Connect (OSTI)

    Horwat, D.; Endrino, J.L.; Boreave, A.; Karoum,R.; Pierson, J.F.; Weber, S.; Anders, A.; Vernoux, Ph.

    2008-12-12

    Methane conversion tests were performed on Pd, PdOy, Pd0.6Pt0.4Oy and Pd0.4Pt0.6Oy thin films deposited on yttria stabilized zirconia (YSZ) substrates. Pt containing films exhibited poor activity and high reducibility. As-deposited Pd and PdOy films showed good activity and transformed, during the cycling process, to particles dispersed on the YSZ substrates. The higher reaction rate of initially PdOy films was explained by a better dispersion of the catalyst. A drop of the reaction rate was observed when the temperature exceeded 735oC and 725oC for initially Pd and PdOy, respectively, which can be associated with the high-temperature reduction of PdO into Pd.

  6. Methane Hydrate Field Program

    SciTech Connect (OSTI)

    2013-12-31

    This final report document summarizes the activities undertaken and the output from three primary deliverables generated during this project. This fifteen month effort comprised numerous key steps including the creation of an international methane hydrate science team, determining and reporting the current state of marine methane hydrate research, convening an international workshop to collect the ideas needed to write a comprehensive Marine Methane Hydrate Field Research Plan and the development and publication of that plan. The following documents represent the primary deliverables of this project and are discussed in summary level detail in this final report. • Historical Methane Hydrate Project Review Report • Methane Hydrate Workshop Report • Topical Report: Marine Methane Hydrate Field Research Plan • Final Scientific/Technical Report

  7. Methane Hydrate Program

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Fiscal Year 2012 Methane Hydrate Program Report to Congress August 2013 United States Department of Energy Washington, DC 20585 Department of Energy | August 2013 Fiscal Year 2012 Methane Hydrate Program Report to Congress | Page ii Message from the Secretary Section 968 of the Energy Policy Act of 2005 requires the Department of Energy to submit to Congress an annual report on the actions taken to carry out methane hydrate research. I am pleased to submit the enclosed report, entitled U.S.

  8. Methane Hydrate Field Studies

    Office of Energy Efficiency and Renewable Energy (EERE)

    Since 2001, DOE has conducted field trials of exploration and production technology in the Alaska North Slope. Although Alaska methane hydrate resources are smaller than marine deposits and...

  9. Oxide

    SciTech Connect (OSTI)

    2014-07-15

    Oxide is a modular framework for feature extraction and analysis of executable files. Oxide is useful in a variety of reverse engineering and categorization tasks relating to executable content.

  10. The future of methane

    SciTech Connect (OSTI)

    Howell, D.G.

    1995-12-31

    Natural gas, mainly methane, produces lower CO{sub 2}, CO, NO{sub x}, SO{sub 2} and particulate emissions than either oil or coal; thus further substitutions of methane for these fuels could help mitigate air pollution. Methane is, however, a potent greenhouse gas and the domestication of ruminants, cultivation of rice, mining of coal, drilling for oil, and transportation of natural gas have all contributed to a doubling of the amount of atmospheric methane since 1800. Today nearly 300,000 wells yearly produce ca. 21 trillion cubic feet of methane. Known reserves suggest about a 10 year supply at the above rates of recovery; and the potential for undiscovered resources is obscured by uncertainty involving price, new technologies, and environmental restrictions steming from the need to drill an enormous number of wells, many in ecologically sensitive areas. Until all these aspects of methane are better understood, its future role in the world`s energy mix will remain uncertain. The atomic simplicity of methane, composed of one carbon and four hydrogen atoms, may mask the complexity and importance of this, the most basic of organic molecules. Within the Earth, methane is produced through thermochemical alteration of organic materials, and by biochemical reactions mediated by metabolic processes of archaebacteria; some methane may even be primordial, a residue of planetary accretion. Methane also occurs in smaller volumes in landfills, rice paddies, termite complexes, ruminants, and even many humans. As an energy source, its full energy potential is controversial. Methane is touted by some as a viable bridge to future energy systems, fueled by the sun and uranium and carried by electricity and hydrogen.

  11. Fact #825: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Gases Plus Nitrogen Oxide Emission Standards, Model Years 2017-2025 Fact 825: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus Nitrogen Oxide Emission Standards, Model Years ...

  12. Methanation assembly using multiple reactors

    DOE Patents [OSTI]

    Jahnke, Fred C.; Parab, Sanjay C.

    2007-07-24

    A methanation assembly for use with a water supply and a gas supply containing gas to be methanated in which a reactor assembly has a plurality of methanation reactors each for methanating gas input to the assembly and a gas delivery and cooling assembly adapted to deliver gas from the gas supply to each of said methanation reactors and to combine water from the water supply with the output of each methanation reactor being conveyed to a next methanation reactor and carry the mixture to such next methanation reactor.

  13. Plasma catalytic reforming of methane

    SciTech Connect (OSTI)

    Bromberg, L.; Cohn, D.R.; Rabinovich, A.; Alexeev, N.

    1998-08-01

    Thermal plasma technology can be efficiently used in the production of hydrogen and hydrogen-rich gases from methane and a variety of fuels. This paper describes progress in plasma reforming experiments and calculations of high temperature conversion of methane using heterogeneous processes. The thermal plasma is a highly energetic state of matter that is characterized by extremely high temperatures (several thousand degrees Celsius) and high degree of dissociation and substantial degree of ionization. The high temperatures accelerate the reactions involved in the reforming process. Hydrogen-rich gas (50% H{sub 2}, 17% CO and 33% N{sub 2}, for partial oxidation/water shifting) can be efficiently made in compact plasma reformers. Experiments have been carried out in a small device (2--3 kW) and without the use of efficient heat regeneration. For partial oxidation/water shifting, it was determined that the specific energy consumption in the plasma reforming processes is 16 MJ/kg H{sub 2} with high conversion efficiencies. Larger plasmatrons, better reactor thermal insulation, efficient heat regeneration and improved plasma catalysis could also play a major role in specific energy consumption reduction and increasing the methane conversion. A system has been demonstrated for hydrogen production with low CO content ({approximately} 1.5%) with power densities of {approximately} 30 kW (H{sub 2} HHV)/liter of reactor, or {approximately} 10 m{sup 3}/hr H{sub 2} per liter of reactor. Power density should further increase with increased power and improved design.

  14. Methane Hydrate Advisory Committee Meeting Minutes | Department...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Methane Hydrate Advisory Committee Meeting Minutes Methane Hydrate Advisory Committee Meeting Minutes Methane Hydrate Advisory Committee Meeting Minutes May 15, 2014 Washington, DC...

  15. Oklahoma Coalbed Methane Production (Billion Cubic Feet)

    Annual Energy Outlook

    Production (Billion Cubic Feet) Oklahoma Coalbed Methane Production (Billion Cubic Feet) ... Referring Pages: Coalbed Methane Estimated Production Oklahoma Coalbed Methane Proved ...

  16. Science on the Hill: Methane cloud hunting

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Methane cloud hunting Science on the Hill: Methane cloud hunting Los Alamos researchers go ... Science on the Hill: Methane cloud hunting When our team from Los Alamos National ...

  17. Methane Hydrate Program Reports | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Program Reports Methane Hydrate Program Reports PDF icon Secretary of Energy Advisory Board Task Force Report on Methane Hydrate PDF icon FY14 Methane Hydrate Report to Congress ...

  18. ARM - Measurement - Methane concentration

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    concentration ARM Data Discovery Browse Data Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Measurement : Methane concentration The amount of methane, a greenhouse gas, per unit of volume. Categories Atmospheric Carbon Instruments The above measurement is considered scientifically relevant for the following instruments. Refer to the datastream (netcdf) file headers of each instrument for a list of all available measurements, including those

  19. ARM - Measurement - Methane flux

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    flux ARM Data Discovery Browse Data Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Measurement : Methane flux Vertical flux of methane near the surface due to turbulent transport. Categories Surface Properties, Atmospheric Carbon Instruments The above measurement is considered scientifically relevant for the following instruments. Refer to the datastream (netcdf) file headers of each instrument for a list of all available measurements, including

  20. Completed Methane Hydrate Projects

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Completed Methane Hydrate Projects Active Projects | Completed Projects Completed Methane Hydrate Projects Project Number Project Name Primary Performer DE-FE0002911 Natural Gas Hydrates in Permafrost and Marine Settings: Resources, Properties, and Environmental Issues U.S. Geological Survey at Woods Hole DE-FE0013565 Hydrate Evolution in Response to Ongoing Environmental Shifts University of Oregon DE-FE0013889 THCM Coupled Model for Hydrate-bearing Sediments: Data Analysis and Design of New

  1. Fact #825: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus Nitrogen

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Oxide Emission Standards, Model Years 2017-2025 | Department of Energy 5: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus Nitrogen Oxide Emission Standards, Model Years 2017-2025 Fact #825: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus Nitrogen Oxide Emission Standards, Model Years 2017-2025 The Environmental Protection Agency finalized Tier 3 emission standards in a rule issued in March 2014. One effect of the rule is a decrease in the combined amount of non-methane organic gases

  2. Coalbed Methane | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Coalbed Methane Coalbed Methane Coalbed methane is natural gas found in coal deposits. It was once considered a nuisance and mine safety hazard, but today has become a valuable part of the U.S. energy portfolio. A major reason for this is resource characterization and the establishment of efficient recovery methods pioneered by Office of Fossil Energy R&D. Fossil Energy Research Benefits - Coalbed Methane (920.32 KB) More Documents & Publications Before the Senate Energy and Natural

  3. Direct Aromaization of Methane

    SciTech Connect (OSTI)

    George Marcelin

    1997-01-15

    The thermal decomposition of methane offers significant potential as a means of producing higher unsaturated and aromatic hydrocarbons when the extent of reaction is limited. Work in the literature previous to this project had shown that cooling the product and reacting gases as the reaction proceeds would significantly reduce or eliminate the formation of solid carbon or heavier (Clo+) materials. This project studied the effect and optimization of the quenching process as a means of increasing the amount of value added products during the pyrolysis of methane. A reactor was designed to rapidly quench the free-radical combustion reaction so as to maximize the yield of aromatics. The use of free-radical generators and catalysts were studied as a means of lowering the reaction temperature. A lower reaction temperature would have the benefits of more rapid quenching as well as a more feasible commercial process due to savings realized in energy and material of construction costs. It was the goal of the project to identify promising routes from methane to higher hydrocarbons based on the pyrolysis of methane.

  4. Dense ceramic membranes for methane conversion

    SciTech Connect (OSTI)

    Balachandran, U.; Mieville, R.L.; Ma, B.; Udovich, C.A.

    1996-05-01

    This report focuses on a mechanism for oxygen transport through mixed- oxide conductors as used in dense ceramic membrane reactors for the partial oxidation of methane to syngas (CO and H{sub 2}). The in-situ separation of O{sub 2} from air by the membrane reactor saves the costly cryogenic separation step that is required in conventional syngas production. The mixed oxide of choice is SrCo{sub 0.5}FeO{sub x}, which exhibits high oxygen permeability and has been shown in previous studies to possess high stability in both oxidizing and reducing conditions; in addition, it can be readily formed into reactor configurations such as tubes. An understanding of the electrical properties and the defect dynamics in this material is essential and will help us to find the optimal operating conditions for the conversion reactor. In this paper, we discuss the conductivities of the SrFeCo{sub 0.5}O{sub x} system that are dependent on temperature and partial pressure of oxygen. Based on the experimental results, a defect model is proposed to explain the electrical properties of this system. The oxygen permeability of SrFeCo{sub 0.5}O{sub x} is estimated by using conductivity data and is compared with that obtained from methane conversion reaction.

  5. Louisiana--North Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Louisiana--North Coalbed Methane ... Coalbed Methane Proved Reserves as of Dec. 31 North Louisiana Coalbed Methane Proved ...

  6. Project identification for methane reduction options

    SciTech Connect (OSTI)

    Kerr, T.

    1996-12-31

    This paper discusses efforts directed at reduction in emission of methane to the atmosphere. Methane is a potent greenhouse gas, which on a 20 year timeframe may present a similar problem to carbon dioxide. In addition, methane causes additional problems in the form of smog and its longer atmospheric lifetime. The author discusses strategies for reducing methane emission from several major sources. This includes landfill methane recovery, coalbed methane recovery, livestock methane reduction - in the form of ruminant methane reduction and manure methane recovery. The author presents examples of projects which have implemented these ideas, the economics of the projects, and additional gains which come from the projects.

  7. Coal Bed Methane Primer

    SciTech Connect (OSTI)

    Dan Arthur; Bruce Langhus; Jon Seekins

    2005-05-25

    During the second half of the 1990's Coal Bed Methane (CBM) production increased dramatically nationwide to represent a significant new source of income and natural gas for many independent and established producers. Matching these soaring production rates during this period was a heightened public awareness of environmental concerns. These concerns left unexplained and under-addressed have created a significant growth in public involvement generating literally thousands of unfocused project comments for various regional NEPA efforts resulting in the delayed development of public and fee lands. The accelerating interest in CBM development coupled to the growth in public involvement has prompted the conceptualization of this project for the development of a CBM Primer. The Primer is designed to serve as a summary document, which introduces and encapsulates information pertinent to the development of Coal Bed Methane (CBM), including focused discussions of coal deposits, methane as a natural formed gas, split mineral estates, development techniques, operational issues, producing methods, applicable regulatory frameworks, land and resource management, mitigation measures, preparation of project plans, data availability, Indian Trust issues and relevant environmental technologies. An important aspect of gaining access to federal, state, tribal, or fee lands involves education of a broad array of stakeholders, including land and mineral owners, regulators, conservationists, tribal governments, special interest groups, and numerous others that could be impacted by the development of coal bed methane. Perhaps the most crucial aspect of successfully developing CBM resources is stakeholder education. Currently, an inconsistent picture of CBM exists. There is a significant lack of understanding on the parts of nearly all stakeholders, including industry, government, special interest groups, and land owners. It is envisioned the Primer would being used by a variety of

  8. Fluxes of methane between landfills and the atmosphere: Natural and engineered controls

    SciTech Connect (OSTI)

    Bogner, J.; Meadows, M.; Czepiel, P.

    1997-08-01

    Field measurement of landfill methane emissions indicates natural variability spanning more than 2 seven orders of magnitude, from approximately 0.0004 to more than 4000 g m{sub -2} day{sup -1}. This wide range reflects net emissions resulting from production (methanogenesis), consumption (methanotrophic oxidation), and gaseous transport processes. The determination of an {open_quotes}average{close_quotes} emission rate for a given field site requires sampling designs and statistical techniques which consider spatial and temporal variability. Moreover, particularly at sites with pumped gas recovery systems, it is possible for methanotrophic microorganisms in aerated cover soils to oxidize all of the methane from landfill sources below and, additionally, to oxidize methane diffusing into cover soils from atmospheric sources above. In such cases, a reversed soil gas concentration gradient is observed in shallow cover soils, indicating bidirectional diffusional transport to the depth of optimum methane oxidation. Rates of landfill methane oxidation from field and laboratory incubation studies range up to 166 g m{sup -2} day{sup -1} among the highest for any natural setting, providing an effective natural control on net emissions. Estimates of worldwide landfill methane emissions to the atmosphere have ranged from 9 to 70 Tg yr{sup -1}, differing mainly in assumed methane yields from estimated quantities of landfilled refuse. At highly controlled landfill sites in developed countries, landfill methane is often collected via vertical wells or horizontal collectors. Recovery of landfill methane through engineered systems can provide both environmental and energy benefits by mitigating subsurface migration, reducing surface emissions, and providing an alternative energy resource for industrial boiler use, on-site electrical generation, or upgrading to a substitute natural gas.

  9. Methane/nitrogen separation process

    DOE Patents [OSTI]

    Baker, Richard W.; Lokhandwala, Kaaeid A.; Pinnau, Ingo; Segelke, Scott

    1997-01-01

    A membrane separation process for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. We have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen.

  10. Methane/nitrogen separation process

    DOE Patents [OSTI]

    Baker, R.W.; Lokhandwala, K.A.; Pinnau, I.; Segelke, S.

    1997-09-23

    A membrane separation process is described for treating a gas stream containing methane and nitrogen, for example, natural gas. The separation process works by preferentially permeating methane and rejecting nitrogen. The authors have found that the process is able to meet natural gas pipeline specifications for nitrogen, with acceptably small methane loss, so long as the membrane can exhibit a methane/nitrogen selectivity of about 4, 5 or more. This selectivity can be achieved with some rubbery and super-glassy membranes at low temperatures. The process can also be used for separating ethylene from nitrogen. 11 figs.

  11. Capture and Use of Coal Mine Ventilation Air Methane

    SciTech Connect (OSTI)

    Deborah Kosmack

    2008-10-31

    CONSOL Energy Inc., in conjunction with MEGTEC Systems, Inc., and the U.S. Department of Energy with the U.S. Environmental Protection Agency, designed, built, and operated a commercial-size thermal flow reversal reactor (TFRR) to evaluate its suitability to oxidize coal mine ventilation air methane (VAM). Coal mining, and particularly coal mine ventilation air, is a major source of anthropogenic methane emissions, a greenhouse gas. Ventilation air volumes are large and the concentration of methane in the ventilation air is low; thus making it difficult to use or abate these emissions. This test program was conducted with simulated coal mine VAM in advance of deploying the technology on active coal mine ventilation fans. The demonstration project team installed and operated a 30,000 cfm MEGTEC VOCSIDIZER oxidation system on an inactive coal mine in West Liberty, WV. The performance of the unit was monitored and evaluated during months of unmanned operation at mostly constant conditions. The operating and maintenance history and how it impacts the implementation of the technology on mine fans were investigated. Emission tests showed very low levels of all criteria pollutants at the stack. Parametric studies showed that the equipment can successfully operate at the design specification limits. The results verified the ability of the TFRR to oxidize {ge}95% of the low and variable concentration of methane in the ventilation air. This technology provides new opportunities to reduce greenhouse gas emissions by the reduction of methane emissions from coal mine ventilation air. A large commercial-size installation (180,000 cfm) on a single typical mine ventilation bleeder fan would reduce methane emissions by 11,000 to 22,100 short tons per year (the equivalent of 183,000 to 366,000 metric tonnes carbon dioxide).

  12. Functionally gradient material for membrane reactors to convert methane gas into value-added products

    DOE Patents [OSTI]

    Balachandran, U.; Dusek, J.T.; Kleefisch, M.S.; Kobylinski, T.P.

    1996-11-12

    A functionally gradient material for a membrane reactor for converting methane gas into value-added-products includes an outer tube of perovskite, which contacts air; an inner tube which contacts methane gas, of zirconium oxide, and a bonding layer between the perovskite and zirconium oxide layers. The bonding layer has one or more layers of a mixture of perovskite and zirconium oxide, with the layers transitioning from an excess of perovskite to an excess of zirconium oxide. The transition layers match thermal expansion coefficients and other physical properties between the two different materials. 7 figs.

  13. Functionally gradient material for membrane reactors to convert methane gas into value-added products

    DOE Patents [OSTI]

    Balachandran, Uthamalingam; Dusek, Joseph T.; Kleefisch, Mark S.; Kobylinski, Thadeus P.

    1996-01-01

    A functionally gradient material for a membrane reactor for converting methane gas into value-added-products includes an outer tube of perovskite, which contacts air; an inner tube which contacts methane gas, of zirconium oxide, and a bonding layer between the perovskite and zirconium oxide layers. The bonding layer has one or more layers of a mixture of perovskite and zirconium oxide, with the layers transitioning from an excess of perovskite to an excess of zirconium oxide. The transition layers match thermal expansion coefficients and other physical properties between the two different materials.

  14. ARM - Oxides of Nitrogen

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Oxides of Nitrogen Outreach Home Room News Publications Traditional Knowledge Kiosks Barrow, Alaska Tropical Western Pacific Site Tours Contacts Students Study Hall About ARM Global Warming FAQ Just for Fun Meet our Friends Cool Sites Teachers Teachers' Toolbox Lesson Plans Oxides of Nitrogen Oxides of nitrogen, chlorofluorocarbons (CFCs), and ozone have a lesser effect on the atmosphere than carbon dioxide and methane, but as you will see they are important contributors to the greenhouse

  15. Methane Hydrate Advisory Committee Meeting Minutes | Department...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    2012 Houston, TX PDF icon July 26, 2012 Meeting Minutes More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes Methane Hydrate Advisory Committee Meeting...

  16. Methane Hydrate Advisory Committee Meeting Minutes | Department...

    Office of Environmental Management (EM)

    Washington, DC PDF icon July 16, 2013 Meeting Minutes More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes Methane Hydrate Advisory Committee Meeting...

  17. Methane Hydrate Advisory Committee Meeting Minutes | Department...

    Energy Savers

    DC PDF icon March 27-28, 2014, Meeting Minutes More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes, March 2010 Methane Hydrate Advisory...

  18. Methane Power Inc | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    Power Inc Jump to: navigation, search Logo: Methane Power Inc. Name: Methane Power Inc. Address: 121 Edinburgh South Drive Place: Cary, NC Zip: 27511 Sector: Renewable Energy...

  19. Methane Hydrate Advisory Committee Meeting Minutes | Department...

    Energy.gov (indexed) [DOE]

    June 6th - 7th, 2013 Meeting Minutes More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes, June 6th-7th, 2013 Methane Hydrate Advisory Committee Meeting...

  20. Florida Coalbed Methane Production (Billion Cubic Feet)

    Annual Energy Outlook

    Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane Estimated Production Florida Coalbed Methane Proved Reserves, Reserves Changes, and ...

  1. Methane Hydrate Advisory Committee Charter | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Charter Methane Hydrate Advisory Committee Charter Methane Hydrate Advisory Committee Charter Methane Hydrate Advisory Committee Charter (140.43 KB) More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes, March 2010 Methane Hydrate Advisory Committee Meeting Minutes, January

  2. Catalyst for the methanation of carbon monoxide in sour gas

    DOE Patents [OSTI]

    Kustes, William A. (Louisville, KY); Hausberger, Arthur L. (Louisville, KY)

    1985-01-01

    The invention involves the synergistic effect of the specific catalytic constituents on a specific series of carriers for the methanation of carbon monoxide in the presence of sulfur at relatively high temperatures and at low steam to gas ratios in the range of 0.2:1 or less. This effect was obtained with catalysts comprising the mixed sulfides and oxides of nickel and chromium supported on carriers comprising magnesium aluminate and magnesium silicate. Conversion of carbon monoxide to methane was in the range of from 40 to 80%. Tests of this combination of metal oxides and sulfides on other carriers and tests of other metal oxides and sulfides on the same carrier produced a much lower level of conversion.

  3. Reducing Open Cell Landfill Methane Emissions with a Bioactive Alternative Daily

    SciTech Connect (OSTI)

    Helene Hilger; James Oliver; Jean Bogner; David Jones

    2009-03-31

    Methane and carbon dioxide are formed in landfills as wastes degrade. Molecule-for-molecule, methane is about 20 times more potent than carbon dioxide at trapping heat in the earth's atmosphere, and thus, it is the methane emissions from landfills that are scrutinized. For example, if emissions composed of 60% methane and 40% carbon dioxide were changed to a mix that was 40% methane and 60% carbon dioxide, a 30% reduction in the landfill's global warming potential would result. A 10% methane, 90% carbon dioxide ratio will result in a 75% reduction in global warming potential compared to the baseline. Gas collection from a closed landfill can reduce emissions, and it is sometimes combined with a biocover, an engineered system where methane oxidizing bacteria living in a medium such as compost, convert landfill methane to carbon dioxide and water. Although methane oxidizing bacteria merely convert one greenhouse gas (methane) to another (carbon dioxide), this conversion can offer significant reductions in the overall greenhouse gas contribution, or global warming potential, associated with the landfill. What has not been addressed to date is the fact that methane can also escape from a landfill when the active cell is being filled with waste. Federal regulations require that newly deposited solid waste to be covered daily with a 6 in layer of soil or an alternative daily cover (ADC), such as a canvas tarp. The aim of this study was to assess the feasibility of immobilizing methane oxidizing bacteria into a tarp-like matrix that could be used for alternative daily cover at open landfill cells to prevent methane emissions. A unique method of isolating methanotrophs from landfill cover soil was used to create a liquid culture of mixed methanotrophs. A variety of prospective immobilization techniques were used to affix the bacteria in a tarp-like matrix. Both gel encapsulation of methanotrophs and gels with liquid cores containing methanotrophs were readily made but

  4. Coal mine methane global review

    SciTech Connect (OSTI)

    2008-07-01

    This is the second edition of the Coal Mine Methane Global Overview, updated in the summer of 2008. This document contains individual, comprehensive profiles that characterize the coal and coal mine methane sectors of 33 countries - 22 methane to market partners and an additional 11 coal-producing nations. The executive summary provides summary tables that include statistics on coal reserves, coal production, methane emissions, and CMM projects activity. An International Coal Mine Methane Projects Database accompanies this overview. It contains more detailed and comprehensive information on over two hundred CMM recovery and utilization projects around the world. Project information in the database is updated regularly. This document will be updated annually. Suggestions for updates and revisions can be submitted to the Administrative Support Group and will be incorporate into the document as appropriate.

  5. Coalbed Methane Production

    U.S. Energy Information Administration (EIA) (indexed site)

    Methane Production (Billion Cubic Feet) Period: Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes 2009 2010 2011 2012 2013 2014 View History U.S. 1,914 1,886 1,763 1,655 1,466 1,404 1989-2014 Alabama 105 102 98 91 62 78 1989-2014 Alaska 0 0 0 0 0 0 2005-2014 Arkansas 3 3 4 2 2 2 2005-2014 California 0 0 0 0 0 0 2005-2014 Colorado 498 533 516 486 444 412 1989-2014 Florida 0 0 0 0 0 0 2005-2014 Kansas 43 41 37 34 30 27

  6. Coalbed Methane Production

    Gasoline and Diesel Fuel Update

    Methane Production (Billion Cubic Feet) Period: Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes 2009 2010 2011 2012 2013 2014 View History U.S. 1,914 1,886 1,763 1,655 1,466 1,404 1989-2014 Alabama 105 102 98 91 62 78 1989-2014 Alaska 0 0 0 0 0 0 2005-2014 Arkansas 3 3 4 2 2 2 2005-2014 California 0 0 0 0 0 0 2005-2014 Colorado 498 533 516 486 444 412 1989-2014 Florida 0 0 0 0 0 0 2005-2014 Kansas 43 41 37 34 30 27

  7. Methane Stakeholder Roundtables | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Methane Stakeholder Roundtables Methane Stakeholder Roundtables April 24, 2014 - 3:00pm Addthis Methane Stakeholder Roundtables Advancing the Interagency Methane Strategy As directed by President Obama in his Climate Action Plan, the Department of Energy (DOE) collaborated with other Federal agencies to develop a Strategy to Reduce Methane Emissions, which was formally announced by the White House last month. To advance this strategy, DOE is now working with other Federal agencies and the White

  8. methane hydrates | netl.doe.gov

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    methane hydrates methane-hydrates.jpg Maintaining a focused vision on what's next is one trait that makes NETL a lab of the future, and methane hydrates are one "cool" part of that vision. Found in Arctic and deep-water marine environments, methane hydrates are an untapped abundant source of natural gas. A hydrate comprises a crystal structure in which frozen water creates a cage that traps molecules of primarily methane (natural gas). NETL researchers are exploring and developing

  9. Science on the Hill: Methane cloud hunting

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Methane cloud hunting Methane cloud hunting Los Alamos researchers go hunting for methane gas over the Four Corners area of northwest New Mexico and find a strange daily pattern. July 12, 2015 methane map Methane, the primary component of natural gas, is also a potent greenhouse gas, trapping energy in the atmosphere. Last year NASA released satellite images showing a hot spot in the area where New Mexico, Colorado, Utah and Arizona meet, prompting scientists to go in search of the sources.

  10. Release of Methane from Bering Sea Sediments During the Last Glacial Period

    SciTech Connect (OSTI)

    Mea Cook; Lloyd Keigwin

    2007-11-30

    Several lines of evidence suggest that during times of elevated methane flux the sulfate-methane transition zone (SMTZ) was positioned near the sediment-water interface. We studied two cores (from 700 m and 1457 m water depth) from the Umnak Plateau region. Anomalously low d13C and high d18O in benthic and planktonic foraminifera in these cores are the consequence of diagenetic overgrowths of authigenic carbonates. There are multiple layers of authigenic-carbonate-rich sediment in these cores, and the stable isotope compositions of the carbonates are consistent with those formed during anaerobic oxidation of methane (AOM). The carbonate-rich layers are associated with biomarkers produced by methane-oxidizing archaea, archaeol and glyceryl dibiphytanyl glyceryl tetraether (GDGT). The d13C of the archaeol and certain GDGTs are isotopically depleted. These carbonate- and AOM-biomarker-rich layers were emplaced in the SMTZ during episodes when there was a high flux of methane or methane-rich fluids upward in the sediment column. The sediment methane in the Umnak Plateau region appears to have been very dynamic during the glacial period, and interacted with the ocean-atmosphere system at millennial time scales. The upper-most carbonate-rich layers are in radiocarbon-dated sediment deposited during interstitials 2 and 3, 28-20 ka, and may be associated with the climate warming during this time.

  11. Assessing the Efficacy of the Aerobic Methanotrophic Biofilter in Methane Hydrate Environments

    SciTech Connect (OSTI)

    Valentine, David

    2012-09-30

    In October 2008 the University of California at Santa Barbara (UCSB) initiated investigations of water column methane oxidation in methane hydrate environments, through a project funded by the National Energy Technology Laboratory (NETL) entitled: assessing the efficacy of the aerobic methanotrophic biofilter in methane hydrate environments. This Final Report describes the scientific advances and discoveries made under this award as well as the importance of these discoveries in the broader context of the research area. Benthic microbial mats inhabit the sea floor in areas where reduced chemicals such as sulfide reach the more oxidizing water that overlies the sediment. We set out to investigate the role that methanotrophs play in such mats at locations where methane reaches the sea floor along with sulfide. Mats were sampled from several seep environments and multiple sets were grown in-situ at a hydrocarbon seep in the Santa Barbara Basin. Mats grown in-situ were returned to the laboratory and used to perform stable isotope probing experiments in which they were treated with 13C-enriched methane. The microbial community was analyzed, demonstrating that three or more microbial groups became enriched in methane?s carbon: methanotrophs that presumably utilize methane directly, methylotrophs that presumably consume methanol excreted by the methanotrophs, and sulfide oxidizers that presumably consume carbon dioxide released by the methanotrophs and methylotrophs. Methanotrophs reached high relative abundance in mats grown on methane, but other bacterial processes include sulfide oxidation appeared to dominate mats, indicating that methanotrophy is not a dominant process in sustaining these benthic mats, but rather a secondary function modulated by methane availability. Methane that escapes the sediment in the deep ocean typically dissolved into the overlying water where it is available to methanotrophic bacteria. We set out to better understand the efficacy of this

  12. Methane Hydrate Advisory Committee Meeting

    Energy.gov (indexed) [DOE]

    Methane Hydrate Advisory Committee Meeting May 15, 2014 11:00am - 12:30pm (EDT) Public Access U.S. Department of Energy Forrestal Building, Room 3G-043 1000 Independence Ave., SW...

  13. May 15, 2014 Methane Hydrates Committee Meeting Agenda | Department...

    Office of Environmental Management (EM)

    May 15, 2014 Methane Hydrates Committee Meeting Agenda May 15, 2014 Methane Hydrates Committee Meeting Agenda May 15, 2014 Methane Hydrates Committee Meeting Agenda PDF icon...

  14. Methane Hydrate Advisory Committee Meeting Minutes, March 2010...

    Energy Savers

    March 2010 Methane Hydrate Advisory Committee Meeting Minutes, March 2010 Methane Hydrate Advisory Committee Meeting Minutes March 2010 Washington, DC PDF icon Methane Hydrate...

  15. Methane Hydrate Advisory Committee Meeting Minutes, January 2010...

    Energy.gov (indexed) [DOE]

    0 Atlanta, GA Methane Hydrate Advisory Committee Meeting Minutes, January 2010 More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes, March 2010 Methane...

  16. Methane Hydrate Advisory Committee Meeting Minutes, June 6th...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Methane Hydrate Advisory Committee Meeting Minutes, June 6th-7th, 2013 Methane Hydrate Advisory Committee Meeting Minutes, June 6th-7th, 2013 Methane Hydrate Advisory Committee...

  17. China United Coalbed Methane Co Ltd | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    Coalbed Methane Co Ltd Jump to: navigation, search Name: China United Coalbed Methane Co Ltd Place: Beijing Municipality, China Zip: 100011 Product: Coal bed methane developer in...

  18. Metro Methane Recovery Facility Biomass Facility | Open Energy...

    Open Energy Information (Open El) [EERE & EIA]

    Methane Recovery Facility Biomass Facility Jump to: navigation, search Name Metro Methane Recovery Facility Biomass Facility Facility Metro Methane Recovery Facility Sector Biomass...

  19. Methane Hydrates and Climate Change | Department of Energy

    Energy Savers

    Hydrates and Climate Change Methane Hydrates and Climate Change Methane hydrates store huge volumes of methane formed by the bacterial decay of organic matter or leaked from ...

  20. Texas (with State Offshore) Coalbed Methane Production (Billion...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Production ... Referring Pages: Coalbed Methane Estimated Production Texas Coalbed Methane Proved ...

  1. New Mexico Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) New Mexico Coalbed Methane Production (Billion Cubic Feet) ... Referring Pages: Coalbed Methane Estimated Production New Mexico Coalbed Methane Proved ...

  2. New Mexico Coalbed Methane Proved Reserves (Billion Cubic Feet...

    Annual Energy Outlook

    Proved Reserves (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves (Billion ... Coalbed Methane Proved Reserves as of Dec. 31 New Mexico Coalbed Methane Proved Reserves, ...

  3. Methane Hydrate Research and Development Act of 2000 | Department...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Research and Development Act of 2000 Methane Hydrate Research and Development Act of 2000 Methane Hydrate Research and Development Act of 2000 PDF icon Methane Hydrate Research and ...

  4. North Dakota Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    North Dakota Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 ... Coalbed Methane Proved Reserves as of Dec. 31 North Dakota Coalbed Methane Proved ...

  5. Catalysts for conversion of methane to higher hydrocarbons

    DOE Patents [OSTI]

    Siriwardane, Ranjani V.

    1993-01-01

    Catalysts for converting methane to higher hydrocarbons such as ethane and ethylene in the presence of oxygen at temperatures in the range of about 700.degree. to 900.degree. C. are described. These catalysts comprise calcium oxide or gadolinium oxide respectively promoted with about 0.025-0.4 mole and about 0.1-0.7 mole sodium pyrophosphate. A preferred reaction temperature in a range of about 800.degree. to 850.degree. C. with a preferred oxygen-to-methane ratio of about 2:1 provides an essentially constant C.sub.2 hydrocarbon yield in the range of about 12 to 19 percent over a period of time greater than about 20 hours.

  6. Methane generation from animal wastes

    SciTech Connect (OSTI)

    Fulton, E.L.

    1980-06-01

    The conversion of manure to biogas via anaerobic digestion is described. The effluent resulting from the conversion retains fertilizer value and is environmentally acceptable. Discussion is presented under the headings: methane formation in the digester; the Tarleton State Poultry Waste to Methane production system; operating experience at Tarleton State; economics of biogas production from poultry waste; construction cost and biogas value; energy uses; feed and waste processing; and advantages of anaerobic digestion. (DMC)

  7. Methane Hydrate Annual Reports | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Annual Reports Methane Hydrate Annual Reports Section 968 of the Energy Policy Act of 2005 requires the Department of Energy to submit to Congress an annual report on the results of Methane Hydrate research. Listed are the Annual Reports per Fiscal Year. FY 14 Methane Hydrate Program Report to Congress (10.92 MB) FY 13 Methane Hydrates Annual Report to Congress (960.13 KB) FY 12 Methane Hydrates Annual Report to Congress (1.09 MB) FY 11 Methane Hydrates Annual Report to Congress (953.09 KB) FY

  8. Methane Hydrate Reservoir Simulator Code Comparison Study

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Annual Reports Methane Hydrate Annual Reports Section 968 of the Energy Policy Act of 2005 requires the Department of Energy to submit to Congress an annual report on the results of Methane Hydrate research. Listed are the Annual Reports per Fiscal Year. FY 14 Methane Hydrate Program Report to Congress (10.92 MB) FY 13 Methane Hydrates Annual Report to Congress (960.13 KB) FY 12 Methane Hydrates Annual Report to Congress (1.09 MB) FY 11 Methane Hydrates Annual Report to Congress (953.09 KB) FY

  9. METHANE HYDRATE ADVISORY COMMITTEE U.S. Department of Energy

    Energy.gov (indexed) [DOE]

    METHANE HYDRATE ADVISORY COMMITTEE U.S. Department of Energy Advisory Committee Charter - - - - ---- ---- ------ 1. Committee's Official Designation. Methane Hydrate Advisory...

  10. File:Methane.pdf | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    Methane.pdf Jump to: navigation, search File File history File usage File:Methane.pdf Size of this preview: 448 600 pixels. Go to page 1 2 3 4 5 Go next page next page ...

  11. Methane Gas Conversion Property Tax Exemption

    Office of Energy Efficiency and Renewable Energy (EERE)

    Under Iowa's methane gas conversion property tax exemption, real and personal property used to decompose waste and convert the waste to gas, collect the methane or other gases, convert the gas to...

  12. Miscellaneous States Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Miscellaneous States Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 ...

  13. Valuing the ozone-related health benefits of methane emission controls

    DOE PAGES-Beta [OSTI]

    Sarofim, Marcus C.; Waldhoff, Stephanie T.; Anenberg, Susan C.

    2015-06-29

    Methane is a greenhouse gas that oxidizes to form ground-level ozone, itself a greenhouse gas and a health-harmful air pollutant. Reducing methane emissions will both slow anthropogenic climate change and reduce ozone-related mortality. We estimate the benefits of reducing methane emissions anywhere in the world for ozone-related premature mortality globally and for eight geographic regions. Our methods are consistent with those used by the US Government to estimate the social cost of carbon (SCC). We find that the global short- and long-term premature mortality benefits due to reduced ozone production from methane mitigation are (2011) $790 and $1775 per tonnemore » methane, respectively. These correspond to approximately 70 and 150 % of the valuation of methane’s global climate impacts using the SCC after extrapolating from carbon dioxide to methane using global warming potential estimates. Results for monetized benefits are sensitive to a number of factors, particularly the choice of elasticity to income growth used when calculating the value of a statistical life. The benefits increase for emission years further in the future. Regionally, most of the global mortality benefits accrue in Asia, but 10 % accrue in the United States. As a result, this methodology can be used to assess the benefits of methane emission reductions anywhere in the world, including those achieved by national and multinational policies.« less

  14. Valuing the ozone-related health benefits of methane emission controls

    SciTech Connect (OSTI)

    Sarofim, Marcus C.; Waldhoff, Stephanie T.; Anenberg, Susan C.

    2015-06-29

    Methane is a greenhouse gas that oxidizes to form ground-level ozone, itself a greenhouse gas and a health-harmful air pollutant. Reducing methane emissions will both slow anthropogenic climate change and reduce ozone-related mortality. We estimate the benefits of reducing methane emissions anywhere in the world for ozone-related premature mortality globally and for eight geographic regions. Our methods are consistent with those used by the US Government to estimate the social cost of carbon (SCC). We find that the global short- and long-term premature mortality benefits due to reduced ozone production from methane mitigation are (2011) $790 and $1775 per tonne methane, respectively. These correspond to approximately 70 and 150 % of the valuation of methane’s global climate impacts using the SCC after extrapolating from carbon dioxide to methane using global warming potential estimates. Results for monetized benefits are sensitive to a number of factors, particularly the choice of elasticity to income growth used when calculating the value of a statistical life. The benefits increase for emission years further in the future. Regionally, most of the global mortality benefits accrue in Asia, but 10 % accrue in the United States. As a result, this methodology can be used to assess the benefits of methane emission reductions anywhere in the world, including those achieved by national and multinational policies.

  15. Methane Hydrate Production Feasibility | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Production Feasibility Methane Hydrate Production Feasibility The red curves are temperature profiles for various water depths; the blue line shows methane hydrate stability relative to temperature and pressure. The area enclosed by the two curves represents the area of methane hydrate stability. The red curves are temperature profiles for various water depths; the blue line shows methane hydrate stability relative to temperature and pressure. The area enclosed by the two curves represents the

  16. Method for the photocatalytic conversion of methane

    DOE Patents [OSTI]

    Noceti, R.P.; Taylor, C.E.; D`Este, J.R.

    1998-02-24

    A method for converting methane to methanol is provided comprising subjecting the methane to visible light in the presence of a catalyst and an electron transfer agent. Another embodiment of the invention provides for a method for reacting methane and water to produce methanol and hydrogen comprising preparing a fluid containing methane, an electron transfer agent and a photolysis catalyst, and subjecting said fluid to visible light for an effective period of time. 3 figs.

  17. Method for the photocatalytic conversion of methane

    DOE Patents [OSTI]

    Noceti, Richard P.; Taylor, Charles E.; D'Este, Joseph R.

    1998-01-01

    A method for converting methane to methanol is provided comprising subjecting the methane to visible light in the presence of a catalyst and an electron transfer agent. Another embodiment of the invention provides for a method for reacting methane and water to produce methanol and hydrogen comprising preparing a fluid containing methane, an electron transfer agent and a photolysis catalyst, and subjecting said fluid to visible light for an effective period of time.

  18. General Equilibrium Model for Economy - Energy - Environment...

    Open Energy Information (Open El) [EERE & EIA]

    and non-energy related emissions of carbon dioxide (CO2), other GHG such as methane (CH4), nitrous oxide (N20) sulfur hexafluoride (SF6), hydrofluorocarbon (HFC), and...

  19. State-level Greenhouse Gas Emission Factors for Electricity Generation, Updated 2002

    Reports and Publications

    2002-01-01

    This report documents the preparation of updated state-level electricity coefficients for carbon dioxide (CO ), methane (CH ), and nitrous oxide (NO), which represent a three-year weighted average for 1998-2000.

  20. Activation of methane by transition metal-substituted aluminophosphate molecular sieves

    DOE Patents [OSTI]

    Iton, Lennox E.; Maroni, Victor A.

    1991-01-01

    Aluminophosphate molecular sieves substituted with cobalt, manganese or iron and having the AlPO.sub.4 -34 or AlPO.sub.4 -5, or related AlPO.sub.4 structure activate methane starting at approximately 350.degree. C. Between 400.degree. and 500.degree. C. and at methane pressures .ltoreq.1 atmosphere the rate of methane conversion increases steadily with typical conversion efficiencies at 500.degree. C. approaching 50% and selectivity to the production of C.sub.2+ hydrocarbons approaching 100%. The activation mechanism is based on reduction of the transition metal(III) form of the molecular sieve to the transition metal(II) form with accompanying oxidative dehydrogenation of the methane. Reoxidation of the - transition metal(II) form to the transition metal(III) form can be done either chemically (e.g., using O.sub.2) or electrochemically.

  1. Methane sources and emissions in Italy

    SciTech Connect (OSTI)

    Guidotti, G.R.; Castagnola, A.M.

    1994-12-31

    Methane emissions in Italy were assessed in the framework of the measures taken to follow out the commitments undertaken at the 1992 U.N. Conference for Environment and Development. Methane emissions of anthropic origin were estimated to be in the range of 1.6 to 2.3 million ton of methane per year. Some of these methane sources (natural gas production, transmission and distribution; rice paddies; managed livestock enteric fermentation and waste; solid waste landfills) are given here particular care as they mainly contribute to the total methane emission budget.

  2. Methane generation from waste materials

    SciTech Connect (OSTI)

    Samani, Zohrab A.; Hanson, Adrian T.; Macias-Corral, Maritza

    2010-03-23

    An organic solid waste digester for producing methane from solid waste, the digester comprising a reactor vessel for holding solid waste, a sprinkler system for distributing water, bacteria, and nutrients over and through the solid waste, and a drainage system for capturing leachate that is then recirculated through the sprinkler system.

  3. Methane production by attached film

    DOE Patents [OSTI]

    Jewell, William J.

    1981-01-01

    A method for purifying wastewater of biodegradable organics by converting the organics to methane and carbon dioxide gases is disclosed, characterized by the use of an anaerobic attached film expanded bed reactor for the reaction process. Dilute organic waste material is initially seeded with a heterogeneous anaerobic bacteria population including a methane-producing bacteria. The seeded organic waste material is introduced into the bottom of the expanded bed reactor which includes a particulate support media coated with a polysaccharide film. A low-velocity upward flow of the organic waste material is established through the bed during which the attached bacterial film reacts with the organic material to produce methane and carbon dioxide gases, purified water, and a small amount of residual effluent material. The residual effluent material is filtered by the film as it flows upwardly through the reactor bed. In a preferred embodiment, partially treated effluent material is recycled from the top of the bed to the bottom of the bed for further treatment. The methane and carbon dioxide gases are then separated from the residual effluent material and purified water.

  4. Strategies to Optimize Microbially-Mediated Mitigation of Greenhouse Gas Emissions from Landfill Cover Soils

    SciTech Connect (OSTI)

    Jeremy Semrau; Sung-Woo Lee; Jeongdae Im; Sukhwan Yoon; Michael Barcelona

    2010-09-30

    The overall objective of this project, 'Strategies to Optimize Microbially-Mediated Mitigation of Greenhouse Gas Emissions from Landfill Cover Soils' was to develop effective, efficient, and economic methodologies by which microbial production of nitrous oxide can be minimized while also maximizing microbial consumption of methane in landfill cover soils. A combination of laboratory and field site experiments found that the addition of nitrogen and phenylacetylene stimulated in situ methane oxidation while minimizing nitrous oxide production. Molecular analyses also indicated that methane-oxidizing bacteria may play a significant role in not only removing methane, but in nitrous oxide production as well, although the contribution of ammonia-oxidizing archaea to nitrous oxide production can not be excluded at this time. Future efforts to control both methane and nitrous oxide emissions from landfills as well as from other environments (e.g., agricultural soils) should consider these issues. Finally, a methanotrophic biofiltration system was designed and modeled for the promotion of methanotrophic activity in local methane 'hotspots' such as landfills. Model results as well as economic analyses of these biofilters indicate that the use of methanotrophic biofilters for controlling methane emissions is technically feasible, and provided either the costs of biofilter construction and operation are reduced or the value of CO{sub 2} credits is increased, can also be economically attractive.

  5. Table 11.4 Nitrous Oxide Emissions, 1980-2009 (Thousand Metric...

    U.S. Energy Information Administration (EIA) (indexed site)

    ... Protection Agency's Inventory of U.S. Greenhouse Gas Emissions and Sinks: 19902008 (April 2010)see http:www.epa.govclimatechangeemissionsusinventoryreport.html.

  6. Turbulent burning rates of methane and methane-hydrogen mixtures

    SciTech Connect (OSTI)

    Fairweather, M. [School of Process, Environmental and Materials Engineering, University of Leeds, Leeds LS2 9JT (United Kingdom); Ormsby, M.P.; Sheppard, C.G.W. [School of Mechanical Engineering, University of Leeds, Leeds LS2 9JT (United Kingdom); Woolley, R. [Department of Mechanical Engineering, University of Sheffield, Sheffield S1 3JD (United Kingdom)

    2009-04-15

    Methane and methane-hydrogen (10%, 20% and 50% hydrogen by volume) mixtures have been ignited in a fan stirred bomb in turbulence and filmed using high speed cine schlieren imaging. Measurements were performed at 0.1 MPa (absolute) and 360 K. A turbulent burning velocity was determined for a range of turbulence velocities and equivalence ratios. Experimental laminar burning velocities and Markstein numbers were also derived. For all fuels the turbulent burning velocity increased with turbulence velocity. The addition of hydrogen generally resulted in increased turbulent and laminar burning velocity and decreased Markstein number. Those flames that were less sensitive to stretch (lower Markstein number) burned faster under turbulent conditions, especially as the turbulence levels were increased, compared to stretch-sensitive (high Markstein number) flames. (author)

  7. The Methane to Markets Coal Mine Methane Subcommittee meeting

    SciTech Connect (OSTI)

    2008-07-01

    The presentations (overheads/viewgraphs) include: a report from the Administrative Support Group; strategy updates from Australia, India, Italy, Mexico, Nigeria, Poland and the USA; coal mine methane update and IEA's strategy and activities; the power of VAM - technology application update; the emissions trading market; the voluntary emissions reduction market - creating profitable CMM projects in the USA; an Italian perspective towards a zero emission strategies; and the wrap-up and summary.

  8. Stable, Ultra-Low Residence Time Partial Oxidation

    DOE Patents [OSTI]

    Schmidt, Lanny D.; Hickman, Daniel A.

    1997-07-15

    A process for the catalytic partial oxidation of methane in gas phase at very short residence time (800,000 to 12,000,000 hr.sup.-1) by contacting a gas stream containing methane and oxygen with a metal supported catalyst, such as platinum deposited on a ceramic monolith.

  9. Systems level insights into alternate methane cycling modes in a freshwater lake via community transcriptomics, metabolomics and nano-SIMS analysis

    SciTech Connect (OSTI)

    Lidstrom, Mary E.; Chistoserdova, Ludmila; Kalyuzhnaya, Marina G.; Orphan, Victoria J.; Beck, David A.

    2014-08-07

    The research conducted as part of this project contributes significantly to the understanding of the microbes and their activities involved in methane metabolism in freshwater lake sediments and in the environment in a more global sense. Significant new insights have been gained into the identity of the species that are most active in methane oxidation. New concepts have been developed based on the new data on how these organisms metabolize methane, impacting not only environmental microbiology but also biotechnology, including biotechnology of next generation biofuels. Novel approaches have been developed for studying functional microbial communities, via holistic approaches, such as metagenomics, metatrancriptomics and metabolite analysis. As a result, a novel outlook has been obtained at how such communities operate in nature. Understanding methane-oxidizing communities in lakes and other environments is of significant benefit to the public, in terms of methane emission mitigation and in terms of potential biotechnological applications.

  10. Clay enhancement of methane, low molecular weight hydrocarbon and halocarbon conversion by methanotrophic bacteria

    DOE Patents [OSTI]

    Apel, William A.; Dugan, Patrick R.

    1995-01-01

    An apparatus and method for increasing the rate of oxidation of toxic vapors by methanotrophic bacteria. The toxic vapors of interest are methane and trichloroethylene. The apparatus includes a gas phase bioreactor within a closed loop pumping system or a single pass system. The methanotrophic bacteria include Methylomonas methanica, Methylosinus trichosporium, and uncharacterized environmental enrichments.

  11. Clay enhancement of methane, low molecular weight hydrocarbon and halocarbon conversion by methanotrophic bacteria

    DOE Patents [OSTI]

    Apel, William A.; Dugan, Patrick R.

    1995-04-04

    An apparatus and method for increasing the rate of oxidation of toxic vapors by methanotrophic bacteria. The toxic vapors of interest are methane and trichloroethylene. The apparatus includes a gas phase bioreactor within a closed loop pumping system or a single pass system. The methanotrophic bacteria include Methylomonas methanica, Methylosinus trichosporium, and uncharacterized environmental enrichments.

  12. Coalbed Methane (CBM) is natural

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Coalbed Methane (CBM) is natural gas found in coal deposits. It was once considered a nuisance and mine safety hazard, but today has become a valuable part of the U.S. energy portfolio. A major reason for this is resource characterization and the establishment of efficient recovery methods pioneered by Office of Fossil Energy (FE) research and development. CBM proved reserves and production have grown nearly every year since 1989. Today it accounts for 9 percent of total domestic natural gas

  13. Methane Hydrate Program Annual Report to Congress

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    FY 2010 Methane Hydrate Program Annual Report to Congress September 2011 U.S. Department of ENERGY United States Department of Energy Washington, DC 20585 Department of Energy | September 2011 FY 2010 Methane Hydrate Program Annual Report to Congress | Page 2 Message from the Secretary Section 968 of the Energy Policy Act of 2005 requires the Department of Energy to submit to Congress an annual report on the results of methane hydrate research. I am pleased to submit the enclosed report

  14. Modeling Methane Adsorption in Interpenetrating Porous Polymer...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Modeling Methane Adsorption in Interpenetrating Porous Polymer Networks Previous Next List Richard L. Martin, Mahdi Niknam Shahrak, Joseph A. Swisher, Cory M. Simon, Julian P....

  15. EIA - Greenhouse Gas Emissions - Methane Emissions

    Gasoline and Diesel Fuel Update

    3. Methane Emissions 3.1. Total emissions The major sources of U.S. methane emissions are energy production, distribution, and use; agriculture; and waste management (Figure 17). U.S. methane emissions in 2009 totaled 731 MMTCO2e, 0.9 percent higher than the 2008 total of 724 MMTCO2e (Table 17). Methane emissions declined steadily from 1990 to 2001, as emissions from coal mining and landfills fell, then rose from 2002 to 2009 as a result of moderate increases in emissions related to energy,

  16. Capping methane leaks a win-win

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Capping methane leaks a win-win Capping methane leaks a win-win As special correspondent Kathleen McCleery explains, that's why both environmentalists and the energy industry are trying to find ways to capture leaks from oil and gas facilities. November 13, 2015 Capping methane leaks a win-win Methane, the primary component of natural gas, is also a potent greenhouse gas, trapping energy in the atmosphere. Last year NASA released satellite images showing a hot spot in the area where New Mexico,

  17. New Methane Hydrate Research: Investing in Our Energy Future...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    New Methane Hydrate Research: Investing in Our Energy Future New Methane Hydrate Research: Investing in Our Energy Future August 31, 2012 - 1:37pm Addthis Methane hydrates are 3D ...

  18. Mechanism of Methane Chemical Looping Combustion with Hematite Promoted with CeO2

    SciTech Connect (OSTI)

    Miller, Duane D.; Siriwardane, Ranjani

    2013-08-01

    Chemical looping combustion (CLC) is a promising technology for fossil fuel combustion that produces sequestration-ready CO{sub 2} stream, reducing the energy penalty of CO{sub 2} separation from flue gases. An effective oxygen carrier for CLC will readily react with the fuel gas and will be reoxidized upon contact with oxygen. This study investigated the development of a CeO{sub 2}-promoted Fe{sub 2}O{sub 3}?hematite oxygen carrier suitable for the methane CLC process. Composition of CeO{sub 2} is between 5 and 25 wt % and is lower than what is generally used for supports in Fe{sub 2}O{sub 3} carrier preparations. The incorporation of CeO{sub 2} to the natural ore hematite strongly modifies the reduction behavior in comparison to that of CeO{sub 2} and hematite alone. Temperature-programmed reaction studies revealed that the addition of even 5 wt % CeO{sub 2} enhances the reaction capacity of the Fe{sub 2}O{sub 3} oxygen carrier by promoting the decomposition and partial oxidation of methane. Fixed-bed reactor data showed that the 5 wt % cerium oxides with 95 wt % iron oxide produce 2 times as much carbon dioxide in comparison to the sum of carbon dioxide produced when the oxides were tested separately. This effect is likely due to the reaction of CeO{sub 2} with methane forming intermediates, which are reactive for extracting oxygen from Fe{sub 2}O{sub 3} at a considerably faster rate than the rate of the direct reaction of Fe{sub 2}O{sub 3} with methane. These studies reveal that 5 wt % CeO{sub 2}/Fe{sub 2}O{sub 3} gives stable conversions over 15 reduction/oxidation cycles. Lab-scale reactor studies (pulsed mode) suggest the methane reacts initially with CeO{sub 2} lattice oxygen to form partial oxidation products (CO + H{sub 2}), which continue to react with oxygen from neighboring Fe{sub 2}O{sub 3}, leading to its complete oxidation to form CO{sub 2}. The reduced cerium oxide promotes the methane decomposition reaction to form C + H{sub 2}, which continue to

  19. Methane Hydrate Advisory Committee Meeting Minutes, October 2011...

    Office of Environmental Management (EM)

    October 2011 Methane Hydrate Advisory Committee Meeting Minutes, October 2011 Methane Hydrate Advisory Committee Meeting Minutes October 2011 Washington, DC PDF icon Advisory...

  20. Landfill Methane Project Development Handbook | Open Energy Informatio...

    Open Energy Information (Open El) [EERE & EIA]

    Methane Project Development Handbook Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Landfill Methane Project Development Handbook AgencyCompany Organization: United...

  1. US EPA Landfill Methane Outreach Program | Open Energy Information

    Open Energy Information (Open El) [EERE & EIA]

    EPA Landfill Methane Outreach Program Jump to: navigation, search Name US EPA Landfill Methane Outreach Program AgencyCompany Organization United States Environmental Protection...

  2. Data from Innovative Methane Hydrate Test on Alaska's North Slope...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Data from Innovative Methane Hydrate Test on Alaska's North Slope Now Available on NETL Website Data from Innovative Methane Hydrate Test on Alaska's North Slope Now Available on ...

  3. Natural Gas Infrastructure R&D and Methane Emissions Mitigation...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Workshops Natural Gas Infrastructure R&D and Methane Emissions Mitigation Workshop Natural Gas Infrastructure R&D and Methane Emissions Mitigation Workshop The Advanced ...

  4. Florida Coalbed Methane Proved Reserves (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Florida Coalbed Methane Proved Reserves, Reserves Changes, and ...

  5. ,"Florida Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Florida Coalbed Methane Proved Reserves (Billion ... 7:23:10 AM" "Back to Contents","Data 1: Florida Coalbed Methane Proved Reserves (Billion ...

  6. Louisiana--State Offshore Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Louisiana--State Offshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade ...312016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 LA, State Offshore

  7. ,"Lower 48 Federal Offshore Coalbed Methane Proved Reserves ...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Lower 48 Federal Offshore Coalbed Methane Proved Reserves (Billion ... to Contents","Data 1: Lower 48 Federal Offshore Coalbed Methane Proved Reserves (Billion ...

  8. Lower 48 Federal Offshore Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Lower 48 Federal Offshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade ...2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Federal Offshore U.S.

  9. ,"Texas (with State Offshore) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Texas (with State Offshore) Coalbed Methane Proved Reserves ... to Contents","Data 1: Texas (with State Offshore) Coalbed Methane Proved Reserves ...

  10. ,"Alaska (with Total Offshore) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Alaska (with Total Offshore) Coalbed Methane Proved Reserves ... to Contents","Data 1: Alaska (with Total Offshore) Coalbed Methane Proved Reserves ...

  11. ,"Louisiana--State Offshore Coalbed Methane Proved Reserves ...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Louisiana--State Offshore Coalbed Methane Proved Reserves (Billion ... to Contents","Data 1: Louisiana--State Offshore Coalbed Methane Proved Reserves (Billion ...

  12. ,"Federal Offshore--Texas Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Federal Offshore--Texas Coalbed Methane Proved Reserves ... AM" "Back to Contents","Data 1: Federal Offshore--Texas Coalbed Methane Proved Reserves ...

  13. ,"Louisiana (with State Offshore) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    for" ,"Data 1","Louisiana (with State Offshore) Coalbed Methane Proved Reserves ... Contents","Data 1: Louisiana (with State Offshore) Coalbed Methane Proved Reserves ...

  14. ,"Texas--State Offshore Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Texas--State Offshore Coalbed Methane Proved Reserves (Billion ... "Back to Contents","Data 1: Texas--State Offshore Coalbed Methane Proved Reserves (Billion ...

  15. Estimating global and North American methane emissions with high...

    Office of Scientific and Technical Information (OSTI)

    methane emissions with high spatial resolution using GOSAT satellite data Citation Details In-Document Search Title: Estimating global and North American methane emissions ...

  16. New York Coalbed Methane Proved Reserves (Billion Cubic Feet...

    Annual Energy Outlook

    Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 New York Coalbed Methane Proved Reserves, Reserves Changes, ...

  17. Louisiana--South Onshore Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    South Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  18. Alaska (with Total Offshore) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  19. U.S. Coalbed Methane Proved Reserves Extensions (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Extensions (Billion ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  20. U.S. Coalbed Methane Proved Reserves New Reservoir Discoveries...

    U.S. Energy Information Administration (EIA) (indexed site)

    New Reservoir Discoveries in Old Fields (Billion Cubic Feet) U.S. Coalbed Methane Proved ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  1. ,"Alabama Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at ... Data for" ,"Data 1","Alabama Coalbed Methane Proved Reserves (Billion Cubic ...

  2. U.S. Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) U.S. Coalbed Methane Production (Billion Cubic Feet) ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  3. Texas--RRC District 5 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    5 Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  4. Texas--RRC District 1 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    1 Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  5. Towards a Computational Model of a Methane Producing Archaeum...

    Office of Scientific and Technical Information (OSTI)

    Towards a Computational Model of a Methane Producing Archaeum Citation Details In-Document Search Title: Towards a Computational Model of a Methane Producing Archaeum Authors: ...

  6. Texas--RRC District 9 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    9 Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  7. U.S. Coalbed Methane Proved Reserves Revision Increases (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Increases (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Revision Increases ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  8. ,"Wyoming Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at ... Data for" ,"Data 1","Wyoming Coalbed Methane Proved Reserves (Billion Cubic ...

  9. Michigan Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Michigan Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  10. U.S. Coalbed Methane Proved Reserves Revision Decreases (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Decreases (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Revision Decreases ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  11. Texas--RRC District 8 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  12. U.S. Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  13. U.S. Coalbed Methane Proved Reserves Adjustments (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Adjustments (Billion ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  14. Mississippi (with State off) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Mississippi (with State off) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  15. ,"Utah Coalbed Methane Proved Reserves (Billion Cubic Feet)"

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at ... Data for" ,"Data 1","Utah Coalbed Methane Proved Reserves (Billion Cubic ...

  16. U.S. Coalbed Methane Proved Reserves Acquisitions (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Acquisitions ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  17. Process for separating nitrogen from methane using microchannel...

    Office of Scientific and Technical Information (OSTI)

    Process for separating nitrogen from methane using microchannel process technology Citation Details In-Document Search Title: Process for separating nitrogen from methane using ...

  18. ,"Colorado Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at ... Data for" ,"Data 1","Colorado Coalbed Methane Proved Reserves (Billion Cubic ...

  19. Texas--RRC District 6 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    6 Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  20. ,"North Dakota Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","North Dakota Coalbed Methane Proved Reserves ... 9:22:44 AM" "Back to Contents","Data 1: North Dakota Coalbed Methane Proved Reserves ...

  1. ,"Louisiana--North Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","Louisiana--North Coalbed Methane Proved Reserves (Billion ... "Back to Contents","Data 1: Louisiana--North Coalbed Methane Proved Reserves (Billion ...

  2. Methane and Methanotrophic Bacteria as a Biotechnological Platform...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Methane and Methanotrophic Bacteria as a Biotechnological Platform Methane and Methanotrophic Bacteria as a Biotechnological Platform Breakout Session 2-B: NewEmerging Pathways ...

  3. Methane

    Energy Savers

    ... implications for resource use efficiency, worker and public safety, air pollution, and human health (4), and for the climate impact of NG as a large and growing source of energy. ...

  4. May 15, 2014 Methane Hydrates Committee Meeting Agenda | Department of

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Energy May 15, 2014 Methane Hydrates Committee Meeting Agenda May 15, 2014 Methane Hydrates Committee Meeting Agenda May 15, 2014 Methane Hydrates Committee Meeting Agenda Meeting Agenda (443.71 KB) More Documents & Publications Advisory Committee Meeting Minutes, May 7, 2015 Report of the Task Force on Methane Hydrates Presentations from the May 7, 2015 Advisory Committee Meeting

  5. Department of Energy Advance Methane Hydrates Science and Technology Projects

    Energy.gov [DOE]

    Descriptions for Energy Department Methane Hydrates Science and Technology Projects, August 31, 2012

  6. Enhanced Renewable Methane Production System | Argonne National Laboratory

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Enhanced Renewable Methane Production System Technology available for licensing: Enhanced renewable methane production system provides a low-cost process that accelerates biological methane production rates at least fivefold. Low cost Delivers near-pipeline-quality gas and eliminates carbon dioxide emissions PDF icon methane_production_system

  7. Arkansas Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Arkansas Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 2 3 3 3 3 2010's 3 4 2 2 2 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Arkansas Coalbed Methane Proved Reserves, Reserves Changes, and

  8. Kansas Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Kansas Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 17 25 38 47 43 2010's 41 37 34 30 27 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Kansas Coalbed Methane Proved Reserves, Reserves Changes,

  9. Kentucky Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Kentucky Coalbed Methane Proved Reserves, Reserves Changes, and Production Coalbed Methane Production

  10. International Cooperation in Methane Hydrates | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Oil & Gas » Methane Hydrate » International Cooperation in Methane Hydrates International Cooperation in Methane Hydrates In 1982 the multi-national Deep Sea Drilling Program (DSDP) recovered the first subsea substantial methane hydrate deposits, which spurred methane hydrate research in the US and other countries. The successor programs, the Ocean Drilling Program (ODP) and the Integrated Ocean Drilling Program (IODP) sampled hydrate deposits off Oregon (ODP 204, 2002) and in the Cascadia

  11. METHOD FOR PRODUCING ISOTOPIC METHANES AND PARTIALLY HALOGENATED DERIVATIVES THEROF

    DOE Patents [OSTI]

    Frazer, J.W.

    1959-08-18

    A method is given for producing isotopic methanes and/ or partially halogenated derivatives. Lithium hydride, deuteride, or tritide is reacted with a halogenated methane or with a halogenated methane in combination with free halogen. The process is conveniently carried out by passing a halogenated methane preferably at low pressures or in an admixture with an inert gas through a fixed bed of finely divided lithium hydride heated initially to temperatures of 100 to 200 deg C depending upon the halogenated methane used.

  12. Towards quantifying the reaction network around the sulfate–methane-transition-zone in the Ulleung Basin, East Sea, with a kinetic modeling approach

    SciTech Connect (OSTI)

    Hong, Wei-Li; Torres, Marta E.; Kim, Ji-Hoon; Choi, Jiyoung; Bahk, Jang-Jun

    2014-09-01

    We present a kinetic model based upon pore water data collected from eight sites drilled during the second Ulleung Basin gas hydrate drilling expedition (UBGH2) in 2010. Three sites were drilled at locations where acoustic chimneys were identified in seismic data, and the rest were drilled on non-chimney (i.e. background) environments. Our model, coupled a comprehensive compositional and isotopic data set, is used to illustrate the different biogeochemical processes at play in those two environments, in terms of reactions around the sulfate-methane-transition-zone (SMTZ). Organic matter decomposition is an important process for production of methane, dissolved inorganic carbon (DIC) and consumption of sulfate in the non-chimney sites, whereas anaerobic oxidation of methane (AOM) dominates both carbon and sulfur cycles in the chimney environment. Different sources of methane mediate AOM in the two settings. Internally produced methane through CO₂ reduction (CR) and methanogenesis fuels AOM in the non-chimney sites, whereas AOM is sustained by methane from external sources in the chimney sites. We also simulate the system evolution from non-chimney to chimney conditions by increasing the bottom methane supply to a non-chimney setting. We show that the higher CH₄ flux leads to a higher microbial activity of AOM, and more organic matter decomposition through methanogenesis. A higher methanogenesis rate and a smaller CR contribution relative to AOM in the chimney sites is responsible for the isotopically light DIC and heavy methane in this environment, relative to the non-chimney sites.

  13. Reduction of Non-CO2 Gas Emissions Through The In Situ Bioconversion of Methane

    SciTech Connect (OSTI)

    Scott, A R; Mukhopadhyay, B; Balin, D F

    2012-09-06

    The primary objectives of this research were to seek previously unidentified anaerobic methanotrophs and other microorganisms to be collected from methane seeps associated with coal outcrops. Subsurface application of these microbes into anaerobic environments has the potential to reduce methane seepage along coal outcrop belts and in coal mines, thereby preventing hazardous explosions. Depending upon the types and characteristics of the methanotrophs identified, it may be possible to apply the microbes to other sources of methane emissions, which include landfills, rice cultivation, and industrial sources where methane can accumulate under buildings. Finally, the microbes collected and identified during this research also had the potential for useful applications in the chemical industry, as well as in a variety of microbial processes. Sample collection focused on the South Fork of Texas Creek located approximately 15 miles east of Durango, Colorado. The creek is located near the subsurface contact between the coal-bearing Fruitland Formation and the underlying Pictured Cliffs Sandstone. The methane seeps occur within the creek and in areas adjacent to the creek where faulting may allow fluids and gases to migrate to the surface. These seeps appear to have been there prior to coalbed methane development as extensive microbial soils have developed. Our investigations screened more than 500 enrichments but were unable to convince us that anaerobic methane oxidation (AMO) was occurring and that anaerobic methanotrophs may not have been present in the samples collected. In all cases, visual and microscopic observations noted that the early stage enrichments contained viable microbial cells. However, as the levels of the readily substrates that were present in the environmental samples were progressively lowered through serial transfers, the numbers of cells in the enrichments sharply dropped and were eliminated. While the results were disappointing we acknowledge that

  14. Ohio Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 - No Data Reported; -- ...

  15. Utah Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Utah Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 74 83 103...

  16. Montana Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Montana Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 12 12 13...

  17. Methane storage capabilities of diamond analogues

    SciTech Connect (OSTI)

    Haranczyk, M; Lin, LC; Lee, K; Martin, RL; Neaton, JB; Smit, B

    2013-01-01

    Methane can be an alternative fuel for vehicular usage provided that new porous materials are developed for its efficient adsorption-based storage. Herein, we search for materials for this application within the family of diamond analogues. We used density functional theory to investigate structures in which tetrahedral C atoms of diamond are separated by-CC-or-BN-groups, as well as ones involving substitution of tetrahedral C atoms with Si and Ge atoms. The adsorptive and diffusive properties of methane are studied using classical molecular simulations. Our results suggest that the all-carbon structure has the highest volumetric methane uptake of 280 VSTP/V at p = 35 bar and T = 298 K. However, it suffers from limited methane diffusion. Alternatively, the considered Si and Ge-containing analogies have fast diffusive properties but their adsorption is lower, ca. 172-179 VSTP/V, at the same conditions.

  18. Virginia Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Virginia Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 56 81...

  19. Pennsylvania Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Pennsylvania Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 3 5...

  20. Wyoming Coalbed Methane Production (Billion Cubic Feet)

    Annual Energy Outlook

    Production (Billion Cubic Feet) Wyoming Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 133 278...

  1. Methane Hydrates R&D Program

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    they contain perhaps more organic carbon that all the world's oil, gas, and coal combined. ... Fire in the Ice: A periodical highlighting the National Methane Hydrate R&D Program http:...

  2. Discovery of New Materials to Capture Methane | U.S. DOE Office...

    Office of Science (SC) [DOE]

    Discovery of New Materials to Capture Methane Predicted materials could economically produce high-purity methane from natural gas systems and separate methane from coal mine ...

  3. New Methane Hydrate Research: Investing in Our Energy Future | Department

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    of Energy Methane Hydrate Research: Investing in Our Energy Future New Methane Hydrate Research: Investing in Our Energy Future August 31, 2012 - 1:37pm Addthis Methane hydrates are 3D ice-lattice structures with natural gas locked inside. If methane hydrate is either warmed or depressurized, it will release the trapped natural gas. Methane hydrates are 3D ice-lattice structures with natural gas locked inside. If methane hydrate is either warmed or depressurized, it will release the trapped

  4. An active atmospheric methane sink in high Arctic mineral cryosols

    SciTech Connect (OSTI)

    Lau, Maggie C.Y.; Stackhouse, B.; Layton, Alice C.; Chauhan, Archana; Vishnivetskaya, T. A.; Chourey, Karuna; Mykytczuk, N. C.S.; Bennett, Phil C.; Lamarche-Gagnon, G.; Burton, N.; Renholm, J.; Hettich, R. L.; Pollard, W. H.; Omelon, C. R.; Medvigy, David M.; Pffifner, Susan M.; Whyte, L. G.; Onstott, T. C.

    2015-04-14

    The transition of Arctic carbon-rich cryosols into methane (CH₄)-emitting wetlands due to global warming is a rising concern. However, the spatially predominant mineral cryosols and their CH₄ emission potential are poorly understood. Fluxes measured in situ and estimated under laboratory conditions coupled with -omics analysis indicate (1) mineral cryosols in the Canadian high Arctic contain atmospheric CH₄-oxidizing bacteria; (2) the atmospheric CH⁺ uptake flux increases with ground temperature; and, as a result, (3) the atmospheric CH₄ sink strength will increase by a factor of 5-30 as the Arctic warms by 5-15 °C over a century. We demonstrated that acidic mineral cryosols have previously unrecognized potential of negative CH₄ feedback.

  5. An active atmospheric methane sink in high Arctic mineral cryosols

    DOE PAGES-Beta [OSTI]

    Lau, Maggie C.Y.; Stackhouse, B.; Layton, Alice C.; Chauhan, Archana; Vishnivetskaya, T. A.; Chourey, Karuna; Mykytczuk, N. C.S.; Bennett, Phil C.; Lamarche-Gagnon, G.; Burton, N.; et al

    2015-01-01

    The transition of Arctic carbon-rich cryosols into methane (CH₄)-emitting wetlands due to global warming is a rising concern. However, the spatially predominant mineral cryosols and their CH₄ emission potential are poorly understood. Fluxes measured in situ and estimated under laboratory conditions coupled with -omics analysis indicate (1) mineral cryosols in the Canadian high Arctic contain atmospheric CH₄-oxidizing bacteria; (2) the atmospheric CH⁺ uptake flux increases with ground temperature; and, as a result, (3) the atmospheric CH₄ sink strength will increase by a factor of 5-30 as the Arctic warms by 5-15 °C over a century. We demonstrated that acidic mineralmore » cryosols have previously unrecognized potential of negative CH₄ feedback.« less

  6. An active atmospheric methane sink in high Arctic mineral cryosols

    SciTech Connect (OSTI)

    Lau, Maggie C.Y.; Stackhouse, B.; Layton, Alice C.; Chauhan, Archana; Vishnivetskaya, T. A.; Chourey, Karuna; Mykytczuk, N. C.S.; Bennett, Phil C.; Lamarche-Gagnon, G.; Burton, N.; Renholm, J.; Hettich, R. L.; Pollard, W. H.; Omelon, C. R.; Medvigy, David M.; Pffifner, Susan M.; Whyte, L. G.; Onstott, T. C.

    2015-01-01

    The transition of Arctic carbon-rich cryosols into methane (CH₄)-emitting wetlands due to global warming is a rising concern. However, the spatially predominant mineral cryosols and their CH₄ emission potential are poorly understood. Fluxes measured in situ and estimated under laboratory conditions coupled with -omics analysis indicate (1) mineral cryosols in the Canadian high Arctic contain atmospheric CH₄-oxidizing bacteria; (2) the atmospheric CH⁺ uptake flux increases with ground temperature; and, as a result, (3) the atmospheric CH₄ sink strength will increase by a factor of 5-30 as the Arctic warms by 5-15 °C over a century. We demonstrated that acidic mineral cryosols have previously unrecognized potential of negative CH₄ feedback.

  7. Absorption spectrum and solar photodissociation of gaseous nitrous acid in the actinic wavelength region

    SciTech Connect (OSTI)

    Vasudev, R. )

    1990-11-01

    The absorption cross section of gaseous nitrous acid (HONO) in the actinic wavelength region ({lambda} {ge} 290 nm) of the solar radiation is mapped through laser photodissociation experiments, HONO is photodissociated by a tunable ultraviolet beam, and the OH product is monitored through fluorescence induced by a frequency-double dye laser. The absorption of HONO is mapped by scanning the photolysis wavelength. Since this technique yields relative cross-sections, the authors calibrate the measurements with previous measurements of absolute cross-section at 354 nm (because there is reasonable agreement among previous measurements at this wavelength). The present experimental approach is insensitive to the presence of NO{sub 2}, which apparently contributed to inaccuracies in some of the previous conventional measurements on HONO absorption.

  8. Synthesis and characterization of complexes of rare earth picrates and rac-bis(ethylsulfinyl)methane

    SciTech Connect (OSTI)

    Andrade Da Silva, M.A.; Zaim, M.H.; Isolani, P.C.

    1995-12-31

    The compound {beta}-dissulfoxide bis(ethylsufinyl)methane (besm) was prepared by oxidation of bis(ethylthio)methane with hydrogen peroxide in acetic acid, and obtained as a mixture of its meso and d,1 diastereomers. An analytical sample was obtained by recrystallization from chloroform-diethyl ether. The racemic-bis(ethylsulfinyl)methane was characterized and studied by CHS elemental analysis, high resolution mass spectrometry, infrared spectra, {sup 1}H and {sup 13}C NMR. A series of compounds with composition RE(pic){sub 3}2rac-besm [RE = La, Ce, Nd, Eu, Gd, Er, Tm, Yb, Lu and Y; pic = picrate and rac-besm = racemic-bis(ethylsulfinyl)methane] were synthesized and characterized by CHNS elemental analysis and rare earths complexometric titration with EDTA, conductance measurements, X-ray powder patterns, infrared spectra, visible absorption of the neodymium and emission spectra of the europium materials. The coordination polyhedron around the Eu{sup 3+} center is probably a dodecahedron with coordination number eight. 19 refs., 2 figs., 4 tabs.

  9. Federal Offshore--Texas Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Offshore--Texas Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 ... Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Federal Offshore, Gulf of ...

  10. Solubility of methane in water under natural conditions: a laboratory...

    Office of Scientific and Technical Information (OSTI)

    302sup 0F. Also the solubility of crude oil and water in methane has been determined ... Increasing pressure increases the solubility of crude oil in methane gas. At an elevated ...

  11. ,"New York Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    ...","Frequency","Latest Data for" ,"Data 1","New York Coalbed Methane Proved Reserves ... 8:49:43 AM" "Back to Contents","Data 1: New York Coalbed Methane Proved Reserves ...

  12. ,"New Mexico--West Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    ...","Frequency","Latest Data for" ,"Data 1","New Mexico--West Coalbed Methane Proved ... 8:49:40 AM" "Back to Contents","Data 1: New Mexico--West Coalbed Methane Proved ...

  13. ,"New Mexico Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    ...","Frequency","Latest Data for" ,"Data 1","New Mexico Coalbed Methane Proved Reserves ... 9:00:33 AM" "Back to Contents","Data 1: New Mexico Coalbed Methane Proved Reserves ...

  14. ,"New Mexico--East Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    ...","Frequency","Latest Data for" ,"Data 1","New Mexico--East Coalbed Methane Proved ... 8:49:39 AM" "Back to Contents","Data 1: New Mexico--East Coalbed Methane Proved ...

  15. Ohio Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Ohio Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  16. Louisiana (with State Offshore) Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Louisiana (with State Offshore) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 ...

  17. Colorado Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  18. Lower 48 States Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 ...

  19. Texas--RRC District 4 Onshore Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    4 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Texas--RRC District 4 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ...

  20. Oklahoma Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  1. Virginia Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  2. Montana Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Montana Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  3. Pennsylvania Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 ...

  4. Kentucky Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Kentucky Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  5. Kansas Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Kansas Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  6. Wyoming Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  7. Texas--RRC District 2 Onshore Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Texas--RRC District 2 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 ...

  8. Utah Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  9. Texas (with State Offshore) Coalbed Methane Proved Reserves ...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 ...

  10. Arkansas Coalbed Methane Proved Reserves (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  11. Texas--RRC District 3 Onshore Coalbed Methane Proved Reserves...

    U.S. Energy Information Administration (EIA) (indexed site)

    3 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Texas--RRC District 3 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ...

  12. ,"U.S. Coalbed Methane Proved Reserves (Billion Cubic Feet)"

    U.S. Energy Information Administration (EIA) (indexed site)

    Data for" ,"Data 1","U.S. Coalbed Methane Proved Reserves (Billion Cubic ... "Back to Contents","Data 1: U.S. Coalbed Methane Proved Reserves (Billion Cubic Feet)" ...

  13. Alabama Coalbed Methane Proved Reserves (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Alabama Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 ...

  14. West Virginia Coalbed Methane Proved Reserves (Billion Cubic...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 ...

  15. Texas--RRC District 10 Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed Methane Proved Reserves (Billion Cubic Feet) Texas--RRC District 10 Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 ...

  16. Direct use of methane in coal liquefaction

    DOE Patents [OSTI]

    Sundaram, M.S.; Steinberg, M.

    1985-06-19

    This invention relates to a process for converting solid carbonaceous material, such as coal, to liquid and gaseous hydrocarbons utilizing methane, generally at a residence time of about 20 to 120 minutes at a temperature of 250 to 750/sup 0/C, preferably 350 to 450/sup 0/C, pressurized up to 6000 psi, and preferably in the 1000 to 2500 psi range, preferably directly utilizing methane 50 to 100% by volume in a mix of methane and hydrogen. A hydrogen donor solvent or liquid vehicle such as tetralin, tetrahydroquinoline, piperidine, and pyrolidine may be used in a slurry mix where the solvent feed is 0 to 100% by weight of the coal or carbonaceous feed. Carbonaceous feed material can either be natural, such as coal, wood, oil shale, petroleum, tar sands, etc., or man-made residual oils, tars, and heavy hydrocarbon residues from other processing systems. 1 fig.

  17. Direct use of methane in coal liquefaction

    DOE Patents [OSTI]

    Sundaram, Muthu S.; Steinberg, Meyer

    1987-01-01

    This invention relates to a process for converting solid carbonaceous material, such as coal, to liquid and gaseous hydrocarbons utilizing methane, generally at a residence time of about 20-120 minutes at a temperature of 250.degree.-750.degree. C., preferably 350.degree.-450.degree. C., pressurized up to 6000 psi, and preferably in the 1000-2500 psi range, preferably directly utilizing methane 50-100% by volume in a mix of methane and hydrogen. A hydrogen donor solvent or liquid vehicle such as tetralin, tetrahydroquinoline, piperidine, and pyrolidine may be used in a slurry mix where the solvent feed is 0-100% by weight of the coal or carbonaceous feed. Carbonaceous feed material can either be natural, such as coal, wood, oil shale, petroleum, tar sands, etc., or man-made residual oils, tars, and heavy hydrocarbon residues from other processing systems.

  18. Impact of mammalian megaherbivores on global methane examined

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    function and potential climate effects resulting from methane concentration changes. ... Panel on Climate Change (IPCC) inventories for climate model simulations. ...

  19. 7.4 Landfill Methane Utilization | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    7.4 Landfill Methane Utilization 7.4 Landfill Methane Utilization A chapter on Landfill Methane Utilization from the Clean Energy Strategies for Local Governments publication. 7.4_landfill_methane_utilization.pdf (484.59 KB) More Documents & Publications CHP and Bioenergy for Landfills and Wastewater Treatment Plants: Market Opportunities Powering Microturbines With Landfill Gas, October 2002 Barriers to CHP with Renewable Portfolio Standards, Draft White Paper, September 2007

  20. Report of the Task Force on Methane Hydrates

    Office of Energy Efficiency and Renewable Energy (EERE)

    This report presents the findings and recommendations for the Secretary of Energy Advisory Board (SEAB) Task Force on Methane Hydrates.

  1. Draft Report of the Task Force on Methane Hydrates

    Energy.gov [DOE]

    This report presents the findings and recommendations for the Secretary of Energy Advisory Board (SEAB) Task Force on Methane Hydrates.

  2. DOE/NETL Methane Hydrate Projects | netl.doe.gov

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Methane Hydrate Projects Active Projects | Completed Projects Active Methane Hydrate Projects Project Number Project Name Primary Performer DE-FE0023919 Deepwater Methane Hydrate Characterization and Scientific Assessment University of Texas at Austin DE-FE0025387 Support for Methane Hydrate Research on the Alaska North Slope Petrotechnical Resources of Alaska DE-FE0009897 Hydrate-Bearing Clayey Sediments: Morphology, Physical Properties, Production and Engineering/Geological Implications

  3. Alabama Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Alabama Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 23 1990's 36 68 89 103 108 109 98 111 123 108 2000's 109 111 117 98 121 113 114 114 107 105 2010's 102 98 91 62 78 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane

  4. Method for removal of methane from coalbeds

    DOE Patents [OSTI]

    Pasini, III, Joseph; Overbey, Jr., William K.

    1976-01-01

    A method for removing methane gas from underground coalbeds prior to mining the coal which comprises drilling at least one borehole from the surface into the coalbed. The borehole is started at a slant rather than directly vertically, and as it descends, a gradual curve is followed until a horizontal position is reached where the desired portion of the coalbed is intersected. Approaching the coalbed in this manner and fracturing the coalbed in the major natural fraction direction cause release of large amounts of the trapped methane gas.

  5. Methane recovery from landfill in China

    SciTech Connect (OSTI)

    Gaolai, L.

    1996-12-31

    GEF has approved a special project for a demonstration project for Methane Recovery from the Urban Refuse Land Fill. This paper will introduce the possibility of GHG reduction from the landfill in China, describe the activities of the GEF project, and the priorities for international cooperation in this field. The Global Environment Facility (GEF) approved the project, China Promoting Methane Recovery and Unlization from Mixed Municipal Refuse, at its Council meeting in last April. This project is the first one supported by international organization in this field.

  6. Formation and retention of methane in coal

    SciTech Connect (OSTI)

    Hucka, V.J.; Bodily, D.M.; Huang, H.

    1992-05-15

    The formation and retention of methane in coalbeds was studied for ten Utah coal samples, one Colorado coal sample and eight coal samples from the Argonne Premium Coal Sample Bank.Methane gas content of the Utah and Colorado coals varied from zero to 9 cm{sup 3}/g. The Utah coals were all high volatile bituminous coals. The Colorado coal was a gassy medium volatile bituminous coal. The Argonne coals cover a range or rank from lignite to low volatile bituminous coal and were used to determine the effect of rank in laboratory studies. The methane content of six selected Utah coal seams and the Colorado coal seam was measured in situ using a special sample collection device and a bubble desorbometer. Coal samples were collected at each measurement site for laboratory analysis. The cleat and joint system was evaluated for the coal and surrounding rocks and geological conditions were noted. Permeability measurements were performed on selected samples and all samples were analyzed for proximate and ultimate analysis, petrographic analysis, {sup 13}C NMR dipolar-dephasing spectroscopy, and density analysis. The observed methane adsorption behavior was correlated with the chemical structure and physical properties of the coals.

  7. Generating power with drained coal mine methane

    SciTech Connect (OSTI)

    2005-09-01

    The article describes the three technologies most commonly used for generating electricity from coal mine methane: internal combustion engines, gas turbines, and microturbines. The most critical characteristics and features of these technologies, such as efficiency, output and size are highlighted. 5 refs.

  8. Enhancement of Biogenic Coalbed Methane Production and Back Injection of Coalbed Methane Co-Produced Water

    SciTech Connect (OSTI)

    Song Jin

    2007-05-31

    Biogenic methane is a common constituent in deep subsurface environments such as coalbeds and oil shale beds. Coalbed methane (CBM) makes significant contributions to world natural gas industry and CBM production continues to increase. With increasing CBM production, the production of CBM co-produced water increases, which is an environmental concern. This study investigated the feasibility in re-using CBM co-produced water and other high sodic/saline water to enhance biogenic methane production from coal and other unconventional sources, such as oil shale. Microcosms were established with the selected carbon sources which included coal, oil shale, lignite, peat, and diesel-contaminated soil. Each microcosm contained either CBM coproduced water or groundwater with various enhancement and inhibitor combinations. Results indicated that the addition of nutrients and nutrients with additional carbon can enhance biogenic methane production from coal and oil shale. Methane production from oil shale was much greater than that from coal, which is possibly due to the greater amount of available Dissolved Organic Carbon (DOC) from oil shale. Inconclusive results were observed from the other sources since the incubation period was too low. WRI is continuing studies with biogenic methane production from oil shale.

  9. Geochemistry of clathrate-derived methane in Arctic Ocean waters

    SciTech Connect (OSTI)

    Elliott, S.M.; Reagan, M.T.; Moridis, G.J.; Cameron-Smith, P.J.

    2010-03-15

    Alterations to the composition of seawater are estimated for microbial oxidation of methane from large polar clathrate destabilizations, which may arise in the coming century. Gas fluxes are taken from porous flow models of warming Arctic sediment. Plume spread parameters are then used to bracket the volume of dilution. Consumption stoichiometries for the marine methanotrophs are based on growth efficiency and elemental/enzyme composition data. The nutritional demand implied by extra CH{sub 4} removal is compared with supply in various high latitude water masses. For emissions sized to fit the shelf break, reaction potential begins at one hundred micromolar and falls to order ten a thousand kilometers downstream. Oxygen loss and carbon dioxide production are sufficient respectively to hypoxify and acidify poorly ventilated basins. Nitrogen and the monooxygenase transition metals may be depleted in some locations as well. Deprivation is implied relative to existing ecosystems, along with dispersal of the excess dissolved gas. Physical uncertainties are inherent in the clathrate abundance, patch size, outflow buoyancy and mixing rate. Microbial ecology is even less defined but may involve nutrient recycling and anaerobic oxidizers.

  10. Thermodynamic properties and diffusion of water + methane binary mixtures

    SciTech Connect (OSTI)

    Shvab, I.; Sadus, Richard J.

    2014-03-14

    Thermodynamic and diffusion properties of water + methane mixtures in a single liquid phase are studied using NVT molecular dynamics. An extensive comparison is reported for the thermal pressure coefficient, compressibilities, expansion coefficients, heat capacities, Joule-Thomson coefficient, zero frequency speed of sound, and diffusion coefficient at methane concentrations up to 15% in the temperature range of 298650 K. The simulations reveal a complex concentration dependence of the thermodynamic properties of water + methane mixtures. The compressibilities, heat capacities, and diffusion coefficients decrease with increasing methane concentration, whereas values of the thermal expansion coefficients and speed of sound increase. Increasing methane concentration considerably retards the self-diffusion of both water and methane in the mixture. These effects are caused by changes in hydrogen bond network, solvation shell structure, and dynamics of water molecules induced by the solvation of methane at constant volume conditions.

  11. Effect of bubble size and density on methane conversion to hydrate

    SciTech Connect (OSTI)

    Leske, J.; Taylor, C.E.; Ladner, E.P.

    2007-03-01

    Research is underway at NETL to understand the physical properties of methane hydrates. One area of investigation is the storage of methane as methane hydrates. An economical and efficient means of storing methane in hydrates opens many commercial opportunities such as transport of stranded gas, off-peak storage of line gas, etc.We have observed during our investigations that the ability to convert methane to methane hydrate is enhanced by foaming of the methanewater solution using a surfactant. The density of the foam, along with the bubble size, is important in the conversion of methane to methane hydrate.

  12. Cross Sections for Electron Collisions with Methane

    SciTech Connect (OSTI)

    Song, Mi-Young Yoon, Jung-Sik; Cho, Hyuck; Itikawa, Yukikazu; Karwasz, Grzegorz P.; Kokoouline, Viatcheslav; Nakamura, Yoshiharu; Tennyson, Jonathan

    2015-06-15

    Cross section data are compiled from the literature for electron collisions with methane (CH{sub 4}) molecules. Cross sections are collected and reviewed for total scattering, elastic scattering, momentum transfer, excitations of rotational and vibrational states, dissociation, ionization, and dissociative attachment. The data derived from swarm experiments are also considered. For each of these processes, the recommended values of the cross sections are presented. The literature has been surveyed through early 2014.

  13. TITAN'S TRANSPORT-DRIVEN METHANE CYCLE

    SciTech Connect (OSTI)

    Mitchell, Jonathan L.

    2012-09-10

    The mechanisms behind the occurrence of large cloud outbursts and precipitation on Titan have been disputed. A global- and annual-mean estimate of surface fluxes indicated only 1% of the insolation, or {approx}0.04 W m{sup -2}, is exchanged as sensible and/or latent fluxes. Since these fluxes are responsible for driving atmospheric convection, it has been argued that moist convection should be quite rare and precipitation even rarer, even if evaporation globally dominates the surface-atmosphere energy exchange. In contrast, climate simulations indicate substantial cloud formation and/or precipitation. We argue that the top-of-atmosphere (TOA) radiative imbalance is diagnostic of horizontal heat transport by Titan's atmosphere, and thus constrains the strength of the methane cycle. Simple calculations show the TOA radiative imbalance is {approx}0.5-1 W m{sup -2} in Titan's equatorial region, which implies 2-3 MW of latitudinal heat transport by the atmosphere. Our simulation of Titan's climate suggests this transport may occur primarily as latent heat, with net evaporation at the equator and net accumulation at higher latitudes. Thus, the methane cycle could be 10-20 times previous estimates. Opposing seasonal transport at solstices, compensation by sensible heat transport, and focusing of precipitation by large-scale dynamics could further enhance the local, instantaneous strength of Titan's methane cycle by a factor of several. A limited supply of surface liquids in regions of large surface radiative imbalance may throttle the methane cycle, and if so, we predict more frequent large storms over the lakes district during Titan's northern summer.

  14. Enhanced carbon monoxide utilization in methanation process

    DOE Patents [OSTI]

    Elek, Louis F.; Frost, Albert C.

    1984-01-01

    Carbon monoxide - containing gas streams are passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. The active carbon is subsequently reacted with steam or hydrogen to form methane. Surprisingly, hydrogen and water vapor present in the feed gas do not adversely affect CO utilization significantly, and such hydrogen actually results in a significant increase in CO utilization.

  15. Process for separating nitrogen from methane using microchannel process technology

    DOE Patents [OSTI]

    Tonkovich, Anna Lee; Qiu, Dongming; Dritz, Terence Andrew; Neagle, Paul; Litt, Robert Dwayne; Arora, Ravi; Lamont, Michael Jay; Pagnotto, Kristina M.

    2007-07-31

    The disclosed invention relates to a process for separating methane or nitrogen from a fluid mixture comprising methane and nitrogen, the process comprising: (A) flowing the fluid mixture into a microchannel separator, the microchannel separator comprising a plurality of process microchannels containing a sorption medium, the fluid mixture being maintained in the microchannel separator until at least part of the methane or nitrogen is sorbed by the sorption medium, and removing non-sorbed parts of the fluid mixture from the microchannel separator; and (B) desorbing the methane or nitrogen from the sorption medium and removing the desorbed methane or nitrogen from the microchannel separator. The process is suitable for upgrading methane from coal mines, landfills, and other sub-quality sources.

  16. Towards quantifying the reaction network around the sulfate–methane-transition-zone in the Ulleung Basin, East Sea, with a kinetic modeling approach

    DOE PAGES-Beta [OSTI]

    Hong, Wei-Li; Torres, Marta E.; Kim, Ji-Hoon; Choi, Jiyoung; Bahk, Jang-Jun

    2014-09-01

    We present a kinetic model based upon pore water data collected from eight sites drilled during the second Ulleung Basin gas hydrate drilling expedition (UBGH2) in 2010. Three sites were drilled at locations where acoustic chimneys were identified in seismic data, and the rest were drilled on non-chimney (i.e. background) environments. Our model, coupled a comprehensive compositional and isotopic data set, is used to illustrate the different biogeochemical processes at play in those two environments, in terms of reactions around the sulfate-methane-transition-zone (SMTZ). Organic matter decomposition is an important process for production of methane, dissolved inorganic carbon (DIC) and consumptionmore » of sulfate in the non-chimney sites, whereas anaerobic oxidation of methane (AOM) dominates both carbon and sulfur cycles in the chimney environment. Different sources of methane mediate AOM in the two settings. Internally produced methane through CO₂ reduction (CR) and methanogenesis fuels AOM in the non-chimney sites, whereas AOM is sustained by methane from external sources in the chimney sites. We also simulate the system evolution from non-chimney to chimney conditions by increasing the bottom methane supply to a non-chimney setting. We show that the higher CH₄ flux leads to a higher microbial activity of AOM, and more organic matter decomposition through methanogenesis. A higher methanogenesis rate and a smaller CR contribution relative to AOM in the chimney sites is responsible for the isotopically light DIC and heavy methane in this environment, relative to the non-chimney sites.« less

  17. Lean methane premixed laminar flames doped by components of diesel fuel II: n-propylcyclohexane

    SciTech Connect (OSTI)

    Pousse, E.; Porter, R.; Warth, V.; Glaude, P.A.; Fournet, R.; Battin-Leclerc, F. [Departement de Chimie-Physique des Reactions, Nancy Universite, CNRS, ENSIC, 1 rue Grandville, BP 20451, 54001 Nancy Cedex (France)

    2010-01-15

    For a better understanding of the chemistry involved during the combustion of components of diesel fuel, the structure of a laminar lean premixed methane flame doped with n-propylcyclohexane has been investigated. The inlet gases contained 7.1% (molar) methane, 36.8% oxygen, and 0.81% n-propylcyclohexane (C{sub 9}H{sub 18}), corresponding to an equivalence ratio of 0.68 and a C{sub 9}H{sub 18}/CH{sub 4} ratio of 11.4%. The flame has been stabilized on a burner at a pressure of 6.7 kPa (50 Torr) using argon as diluent, with a gas velocity at the burner of 49.2 cm/s at 333 K. Quantified species included the usual methane C{sub 0}-C{sub 2} combustion products, but also 17 C{sub 3}-C{sub 5} hydrocarbons, seven C{sub 1}-C{sub 3} oxygenated compounds, and only four cyclic C{sub 6+} compounds, namely benzene, 1,3-cyclohexadiene, cyclohexene, and methylenecyclohexane. A new mechanism for the oxidation of n-propylcyclohexane has been proposed. It allows the proper simulation of profiles of most of the products measured in flames, as well as the satisfactory reproduction of experimental results obtained in a jet-stirred reactor. The main reaction pathways of consumption of n-propylcyclohexane have been derived from rate-of-production analysis. (author)

  18. A lean methane premixed laminar flame doped with components of diesel fuel. I. n-Butylbenzene

    SciTech Connect (OSTI)

    Pousse, E.; Glaude, P.A.; Fournet, R.; Battin-Leclerc, F. [Departement de Chimie-Physique des Reactions, Nancy Universite, CNRS, ENSIC, 1 rue Grandville, BP 20451, 54001 Nancy Cedex (France)

    2009-05-15

    To better understand the chemistry involved in the combustion of components of diesel fuel, the structure of a laminar lean premixed methane flame doped with n-butylbenzene has been investigated. The inlet gases contained 7.1% (molar) methane, 36.8% oxygen, and 0.96% n-butylbenzene corresponding to an equivalence ratio of 0.74 and a ratio C{sub 10}H{sub 14}/CH{sub 4} of 13.5%. The flame has been stabilized on a burner at a pressure of 6.7 kPa using argon as diluent, with a gas velocity at the burner of 49.2 cm/s at 333 K. Quantified species included the usual methane C{sub 0}-C{sub 2} combustion products, but also 16 C{sub 3}-C{sub 5} hydrocarbons, and 7 C{sub 1}-C{sub 3} oxygenated compounds, as well as 20 aromatic products. A new mechanism for the oxidation of n-butylbenzene is proposed whose predictions are in satisfactory agreement with measured species profiles in flames and flow reactor experiments. The main reaction pathways of consumption of n-butylbenzene have been derived from flow rate analyses. (author)

  19. Implications of Representative Concentration Pathway 4.5 Methane Emissions to Stabilize Radiative Forcing

    SciTech Connect (OSTI)

    Emanuel, William R.; Janetos, Anthony C.

    2013-02-01

    Increases in the abundance of methane (CH4) in the Earth’s atmosphere are responsible for significant radiative forcing of climate change (Forster et al., 2007; Wuebbles and Hayhoe, 2002). Since 1750, a 2.5 fold increase in atmospheric CH4 contributed 0.5 W/m2 to direct radiative forcing and an additional 0.2 W/m2 indirectly through changes in atmospheric chemistry. Next to water and carbon dioxide (CO2), methane is the most abundant greenhouse gas in the troposphere. Additionally, CH4 is significantly more effective as a greenhouse gas on a per molecule basis than is CO2, and increasing atmospheric CH4 has been second only to CO2 in radiative forcing (Forster et al., 2007). The chemical reactivity of CH4 is important to both tropospheric and stratospheric chemistry. Along with carbon monoxide, methane helps control the amount of the hydroxyl radical (OH) in the troposphere where oxidation of CH4 by OH leads to the formation of formaldehyde, carbon monoxide, and ozone.

  20. Process for producing methane from gas streams containing carbon monoxide and hydrogen

    DOE Patents [OSTI]

    Frost, Albert C.

    1980-01-01

    Carbon monoxide-containing gas streams are passed over a catalyst capable of catalyzing the disproportionation of carbon monoxide so as to deposit a surface layer of active surface carbon on the catalyst essentially without formation of inactive coke thereon. The surface layer is contacted with steam and is thus converted to methane and CO.sub.2, from which a relatively pure methane product may be obtained. While carbon monoxide-containing gas streams having hydrogen or water present therein can be used only the carbon monoxide available after reaction with said hydrogen or water is decomposed to form said active surface carbon. Although hydrogen or water will be converted, partially or completely, to methane that can be utilized in a combustion zone to generate heat for steam production or other energy recovery purposes, said hydrogen is selectively removed from a CO--H.sub.2 -containing feed stream by partial oxidation thereof prior to disproportionation of the CO content of said stream.

  1. Methane and Methanotrophic Bacteria as a Biotechnological Platform |

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Department of Energy Methane and Methanotrophic Bacteria as a Biotechnological Platform Methane and Methanotrophic Bacteria as a Biotechnological Platform Breakout Session 2-B: New/Emerging Pathways Methane and Methanotrophic Bacteria as a Biotechnological Platform Dr. Lori Giver, Vice President of Biological Engineering, Calysta Energy, Inc. giver_bioenergy_2015.pdf (1.68 MB) More Documents & Publications CX-100166 Categorical Exclusion Determination Biobased Chemicals Landscape in

  2. Enhanced Renewable Methane Production System Benefits Wastewater Treatment

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Plants, Farms, and Landfills - Energy Innovation Portal Biomass and Biofuels Biomass and Biofuels Find More Like This Return to Search Enhanced Renewable Methane Production System Benefits Wastewater Treatment Plants, Farms, and Landfills Argonne National Laboratory Contact ANL About This Technology <p> Argonne&rsquo;s Enhanced Renewable Methane Production System &mdash; Process Schematic.</p> Argonne's Enhanced Renewable Methane Production System - Process Schematic.

  3. DOE Announces $2 Million Funding for Methane Hydrates Projects | Department

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    of Energy 2 Million Funding for Methane Hydrates Projects DOE Announces $2 Million Funding for Methane Hydrates Projects November 7, 2005 - 12:43pm Addthis Seeks to Unlock World's Biggest Potential Source of "Ice That Burns" WASHINGTON, DC - The Department of Energy (DOE) today announced a total of $2 million in funding to five research projects that will assess the energy potential, safety, and environmental aspects of methane hydrate exploration and development. Termed the

  4. Western States Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Western States Coalbed Methane Production (Billion Cubic Feet) Western States Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 4 14 33 51 77 89 108 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Production

  5. UPGRADING METHANE USING ULTRA-FAST THERMAL SWING ADSORPTION

    SciTech Connect (OSTI)

    Anna Lee Tonkovich

    2004-01-01

    The purpose of this project is to design and demonstrate an approach to upgrade low-BTU methane streams from coal mines to pipeline-quality natural gas. The objective of Phase I of the project was to assess the feasibility of upgrading low-Btu methane streams using ultra-fast thermal swing adsorption (TSA) using Velocys' modular microchannel process technology. The project is on schedule and under budget. For Task 1.1, the open literature, patent information, and vendor contacts were surveyed to identify adsorbent candidates for experimental validation and subsequent demonstration in an MPT-based ultra-fast TSA separation for methane upgrading. The leading candidates for preferential adsorption of methane over nitrogen are highly microporous carbons. A Molecular Gate{trademark} zeolite from Engelhard Corporation has emerged as a candidate. For Task 1.2, experimental evaluation of adsorbents was initiated, and data were collected on carbon (MGN-101) from PICA, Inc. This carbon demonstrated a preferential capacity for methane over nitrogen, as well as a reasonable thermal swing differential capacity for a 90% methane and 10% nitrogen mixture. A similar methane swing capacity at 2 psig was measured. The mixture composition is relevant because gob gas contains nearly 85% methane and must be purified to 97% methane for pipeline quality.

  6. High Methane Storage Capacity in Aluminum Metal-Organic Frameworks...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    High Methane Storage Capacity in Aluminum Metal-Organic Frameworks Previous Next List Felipe Gndara, Hiroyasu Furukawa, Seungkyu Lee, and Omar M. Yaghi, J. Am. Chem. Soc., 136,...

  7. ,"U.S. Coalbed Methane Proved Reserves, Reserves Changes, and...

    U.S. Energy Information Administration (EIA) (indexed site)

    ame","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Coalbed Methane Proved Reserves, Reserves Changes, and Production",10,"Annual",2013,"06301989"...

  8. Controlling Methane Emissions in the Natural Gas Sector: A Review...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Controlling Methane Emissions in the Natural Gas Sector: A Review of Federal & State Regulatory Frameworks Governing Production, Processing, Transmission, and Distribution ...

  9. DOE Announces $13 Million to Quantify and Mitigate Methane Emissions...

    Energy.gov (indexed) [DOE]

    to twelve multi-year research projects intended to develop cost efficient and effective ways to mitigate methane emissions from natural gas pipeline and storage infrastructure. ...

  10. Critical Factors Driving the High Volumetric Uptake of Methane...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Critical Factors Driving the High Volumetric Uptake of Methane in Cu-3(btc)(2) Previous Next List Hulvey, Zeric; Vlaisavljevich, Bess; Mason, Jarad A.; Tsivion, Ehud; Dougherty,...

  11. Bioconversion of methane to lactate by an obligate methanotrophic bacterium

    DOE PAGES-Beta [OSTI]

    Henard, Calvin A.; Smith, Holly; Dowe, Nancy; Kalyuzhnaya, Marina G.; Pienkos, Philip T.; Guarnieri, Michael T.

    2016-02-23

    Methane is the second most abundant greenhouse gas (GHG), with nearly 60% of emissions derived from anthropogenic sources. Microbial conversion of methane to fuels and value-added chemicals offers a means to reduce GHG emissions, while also valorizing this otherwise squandered high-volume, high-energy gas. However, to date, advances in methane biocatalysis have been constrained by the low-productivity and limited genetic tractability of natural methane-consuming microbes. Here, leveraging recent identification of a novel, tractable methanotrophic bacterium, Methylomicrobium buryatense, we demonstrate microbial biocatalysis of methane to lactate, an industrial platform chemical. Heterologous overexpression of a Lactobacillus helveticus L-lactate dehydrogenase in M. buryatense resultedmore » in an initial titer of 0.06 g lactate/L from methane. Cultivation in a 5 L continuously stirred tank bioreactor enabled production of 0.8 g lactate/L, representing a 13-fold improvement compared to the initial titer. The yields (0.05 g lactate/g methane) and productivity (0.008 g lactate/L/h) indicate the need and opportunity for future strain improvement. Additionally, real-time analysis of methane utilization implicated gas-to-liquid transfer and/or microbial methane consumption as process limitations. This work opens the door to develop an array of methanotrophic bacterial strain-engineering strategies currently employed for biocatalytic sugar upgrading to “green” chemicals and fuels.« less

  12. Minimizing the formation of coke and methane on Co nanoparticles...

    Office of Scientific and Technical Information (OSTI)

    that leads to high hydrogen selectivity and low methane formation on Co-based catalysts. ... We gratefully acknowledge the financial support from U. S. Department of Energy (DOE), ...

  13. Scientists detect methane levels three times larger than expected...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    "We attribute this hot spot to fugitive leaks from coal-bed methane that actually preceded recent concerns about potential emissions from fracking," Dubey said. Scientists detect ...

  14. Rapid Production of Methane Hydrates | netl.doe.gov

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    ... The high velocities of both the water and gas feeds within the small mixing zone ... methane content), cold energy storage, transportation fuels, and desalination processes. ...

  15. Table 16. Coalbed methane proved reserves, reserves changes,...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed methane proved reserves, reserves changes, and production, 2014" "billion cubic feet" ,,"Changes in Reserves During 2014" ,"Published",,,..."New Reservoir" ...

  16. Table 15. Coalbed methane proved reserves and production, 2010...

    U.S. Energy Information Administration (EIA) (indexed site)

    Coalbed methane proved reserves and production, 2010-14" "billion cubic feet" ,,"Reserves",,,,,,"Production" "State and Subdivision",,2010,2011,2012,2013,2014,,2010,2011,2012,2013,...

  17. Remote Sensing and Sea-Truth Measurements of Methane Flux to the Atmosphere (HYFLUX project)

    SciTech Connect (OSTI)

    Ian MacDonald

    2011-05-31

    A multi-disciplinary investigation of distribution and magnitude of methane fluxes from seafloor gas hydrate deposits in the Gulf of Mexico was conducted based on results obtained from satellite synthetic aperture radar (SAR) remote sensing and from sampling conducted during a research expedition to three sites where gas hydrate occurs (MC118, GC600, and GC185). Samples of sediments, water, and air were collected from the ship and from an ROV submersible using sediments cores, niskin bottles attached to the ROV and to a rosette, and an automated sea-air interface collector. The SAR images were used to quantify the magnitude and distribution of natural oil and gas seeps that produced perennial oil slicks on the ocean surface. A total of 176 SAR images were processed using a texture classifying neural network algorithm, which segmented the ocean surface into oil-free and oil-covered water. Geostatistical analysis indicates that there are a total of 1081 seep formations distributed over the entire Gulf of Mexico basin. Oil-covered water comprised an average of 780.0 sq. km (sd 86.03) distributed with an area of 147,370 sq. km. Persistent oil and gas seeps were also detected with SAR sampling on other ocean margins located in the Black Sea, western coast of Africa, and offshore Pakistan. Analysis of sediment cores from all three sites show profiles of sulfate, sulfide, calcium and alkalinity that indicated anaerobic oxidation of methane with precipitation of authigenic carbonates. Difference among the three sampling sites may reflect the relative magnitude of methane flux. Methane concentrations in water column samples collected by ROV and rosette deployments from MC118 ranged from {approx}33,000 nM at the seafloor to {approx}12 nM in the mixed layer with isolated peaks up to {approx}13,670 nM coincident with the top of the gas hydrate stability field. Average plume methane, ethane, and propane concentrations in the mixed layer are 7, 630, and 9,540 times saturation

  18. A Path to Reduce Methane Emissions from Gas Systems | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    A Path to Reduce Methane Emissions from Gas Systems A Path to Reduce Methane Emissions from Gas Systems July 29, 2014 - 3:33pm Addthis A researcher evaluates methane produced in a unique conservation process. Methane is both a potent greenhouse gas and valuable energy resource.| Photo courtesy of the Energy Department. A researcher evaluates methane produced in a unique conservation process. Methane is both a potent greenhouse gas and valuable energy resource.| Photo courtesy of the Energy

  19. Emissions Of Greenhouse Gases From Rice Agriculture

    SciTech Connect (OSTI)

    M. Aslam K. Khalil

    2009-07-16

    This project produced detailed data on the processes that affect methane and nitrous oxide emissions from rice agriculture and their inter-relationships. It defines the shifting roles and potential future of these gases in causing global warming and the benefits and tradeoffs of reducing emissions. The major results include: 1). Mechanisms and Processes Leading to Methane Emissions are Delineated. Our experiments have tested the standard model of methane emissions from rice fields and found new results on the processes that control the flux. A mathematical mass balance model was used to unravel the production, oxidation and transport of methane from rice. The results suggested that when large amounts of organic matter are applied, the additional flux that is observed is due to both greater production and reduced oxidation of methane. 2). Methane Emissions From China Have Been Decreasing Over the Last Two Decades. We have calculated that methane emissions from rice fields have been falling in recent decades. This decrease is particularly large in China. While some of this is due to reduced area of rice agriculture, the bigger effect is from the reduction in the emission factor which is the annual amount of methane emitted per hectare of rice. The two most important changes that cause this decreasing emission from China are the reduced use of organic amendments which have been replaced by commercial nitrogen fertilizers, and the increased practice of intermittent flooding as greater demands are placed on water resources. 3). Global Methane Emissions Have Been Constant For More Than 20 Years. While the concentrations of methane in the atmosphere have been leveling off in recent years, our studies show that this is caused by a near constant total global source of methane for the last 20 years or more. This is probably because as some anthropogenic sources have increased, others, such as the rice agriculture source, have fallen. Changes in natural emissions appear small

  20. Exploiting coalbed methane and protecting the global environment

    SciTech Connect (OSTI)

    Yuheng, Gao

    1996-12-31

    The global climate change caused by greenhouse gases (GHGs) emission has received wide attention from all countries in the world. Global environmental protection as a common problem has confronted the human being. As a main component of coalbed methane, methane is an important factor influencing the production safety of coal mine and threatens the lives of miners. The recent research on environment science shows that methane is a very harmful GHG. Although methane gas has very little proportion in the GHGs emission and its stayed period is also very short, it has very obvious impact on the climate change. From the estimation, methane emission in the coal-mining process is only 10% of the total emission from human`s activities. As a clean energy, Methane has mature recovery technique before, during and after the process of mining. Thus, coalbed methane is the sole GHG generated in the human`s activities and being possible to be reclaimed and utilized. Compared with the global greenhouse effect of other GHGs emission abatement, coalbed methane emission abatement can be done in very low cost with many other benefits: (1) to protect global environment; (2) to improve obviously the safety of coal mine; and (3) to obtain a new kind of clean energy. Coal is the main energy in China, and coalbed contains very rich methane. According to the exploration result in recent years, about 30000{approximately}35000 billion m{sup 2} methane is contained in the coalbed below 2000 m in depth. China has formed a good development base in the field of reclamation and utilization of coalbed methane. The author hopes that wider international technical exchange and cooperation in the field will be carried out.

  1. Presentations from the March 27th - 28th Methane Hydrates Advisory...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    the March 27th - 28th Methane Hydrates Advisory Committee Meeting Presentations from the March 27th - 28th Methane Hydrates Advisory Committee Meeting PDF icon International Gas ...

  2. U.S. Coalbed Methane Proved Reserves Sales (Billion Cubic Feet...

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) U.S. Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  3. U.S. Coalbed Methane Proved Reserves New Field Discoveries (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    U.S. Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  4. Texas--RRC District 8A Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    A Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  5. Texas--RRC District 7C Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    C Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  6. Texas--RRC District 7B Coalbed Methane Proved Reserves (Billion...

    U.S. Energy Information Administration (EIA) (indexed site)

    B Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 ... Release Date: 11192015 Next Release Date: 12312016 Referring Pages: Coalbed Methane ...

  7. Methanation process utilizing split cold gas recycle

    DOE Patents [OSTI]

    Tajbl, Daniel G.; Lee, Bernard S.; Schora, Jr., Frank C.; Lam, Henry W.

    1976-07-06

    In the methanation of feed gas comprising carbon monoxide and hydrogen in multiple stages, the feed gas, cold recycle gas and hot product gas is mixed in such proportions that the mixture is at a temperature sufficiently high to avoid carbonyl formation and to initiate the reaction and, so that upon complete reaction of the carbon monoxide and hydrogen, an excessive adiabatic temperature will not be reached. Catalyst damage by high or low temperatures is thereby avoided with a process that utilizes extraordinarily low recycle ratios and a minimum of investment in operating costs.

  8. Colorado Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Colorado Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 12 1990's 26 48 82 125 179 226 274 312 401 432 2000's 451 490 520 488 520 515 477 519 497 498 2010's 533 516 486 444 412 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed

  9. Methane Hydrate Advisory Committee (MHAC) Meeting

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Hydrate Advisory Committee (MHAC) Meeting May 7, 2015 1:00 - 3:00PM (EDT) Via Teleconference MEETING SUMMARY Attached are the meeting agenda and the list of attendees; a quorum of Committee members was present. DFO Welcome and Introductions - Paula A. Gant, DFO The meeting was called to order at 1:00PM EDT by Paula A. Gant, Deputy Assistant Secretary (DAS) for Oil and Gas within the U.S. Department of Energy (DOE) and Designated Federal Officer (DFO) for the Methane Hydrate Advisory Committee

  10. MethaneHydrateRD_FC.indd

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    gas is an important energy resource for the United States, providing nearly one-quarter of total energy use. The Department of Energy's Office of Fossil Energy (FE) has played a major role in developing technologies to help tap new, unconventional sources of natural gas. FOSSIL ENERGY RESEARCH BENEFITS Methane Hydrate R&D "The (DOE) Program has supported and managed a high-quality research portf olio that has enabled signifi cant progress toward the (DOE) Program's long-term

  11. Microbial conversion of biomass to methane

    SciTech Connect (OSTI)

    Chynoweth, D.P.

    1981-01-01

    Laboratory studies have investigated the anaerobic digestion of a variety of feedstocks including sea kelp, water hyacinth, terrestrial herbaceous and woody plants, sewage sludge, municipal solid waste, and biomass-organic waste blends. The results of these and other studies are used to illustrate key factors which influence methane production rates and yields, including feed organic composition, nutrients, inoculum, temperature, retention time, feed concentration, particle size, and mixing. A new process recently developed which combines biological and thermal operations for conversion of biomass to substitute natural gas is described.

  12. Enhanced Microbial Pathways for Methane Production from Oil Shale

    SciTech Connect (OSTI)

    Paul Fallgren

    2009-02-15

    Methane from oil shale can potentially provide a significant contribution to natural gas industry, and it may be possible to increase and continue methane production by artificially enhancing methanogenic activity through the addition of various substrate and nutrient treatments. Western Research Institute in conjunction with Pick & Shovel Inc. and the U.S. Department of Energy conducted microcosm and scaled-up reactor studies to investigate the feasibility and optimization of biogenic methane production from oil shale. The microcosm study involving crushed oil shale showed the highest yield of methane was produced from oil shale pretreated with a basic solution and treated with nutrients. Incubation at 30 C, which is the estimated temperature in the subsurface where the oil shale originated, caused and increase in methane production. The methane production eventually decreased when pH of the system was above 9.00. In the scaled-up reactor study, pretreatment of the oil shale with a basic solution, nutrient enhancements, incubation at 30 C, and maintaining pH at circumneutral levels yielded the highest rate of biogenic methane production. From this study, the annual biogenic methane production rate was determined to be as high as 6042 cu. ft/ton oil shale.

  13. Methane production from grape skins. Final technical report

    SciTech Connect (OSTI)

    Yunghans, W.N.

    1981-10-09

    Methane production from grape pomace was measured for a 50-day digestion period. Gas production was calculated to be 2400 ft/sup 3//10 d/ton at 53% methane content. Microorganisms particularly a fungus which grows on grape pomace and lignin was isolated. Lignin content of pomace was measured at approximately 60%. Lignin is slowly digested and may represent a residue which requires long term digestion. Research is continuing on isolation of anaerobic methane bacteria and codigestion of pomace with enzymes as cellulase and pectinase. The sewage sludge functioned adequately as a mixed source of organisms capable of digesting grape pomace. A sediment from stored grape juice produced significant amounts of methane and represents a nutrient substrate for additional studies on continuous flow methane production. 3 figs.

  14. METHANE AND NITROGEN ABUNDANCES ON PLUTO AND ERIS

    SciTech Connect (OSTI)

    Tegler, S. C.; Cornelison, D. M.; Abernathy, M. R.; Bovyn, M. J.; Burt, J. A.; Evans, D. E.; Maleszewski, C. K.; Thompson, Z.; Grundy, W. M.; Romanishin, W.; Vilas, F. E-mail: David.Cornelison@nau.ed E-mail: wjr@nhn.ou.ed

    2010-12-10

    We present spectra of Eris from the MMT 6.5 m Telescope and Red Channel Spectrograph (5700-9800 A, 5 A pixel{sup -1}) on Mt. Hopkins, AZ, and of Pluto from the Steward Observatory 2.3 m Telescope and Boller and Chivens Spectrograph (7100-9400 A, 2 A pixel{sup -1}) on Kitt Peak, AZ. In addition, we present laboratory transmission spectra of methane-nitrogen and methane-argon ice mixtures. By anchoring our analysis in methane and nitrogen solubilities in one another as expressed in the phase diagram of Prokhvatilov and Yantsevich, and comparing methane bands in our Eris and Pluto spectra and methane bands in our laboratory spectra of methane and nitrogen ice mixtures, we find Eris' bulk methane and nitrogen abundances are {approx}10% and {approx}90% and Pluto's bulk methane and nitrogen abundances are {approx}3% and {approx}97%. Such abundances for Pluto are consistent with values reported in the literature. It appears that the bulk volatile composition of Eris is similar to the bulk volatile composition of Pluto. Both objects appear to be dominated by nitrogen ice. Our analysis also suggests, unlike previous work reported in the literature, that the methane and nitrogen stoichiometry is constant with depth into the surface of Eris. Finally, we point out that our Eris spectrum is also consistent with a laboratory ice mixture consisting of 40% methane and 60% argon. Although we cannot rule out an argon-rich surface, it seems more likely that nitrogen is the dominant species on Eris because the nitrogen ice 2.15 {mu}m band is seen in spectra of Pluto and Triton.

  15. Table 11.3 Methane Emissions, 1980-2009 (Million Metric Tons of Methane)

    U.S. Energy Information Administration (EIA) (indexed site)

    Methane Emissions, 1980-2009 (Million Metric Tons of Methane) Year Energy Sources Waste Management Agricultural Sources Industrial Processes 9 Total 5 Coal Mining Natural Gas Systems 1 Petroleum Systems 2 Mobile Com- bustion 3 Stationary Com- bustion 4 Total 5 Landfills Waste- water Treatment 6 Total 5 Enteric Fermen- tation 7 Animal Waste 8 Rice Cultivation Crop Residue Burning Total 5 1980 3.06 4.42 NA 0.28 0.45 8.20 10.52 0.52 11.04 5.47 2.87 0.48 0.04 8.86 0.17 28.27 1981 2.81 5.02 NA .27

  16. Oxidation of coal-water slurry feed to hydrogasifier

    DOE Patents [OSTI]

    Lee, Bernard S.

    1976-01-01

    An aqueous coal slurry is preheated, subjected to partial oxidation and vaporization by injection of high pressure oxygen and is introduced into a top section of a hydrogasifier in direct contact with hot methane-containing effluent gases where vaporization of the slurry is completed. The resulting solids are reacted in the hydrogasifier and the combined gases and vapors are withdrawn and subjected to purification and methanation to provide pipeline gas. The amount of oxygen injected into the slurry is controlled to provide the proper thermal balance whereby all of the water in the slurry can be evaporated in contact with the hot effluent gases from the hydrogasifier.

  17. Methane Recovery from Hydrate-bearing Sediments

    SciTech Connect (OSTI)

    J. Carlos Santamarina; Costas Tsouris

    2011-04-30

    Gas hydrates are crystalline compounds made of gas and water molecules. Methane hydrates are found in marine sediments and permafrost regions; extensive amounts of methane are trapped in the form of hydrates. Methane hydrate can be an energy resource, contribute to global warming, or cause seafloor instability. This study placed emphasis on gas recovery from hydrate bearing sediments and related phenomena. The unique behavior of hydrate-bearing sediments required the development of special research tools, including new numerical algorithms (tube- and pore-network models) and experimental devices (high pressure chambers and micromodels). Therefore, the research methodology combined experimental studies, particle-scale numerical simulations, and macro-scale analyses of coupled processes. Research conducted as part of this project started with hydrate formation in sediment pores and extended to production methods and emergent phenomena. In particular, the scope of the work addressed: (1) hydrate formation and growth in pores, the assessment of formation rate, tensile/adhesive strength and their impact on sediment-scale properties, including volume change during hydrate formation and dissociation; (2) the effect of physical properties such as gas solubility, salinity, pore size, and mixed gas conditions on hydrate formation and dissociation, and it implications such as oscillatory transient hydrate formation, dissolution within the hydrate stability field, initial hydrate lens formation, and phase boundary changes in real field situations; (3) fluid conductivity in relation to pore size distribution and spatial correlation and the emergence of phenomena such as flow focusing; (4) mixed fluid flow, with special emphasis on differences between invading gas and nucleating gas, implications on relative gas conductivity for reservoir simulations, and gas recovery efficiency; (5) identification of advantages and limitations in different gas production strategies with

  18. Studying methane migration mechanisms at Walker Ridge, Gulf of Mexico, via 3D methane hydrate reservoir modeling

    SciTech Connect (OSTI)

    Nole, Michael; Daigle, Hugh; Mohanty, Kishore; Cook, Ann; Hillman, Jess

    2015-12-15

    We have developed a 3D methane hydrate reservoir simulator to model marine methane hydrate systems. Our simulator couples highly nonlinear heat and mass transport equations and includes heterogeneous sedimentation, in-situ microbial methanogenesis, the influence of pore size contrast on solubility gradients, and the impact of salt exclusion from the hydrate phase on dissolved methane equilibrium in pore water. Using environmental parameters from Walker Ridge in the Gulf of Mexico, we first simulate hydrate formation in and around a thin, dipping, planar sand stratum surrounded by clay lithology as it is buried to 295mbsf. We find that with sufficient methane being supplied by organic methanogenesis in the clays, a 200x pore size contrast between clays and sands allows for a strong enough concentration gradient to significantly drop the concentration of methane hydrate in clays immediately surrounding a thin sand layer, a phenomenon that is observed in well log data. Building upon previous work, our simulations account for the increase in sand-clay solubility contrast with depth from about 1.6% near the top of the sediment column to 8.6% at depth, which leads to a progressive strengthening of the diffusive flux of methane with time. By including an exponentially decaying organic methanogenesis input to the clay lithology with depth, we see a decrease in the aqueous methane supplied to the clays surrounding the sand layer with time, which works to further enhance the contrast in hydrate saturation between the sand and surrounding clays. Significant diffusive methane transport is observed in a clay interval of about 11m above the sand layer and about 4m below it, which matches well log observations. The clay-sand pore size contrast alone is not enough to completely eliminate hydrate (as observed in logs), because the diffusive flux of aqueous methane due to a contrast in pore size occurs slower than the rate at which methane is supplied via organic methanogenesis

  19. Lower 48 States Coalbed Methane Proved Reserves New Field Discoveries

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) States Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane New Field Discoveries Lower 48 States Coalbed Methane Proved Reserves,

  20. New Mexico Coalbed Methane Proved Reserves New Field Discoveries (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane New Field Discoveries New Mexico Coalbed Methane Proved Reserves, Reserves

  1. Alaska (with Total Offshore) Coalbed Methane Production (Billion Cubic

    Gasoline and Diesel Fuel Update

    Feet) Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Alaska Coalbed Methane Proved Reserves, Reserves Changes, and Production Coalbed Methane Production

  2. California (with State off) Coalbed Methane Production (Billion Cubic Feet)

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production California Coalbed Methane Proved Reserves, Reserves Changes, and Production Coalbed Methane Production

  3. California (with State off) Coalbed Methane Proved Reserves (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 California Coalbed Methane

  4. California - Coastal Region Coalbed Methane Proved Reserves (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 CA, Coastal Region Onshore Coalbed Methane Proved Reserves, Reserves Changes, and

  5. California - Los Angeles Basin Onshore Coalbed Methane Proved Reserves

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 CA, Los Angeles Basin Onshore Coalbed Methane Proved Reserves,

  6. California--State Offshore Coalbed Methane Proved Reserves (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 CA, State Offshore Coalbed Methane Proved Reserves, Reserves

  7. Federal Offshore California Coalbed Methane Proved Reserves (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Federal Offshore California Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Federal Offshore, Pacific (California) Coalbed Methane

  8. Methane recovery from animal manures: A current opportunities casebook

    SciTech Connect (OSTI)

    1995-08-01

    This Casebook examines some of the current opportunities for the recovery of methane from the anaerobic digestion of animal manures US livestock operations currently employ four types of anaerobic digester technology: Slurry, plug flow, complete mix, and covered lagoon. An introduction to the engineering economies of these technologies is provided, and possible end-use applications for the methane gas generated by the digestion process are discussed. The economic evaluations are based on engineering studies of digesters that generate electricity from the recovered methane. Regression models, which can be used to estimate digester cost and internal rate of return, are developed from the evaluations.

  9. Wyoming Coalbed Methane Proved Reserves New Field Discoveries (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane New Field Discoveries Wyoming Coalbed Methane Proved Reserves, Reserves

  10. Oklahoma Coalbed Methane Proved Reserves New Field Discoveries (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane New Field Discoveries Oklahoma Coalbed Methane Proved Reserves, Reserves

  11. Utah Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Coalbed Methane Proved Reserves New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane New Field Discoveries Utah Coalbed Methane Proved Reserves, Reserves Changes, and Production

  12. Louisiana (with State Offshore) Coalbed Methane Production (Billion Cubic

    Gasoline and Diesel Fuel Update

    Feet) Production (Billion Cubic Feet) Louisiana (with State Offshore) Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 1 1 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Louisiana Coalbed Methane Proved

  13. Mississippi (with State off) Coalbed Methane Production (Billion Cubic

    Gasoline and Diesel Fuel Update

    Feet) Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production Mississippi Coalbed Methane Proved Reserves, Reserves Changes, and Production Coalbed Methane Production

  14. Economic analysis of vertical wells for coalbed methane recovery

    SciTech Connect (OSTI)

    Not Available

    1981-04-01

    Previous economic studies of the recovery and utilization of methane from coalbeds using vertical wells were based on drainage in advance of mining where a single seam is drained with well spacing designed for rapid predrainage. This study extends the earlier work and shows that methane recovery costs can be reduced significantly by increasing well spacing and draining multiple coalbeds. A favorable return on investment can be realized in many geologic settings using this method. Sensitivity of recovery economics to certain development costs and parametric variations are also examined as are the economics of three methane utilization options.

  15. The Secretary of Energy Advisory Board (SEAB) Task Force on Methane

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Hydrates | Department of Energy Methane Hydrates The Secretary of Energy Advisory Board (SEAB) Task Force on Methane Hydrates The Secretary of Energy Advisory Board (SEAB) Task Force on Methane Hydrates is composed of SEAB members and independent experts charged with recommending a framework for DOE methane hydrate research programs. Purpose of the Task Force: The purpose of this task force is to provide a framework for DOE's pre-commercial methane hydrate research effort, in particular, the

  16. Emissions of greenhouse gases in the United States 1995

    SciTech Connect (OSTI)

    1996-10-01

    This is the fourth Energy Information Administration (EIA) annual report on US emissions of greenhouse gases. This report presents estimates of US anthropogenic (human-caused) emissions of carbon dioxide, methane, nitrous oxide, and several other greenhouse gases for 1988 through 1994. Estimates of 1995 carbon dioxide, nitrous oxide, and halocarbon emissions are also provided, although complete 1995 estimates for methane are not yet available. Emissions of carbon dioxide increased by 1.9% from 1993 to 1994 and by an additional 0.8% from 1994 to 1995. Most carbon dioxide emissions are caused by the burning of fossil fuels for energy consumption, which is strongly related to economic growth, energy prices, and weather. The US economy grew rapidly in 1994 and slowed in 1995. Estimated emissions of methane increased slightly in 1994, as a result of a rise in emissions from energy and agricultural sources. Estimated nitrous oxide emissions increased by 1.8% in 1995, primarily due to increased use of nitrogen fertilizers and higher output of chemicals linked to nitrous oxide emissions. Estimated emissions of hydrofluorocarbons (HFCs) and perfluorocarbons (PFCs), which are known to contribute to global warming, increased by nearly 11% in 1995, primarily as a result of increasing substitution for chlorofluorocarbons (CFCs). With the exception of methane, the historical emissions estimates presented in this report are only slightly revised from those in last year`s report.

  17. Lower 48 States Coalbed Methane Production (Billion Cubic Feet...

    Annual Energy Outlook

    Production (Billion Cubic Feet) Lower 48 States Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's...

  18. West Virginia Coalbed Methane Production (Billion Cubic Feet...

    Annual Energy Outlook

    Production (Billion Cubic Feet) West Virginia Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 30...

  19. Louisiana--North Coalbed Methane Production (Billion Cubic Feet...

    Annual Energy Outlook

    Production (Billion Cubic Feet) Louisiana--North Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's...

  20. Methane storage in advanced porous materials | Center for Gas...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Methane storage in advanced porous materials Previous Next List Trevor A. Makal, Jian-Rong Li, Weigang Lu and Hong-Cai Zhou, Chem. Soc. Rev., 2012,41, 7761-7779 DOI: 10.1039...

  1. Critical Factors Driving the High Volumetric Uptake of Methane...

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    carried out to elucidate the mechanistic reasons for the high volumetric uptake of methane in the metal-organic framework Cu3(btc)2 (btc3- 1,3,5-benzenetricarboxylate; HKUST-1). ...

  2. Commodity chemicals from natural gas by methane chlorination

    SciTech Connect (OSTI)

    Che, S.C.; Minet, R.G.; Giacobbe, F.; Mullick, S.L.

    1987-01-01

    Ethylene and vinyl chloride monomer (VCM) can be produced from natural gas through methane chlorination by reacting methane and chlorine at 900/sup 0/C or higher. Experimental results indicate total ethylene equivalent yield from methane of 45%(wt) and marginal process economics. Fundamental kinetic modeling predicts improved C/sub 2/ yields of up to 70%(wt) at optimum reaction conditions. This optimum condition established the basis for the process design study to evaluate the potential for producing ethylene and VCM from natural gas. HCl by-product is recycled for economic viability. Using the Kel-Chlor process for recycling HCl, the proposed plant produces 27,200 TPA of C/sub 2/H/sub 4/ and 383,800 TPA of VCM. The Midwest is an ethylene consumption area requiring imports of ethylene derivatives from other regions. A methane chlorination plant located on a Midwestern natural gas pipeline network has a good commercial potential.

  3. Texas--RRC District 10 Coalbed Methane Production (Billion Cubic...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Texas--RRC District 10 Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 ...

  4. Texas--RRC District 2 Onshore Coalbed Methane Production (Billion...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Texas--RRC District 2 Onshore Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  5. Texas--RRC District 3 Onshore Coalbed Methane Production (Billion...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) Texas--RRC District 3 Onshore Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  6. New Mexico--West Coalbed Methane Production (Billion Cubic Feet...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) New Mexico--West Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's ...

  7. New Mexico--West Coalbed Methane Proved Reserves (Billion Cubic...

    Annual Energy Outlook

    Proved Reserves (Billion Cubic Feet) New Mexico--West Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  8. New Mexico--East Coalbed Methane Proved Reserves (Billion Cubic...

    Gasoline and Diesel Fuel Update

    Proved Reserves (Billion Cubic Feet) New Mexico--East Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 ...

  9. New Mexico--East Coalbed Methane Production (Billion Cubic Feet...

    Gasoline and Diesel Fuel Update

    Production (Billion Cubic Feet) New Mexico--East Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's ...

  10. Controlling Methane Emissions in the Natural Gas Sector: A Review...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    ... Rather, methane emission reductions from this sector have typically occurred as a co-benefit of policies that target air pollution (such as smog) and improve safety. In general, ...

  11. Biomass Gasification and Methane Digester Property Tax Exemption

    Energy.gov [DOE]

    In order to be eligible for the exemption, methane digester equipment must be certified by the Michigan Department of Agriculture (MDA) and the farm must be verified as compliant under the Michig...

  12. DEVELOPMENT OF IMPROVED CATALYSTS FOR THE SELECTIVE CATALYTIC REDUCTION OF NITROGEN OXIDES WITH HYDROCARBONS

    SciTech Connect (OSTI)

    Dr. Ates Akyurlu; Dr. Jale F. Akyurtlu

    2003-01-28

    Significant work has been done by the investigators on the cerium oxide-copper oxide based sorbent/catalysts for the combined removal of sulfur and nitrogen oxides from the flue gases of stationary sources. A relatively wide temperature window was established for the use of alumina-supported cerium oxide-copper oxide mixtures as regenerable sorbents for SO{sub 2} removal. Evaluation of these sorbents as catalysts for the selective reduction of NO{sub x} gave promising results with methane. Since the replacement of ammonia by methane is commercially very attractive, in this project, it was planned to investigate the effect of promoters on the activity and selectivity of copper oxide/cerium oxide-based catalysts and to obtain data on the reaction mechanism for the SCR with methane. The investigation of the reaction mechanism will help in the selection of promoters to improve the catalytic activity and selectivity of the sorbents in the SCR with methane. This will result in new catalyst formulations. The last component of the project involves our industrial partner TDA Research, and the objective is to evaluate long- term stability and durability of the prepared sorbent/catalysts. In the second year of the project, the catalysts were investigated for their SCR activity with methane in a microreactor setup and also, by the temperature-programmed desorption (TPD) technique. The results from the SCR experiments indicated that manganese is a more effective promoter than rhodium on the supported copper oxide-ceria catalysts under study; the effectiveness of the promoter increases with the increase in Ce/Cu ratio. The TPD profiles of the unpromoted catalyst (Cu/Ce=3) is different than those promoted with 0.1% rhodium. In the current reporting period, the screening of the promoted catalysts were completed, sufficient amount of the selected catalysts were prepared and delivered to TDA for long term deactivation testing.

  13. NREL Research Helps Convert Overabundant Methane into Useful Products |

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    Bioenergy | NREL Research Helps Convert Overabundant Methane into Useful Products March 18, 2016 Photo of a fermentation vessel cultivating our bacteria to produce lactic acid. Using fermentation vessels such as the one pictured here, NREL researchers have discovered how to cultivate genetically engineered methanotrophic bacteria to produce lactic acid, a high-value precursor to bioplastics. Photo by Holly Smith, NREL Methane is Earth's second most abundant greenhouse gas (GHG) after carbon

  14. Impact of mammalian megaherbivores on global methane examined

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    December » Impact of mammalian megaherbivores on global methane examined Impact of mammalian megaherbivores on global methane examined Examining the past consequences of large herbivore loss yields insights into contemporary ecosystem function. December 21, 2015 Artist's depiction of the late Pleistocene landscape with some of the megaherbivores that became extinct. Artist's depiction of the late Pleistocene landscape with some of the megaherbivores that became extinct. Communications Office

  15. Methane Hydrate R&D | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    R&D Methane Hydrate R&D Natural gas is an important energy resource for the United States, providing nearly one-quarter of total energy use. The Department of Energy's Office of Fossil Energy has played a major role in developing technologies to help tap new, unconventional sources of natural gas. Fossil Energy Research Benefits - Methane Hydrate (1.01 MB) More Documents & Publications Idaho Operations AMWTP Fact Sheet Greenpower Trap Mufflerl System CERTIFIED REALTY SPECIALIST

  16. Membrane-augmented cryogenic methane/nitrogen separation

    DOE Patents [OSTI]

    Lokhandwala, K.

    1997-07-15

    A membrane separation process is described which is combined with a cryogenic separation process for treating a gas stream containing methane, nitrogen and at least one other component. The membrane separation process works by preferentially permeating methane and the other component and rejecting nitrogen. The process is particularly useful in removing components such as water, carbon dioxide or C{sub +2} hydrocarbons that might otherwise freeze and plug the cryogenic equipment. 10 figs.

  17. Membrane-augmented cryogenic methane/nitrogen separation

    DOE Patents [OSTI]

    Lokhandwala, Kaaeid

    1997-01-01

    A membrane separation process combined with a cryogenic separation process for treating a gas stream containing methane, nitrogen and at least one other component. The membrane separation process works by preferentially permeating methane and the other component and rejecting nitrogen. The process is particularly useful in removing components such as water, carbon dioxide or C.sub.3+ hydrocarbons that might otherwise freeze and plug the cryogenic equipment.

  18. Miscellaneous States Coalbed Methane Production (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Production (Billion Cubic Feet) Miscellaneous States Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1 1 1 1 1 2010's 1 1 1 3 1 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Estimated Production

  19. Montana Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Montana Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 11 -30 17 10 -3 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  20. Montana Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Montana Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 3 2010's 3 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  1. New Mexico Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's -9 2010's 261 -170 56 41 701 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  2. New Mexico Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 37 2010's 42 80 60 22 68 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  3. Ownership questions can stymie development of coalbed methane

    SciTech Connect (OSTI)

    Counts, R.A. )

    1990-01-01

    Although the technology exists for commercial recovery of coalbed methane, production has been hindered because of the legal quandary as to ownership. The author discusses how claims to ownership of coalbed methane can and have been made by the coal owner or lessee, the oil and gas owner or lessee, the surface owner, or any combination thereof. The federal perspective on this question of ownership is described and several state rulings are assessed.

  4. Arkansas Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 22 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  5. Arkansas Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 1 0 0 0 1 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  6. Arkansas Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 31 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  7. Colorado Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 1,021 0 0 60 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  8. Colorado Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 106 73 181 75 66 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  9. Colorado Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 48 2010's 184 220 22 2 34 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  10. Colorado Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 1,034 0 82 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  11. Methane Hydrate Advisory Committee Meetings | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    Meetings Methane Hydrate Advisory Committee Meetings October 19, 2016 Advisory Committee Meeting Federal Register Notice for October 19, 2016 Meeting Methane Hydrate Committee Meeting Agenda Presentations from the Advisory Committee Meeting May 7, 2015 Advisory Committee Meeting Presentations from the Advisory Committee Meeting May 21, 2014 Committee Recommendations to Secretary of Energy Advisory Committee Meeting Minutes, May 7, 2015 Federal Register Notice for May 7, 2015 Meeting May 15, 2014

  12. Wyoming Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 59 123 36 0 3 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  13. Wyoming Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's -4 2010's 329 98 -32 -84 -50 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  14. Wyoming Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 226 2010's 180 370 80 182 67 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  15. Wyoming Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 111 2010's 82 194 162 0 3 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  16. New Mexico Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 33 2010's 12 221 0 440 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  17. Ohio Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Revision Decreases (Billion Cubic Feet) Ohio Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1 2010's 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  18. Oklahoma Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 11 1 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  19. Oklahoma Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1 2010's 27 27 764 -200 160 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  20. Oklahoma Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 22 2010's 2 1 1 1 21 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  1. Oklahoma Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 6 2010's 6 40 21 3 4 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  2. Pennsylvania Coalbed Methane Proved Reserves Adjustments (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Adjustments (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's -1 1 120 68 8 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  3. Pennsylvania Coalbed Methane Proved Reserves Extensions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Extensions (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 34 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  4. Pennsylvania Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 17 2010's 0 1 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  5. Utah Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 125 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  6. Utah Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 8 9 7 -3 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  7. Utah Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 4 2 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  8. Utah Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 130 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  9. Virginia Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Acquisitions (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 534 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  10. Virginia Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 1 26 49 -12 341 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  11. Virginia Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 302 2010's 30 57 3 71 179 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  12. Virginia Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 334 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  13. West Virginia Coalbed Methane Proved Reserves Sales (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Sales (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 50 17 0 99 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  14. NREL Research Helps Convert Overabundant Methane into Useful Products -

    U.S. Department of Energy (DOE) all webpages (Extended Search)

    News Releases | NREL Research Helps Convert Overabundant Methane into Useful Products March 18, 2016 Photo of a fermentation vessel cultivating our bacteria to produce lactic acid. Using fermentation vessels such as the one pictured here, NREL researchers have discovered how to cultivate genetically engineered methanotrophic bacteria to produce lactic acid, a high-value precursor to bioplastics. Photo by Holly Smith, NREL Methane is Earth's second most abundant greenhouse gas (GHG) after

  15. Kansas Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Kansas Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's -3 2010's -22 -6 53 -35 -24 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  16. Kansas Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Extensions (Billion Cubic Feet) Kansas Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 7 2010's 1 3 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  17. Kentucky Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)

    U.S. Energy Information Administration (EIA) (indexed site)

    Adjustments (Billion Cubic Feet) Kentucky Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 6 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  18. Source Characterization and Temporal Variation of Methane Seepage from Thermokarst Lakes on the Alaska North Slope in Response to Arctic Climate Change

    SciTech Connect (OSTI)

    None, None

    2012-09-30

    reconnaissance surveys provided a strong impetus to visit this area in 2010. The seismic methods applied in Lake Teshekpuk were able to image pockmarks, widespread shallow gas in the sediments, and the relationship among different sediment packages on the lake's bottom, but even boomer seismics did not detect permafrost beneath the northern part of the lake. By characterizing the biogeochemistry of shallow TKL with methane seeps we showed that the radical seasonal shifts in ice cover and temperature. These seasonal environmental differences result in distinct consumption and production processes of biologically-relevant compounds. The combined effects of temperature, ice-volume and other lithological factors linked to seepage from the lake are manifest in the distribution of sedimentary methane in Lake Q during icecovered and ice-free conditions. The biogeochemistry results illustrated very active methanotrophy in TKLs. Substantial effort was subsequently made to characterize the nature of methanotrophic communities in TKLs. We applied stable isotope probing approaches to genetically characterize the methanotrophs most active in utilizing methane in TKLs. Our study is the first to identify methane oxidizing organisms active in arctic TKLs, and revealing that type I methanotrophs and type II methanotrophs are abundant and active in assimilating methane in TKLs. These organisms play an important role in limiting the flux of methane from these sites. Our investigations indicate that as temperatures increase in the Arctic, oxidation rates and active methanotrophic populations will also shift. Whether these changes can offset predicted increases in methanogenesis is an important question underlying models of future methane flux and resultant climate change. Overall our findings indicate that TKLs and their ability to act as both source and sink of methane are exceedingly sensitive to environmental change.

  19. Methods for applying microchannels to separate methane using liquid absorbents, especially ionic liquid absorbents from a mixture comprising methane and nitrogen

    DOE Patents [OSTI]

    Tonkovich, Anna Lee Y.; Litt, Robert D.; Dongming, Qiu; Silva, Laura J.; Lamont, Micheal Jay; Fanelli, Maddalena; Simmons, Wayne W.; Perry, Steven

    2011-10-04

    Methods of using microchannel separation systems including absorbents to improve thermal efficiency and reduce parasitic power loss. Energy is typically added to desorb methane and then energy or heat is removed to absorb methane using a working solution. The working solution or absorbent may comprise an ionic liquid, or other fluids that demonstrate a difference in affinity between methane and nitrogen in a solution.

  20. Thermal and catalytic upgrading of extra heavy crude oil using methane as a source of hydrogen

    SciTech Connect (OSTI)

    Ovalles, C.; Hamana, A.; Bolivar, R.A.

    1995-12-31

    The upgrading of Orinoco-belt extra-heavy crude oil by reaction with methane as a source of hydrogen was studied under thermal and catalytic conditions. The reactions were carried out in a 300-mL batch reactor at 380{degrees}C, 1600 psi of final pressure for a 4-h period. An alumina supported molybdenum-nickel catalyst was used and activated in situ using carbon disulfide at 350{degrees}C and 100 psi of hydrogen for 2 h. In the presence of an alumina supported molybdenum-nickel catalyst, higher percentage of desulfurization (28%) and lower percentage of asphaltenes (9.3%) were found than those found in the absence of the catalysts (11% and 11.8%, respectively). These results indicate that methane is, most probably, activated by the metal catalyst via oxidative addition producing hydrogen and methyl groups adsorbed on the surface. Finally, the observed relative order of reactivity for the thermal and catalytic upgrading of Hamaca crude oil is: H{sub 2} {>=} CH{sub 4} > N{sub 2}.

  1. LANDFILL OPERATION FOR CARBON SEQUESTRATION AND MAXIMUM METHANE EMISSION CONTROL

    SciTech Connect (OSTI)

    Don Augenstein; Ramin Yazdani; Rick Moore; Michelle Byars; Jeff Kieffer; Professor Morton Barlaz; Rinav Mehta

    2000-02-26

    Controlled landfilling is an approach to manage solid waste landfills, so as to rapidly complete methane generation, while maximizing gas capture and minimizing the usual emissions of methane to the atmosphere. With controlled landfilling, methane generation is accelerated to more rapid and earlier completion to full potential by improving conditions (principally moisture, but also temperature) to optimize biological processes occurring within the landfill. Gas is contained through use of surface membrane cover. Gas is captured via porous layers, under the cover, operated at slight vacuum. A field demonstration project has been ongoing under NETL sponsorship for the past several years near Davis, CA. Results have been extremely encouraging. Two major benefits of the technology are reduction of landfill methane emissions to minuscule levels, and the recovery of greater amounts of landfill methane energy in much shorter times, more predictably, than with conventional landfill practice. With the large amount of US landfill methane generated, and greenhouse potency of methane, better landfill methane control can play a substantial role both in reduction of US greenhouse gas emissions and in US renewable energy. The work described in this report, to demonstrate and advance this technology, has used two demonstration-scale cells of size (8000 metric tons [tonnes]), sufficient to replicate many heat and compaction characteristics of larger ''full-scale'' landfills. An enhanced demonstration cell has received moisture supplementation to field capacity. This is the maximum moisture waste can hold while still limiting liquid drainage rate to minimal and safely manageable levels. The enhanced landfill module was compared to a parallel control landfill module receiving no moisture additions. Gas recovery has continued for a period of over 4 years. It is quite encouraging that the enhanced cell methane recovery has been close to 10-fold that experienced with conventional

  2. Field Exploration of Methane Seep Near Atqasuk

    SciTech Connect (OSTI)

    Katey Walter, Dennis Witmer, Gwen Holdmann

    2008-12-31

    Methane (CH{sub 4}) in natural gas is a major energy source in the U.S., and is used extensively on Alaska's North Slope, including the oilfields in Prudhoe Bay, the community of Barrow, and the National Petroleum Reserve, Alaska (NPRA). Smaller villages, however, are dependent on imported diesel fuel for both power and heating, resulting in some of the highest energy costs in the U.S. and crippling local economies. Numerous CH{sub 4} gas seeps have been observed on wetlands near Atqasuk, Alaska (in the NPRA), and initial measurements have indicated flow rates of 3,000-5,000 ft{sup 3} day{sup -1} (60-100 kg CH{sub 4} day{sup -1}). Gas samples collected in 1996 indicated biogenic origin, although more recent sampling indicated a mixture of biogenic and thermogenic gas. In this study, we (1) quantified the amount of CH{sub 4} generated by several seeps and evaluated their potential use as an unconventional gas source for the village of Atqasuk; (2) collected gas and analyzed its composition from multiple seeps several miles apart to see if the source is the same, or if gas is being generated locally from isolated biogenic sources; and (3) assessed the potential magnitude of natural CH{sub 4} gas seeps for future use in climate change modeling.

  3. IN-SITU SAMPLING AND CHARACTERIZATION OF NATURALLY OCCURRING MARINE METHANE HYDRATE USING THE D/V JOIDES RESOLUTION

    SciTech Connect (OSTI)

    Frank R. Rack; Tim Francis; Peter Schultheiss; Philip E. Long; Barry M. Freifeld

    2005-04-01

    The primary activities accomplished during this quarter were continued efforts to develop plans for Phase 2 of this cooperative agreement based on the evolving operational planning for IODP Expedition 311, which will use the JOIDES Resolution to study marine methane hydrates along the Cascadia margin, offshore Vancouver Island. IODP Expedition 311 has been designed to further constrain the models for the formation of marine gas hydrate in subduction zone accretionary prisms. The objectives include characterizing the deep origin of the methane, its upward transport, its incorporation in gas hydrate, and its subsequent loss to the seafloor. The main attention of this expedition is on the widespread seafloor-parallel layer of dispersed gas hydrate located just above the base of the predicted stability field. In a gas hydrate formation model, methane is carried upward through regional sediment or small-scale fracture permeability, driven by the tectonic consolidation of the accretionary prism. The upward moving methane is incorporated into the gas hydrate clathrate as it enters the methane hydrate stability zone. Also important is the focusing of a portion of the upward methane flux into localized plumes or channels to form concentrations of near-seafloor gas hydrate. The amount of gas hydrate in local concentrations near the seafloor is especially important for understanding the response of marine gas hydrate to climate change. The expedition includes coring and downhole measurements at five sites across the Northern Cascadia accretionary prism. The sites will track the history of methane in an accretionary prism from (1) its production by mainly microbiological processes over a thick sediment vertical extent, (2) its upward transport through regional or locally focused fluid flow, (3) its incorporation in the regional hydrate layer above the BSR or in local concentrations at or near the seafloor, (4) methane loss from the hydrate by upward diffusion, and (5) methane

  4. Microbial distributions detected by an oligonucleotide microarray across geochemical zones associated with methane in marine sediments from the Ulleung Basin

    SciTech Connect (OSTI)

    Briggs, Brandon R.; Graw, Michael; Brodie, Eoin L.; Bahk, Jang-Jun; Kim, Sung-Han; Hyun, Jung-Ho; Kim, Ji-Hoon; Torres, Marta; Colwell, Frederick S.

    2013-11-01

    The biogeochemical processes that occur in marine sediments on continental margins are complex; however, from one perspective they can be considered with respect to three geochemical zones based on the presence and form of methane: sulfatemethane transition (SMTZ), gas hydrate stability zone (GHSZ), and free gas zone (FGZ). These geochemical zones may harbor distinct microbial communities that are important in biogeochemical carbon cycles. The objective of this study was to describe the microbial communities in sediments from the SMTZ, GHSZ, and FGZ using molecular ecology methods (i.e. PhyloChip microarray analysis and terminal restriction fragment length polymorphism (T-RFLP)) and examining the results in the context of non-biological parameters in the sediments. Non-metric multidimensional scaling and multi-response permutation procedures were used to determine whether microbial community compositions were significantly different in the three geochemical zones and to correlate samples with abiotic characteristics of the sediments. This analysis indicated that microbial communities from all three zones were distinct from one another and that variables such as sulfate concentration, hydrate saturation of the nearest gas hydrate layer, and depth (or unmeasured variables associated with depth e.g. temperature, pressure) were correlated to differences between the three zones. The archaeal anaerobic methanotrophs typically attributed to performing anaerobic oxidation of methane were not detected in the SMTZ; however, the marine benthic group-B, which is often found in SMTZ, was detected. Within the GHSZ, samples that were typically closer to layers that contained higher hydrate saturation had indicator sequences related to Vibrio-type taxa. These results suggest that the biogeographic patterns of microbial communities in marine sediments are distinct based on geochemical zones defined by methane.

  5. Methane Hydrate Field Program. Development of a Scientific Plan for a Methane Hydrate-Focused Marine Drilling, Logging and Coring Program

    SciTech Connect (OSTI)

    Collett, Tim; Bahk, Jang-Jun; Frye, Matt; Goldberg, Dave; Husebo, Jarle; Koh, Carolyn; Malone, Mitch; Shipp, Craig; Torres, Marta; Myers, Greg; Divins, David; Morell, Margo

    2013-12-31

    This topical report represents a pathway toward better understanding of the impact of marine methane hydrates on safety and seafloor stability and future collection of data that can be used by scientists, engineers, managers and planners to study climate change and to assess the feasibility of marine methane hydrate as a potential future energy resource. Our understanding of the occurrence, distribution and characteristics of marine methane hydrates is incomplete; therefore, research must continue to expand if methane hydrates are to be used as a future energy source. Exploring basins with methane hydrates has been occurring for over 30 years, but these efforts have been episodic in nature. To further our understanding, these efforts must be more regular and employ new techniques to capture more data. This plan identifies incomplete areas of methane hydrate research and offers solutions by systematically reviewing known methane hydrate “Science Challenges” and linking them with “Technical Challenges” and potential field program locations.

  6. Regional analysis of non-methane hydrocarbons and meteorology of the rural southeast United States

    SciTech Connect (OSTI)

    Hagerman, L.M.

    1996-11-01

    Measurements of non-methane hydrocarbons, as well as ozone, meteorological and trace gas data, were made at four rural sites located within the southeastern United States as a part of the Southern Oxidants Study. Fifty-six C2-C10 hydrocarbons were collected from 1200-1300 local time, once every six days from September 1992 through October 1993. The measurements were made in an effort to enhance the understanding of the behavior and trends of ozone and other photochemical oxidants in this region. The light molecular weight alkanes (ethane, propane, n-butane, iso-butane), ethene and acetylene display a seasonal variation with a winter maximum and summer minimum. Isoprene was virtually non-existent during the winter at all sites, and averaged from 9.8 ppbC (Yorkville, GA) to 21.15 ppbC (Centreville, AL) during the summer. The terpene concentration was greatest in the summer with averages ranging between 3.19 ppbC (Centreville, AL) to 6.38 ppbC (Oak Grove, MS), but was also emitted during the winter months, with a range of 1.25 to 1.9 ppbC for all sites. Propylene-equivalent concentrations were calculated to account for differences in reaction rates between the hydroxyl radical and individual hydrocarbons, and to thereby estimate their relative contribution to ozone, especially in regards to the highly reactive biogenic compounds such as isoprene. It was calculated that biogenics represent at least 65% of the total non-methane hydrocarbon sum at these four sites during the summer season when considering propylene-equivalent concentrations. An ozone episode which occurred from July 20 to July 24 1993 was used as an example to show ozone profiles at each of the sites, and to show the effect of synoptic meteorology on high ozone by examining NOAA daily weather maps and climatic data.

  7. Sources of biogenic methane to form marine gas hydrates: In situ production or upward migration?

    SciTech Connect (OSTI)

    Paull, C.K.; Ussler, W. III; Borowski, W.S.

    1993-09-01

    Potential sources of biogenic methane in the Carolina Continental Rise -- Blake Ridge sediments have been examined. Two models were used to estimate the potential for biogenic methane production: (1) construction of sedimentary organic carbon budgets, and (2) depth extrapolation of modern microbial production rates. While closed-system estimates predict some gas hydrate formation, it is unlikely that >3% of the sediment volume could be filled by hydrate from methane produced in situ. Formation of greater amounts requires migration of methane from the underlying continental rise sediment prism. Methane may be recycled from below the base of the gas hydrate stability zone by gas hydrate decomposition, upward migration of the methane gas, and recrystallization of gas hydrate within the overlying stability zone. Methane bubbles may also form in the sediment column below the depth of gas hydrate stability because the methane saturation concentration of the pore fluids decreases with increasing depth. Upward migration of methane bubbles from these deeper sediments can add methane to the hydrate stability zone. From these models it appears that recycling and upward migration of methane is essential in forming significant gas hydrate concentrations. In addition, the depth distribution profiles of methane hydrate will differ if the majority of the methane has migrated upward rather than having been produced in situ.

  8. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Richard Sigal; Kent Newsham; Thomas Williams; Barry Freifeld; Timothy Kneafsey; Carl Sondergeld; Shandra Rai; Jonathan Kwan; Stephen Kirby; Robert Kleinberg; Doug Griffin

    2005-02-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. The work scope drilled and cored a well The Hot Ice No. 1 on Anadarko leases beginning in FY 2003 and completed in 2004. An on-site core analysis laboratory was built and utilized for determining the physical characteristics of the hydrates and surrounding rock. The well was drilled from a new Anadarko Arctic Platform that has a minimal footprint and environmental impact. The final efforts of the project are to correlate geology, geophysics, logs, and drilling and production data and provide this information to scientists developing reservoir models. No gas hydrates were encountered in this well; however, a wealth of information was generated and is contained in this report. The Hot Ice No. 1 well was drilled from the surface to a measured depth of 2300 ft. There was almost 100% core recovery from the bottom of surface casing at 107 ft to total depth. Based on the best estimate of the bottom of the methane hydrate stability zone (which used new data obtained from Hot Ice No. 1 and new analysis of data from adjacent wells), core was recovered over its complete range. Approximately 580 ft of porous, mostly frozen, sandstone and 155 of conglomerate were recovered in the Ugnu Formation and approximately 215 ft of porous sandstone were recovered in the West Sak Formation. There were gas shows in the bottom

  9. Production of methane by anaerobic fermentation of waste materials

    SciTech Connect (OSTI)

    Hitzman, D.O.

    1989-01-17

    This patent describes an apparatus for producing methane by anaerobic fermentation of waste material, comprising: cavity means in the earth for holding a quantity of the waste material; means for covering a quantity of the waste material in the cavity means and thereby separating the quantity of the waste material from the atmosphere; first conduit means communicating between the waste material in the cavity means and a location remote from the cavity means for conveying gas comprising carbon dioxide and methane from the cavity means to the location; gas separation means communicating with the first conduit means at the location for separating carbon dioxide from methane, the first conduit means including at least one pipe having a plurality of apertures therein and disposed in the cavity means extending into and in fluid flow communication with the waste material for receiving gas liberated by the anaerobic fermentation of the waste material and comprising carbon dioxide and methane, through the apertures therein for conveyance via the first conduit means to the gas separation means; second conduit means communicating between the gas separation means and the waste material in the cavity means for conveying carbon dioxide from the gas separation means to the waste material; and third conduit means communicating with the gas separation means for conveying methane from the gas separation means.

  10. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Thomas E. Williams; Keith Millheim; Buddy King

    2004-06-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project is in the final stages of a cost shared partnership between Maurer Technology, Noble Corporation, Anadarko Petroleum, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. The work scope drilled and cored a well The HOT ICE No.1 on Anadarko leases beginning in FY 2003 and completed in 2004. An on-site core analysis laboratory was built and utilized for determining the physical characteristics of the hydrates and surrounding rock. The well was drilled from a new Anadarko Arctic Platform that has a minimal footprint and environmental impact. The final efforts of the project are to correlate geology, geophysics, logs, and drilling and production data and provide this information to scientists developing reservoir models. No gas hydrates were encountered in this well; however, a wealth of information was generated and is contained in this report.

  11. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Thomas E. Williams; Keith Millheim; Bill Liddell

    2005-03-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Oil-field engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in Arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrates agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project is a cost-shared partnership between Maurer Technology, Anadarko Petroleum, Noble Corporation, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to help identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. As part of the project work scope, team members drilled and cored the HOT ICE No. 1 on Anadarko leases beginning in January 2003 and completed in March 2004. Due to scheduling constraints imposed by the Arctic drilling season, operations at the site were suspended between April 21, 2003 and January 30, 2004. An on-site core analysis laboratory was designed, constructed and used for determining physical characteristics of frozen core immediately after it was retrieved from the well. The well was drilled from a new and innovative Anadarko Arctic Platform that has a greatly reduced footprint and environmental impact. Final efforts of the project were to correlate geology, geophysics, logs, and drilling and production data and provide this information to scientists for future hydrate operations. Unfortunately, no gas hydrates were encountered in this well; however, a wealth of information was generated and is

  12. DOE-Sponsored Beaufort Sea Expedition Studies Methane's Role in Global Climate Cycle

    Energy.gov [DOE]

    Washington, D.C. -- Increased understanding of methane's role in the global climate cycle and the potential of methane hydrate as a future energy resource could result from a recent joint research...

  13. Final report for the Iowa Livestock Industry Waste Characterization and Methane Recovery Information Dissemination Project

    SciTech Connect (OSTI)

    Garrison, M.V.; Richard, Thomas L

    2001-11-13

    This report summarizes analytical methods, characterizes Iowa livestock wastes, determines fossil fuel displacement by methane use, assesses the market potential, and offers recommendations for the implementation of methane recovery technologies.

  14. Presentations from June 6-7 2013 Methane Hydrates Advisory Meeting...

    Office of Energy Efficiency and Renewable Energy (EERE) (indexed site)

    June 6-7 2013 Methane Hydrates Advisory Meeting Presentations from June 6-7 2013 Methane Hydrates Advisory Meeting PDF icon ConocoPhillips test results and data analysis PDF icon ...

  15. The Young Planet-mass Ob ject 2M1207b: A cool, cloudy, and methane...

    Office of Scientific and Technical Information (OSTI)

    A cool, cloudy, and methane-poor atmosphere Citation Details In-Document Search Title: The Young Planet-mass Ob ject 2M1207b: A cool, cloudy, and methane-poor atmosphere You ...

  16. Methane activation using Kr and Xe in a dielectric barrier discharge reactor

    SciTech Connect (OSTI)

    Jo, Sungkwon; Lee, Dae Hoon Kim, Kwan-Tae; Kang, Woo Seok; Song, Young-Hoon

    2014-10-15

    Methane has interested many researchers as a possible new energy source, but the high stability of methane causes a bottleneck in methane activation, limiting its practical utilization. To determine how to effectively activate methane using non-thermal plasma, the conversion of methane is measured in a planar-type dielectric barrier discharge reactor using three different noble gases—Ar, Kr, and Xe—as additives. In addition to the methane conversion results at various applied voltages, the discharge characteristics such as electron temperature and electron density were calculated through zero-dimensional calculations. Moreover, the threshold energies of excitation and ionization were used to distinguish the dominant particle for activating methane between electrons, excited atoms, and ionized atoms. From the experiments and calculations, the selection of the additive noble gas is found to affect not only the conversion of methane but also the selectivity of product gases even under similar electron temperature and electron density conditions.

  17. Methane drainage with horizontal boreholes in advance of longwall mining: an analysis. Final report

    SciTech Connect (OSTI)

    Gabello, D.P.; Felts, L.L.; Hayoz, F.P.

    1981-05-01

    The US Department of Energy (DOE) Morgantown Energy Technology Center has implemented a comprehensive program to demonstrate the technical and economic viability of coalbed methane as an energy resource. The program is directed toward solution of technical and institutional problems impeding the recovery and use of large quantities of methane contained in the nation's minable and unminable coalbeds. Conducted in direct support of the DOE Methane Recovery from Coalbeds Project, this study analyzes the economic aspects of a horizontal borehole methane recovery system integrated as part of a longwall mine operation. It establishes relationships between methane selling price and annual mine production, methane production rate, and the methane drainage system capital investment. Results are encouraging, indicating that an annual coal production increase of approximately eight percent would offset all associated drainage costs over the range of methane production rates and capital investments considered.

  18. Dewatering of coalbed methane wells with hydraulic gas pump

    SciTech Connect (OSTI)

    Amani, M.; Juvkam-Wold, H.C.

    1995-12-31

    The coalbed methane industry has become an important source of natural gas production. Proper dewatering of coalbed methane (CBM) wells is the key to efficient gas production from these reservoirs. This paper presents the Hydraulic Gas Pump as a new alternative dewatering system for CBM wells. The Hydraulic Gas Pump (HGP) concept offers several operational advantages for CBM wells. Gas interference does not affect its operation. It resists solids damage by eliminating the lift mechanism and reducing the number of moving parts. The HGP has a flexible production rate and is suitable for all production phases of CBM wells. It can also be designed as a wireline retrievable system. We conclude that the Hydraulic Gas Pump is a suitable dewatering system for coalbed methane wells.

  19. Investigation of Compton profiles of molecular methane and ethane

    SciTech Connect (OSTI)

    Zhao, Xiao-Li; Xu, Long-Quan; Kang, Xu; Liu, Ya-Wei; Ni, Dong-Dong; Zhu, Lin-Fan; Yang, Ke Ma, Yong-Peng; Yan, Shuai

    2015-02-28

    The Compton profiles of methane and ethane molecules have been determined at an incident photon energy of 20 keV based on the third generation synchrotron radiation, and the statistical accuracy of 0.2% is achieved near p{sub z} = 0. The density functional theory with aug-cc-pVTZ basis set was used to calculate the Compton profiles of methane and ethane. The present experimental Compton profiles are in better agreement with the theoretical calculations in the whole p{sub z} region than the previous experimental results, which indicates that the present experimental Compton profiles are accurate enough to serve as the benchmark data for methane and ethane molecules.

  20. Methanation of gas streams containing carbon monoxide and hydrogen

    DOE Patents [OSTI]

    Frost, Albert C.

    1983-01-01

    Carbon monoxide-containing gas streams having a relatively high concentration of hydrogen are pretreated so as to remove the hydrogen in a recoverable form for use in the second step of a cyclic, essentially two-step process for the production of methane. The thus-treated streams are then passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. This active carbon is reacted with said hydrogen removed from the feed gas stream to form methane. The utilization of the CO in the feed gas stream is appreciably increased, enhancing the overall process for the production of relatively pure, low-cost methane from CO-containing waste gas streams.

  1. Benefits and hurdles for biological methane upgrading; NREL (National Renewable Energy Laboratory)

    SciTech Connect (OSTI)

    Fei, Qiang

    2015-09-01

    The presentation will focus on the technical hurdles for bioconversion of methane into chemical and liquid fuel.

  2. Coupling of oxidative dehydrogenation and aromatization reactions of butane

    SciTech Connect (OSTI)

    Xu, Wen-Qing; Suib, S.L. )

    1994-01-01

    Coupling of oxidative dehydrogenation and aromatization of butane by using a dual function catalyst has led to a significant enhancement of the yields (from 25 to 40%) and selectivities to aromatics (from 39 to 64%). Butane is converted to aromatics by using either zinc-promoted [Ga]-ZSM-5 or zinc and gallium copromoted [Fe]-ZSM-5 zeolite as a catalyst. However, the formation of aromatics is severely limited by hydrocracking of butane to methane, ethane, and propane due to the hydrogen formed during aromatization reactions. On the other hand, the oxidative dehydrogenation of butane to butene over molybdate catalysts is found to be accompanied by a concurrent undesirable reaction, i.e., total oxidation. When two of these reactions (oxidative dehydrogenation and aromatization of butane) are coupled by using a dual function catalyst they have shown to complement each other. It is believed that the rate-limiting step for aromatization (butane to butene) is increased by adding an oxidative dehydrogenation catalyst (Ga-Zn-Mg-Mo-O). The formation of methane, ethane, and propane was suppressed due to the removal of hydrogen initially formed as water. Studies of ammonia TPD show that the acidities of [Fe]-ZSM-5 are greatly affected by the existence of metal oxides such as Ga[sub 2]O[sub 3], MgO, ZnO, and MoO[sub 3]. 40 refs., 9 figs., 1 tab.

  3. Lower 48 States Coalbed Methane Proved Reserves Acquisitions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Acquisitions (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 24 2010's 226 1,710 36 42 680 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  4. Lower 48 States Coalbed Methane Proved Reserves Adjustments (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Adjustments (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's -14 2010's 784 -15 1,327 -309 1,796 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  5. Lower 48 States Coalbed Methane Proved Reserves Extensions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Extensions (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 724 2010's 497 736 166 278 395 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  6. Lower 48 States Coalbed Methane Proved Reserves Revision Decreases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Decreases (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 2,486 2010's 2,914 1,668 3,871 1,998 1,020 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision

  7. Lower 48 States Coalbed Methane Proved Reserves Revision Increases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Increases (Billion Cubic Feet) Lower 48 States Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1,563 2010's 2,589 2,071 971 3,123 3,299 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision I

  8. Miscellaneous States Coalbed Methane Proved Reserves Adjustments (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Adjustments (Billion Cubic Feet) Miscellaneous States Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1 2010's 2 3 -2 13 -12 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  9. Miscellaneous States Coalbed Methane Proved Reserves Revision Decreases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Decreases (Billion Cubic Feet) Miscellaneous States Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 24 2010's 2 0 1 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  10. Miscellaneous States Coalbed Methane Proved Reserves Revision Increases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Increases (Billion Cubic Feet) Miscellaneous States Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 1 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  11. Miscellaneous States Coalbed Methane Proved Reserves Sales (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Sales (Billion Cubic Feet) Miscellaneous States Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 1 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  12. Montana Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Montana Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 29 2010's 0 3 28 4 2 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  13. Montana Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Montana Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 23 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  14. New Mexico Coalbed Methane Proved Reserves Acquisitions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Acquisitions (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 2 2010's 0 221 0 42 11 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  15. New Mexico Coalbed Methane Proved Reserves Revision Decreases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Decreases (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 353 2010's 565 279 602 587 532 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  16. ISOTOPIC RATIOS IN TITAN's METHANE: MEASUREMENTS AND MODELING

    SciTech Connect (OSTI)

    Nixon, C. A.; Achterberg, R. K.; Temelso, B.; Vinatier, S.; Bezard, B.; Coustenis, A.; Teanby, N. A.; Mandt, K. E.; Sherrill, C. D.; Irwin, P. G. J.; Jennings, D. E.; Romani, P. N.; Flasar, F. M.

    2012-04-20

    The existence of methane in Titan's atmosphere ({approx}6% level at the surface) presents a unique enigma, as photochemical models predict that the current inventory will be entirely depleted by photochemistry in a timescale of {approx}20 Myr. In this paper, we examine the clues available from isotopic ratios ({sup 12}C/{sup 13}C and D/H) in Titan's methane as to the past atmosphere history of this species. We first analyze recent infrared spectra of CH{sub 4} collected by the Cassini Composite Infrared Spectrometer, measuring simultaneously for the first time the abundances of all three detected minor isotopologues: {sup 13}CH{sub 4}, {sup 12}CH{sub 3}D, and {sup 13}CH{sub 3}D. From these we compute estimates of {sup 12}C/{sup 13}C = 86.5 {+-} 8.2 and D/H = (1.59 {+-} 0.33) Multiplication-Sign 10{sup -4}, in agreement with recent results from the Huygens GCMS and Cassini INMS instruments. We also use the transition state theory to estimate the fractionation that occurs in carbon and hydrogen during a critical reaction that plays a key role in the chemical depletion of Titan's methane: CH{sub 4} + C{sub 2}H {yields} CH{sub 3} + C{sub 2}H{sub 2}. Using these new measurements and predictions we proceed to model the time evolution of {sup 12}C/{sup 13}C and D/H in Titan's methane under several prototypical replenishment scenarios. In our Model 1 (no resupply of CH{sub 4}), we find that the present-day {sup 12}C/{sup 13}C implies that the CH{sub 4} entered the atmosphere 60-1600 Myr ago if methane is depleted by chemistry and photolysis alone, but much more recently-most likely less than 10 Myr ago-if hydrodynamic escape is also occurring. On the other hand, if methane has been continuously supplied at the replenishment rate then the isotopic ratios provide no constraints, and likewise for the case where atmospheric methane is increasing. We conclude by discussing how these findings may be combined with other evidence to constrain the overall history of the atmospheric

  17. Alabama (with State Offshore) Coalbed Methane Proved Reserves Acquisitions

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Acquisitions (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 151 219 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  18. Alabama (with State Offshore) Coalbed Methane Proved Reserves Adjustments

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Adjustments (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 61 -45 21 -166 641 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  19. Alabama (with State Offshore) Coalbed Methane Proved Reserves Extensions

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Extensions (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 21 2010's 29 3 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  20. Alabama (with State Offshore) Coalbed Methane Proved Reserves Revision

    U.S. Energy Information Administration (EIA) (indexed site)

    Decreases (Billion Cubic Feet) Decreases (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 316 2010's 51 86 150 54 40 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves

  1. Alabama (with State Offshore) Coalbed Methane Proved Reserves Revision

    U.S. Energy Information Administration (EIA) (indexed site)

    Increases (Billion Cubic Feet) Increases (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 17 2010's 134 23 16 33 42 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves

  2. Alabama (with State Offshore) Coalbed Methane Proved Reserves Sales

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Sales (Billion Cubic Feet) Alabama (with State Offshore) Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 2 2010's 266 104 0 344 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  3. Arkansas Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 1 3 10 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  4. Arkansas Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Arkansas Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 3 2010's 9 0 1 5 3 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  5. Colorado Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 566 2010's 1,557 367 1,566 1,023 198 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  6. Colorado Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Colorado Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 126 2010's 937 698 343 789 1,162 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  7. California - San Joaquin Basin Onshore Coalbed Methane Proved Reserves

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) San Joaquin Basin Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 CA, San Joaquin Basin Onshore Coalbed

  8. Wyoming Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 725 2010's 140 539 541 105 186 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  9. Wyoming Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Wyoming Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 609 2010's 575 504 242 412 195 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  10. New Mexico Coalbed Methane Proved Reserves Revision Increases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Increases (Billion Cubic Feet) New Mexico Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 443 2010's 562 562 255 1,362 1,389 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  11. New Mexico--East Coalbed Methane Proved Reserves Revision Decreases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Decreases (Billion Cubic Feet) New Mexico--East Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 30 2010's 0 2 117 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  12. New Mexico--East Coalbed Methane Proved Reserves Revision Increases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Increases (Billion Cubic Feet) New Mexico--East Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 72 11 0 71 46 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  13. New Mexico--West Coalbed Methane Proved Reserves Acquisitions (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Acquisitions (Billion Cubic Feet) New Mexico--West Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 2 2010's 0 221 0 42 11 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  14. New Mexico--West Coalbed Methane Proved Reserves Revision Decreases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Decreases (Billion Cubic Feet) New Mexico--West Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 323 2010's 565 277 485 587 532 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision D

  15. New Mexico--West Coalbed Methane Proved Reserves Revision Increases

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Increases (Billion Cubic Feet) New Mexico--West Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 443 2010's 490 551 255 1,291 1,343 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision

  16. Oklahoma Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 216 2010's 84 98 550 12 43 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  17. Oklahoma Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Oklahoma Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 81 2010's 82 91 39 280 89 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  18. Pennsylvania Coalbed Methane Proved Reserves Revision Decreases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Decreases (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 1 2010's 0 2 123 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  19. Pennsylvania Coalbed Methane Proved Reserves Revision Increases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Increases (Billion Cubic Feet) Pennsylvania Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 29 2010's 2 1 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  20. Texas (with State Offshore) Coalbed Methane Proved Reserves Adjustments

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Adjustments (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 92 -16 -37 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  1. Texas (with State Offshore) Coalbed Methane Proved Reserves Extensions

    U.S. Energy Information Administration (EIA) (indexed site)

    (Billion Cubic Feet) Extensions (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 26 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  2. Texas (with State Offshore) Coalbed Methane Proved Reserves Revision

    U.S. Energy Information Administration (EIA) (indexed site)

    Decreases (Billion Cubic Feet) Decreases (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 4 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision

  3. Texas (with State Offshore) Coalbed Methane Proved Reserves Revision

    U.S. Energy Information Administration (EIA) (indexed site)

    Increases (Billion Cubic Feet) Increases (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 30 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision

  4. Texas (with State Offshore) Coalbed Methane Proved Reserves Sales (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Sales (Billion Cubic Feet) Texas (with State Offshore) Coalbed Methane Proved Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 2 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Sales

  5. Utah Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 110 2010's 30 31 134 11 6 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  6. Utah Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 9 2010's 77 46 21 69 68 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  7. Virginia Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 459 199 71 201 9 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  8. Virginia Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Virginia Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 219 2010's 16 87 30 87 243 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  9. West Virginia Coalbed Methane Proved Reserves Acquisitions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Acquisitions (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 5 0 0 0 72 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Acquisitions

  10. West Virginia Coalbed Methane Proved Reserves Adjustments (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Adjustments (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 -1 1 0 -2 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Adjustments

  11. West Virginia Coalbed Methane Proved Reserves Extensions (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Extensions (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 24 2010's 22 0 0 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Extensions

  12. West Virginia Coalbed Methane Proved Reserves Revision Decreases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Decreases (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 38 2010's 25 47 10 1 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  13. West Virginia Coalbed Methane Proved Reserves Revision Increases (Billion

    U.S. Energy Information Administration (EIA) (indexed site)

    Cubic Feet) Increases (Billion Cubic Feet) West Virginia Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 19 2010's 15 35 3 15 3 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  14. Kansas Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Decreases (Billion Cubic Feet) Kansas Coalbed Methane Proved Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 107 2010's 0 14 85 0 0 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Decreases

  15. Kansas Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Increases (Billion Cubic Feet) Kansas Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 8 2010's 157 24 21 71 73 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  16. Kentucky Coalbed Methane Proved Reserves Revision Increases (Billion Cubic

    U.S. Energy Information Administration (EIA) (indexed site)

    Feet) Revision Increases (Billion Cubic Feet) Kentucky Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 2010's 0 0 0 0 1 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 11/19/2015 Next Release Date: 12/31/2016 Referring Pages: Coalbed Methane Reserves Revision Increases

  17. Understanding the nature of methane emission from rice ecosystems as basis of mitigation strategies

    SciTech Connect (OSTI)

    Buendia, L.V.; Neue, H.U.; Wassmann, R.

    1996-12-31

    Methane is considered as an important Greenhouse gas and rice fields are one of the major atmospheric methane sources. The paper aims to develop sampling strategies and formulate mitigation options based on diel (day and night) and seasonal pattern of methane emission. The study was conducted in 4 countries to measure methane flux using an automatic closed chamber system. A 24-hour bihourly methane emissions were continuously obtained during the whole growing season. Daily and seasonal pattern of methane fluxes from different rice ecosystems were evaluated. Diel pattern of methane emission from irrigated rice fields, in all sites, displayed similar pattern from planting to flowering. Fluxes at 0600, 1200, and 1800 h were important components of the total diel flux. A proposed sampling frequency to accurately estimate methane emission within the growing season was designed based on the magnitude of daily flux variation. Total methane emission from different ecosystems follow the order: deepwater rice > irrigated rice > rainfed rice. Application of pig manure increased total emission by 10 times of that without manure. Green manure application increased emission by 49% of that applied only with inorganic fertilizer. Removal of floodwater at 10 DAP and 35 DAP, within a period of 4 days, inhibited production and emission of methane. The level of variation in daily methane emission and seasonal emission pattern provides useful information for accurate determination of methane fluxes. Characterization of seasonal emission pattern as to ecologies, fertilizer amendments, and water management gives an idea of where to focus mitigation strategies for sustainable rice production.

  18. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Thomas E. Williams; Keith Millheim; Bill Liddell

    2004-11-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project is a cost-shared partnership between Maurer Technology, Anadarko Petroleum, Noble Corporation, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to help identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. As part of the project work scope, team members drilled and cored a well (the Hot Ice No. 1) on Anadarko leases beginning in January 2003 and completed in March 2004. Due to scheduling constraints imposed by the Arctic drilling season, operations at the site were suspended between April 21, 2003 and January 30, 2004. An on-site core analysis laboratory was constructed and used for determining physical characteristics of frozen core immediately after it was retrieved from the well. The well was drilled from a new and innovative Anadarko Arctic Platform that has a greatly reduced footprint and environmental impact. Final efforts of the project were to correlate geology, geophysics, logs, and drilling and production data and provide this information to scientists for future hydrate operations. No gas hydrates were encountered in this well; however, a wealth of information was generated and is contained in the

  19. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Steve Runyon; Mike Globe; Kent Newsham; Robert Kleinberg; Doug Griffin

    2005-02-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project was a cost-shared partnership between Maurer Technology, Noble Corporation, Anadarko Petroleum, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. The work scope included drilling and coring a well (Hot Ice No. 1) on Anadarko leases beginning in FY 2003 and completed in 2004. During the first drilling season, operations were conducted at the site between January 28, 2003 to April 30, 2003. The well was spudded and drilled to a depth of 1403 ft. Due to the onset of warmer weather, work was then suspended for the season. Operations at the site were continued after the tundra was re-opened the following season. Between January 12, 2004 and March 19, 2004, the well was drilled and cored to a final depth of 2300 ft. An on-site core analysis laboratory was built and utilized for determining the physical characteristics of the hydrates and surrounding rock. The well was drilled from a new Anadarko Arctic Platform that has a minimal footprint and environmental impact. The final efforts of the project are to correlate geology, geophysics, logs, and drilling and

  20. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Donn McGuire; Steve Runyon; Richard Sigal; Bill Liddell; Thomas Williams; George Moridis

    2005-02-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project is in the final stages of a cost-shared partnership between Maurer Technology, Noble Corporation, Anadarko Petroleum, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. Hot Ice No. 1 was planned to test the Ugnu and West Sak sequences for gas hydrates and a concomitant free gas accumulation on Anadarko's 100% working interest acreage in section 30 of Township 9N, Range 8E of the Harrison Bay quadrangle of the North Slope of Alaska. The Ugnu and West Sak intervals are favorably positioned in the hydrate-stability zone over an area extending from Anadarko's acreage westward to the vicinity of the aforementioned gas-hydrate occurrences. This suggests that a large, north-to-south trending gas-hydrate accumulation may exist in that area. The presence of gas shows in the Ugnu and West Sak reservoirs in wells situated eastward and down dip of the Hot Ice location indicate that a free-gas accumulation may be trapped by gas hydrates. The Hot Ice No. 1 well was designed to core from the surface to the base of the West Sak interval using the revolutionary and new

  1. METHANE HYDRATE PRODUCTION FROM ALASKAN PERMAFROST

    SciTech Connect (OSTI)

    Ali Kadaster; Bill Liddell; Tommy Thompson; Thomas Williams; Michael Niedermayr

    2005-02-01

    Natural-gas hydrates have been encountered beneath the permafrost and considered a nuisance by the oil and gas industry for years. Engineers working in Russia, Canada and the USA have documented numerous drilling problems, including kicks and uncontrolled gas releases, in arctic regions. Information has been generated in laboratory studies pertaining to the extent, volume, chemistry and phase behavior of gas hydrates. Scientists studying hydrate potential agree that the potential is great--on the North Slope of Alaska alone, it has been estimated at 590 TCF. However, little information has been obtained on physical samples taken from actual rock containing hydrates. This gas-hydrate project was a cost-shared partnership between Maurer Technology, Noble Corporation, Anadarko Petroleum, and the U.S. Department of Energy's Methane Hydrate R&D program. The purpose of the project is to build on previous and ongoing R&D in the area of onshore hydrate deposition to identify, quantify and predict production potential for hydrates located on the North Slope of Alaska. The work scope included drilling and coring a well (Hot Ice No. 1) on Anadarko leases beginning in FY 2003 and completed in 2004. During the first drilling season, operations were conducted at the site between January 28, 2003 to April 30, 2003. The well was spudded and drilled to a depth of 1403 ft. Due to the onset of warmer weather, work was then suspended for the season. Operations at the site were continued after the tundra was re-opened the following season. Between January 12, 2004 and March 19, 2004, the well was drilled and cored to a final depth of 2300 ft. An on-site core analysis laboratory was built and implemented for determining physical characteristics of the hydrates and surrounding rock. The well was drilled from a new Anadarko Arctic Platform that has a minimal footprint and environmental impact. Final efforts of the project are to correlate geology, geophysics, logs, and drilling and

  2. Role of metal-support interactions on the activity of Pt and Rh catalysts for reforming methane and butane.

    SciTech Connect (OSTI)

    Rossignol, C.; Krause, T.; Krumpelt, M.

    2002-01-11

    For residential fuel cell systems, reforming of natural gas is one option being considered for providing the H{sub 2} necessary for the fuel cell to operate. Industrially, natural gas is reformed using Ni-based catalysts supported on an alumina substrate, which has been modified to inhibit coke formation. At Argonne National Laboratory, we have developed a new family of catalysts derived from solid oxide fuel cell technology for reforming hydrocarbon fuels to generate H{sub 2}. These catalysts consist of a transition metal supported on an oxide-ion-conducting substrate, such as ceria, that has been doped with a small amount of a non-reducible element, such as gadolinium, samarium, or zirconium. Unlike alumina, the oxide-ion-conducting substrate has been shown to induce strong metal-support interactions. Metal-support interactions are known to play an important role in influencing the catalytic activity of many metals supported on oxide supports. Based on results from temperature-programmed reduction/oxidation and kinetic reaction studies, this paper discusses the role of the metal and the substrate in the metal-support interactions, and how these interactions influence the activity and the selectivity of the catalyst in reforming methane and butane to hydrogen for use in fuel cell power systems.

  3. Oxidation catalysts comprising metal exchanged hexaaluminate wherein the metal is Sr, Pd, La, and/or Mn

    DOE Patents [OSTI]

    Wickham, David; Cook, Ronald

    2008-10-28

    The present invention provides metal-exchanged hexaaluminate catalysts that exhibit good catalytic activity and/or stability at high temperatures for extended periods with retention of activity as combustion catalysts, and more generally as oxidation catalysts, that make them eminently suitable for use in methane combustion, particularly for use in natural gas fired gas turbines. The hexaaluminate catalysts of this invention are of particular interest for methane combustion processes for minimization of the generation of undesired levels (less than about 10 ppm) of NOx species. Metal exchanged hexaaluminate oxidation catalysts are also useful for oxidation of volatile organic compounds (VOC), particularly hydrocarbons. Metal exchanged hexaaluminate oxidation catalysts are further useful for partial oxidation, particularly at high temperatures, of reduced species, particularly hydrocarbons (alkanes and alkenes).

  4. Formation and retention of methane in coal. Final report

    SciTech Connect (OSTI)

    Hucka, V.J.; Bodily, D.M.; Huang, H.

    1992-05-15

    The formation and retention of methane in coalbeds was studied for ten Utah coal samples, one Colorado coal sample and eight coal samples from the Argonne Premium Coal Sample Bank.Methane gas content of the Utah and Colorado coals varied from zero to 9 cm{sup 3}/g. The Utah coals were all high volatile bituminous coals. The Colorado coal was a gassy medium volatile bituminous coal. The Argonne coals cover a range or rank from lignite to low volatile bituminous coal and were used to determine the effect of rank in laboratory studies. The methane content of six selected Utah coal seams and the Colorado coal seam was measured in situ using a special sample collection device and a bubble desorbometer. Coal samples were collected at each measurement site for laboratory analysis. The cleat and joint system was evaluated for the coal and surrounding rocks and geological conditions were noted. Permeability measurements were performed on selected samples and all samples were analyzed for proximate and ultimate analysis, petrographic analysis, {sup 13}C NMR dipolar-dephasing spectroscopy, and density analysis. The observed methane adsorption behavior was correlated with the chemical structure and physical properties of the coals.

  5. Gettering of hydrogen and methane from a helium gas mixture

    SciTech Connect (OSTI)

    Crdenas, Rosa Elia; Stewart, Kenneth D.; Cowgill, Donald F.

    2014-11-01

    In this study, the authors developed an approach for accurately quantifying the helium content in a gas mixture also containing hydrogen and methane using commercially available getters. The authors performed a systematic study to examine how both H{sub 2} and CH{sub 4} can be removed simultaneously from the mixture using two SAES St 172{sup } getters operating at different temperatures. The remaining He within the gas mixture can then be measured directly using a capacitance manometer. The optimum combination involved operating one getter at 650?C to decompose the methane, and the second at 110?C to remove the hydrogen. This approach eliminated the need to reactivate the getters between measurements, thereby enabling multiple measurements to be made within a short time interval, with accuracy better than 1%. The authors anticipate that such an approach will be particularly useful for quantifying the He-3 in mixtures that include tritium, tritiated methane, and helium-3. The presence of tritiated methane, generated by tritium activity, often complicates such measurements.

  6. Texas--RRC District 4 Onshore Coalbed Methane Production (Billion...

    Annual Energy Outlook

    4 Onshore Coalbed Methane Production (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 2000's 0 0 0 0 0 2010's 0 0 0 0 0 - No Data...

  7. Methane-derived hydrocarbons produced under upper-mantle conditions

    SciTech Connect (OSTI)

    Kolesnikov, Anton; Kutcherov, Vladimir G.; Goncharov, Alexander F.

    2009-08-13

    There is widespread evidence that petroleum originates from biological processes. Whether hydrocarbons can also be produced from abiogenic precursor molecules under the high-pressure, high-temperature conditions characteristic of the upper mantle remains an open question. It has been proposed that hydrocarbons generated in the upper mantle could be transported through deep faults to shallower regions in the Earth's crust, and contribute to petroleum reserves. Here we use in situ Raman spectroscopy in laser-heated diamond anvil cells to monitor the chemical reactivity of methane and ethane under upper-mantle conditions. We show that when methane is exposed to pressures higher than 2 GPa, and to temperatures in the range of 1,000-1,500 K, it partially reacts to form saturated hydrocarbons containing 2-4 carbons (ethane, propane and butane) and molecular hydrogen and graphite. Conversely, exposure of ethane to similar conditions results in the production of methane, suggesting that the synthesis of saturated hydrocarbons is reversible. Our results support the suggestion that hydrocarbons heavier than methane can be produced by abiogenic processes in the upper mantle.

  8. Gettering of Hydrogen and Methane from a Helium Gas Mixture

    DOE PAGES-Beta [OSTI]

    Cardenas, Rosa E.; Stewart, Kenneth D.; Cowgill, Donald F.

    2014-10-21

    In our study, the authors developed an approach for accurately quantifying the helium content in a gas mixture also containing hydrogen and methane using commercially available getters. The authors performed a systematic study to examine how both H2 and CH4 can be removed simultaneously from the mixture using two SAES St 172® getters operating at different temperatures. The remaining He within the gas mixture can then be measured directly using a capacitance manometer. Moreover, the optimum combination involved operating one getter at 650°C to decompose the methane, and the second at 110°C to remove the hydrogen. Finally, this approach eliminatedmore » the need to reactivate the getters between measurements, thereby enabling multiple measurements to be made within a short time interval, with accuracy better than 1%. The authors anticipate that such an approach will be particularly useful for quantifying the He-3 in mixtures that include tritium, tritiated methane, and helium-3. The presence of tritiated methane, generated by tritium activity, often complicates such measurements.« less

  9. Gettering of Hydrogen and Methane from a Helium Gas Mixture

    SciTech Connect (OSTI)

    Cardenas, Rosa E.; Stewart, Kenneth D.; Cowgill, Donald F.

    2014-10-21

    In our study, the authors developed an approach for accurately quantifying the helium content in a gas mixture also containing hydrogen and methane using commercially available getters. The authors performed a systematic study to examine how both H2 and CH4 can be removed simultaneously from the mixture using two SAES St 172® getters operating at different temperatures. The remaining He within the gas mixture can then be measured directly using a capacitance manometer. Moreover, the optimum combination involved operating one getter at 650°C to decompose the methane, and the second at 110°C to remove the hydrogen. Finally, this approach eliminated the need to reactivate the getters between measurements, thereby enabling multiple measurements to be made within a short time interval, with accuracy better than 1%. The authors anticipate that such an approach will be particularly useful for quantifying the He-3 in mixtures that include tritium, tritiated methane, and helium-3. The presence of tritiated methane, generated by tritium activity, often complicates such measurements.

  10. Detection and Production of Methane Hydrate

    SciTech Connect (OSTI)

    George Hirasaki; Walter Chapman; Gerald Dickens; Colin Zelt; Brandon Dugan; Kishore Mohanty; Priyank Jaiswal

    2011-12-31

    This project seeks to understand regional differences in gas hydrate systems from the perspective of as an energy resource, geohazard, and long-term climate influence. Specifically, the effort will: (1) collect data and conceptual models that targets causes of gas hydrate variance, (2) construct numerical models that explain and predict regional-scale gas hydrate differences in 2-dimensions with minimal 'free parameters', (3) simulate hydrocarbon production from various gas hydrate systems to establish promising resource characteristics, (4) perturb different gas hydrate systems to assess potential impacts of hot fluids on seafloor stability and well stability, and (5) develop geophysical approaches that enable remote quantification of gas hydrate heterogeneities so that they can be characterized with minimal costly drilling. Our integrated program takes advantage of the fact that we have a close working team comprised of experts in distinct disciplines. The expected outcomes of this project are improved exploration and production technology for production of natural gas from methane hydrates and improved safety through understanding of seafloor and well bore stability in the presence of hydrates. The scope of this project was to more fully characterize, understand, and appreciate fundamental differences in the amount and distribution of gas hydrate and how this would affect the production potential of a hydrate accumulation in the marine environment. The effort combines existing information from locations in the ocean that are dominated by low permeability sediments with small amounts of high permeability sediments, one permafrost location where extensive hydrates exist in reservoir quality rocks and other locations deemed by mutual agreement of DOE and Rice to be appropriate. The initial ocean locations were Blake Ridge, Hydrate Ridge, Peru Margin and GOM. The permafrost location was Mallik. Although the ultimate goal of the project was to understand processes

  11. Mechanistic studies of the reaction of reduced methane monooxygenase hydroxylase with dioxygen and substrates

    SciTech Connect (OSTI)

    Valentine, A.M.; Stahl, S.S.; Lippard, S.J.

    1999-04-28

    Soluble methane monooxygenase (sMMO) catalyzes the oxidation of methane to methanol. Single-turnover reactions of sMMO from Methylococcus capsulatus (Bath) were studied by stopped-flow optical spectroscopy to examine further the activated dioxygen intermediates and their reactions with hydrocarbon substrates. A diiron(III) peroxo species designated H{sub peroxo} is the first intermediate observed in the reaction between the chemically reduced hydroxylase (H{sub red}) and dioxygen. The optical spectrum of this species determined by diode array detection is presented for the first time and exhibits visible absorption bands with {lambda}{sub max} {approx} 420 nm ({epsilon} = 4,000 M{sup {minus}1} cm{sup {minus}1}) and {lambda}{sub max} = 725 nm ({epsilon} = 1,800 M{sup {minus}1} cm{sup {minus}1}). The temperature dependences of the rate constants for formation and decay of H{sub peroxo} and for the subsequent intermediate, Q, were examined in the absence and in the presence of hydrocarbon substrates, and activation parameters for these reactions were determined. For single-turnover reaction kinetics monitored at 420 nm, the {lambda}{sub max} for Q, a nonlinear Eyring plot was obtained when acetylene or methane was present in sufficiently high concentration. This behavior reflects a two-step mechanism, Q formation followed by Q decay, in which the rate-determining step changes depending on the temperature. The rate of H{sub peroxo} formation does not depend on dioxygen concentration, indicating that an effectively irreversible step involving dioxygen precedes formation of the diiron(III) peroxo species. The rate constant observed at 4 C for H{sub peroxo} formation, 1--2 s{sup {minus}1}, is slower than that determined previously by Moessbauer and optical spectroscopy, {approximately}20--25 s{sup {minus}1} (Liu, K. E., et al. J. Am. Chem. Soc. 1995, 117, 4997--4998; 10174--10185). Possible explanations for this discrepancy include the existence of two distinct peroxo

  12. Modeling the impediment of methane ebullition bubbles by seasonal lake ice

    DOE PAGES-Beta [OSTI]

    Greene, S.; Walter Anthony, K. M.; Archer, D.; Sepulveda-Jauregui, A.; Martinez-Cruz, K.

    2014-07-15

    Microbial methane (CH4) ebullition (bubbling) from anoxic lake sediments comprises a globally significant flux to the atmosphere, but ebullition bubbles in temperate and polar lakes can be trapped by winter ice cover and later released during spring thaw. This "ice-bubble storage" (IBS) constitutes a novel mode of CH4 emission. Before bubbles are encapsulated by downward-growing ice, some of their CH4 dissolves into the lake water, where it may be subject to oxidation. We present field characterization and a model of the annual CH4 cycle in Goldstream Lake, a thermokarst (thaw) lake in interior Alaska. We find that summertime ebullition dominatesmore » annual CH4 emissions to the atmosphere. Eighty percent of CH4 in bubbles trapped by ice dissolves into the lake water column in winter, and about half of that is oxidized. The ice growth rate and the magnitude of the CH4 ebullition flux are important controlling factors of bubble dissolution. Seven percent of annual ebullition CH4 is trapped as IBS and later emitted as ice melts. In a future warmer climate, there will likely be less seasonal ice cover, less IBS, less CH4 dissolution from trapped bubbles, and greater CH4 emissions from northern lakes.« less

  13. Modeling the impediment of methane ebullition bubbles by seasonal lake ice

    DOE PAGES-Beta [OSTI]

    Greene, S.; Walter Anthony, K. M.; Archer, D.; Sepulveda-Jauregui, A.; Martinez-Cruz, K.

    2014-12-08

    Microbial methane (CH4) ebullition (bubbling) from anoxic lake sediments comprises a globally significant flux to the atmosphere, but ebullition bubbles in temperate and polar lakes can be trapped by winter ice cover and later released during spring thaw. This "ice-bubble storage" (IBS) constitutes a novel mode of CH4 emission. Before bubbles are encapsulated by downward-growing ice, some of their CH4 dissolves into the lake water, where it may be subject to oxidation. We present field characterization and a model of the annual CH4 cycle in Goldstream Lake, a thermokarst (thaw) lake in interior Alaska. We find that summertime ebullition dominatesmore » annual CH4 emissions to the atmosphere. Eighty percent of CH4 in bubbles trapped by ice dissolves into the lake water column in winter, and about half of that is oxidized. The ice growth rate and the magnitude of the CH4 ebullition flux are important controlling factors of bubble dissolution. Seven percent of annual ebullition CH4 is trapped as IBS and later emitted as ice melts. In a future warmer climate, there will likely be less seasonal ice cover, less IBS, less CH4 dissolution from trapped bubbles, and greater CH4 emissions from northern lakes.« less

  14. State-of-the-art in coalbed methane drilling fluids

    SciTech Connect (OSTI)

    Baltoiu, L.V.; Warren, B.K.; Natras, T.A.

    2008-09-15

    The production of methane from wet coalbeds is often associated with the production of significant amounts of water. While producing water is necessary to desorb the methane from the coal, the damage from the drilling fluids used is difficult to assess, because the gas production follows weeks to months after the well is drilled. Commonly asked questions include the following: What are the important parameters for drilling an organic reservoir rock that is both the source and the trap for the methane? Has the drilling fluid affected the gas production? Are the cleats plugged? Does the 'filtercake' have an impact on the flow of water and gas? Are stimulation techniques compatible with the drilling fluids used? This paper describes the development of a unique drilling fluid to drill coalbed methane wells with a special emphasis on horizontal applications. The fluid design incorporates products to match the delicate surface chemistry on the coal, a matting system to provide both borehole stability and minimize fluid losses to the cleats, and a breaker method of removing the matting system once drilling is completed. This paper also discusses how coal geology impacts drilling planning, drilling practices, the choice of drilling fluid, and completion/stimulation techniques for Upper Cretaceous Mannville-type coals drilled within the Western Canadian Sedimentary Basin. A focus on horizontal coalbed methane (CBM) wells is presented. Field results from three horizontal wells are discussed, two of which were drilled with the new drilling fluid system. The wells demonstrated exceptional stability in coal for lengths to 1000 m, controlled drilling rates and ease of running slotted liners. Methods for, and results of, placing the breaker in the horizontal wells are covered in depth.

  15. Effect of industrial by-products containing electron acceptors on mitigating methane emission during rice cultivation

    SciTech Connect (OSTI)

    Ali, Muhammad Aslam; Lee, Chang Hoon; Kim, Sang Yoon; Kim, Pil Joo

    2009-10-15

    Three industrial by-products (fly ash, phosphogypsum and blast furnace slag), were evaluated for their potential re-use as soil amendments to reduce methane (CH{sub 4}) emission resulting from rice cultivation. In laboratory incubations, CH{sub 4} production rates from anoxic soil slurries were significantly reduced at amendment levels of 0.5%, 1%, 2% and 5% (wt wt{sup -1}), while observed CO{sub 2} production rates were enhanced. The level of suppression in methane production was the highest for phosphogypsum, followed by blast slag and then fly ash. In the greenhouse experiment, CH{sub 4} emission rates from the rice planted potted soils significantly decreased with the increasing levels (2-20 Mg ha{sup -1}) of the selected amendments applied, while rice yield simultaneously increased compared to the control treatment. At 10 Mg ha{sup -1} application level of the amendments, total seasonal CH{sub 4} emissions were reduced by 20%, 27% and 25%, while rice grain yields were increased by 17%, 15% and 23% over the control with fly ash, phosphogypsum, and blast slag amendments, respectively. The suppression of CH{sub 4} production rates as well as total seasonal CH{sub 4} flux could be due to the increased concentrations of active iron, free iron, manganese oxides, and sulfate in the amended soil, which acted as electron acceptors and controlled methanogens' activity by limiting substrates availability. Among the amendments, blast furnace slag and fly ash contributed mainly to improve the soil nutrients balance and increased the soil pH level towards neutral point, but soil acidity was developed with phosphogypsum application. Conclusively, blast slag among the selected amendments would be a suitable soil amendment for reducing CH{sub 4} emissions as well as sustaining rice productivity.

  16. Integrating catalytic coal gasifiers with solid oxide fuel cells

    SciTech Connect (OSTI)

    Siefert, N.; Shamsi, A.; Shekhawat, D.; Berry, D.

    2010-01-01

    A review was conducted for coal gasification technologies that integrate with solid oxide fuel cells (SOFC) to achieve system efficiencies near 60% while capturing and sequestering >90% of the carbon dioxide [1-2]. The overall system efficiency can reach 60% when a) the coal gasifier produces a syngas with a methane composition of roughly 25% on a dry volume basis, b) the carbon dioxide is separated from the methane-rich synthesis gas, c) the methane-rich syngas is sent to a SOFC, and d) the off-gases from the SOFC are recycled back to coal gasifier. The thermodynamics of this process will be reviewed and compared to conventional processes in order to highlight where available work (i.e. exergy) is lost in entrained-flow, high-temperature gasification, and where exergy is lost in hydrogen oxidation within the SOFC. The main advantage of steam gasification of coal to methane and carbon dioxide is that the amount of exergy consumed in the gasifier is small compared to conventional, high temperature, oxygen-blown gasifiers. However, the goal of limiting the amount of exergy destruction in the gasifier has the effect of limiting the rates of chemical reactions. Thus, one of the main advantages of steam gasification leads to one of its main problems: slow reaction kinetics. While conventional entrained-flow, high-temperature gasifiers consume a sizable portion of the available work in the coal oxidation, the consumed exergy speeds up the rates of reactions. And while the rates of steam gasification reactions can be increased through the use of catalysts, only a few catalysts can meet cost requirements because there is often significant deactivation due to chemical reactions between the inorganic species in the coal and the catalyst. Previous research into increasing the kinetics of steam gasification will be reviewed. The goal of this paper is to highlight both the challenges and advantages of integrating catalytic coal gasifiers with SOFCs.

  17. Development of METHANE de-NOX Reburn Process for Wood Waste and Biomass Fired Stoker Boilers - Final Report - METHANE de-NOX Reburn Technology Manual

    SciTech Connect (OSTI)

    J. Rabovitser; B. Bryan; S. Wohadlo; S. Nester; J. Vaught; M. Tartan L. Szymanski; R. Glickert

    2007-12-31

    The overall objective of this project was to demonstrate the effectiveness of the METHANE de-NOX® (MdN) Reburn process in the Forest Products Industry (FPI) to provide more efficient use of wood and sludge waste (biosolids) combustion for both energy generation and emissions reduction (specifically from nitrogen oxides (NOx)) and to promote the transfer of the technology to the wide range of wood waste-fired stoker boilers populating the FPI. This document, MdN Reburn Commercial Technology Manual, was prepared to be a resource to promote technology transfer and commercialization activities of MdN in the industry and to assist potential users understand its application and installation requirements. The Manual includes a compilation of MdN commercial design data from four different stoker boiler designs that were baseline tested as part of the development effort. Design information in the Manual include boiler CFD model studies, process design protocols, engineering data sheets and commercial installation drawings. Each design package is unique and implemented in a manner to meet specific mill requirements.

  18. Synergetic effects of mixed copper-iron oxides oxygen carriers in chemical looping combustion

    SciTech Connect (OSTI)

    Siriwardane, Ranjani; Tian, Hanjing; Simonyi, Thomas; Poston, James

    2013-06-01

    Chemical looping combustion (CLC) is an emerging technology for clean energy production from fuels. CLC produces sequestration-ready CO{sub 2}-streams without a significant energy penalty. Development of efficient oxygen carriers is essential to successfully operate a CLC system. Copper and iron oxides are promising candidates for CLC. Copper oxide possesses high reactivity but it has issues with particle agglomeration due to its low melting point. Even though iron oxide is an inexpensive oxygen carrier it has a slower reactivity. In this study, mixed metal oxide carriers containing iron and copper oxides were evaluated for coal and methane CLC. The components of CuO and Fe{sub 2}O{sub 3} were optimized to obtain good reactivity while maintaining physical and chemical stability during cyclic reactions for methane-CLC and solid-fuel CLC. Compared with single metal oxygen carriers, the optimized Cu–Fe mixed oxide oxygen carriers demonstrated high reaction rate, better combustion conversion, greater oxygen usage and improved physical stability. Thermodynamic calculations, XRD, TGA, flow reactor studies and TPR experiments suggested that there is a strong interaction between CuO and Fe{sub 2}O{sub 3} contributing to a synergistic effect during CLC reactions. The amount of oxygen release of the mixed oxide carrier in the absence of a fuel was similar to that of the single metal oxides. However, in the presence of fuels, the oxygen consumption and the reaction profiles of the mixed oxide carriers were significantly better than that of the single metal oxides. The nature of the fuel not only influenced the reactivity, but also the final reduction status of the oxygen carriers during chemical looping combustion. Cu oxide of the mixed oxide was fully reduced metallic copper with both coal and methane. Fe oxide of the mixed oxide was fully reduced Fe metal with methane but it was reduced to only FeO with coal. Possible mechanisms of how the presence of CuO enhances the

  19. Oxidation catalyst

    DOE Patents [OSTI]

    Ceyer, Sylvia T.; Lahr, David L.

    2010-11-09

    The present invention generally relates to catalyst systems and methods for oxidation of carbon monoxide. The invention involves catalyst compositions which may be advantageously altered by, for example, modification of the catalyst surface to enhance catalyst performance. Catalyst systems of the present invention may be capable of performing the oxidation of carbon monoxide at relatively lower temperatures (e.g., 200 K and below) and at relatively higher reaction rates than known catalysts. Additionally, catalyst systems disclosed herein may be substantially lower in cost than current commercial catalysts. Such catalyst systems may be useful in, for example, catalytic converters, fuel cells, sensors, and the like.

  20. Methane Recovery from Animal Manures The Current Opportunities Casebook

    SciTech Connect (OSTI)

    Lusk, P.

    1998-09-22

    Growth and concentration of the livestock industry create opportunities for the proper disposal of the large quantities of manures generated at dairy, swine, and poultry farms. Pollutants from unmanaged livestock wastes can degrade the environment, and methane emitted from decomposing manure may contribute to global climate change. One management system not only helps prevent pollution but can also convert a manure problem into a new profit center. Economic evaluations and case studies of operating systems indicate that the anaerobic digestion of livestock manures is a commercially viable conversion technology with considerable potential for providing profitable coproducts, including a cost-effective renewable fuel for livestock production operations. This casebook examines some of the current opportunities for recovering methane from anaerobic digestion animal manures.