Powered by Deep Web Technologies
Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

Methane and Nitrous Oxide: Their Effects on the Terrestrial Climate  

Science Conference Proceedings (OSTI)

Simplified band models are developed for methane (CH4) and nitrous oxide (N2O) bands in the longwave radiation spectrum. The band models are then employed in a radiation model to calculate the seasonally and latitudinally varying contributions of ...

L. Donner; V. Ramanathan

1980-01-01T23:59:59.000Z

2

EMISSIONS OF NITROUS OXIDE AND METHANE FROM CONVENTIONAL AND ALTERNATIVE FUEL MOTOR VEHICLES  

E-Print Network (OSTI)

EMISSIONS OF NITROUS OXIDE AND METHANE FROM CONVENTIONAL AND ALTERNATIVE FUEL MOTOR VEHICLES from motor vehicles because unlike emissions of CO2, which are relatively easy to estimate, emissions-related emissions. In the U.S., for example, emissions of carbon dioxide (CO2) from the production and use of motor

Kammen, Daniel M.

3

Soil–Atmosphere Exchange of Nitrous Oxide, Nitric Oxide, Methane, and Carbon Dioxide in Logged and Undisturbed Forest in the Tapajos National Forest, Brazil  

Science Conference Proceedings (OSTI)

Selective logging is an extensive land use in the Brazilian Amazon region. The soil–atmosphere fluxes of nitrous oxide (N2O), nitric oxide (NO), methane (CH4), and carbon dioxide (CO2) are studied on two soil types (clay Oxisol and sandy loam ...

Michael Keller; Ruth Varner; Jadson D. Dias; Hudson Silva; Patrick Crill; Raimundo Cosme de Oliveira Jr.; Gregory P. Asner

2005-11-01T23:59:59.000Z

4

EIA - Greenhouse Gas Emissions - Nitrous Oxide Emissions  

Annual Energy Outlook 2012 (EIA)

nitrous oxide emisssions from industrial sources, 1990, 2005, 2008, and 2009 4.5. Waste management sources In 2009, treatment of residential and commercial wastewater produced 92...

5

EIA - Greenhouse Gas Emissions - Nitrous Oxide Emissions  

Gasoline and Diesel Fuel Update (EIA)

4. Nitrous Oxide Emissions 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 percent). U.S. nitrous oxide emissions rose from 1990 to 1994, fell from 1994 to 2002, and returned to an upward trajectory from 2003 to 2007, largely as a result of increased use of synthetic fertilizers. Fertilizers are the primary contributor of emissions from nitrogen fertilization of soils, which grew by more than 30 percent from

6

The biogeochemistry of marine nitrous oxide  

E-Print Network (OSTI)

Atmospheric nitrous oxide N?O concentrations have been rising steadily for the past century as a result of human activities. In particular, human perturbation of the nitrogen cycle has increased the N?O production rates ...

Frame, Caitlin H

2011-01-01T23:59:59.000Z

7

Low temperature plasma enhanced chemical vapor deposition of silicon oxide films using disilane and nitrous oxide  

Science Conference Proceedings (OSTI)

Keywords: disilane, low temperature, nitrous oxide, plasma enhanced chemical vapor deposition, silicon oxide

Juho Song; G. S. Lee; P. K. Ajmera

1995-10-01T23:59:59.000Z

8

Process Modeling of Global Soil Nitrous Oxide Emissions  

E-Print Network (OSTI)

Nitrous oxide is an important greenhouse gas and is a major ozone-depleting substance. To understand and

Saikawa, E.

2011-09-01T23:59:59.000Z

9

Spatiotemporal modelling in estimation of nitrous oxide emissions from soil.  

E-Print Network (OSTI)

??Nitrous oxide is a major greenhouse gas emission. The aim of this research was to develop and apply statistical models to characterize the complex spatial… (more)

Huang, Xiaodong

2013-01-01T23:59:59.000Z

10

Selective methane oxidation over promoted oxide catalysts  

DOE Green Energy (OSTI)

Objective was to selectively oxidize methane to C{sub 2} hydrocarbons and to oxygenates, in particular formaldehyde and methanol, in high space time yields under relatively mild reaction conditions. Results in this document are reported under the headings: methane oxidation over silica, methane oxidation over Sr/La{sub 2}O{sub 3} catalysts, and oxidative coupling of methane over sulfate-doped Sr/La{sub 2}O{sub 3} catalysts. 24 refs, 10 figs, 4 tabs.

Klier, K.; Herman, R.G.

1993-12-31T23:59:59.000Z

11

Why Sequence a Methane-Oxidizing Archaean?  

NLE Websites -- All DOE Office Websites (Extended Search)

a Methane-Oxidizing Archaeon? a Methane-Oxidizing Archaeon? Methane is a potent greenhouse gas whose atmospheric concentration has increased significantly because of anthropogenic activities and fluctuated naturally over glacial and interglacial cycles. While the importance of methane in Earth's climate dynamics has been well established, the global processes regulating its oceanic cycling remain poorly understood. Although there are high rates of methane production in many marine sedimentary environments (including a number that have been targeted as petroleum reserves), net methane sources from the ocean to the atmosphere appear to be small. This is due in large part to a biogeochemical process known as the anaerobic oxidation of methane (AOM). Microbially mediated AOM reduces methane flux from ocean to atmosphere, stimulates subsurface microbial

12

Selective methane oxidation over promoted oxide catalysts. Quarterly report, September 1 - November 30, 1995  

DOE Green Energy (OSTI)

The objective of this research is the selective oxidation of methane to C{sub 2}H{sub 4} hydrocarbons and to oxygenates, in particular formaldehyde and methanol. Air, oxygen, or carbon dioxide rather than nitrous oxide, are utilized as the oxidizing gas at high gas hourly space velocity but mild reaction conditions (500-700{degrees}C, 1 atm total pressure). All the investigated processes are catalytic, aiming at minimizing gas phase reactions that are difficult to control. During this quarter, solid state {sup 51}V NMR and double catalyst bed experiments were conducted to demonstrate the unfavorable effect of the presence of bulk crystalline V{sub 2}O{sub 5} in V{sub 2}O{sub 5}-SiO{sub 2} xerogel catalysts on selective oxidation of methane to methanol and formaldehyde. Results are discussed.

Klier, Kamil; Herman, R.G.; Wang, C.B. [USDOE Morgantown Energy Technology Center, WV (United States)

1995-12-31T23:59:59.000Z

13

On-farm Assessment of Nitrogen Fertilizer application to corn on Nitrous Oxide Emissions  

E-Print Network (OSTI)

mitigation of greenhouse gas emissions by agriculture. Nutr.1998. Nitrous oxide emission in three years as affected by2008. Soil-surface gas emissions. p.851-861. In: M.R. Carter

2009-01-01T23:59:59.000Z

14

A kinetics study of the atmospheric pressure CVD reaction of silane and nitrous oxide  

SciTech Connect

A mechanistic study of oxide deposition from silane and nitrous oxide between 495{sup 0}C and 690{sup 0}C was performed in a laminar flow, cool wall reactor. Results indicate the existence of two distinct chemical pathways. At high nitrous oxide concentrations, the deposition reaction is dominated by radical chain chemistry initiated by the decomposition of N/sub 2/O. At lower N/sub 2/O concentrations, the decomposition of silane to form silylene (SiH/sub 2/) initiates the deposition. Studies of the reaction of disilane and nitrous oxide confirmed the role of SiH/sub 2/ in the deposition. Reactions involving SiH/sub 2/ are used to explain the observed growth of sub-stoichiometric oxides under low N/sub 2/O conditions.

Chapple-Sokol, J.D.; Giunta, C.J.; Gordon, R.G. (Harvard Univ., Cambridge, MA (USA). Dept. of Chemistry)

1989-10-01T23:59:59.000Z

15

Selective methane oxidation over promoted oxide catalysts  

DOE Green Energy (OSTI)

Principal accomplishments have been achieved in all three areas of selective catalytic oxidation of methane that have been pursued in this research project. These accomplishments are centered on the development of catalyst systems that produce high space time yields of C{sub 2} hydrocarbon products, formaldehyde, and methanol from methane/air mixtures at moderate temperatures and at ambient pressure. The accomplishments can be summarized as the following: the SO{sub 4}{sup 2{minus}}/SrO/La{sub 2}O{sub 3} catalyst developed here has been further optimized to produce 2 kg of C{sub 2} hydrocarbons/kg catalyst/hr at 550C; V{sub 2}O{sub 5}SiO{sub 2} catalysts have been prepared that produce up to 1.5 kg formaldehyde/kg catalyst/hr at 630C with CO{sub 2} selectivities; and a novel dual bed catalyst system has been designed and tested that produces over 100 g methanol/kg catalyst/hr at 600C.

Klier, K.; Herman, R.G.

1995-06-01T23:59:59.000Z

16

Selective methane oxidation over promoted oxide catalysts. Quarterly report, March--May 1995  

DOE Green Energy (OSTI)

The objective of this research is the selective oxidative coupling of methane to C{sub 2}H{sub 4} hydrocarbons and oxygenates, in particular formaldehyde and methanol. Air, oxygen or carbon dioxide, rather than nitrous oxide will be utilized as the oxidizing gas at high gas hourly space velocity, but mild reaction conditions (500-700 {degrees}C, 1 atm total pressure). All the investigated processes are catalytic, aiming at minimizing gas phase reactions that are difficult to control. The research is divided into the following three tasks: (1) maximizing selective methane oxidation to C{sub 2}H{sub 4} products over promoted Sr/La{sub 2}O{sub 3}; (2) selective methane oxidation to oxygenates; and (3) catalyst characterization and optimization. Task 1 dealt with the preparation, testing, and optimization of acidic promoted lanthana-based catalysts for the synthesis of C{sub 2}H{sub 4} hydrocarbons and is essentially completed. Task 2 aims at the formation and optimization of promoted catalysts for the synthesis of oxygenates, in particular formaldehyde and methanol. Task 3 involves characterization of the most promising catalysts so that optimization can be achieved under Task 2. Accomplishments for this period are presented.

Klier, K.; Herman, R.G.; Wang, Chaun-Bao; Shi, Chunlei; Sun, Qun

1995-08-01T23:59:59.000Z

17

Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core  

NLE Websites -- All DOE Office Websites (Extended Search)

Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core Record from Law Dome, Antarctica Introduction This page provides an introduction and links to records of atmospheric nitrous oxide (N2O) over the last 2000 years, emphasizing large data bases each representing currently active stations. Records in recent decades (time period depending on location) have been obtained from samples of ambient-air at remote locations, which represent changing global atmospheric conditions rather than influences of local sources. The longer (2000-year) record is from the Law Dome ice core in Antarctica. The ice-core record has been merged with modern annual data from Cape Grim, Tasmania to provide a 2000-year time series of annual values. A spline function has been fit to the data to provide a continuous time series of

18

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

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.

Egbert Schwartz

2008-12-15T23:59:59.000Z

19

Nitrous oxide (N?O) isotopic composition in the troposphere : instrumentation, observations at Mace Head, Ireland, and regional modeling  

E-Print Network (OSTI)

Nitrous oxide (N?O) is a significant greenhouse gas and main contributor to stratospheric ozone destruction. Surface measurements of N?O mole fractions have been used to attribute source and sink strengths, but large ...

Potter, Katherine Ellison

2011-01-01T23:59:59.000Z

20

Biomass burning sources of nitrogen oxides, carbon monoxide, and non-methane hydrocarbons  

SciTech Connect

Biomass burning is an important source of many key tropospheric species, including aerosols, carbon dioxide (CO{sub 2}), nitrogen oxides (NO{sub {times}}=NO+NO{sub 2}), carbon monoxide (CO), methane (CH{sub 4}), nitrous oxide (N{sub 2}O), methyl bromide (CH{sub 3}Br), ammonia (NH{sub 3}), non-methane hydrocarbons (NMHCs) and other species. These emissions and their subsequent products act as pollutants and affect greenhouse warming of the atmosphere. One important by-product of biomass burning is tropospheric ozone, which is a pollutant that also absorbs infrared radiation. Ozone is formed when CO, CH{sub 4}, and NMHCs react in the presence of NO{sub {times}} and sunlight. Ozone concentrations in tropical regions (where the bulk of biomass burning occurs) may increase due to biomass burning. Additionally, biomass burning can increase the concentration of nitric acid (HNO{sub 3}), a key component of acid rain.

Atherton, C.S.

1995-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Vibrational Infrared Lifetime of the Anesthetic nitrous oxide gas in solution  

E-Print Network (OSTI)

The lifetime of the asymmetric fundamental stretching 2218 cm$^{-1}$ vibration of the anesthetic gas nitrous oxide (N$_2$O) dissolved in octanol and olive oil is reported. These solvents are model systems commonly used to assess anesthetic potency. Picosecond time-scale molecular dynamics simulations have suggested that protein dynamics or membrane dynamics play a role in the molecular mechanism of anesthetic action. Ultrafast infrared spectroscopy with 100 fs time resolution is an ideal tool to probe dynamics of anesthetic molecules on such timescales. Pump-probe studies at the peak of the vibrational band yield a lifetime of $55 \\pm 1$ ps in olive oil and $52 \\pm 1 ps$ in octanol. The similarity of lifetimes suggests that energy relaxation of the anesthetic is determined primarily by the hydrophobic nature of the environment, consistent with models of anesthetic action. The results show that nitrous oxide is a good model system for probing anesthetic-solvent interactions using nonlinear infrared spectroscop...

Chieffo, Logan; Shattuck, Jeffrey; Hong, Mi K; Ziegler, Lawrence; Erramilli, Shyamsunder

2006-01-01T23:59:59.000Z

22

Nitric oxide reburning with methane  

SciTech Connect

This paper deals with initial findings from the ongoing, three-year DOE program that began on 02/01/1995. The program involves computer simulation studies to aid in planning and conducting a series of experiments that will extend the knowledge of reburning process. The objective of this work is to find nitric oxide reduction effectiveness for various reburning fuels and identify both homogeneous and heterogeneous reaction mechanisms characterizing NO reduction.

Kumpaty, S.K. [Rust Coll., Holly Springs, MS (United States); Subramanian, K. [Subramanian (Kannikeswaran), Houston, TX (United States)

1996-12-31T23:59:59.000Z

23

Methane oxidation over dual redox catalysts  

SciTech Connect

The objective of this research is to develop approaches to direct catalytic oxidation of methane over oxides that are doubly doped with transition metal ions. The desired process aims at employing a double redox mechanism, where one redox couple is utilized for activation of oxygen and another for the trapping of CH{sub 3} radicals. The methyl radicals can either recombine, giving C{sub 2} hydrocarbons, or be converted, via electron transfer reaction, to carbocations. The latter species can react with surface OH{sup {minus}} groups to form methanol or formaldehyde. To choose from several possible catalytic systems, this research initially involved the characterization of the micromorphology and crystalline dimensions of zinc oxide catalysts doped with Cu, Fe, and Sn by scanning electron microscopy. In addition, the determination of surface composition and oxidation states by X-ray photoelectron spectroscopy was carried out. A newly constructed high temperature catalytic testing system has been calibrated (flow meters and temperature controllers), tested for possible gas leaks and integrated with a gas chromatographic analytical unit. A preliminary catalytic test study over a Cu/Fe/ZnO sample was performed. The following products of the methane coupling reaction was found: C{sub 2}H{sub 6}, C{sub 2}H{sub 4} and H{sub 2}O together with CO{sub 2}. The maximum space time yield of 14 mmol C{sub 2} hydrocarbons/g cat/h was obtained at 848{degrees}C.

Klier, K.; Herman, R.G.; Sojka, Z.

1989-09-01T23:59:59.000Z

24

Decomposition of methane during oxide reduction using Natural gas  

Science Conference Proceedings (OSTI)

Decomposition of methane during oxide reduction using Natural gas · DELIVERING ... Reaction mechanism and reaction rate of Sn evaporation from liquid steel.

25

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

DOE Green Energy (OSTI)

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.

Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. [Westinghouse Savannah River Co., Aiken, SC (United States); Meisel, D. [Argonne National Lab., IL (United States)

1992-07-01T23:59:59.000Z

26

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

DOE Green Energy (OSTI)

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.

Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. (Westinghouse Savannah River Co., Aiken, SC (United States)); Meisel, D. (Argonne National Lab., IL (United States))

1992-01-01T23:59:59.000Z

27

Complete oxidation of methane on palladium catalysts. Final Report  

DOE Green Energy (OSTI)

This is the final report for grant DE-FG02-00ER15026. It summarizes all the accomplishments in these 8 sections: (1) Adaptations on Existing Unit and Construction of New Unit; (2) Turnover Rate and Reaction Orders for the Complete Oxidation of Methane on a Palladium Foil in Excess Dioxygen; (3) Surface area increase on Pd foils after oxidation in excess methane; (4) UV Raman spectroscopic study of hydrogen bonding in gibbsite and bayerite between 93 and 453 K; (5) Coverage of Palladium Catalysts by Oxidized Silicon During Complete Oxidation of Methane; (6) Kinetics of Methane Oxidation under lean conditions over Pd and PdO; (7) An Explanation for the Hysteresis on the Oxidation of Methane; and (8) Structure of Pd(111) after oxidation in O{sub 2}.

Ribeiro, Fabio H.

2003-07-17T23:59:59.000Z

28

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This final project report describes a three-year long EPRI supplemental project entitled "Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions." This EPRI-sponsored project investigated an innovative approach to developing large-scale, cost-effective greenhouse gas (GHG) emissions offsets that potentially can be implemented across broad geographic areas of the United States and internationally.

2009-12-17T23:59:59.000Z

29

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This Technical Update covers the first year of a three-year-long EPRI research project entitled Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production. The report provides a project overview and explains the preliminary results yielded from the first year of on-farm research.

2007-10-30T23:59:59.000Z

30

Non-oxidative conversion of methane with continuous hydorgen removal  

SciTech Connect

The objective is to overcome the restrictions of non-oxidative methane pyrolysis and oxidative coupling of methane by transferring hydrogen across a selective inorganic membrane between methane and air streams, without simultaneous transport of hydrocarbon reactants or products. This will make the overall reaction system exothermic, remove the thermodynamic barrier to high conversion, and eliminate the formation of carbon oxides. Our approach is to couple C-H bond activation and hydrogen removal by passage of hydrogen atoms through a dense ceramic membrane. In our membrane reactor, catalytic methane pyrolysis produces C2+ hydrogen carbons and aromatics on the one side of the membrane and hydrogen is removed through an oxide film and combusted with air on the opposite side. This process leads to a net reaction with the stoichiometry and thermodynamic properties of oxidative coupling, but without contact between the carbon atoms and oxygen species.

Borry, R.W. III [California Univ., Berkeley, CA (United States). Dept. of Chemical Engineering; Iglesia, E. [California Univ., Berkeley, CA (United States). Lawrence Berkeley Lab.

1997-12-31T23:59:59.000Z

31

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This report covers the first two years of a three-year long project entitled "Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions." This EPRI-sponsored project is investigating an innovative approach to developing large-scale and potentially cost-effective greenhouse gas (GHG) emissions offsets that could be implemented across broad geographic areas of the U.S. and internationally. The tools and information developed in this project will broaden the GHG emissions offset ...

2008-11-11T23:59:59.000Z

32

New constraints on methane fluxes and rates of anaerobic methane oxidation in a Gulf of Mexico brine pool via in situ mass spectrometry  

E-Print Network (OSTI)

New constraints on methane fluxes and rates of anaerobic methane oxidation in a Gulf of Mexico Keywords: Methane flux Mass spectrometer Brine pool Methane oxidation Gulf of Mexico a b s t r a c t Deep report direct measurements of methane concentrations made in a Gulf of Mexico brine pool located

Girguis, Peter R.

33

Regional Sources of Nitrous Oxide over the United States: Seasonal Variation and Spatial Distribution  

SciTech Connect

This paper presents top-down constraints on the magnitude, spatial distribution, and seasonality of nitrous oxide (N{sub 2}O) emissions over the central United States. We analyze data from tall towers in 2004 and 2008 using a high resolution Lagrangian particle dispersion model paired with both geostatistical and Bayesian inversions. Our results indicate peak N{sub 2}O emissions in June with a strong seasonal cycle. The spatial distribution of sources closely mirrors data on fertilizer application with particularly large N{sub 2}O sources over the US Cornbelt. Existing inventories for N{sub 2}O predict emissions that differ substantially from the inverse model results in both seasonal cycle and magnitude. We estimate a total annual N{sub 2}O budget over the central US of 0.9-1.2 TgN/yr and an extrapolated budget for the entire US and Canada of 2.1-2.6 TgN/yr. By this estimate, the US and Canada account for 12-15% of the total global N{sub 2}O source or 32-39% of the global anthropogenic source as reported by the Intergovernmental Panel on Climate Change in 2007.

Miller, S. M.; Kort, E. A.; Hirsch, A. I.; Dlugokencky, E. J.; Andrews, A. E.; Xu, X.; Tian, H.; Nehrkorn, T.; Eluszkiewicz, J.; Michalak, A. M.; Wofsy, S. C.

2012-01-01T23:59:59.000Z

34

Combined Steam Reforming and Partial Oxidation of Methane to Synthesis Gas under Electrical Discharge  

E-Print Network (OSTI)

Combined Steam Reforming and Partial Oxidation of Methane to Synthesis Gas under Electrical production from simultaneous steam reforming and partial oxidation of methane using an ac corona discharge and steam reforming has a benefit in terms of balancing the heat load. Methane conversions can be achieved

Mallinson, Richard

35

OXIDATIVE COUPLING OF METHANE USING INORGANIC MEMBRANE REACTORS  

Science Conference Proceedings (OSTI)

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.

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

1998-04-01T23:59:59.000Z

36

Microbial oxidation of methane from old landfills in biofilters  

Science Conference Proceedings (OSTI)

Landfill gas emissions are among the largest sources of the greenhouse gas methane. For this reason, the possibilities of microbial methane degradation in biofilters were investigated. Different filter materials were tested in two experimental plants, a bench-scale plant (total filter volume 51 l) and a pilot plant (total filter volume 4 m{sup 3}). Three months after the beginning of the experiment, very high degradation rates of up to 63 g CH{sub 4}/(m{sup 3}h) were observed in the bench-scale plant at mean methane concentrations of 2.5% v/v and with fine-grained compost as biofilter material. However, the degradation rates of the compost biofilter decreased in the fifth month of the experiment, probably due to the accumulation of exopolymeric substances formed by the microorganisms. A mixture of compost, peat, and wood fibers showed stable and satisfactory degradation rates around 20 g/(m{sup 3}h) at mean concentrations of 3% v/v over a period of one year. In this material, the wood fibers served as a structural material and prevented clogging of the biofilter. Extrapolation of the experimental data indicates that biofilters for methane oxidation have to be at least 100 times the volume of biofilters for odor control to obtain the same cleaning efficiency per unit volume flow of feed gas.

Streese, J.; Stegmann, R

2003-07-01T23:59:59.000Z

37

Mechanisms and controlling characteristics of the catalytic oxidation of methane  

DOE Green Energy (OSTI)

We have demonstrated in this work (1) that methane is readily activated at mild conditions (100[degree]C, 1 torr) over a relatively noble metal, Pd. This was observed using a stepped and kinked Pd(679) crystal (1), and other crystal faces are now being investigated to establish whether the cracking of the C-H bond of methane on Pd is structure sensitive or structure insensitive. Oxygen chemisorption is extremely structure sensitive: weakly bonded, highly reactive oxygen overlayers form on Pd(100) surface (2), while strongly bonded, moderately reactive oxygen overlayers form on Pd(111) and Pd(679). Reaction of the weakly bonded oxygen with surface carbide gives rise to CO[sub 2] over clean Pd(100) but to CO over halogen-doped Pd(100) (3--5). The effect of halogens is primarily ensemble-controlling, or oxygen-supply restricting, but long range influence of surface Cl on the strength of the Pd-O bond has also been observed (3). Because the overall chemistry of methane activation with the subsequent oxidation gives rise to the very important oxidative reforming CH[sub 4] + 1/2 O[sub 2] [yields][sub Pd/Cl] CO + 2 H[sub 2], Pd/Cl we plan to continue our study of this reaction in detail over Pd(100) (completed), Pd(111) (initiated), Pd(311) (initiated), Pd(110) (to be initiated), and Pd(679) (completed), without and with the halogen modifiers.

Klier, K.; Simmons, G.W.; Herman, R.G.; Miller, A.C.

1992-01-01T23:59:59.000Z

38

Performance comparison between partial oxidation and methane steam reforming processes for solid oxide fuel cell (SOFC) micro combined heat and  

E-Print Network (OSTI)

Performance comparison between partial oxidation and methane steam reforming processes for solid recirculation are used along with steam methane reforming. Further Steam Methane Reforming process produces Cell fueled by natural gas with two different types of pre-reforming systems, namely Steam Reforming

Liso, Vincenzo

39

APPENDIX F: EMISSIONS OF NITROUS OXIDE AND METHANE FROM ALTERNATIVE FUELS FOR MOTOR  

E-Print Network (OSTI)

for Improving Efficiency and Versatility of Dye-Sensitized Solar Cells ... PM 307 (Convention Center ) Pisist The operation and efficiency of dye-sensitized solar cells (DSSCs) ... Macromolecular Crowding Effects by Supported Wox/SiO2 Catalysts ... Center ) Israel E. Wachs1, Soe Lwin1, Wu Zhou2, Chris K. Kiely3, Nikolaos

Delucchi, Mark

40

Application of the GRI 1.2 methane oxidation model to methane and methanol oxidation in supercritical water  

SciTech Connect

The GRI 1.2 mechanism is used to predict the oxidation rates of methane and methanol by oxygen in supercritical water at 250 bar and temperatures ranging from 420--630 C. Using the Chemkin II computational package which assumes an ideal gas equation of state, the GRI model does very well in representing the available experimental results on methane over a wide temperature and concentration rate. However, the model may lack key CH{sub 3}O{sub 2} reactions needed for a complete description in the < 450 C region. The oxidation of methanol and formation of formaldehyde is not well represented by the GRI mechanism when left unchanged. If two important modifications are made to the reactivity of HO{sub 2}, good agreement with the methanol oxidation results is achieved. This paper illustrates that the carefully-assembled GRI 1.2 mechanism, although designed for conventional combustion conditions, can be successfully extended with very little modification to much lower temperature and extreme pressure conditions. The purpose of this study is to understand the operative chemical kinetics of supercritical water oxidation required for the more efficient application of this technology to treatment of hazardous wastes, obsolete munitions, rocket motors, and chemical warfare agents.

Rice, S.F. [Sandia National Labs., Livermore, CA (United States). Combustion Research Facility

1996-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Production of Organic Oxygenates in the Partial Oxidation of Methane in a Silent Electric Discharge Reactor  

E-Print Network (OSTI)

Significant amounts of these reserves are located in remote areas. Steam reforming to synthesis gasProduction of Organic Oxygenates in the Partial Oxidation of Methane in a Silent Electric Discharge, Room T 335, Norman, Oklahoma 73019 This study on the partial oxidation of methane in a silent electric

Mallinson, Richard

42

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

SciTech Connect

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 and diffusive ingress of atmospheric air. For one material with elevated levels of fine particles and high organic matter content, methane production impeded the quantification of methane oxidation potentials. Regarding the design of landfill cover layers it was concluded that the magnitude of the expected methane load, the texture and expected compaction of the cover material are key variables that need to be known. Based on these, a column study can serve as an appropriate testing system to determine the methane oxidation capacity of a soil intended as landfill cover material.

Rachor, Ingke, E-mail: i.rachor@ifb.uni-hamburg.de [University of Hamburg, Institute of Soil Science, Allende-Platz 2, 20146 Hamburg (Germany); Gebert, Julia; Groengroeft, Alexander; Pfeiffer, Eva-Maria [University of Hamburg, Institute of Soil Science, Allende-Platz 2, 20146 Hamburg (Germany)

2011-05-15T23:59:59.000Z

43

Steady-state and transient catalytic oxidation and coupling of methane  

DOE Green Energy (OSTI)

This project addresses the conversion of methane from natural gas into ethane, ethylene and higher hydrocarbons. Our research explores the mechanistic and practical implications of carrying out the methane oxidative coupling reaction in reactor designs other than conventional packed-beds with co-fed reactants. These alternate reactor designs are needed to prevent the full oxidation of methane, which limits C{sub 2}, yields in methane oxidative coupling reactions. The research strategy focuses on preventing contact between the 0{sub 2} reactant required for favorable overall thermodynamics and the C{sub 2+} products of methane coupling. The behavior of various reactor designs are simulated using detailed kinetic transport models. These simulations have suggested that the best way to prevent high C0{sub 2} yields is to separate the oxygen and hydrocarbon streams altogether. As a result, the project has focused on the experimental demonstration of proton transport membrane reactors for the selective conversion of methane into higher hydrocarbons.

Iglesia, E.; Perry, D.L.; Heinemann, H.

1995-06-01T23:59:59.000Z

44

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production: Experience Validating a New GHG Offset Protocol  

Science Conference Proceedings (OSTI)

This project report describes in part the second phase (years four through six, 2010–2012) of a two-phase, six-year long EPRI-sponsored research project entitled “Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions.” This project investigated an innovative approach to developing large-scale, cost-effective greenhouse gas (GHG) emissions offsets that potentially can be implemented across broad geographic areas of the ...

2013-05-28T23:59:59.000Z

45

Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Proto col for US Midwest Agriculture  

Science Conference Proceedings (OSTI)

Status: Published Citation: Millar, N; Robertson, GP; Grace, PR; Gehl, RJ; and Hoben, JP. 2010. Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Protocol for US Midwest Agriculture. In Journal of Mitigation and Adaptation Strategies for Global Change,Volume 15, Number 2, 2010, pp. 185-204. Link to Journal Publication: See Journal of Mitigation and Adaptation Strategies for Global Change.

2010-09-03T23:59:59.000Z

46

Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Redu ction Protocol for U.S. Midwest Agriculture  

Science Conference Proceedings (OSTI)

Status: Published Citation: Millar, N; Robertson, GP; Grace, PR; Gehl, RJ; and Hoben; JP. 2010. Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Protocol for U.S. Midwest Agriculture. In Mitigation and Adaptation Strategies for Global Change, Volume 15, Number 2, 2010, pp. 185-204. A peer-reviewed journal article that identifies, describes and analyzes socio-economic factors that may encourage or inhibit farmers from participat...

2009-12-17T23:59:59.000Z

47

Selective methane oxidation over promoted oxide catalysts. Topical report, September 8, 1992--September 7, 1996  

DOE Green Energy (OSTI)

The objective of this research was to selectively oxidize methane to C{sub 2} hydrocarbons and to oxygenates, in particular formaldehyde and methanol, in high space time yields using air at the oxidant under milder reaction conditions that heretofore employed over industrially practical oxide catalysts. The research carried out under this US DOE-METC contract was divided into the following three tasks: Task 1, maximizing selective methane oxidation to C{sub 2}{sup +} products over promoted SrO/La{sub 2}O{sub 3} catalysts; Task 2, selective methane oxidation to oxygenates; and Task 3, catalyst characterization and optimization. Principal accomplishments include the following: the 1 wt% SO{sub 4}{sup 2{minus}}/SrO/La{sub 2}O{sub 3} promoted catalyst developed here produced over 2 kg of C{sub 2} hydrocarbons/kg catalyst/hr at 550 C; V{sub 2}O{sub 5}/SiO{sub 2} catalysts have been prepared that produce up to 1.5 kg formaldehyde/kg catalyst/hr at 630 C with low CO{sub 2} selectivities; and a novel dual bed catalyst system has been designed and utilized to produce over 100 g methanol/kg catalyst/hr at 600 C with the presence of steam in the reactant mixture.

Klier, K.; Herman, R.G.

1996-12-31T23:59:59.000Z

48

Oxygen Pathways and Carbon Dioxide Utilization in Methane Partial Oxidation in Ambient Temperature  

E-Print Network (OSTI)

- ronmental impact. Present technology uses steam reforming to produce synthesis gas which is converted into enhance- ment of the carbon balance of methane conversion by reforming with CO2 in order to "recycleOxygen Pathways and Carbon Dioxide Utilization in Methane Partial Oxidation in Ambient Temperature

Mallinson, Richard

49

CH Activation and Oxidation of Methane to Methanol in High Yield...  

NLE Websites -- All DOE Office Websites (Extended Search)

CH Activation and Oxidation of Methane to Methanol in High Yield with Novel Pt Complexes Speaker(s): Roy Periana Date: April 27, 1999 - 12:00pm Location: Bldg. 90 Seminar Host...

50

Steady-state and transient catalytic oxidation and coupling of methane  

DOE Green Energy (OSTI)

Four papers have been published on mechanisms and site requirements for oxidative coupling of methane to ethane and ethylene and on synthesis of thin catalytic films during fiscal 1993. These publications also describe a unique inhibiting effect of water on the rate of undesired full oxidation pathways during oxidative coupling. Five quarterly reports have been written and submitted during the covered period. These findings and recently reported models of surface and gas phase reactions of methane suggest the use of membrane reactors and of cyclic methane decomposition schemes in order to avoid deleterious full oxidation reactions and to increase C{sub 2} yields above 25%. In fiscal 1994, we will proceed with the testing of proton-conducting membranes that we have recently fabricated. We will also continue our emerging effort in cyclic decomposition of methane and scavenging of fragments on supported metal catalysts.

Heinemann, H.; Iglesia, E.; Perry, D.L.

1993-12-31T23:59:59.000Z

51

Scaling methane oxidation: From laboratory incubation experiments to landfill cover field conditions  

SciTech Connect

Evaluating field-scale methane oxidation in landfill cover soils using numerical models is gaining interest in the solid waste industry as research has made it clear that methane oxidation in the field is a complex function of climatic conditions, soil type, cover design, and incoming flux of landfill gas from the waste mass. Numerical models can account for these parameters as they change with time and space under field conditions. In this study, we developed temperature, and water content correction factors for methane oxidation parameters. We also introduced a possible correction to account for the different soil structure under field conditions. These parameters were defined in laboratory incubation experiments performed on homogenized soil specimens and were used to predict the actual methane oxidation rates to be expected under field conditions. Water content and temperature corrections factors were obtained for the methane oxidation rate parameter to be used when modeling methane oxidation in the field. To predict in situ measured rates of methane with the model it was necessary to set the half saturation constant of methane and oxygen, K{sub m}, to 5%, approximately five times larger than laboratory measured values. We hypothesize that this discrepancy reflects differences in soil structure between homogenized soil conditions in the lab and actual aggregated soil structure in the field. When all of these correction factors were re-introduced into the oxidation module of our model, it was able to reproduce surface emissions (as measured by static flux chambers) and percent oxidation (as measured by stable isotope techniques) within the range measured in the field.

Abichou, Tarek, E-mail: abichou@eng.fsu.edu [Florida State University, Tallahassee, FL 32311 (United States); Mahieu, Koenraad; Chanton, Jeff [Florida State University, Tallahassee, FL 32311 (United States); Romdhane, Mehrez; Mansouri, Imane [Unite de Recherche M.A.C.S., Ecole Nationale d'Ingenieurs de Gabes, Route de Medenine, 6029 Gabes (Tunisia)

2011-05-15T23:59:59.000Z

52

Mechanisms and controlling characteristics of the catalytic oxidation of methane  

DOE Green Energy (OSTI)

Progress has included (1) construction and installation of an ultraviolet photoelectron spectrometer (UPS) with power supply and pumping system that has been added as an attachment to the SCIENTA ESCA-300 instrument, (2) modification of the high resolution electron energy loss spectrometer (HREELS) to produce a stable ultra high vacuum (UHV) environment for initial experiments with a Pd(311) single crystal, (3) construction of a separate high vacuum system for preparation of surface doped model catalysts by chemical vapor deposition and pretreatment of a Pd(100) single crystal in this system, (4) carried out detailed experiments of methane activation and oxidation on Pd(679) using a high pressure reaction cell contained in a third ultra high vacuum system, (5) completion of adsorption/desorption studies of H{sub 2}, CO, and O{sub 2} on Pd(679), (6) utilized angle-resolved XPS to probe the diffraction characteristics and structure of the Pd(100) surface, (7) determination of the electronic surface structure of Pd(100) using angle-resolved UPS, and (8) computational analysis of oxygen overlayers on the PD(100) surface. Each of these is discussed in further detail below.

Klier, K.

1990-01-01T23:59:59.000Z

53

GRI methane chemistry program review meeting  

SciTech Connect

Methane is an important greenhouse gas which affects the atmosphere directly by the absorption and re-emission of infrared radiation as well as indirectly, through chemical interactions. Emissions of several important greenhouse gases (GHGS) including methane are increasing, mainly due to human activity. Higher concentrations of these gases in the atmosphere are projected to cause a decrease in the amount of infrared radiation escaping to space, and a subsequent warming of global climate. It is therefore vital to understand not only the causes of increased production of methane and other GHGS, but the effect of higher GHG concentrations on climate, and the possibilities for reductions of these emissions. In GRI-UIUC methane project, the role of methane in climate change and greenhouse gas abatement strategies is being studied using several distinct approaches. First, a detailed treatment of the mechanisms controlling each important methane source and sink, and hence the atmospheric concentration of methane, is being developed for use with the UIUC Integrated Science Assessment Model. The focus of this study is to resolve the factors which determine methane emissions and removal, including human population, land use, energy demand, global temperature, and regional concentrations of the hydroxyl radical, carbon monoxide, nitrous oxides, non-methane hydrocarbons, water vapor, tropospheric and stratospheric ozone.

Dignon, J.; Grant, K.; Grossman, A.; Wuebles, D.; Brasseur, G.; Madronich, S.; Huang, T.; Chang, J.; Lott, B.

1997-02-01T23:59:59.000Z

54

Selective methane oxidation over promoted oxide catalysts. Quarterly report, March 1 - May 31, 1996  

DOE Green Energy (OSTI)

Series of catalysts consisting of MoO{sub 3}, V{sub 2}O{sub 5}, TiO{sub 2}, and SnO{sub 2} impregnated onto oxide supports consisting of SiO{sub 2} (Cab-O-Sil), TiO{sub 2} or SnO{sub 2} were previously prepared and tested for the selective oxidation of methane to oxygenates, and it was found that the V{sub 2}O{sub 5}/SiO{sub 2} catalyst was the most active and most selective toward the formation of formaldehyde. These catalysts have been characterized by laser Raman spectroscopy after dehydration and during the methane oxidation reaction with a CH{sub 4}/02 = 10/1 reaction mixture at 500{degrees}C in a continuous flow in situ reaction cell. With the V{sub 2}O{sub 5}/SiO{sub 2} catalyst (the most active catalyst among those studied), no significant structural changes were revealed by in situ Raman analyses, indicating that the fully oxidized surface sites were related to the high formaldehyde selectivivity. Over the V{sub 2}O{sub 5}/TiO{sub 2} and V{sub 2}O{sub 5}/SnO{sub 2} catalysts, CO and CO{sub 2} were the principal products produced by oxidation of methane. For the first time, in situ Raman analysis clearly showed that for these latter catalysts, the surface vanadium(V) oxide species were partially reduced under the steady-state reaction conditions. The performance of the V{sub 2}O{sub 5}/TiO{sub 2}/SiO{sub 2} catalyst was similar to that of the V{sub 2}O{sub 5}TiO{sub 2} catalyst, consistent with the earlier observation that vanadia was largely bound to the titania overlayer. It appears that formaldehyde selectivity decreased with increasing catalyst reducibility, but no direct correlation of catalyst activity with reductibility was observed.

Klier, K.; Herman, R.G.; Wang, C.-B.

1996-12-31T23:59:59.000Z

55

Effect of fresh green waste and green waste compost on mineral nitrogen, nitrous oxide and carbon dioxide from a Vertisol  

Science Conference Proceedings (OSTI)

Incorporation of organic waste amendments to a horticultural soil, prior to expected risk periods, could immobilise mineral N, ultimately reducing nitrogen (N) losses as nitrous oxide (N{sub 2}O) and leaching. Two organic waste amendments were selected, a fresh green waste (FGW) and green waste compost (GWC) as they had suitable biochemical attributes to initiate N immobilisation into the microbial biomass and organic N forms. These characteristics include a high C:N ratio (FGW 44:1, GWC 35:1), low total N (14%). Both products were applied at 3 t C/ha to a high N (plus N fertiliser) or low N (no fertiliser addition) Vertisol soil in PVC columns. Cumulative N{sub 2}O production over the 28 day incubation from the control soil was 1.5 mg/N{sub 2}O/m{sup 2}, and 11 mg/N{sub 2}O/m{sup 2} from the control + N. The N{sub 2}O emission decreased with GWC addition (P < 0.05) for the high N soil, reducing cumulative N{sub 2}O emissions by 38% by the conclusion of the incubation. Analysis of mineral N concentrations at 7, 14 and 28 days identified that both FGW and GWC induced microbial immobilisation of N in the first 7 days of incubation regardless of whether the soil environment was initially high or low in N; with the FGW immobilising up to 30% of available N. It is likely that the reduced mineral N due to N immobilisation led to a reduced substrate for N{sub 2}O production during the first week of the trial, when soil N{sub 2}O emissions peaked. An additional finding was that FGW + N did not decrease cumulative N{sub 2}O emissions compared to the control + N, potentially due to the fact that it stimulated microbial respiration resulting in anaerobic micro sites in the soil and ultimately N{sub 2}O production via denitrification. Therefore, both materials could be used as post harvest amendments in horticulture to minimise N loss through nitrate-N leaching in the risk periods between crop rotations. The mature GWC has potential to reduce N{sub 2}O, an important greenhouse gas.

Vaughan, Sarah M., E-mail: s.vaughan@uq.edu.au [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia); Dalal, Ram C. [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia); Department of Environment and Resource Management, 80 Meiers Rd., Indooroopilly, QLD 4068 (Australia); Harper, Stephen M. [Department of Employment, Economic Development and Innovation, Warrego Highway, Gatton, QLD 4343 (Australia); Menzies, Neal W. [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia)

2011-08-15T23:59:59.000Z

56

Laser-initiated chain reactions in the partial oxidation of methane  

DOE Green Energy (OSTI)

Using laser photolysis of suitable precursor molecules to produce gas-phase free radicals, we have been studying important kinetic processes in the partial oxidation of methane. Prompt production of a relatively high concentration of free radicals via laser photolysis makes it possible to separate the thermal initiation step from the subsequent chain propagation steps. Since the conditions (temperature, pressure, and mixture composition) for rapid thermal initiation and optimum production may differ, this provides an exciting potential application for laser-induced chemistry where the laser acts as the initiation source. We report our results on the partial oxidation of methane by oxygen at moderate temperatures. A trace amount of acetone is photolyzed at 193 nm a prompt source of methyl radicals in methane-oxygen mixtures. Details of the proposed mechanism are discussed as well as application of the technique to technologies for methane conversion to transportable fuels such as methanol. 15 refs., 6 figs.

Baughcum, S.L.; Oldenborg, R.C.; Danen, W.C.; Streit, G.E.; Rofer, C.

1986-01-01T23:59:59.000Z

57

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

DOE Green Energy (OSTI)

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.

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

1996-02-01T23:59:59.000Z

58

A simulated countercurrent moving-bed chromatographic reactor for the oxidative coupling of methane: Experimental results  

DOE Green Energy (OSTI)

The oxidative coupling reaction of methane (OCM) represents a potential commercial ethylene production route. However, the highest reported yields do not exceed 20%. The methane coupling reaction is accompanied by the undesired conversion of methane to carbon oxides. The relative amount of oxygen and methane along with other parameters, including temperature, determine the favored reaction pathway. High hydrocarbon to oxygen feed ratios give high ethane/ethylene selectivities but at the expense of the hydrocarbon conversion. When the methane to oxygen feed ratio is low, combustion is favored. The simulated countercurrent moving-bed chromatographic reactor (SCMCR) is applied to the OCM. A modified experimental configuration is designed and evaluated. A four-section apparatus, each containing a reaction and two separation columns, is used to quickly separate the reactants and products using the principles of simulated countercurrent flow. Simultaneous reaction and separation of the reactive products column is desired, but unattainable because of an incompatibility between OCM reaction and separation temperatures. Microreactor yields with a samarium oxide catalyst gives yields between 2% and 10%. Yields as high as 50% are observed with the same catalyst and run conditions in the SCMCR. These yields are significantly higher than previously reported values. The effects of temperature, feed switching time, and methane to oxygen feed ratio have been investigated. The reactor, while not fully optimized, does give promise as an alternative production method for ethylene.

Tonkovich, A.L.Y. [Pacific Northwest Lab., Richland, WA (United States); Carr, R.W. [Univ. of Minnesota, Minneapolis, MN (United States). Dept. of Chemical Engineering and Materials Sciences

1994-09-01T23:59:59.000Z

59

Nitrous oxide emissions  

SciTech Connect

The purpose of this paper is to report the effect of key operating parameters, the relative importance of coal type, and the potentially significant coal properties for producing N{sub 2}O emissions in an atmospheric circulating fluidized-bed combustor (CFBC) and pressurized bubbling fluidized-bed combustor (PFBC). The generation of N{sub 2}O emissions is quantified in an empirical model based on the experimental data.

Mann, M.D.; Collings, M.E.; Young, B.C.

1992-12-01T23:59:59.000Z

60

Nitrous oxide emissions  

SciTech Connect

The purpose of this paper is to report the effect of key operating parameters, the relative importance of coal type, and the potentially significant coal properties for producing N[sub 2]O emissions in an atmospheric circulating fluidized-bed combustor (CFBC) and pressurized bubbling fluidized-bed combustor (PFBC). The generation of N[sub 2]O emissions is quantified in an empirical model based on the experimental data.

Mann, M.D.; Collings, M.E.; Young, B.C.

1992-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Kinetics of biological methane oxidation in the presence of non-methane organic compounds in landfill bio-covers  

SciTech Connect

In this experimental program, the effects of non-methane organic compounds (NMOCs) on the biological methane (CH{sub 4}) oxidation process were examined. The investigation was performed on compost experiments incubated with CH{sub 4} and selected NMOCs under different environmental conditions. The selected NMOCs had different concentrations and their effects were tested as single compounds and mixtures of compounds. The results from all experimental sets showed a decrease in CH{sub 4} oxidation capacity of the landfill bio-cover with the increase in NMOCs concentrations. For example, in the experiment using compost with 100% moisture content at 35 deg. C without any NMOCs the V{sub max} value was 35.0 mug CH{sub 4}h{sup -1}g{sub wetwt}{sup -1}. This value was reduced to 19.1 mug CH{sub 4}h{sup -1}g{sub wetwt}{sup -1} when mixed NMOCs were present in the batch reactors under the same environmental conditions. The experimental oxidation rates of CH{sub 4} in the presence of single and mixed NMOCs were modeled using the uncompetitive inhibition model and kinetic parameters, including the dissociation constants, were obtained. Additionally, the degradation rates of the NMOCs and co-metabolic abilities of methanotrophic bacteria were estimated.

Albanna, Muna, E-mail: muna.albanna@gju.edu.j [Department of Civil Engineering, University of Ottawa, 161 Louis Pasteur St., Ottawa, Ontario, K1N 6N5 (Canada); Warith, Mostafa; Fernandes, Leta [Department of Civil Engineering, University of Ottawa, 161 Louis Pasteur St., Ottawa, Ontario, K1N 6N5 (Canada)

2010-02-15T23:59:59.000Z

62

Selective methane oxidation over promoted oxide catalysts. Quarterly report, December 1, 1995--February 29, 1996  

DOE Green Energy (OSTI)

In a systematic study with a CH{sub 4}/air reactant mixture at 600 C and 0.1 MPa, it is demonstrated that among eight Cab-O-Sil supported redox transition metal oxide catalysts, a V{sub 2}O{sub 5}/SiO{sub 2} catalyst exhibited the highest productivities of formaldehyde and methanol. The effect of steam on enhancing the space time yields of the oxygenates was observed with the catalysts that were studied with this third component in the reaction mixture. With the vanadia-containing catalyst, it was shown that a loading of 2 wt% of V{sub 2}O{sub 5} on SiO{sub 2} produced the highest conversion of methane from a CH{sub 4}/air/steam = 4/1/1 reactant mixture and the highest productivities of both CH{sub 3}OH and HCHO. It was also shown that increasing the reactant flow rate (thereby decreasing the contact time) increased the space time yield of methanol but decreased the overall methane conversion level.

Klier, K.; Herman, R.G.; Wang, C.B.; Shi, C.

1996-12-31T23:59:59.000Z

63

TCE degradation by methane-oxidizing cultures grown with various nitrogen sources  

SciTech Connect

Methane-oxidizing microorganisms exhibit great potential for vadose zone bioremediation. This paper reports the effects of supplying nitrogen as nitrate, ammonia, and molecular nitrogen on the growth, trichloroethylene (TCE) degradation capacity, and energy storage capacity of a mixed methane-oxidizing culture. Cells inoculated from a nitrate-supplied methane-oxidizing culture grew fastest while fixing atmospheric nitrogen when oxygen partial pressures were kept less than 8%. Cell growth and methane oxidation were more rapid for ammonia-supplied cells than for nitrate-supplied or nitrogen-fixing cells. However, nitrogen-fixing cells were capable of oxidizing TCE as efficiently as nitrate or ammonia-supplied cells, and they exhibited the highest TCE transformation capacity of all three cultures both with and without formate as an exogenous reducing energy source. The TCE product toxicity was not as pronounced for the nitrogen fixing cells as for the nitrate- or ammonia-supplied cells after exposure to high (20 mg/L) or low (2 mg/L) TCE concentrations. Energy storage in the form of poly-{beta}- hydroxybutyrate was 20% to 30% higher for nitrogen-fixing cells; increased energy storage may be responsible for the higher transformation capacity of nitrogen-fixing cells when no external reducing energy was available. 35 refs., 4 figs., 2 tabs.

Chu, K.H.; Alvarez-Cohen, L. [Univ. of California, Berkeley, CA (United States)

1996-01-01T23:59:59.000Z

64

Synthesis Gas Production from Partial Oxidation of Methane with Air in AC Electric Gas Discharge  

E-Print Network (OSTI)

depending on the ratio of hydrogen to carbon monoxide. Most synthesis gas is produced by the steam reform reaction. Industrially, steam reforming is performed over a Ni/ Al2O3 catalyst.9 The typical problemSynthesis Gas Production from Partial Oxidation of Methane with Air in AC Electric Gas Discharge K

Mallinson, Richard

65

Selective methane oxidation over promoted oxide catalysts. Quarterly technical progress report, September 8, 1992--November 30, 1992  

DOE Green Energy (OSTI)

Support effects on catalytic reactions, especially of highly exothermic oxidation reactions, can be very significant. Since we had shown that a MoO{sub 3}/SiO{sub 2} catalyst, especially when used in a double bed configuration with a Sr/La{sub 2}O{sub 3} catalyst, can selectively oxidize methane to formaldehyde, the role of the SiO{sub 2} support was investigated. Therefore, partial oxidation of methane by oxygen to form formaldehyde, carbon oxides, and C{sub 2} products (ethane and ethene) has been studied over silica catalyst supports (fumed Cabosil and Grace 636 silica gel) in the 630-780{degrees}C temperature range under ambient pressure. When relatively high gas hourly space velocities (GHSV) were utilized, the silica catalysts exhibit high space time yields (at low conversions) for methane partial oxidation to formaldehyde, and the C{sub 2} hydrocarbons were found to be parallel products with formaldehyde. In general, the selectivities toward CO were high while those toward CO{sub 2} were low. Based on the present results obtained by a double catalyst bed experiment, the observations of product composition dependence on the variation of GHSV (i.e. gas residence time), and differences in apparent activation energies of formation of C{sub 2}H{sub 6}, and CH{sub 2}O, a reaction mechanism is proposed for the activation of methane over the silica surface. This mechanism can explain the observed product distribution patterns (specifically the parallel formation of formaldehyde and C{sub 2} hydrocarbons).

Klier, K.; Herman, R.G.; Sun, Q.; Sarkany, J.

1993-01-01T23:59:59.000Z

66

Selective methane oxidation over promoted oxide catalysts. Quarterly report, September--November, 1994  

DOE Green Energy (OSTI)

Experimental research in the direct conversion of methane to methanol using a double bed reactor and with gaseous steam as cofeed with the CH{sub 4}/air reactant mixture continued during this quarter in order to improve the methanol space time yield. Work was carried out along several pathways that included a stability test of the second bed catalyst 1%V{sub 2}O{sub 5}/SiO{sub 2} that yielded up to 100 g methanol/kg cat/hr and investigation of the effect of pressure on methanol yields. Redox dopants were put onto several metal oxide supports in an attempt to find better second bed catalysts. A catalyst that was reasonably selective towards oxygenates was obtained when SiO{sub 2} was used as the support and low quantities of Fe or Cu were utilized. Attempts were also made to incorporate alkali ions into the catalysts to improve the surface hydrolyzability. Experiments were carried out to examine the effect of pressure and temperature on the oxygenate productivity over a double-layered catalyst bed of 0.1 g 1 wt% SO{sub 4}{sup 2{minus}}/Sr/La{sub 2}O{sub 3} as the first bed and 0.1 g 1 wt% V{sub 2}O{sub 5}/SiO{sub 2} as the second bed without H{sub 2}O cofeed in a glass-lined tubular down-flow reactor at pressures of 0.1--3.2 MPa (14.7--460 psig), temperatures of 450--500 C, and with a reactant flow rate having a ratio of CH{sub 4}/air = 150/50 ml/min. Reaction products observed were methanol, formaldehyde, carbon dioxide, acetylene, ethylene, and ethane. The overall activity of the catalyst increased at low pressures and high temperature. However, testing at low temperature and high pressure was found to favor methanol production.

Klier, K.; Herman, R.G.; Shi, C.; Wang, C.B.; Sun, Q.

1994-12-01T23:59:59.000Z

67

Induction of enhanced methane oxidation in compost: Temperature and moisture response  

Science Conference Proceedings (OSTI)

Landfilling is one of the most common ways of municipal solid waste disposal. Degradation of organic waste produces CH{sub 4} and other landfill gases that significantly contribute to global warming. However, before entering the atmosphere, part of the produced CH{sub 4} can be oxidised while passing through the landfill cover. In the present study, the oxidation rate of CH{sub 4} was studied with various types of compost as possible landfill cover. The influence of incubation time, moisture content and temperature on the CH{sub 4} oxidation capacity of different types of compost was examined. It was observed that the influence of moisture content and temperature on methane oxidation is time-dependent. Maximum oxidation rates were observed at moisture contents ranging from 45% to 110% (dry weight basis), while the optimum temperature ranged from 15 to 30 deg. C.

Mor, Suman [Centre for Energy Studies, Indian Institute of Technology Delhi, Hauz Khas, New Delhi-110016 (India) and Department of Applied Analytical and Physical Chemistry, Ghent University, Coupure Links 653, B-9000 Ghent (Belgium)]. E-mail: sumanmor@yahoo.com; Visscher, Alex de [Department of Applied Analytical and Physical Chemistry, Ghent University, Coupure Links 653, B-9000 Ghent (Belgium); Ravindra, Khaiwal [Micro and Trace Analysis Centre, Department of Chemistry, University of Antwerp, Universiteitsplein 1, B-2610 Antwerp (Belgium); Dahiya, R.P. [Centre for Energy Studies, Indian Institute of Technology Delhi, Hauz Khas, New Delhi-110016 (India); Chandra, A. [Centre for Energy Studies, Indian Institute of Technology Delhi, Hauz Khas, New Delhi-110016 (India); Cleemput, Oswald van [Department of Applied Analytical and Physical Chemistry, Ghent University, Coupure Links 653, B-9000 Ghent (Belgium)

2006-07-01T23:59:59.000Z

68

Methane oxidation over dual redox catalysts. Quarterly technical progress report, July--September 1989  

SciTech Connect

The objective of this research is to develop approaches to direct catalytic oxidation of methane over oxides that are doubly doped with transition metal ions. The desired process aims at employing a double redox mechanism, where one redox couple is utilized for activation of oxygen and another for the trapping of CH{sub 3} radicals. The methyl radicals can either recombine, giving C{sub 2} hydrocarbons, or be converted, via electron transfer reaction, to carbocations. The latter species can react with surface OH{sup {minus}} groups to form methanol or formaldehyde. To choose from several possible catalytic systems, this research initially involved the characterization of the micromorphology and crystalline dimensions of zinc oxide catalysts doped with Cu, Fe, and Sn by scanning electron microscopy. In addition, the determination of surface composition and oxidation states by X-ray photoelectron spectroscopy was carried out. A newly constructed high temperature catalytic testing system has been calibrated (flow meters and temperature controllers), tested for possible gas leaks and integrated with a gas chromatographic analytical unit. A preliminary catalytic test study over a Cu/Fe/ZnO sample was performed. The following products of the methane coupling reaction was found: C{sub 2}H{sub 6}, C{sub 2}H{sub 4} and H{sub 2}O together with CO{sub 2}. The maximum space time yield of 14 mmol C{sub 2} hydrocarbons/g cat/h was obtained at 848{degrees}C.

Klier, K.; Herman, R.G.; Sojka, Z.

1989-09-01T23:59:59.000Z

69

Selective methane oxidation over promoted oxide catalysts. Quarterly report, June 1 - August 31, 1996  

DOE Green Energy (OSTI)

Further data analysis for the conversion of methane to oxygenates over high surface are V{sub 2}O{sub 5}/SiO{sub 2} xerogel catalysts that were synthesized by a sol-gel process have been carried out. As previously described the vanadia loading of the catalysts was varied between 0-25 wt%. Turnover numbers (T.O.N.) have been calculated for methane conversion to products and for the synthesis of methanol and formaldehyde, where T.O.N. is defined as molecules converted or formed per dispersed tetrahedrally coordinated vanadium atom ad determined by {sup 51}V NMR analyses. It is found that highly dispersed tetrahedrally coordinated V{sup 5+} is the active site for the selective conversion of methane to methanol and formaldehyde.

Klier, K.; German, R.G.; Wang, C.

1996-12-31T23:59:59.000Z

70

METHANE AND n-BUTANE OXIDATION WITH CO2 UNDER RADIOFREQUENCY PLASMAS OF MODERATE PRESSURES (*)  

E-Print Network (OSTI)

1205 METHANE AND n-BUTANE OXIDATION WITH CO2 UNDER RADIOFREQUENCY PLASMAS OF MODERATE PRESSURES) Résumé. 2014 L'oxydation du méthane et du n-butane avec CO2 a été étudiée dans des décharges électriques intermédiaires en C2 (C2H2, C2H4, C2H6) qui est la voie principale pour convertir mé- thane et n-butane en CO

Paris-Sud XI, Université de

71

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

DOE Green Energy (OSTI)

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.

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

1996-12-01T23:59:59.000Z

72

Methane flux and oxidation at two types of intermediate landfill covers  

SciTech Connect

Methane emissions were measured on two areas at a Florida (USA) landfill using the static chamber technique. Because existing literature contains few measurements of methane emissions and oxidation in intermediate cover areas, this study focused on field measurement of emissions at 15-cm-thick non-vegetated intermediate cover overlying 1-year-old waste and a 45-cm-thick vegetated intermediate cover overlying 7-year-old waste. The 45 cm thick cover can also simulate non-engineered covers associated with older closed landfills. Oxidation of the emitted methane was evaluated using stable isotope techniques. The arithmetic means of the measured fluxes were 54 and 22 g CH{sub 4} m{sup -2} d{sup -1} from the thin cover and the thick cover, respectively. The peak flux was 596 g m{sup -2} d{sup -1} for the thin cover and 330 g m{sup -2} d{sup -1} for the thick cover. The mean percent oxidation was significantly greater (25%) at the thick cover relative to the thin cover (14%). This difference only partly accounted for the difference in emissions from the two sites. Inverse distance weighing was used to describe the spatial variation of flux emissions from each cover type. The geospatial mean flux was 21.6 g m{sup -2} d{sup -1} for the thick intermediate cover and 50.0 g m{sup -2} d{sup -1} for the thin intermediate cover. High emission zones in the thick cover were fewer and more isolated, while high emission zones in the thin cover were continuous and covered a larger area. These differences in the emission patterns suggest that different CH{sub 4} mitigation techniques should be applied to the two areas. For the thick intermediate cover, we suggest that effective mitigation of methane emissions could be achieved by placement of individualized compost cells over high emission zones. Emissions from the thin intermediate cover, on the other hand, can be mitigated by placing a compost layer over the entire area.

Abichou, Tarek [Department of Civil and Environmental Engineering, Florida A and M University, Florida State University, College of Engineering, Tallahassee, FL 32310 (United States)]. E-mail: abichou@eng.fsu.edu; Chanton, Jeffery [Department of Oceanography, Florida State University, Tallahassee, FL 32306 (United States); Powelson, David [Department of Oceanography, Florida State University, Tallahassee, FL 32306 (United States); Fleiger, Jill [Department of Oceanography, Florida State University, Tallahassee, FL 32306 (United States); Escoriaza, Sharon [Department of Civil and Environmental Engineering, Florida A and M University, Florida State University, College of Engineering, Tallahassee, FL 32310 (United States); Lei, Yuan [Department of Civil and Environmental Engineering, Florida A and M University, Florida State University, College of Engineering, Tallahassee, FL 32310 (United States); Stern, Jennifer [Department of Geology, Florida State University, Tallahassee, FL 32306 (United States)

2006-07-01T23:59:59.000Z

73

Fabrication and characterization of dense ceramic membranes for partial oxidation of methane  

DOE Green Energy (OSTI)

In this technology, air is used as the oxidant for methane conversion reactions, thiu eliminating tne need for an expensive oxygen plant. Mixed-conducting ceramic materials have been produced from mixed-oxide system of the La-Sr-Fe-Co-O (SFC) type, in the form of tubes and bars. Thermodynamic stability of the tubes was studied vs oxygen partial pressure by high-temperature XRD. Mechanical properties of the SFC-2 (SrFeCo{sub 0.5}O{sub x}) material were adequate for reactor use. Electronic and ionic conductivities showed that SFC-2 is unique in that its ratio of ionic to electronic conductance is close to unity. Performance of the membrane tubes was good only with SFC-2. Fracture of other SFC tubes was consequence of an oxygen gradient that introduced a volumetric lattice difference between the inner and outer walls. SFC-2 tubes provided methane conversion efficiencies >99% in a reactor and have operated successfully for >1000 h.

Balachandran, U.; Ma, B.; Dusek, J.T.; Picciolo, J.J.; Mieville, R.L.; Maiya, P.S. [Argonne National Lab., IL (United States); Kleefisch, M.S.; Udovich, C.A. [Amoco Research Center, Naperville, IL (United States)

1995-06-01T23:59:59.000Z

74

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

SciTech Connect

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.

Yongchun Tang; John (Qisheng) Ma

2012-03-23T23:59:59.000Z

75

THE EFFECT OF SULFUR ON METHANE PARTIAL OXIDATION AND REFORMING PROCESSES FOR LEAN NOX TRAP CATALYSIS  

Science Conference Proceedings (OSTI)

Lean NOx trap catalysis has demonstrated the ability to reduce NOx emissions from lean natural gas reciprocating engines by >90%. The technology operates in a cyclic fashion where NOx is trapped on the catalyst during lean operation and released and reduced to N2 under rich exhaust conditions; the rich cleansing operation of the cycle is referred to as "regeneration" since the catalyst is reactivated for more NOx trapping after NOx purge. Creating the rich exhaust conditions for regeneration can be accomplished by catalytic partial oxidation of methane in the exhaust system. Furthermore, catalytic reforming of partial oxidation exhaust can enable increased quantities of H2 which is an excellent reductant for lean NOx trap regeneration. It is critical to maintain clean and efficient partial oxidation and reforming processes to keep the lean NOx trap functioning properly and to reduce extra fuel consumption from the regeneration process. Although most exhaust constituents do not impede partial oxidation and reforming, some exhaust constituents may negatively affect the catalysts and result in loss of catalytic efficiency. Of particular concern are common catalyst poisons sulfur, zinc, and phosphorous. These poisons form in the exhaust through combustion of fuel and oil, and although they are present at low concentrations, they can accumulate to significant levels over the life of an engine system. In the work presented here, the effects of sulfur on the partial oxidation and reforming catalytic processes were studied to determine any durability limitations on the production of reductants for lean NOx trap catalyst regeneration.

Parks, II, James E [ORNL; Ponnusamy, Senthil [ORNL

2006-01-01T23:59:59.000Z

76

The landfill methane balance: Model and practical applications  

SciTech Connect

A rational mass-balance framework is described for improved quantification of landfill methane processes at a given site. The methane balance model examines the partitioning of methane generated into methane recovered (via extraction systems), methane emitted, methane oxidized, methane migrated, and methane storage. This model encourages use of field-based data to better quantify rates of methane recovery and emissions.

Bogner, J.; Spokas, K.

1995-10-01T23:59:59.000Z

77

Quantifying methane oxidation in a landfill-cover soil by gas push-pull tests  

SciTech Connect

Methane (CH{sub 4}) oxidation by aerobic methanotrophs in landfill-cover soils decreases emissions of landfill-produced CH{sub 4} to the atmosphere. To quantify in situ rates of CH{sub 4} oxidation we performed five gas push-pull tests (GPPTs) at each of two locations in the cover soil of the Lindenstock landfill (Liestal, Switzerland) over a 4 week period. GPPTs consist of the injection of a gas mixture containing CH{sub 4}, O{sub 2} and noble gas tracers followed by extraction from the same location. Quantification of first-order rate constants was based upon comparison of breakthrough curves of CH{sub 4} with either Ar or CH{sub 4} itself from a subsequent inactive GPPT containing acetylene as an inhibitor of CH{sub 4} oxidation. The maximum calculated first-order rate constant was 24.8 {+-} 0.8 h{sup -1} at location 1 and 18.9 {+-} 0.6 h{sup -1} at location 2. In general, location 2 had higher background CH{sub 4} concentrations in vertical profile samples than location 1. High background CH{sub 4} concentrations in the cover soil during some experiments adversely affected GPPT breakthrough curves and data interpretation. Real-time PCR verified the presence of a large population of methanotrophs at the two GPPT locations and comparison of stable carbon isotope fractionation of CH{sub 4} in an active GPPT and a subsequent inactive GPPT confirmed that microbial activity was responsible for the CH{sub 4} oxidation. The GPPT was shown to be a useful tool to reproducibly estimate in situ rates of CH{sub 4} oxidation in a landfill-cover soil when background CH{sub 4} concentrations were low.

Gomez, K.E. [Institute of Biogeochemistry and Pollutant Dynamics, ETH Zuerich, Universitaetstrasse 16, 8092 Zuerich (Switzerland)], E-mail: gomezke@hotmail.com; Gonzalez-Gil, G.; Lazzaro, A. [Institute of Biogeochemistry and Pollutant Dynamics, ETH Zuerich, Universitaetstrasse 16, 8092 Zuerich (Switzerland); Schroth, M.H. [Institute of Biogeochemistry and Pollutant Dynamics, ETH Zuerich, Universitaetstrasse 16, 8092 Zuerich (Switzerland)], E-mail: martin.schroth@env.ethz.ch

2009-09-15T23:59:59.000Z

78

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, October 1, 1994--December 31, 1994  

SciTech Connect

This report describes research on the oxidative coupling of methane and catalysts involved in coal gasification. Topics include methane pyrolysis and catalysts, and magnetic properties of the coal gasification catalyst Ca-Ni-K-O system.

Iglesia, E.; Perry, D.L.; Heinemann, H.

1994-12-01T23:59:59.000Z

79

Catalytic partial oxidation of methane to synthesis gas over Ni-based catalysts. 2: Transient, FTIR, and XRD measurements  

SciTech Connect

Ni/La{sub 2}O{sub 3} and Ni/Al{sub 2}O{sub 3} catalysts were studied under conditions of partial oxidation of methane to synthesis gas. Temperature-programmed oxidation and hydrogenation experiments have shown that carbon accumulation over Ni/La{sub 2}O{sub 3} during CPO remains essentially constant after 2 h time on-stream, while over Ni/Al{sub 2}O{sub 3} it increases during the initial several hours. FTIR spectroscopy of surface species formed over the Ni/La{sub 2}O{sub 3} catalyst under reaction conditions indicates that the carbonate species formed over the support do not decompose under He and O{sub 2} treatment at 600 C. XRD spectra obtained following high ({approximately}90%) or low (<10%) methane conversions show that Ni, La{sub 2}O{sub 3}, La{sub 2}O{sub 2}CO{sub 3}, NiO, and Ni{sub 3}C phases are present in the case of high methane and complete oxygen conversions, while nickel oxide, nickel carbide and, to a small extent, La{sub 2}O{sub 2}CO{sub 3} phases are present in the case of low CH{sub 4} and incomplete oxygen conversions.

Tsipouriari, V.A.; Verykios, X.E. [Univ. of Patras (Greece). Dept. of Chemical Engineering

1998-10-01T23:59:59.000Z

80

Mechanisms and controlling characteristics of the catalytic oxidation of methane. Progress report  

DOE Green Energy (OSTI)

Progress has included (1) construction and installation of an ultraviolet photoelectron spectrometer (UPS) with power supply and pumping system that has been added as an attachment to the SCIENTA ESCA-300 instrument, (2) modification of the high resolution electron energy loss spectrometer (HREELS) to produce a stable ultra high vacuum (UHV) environment for initial experiments with a Pd(311) single crystal, (3) construction of a separate high vacuum system for preparation of surface doped model catalysts by chemical vapor deposition and pretreatment of a Pd(100) single crystal in this system, (4) carried out detailed experiments of methane activation and oxidation on Pd(679) using a high pressure reaction cell contained in a third ultra high vacuum system, (5) completion of adsorption/desorption studies of H{sub 2}, CO, and O{sub 2} on Pd(679), (6) utilized angle-resolved XPS to probe the diffraction characteristics and structure of the Pd(100) surface, (7) determination of the electronic surface structure of Pd(100) using angle-resolved UPS, and (8) computational analysis of oxygen overlayers on the PD(100) surface. Each of these is discussed in further detail below.

Klier, K.

1990-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Catalytic performance of vanadium incorporated MCM-41 catalysts for the partial oxidation of methane to formaldehyde  

E-Print Network (OSTI)

steam reforming of methane to syngas (CO and H2), (ii) high pressure conversion to methanol and (iii disadvantages, e.g. the energy requirements of the endothermic steam reforming of the first step, the high of methane to formaldehyde Guoan Du, Sangyun Lim, Yanhui Yang, Chuan Wang, Lisa Pfefferle, Gary L. Haller

Haller, Gary L.

82

Mechanisms and controlling characteristics of the catalytic oxidation of methane. Technical progress report, June 15, 1990--December 14, 1992  

DOE Green Energy (OSTI)

We have demonstrated in this work (1) that methane is readily activated at mild conditions (100{degree}C, 1 torr) over a relatively noble metal, Pd. This was observed using a stepped and kinked Pd(679) crystal (1), and other crystal faces are now being investigated to establish whether the cracking of the C-H bond of methane on Pd is structure sensitive or structure insensitive. Oxygen chemisorption is extremely structure sensitive: weakly bonded, highly reactive oxygen overlayers form on Pd(100) surface (2), while strongly bonded, moderately reactive oxygen overlayers form on Pd(111) and Pd(679). Reaction of the weakly bonded oxygen with surface carbide gives rise to CO{sub 2} over clean Pd(100) but to CO over halogen-doped Pd(100) (3--5). The effect of halogens is primarily ensemble-controlling, or oxygen-supply restricting, but long range influence of surface Cl on the strength of the Pd-O bond has also been observed (3). Because the overall chemistry of methane activation with the subsequent oxidation gives rise to the very important oxidative reforming CH{sub 4} + 1/2 O{sub 2} {yields}{sub Pd/Cl} CO + 2 H{sub 2}, Pd/Cl we plan to continue our study of this reaction in detail over Pd(100) (completed), Pd(111) (initiated), Pd(311) (initiated), Pd(110) (to be initiated), and Pd(679) (completed), without and with the halogen modifiers.

Klier, K.; Simmons, G.W.; Herman, R.G.; Miller, A.C.

1992-12-31T23:59:59.000Z

83

Development of vanidum-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report, 1996  

DOE Green Energy (OSTI)

Activities this past quarter, focused on acquisition of kinetic data for oxidation of formaldehyde and methanol on these catalysts. In the next quarter these results will be used to propose a simple reaction network and kinetic model. To date we have completed Task 1: Laboratory Setup and Task 2: Process Variable Study. Activities in the current quarter focused on finalizing these tasks and on Task 3: Promoters and Supports, this task is approximately 50% completed. Task 4: Advanced Catalysts is to be initiated in the next quarter. Specific accomplishments this quarter include: finalizing and calibrating a new reaction product analytical system with markedly improved precision and accuracy relative to older. approaches; development of procedures for accurately feeding formaldehyde to the reactor; examination of formaldehyde and methanol oxidation kinetics over vanadyl pyrophosphate at a range of temperatures; and preliminary studies of methane oxidation over a silica support.

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

1996-06-01T23:59:59.000Z

84

Investigation of H{sub 2}O and CO{sub 2} reforming and partial oxidation of methane: catalytic effects of coal char and coal ash  

Science Conference Proceedings (OSTI)

Methane reforming and partial oxidation was studied to evaluate the catalytic effects of coal chars and coal ashes on methane (CH{sub 4}) conversion, sum selectivity (the sum of H{sub 2} and CO), and ratio selectivity (the ratio of H{sub 2}/CO) in an atmospheric fluidized bed. The kinetics study presented the possibility of CH{sub 4} reforming and partial oxidation with a favorable H{sub 2}/CO ratio, greater than 5. The higher H{sub 2}/CO ratio in CH{sub 4} reforming and the partial-oxidation process can reduce the consumption of CH{sub 4} needed to adjust the H{sub 2}/CO ratio during combined coal gasification and methane reforming. Coal ashes failed to be good candidates of catalysts on CH{sub 4} reforming and partial oxidation because of their very low specific surface area available for catalytic reactions. However, coal chars presented very promising catalytic performance on CH{sub 4} reforming and partial oxidation because of their larger specific surface area. In this study, no other constituents in coal fly ash or special surface properties of coal chars were correlated with the enhanced methane-conversion efficiency. It seems that the specific surface area is only variable in controlling methane-conversion efficiency. 16 refs., 9 figs.

Hongcang Zhou; Yan Cao; Houyin Zhao; Hongying Liu; Wei-Ping Pan [Western Kentucky University, Bowling Green, KY (United States). Institute for Combustion Science and Environmental Technology

2008-07-15T23:59:59.000Z

85

Kinetic Consequences of Chemisorbed Oxygen Atoms during Methane Oxidation on Group VIII Metal Clusters  

E-Print Network (OSTI)

v for the oxidation of bulk Pt metals. The bulk oxidation isbulk, cluster size and metal coordination effects on thermodynamic tendencies of bulk oxidation,O s * sites at metal surfaces. Bulk oxidation exposes Pd 2+

Chin, Ya Huei

2011-01-01T23:59:59.000Z

86

Biomimetic methane oxidation. Final report, October 1, 1989--June 1, 1995  

DOE Green Energy (OSTI)

Transportation fuels are a critical energy commodity and they impact nearly every sector of this country. The need for transportation fuels is projected well into the next century. Consequently, there is a strong emphasis on the economical conversion of other domestic fossil energy resources to liquid hydrocarbons that can be used as transportation fuels. Natural gas is currently a readily available resource that has a positive future outlook considering its known and anticipated reserves. There is intense government and industrial interest in developing economic technologies to convert natural gas to liquid fuels. Methane, CH{sub 4}, is the primary hydrocarbon (85-95%) in natural gas. This document covers the following: production soluable of methane monooxygenase; production of particulate methane monooxygenase; production of methane monooxygenase in continuous culture; subunit resolution for active site identification of methylosinus trichosporium OB3b soluble methane monooxygenase; the synthesis and characterization of new copper coordination complexes contairing the asymmetric coordinating chelate ligand application to enzyme active site modeling; the synthesis and characterization of new iron coordination complexes utilizing an asymmetric coordinating chelate ligand; further characterization of new bionuclear iron complexes.

Watkins, B.E.; Satcher, J.H. Jr.; Droege, M.W.; Taylor, R.T.

1995-07-01T23:59:59.000Z

87

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, April 1, 1992--June 30, 1992  

DOE Green Energy (OSTI)

Work continued on the catalytic conversion of methane to produce C{sub 2}, C{sub 3},and C{sub 4} hydrocarbons. Progress is reported on the catalytic effects of Lithium Oxide and Magnesium Oxide catalysts.

Heinemann, H.; Somorjai, G.A.; Perry, D.L.

1992-06-01T23:59:59.000Z

88

Methane to methanol conversion  

DOE Green Energy (OSTI)

The purpose of this project is to develop a novel process by which natural gas or methane from coal gasification products can be converted to a transportable liquid fuel. It is proposed that methanol can be produced by the direct, partial oxidation of methane utilizing air or oxygen. It is anticipated that, compared to present technologies, the new process might offer significant economic advantages with respect to capital investment and methane feedstock purity requirements. Results to date are discussed. 6 refs.

Finch, F.T.; Danen, W.C.; Lyman, J.L.; Oldenborg, R.C.; Rofer, C.K.; Ferris, M.J.

1990-01-01T23:59:59.000Z

89

Methane Main  

NLE Websites -- All DOE Office Websites (Extended Search)

the the Methane Hydrate Advisory Committee on Methane Hydrate Issues and Opportunities Including Assessment of Uncertainty of the Impact of Methane Hydrate on Global Climate Change December 2002 Report of the Methane Hydrate Advisory Committee on Methane Hydrate Issues and Opportunities Including Assessment of Uncertainty of the Impact of Methane Hydrate on Global Climate Change December 2002 i CONTENTS What is Methane Hydrate? ............................................................................................. 1 Why Methane Hydrate Matters for the United States? ..................................................... 4 Resource Potential of Methane Hydrate .......................................................................... 5 Implications of Methane Hydrate on Safety and Seafloor Stability

90

Electrochemical methane sensor  

DOE Patents (OSTI)

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.

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

1984-08-27T23:59:59.000Z

91

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report 10, July 1, 1995--September 31, 1995  

DOE Green Energy (OSTI)

This document is the tenth quarterly technical progress report under Contract No. DE-AC22-92PC92110 {open_quotes}Development of Vanadium-Phosphate Catalysts for Methanol Production by Selective Oxidation of Methane{close_quotes}. Activities focused on testing of additional modified and promoted catalysts and characterization of these materials. Attempts at improving the sensitivity of our GC based analytical systems were also made with some success. Methanol oxidation studies were initiated. These results are reported. Specific accomplishments include: (1) Methane oxidation testing of a suite of catalysts promoted with most of the first row transition metals was completed. Several of these materials produced low, difficult to quantify yields of formaldehyde. (2) Characterization of these materials by XRD and FTIR was performed with the goal of correlating activity and selectivity with catalyst properties. (3) We began to characterize catalysts prepared via modified synthesis methods designed to enhance acidity using TGA measurements of acetonitrile chemisorption and methanol dehydration to dimethyl ether as a test reaction. (4) A catalyst prepared in the presence of naphthalene methanol as a structural disrupter was tested for activity in methane oxidation. It was found that this material produced low yields of formaldehyde which were difficult to quantify. (5) Preparation of catalysts with no Bronsted acid sites. This was accomplished by replacement of exchangeable protons with potassium, and (6) Methanol oxidation studies were initiated to provide an indication of catalyst activity for decomposition of this desired product and as a method of characterizing the catalyst surface.

McCormick, R.L.

1995-12-07T23:59:59.000Z

92

Catalytic partial oxidation of methane to synthesis gas over Ni-based catalysts. 1: Catalyst performance characteristics  

SciTech Connect

The catalytic partial oxidation of methane to synthesis gas was studied over various Ni-based catalysts. It was found that, in contrast to conventional Ni catalysts which show continuous deactivation with time on stream, the Ni/La{sub 2}O{sub 3} catalyst exhibits good activity and excellent stability, using the stoichiometric ratio of CH{sub 4}/O{sub 2} (=2). Kinetic results indicate that the reaction over the Ni/La{sub 2}O{sub 3} catalyst follows mainly the sequence of total oxidation to CO{sub 2} and H{sub 2}O, followed by reforming reactions to synthesis gas, while CO formation via the direct route is observed at very low oxygen partial pressures. Chemisorption and FTIR studies show that the enhanced stability of the Ni/La{sub 2}O{sub 3} catalyst is related to decoration of the Ni crystallites with lanthanum species, primarily oxycarbonates, which favor removal of excess carbon deposition and impart the catalyst its stability characteristics.

Tsipouriari, V.A.; Zhang, Z.; Verykios, X.E. [Univ. of Patras (Greece). Dept. of Chemical Engineering

1998-10-01T23:59:59.000Z

93

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

SciTech Connect

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 (â??Methane in the Arctic Shelfâ?ť 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 (â??metagenomesâ?ť). 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 anaerobic methane oxidation.

David Kirchman

2011-12-31T23:59:59.000Z

94

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report 13, April--June, 1996  

DOE Green Energy (OSTI)

The specific objectives of this project are: to determine optimum conditions for methanol and formaldehyde production from methane using VPO catalysts, in particular to 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; to utilize promoters and catalyst supports to improve oxygenate yield relative to the base case catalysts; to provide a preliminary understanding of how these promoters and supports actually effect catalyst properties; and use the information obtained to prepare advanced catalysts which will be tested for activity, selectivity, and stability. Activities this quarter included analysis of all previously acquired data for methane, methanol, and formaldehyde oxidation over vanadyl pyrophosphate and testing of supported, promoted, and iron phosphate catalysts. Some experiments have been conducted with a small percentage of butane in the feed gas to help retain the catalyst in a reduced state and these results are reported. Iron phosphate, and iron phosphate supported on silica have also been tested in a preliminary way.

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

1996-07-30T23:59:59.000Z

95

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

as described by Dillon, et al. (1998). Failure would be accompanied by the release of methane gas, but a portion of the methane is likely to be oxidized unless the gas release is...

96

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report 8, January--March, 1995  

DOE Green Energy (OSTI)

Activities during this quarter focused on fine tuning of catalyst characterization and synthesis techniques. Improvements in catalyst activity test methods were also implemented but more remains to be done. Specific accomplishments include: improved characterization of vanadyl pyrophosphate (VPO) and Si promoted VPO by FTIR and FTIR of chemisorbed bases; several minor improvements in catalyst preparation technique resulting in enhanced catalyst yield, better control of catalyst composition, and generation of less waste; preliminary pulsed reaction data on methane oxidation were also acquired. Preliminary activity measurements for methane conversion (without oxygen) in a pulsed reactor over VPO indicate that the primary reaction product is CO. Carbon dioxide is also formed but selectivity to CO{sub 2} decreases with number of pulses. These results suggest that selectivity to partially oxidized products improves with catalyst reduction and suggest that some surface modification will be required to obtain oxidized hydrocarbon products. Note that catalyst activation (conversion from the precursor to VPO) has been carried out using air. For butane oxidation catalysts VPO is activated in a 1% butane/air mixture which produces a slightly reduced catalyst.

McCormick, R.L.

1995-05-25T23:59:59.000Z

97

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, 1 January--31 March 1994  

DOE Green Energy (OSTI)

This report describes work in progress on three tasks: (1) Catalytic steam gasification of coals and cokes; (2) Oxidative coupling of methane; and (3) Synthesis and characterization of catalysts. Since Task 1 is complete, a final report has been written. This report describes membrane reactors, cyclic methane conversion reactors, theoretical descriptions of reaction-separation schemes, and time-space relationships in cyclic and membrane reactors, all subtasks of Task 2. Initial studies under Task 3 are briefly described.

Iglesia, E.; Heinemann, H.; Perry, D.L. [Lawrence Berkeley Lab., CA (United States). Center for Advanced Materials

1994-03-01T23:59:59.000Z

98

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

SciTech Connect

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.

Liang, B.; Suzuki, T.; Hamamoto, K.; Yamaguchi, T.; Sumi, H.; Fujishiro, Y.; Ingram, B. J.; Carter, J. D. (Chemical Sciences and Engineering Division); (National Institute of Advanced Industrial Science and Technology)

2012-03-15T23:59:59.000Z

99

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report No. 9, April 1995--June 1995  

DOE Green Energy (OSTI)

This document is the ninth quarterly technical progress report under Contract No. DE-AC22-92PC92110 {open_quotes}Development of Vanadium-Phosphate Catalysts for Methanol Production by Selective Oxidation of Methane{close_quotes}. Activities were focused on fine tuning of the microreactor system by elimination of transport effects and improvements in the analytical system. Process variable studies were conducted on vanadyl pyrophosphate and screening studies were conducted on several modified catalyst. One additional catalyst was prepared and characterization studies continued. These results are reported.

McCormick, R.L.

1995-09-14T23:59:59.000Z

100

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report 11, October--December 1995  

DOE Green Energy (OSTI)

Activities during this report period focused on testing of additional modified and promoted catalysts and characterization of these materials. Methanol oxidation studies were performed as a method of acid site characterization. Improvements to the product gas analysis system continued to be developed. These results are reported. Specific accomplishments include: (1) Obtaining and interpreting infrared spectra of modified catalysts prepared to enhance surface acidity. (2) Testing of these catalysts in methanol oxidation as a method of acid site characterization and to determine catalytic activity for conversion of this desired product. Catalysts were quite active for methanol conversion to dimethyl ether. Two of the modified catalysts prepared in this work exhibited the highest activity for this reaction, presumably because of their higher surface areas. (3) Determination that acidity modifications had no effect on activity for methane conversion.

McCormick, R.L.

1996-04-16T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Evaluation of three catalysts formulated for methane oxidation on a cng-fueled pickup truck. Technical report  

Science Conference Proceedings (OSTI)

The report describes the exhaust emission results obtained from the evaluation of three specialized methane catalytic converters supplied by three different catalysts manufacturers. The catalytic converters were evaluated using a compressed natural gas-fueled Dodge Dakota pickup truck. The report includes a description of the catalytic converters, the test vehicle, test facilities and test procedures.

Piotrowski, G.K.; Schaefer, R.M.

1993-12-01T23:59:59.000Z

102

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, October 1--December 31, 1993  

SciTech Connect

This report covers the time period from October 1 through December 31, 1993. A description of tasks for fiscal year 1994 is included in this report. Highlights and progress of work performed during this quarter is reported in (a) catalytic steam gasification of coals and cokes; (b) oxidative coupling of methane; and (c) synthesis and characterization of catalysts. Attached to this report is a copy of a manuscript submitted to Proceeding of Fuels Technology Contractors Meeting {open_quotes}Steady-State and Transient Catalytic Oxidation and Coupling of Methane{close_quotes} by Heinemann, Iglesia, and Perry.

Heinemann, H.; Iglesia, E.; Perry, D.L.

1993-12-01T23:59:59.000Z

103

Measuring Hydroxyl Radicals during the Oxidation of Methane, Ethane, Ethylene, and Acetylene in a Shock Tube Using UV Absorption Spectroscopy  

E-Print Network (OSTI)

The hydroxyl (OH) radical is a common intermediate species in any hydrogen- or hydrocarbon-based flame. Investigating OH at elevated temperatures and pressures is not a trivial task, and many considerations must be made to fully study the molecule. Shock tubes can provide the experimenter with a wide range of temperatures and pressures to investigate a variety of combustion characteristics including, but not limited to, OH kinetic profiles. Described in this dissertation is the diagnostic used to measure OH within a shock tube using UV absorption spectroscopy from an enhanced UV Xenon lamp passed through a spectrometer. OH absorption was made over a narrow range of wavelengths around 309.551 nm within the widely studied OH X?A ground vibrational transition region. Experiments have been performed in the shock-tube facility at Texas A&M University using this OH absorption diagnostic. A calibration mixture of stoichiometric H2/O2 diluted in 98% argon by volume was tested initially and compared with a well-known hydrogen-based kinetics mechanism to generate an absorption coefficient correlation. This correlation is valid over the range of conditions observed in the experiments at two pressures near 2 and 13 atm and temperatures from 1182 to 2017 K. Tests were completed using the absorption coefficient correlation on stoichiometric mixtures of methane, methane and water, ethane, ethylene, and acetylene to compare against a comprehensive, detailed chemical kinetics mechanism which considers up through C5 hydrocarbons. Measurements of methane show good agreement in peak OH formation and ignition delay time when compared with the mechanism. Improvements can be made in the shape of the methane-oxygen OH profile, and sensitivity and rate of production analyses were performed with the mechanism to identify key reactions for tuning. Similar results were found for methane-water-oxygen mixtures with no difference in profile shape or ignition delay time noted. There is room for improvement between the mechanism and measured values of OH for ethane-, ethylene-, and acetylene-based mixtures, although interesting pre-ignition features are nonetheless captured relatively well by the mechanism. Uncertainty in the measurement comes from the inherent noise in the photomultiplier tube signal and is ±25-150 ppm for the 2-atm experiments and ±6-25 ppm for the 13-atm experiments.

Aul, Christopher J

2013-05-01T23:59:59.000Z

104

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, July 1, 1994--September 30, 1994  

SciTech Connect

Research continued on the study of catalysts and membrane materials involved in the oxidative coupling of methane and coal gasification processes. Membranes studied and fabricated included Sr-Zr-Y-O, Sr-Zr-Y, and Sr-Ce-Y-O systems.

Iglesia, E.; Perry, D.L.; Heinemann, H.

1994-09-01T23:59:59.000Z

105

Methane conversion to methanol  

DOE Green Energy (OSTI)

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.

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

1992-06-01T23:59:59.000Z

106

Coalbed Methane  

Energy.gov (U.S. Department of Energy (DOE))

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.

107

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

SciTech Connect

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.

Recknagle, Kurtis P.; Khaleel, Mohammad A.

2009-03-01T23:59:59.000Z

108

Converting Methane to Methanol: Structural Insight into the Reaction...  

NLE Websites -- All DOE Office Websites (Extended Search)

Biology, Wayne State University, School of Medicine, Detroit, Michigan 48201, USA. Methane-oxidizing bacteria (methanotrophs) are extremely attractive from a chemist's...

109

NETL: Methane Hydrates - DOE/NETL Projects - Reconstructing Paleo...  

NLE Websites -- All DOE Office Websites (Extended Search)

to track diagenetic changes that are associated with the anaerobic oxidation of methane. To achieve this goal, this project aims to (1) reconstruct the paleo-positions of...

110

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, January 1, 1995--March 31, 1995  

DOE Green Energy (OSTI)

The synthesis of ethane and ethylene from methane and oxygen will be carried out in novel hydrogen transport inorganic membranes and in cyclic reactors in order to prevent undesirable secondary reactions of C{sub 2} molecules to CO and CO{sub 2}. Neither inorganic membrane reactors nor cyclic tubular reactors are presently used in commercial processes. Their application to catalytic reactions represents a novel application of engineering and solid-state chemistry concepts to catalytic reactions. Our approach combines high temperature membrane and cyclic experimental reactors, synthesis and characterization of thin membrane films and of high surface area catalysts, and detailed models of complex gas phase and surface reactions involved in oxidative coupling. We anticipate that this approach will lead to novel reactors for carrying our kinetic-controlled sequential reactions, such as the oxidative coupling of methane. Careful spectrographic and wet chemical analyses of fresh and silent catalysts have shown considerable differences which have permitted conclusions as to the source of deactivation. Our activities in the first quarter FYI 995 have focused on the synthesis, structural characterization, and catalytic evaluation of membrane films, disks, and reactors. We have also continued to exploit reaction-transport models to predict the performance of membrane, cyclic, and recycle reactors in the oxidative coupling of methane.

Iglesia, E.; Perry, D.L.; Heinemann, H.

1995-03-01T23:59:59.000Z

111

Detailed modeling and laser-induced fluorescence imaging of nitric oxide in a NH(i)-seeded non-premixed methane/air flame  

Science Conference Proceedings (OSTI)

In this paper we study the formation of NO in laminar, nitrogen diluted methane diffusion flames that are seeded with ammonia in the fuel stream. We have performed numerical simulations with detailed chemistry as well as laser-induced fluorescence imaging measurements for a range of ammonia injection rates. For comparison with the experimental data, synthetic LIF images are calculated based on the numerical data accounting for temperature and fluorescence quenching effects. We demonstrate good agreement between measurements and computations. The LIF corrections inferred from the simulation are then used to calculate absolute NO mole fractions from the measured signal.The NO formation in both doped and undoped flames occurs in the flame sheet. In the undoped flame, four different mechanisms including thermal and prompt NO appear to contribute to NO formation. As the NH3 seeding level increases, fuel-NO becomes the dominant mechanism and N2 shifts from being a net reactant to being a net product. Nitric oxide in the undoped flame as well as in the core region of the doped flames are underpredicted by the model; we attribute this mainly to inaccuracies in the NO recycling chemistry on the fuel-rich side of the flame sheet.

Bell, John B.; Day, Marcus S.; Grcar, Joseph F.; Bessler, Wolfgang G.; Schulz, Christof; Glarborg, Peter; Jensen, Anker D.

2001-12-14T23:59:59.000Z

112

Capture and Use of Coal Mine Ventilation-Air Methane  

NLE Websites -- All DOE Office Websites (Extended Search)

Capture and use of Coal Mine Capture and use of Coal Mine Ventilation - air Methane Background Methane emissions from coal mines represent about 10 percent of the U.S. anthropogenic methane released to the atmosphere. Methane-the second most important non-water greenhouse gas-is 21 times as powerful as carbon dioxide (CO 2 ) in its global warming potential. Ventilation-air methane (VAM)-the exhaust air from underground coal mines-is the largest source of coal mine methane, accounting for about half of the methane emitted from coal mines in the United States. Unfortunately, because of the low methane concentration (0.3-1.5 percent) in ventilation air, its beneficial use is difficult. However, oxidizing the methane to CO 2 and water reduces its global warming potential by 87 percent. A thermal

113

Methane (CH4)  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane (CH4) Gateway Pages to Methane Data Modern Records of Atmospheric Methane (CH4) and a 2000-year Ice-core Record from Law Dome, Antarctica 800,000-year Ice-Core Records of...

114

NIST: Methane Symmetry Operations  

Science Conference Proceedings (OSTI)

*. Bookmark and Share. Version History Methane Symmetry Operations. JT Hougen Optical Technology Division Gloria Wiersma ...

2010-10-05T23:59:59.000Z

115

Journal of Molecular Catalysis A: Chemical 163 (2000) 918 Methane activation on Ni and Ru model catalysts  

E-Print Network (OSTI)

these intermediates play in important methane reactions such as steam reforming, partial oxidation and homologation, methane activation represents a great challenge to researchers all over the world. Currently steam reforming of methane represents the primary route for methane conversion [8,9]. This highly endothermic

Goodman, Wayne

116

The Effect of Oxygen to Methane Ratio on the Methane-wet Air Autothermal Reforming and Carbon Deposition in the Micro-chamber  

Science Conference Proceedings (OSTI)

Considering the problems of catalyst carbon deposition and reforming endothermic reaction in micro-reforming chamber, coupled methane catalyst partial oxidation and steam methane reforming can make the micro-reforming system auto-supply heat and inhibit ... Keywords: micro-chamber, autothermal reforming, carbon deposition, oxygen to methane ratio

Ran Jingyu; Tu Weifeng

2011-01-01T23:59:59.000Z

117

Premixed Carbon Monoxide–Nitrous Oxide–Hydrogen Flames ...  

Science Conference Proceedings (OSTI)

... the combustion emission charac- teristics of stationary and mobile power plants. ... present data are in good agreement with the low-hydro- gen data ...

2012-12-06T23:59:59.000Z

118

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  

Science Conference Proceedings (OSTI)

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.

Widory, D., E-mail: d.widory@brgm.fr [BRGM, 3 ave Claude Guillemin, 45000 Orleans (France); Proust, E.; Bellenfant, G. [BRGM, 3 ave Claude Guillemin, 45000 Orleans (France); Bour, O. [INERIS, Parc Technologique ALATA, 60550 Verneuil-en-Halatte (France)

2012-09-15T23:59:59.000Z

119

Heat pipe methanator  

DOE Patents (OSTI)

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.

Ranken, William A. (Los Alamos, NM); Kemme, Joseph E. (Los Alamos, NM)

1976-07-27T23:59:59.000Z

120

NETL: Methane Hydrates - Methane Hydrate Reference Shelf  

NLE Websites -- All DOE Office Websites (Extended Search)

Reference Shelf Reference Shelf The Methane Hydrate Reference Shelf was created to provide a repository for information collected from projects funded as part of the National Methane Hydrate R&D Program. As output from the projects is received, it will be reviewed and then placed onto the reference shelf to be available to other methane hydrate researchers. Projects: DOE/NETL Projects : These pages contain detailed information on methane hydrate projects funded through the National Energy Technology Laboratory. Publications: Newsletter | Bibliography | Software | Reports | Program Publications | Photo Gallery Newsletter: Fire in the Ice: A publication highlighting the National Methane Hydrate R&D Program Bibliography: "Project Reports Bibliography"[PDF]: The bibliography lists publications resulting from DOE/NETL-sponsored

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

New manganese catalyst for light alkane oxidation  

DOE Patents (OSTI)

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

Durante, Vincent A. (West Chester, PA); Lyons, James E. (Wallingford, PA); Walker, Darrell W. (Visalia, CA); Marcus, Bonita K. (Radnor, PA)

1994-01-01T23:59:59.000Z

122

Integrated autothermal reactor concepts for oxidative coupling and reforming of  

E-Print Network (OSTI)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . 4 1.3 Oxidative coupling and steam reforming of methane . . . . . . . . . . 5 1.4 This thesis of methane . . . . . . . . . . . . . . . . . . . 23 2.4 Only steam reforming of methane#12;Integrated autothermal reactor concepts for oxidative coupling and reforming of methane #12

Twente, Universiteit

123

NETL: Methane Hydrates - Methane Hydrate Library  

NLE Websites -- All DOE Office Websites (Extended Search)

Ridge region Ongoing areas of study in the Hydrate Ridge region Map showing where gas hydrates occur off the Cascadia Margin Locations of methane hydrate off the Cascadia Margin...

124

NETL: Methane Hydrates - Methane Hydrate Reference Shelf  

NLE Websites -- All DOE Office Websites (Extended Search)

Hydrates Primer provides background and general information about the history of hydrate R&D, the science of methane hydrates, their occurrences, and R&D related issues. Photo...

125

Method of determining methane and electrochemical sensor therefor  

DOE Patents (OSTI)

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.

Zaromb, Solomon (Hinsdale, IL); Otagawa, Takaaki (Westmont, IL); Stetter, Joseph R. (Naperville, IL)

1986-01-01T23:59:59.000Z

126

Why not methane--5. Delivering methane  

SciTech Connect

A discussion showed that the methane delivery system in the U.S. consists of 350,000 mi of underground high-pressure pipelines, 650,000 mi of distribution mains and connections to 45 million energy users. This delivery system now carries much less natural gas than it could carry because of the regulation-caused shortages of recent years. The delivery system is also connected to an efficient storage system of exhausted underground gas wells into which methane from any source (e.g., gasification of coal or vegetation) could be pumped and then recovered as needed. This storage system could be readily expanded and could thus be used for strategic storage of methane. Enough methane could be stored to replace foreign oil if the foreign supply should be interrupted; and methane can be quickly delivered nation-wide, whereas strategic oil storage requires unusual and expensive provisions for delivery. Natural gas usage could be increased by 20Vertical Bar3< in two years and would reduce payments for imported oil by about $10 billion. Doubling the amount of methane used in the U.S. would eliminate the need for foreign oil entirely.

Luntey, E.

1979-01-01T23:59:59.000Z

127

How Portfolio Manager calculates greenhouse gas emissions | ENERGY...  

NLE Websites -- All DOE Office Websites (Extended Search)

methane, and nitrous oxide) from on-site fuel combustion and purchased electricity and district heating and cooling. Portfolio Manager also enables tracking of avoided emissions...

128

Katharine Gebbie GHG Emissions Speech ? June 2, 2010 ...  

Science Conference Proceedings (OSTI)

... 2. We are also releasing other gases – methane, nitrous oxide, sulfur hexafluoride – into the atmosphere that trap heat more effectively than CO ...

2012-05-10T23:59:59.000Z

129

Global Warming and Greenhouse Gases  

Science Conference Proceedings (OSTI)

... NIST is producing new suites of primary gas standards for carbon dioxide, methane, carbon monoxide, and nitrous oxide in air at atmospheric levels ...

2013-09-20T23:59:59.000Z

130

NIST Kevin Douglass  

Science Conference Proceedings (OSTI)

... 1.6 micron atmospheric window region where three critical greenhouse gases, carbon dioxide (CO 2 ), nitrous oxide (N 2 O), and methane (CH 4 ...

2013-04-01T23:59:59.000Z

131

OIAF Products and Data Analyses Brochure, May 2000  

U.S. Energy Information Administration (EIA)

As required by the Energy Policy Act of 1992,this report presents the annual estimates of U.S.emissions for carbon dioxide, methane, nitrous oxide, ...

132

Methane cracking over a bituminous coal char  

Science Conference Proceedings (OSTI)

Methane cracking over a bed of Chinese bituminous coal char was studied using a fixed-bed reactor at atmospheric pressure and temperatures between 1073 and 1223 K. Methane conversion over the fresh char increased with increasing temperature to 90% at 1223 K. Hydrogen was the only gas-phase product that was detected during the experimentation. The char was shown to exert a significant catalytic effect on methane cracking by comparing results from experiments with the raw char and demineralised char as well as from blank experiments using quartz. It was further shown that the ash was not the source of the catalytic effect of the char. However, both methane conversion and hydrogen yield decreased with increasing reaction time, irrespective of other experimental conditions, indicating that the char rapidly became deactivated following the exposure to methane. It was speculated that the deposition of carbon from methane cracking was responsible for this deactivation, which is supported by scanning electron microscopy (SEM) image analysis. It was demonstrated that the catalytic activity of the deactivated char can be partially recovered by burning off the carbon deposits with an oxidizing gas mixture containing 0.46% oxygen. 10 refs., 11 figs., 1 tab.

Zhi-qiang Sun; Jin-hu Wu; Mohammad Haghighi; John Bromly; Esther Ng; Hui Ling Wee; Yang Wang; Dong-ke Zhang [Chinese Academy of Sciences, Taiyuan (China). Institute of Coal Chemistry

2007-06-15T23:59:59.000Z

133

Trends Online Methane Emissions  

NLE Websites -- All DOE Office Websites (Extended Search)

Emissions Introduction Annual Estimates of Global Anthropogenic Methane Emissions: 1860-1994 - D.I. Stern and R.K. Kaufmann Contents-Trends | CDIAC Home 102001...

134

Coalbed Methane Production  

Gasoline and Diesel Fuel Update (EIA)

Methane Production (Billion Cubic Feet) Period: Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes 2006 2007 2008 2009...

135

Plasma—Methane Reformation  

INL thermal plasma methane reformation process produces hydrogen and elemental carbon from natural gas and other hydrocarbons, such as natural gas or ...

136

NIST: Methane Symmetry Operations - Introduction  

Science Conference Proceedings (OSTI)

Methane Symmetry Operations. ... At least three T d symmetry classification systems are widely used at present in the methane literature [5-13]. ...

137

Methane Hydrate Advisory Committee Charter | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Charter Methane Hydrate Advisory Committee Charter Methane Hydrate Advisory Committee Charter Methane Hydrate Advisory Committee Charter...

138

Fundamental studies of the mechanism of catalytic reactions with catalysts effective in the gasification of carbon solids and the oxidative coupling of methane. Quarterly report, April 1, 1994--June 30, 1994  

DOE Green Energy (OSTI)

Catalytic gasification work has been completed and no other work is planned in the general area of catalytic gasification of coals and chars has operated without a post-doctoral fellow because of budget limitations during the first two quarters of FY1994. Dr. S. Sundararajan joined the group in April 1994 and will be assigned to the project throughout the remaining of the fiscal year. Results published by Hamakawa, et al. in The Journal of the Electrochemical Society have confirmed the concept of methane coupling via a membrane reactor. These findings confirm our previous conclusion that thinner membranes and increased surface activity for C-H bond activation at low temperatures are required in order to reach commercially attractive rates of reaction. The initial analysis of a theoretical model comparing the membrane and cyclic processes has been completed. The results indicate that perovskite membranes on the order of 50 microns will be needed for the membrane operation to be superior to a cyclic one. Two techniques, laser ablation and spin-coating/sol-gel chemistry are being tried to prepare the thin membranes described above. Studies of the magnetochemical properties of the calcium-nickel-potassium oxide powdered catalysts have been concluded and a manuscript describing the work has been completed. Synchrotron x-ray fluorescence microprobe data for calcium-nickel-potassium films have been analyzed and an abstract of the results has been submitted for presentation at the Fall Meeting of the Materials Research Society. Initial films of strontium-zirconium oxide, using yttria-stabilized zirconia as a buffer layer, have been fabricated using pulsed laser deposition. X-ray diffraction data have been obtained for several of the strontium-zirconium-yttrium oxide films.

Iglesia, E.; Perry, D.L.; Heinemann, H.

1994-06-01T23:59:59.000Z

139

Extracting value from coal mine methane  

Science Conference Proceedings (OSTI)

Emerging US policy to regulate greenhouse gas (GHG) emissions through a cap-and-trade program presents mine managers with a new opportunity to explore and develop methane utilization or abatement projects that generate value from the anodization of carbon offset credits. In addition, the rising focus on US energy security and domestic energy supply is promoting mine managers and engineers to give further consideration to the importance of their methane gas by-products. The market through which coal mine methane offset projects can be developed and carbon offset credits monetized is quickly maturing. While many methane utilization projects have previously been uneconomical, the carbon offset credit market provides a new set of financing tools for mine engineers to capitalize these projects today. Currently , there are two certification programs that have approved project protocols for CMM projects. The Voluntary Carbon Standard (VCS) offers a methodology approved under the Clean Development Mechanism, the international compliance based offset market under the Kyoto Protocol. The VCS protocol is applicable to projects that combust ventilation air methane (VAM) and methane extracted from pre-and post-mine drainage systems. The Chicago Climate Exchange (CCX), which operates a voluntary yet binding cap-and-trade market, also has an approved protocol for CMM projects. CCX's protocol can be applied to projects combusting VAM, and methane extracted from pre-and-post-mine drainage systems, as well as abandoned mines. The article describes two case studies - Developing a gob gas utilization project financed by carbon offset credits and First VAM oxidation system to be commissioned at an operating mine in the US. 1 tab., 4 photos.

Liebert, B. [Verdao Group (United States)

2009-06-15T23:59:59.000Z

140

Methane Hydrates - Methane Hydrate Graduate Fellowship  

NLE Websites -- All DOE Office Websites (Extended Search)

Future Supply and Emerging Resources Future Supply and Emerging Resources The National Methane Hydrates R&D Program - Graduate Fellowship Program Methane Hydrate Graduate Fellowship Program Jeffrey James Marlow, a graduate student in Geobiology at the California Institute of Technology, was recently selected as the 2012 recipient of the NETL-National Academy of Sciences (NAS) Methane Hydrate Research Fellowship. Please see page 15 of the March 2013 issue (Vol. 13, Issue 1) of Fire in the Ice for more information on the recipient. The Department of Energy has a long history of building synergistic relationships with research universities. Funding academic research is a "win-win-win" situation. The U.S. government is able to tap into some of the best minds available for solving national energy problems, the universities get the support they need to maintain cutting edge faculty and laboratories, and the students involved are provided with opportunities that help them along their chosen path of study, strengthening the national pool of scientists and engineers. According to Samuel Bodman, speaking about graduate research in methane hydrates, "Students are the foundation of our energy future, bringing new ideas and fresh perspectives to the energy industry. What better way to assure technology innovation than to encourage students working on the development of a resource that has the potential to tip our energy balance toward clean-burning, domestic fuels."

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Dense ceramic membranes for converting methane to syngas  

DOE Green Energy (OSTI)

Dense mixed-oxide ceramics capable of conducting both electrons and oxygen ions are promising materials for partial oxygenation of methane to syngas. We are particularly interested in an oxide based on the Sr-Fe-Co-O system. Dense ceramic membrane tubes have been fabricated by a plastic extrusion technique. The sintered tubes were then used to selectively transport oxygen from air through the membrane to make syngas without the use of external electrodes. The sintered tubes have operated for >1000 h, and methane conversion efficiencies of >98% have been observed. Mechanical properties, structural integrity of the tubes during reactor operation, results of methane conversion, selectivity of methane conversion products, oxygen permeation, and fabrication of multichannel configurations for large-scale production of syngas will be presented.

Balachandran, U.; Dusek, J.T.; Picciolo, J.J.; Ma, B.; Maiya, P.S.; Mieville, R.L. [Argonne National Lab., IL (United States); Kleefisch, M.S.; Udovich, C.A. [Amoco Exploration/Production, Naperville, IL (United States)

1995-07-01T23:59:59.000Z

142

Methane Hydrate Program  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

FY 2011 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 Hydrate Program Report to Congress. The report was prepared by the Department of Energy's Office of Fossil Energy and summarizes the progress being made in this important area of research. Pursuant to statutory requirements, this report is being provided to the following

143

Methane Hydrate Annual Reports  

Energy.gov (U.S. Department of Energy (DOE))

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...

144

Methane Hydrate Program  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Fiscal Year 2012 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. Department of Energy Fiscal Year 2012 Methane Hydrate Program Report to Congress. The report was prepared by the Department of Energy's Office of Fossil Energy and summarizes the progress being made in this important area

145

Methane Hydrate Advisory Committee Meeting Minutes | Department...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

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

146

Direct conversion of methane to C sub 2 's and liquid fuels  

DOE Green Energy (OSTI)

Research on promoted metal oxide catalysts has continued with the study of alkaline earth/metal oxide halide catalysts. A barium bromide/alumina catalyst was comparable in methane conversion and selectivity to C{sub 2}'s to barium chloride/alumina catalysts. The effects of varying methane to oxygen feed ratios were explored for one of the best alkaline earth catalysts and one of the best literature catalysts (Li/MgO). A significant decrease in the selectivity to C{sub 2}'s is observed upon addition of ethane to the feed gas (feed gas methane/ethane ratio of 3). This observation demonstrates that a significant amount of ethane should not be recycled during methane oxidation over these types of catalysts under process conditions used. Methane oxidation over barium carbonate alone results in high enough selectivities and methane conversions to suggest an oxidized barium species may be responsible for methane oxidation on barium/metal oxide catalysts. Methane coupling studies have continued using layered perovskite catalysts in the cofeed mode and double perovskite catalysts in the sequential mode. Addition of sodium to the double perovskite LaCaMnCoO{sub 6} resulted in a catalyst with improved selectivity over the one without sodium. A reactor system containing two reactors in under construction. These reactors will be used to study different feed diluents, including steam. One reactor will be used to study the effects of pressure on the reaction. Process economics were explored for a hypothetical methane coupling scheme employing a feed mixture of 7/2/1 nitrogen/methane/oxygen. Economic evaluations of the first two of a series of cases based on extrapolations of Union Carbide methane coupling results have been completed. 33 refs., 17 figs., 2 tabs.

Warren, B.K.; Campbell, K.D.; Matherne, J.L.

1990-02-14T23:59:59.000Z

147

TRENDS: METHANE EMISSIONS - INTRODUCTION  

NLE Websites -- All DOE Office Websites (Extended Search)

Of the total direct radiative forcing of long-lived greenhouse gases (2.45 Of the total direct radiative forcing of long-lived greenhouse gases (2.45 Wm-2), almost 20% is attributable to methane (CH4), according to the 1995 report of the Intergovernmental Panel on Climate Change (IPCC 1995). Since the mid-1700s, the atmospheric concentration of methane has increased by about 145% (IPCC 1995). Thus, an understanding of the various sources of methane is important. Atmospheric methane is produced both from natural sources (e.g., wetlands) and from human activities (see global methane cycle, from Professor W.S. Reeburgh at the University of California Irvine). Total sources of methane to the atmosphere for the period 1980-1990 were about 535 (range of 410-660) Tg (1 Teragram = 1 million metric tons) CH4 per year, of which 160 (110-210) Tg CH4/yr were from natural sources and 375 (300-450) Tg CH4/yr

148

Methane Hydrate | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Methane Hydrate 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 generally occur in two types of settings: under Arctic permafrost, and beneath the ocean floor. Methane that forms hydrate can be both biogenic, created by biological activity in sediments, and thermogenic, created by geological processes deeper within the earth.

149

Methane coupling by membrane reactor. Quarterly technical progress report, June 25, 1994--September 24, 1994  

DOE Green Energy (OSTI)

This quarterly report describes results from the experimental studies on oxidative coupling of methane, oxygen conducting perovskite dense membrane synthesis and modeling studies of the methane coupling reaction. The focus of the experimental study is to explore the effects of varying catalyst loading, varying methane to oxygen ratios and feed conditions when the oxygen conversion is much less than 100%. Results from these studies help in understanding the effects of various parameters controlling methane coupling. Dense membrane synthesis and characterization results are presented which describe new approaches to the synthesis and characterization of these membranes. The modeling results described in this report present a theoretical fit to the experimental data on oxidative coupling of methane in fixed bed reactors. The parameters from the fit are used to predict the trends in experimental data obtained from VYCOR membrane reactors. The predicted trends are based on a theoretical model employing simplified methane coupling kinetics.

Ma, Yi Hua

1995-01-04T23:59:59.000Z

150

NETL: Methane Hydrates - Global Assessment of Methane Gas Hydrates  

NLE Websites -- All DOE Office Websites (Extended Search)

Assessment of Methane Gas Hydrates Last Reviewed 6142013 DE-FE0003060 Goal The goal of this project is to develop a global assessment of methane gas hydrates that will facilitate...

151

The basics of coalbed methane  

Science Conference Proceedings (OSTI)

The report is an overview of coalbed methane (CBM), also known as coal seam gas. It provides an overview of what coalbed methane is and the current status of global coalbed methane exploration and production. Topics covered in the report include: An analysis of the natural gas industry, including current and future production, consumption, and reserves; A detailed description of coalbed methane, its characteristics, and future potential; An analysis of the key business factors that are driving the increased interest in coalbed methane; An analysis of the barriers that are hindering the development of coalbed methane; An overview of the technologies used for coalbed methane production and water treatment; and Profiles of key coalbed methane producing countries. 25 figs., 5 tabs., 1 app.

NONE

2006-12-15T23:59:59.000Z

152

Methane Emissions - Energy Information Administration  

U.S. Energy Information Administration (EIA)

Carbon Dioxide Equivalent; Estimated 2003 ... for about 8.7 percent of total U.S. greenhouse gas emissions when weighted by methane’s global warming potential factor.

153

Enhanced coalbed methane recovery  

SciTech Connect

The recovery of coalbed methane can be enhanced by injecting CO{sub 2} in the coal seam at supercritical conditions. Through an in situ adsorption/desorption process the displaced methane is produced and the adsorbed CO{sub 2} is permanently stored. This is called enhanced coalbed methane recovery (ECBM) and it is a technique under investigation as a possible approach to the geological storage of CO{sub 2} in a carbon dioxide capture and storage system. This work reviews the state of the art on fundamental and practical aspects of the technology and summarizes the results of ECBM field tests. These prove the feasibility of ECBM recovery and highlight substantial opportunities for interdisciplinary research at the interface between earth sciences and chemical engineering.

Mazzotti, M.; Pini, R.; Storti, G. [ETH, Zurich (Switzerland). Inst. of Process Engineering

2009-01-15T23:59:59.000Z

154

Voluntary Reporting of Greenhouse Gases Program - Electricity Factors  

U.S. Energy Information Administration (EIA) Indexed Site

Voluntary Reporting Program > Coefficients Voluntary Reporting Program > Coefficients Voluntary Reporting of Greenhouse Gases Program (Voluntary Reporting of Greenhouse Gases Program Fuel Carbon Dioxide Emission Coefficients) Voluntary Reporting of Greenhouse Gases Program Fuel Emission Coefficients Table 1: Carbon Dioxide Emission Factors for Stationary Combustion Table 2: Carbon Dioxide Emission Factors for Transportation Fuels Table 3: Generic Methane and Nitrous Oxide Emission Factors for Stationary Fuel Combustion Table 4: Specific Methane and Nitrous Oxide Emission Factors for Biogenic Fuel Sources Table 5: Methane and Nitrous Oxide Emissions Factors for Highway Vehicles Table 6: Methane and Nitrous Oxide Emission Factors for Alternative Fuel Vehicles Table 7: Methane and Nitrous Oxide Emission Factors for Non-Highway Mobile Combustion

155

Development of vanadium-phosphate catalysts for methanol production by selective oxidation of methane. Quarterly technical progress report No. 6, July--September 1994  

DOE Green Energy (OSTI)

This is the eighth quarterly technical progress report. During this quarter the project was initiated, after transfer via a novation agreement, at the Colorado School of Mines. Project initiation activities have included: set up of catalyst synthesis apparatus; training on x-ray diffraction and FTIR apparatus; set up of catalyst testing reactor; set up of reactor product analytical systems; and set up of method development for measuring catalyst acidity via FTIR. At the end of this quarter significant progress had been made towards completion of these initiation activities. Several catalyst syntheses have been performed and the catalysts characterized by x-ray diffraction and FTIR. The catalyst testing reactor system is operational. Reactor product analysis system is nearing completion. Initiation of this system was delayed by the unavailability of a Valco valve which has just recently arrived. Set up of the in-situ FTIR cell for catalyst acidity studies has begun. In this report the results of several catalyst syntheses are reported along with characterization results. In particular, impregnation of vanadyl pyrophosphate with potassim nitrate dramatically reduced the number of surface hydroxyl groups. Such groups may be important in the non-selective, total oxidation of hydrocarbons. Also, preliminary experimental results on FTIR spectra of adsorbed pyridine are presented. It is shown that pyridine adsorbed on the catalyst surface can be easily observed by the diffuse reflectance IR technique. We plan to apply this technique to measurement of the acid site strength of surfaces modified with promoters.

McCormick, R.L.

1995-01-10T23:59:59.000Z

156

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 5, November 16, 1987--January 15, 1988  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that later can be converted to either liquid fuels or value-added chemicals, as economics dictate. During this reporting period, we have synthesized and tested several novel catalysts for methane reforming (Tasks 1 and 2) and for partial oxidation of methane (Tasks 3 and 4). We started to test a mixed metal system, an FeRu{sub 3} cluster. This catalyst was supported both on zeolite and on magnesium oxide and the systems were tested for methane reforming at various reaction temperatures. We also prepared and tested a monomeric ruthenium catalyst supported on magnesium oxide. We found that methane is activated at a lower temperature with the basic magnesium oxide support than with acidic supports such as zeolite or alumina. Methane conversions increased with temperature, but the production of coke also increased. We prepared a sterically hindered ruthenium porphyrin encapsulated in a zeolite supercage for catalysis of methane oxidation. The results showed that only carbon dioxide was produced. Addition of axial base to this catalyst gave similar results. Another type of catalyst, cobalt Schiff base complexes, was also prepared and tested for methane oxidation. In this case, no methane conversion was observed at temperatures ranging from 200 to 450{degrees}C. These complexes do not appear to be stable under the reaction conditions.

Wilson, R.B. Jr.; Chan Yee Wai

1988-02-05T23:59:59.000Z

157

Predicting methane fermentation biodegradability  

Science Conference Proceedings (OSTI)

Estimation of the feedstock digestibility in cows by procedures developed by Van Soest was performed. By feeding cows feedstuff of different lignin content, cell wall digestibility can be estimated. In this article a digestibility model has been employed and tested along with other models for the rapid prediction of substrate methane fermentation biodegradability.

Chandler, J.A.; Jewell, W.J.; Gossett, J.M.; Van Soest, P.J.; Robertson, J.B.

1980-01-01T23:59:59.000Z

158

Methane emissions from natural wetlands  

SciTech Connect

Analyses of air trapped in polar ice cores in conjunction with recent atmospheric measurements, indicate that the atmospheric methane concentration increased by about 250% during the past two or three hundred years (Rasmussen and Khalil, 1984). Because methane is a potent ``greenhouse`` gas, the increasing concentrations are expected to contribute to global warning (Dickinson and Cicerone, 1986). The timing of the methane increase suggests that it is related to the rapid growth of the human population and associated industrialization and agricultural development. The specific causes of the atmospheric methane concentration increase are not well known, but may relate to either increases in methane sources, decreases in the strengths of the sinks, or both.

Meyer, J.L. [Georgia Univ., Athens, GA (United States); Burke, R.A. Jr. [Environmental Protection Agency, Athens, GA (United States). Environmental Research Lab.

1993-09-01T23:59:59.000Z

159

Shock-Tube Study of Methane Ignition with NO2 and N2O  

E-Print Network (OSTI)

NOx produced during combustion can persist in the exhaust gases of a gas turbine engine in quantities significant to induce regulatory concerns. There has been much research which has led to important insights into NOx chemistry. One method of NOx reduction is exhaust gas recirculation. In exhaust gas recirculation, a portion of the exhaust gases that exit are redirected to the inlet air stream that enters the combustion chamber, along with fuel. Due to the presence of NOx in the exhaust gases which are subsequently introduced into the burner, knowledge of the effects of NOx on combustion is advantageous. Contrary to general NOx research, little has been conducted to investigate the sensitizing effects of NO2 and N2O addition to methane/oxygen combustion. Experiments were made with dilute and real fuel air mixtures of CH4/O2/Ar with the addition of NO2 and N2O. The real fuel air concentrations were made with the addition of NO2 only. The equivalence ratios of mixtures made were 0.5, 1 and 2. The experimental pressure range was 1 - 44 atm and the temperature range tested was 1177 – 2095 K. The additives NO2 and N2O were added in concentrations from 831 ppm to 3539 ppm. The results of the mixtures with NO2 have a reduction in ignition delay time across the pressure ranges tested, and the mixtures with N2O show a similar trend. At 1.3 atm, the NO2 831 ppm mixture shows a 65% reduction and shows a 75% reduction at 30 atm. The NO2 mixtures showed a higher decrease in ignition time than the N2O mixtures. The real fuel air mixture also showed a reduction. Sensitivity Analyses were performed. The two most dominant reactions in the NO2 mixtures are the reaction O+H2 = O+OH and the reaction CH3+NO2 = CH3O+NO. The presence of this second reaction is the means by which NO2 decreases ignition delay time, which is indicated in the experimental results. The reaction produces CH3O which is reactive and can participate in chain propagating reactions, speeding up ignition. The two dominant reactions for the N2O mixture are the reaction O+H2 = O+OH and, interestingly, the other dominant reaction is the reverse of the initiation reaction in the N2O-mechanism: O+N2+M = N2O+M. The reverse of this reaction is the direct oxidation of nitrous oxide. The O produced in this reaction can then speed up ignition by partaking in propagation reactions, which was experimentally observed.

Pemelton, John

2011-08-01T23:59:59.000Z

160

Dense ceramic membranes for methane conversion  

DOE Green Energy (OSTI)

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.

Balachandran, U.; Mieville, R.L.; Ma, B. [Argonne National Lab., IL (United States); Udovich, C.A. [Amoco Oil Co., Naperville, IL (United States)

1996-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

Synthesis of High-Surface Area Cathode Materials for Solid Oxide ...  

Science Conference Proceedings (OSTI)

Cu-Pd/CeO2 Cermet Anodes for Direct Oxidation of Methane in LSGM Electrolyte -Supported SOFCs · Deposition of Porous Anode Film of Solid Oxide Fuel Cell ...

162

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

DOE Patents (OSTI)

The invention described in this report relates to a combined system of an apparatus and a method of increasing the rates of oxidation of gases and hazardous vapors by methanotrophic and other bacteria. The gases of interest are methane and trichlorethylene and other hazardous vapors. In a preferred embodiment, the oxidation rate of methane is improved by the addition of clays, e.g., kaolin, sometimes called ``China clay.``

Apel, W.A.; Dugan, P.R.

1991-12-31T23:59:59.000Z

163

Coal Bed Methane Primer  

SciTech Connect

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 stakeholders to present a consistent and complete synopsis of the key issues involved with CBM. In light of the numerous CBM NEPA documents under development this Primer could be used to support various public scoping meetings and required public hearings throughout the Western States in the coming years.

Dan Arthur; Bruce Langhus; Jon Seekins

2005-05-25T23:59:59.000Z

164

NETL: Methane Hydrates - Interagency Coordination  

NLE Websites -- All DOE Office Websites (Extended Search)

Links to interagency pdf. The multi-faceted issues associated with naturally occurring methane hydrates demand a coordinated approach to studying (1) the potential of this resource...

165

Methane/nitrogen separation process  

DOE Patents (OSTI)

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.

Baker, Richard W. (Palo Alto, CA); Lokhandwala, Kaaeid A. (Menlo Park, CA); Pinnau, Ingo (Palo Alto, CA); Segelke, Scott (Mountain View, CA)

1997-01-01T23:59:59.000Z

166

Methane/nitrogen separation process  

DOE Patents (OSTI)

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.

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

1997-09-23T23:59:59.000Z

167

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

SciTech Connect

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.

Bogner, J. [Argonne National Lab., IL (United States); Meadows, M. [ETSU, Harwell, Oxfordshire (United Kingdom); Czepiel, P. [Harvard Univ., Cambridge, MA (United States)

1997-08-01T23:59:59.000Z

168

Capture and Use of Coal Mine Ventilation Air Methane  

Science Conference Proceedings (OSTI)

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).

Deborah Kosmack

2008-10-31T23:59:59.000Z

169

Quantification of multiple methane emission sources at landfills using a double tracer technique  

SciTech Connect

Research highlights: > Precise and reliable measurements of emissions from landfills are needed. > A tracer technique involving simultaneous release of two tracers was proven successful. > Measurements to be performed at times with low changing trends in barometric pressure. - Abstract: A double tracer technique was used successfully to quantify whole-site methane (CH{sub 4}) emissions from Fakse Landfill. Emissions from different sections of the landfill were quantified by using two different tracers. A scaled-down version of the tracer technique measuring close-by to localized sources having limited areal extent was also used to quantify emissions from on-site sources at the landfill facility, including a composting area and a sewage sludge storage pit. Three field campaigns were performed. At all three field campaigns an overall leak search showed that the CH{sub 4} emissions from the old landfill section were localized to the leachate collection wells and slope areas. The average CH{sub 4} emissions from the old landfill section were quantified to be 32.6 {+-} 7.4 kg CH{sub 4} h{sup -1}, whereas the source at the new section was quantified to be 10.3 {+-} 5.3 kg CH{sub 4} h{sup -1}. The CH{sub 4} emission from the compost area was 0.5 {+-} 0.25 kg CH{sub 4} h{sup -1}, whereas the carbon dioxide (CO{sub 2}) and nitrous oxide (N{sub 2}O) flux was quantified to be in the order of 332 {+-} 166 kg CO{sub 2} h{sup -1} and 0.06 {+-} 0.03 kg N{sub 2}O h{sup -1}, respectively. The sludge pit located west of the compost material was quantified to have an emission of 2.4 {+-} 0.63 kg h{sup -1} CH{sub 4}, and 0.03 {+-} 0.01 kg h{sup -1} N{sub 2}O.

Scheutz, C., E-mail: chs@env.dtu.dk [Department of Environmental Engineering, Technical University of Denmark, Miljovej, Building 113, 2800 Kongens Lyngby (Denmark); Samuelsson, J., E-mail: jerker.samuelsson@fluxsense.se [Chalmers University of Technology/FluxSense AB, SE-412 96 Goeteborg (Sweden); Fredenslund, A.M., E-mail: amf@env.dtu.dk [Department of Environmental Engineering, Technical University of Denmark, Miljovej, Building 113, 2800 Kongens Lyngby (Denmark); Kjeldsen, P., E-mail: pk@env.dtu.dk [Department of Environmental Engineering, Technical University of Denmark, Miljovej, Building 113, 2800 Kongens Lyngby (Denmark)

2011-05-15T23:59:59.000Z

170

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

DOE Patents (OSTI)

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.

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

1996-11-12T23:59:59.000Z

171

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

DOE Patents (OSTI)

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.

Balachandran, Uthamalingam (Hinsdale, IL); Dusek, Joseph T. (Lombard, IL); Kleefisch, Mark S. (Napersville, IL); Kobylinski, Thadeus P. (Lisle, IL)

1996-01-01T23:59:59.000Z

172

Florida Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Florida Coalbed Methane Proved Reserves, Reserves Changes, and...

173

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

with sampling and observation from the surface ship. Activities included collection of methane hydrate, sediment, water, and other materials from methane hydrate and seep sites...

174

NIST: Methane Symmetry Operations - Td Symmetry Species  

Science Conference Proceedings (OSTI)

Table of Contents Methane Symmetry Operations. 11. ... Magnetic-dipole transitions are observed in molecular-beam studies of methane [42]. ...

175

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

represent components of dynamic biogeochemical environments with inputs and outputs of methane, accurate rates of biological methane production are poorly understood. Recent...

176

Michigan Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Michigan Coalbed Methane Proved Reserves, Reserves Changes, and...

177

Kentucky Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Kentucky Coalbed Methane Proved Reserves, Reserves Changes, and...

178

Enhanced Renewable Methane Production System | Argonne National...  

NLE Websites -- All DOE Office Websites (Extended Search)

Enhanced Renewable Methane Production System Technology available for licensing: Enhanced renewable methane production system provides a low-cost process that accelerates...

179

MethaneHydrateRD_FC.indd  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Academies 2010 One of these is methane hydrate - molecules of natural gas trapped in ice crystals. Containing vast amounts of natural gas, methane hydrate occurs in a variety...

180

New Materials Make Methane Capture Possible  

Science Conference Proceedings (OSTI)

May 8, 2013... SBN, captured enough medium source methane to turn it to high purity methane, which in turn could be used to generate efficient electricity.

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

Oxidation of Flash Reduced Iron Particles in Various Gas Mixtures ...  

Science Conference Proceedings (OSTI)

Decomposition of Methane during Oxide Reduction Using Natural gas · Delivering a National Process Design Unit with Industry Support · Development of a ...

182

Biomass Burning and the Production of Greenhouse Gases  

Science Conference Proceedings (OSTI)

Biomass burning is a source of greenhouse gases, carbon dioxide, methane, and nitrous oxide. In addition, biomass burning is a source of chemically active gases, including carbon monoxide, nonmethane hydrocarbons, and nitric oxide. These gases, along ...

Levine J. S.

1994-01-01T23:59:59.000Z

183

Coal mine methane global review  

Science Conference Proceedings (OSTI)

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.

NONE

2008-07-01T23:59:59.000Z

184

Reducing Open Cell Landfill Methane Emissions with a Bioactive Alternative Daily  

Science Conference Proceedings (OSTI)

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 prone to rapid desiccation. Bacterial adsorption onto foam padding, natural sponge, and geotextile was successful. The most important factor for success appeared to be water holding capacity. Prototype biotarps made with geotextiles plus adsorbed methane oxidizing bacteria were tested for their responses to temperature, intermittent starvation, and washing (to simulate rainfall). The prototypes were mesophilic, and methane oxidation activity remained strong after one cycle of starvation but then declined with repeated cycles. Many of the cells detached with vigorous washing, but at least 30% appeared resistant to sloughing. While laboratory landfill simulations showed that four-layer composite biotarps made with two different types of geotextile could remove up to 50% of influent methane introduced at a flux rate of 22 g m{sup -2} d{sup -1}, field experiments did not yield high activity levels. Tests revealed that there were high hour-to-hour flux variations in the field, which, together with frequent rainfall events, confounded the field testing. Overall, the findings suggest that a methanotroph embedded biotarp appears to be a feasible strategy to mitigate methane emission from landfill cells, although the performance of field-tested biotarps was not robust here. Tarps will likely be best suited for spring and summer use, although the methane oxidizer population may be able to shift and adapt to lower temperatures. The starvation cycling of the tarp may require the capacity for intermittent reinoculation of the cells, although it is also possible that a subpopulation will adapt to the cycling and become dominant. Rainfall is not expected to be a major factor, because a baseline biofilm will be present to repopulate the tarp. If strong performance can be achieved and documented, the biotarp concept could be extended to include interception of other compounds beyond methane, such as volatile aromatic hydrocarbons and chlorinated solvents.

Helene Hilger; James Oliver; Jean Bogner; David Jones

2009-03-31T23:59:59.000Z

185

Methane activation on ruthenium: the nature of the surface intermediates T.V. Choudhary and D.W. Goodman*  

E-Print Network (OSTI)

) by steam reforming [1,2], partial oxidation [3,4], autothermal reforming [2,5] or CO2 reforming [6,20]. In a similar fashion, we have investigated step- wise methane reforming (methane decomposition in step IMethane activation on ruthenium: the nature of the surface intermediates T.V. Choudhary and D

Goodman, Wayne

186

Catalysis Letters 59 (1999) 9394 93 Stepwise methane steam reforming: a route to CO-free hydrogen  

E-Print Network (OSTI)

Catalysis Letters 59 (1999) 93­94 93 Stepwise methane steam reforming: a route to CO-free hydrogen-free hydrogen. Keywords: methane decomposition, Ni/zirconia, steam gasification In order to utilize hydrogen of impurities, particularly carbon monoxide. Steam reforming, partial oxidation and au- tothermal reforming [1

Goodman, Wayne

187

Microchannel Process Technology for Compact Methane Steam Reforming  

Science Conference Proceedings (OSTI)

The study of microchannel reaction engineering and applications to compact chemical reactors has expanded rapidly both academically and industrially in recent years. Velocys{reg_sign}, a spin-out company from Battelle Memorial Institute, is commercializing microchannel process technology for large-scale chemical processing. Hydrogen production at industrial rates in compact Velocys hardware is made possible through increases in both heat and mass transfer rates for highly active and novel catalysts. In one example, a microchannel methane steam reforming reactor is presented with integrated catalytic partial oxidation of methane prior to catalytic combustion with low excess air (25%) to generate the required energy for undothermic methane steam reforming in adjacent channels. Heat transfer rates from the exothermic reactions exceed 18 W/cm{sup 2} of interplanar heat transfer surface area and exceed 65 W/cm{sup 3} of total reaction volume for a methane steam reforming contact time near 4 milliseconds. The process intensity of the Velocys methane steam reformer well exceeds that of conventional steam reformers, which have a typical volumetric heat flux below 1 W/cm{sup 3}. The integration of multiple unit operations and improvements in process intensification result in significant capital and operating cost savings for commercial applications.

Tonkovich, A L.; Perry, Steve; Wang, Yong; Qiu, Dongming; LaPlante, Timothy J.; Rogers, William A.

2004-12-01T23:59:59.000Z

188

Methane coupling by membrane reactor. Quarterly technical progress report, December 25, 1994--March 24, 1995  

DOE Green Energy (OSTI)

Research efforts during this quarter concentrated on two issues. The first issue is related to the chemistry of oxygen conducting materials that could be used as dense membranes in the membrane reactors. Mixed oxides of La, Sr, Fe, Ce, Yb etc., were synthesized, characterized and studied for their catalytic activity towards the oxidative coupling of methane. Heavy metal oxides of lanthanum, strontium and iron, which form good oxygen conductors, showed very poor methane coupling activity. Perovskites of the Strontium-Cerium-Yitribium series showed moderate activity for methane coupling. These could be potential candidates for dense membrane synthesis, since they also have moderate oxygen conduction properties. The second area of research focus was the development of a radial flow catalytic membrane reactor in which methane coupling was carried out over a catalyst that was deposited inside the pores of a ceramic porous membrane. Catalytic results from the high temperature oxidative coupling of methane in these radial flow membrane reactors are presented in this report. By exploring the reactor performance in membranes of pore diameters of 2.0{mu}m, 0.2{mu}m, and 0.02{mu}m, the effect of the diffusional regime on the methane. coupling activity was demonstrated. The smallest pore diameter membranes exhibited lowest hydrocarbon selectivities.

Ma, Hua Yi

1995-06-06T23:59:59.000Z

189

Conversion of methane to higher hydrocarbons (Biomimetic catalysis of the conversion of methane to methanol). Final report  

DOE Green Energy (OSTI)

In addition to inorganic catalysts that react with methane, it is well-known that a select group of aerobic soil/water bacteria called methanotrophs can efficiently and selectively utilize methane as the sole source of their energy and carbon for cellular growth. The first reaction in this metabolic pathway is catalyzed by the enzyme methane monooxygenase (MMO) forming methanol. Methanol is a technology important product from this partial oxidation of methane since it can be easily converted to liquid hydrocarbon transportation fuels (gasoline), used directly as a liquid fuel or fuel additive itself, or serve as a feedstock for chemicals production. This naturally occurring biocatalyst (MMO) is accomplishing a technologically important transformation (methane directly to methanol) for which there is currently no analogous chemical (non-biological) process. The authors approach has been to use the biocatalyst, MMO, as the initial focus in the development of discrete chemical catalysts (biomimetic complexes) for methane conversion. The advantage of this approach is that it exploits a biocatalytic system already performing a desired transformation of methane. In addition, this approach generated needed new experimental information on catalyst structure and function in order to develop new catalysts rationally and systematically. The first task is a comparative mechanistic, biochemical, and spectroscopic investigation of MMO enzyme systems. This work was directed at developing a description of the structure and function of the catalytically active sites in sufficient detail to generate a biomimetic material. The second task involves the synthesis, characterization, and chemical reactions of discrete complexes that mimic the enzymatic active site. These complexes were synthesized based on their best current understanding of the MMO active site structure.

Watkins, B.E.; Taylor, R.T.; Satcher, J.H. [and others

1993-09-01T23:59:59.000Z

190

NETL: Methane Hydrates - DOE/NETL Projects - Controls On Methane...  

NLE Websites -- All DOE Office Websites (Extended Search)

On Methane Expulsion During Melting Of Natural Gas Hydrate Systems Last Reviewed 6242013 DE-FE0010406 Goal The project goal is to predict, given characteristic climate-induced...

191

Development of dense ceramic membranes for methane conversion  

DOE Green Energy (OSTI)

The most significant cost associated with partial oxidation of methane to syngas is that of the oxygen plant. In this paper, the authors offer a technology, based on dense ceramic membranes, that uses air as the oxidant for methane conversion reactions, thus eliminating the need for the oxygen plant. Certain ceramic materials exhibit both electronic and ionic conductivities (of particular interest is oxygen-ion conductivity). These materials transport not only oxygen ions (functioning as selective oxygen separators) but also electrons back from the reactor side to the oxygen/reduction interface. No external electrodes are required, and, if the driving potential of transport is adequate, the partial oxidation reactions should be spontaneous. Such a system will operate without an externally applied potential. Oxygen is transported across the ceramic material in the form of oxygen ions, not oxygen molecules. Recent reports in the literature suggest that dense ceramic membranes made of these mixed conductors can successfully separate oxygen from air at flux rates that could be considered commercially feasible. Thus, these membranes have the potential to improve the economics of methane conversion processes. In principle, the dense ceramic materials can be shaped into hollow-tube reactors, in which air passes over the outside of the membrane and methane flows through the inside. The surfaces can also be reversed. The membrane is permeable to oxygen at high temperatures, but not to nitrogen or other gases. Thus, only oxygen from air can be transported through the membrane to the inside of the reactor surface, where it reacts with methane. Other geometric forms, such as honeycombs or corrugations, of the reactor are possible and can provide substantially greater surface areas for reaction.

Balachandran, U.; Dusek, J.T.; Maiya, P.S.; Ma, B.; Mieville, R.L. [Argonne National Lab., IL (United States). Energy Technology Div.; Kleefisch, M.S.; Udovich, C.A.; Fleisch, T.H. [Amoco Exploration/Production, Naperville, IL (United States); Bose, A.C. [USDOE Pittsburgh Energy Technology Center, PA (United States)

1995-06-01T23:59:59.000Z

192

Methane Credit | Open Energy Information  

Open Energy Info (EERE)

Methane Credit Methane Credit Jump to: navigation, search Name Methane Credit Place Charlotte, North Carolina Zip 28273 Product Specialises in utilising methane produced on municipal landfill sites. Coordinates 35.2225°, -80.837539° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":35.2225,"lon":-80.837539,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

193

NETL: Methane Hydrates - Hydrate Newsletter  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrate R&D Program Newsletter Methane Hydrate R&D Program Newsletter An image of a hydrate burning overlayed with the Newsletter Title: Fire in the Ice The methane hydrate newsletter, Fire in the Ice, is a bi-annual publication highlighting the latest developments in international gas hydrates R&D. Fire in the Ice promotes the exchange of information amoung those involved in gas hydrates research and development, and also recognizes the efforts of a hydrate researcher in each issue. The newsletter now reaches nearly 1300 scientists and other interested individuals in sixteen countries. To subscribe electronically to Fire in the Ice please send an email to karl.lang@contr.netl.doe.gov Please click on the links below to access issues of "Fire in the Ice". More on Methane Hydrates

194

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

SciTech Connect

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 process as a biofilter by studying the distribution of methane oxidation and disposition of methanotrophic populations in the Pacific Ocean. We investigated several environments including the basins offshore California, the continental margin off Central America, and the shallow waters around gas seeps. We succeeded in identifying the distributions of activity in these environments, identified potential physical and chemical controls on methanotrophic activity, we further revealed details about the methanotrophic communities active in these settings, and we developed new approaches to study methanotrophic communities. These findings should improve our capacity to predict the methanotrophic response in ocean waters, and further our ability to generate specific hypotheses as to the ecology and efficacy of pelagic methanotrophic communites. The discharge of methane and other hydrocarbons to Gulf of Mexico that followed the sinking of the Deepwater Horizon provided a unique opportunity to study the methanotorphic biofilter in the deep ocean environment. We set out to understand the consumption of methane and the bloom of methanotrophs resulting from this event, as a window into the regional scale release of gas hydrate under rapid warming scenarios. We found that other hydrocarbon gases, notably propane and ethane, were preferred for consumption over methane, but that methane consumption accelerated rapidly and drove the depletion of methane within a matter of months after initial release. These results revealed the identity of the responsible community, and point to the importance of the seed population in determining the rate at which a methanotrophic community is able to respond to an input of methane. Collectively, these results provide a significant advance in our understanding of the marine methanotrohic biofilter, and further provide direction and context for future investigations of this important phenomenon. This project has resulted in fourteen publications to date, with five more circulating in draft form, and several others planned.

Valentine, David

2012-09-30T23:59:59.000Z

195

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

Energy.gov (U.S. Department of Energy (DOE)) 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...

196

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

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

197

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

January 2010 Methane Hydrate Advisory Committee Meeting Minutes, January 2010 Methane Hydrate Advisory Committee Meeting Minutes January, 2010 Atlanta, GA Methane Hydrate Advisory...

198

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Advance Methane Hydrates Science and Technology Projects Department of Energy Advance Methane Hydrates Science and Technology Projects Descriptions for Energy Department Methane...

199

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

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

200

Direct catalytic conversion of methane and light hydrocarbon gases. Final report, October 1, 1986--July 31, 1989  

DOE Green Energy (OSTI)

This project explored conversion of methane to useful products by two techniques that do not involve oxidative coupling. The first approach was direct catalytic dehydrocoupling of methane to give hydrocarbons and hydrogen. The second approach was oxidation of methane to methanol by using heterogenized versions of catalysts that were developed as homogeneous models of cytochrome-P450, an enzyme that actively hydroxylates hydrocarbons by using molecular oxygen. Two possibilities exist for dehydrocoupling of methane to higher hydrocarbons: The first, oxidative coupling to ethane/ethylene and water, is the subject of intense current interest. Nonoxidative coupling to higher hydrocarbons and hydrogen is endothermic, but in the absence of coke formation the theoretical thermodynamic equilibrium yield of hydrocarbons varies from 25% at 827{degrees}C to 65% at 1100{degrees}C (at atmospheric pressure). In this project we synthesized novel, highly dispersed metal catalysts by attaching metal clusters to inorganic supports. The second approach mimics microbial metabolism of methane to produce methanol. The methane mono-oxygenase enzyme responsible for the oxidation of methane to methanol in biological systems has exceptional selectivity and very good rates. Enzyme mimics are systems that function as the enzymes do but overcome the problems of slow rates and poor stability. Most of that effort has focused on mimics of cytochrome P-450, which is a very active selective oxidation enzyme and has a metalloporphyrin at the active site. The interest in nonporphyrin mimics coincides with the interest in methane mono-oxygenase, whose active site has been identified as a {mu}-oxo dinuclear iron complex.We employed mimics of cytochrome P-450, heterogenized to provide additional stability. The oxidation of methane with molecular oxygen was investigated in a fixed-bed, down-flow reactor with various anchored metal phthalocyanines (PC) and porphyrins (TPP) as the catalysts.

Wilson, R.B. Jr.; Posin, B.M.; Chan, Yee-Wai

1995-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Catalysts for conversion of methane to higher hydrocarbons  

DOE Patents (OSTI)

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.

Siriwardane, Ranjani V. (Morgantown, WV)

1993-01-01T23:59:59.000Z

202

Catalysts for conversion of methane to higher hydrocarbons  

DOE Patents (OSTI)

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 to 900{degrees}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 to 850{degrees}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.

Siriwardane, R.V.

1991-05-15T23:59:59.000Z

203

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 6, January 16, 1988--April 15, 1988  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that later can be converted to either liquid fuels or value-added chemicals, as economics dictate. During this reporting period, we synthesized several phthalocyanine catalysts supported on magnesia (MgO) in Task 3. In Task 4 we have tested these catalysts for oxidation of methane and did a number of blank experiments to determine the cause of the low methanol yield we have observed. Magnesia supported catalysts were prepared by first synthesizing the various metal tetrasulfophthalocyanines (TSPCs), converting them to the acid form, and then supporting these complexes on a basic support (MgO) by a neutralization reaction. The metals used were Ru, Pd, Cu, Fe, Co, Mn, and Mo. CoTSPC was also synthesized in zeolite Y using our standard template techniques described in Quarterly Report No. 1. These complexes were examined for catalytic activity in the oxidation of methane. The PdTSPC/MgO had greater activity, and oxidized some of the methane (selectivity of 2.8% from the methane oxidized at 375{degrees}C) to ethane. This is a much lower temperature for this reaction than previously reported in the literature. We also examined the reactivity of various components of the system in the oxidation of the product methanol. The reactor showed some activity for the oxidation of methanol to carbon dioxide. When zeolite or magnesia were added, this activity increased. The magnesia oxidized most of the methanol to carbon dioxide, while the zeolite reduced some of the methanol to hydrocarbons. With oxygen in the feed gas stream (i.e., the conditions of our methane oxidation), a very large fraction of the methanol was oxidized to carbon dioxide when passed over magnesia. From this, we can conclude that any methanol formed in the oxidation of methane would probably be destroyed very quickly on the catalyst bed.

Wilson, R.B. Jr.; Chan, Yee Wai; Posin, B.M.

1988-05-20T23:59:59.000Z

204

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Gas Hydrate Research in Deep Sea Sediments - New Zealand Task Gas Hydrate Research in Deep Sea Sediments - New Zealand Task DE-AI26-06NT42878 Goal The objective of this research is to determine the extent and dynamics of gas hydrate deposits and their relation to areas of focused fluid flux at and beneath the seafloor. Specific objectives include: a). Refine geophysical, geochemical and microbiological technologies for prospecting hydrate distribution and content; b). Contribute to establishing high-priority geographical regions of prospective interest, in terms of methane volume estimates; c). Prediction of environmental effects and geologic risks at the continental margin associated to the natural resource occurrence and resource exploitation; and d). Expand understanding of the biogeochemical parameters and associated microbial community diversity in shallow sediments that influence the porewater sulfate gradient observed through anaerobic oxidation of methane. To accomplish these objectives, the Naval Research Laboratory (NRL) collaborated with New ZealandÂ’s Institute of Geological and Nuclear Sciences (GNS) in a research cruise off the coast of New Zealand. NRL has conducted similar research cruises off the west coast and east coast of the United States, in the Gulf of Mexico and off the coast of Chile.

205

Coalbed Methane Proved Reserves  

Gasoline and Diesel Fuel Update (EIA)

Coalbed Methane Proved Reserves (Billion Cubic Feet) Period: Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes 2003 2004 2005 2006 2007 2008 View History U.S. 18,743 18,390 19,892 19,620 21,874 20,798 1989-2008 Alabama 1,665 1,900 1,773 2,068 2,126 1,727 1989-2008 Alaska 0 0 2007-2008 Arkansas 31 31 2007-2008 California 0 0 2007-2008 Colorado 6,473 5,787 6,772 6,344 7,869 8,238 1989-2008 Florida 0 0 2007-2008 Kansas 340 301 2007-2008 Kentucky 0 0 2007-2008 Louisiana 7 9 2007-2008 North 7 9 2007-2008 South Onshore 0 0 2007-2008 South Offshore 0 0 2007-2008 Michigan 0 0 2007-2008 Mississippi 0 0 2007-2008 Montana 66 75 2007-2008 New Mexico 4,396 5,166 5,249 4,894 4,169 3,991 1989-2008

206

Mixed-conducting ceramic membranes for partial oxygenation of methane  

DOE Green Energy (OSTI)

The most significant cost associated with the conventional partial oxidation of methane is that of an oxygen plant. Our new technology offers a way to lower this cost, and in this paper we explore the technology that is based on dense ceramic membranes and that uses air as the oxidant for methane-conversion reactions. Mixed-conducting ceramic materials have been produced from mixed-oxide systems of the La-Sr-Fe-Co-O (SFC) type, in the form of tubes and bars. Thermodynamic stability of the tubes was studied as a function of oxygen partial pressure by high-temperature XRD. Mechanical properties were measured and found to be adequate for a reactor in the case of SFC-2: Electronic and ionic conductivities were measured; SFC-2 is unique in the sense that the ratio of ionic to electronic conductance is close to unity. Performance of the membrane tubes was good only with SFC-2. Fracture of other SFC tubes was the consequence of an oxygen gradient that introduced a volumetric lattice difference between the inner and outer walls. SFC-2 tubes provided methane conversion efficiencies of >99% in a reactor. These tubes have operated for >1000 h.

Balachandran, U.; Dusek, J.T.; Maiya, P.S.; Mieville, R.L. [Argonne National Lab., IL (United States); Kleefisch, M.S.; Udovich, C.A. [Amoco Corp., Naperville, IL (United States); Bose, A.C. [USDOE Pittsburgh Energy Technology Center, PA (United States)

1995-05-01T23:59:59.000Z

207

NETL: Methane Hydrates - Global Assessment of Methane Gas Hydrates  

NLE Websites -- All DOE Office Websites (Extended Search)

Global Assessment of Methane Gas Hydrates Last Reviewed 12/18/2013 Global Assessment of Methane Gas Hydrates Last Reviewed 12/18/2013 DE-FE0003060 Goal The goal of this project is to develop a global assessment of methane gas hydrates that will facilitate informed decision-making regarding the potential development of gas hydrate resources between the scientific community and other stakeholders/decision makers. The Assessment will provide science-based information on the role of gas hydrates in natural climate change and the carbon cycle, their sensitivity to climate change, and the potential environmental and socio-economic impacts of hydrate production. Performers Stiftelsen GRID-Arendal, Arendal, Norway Funding Institutions United Nations Environment Programme (UNEP) Statoil Schlumberger United States Department of Energy (USDOE)

208

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Assessing the Efficacy of the Aerobic Methanotropic Biofilter in Methane Hydrate Environments Last Reviewed 1/8/2013 Assessing the Efficacy of the Aerobic Methanotropic Biofilter in Methane Hydrate Environments Last Reviewed 1/8/2013 DE-NT0005667 Goal The goal of this project is to assess the efficacy of aerobic methanotrophy in preventing the escape of methane from marine, hydrate-bearing reservoirs to the atmosphere and ultimately to better define the role of aerobic methanotrophy in the global carbon cycle. Graph overlayed on photo - Methane seeps with the resulting methane plume Methane seeps with the resulting methane plume, Geophysical Research Letters, November 2007 Performers University of California – Santa Barbara, Santa Barbara (UCSB), CA 93106 Background The global methane reservoir in the form of gas hydrate is estimated at 500–10,000 Gt (KVENVOLDEN, 1995; MILKOV, 2004). This pool of carbon

209

Miscellaneous States Coalbed Methane Proved Reserves (Billion...  

Gasoline and Diesel Fuel Update (EIA)

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...

210

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Degradation and Methane-Degrading Microbes in Alaska Coastal Waters Last Reviewed 5152012 DE-NT0005666 Goal The goal of this project is gain a better understanding of...

211

NETL: News Release - Methane Hydrate Production Technologies...  

NLE Websites -- All DOE Office Websites (Extended Search)

of CO2 molecules for methane molecules in the solid-water hydrate lattice, the release of methane gas, and the permanent storage of CO2 in the formation. This field experiment will...

212

coalbed methane | OpenEI  

Open Energy Info (EERE)

coalbed methane coalbed methane Dataset Summary Description (Abstract): Each TMY is a data set of hourly values of solar radiation and meteorological elements for a 1-year period. Solar radiation is modeled using the NREL METSTAT model, with surface observed cloud cover being the principal model input. The container file contains one TMY file for each selected station in the region, plus documentation files and a TMY data reader file for use with Microsoft Excel. (Purpose): Simulations Source NREL Date Released April 30th, 2005 (9 years ago) Date Updated November 07th, 2007 (7 years ago) Keywords coalbed methane GEF Kenya NREL SWERA TMY UNEP Data application/zip icon Download Data (zip, 5.4 MiB) Quality Metrics Level of Review Some Review Comment Temporal and Spatial Coverage

213

Dense ceramic membranes for partial oxygenation of methane  

DOE Green Energy (OSTI)

The most significant cost associated with partial oxidation of methane to syngas is that of the oxygen plant. In this paper, the authors offer a technology that is based on dense ceramic membranes and that uses air as the oxidant for methane-conversion reactions, thus eliminating the need for the oxygen plant. Certain ceramic materials exhibit both electronic and ionic conductivities (of particular interest is oxygen-ion conductivity). These materials transport not only oxygen ions (functioning as selective oxygen separators) but also electrons back from the reactor side to the oxygen/reduction interface. No external electrodes are required and if the driving potential of transport is sufficient, the partial oxidation reactions should be spontaneous. Such a system will operate without an externally applied potential. Oxygen is transported across the ceramic material in the form of oxygen anions, not oxygen molecules. In principle, the dense ceramic materials can be shaped into a hollow-tube reactor, with air passed over the outside of the membrane and methane through the inside. The membrane is permeable to oxygen at high temperatures, but not to nitrogen or any other gas. Long tubes of La-Sr-Fe-Co-O (SFC) membrane were fabricated by plastic extrusion, and thermal stability of the tubes was studied as a function of oxygen partial pressure by high-temperature XRD. Mechanical properties were measured and found to be acceptable for a reactor material. Fracture of certain SFC tubes was the consequence of an oxygen gradient that introduced a volumetric lattice difference between the inner and outer walls. However, tubes made with a particular stoichiometry (SFC-2) provided methane conversion efficiencies of >99% in a reactor. Some of the reactor tubes have operated for up to {approx} 1,000 h.

Balachandran, U.; Dusek, J.T.; Sweeney, S.M.; Mieville, R.L.; Maiya, P.S. [Argonne National Lab., IL (United States). Energy Technology Div.; Kleefisch, M.S.; Pei, S.; Kobylinski, T.P. [Amoco Research Center, Naperville, IL (United States); Bose, A.C. [USDOE Pittsburgh Energy Technology Center, PA (United States)

1994-05-01T23:59:59.000Z

214

Method for the photocatalytic conversion of methane  

DOE Patents (OSTI)

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.

Noceti, Richard P. (Pittsburgh, PA); Taylor, Charles E. (Pittsburgh, PA); D' Este, Joseph R. (Pittsburgh, PA)

1998-01-01T23:59:59.000Z

215

Method for the photocatalytic conversion of methane  

DOE Patents (OSTI)

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.

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

1998-02-24T23:59:59.000Z

216

QUEST FOR NEW MATERIALS FOR METHANE STORAGE ...  

Science Conference Proceedings (OSTI)

Quest for New Materials for Methane Storage: Gas Adsorption and Neutron Diffraction Measurements. Yang Peng, 1,2 Vaiva ...

217

EIA - Greenhouse Gas Emissions - Methane Emissions  

U.S. Energy Information Administration (EIA)

Residential wood consumption accounted for just over 45 percent of U.S. methane emissions from stationary combustion in 2009.

218

NIST: Methane Symmetry Operations - Nuclear spin functions  

Science Conference Proceedings (OSTI)

Methane Symmetry Operations. 9. Symmetry Properties of Laboratory-Fixed Nuclear Spin Functions, Nuclear Spin Statistics, and Parities. ...

219

Meridional Distribution of Stratospheric Trace Constituents  

Science Conference Proceedings (OSTI)

Vertically stratified stratospheric tracers such as methane and nitrous oxide tend to have constant mixing ratio surfaces that slope downward toward the poles in the meridional plane. The equilibrium tracer slope results from the competition ...

James R. Holton

1986-06-01T23:59:59.000Z

220

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

Reports and Publications (EIA)

This report documents the preparation of updated state-level electricity coefficients for carbon dioxide (CO ), methane (CH ), and nitrous oxide (N O), which represent a three-year weighted average for 1998-2000.

Information Center

2002-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


221

Power Technologies Energy Data Book: Fourth Edition, Chapter...  

NLE Websites -- All DOE Office Websites (Extended Search)

Table 12.7 - Global Warming Potentials (GWP) (100-year time horizon) Gas GWP SAR 900 Carbon dioxide (CO2) 1 Methane (CH 4 ) 1 21 Nitrous oxide (N 2 O) 310 HFC-23 11,700 HFC-32 650...

222

Emissions of Greenhouse Gases in the United States, 2004  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2005-12-19T23:59:59.000Z

223

Emissions of Greenhouse Gases in the United States, 2002  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2003-10-01T23:59:59.000Z

224

Emissions of Greenhouse Gases in the United States, 2005  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2006-11-14T23:59:59.000Z

225

Emissions of Greenhouse Gases in the United States, 1996  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1997-10-01T23:59:59.000Z

226

Emissions of Greenhouse Gases in the United States, 1995  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1996-10-01T23:59:59.000Z

227

Emissions of Greenhouse Gases in the United States, 1994  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1995-09-01T23:59:59.000Z

228

Emissions of Greenhouse Gases in the United States, 1999  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2000-10-01T23:59:59.000Z

229

Emissions of Greenhouse Gases in the United States, 2000  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2001-11-01T23:59:59.000Z

230

Emissions of Greenhouse Gases in the United States, 1997  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1998-10-01T23:59:59.000Z

231

Emissions of Greenhouse Gases in the United States, 1998  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1999-10-01T23:59:59.000Z

232

Emissions of Greenhouse Gases in the United States, 2001  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2002-12-01T23:59:59.000Z

233

Emissions of Greenhouse Gases in the United States, 2003  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2004-12-01T23:59:59.000Z

234

Emissions of Greenhouse Gases in the United States, 2000 Executive Summary  

Reports and Publications (EIA)

Executive Summary on the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2001-11-01T23:59:59.000Z

235

Methane Emissions from Rice Fields - Final Report  

SciTech Connect

Methane (Ch4) is a greenhouse gas regarded second only to carbon dioxide in its ability to cause global warming. Methane is important because of its relatively fast increase, and also because it is, per molecule, some 60 times more effective than carbon dioxide in causing global warming. The largest present anthropogenic sources of methane are rice fields, cattle and biomass burning.

Khalil, M. Aslam; Rasmussen,Reinhold A.

2002-12-03T23:59:59.000Z

236

Biogeochemistry of Microbial Coal-Bed Methane  

E-Print Network (OSTI)

Biogeochemistry of Microbial Coal-Bed Methane Dariusz Strapo´c,1, Maria Mastalerz,2 Katherine, biodegradation Abstract Microbial methane accumulations have been discovered in multiple coal- bearing basins low-maturity coals with predominantly microbial methane gas or uplifted coals containing older

Macalady, Jenn

237

Methane coupling by membrane reactor. Quarterly technical progress report, March 25, 1995--June 24, 1995  

DOE Green Energy (OSTI)

Research focus, for the development of a radial flow catalytic membrane reactor for studying methane coupling concentrated on understanding the effects of pore size on improving the hydrocarbon selectivity for the reaction. The effect of pressure on the reaction was also investigated. Experimental results from the catalytic studies of oxidative coupling of methane in the radial flow membrane reactors presented in this report augment earlier work on membranes of pore diameters of 2.0{mu}m, 0.2{mu}m, and 0.02{mu}m, indicating better performance with the larger pore diameter membranes. Higher operating pressures seem to enhance gas phase non-selective reactions during methane coupling. The chemistry of oxygen conducting materials that could be used as dense membranes in the membrane reactors was investigated by studying the catalytic activity of several oxygen conducting perovskites for methane coupling. Heavy metal oxides of lanthanum, strontium and iron, which form good oxygen conductors, showed very poor methane coupling activity. Perovskites of the Strontium-Cerium-Yttribium series showed moderate activity for methane coupling. These could serve as candidates for dense membrane synthesis, since they also have moderate oxygen conduction properties.

Yi Hua Ma

1995-10-11T23:59:59.000Z

238

Methane coupling by membrane reactor. Quarterly technical progress report, December 25, 1995--March 24, 1996  

DOE Green Energy (OSTI)

Methane oxidative coupling experiments were conducted in a packed-bed reactor using La/MgO catalyst. The results were in agreement with those reported in the literature. Oxygen permeability through an oxygen-conductive dense membrane was measured. The oxygen permeability was about 20% of the reported values and increased with the sweep flow rate of helium in the tube side. Blank runs under methane coupling conditions were carried out with no catalyst packed in the dense membrane tube. Nearly 100% CO{sub 2} selectivity was observed, suggesting that the membrane material is a facile total oxidation catalyst. After the experiment the membrane tube was analyzed by scanning electron microscopy.

NONE

1996-05-28T23:59:59.000Z

239

Activation of methane by transition metal-substituted aluminophosphate molecular sieves  

DOE Patents (OSTI)

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.

Iton, Lennox E. (Downers Grove, IL); Maroni, Victor A. (Naperville, IL)

1991-01-01T23:59:59.000Z

240

The eects of CO2, CO and H2 co-reactants on methane reactions catalyzed by Mo/H-ZSM-5  

E-Print Network (OSTI)

partial oxidation and autothermal or steam reforming is currently practiced [1±4]. Catalytic pyrolysisThe eects of CO2, CO and H2 co-reactants on methane reactions catalyzed by Mo/H-ZSM-5 Zheng Liu-reactants; methane reactions; Mo/H-ZSM-5 catalyst. 1. Introduction The direct conversion of natural gas

Iglesia, Enrique

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

800,000 Year Ice-Core Records of Atmospheric Nitrous Oxide (N2O...  

NLE Websites -- All DOE Office Websites (Extended Search)

create a long-term record to the present. These records are maintained by the World Data Center for Paleoclimatology, National Oceanic and Atmospheric Administration (NOAA), and...

242

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

U.S. Energy Information Administration (EIA)

States 2009 (March 2011), Table 22; and EIA estimates based on the Intergovernmental Panel on Climate Change's Guidelines for National Greenhouse Gas Inventories ...

243

On-farm Assessment of Nitrogen Fertilizer application to corn on Nitrous Oxide Emissions  

E-Print Network (OSTI)

in soils cropped to corn with varying N fertilization. Can.as affected by tillage, corn-soybean-alfalfa rotations, andsoil nitrogen mineralization for corn production in eastern

2009-01-01T23:59:59.000Z

244

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

U.S. Energy Information Administration (EIA)

Short-Term Energy Outlook › Annual Energy Outlook › Energy Disruptions › International Energy Outlook ... 1984: 86: 45: 132: 1: 11: 11: 355: 2: 74: 431: 87: 661:

245

Quantification of and Controls on Dinitrogen and Nitrous Oxide Fluxes from Terrestrial Ecosystems  

E-Print Network (OSTI)

and then 100 g was weighed into each sample jar (490 mL).The jars were sealed on viton gaskets with aluminum lidssepta for gas sampling. The jars were flushed with N 2 for

Yang, Wendy Hui-I

2010-01-01T23:59:59.000Z

246

Methane generation from waste materials  

DOE Patents (OSTI)

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.

Samani, Zohrab A. (Las Cruces, NM); Hanson, Adrian T. (Las Cruces, NM); Macias-Corral, Maritza (Las Cruces, NM)

2010-03-23T23:59:59.000Z

247

Methane production by attached film  

DOE Patents (OSTI)

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.

Jewell, William J. (202 Eastwood Ave., Ithaca, NY 14850)

1981-01-01T23:59:59.000Z

248

Methane coupling by membrane reactor. Quarterly technical progress report, June 25, 1995--September 24, 1995  

DOE Green Energy (OSTI)

The research focus, for the development of a radial flow catalytic membrane reactor for studying methane coupling, concentrated on understanding the effects of pore size, catalyst loading and catalyst distribution inside the membrane, on the hydrocarbon selectivity. The experimental results from the catalytic studies of oxidative coupling of methane in the radial flow membrane reactors are summarized in this report and the reactor performances of three radial flow reactors with pore sizes of 0.02 {mu}m are interpreted by the energy dispersive X-ray digital mapping (EDX) technique. A conventional fixed bed catalytic reactor was set up and run under the same conditions as were used for the radial flow reactor studies. Two sources of samarium oxide catalysts were used in these experiments and their performances were compared in terms of C{sub 2} selectivity at same methane conversion. Compared to the monoclinic form of samarium oxide, the catalyst with cubic form was more active and selective for methane oxidative coupling. A general reactor model for oxidation reactions with distributed feed of oxygen and product removal strategies was proposed. Six types of feeding modes were analyzed and their feed distributions were optimized such that the desired product yields at the reactor outlet were maximized.

NONE

1995-12-12T23:59:59.000Z

249

Methane Hydrate Advisory Committee | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Methane Hydrate Advisory Methane Hydrate Advisory Committee Methane Hydrate Advisory Committee The Methane Hydrate Advisory Committee was created in response to provisions of the Methane Hydrate Research and Development Act of 2000 and reauthorized by the Energy Policy Act of 2005. The Committee is to advise the Secretary of Energy on potential applications of methane hydrate; assist in developing recommendations and priorities for the methane hydrate research and development program; and submit to Congress one or more reports on an assessment of the research program and an assessment of the DOE 5-year research plan. The Committee's charter stipulates that up to 15 members can be appointed by the Secretary of Energy, representing institutions of higher education, industrial enterprises and oceanographic institutions and state agencies.

250

Methane Hydrate Production Feasibility | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Production Feasibility 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 area of methane hydrate stability. Methane, the predominant component of natural gas, forms hydrate in the presence of water, low temperatures and high pressures. Alternatively, when the temperature is increased or the pressure decreased so that hydrates are outside their stability field, they dissociate into methane and water.

251

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

SciTech Connect

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.

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

2010-09-30T23:59:59.000Z

252

Methane Digesters and Biogas Recovery - Masking the Environmental Consequences of Industrial Concentrated Livestock Production  

E-Print Network (OSTI)

Methane Digesters and Biogas Recovery-Masking theII. METHANE DIGESTERS AND BIOGAs RECOVERY- IN THE2011] METHANE DIGESTERS AND BIOGAS RECOVERY methane, and 64%

Di Camillo, Nicole G.

2011-01-01T23:59:59.000Z

253

Turbulent burning rates of methane and methane-hydrogen mixtures  

Science Conference Proceedings (OSTI)

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)

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)

2009-04-15T23:59:59.000Z

254

A decrease in NiO-MgO phase through its solid solution equilibrium with tetragonal (La1-zSrz)2Ni1-yMgyO4-?: effect on catalytic partial oxidation of methane  

Science Conference Proceedings (OSTI)

Calcination of an oxide mixture consisting of 0.4 La2O3, 0.2 SrCO2, (1 - x)NiO, and xMgO at 800°C results in an equilibrium between tetragonal (La1-zSrz)2Ni1-yMgyO4-? ...

Xiong Yin; Liang Hong; Zhengliang Gong

2012-01-01T23:59:59.000Z

255

Utilization of ventilation air methane as a supplementary fuel at a circulating fluidized bed combustion boiler  

Science Conference Proceedings (OSTI)

Ventilation air methane (VAM) accounts for 60-80% of the total emissions from underground coal mining activities in China, which is of serious greenhouse gas concerns as well as a waste of valuable fuel sources. This contribution evaluates the use of the VAM utilization methods as a supplementary fuel at a circulating fluidized bed combustion boiler. The paper describes the system design and discusses some potential technical challenges such as methane oxidation rate, corrosion, and efficiency. Laboratory experimentation has shown that the VAM can be burnt completely in circulated fluidized bed furnaces, and the VAM oxidation does not obviously affect the boiler operation when the methane concentration is less than 0.6%. The VAM decreased the incomplete combustion loss for the circulating fluidized bed combustion furnace. The economic benefit from the coal saving insures that the proposed system is more economically feasible. 17 refs., 3 figs., 1 tab.

Changfu You; Xuchang Xu [Tsinghua University, Beijing (China). Key Laboratory for Thermal Science and Power Engineering of Ministry of Education

2008-04-01T23:59:59.000Z

256

Development of mixed-conducting ceramic membranes for converting methane to syngas  

DOE Green Energy (OSTI)

The abundantly available natural gas (mostly methane) discovered in remote areas has stimulated considerable research on upgrading this gas to high-value-added clean-burning fuels such as dimethyl ether and alcohols and to pollution-fighting additives. Of the two routes to convert methane to valuable products direct and indirect, the direct route involving partial oxidation of methane to syngas (CO + H{sub 2}) by air is preferred. Syngas is the key intermediate product used to form a variety of petrochemicals and transportation fuels. This paper is concerned with the selective transport of oxygen from air for converting methane to syngas by means of a mixed-conducting ceramic oxide membrane prepared from Sr-Fe-Co-O oxide. While both perovskite and nonperovskite type Sr-Fe-Co-O oxides permeate large amounts of oxygen when the membrane tube is subjected to oxygen pressure gradients, the work shows that the nonperovskite SrFeCo{sub 0.5}O{sub x} exhibits remarkable stability during oxygen permeation. More particularly, extruded and sintered tubes from SrFeCo{sub 0.5}O{sub x} have been evaluated in a reactor operating at {approx} 850 C for conversion of methane into syngas in the presence of a reforming catalyst. Methane conversion efficiencies of {approx} 99% were observed. In addition, oxygen permeability of SrFeCo{sub 0.5}O{sub x} was measured as a function of oxygen partial pressure gradient and temperature in a gas-tight electrochemical cell. Oxygen permeability has also been calculated from conductivity data and the results are compared and discussed.

Balachandran, U.; Maiya, P.S.; Ma, B.; Dusek, J.T.; Mieville, R.L.; Picciolo, J.J.

1997-04-01T23:59:59.000Z

257

Dairy methane generator. Final report  

Science Conference Proceedings (OSTI)

Details of the work completed under this contract are presented. During the winter of 1979-80 three students enrolled, in the Mechanical Design Engineering Technology program at the Pennsylvania State University's Capitol Campus (Middletown, PA), undertook a feasibility study for the utilization of the manure generated by the dairy cows located on Mr. Thomas B. Williams farm for the generation and use of methane gas. The results of their effort was the design of an Anaerobic Digester/Electric Generation System. This preliminary designed system was later changed and improved by another group of P.S.U. MDET students in the spring of 1980. The final design included working drawings and an economic analysis of the estimated investment necessary to complete the Methane Generator/Electric Power Generation System.

Williams, T.B.

1981-09-30T23:59:59.000Z

258

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

DOE Patents (OSTI)

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.

Apel, William A. (Idaho Falls, ID); Dugan, Patrick R. (Idaho Falls, ID)

1995-01-01T23:59:59.000Z

259

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Characterization and Decomposition Kinetic Studies of Methane Hydrate in Host Sediments under Subsurface Mimic Conditions Last Reviewed 02/17/2010 Characterization and Decomposition Kinetic Studies of Methane Hydrate in Host Sediments under Subsurface Mimic Conditions Last Reviewed 02/17/2010 EST-380-NEDA Goal The purpose of this study is to establish sediment lithology and quantification of methane in hydrates hosted in fine-grained sediments from the Gulf of Mexico (GoM), a marine site of methane hydrate occurrence. The results will help establish a correlation between laboratory data and hydrate accumulation field data on dispersed hydrates in the natural environment. Performer Brookhaven National Laboratory (BNL), Upton, New York 11973 Background Gas hydrates are located in permafrost and marine environments and show potential as a vast methane source worldwide. However, methane is about 17 times more potent a greenhouse gas than CO2 and the inherent instability of

260

Methane Hydrates R&D Program  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrates R&D Program Methane Hydrates R&D Program Gas hydrates are a naturally-occurring combination of methane gas and water that form under specific conditions of low temperature and high pressure. Once thought to be rare in nature, gas hydrates are now known to occur in great abundance in association with arctic permafrost and in the shallow sediments of the deep-water continental shelves. The most recent estimates of gas hydrate abundance suggest that they contain

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Table 16. Coalbed Methane Proved Reserves, Reserves ...  

U.S. Energy Information Administration (EIA)

aIncludes Illinois and Indiana. Note: The above table is based on coalbed methane proved reserves and production volumes as reported to the EIA on ...

262

NETL: Methane Hydrates - Hydrate Model Code Comparison  

NLE Websites -- All DOE Office Websites (Extended Search)

Reservoir Simulator Code Comparison Study An International Effort to Compare Methane Hydrate Reservoir Simulators Code Comparison Logo The National Energy Technology Laboratory...

263

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

of gas hydrates. The effort aims to quantify the mechanical characteristics of methane hydrate and hydrate cemented sediments for use in models of the dynamic behavior of...

264

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

in Support of Characterization of Recoverable Resources from Methane Hydrate Deposits Last Reviewed 5102012 ESD05-048 Goal The project is bringing new laboratory measurements and...

265

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrate Projects If you need help finding information on a particular project, please contact the content manager. Search Hydrates Projects Active Projects | Completed...

266

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

characterization and temporal variation of methane seepage from thermokarst lakes on the Alaska North Slope in response to Arctic climate change Last Reviewed 632013 DE-NT0005665...

267

,"California - Coastal Region Coalbed Methane Proved Reserves...  

U.S. Energy Information Administration (EIA) Indexed Site

- Coastal Region Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","...

268

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

in the Gulf of Mexico and 2) NRL's Advanced Research Initiative on shallow sediment methane seeps. Geochemical data coupled with heat flow probe data were used to estimate...

269

Methane Hydrate Advisory Committee Meeting Minutes | Department...  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

16, 2013 Washington, DC July 16, 2013 Meeting Minutes More Documents & Publications Methane Hydrate Advisory Committee Meeting Minutes Electricity Advisory Committee Notice of Open...

270

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

late Quaternary. An investigation of the nature of deposition and alteration of the methane hydrate in cores from the Umnak Plateau in the southeastern Bering Sea was conducted...

271

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

establishing high-priority geographical regions of prospective interest, in terms of methane volume estimates; c). Prediction of environmental effects and geologic risks at the...

272

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

goal was to develop new methodologies to characterize the physical properties of methane hydrate and hydrate sediment systems. Performers Westport Technology Center...

273

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

during NGHP Expedition 01 Background Gas hydrate distribution in sediments depends on methane supply, which in turn depends on fluid flow. When drilling data are available to...

274

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrate Research - Geoscience Evaluations and Field Studies Last Reviewed 3182013 Project Goals The primary goals of the DOENETL Natural Gas Hydrate Field Studies...

275

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

(RUS) technique to examine hydrate formationdissociation processes. For determining methane abundance and location on a grain-to-grain scale, a completely new method of...

276

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

natural and simulated sediment samples, and to use these sediments as hosts to form methane hydrate and to investigate the kinetics of hydrate formation and dissociation...

277

,"Federal Offshore California Coalbed Methane Proved Reserves...  

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

278

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

for this sample, but Raman bands from both samples were essentially identical: methane and ethane along with trace amounts of isobutene and trans-butane. Small angle...

279

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

on the behavior of gas hydrates in their natural environment under either production (methane gas extraction) or climate change scenarios. This research is closely linked with...

280

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Determine the potential impacts of gas hydrate instability in terms of the release of methane into seafloor sediments, the ocean and the atmosphere. Performers University of...

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Decomposition Kinetic Studies of Methane Hydrate in Host Sediments under Subsurface Mimic Conditions Last Reviewed 02172010 EST-380-NEDA Goal The purpose of this study is to...

282

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

and presentations as well as a listing of funded students can be found in the Methane Hydrate Program Bibliography PDF. A final report is available by request. Contact...

283

,"Miscellaneous States Coalbed Methane Proved Reserves (Billion...  

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

284

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

and presentations as well as a listing of funded students can be found in the Methane Hydrate Program Bibliography PDF. Final Project Report PDF-23MB - October, 2009...

285

,"Pennsylvania Coalbed Methane Proved Reserves (Billion Cubic...  

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

286

NETL: Methane Hydrates - ANS Research Project  

NLE Websites -- All DOE Office Websites (Extended Search)

Characterization project has resulted in a characterization of two large prospective methane hydrate accumulations (or trends); the Eileen Trend, which underlies but extends well...

287

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Structure and Physical Properties of Methane Hydrate Deposit at Blake Ridge Last Reviewed 02052010 Bathymetric location map of the Blake Ridge study area Bathymetric location map...

288

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Horizon spill approximately 10 miles from the observatory showed increased levels of methane at two depths where detectable levels had not been seen in the past. The evidence...

289

NETL: Methane Hydrates - ANS Research Project  

NLE Websites -- All DOE Office Websites (Extended Search)

Slope represents an important milestone in an ongoing evaluation of Alaskan Arctic methane hydrate potential. This evaluation, a joint effort of DOE, USGS, BP Exploration...

290

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Survey, Woods Hole Field Center Location Woods Hole Massachusetts Background Oceanic methane hydrates are a major emerging research topic spanning energy resource issues, global...

291

New Materials Make Methane Capture Possible  

Science Conference Proceedings (OSTI)

May 8, 2013... and FER, were able to concentrate dilute methane streams into moderate concentrations that could be used to treat coal-mine ventilation air.

292

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

NETL ORD Methane Hydrate Research - Thermal Properties of Hydrate Tool Development Last Reviewed 3182013 Project Goal The goal of this project is increased understanding of...

293

Coal bed methane reservoir simulation studies.  

E-Print Network (OSTI)

??The purpose of this study is to perform simulation studies for a specific coal bed methane reservoir. First, the theory and reservoir engineering aspects of… (more)

Karimi, Kaveh

2005-01-01T23:59:59.000Z

294

EIA - Greenhouse Gas Emissions - Methane Emissions  

Gasoline and Diesel Fuel Update (EIA)

oil production dropping by 28 percent from 1990 to 2009, methane emissions from petroleum exploration and production have declined by the same percentage. Residential wood...

295

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Seol, Y. and T. J. Kneafsey, Methane hydrate induced permeability modification for multiphase flow in unsaturated porous media, Journal of Geophysical Research, 2011, In...

296

methane hydrate science plan-final.indd  

NLE Websites -- All DOE Office Websites (Extended Search)

Industrial Revolu on. Methane in the atmosphere comes from many sources, including wetlands, rice cul va on, termites, cows and other ruminants, forest fi res, and fossil fuel...

297

Method for the photocatalytic conversion of methane  

DOE Patents (OSTI)

The invention relates to a method for converting methane and water to methanol and hydrogen using visible light and a catalyst.

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

1996-12-01T23:59:59.000Z

298

Biomass burning and the production of greenhouse gases, in Climate Biosphere Interaction: Biogenic Emissions and the Environmental Effects of Climate Change, edited by  

E-Print Network (OSTI)

Biomass burning is a source of greenhouse gases, carbon dioxide, methane, and nitrous oxide. In addition, biomass burning is a source of chemically active gases, including carbon monoxide, nonmethane hydrocarbons, and nitric oxide. These gases, along with methane, lead to the chemical production of tropospheric ozone (another greenhouse gas) as well as control the concentration of the

Joel S. Levine

1994-01-01T23:59:59.000Z

299

Stable, Ultra-Low Residence Time Partial Oxidation  

DOE Patents (OSTI)

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.

Schmidt, Lanny D. (Minneapolis, MN); Hickman, Daniel A. (Midland, MI)

1997-07-15T23:59:59.000Z

300

A conduit dilation model of methane venting from lake sediments  

E-Print Network (OSTI)

Methane is a potent greenhouse gas, but its effects on Earth's climate remain poorly constrained, in part due to uncertainties in global methane fluxes to the atmosphere. An important source of atmospheric methane is the ...

Ruppel, Carolyn

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

Methane coupling by membrane reactor. Quarterly technical progress report: June 25, 1993--September 24, 1993  

DOE Green Energy (OSTI)

Several membranes have been investigated for use in a membrane reactor. Porous VYCOR has been tested for permeability changes with temperature. Three-sectional VYCOR membranes, with a porous central section, have been fabricated and tested in the experimental setup. Catalysts for methane coupling have been reviewed in the literature and five catalysts have been selected. Modeling studies of the methane oxidative coupling reaction in different reactor configurations shows higher C{sub 2} selectivity and yield with membrane reactors as compared to conventional packed bed reactors.

Ma, Yi Hua

1993-10-28T23:59:59.000Z

302

Method of making compost and spawned compost, mushroom spawn and generating methane gas  

Science Conference Proceedings (OSTI)

Newly designed ribbon-type mixers provide an improved method for making composts, aerating composts, growing mushroom spawn, generating methane gas, and filling conveyors in the mushroom-growing industry. The mixers may be the double-ribbon type for purely mixing operations or the single-ribbon type for moving the material from one place to another. Both types can operate under pressure. In preparing compost for mushroom growing, operators can first use the airtight mixers for a preliminary anaerobic fermentation to produce methane, then by changing the atmosphere to an oxidizing one, complete the compost preparation under the necessary aerobic conditions.

Stoller, B.B.

1981-04-28T23:59:59.000Z

303

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

U.S. Energy Information Administration (EIA) Indexed Site

Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane New Field Discoveries Utah Coalbed Methane Proved Reserves, Reserves Changes, and Production...

304

Louisiana--South Onshore Coalbed Methane Production (Billion...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production LA, South Onshore Coalbed Methane Proved Reserves, Reserves...

305

California (with State off) Coalbed Methane Production (Billion...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production California Coalbed Methane Proved Reserves, Reserves Changes,...

306

Other States Natural Gas Coalbed Methane, Reserves Based Production...  

Gasoline and Diesel Fuel Update (EIA)

Other States Natural Gas Coalbed Methane, Reserves Based Production (Billion Cubic Feet) Other States Natural Gas Coalbed Methane, Reserves Based Production (Billion Cubic Feet)...

307

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Texas Coalbed Methane Proved Reserves, Reserves Changes, and...

308

Texas--RRC District 8 Coalbed Methane Production (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 8 Coalbed Methane Proved Reserves, Reserves...

309

Texas--RRC District 5 Coalbed Methane Production (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 5 Coalbed Methane Proved Reserves, Reserves...

310

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 3 Onshore Coalbed Methane Proved...

311

Texas--RRC District 6 Coalbed Methane Production (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 6 Coalbed Methane Proved Reserves, Reserves...

312

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 5 Coalbed Methane Proved Reserves,...

313

Lower 48 Federal Offshore Coalbed Methane Production (Billion...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Federal Offshore U.S. Coalbed Methane Proved Reserves, Reserves...

314

Texas--RRC District 9 Coalbed Methane Production (Billion Cubic...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 9 Coalbed Methane Proved Reserves, Reserves...

315

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 LA, South Onshore Coalbed Methane Proved Reserves,...

316

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Alaska Coalbed Methane Proved Reserves, Reserves...

317

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 6 Coalbed Methane Proved Reserves,...

318

Texas--RRC District 3 Onshore Coalbed Methane Production (Billion...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 3 Onshore Coalbed Methane Proved Reserves,...

319

Texas--RRC District 4 Onshore Coalbed Methane Production (Billion...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 4 Onshore Coalbed Methane Proved Reserves,...

320

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 North Dakota Coalbed Methane Proved Reserves, Reserves...

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 10 Coalbed Methane Proved Reserves,...

322

Texas--RRC District 1 Coalbed Methane Production (Billion Cubic...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 1 Coalbed Methane Proved Reserves, Reserves...

323

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 4 Onshore Coalbed Methane Proved...

324

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 1 Coalbed Methane Proved Reserves,...

325

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

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

326

New York Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production New York Coalbed Methane Proved Reserves, Reserves Changes, and...

327

Texas--RRC District 10 Coalbed Methane Production (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 10 Coalbed Methane Proved Reserves, Reserves...

328

North Dakota Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production North Dakota Coalbed Methane Proved Reserves, Reserves Changes,...

329

Louisiana--State Offshore Coalbed Methane Production (Billion...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production LA, State Offshore Coalbed Methane Proved Reserves, Reserves...

330

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 9 Coalbed Methane Proved Reserves,...

331

Texas--RRC District 2 Onshore Coalbed Methane Production (Billion...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, RRC District 2 Onshore Coalbed Methane Proved Reserves,...

332

Texas--State Offshore Coalbed Methane Proved Reserves (Billion...  

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, State Offshore Coalbed Methane Proved Reserves,...

333

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Alaska Coalbed Methane Proved Reserves, Reserves Changes, and...

334

Texas--State Offshore Coalbed Methane Production (Billion Cubic...  

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production TX, State Offshore Coalbed Methane Proved Reserves, Reserves...

335

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Mississippi Coalbed Methane Proved Reserves, Reserves...

336

Why sequence functional metagenomics of methane and nitrogen...  

NLE Websites -- All DOE Office Websites (Extended Search)

functional metagenomics of methane and nitrogen cycles in freshwater lakes? Methane is a more potent greenhouse gas than carbon dioxide, but it is also a potential source of...

337

Airborne observations of methane emissions from rice cultivation...  

NLE Websites -- All DOE Office Websites (Extended Search)

Airborne observations of methane emissions from rice cultivation in the Sacramento Valley of California Title Airborne observations of methane emissions from rice cultivation in...

338

METHANE HYDRATE ADVISORY COMMITTEE U.S. DEPARTMENT OF ENERGY  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

METHANE HYDRATE ADVISORY COMMITTEE U.S. DEPARTMENT OF ENERGY Advisory Committee Charter 1. Committee's Official Designation. Methane Hydrate Advisory Committee (MHAC) 2. Authority....

339

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 Kentucky Coalbed Methane Proved Reserves, Reserves...

340

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

Gasoline and Diesel Fuel Update (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Proved Reserves as of Dec. 31 TX, RRC District 8 Coalbed Methane Proved Reserves,...

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

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

Annual Energy Outlook 2012 (EIA)

data. Release Date: 812013 Next Release Date: 812014 Referring Pages: Coalbed Methane Estimated Production Mississippi Coalbed Methane Proved Reserves, Reserves Changes,...

342

Other States Natural Gas Coalbed Methane, Proved Reserves (Billion...  

Gasoline and Diesel Fuel Update (EIA)

Other States Natural Gas Coalbed Methane, Proved Reserves (Billion Cubic Feet) Other States Natural Gas Coalbed Methane, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1...

343

NETL: Methane Hydrates - DOE/NETL Projects - Application of Crunch...  

NLE Websites -- All DOE Office Websites (Extended Search)

multi-dimensional reactive transport simulation code to constrain modern day methane fluxes and to reconstruct past episodes of methane flux that can be correlated with...

344

Changes related to "Coal Bed Methane Protection Act (Montana...  

Open Energy Info (EERE)

Special page Share this page on Facebook icon Twitter icon Changes related to "Coal Bed Methane Protection Act (Montana)" Coal Bed Methane Protection Act (Montana)...

345

Pages that link to "Coal Bed Methane Protection Act (Montana...  

Open Energy Info (EERE)

Edit History Share this page on Facebook icon Twitter icon Pages that link to "Coal Bed Methane Protection Act (Montana)" Coal Bed Methane Protection Act (Montana)...

346

Manifold methods for methane combustion  

SciTech Connect

Objective is to develop a new method for studying realistic chemistry in turbulent methane combustion with NO{sub x} mechanism. The realistic chemistry is a simplification to a more detailed chemistry based on the manifold method; accuracy is determined by interaction between the transport process and the chemical reaction. In this new (tree) method, probability density function or partially stirred reactor calculations are performed. Compared with the reduced mechanism, manifold, and tabulation methods, the new method overcomes drawbacks of the reduced mechanism method and preserves the advantages of the manifold method. Accuracy is achieved by specifying the size of the cell.

Yang, B.; Pope, S.B. [Cornell Univ., Ithaca, NY (United States)

1995-12-31T23:59:59.000Z

347

Catalyst for utilization of methane in selective catalytic reduction of NO{sub x}, Task 2.6  

DOE Green Energy (OSTI)

Selective catalytic reduction (SCR) of nitrogen oxides(NO{sub x}) in flue gas or engine exhaust gas with hydrocarbons as the reductant has great potential for less expense, less pollution, and easier operation than SCR with ammonia. Methane is the preferred reducing gas because of its low cost and low toxicity. Stable, low-cost catalysts for SCR with methane are required to demonstrate this technology for controlling NO{sub x} emissions. Several cobalt and nickel catalysts on synthetic clay and uranium oxide supports were investigated for their activities in reducing NO{sub x} with methane in the presence of air. The efficiency of the synthetic clay-supported nickel and cobalt catalysts for nitric oxide (NO) reduction with methane as the reducing gas was poor. The nickel oxide-uranium oxide catalyst, which was chosen for its high stability, was also ineffective. Results from the two-step experiments conducted at two-temperatures produced some interesting information on the reactions of methane with the catalysts and the reactivity of the carbonaceous intermediate. The carbonaceous material formed from methane dissociation at 450{degrees}C not only reduces NO to N{sub 2}O at lower temperatures, but also prevents oxidation of NO to NO{sub 2}. Unfortunately, the carbonaceous forms that reduce the NO are not available for reactions at 400{degrees}C in the presence of oxygen. A two-step process employing this chemistry would be difficult because the catalyst would have to be cycled between the two temperatures. Also the desired reduction to nitrogen is not very efficient.

Olson, E.S.; Sharma, R.K.

1996-02-01T23:59:59.000Z

348

Arctic Methane, Hydrates, and Global Climate  

NLE Websites -- All DOE Office Websites (Extended Search)

Arctic Methane, Hydrates, and Global Climate Arctic Methane, Hydrates, and Global Climate Speaker(s): Matthew T. Reagan Date: March 17, 2010 - 12:00pm Location: 90-3122 Paleooceanographic evidence has been used to postulate that methane may have had a significant role in regulating past climate. However, the behavior of contemporary permafrost deposits and oceanic methane hydrate deposits subjected to rapid temperature changes, like those now occurring in the arctic and those predicted under future climate change scenarios, has only recently been investigated. A recent expedition to the west coast of Spitsbergen discovered substantial methane gas plumes exiting the seafloor at depths that correspond to the upper limit of the receding gas hydrate stability zone. It has been suggested that these plumes may be the

349

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Recovery from Hydrate-bearing Sediments Last Reviewed 11/30/2011 Methane Recovery from Hydrate-bearing Sediments Last Reviewed 11/30/2011 DE-FC26-06NT42963 Goal The goal of this project is to develop observational and experimental data that can provide a better understanding of the basic mechanisms at work in a methane hydrate reservoir that is under production. To this end, a thorough physical understanding of underlying phenomena associated with methane hydrate production will be acquired through unique, multi-scale experiments and associated analyses. In addition, one or more mathematical models that account for the observed phenomena and provide insights that may help to optimize methane hydrate production methods will be developed. Performers Georgia Tech Research Corporation, Atlanta, Georgia 30332 Oak Ridge National Laboratory (ORNL), Oak Ridge, Tennessee 37831

350

Analysis of Percent On-Cell Reformation of Methane in SOFC Stacks: Thermal, Electrical and Stress Analysis  

DOE Green Energy (OSTI)

This report summarizes a parametric analysis performed to determine the effect of varying the percent on-cell reformation (OCR) of methane on the thermal and electrical performance for a generic, planar solid oxide fuel cell (SOFC) stack design. OCR of methane can be beneficial to an SOFC stack because the reaction (steam-methane reformation) is endothermic and can remove excess heat generated by the electrochemical reactions directly from the cell. The heat removed is proportional to the amount of methane reformed on the cell. Methane can be partially pre-reformed externally, then supplied to the stack, where rapid reaction kinetics on the anode ensures complete conversion. Thus, the thermal load varies with methane concentration entering the stack, as does the coupled scalar distributions, including the temperature and electrical current density. The endotherm due to the reformation reaction can cause a temperature depression on the anode near the fuel inlet, resulting in large thermal gradients. This effect depends on factors that include methane concentration, local temperature, and stack geometry.

Recknagle, Kurtis P.; Yokuda, Satoru T.; Jarboe, Daniel T.; Khaleel, Mohammad A.

2006-04-07T23:59:59.000Z

351

Direct conversion of methane to C sub 2 's and liquid fuels  

DOE Green Energy (OSTI)

Objectives of the project are to discover and evaluate novel catalytic systems for the conversion of methane or by-product light hydrocarbon gases either indirectly (through intermediate light gases rich in C{sub 2}'s) or directly to liquid hydrocarbon fuels, and to evaluate, from an engineering perspective, different conceptualized schemes. The approach is to carry out catalyst testing on several specific classes of potential catalysts for the conversion of methane selectively to C{sub 2} products. Promoted metal oxide catalysts were tested. Several of these exhibited similar high ethylene to ethane ratios and low carbon dioxide to carbon monoxide ratios observed for the NaCl/{alpha}-alumina catalyst system reported earlier. Research on catalysts containing potentially activated metals began with testing of metal molecular sieves. Silver catalysts were shown to be promising as low temperature catalysts. Perovskites were tested as potential methane coupling catalysts. A layered perovskite (K{sub 2}La{sub 2}Ti{sub 3}O{sub 10}) gave the highest C{sub 2} yield. Work continued on the economic evaluation of a hypothetical process converting methane to ethylene. An engineering model of the methane coupling system has been prepared. 47 refs., 17 figs., 57 tabs.

Warren, B.K.; Campbell, K.D.

1989-11-22T23:59:59.000Z

352

Remote sensor improves methane leakage surveys  

SciTech Connect

The remote sensing methane detector (RSMD) described in this paper is the result of a twelve year cooperative research program sponsored by the Columbia Gas System Service Corp., Environmental Research and Technology, Inc. and the Gas Research Institute. It is a hand-held, rechargeable battery-powered sensor that operates eight hours on one charge with a sensitivity very specific to methane. It can be scanned along the right of way to detect any methane in its path, up to at least 50 feet away. The RSMD is methane specific in that it only sense methane with minor sensitivity to ethane. This makes it particularly useful in industrial areas where present instruments are confused by solvents. It cannot be poisoned by silicones or leaded gasoline, since it is an optical system. When a cloud of methane has been detected by the RSMD, a sample cell attachment can be used to determine methane concentration in parts per million. A low power microcomputer is used in the RSMD to control its operation.

Eberle, A.C.; Kebabian, P.L.; Kruse, J.R.

1984-12-01T23:59:59.000Z

353

Department of Energy Advance Methane Hydrates Science and Technology Projects  

Energy.gov (U.S. Department of Energy (DOE))

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

354

Diffusive Accumulation of Methane Bubbles in Seabed  

E-Print Network (OSTI)

We consider seabed bearing methane bubbles. In the absence of fractures the bubbles are immovably trapped in a porous matrix by surface tension forces; therefore the dominant mechanism of transfer of gas mass becomes the diffusion of gas molecules through the liquid. The adequate description of this process requires accounting "other-than-normal" (non-Fickian) diffusion effects, thermodiffusion and gravity action. We evaluate the diffusive flux of aqueous methane and predict the possibility of existence of bubble mass accumulation zones (which can appear independently from the presence/absence of hydrate stability zone) and effect of non-Fickian drift on the capacity of shallow and deep methane-hydrate deposits.

Goldobin, D S; Levesley, J; Lovell, M A; Rochelle, C A; Jackson, P; Haywood, A; Hunter, S; Rees, J

2010-01-01T23:59:59.000Z

355

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

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Methane Hydrate Research: Investing in Our Energy Future 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 natural gas. Jenny Hakun What Are Methane Hydrates? Methane hydrates are 3D ice-lattice structures with natural gas locked inside. The substance looks remarkably like white ice, but it does not behave like ice. If methane hydrate is either warmed or depressurized, it will release the trapped natural gas.

356

Methane Hydrates and Climate Change | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Hydrates and Climate Change 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 underlying oil and natural gas deposits. The active formation of methane hydrates in the shallow crust prevents methane, a greenhouse gas, from entering the atmosphere. On the other hand, warming of arctic sediments or ocean waters has the potential to cause methane hydrate to dissociate, releasing methane into the deepwater sediments, the ocean or atmosphere. DOE is conducting research to understand the mechanisms and volumes involved in these little-studied processes. DOE environmental and climate change research projects related to Arctic methane hydrate deposits include: Characterization of Methane Degradation and Methane-Degrading

357

Direct methane conversion to methanol. Final report, July 19, 1990--May 18, 1996  

DOE Green Energy (OSTI)

One objective of this project was to demonstrate the effectiveness of a catalytic membrane reactor (a ceramic membrane combined with a catalyst) to selectively produce methanol by partial oxidation of methane. Methanol is used as a chemical feed stock, gasoline additive, and turbine fuel. Methane partial oxidation using a catalytic membrane reactor has been determined as one of the promising approaches for methanol synthesis from methane. Methanol synthesis and separation in one step would also make methane valuable for producing chemicals and fuels. Another valuable fuel product is H{sub 2}. Its separation from other gasification products would make it very valuable as a chemical feedstock and clean fuel for fuel cells. Gasification of coal or other organic fuels as a source of H{sub 2} produces compounds (CO, CO{sub 2}, and H{sub 2}O) that require high temperature (1000-1500{degrees}F) and high pressure (600-1000 psia) separations. A zeolite membrane layer on a mechanically stable ceramic or stainless steel support would have ideal applications for this type of separation. Separations using zeolite membrane was also evaluated for use in the production in the above fuels. 20 refs., 20 figs., 1 tab.

NONE

1998-12-31T23:59:59.000Z

358

METHOD FOR PRODUCING ISOTOPIC METHANES AND PARTIALLY HALOGENATED DERIVATIVES THEROF  

DOE Patents (OSTI)

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.

Frazer, J.W.

1959-08-18T23:59:59.000Z

359

Methane Digester Loan Program | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Methane Digester Loan Program Methane Digester Loan Program Methane Digester Loan Program < Back Eligibility Agricultural Savings Category Bioenergy Maximum Rebate RFA can provide up to $250,000 of loan principal Program Info Funding Source Minnesota Rural Finance Authority (RFA) State Minnesota Program Type State Loan Program Rebate Amount RFA participation limited to 45% of loan principal Provider Minnesota Department of Agriculture Established in 1998, the Minnesota Dept. of Agriculture Methane Digester Loan Program helps livestock producers install on-farm anaerobic digesters used for the production of electricity by providing zero-interest loans to eligible borrowers. The loan program is part of the Rural Finance Authority (RFA) revolving loan fund, through which farmers can receive financial aid

360

Methane Hydrate Program Annual Report to Congress  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

FY 2010 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 entitled, U.S. Department of Energy FY 2010 Methane Hydrate Program Report to Congress. The report was prepared by the Department of Energy's Office of Fossil Energy and summarizes the progress being made in this important area of

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Seismic-Scale Rock Physics of Methane Hydrate Seismic-Scale Rock Physics of Methane Hydrate DE-FC26-05NT42663 Goal The goal of this project was to establish rock physics models for use in generating synthetic seismic signatures of methane hydrate reservoirs. Ultimately, the intent was to improve seismic detection and quantification of offshore and onshore methane hydrate accumulations. Performer Stanford University, Stanford, CA 94305 Background Gas hydrate reservoir characterization is, in principle, no different from traditional hydrocarbon reservoir characterization. The seismic response of the subsurface is determined by the spatial distribution of the elastic properties (properties of the subsurface that deform as seismic waves pass through it) and attenuation. By mapping changes in the elastic properties, scientists can identify geologic features, including hydrocarbon reservoirs.

362

Arkansas Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

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...

363

Alabama Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

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...

364

Kansas Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

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...

365

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Sampling and Characterization of Naturally Occurring Methane Hydrate Using the DV JOIDES Resolution Last Reviewed 02052010 DE-FC26-01NT41329 photo of a man showing the pressure...

366

Virginia Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

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...

367

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

that the hydrate in this region occurs in patchy deposits and may require a high methane flux from the subsurface in order to form more continuous drilling prospects. Project...

368

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

DE-AF26-01NT00370 Goal The goal of the project is to better characterize potential methane hydrate drilling sites in the Gulf of Mexico for the Ocean Drilling Program....

369

Wyoming Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

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...

370

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

area, known as Mississippi Canyon lease block 118, is well-known for the occurrence of methane hydrate and is the location of the University of Mississippis gas hydrate...

371

Oklahoma Coalbed Methane Production (Billion Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Production (Billion Cubic Feet) Oklahoma 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 58 68...

372

Methane Hydrates - Mt. Elbert Well Log Data  

NLE Websites -- All DOE Office Websites (Extended Search)

more. Project background information - Alaska North Slope Gas Hydrate Reservoir Characterization - DE-FC26-01NT41332 More information on the National Methane Hydrates R&D Program...

373

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

FWP-4340-60 and FWP-42C1-01 Goal Determine the presence and activity of methanogens in methane hydrate-bearing sediments. Background The project was set up to determine a...

374

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

of high chloride concentration and no sulfate reduction zone, indicating areas of high methane flux. The February 2005 RV Pelican cruise was a follow-up to the May 2004 cruise....

375

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Efficacy of the Aerobic Methanotropic Biofilter in Methane Hydrate Environments Last Reviewed 182013 DE-NT0005667 Goal The goal of this project is to assess the efficacy of...

376

Montana Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

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...

377

Pennsylvania Coalbed Methane Production (Billion Cubic Feet)  

Annual Energy Outlook 2012 (EIA)

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...

378

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

to develop a two-dimensional, basin-scale model for the deep sediment biosphere with methane dynamics to provide a better picture of the distribution of hydrates on the sea floor...

379

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Goal The overall objective of this project is to develop a new method to assess methane hydrate distribution using 3-D seismic data calibrated to wellbore data. The method...

380

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Production of Methane Hydrate Last Reviewed 5152012 DE-FC26-06NT42960 Goal The goal of this project is to improve the understanding of regional and local differences in gas...

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

The role of methane in tropospheric chemistry  

E-Print Network (OSTI)

While methane is chemically quite inert to reactions with atmospheric molecular species, it does react with atomic species and molecular radicals. Because of its relatively large abundance in the global troposphere and ...

Golomb, D.

1989-01-01T23:59:59.000Z

382

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Laboratory Studies in Support of Characterization of Recoverable Resources from Methane Hydrate Deposits Last Reviewed 5/10/2012 Laboratory Studies in Support of Characterization of Recoverable Resources from Methane Hydrate Deposits Last Reviewed 5/10/2012 ESD05-048 Goal The project is bringing new laboratory measurements and evaluation techniques to bear on the difficult problems of characterization and gas recovery from methane hydrate deposits. Performer Lawrence Berkeley National Laboratory, Berkeley, CA 94720 Background LBNL is performing laboratory tests to provide data to support the characterization and development of methane hydrate deposits. Major areas of research underway include hydrologic measurements, combined geomechanical/geophysical measurements, and synthetic hydrate formation studies. Hydrologic Measurements Relatively little research has been done to experimentally determine

383

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Collection and Microbiological Analysis of Gas Hydrate Cores Collection and Microbiological Analysis of Gas Hydrate Cores FWP-4340-60 and FWP-42C1-01 Goal Determine the presence and activity of methanogens in methane hydrate-bearing sediments. Background The project was set up to determine a fundamental modeling parameter - the amount of methane generated in deep sediments by methanogenic microorganisms. This would allow methane distribution models of gas hydrate reservoirs to accurately reflect an unknown volume and the distribution of biogenic methane within in a reservoir. The personnel at INEL have experience in similar biologic research and are considered to be experts by their global peers. Performer Idaho National Engineering and Environmental Laboratory (INEEL) - sample collection and analysis Location

384

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

SciTech Connect

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 anaerobic methane oxidizing (AOM) microorganisms are predominantly found in marine habitats and grow poorly under most laboratory conditions. One path for future research would be to use a small rotary rig to collect samples from deeper soil horizons, possibly adjacent to the coal-bearing horizons that may be more anaerobic.

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

2012-09-06T23:59:59.000Z

385

Methane level rise blamed in greenhouse effect  

SciTech Connect

As scientists continue to probe effects of global warming trends and the greenhouse effect, increasing attention is being placed on the impact of methane. Last year, scientists at the University of California in Irvine found there were almost 1.7 parts per million of methane in the troposphere- 11% higher that a decade ago and climbing at 1% annually. European scientists came up with similar analyses, and the belief is that methane is currently 2.4 times higher than it has ever been in the last 160,000 years. The big challenge now is to identify the sources of the methane. About 15 to 20% can be traced to oil and gas wells, coal mining and other tapping of the gas trapped in the planet's crust. Other sources are bacteria working in tropical rain forests, burned-off clearings, etc. Cattle figure high on the list of methane generators. When domesticated herds of sheep, goats, pigs, etc. are figured, the total rises to 73 million metric tons per year- a 435% increase since 1890. Rice paddies are also rated a major source of methane. It's estimated that 115 million metric tons rise from rice paddies a year, as much as is coming from natural swamps and wetlands. When scientists added up all the published estimates of methane production, the total ranged from 400 million to 640 million metric tons a year. Estimates of how much methane the atmosphere can handle are similarly uncertain, ranging from 300 million to 650 million metric tons a year.

1989-01-01T23:59:59.000Z

386

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 1, October 16, 1986--January 15, 1987  

DOE Green Energy (OSTI)

The United States will need to be able to convert coal to liquid fuels should current supplies be interrupted. The indirect method for producing fuel liquids is the gasification of the coal to synthesis gas (syngas) followed by Fischer-Tropsch synthesis to convert syngas to hydrocarbons. However, both the gasifier and the FTS processes result in the production of methane and/or light hydrocarbon by-product that negatively affect the economics of the production of liquid fuel from coal. The goal of SRI`s research is thus to develop catalysts that directly convert methane and light hydrocarbons to intermediates that can, as economics dictate, be subsequently converted either to liquid fuels or value-added chemicals. SRI project 2678 is exploring two approaches to achieving the stated goal. The first approach consists of developing advanced catalysts for reforming methane. We will prepare the catalysts by reacting organometallic complexes of transition metals (Fe, Ru, Rh, and Re) with zeolitic and rare earth exchanged zeolitic supports to produce surfaceconfined metal complexes in the zeolite pores. We will then decompose the organometallic complexes to obtain very stable, highly dispersed catalysts. Our second approach entails synthesizing the porphyrin and phthalocyanine complexes of Cr, Mn, Ru, Fe, and/or Co within the pores of zeolitic supports for use as selective oxidation catalysts for methane and light hydrocarbons. We will test the catalysts in a fixed-bed isothermal microreactor in a downflow mode at {approximately}100 psi. During the first quarter of this project, we have concentrated on methane oxidation to methanol. We have synthesized phthalocyanine oxidation catalysts containing different metals (Co, Fe, and Ru) within zeolite pores. our examination of their ability to oxidize methane to methanol has indicated preliminary positive results.

Wilson, R.B. Jr.; Chan, Yee Wai

1987-02-23T23:59:59.000Z

387

Production and Ebullition of Methane in a Shallow Eutrophic Lake (Lake Elsinore, CA)  

E-Print Network (OSTI)

monoxide, methane, carbon dioxide and total gaseous mercuryFluxes of methane and carbon dioxide from a small productiveebullition of methane and carbon dioxide from a eutrophied

Martinez, Denise Nicole

2012-01-01T23:59:59.000Z

388

Hydrogen Safety Issues Compared to Safety Issues with Methane and Propane  

E-Print Network (OSTI)

Issues with Methane and Propane Michael A. Green LawrenceSAFETY ISSUES WITH METHANE AND PROPANE M. A. Green Lawrencehydrogen. Methane and propane are commonly used by ordinary

Green, Michael A.

2005-01-01T23:59:59.000Z

389

Separation and Purification of Methane from coal-Bed Methane via the Hydrate Technology  

Science Conference Proceedings (OSTI)

The separation of methane from coal-bed methane (CBM) via hydrate process using tetrahydrofuran (THF) + sodium dodecyl sulfate (SDS) as additives was investigated in this work. The effect of additives, the concentration of the additives and hydrate memory ... Keywords: CBM, hydrate, separation, THF, SDS

Cai Jing; Chen Zhaoyang; Li Xiaosen; Xu Chungang

2010-12-01T23:59:59.000Z

390

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 2, January 16, 1987--April 15, 1987  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that can, as economics dictate, be subsequently converted either to liquid fuels or value-added chemicals. In this program we are exploring two approaches to developing such catalysts. The first approach consists of developing advanced catalysts for reforming methane. We will prepare the catalysts by reacting organometallic complexes of transition metals (Fe, Ru, Rh, and Re) with zeolitic and rare-earth-exchanged zeolitic supports to produce surfaceconfined metal complexes in the zeolite pores. Our second approach entails synthesizing the porphyrin and phthalocyanine complexes of Cr, Mn, Ru, Fe, and/or Co within the pores of zeolitic supports for use as selective oxidation catalysts for methane and light hydrocarbons. During the second quarter of this project, we concentrated on methane reforming. Two ruthenium clusters (Ru{sub 4} and Ru{sub 6}) supported on three types of support materials ({beta}-alumina, 5 {Angstrom} molecular sieves, and {gamma}-zeolite) were tested for methane reforming. The effects of cluster size, supporting material, and reaction conditions were evaluated. The methane conversions range from 1.74 to 10.11% at 750{degrees}C. The reaction product contains hydrogen, C{sub 2} hydrocarbons, and C{sub 6} or higher hydrocarbons. Up to 48.34% yield of hydrocarbon (C{sub 2}+) is obtained based on reacted methane. Some of these catalysts show very good coking resistance compared with a commercial ruthenium catalyst. Addition of oxygen to these reactions significantly increases the percent methane conversion at lower reaction temperature. However, carbon dioxide and water are the major products in the presence of oxygen.

Wilson, R.B. Jr.; Chan, Yee Wai

1987-05-21T23:59:59.000Z

391

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 3, April 16--July 15, 1987  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that can, as economics dictate, be subsequently converted either to liquid fuels or value-added chemicals. In this program we are exploring two approaches to developing such catalysts. The first approach consists of developing advanced catalysts for reforming methane. We will prepare the catalysts by reacting organometallic complexes of transition metals (Fe, Ru, Rh, and Re) with zeolitic and rare-earth-exchanged zeolitic supports to produce surface-confined metal complexes in the zeolite pores. Our second approach entails synthesizing the porphyrin and phthalocyanine complexes of Cr, Mn, Ru, Fe, and/or Co within the pores of zeolitic supports for use as selective oxidation catalysts for methane and light hydrocarbons. During this reporting period, we concentrated on synthesizing and testing methane oxidation catalysts using the automated GC sampling system. We modified our preparation method of zeolite-encapsulated phthalocyanines (PC). The catalysts have higher complex loading, and the uncomplexed metal ions were back-exchanged by sodium ions (to remove any uncomplexed metal ions). Four metal ions were used: cobalt, iron, ruthenium, and manganese. We also synthesized four zeolite-encapsulated tetraphenylporphyrin (TPP) complexes using the same metals. These catalysts were tested for methane oxidation in the temperature range from 300{degrees} to 500{degrees}C at 50 psig pressure. The RUPC, COTPP, and MNTPP showed activity toward the formation of methanol. The RUPC zeolite gave the best methanol yield. The methane conversion was 4.8%, and the selectivity to methanol is 11.3% at 375{degrees}C. Again, the major products are carbon dioxide and water in every catalyst we tested during this reporting period.

Wilson, R.B. Jr.; Chan, Yee Wai

1987-08-28T23:59:59.000Z

392

Methane Power Inc | Open Energy Information  

Open Energy Info (EERE)

Methane Power Inc Methane 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 Product Methane Power is a renewable energy project developer that focuses on landfill gas-to-energy projects. Currently, they are a supplier of landfill gas generated energy to Duke Energy in North Carolina. Phone number 919-297-7206 Website http://www.methanepower.net Coordinates 35.7395875°, -78.8029226° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":35.7395875,"lon":-78.8029226,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

393

Coal bed methane global market potential  

Science Conference Proceedings (OSTI)

Worldwide increases in energy prices, as well as the increased potential for project financing derived from emissions credits, have renewed focus on coal bed methane (CBM) and coal mine methane (CMM) projects in coal-producing countries around the world. Globally, CBM utilization projects (in the operational, development, or planning stages) capture and utilize methane from gassy underground coal mines in at least 13 countries. The total methane emission reductions that could be achieved by these projects are approximately 135 billion cubic feet per year (equal to 14.8 million tons of carbon equivalent per year). This global activity level reflects a growing awareness of the technological practicality and the economic attractiveness of coal mine methane recovery and use. This report outlines the potential of the global CBM market. Contents: An overview of CBM; Challenges and issues; Technologies to generate power from CAM; Global CBM/CMM utilization; Country highlights; Ranking of countries with the largest CMM development potential (Australia, Canada, China, Germany, Mexico, Poland, Russia, Ukraine, United Kingdom, USA, Bulgaria, Czech Republic, France, India, Japan, Kazakhstan, South Africa); Planning CBM/CMM projects; Pre-feasibility and feasibility studies; Demonstration projects; Development plan and application process; Equity and debt; Carbon financing; Government sponsors; Private sponsors; Project risk reduction support; Examples of integrated project financing; Glossary.

Drazga, B. (ed.)

2007-01-16T23:59:59.000Z

394

Activation of methane by transition metal-substituted aluminophosphate molecular sieves  

DOE Patents (OSTI)

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 and 500{degree}C and at methane pressures {le} 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 cobalt substituted AlPO{sub 4}-34 structure (CoAPSO-34) produces ethylene, ethane, propylene, and propane in varying proportions, depending on reaction conditions. The cobalt-substituted AlPO{sub 4}-5 (CoAPSO-5) produces polypropylene in very high yield, with ethane, ethylene, and propane also produced. The activation mechanism is based on reduction of the transition metal (III) from 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. 4 figs.

Iton, L.E.; Maroni, V.A.

1990-03-16T23:59:59.000Z

395

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...

396

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...

397

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...

398

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane 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...

399

Eastern States Coalbed Methane Proved Reserves (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

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

400

Western States Coalbed Methane Proved Reserves (Billion Cubic...  

Annual Energy Outlook 2012 (EIA)

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

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

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

U.S. Energy Information Administration (EIA) Indexed Site

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

402

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...

403

Eastern States Coalbed Methane Production (Billion Cubic Feet...  

Annual Energy Outlook 2012 (EIA)

Coalbed Methane Production (Billion Cubic Feet) Eastern 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...

404

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

Annual Energy Outlook 2012 (EIA)

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...

405

On the Sources of Methane to the Los Angeles Atmosphere  

NLE Websites -- All DOE Office Websites (Extended Search)

On the Sources of Methane to the Los Angeles Atmosphere Title On the Sources of Methane to the Los Angeles Atmosphere Publication Type Journal Article Year of Publication 2012...

406

MARINE BIOMASS SYSTEM: ANAEROBIC DIGESTION AND PRODUCTION OF METHANE  

E-Print Network (OSTI)

The basic energy conversion system being considered in thisEnergy Fixation and Conversion with Algal Bacterial Systems/energy producer based on current methane prices. bility of a kelp to methane conversion system

Haven, Kendall F.

2011-01-01T23:59:59.000Z

407

ANALYSIS OF METHANE PRODUCING COMMUNITIES WITHIN UNDERGROUND COAL BEDS  

E-Print Network (OSTI)

ANALYSIS OF METHANE PRODUCING COMMUNITIES WITHIN UNDERGROUND COAL BEDS by Elliott Paul Barnhart.........................................................................................8 Coal and Metabolite Enrichment Studies ..................................................................................14 Ability of the Consortium to Produce Methane from Coal and Metabolites ................16

Maxwell, Bruce D.

408

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Gas Hydrate Production Trial Using CO2 / CH4 Exchange Completed Gas Hydrate Production Trial Using CO2 / CH4 Exchange Completed DE-NT0006553 Goal The goal of this project is to define, plan, conduct and evaluate the results of a field trial of a methane hydrate production methodology whereby carbon dioxide (CO2) molecules are exchanged in situ for methane (CH4) molecules within a hydrate structure, releasing the methane for production. The objective is to evaluate the viability of this hydrate production technique and to understand the implications of the process at a field scale. image showing Conceptual rendering of proposed CO2 - CH4 exchange methodology for the production of natural gas from hydrates Conceptual rendering of proposed CO2 - CH4 exchange methodology for the

409

MethaneHydrateRD_FC.indd  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

gas is an important energy 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 goals." The Nati onal Academies 2010 One of these is methane hydrate - molecules of natural gas trapped in ice crystals. Containing vast amounts of natural gas, methane hydrate occurs in a variety of forms in sediments within and below thick permafrost in Arctic regions, and in the

410

SCREENING TESTS FOR IMPROVED METHANE CRACKING MATERIALS  

DOE Green Energy (OSTI)

Bench scale (1 to 6 gram) methane cracking tests have been performed on a variety of pure elements, some alloys, and SAES{reg_sign} commercial getters St 101, St 198, St 707, St 737, and St 909 to determine methane cracking performance (MCP) of 5% methane in a helium carrier at 700 C, 101.3 kPa (760 torr) with a 10 sccm feed. The MCP was almost absent from some materials tested while others showed varying degrees of MCP. Re, Cr, V, Gd, and Mo powders had good MCP, but limited capacities. Nickel supported on kieselguhr (Ni/k), a Zr-Ni alloy, and the SAES{reg_sign} getters had good MCP in a helium carrier. The MCP of these same materials was suppressed in a hydrogen carrier stream and the MCP of the Zr-based materials was reduced by nitride formation when tested with a nitrogen carrier gas.

Klein, J; Jeffrey Holder, J

2007-07-16T23:59:59.000Z

411

Direct use of methane in coal liquefaction  

DOE Patents (OSTI)

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.

Sundaram, Muthu S. (Shoreham, NY); Steinberg, Meyer (Melville, NY)

1987-01-01T23:59:59.000Z

412

Direct use of methane in coal liquefaction  

DOE Patents (OSTI)

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.

Sundaram, M.S.; Steinberg, M.

1985-06-19T23:59:59.000Z

413

CFD Modeling of Methane Production from Hydrate-Bearing Reservoir  

Science Conference Proceedings (OSTI)

Methane hydrate is being examined as a next-generation energy resource to replace oil and natural gas. The U.S. Geological Survey estimates that methane hydrate may contain more organic carbon the the world's coal, oil, and natural gas combined. To assist in developing this unfamiliar resource, the National Energy Technology Laboratory has undertaken intensive research in understanding the fate of methane hydrate in geological reservoirs. This presentation reports preliminary computational fluid dynamics predictions of methane production from a subsurface reservoir.

Gamwo, I.K.; Myshakin, E.M.; Warzinski, R.P.

2007-04-01T23:59:59.000Z

414

Detection and Production of Methane Hydrate  

NLE Websites -- All DOE Office Websites (Extended Search)

July-September 2007 July-September 2007 Detection and Production of Methane Hydrate Submitted by: Rice University University of Houston George J. Hirasaki Department of Chemical and Biomolecular Engineering Rice University - MS 362 6100 Main St. Houston, TX 77251-1892 Phone: 713-348-5416; FAX: 713-348-5478; Email: gjh@rice.edu Prepared for: United States Department of Energy National Energy Technology Laboratory December, 2007 Office of Fossil Energy Table of Contents DOE Methane Hydrate Program Peer Review.................................................. 3 Task 5: Carbon Inputs and Outputs to Gas Hydrate Systems ........................... 3 Task 6: Numerical Models for Quantification of Hydrate and Free Gas Accumulations....................................................................................................

415

Method for removal of methane from coalbeds  

DOE Patents (OSTI)

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.

Pasini, III, Joseph (Morgantown, WV); Overbey, Jr., William K. (Morgantown, WV)

1976-01-01T23:59:59.000Z

416

Multivariate statistical evaluation of equilibrium methane adsorption isotherms of coal  

SciTech Connect

The adsorption of methane by coals varies over a broad range of values and appears to depend on a complex function related to coal rank. In order to evaluate these variations in methane adsorption 100 coal samples were analyzed. The paper presents some preliminary results of this study based on multivariate statistical evaluation of equilibrium methane adsorption isotherm data, coal petrology, and vitrinite reflectance.

Schwarzer, R.S.; Bayliss, G.S.

1982-01-01T23:59:59.000Z

417

Renewable Energy 32 (2007) 12431257 Methane generation in landfills  

E-Print Network (OSTI)

2006 Abstract Methane gas is a by-product of landfilling municipal solid wastes (MSW). Most tonnes of methane annually, 70% of which is used to generate heat and/or electricity. The landfill gas. All rights reserved. Keywords: Landfill gas; Renewable energy; Municipal solid waste; Biogas; Methane

Columbia University

418

Novel Anode Materials For Solid Oxide Fuel Cells Dissertation committee  

E-Print Network (OSTI)

and fabrication of alternative anodes for direct methane oxidation in SOFC". Publisher: Twente University Press, P cells (SOFC). The principles and materials employed for SOFC are described. Emphasis is on the anode (PAFC), · the molten carbonate fuel cell (MCFC), · the solid oxide fuel cell (SOFC). Each type of fuel

Verweij, Henk

419

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 9, October 1--December 31, 1988  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that later can be converted to either liquid fuels or value-added chemicals, as economics dictate. During this reporting period, we completed our IR spectroscopic examination of the Ru{sub 4}/MgO and FeRu{sub 3}/MgO systems under nitrogen and methane by examining FeRu{sub 3}/MgO under methane. This system behaved quite differently than the same system under nitrogen. Under methane, only one very broad peak is observed at room temperature. Upon heating, the catalyst transformed so that by 300{degrees}C, the spectrum of FeRu{sub 3}/MgO under methane was the same as that of Ru{sub 4}/MgO. This suggests that methane promotes the segregation of the metals in the mixed metal system. The differences in catalytic activity between the FeRu{sub 3}/MgO and Ru{sub 4}/MgO systems may then be due to the presence of IR transparent species such as iron ions which cause different nucleation in the ruthenium clusters. We examined several systems for activity in the methane dehydrogenation reaction. Focusing on systems which produce C{sub 6} hydrocarbons since this is the most useful product. These systems all displayed low activity so that the amount of hydrocarbon product is very low. Some C{sub 6} hydrocarbon is observed over zeolite supports, but its production ceases after the first few hours of reaction. We prepared a new system, Ru{sub 4} supported on carbon, and examined its reactivity. Its activity was very low and in fact the carbon support had the same level of activity. We synthesized four new systems for examination as catalysts in the partial oxidation of methane. Three of these (PtTSPC/MgO, PtTSPC and PdTSPC on carbon) are analogs of PdTSPC/MgO. This system is of interest because we have observed the production of ethane from methane oxidation over PdTSPC/MgO at relatively low temperatures and we wished to explore its generality among close analogs.

Wilson, R.B. Jr.; Posin, B.M.; Chan, Yee Wai

1989-03-10T23:59:59.000Z

420

OXIDATION OF DRY HYDROCARBONS AT HIGH-POWER DENSITY ANODES  

DOE Green Energy (OSTI)

This work builds upon discoveries by the University of Pennsylvania and others pertaining to the oxidation of dry hydrocarbon fuels in high temperature solid oxide fuel cells. The work reported here was restricted primarily to dry methane and confirms that YSZ-based cells, having ceria in the anode as a catalyst and copper in the anode as a current collector, can operate on dry methane for extended periods. Thirty-three lab-scale cells of various designs were fabricated and operated under a variety of conditions. The longest-lived cell gave stable performance on dry methane at 800 C for over 305 hours. Only slight carbon deposition was noted at the completion of the test. A corresponding nickel/YSZ-based anode would have lasted for less than an hour under these test conditions (which included open circuit potential measurements) before carbon fouling essentially destroyed the cell. The best performing cell achieved 112 mW/cm{sub 2} on dry methane at 800 C. Several problems were encountered with carbon fouling and declining open circuit voltages in many of the test cells after switching from operation on hydrogen to dry methane. Although not rigorously confirmed by experimentation, the results suggested that air infiltration through less than perfect perimeter seals or pinholes in the electrolytes, or both gave rise to conditions that caused the carbon fouling and OCV decline. Small amounts of air reacting with methane in a partial oxidation reaction could produce carbon monoxide that, in turn, would deposit the carbon. If this mechanism is confirmed, it implies that near perfect hardware is required for extended operation. Some evidence was also found for the formation of electrical shorts, probably from carbon deposits bridging the electrolyte. Work with odorized methane and with methane containing 100-ppm hydrogen sulfide confirmed that copper is stable at 800 C in dry hydrocarbon fuels in the presence of sulfur. In a number of cases, but not exclusively, the performance life on dry methane with sulfur compounds was much longer than with dry methane alone. The effect of sulfur compounds in these cases appeared to correlate with inhibition of carbon deposition. Mixed results were obtained for the effect of the sulfur compounds on power density. Progress also was made in understanding the mechanisms involved in direct utilization of dry natural gas. Evidence was developed for three possible mechanisms for dry methane utilization in addition to the usually cited mechanism--direct oxidation of methane by oxygen anions. Further work is required at a fundamental level before the knowledge gained here can be translated into higher levels of performance.

K.Krist; O. Spaldon-Stewart; R. Remick

2004-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Unconventional gas resources. [Eastern Gas Shales, Western Gas Sands, Coalbed Methane, Methane from Geopressured Systems  

DOE Green Energy (OSTI)

This document describes the program goals, research activities, and the role of the Federal Government in a strategic plan to reduce the uncertainties surrounding the reserve potential of the unconventional gas resources, namely, the Eastern Gas Shales, the Western Gas Sands, Coalbed Methane, and methane from Geopressured Aquifers. The intent is to provide a concise overview of the program and to identify the technical activities that must be completed in the successful achievement of the objectives.

Komar, C.A. (ed.)

1980-01-01T23:59:59.000Z

422

File:Methane.pdf | Open Energy Information  

Open Energy Info (EERE)

Methane.pdf 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 → Full resolution ‎(1,218 × 1,630 pixels, file size: 929 KB, MIME type: application/pdf, 5 pages) File history Click on a date/time to view the file as it appeared at that time. Date/Time Thumbnail Dimensions User Comment current 15:51, 9 February 2012 Thumbnail for version as of 15:51, 9 February 2012 1,218 × 1,630, 5 pages (929 KB) Graham7781 (Talk | contribs) You cannot overwrite this file. Edit this file using an external application (See the setup instructions for more information) File usage The following page links to this file: Hydraulic Fracturing Retrieved from "http://en.openei.org/w/index.php?title=File:Methane.pdf&oldid=404017"

423

California - Coastal Region Coalbed Methane Proved Reserves ...  

Annual Energy Outlook 2012 (EIA)

Coastal Region 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 - No...

424

Federal Offshore California Coalbed Methane Proved Reserves ...  

Annual Energy Outlook 2012 (EIA)

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 -...

425

Generating power with drained coal mine methane  

SciTech Connect

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.

NONE

2005-09-01T23:59:59.000Z

426

Methane Hydrates R&D U S  

NLE Websites -- All DOE Office Websites (Extended Search)

the Power of Working Together Interagency Coordination on Methane Hydrates R&D U . S . D e p a r t m e n t o f E n e r g y * O f f i c e o f F o s s i l E n e r g y N a t i o n a l...

427

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

Science Conference Proceedings (OSTI)

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.

Song Jin

2007-05-31T23:59:59.000Z

428

SAES ST 909 PILOT SCALE METHANE CRACKING TESTS  

DOE Green Energy (OSTI)

Pilot scale (500 gram) SAES St 909 methane cracking tests were conducted to determine material performance for tritium process applications. Tests that ran up to 1400 hours have been performed at 700 C, 202.7 kPa (1520 torr) with a 30 sccm feed of methane, with various impurities, in a 20 vol% hydrogen, balance helium, stream. A 2.5 vol% methane feed was reduced below 30 ppm for 631 hours. A feed of 1.1 vol% methane plus 1.4 vol% carbon dioxide was reduced below 30 ppm for 513 hours. The amount of carbon dioxide gettered by St 909 can be equated to an equivalent amount of methane gettered to estimate a reduced bed life for methane cracking. The effect of 0.4 vol % and 2.1 vol% nitrogen in the feed reduced the time to exceed 30 ppm methane to 362 and 45 hours, respectively, but the nitrogen equivalence to reduced methane gettering capacity was found to be dependent on the nitrogen feed composition. Decreased hydrogen concentrations increased methane getter rates while a drop of 30 C in one bed zone increased methane emissions by over a factor of 30. The impact of gettered nitrogen can be somewhat minimized if the nitrogen feed to the bed has been stopped and sufficient time given to recover the methane cracking rate.

Klein, J; Henry Sessions, H

2007-07-02T23:59:59.000Z

429

Coal Bed Methane Protection Act (Montana) | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Coal Bed Methane Protection Act (Montana) Coal Bed Methane Protection Act (Montana) Coal Bed Methane Protection Act (Montana) < Back Eligibility Utility Fed. Government Commercial Agricultural Investor-Owned Utility State/Provincial Govt Industrial Construction Municipal/Public Utility Local Government Rural Electric Cooperative Tribal Government Institutional Fuel Distributor Program Info State Montana Program Type Environmental Regulations Provider Montana Department of Natural Resources and Conservation The Coal Bed Methane Protection Act establishes a long-term coal bed methane protection account and a coal bed methane protection program for the purpose of compensating private landowners and water right holders for damage to land and to water quality and availability that is attributable to the development of coal bed methane wells. The Act aims to provide for

430

Methane Hydrates - The National R&D Program  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrates R&D Program Methane Hydrates R&D Program The National Methane Hydrates R&D Program Welcome to the information portal for the National Methane Hydrate R&D Program. Over the past eight years, research carried out under this program has resulted in significant advances in our understanding of methane hydrates, their role in nature, and their potential as a future energy resource. This success is largely due to an unprecedented level of cooperation between federal agencies, industry, national laboratories, and academic institutions. For a quick introduction to methane hydrate and its potential as a fuel source, please read the 2011 Methane Hydrates Primer. Information on other elements of the program can be found under the remaining Key Links. Read More.

431

The Effects of Dissolved Methane upon Liquid Argon Scintillation Light  

E-Print Network (OSTI)

In this paper we report on measurements of the effects of dissolved methane upon argon scintillation light. We monitor the light yield from an alpha source held 20 cm from a cryogenic photomultiplier tube (PMT) assembly as methane is injected into a high-purity liquid argon volume. We observe significant suppression of the scintillation light yield by dissolved methane at the 10 part per billion (ppb) level. By examining the late scintillation light time constant, we determine that this loss is caused by an absorption process and also see some evidence of methane-induced scintillation quenching at higher concentrations (50-100 ppb). Using a second PMT assembly we look for visible re-emission features from the dissolved methane which have been reported in gas-phase argon methane mixtures, and we find no evidence of visible re-emission from liquid-phase argon methane mixtures at concentrations between 10 ppb and 0.1%.

B. J. P. Jones; T. Alexander; H. O. Back; G. Collin; J. M. Conrad; A. Greene; T. Katori; S. Pordes; M. Toups

2013-08-16T23:59:59.000Z

432

Operation of an aircraft engine using liquefied methane fuel  

SciTech Connect

The operation of a reciprocating aircraft engine on methane fuel is demonstrated. Since storage of the methane fuel in the gaseous state would impractical for a flight fuel system, a liquid storage system was used. System valving was configured to deliver only liquid methane to the engine supply line. The equipment description includes photo and diagram illustrations of the liquid methane storage dewar, and photos of the methane heat exchanger, pressure regulator and air-fuel mixer. The engine test results are presented for gasoline and methane in terms of RPM, horsepower, fuel flow, specific energy consumption and standard conditions horsepower. Conclusions include the finding that conversion of an aircraft reciprocating engine to operate on liquified methane is possible with very satisfactory results.

Raymer, J.A.

1982-01-01T23:59:59.000Z

433

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

D6), doi:10.1029/1096JD03382. Volk, C. M. , et al. (1996),CIRS, Icarus , 191 , 712-721. Volk, C. M. , et al. (1996),Mass Spectrom. , 22, 603-312. Volk, C. M. , et al. (1996),

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

434

Nitrous oxide as a substitute for sulfur hexafluoride in the ANSI/ASHRAE 110 Method of hood performance evaluation.  

E-Print Network (OSTI)

??The ANSI/ASHRAE 110 Method is the standard test for laboratory hood containment performance. Sulfur hexafluoride is specified as the gas most suitable for this test… (more)

Guffey, Eric J. (Eric Jemison)

2011-01-01T23:59:59.000Z

435

Nitrous oxide as a substitute for sulfur hexafluoride in the ANSI/ASHRAE 110 Method of hood performance evaluation  

E-Print Network (OSTI)

The ANSI/ASHRAE 110 Method is the standard test for laboratory hood containment performance. Sulfur hexafluoride is specified as the gas most suitable for this test and is most commonly used. Sulfur hexafluoride use has ...

Guffey, Eric J. (Eric Jemison)

2011-01-01T23:59:59.000Z

436

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

not included here). The solar spectrum at 625 km in Earth’ssee if structure in the solar spectrum changes the ratio ofnot included here). The solar spectrum at 625 km in Earth’s

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

437

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

through biomass and fossil fuel combustion, which show thatof industrial combustion or biomass burning processes butbiomass burning, based on recent measurements of a combustion

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

438

Geochemistry of clathrate-derived methane in Arctic Ocean waters  

SciTech Connect

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.

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

2010-03-15T23:59:59.000Z

439

Methane coupling by membrane reactor. Quarterly report, June 25--September 24, 1996  

DOE Green Energy (OSTI)

To prevent the deep oxidation of methane catalyzed by the direct contact between methane and the dense membrane material (SrFeCo{sub 0.5}O{sub 3{minus}x}), BaCe{sub 0.6}Sm{sub 0.4}O{sub 3} perovskite was coated on the inner surface of the dense membrane tube by the sol-gel technique. Different pretreatment methods were tested to compare their effects on the coated film. The morphology of the coated membrane was studied by SEM. The BaCe{sub 0.6}Sm{sub 0.4}O{sub 3}-coated membrane which was pretreated with a basic solution before coating was more evenly covered by the coating material. The oxygen permanence through the modified membrane tube were measured at different temperatures. The oxygen permanence were found to be about 70% lower than those of the unmodified tubes. The catalytic runs were carried out with La/MgO catalyst packed inside the membrane tube. The C{sub 2} yields obtained using the dense membrane reactor were less than 4%. This may have resulted from the fact that the methane fed to the tube side was still exposed to the uncoated area of the dense membrane surface due to the incomplete coverage of the coating material (BaCe{sub 0.6}Sm{sub 0.4}O{sub 3}). A hybrid dense membrane reactor, in which the oxygen was supplied by co-feeding oxygen with methane to the tube side and feeding air to the shell side, was used for the oxidative coupling of methane. Again, the inner surface of the membrane tube was coated with BaCe{sub 0.6}Sm{sub 0.4}O{sub 3} by the sol-gel technique, and the La/MgO catalyst was packed inside the membrane tube. The oxygen permanence through the membrane tube was found to be about ten times higher than that under non-reaction conditions. C{sub 2} yields up to 12% were obtained using the coated dense membrane reactor. These yields are higher than those obtained in an uncoated dense membrane reactor setup with methane and oxygen co-fed into the tube side, where the same catalyst was packed.

Ma, Y.H.

1996-12-28T23:59:59.000Z

440

Regulation of methane genes and genome expression  

DOE Green Energy (OSTI)

At the start of this project, it was known that methanogens were Archaeabacteria (now Archaea) and were therefore predicted to have gene expression and regulatory systems different from Bacteria, but few of the molecular biology details were established. The goals were then to establish the structures and organizations of genes in methanogens, and to develop the genetic technologies needed to investigate and dissect methanogen gene expression and regulation in vivo. By cloning and sequencing, we established the gene and operon structures of all of the “methane” genes that encode the enzymes that catalyze methane biosynthesis from carbon dioxide and hydrogen. This work identified unique sequences in the methane gene that we designated mcrA, that encodes the largest subunit of methyl-coenzyme M reductase, that could be used to identify methanogen DNA and establish methanogen phylogenetic relationships. McrA sequences are now the accepted standard and used extensively as hybridization probes to identify and quantify methanogens in environmental research. With the methane genes in hand, we used northern blot and then later whole-genome microarray hybridization analyses to establish how growth phase and substrate availability regulated methane gene expression in Methanobacterium thermautotrophicus ?H (now Methanothermobacter thermautotrophicus). Isoenzymes or pairs of functionally equivalent enzymes catalyze several steps in the hydrogen-dependent reduction of carbon dioxide to methane. We established that hydrogen availability determine which of these pairs of methane genes is expressed and therefore which of the alternative enzymes is employed to catalyze methane biosynthesis under different environmental conditions. As were unable to establish a reliable genetic system for M. thermautotrophicus, we developed in vitro transcription as an alternative system to investigate methanogen gene expression and regulation. This led to the discovery that an archaeal protein, designated TFE, that had sequences in common with the eukaryotic general transcription factor TFIIE, stimulated archaeal transcription initiation and that the archaeal TATA-box binding protein (TBP) remained attached to the promoter region whereas the transcription factor TFB dissociated from the template DNA following initiation. DNA sequences that directed the localized assembly of archaeal histones into archaeal nucleosomes were identified, and we established that transcription by an archaeal RNA polymerase was slowed but not blocked by archaeal nucleosomes. We developed a new protocol to purify archaeal RNA polymerases and with this enzyme and additional improvements to the in vitro transcription system, we established the template requirements for archaeal transcription termination, investigated the activities of proteins predicted to be methane gene regulators, and established how TrpY, a novel archaeal regulator of expression of the tryptophan biosynthetic operon functions in M. thermautotrophicus. This also resulted in the discovery that almost all M. thermautotrophicus mutants isolated as spontaneously resistant to 5-methyl tryptophan (5MTR) had mutations in trpY and were therefore 5MTR through de-repressed trp operon expression. This established a very simple, practical procedure to determine and quantify the DNA sequence changes that result from exposure of this Archaeon to any experimental mutagenesis protocol. Following the discovery that the Thermococcus kodakaraensis was amenable to genetic manipulation, we established this technology at OSU and subsequently added plasmid expression, a reporter system and additional genetic selections to the T. kodakaraensis genetic toolbox. We established that transcription and translation are coupled in this Archaeon, and by combining in vitro transcription and in vivo genetics, we documented that both TFB1 and TFB2 support transcription initiation in T. kodakaraensis. We quantified the roles of ribosome binding sequences and alternative initiation codons in translation initiation, established that polarity e

John N. Reeve

2009-09-09T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

In Situ Sampling and Characterization of Naturally Occurring Methane Hydrate Using the D/V JOIDES Resolution Last Reviewed 02/05/2010 In Situ Sampling and Characterization of Naturally Occurring Methane Hydrate Using the D/V JOIDES Resolution Last Reviewed 02/05/2010 DE-FC26-01NT41329 photo of a man showing the pressure core sampler on the deck of JOIDES Resolution Pressure core sampler on deck courtesy Texas A&M University Goal The goal of the project was to characterize hydrate accumulation at Hydrate Ridge (offshore Oregon) and improve the ability to use geophysical and subsurface logging to identify hydrates. A follow-on goal was to characterize hydrate accumulation at offshore Vancouver Island, BC, Canada. Background This project focused on physically verifying the existence of hydrates at Hydrate Ridge through the collection of pressurized and non-pressurized core samples and logging data. This study developed and tested tools to

442

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Detection and Production of Methane Hydrate Last Reviewed 5/15/2012 Detection and Production of Methane Hydrate Last Reviewed 5/15/2012 DE-FC26-06NT42960 Goal The goal of this project is to improve the understanding of regional and local differences in gas hydrate systems from three perspectives: as an energy resource, as a geohazard, and as a long-term influence on global climate. Performers Rice University, Houston, TX University of Texas, Austin, TX Oklahoma State University, Stillwater, OK Background Heterogeneity in the distribution of gas hydrate accumulations impacts all aspects of research into gas hydrate natural systems. The challenge is to delineate, understand, and appreciate these differences at the regional and local scales, where differences in in situ concentrations are relevant to the importance of gas hydrate as a resource, a geohazard, and a factor in

443

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

- Methane Hydrate Research - Geoscience Evaluations and Field Studies Last Reviewed 3/18/2013 - Methane Hydrate Research - Geoscience Evaluations and Field Studies Last Reviewed 3/18/2013 Project Goals The primary goals of the DOE/NETL Natural Gas Hydrate Field Studies (NGHFS) project are: Conduct field-based studies that advance the ability to predict, detect, characterize, and understand distribution of and controls on natural gas hydrate occurrences. Analyze geologic, geochemical, and microbiologic data for indications of past and current changes to the stability of natural gas hydrate in marine settings. Develop links between the U.S. Gas Hydrate Program and international R&D efforts through direct participation in international field programs and workshops. Evaluate the potential role natural gas hydrates may play in the global carbon cycle through analysis of modern and paleo-natural gas

444

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

– Formation and Dissociation of Methane Hydrates Last Reviewed 07/7/2011 – Formation and Dissociation of Methane Hydrates Last Reviewed 07/7/2011 Project Objective Observe hydrate formation and dissociation phenomena in various porous media and characterize hydrate-bearing sediments by estimating physical properties (kinetic parameters for hydrate formation and dissociation, thermal conductivity, permeability, relative permeability, and mechanical strength) to enhance fundamental understanding on hydrate formation and accumulation and to support numerical simulations and potential gas hydrate production Project Performers Yongkoo Seol – NETL Office of Research & Development Jeong Choi – Oak Ridge Institute for Science and Education Jongho Cha-Virginia Polytech Institute Project Location National Energy Technology Laboratory - Morgantown, West Virginia

445

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Phase 1 - Characterization and Qualification of the Methane Hydrate Resource Potential Associated with the Barrow Gas Fields Phase 1 - Characterization and Qualification of the Methane Hydrate Resource Potential Associated with the Barrow Gas Fields DE-FC26-06NT42962 Goal The goal of this project is to characterize and quantify the postulated gas hydrate resource associated with the Barrow Gas Fields – three producing fields located in a permafrost region near Barrow, the North Slope's biggest population center and economic hub. Map of the North Slope Borough showing the location of its eight major communities, including Barrow, the site of this research project. Map of the North Slope Borough showing the location of its eight major communities, including Barrow, the site of this research project. Performers North Slope Borough, Barrow, Alaska (North Slope Borough) 99723

446

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Methane Hydrate Production from Alaskan Permafrost Last Reviewed 02/05/2010 Methane Hydrate Production from Alaskan Permafrost Last Reviewed 02/05/2010 DE-FC26-01NT41331 photo of new Anadarko drilling rig in place at Hot Ice No.1 on Alaska's North Slope Hot Ice No. 1 Drilling Platform courtesy Anadarko Petroleum Corp. Goal The goal of the project was to develop technologies for drilling and recovering hydrates in arctic areas. The specific objectives were to drill, core, and test a well through the hydrate stability zone in northern Alaska Performers Maurer Technology, Inc.* - Project coordination with DOE Anadarko Petroleum Corporation - Overall project management for the design, construction, and operation of the Arctic Drilling Platform and mobile core lab, and field coring operations Noble Engineering and Development* - Real time data collection and

447

Detection and Production of Methane Hydrate  

NLE Websites -- All DOE Office Websites (Extended Search)

Oil & Natural Gas Technology Oil & Natural Gas Technology DOE Award No.: DE-FC26-06NT42960 Quarterly Progress Report Reporting Period: April-June 2007 Detection and Production of Methane Hydrate Submitted by: Department of Chemical and Biomolecular Engineering Rice University - MS 362 6100 Main St. Houston, TX 77251-1892 Prepared for: United States Department of Energy National Energy Technology Laboratory August, 2007 Office of Fossil Energy Detection and Production of Methane Hydrate Quarterly Progress Report Reporting Period: April-June 2007 Prepared by: George Hirasaki Rice University August 2007 CONTRACT NO. DE-FC26-06NT42960 Department of Chemical and Biomolecular Engineering Rice University - MS 362 6100 Main St. Houston, TX 77251-1892 Phone: 713-348-5416; Fax: 713-348-5478; Email: gjh@rice.edu

448

Methane Hydrate Field Studies | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Field Studies Field Studies Methane Hydrate Field Studies Arctic/Alaska North Slope Field Studies 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 currently lack outlets to commercial markets, Alaska provides an excellent laboratory to study E&P technology. The research also has implications for various Alaska resources, including potential gas hydrate resources for local communities, conventional "stranded" gas, as well as Alaska's large unconventional oil resources. The hydrate deposits have been delineated in the process of developing underlying oil fields, and drilling costs are much lower than offshore. DOE-BP Project

449

Effect of bubble size and density on methane conversion to hydrate  

SciTech Connect

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 methane–water solution using a surfactant. The density of the foam, along with the bubble size, is important in the conversion of methane to methane hydrate.

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

2007-03-01T23:59:59.000Z

450

TITAN'S TRANSPORT-DRIVEN METHANE CYCLE  

SciTech Connect

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.

Mitchell, Jonathan L. [Department of Earth and Space Sciences, Department of Atmospheric and Oceanic Sciences, University of California, Los Angeles, CA 90095 (United States)

2012-09-10T23:59:59.000Z

451

Thermal Conversion of Methane to Acetylene  

DOE Green Energy (OSTI)

This report describes the experimental demonstration of a process for the direct thermal conversion of methane to acetylene. The process utilizes a thermal plasma heat source to dissociation products react to form a mixture of acetylene and hydrogen. The use of a supersonic expansion of the hot gas is investigated as a method of rapidly cooling (quenching) the product stream to prevent further reaction or thermal decomposition of the acetylene which can lower the overall efficiency of the process.

Fincke, James Russell; Anderson, Raymond Paul; Hyde, Timothy Allen; Wright, Randy Ben; Bewley, Randy Lee; Haggard, Delon C; Swank, William David

2000-01-01T23:59:59.000Z

452

Enhanced carbon monoxide utilization in methanation process  

DOE Green Energy (OSTI)

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.

Elek, Louis F. (Peekskill, NY); Frost, Albert C. (Congers, NY)

1984-01-01T23:59:59.000Z

453

Methane Detection by MIM Sensor Devices Based on Nano ZnO Thin Films Obtained by Sol-Gel and by Anodization: A Comparative Study  

Science Conference Proceedings (OSTI)

Amongst various gas sensor structures developed so far probably the least investigated one is the Metal- (Active) Insulator-Metal or (MIM) structure. It has been reported that the vertical electron transport mechanism of this structure offers high response ... Keywords: Nanocrystalline, Nanoporous, Zinc Oxide, MIM, Methane sensor, Pd-Ag Catalytic contact

Partha Bhattacharyya; Palash Kumar Basu; Sukumar Basu

2010-07-01T23:59:59.000Z

454

NETL: Methane Hydrates - DOE/NETL Projects  

NLE Websites -- All DOE Office Websites (Extended Search)

Support of Gulf of Mexico Hydrate Research Consortium: Activities to Support Establishment of Sea Floor Monitoring Station Support of Gulf of Mexico Hydrate Research Consortium: Activities to Support Establishment of Sea Floor Monitoring Station DE-FC26-02NT41328 Goal Determine the potential impacts of gas hydrate instability in terms of the release of methane into seafloor sediments, the ocean and the atmosphere. Performers University of California, San Diego (Scripps Institution of Oceanography) - manage geochemical, hydrological and sedimentological investigations Texas A&M University - manage field monitoring program Location La Jolla, California 92093 Background This project will monitor, characterize, and quantify the rates of formation and dissociation of methane gas hydrates at and near the seafloor in the northern Gulf of Mexico, and determine linkages between formation/dissociation and physical/chemical parameters of the deposits over the course of a year. The stability and response of shallow gas hydrates to temperature and chemical perturbations will be monitored in situ, and localized seafloor and water column environmental impacts of hydrate formation and dissociation characterized. The following will be determined: 1) The equilibrium/steady state conditions for structure II methane gas hydrates at the field site,2) whether the system is in dynamic equilibrium and the local hydrology is characterized by steady state episodic fluid flow, and 3) how fluid fluxes and fluid composition work together to dynamically influence gas hydrate stability.

455

International Cooperation in Methane Hydrates | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Oil & Gas » Methane Hydrate » 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 Margin off Vancouver Island, Canada (ODP 146, 1992 and IODP 311, 2005). In the Atlantic Ocean off the US, ODP Leg 146 sampled hydrate deposits on the Blake Ridge and Carolina Rise in 1995. International cooperation helps scientists in the US and other countries

456

METHANE HYDRATE ADVISORY COMMITTEE U.S. Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

METHANE HYDRATE ADVISORY COMMITTEE METHANE HYDRATE ADVISORY COMMITTEE U.S. Department of Energy Advisory Committee Charter - - - - ---- ---- ------~ 1. Committee's Official Designation. Methane Hydrate Advisory Committee (MHAC) 2. Authority:. This charter establishes the Methane Hydrate Advisory Committee (Committee) pursuant to Title IX, Subtitle F, Section 968, Methane Hydrate Research of the Energy Policy Act of 2005 (EPACT), Public Law 109-58. This charter establishes the MHAC under the authority of the Department of Energy (DOE). The MHAC is being renewed in accordance with the provisions of the Federal Advisory Committee Act (FACA), as amended, 5 U.S.C., App.2. 3. Objectives and Scope of Activities. The Committee provides advice to the Secretary of Energy by developing recommendations and broad programmatic priorities for the methane

457

Process for separating nitrogen from methane using microchannel process technology  

DOE Patents (OSTI)

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.

Tonkovich, Anna Lee (Marysville, OH); Qiu, Dongming (Dublin, OH); Dritz, Terence Andrew (Worthington, OH); Neagle, Paul (Westerville, OH); Litt, Robert Dwayne (Westerville, OH); Arora, Ravi (Dublin, OH); Lamont, Michael Jay (Hilliard, OH); Pagnotto, Kristina M. (Cincinnati, OH)

2007-07-31T23:59:59.000Z

458

Direct conversion of methane to C sub 2 's and liquid fuels  

DOE Green Energy (OSTI)

The objectives of the project are to discover and evaluate novel catalytic systems for the conversion of methane or by-product light hydrocarbon gases either indirectly (through intermediate light gases rich in C{sub 2}'s) or directly to liquid hydrocarbon fuels, and to evaluate, from an engineering perspective, different conceptualized schemes. The approach is to carry out catalyst testing on several specific classes of potential catalysts for the conversion of methane selectively to C{sub 2} products. The behavior of alkaline earth/metal oxide/halide catalysts containing strontium was found to be different from the behavior of catalysts containing barium. Two approaches were pursued to avoid the heterogeneous/homogeneous mechanism in order to achieve higher C{sub 2} selectivity/methane conversion combinations. One approach was to eliminate or minimize the typical gas phase combustion chemistry and make more of the reaction occur on the surface of the catalyst by using silver. Another approach was to change the gas phase chemistry to depart from the typical combustion reaction network by using vapor-phase catalysts. The layered perovskite K{sub 2}La{sub 2}Ti{sub 3}O{sub 10} was further studied. Modifications of process and catalyst variables for LaCaMnCoO{sub 6} catalysts resulted in catalysts with superior performance. Results obtained with a literature catalyst Na{sub 2}CO{sub 3}/Pr{sub 6}O{sub 11} were better than those obtained with NaCO{sub 3}/Pr-Ce oxide or Na{sub 2}CO{sub 3}/Ag-Pr-Ce oxide. 52 refs., 15 figs., 9 tabs.

Warren, B.K.; Campbell, K.D.; Matherne, J.L.; Kinkade, N.E.

1990-03-12T23:59:59.000Z

459

Methane coupling by membrane reactor. Quarterly technical progress report, March 25--June 24, 1996  

DOE Green Energy (OSTI)

The experimental study was continued on methane oxidative coupling using an oxygen-permeable dense membrane reactor. The oxygen permeance through the dense membrane was measured and preliminary experiments were conducted with the catalytic membrane reactor. The oxygen permeance was found to be similar to that obtained earlier without catalyst packing. No C{sub 2} hydrocarbons were observed in the catalytic membrane reactor for methane coupling. In order to reduce the non-selective, total oxidation activity of the dense membrane material, the inner surface of the dense membrane tube was deposited by the sol-gel technique with BaCe{sub 0.6}Sm{sub 0.4}O{sub 3}, which is a catalytic, oxygen-conductive material without total oxidation catalytic activity. The dense membrane tube was examined by XRD before and after the deposition. Catalytic experiments with the coated dense membrane reactor were carried out and higher C{sub 2} selectivity was observed than with the co-feed reactor.

NONE

1996-08-28T23:59:59.000Z

460

Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 8, July 16--September 30, 1988  

DOE Green Energy (OSTI)

The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that later can be converted to either liquid fuels or value-added chemicals, as economics dictate. During this reporting period, we investigated the behavior of some of our catalysts under working conditions using diffuse reflectance fourier transform infrared spectroscopy (DRIFT). Two catalysts (FeRu{sub 3} and Ru{sub 4} on magnesia) were examined under nitrogen, and the Ru{sub 4}/MgO system was examined under a methane/argon mixture. We synthesized ruthenium clusters supported on carbon as catalysts for methane reforming and new phthalocyanines to be used as catalyst precursors for oxidizing methane to methanol. The Ru{sub 4} and FeRu{sub 3} complexes supported on magnesia exhibited very different behavior in the DRIFT cell when heated under nitrogen. The FeRu{sub 3}/MgO system was completely decarbonylated by 400{degrees}C, while spectrum of the Ru{sub 4} system displayed carbonyl peaks until the temperature rose to over 600{degrees}C. The ru{sub 4}/MgO system behaved almost identically under methane/argon as it did under nitrogen in the carbonyl region. In the C-H region of the spectrum (2800-3100 cm{sup {minus}1}), peaks were observed under methane but not under nitrogen. The intensity of these peaks did not vary with temperature. We synthesized new catalysts by supporting the Ru{sub 4} and Ru{sub 6} clusters on carbon. Both acidic zeolites (Type Y or 5A) and basic magnesia (MgO) have been observed to react with hydrocarbons at high temperatures; these reactions generally lead to coking, then deactivation of the catalyst contained on these supports. We expect carbon to be a truly inert support.

Wilson, R.B. Jr.; Posin, B.M.; Chan, Yee Wai

1989-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

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

DOE Patents (OSTI)

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.

Frost, Albert C. (Congers, NY)

1980-01-01T23:59:59.000Z

462

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

SciTech Connect

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.

Emanuel, William R.; Janetos, Anthony C.

2013-02-01T23:59:59.000Z

463

Utah Coalbed Methane Proved Reserves New Reservoir Discoveries...  

U.S. Energy Information Administration (EIA) Indexed Site

New Reservoir Discoveries in Old Fields (Billion Cubic Feet) Utah Coalbed Methane Proved Reserves New Reservoir Discoveries in Old Fields (Billion Cubic Feet) Decade Year-0 Year-1...

464

,"Utah Coalbed Methane Proved Reserves, Reserves Changes, and...  

U.S. Energy Information Administration (EIA) Indexed Site

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Utah Coalbed Methane Proved Reserves, Reserves Changes, and Production",10,"Annual",2011,"6...

465

LANDFILL OPERATION FOR CARBON SEQUESTRATION AND MAXIMUM METHANE EMISSION CONTROL  

SciTech Connect

''Conventional'' waste landfills emit methane, a potent greenhouse gas, in quantities such that landfill methane is a major factor in global climate change. Controlled landfilling is a novel approach to manage landfills for rapid completion of total gas generation, maximizing gas capture and minimizing emissions of methane to the atmosphere. With controlled landfilling, methane generation is accelerated and brought to much earlier completion by improving conditions for biological processes (principally moisture levels) in the landfill. Gas recovery efficiency approaches 100% through use of surface membrane cover over porous gas recovery layers operated at slight vacuum. A field demonstration project's results at the Yolo County Central Landfill near Davis, California are, to date, highly encouraging. Two major controlled landfilling benefits would be the reduction of landfill methane emissions to minuscule levels, and the recovery of greater amounts of landfill methane energy in much shorter times 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 in reduction of US greenhouse gas emissions.

Don Augenstein

1999-01-11T23:59:59.000Z

466

NETL: Methane Hydrates - DOE/NETL Projects - Advanced Hydrate...  

NLE Websites -- All DOE Office Websites (Extended Search)

is to develop analytical techniques capable of quantitatively evaluating the nature of methane hydrate reservoir systems through modeling of their acoustic response using...

467

,"Texas--RRC District 2 Onshore Coalbed Methane Proved Reserves...  

U.S. Energy Information Administration (EIA) Indexed Site

2 Onshore Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest...

468

NETL: Methane Hydrates - DOE/NETL Projects - GAS HYDRATE DYNAMICS...  

NLE Websites -- All DOE Office Websites (Extended Search)

the first systematic geochemical and microbiological data to constrain subseafloor methane sinks and the spatio-temporal changes in the nature of microbial systems and pore...

469

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

470

,"U.S. Coalbed Methane Proved Reserves Adjustments (Billion Cubic...  

U.S. Energy Information Administration (EIA) Indexed Site

ame","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Coalbed Methane Proved Reserves Adjustments (Billion Cubic Feet)",1,"Annual",2011 ,"Release...

471

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

U.S. Energy Information Administration (EIA) Indexed Site

ame","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Coalbed Methane Proved Reserves (Billion Cubic Feet)",1,"Annual",2011 ,"Release Date:","812013"...

472

,"Oklahoma 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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

473

,"California - Los Angeles Basin Onshore Coalbed Methane Proved...  

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

474

,"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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

475

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

476

,"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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

477

,"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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

478

Table 16: Coalbed methane proved reserves and production, 2007...  

U.S. Energy Information Administration (EIA) Indexed Site

: Coalbed methane proved reserves and production, 2007 - 2011" "billion cubic feet" ,,"Reserves",,,,,,"Production" "State and Subdivision",,2007,2008,2009,2010,2011,,2007,2008,2009...

479

,"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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

480

NETL-ORD Methane Hydrate Project - Micro XCT Characterization...  

NLE Websites -- All DOE Office Websites (Extended Search)

the experimental systempressure vessel development and system parameter optimization, methane hydrate will be formed and dissociated in packed sediments. Micro-XCT scans will be...

Note: This page contains sample records for the topic "methane nitrous oxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

,"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",2011,"6301989"...

482

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

483

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

484

,"Michigan 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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

485

,"Virginia 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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

486

,"Montana 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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

487

,"Kansas 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 bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...

488

,"U.S. Coalbed Methane Proved Reserves Revision Increases (Billion...  

U.S. Energy Information Administration (EIA) Indexed Site

ame","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Coalbed Methane Proved Reserves Revision Increases (Billion Cubic Feet)",1,"Annual",2011 ,"Release...

489

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

U.S. Energy Information Administration (EIA) Indexed Site

Coalbed Methane Proved Reserves (Billion Cubic Feet)" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for"...