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1

Aqueous Phase Glycerol Reforming by PtMo Bimetallic Nano-Particle Catalyst: Product Selectivity and Structural Characterization  

Science Conference Proceedings (OSTI)

A carbon supported PtMo aqueous phase reforming catalyst for producing hydrogen from glycerol was characterized by analysis of the reaction products and pathway, TEM, XPS and XAS spectroscopy. Operando X-ray absorption spectroscopy (XAS) indicates the catalyst consists of bimetallic nano-particles with a Pt rich core and a Mo rich surface. XAS of adsorbed CO indicates that approximately 25% of the surface atoms are Pt. X-ray photoelectron spectroscopy indicates that there is unreduced and partially reduced Mo oxide (MoO{sub 3} and MoO{sub 2}), and Pt-rich PtMo bimetallic nano-particles. The average size measured by transmission electron microscopy of the fresh PtMo nano-particles is about 2 nm, which increases in size to 5 nm after 30 days of glycerol reforming at 31 bar and 503 K. The catalyst structure differs from the most energetically stable structure predicted by density functional theory (DFT) calculations for metallic Pt and Mo atoms. However, DFT indicates that for nano-particles composed of metallic Pt and Mo oxide, the Mo oxide is at the particle surface. Subsequent reduction would lead to the experimentally observed structure. The aqueous phase reforming reaction products and intermediates are consistent with both C-C and C-OH bond cleavage to generate H{sub 2}/CO{sub 2} or the side product CH{sub 4}. While the H{sub 2} selectivity at low conversion is about 75%, cleavage of C-OH bonds leads to liquid products with saturated carbon atoms. At high conversions (to gas), these will produced additional CH{sub 4} reducing the H{sub 2} yield and selectivity.

Stach E. A.; Dietrich, P.J.; Lobo-Lapidus, R.J.; Wu, T.; Sumer, A.; Akatay, M.C.; Fingland, B.R.; Guo, N.; Dumesic, J.A.; Marshall, C.L.; Jellinek, J.; Delgass, W.N.; Ribeiro, F.H.; Miller, J.T.

2012-03-01T23:59:59.000Z

2

Method for aqueous phase reactions  

DOE Patents (OSTI)

A method for converting liquid organic material in a mixture into a product utilizing a catalyst in the form of a plurality of porous particles wherein each particle is a support having nickel metal catalytic phase or reduced nickel deposited thereon in a first dispersed phase and an additional metal deposited onto the support in a second dispersed phase. The additional metal is effective in retarding or reducing agglomeration or sintering of the nickel metal catalytic phase without substantially affecting the catalytic activity, thereby increasing the life time of the catalyst.

Elliott, Douglas C. (Richland, WA); Hart, Todd R. (Kennewick, WA)

2000-01-01T23:59:59.000Z

3

Phase behavior of DODAB aqueous solution  

SciTech Connect

Phase behavior of DODAB aqueous solution, prepared without sonication, was studied by adiabatic scanning calorimetry. Measurements revealed four phase transitions with the temperatures 35.2, 39.6, 44.6, and 52.4 Degree-Sign C at heating and one transition at the temperature 40.4 Degree-Sign C at cooling. The first three transitions at heating occur in unilamellar vesicles. The first and third transitions correspond to the subgel-gel and gelliquid phase transitions, corresponding enthalpy jumps are equal to 33 and 49 kJ/mol. The second transition appears after some aging and is similar to gel-ripple phase transition in a DPPC solution, with the enthalpy jump under the transition exceeding 7.4 kJ/mol. The transition occurs in unilamellar vesicles. The transition at the temperature 52.4 Degree-Sign C occurs in another subsystem of the solution, which we believe to be multilamellar vesicles. The enthalpy jump at this transition is equal to 97 kJ/mol, and data analysis suggests that this is a subgel-liquid transition. The phase transition at cooling is the liquid-gel transition in unilamellar vesicles. During the measurements, a slow evolution of the solution occurs, consisting in a change of concentrations of unilamellar and multilamellar vesicles. This transformation mainly occurs at low temperatures.

Voronov, V. P.; Kuryakov, V. N.; Muratov, A. R., E-mail: muratov@ogri.ru [Russian Academy of Sciences, Oil and Gas Research Institute (Russian Federation)

2012-12-15T23:59:59.000Z

4

Multi-fuel reformers for fuel cells used in transportation. Multi-fuel reformers: Phase 1 -- Final report  

DOE Green Energy (OSTI)

DOE has established the goal, through the Fuel Cells in Transportation Program, of fostering the rapid development and commercialization of fuel cells as economic competitors for the internal combustion engine. Central to this goal is a safe feasible means of supplying hydrogen of the required purity to the vehicular fuel cell system. Two basic strategies are being considered: (1) on-board fuel processing whereby alternative fuels such as methanol, ethanol or natural gas stored on the vehicle undergo reformation and subsequent processing to produce hydrogen, and (2) on-board storage of pure hydrogen provided by stationary fuel processing plants. This report analyzes fuel processor technologies, types of fuel and fuel cell options for on-board reformation. As the Phase 1 of a multi-phased program to develop a prototype multi-fuel reformer system for a fuel cell powered vehicle, the objective of this program was to evaluate the feasibility of a multi-fuel reformer concept and to select a reforming technology for further development in the Phase 2 program, with the ultimate goal of integration with a DOE-designated fuel cell and vehicle configuration. The basic reformer processes examined in this study included catalytic steam reforming (SR), non-catalytic partial oxidation (POX) and catalytic partial oxidation (also known as Autothermal Reforming, or ATR). Fuels under consideration in this study included methanol, ethanol, and natural gas. A systematic evaluation of reforming technologies, fuels, and transportation fuel cell applications was conducted for the purpose of selecting a suitable multi-fuel processor for further development and demonstration in a transportation application.

Not Available

1994-05-01T23:59:59.000Z

5

Biomass-Derived Liquids Distributed (Aqueous Phase) Reforming...  

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

required to meet the target G G G G G Introduction This project focuses on the APR of biomass-derived liquids for the production of hydrogen. We target the development of...

6

Steam Reforming Solidification of Cesium and Strontium Separations Product from Advanced Aqueous Processing of Spent Nuclear Fuel  

SciTech Connect

The Advanced Fuel Cycle Initiative program is conducting research on aqueous separations processes for the nuclear fuel cycle. This research includes development of solvent extraction processes for the separation of cesium and strontium from dissolved spent nuclear fuel solutions to reduce the short-term decay heat load. The cesium/strontium strip solution from candidate separation processes will require treatment and solidification for managed storage. Steam reforming is currently being investigated for stabilization of these streams because it can potentially destroy the nitrates and organics present in these aqueous, nitrate-bearing solutions, while converting the cesium and strontium into leach-resistant aluminosilicate minerals, such as pollucite. These ongoing experimental studies are being conducted to evaluate the effectiveness of steam reforming for this application.

Julia L. Tripp; T. G. Garn; R. D. Boardman; J. D. Law

2006-02-01T23:59:59.000Z

7

Catalyst and method for aqueous phase reactions  

DOE Patents (OSTI)

The present invention is a catalyst in the form of a plurality of porous particles wherein each particle is a support having nickel metal catalytic phase or reduced nickel deposited thereon in a first dispersed phase and an additional metal deposited onto the support in a second dispersed phase. The additional metal is effective in retarding or reducing agglomeration or sintering of the nickel metal catalytic phase without substantially affecting the catalytic activity, thereby increasing the life time of the catalyst.

Elliott, Douglas C. (Richland, WA); Hart, Todd R. (Kennewick, WA)

1999-01-01T23:59:59.000Z

8

On-demand generation of aqueous two-phase microdroplets with reversible phase transitions  

Science Conference Proceedings (OSTI)

Aqueous two-phase systems contained entirely within microdroplets enable a bottom-up approach to mimicking the dynamic microcompartmentation of biomaterial that naturally occurs within the cytoplasm of cells. Here, we demonstrate the on-demand generation of femtolitre aqueous two-phase droplets within a microfluidic oil channel. Gated pressure pulses were used to generate individual, stationary two-phase microdroplets with a well-defined time zero for carrying out controlled and sequential phase transformations over time. Reversible phase transitions between single-phase, two-phase, and core-shell microgel states were obtained via evaporation-induced dehydration and on-demand water rehydration. In contrast to other microfluidic aqueous two-phase droplets, which require continuous flows and high-frequency droplet formation, our system enables the controlled isolation and reversible transformation of a single microdroplet and is expected to be useful for future studies in dynamic microcompartmentation and affinity partitioning.

Boreyko, Jonathan B [ORNL; Mruetusatorn, Prachya [ORNL; Retterer, Scott T [ORNL; Collier, Pat [ORNL

2013-01-01T23:59:59.000Z

9

Development of Steam Reforming for the Solidification of the Cesium and Stronitum Separations Product from Advanced Aqueous Reprocessing of Spent Nuclear Fuel  

SciTech Connect

Steam reforming is one option currently being investigated for stabilization of the cesium/strontium strip products from spent fuel reprocessing solvent extraction processes because it can potentially destroy the nitrates and organics present in these aqueous, nitrate-bearing solutions, while converting the cesium and strontium into leach resistant aluminosilicate minerals, such as pollucite. To produce pollucite and other mineral analogs of the alkaline metals, the feeds must be mixed with aluminosilicate compounds and thermally sintered or calcined to activate solid-state crystal formation. Scoping tests completed indicated that the cesium/strontium in these organic and acid solutions can be converted into aluminosilicate materials using steam reforming.

Julia L. Tripp; T. Garn; R. Boardman; J. Law

2006-10-01T23:59:59.000Z

10

National Environmenal Policy Act Contracting Reform Guidance: Phase 1  

Science Conference Proceedings (OSTI)

The NEPA Contracting Quality Improvement Team identified several contracting improvements to reduce the cost and time for the NEPA process. The team`s February 1995 report recommended a series of steps to achieve the improvements, including issuance of contracting guidance. The guidance will be issued in three phases. This Phase I guidance implements the team`s short-term recommendations. It provides model statements of work and a sample schedule of contractor deliverables, establishes a pilot program for evaluating performance of NEPA support contractors, and describes information resources available on the DOE NEPA Web.

NONE

1995-08-01T23:59:59.000Z

11

Glycine phases formed from frozen aqueous solutions: Revisited  

SciTech Connect

Glycine phases formed when aqueous solutions were frozen and subsequently heated under different conditions were studied by Raman scattering, x-ray diffraction, and differential scanning calorimetry (DSC) techniques. Crystallization of ice I{sub h} was observed in all the cases. On cooling at the rates of 0.5 K/min and 5 K/min, glassy glycine was formed as an intermediate phase which lived about 1 min or less only, and then transformed into {beta}-polymorph of glycine. Quench cooling of glycine solutions (15% w/w) in liquid nitrogen resulted in the formation of a mixture of crystalline water ice I{sub h} and a glassy glycine, which could be preserved at cryogenic temperatures (80 K) for an indefinitely long time. This mixture remained also quite stable for some time after heating above the cryogenic temperature. Subsequent heating under various conditions resulted in the transformation of the glycine glass into an unknown crystalline phase (glycine 'X-phase') at 209-216 K, which at 218-226 K transformed into {beta}-polymorph of glycine. The 'X-phase' was characterized by Raman spectroscopy; it could be obtained in noticeable amounts using a special preparation technique and tentatively characterized by x-ray powder diffraction (P2, a= 6.648 A, b= 25.867 A, c= 5.610 A, {beta}= 113.12 Masculine-Ordinal-Indicator ); the formation of 'X-phase' from the glycine glassy phase and its transformation into {beta}-polymorph were followed by DSC. Raman scattering technique with its power for unambiguous identification of the crystalline and glassy polymorphs without limitation on the crystallite size helped us to follow the phase transformations during quenching, heating, and annealing. The experimental findings are considered in relation to the problem of control of glycine polymorphism on crystallization.

Surovtsev, N. V. [Institute of Automation and Electrometry, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Adichtchev, S. V.; Malinovsky, V. K. [Institute of Automation and Electrometry, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Ogienko, A. G.; Manakov, A. Yu. [Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Nikolaev Institute of Inorganic Chemistry, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Drebushchak, V. A. [Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Institute of Geology and Mineralogy, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Ancharov, A. I.; Boldyreva, E. V. [Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Institute of Solid Chemistry and Mechanochemistry, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation); Yunoshev, A. S. [Novosibirsk State University, Novosibirsk 630090 (Russian Federation); Lavrentiev Institute of Hydrodynamics, Siberian Branch of Russian Academy of Sciences, Novosibirsk 630090 (Russian Federation)

2012-08-14T23:59:59.000Z

12

Phase 2 THOR Steam Reforming Tests for Sodium Bearing Waste Treatment  

Science Conference Proceedings (OSTI)

About one million gallons of acidic, hazardous, and radioactive sodium-bearing waste is stored in stainless steel tanks at the Idaho Nuclear Technology and Engineering Center (INTEC), which is a major operating facility of the Idaho National Engineering and Environmental Laboratory. Steam reforming is a candidate technology being investigated for converting the waste into a road ready waste form that can be shipped to the Waste Isolation Pilot Plant in New Mexico for interment. A steam reforming technology patented by Studsvik, Inc., and licensed to THOR Treatment Technologies has been tested in two phases using a Department of Energy-owned fluidized bed test system located at the Science Applications International Corporation (SAIC) Science and Technology Applications Research Center located in Idaho Falls, Idaho. The Phase 1 tests were reported earlier in 2003. The Phase 2 tests are reported here. For Phase 2, the process feed rate, stoichiometry, and chemistry were varied to identify and demonstrate process operation and product characteristics under different operating conditions. Two test series were performed. During the first series, the process chemistry was designed to produce a sodium carbonate product. The second series was designed to produce a more leach-resistant, mineralized sodium aluminosilicate product. The tests also demonstrated the performance of a MACT-compliant off-gas system.

Nicholas R. Soelberg

2004-01-01T23:59:59.000Z

13

Phase 2 TWR Steam Reforming Test for Sodium-Bearing Waste Treatment  

SciTech Connect

About one million gallons of acidic, hazardous, and radioactive sodium-bearing waste (SBW) is stored in stainless steel tanks a the Idaho Nuclear Technology and Engineering Center (INTEC), which is a major operating facility of the Idaho National Engineering and Environmental Laboratory (INEEL). Steam reforming is a candidate technology being investigated for converting the SBW into a road ready waste form that can be shipped to the Waste Isolation Pilot Plant in New Mexico for interment. Fluidized bed steam reforming technology, licensed to ThermoChem Waste Remediation, LLC (TWR) by Manufacturing Technology Conversion International, was tested in two phases using an INEEL (Department of Energy) fluidized bed test system located at the Science Applications International Corporation (SAIC) Science and Technology Applications Research Center in Idaho Falls, Idaho. The Phase 1 tests were reported earlier. The Phase 2 tests are reported here. For Phase 2, the process feed rate, reductant stoichiometry, and process temperature were varied to identify and demonstrate how the process might be optimized to improve operation and product characteristics. The first week of testing was devoted primarily to process chemistry and the second week was devoted more toward bed stability and particle size control.

Nicholas R. Soelberg; Doug Marshall; Dean Taylor; Steven Bates

2004-01-01T23:59:59.000Z

14

Novel Reforming Catalysts  

Science Conference Proceedings (OSTI)

Aqueous phase reforming is useful for processing oxygenated hydrocarbons to hydrogen and other more useful products. Current processing is hampered by the fact that oxide based catalysts are not stable under high temperature hydrothermal conditions. Silica in the form of structured MCM-41 is thermally a more stable support for Co and Ni than conventional high surface area amorphous silica but hydrothermal stability is not demonstrated. Carbon nanotube supports, in contrast, are highly stable under hydrothermal reaction conditions. In this project we show that carbon nanotubes are stable high activity/selectivity supports for the conversion of ethylene glycol to hydrogen.

Pfefferle, Lisa D; Haller, Gary L

2012-10-16T23:59:59.000Z

15

Aerosol–Cloud Interactions in a Mesoscale Model. Part II: Sensitivity to Aqueous-Phase Chemistry  

Science Conference Proceedings (OSTI)

The feedbacks between aerosols, cloud microphysics, and cloud chemistry are investigated in a mesoscale model. A simple bulk aqueous-phase sulfur chemistry scheme was fully coupled to the existing aerosol and microphysics schemes. The ...

Irena T. Ivanova; Henry G. Leighton

2008-02-01T23:59:59.000Z

16

Smoothed particle hydrodynamics model of non-aqueous phase liquid flow and dissolution  

Science Conference Proceedings (OSTI)

A smoothed particle hydrodynamics model was developed to simulate the flow of mixtures of aqueous and non-aqueous phase liquids in porous media and the dissolution of the non-aqueous phase in the aqueous phase. The model was used to study the effects of pore-scale heterogeneity and anisotropy on the steady state dense non-aqueous phase liquid (DNAPL) saturation when gravity driven DNAPL displaces water from initially water saturated porous media. Pore-scale anisotropy was created by using co-oriented non overlapping elliptically shaped grains to represent the porous media. After a steady state DNAPL saturation was reached, water was injected until a new steady state DNAPL saturation was reached. The amount of trapped DNAPL was found to be greater when DNAPL is displaced in the direction of the major axes of the soil grains than when it is displaced in the direction of the minor axes of the soil grains. The amount of trapped DNAPL was also found to increase with decreasing initial saturation of the continuous DNAPL phase. For the conditions used in our simulations, the saturation of the trapped NAPL with a smaller initial DNAPL saturation was more than 3 times larger than the amount of trapped DNAPL with a larger initial saturation. These simulations were carried out assuming that the DNAPL did not dissolve in water. Simulations including the effect of dissolution of DNAPL in the aqueous phase were also performed, and effective (macroscopic) mass transfer coefficients were determined.

Tartakovsky, Alexandre M.; Meakin, Paul; Ward, Anderson L.

2009-01-01T23:59:59.000Z

17

Nickel/ruthenium catalyst and method for aqueous phase reactions  

DOE Patents (OSTI)

A method of hydrogenation using a catalyst in the form of a plurality of porous particles wherein each particle is a support having nickel metal catalytic phase or reduced nickel deposited thereon in a first dispersed phase and an additional ruthenium metal deposited onto the support in a second dispersed phase. The additional ruthenium metal is effective in retarding or reducing agglomeration or sintering of the nickel metal catalytic phase thereby increasing the life time of the catalyst during hydrogenation reactions.

Elliott, Douglas C. (Richland, WA); Sealock, John L. (West Richland, WA)

1998-01-01T23:59:59.000Z

18

Preparation and initial characterization of fluidized bed steam reforming pure-phase standards  

SciTech Connect

Hanford is investigating the Fluidized Bed Steam Reforming (FBSR) process for their Low Activity Waste. The FBSR process offers a low-temperature continuous method by which liquid waste can be processed with the addition of clay into a sodium aluminosilicate (NAS) waste form. The NAS waste form is mainly comprised of nepheline (NaAlSiO{sub 4}), sodalite (Na{sub 8}[AlSiO{sub 4}]{sub 6}Cl{sub 2}), and nosean (Na{sub 8}[AlSiO{sub 4}]{sub 6}SO{sub 4}). Anions such as perrhenate (ReO{sub 4}{sup -}), pertechnetate (TcO{sub 4}{sup -}), and iodine (I{sup -}) are expected to replace sulfate in the nosean structure and/or chloride in the sodalite mineral structure (atomically bonded inside the aluminosilicate cages that these mineral structures possess). In the FBSR waste form, each of these phases can exist in a variety of solid solutions that differ from the idealized forms observed in single crystals in nature. The lack of understanding of the durability of these stoichiometric or idealized mineral phases complicates the ability to deconvolute the durability of the mixed phase FBSR product since it is a combination of different NAS phases. To better understand the behavior, fabrication and testing of the individual phases of the FBSR product is required. Analytical Development (AD) of the Science and Technology directorate of the Savannah River National Laboratory (SRNL) was requested to prepare the series of phase-pure standards, consisting of nepheline, nosean, and Cl, Re, and I sodalite. Once prepared, X-ray Diffraction (XRD) analyses were used to confirm the products were phase pure. These standards are being used for subsequent characterization studies consisting of the following: single-pass flow-through (SPFT) testing, development of thermodynamic data, and x-ray diffraction (XRD) calibration curves. In addition to the above mentioned phase-pure standards, AD was tasked with fabricating a mixed Tc-Re sodalite.

Missimer, D. M.; Rutherford, R. L.

2013-03-21T23:59:59.000Z

19

PHASE BEHAVIOR OF LIGHT GASES IN HYDROCARBON AND AQUEOUS SOLVENTS  

Science Conference Proceedings (OSTI)

Under previous support from the Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present period, the Park-Gasem-Robinson (PGR) equation of state (EOS) has been modified to improve its volumetric and equilibrium predictions. Specifically, the attractive term of the PGR equation was modified to enhance the flexibility of the model, and a new expression was developed for the temperature dependence of the attractive term in this segment-segment interaction model. The predictive capability of the modified PGR EOS for vapor pressure, and saturated liquid and vapor densities was evaluated for selected normal paraffins, normal alkenes, cyclo-paraffins, light aromatics, argon, carbon dioxide and water. The generalized EOS constants and substance-specific characteristic parameters in the modified PGR EOS were obtained from the pure component vapor pressures, and saturated liquid and vapor molar volumes. The calculated phase properties were compared to those of the Peng-Robinson (PR), the simplified-perturbed-hard-chain theory (SPHCT) and the original PGR equations. Generally, the performance of the proposed EOS was better than the PR, SPHCT and original PGR equations in predicting the pure fluid properties (%AAD of 1.3, 2.8 and 3.7 for vapor pressure, saturated liquid and vapor densities, respectively).

KHALED A.M. GASEM; ROBERT L. ROBINSON, JR.

1998-08-31T23:59:59.000Z

20

Phase Behavior of Light Gases in Hydrocarbon and Aqueous Solvents  

Science Conference Proceedings (OSTI)

Under previous support from the Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present reporting period, our solubility apparatus was refurbished and restored to full service. To test the experimental apparatus and procedures used, measurements were obtained for the solubility Of C0{sub 2} in benzene at 160{degrees}F. Having confirmed the accuracy of the newly acquired data in comparison with our previous measurements and data reported in the literature for this test system, we have begun to measure the solubility of hydrogen in hexane. The measurements for this system will cover the temperature range from 160 to 280{degrees}F at pressures to 2,500 psia. As part of our model evaluation efforts, we examined the predictive abilities of an alternative approach we have proposed for calculating the phase behavior properties of highly non-ideal systems. Using this approach, the liquid phase fugacities generated from an equation of state (EOS) are augmented by a fugacity deviation function correction. The correlative abilities of this approach are compared with those of an EOS equipped with the recently introduced Wong-Sandler (MWS) mixing rules. These two approaches are compared with the current methods for vapor-liquid equilibrium (VLE) calculations, i.e., the EOS (0/0) approach with the van der Waals mixing rules and the split (y/0) approach. The evaluations were conducted on a database comprised of non-ideal low pressure binary systems as well as asymmetric high pressure binary systems. These systems are of interest in the coal liquefaction and utilization processes. The Peng-Robinson EOS was selected for the purposes of this evaluation.

Gasem, K.A.M.; Robinson, R.L., Jr.; Trvedi, N.J., Gao, W.

1997-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Aqueous-phase hydrogenation of acetic acid over transition metal catalysts  

SciTech Connect

Catalytic hydrogenation of acetic acid to ethanol has been carried out in aqueous phase on several metals, with ruthenium being the most active and selective. DFT calculations suggest that the initial CO bond scission yielding acetyl is the key step and that the intrinsic reactivity of the metals accounts for the observed activity.

Olcay, Hakan [University of Massachusetts, Amherst; Xu, Lijun [ORNL; Xu, Ye [ORNL; Huber, George [University of Massachusetts, Amherst

2010-01-01T23:59:59.000Z

22

PHASE BEHAVIOR OF LIGHT GASES IN HYDROGEN AND AQUEOUS SOLVENTS  

DOE Green Energy (OSTI)

Under previous support from the US Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present reporting period, the solubilities of hydrogen in n-hexane, carbon monoxide in cyclohexane, and nitrogen in phenanthrene and pyrene were measured using a static equilibrium cell over the temperature range from 344.3 to 433.2 K and pressures to 22.8 MPa. The uncertainty in these new solubility measurements is estimated to be less than 0.001 in mole fraction. The data were analyzed using the Peng-Robinson (PR) equation of state (EOS). In general, the PR EOS represents the experimental data well when a single interaction parameter (C{sub ij}) is used for each isotherm. In addition, the predictive capability of the modified Park-Gasem-Robinson (PGR) equation of state (EOS) was evaluated for selected carbon dioxide + normal paraffins, ethane + normal paraffins, and hydrogen + normal paraffins. A set of mixing rules was proposed for the modified EOS to extend its predictive capabilities to mixtures. The predicted bubble point pressures for the ethane + n-paraffin and carbon dioxide + n-paraffin binaries were compared to those of the Peng-Robinson (PR), simplified-perturbed-hard-chain theory (SPHCT) and original PGR equations. The predictive capability of the proposed equation is better or comparable to the PR, SPHCT and original PGR equations of state for the ethane binaries (%AAD of 1.9) and carbon dioxide binaries (%AAD of 2.0). For the hydrogen binaries, the modified PGR EOS showed much better performance (%AAD of 1.7) than the original PGR equation and comparable to the PR equation.

KHALED A.M. GASEM; ROBERT L. ROBINSON, JR.

1999-03-31T23:59:59.000Z

23

Modeling of aqueous and organic phase speciation for solvent extraction systems  

SciTech Connect

The TRUEX (TRansUranic EXtraction) solvent extraction process has the ability to remove, separate, and recover transuranic (TRU) elements from acidic nuclear waste solutions. A computer model of the TRUEX process is currently being developed for use in flowsheet design and process optimization. The correlations that are to be used in the model for generating extraction distribution ratios are based on chemical mass action principles and require calculation of aqueous and organic phase speciation. Aqueous phase activity coefficients are calculated using methods available in the literature, while the organic phase species are treated in terms of ideal associated solution theory. This approach is demonstrated for the extraction of HNO/sub 3/, HTcO/sub 4/, and americium nitrate by n-octyl(phenyl)-N,N-diisobutylcarbamoyl-methylphosphine oxide (CMPO)---the primary metal extractant in the TRUEX solvent. 23 refs., 5 figs.

Chaiko, D.J.; Tse, Pui-Kwan; Vandegrift, G.F

1988-11-01T23:59:59.000Z

24

Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report-January through March 2003  

Office of Legacy Management (LM)

4-TAC 4-TAC GJO-PIN 13.5.1-1 Pinellas Environmental Restoration Project January through March 2003 Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report April 2003 Grand Junction Office U.S. Department of Energy Work Performed Under DOE Contract No. for the U.S. Department of Energy DE-AC13-02GJ79491 Approved for public release; distribution is unlimited. N0060900 GJO-2003-434-TAC GJO-PIN 13.5.1-1 Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report January through March 2003 April 2003 Prepared by U.S. Department of Energy Grand Junction Office Grand Junction, Colorado Work Performed Under DOE Contract Number DE-AC13-02GJ79491 Task Order Number ST03-107

25

Method and device for removing a non-aqueous phase liquid from a groundwater system  

DOE Patents (OSTI)

A device for removing a non-aqueous phase liquid from a groundwater system includes a generally cylindrical push-rod defining an internal recess therein. The push-rod includes first and second end portions and an external liquid collection surface. A liquid collection member is detachably connected to the push-rod at one of the first and second end portions thereof. The method of the present invention for removing a non-aqueous phase liquid from a contaminated groundwater system includes providing a lance including an external hydrophobic liquid collection surface, an internal recess, and a collection chamber at the bottom end thereof. The lance is extended into the groundwater system such that the top end thereof remains above the ground surface. The liquid is then allowed to collect on the liquid collection surface, and flow downwardly by gravity into the collection chamber to be pumped upwardly through the internal recess in the lance.

Looney, Brian B. (Aiken, SC); Rossabi, Joseph (Aiken, SC); Riha, Brian D. (Augusta, GA)

2002-01-01T23:59:59.000Z

26

Ruthenium on rutile catalyst, catalytic system, and method for aqueous phase hydrogenations  

DOE Patents (OSTI)

An essentially nickel- and rhenium-free catalyst is described comprising ruthenium on a titania support where the titania is greater than 75% rutile. A catalytic system containing a nickel-free catalyst comprising ruthenium on a titania support where the titania is greater than 75% rutile, and a method using this catalyst in the hydrogenation of an organic compound in the aqueous phase is also described.

Elliot, Douglas C. (Richland, WA); Werpy, Todd A. (West Richland, WA); Wang, Yong (Richland, WA); Frye, Jr., John G. (Richland, WA)

2001-01-01T23:59:59.000Z

27

Technical and Economic Evaluation of Coal Tar Dense Non-Aqueous Phase Liquid (DNAPL) Pumping Techniques  

Science Conference Proceedings (OSTI)

The utility industry has become aware of potential environmental issues at some sites resulting from process residues or byproducts at former manufactured gas plant (MGP) sites. One of the greatest challenges utility managers face in the management of these sites is the subsurface presence of coal tar, dense-non aqueous phase liquid (DNAPL). This report, which explores the technical feasibility and life cycle costs for several coal tar DNAPL pumping alternatives, is intended to assist utilities in evalua...

2000-03-07T23:59:59.000Z

28

Catalytic Reforming  

Science Conference Proceedings (OSTI)

Don Little's Catalytic Reforming deals exclusively with reforming. With the increasing need for unleaded gasoline, the importance of this volume has escalated since it combines various related aspects of reforming technology into a single publication. For those with no practical knowledge of catalytic reforming, the chemical reactions, flow schemes and how the cat reformer fits into the overall refinery process will be of interest. Contents include: Catalytic reforming in refinery processing: How catalytic reformers work - chemical reactions; Process design; The catalyst, process variables and unit operation; Commercial processes; BTX operation; Feed preparation; naphtha hydrotreating and catalytic reforming; Index.

Little, D.M.

1985-01-01T23:59:59.000Z

29

A swollen phase observed between the liquid-crystalline phase and the interdigitated phase induced by pressure and/or adding ethanol in DPPC aqueous solution  

E-Print Network (OSTI)

A swollen phase, in which the mean repeat distance of lipid bilayers is larger than the other phases, is found between the liquid-crystalline phase and the interdigitated gel phase in DPPC aqueous solution. Temperature, pressure and ethanol concentration dependences of the structure were investigated by small-angle neutron scattering, and a bending rigidity of lipid bilayers was by neutron spin echo. The nature of the swollen phase is similar to the anomalous swelling reported previously. However, the temperature dependence of the mean repeat distance and the bending rigidity of lipid bilayers are different. This phase could be a precursor to the interdigitated gel phase induced by pressure and/or adding ethanol.

H. Seto; M. Hishida; H. Nobutou; N. L. Yamada; M. Nagao; T. Takeda

2006-02-21T23:59:59.000Z

30

Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report October through December 2002  

Office of Legacy Management (LM)

700 700 GJO-2003-411-TAC GJO-PIN 13.5.1-1 Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report October through December 2002 January 2003 Prepared by U.S. Department of Energy Grand Junction Office Grand Junction, Colorado Work Performed Under DOE Contract Number DE-AC13-02GJ79491 Task Order Number ST03-107 Document Number N0057700 Contents DOE/Grand Junction Office Northeast Site NAPL Interim Measures Progress Report January 2003 Page ii Contents Acronyms and Abbreviations ........................................................................................................ iii 1.0 Introduction ............................................................................................................................1

31

Platinum-Modulated Cobalt Nanocatalysts for Low-Temperature Aqueous-Phase Fischer Tropsch Synthesis  

Science Conference Proceedings (OSTI)

Fischer Tropsch synthesis (FTS) is an important catalytic process for liquid fuel generation, which converts coal/shale gas/biomass-derived syngas (a mixture of CO and H2) to oil. While FTS is thermodynamically favored at low temperature, it is desirable to develop a new catalytic system that could allow working at a relatively low reaction temperature. In this article, we present a one-step hydrogenation reduction route for the synthesis of Pt Co nanoparticles (NPs) which were found to be excellent catalysts for aqueous-phase FTS at 433 K. Coupling with atomic-resolution scanning transmission electron microscopy (STEM) and theoretical calculations, the outstanding activity is rationalized by the formation of Co overlayer structures on Pt NPs or Pt Co alloy NPs. The improved energetics and kinetics from the change of the transition states imposed by the lattice mismatch between the two metals are concluded to be the key factors responsible for the dramatically improved FTS performance.

Wang, Hang [Peking University; Zhou, Wu [ORNL; Liu, JinXun [Dalian Institute of Chemical Physics; Si, Rui [Brookhaven National Laboratory (BNL); Sun, Geng [Peking University; Zhong, Mengqi [Peking University; Su, Haiyan [Peking University; Zhao, Huabo [Peking University; Rodrigues, Jose [Brookhaven National Laboratory (BNL); Pennycook, Stephen J [ORNL; Idrobo Tapia, Juan C [ORNL; Li, Weixue [Dalian Institute of Chemical Physics; Kou, Yuan [Peking University; Ma, Ding [Peking University

2013-01-01T23:59:59.000Z

32

Confounding effects of aqueous-phase impinger chemistry on apparent oxidation of mercury in flue gases  

SciTech Connect

Gas-phase reactions between elemental mercury and chlorine are a possible pathway to producing oxidized mercury species such as mercuric chloride in combustion systems. This study examines the effect of the chemistry of a commonly used sample conditioning system on apparent and actual levels of mercury oxidation in a methane-fired, 0.3 kW, quartz-lined reactor in which gas composition (HCl, Cl{sub 2}, NOx, SO{sub 2}) and quench rate were varied. The sample conditioning system included two impingers in parallel: one containing an aqueous solution of KCl to trap HgCl{sub 2}, and one containing an aqueous solution of SnCl{sub 2} to reduce HgCl{sub 2} to elemental mercury (Hg{sup 0}). Gas-phase concentrations of Cl{sub 2} as low as 1.5 ppmv were sufficient to oxidize a significant fraction of the elemental mercury in the KCl impinger via the hypochlorite ion. Furthermore, these low, but interfering levels of Cl{sub 2} appeared to persist in flue gases from several doped rapidly mixed flames with varied post flame temperature quench rates. The addition of 0.5 wt% sodium thiosulfate to the KCl solution completely prevented the oxidation from occurring in the impinger. The addition of thiosulfate did not inhibit the KCl impinger's ability to capture HgCl{sub 2}. The effectiveness of the thiosulfate was unchanged by NO or SO{sub 2}. These results bring into question laboratory scale experimental data on mercury oxidation where wet chemistry was used to partition metallic and oxidized mercury without the presence of sufficient levels of SO{sub 2}. 23 refs., 5 figs., 1 tab.

Brydger Cauch; Geoffrey D. Silcox; Joann S. Lighty; Jost O.L. Wendt; Andrew Fry; Constance L. Senior [University of Utah, Salt Lake City, UT (United States). Department of Chemical Engineering

2008-04-01T23:59:59.000Z

33

CROWTM PROCESS APPLICATION FOR SITES CONTAMINATED WITH LIGHT NON-AQUEOUS PHASE LIQUIDS AND CHLORINATED HYDROCARBONS  

DOE Green Energy (OSTI)

Western Research Institute (WRI) has successfully applied the CROWTM (Contained Recovery of Oily Wastes) process at two former manufactured gas plants (MGPs), and a large wood treatment site. The three CROW process applications have all occurred at sites contaminated with coal tars or fuel oil and pentachlorophenol (PCP) mixtures, which are generally denser than water and are classified as dense non-aqueous phase liquids (DNAPLs). While these types of sites are abundant, there are also many sites contaminated with gasoline, diesel fuel, or fuel oil, which are lighter than water and lie on top of an aquifer. A third site type occurs where chlorinated hydrocarbons have contaminated the aquifer. Unlike the DNAPLs found at MGP and wood treatment sites, chlorinated hydrocarbons are approximately one and a half times more dense than water and have fairly low viscosities. These contaminants tend to accumulate very rapidly at the bottom of an aquifer. Trichloroethylene (TCE) and perchloroethylene, or tetrachloroethylene (PCE), are the major industrial chlorinated solvents that have been found contaminating soils and aquifers. The objective of this program was to demonstrate the effectiveness of applying the CROW process to sites contaminated with light non-aqueous phase liquids (LNAPLs) and chlorinated hydrocarbons. Individual objectives were to determine a range of operating conditions necessary to optimize LNAPL and chlorinated hydrocarbon recovery, to conduct numerical simulations to match the laboratory experiments and determine field-scale recoveries, and determine if chemical addition will increase the process efficiency for LNAPLs. The testing consisted of twelve TCE tests; eight tests with PCE, diesel, and wood treatment waste; and four tests with a fuel oil-diesel blend. Testing was conducted with both vertical and horizontal orientations and with ambient to 211 F (99 C) water or steam. Residual saturations for the horizontal tests ranged from 23.6% PV to 0.3% PV. Also conducted was screening of 13 chemicals to determine their relative effectiveness and the selection of three chemicals for further testing.

L.A. Johnson, Jr.

2003-06-30T23:59:59.000Z

34

Formation of Hydrates from Single-Phase Aqueous Solutions and Implications for Oceanic Sequestration of CO2  

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

Formation of Hydrates from Single-Phase Aqueous Solutions Formation of Hydrates from Single-Phase Aqueous Solutions and Implications for Oceanic Sequestration of CO 2 . G. Holder (holder@engrng.pitt.edu) 412-624-9809 L. Mokka (lakshmi.mokka@netl.doe.gov) 412-386-6019 Department of Chemical and Petroleum Engineering University of Pittsburgh Pittsburgh, PA 15261 R. Warzinski* (robert.warzinski@netl.doe.gov) 412-386-5863 U.S. Department of Energy National Energy Technology Laboratory P.O. Box 10940 Pittsburgh, PA 15236-0940 Introduction a Gas hydrates are crystalline solids formed from mixtures of water and low molecular weight compounds, referred to as hydrate formers, that typically are gases at ambient conditions (1). Generally, hydrates are formed in the laboratory from two-phase systems by contacting a hydrate former or formers in the gas or liquid phase with liquid water and increasing the pressure until

35

Hydrogen Generation from Biomass-Derived Surgar Alcohols via the Aqueous-Phase Carbohydrate Reforming (ACR) Process  

DOE Green Energy (OSTI)

This project involved the investigation and development of catalysts and reactor systems that will be cost-effective to generate hydrogen from potential sorbitol streams. The intention was to identify the required catalysts and reactors systems as well as the design, construction, and operation of a 300 grams per hour hydrogen system. Virent was able to accomplish this objective with a system that generates 2.2 kgs an hour of gas containing both hydrogen and alkanes that relied directly on the work performed under this grant. This system, funded in part by the local Madison utility, Madison, Gas & Electric (MGE), is described further in the report. The design and development of this system should provide the necessary scale-up information for the generation of hydrogen from corn-derived sorbitol.

Randy Cortright

2006-06-30T23:59:59.000Z

36

Coal Tar Treatability Test Program: Chemical Oxidation Effects on Dense Non-Aqueous Phase Liquid Using Potassium Permanganate  

Science Conference Proceedings (OSTI)

EPRI has initiated a progressive program to investigate the effectiveness of using potassium permanganate to mitigate the impact of coal tar on groundwater at former manufactured gas plant (MGP) sites. This study evaluated the effectiveness of using potassium permanganate to reduce the rate of dissolution of chemical constituents present in coal-tar-derived dense non-aqueous phase liquid (DNAPL) into the surrounding groundwater. The focus of the research was 1) to develop a proof of concept for using pot...

2004-03-31T23:59:59.000Z

37

Technical Protocols for Assessing Dense Non-Aqueous Phase Liquid Mobility in the Subsurface at Manufactured Gas Plant Sites  

Science Conference Proceedings (OSTI)

This report summarizes Electric Power Research Institute (EPRI) research that has been conducted on dense non-aqueous phase liquid (DNAPL) mobility at manufactured gas plant (MGP) sites and presents technical protocols for conducting DNAPL mobility assessments at MGP sites using currently available methodologies and/or technologies. The technical protocols address each of the primary zones of the subsurface environment: vadose zone, saturated zone, and bedrock (both competent and fractured). The report a...

2011-12-12T23:59:59.000Z

38

Catalytic reforming  

Science Conference Proceedings (OSTI)

This patent describes a process for the catalytic reforming of a feedstock which contains at least one reformable organic compound. The process consists of contacting the feedstock under suitable reforming conditions with a catalyst composition selected from the group consisting of a catalyst. The catalyst essentially consists of zinc oxide and a spinel structure alumina. Another catalyst consists essentially of a physical mixture of zinc titanate and a spinel structure alumina in the presence of sufficient added hydrogen to substantially prevent the formation of coke. Insufficient zinc is present in the catalyst composition for the formation of a bulk zinc aluminate.

Aldag, A.W. Jr.

1986-01-28T23:59:59.000Z

39

Mass-transport considerations pertinent to aqueous-phase reactions of gases in liquid-water clouds  

SciTech Connect

Reactions of gases in liquid-water clouds are potentially important in the transformation of atmospheric pollutants affecting their transport in the atmosphere and subsequent removal and deposition to the surface. Such processes consist of the following sequence of steps. Mass-transport of the reagent gas or gases to the air-water interface; transfer across the interface and establishment of solubility equilibria locally at the interface; mass-transport of the dissolved gas or gases within the aqeuous phase; aqueous-phase chemical reactions(s); mass-transport of reaction product(s) and possible subsequent evolution into the gas-phase. Description of the rate of the overall process requires identification of the rate-limiting step (or steps) and evaluation of the rate of such step(s). Identification of the rate-limiting step may be achieved by evaluation and comparison of the characteristic times pertinent to the several processes and may be readily carried out by methods outlined herein, for known or assumed reagent concentrations, drop size, and fundamental constants as follows: gas- and aqueous-phase diffusion coefficients; Henry's law coefficient and other pertinent equilibrium constants; interfacial mass-transfer accommodation coefficient; aqueous-phase reaction rate constant(s). A graphical method is described whereby it may be ascertained whether a given reaction is controlled solely by reagent solubility and intrinsic chemical kinetics or is mass-transport limited by one or another of the above processes. In the absence of mass-transport limitation, reaction rates may be evaluated uniformly for the entire liquid-water content of the cloud using equilibrium reagent concentrations. In contrast, where appreciable mass-transport limitation is indicated, evaluation of the overall rate requires knowledge of and integration over the drop-size distribution characterizing the cloud. 68 references, 16 figures.

Schwartz, S.E.

1983-01-01T23:59:59.000Z

40

Multi-fuel reformers for fuel cells used in transportation: Assessment of hydrogen storage technologies. Phase 1, Final report  

DOE Green Energy (OSTI)

This report documents a portion of the work performed Multi-fuel Reformers for Fuel Cells Used in Transportation. One objective for development is to develop advanced fuel processing systems to reform methanol, ethanol, natural gas, and other hydrocarbons into hydrogen for use in transportation fuel cell systems, while a second objective is to develop better systems for on-board hydrogen storage. This report examines techniques and technology available for storage of pure hydrogen on board a vehicle as pure hydrogen of hydrides. The report focuses separately on near- and far-term technologies, with particular emphasis on the former. Development of lighter, more compact near-term storage systems is recommended to enhance competitiveness and simplify fuel cell design. The far-term storage technologies require substantial applied research in order to become serious contenders.

Not Available

1994-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Electrical resistivity for detecting subsurface non-aqueous phase liquids: A progress report  

SciTech Connect

Soils and groundwater have been contaminated by hazardous substances at many places in the United States and many other countries. The contaminants are commonly either petroleum products or industrial solvents with very low solubility in water. These contaminants are usually called non-aqueous phase liquids (NAPLs). The cost of cleaning up the affected sites in the United States is estimated to be of the order of 100 billion dollars. In spite of the expenditure of several billion dollars during the last 15 years, to date, very few, if any major contaminated site has been restored. The presence of NAPL pools in the subsurface is believed to be the main cause for the failure of previous cleanup activities. Due to their relatively low water solubility, and depending on their volume, it takes tens or even hundreds of years to deplete the NAPL sources if they are not removed from the subsurface. The intrinsic electrical resistivity of most NAPLs is typically in the range of 10{sup 7} to 10{sup 12}{Omega}-m, which is several orders of magnitude higher than that of groundwater containing dissolved solids (usually in the range of a few {Omega}-m to a few thousand {Omega}-m). Although a dry soil is very resistive, the electrical resistivity of a wet soil is on the order of 100 {Omega}-m and is dependent on the extent of water saturation. For a given soil, the electrical resistivity increases with decrease of water saturation. Therefore, if part of the pore water is replaced by a NAPL, the electrical resistivity will increase. At many NAPL sites, both the vadose and phreatic zones can be partially occupied by NAPL pools. It is the great contrast in electrical resistivity between the NAPLs and groundwater that may render the method to be effective in detecting subsurface NAPLs at contaminated sites. The following experiments were conducted to investigate the change of the electrical resistivity of porous media when diesel fuel (NAPL) replaces part of the water.

Lee, K.H.; Shan, C.; Javandel, I.

1995-06-01T23:59:59.000Z

42

Attrition resistant fluidizable reforming catalyst  

DOE Patents (OSTI)

A method of preparing a steam reforming catalyst characterized by improved resistance to attrition loss when used for cracking, reforming, water gas shift and gasification reactions on feedstock in a fluidized bed reactor, comprising: fabricating the ceramic support particle, coating a ceramic support by adding an aqueous solution of a precursor salt of a metal selected from the group consisting of Ni, Pt, Pd, Ru, Rh, Cr, Co, Mn, Mg, K, La and Fe and mixtures thereof to the ceramic support and calcining the coated ceramic in air to convert the metal salts to metal oxides.

Parent, Yves O. (Golden, CO); Magrini, Kim (Golden, CO); Landin, Steven M. (Conifer, CO); Ritland, Marcus A. (Palm Beach Shores, FL)

2011-03-29T23:59:59.000Z

43

Cost Analysis of Bio-Derived Liquids Reforming  

E-Print Network (OSTI)

) steam reforming C2H5OH + H2O Ă? 2CO + 4H2 6) Water gas shift 7) Methanation 8) Coking from CH4 (methane Ethanol Reforming Options Gas Phase Liquid Phase Virent Steam Partial Oxidation Reforming GE (SCPO) decomposition C2H5OH Ă? CH4 + CO + H2 steam reforming CH4 + 2H2O Ă? 4H2 + CO2 3) C2H5OH dehydrogenation

44

Hiring Reform | Department of Energy  

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

Hiring Reform Hiring Reform Hiring Reform President Obama's Memorandum dated May 11, 2010, Improving the Federal Recruitment and Hiring Process, is Phase I of the Administration's comprehensive initiative to address major, long-standing impediments to recruiting and hiring the best and the brightest into the Federal civilian workforce. The Memorandum is based on issues that DOE and others brought to the attention of OPM, and it is designed to help Agencies build the workforce you need to achieve your goals. The Presidential Memorandum launches the Obama Administration's flagship personnel policy reform initiative. It builds on a nearly year-long collaboration between OPM and Agencies aimed at streamlining the hiring process and recruiting top talent, especially for mission-critical jobs.

45

Irreversible Aging Dynamics and Generic Phase Behavior of Aqueous Suspensions of Laponite  

E-Print Network (OSTI)

In this work we study the aging behavior of aqueous suspension of Laponite having 2.8 weight % concentration using rheological tools. At various salt concentration all the samples demonstrate orientational order when observed using crossed polarizers. In rheological experiments we observe inherent irreversibility in the aging dynamics which forces the system not to rejuvenate to the same state in the shear melting experiment carried out at a later date since preparation. The extensive rheological experiments carried out as a function of time elapsed since preparation demonstrate the self similar trend in the aging behavior irrespective of the concentration of salt. We observe that the exploration of the low energy states as a function of aging time is only kinetically affected by the presence of salt. We estimate that the energy barrier to attain the low energy states decreases linearly with increase in the concentration of salt. The observed superposition of all the elapsed time and the salt concentration dependent data suggests that the aging that occurs in low salt concentration systems over a very long period is qualitatively similar to the aging behavior observed in systems with high salt concentration over a shorter period.

A. Shahin; Yogesh M. Joshi

2010-01-26T23:59:59.000Z

46

Environmental fiscal reform (EFR) | Open Energy Information  

Open Energy Info (EERE)

Environmental fiscal reform (EFR) Environmental fiscal reform (EFR) Jump to: navigation, search Tool Summary Name: Environmental fiscal reform (EFR) Agency/Company /Organization: Global Subsidies Initiative (GSI), International Institute for Sustainable Development (IISD), World Bank Phase: Develop Goals, Prepare a Plan, Develop Finance and Implement Projects Topics: Co-benefits assessment, Finance, Market analysis, Policies/deployment programs References: Environmental fiscal reform - What should be done and how to achieve it[1] Reforming fiscal policies to close the gap between economic and ecological efficiencies[2] Overview "The term environmental fiscal reform (EFR) refers to: a range of taxation or pricing instruments that can raise revenue, while simultaneously furthering environmental goals. This is achieved by providing economic

47

Multi-fuel reformers for fuel cells used in transportation: Assessment of hydrogen storage technologies. Phase 2: Final report  

DOE Green Energy (OSTI)

During Phase 1 of this program, the authors evaluated all known hydrogen storage technologies (including those that are now practiced and those that are development) in the context of fuel cell vehicles. They determined that among the development technologies, carbon sorbents could most benefit from closer scrutiny. During Phase 2 of this program, they tested ten different carbon sorbents at various practical temperatures and pressures, and developed the concept of the usable Capacity Ratio, which is the ratio of the mass of hydrogen that can be released from a carbon-filled tank to the mass of hydrogen that can be released from an empty tank. The authors also commissioned the design, fabrication, and NGV2 (Natural Gas Vehicle) testing of an aluminum-lined, carbon-composite, full-wrapped pressure vessel to store hydrogen at 78 K and 3,000 psi. They constructed a facility to pressure cycle the tank at 78 K and to temperature cycle the tank at 3,000 psi, tested one such tank, and submitted it for a burst test. Finally, they devised a means by which cryogenic compressed hydrogen gas tanks can be filled and discharged using standard hardware--that is, without using filters, valves, or pressure regulators that must operate at both low temperature and high pressure. This report describes test methods and test results of carbon sorbents and the design of tanks for cold storage. 7 refs., 91 figs., 10 tabs.

NONE

1995-05-01T23:59:59.000Z

48

Residual Saturation of Coal Tar, a Non-Aqueous Phase Liquid (NAPL), in Soils at MGP Sites: March 2002 Interim Report  

Science Conference Proceedings (OSTI)

Coal tar, a non-aqueous phase liquid (NAPL), is present in the subsurface at former manufactured gas plant (MGP) sites. EPRI initiated this research project to compile and synthesize available data on residual saturation of various NAPLs, as well as to summarize available data on groundwater quality and soil concentrations of coal tar constituents found at a number of MGP sites. The continuing EPRI research will carry out laboratory experiments to generate residual saturation values for a number of soil-...

2002-02-28T23:59:59.000Z

49

Process for catalytic reforming  

Science Conference Proceedings (OSTI)

An improved catalytic reforming process is disclosed wherein hydrogen and light hydrocarbons generated in the catalytic reaction zone are passed to a hydrogen production/purification zone and and reacted and processed therein to produce substantially pure hydrogen. A portion of the hydrogen is then admixed with the charge stock to the catalytic reforming zone to provide the hydrogen requirements of the catalytic reforming reaction zone.

James, R. B. Jr.

1984-11-20T23:59:59.000Z

50

Systemic Reform Bibliography  

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

(5) support local initiatives and model sites; (6) align state policy; (7) reform higher education and teacher preparation; and (8) mobilize public and professional...

51

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 ...

52

Catalytic reforming process  

Science Conference Proceedings (OSTI)

A catalytic reforming process is disclosed in which substantially all of the heat requirements of the product stabilizer column is supplied by multiple indirect heat exchange.

Peters, K.D.

1983-10-11T23:59:59.000Z

53

Security and Suitability Process Reform  

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

Security and Suitability Process Reform December 2008 Provided by the Joint Security and Suitability Reform Team EXECUTIVE OFFICE OF THE PRESIDENT OFFICE OF MANAGEMENT AND BUDGET...

54

Copyright reform step zero  

Science Conference Proceedings (OSTI)

'A reasonable person might well think it's a fool's errand to contemplate a [copyright] reform project of any sort.' The US Copyright Act of 1976 and its subsequent amendments is contained in over 200 pages of incomprehensible, sometimes inconsistent, ... Keywords: US copyright law, administrative law, copyright reform, institutional frameworks

Terry Hart

2010-06-01T23:59:59.000Z

55

Catalytic reforming process  

Science Conference Proceedings (OSTI)

A catalytic reforming process is disclosed wherein the reboiler heat requirements of the stabilizer column are supplied by means of indirect heat exchange with hot combustion gases in the reforming reactants fired heater convection heating section. Heat in excess of the reboiler requirements is passed to the stabilizer column with control being effected by removal of excess heat from the column.

James, R.B. Jr.

1984-02-14T23:59:59.000Z

56

Catalytic reforming methods  

DOE Patents (OSTI)

A catalytic reforming method is disclosed herein. The method includes sequentially supplying a plurality of feedstocks of variable compositions to a reformer. The method further includes adding a respective predetermined co-reactant to each of the plurality of feedstocks to obtain a substantially constant output from the reformer for the plurality of feedstocks. The respective predetermined co-reactant is based on a C/H/O atomic composition for a respective one of the plurality of feedstocks and a predetermined C/H/O atomic composition for the substantially constant output.

Tadd, Andrew R; Schwank, Johannes

2013-05-14T23:59:59.000Z

57

Separation of hydrogen from a catalytic reforming zone effluent stream  

Science Conference Proceedings (OSTI)

A process for the catalytic reforming of a hydrocarbonaceous feedstock at reforming conditions including a pressure of from about 50 to about 250 psig. Is disclosed. A portion of the hydrogen-rich vapor phase recovered from the reforming zone effluent at a relatively low pressure is compressed and recycled to the reforming zone without further purification. The balance of said hydrogen-rich vapor phase, or the net hydrogen, is compressed to a relatively high pressure and recontacted with at least a portion of the liquid hydrocarbon phase recovered from said low pressure separation to effect a further purification of said net hydrogen and to maximize the recovery of C/sub 3/-C/sub 6/+ the liquid phase.

Schmelzer, E.; Tagamolila, C.P.

1983-02-22T23:59:59.000Z

58

Multizone naphtha reforming process  

Science Conference Proceedings (OSTI)

This patent describes a catalytic reforming process for conversion of a naphtha hydrocarbon at reforming conditions having at least two segregated catalyst zones. The improvement comprises contacting the hydrocarbon in a first zone with a first catalyst comprising tin and at least one platinum group metal deposited on a solid catalyst support followed by contacting in a second zone with a second catalyst comprising at least one metal selected from the group consisting of platinum group metals deposited on a solid catalyst support.

Fleming, B.

1987-05-05T23:59:59.000Z

59

Morphological and phase evolution of TiO{sub 2} nanocrystals prepared from peroxotitanate complex aqueous solution: Influence of acetic acid  

Science Conference Proceedings (OSTI)

Nanosized anatase and rutile TiO{sub 2} having different shape, phase and size have been prepared from aqueous solutions of peroxo titanium complex starting from titanium(IV) isopropoxide (TTIP), acetic acid and hydrogen peroxide (H{sub 2}O{sub 2}) in water/isopropanol media by a facile sol-gel process. The TiO{sub 2} nanocrystals are characterized by powder X-ray diffraction (XRD), Raman spectroscopy, FT-IR spectroscopy, TEM, high resolution transmission electron microscopy (HRTEM) and selected area electron diffraction (SAED) techniques. The influence of pH and the sequence of addition of reaction contents on the phase and morphology of TiO{sub 2} are studied. The reasons for the observation of only anatase and/or mixture of anatase and rutile are given. - Graphical abstract: The morphology of TiO{sub 2} depends on the sequence of addition of AcOH and H{sub 2}O{sub 2} from the system of titanium isopropoxide and acetic acid (AcOH) in the presence of H{sub 2}O{sub 2}.

Chang, Jeong Ah; Vithal, Muga; Baek, In Chan [KRICT-EPFL Global Research Laboratory, Advanced Materials Division, Korea Research Institute of Chemical Technology, 19 Sinseongno, Yuseong, Daejeon 305-600 (Korea, Republic of); Seok, Sang Il, E-mail: seoksi@krict.re.k [KRICT-EPFL Global Research Laboratory, Advanced Materials Division, Korea Research Institute of Chemical Technology, 19 Sinseongno, Yuseong, Daejeon 305-600 (Korea, Republic of)

2009-04-15T23:59:59.000Z

60

Catalytic reforming process  

Science Conference Proceedings (OSTI)

This patent describes a catalytic reforming process which comprises contacting a naphtha range feed with a low acidity extrudate comprising an intermediate and/or a large pore acidic zeolite bound with a low acidity refractory oxide under reforming conditions to provide a reaction product of increased aromatic content, the extrudate having been prepared with at least an extrusion-facilitating amount of a low acidity refractory oxide in colloidal form and containing at least one metal species selected from the platinum group metals.

Absil, R.P.; Huss, A. Jr.; McHale, W.D.; Partridge, R.D.

1989-06-13T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

REMOVAL OF CHLORIDE FROM AQUEOUS SOLUTIONS  

DOE Patents (OSTI)

The removal of chlorides from aqueons solutions is described. The process involves contacting the aqueous chloride containing solution with a benzene solution about 0.005 M in phenyl mercuric acetate whereby the chloride anions are taken up by the organic phase and separating the organic phase from the aqueous solutions.

Schulz, W.W.

1959-08-01T23:59:59.000Z

62

Multifuel reformer R D  

DOE Green Energy (OSTI)

The on-board fuel for fuel cell powered vehicles may be one or more of hydrogen, methanol, ethanol, natural gas, propane, or other liquified petroleum gases. To use hydrogen as the fuel, suitable means of storing, and subsequently delivering, adequate quantities of the gas must be developed. For all other fuels suitable reformers must be developed to convert the fuel to hydrogen or a hydrogen-rich gas mixture at rates corresponding to the varying power demand rates of the automotive system; this is especially true for the lower temperature fuel cells, such as the polymer electrolyte fuel cell which operates at 80{degrees}C and the phosphoric acid fuel cell which operates at 190{degrees}C. This paper discusses the key design and performance characteristics of such hydrogen storage and fuel reformer systems for use in stand-alone fuel cell automotive applications.

Kumar, R.; Ahmed, S.

1991-01-01T23:59:59.000Z

63

Methanol partial oxidation reformer  

DOE Patents (OSTI)

A partial oxidation reformer is described comprising a longitudinally extending chamber having a methanol, water and an air inlet and an outlet. An igniter mechanism is near the inlets for igniting a mixture of methanol and air, while a partial oxidation catalyst in the chamber is spaced from the inlets and converts methanol and oxygen to carbon dioxide and hydrogen. Controlling the oxygen to methanol mole ratio provides continuous slightly exothermic partial oxidation reactions of methanol and air producing hydrogen gas. The liquid is preferably injected in droplets having diameters less than 100 micrometers. The reformer is useful in a propulsion system for a vehicle which supplies a hydrogen-containing gas to the negative electrode of a fuel cell. 7 figs.

Ahmed, S.; Kumar, R.; Krumpelt, M.

1999-08-24T23:59:59.000Z

64

Methanol partial oxidation reformer  

DOE Patents (OSTI)

A partial oxidation reformer is described comprising a longitudinally extending chamber having a methanol, water and an air inlet and an outlet. An igniter mechanism is near the inlets for igniting a mixture of methanol and air, while a partial oxidation catalyst in the chamber is spaced from the inlets and converts methanol and oxygen to carbon dioxide and hydrogen. Controlling the oxygen to methanol mole ratio provides continuous slightly exothermic partial oxidation reactions of methanol and air producing hydrogen gas. The liquid is preferably injected in droplets having diameters less than 100 micrometers. The reformer is useful in a propulsion system for a vehicle which supplies a hydrogen-containing gas to the negative electrode of a fuel cell. 7 figs.

Ahmed, S.; Kumar, R.; Krumpelt, M.

1999-08-17T23:59:59.000Z

65

Catalytic reforming catalyst  

Science Conference Proceedings (OSTI)

An improved catalyst, having a reduced fouling rate when used in a catalytic reforming process, said catalyst comprising platinum disposed on an alumina support wherein the alumina support is obtained by removing water from aluminum hydroxide produced as a by-product from a ziegler higher alcohol synthesis reaction, and wherein the alumina is calcined at a temperature of 1100-1400/sup 0/F so as to have a surface area of 165 to 215 square meters per gram.

Buss, W.C.; Kluksdahl, H.E.

1980-12-09T23:59:59.000Z

66

Steam reformer with catalytic combustor  

DOE Patents (OSTI)

A steam reformer is disclosed having an annular steam reforming catalyst bed formed by concentric cylinders and having a catalytic combustor located at the center of the innermost cylinder. Fuel is fed into the interior of the catalytic combustor and air is directed at the top of the combustor, creating a catalytic reaction which provides sufficient heat so as to maintain the catalytic reaction in the steam reforming catalyst bed. Alternatively, air is fed into the interior of the catalytic combustor and a fuel mixture is directed at the top. The catalytic combustor provides enhanced radiant and convective heat transfer to the reformer catalyst bed.

Voecks, Gerald E. (La Crescenta, CA)

1990-03-20T23:59:59.000Z

67

Autothermal reforming catalyst having perovskite structure  

DOE Patents (OSTI)

The invention addressed two critical issues in fuel processing for fuel cell application, i.e. catalyst cost and operating stability. The existing state-of-the-art fuel reforming catalyst uses Rh and platinum supported over refractory oxide which add significant cost to the fuel cell system. Supported metals agglomerate under elevated temperature during reforming and decrease the catalyst activity. The catalyst is a perovskite oxide or a Ruddlesden-Popper type oxide containing rare-earth elements, catalytically active firs row transition metal elements, and stabilizing elements, such that the catalyst is a single phase in high temperature oxidizing conditions and maintains a primarily perovskite or Ruddlesden-Popper structure under high temperature reducing conditions. The catalyst can also contain alkaline earth dopants, which enhance the catalytic activity of the catalyst, but do not compromise the stability of the perovskite structure.

Krumpel, Michael (Naperville, IL); Liu, Di-Jia (Naperville, IL)

2009-03-24T23:59:59.000Z

68

NEPA Contracting Reform Guidance  

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

defining early what contractors should accomplish < establishing contracts ahead of time < minimizing cost while maintaining quality by * maximizing competition and use of incentives * using past performance information in awarding work * managing the NEPA process as a project This guidance provides: < model statements of work < information on contract types and incentives < direction on effective NEPA contract management by the NEPA Document Manager < a system for measuring NEPA process costs < NEPA contractor evaluation procedures < details on the DOE NEPA Web site U.S. Department of Energy, Office of NEPA Policy and Assistance, December 1996 NEPA CONTRACTING REFORM GUIDANCE Table of Contents 1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

69

Multizone catalytic reforming process  

Science Conference Proceedings (OSTI)

This patent describes a process for the catalytic reforming of hydrocarbons comprising contacting the hydrocarbon feed in two sequential catalyst zones. It comprises: a first catalyst zone contains a first catalytic composite consisting essentially of a platinum component, a germanium component, a refractory inorganic oxide, and a halogen component; and a second catalyst zone contains a second catalytic composite comprising a platinum component, a germanium component, a refractory inorganic oxide, a halogen component, and catalytically effective amounts of a metal promoter selected from rhenium, rhodium, ruthenium, cobalt, nickel, and iridium, and mixtures thereof.

Moser, M.C.; Lawson, R.J.; Antos, G.J.; Wang, L.; Parulekar, V.N.

1990-05-29T23:59:59.000Z

70

Patent Counsel - Patent Reform | Department of Energy  

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

Patent Counsel - Patent Reform Patent Counsel - Patent Reform America invents Act 20112.pdf More Documents & Publications PETITION FOR ADVANCE WAIVER OF PATENT RIGHTS Office of...

71

Attrition resistant fluidizable reforming catalyst - Energy ...  

A method of preparing a steam reforming catalyst characterized by improved resistance to attrition loss when used for cracking, reforming, water gas shift and ...

72

Catalytic reforming optimization  

Science Conference Proceedings (OSTI)

The authors have previously examined correlations between catalytic reforming parameters for an L-35-6 unit at the Gor'knefteorgsintez Industrial Association. Experimental design was used to derive polynomial equations describing the correlations for each reactor. Further research on optimizing the reforming has been based on these results. They adopted the following strategy to define the best working parameters: they define a temperature that would provide the maximum target-product yield while maintaining a given working life. Most of the aromatic hydrocarbons are formed by the naphthene dehydrogenation, which is endothermic, so the greater the temperature drop over the height, the more rapid the process. The temperature difference thus indicates the current catalyst activity. To increase the target-product yield, one must raise the inlet temperature and ensure the largest drop across the catalyst. They examined an algorithm with fixed inlet conditions as regards flow rate and raw material composition. This algorithm provides the basis of software for the automatic control of the L-35-6 reactor unit at the Gor'knefteorgsintez Industrial Association. The system has been checked out and put into experimental operation.

Mazina, S.G.; Rybtsov, V.V.; Priss-Titarenko, T.A.

1988-11-10T23:59:59.000Z

73

High severity catalytic reforming process  

Science Conference Proceedings (OSTI)

A high-severity catalytic reforming process is described comprising: (a) passing a mixture comprising a catalytic reforming feed stream and a recycle stream into a catalytic reforming reaction zone which is maintained at high-severity reforming conditions; (b) cooling an effluent stream comprising hydrogen and hydrocarbonaceous catalytic reforming reaction products which is withdrawn from the reaction zone; (c) passing the cooled effluent stream into a vapor-liquid separation zone and recovering therefrom a liquid stream comprising hydrocarbons and a hydrogen-rich gas stream; (d) passing the hydrogen-rich gas stream through an adsorption zone wherein the gas is contacted with a treating material which removes polycyclic aromatic compounds from the gas stream, the compounds remaining in the adsorption zone; (e) mixing a portion of the hydrogen-rich gas stream, which is the recycle stream, with the feed stream to form the charge stock mixture and withdrawing the balance of the hydrogen-rich gas stream, which is denoted as net hydrogen, from the catalytic reforming area, all of the hydrogen-rich gas stream being substantially free of polycyclic aromatic compounds; and (f) fractionating the liquid stream and recovering an overhead product comprising light hydrocarbons and a bottoms product comprising reformate.

Bennett, R.W.; Cottrell, P.R.; Gilsdorf, N.L.; Winfield, M.D.

1988-03-22T23:59:59.000Z

74

Liquid fuel reformer development.  

DOE Green Energy (OSTI)

At Argonne National Laboratory we are developing a process to convert hydrocarbon fuels to a clean hydrogen feed for a fuel cell. The process incorporates a partial oxidation/steam reforming catalyst that can process hydrocarbon feeds at lower temperatures than existing commercial catalysts. We have tested the catalyst with three diesel-type fuels: hexadecane, low-sulfur diesel fuel, and a regular diesel fuel. We achieved complete conversion of the feed to products. Hexadecane yielded products containing 60% hydrogen on a dry, nitrogen-free basis at 800 C. For the two diesel fuels, higher temperatures, >850 C, were required to approach similar levels of hydrogen in the product stream. At 800 C, hydrogen yield of the low sulfur diesel was 32%, while that of the regular diesel was 52%. Residual products in both cases included CO, CO{sub 2}, ethane, ethylene, and methane.

Ahmed, S.; Krumpelt, M.; Pereira, C.; Wilkenhoener, R.

1999-07-30T23:59:59.000Z

75

Multizone catalytic reforming process  

Science Conference Proceedings (OSTI)

This patent describes a process for the catalytic reforming of hydrocarbons comprising contacting the hydrocarbon feed in two sequential catalyst zones. It comprises: an initial catalyst zone which is a fixed-bed system and contains an initial catalytic composite comprising a platinum component, a germanium component, a refractory inorganic oxide, and a halogen component; and a terminal catalyst zone which is a moving-bed system with associated continuous catalyst regeneration and contains a terminal catalytic composite having the essential absence of germanium and comprising a platinum component, a refractory inorganic oxide, a halogen component, and catalytically effective amounts of a metal promoter selected from one or more of the rhenium, tin, indium, rhodium, ruthenium, cobalt, nickel, and iridium.

Moser, M.; Lawson, R.J.; Wang, L.; Parulekar, V.; Peer, R.L.; Hamlin, C.R.

1991-01-15T23:59:59.000Z

76

Puerto Rico Refinery Catalytic Reforming Downstream Charge ...  

U.S. Energy Information Administration (EIA)

Puerto Rico Refinery Catalytic Reforming Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

77

Mississippi Refinery Catalytic Reforming Downstream Charge ...  

U.S. Energy Information Administration (EIA)

Mississippi Refinery Catalytic Reforming Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

78

Louisiana Refinery Catalytic Reforming Downstream Charge Capacity ...  

U.S. Energy Information Administration (EIA)

Louisiana Refinery Catalytic Reforming Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

79

Corrosion protection of reforming equipment during regeneration of the catalyst  

Science Conference Proceedings (OSTI)

The authors discuss the important process of catalytic reforming to produce the basic components of high-octane gasolines and aromatic hydrocarbons in petroleum chemistry. Wide use is made of two-stage oxidative regeneration--coke burning and oxychlorination. This increases the activity of the catalysts. The authors developed a two-stage industrial method of corrosion protection for the low-temperature equipment of catalytic reforming plants during catalyst regeneration. The system is washed, before catalyst regeneration, with an aqueous solution of KLOE-15 in order to remove corrosion products already present. During catalyst regeneration, KLOE-15 and a neutralizing additive are fed in. The method is technically simple and economically effective, and has been introduced in a number of petroleum refineries.

Altsybeeva, A.I.; Andreeva, G.A.; Prasolova, O.N.; Ratner, E.M.; Reshetnikov, S.M.; Teslya, B.M.

1986-01-01T23:59:59.000Z

80

Applications of solar reforming technology  

DOE Green Energy (OSTI)

Research in recent years has demonstrated the efficient use of solar thermal energy for driving endothermic chemical reforming reactions in which hydrocarbons are reacted to form synthesis gas (syngas). Closed-loop reforming/methanation systems can be used for storage and transport of process heat and for short-term storage for peaking power generation. Open-loop systems can be used for direct fuel production; for production of syngas feedstock for further processing to specialty chemicals and plastics and bulk ammonia, hydrogen, and liquid fuels; and directly for industrial processes such as iron ore reduction. In addition, reforming of organic chemical wastes and hazardous materials can be accomplished using the high-efficiency destruction capabilities of steam reforming. To help identify the most promising areas for future development of this technology, we discuss in this paper the economics and market potential of these applications.

Spiewak, I. [Weizmann Inst. of Science, Rehovoth (Israel); Tyner, C.E. [Sandia National Labs., Albuquerque, NM (United States); Langnickel, U. [Deutsche Forschungsanstalt fuer Luft- und Raumfahrt e.V. (DLR), Koeln (Germany)

1993-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Partial oxidation reforming of methanol  

DOE Green Energy (OSTI)

Methanol is an attractive fuel for fuel cell-powered vehicles because it has a fairly high energy density, can be pumped into the tank of a vehicle mush like gasoline, and is relatively easy to reform. For on-board reforming, the reformer must be compact and lightweight, and have rapid start-up and good dynamic response. Steam reforming reactors with the tube-and-shell geometry that was used on the prototype fuel cell-powered buses are heat transfer limited. To reach their normal operating temperature, these types of reactors need 45 minutes from ambient temperature start-up. The dynamic response is poor due to temperature control problems. To overcome the limitations of steam reforming, ANL explored the partial oxidation concept used in the petroleum industry to process crude oils. In contrast to the endothermic steam reforming reaction, partial oxidations is exothermic. Fuel and air are passed together over a catalyst or reacted thermally, yielding a hydrogen-rich gas. Since the operating temperature of such a reactor can be controlled by the oxygen-to- methanol ratio, the rates of reaction are not heat transfer limited. Start-up and transient response should be rapid, and the mass and volume are expected to be small by comparison.

Krumpelt, M.; Ahmed, S.; Kumar, R.

1996-04-01T23:59:59.000Z

82

Before House Committee on Oversight and Government Reform | Department...  

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

House Committee on Oversight and Government Reform Before House Committee on Oversight and Government Reform Before House Committee on Oversight and Government Reform By: Secretary...

83

Before the House Committee on Oversight and Government Reform...  

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

Oversight and Government Reform Before the House Committee on Oversight and Government Reform Before the Committee on Oversight and Government Reform, U.S. House of Representatives...

84

Before the House Oversight and Government Reform Subcommittee...  

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

Information Policy, Intergovernmental Relations, and Procurement Reform Before the House Oversight and Government Reform Subcommittee on Technology, Information Policy,...

85

Safety and Security Directives Reform  

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

Reforming a "Mountain" of Policy Reforming a "Mountain" of Policy Beginning with his confirmation hearings in January 2009, Energy Secretary Steven Chu challenged the Department of Energy to take a fresh look at how we conduct business. This challenge provided the opportunity for DOE to put in place the most effective and efficient strategies to accomplish the Department's missions safely and securely. In response to the Secretary's challenge and building on the results of Deputy Secretary Poneman's Safety and Security Reform studies, the Office of Health, Safety and Security (HSS) broadened its directives review activities during 2009. By November 2009 HSS had initiated a disciplined review of all health, safety, and security directives, which included a systematic review of the Department's safety and security regulatory model.

86

Evaluate reformer performance at a glance  

Science Conference Proceedings (OSTI)

Catalytic reforming is becoming increasingly important in replacing octane lost as the removal of lead from worldwide gasoline pools continues. A method has been developed that can quickly evaluate the performance of any catalytic reformer. The catalytic naphtha reforming process primarily involves three well-known reactions. These are aromatization of naphthenes, cyclization of paraffins and hydrocracking of paraffins. Hydrogen is produced in the process of aromatization and dehydrocyclization of paraffins. Reformer performance is normally evaluated with a reformate analysis (PONA) and yield of C{sub 5{sup +}} reformate. This method of quick evaluation of reformer performance is based upon the main assumption that the increase in hydrocarbon moles in the process is equal to the number of C{single_bond}C bond ruptures and one mole of hydrogen is absorbed to saturate the same. This new method calculates aromatization efficiency, paraffin conversion, aromatic selectivity and finally the paraffin, naphthene and aromatic content of C{sub 5{sup +}} reformate.

Nag, A. [Indian Oil Corporation Ltd., Gujarat (India)

1996-02-01T23:59:59.000Z

87

Bringing electricity reform to the Philippines  

SciTech Connect

Electricity reforms will not translate to competition overnight. But reforms are inching their way forward in institutions and stakeholders of the Philippine electricity industry, through regulatory and competition frameworks, processes, and systems promulgated and implemented. (author)

Fe Villamejor-Mendoza, Maria

2008-12-15T23:59:59.000Z

88

Fluidized Bed Steam Reforming Technology Overview  

Coal added as reductant and for energy • What happens inside the reformer? Water evaporates Nitrates reduced to nitrogen gas

89

Method of steam reforming methanol to hydrogen  

DOE Patents (OSTI)

The production of hydrogen by the catalyzed steam reforming of methanol is accomplished using a reformer of greatly reduced size and cost wherein a mixture of water and methanol is superheated to the gaseous state at temperatures of about 800.degree. to about 1,100.degree. F. and then fed to a reformer in direct contact with the catalyst bed contained therein, whereby the heat for the endothermic steam reforming reaction is derived directly from the superheated steam/methanol mixture.

Beshty, Bahjat S. (Lower Makefield, PA)

1990-01-01T23:59:59.000Z

90

Olefins from High Yield Autothermal Reforming Process ...  

Isobutylene is used to produce fuel additives. The autothermal reforming process can produce isobutylene and requires no external energy input ...

91

Accelerated Weathering of Fluidized Bed Steam Reformation ...  

Science Conference Proceedings (OSTI)

Sep 16, 2007 ... Accelerated Weathering of Fluidized Bed Steam Reformation Material Under Hydraulically Unsaturated Conditions by E.M. Pierce ...

92

Continuing Management Reform | National Nuclear Security Administratio...  

National Nuclear Security Administration (NNSA)

Continuing Management Reform | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response...

93

INTEGRAL CATALYTIC COMBUSTION/FUEL REFORMING  

E-Print Network (OSTI)

INTEGRAL CATALYTIC COMBUSTION/FUEL REFORMING FOR GAS TURBINE Prepared For: California Energy REPORT (FAR) INTEGRAL CATALYTIC COMBUSTION/FUEL REFORMING FOR GAS TURBINE CYCLES EISG AWARDEE University://www.energy.ca.gov/research/index.html. #12;Page 1 Integral Catalytic Combustion/Fuel Reforming for Gas Turbine Cycles EISG Grant # 99

94

Unfunded Mandates Reform Act; Intergovernmental Consultation | Department  

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

Unfunded Mandates Reform Act; Intergovernmental Consultation Unfunded Mandates Reform Act; Intergovernmental Consultation Unfunded Mandates Reform Act; Intergovernmental Consultation The Department of Energy (DOE) today publishes a final statement of policy on intergovernmental consultation under the Unfunded Mandates Reform Act of 1995. The policy reflects the guidelines and instructions that the Director of the Office of Management and Budget (OMB) provided to each agency to develop, with input from State, local, and tribal officials, an intergovernmental consultation process with regard to significant intergovernmental mandates contained in a notice of proposed rulemaking. Unfunded Mandates Reform Act; Intergovernmental Consultation More Documents & Publications TEC Working Group Topic Groups Tribal Key Documents

95

NEPA Contracting Reform Guidance | Department of Energy  

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

Contracting Reform Guidance Contracting Reform Guidance NEPA Contracting Reform Guidance This documents provides guidance on NEPA contracting strategy, including: defining the work of the contractor; establishing contracts ahead of time; minimizing cost while maintaining quality. Guidance also provides: model statements of work, direction on NEPA contract management by NEPA Document Manager; a system for measuring NEPA costs and for evaluating contractor procedures; details on the DOE NEPA website. NEPA Contracting Reform Guidance More Documents & Publications NEPA Contracting Reform Guidance (December 1996) Statement of Work-National Environmental Policy Act (NEPA) Support Services Acquisition: Preparation and Review of Environmental Impact Statements, Environmental Assessments, Environmental Reports, and other Environmental

96

Unfunded Mandates Reform Act; Intergovernmental Consultation | Department  

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

Unfunded Mandates Reform Act; Intergovernmental Consultation Unfunded Mandates Reform Act; Intergovernmental Consultation Unfunded Mandates Reform Act; Intergovernmental Consultation The Department of Energy (DOE) today publishes a final statement of policy on intergovernmental consultation under the Unfunded Mandates Reform Act of 1995. The policy reflects the guidelines and instructions that the Director of the Office of Management and Budget (OMB) provided to each agency to develop, with input from State, local, and tribal officials, an intergovernmental consultation process with regard to significant intergovernmental mandates contained in a notice of proposed rulemaking. Unfunded Mandates Reform Act; Intergovernmental Consultation More Documents & Publications TEC Working Group Topic Groups Tribal Key Documents

97

Synchrotron x-ray spectroscopy of Eu/HNO{sub 3} aqueous solutions at high temperatures and pressures and Nb-bearing silicate melt phases coexisting with hydrothermal fluids using a modified hydrothermal diamond anvil cell and rail assembly  

Science Conference Proceedings (OSTI)

A modified hydrothermal diamond anvil cell (HDAC) rail assembly has been constructed for making synchrotron x-ray absorption spectroscopy, x-ray fluorescence, and x-ray mapping measurements on fluids or solid phases in contact with hydrothermal fluids up to {approx}900 deg. C and 700 MPa. The diamond anvils of the HDAC are modified by laser milling grooves or holes, for the reduction of attenuation of incident and fluorescent x rays and sample cavities. The modified HDAC rail assembly has flexibility in design for measurement of light elements at low concentrations or heavy elements at trace levels in the sample and the capability to probe minute individual phases of a multiphase fluid-based system using focused x-ray microbeam. The supporting rail allows for uniform translation of the HDAC, rotation and tilt stages, and a focusing mirror, which is used to illuminate the sample for visual observation using a microscope, relative to the direction of the incident x-ray beam. A structure study of Eu(III) aqua ion behavior in high-temperature aqueous solutions and a study of Nb partitioning and coordination in a silicate melt in contact with a hydrothermal fluid are described as applications utilizing the modified HDAC rail assembly.

Mayanovic, Robert A.; Anderson, Alan J.; Bassett, William A.; Chou, I-Ming [Department of Physics, Astronomy and Materials Science, Missouri State University, Springfield, Missouri 65897 (United States); Department of Earth Sciences, St. Francis Xavier University, P.O. Box 5000, Antigonish, Nova Scotia B2G 2W5 (Canada); Department of Earth and Atmospheric Sciences, Cornell University, Ithaca, New York 14853 (United States); MS 954, U.S. Geological Survey, Reston, Virginia 20192 (United States)

2007-05-15T23:59:59.000Z

98

Plasma-catalyzed fuel reformer  

DOE Patents (OSTI)

A reformer is disclosed that includes a plasma zone to receive a pre-heated mixture of reactants and ionize the reactants by applying an electrical potential thereto. A first thermally conductive surface surrounds the plasma zone and is configured to transfer heat from an external heat source into the plasma zone. The reformer further includes a reaction zone to chemically transform the ionized reactants into synthesis gas comprising hydrogen and carbon monoxide. A second thermally conductive surface surrounds the reaction zone and is configured to transfer heat from the external heat source into the reaction zone. The first thermally conductive surface and second thermally conductive surface are both directly exposed to the external heat source. A corresponding method and system are also disclosed and claimed herein.

Hartvigsen, Joseph J.; Elangovan, S.; Czernichowski, Piotr; Hollist, Michele

2013-06-11T23:59:59.000Z

99

Fuel Reformation: Microchannel Reactor Design  

DOE Green Energy (OSTI)

Fuel processing is used to extract hydrogen from conventional vehicle fuel and allow fuel cell powered vehicles to use the existing petroleum fuel infrastructure. Kilowatt scale micro-channel steam reforming, water-gas shift and preferential oxida-tion reactors have been developed capable of achieving DOE required system performance metrics. Use of a microchannel design effectively supplies heat to the highly endothermic steam reforming reactor to maintain high conversions, controls the temperature profile for the exothermic water gas shift reactor, which optimizes the overall reaction conversion, and removes heat to prevent the unwanted hydrogen oxidation in the prefer-ential oxidation reactor. The reactors combined with micro-channel heat exchangers, when scaled to a full sized 50 kWe automotive system, will be less than 21 L in volume and 52 kg in weight.

Brooks, Kriston P.; Davis, James M.; Fischer, Christopher M.; King, David L.; Pederson, Larry R.; Rawlings, Gregg C.; Stenkamp, Victoria S.; TeGrotenhuis, Ward E.; Wegeng, Robert S.; Whyatt, Greg A.

2005-09-01T23:59:59.000Z

100

Thermochemical Fuel Reformer Development Project  

Science Conference Proceedings (OSTI)

Thermochemical Fuel Reforming (TCFR) is the recovery of internal combustion engine exhaust heat to chemically convert natural gas into a higher calorific flow fuel stream containing a significant concentration of hydrogen. This technique of recycling the engine exhaust heat can reduce fuel use (heat rate). In addition, the hydrogen enhanced combustion also allows stable engine operation at a higher air-fuel ratio (leaner combustion) which results in very low NOx production. This interim report covers two...

2006-12-11T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Status of Power Sector Reform in Africa: Impact on the Poor | Open Energy  

Open Energy Info (EERE)

Status of Power Sector Reform in Africa: Impact on the Poor Status of Power Sector Reform in Africa: Impact on the Poor Jump to: navigation, search Tool Summary Name: Status of Power Sector Reform in Africa: Impact on the Poor Agency/Company /Organization: Stephen Karekezi and John Kimani Sector: Energy Focus Area: Renewable Energy, Energy Efficiency, People and Policy Phase: Create a Vision Topics: Co-benefits assessment, - Energy Access Resource Type: Publications User Interface: Website Website: www.sciencedirect.com/science/article/pii/S0301421502000484 Cost: Free UN Region: Eastern Africa, Southern Africa Language: English This article is based on a regional study by the authors reviewing the status, challenges and prospects of ongoing and planned power sector reform in eastern and southern Africa with special emphasis on the implications

102

Effect of reformer conditions on catalytic reforming of biomass-gasification tars  

Science Conference Proceedings (OSTI)

Parametric tests on catalytic reforming of tars produced in biomass gasification are performed using a bench-scale, fluid-bed catalytic reformer containing a commercial nickel-based catalyst. The product gas composition and yield vary with reformer temperature, space time, and steam: biomass ratio. Under certain catalytic tar reforming conditions, the gas yield increases by 70%; 97% of the tars are cracked into gases; and benzene and naphthalene, the predominant tar species, are virtually eliminated from the product gas.

Kinoshita, C.M.; Wang, Y.; Zhou, J. [Univ. of Hawaii, Honolulu, HI (United States)

1995-09-01T23:59:59.000Z

103

Distributed Bio-Oil Reforming (Presentation)  

DOE Green Energy (OSTI)

This presentation by Bob Evans at the 2007 DOE Hydrogen Program Annual Merit Review Meeting provides information about NREL's distributed bio-oil reforming efforts.

Evans, R. J.; Czernik, S.; French, R.; Ratcliff, M.; Marda, J.; Dean, A. M.

2007-05-15T23:59:59.000Z

104

TransForum v4n2 - Diesel Reformer  

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

1 ARGONNE SCIENTISTS TEAM UP TO DEVELOP NEW DIESEL REFORMER Liu tests diesel reformer Argonne's Di-Jia Liu conducted extensive testing of the diesel reformer; his experiments are...

105

SEPARATION OF RUTHENIUM FROM AQUEOUS SOLUTIONS  

DOE Patents (OSTI)

>The separation of ruthenium from aqueous solutions containing uranium plutonium, ruthenium, and fission products is described. The separation is accomplished by providing a nitric acid solution of plutonium, uranium, ruthenium, and fission products, oxidizing plutonium to the hexavalent state with sodium dichromate, contacting the solution with a water-immiscible organic solvent, such as hexone, to extract plutonyl, uranyl, ruthenium, and fission products, reducing with sodium ferrite the plutonyl in the solvent phase to trivalent plutonium, reextracting from the solvent phase the trivalent plutonium, ruthenium, and some fission products with an aqueous solution containing a salting out agent, introducing ozone into the aqueous acid solution to oxidize plutonium to the hexavalent state and ruthenium to ruthenium tetraoxide, and volatizing off the ruthenium tetraoxide.

Callis, C.F.; Moore, R.L.

1959-09-01T23:59:59.000Z

106

Plant Cell Walls: Basics of Structure, Chemistry, Accessibility and the Influence on Conversion - Aqueous Pretreatment of Plant Biomass for Biological and Chemical Conversion to Fuels and Chemicals  

SciTech Connect

This book is focused on the pretreatment of biomass, a necessary step for efficient conversion of the plant cell wall materials to fuels and other products. Pretreatment is required because it is difficult to access, separate, and release the monomeric sugars comprising the biopolymers within the biomass that can be further upgraded to products through chemical processes such as aqueous phase reforming or biological routes such as fermentation of the sugars to ethanol This resistance to degradation or difficulty to release the monomers (mostly sugars) is commonly referred to as recalcitrance. There are many methods to overcome plant recalcitrance, but the underlying cause of the recalcitrance lies in the complex combination of chemical and structural features of the plant cell walls.

Davison, Brian H [ORNL; Davis, Dr. Mark F. [National Renewable Energy Laboratory (NREL); Parks, Jerry M [ORNL; Donohoe, Bryan [National Renewable Energy Laboratory (NREL)

2013-01-01T23:59:59.000Z

107

An update on catalytic reforming  

Science Conference Proceedings (OSTI)

The UOP Platforming process is a catalytic reforming process in widespread use throughout the petroleum and petrochemical industries. Since the first unit went onstream in 1949, the process has become a standard feature in refineries worldwide. Over the years, significant improvements have been made in process catalysts and process design. The most recent improvement is the combination of a catalyst called R-72 with a new patented flow scheme, R-72 staged loading, which gives significantly higher yields and provides increased catalyst stability. In this article, the authors describe two types of Platforming processes and the new R-72 staged loading scheme.

Wei, D.H.; Moser, M.D.; Haizmann, R.S.

1996-10-01T23:59:59.000Z

108

Before House Committee on Oversight and Government Reform | Department...  

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

Oversight and Government Reform Before House Committee on Oversight and Government Reform Testimony of Daniel Poneman, Deputy Secretary of Energy Before House Committee on...

109

Bio-Derived Liquids to Hydrogen Distributed Reforming Targets...  

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

Group includes individuals from DOE, the national laboratories, industry, and academia. Corn Stover Harvest Bio-Derived Liquids Reforming Distributed reforming of biomass derived...

110

Regulatory and Financial Reform of Federal Research Policy: Recommenda...  

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

and Financial Reform of Federal Research Policy: Recommendations to the NRC Committee on Research Universities Regulatory and Financial Reform of Federal Research Policy:...

111

Guidance_Application_Federal_Vacancies_Reform_Act_1998.pdf |...  

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

nceApplicationFederalVacanciesReformAct1998.pdf More Documents & Publications Intelligence Reform and Terroroism Prevention Act - December 17, 2004 Bond Amendment, Security...

112

Diesel Reforming for Fuel Cell Auxiliary Power Units  

DOE Green Energy (OSTI)

This objective of this project was to develop technology suitable for onboard reforming of diesel. The approach was to examine catalytic partial oxidation and steam reforming.

Borup, R.; Parkinson, W. J.; Inbody, M.; Brosha, E.L.; Guidry, D.R.

2005-01-27T23:59:59.000Z

113

Fuel cell integrated with steam reformer  

DOE Patents (OSTI)

A H.sub.2 -air fuel cell integrated with a steam reformer is disclosed wherein a superheated water/methanol mixture is fed to a catalytic reformer to provide a continuous supply of hydrogen to the fuel cell, the gases exhausted from the anode of the fuel cell providing the thermal energy, via combustion, for superheating the water/methanol mixture.

Beshty, Bahjat S. (Lower Makefield, PA); Whelan, James A. (Bricktown, NJ)

1987-01-01T23:59:59.000Z

114

School Finance Reform: Assessing General Equilibrium Effects  

E-Print Network (OSTI)

In 1994 the state of Michigan implemented one of the most comprehensive school finance reforms undertaken to date in any of the states. Understanding the effects of the reform is thus of value in informing other potential reform initiatives. In addition, the reform and associated changes in the economic environment provide an opportunity to assess whether a simple general equilibrium model can be of value in framing the study of such reform initiatives. In this paper, we present and use such a model to derive predictions about the effects of the reform on housing prices and neighborhood demographic compositions. Broadly, our analysis implies that the effects of the reform and changes in the economic environment are likely to have been reflected primarily in housing prices and only modestly on neighborhood demographics. We find that evidence for the Detroit metropolitan area from the decade encompassing the reform is largely consistent with the predictions of the model (JEL codes: H42, H71, H73, I22).

Maria Marta Ferreyra

2007-01-01T23:59:59.000Z

115

Octane Number Prediction in a Reforming Plant  

Science Conference Proceedings (OSTI)

In this work a neural network for the prediction of the complex and non-linear behavior of a Catalytic Reforming of a refinery has been developed. In a fuel, refinery reforming is a conversion process to increase octane number (RON) of the desulphurated ...

E. Chibaro

2000-07-01T23:59:59.000Z

116

Methanol Steam Reformer on a Silicon Wafer  

DOE Green Energy (OSTI)

A study of the reforming rates, heat transfer and flow through a methanol reforming catalytic microreactor fabricated on a silicon wafer are presented. Comparison of computed and measured conversion efficiencies are shown to be favorable. Concepts for insulating the reactor while maintaining small overall size and starting operation from ambient temperature are analyzed.

Park, H; Malen, J; Piggott, T; Morse, J; Sopchak, D; Greif, R; Grigoropoulos, C; Havstad, M; Upadhye, R

2004-04-15T23:59:59.000Z

117

Method and apparatus for destroying organic contaminants in aqueous liquids  

DOE Patents (OSTI)

A method and apparatus for destroying organic contaminants, such as trichloroethylene, in aqueous liquids, such as groundwater, utilizing steam stripping integrated with biodegradation. The contaminated aqueous liquid is fed into a steam stripper causing the volatilization of essentially all of the organic contaminants and a portion of the aqueous liquid. The majority of the aqueous liquid is discharged from the steam stripper. The volatilized vapors are then condensed to the liquid phase and introduced into a bioreactor. The bioreactor contains methanotrophic microorganisms which convert the organic contaminants into mainly carbon dioxide. The effluent from the bioreactor is then recycled back to the steam stripper for further processing.

Donaldson, Terrence L. (Lenior City, TN); Wilson, James H. (Oak Ridge, TN)

1993-01-01T23:59:59.000Z

118

Method and apparatus for destroying organic contaminants in aqueous liquids  

DOE Patents (OSTI)

A method and apparatus for destroying organic contaminants, such as trichloroethylene, in aqueous liquids, such as groundwater, utilizing steam stripping integrated with biodegradation. The contaminated aqueous liquid is fed into a steam stripper causing the volatilization of essentially all of the organic contaminants and a portion of the aqueous liquid. The majority of the aqueous liquid is discharged from the steam stripper. The volatilized vapors are then condensed to the liquid phase and introduced into a bioreactor. The bioreactor contains methanotrophic microorganisms which convert the organic contaminants into mainly carbon dioxide. The effluent from the bioreactor is then recycled back to the steam stripper for further processing. 2 figures.

Donaldson, T.L.; Wilson, J.H.

1993-09-21T23:59:59.000Z

119

New model accurately predicts reformate composition  

Science Conference Proceedings (OSTI)

Although naphtha reforming is a well-known process, the evolution of catalyst formulation, as well as new trends in gasoline specifications, have led to rapid evolution of the process, including: reactor design, regeneration mode, and operating conditions. Mathematical modeling of the reforming process is an increasingly important tool. It is fundamental to the proper design of new reactors and revamp of existing ones. Modeling can be used to optimize operating conditions, analyze the effects of process variables, and enhance unit performance. Instituto Mexicano del Petroleo has developed a model of the catalytic reforming process that accurately predicts reformate composition at the higher-severity conditions at which new reformers are being designed. The new AA model is more accurate than previous proposals because it takes into account the effects of temperature and pressure on the rate constants of each chemical reaction.

Ancheyta-Juarez, J.; Aguilar-Rodriguez, E. (Inst. Mexicano del Petroleo, Mexico City (Mexico))

1994-01-31T23:59:59.000Z

120

Aqueous coal slurry  

DOE Patents (OSTI)

A principal object of the invention is the provision of an aqueous coal slurry containing a dispersant, which is of low-cost and which contains very low or no levels of sodium, potassium, sulfur and other contaminants. In connection with the foregoing object, it is an object of the invention to provide an aqueous slurry containing coal and dextrin as a dispersant and to provide a method of preparing an aqueous coal slurry which includes the step of adding an effective amount of dextrin as a dispersant. The invention consists of certain novel features and a combination of parts hereinafter fully described, and particularly pointed out in the appended claims. 6 tabs.

Berggren, M.H.; Smit, F.J.; Swanson, W.W.

1989-10-30T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Prediction of solid-aqueous equilibria: Scheme to combine first-principles calculations of solids with experimental aqueous states  

E-Print Network (OSTI)

We present an efficient scheme for combining ab initio calculated solid states with experimental aqueous states through a framework of consistent reference energies. Our work enables accurate prediction of phase stability ...

Persson, Kristin A.

122

Aqueous coal slurry  

DOE Patents (OSTI)

An aqueous slurry containing coal and dextrin as a dispersant. The slurry, in addition to containing dextrin, may contain a conventional dispersant or, alternatively, a pH controlling reagent.

Berggren, Mark H. (Golden, CO); Smit, Francis J. (Arvada, CO); Swanson, Wilbur W. (Golden, CO)

1993-01-01T23:59:59.000Z

123

Autothermal Cyclic Reforming Based H2 Generating & Dispensing System  

E-Print Network (OSTI)

Pressure Reforming Comp- ressor 100 psig 100 psig Reformer H2 PSA SyngasNatural Gas Low Pressure Reforming CMP Syngas 5 psig5 psig Reformer CMP 100 psig H2 PSA Natural Gas Syngas CMP HX CMP HX Thermal Reliability (Eliminates Syngas Compressor) Advantages 70-80%70-80%Thermal Efficiency (Excludes Electricity

124

Electricity reform in developing and transition countries: A reappraisal  

E-Print Network (OSTI)

Electricity reform in developing and transition countries: A reappraisal J.H. Williams, R. Ghanadan-oriented reforms in their electric power sectors. Despite the widespread adoption of a standard policy model features of non-OECD electricity reform and reappraises reform policies and underlying assumptions

Kammen, Daniel M.

125

Diesel Reforming for Solid Oxide Fuel Cell Application  

DOE Green Energy (OSTI)

This presentation discusses the development of a diesel reforming catalyst and catalytic system development.

Liu, D-J.; Sheen, S-H.; Krumpelt, M.

2005-01-27T23:59:59.000Z

126

Before the House Oversight and Government Reform Subcommittee on  

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

Oversight and Government Reform Subcommittee on Oversight and Government Reform Subcommittee on Technology, Information Policy, Intergovernmental Relations, and Procurement Reform Before the House Oversight and Government Reform Subcommittee on Technology, Information Policy, Intergovernmental Relations, and Procurement Reform Before the Subcommittee on Technology, Information Policy, Intergovernmental Relations and Procurement Reform, Committee on Oversight and Government Reform, United States House of Representatives Written Statement By: Owen Barwell, Acting Chief Financial Officer, United States Department of Energy Subject: DOE Financial Information Systems Final_Testimony_for_Owen_Barwell.pdf More Documents & Publications AL2010-03.pdf Request for Information - Operations and Maintenance (O & M) Support

127

Internal reforming fuel cell assembly with simplified fuel feed  

DOE Patents (OSTI)

A fuel cell assembly in which fuel cells adapted to internally reform fuel and fuel reformers for reforming fuel are arranged in a fuel cell stack. The fuel inlet ports of the fuel cells and the fuel inlet ports and reformed fuel outlet ports of the fuel reformers are arranged on one face of the fuel cell stack. A manifold sealing encloses this face of the stack and a reformer fuel delivery system is arranged entirely within the region between the manifold and the one face of the stack. The fuel reformer has a foil wrapping and a cover member forming with the foil wrapping an enclosed structure.

Farooque, Mohammad (Huntington, CT); Novacco, Lawrence J. (Brookfield, CT); Allen, Jeffrey P. (Naugatuck, CT)

2001-01-01T23:59:59.000Z

128

Computational Fluid Dynamics Simulation of Steam Reforming and Autothermal Reforming for Fuel Cell Applications.  

E-Print Network (OSTI)

??With the increasing demand for fuel cell applications in transportation, the performance of reformers using gasoline or diesel as the fuel needs to be optimized.… (more)

Shi, Liming

2009-01-01T23:59:59.000Z

129

Bank Regulation and Mortgage Market Reform  

E-Print Network (OSTI)

America’s Housing Finance Market: A Report To Congress”,Subordinated Debt: A Capital Markets Approach to BankBank Regulation and Mortgage Market Reform Dwight M. Jaffee

Jaffee, Dwight M.

2011-01-01T23:59:59.000Z

130

Electricity reform abroad and US investment  

SciTech Connect

This report reviews and analyzes the recent electricity reforms in Argentina, Australia, and the United Kingdom (UK) to illustrate how different models of privatization and reform have worked in practice. This report also analyzes the motivations of the U.S. companies who have invested in the electricity industries in these countries, which have become the largest targets of U.S. foreign investment in electricity. Two calculations of foreign investment are used. One is the foreign direct investment series produced by the U.S. Department of Commerce. The other is based on transactions in electric utilities of the three countries. The electricity reform and privatization experiences reviewed may offer some insight as to how the U.S. electricity industry might develop as a result of recent domestic reform efforts and deregulation at the state and national levels. 126 refs., 23 figs., 27 tabs.

1997-10-01T23:59:59.000Z

131

Distributed Reforming of Biomass Pyrolysis Oils (Presentation...  

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

gas (0.5% H 2 ) System Definition (1500 kgday station used for H2A analysis) Capital Costs Bio-Oil Reforming H2A Analysis Bio-Oil Case (Ethanol Case) Bio-oil Storage Tank...

132

Device for cooling and humidifying reformate  

Science Conference Proceedings (OSTI)

Devices for cooling and humidifying a reformate stream from a reforming reactor as well as related methods, modules and systems includes a heat exchanger and a sprayer. The heat exchanger has an inlet, an outlet, and a conduit between the inlet and the outlet. The heat exchanger is adapted to allow a flow of a first fluid (e.g. water) inside the conduit and to establish a heat exchange relationship between the first fluid and a second fluid (e.g. reformate from a reforming reactor) flowing outside the conduit. The sprayer is coupled to the outlet of the heat exchanger for spraying the first fluid exiting the heat exchanger into the second fluid.

Zhao, Jian Lian (Belmont, MA); Northrop, William F. (Ann Arbor, MI)

2008-04-08T23:59:59.000Z

133

Liquid fuel reformer development: Autothermal reforming of Diesel fuel  

DOE Green Energy (OSTI)

Argonne National Laboratory is developing a process to convert hydrocarbon fuels to clean hydrogen feeds for a polymer electrolyte fuel cell. The process incorporates an autothermal reforming catalyst that can process hydrocarbon feeds at lower temperatures than existing commercial catalysts. The authors have tested the catalyst with three diesel-type fuels: hexadecane, certified low-sulfur grade 1 diesel, and a standard grade 2 diesel. Hexadecane yielded products containing 60% hydrogen on a dry, nitrogen-free basis at 850 C, while maximum hydrogen product yields for the two diesel fuels were near 50%. Residual products in all cases included CO, CO{sub 2}, ethane, and methane. Further studies with grade 1 diesel showed improved conversion as the water:fuel ratio was increased from 1 to 2 at 850 C. Soot formation was reduced when the oxygen:carbon ratio was maintained at 1 at 850 C. There were no significant changes in hydrogen yield as the space velocity and the oxygen:fuel ratio were varied. Tests with a microchannel monolithic catalyst yielded similar or improved hydrogen levels at higher space velocities than with extruded pellets in a packed bed.

Pereira, C.; Bae, J-M.; Ahmed, S.; Krumpelt, M.

2000-07-24T23:59:59.000Z

134

Reforming of fuel inside fuel cell generator  

DOE Patents (OSTI)

Disclosed is an improved method of reforming a gaseous reformable fuel within a solid oxide fuel cell generator, wherein the solid oxide fuel cell generator has a plurality of individual fuel cells in a refractory container, the fuel cells generating a partially spent fuel stream and a partially spent oxidant stream. The partially spent fuel stream is divided into two streams, spent fuel stream 1 and spent fuel stream 2. Spent fuel stream 1 is burned with the partially spent oxidant stream inside the refractory container to produce an exhaust stream. The exhaust stream is divided into two streams, exhaust stream 1 and exhaust stream 2, and exhaust stream 1 is vented. Exhaust stream 2 is mixed with spent fuel stream 2 to form a recycle stream. The recycle stream is mixed with the gaseous reformable fuel within the refractory container to form a fuel stream which is supplied to the fuel cells. Also disclosed is an improved apparatus which permits the reforming of a reformable gaseous fuel within such a solid oxide fuel cell generator. The apparatus comprises a mixing chamber within the refractory container, means for diverting a portion of the partially spent fuel stream to the mixing chamber, means for diverting a portion of exhaust gas to the mixing chamber where it is mixed with the portion of the partially spent fuel stream to form a recycle stream, means for injecting the reformable gaseous fuel into the recycle stream, and means for circulating the recycle stream back to the fuel cells. 1 fig.

Grimble, R.E.

1988-03-08T23:59:59.000Z

135

Reforming of fuel inside fuel cell generator  

DOE Patents (OSTI)

Disclosed is an improved method of reforming a gaseous reformable fuel within a solid oxide fuel cell generator, wherein the solid oxide fuel cell generator has a plurality of individual fuel cells in a refractory container, the fuel cells generating a partially spent fuel stream and a partially spent oxidant stream. The partially spent fuel stream is divided into two streams, spent fuel stream I and spent fuel stream II. Spent fuel stream I is burned with the partially spent oxidant stream inside the refractory container to produce an exhaust stream. The exhaust stream is divided into two streams, exhaust stream I and exhaust stream II, and exhaust stream I is vented. Exhaust stream II is mixed with spent fuel stream II to form a recycle stream. The recycle stream is mixed with the gaseous reformable fuel within the refractory container to form a fuel stream which is supplied to the fuel cells. Also disclosed is an improved apparatus which permits the reforming of a reformable gaseous fuel within such a solid oxide fuel cell generator. The apparatus comprises a mixing chamber within the refractory container, means for diverting a portion of the partially spent fuel stream to the mixing chamber, means for diverting a portion of exhaust gas to the mixing chamber where it is mixed with the portion of the partially spent fuel stream to form a recycle stream, means for injecting the reformable gaseous fuel into the recycle stream, and means for circulating the recycle stream back to the fuel cells.

Grimble, Ralph E. (Finleyville, PA)

1988-01-01T23:59:59.000Z

136

Heat Transfer Limitations in Hydrogen Production Via Steam Reformation: The Effect of Reactor Geometry  

E-Print Network (OSTI)

Ratio Parameters in Steam-Reforming Hydrogen productionan Insufficient Parameter in the Steam-Reforming Process,”Impurities on the Methanol Steam-Reforming Process for Fuel

Vernon, David R.; Davieau, David D.; Dudgeon, Bryce A.; Erickson, Paul A.

2006-01-01T23:59:59.000Z

137

Process and apparatus for the production of hydrogen by steam reforming of hydrocarbon  

DOE Patents (OSTI)

In the steam reforming of hydrocarbon, particularly methane, under elevated temperature and pressure to produce hydrogen, a feed of steam and hydrocarbon is fed into a first reaction volume containing essentially only reforming catalyst to partially reform the feed. The balance of the feed and the reaction products of carbon dioxide and hydrogen are then fed into a second reaction volume containing a mixture of catalyst and adsorbent which removes the carbon dioxide from the reaction zone as it is formed. The process is conducted in a cycle which includes these reactions followed by countercurrent depressurization and purge of the adsorbent to regenerate it and repressurization of the reaction volumes preparatory to repeating the reaction-sorption phase of the cycle.

Sircar, Shivaji (Wescosville, PA); Hufton, Jeffrey Raymond (Fogelsville, PA); Nataraj, Shankar (Allentown, PA)

2000-01-01T23:59:59.000Z

138

A thermodynamic model for aqueous solutions of liquid-like density  

DOE Green Energy (OSTI)

The paper describes a model for the prediction of the thermodynamic properties of multicomponent aqueous solutions and discusses its applications. The model was initially developed for solutions near room temperature, but has been found to be applicable to aqueous systems up to 300/sup 0/C or slightly higher. A liquid-like density and relatively small compressibility are assumed. A typical application is the prediction of the equilibrium between an aqueous phase (brine) and one or more solid phases (minerals). (ACR)

Pitzer, K.S.

1987-06-01T23:59:59.000Z

139

Continuous aqueous tritium monitor  

DOE Patents (OSTI)

An apparatus for a selective on-line determination of aqueous tritium concentration is disclosed. A moist air stream of the liquid solution being analyzed is passed through a permeation dryer where the tritium and moisture and selectively removed to a purge air stream. The purge air stream is then analyzed for tritium concentration, humidity, and temperature, which allows computation of liquid tritium concentration.

McManus, Gary J. (Idaho Falls, ID); Weesner, Forrest J. (Idaho Falls, ID)

1989-05-30T23:59:59.000Z

140

Hydrogen generation utilizing integrated CO2 removal with steam reforming  

DOE Patents (OSTI)

A steam reformer may comprise fluid inlet and outlet connections and have a substantially cylindrical geometry divided into reforming segments and reforming compartments extending longitudinally within the reformer, each being in fluid communication. With the fluid inlets and outlets. Further, methods for generating hydrogen may comprise steam reformation and material adsorption in one operation followed by regeneration of adsorbers in another operation. Cathode off-gas from a fuel cell may be used to regenerate and sweep the adsorbers, and the operations may cycle among a plurality of adsorption enhanced reformers to provide a continuous flow of hydrogen.

Duraiswamy, Kandaswamy; Chellappa, Anand S

2013-07-23T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Columbia River Hatchery Reform System-Wide Report.  

SciTech Connect

The US Congress funded the Puget Sound and Coastal Washington Hatchery Reform Project via annual appropriations to the US Fish and Wildlife Service (USFWS) beginning in fiscal year 2000. Congress established the project because it recognized that while hatcheries have a necessary role to play in meeting harvest and conservation goals for Pacific Northwest salmonids, the hatchery system was in need of comprehensive reform. Most hatcheries were producing fish for harvest primarily to mitigate for past habitat loss (rather than for conservation of at-risk populations) and were not taking into account the effects of their programs on naturally spawning populations. With numerous species listed as threatened or endangered under the Endangered Species Act (ESA), conservation of salmon in the Puget Sound area was a high priority. Genetic resources in the region were at risk and many hatchery programs as currently operated were contributing to those risks. Central to the project was the creation of a nine-member independent scientific review panel called the Hatchery Scientific Review Group (HSRG). The HSRG was charged by Congress with reviewing all state, tribal and federal hatchery programs in Puget Sound and Coastal Washington as part of a comprehensive hatchery reform effort to: conserve indigenous salmonid genetic resources; assist with the recovery of naturally spawning salmonid populations; provide sustainable fisheries; and improve the quality and cost-effectiveness of hatchery programs. The HSRG worked closely with the state, tribal and federal managers of the hatchery system, with facilitation provided by the non-profit organization Long Live the Kings and the law firm Gordon, Thomas, Honeywell, to successfully complete reviews of over 200 hatchery programs at more than 100 hatcheries across western Washington. That phase of the project culminated in 2004 with the publication of reports containing the HSRG's principles for hatchery reform and recommendations for Puget Sound/Coastal Washington hatchery programs, followed by the development in 2005 of a suite of analytical tools to support application of the principles (all reports and tools are available at www.hatcheryreform.us). In 2005, Congress directed the National Oceanic and Atmospheric Administration-Fisheries (NOAA Fisheries) to replicate the Puget Sound and Coastal Washington Hatchery Reform Project in the Columbia River Basin. The HSRG was expanded to 14 members to include individuals with specific knowledge about the Columbia River salmon and steelhead populations. This second phase was initially envisioned as a one-year review, with emphasis on the Lower Columbia River hatchery programs. It became clear however, that the Columbia River Basin needed to be viewed as an inter-connected ecosystem in order for the review to be useful. The project scope was subsequently expanded to include the entire Basin, with funding for a second year provided by the Bonneville Power Administration (BPA) under the auspices of the Northwest Power and Conservation Council's (NPCC) Fish and Wildlife Program. The objective of the HSRG's Columbia River Basin review was to change the focus of the Columbia River hatchery system. In the past, these hatchery programs have been aimed at supplying adequate numbers of fish for harvest as mitigation primarily for hydropower development in the Basin. A new, ecosystem-based approach is founded on the idea that harvest goals are sustainable only if they are compatible with conservation goals. The challenge before the HSRG was to determine whether or not conservation and harvest goals could be met by fishery managers and, if so, how. The HSRG determined that in order to address these twin goals, both hatchery and harvest reforms are necessary. The HSRG approach represents an important change of direction in managing hatcheries in the region. It provides a clear demonstration that current hatchery programs can indeed be redirected to better meet both conservation and harvest goals. For each Columbia River Basin Environmentally Si

Warren, Dan [Hatchery Scientific Review Group

2009-04-16T23:59:59.000Z

142

Columbia River Hatchery Reform System-Wide Report.  

DOE Green Energy (OSTI)

The US Congress funded the Puget Sound and Coastal Washington Hatchery Reform Project via annual appropriations to the US Fish and Wildlife Service (USFWS) beginning in fiscal year 2000. Congress established the project because it recognized that while hatcheries have a necessary role to play in meeting harvest and conservation goals for Pacific Northwest salmonids, the hatchery system was in need of comprehensive reform. Most hatcheries were producing fish for harvest primarily to mitigate for past habitat loss (rather than for conservation of at-risk populations) and were not taking into account the effects of their programs on naturally spawning populations. With numerous species listed as threatened or endangered under the Endangered Species Act (ESA), conservation of salmon in the Puget Sound area was a high priority. Genetic resources in the region were at risk and many hatchery programs as currently operated were contributing to those risks. Central to the project was the creation of a nine-member independent scientific review panel called the Hatchery Scientific Review Group (HSRG). The HSRG was charged by Congress with reviewing all state, tribal and federal hatchery programs in Puget Sound and Coastal Washington as part of a comprehensive hatchery reform effort to: conserve indigenous salmonid genetic resources; assist with the recovery of naturally spawning salmonid populations; provide sustainable fisheries; and improve the quality and cost-effectiveness of hatchery programs. The HSRG worked closely with the state, tribal and federal managers of the hatchery system, with facilitation provided by the non-profit organization Long Live the Kings and the law firm Gordon, Thomas, Honeywell, to successfully complete reviews of over 200 hatchery programs at more than 100 hatcheries across western Washington. That phase of the project culminated in 2004 with the publication of reports containing the HSRG's principles for hatchery reform and recommendations for Puget Sound/Coastal Washington hatchery programs, followed by the development in 2005 of a suite of analytical tools to support application of the principles (all reports and tools are available at www.hatcheryreform.us). In 2005, Congress directed the National Oceanic and Atmospheric Administration-Fisheries (NOAA Fisheries) to replicate the Puget Sound and Coastal Washington Hatchery Reform Project in the Columbia River Basin. The HSRG was expanded to 14 members to include individuals with specific knowledge about the Columbia River salmon and steelhead populations. This second phase was initially envisioned as a one-year review, with emphasis on the Lower Columbia River hatchery programs. It became clear however, that the Columbia River Basin needed to be viewed as an inter-connected ecosystem in order for the review to be useful. The project scope was subsequently expanded to include the entire Basin, with funding for a second year provided by the Bonneville Power Administration (BPA) under the auspices of the Northwest Power and Conservation Council's (NPCC) Fish and Wildlife Program. The objective of the HSRG's Columbia River Basin review was to change the focus of the Columbia River hatchery system. In the past, these hatchery programs have been aimed at supplying adequate numbers of fish for harvest as mitigation primarily for hydropower development in the Basin. A new, ecosystem-based approach is founded on the idea that harvest goals are sustainable only if they are compatible with conservation goals. The challenge before the HSRG was to determine whether or not conservation and harvest goals could be met by fishery managers and, if so, how. The HSRG determined that in order to address these twin goals, both hatchery and harvest reforms are necessary. The HSRG approach represents an important change of direction in managing hatcheries in the region. It provides a clear demonstration that current hatchery programs can indeed be redirected to better meet both conservation and harvest goals. For each Columbia River Basin Environmentally Significant Unit

Warren, Dan [Hatchery Scientific Review Group

2009-04-16T23:59:59.000Z

143

Suppressant:Water & Aqueous Solutions  

Science Conference Proceedings (OSTI)

Suppressant:Water & Aqueous Solutions. ... Reuther, JJ; 1991. Fine Water Sprays for Fire Protection: A Halon Replacement Option.. ...

2011-10-28T23:59:59.000Z

144

RADIOACTIVE DEMONSTRATION OF FINAL MINERALIZED WASTE FORMS FOR HANFORD WASTE TREATMENT PLANT SECONDARY WASTE BY FLUIDIZED BED STEAM REFORMING USING THE BENCH SCALE REFORMER PLATFORM  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy's Office of River Protection (ORP) is responsible for the retrieval, treatment, immobilization, and disposal of Hanford's tank waste. Currently there are approximately 56 million gallons of highly radioactive mixed wastes awaiting treatment. A key aspect of the River Protection Project (RPP) cleanup mission is to construct and operate the Waste Treatment and Immobilization Plant (WTP). The WTP will separate the tank waste into high-level and low-activity waste (LAW) fractions, both of which will subsequently be vitrified. The projected throughput capacity of the WTP LAW Vitrification Facility is insufficient to complete the RPP mission in the time frame required by the Hanford Federal Facility Agreement and Consent Order, also known as the Tri-Party Agreement (TPA), i.e. December 31, 2047. Therefore, Supplemental Treatment is required both to meet the TPA treatment requirements as well as to more cost effectively complete the tank waste treatment mission. In addition, the WTP LAW vitrification facility off-gas condensate known as WTP Secondary Waste (WTP-SW) will be generated and enriched in volatile components such as {sup 137}Cs, {sup 129}I, {sup 99}Tc, Cl, F, and SO{sub 4} that volatilize at the vitrification temperature of 1150 C in the absence of a continuous cold cap (that could minimize volatilization). The current waste disposal path for the WTP-SW is to process it through the Effluent Treatment Facility (ETF). Fluidized Bed Steam Reforming (FBSR) is being considered for immobilization of the ETF concentrate that would be generated by processing the WTP-SW. The focus of this current report is the WTP-SW. FBSR offers a moderate temperature (700-750 C) continuous method by which WTP-SW wastes can be processed irrespective of whether they contain organics, nitrates, sulfates/sulfides, chlorides, fluorides, volatile radionuclides or other aqueous components. The FBSR technology can process these wastes into a crystalline ceramic (mineral) waste form. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be as durable as LAW glass. Monolithing of the granular FBSR product is being investigated to prevent dispersion during transport or burial/storage, but is not necessary for performance. A Benchscale Steam Reformer (BSR) was designed and constructed at the SRNL to treat actual radioactive wastes to confirm the findings of the non-radioactive FBSR pilot scale tests and to qualify the waste form for applications at Hanford. BSR testing with WTP SW waste surrogates and associated analytical analyses and tests of granular products (GP) and monoliths began in the Fall of 2009, and then was continued from the Fall of 2010 through the Spring of 2011. Radioactive testing commenced in 2010 with a demonstration of Hanford's WTP-SW where Savannah River Site (SRS) High Level Waste (HLW) secondary waste from the Defense Waste Processing Facility (DWPF) was shimmed with a mixture of {sup 125/129}I and {sup 99}Tc to chemically resemble WTP-SW. Prior to these radioactive feed tests, non-radioactive simulants were also processed. Ninety six grams of radioactive granular product were made for testing and comparison to the non-radioactive pilot scale tests. The same mineral phases were found in the radioactive and non-radioactive testing.

Crawford, C.; Burket, P.; Cozzi, A.; Daniel, W.; Jantzen, C.; Missimer, D.

2012-02-02T23:59:59.000Z

145

Interactions of Cl- and OH Radical in Aqueous Solution  

Science Conference Proceedings (OSTI)

Fundamental understanding of ion-radical interactions in aqueous solutions is of significant relevance to many environmentally important applications. An important example can be found in the problem involving the excess production of molecular chlorine in marine layer, where interactions between OH radical and Cl- species have been implicated as the main reason for the unexpectedly high concentration of Cl2. Current understanding of this process is hindered due to uncertainty regarding the nature of the [OHCl]- complex in aqueous phase.

Valiev, Marat; D'Auria, Rafaella; Tobias, Douglas J.; Garrett, Bruce C.

2009-08-06T23:59:59.000Z

146

DURABILITY TESTING OF FLUIDIZED BED STEAM REFORMER (FBSR) WASTE FORMS  

SciTech Connect

Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium aqueous radioactive wastes. The addition of clay and a catalyst as co-reactants converts high sodium aqueous low activity wastes (LAW) such as those existing at the Hanford and Idaho DOE sites to a granular ''mineralized'' waste form that may be made into a monolith form if necessary. Simulant Hanford and Idaho high sodium wastes were processed in a pilot scale FBSR at Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low-activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium-bearing waste (SBW). The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The durability of the FBSR waste form products was tested in order to compare the measured durability to previous FBSR waste form testing on Hanford Envelope C waste forms that were made by THOR Treatment Technologies (TTT) and to compare the FBSR durability to vitreous LAW waste forms, specifically the Hanford low activity waste (LAW) glass known as the Low-activity Reference Material (LRM). The durability of the FBSR waste form is comparable to that of the LRM glass for the test responses studied.

Jantzen, C

2006-01-06T23:59:59.000Z

147

Thermally integrated staged methanol reformer and method  

DOE Green Energy (OSTI)

A thermally integrated two-stage methanol reformer including a heat exchanger and first and second reactors colocated in a common housing in which a gaseous heat transfer medium circulates to carry heat from the heat exchanger into the reactors. The heat transfer medium comprises principally hydrogen, carbon dioxide, methanol vapor and water vapor formed in a first stage reforming reaction. A small portion of the circulating heat transfer medium is drawn off and reacted in a second stage reforming reaction which substantially completes the reaction of the methanol and water remaining in the drawn-off portion. Preferably, a PrOx reactor will be included in the housing upstream of the heat exchanger to supplement the heat provided by the heat exchanger.

Skala, Glenn William (Churchville, NY); Hart-Predmore, David James (Rochester, NY); Pettit, William Henry (Rochester, NY); Borup, Rodney Lynn (East Rochester, NY)

2001-01-01T23:59:59.000Z

148

Fundamental kinetic modeling of the catalytic reforming process  

Science Conference Proceedings (OSTI)

In this work, a fundamental kinetic model for the catalytic reforming process has been developed. The complex network of elementary steps and molecular reactions occurring in catalytic reforming has been generated through a computer algorithm characterizing ...

Rogelio Sotelo-Boyas / Gilbert F. Froment; Rayford G. Anthony

2005-01-01T23:59:59.000Z

149

Electricity reform in Chile : lessons for developing countries  

E-Print Network (OSTI)

Chile was the first country in the world to implement a comprehensive reform of its electricity sector in the recent period. Among developing countries only Argentina has had a comparably comprehensive and successful reform. ...

Pollitt, Michael G.

2004-01-01T23:59:59.000Z

150

REFORMING PROCESSES FOR MICRO COMBINED HEAT AND POWER SYSTEM BASED ON SOLID OXIDE FUEL CELL  

E-Print Network (OSTI)

and energy balance, different types of fuel reforming including steam reforming, autothermal reforming technologies. Steam reforming, partial oxidation and autothermal reforming are the three major fuel of an activated carbon bed. Prior to enter the SOFC stack, the fuel is pre-reformed (methane is partially

Liso, Vincenzo

151

Continuous aqueous tritium monitor  

DOE Patents (OSTI)

An apparatus for a selective on-line determination of aqueous tritium concentration is disclosed. A moist air stream of the liquid solution being analyzed is passed through a permeation dryer where the tritium and moisture are selectively removed to a purge air stream. The purge air stream is then analyzed for tritium concentration, humidity, and temperature, which allows computation of liquid tritium concentration. 2 figs.

McManus, G.J.; Weesner, F.J.

1987-10-19T23:59:59.000Z

152

Before the House Oversight and Government Reform Subcommittee...  

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

Government Management, Organization, and Procurement Before the House Oversight and Government Reform Subcommittee on Government Management, Organization, and Procurement Before...

153

New Jersey Refinery Catalytic Reforming/High Pressure Downstream ...  

U.S. Energy Information Administration (EIA)

New Jersey Refinery Catalytic Reforming/High Pressure Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

154

Arkansas Refinery Catalytic Reforming/High Pressure Downstream ...  

U.S. Energy Information Administration (EIA)

Arkansas Refinery Catalytic Reforming/High Pressure Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

155

Simulation of terrace wall methane-steam reforming reactors  

Science Conference Proceedings (OSTI)

Terrace wall arrangement is one of the most common arrangements for methane-steam reforming reactor furnaces. In this work, a mathematical model of heat transfer in terrace wall furnaces has been developed. The model has been coupled with a reliable ... Keywords: heat transfer modeling, methane-steam reforming, reformer simulation, terrace wall furnace

J. S. Soltan Mohammadzadeh; A. Zamaniyan

2002-08-01T23:59:59.000Z

156

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

157

Bioethanol production from lignocellulosic feedstock using aqueous ammonia pretreatment and simultaneous saccharification and fermentation (SSF): process development and optimization.  

E-Print Network (OSTI)

??An integrated bioconversion process, which incorporated soaking in aqueous ammonia (SAA) pretreatment and two-phase simultaneous saccharification and fermentation (TPSSF), was investigated. The TPSSF process consists… (more)

Li, Xuan

2010-01-01T23:59:59.000Z

158

Legal aspects of Internet governance reform  

Science Conference Proceedings (OSTI)

The Internet has moved on from its early almost lawless nature. There are now multiple organisations and legal aspects associated with Internet governance. Whether the issue on the Internet is network security, intellectual property rights (IPRs), e-commerce, ... Keywords: ICANN, WGIG, WSIS, cybercrime, framework, governance, internet, law, reform, treaty

David Satola

2007-01-01T23:59:59.000Z

159

Catalytic partial oxidation reforming of hydrocarbon fuels.  

DOE Green Energy (OSTI)

The polymer electrolyte fuel cell (PEFC) is the primary candidate as the power source for light-duty transportation systems. On-board conversion of fuels (reforming) to supply the required hydrogen has the potential to provide the driving range that is typical of today's automobiles. Petroleum-derived fuels, gasoline or some distillate similar to it, are attractive because of their existing production, distribution, and retailing infrastructure. The fuel may be either petroleum-derived or other alternative fuels such as methanol, ethanol, natural gas, etc. [1]. The ability to use a variety of fuels is also attractive for stationary distributed power generation [2], such as in buildings, or for portable power in remote locations. Argonne National Laboratory has developed a catalytic reactor based on partial oxidation reforming that is suitable for use in light-duty vehicles powered by fuel cells. The reactor has shown the ability to convert a wide variety of fuels to a hydrogen-rich gas at less than 800 C, temperatures that are several hundreds of degrees lower than alternative noncatalytic processes. The fuel may be methanol, ethanol, natural gas, or petroleum-derived fuels that are blends of various hydrocarbons such as paraffins, olefins, aromatics, etc., as in gasoline. This paper will discuss the results obtained from a bench-scale (3-kWe) reactor., where the reforming of gasoline and natural gas generated a product gas that contained 38% and 42% hydrogen on a dry basis at the reformer exit, respectively.

Ahmed, S.

1998-09-21T23:59:59.000Z

160

Behavior of americium in aqueous carbonate systems  

Science Conference Proceedings (OSTI)

The solubilities of crystalline Am(OH)/sub 3/ and AmOHCO/sub 3/ were measured at 25/sup 0/C in aqueous solutions of 0.1 M NaClO/sub 4/ by determination of the solution concentrations of Am. Prior to use in the measurements, the solid materials were characterized by their x-ray powder diffraction patterns. The solubility product quotients were calculated from the experimental data. The hydrolysis quotients of Am/sup 3 +/ were also estimated from the hydroxide solubility data. Using the thermodynamic data derived from these experiments and the recently reported formation constants for the Am/sup 3 +/ carbonate complexes, the solid phases and concentrations of solution species of americium in several aqueous carbonate systems were calculated using the computer code MINEQL. 20 references, 1 figure, 1 table.

Silva, R.J.

1983-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" from the National Library of EnergyBeta (NLEBeta).
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161

March 16, 2010, Safety and Security Reform Roundtable - Agenda  

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

Safety and Security Reform Roundtable Safety and Security Reform Roundtable Forrestal Building, Washington, DC March 16 th , 2010 1:00 PM (EST) AGENDA * Introduction of Union Leaders Glenn Podonsky, Chief Health, Safety and Security Officer * Welcome/Introductory Remarks on Reform Goals Dan Poneman, Deputy Secretary * Reform Status and Approach - Oversight, Directives, Mission Support Glenn Podonsky, Chief Health, Safety and Security Officer * Discussion Forum - Union Feedback - Feedback on oversight reform initiatives - Priority safety issues - Experience in collaborative focus group efforts - Recommendations for a path forward * Operating Organization Perspectives 1. Tom D'Agostino Administrator, National Nuclear Security Administration 2. Steven Koonin Under Secretary for Science

162

Bio-Derived Liquids to Hydrogen Distributed Reforming Targets (Presentation)  

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

Distributed Reforming Targets Arlene F. Anderson Technology Development Manager, U.S. DOE Office of Energy Efficiency and Renewable Energy Hydrogen, Fuel Cells and Infrastructure Technologies Program Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group and Hydrogen Production Technical Team Review November 6, 2007 Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG) The Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG), launched in October 2006, provides a forum for effective communication and collaboration among participants in DOE Hydrogen, Fuel Cells, and Infrastructure Technologies Program (HFCIT) cost-shared research directed at distributed bio-liquid reforming. The Working Group includes

163

Synergize fuel and petrochemical processing plans with catalytic reforming  

Science Conference Proceedings (OSTI)

Depending on the market, refiner`s plans to produce clean fuels and higher value petrochemicals will weigh heavily on the catalytic reformer`s flexibility. It seems that as soon as a timely article related to catalytic reforming operations is published, a new {open_quotes}boutique{close_quotes} gasoline fuel specification is slapped on to existing fuel standards, affecting reformer operations and processing objectives. Just as importantly, the petrochemical market (such as aromatics) that refiners are targeting, can be very fickle. That`s why process engineers have endeavored to maintain an awareness of the flexibility that technology suppliers are building into modern catalytic reformers.

NONE

1997-03-01T23:59:59.000Z

164

Effect of reaction pressure on octane number and reformate and hydrogen yields in catalytic reforming  

Science Conference Proceedings (OSTI)

The effect of reaction pressure in catalytic reforming was studied in a pilot reactor with a commercial Pt-Re/Al{sub 2}O{sub 3} reforming catalyst and a hydrotreated naphtha from a North Sea crude. Reformate and hydrogen yields, research octane numbers (RON), and reformate composition at reactor pressures in the range of 12--25 bar were measured as a function of temperature in the range of 95--105 RON. Reformate and hydrogen yields increased as the pressure range. For the lower reaction pressures the hydrogen yields increased with increasing severity, but for the higher pressures the hydrogen yields started to decline above certain severities. RON was linearly dependent on the concentration of aromatics in the reformate, although the selectivity toward aromatics depends on both pressure and temperature. Less hydro dealkylation of C{sub 8} and heavier aromatics to benzene and toluene resulted in a shift toward xylenes and heavier aromatic components when pressure was lowered. Variations in the degree of paraffin isomerization did not influence RON significantly at those severities.

Moljord, K.; Hellenes, H.G.; Hoff, A.; Tanem, I. [SINTEF Applied Chemistry, Trondheim (Norway); Grande, K. [Statoil Research Centre, Trondheim (Norway); Holmen, A. [Univ. of Trondheim (Norway). Dept. Industrial Chemistry

1996-01-01T23:59:59.000Z

165

A method for separating water soluble organics from a process stream by aqueous biphasic extraction  

DOE Patents (OSTI)

The present invention relates to a method for separating water-miscible organic species from a process stream by aqueous biphasic extraction. In particular, the method includes extracting the organic species into a polymer-rich phase of an aqueous biphase system in which the process stream comprises the salt-rich phase, and, next, separating the polymer from the extracted organic species by contacting the loaded, polymer-rich phase with a water-immiscible organic phase. Alternatively, the polymer can be separated from the extracted organic species by raising the temperature of the loaded, polymer-rich phase above the cloud point, such that the polymer and the water-soluble organic species separate into two distinct aqueous phases. In either case, a substantially salt-free, concentrated aqueous solution containing the organic species is recovered.

Chaiko, David J.; Mego, William A.

1997-12-01T23:59:59.000Z

166

Membrane reactor advantages for methanol reforming and similar reactions  

Science Conference Proceedings (OSTI)

Membrane reactors achieve efficiencies by combining in one unit a reactor that generates a product with a semipermeable membrane that extracts it. One well-known benefit of this is greater conversion, as removal of a product drives reactions toward completion, but there are several potentially larger advantages that have been largely ignored. Because a membrane reactor tends to limit the partial pressure of the extracted product, it fundamentally changes the way that total pressure in the reactor affects equilibrium conversion. Thus, many gas-phase reactions that are preferentially performed at low pressures in a conventional reactor are found to have maximum conversion at high pressures in a membrane reactor. These higher pressures and reaction conversions allow greatly enhanced product extraction as well. Further, membrane reactors provide unique opportunities for temperature management which have not been discussed previously. These benefits are illustrated for methanol reforming to hydrogen for use with PEM (polymer electrolyte membrane) fuel cells.

Buxbaum, R.E. [REB Research and Consulting Co., Ferndale, MI (United States)

1999-07-01T23:59:59.000Z

167

Hydrocarbon reforming catalyst material and configuration of the same  

DOE Patents (OSTI)

A hydrocarbon reforming catalyst material comprising a catalyst support impregnated with catalyst is provided for reforming hydrocarbon fuel gases in an electrochemical generator. Elongated electrochemical cells convert the fuel to electrical power in the presence of an oxidant, after which the spent fuel is recirculated and combined with a fresh hydrocarbon feed fuel forming the reformable gas mixture which is fed to a reforming chamber containing a reforming catalyst material, where the reforming catalyst material includes discrete passageways integrally formed along the length of the catalyst support in the direction of reformable gas flow. The spent fuel and/or combusted exhaust gases discharged from the generator chamber transfer heat to the catalyst support, which in turn transfers heat to the reformable gas and to the catalyst, preferably via a number of discrete passageways disposed adjacent one another in the reforming catalyst support. The passageways can be slots extending inwardly from an outer surface of the support body, which slots are partly defined by an exterior confining wall. According to a preferred embodiment, the catalyst support is non-rigid, porous, fibrous alumina, wherein the fibers are substantially unsintered and compressible, and the reforming catalyst support is impregnated, at least in the discrete passageways with Ni and MgO, and has a number of internal slot passageways for reformable gas, the slot passageways being partly closed by a containing outer wall. 5 figs.

Singh, P.; Shockling, L.A.; George, R.A.; Basel, R.A.

1996-06-18T23:59:59.000Z

168

Hydrocarbon reforming catalyst material and configuration of the same  

DOE Patents (OSTI)

A hydrocarbon reforming catalyst material comprising a catalyst support impregnated with catalyst is provided for reforming hydrocarbon fuel gases in an electrochemical generator. Elongated electrochemical cells convert the fuel to electrical power in the presence of an oxidant, after which the spent fuel is recirculated and combined with a fresh hydrocarbon feed fuel forming the reformable gas mixture which is fed to a reforming chamber containing a reforming catalyst material, where the reforming catalyst material includes discrete passageways integrally formed along the length of the catalyst support in the direction of reformable gas flow. The spent fuel and/or combusted exhaust gases discharged from the generator chamber transfer heat to the catalyst support, which in turn transfers heat to the reformable gas and to the catalyst, preferably via a number of discrete passageways disposed adjacent one another in the reforming catalyst support. The passageways can be slots extending inwardly from an outer surface of the support body, which slots are partly defined by an exterior confining wall. According to a preferred embodiment, the catalyst support is non-rigid, porous, fibrous alumina, wherein the fibers are substantially unsintered and compressible, and the reforming catalyst support is impregnated, at least in the discrete passageways with Ni and MgO, and has a number of internal slot passageways for reformable gas, the slot passageways being partly closed by a containing outer wall.

Singh, Prabhakar (Export, PA); Shockling, Larry A. (Plum Borough, PA); George, Raymond A. (Pittsburgh, PA); Basel, Richard A. (Plub Borough, PA)

1996-01-01T23:59:59.000Z

169

Thermal conductivity of aqueous foam  

Science Conference Proceedings (OSTI)

Thermal conductivity plays an important part in the response of aqueous foams used as geothermal drilling fluids. The thermal conductivity of these foams was measured at ambient conditions using the thermal conductivity probe technique. Foam densities studied were from 0.03 to 0.2 g/cm/sup 3/, corresponding to liquid volume fractions of the same magnitude. Microscopy of the foams indicated bubble sizes in the range 50 to 300 ..mu..m for nitrogen foams, and 30 to 150 ..mu..m for helium foams. Bubble shapes were observed to be polyhedral at low foam densities and spherical at the higher densities. The measured conductivity values ranged from 0.05 to 0.12 W/m-K for the foams studied. The predicted behavior in foam conductivity caused by a change in the conductivity of the discontinuous gas phase was observed using nitrogen or helium gas in the foams. Analysis of the probe response data required an interpretation using the full intergral solution to the heat conduction equation, since the thermal capacity of the foam was small relative to the thermal mass of the probe. The measurements of the thermal conductivity of the foams were influenced by experimental effects such as the probe input power, foam drainage, and the orientation of the probe and test cell. For nitrogen foams, the thermal conductivity vs liquid volume fraction was observed to fall between predictions based on the parallel ordering and Russell models for thermal conduction in heterogeneous materials.

Drotning, W.D.; Ortega, A.; Havey, P.E.

1982-05-01T23:59:59.000Z

170

Aqueous Solvation Free Energies of Ions and Ion?Water Clusters Based on an Accurate Value for the Absolute Aqueous Solvation Free Energy of the Proton  

E-Print Network (OSTI)

TITLE RUNNING HEAD: Aqueous solvation free energies of ions and ion?water clusters Abstract: Thermochemical cycles that involve pKa, gas-phase acidities, aqueous solvation free energies of neutral species, and gas-phase clustering free energies have been used with the cluster pair approximation to determine the absolute aqueous solvation free energy of the proton. The best value obtained in this work is in good agreement with the value reported by Tissandier et al. (Tissandier, M. D.; Cowen, K. A.;

Christopher J. Cramer; Donald G. Truhlar

2006-01-01T23:59:59.000Z

171

Hydrocarbon Reformers for Fuel Cell Systems  

Science Conference Proceedings (OSTI)

Several new or emerging technologies are vying to compete in the distributed resources market; notably, fuel cells and microturbines. Fuel cells represent an idealized power generation technology with tremendous long-term promise. As a hydrogen-fueled system, however, fuel cells need either a hydrogen fuel supply infrastructure or fuel processing (reforming and clean-up) technology to convert conventional fossil fuels to a hydrogen-rich energy source. This report provides an overview of fuel processing t...

2000-11-30T23:59:59.000Z

172

The heat transfer mechanism in aqueous foam flow in a channel  

Science Conference Proceedings (OSTI)

The Heat transfer mechanism in two-phase aqueous foam flow was investigated for developing energy-efficient heat exchangers. Such heat exchangers can provide low consumption of energy resources due to enhanced heat transfer rates. An enhanced heat transfer ... Keywords: aqueous foam flow, heat exchangers, heat transfer

Irena Gabrielaitien?; Jonas Gylys; Rolandas Jonynas; Tadas Ždankus

2011-12-01T23:59:59.000Z

173

Purification of reformer streams by catalytic hydrogenation  

Science Conference Proceedings (OSTI)

Catalytic Reforming is one of the most important processes to produce high grade motor gasolines. Feedstocks are mainly gasoline and naphtha streams from the crude oil distillation boiling in the range of 212 F to 350 F. By catalytic reforming the octane number of these gasoline components is increased from 40--60 RON to 95--100 RON. Besides isomerization and dehydrocyclization reactions mainly formation of aromatics by dehydrogenation of naphthenes occur. Thus, catalytic reformers within refineries are an important source of BTX--aromatics (benzene, toluene, xylenes). Frequently, high purity aromatics are recovered from these streams using modern extractive distillation or liquid extraction processes, e.g. the Krupp-Koppers MORPHYLANE{reg_sign} process. Aromatics product specifications, notably bromine index and acid wash color, have obligated producers to utilize clay treatment to remove trace impurities of diolefins and/or olefins. The conventional clay treatment is a multiple vessel batch process which periodically requires disposal of the spent clay in a suitable environmental manner. BASF, in close cooperation with Krupp-Koppers, has developed a continuous Selective Catalytic Hydrogenation Process (SCHP) as an alternative to clay treatment which is very efficient, cost effective and environmentally compatible. In the following the main process aspects including the process scheme catalyst and operating conditions is described.

Polanek, P.J. [BASF Corp., Geismar, LA (United States); Hooper, H.M. [Krupp Wilputte Corp., Bridgeville, PA (United States); Mueller, J.; Walter, M. [BASF AG, Ludwigshafen (Germany); Emmrich, G. [Krupp Koppers GmbH, Essen (Germany)

1996-12-01T23:59:59.000Z

174

IFP solutions for revamping catalytic reforming units  

Science Conference Proceedings (OSTI)

The decision-making process for the refiner considering a revamp of a catalytic reforming unit comprises many factors. These may be grouped in two broad areas: technical and economic. This paper presents the results of a study performed by IFP that illustrates catalytic reforming unit revamp options. Three IFP processes are described and operating conditions, expected yields, and economic data are presented. The following options are discussed: base case Conventional, fixed-bed, semi-regenerative catalytic reformer; Case 1--revamp using IFP Dualforming technology; Case 2--revamp using IFP Dualforming Plus technology; and Case 3--revamp to IFP Octanizing technology. The study illustrates various options for the refiner to balance unit performance improvements with equipment, site, and economic constraints. The study was performed assuming design feedrate of 98.2 tons/hour (20,000 BPSD) in all cases. Because of the increased need for octane in many refineries, the study assumed that operating severity was set at a design value of 100 research octane number clear (RON). In all of the cases in this study, it was assumed that the existing recycle compressor was reused. Operating pressure differences between the cases is discussed separately. Also, in all cases, a booster compressor was included in order to return export hydrogen pressure to that of the conventional unit.

Gendler, J.L. [HRI, Inc., Princeton, NJ (United States); Domergue, B.; Mank, L. [Inst. Francais du Petrole, Rueil Malmaison (France)

1996-12-01T23:59:59.000Z

175

BENCH-SCALE STEAM REFORMING OF ACTUAL TANK 48H WASTE  

Science Conference Proceedings (OSTI)

Fluidized Bed Steam Reforming (FBSR) has been demonstrated to be a viable technology to remove >99% of the organics from Tank 48H simulant, to remove >99% of the nitrate/nitrite from Tank 48H simulant, and to form a solid product that is primarily carbonate based. The technology was demonstrated in October of 2006 in the Engineering Scale Test Demonstration Fluidized Bed Steam Reformer1 (ESTD FBSR) at the Hazen Research Inc. (HRI) facility in Golden, CO. The purpose of the Bench-scale Steam Reformer (BSR) testing was to demonstrate that the same reactions occur and the same product is formed when steam reforming actual radioactive Tank 48H waste. The approach used in the current study was to test the BSR with the same Tank 48H simulant and same Erwin coal as was used at the ESTD FBSR under the same operating conditions. This comparison would allow verification that the same chemical reactions occur in both the BSR and ESTD FBSR. Then, actual radioactive Tank 48H material would be steam reformed in the BSR to verify that the actual tank 48H sample reacts the same way chemically as the simulant Tank 48H material. The conclusions from the BSR study and comparison to the ESTD FBSR are the following: (1) A Bench-scale Steam Reforming (BSR) unit was successfully designed and built that: (a) Emulated the chemistry of the ESTD FBSR Denitration Mineralization Reformer (DMR) and Carbon Reduction Reformer (CRR) known collectively as the dual reformer flowsheet. (b) Measured and controlled the off-gas stream. (c) Processed real (radioactive) Tank 48H waste. (d) Met the standards and specifications for radiological testing in the Savannah River National Laboratory (SRNL) Shielded Cells Facility (SCF). (2) Three runs with radioactive Tank 48H material were performed. (3) The Tetraphenylborate (TPB) was destroyed to > 99% for all radioactive Bench-scale tests. (4) The feed nitrate/nitrite was destroyed to >99% for all radioactive BSR tests the same as the ESTD FBSR. (5) The radioactive Tank 48H DMR product was primarily made up of soluble carbonates. The three most abundant species were thermonatrite, [Na{sub 2}CO{sub 3} {center_dot} H{sub 2}O], sodium carbonate, [Na{sub 2}CO{sub 3}], and trona, [Na{sub 3}H(CO{sub 3}){sub 2} {center_dot} 2H{sub 2}O] the same as the ESTD FBSR. (6) Insoluble solids analyzed by X-Ray Diffraction (XRD) did not detect insoluble carbonate species. However, they still may be present at levels below 2 wt%, the sensitivity of the XRD methodology. Insoluble solids XRD characterization indicated that various Fe/Ni/Cr/Mn phases are present. These crystalline phases are associated with the insoluble sludge components of Tank 48H slurry and impurities in the Erwin coal ash. The percent insoluble solids, which mainly consist of un-burnt coal and coal ash, in the products were 4 to 11 wt% for the radioactive runs. (7) The Fe{sup +2}/Fe{sub total} REDOX measurements ranged from 0.58 to 1 for the three radioactive Bench-scale tests. REDOX measurements > 0.5 showed a reducing atmosphere was maintained in the DMR indicating that pyrolysis was occurring. (8) Greater than 90% of the radioactivity was captured in the product for all three runs. (9) The collective results from the FBSR simulant tests and the BSR simulant tests indicate that the same chemistry occurs in the two reactors. (10) The collective results from the BSR simulant runs and the BSR radioactive waste runs indicates that the same chemistry occurs in the simulant as in the real waste. The FBSR technology has been proven to destroy the organics and nitrates in the Tank 48H waste and form the anticipated solid carbonate phases as expected.

Burket, P; Gene Daniel, G; Charles Nash, C; Carol Jantzen, C; Michael Williams, M

2008-09-25T23:59:59.000Z

176

Methods of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts  

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

of Reforming Hydrocarbon Fuels Using of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts Contact NETL Technology Transfer Group techtransfer@netl.doe.gov May 2012 Opportunity Research is currently active on the technology "Methods of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts." The technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory. Overview This invention discloses a method to reform hydrocarbon fuels using hexa- aluminate catalysts. In general, the method successfully disrupts the forma- tion of carbon that leads to the deactivation of the catalyst, a key element in the reforming of hydrocarbon fuels. When researchers are designing catalysts to reform hydrocarbon fuels, one

177

Partial oxidation fuel reforming for automotive power systems.  

DOE Green Energy (OSTI)

For widespread use of fuel cells to power automobiles in the near future, it is necessary to convert gasoline or other transportation fuels to hydrogen on-board the vehicle. Partial oxidation reforming is particularly suited to this application as it eliminates the need for heat exchange at high temperatures. Such reformers offer rapid start and good dynamic performance. Lowering the temperature of the partial oxidation process, which requires the development of a suitable catalyst, can increase the reforming efficiency. Catalytic partial oxidation (or autothermal) reformers and non-catalytic partial oxidation reformers developed by various organizations are presently undergoing testing and demonstration. This paper summarizes the process chemistries as well as recent test data from several different reformers operating on gasoline, methanol, and other fuels.

Ahmed, S.; Chalk, S.; Krumpelt, M.; Kumar, R.; Milliken, J.

1999-09-07T23:59:59.000Z

178

Autothermal Reforming of Natural Gas to Synthesis Gas  

DOE Green Energy (OSTI)

This Project Final Report serves to document the project structure and technical results achieved during the 3-year project titled Advanced Autothermal Reformer for US Dept of Energy Office of Industrial Technology. The project was initiated in December 2001 and was completed March 2005. It was a joint effort between Sandia National Laboratories (Livermore, CA), Kellogg Brown & Root LLC (KBR) (Houston, TX) and Süd-Chemie (Louisville, KY). The purpose of the project was to develop an experimental capability that could be used to examine the propensity for soot production in an Autothermal Reformer (ATR) during the production of hydrogen-carbon monoxide synthesis gas intended for Gas-to-Liquids (GTL) applications including ammonia, methanol, and higher hydrocarbons. The project consisted of an initial phase that was focused on developing a laboratory-scale ATR capable of reproducing conditions very similar to a plant scale unit. Due to budget constraints this effort was stopped at the advanced design stages, yielding a careful and detailed design for such a system including ATR vessel design, design of ancillary feed and let down units as well as a PI&D for laboratory installation. The experimental effort was then focused on a series of measurements to evaluate rich, high-pressure burner behavior at pressures as high as 500 psi. The soot formation measurements were based on laser attenuation at a view port downstream of the burner. The results of these experiments and accompanying calculations show that soot formation is primarily dependent on oxidation stoichiometry. However, steam to carbon ratio was found to impact soot production as well as burner stability. The data also showed that raising the operating pressure while holding mass flow rates constant results in considerable soot formation at desirable feed ratios. Elementary reaction modeling designed to illuminate the role of CO2 in the burner feed showed that the conditions in the burner allow for the direct participation of CO2 in the oxidation chemistry.

Steven F. Rice; David P. Mann

2007-04-13T23:59:59.000Z

179

Aqueous complexes in f-element separation science  

SciTech Connect

Powerful and/or selective extractant molecules/sorbents are a necessary component of an efficient ion exchange or solvent extraction separation process. However, selectivity in extraction and efficiency in process design often rely on reactions occurring in or moderated by the aqueous medium. The focus of this report in on the role of the aqueous phase and reaction that occur in aquo in defining separation efficiency and metal ion selectivity. As the programmatic emphasis is on actinide solution chemistry, the separations chemistry of the f-elements will be used to illustrate the principal role of aqueous chemistry in separation science. Most of the arguments developed apply to metal ion separations chemistry and processes in general. The discussion will consider the application of aqueous complexants, incorporation of aqueous complexants into the extracted complex, and the effect of properties of the aqueous medium on separation efficiency and selectivity. Several historically important separations processes will be considered along with recent efforts in these laboratories to design and characterize new water soluble complexants for improved f-element separations.

Nash, K.L. [Argonne National Lab., IL (United States). Chemistry Div.

1997-11-01T23:59:59.000Z

180

Will electricity market reform likely reduce retail rates?  

Science Conference Proceedings (OSTI)

To win public support, proponents for electricity market reform to introduce competition often promise that the post-reform retail rates will be lower than the average embedded cost rates that would have prevailed under the status quo of a regulated monopoly. A simple economic analysis shows that such a promise is unlikely to occur without the critical assumption that the post-reform market has marginal costs below average costs. (author)

Woo, C.K.; Zarnikau, Jay

2009-03-15T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Non-aqueous solution preparation of doped and undoped lixmnyoz  

DOE Patents (OSTI)

A method for generation of phase-pure doped and undoped Li.sub.x Mn.sub.y O.sub.z precursors. The method of this invention uses organic solutions instead of aqueous solutions or nonsolution ball milling of dry powders to produce phase-pure precursors. These precursors can be used as cathodes for lithium-polymer electrolyte batteries. Dopants may be homogeneously incorporated to alter the characteristics of the powder.

Boyle, Timothy J. (5801 Eubank, N.E., Apt. #97, Albuquerque, NM 87111); Voigt, James A. (187 Aaramar La., Corrales, NM 87048)

1997-01-01T23:59:59.000Z

182

Microsoft Word - Poster Abstract_2010_NETL_ Oxide-Based Reforming...  

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

Structured Oxide - Based Reforming Catalyst Development U.S. Dept of Energy, National Energy Technology Laboratory, Morgantown, WV 26507 Dushyant Shekhawat Dushyant.Shekhawat@NETL....

183

Compatibility of selected ceramics with steam-methane reformer environments  

DOE Green Energy (OSTI)

Conventional steam reforming of methane to synthesis gas (CO and H{sub 2}) hasa conversion efficiency of about 85%. Replacement of metal tubes in the reformer with ceramic tubes offers the potential for operation at temperatures high enough to increase the efficiency to 98-99%. However, the two candidate ceramic materials being given strongest consideration, sintered alpha Si carbide and Si carbide particulate-strengthened alumina, have been shown to react with components of the reformer environment. Extent of degradation as a function of steam partial pressure and exposure time has been studied, and results suggest limits under which these structural ceramics can be used in advanced steam-methane reformers.

Keiser, J.R.; Howell, M. [Oak Ridge National Lab., TN (United States); Williams, J.J.; Rosenberg, R.A. [Stone and Webster Engineering Corp., Boston, MA (United States)

1996-04-01T23:59:59.000Z

184

Thermodynamic and Experimental Study on the Steam Reforming ...  

Science Conference Proceedings (OSTI)

For improving hydrogen yield, a new system for steam reforming of bio-oil with site ... Kinetic Modeling Study of Oxy-methane Combustion at Ordinary Pressure.

185

Women and the reform of the welfare system: An introduction  

Science Conference Proceedings (OSTI)

This special issue of Gender Issues, one of a three-part series, examines the welfare reform measures initiated a decade ago and their consequences for ...

186

Kinetics of Supercritical Water Reformation of Ethanol to H  

Science Conference Proceedings (OSTI)

Sep 16, 2007 ... Description Kinetics of the supercritical water reformation of ethanol was experimentally studied in a tubular reactor made of Inconel 625 alloy.

187

Catalytic reforming boosts octane for gasoline blending - Today in ...  

U.S. Energy Information Administration (EIA)

Because reformate contains significant amounts of benzene, toluene, and xylene, it also is an important source of feedstock for the petrochemical industry.

188

New process model proves accurate in tests on catalytic reformer  

Science Conference Proceedings (OSTI)

A mathematical model has been devised to represent the process that takes place in a fixed-bed, tubular, adiabatic catalytic reforming reactor. Since its development, the model has been applied to the simulation of a commercial semiregenerative reformer. The development of mass and energy balances for this reformer led to a model that predicts both concentration and temperature profiles along the reactor. A comparison of the model's results with experimental data illustrates its accuracy at predicting product profiles. Simple steps show how the model can be applied to simulate any fixed-bed catalytic reformer.

Aguilar-Rodriguez, E.; Ancheyta-Juarez, J. (Inst. Mexicano del Petroleo, Mexico City (Mexico))

1994-07-25T23:59:59.000Z

189

Analysis of Chemically Reacting Gas Flow and Heat Transfer in Methane Reforming Processes  

Science Conference Proceedings (OSTI)

This paper presents simulation and analysis of gas flow and heat transfer affected by chemical reactions relating to steam reforming of methane in a compact reformer. The reformer conditions such as the combined thermal boundary conditions on solid walls, ...

Guogang Yang; Danting Yue; Xinrong Lv; Jinliang Yuan

2009-10-01T23:59:59.000Z

190

Process for removal of polynuclear aromatics from a hydrocarbon in an endothermic reformer reaction system  

Science Conference Proceedings (OSTI)

A process is described for reforming a hydrocarbon in a multi-stage endothermic reforming series of catalytic reforming reactors where the hydrocarbon is passed through the series of catalytic reforming reactors to form a reformate. The hydrocarbon is heated prior to entry to the next catalytic reforming reactor in the series, which process comprises contact of the hydrocarbon intermediate from the series of catalytic reforming reactors containing reforming catalyst with a polynuclear aromatic adsorbent to adsorb at least a portion of the polynuclear aromatic content from the hydrocarbon prior to entry to each of the next catalytic reforming reactor in the series and recovering a reformate from the last catalytic reforming reactor in the series, the recovered reformate having a reduced content of polynuclear aromatics.

Ngan, D.Y.

1989-02-14T23:59:59.000Z

191

RADIOACTIVE DEMONSTRATIONS OF FLUIDIZED BED STEAM REFORMING (FBSR) WITH HANFORD LOW ACTIVITY WASTES  

SciTech Connect

Several supplemental technologies for treating and immobilizing Hanford low activity waste (LAW) are being evaluated. One immobilization technology being considered is Fluidized Bed Steam Reforming (FBSR) which offers a low temperature (700-750°C) continuous method by which wastes high in organics, nitrates, sulfates/sulfides, or other aqueous components may be processed into a crystalline ceramic (mineral) waste form. The granular waste form produced by co-processing the waste with kaolin clay has been shown to be as durable as LAW glass. The FBSR granular product will be monolithed into a final waste form. The granular component is composed of insoluble sodium aluminosilicate (NAS) feldspathoid minerals such as sodalite. Production of the FBSR mineral product has been demonstrated both at the industrial, engineering, pilot, and laboratory scales on simulants. Radioactive testing at SRNL commenced in late 2010 to demonstrate the technology on radioactive LAW streams which is the focus of this study.

Jantzen, C.; Crawford, C.; Burket, P.; Bannochie, C.; Daniel, G.; Nash, C.; Cozzi, A.; Herman, C.

2012-10-22T23:59:59.000Z

192

Radioactive Demonstrations Of Fluidized Bed Steam Reforming (FBSR) With Hanford Low Activity Wastes  

Science Conference Proceedings (OSTI)

Several supplemental technologies for treating and immobilizing Hanford low activity waste (LAW) are being evaluated. One immobilization technology being considered is Fluidized Bed Steam Reforming (FBSR) which offers a low temperature (700-750?C) continuous method by which wastes high in organics, nitrates, sulfates/sulfides, or other aqueous components may be processed into a crystalline ceramic (mineral) waste form. The granular waste form produced by co-processing the waste with kaolin clay has been shown to be as durable as LAW glass. The FBSR granular product will be monolithed into a final waste form. The granular component is composed of insoluble sodium aluminosilicate (NAS) feldspathoid minerals such as sodalite. Production of the FBSR mineral product has been demonstrated both at the industrial, engineering, pilot, and laboratory scales on simulants. Radioactive testing at SRNL commenced in late 2010 to demonstrate the technology on radioactive LAW streams which is the focus of this study.

Jantzen, C. M.; Crawford, C. L.; Burket, P. R.; Bannochie, C. J.; Daniel, W. G.; Nash, C. A.; Cozzi, A. D.; Herman, C. C.

2012-10-22T23:59:59.000Z

193

Process for separating and recovering an anionic dye from an aqueous solution  

DOE Patents (OSTI)

A solid/liquid phase process for the separation and recovery of an anionic dye from an aqueous solution is disclosed. The solid phase comprises separation particles having surface-bonded poly(ethylene glycol) groups, whereas the aqueous solution from which the anionic dye molecules are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved lyotropic salt. After contact between the aqueous solution and separation particles, the anionic dye is bound to the particles. The bound anionic dye molecules are freed from the separation particles by contacting the anionic dye-bound particles with an aqueous solution that does not contain a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved lyotropic salt to form an aqueous anionic dye solution whose anionic dye concentration is preferably higher than that of the initial dye-containing solution.

Rogers, Robin (DeKalb, IL); Horwitz, E. Philip (Naperville, IL); Bond, Andrew H. (Tallahassee, FL)

1998-01-01T23:59:59.000Z

194

Process for separating and recovering an anionic dye from an aqueous solution  

DOE Patents (OSTI)

A solid/liquid phase process for the separation and recovery of an anionic dye from an aqueous solution is disclosed. The solid phase comprises separation particles having surface-bonded poly(ethylene glycol) groups, whereas the aqueous solution from which the anionic dye molecules are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved lyotropic salt. After contact between the aqueous solution and separation particles, the anionic dye is bound to the particles. The bound anionic dye molecules are freed from the separation particles by contacting the anionic dye-bound particles with an aqueous solution that does not contain a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved lyotropic salt to form an aqueous anionic dye solution whose anionic dye concentration is preferably higher than that of the initial dye-containing solution. 7 figs.

Rogers, R.; Horwitz, E.P.; Bond, A.H.

1998-01-13T23:59:59.000Z

195

Interim report:feasibility of microscale glucose reforming for renewable hydrogen.  

DOE Green Energy (OSTI)

Micro-scale aqueous steam reforming of glucose is suggested as a novel method of H{sub 2} production for micro fuel cells. Compact fuel cell systems are a viable alternative to batteries as a portable electrical power source. Compared with conventional lithium polymer batteries, hydrocarbon powered fuel cells are smaller, weigh less, and have a much higher energy density. The goal of this project is to develop a hydrocarbon powered microfuel processor capable of driving an existing microfuel cell, and this interim report provides a summary of the engineering information for microscale reforming of carbohydrates and the summarizes the work completed as of September 2006. Work on this program will continue. Gas analysis of the gas evolved from glucose breakdown using a quadrupole mass spectrometer is now possible due do significant modifications to the vacuum chamber and to the mass spectrometer electronics. Effective adhesion of Pt/Al{sub 2}O{sub 3} to 316SS microstructured catalyst plates is still under investigation. Electrophoretic and dip coat methods of catalyst deposition have produced coatings with poor adhesion and limited available Pt surface area.

Norman, Kirsten (New Mexico Institute of Mining and Technology, Socorro, NM)

2007-03-01T23:59:59.000Z

196

NEPA Contracting Reform Guidance (December 1996)  

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

defining early what contractors should accomplish defining early what contractors should accomplish < establishing contracts ahead of time < minimizing cost while maintaining quality by * maximizing competition and use of incentives * using past performance information in awarding work * managing the NEPA process as a project This guidance provides: < model statements of work < information on contract types and incentives < direction on effective NEPA contract management by the NEPA Document Manager < a system for measuring NEPA process costs < NEPA contractor evaluation procedures < details on the DOE NEPA Web site U.S. Department of Energy, Office of NEPA Policy and Assistance, December 1996 NEPA CONTRACTING REFORM GUIDANCE Table of Contents 1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . .

197

Noble metal alkaline zeolites for catalytic reforming  

Science Conference Proceedings (OSTI)

This patent describes a method for producing a noble-metal containing zeolite suitable for catalytic reforming contacting a zeolite selected from alkaline faujasites and L zeolites and zeolites and zeolites isostructural thereto, with a noble-metal compound selected from Pt(acetylacetonate){sub 2} and Pd(acetylacetonate){sub 2} for a effective amount of time to incorporate Pt and/or Pd into the pore surface regions of the zeolite, but not to disperse the Pt and/or Pd throughout the entire zeolite; and calcining the so treated zeolite at a temperature from about 250 {degrees} C, to about 600 {degrees} C for an effective amount of time.

Schweizer, A.E.

1991-02-12T23:59:59.000Z

198

Simulator for Subsurface Transport Over Multiple Phases (STOMP ...  

Experimentally verified and supported modeling of dense and light non-aqueous phase liquids ... CO2 exchange technologies for production of natural ga ...

199

Computational Model For Transient And Steady State Analysis Of A 1-dimensional Auto-thermal Reformer.  

E-Print Network (OSTI)

??Kim, Daejong This study presents a 1-dimensional mathematical model of steam reformer to be used with high temperature solid oxide fuel cell (SOFC). Steam reforming… (more)

Honavara-Prasad, Srikanth

2011-01-01T23:59:59.000Z

200

Process for recovering chaotropic anions from an aqueous solution also containing other ions  

DOE Patents (OSTI)

A solid/liquid process for the separation and recovery of chaotropic anions from an aqueous solution is disclosed. The solid support comprises separation particles having surface-bonded poly(ethylene glycol) groups, whereas the aqueous solution from which the chaotropic anions are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved salt (lyotrope). A solid/liquid phase admixture of separation particles containing bound chaotropic anions in such an aqueous solution is also contemplated, as is a chromatography apparatus containing that solid/liquid phase admixture. 19 figs.

Rogers, R.; Horwitz, E.P.; Bond, A.H.

1999-03-30T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Process for recovering chaotropic anions from an aqueous solution also containing other ions  

DOE Patents (OSTI)

A solid/liquid process for the separation and recovery of chaotropic anions from an aqueous solution is disclosed. The solid support comprises separation particles having surface-bonded poly(ethylene glycol) groups, whereas the aqueous solution from which the chaotropic anions are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved salt (lyotrope). A solid/liquid phase admixture of separation particles containing bound chaotropic anions in such an aqueous solution is also contemplated, as is a chromatography apparatus containing that solid/liquid phase admixture.

Rogers, Robin (DeKalb, IL); Horwitz, E. Philip (Naperville, IL); Bond, Andrew H. (Tallahassee, FL)

1999-01-01T23:59:59.000Z

202

Stabilization of Nickel Metal Catalysts for Aqueous ...  

Biomass and Biofuels Stabilization of Nickel Metal Catalysts for Aqueous Processing Systems Pacific Northwest National Laboratory.

203

Sequencing in telecommunications reform: A review of the Turkish case  

Science Conference Proceedings (OSTI)

This paper reviews the Turkish case of telecommunications reform with reference to the evidence from the sequencing literature. Turkey's progress is in line with the proper sequencing of reform suggested by the literature. Accordingly, Turkey has pursued ... Keywords: Industrial policy, Privatisation, Regulation, Telecommunications

Necmiddin Bagdadioglu; Murat Cetinkaya

2010-12-01T23:59:59.000Z

204

Steam reforming of fuel to hydrogen in fuel cells  

DOE Patents (OSTI)

A fuel cell capable of utilizing a hydrocarbon such as methane as fuel and having an internal dual catalyst system within the anode zone, the dual catalyst system including an anode catalyst supporting and in heat conducting relationship with a reforming catalyst with heat for the reforming reaction being supplied by the reaction at the anode catalyst.

Fraioli, Anthony V. (Hawthorne Woods, IL); Young, John E. (Woodridge, IL)

1984-01-01T23:59:59.000Z

205

Steam reforming of fuel to hydrogen in fuel cell  

DOE Patents (OSTI)

A fuel cell is described capable of utilizing a hydrocarbon such as methane as fuel and having an internal dual catalyst system within the anode zone, the dual catalyst system including an anode catalyst supporting and in heat conducting relationship with a reforming catalyst with heat for the reforming reaction being supplied by the reaction at the anode catalyst.

Young, J.E.; Fraioli, A.V.

1983-07-13T23:59:59.000Z

206

Electricity Reform Abroad and U.S. Investment  

Reports and Publications (EIA)

Reviews and analyzes the recent electricity reforms in Argentina, Australia, and the United Kingdom in an attempt to better understand how different models of privatization and reform have worked in practice. This report also analyzes the motivations of the U.S. companies who have invested in the electricity industries of Argentina, Australia, and the UK.

Kevin Lillis

1997-09-01T23:59:59.000Z

207

Reforming naphtha with boron-containing large-pore zeolites  

Science Conference Proceedings (OSTI)

This patent describes a catalytic reforming process. It comprises contacting a hydrocarbonaceous feedstream under catalytic reforming conditions with a composition comprising larger-pore borosilicate zeolites having a pore size greater than 6 and less than 8 angstroms containing less that 1000 parts per million aluminum.

Zones, S.I.; Holtermann, D.L.; Rainis, A.

1992-05-19T23:59:59.000Z

208

Separation and concentration of lower alcohols from dilute aqueous solutions  

DOE Patents (OSTI)

A process for producing, from a dilute aqueous solution of a lower (C.sub.1 -C.sub.5) alcohol, a concentrated liquid solution of the alcohol in an aromatic organic solvent is disclosed. Most of the water is removed from the dilute aqueous solution of alcohol by chilling sufficiently to form ice crystals. Simultaneously, the remaining liquid is extracted at substantially the same low temperature with a liquid organic solvent that is substantially immiscible in aqueous liquids and has an affinity for the alcohol at that temperature, causing the alcohol to transfer to the organic phase. After separating the organic liquid from the ice crystals, the organic liquid can be distilled to enrich the concentration of alcohol therein. Ethanol so separated from water and concentrated in an organic solvent such as toluene is useful as an anti-knock additive for gasoline.

Moore, Raymond H. (Richland, WA); Eakin, David E. (Kennewick, WA); Baker, Eddie G. (Richland, WA); Hallen, Richard T. (Richland, WA)

1991-01-01T23:59:59.000Z

209

Technology Maturation Plan (TMP) Fluidized Bed Steam Reforming (FBSR)  

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

Maturation Plan (TMP) Fluidized Bed Steam Reforming Maturation Plan (TMP) Fluidized Bed Steam Reforming (FBSR) Technology for Tank 48H Treatment Project (TTP) Technology Maturation Plan (TMP) Fluidized Bed Steam Reforming (FBSR) Technology for Tank 48H Treatment Project (TTP) This assessment determines the technology maturity level of the candidate Tank 48H treatment technologies that are being considered for implementation at DOE's SRS - specifically Fluidized Bed Steam Reformer System. Technology Maturation Plan (TMP) Fluidized Bed Steam Reforming (FBSR) Technology for Tank 48H Treatment Project (TTP) More Documents & Publications Technology Maturation Plan (TMP) Wet Air Oxidation (WAO) Technology for Tank 48H Treatment Project (TTP) SRS Tank 48H Waste Treatment Project Technology Readiness Assessment

210

Reforming Power Markets in Developing Countries | Open Energy Information  

Open Energy Info (EERE)

Reforming Power Markets in Developing Countries Reforming Power Markets in Developing Countries Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Reforming Power Markets in Developing Countries Agency/Company /Organization: World Bank Sector: Energy Focus Area: Conventional Energy, Renewable Energy Topics: Policies/deployment programs Resource Type: Publications, Lessons learned/best practices Website: siteresources.worldbank.org/INTENERGY/Resources/Energy19.pdf References: Reforming Power Markets in Developing Countries [1] Summary "This paper complements the World Bank's Operational Guidance Note by compiling lessons of this experience that help in applying the Note's guidance. These lessons are taken from the rapidly growing literature on power market reform in developing countries. They cover the range of issues

211

Electricity Reform in Chile. Lessons for Developing Countries  

E-Print Network (OSTI)

Chile was the first country in the world to implement a comprehensive reform of its electricity sector in the recent period. Among developing countries only Argentina has had a comparably comprehensive and successful reform. This paper traces the history of the Chilean reform, which began in 1982, and assesses its progress and its lessons. We conclude that the reform has been very successful. We suggest lessons for the generation, transmission and distribution sectors, as well as the economic regulation of electricity and the general institutional environment favourable to reform. We note that while the initial market structure and regulatory arrangements did give rise to certain problems, the overall experience argues strongly for the private ownership and operation of the electricity industry.

Michael Pollitt

2004-01-01T23:59:59.000Z

212

Removal of sulfur from recycle gas streams in catalytic reforming  

Science Conference Proceedings (OSTI)

This patent describes improvement in a process for catalytically reforming a hydrocarbonaceous feedstock boiling in the gasoline range, wherein the reforming is conducted in the presence of hydrogen in a reforming process unit under reforming conditions, the process unit comprised of serially connected reactors, each of the reactors containing a reforming catalyst, and which process unit also includes a regeneration circuit for regenerating the catalyst after it becomes coked, the regeneration comprising treatment with a sulfur containing gas, and which process unit also includes a gas/liquid separator wherein a portion of the gas is recycled and the remaining portion is collected as make-gas. The improvement comprises using a sulfur trap, containing a catalyst comprised of about 10 to about 70 wt. % nickel dispersed on a support, between the gas/liquid separator and the first reactor.

Boyle, J.P.

1991-08-27T23:59:59.000Z

213

Advances in the chemistry of catalytic reforming of naphtha  

Science Conference Proceedings (OSTI)

Catalytic reforming of naphtha remains the key process for production of high octane gasoline and aromatics (BTX) which are used as petrochemicals feedstocks. The increased demand for these products has led refiners to investigate ways for improving the performance of the reforming process and its catalysts. Moreover, in order to comply with environmental restrictions, the reduction in lead content would require further increase in the reformate octane number. In response to these requirements, refiners and catalyst manufacturers are examining the role of the catalysts in improving the selectivity to aromatics and in octane enhancement. By understanding the chemistry and the mechanism of the reforming process, higher performance catalysts with longer life on stream and lower cost can be developed. This review covers recent developments in reforming catalysts, process reaction chemistry and mechanism. It also highlights prospective areas of research.

Anabtawi, J.A.; Redwan, D.S.; Al-Jarallah, A.M.; Aitani, A.M. (Petroleum and Gas Technology Div., Research Inst., King Fahd Univ. of Petroleum and Minerals, Dhahran (SA))

1991-01-01T23:59:59.000Z

214

Regulatory and Financial Reform of Federal Research Policy: Recommendations  

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

and Financial Reform of Federal Research Policy: and Financial Reform of Federal Research Policy: Recommendations to the NRC Committee on Research Universities Regulatory and Financial Reform of Federal Research Policy: Recommendations to the NRC Committee on Research Universities At the request of the National Research Council (NRC) Committee on Research Universities, the Council on Governmental Relations (COGR), the Association of American Universities (AAU), and the Association of Public and Land-grant Universities (APLU) have assembled a set of ten recommendations for regulatory reform that would improve research universities' ability to carry out their missions without requiring a significant financial investment by the Federal government. Regulatory and Financial Reform of Federal Research Policy: Recommendations

215

Process Reform, Security and Suitability - December 17, 2008 | Department  

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

Process Reform, Security and Suitability - December 17, 2008 Process Reform, Security and Suitability - December 17, 2008 Process Reform, Security and Suitability - December 17, 2008 December 17, 2008 This is to report on the progress made to improve the timeliness and effectiveness of our hiring and clearing decisions and the specific plan to reform the process further, in accordance with our initial proposals made in April ofthis year. In response to significant, continuing security clearance timeliness concerns, Congress called for improvements and established specific timeliness goals as part of the Intelligence Reform and Terrorism Prevention Act of 2004 (IRTPA). Since the enactment of IRTPA, average timeliness for 90 percent of all clearance determinations reported has been substantially improved, from 265 days (in 2005) to 82 days (4th Quarter,

216

TWR Bench-Scale Steam Reforming Demonstration  

SciTech Connect

The Idaho Nuclear Technology and Engineering Center (INTEC) was home to nuclear fuel reprocessing activities for decades at the Idaho National Engineering and Environmental Laboratory. As a result of the reprocessing activities, INTEC has accumulated approximately one million gallons of acidic, radioactive, sodium-bearing waste (SBW). The purpose of this demonstration was to investigate a reforming technology, offered by ThermoChem Waste Remediation, LLC, (TWR) for treatment of SBW into a ''road ready'' waste form that would meet the waste acceptance criteria for the Waste Isolation Pilot Plant (WIPP). TWR is the licensee of Manufacturing Technology Conservation International (MTCI) steam-reforming technology in the field of radioactive waste treatment. A non-radioactive simulated SBW was used based on the known composition of waste tank WM-180 at INTEC. Rhenium was included as a non-radioactive surrogate for technetium. Data was collected to determine the nature and characteristics of the product, the operability of the technology, the composition of the off-gases, and the fate of key radionuclides (cesium and technetium) and volatile mercury compounds. The product contained a low fraction of elemental carbon residues in the cyclone and filter vessel catches. Mercury was quantitatively stripped from the product but cesium, rhenium (Tc surrogate), and the heavy metals were retained. Nitrate residues were about 400 ppm in the product and NOx destruction exceeded 86%. The demonstration was successful.

Marshall, D.W.; Soelberg, N.R.

2003-05-21T23:59:59.000Z

217

TWR Bench-Scale Steam Reforming Demonstration  

SciTech Connect

The Idaho Nuclear Technology and Engineering Center (INTEC) was home to nuclear fuel reprocessing activities for decades at the Idaho National Engineering and Environmental Laboratory. As a result of the reprocessing activities, INTEC has accumulated approximately one million gallons of acidic, radioactive, sodium-bearing waste (SBW). The purpose of this demonstration was to investigate a reforming technology, offered by ThermoChem Waste Remediation, LLC, (TWR) for treatment of SBW into a "road ready" waste form that would meet the waste acceptance criteria for the Waste Isolation Pilot Plant (WIPP). TWR is the licensee of Manufacturing Technology Conservation International (MTCI) steam-reforming technology in the field of radioactive waste treatment. A non-radioactive simulated SBW was used based on the known composition of waste tank WM-180 at INTEC. Rhenium was included as a non-radioactive surrogate for technetium. Data was collected to determine the nature and characteristics of the product, the operability of the technology, the composition of the off-gases, and the fate of key radionuclides (cesium and technetium) and volatile mercury compounds. The product contained a low fraction of elemental carbon residues in the cyclone and filter vessel catches. Mercury was quantitatively stripped from the product but cesium, rhenium (Tc surrogate), and the heavy metals were retained. Nitrate residues were about 400 ppm in the product and NOx destruction exceeded 86%. The demonstration was successful.

D. W. Marshall; N. R. Soelberg

2003-05-01T23:59:59.000Z

218

Home Production and Social Security Reform ?  

E-Print Network (OSTI)

This paper incorporates home production into a dynamic general equilibrium model of overlapping generations with endogenous retirement to study Social Security reforms. As such, the model differentiates both consumption goods and labor effort according to their respective roles in home production and market activities. Using a calibrated model, we conduct a policy experiment where we eliminate the current pay-as-you-go Social Security System and study the steady state impact. We find that the experiment has important implications for labor supply as well as consumption decisions and that these decisions are influenced by the presence of a home production technology. Comparing our economy to a onegood economy without home production, the welfare gains of eliminating Social Security are magnified significantly. We further demonstrate that the qualitative results hold with the less extreme policy reform where we delay the eligible Social Security benefits claimant age by four years. These policy analyses suggest the importance of modeling home production and distinguishing between both time

Michael Dotsey; Wenli Li; Fang Yang

2012-01-01T23:59:59.000Z

219

Hiring Reform Memoranda and Action Plan  

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

0585 0585 October 7, 2010 MEMORANDUM FOR HEADS OF ALL DEPARTMENTAL ELEMEI\lTS HUMAI\l RESOURCES DIRECTORS FROM: MICHAELC. KANE~~~ CHIEF HUMAN CAPITAL ~ c· SUBJECT: IMPROVING DOE RECRUITMENT AND HIRING PROCESSES This is a follow-up to the Deputy Secretary's Memorandum dated October 6, 2010 where he communicated the need to implement the Action Plan developed to improve the recruitment and hiring processes throughout the Department. One of the central tenets of the President's reform efforts and the Department's Action Plan is management's commitment and attention to an efficient and effective hiring process that yields quality employees. This was clearly articulated in the President's Memorandum dated May 11, 2010 where he directed that management be held accountable through the performance evaluation system for their role

220

Evaluation of Partial Oxidation Reformer Emissions  

DOE Green Energy (OSTI)

In this study, a gasoline fuel processor and an ethanol fuel processor were operated under conditions simulating both startup and normal operation. Emissions were measured before and after the AGB in order to quantify the effectiveness of the burner catalyst in controlling emissions. The emissions sampling system includes CEM for O2, CO2, CO, NOx, and THC. Also, integrated gas samples are collected in evacuated canisters for hydrocarbon speciation analysis via GC. This analysis yields the concentrations of the hydrocarbon species required for the California NMOG calculation. The PM concentration in the anode burner exhaust was measured through the placement of a filter in the exhaust stream. The emissions from vehicles with fully developed on board reformer systems were estimated.

Unnasch, Stefan; Fable, Scott; Waterland, Larry

2006-01-06T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Clean gasoline reforming with superacid catalysts  

DOE Green Energy (OSTI)

The objectives of this project are to: (a) determine if a coal-derived naphtha can be hydrotreated to produce a product with a sufficiently low heteroatom content that can be used for reforming, (b) identify hydrocarbon compounds in the naphtha with concentrations greater than 0.5 wt %, (c) develop a Pt/Al[sub 2]O[sub 3] heavily chlorided catalyst and determine the activity, selectivity and deactivation of this catalyst using model compounds and the hydrotreated naphtha, and (d) develop both a sulfated Pt/ZrO[sub 2] and Fe/Mn/ZrO[sub 2] catalyst formulations and determine the activity, selectivity and deactivation of these catalysts using model compounds and d warranted, the hydrotreated naphtha.

Davis, B.H.

1992-01-01T23:59:59.000Z

222

SOLAR UPGRADE OF METHANE USING DRY REFORMING IN DIRECT CONTACT BUBBLE REACTOR  

E-Print Network (OSTI)

SOLAR UPGRADE OF METHANE USING DRY REFORMING IN DIRECT CONTACT BUBBLE REACTOR Khalid Al-Ali 1 process of a solar reformer of dry methane reforming was proposed to operate in a temperature range of 600:2:2 fulfills our requirements for the direct contact bubble reactor of the solar reformer, in which a CO2-rich

Recanati, Catherine

223

Thermally efficient melting and fuel reforming for glass making  

DOE Patents (OSTI)

An integrated process is described for utilizing waste heat from a glass making furnace. The hot off-gas from the furnace is initially partially cooled, then fed to a reformer. In the reformer, the partially cooled off-gas is further cooled against a hydrocarbon which is thus reformed into a synthesis gas, which is then fed into the glass making furnace as a fuel. The further cooled off-gas is then recycled back to absorb the heat from the hot off-gas to perform the initial cooling. 2 figures.

Chen, M.S.; Painter, C.F.; Pastore, S.P.; Roth, G.S.; Winchester, D.C.

1991-10-15T23:59:59.000Z

224

RADIOACTIVE DEMONSTRATIONS OF FLUIDIZED BED STEAM REFORMING AS A SUPPLEMENTARY TREATMENT FOR HANFORD'S LOW ACTIVITY WASTE AND SECONDARY WASTES  

SciTech Connect

The U.S. Department of Energy's Office of River Protection (ORP) is responsible for the retrieval, treatment, immobilization, and disposal of Hanford's tank waste. Currently there are approximately 56 million gallons of highly radioactive mixed wastes awaiting treatment. A key aspect of the River Protection Project (RPP) cleanup mission is to construct and operate the Waste Treatment and Immobilization Plant (WTP). The WTP will separate the tank waste into high-level and low-activity waste (LAW) fractions, both of which will subsequently be vitrified. The projected throughput capacity of the WTP LAW Vitrification Facility is insufficient to complete the RPP mission in the time frame required by the Hanford Federal Facility Agreement and Consent Order, also known as the Tri-Party Agreement (TPA), i.e. December 31, 2047. Therefore, Supplemental Treatment is required both to meet the TPA treatment requirements as well as to more cost effectively complete the tank waste treatment mission. The Supplemental Treatment chosen will immobilize that portion of the retrieved LAW that is not sent to the WTP's LAW Vitrification facility into a solidified waste form. The solidified waste will then be disposed on the Hanford site in the Integrated Disposal Facility (IDF). In addition, the WTP LAW vitrification facility off-gas condensate known as WTP Secondary Waste (WTP-SW) will be generated and enriched in volatile components such as Cs-137, I-129, Tc-99, Cl, F, and SO4 that volatilize at the vitrification temperature of 1150 C in the absence of a continuous cold cap. The current waste disposal path for the WTP-SW is to recycle it to the supplemental LAW treatment to avoid a large steady state accumulation in the pretreatment-vitrification loop. Fluidized Bed Steam Reforming (FBSR) offers a moderate temperature (700-750 C) continuous method by which LAW and/or WTP-SW wastes can be processed irrespective of whether they contain organics, nitrates, sulfates/sulfides, chlorides, fluorides, volatile radionuclides or other aqueous components. The FBSR technology can process these wastes into a crystalline ceramic (mineral) waste form. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be as durable as LAW glass. Monolithing of the granular FBSR product is being investigated to prevent dispersion during transport or burial/storage but is not necessary for performance. A Benchscale Steam Reformer (BSR) was designed and constructed at the Savannah River National Laboratory (SRNL) to treat actual radioactive wastes to confirm the findings of the non-radioactive FBSR pilot scale tests and to qualify the waste form for applications at Hanford. Radioactive testing commenced in 2010 with a demonstration of Hanford's WTP-SW where Savannah River Site (SRS) High Level Waste (HLW) secondary waste from the Defense Waste Processing Facility (DWPF) was shimmed with a mixture of I-125/129 and Tc-99 to chemically resemble WTP-SW. Ninety six grams of radioactive product were made for testing. The second campaign commenced using SRS LAW chemically trimmed to look like Hanford's LAW. Six hundred grams of radioactive product were made for extensive testing and comparison to the non-radioactive pilot scale tests. The same mineral phases were found in the radioactive and non-radioactive testing.

Jantzen, C.; Crawford, C.; Cozzi, A.; Bannochie, C.; Burket, P.; Daniel, G.

2011-02-24T23:59:59.000Z

225

Page iManaging Investment Climate Reforms: Viet Nam Case Study Table of Contents  

E-Print Network (OSTI)

The primary objective of this study is to learn about Viet Nam’s experience with reforms aimed at facilitating private entry into businesses, and in particular to understand how the reform process itself was managed, what have been the results or outcomes of the reforms, and what lessons have been learned. The focus of the analysis is the Enterprise Law reform episode and related reforms to promote domestic private sector development in Viet Nam.

Viet Nam; Raymond Mallon; Economic Consultant

2004-01-01T23:59:59.000Z

226

Reforming The Government Hiring Process | Department of Energy  

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

Reforming The Government Hiring Process Reforming The Government Hiring Process Reforming The Government Hiring Process November 19, 2010 - 10:10am Addthis Rita Franklin Rita Franklin Deputy Chief Human Capital Officer What does this mean for me? In the video, Deputy Secretary Daniel Poneman highlights the Department's "Time-to-Hire Tracking and Reporting System." The Department reduced the end-to-end time-to-hire from 174 calendar days for Fiscal Year FY 2009 to 100 days for FY 2010. Wednesday, Deputy Secretary Daniel Poneman and I met with leaders from across the Federal government to share our progress in the our Department's hiring reform efforts. Six months ago, President Obama called on all executive departments and federal agencies to overhaul the way we recruit and hire. As the President

227

Intelligence Reform and Terroroism Prevention Act - December 17, 2004 |  

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

Intelligence Reform and Terroroism Prevention Act - December 17, Intelligence Reform and Terroroism Prevention Act - December 17, 2004 Intelligence Reform and Terroroism Prevention Act - December 17, 2004 December 17, 2004 To reform the intelligence community and the intelligence and intelligence-related activities of the United States Government, and for other purposes. SEC. 102. (a) DIRECTOR OF NATIONAL INTELLIGENCE.-(1) There is a Director of National Intelligence who shall be appointed by the President, by and with the advice and consent of the Senate. Any individual nominated for appointment as Director of National Intelligence shall have extensive national security expertise. ''(2) The Director of National Intelligence shall not be located within the Executive Office of the President. ''(b) PRINCIPAL RESPONSIBILITY.-Subject to the authority, direction,

228

Reforming The Government Hiring Process | Department of Energy  

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

Reforming The Government Hiring Process Reforming The Government Hiring Process Reforming The Government Hiring Process November 19, 2010 - 10:10am Addthis Rita Franklin Rita Franklin Deputy Chief Human Capital Officer What does this mean for me? In the video, Deputy Secretary Daniel Poneman highlights the Department's "Time-to-Hire Tracking and Reporting System." The Department reduced the end-to-end time-to-hire from 174 calendar days for Fiscal Year FY 2009 to 100 days for FY 2010. Wednesday, Deputy Secretary Daniel Poneman and I met with leaders from across the Federal government to share our progress in the our Department's hiring reform efforts. Six months ago, President Obama called on all executive departments and federal agencies to overhaul the way we recruit and hire. As the President

229

Chemical simulation of hydrogen generation in a plasma fuel reformer  

E-Print Network (OSTI)

A model for a plasma fuel reformer or plasmatron has been developed. The model was based in a series of experiments realized at the Plasma Science and Fusion Center with such a plasmatron. The device is set up to produce ...

Margarit Bel, Nuria, 1977-

2004-01-01T23:59:59.000Z

230

The stability of coerced economic reform : the case of IPR  

E-Print Network (OSTI)

Theories in international relations posit, and empirical evidence has verified, that unwilling states can be compelled by another state or by an international institution to enact domestic policy reform. However, these ...

Wilcox, Trudy

2005-01-01T23:59:59.000Z

231

Study on Hydrogen-Enriching Gas Reforming in Smelting ... - TMS  

Science Conference Proceedings (OSTI)

May 1, 2007 ... For the two-step smelting reduction iron-making process, the advantages of hydrogen-enriching gas reforming are not only to lower the export ...

232

Hanford Low Activity Waste (LAW) Fluidized Bed Steam Reformer...  

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

Hanford Low Activity Waste (LAW) Fluidized Bed Steam Reformer (FBSR) Na-Al-Si (NAS) Waste Form Qualification C.M. Jantzen and E.M. Pierce November 18, 2010 2 Participating...

233

Hydrogen & Fuel Cells - Hydrogen - Distributed Ethanol Reforming  

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

Hydrogen from Bio-Derived Liquids Hydrogen from Bio-Derived Liquids Bio-derived liquid fuels can be produced from renewable agricultural products, such as wood chips. Background Bio-derived renewable fuels are attractive for their high energy density and ease of transport. One scenario for a sustainable hydrogen economy considers that these bio-derived liquid fuels will be produced at plants close to the biomass resource, and then transported to distributed hydrogen production centers (e.g., hydrogen refueling stations), where the fuels will be reformed via the steam reforming process, similar to the current centralized production of hydrogen by the steam reforming of natural gas. Hydrogen produced by reforming these fuels must first be purified and compressed to appropriate storage and dispensing pressures. Compressing

234

Electrical Generation Tax Reform Act (Montana) | Department of Energy  

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

Generation Tax Reform Act (Montana) Generation Tax Reform Act (Montana) Electrical Generation Tax Reform Act (Montana) < Back Eligibility Utility Fed. Government Commercial Agricultural Investor-Owned Utility State/Provincial Govt Industrial Municipal/Public Utility Local Government Residential Installer/Contractor Rural Electric Cooperative Tribal Government Low-Income Residential Schools Institutional Multi-Family Residential Systems Integrator Nonprofit General Public/Consumer Transportation Savings Category Alternative Fuel Vehicles Hydrogen & Fuel Cells Buying & Making Electricity Water Home Weatherization Solar Wind Program Info State Montana Program Type Fees Provider Montana Department of Revenue This Act reforms taxes paid by electricity generators to reduce tax rates and imposes replacement taxes in response to the 1997 restructuring of the

235

Reforming the Power Sector in Transition: Do Institutions Matter?  

E-Print Network (OSTI)

  tempted  to  add  additional generation capacity through meaningful power sector reforms in the lurch  towards reducing energy dependency.    As  of  1989,  numerous  nuclear  reactors  in  Armenia,  Bulgaria,  Lithuania,  Russia,  Slovakia...  relationship between country level institutions and power sector reforms    Although  the  neoclassical  economic  theory  considers  both  competition  and  privatization  as  the  core  aspects  of  a market  economy;  the  outcomes  cannot  be  guaranteed  to  be  Pareto  efficient  in  the  absence  of  proper  institutional...

Nepal, Rabindra; Jamasb, Tooraj

236

Quick-start catalyzed methanol partial oxidation reformer  

DOE Green Energy (OSTI)

The catalytic methanol partial oxidation reformer described in this paper offers all the necessary attributes for use in transportation fuel cell systems. The bench-scale prototype methanol reformer developed at Argonne is a cylindrical reactor loaded with copper zinc oxide catalyst. Liquid methanol, along with a small amount of water, is injected as a fine spray into a flowing air stream, past an igniter onto the catalyst bed where the partial oxidation reaction takes place.

Ahmed, S.; Kumar, R.

1995-12-01T23:59:59.000Z

237

Catalytic autothermal reforming of hydrocarbon fuels for fuel cells.  

DOE Green Energy (OSTI)

Fuel cell development has seen remarkable progress in the past decade because of an increasing need to improve energy efficiency as well as to address concerns about the environmental consequences of using fossil fuel for producing electricity and for propulsion of vehicles [1]. The lack of an infrastructure for producing and distributing H{sub 2} has led to a research effort to develop on-board fuel processing technology for reforming hydrocarbon fuels to generate H{sub 2} [2]. The primary focus is on reforming gasoline, because a production and distribution infrastructure for gasoline already exists to supply internal combustion engines [3]. Existing reforming technology for the production of H{sub 2} from hydrocarbon feedstocks used in large-scale manufacturing processes, such as ammonia synthesis, is cost prohibitive when scaled down to the size of the fuel processor required for transportation applications (50-80 kWe) nor is it designed to meet the varying power demands and frequent shutoffs and restarts that will be experienced during normal drive cycles. To meet the performance targets required of a fuel processor for transportation applications will require new reforming reactor technology developed to meet the volume, weight, cost, and operational characteristics for transportation applications and the development of new reforming catalysts that exhibit a higher activity and better thermal and mechanical stability than reforming catalysts currently used in the production of H{sub 2} for large-scale manufacturing processes.

Krumpelt, M.; Krause, T.; Kopasz, J.; Carter, D.; Ahmed, S.

2002-01-11T23:59:59.000Z

238

Fractionation of reformate: A new variant of gasoline production technology  

Science Conference Proceedings (OSTI)

The Novo-Ufa Petroleum Refinery is the largest domestic producer of the unique high-octane unleaded automotive gasolines AI-93 and AI-95 and the aviation gasolines B-91/115 and B-92. The base component for these gasolines is obtained by catalytic reforming of wide-cut naphtha; this basic component is usually blended with certain other components that are expensive and in short supply: toluene, xylenes, and alkylate. For example, the unleaded gasoline AI-93 has been prepared by blending reformate, alkylate, and toluene in a 65:20:15 weight ratio; AI-95 gasoline by blending alkylate and xylenes in an 80:20 weight ratio; and B-91/115 gasoline by compounding a reformate obtained with light straight-run feed, plus alkylate and toluene, in a 55:35:10 weight ratio. Toluene and xylenes have been obtained by process schemes that include the following consecutive processes: redistillation of straight-run naphtha cuts to segregate the required narrow fraction; catalytic reforming (Platforming) of the narrow toluene-xylene straight-run fraction; azeotropic distillation of the reformate to recover toluene and xylenes. A new technology based on the use of reformate fractions is proposed.

Karakuts, V.N.; Tanatarov, M.A.; Telyashev, G.G. [and others

1995-07-01T23:59:59.000Z

239

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

240

Experimental investigation into the effect of reformer gas addition on flame speed and flame front propagation in premixed, homogeneous charge gasoline engines  

SciTech Connect

The effect of reformer gas addition to gasoline in internal combustion engines is assessed based on in-cylinder measurement techniques. These include ion sensors, an optical spark plug and heat release analysis from the cylinder pressure. A detailed analysis of these measurements is presented, giving insight into the combustion process and into the energy release. The flame front shape and propagation in the combustion chamber are reconstructed and the flame speed is estimated. The laminar flame speed has been observed to increase linearly with the energy fraction of reformer gas in the fuel blend. From pure gasoline to pure reformer gas the laminar flame speed increases by a factor of 4.4. The relative increase in the turbulent flame speed is lower. These results confirm what can be observed from the heat release analysis, that reformer gas addition mainly shortens the first phase of the combustion process. Different reformer gas compositions were tested, varying the ratio of hydrogen to inert species. Finally, flame propagation and flame speed at EGR-burn limit and at lean-burn limit are investigated. (author)

Conte, Enrico; Boulouchos, Konstantinos [Aerothermochemistry and Combustion Systems Laboratory (LAV), ETH Zurich, CH-8092 (Switzerland)

2006-07-15T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

THOR Bench-Scale Steam Reforming Demonstration  

SciTech Connect

The Idaho Nuclear Technology and Engineering Center (INTEC) was home to nuclear fuel reprocessing activities for decades at the Idaho National Engineering and Environmental Laboratory. As a result of the reprocessing activities, INTEC has accumulated approximately one million gallons of acidic, radioactive, sodium-bearing waste (SBW). The purpose of this demonstration was to investigate a reforming technology, offered by THORsm Treatment Technologies, LLC, for treatment of SBW into a ''road ready'' waste form that would meet the waste acceptance criteria for the Waste Isolation Pilot Plant (WIPP). A non-radioactive simulated SBW was used based on the known composition of waste tank WM-180 at INTEC. Rhenium was included as a non-radioactive surrogate for technetium. Data was collected to determine the nature and characteristics of the product, the operability of the technology, the composition of the off-gases, and the fate of key radionuclides (cesium and technetium) and volatile mercury compounds. The product contained a low fraction of elemental carbon residues in the cyclone and filter vessel catches. Mercury was quantitatively stripped from the product but cesium, rhenium (Tc surrogate), and the heavy metals were retained. Nitrates were not detected in the product and NOx destruction exceeded 98%. The demonstration was successful.

Marshall, D.W.; Soelberg, N.R.; Shaber, K.M.

2003-05-21T23:59:59.000Z

242

THOR Bench-Scale Steam Reforming Demonstration  

SciTech Connect

The Idaho Nuclear Technology and Engineering Center (INTEC) was home to nuclear fuel reprocessing activities for decades at the Idaho National Engineering and Environmental Laboratory. As a result of the reprocessing activities, INTEC has accumulated approximately one million gallons of acidic, radioactive, sodium-bearing waste (SBW). The purpose of this demonstration was to investigate a reforming technology, offered by THORsm Treatment Technologies, LLC, for treatment of SBW into a "road ready" waste form that would meet the waste acceptance criteria for the Waste Isolation Pilot Plant (WIPP). A non-radioactive simulated SBW was used based on the known composition of waste tank WM-180 at INTEC. Rhenium was included as a non-radioactive surrogate for technetium. Data was collected to determine the nature and characteristics of the product, the operability of the technology, the composition of the off-gases, and the fate of key radionuclides (cesium and technetium) and volatile mercury compounds. The product contained a low fraction of elemental carbon residues in the cyclone and filter vessel catches. Mercury was quantitatively stripped from the product but cesium, rhenium (Tc surrogate), and the heavy metals were retained. Nitrates were not detected in the product and NOx destruction exceeded 98%. The demonstration was successful.

D. W. Marshall; N. R. Soelberg; K. M. Shaber

2003-05-01T23:59:59.000Z

243

An Innovative Injection and Mixing System for Diesel Fuel Reforming  

DOE Green Energy (OSTI)

This project focused on fuel stream preparation improvements prior to injection into a solid oxide fuel cell reformer. Each milestone and the results from each milestone are discussed in detail in this report. The first two milestones were the creation of a coking formation test rig and various testing performed on this rig. Initial tests indicated that three anti-carbon coatings showed improvement over an uncoated (bare metal) baseline. However, in follow-up 70 hour tests of the down selected coatings, Scanning Electron Microscope (SEM) analysis revealed that no carbon was generated on the test specimens. These follow-up tests were intended to enable a down selection to a single best anti-carbon coating. Without the formation of carbon it was impossible to draw conclusions as to which anti-carbon coating showed the best performance. The final 70 hour tests did show that AMCX AMC26 demonstrated the lowest discoloration of the metal out of the three down selected anti-carbon coatings. This discoloration did not relate to carbon but could be a useful result when carbon growth rate is not the only concern. Unplanned variations in the series of tests must be considered and may have altered the results. Reliable conclusions could only be drawn from consistent, repeatable testing beyond the allotted time and funding for this project. Milestones 3 and 4 focused on the creation of a preheating pressure atomizer and mixing chamber. A design of experiment test helped identify a configuration of the preheating injector, Build 1, which showed a very uniform fuel spray flow field. This injector was improved upon by the creation of a Build 2 injector. Build 2 of the preheating injector demonstrated promising SMD results with only 22psi fuel pressure and 0.7 in H2O of Air. It was apparent from testing and CFD that this Build 2 has flow field recirculation zones. These recirculation zones may suggest that this Build 2 atomizer and mixer would require steam injection to reduce the auto ignition potential. It is also important to note that to achieve uniform mixing within a short distance, some recirculation is necessary. Milestone 5 generated CFD and FEA results that could be used to optimize the preheating injector. CFD results confirmed the recirculation zones seen in test data and confirmed that the flow field would not change when attached to a reformer. The FEA predicted fuel wetted wall temperatures which led to several suggested improvements that could possibly improve nozzle efficiency. Milestone 6 (originally an optional task) took a different approach than the preheating pressure atomizer. It focused on creation and optimization of a piezoelectric injector which could perform at extremely low fuel pressures. The piezoelectric atomizer showed acceptable SMD results with fuel pressure less than 1.0 psig and air pressure less than 1.0 in H2O. These SMD values were enhanced when a few components were changed, and it is expected would improve further still at elevated air temperatures. It was demonstrated that the piezoelectric injector could accomplish the desired task. The addition of phase tracking and a burst mode to the frequency controller increased the usability of the piezoelectric injector. This injector is ready to move on to the next phase of development. Engine Components has met the required program milestones of this project. Some of the Milestones were adjusted to allow Milestone 6 to be completed in parallel with the other Milestones. Because of this, Task 3.10 and 3.13 were made optional instead of Milestone 6. Engine Components was extremely grateful for the support that was provided by NETL in support of this work.

Spencer Pack

2007-12-31T23:59:59.000Z

244

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

245

Methanol reformers for fuel cell powered vehicles: Some design considerations  

DOE Green Energy (OSTI)

Fuel cells are being developed for use in automotive propulsion systems as alternatives for the internal combustion engine in buses, vans, passenger cars. The two most important operational requirements for a stand-alone fuel cell power system for a vehicle are the ability to start up quickly and the ability to supply the necessary power on demand for the dynamically fluctuating load. Methanol is a likely fuel for use in fuel cells for transportation applications. It is a commodity chemical that is manufactured from coal, natural gas, and other feedstocks. For use in a fuel cell, however, the methanol must first be converted (reformed) to a hydrogen-rich gas mixture. The desired features for a methanol reformer include rapid start-up, good dynamic response, high fuel conversion, small size and weight, simple construction and operation, and low cost. In this paper the present the design considerations that are important for developing such a reformer, namely: (1) a small catalyst bed for quick starting, small size, and low weight; (2) multiple catalysts for optimum operation of the dissociation and reforming reactions; (3) reforming by direct heat transfer partial oxidation for rapid response to fluctuating loads; and (4) thermal independence from the rest of the fuel cell system. 10 refs., 1 fig.

Kumar, R.; Ahmed, S.; Krumpelt, M.; Myles, K.M.

1990-01-01T23:59:59.000Z

246

Reformers for the production of hydrogen from methanol and alternative fuels for fuel cell powered vehicles  

DOE Green Energy (OSTI)

The objective of this study was (i) to assess the present state of technology of reformers that convert methanol (or other alternative fuels) to a hydrogen-rich gas mixture for use in a fuel cell, and (ii) to identify the R D needs for developing reformers for transportation applications. Steam reforming and partial oxidation are the two basic types of fuel reforming processes. The former is endothermic while the latter is exothermic. Reformers are therefore typically designed as heat exchange systems, and the variety of designs used includes shell-and-tube, packed bed, annular, plate, and cyclic bed types. Catalysts used include noble metals and oxides of Cu, Zn, Cr, Al, Ni, and La. For transportation applications a reformer must be compact, lightweight, and rugged. It must also be capable of rapid start-up and good dynamic performance responsive to fluctuating loads. A partial oxidation reformer is likely to be better than a steam reformer based on these considerations, although its fuel conversion efficiency is expected to be lower than that of a steam reformer. A steam reformer better lends itself to thermal integration with the fuel cell system; however, the thermal independence of the reformer from the fuel cell stack is likely to yield much better dynamic performance of the reformer and the fuel cell propulsion power system. For both steam reforming and partial oxidation reforming, research is needed to develop compact, fast start-up, and dynamically responsive reformers. For transportation applications, steam reformers are likely to prove best for fuel cell/battery hybrid power systems, and partial oxidation reformers are likely to be the choice for stand-alone fuel cell power systems.

Kumar, R.; Ahmed, S.; Krumpelt, M.; Myles, K.M.

1992-08-01T23:59:59.000Z

247

Reformers for the production of hydrogen from methanol and alternative fuels for fuel cell powered vehicles  

DOE Green Energy (OSTI)

The objective of this study was (i) to assess the present state of technology of reformers that convert methanol (or other alternative fuels) to a hydrogen-rich gas mixture for use in a fuel cell, and (ii) to identify the R&D needs for developing reformers for transportation applications. Steam reforming and partial oxidation are the two basic types of fuel reforming processes. The former is endothermic while the latter is exothermic. Reformers are therefore typically designed as heat exchange systems, and the variety of designs used includes shell-and-tube, packed bed, annular, plate, and cyclic bed types. Catalysts used include noble metals and oxides of Cu, Zn, Cr, Al, Ni, and La. For transportation applications a reformer must be compact, lightweight, and rugged. It must also be capable of rapid start-up and good dynamic performance responsive to fluctuating loads. A partial oxidation reformer is likely to be better than a steam reformer based on these considerations, although its fuel conversion efficiency is expected to be lower than that of a steam reformer. A steam reformer better lends itself to thermal integration with the fuel cell system; however, the thermal independence of the reformer from the fuel cell stack is likely to yield much better dynamic performance of the reformer and the fuel cell propulsion power system. For both steam reforming and partial oxidation reforming, research is needed to develop compact, fast start-up, and dynamically responsive reformers. For transportation applications, steam reformers are likely to prove best for fuel cell/battery hybrid power systems, and partial oxidation reformers are likely to be the choice for stand-alone fuel cell power systems.

Kumar, R.; Ahmed, S.; Krumpelt, M.; Myles, K.M.

1992-08-01T23:59:59.000Z

248

Aqueous Phase Mercury Removal: Strategies for a Secure ...  

Science Conference Proceedings (OSTI)

... sources of population exposure are coal-fired utility plants, municipal/medical waste incinerators, and commercial/industrial boilers—estimated to ...

2012-08-01T23:59:59.000Z

249

Method for separating water soluble organics from a process stream by aqueous biphasic extraction  

DOE Patents (OSTI)

A method for separating water-miscible organic species from a process stream by aqueous biphasic extraction is provided. An aqueous biphase system is generated by contacting a process stream comprised of water, salt, and organic species with an aqueous polymer solution. The organic species transfer from the salt-rich phase to the polymer-rich phase, and the phases are separated. Next, the polymer is recovered from the loaded polymer phase by selectively extracting the polymer into an organic phase at an elevated temperature, while the organic species remain in a substantially salt-free aqueous solution. Alternatively, the polymer is recovered from the loaded polymer by a temperature induced phase separation (cloud point extraction), whereby the polymer and the organic species separate into two distinct solutions. The method for separating water-miscible organic species is applicable to the treatment of industrial wastewater streams, including the extraction and recovery of complexed metal ions from salt solutions, organic contaminants from mineral processing streams, and colorants from spent dye baths.

Chaiko, David J. (Naperville, IL); Mego, William A. (Naperville, IL)

1999-01-01T23:59:59.000Z

250

Analysis of decontamination solutions of G agents to detect reformation of agent. Final report, December 1991-March 1992  

SciTech Connect

Agents from a full scale binary munition test were decontaminated with caustic in a 300 gal holding tank. Analysis of the contents by standard methods revealed a trace amount of G agent present despite the highly caustic solution. A technical review of the analytical methods was carried out to determine if the G agent was actually present or an artifact of the analysis. A literature search revealed similar concerns when brine solutions from nerve agent decontamination were analyzed using similar analytical methods. This study concluded that nerve agents reformed at reduced PH or in chloroform extracts of the neutralized or slightly acidic brines. Experiments using nuclear magnetic resonance (NMR), gas chromatography (GC), and GC/mass spectrometry (GC/MS) were used to see where, if any, G agent was present during the analysis. Results obtained confirmed G agent reforming in either the neutral aqueous solution or in the chloroform extract but not in chloroform extracts of the caustic solution. No agent was detected using methylene chloride as the extraction solvent as recommended by the earlier study.

Beaudry, W.T.; Buchanan, J.H.; Rohrbaugh, D.K.; Samuel, J.B.; Szafraniec, L.L.

1993-01-01T23:59:59.000Z

251

Forest Tenure Reform in Vietnam | Open Energy Information  

Open Energy Info (EERE)

in Vietnam in Vietnam Jump to: navigation, search Name Forest Tenure Reform in Vietnam Agency/Company /Organization Regional Community Forestry Training Center for Asia and the Pacific Sector Land Focus Area Forestry Topics Resource assessment, Background analysis Resource Type Lessons learned/best practices Website http://recoftc.org/site/filead Country Vietnam UN Region South-Eastern Asia References Forest Tenure Reform in Vietnam[1] Forest Tenure Reform in Vietnam Screenshot Summary "This report presents a synthesis of findings from the two surveys undertaken in Dak Lak (by Dak Lak Department of Agriculture and Rural Development (DARD)) and Hoa Binh by VFU (See Annex A. for a list of members in the two research teams). It was prepared by Nguyen Quang Tan, Nguyen Ba

252

Regulatory and Financial Reform of Federal Research Policy  

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

Regulatory and Financial Reform of Federal Research Policy Regulatory and Financial Reform of Federal Research Policy Recommendations to the NRC Committee on Research Universities January 21, 2011 Introduction At the request of the National Research Council (NRC) Committee on Research Universities, the Council on Governmental Relations (COGR), the Association of American Universities (AAU), and the Association of Public and Land-grant Universities (APLU) have assembled a set of ten recommendations for regulatory reform that would improve research universities' ability to carry out their missions without requiring a significant financial investment by the Federal government. We firmly believe that compliance and regulatory oversight are essential to the conduct of federally-supported research. Rationalizing the Federal regulatory infrastructure is essential to

253

Comments on Request For Information regarding Reducing Regulatory Reform  

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

Comments on Request For Information regarding Reducing Regulatory Comments on Request For Information regarding Reducing Regulatory Reform issued February 3, 2011 (Federal Register /Vol. 76, No. 23 /Thursday, February 3, 2011 /Notices). Comments on Request For Information regarding Reducing Regulatory Reform issued February 3, 2011 (Federal Register /Vol. 76, No. 23 /Thursday, February 3, 2011 /Notices). I have reviewed the Request For Information regarding Reducing Regulatory Reform issued February 3, 2011 (Federal Register /Vol. 76, No. 23 /Thursday, February 3, 2011 /Notices). In the Department of Energy"s (DOE) attempt to meet its obligation to implement Executive Order 13563, ""Improving Regulation and Regulatory Review,"" issued by the President on January 18, 2011, I recommend DOE make a bold move to change

254

Pyrochlore-type catalysts for the reforming of hydrocarbon fuels  

DOE Patents (OSTI)

A method of catalytically reforming a reactant gas mixture using a pyrochlore catalyst material comprised of one or more pyrochlores having the composition A.sub.2-w-xA'.sub.wA''.sub.xB.sub.2-y-zB'.sub.yB''.sub.zO.sub.7-.DELTA.. Distribution of catalytically active metals throughout the structure at the B site creates an active and well dispersed metal locked into place in the crystal structure. This greatly reduces the metal sintering that typically occurs on supported catalysts used in reforming reactions, and reduces deactivation by sulfur and carbon. Further, oxygen mobility may also be enhanced by elemental exchange of promoters at sites in the pyrochlore. The pyrochlore catalyst material may be utilized in catalytic reforming reactions for the conversion of hydrocarbon fuels into synthesis gas (H.sub.2+CO) for fuel cells, among other uses.

Berry, David A. (Morgantown, WV); Shekhawat, Dushyant (Morgantown, WV); Haynes, Daniel (Morgantown, WV); Smith, Mark (Morgantown, WV); Spivey, James J. (Baton Rouge, LA)

2012-03-13T23:59:59.000Z

255

Pyrochlore-type catalysts for the reforming of hydrocarbon fuels  

Science Conference Proceedings (OSTI)

A method of catalytically reforming a reactant gas mixture using a pyrochlore catalyst material comprised of one or more pyrochlores having the composition A.sub.2-w-xA'.sub.wA''.sub.xB.sub.2-y-zB'.sub.yB''.sub.zO.sub.7-.DELTA.. Distribution of catalytically active metals throughout the structure at the B site creates an active and well dispersed metal locked into place in the crystal structure. This greatly reduces the metal sintering that typically occurs on supported catalysts used in reforming reactions, and reduces deactivation by sulfur and carbon. Further, oxygen mobility may also be enhanced by elemental exchange of promoters at sites in the pyrochlore. The pyrochlore catalyst material may be utilized in catalytic reforming reactions for the conversion of hydrocarbon fuels into synthesis gas (H.sub.2+CO) for fuel cells, among other uses.

Berry, David A. (Morgantown, WV); Shekhawat, Dushyant (Morgantown, WV); Haynes, Daniel (Morgantown, WV); Smith, Mark (Morgantown, WV); Spivey, James J. (Baton Rouge, LA)

2012-03-13T23:59:59.000Z

256

Producing Clean Syngas via Catalytic Reforming for Fuels Production  

Science Conference Proceedings (OSTI)

Thermochemical biomass conversion to fuels and chemicals can be achieved through gasification to syngas. The biomass derived raw syngas contains the building blocks of carbon monoxide and hydrogen as well as impurities such as tars, light hydrocarbons, and hydrogen sulfide. These impurities must be removed prior to fuel synthesis. We used catalytic reforming to convert tars and hydrocarbons to additional syngas, which increases biomass carbon utilization. In this work, nickel based, fluidizable tar reforming catalysts were synthesized and evaluated for tar and methane reforming performance with oak and model syngas in two types of pilot scale fluidized reactors (recirculating and recirculating regenerating). Because hydrogen sulfide (present in raw syngas and added to model syngas) reacts with the active nickel surface, regeneration with steam and hydrogen was required. Pre and post catalyst characterization showed changes specific to the syngas type used. Results of this work will be discussed in the context of selecting the best process for pilot scale demonstration.

Magrini, K. A.; Parent, Y.; Jablonski, W.; Yung, M.

2012-01-01T23:59:59.000Z

257

Ghana-REDD Readiness Requires Radical Reform | Open Energy Information  

Open Energy Info (EERE)

Readiness Requires Radical Reform Readiness Requires Radical Reform Jump to: navigation, search Name Ghana-REDD Readiness Requires Radical Reform Agency/Company /Organization UN-REDD Programme Sector Land Focus Area Forestry, Agriculture Topics Implementation, GHG inventory, Policies/deployment programs, Resource assessment, Pathways analysis, Background analysis Resource Type Maps, Guide/manual, Training materials Website http://environment.yale.edu/tf Country Ghana UN Region Western Africa References Ghana-REDD Readiness[1] Summary "The fundamental changes needed for sustainable forest management in Ghana have been known for years, and many large projects have been instigated accordingly. Yet real change has proved elusive. The key challenge now is to get REDD-plus right so that it makes a difference. Dialogue participants

258

High performance internal reforming unit for high temperature fuel cells  

DOE Patents (OSTI)

A fuel reformer having an enclosure with first and second opposing surfaces, a sidewall connecting the first and second opposing surfaces and an inlet port and an outlet port in the sidewall. A plate assembly supporting a catalyst and baffles are also disposed in the enclosure. A main baffle extends into the enclosure from a point of the sidewall between the inlet and outlet ports. The main baffle cooperates with the enclosure and the plate assembly to establish a path for the flow of fuel gas through the reformer from the inlet port to the outlet port. At least a first directing baffle extends in the enclosure from one of the sidewall and the main baffle and cooperates with the plate assembly and the enclosure to alter the gas flow path. Desired graded catalyst loading pattern has been defined for optimized thermal management for the internal reforming high temperature fuel cells so as to achieve high cell performance.

Ma, Zhiwen (Sandy Hook, CT); Venkataraman, Ramakrishnan (New Milford, CT); Novacco, Lawrence J. (Brookfield, CT)

2008-10-07T23:59:59.000Z

259

Cummins Power Generation SECA Phase 1  

DOE Green Energy (OSTI)

The following report documents the progress of the Cummins Power Generation (CPG) SECA Phase 1 SOFC development and final testing under the U.S. Department of Energy Solid State Energy Conversion Alliance (SECA) contract DE-FC26-01NT41244. This report overviews and summarizes CPG and partner research development leading to successful demonstration of the SECA Phase 1 objectives and significant progress towards SOFC commercialization. Significant Phase 1 Milestones: (1) Demonstrated: (a) Operation meeting Phase 1 requirements on commercial natural gas. (b) LPG and Natural Gas CPOX fuel reformers. (c) SOFC systems on dry CPOX reformate. (c) Steam reformed Natural Gas operation. (d) Successful start-up and shut-down of SOFC system without inert gas purge. (e) Utility of stack simulators as a tool for developing balance of plant systems. (2) Developed: (a) Low cost balance of plant concepts and compatible systems designs. (b) Identified low cost, high volume components for balance of plant systems. (c) Demonstrated high efficiency SOFC output power conditioning. (d) Demonstrated SOFC control strategies and tuning methods. The Phase 1 performance test was carried out at the Cummins Power Generation facility in Minneapolis, Minnesota starting on October 2, 2006. Performance testing was successfully completed on January 4, 2007 including the necessary steady-state, transient, efficiency, and peak power operation tests.

Charles Vesely

2007-08-17T23:59:59.000Z

260

GUIDANCE ON APPLICATION OF FEDERAL VACANCIES REFORM ACT OF 1998 Page 1 of 13  

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

APPLICATION OF FEDERAL VACANCIES REFORM ACT OF 1998 Page 1 of 13 APPLICATION OF FEDERAL VACANCIES REFORM ACT OF 1998 Page 1 of 13 GUIDANCE ON APPLICATION OF FEDERAL VACANCIES REFORM ACT OF 1998 This memorandum provides guidance on the application of the Federal Vacancies Reform Act of1998 to vacancies in Senate-confirmed offices within the executive branch. March 22, 1999 MEMORANDUM FOR AGENCY GENERAL COUNSELS On October 21, 1998, the Federal Vacancies Reform Act of 1998 ("Vacancies Reform Act" or "Act") was signed into law. ( ) The Vacancies Reform Act replaces the old Vacancies Act and alters the way in which vacancies in presidentially appointed, Senate- confirmed offices within the executive branch may be filled on a temporary basis. The following Q&As are intended to provide general guidance on the Vacancies Reform Act. If

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261

Controlling Activity and Stability of Ni-YSZ Catalysts for On-Anode Reforming  

DOE Green Energy (OSTI)

The purposes of the project are to develop an effective Ni-YSZ-based anode for on-anode reforming of methane and natural gas and develop methods to control endothermic steam reforming activity.

King, D.L.; Wang, Y.; Chin, Y-H.; Lin, Y.; Roh, H-S.; Rozmiarek, B.

2005-01-27T23:59:59.000Z

262

www.elsevier.com/locate/econbase School finance reform: Assessing general equilibrium effects  

E-Print Network (OSTI)

In 1994 the state of Michigan implemented one of the most comprehensive school finance reforms undertaken to date in any of the states. Understanding the effects of the reform is thus of value in informing other potential reform initiatives. In addition, the reform and associated changes in the economic environment provide an opportunity to assess whether a simple general equilibrium model can be of value in framing the study of such reform initiatives. In this paper, we present and use such a model to derive predictions about the effects of the reform on housing prices and neighborhood demographic compositions. Broadly, our analysis implies that the effects of the reform and changes in the economic environment are likely to have been reflected primarily in housing prices and only modestly on neighborhood demographics. We find that evidence for the Detroit metropolitan area from the decade encompassing the reform is largely consistent with the predictions of the model.

Maria Marta Ferreyra A

2007-01-01T23:59:59.000Z

263

The Lessons of Practice: Domestic Policy Reform as a Way to Address...  

Open Energy Info (EERE)

The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate Change Jump to: navigation, search Tool Summary Name: The Lessons of Practice: Domestic Policy Reform as...

264

From negotiation to auction : Land-Conveyance Reform in China and its institutional and social impacts  

E-Print Network (OSTI)

The land market and the associated land-development-control mechanism in China have been experiencing a series of reforms since the 1990s, of which Land Conveyance Reform (LCR) in 2004 is a very recent and an important ...

Chen, Zhiyu (Zhiyu Jerry)

2007-01-01T23:59:59.000Z

265

ECONOMIC REFORM AND COMMUNIST REGIME SURVIVABILTY: PAST, PRESENT, AND FUTURE  

E-Print Network (OSTI)

While the collapse of communist rule and process of transitioning to democracy in the former-Soviet Union and its numerous satellite states certainly warrants the wealth of attention received, by no means does this signal that the history of communist state rule is ended. Contrary to popular belief—and even belief in academe it sometimes seems—Communism still survives. In fact, a number of Asian states still claim to follow the path to a promised societal utopia under the guidance of their respective Politburos and may be described as not only ‘surviving’ but thriving, experiencing economic stability and enjoying high rates of growth. This study examines the ramifications of economic and political reform policies implemented by four collapsed communist regimes which have transitioned to democratic governance—the former-Soviet Union, Poland, Hungary, and Czechoslovakia—as well as two surviving Asian communist regimes—Vietnam and China—in identifying characteristic patterns of reform that are conducive to regime survival and/or collapse. The end objective herein is to provide projections for the future of the Castro regime in Cuba, which faces a critical juncture in the future with the impending death of its charismatic leader. I hypothesize that economic reform, through consistent implementation, generates credibility for both Communist Party elites and their future reform endeavors. Additionally, reform packages that manage to successfully stabilize the economy bestow an increased measure of legitimacy to the political elite, allowing the Communist Party to maintain political control, thereby avoiding collapse and the transition to democracy. The third and final section contains general discussion and what conclusions can be drawn from the results, as well as analysis of the history of reform efforts to present in the Caribbean island state of Cuba.

Nelson, John

2006-08-16T23:59:59.000Z

266

Aqueous Chemical Growth of Advanced Nanostructured ... - TMS  

Science Conference Proceedings (OSTI)

Feb 1, 2002 ... A novel concept in materials chemistry have been developed as well as an aqueous low temperature thin film growth technique to create a new ...

267

Why are land reforms granting complete property rights politically risky? Electoral outcomes of Mexico's certification program  

E-Print Network (OSTI)

identified adverse political fallouts as the main reason whygains but fear the political fallout of the reform. It helps

de Janvry, Alain; Gonzalez-Navarro, Marco; Sadoulet, Elisabeth

2012-01-01T23:59:59.000Z

268

Tailored Macroporous SiCN and SiC Structures for High-Temperature Fuel Reforming**  

E-Print Network (OSTI)

. The catalytic reforming of hydrocarbons in a microreformer is an attractive approach to supply hydrogen to fuel

Kenis, Paul J. A.

269

Heat exchanger for fuel cell power plant reformer  

DOE Patents (OSTI)

A heat exchanger uses the heat from processed fuel gas from a reformer for a fuel cell to superheat steam, to preheat raw fuel prior to entering the reformer and to heat a water-steam coolant mixture from the fuel cells. The processed fuel gas temperature is thus lowered to a level useful in the fuel cell reaction. The four temperature adjustments are accomplished in a single heat exchanger with only three heat transfer cores. The heat exchanger is preheated by circulating coolant and purge steam from the power section during startup of the latter.

Misage, Robert (Manchester, CT); Scheffler, Glenn W. (Tolland, CT); Setzer, Herbert J. (Ellington, CT); Margiott, Paul R. (Manchester, CT); Parenti, Jr., Edmund K. (Manchester, CT)

1988-01-01T23:59:59.000Z

270

Catalytic reforming of liquid fuels: Deactivation of catalysts  

Science Conference Proceedings (OSTI)

The catalytic reforming of logistic fuels (e.g., diesel) to provide hydrogen-rich gas for various fuel cells is inevitably accompanied by deactivation. This deactivation can be caused by various mechanisms, such as carbon deposition, sintering, and sulfur poisoning. In general, these mechanisms are, not independent—e.g., carbon deposition may affect sulfur poisoning. However, they are typically studied in separate experiments, with relatively little work reported on their interaction at conditions typical of liquid fuel reforming. Recent work at the U.S. Dept. of Energy/NETL and Louisiana State University has shown progress in understanding the interaction of these deactivation processes, and catalysts designed to minimize them.

Spivey, J.J.; Haynes, D.J.; Berry, D.A.; Shekhawat, Dushyant; Gardner, T.H.

2007-10-01T23:59:59.000Z

271

Hydrocarbon autothermal reforming program. Final technical report, 28 September 1979-31 October 1981  

DOE Green Energy (OSTI)

The goal of the PSI program was to understand the mechanisms of the formation of carbon deposits under conditions relevant to authothermal reformers (ATR). The first year of this two year program was dedicated almost entirely to investigations of gas phase soot formation. It was speculated that soot could form in the gas phase and deposit downstream in the catalyst bed. A high temperature experimental test rig was constructed and comptuer models developed to aid in understanding this process. The conclusion of these studies is that soot does not form in the gas phase upstream of the catalyst bed, under ATR conditions, at least, not under well mixed conditions. In the second year, the program was redirected to study carbon formation processes on surfaces and to perform testing and analysis of Engelhard's six inch ATR rig. This work has resulted in an operational computer code for use in modeling the Engelhard ATR. This code requires rate constant information for performance prediction. The PSI laboratory experiments have shown that coke formation on surfaces of nickel catalysts is very rapid, particularly from olefins. Filamentary carbon was formed. Various relevant processes and their relative rates were studied on various nickel surfaces. Coke was not observed when precious metal catalysts were used. Testing on the Engelhard reactor was performed. These preliminary tests show that the Engelhard catalysts can be used to reform number two fuel oil with no problems associated with carbonaceous deposits. Some hydrocarbon breakthrough was observed, increasing at low oxygen to carbon ratio (0.355). These limited data clearly indicate a high potential for a useful ATR. Further testing and analysis are clearly necessary.

Ham, D.O.; Lewis, P.F.; Lord, G.W.; Yarrington, R.M.; Hwang, H.S.

1982-02-01T23:59:59.000Z

272

EFFECT OF H2 PRODUCED THROUGH STEAM-METHANE REFORMING ON CHP PLANT EFFICIENCY  

E-Print Network (OSTI)

1 EFFECT OF H2 PRODUCED THROUGH STEAM-METHANE REFORMING ON CHP PLANT EFFICIENCY O. Le Corre1 , C@emn.fr ABSTRACT In-situ hydrogen production is carried out by a catalytic reformer kit set up into exhaust gases-thermal reforming process is achieved. Hydrogen production is mainly dependent on O2 content in exhaust gases

273

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

274

Catalysts for hydrogen production by steam reforming of dimethyl ether (DME)  

Science Conference Proceedings (OSTI)

Dimethyl ether (DME) is expected as one of clean fuels. We have been studying on DME steam reforming for hydrogen production. Copper alumina catalysts prepared by a sol-gel method produced large quantities of H2 with DME steam reforming. The reason was ... Keywords: DME, alumina, catalyst, clean fuel, copper, dimethyl ether, hydrogen, sol-gel method, steam reforming

Kaoru Takeishi

2010-02-01T23:59:59.000Z

275

Nematic droplets in aqueous dispersions of carbon nanotubes  

E-Print Network (OSTI)

Aqueous dispersions of exfoliated, bile-salt stabilized single-wall carbon nanotubes exhibit a first order transition to a nematic liquid-crystalline phase. The nematic phase presents itself in the form of micron-sized nematic droplets also known as tactoids, freely floating in the isotropic host dispersion. The nematic droplets are spindle shaped and have an aspect ratio of about four, irrespective of their size. We attribute this to a director field that is uniform rather than bipolar, which is confirmed by polarization microscopy. It follows that the ratio of the anchoring strength and the surface tension must be about four, which is quite larger than predicted theoretically but in line with earlier observations of bipolar tactoids. From the scatter in the data we deduce that the surface tension of the coexisting isotropic and nematic phases must be extremely low, that is, of the order of nN/m.

Nicolas Puech; Eric Grelet; Philippe Poulin; Christophe Blanc; Paul van der Schoot

2013-06-23T23:59:59.000Z

276

Solar Reforming of Carbon Dioxide to Produce Diesel Fuel  

SciTech Connect

This project focused on the demonstration of an innovative technology, referred to as the Sunexus CO2 Solar Reformer, which utilizes waste CO2 as a feedstock for the efficient and economical production of synthetic diesel fuel using solar thermal energy as the primary energy input. The Sunexus technology employs a two stage process for the conversion of CO2 to diesel fuel. A solar reforming system, including a specially designed reactor and proprietary CO2 reforming catalyst, was developed and used to convert captured CO2 rich gas streams into syngas (primarily hydrogen and carbon monoxide) using concentrated solar energy at high conversion efficiencies. The second stage of the system (which has been demonstrated under other funding) involves the direct conversion of the syngas into synthetic diesel fuel using a proprietary catalyst (Terra) previously developed and validated by Pacific Renewable Fuels and Chemicals (PRFC). The overall system energy efficiency for conversion of CO2 to diesel fuel is 74%, due to the use of solar energy. The results herein describe modeling, design, construction, and testing of the Sunexus CO2 Solar Reformer. Extensive parametric testing of the solar reformer and candidate catalysts was conducted and chemical kinetic models were developed. Laboratory testing of the Solar Reformer was successfully completed using various gas mixtures, temperatures, and gas flow rates/space velocities to establish performance metrics which can be employed for the design of commercial plants. A variety of laboratory tests were conducted including dry reforming (CO2 and CH{sub 4}), combination dry/steam reforming (CO2, CH{sub 4} & H{sub 2}O), and tri-reforming (CO2, CH{sub 4}, H{sub 2}O & O{sub 2}). CH{sub 4} and CO2 conversions averaged 95-100% and 50-90% per reformer cycle, respectively, depending upon the temperatures and gas space velocities. No formation of carbon deposits (coking) on the catalyst was observed in any of these tests. A 16 ft. diameter, concentrating solar dish was modified to accommodate the Sunexus CO2 Solar Reformer and the integrated system was installed at the Pacific Renewable Fuels and Chemicals test site at McClellan, CA. Several test runs were conducted without catalyst during which the ceramic heat exchanger in the Sunexus Solar Reformer reached temperatures between 1,050 F (566 C) and 2,200 F (1,204 C) during the test period. A dry reforming mixture of CO2/CH{sub 4} (2.0/1.0 molar ratio) was chosen for all of the tests on the integrated solar dish/catalytic reformer during December 2010. Initial tests were carried out to determine heat transfer from the collimated solar beam to the catalytic reactor. The catalyst was operated successfully at a steady-state temperature of 1,125 F (607 C), which was sufficient to convert 35% of the 2/1 CO2/CH{sub 4} mixture to syngas. This conversion efficiency confirmed the results from laboratory testing of this catalyst which provided comparable syngas production efficiencies (40% at 1,200 F [650 C]) with a resulting syngas composition of 20% CO, 16% H{sub 2}, 39% CO2 and 25% CH{sub 4}. As based upon the laboratory results, it is predicted that 90% of the CO2 will be converted to syngas in the solar reformer at 1,440 F (782 C) resulting in a syngas composition of 50% CO: 43% H{sub 2}: 7% CO2: 0% CH{sub 4}. Laboratory tests show that the higher catalyst operating temperature of 1,440 F (782 C) for efficient conversion of CO2 can certainly be achieved by optimizing solar reactor heat transfer, which would result in the projected 90% CO2-to-syngas conversion efficiencies. Further testing will be carried out during 2011, through other funding support, to further optimize the solar dish CO2 reformer. Additional studies carried out in support of this project and described in this report include: (1) An Assessment of Potential Contaminants in Captured CO2 from Various Industrial Processes and Their Possible Effect on Sunexus CO2 Reforming Catalysts; (2) Recommended Measurement Methods for Assessing Contaminant Levels in Captured CO2 Streams; (3) An Asse

Dennis Schuetzle; Robert Schuetzle

2010-12-31T23:59:59.000Z

277

Process for recovering pertechnetate ions from an aqueous solution also containing other ions  

DOE Patents (OSTI)

A solid/liquid process for the separation and recovery of TcO{sub 4}{sup {minus}1} ions from an aqueous solution is disclosed. The solid support comprises separation particles having surface-bonded poly(ethylene glycol) groups; whereas the aqueous solution from which the TcO{sub 4}{sup {minus}1} ions are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved salt. A solid/liquid phase admixture of separation particles containing bound TcO{sub 4}{sup {minus}1} ions in such an aqueous solution that is free from MoO{sub 4}{sup {minus}2} ions is also contemplated, as is a chromatography apparatus containing that solid/liquid phase admixture. 15 figs.

Rogers, R.; Horwitz, E.P.; Bond, A.H.

1997-02-18T23:59:59.000Z

278

Process for recovering pertechnetate ions from an aqueous solution also containing other ions  

DOE Patents (OSTI)

A solid/liquid process for the separation and recovery of TcO.sub.4.sup.-1 ions from an aqueous solution is disclosed. The solid support comprises separation particles having surface-bonded poly(ethylene glycol) groups; whereas the aqueous solution from which the TcO.sub.4.sup.-1 ions are separated contains a poly(ethylene glycol) liquid/liquid biphase-forming amount of a dissolved salt. A solid/liquid phase admixture of separation particles containing bound TcO.sub.4.sup.-1 ions in such an aqueous solution that is free from MoO.sub.4.sup.-2 ions is also contemplated, as is a chromatography apparatus containing that solid/liquid phase admixture.

Rogers, Robin (DeKalb, IL); Horwitz, E. Philip (Naperville, IL); Bond, Andrew H. (Tallahassee, FL)

1997-01-01T23:59:59.000Z

279

Changing the Rules of the 'ROE': A Reform in Waiting  

SciTech Connect

Congress and FERC recognize the need to attract more investment in transmission. FERC promised to increase cash flow for companies investing in transmission and introduced incremental changes in rates of return. But the agency can do better. FERC should enact comprehensive reform of its return-on-equity calculus to conform policy to market reality. (author)

Rokach, Joshua Z.

2006-05-15T23:59:59.000Z

280

Reform and Regulation of the Electricity Sectors in Developing Countries  

E-Print Network (OSTI)

in investment patterns reflect the differences in the reform strategies adopted by the countries in these regions during the 1990s. By and large, the EAP and SA countries opted for power purchase agreements (PPAs) with independent power producers (IPPs) while...

Jamasb, Tooraj; Littlechild, Stephen C

2004-06-16T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Understanding electricity market reforms and the case of Philippine deregulation  

Science Conference Proceedings (OSTI)

The experience of the Philippines offers lessons that should be relevant to any country seeking to deregulate its power industry. Regardless of structure, consumers must face the real price of electricity production and delivery that is closer to marginal cost. Politically motivated prices merely shift the burden from ratepayers to taxpayers. And any reform should work within a reasonable timetable. (author)

Santiago, Andrea; Roxas, Fernando

2010-03-15T23:59:59.000Z

282

Electricity reform and Gains from the reallocation of resources  

SciTech Connect

Perhaps the greatest beneficiary of electricity reform in Australia was the state government of Victoria itself, which was able to reduce debt levels and post budget surpluses even while increasing expenditure and employment levels in education, health care, and law and order. (author)

Abbott, Malcolm

2007-08-15T23:59:59.000Z

283

Communications Technology and Urban Governance Reform: Project Highlights  

E-Print Network (OSTI)

In this paper, we describe highlights of a research project funded by the NSF Digital Government program. The study has examined the impacts of advanced communication technologies in the implementation of a system of neighborhood councils in Los Angeles. It employs social network analysis to chart the development of political networks engendered by the reform and the role of email in shaping these networks.

Christopher Weare

2005-01-01T23:59:59.000Z

284

Financial and ratepayer impacts of nuclear power plant regulatory reform  

SciTech Connect

Three reports - ''The Future Market for Electric Generating Capacity,'' ''Quantitative Analysis of Nuclear Power Plant Licensing Reform,'' and ''Nuclear Rate Increase Study'' are recent studies performed by the Los Alamos National Laboratory that deal with nuclear power. This presents a short summary of these three studies. More detail is given in the reports.

Turpin, A.G.

1985-01-01T23:59:59.000Z

285

Steam Reforming of Low-Level Mixed Waste  

Science Conference Proceedings (OSTI)

Under DOE Contract No. DE-AR21-95MC32091, Steam Reforming of Low-Level Mixed Waste, ThermoChem has successfully designed, fabricated and operated a nominal 90 pound per hour Process Development Unit (PDU) on various low-level mixed waste surrogates. The design construction, and testing of the PDU as well as performance and economic projections for a 500- lb/hr demonstration and commercial system are described. The overall system offers an environmentally safe, non-incinerating, cost-effective, and publicly acceptable method of processing LLMW. The steam-reforming technology was ranked the No. 1 non-incineration technology for destruction of hazardous organic wastes in a study commissioned by the Mixed Waste Focus Area published April 1997.1 The ThermoChem steam-reforming system has been developed over the last 13 years culminating in this successful test campaign on LLMW surrogates. Six surrogates were successfidly tested including a 750-hour test on material simulating a PCB- and Uranium- contaminated solid waste found at the Portsmouth Gaseous Diffusion Plant. The test results indicated essentially total (>99.9999oA) destruction of RCRA and TSCA hazardous halogenated organics, significant levels of volume reduction (> 400 to 1), and retention of radlonuclides in the volume-reduced solids. Cost studies have shown the steam-reforming system to be very cost competitive with more conventional and other emerging technologies.

None

1998-01-01T23:59:59.000Z

286

Fixed-bed reforming with mid-cycle catalyst addition  

Science Conference Proceedings (OSTI)

A fixed-bed catalytic reforming process is described in which on-stream operation is begun with the catalyst retention volume in the first reactor less than 99% full and additional catalyst is added to said reactor while on-stream.

Houston, R.J.; McCoy, C.S.

1981-02-17T23:59:59.000Z

287

Commercialization of a high-performance continuous reforming catalyst  

Science Conference Proceedings (OSTI)

In 1971, the first CCR Platforming process was started up in the US on the Gulf Coast. Twenty-two years later, more than 108 continuous reforming units are operating worldwide. Another 50 CCR Platforming units are in various stages of design, construction, or start-up. Continuous catalytic reforming now represents more than 25% of the world's reforming capacity. Throughout these three decades, the UOP CCR Platforming technology continuously improved in terms of catalyst and process in response to changing industry requirements. Processing conditions in 1993 place tremendous demands on the catalyst in the reforming unit. This paper reviews the challenges and needs of the changing refining industry and the development of a new generation of CCR Platforming catalyst, R-132, and focuses on the first commercial operation of this high-activity, surface-stable catalyst. Case studies show how a refiner can improve margins by using the high activity, yield stability, longer life, and improved chloride retention benefits of this new R-132 Platforming catalyst.

Gilsdorf, N.L.; Doornbos, A.E.; Gevelinger, T.J. (UOP, Des Plaines, IL (United States)); Angelo, C.M.D. (Petrogal Refinaria de Sines (Portugal))

1993-01-01T23:59:59.000Z

288

Tube skin temperature prediction of catalytic reforming unit (CRU) heaters  

Science Conference Proceedings (OSTI)

The maximum duty of reformer heaters is governed by the occurance of maximum tube skin temperature of the heaters. The value of maximum tube skin temperatures of the heaters must not exceed theirs' maximum allowable design temperature. The paper highlights ... Keywords: coke formation, finite element, simulations, tube furnance

Suzana Yusup; Nguyen Duy Vinh; Nurhayati Mellon; Abdullah Hassan

2006-10-01T23:59:59.000Z

289

Separation of normally gaseous hydrocarbons from a catalytic reforming effluent and recovery of purified hydrogen  

Science Conference Proceedings (OSTI)

A process for the catalytic reforming of a hydrocarbonaceous feedstock, preferably to produce high quality gasoline boiling range products, is disclosed. Relatively impure hydrogen is separated from the reforming zone effluent, compressed, and recontacted with at least a portion of the liquid reformate product to provide relatively pure hydrogen, a portion of which is recycled to the reforming zone. The balance is further compressed and recontacted with at least a portion of the liquid reformate product to provide an improved recovery of normally gaseous hydrocarbons as well as an improved recovery of purified hydrogen at a pressure suitable for use in the relatively high pressure hydrotreating of sulfur-containing feedstocks.

Coste, A.C.

1982-06-08T23:59:59.000Z

290

BILIWG Meeting: High Pressure Steam Reforming of Bio-Derived Liquids (Presentation)  

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

High Pressure Steam Reforming of High Pressure Steam Reforming of Bio-Derived Liquids S. Ahmed, S. Lee, D. Papadias, and R. Kumar November 6, 2007 Laurel, MD Research sponsored by the Hydrogen, Fuel Cells, and Infrastructure Technologies Program of DOE's Office of Energy Efficiency and Renewable Energy Rationale and objective Rationale „ Steam reforming of liquid fuels at high pressures can reduce hydrogen compression costs - Much less energy is needed to pressurize liquids (fuel and water) than compressing gases (reformate or H 2 ) „ High pressure reforming is advantageous for subsequent separations and hydrogen purification Objective „ Develop a reformer design that takes advantage of the savings in compression cost in the steam reforming bio-derived liquid fuels - Metric:

291

Investigation of carbon-formation mechanisms and fuel-conversion rates in the adiabatic reformer. Annual report, March 19, 1980-March 19, 1981  

Science Conference Proceedings (OSTI)

Fuel cell power plants may be required to use coal derived liquid fuels or heavy petroleum distillates as fuels. Among the fuel processor candidates, the adiabatic reformer is at the most advanced state of development. The objective of the present program is to establish a reactor model for the adiabatic reformer which will predict process stream compositions and include carbon formation processes. Four subordinate tasks were proposed to achieve the objective. These are: 1) to determine on selected catalysts rate expressions for catalytic reactions occurring in the entrance section of the adiabatic reformer; 2) to determine with microbalance experiments critical conditions for carbon formation on selected catalysts; 3) to establish a reactor model to predict process stream compositions in the adiabatic reformer using data from Task 1 for catalytic reactions and data from the literature for homogeneous gas phase reactions; and 4) to establish a model to predict carbon formation by combination of the model for process stream composition from Task 3 and data for carbon formation from Task 2. Progress is reported. (WHK)

Not Available

1981-01-01T23:59:59.000Z

292

LONG-TERM STABILITY TESTING RESULTS USING SURROGATES AND SORBENTS FOR SAVANNAH RIVER SITE ORGANIC AND AQUEOUS WASTESTREAMS - 10016  

SciTech Connect

The U.S. Department of Energy (DOE) has tasked MSE Technology Applications, Inc. (MSE) with evaluating the long-term stability of various commercially available sorbent materials to solidify two organic surrogate wastestreams (both volatile and nonvolatile), a volatile organic surrogate with a residual aqueous phase, an aqueous surrogate, and an aqueous surrogate with a residual organic phase. The Savannah River Site (SRS) Legacy and F-Canyon plutonium/uranium extraction (PUREX) process waste surrogates constituted the volatile organic surrogates, and various oils constituted the nonvolatile organic surrogates. The aqueous surrogates included a rainwater surrogate and an aqueous organic surrogate. MSE also evaluated the PUREX surrogate with a residual aqueous component with and without aqueous type sorbent materials. Solidification of the various surrogate wastestreams listed above was performed from 2004 to 2006 at the MSE Test Facility located in Butte, Montana. This paper summarizes the comparison of the initial liquid release test (LRT) values with LRT results obtained during subsequent sampling events in an attempt to understand and define the long-term stability characteristics for the solidified wastestreams.

Burns, H.

2009-11-10T23:59:59.000Z

293

RADIOACTIVE DEMONSTRATION OF MINERALIZED WASTE FORMS MADE FROM HANFORD LOW ACTIVITY WASTE (TANK FARM BLEND) BY FLUIDIZED BED STEAM REFORMATION (FBSR)  

Science Conference Proceedings (OSTI)

The U.S. Department of Energy’s Office of River Protection (ORP) is responsible for the retrieval, treatment, immobilization, and disposal of Hanford’s tank waste. A key aspect of the River Protection Project (RPP) cleanup mission is to construct and operate the Hanford Tank Waste Treatment and Immobilization Plant (WTP). The WTP will separate the tank waste into high-level and low-activity waste (LAW) fractions, both of which will subsequently be vitrified. The projected throughput capacity of the WTP LAW Vitrification Facility is insufficient to complete the RPP mission in the time frame required by the Hanford Federal Facility Agreement and Consent Order, also known as the Tri-Party Agreement (TPA), i.e. December 31, 2047. Supplemental Treatment is likely to be required both to meet the TPA treatment requirements as well as to more cost effectively complete the tank waste treatment mission. The Supplemental Treatment chosen will immobilize that portion of the retrieved LAW that is not sent to the WTP’s LAW Vitrification facility into a solidified waste form. The solidified waste will then be disposed on the Hanford site in the Integrated Disposal Facility (IDF). Fluidized Bed Steam Reforming (FBSR) offers a moderate temperature (700-750°C) continuous method by which LAW can be processed irrespective of whether the waste contain organics, nitrates, sulfates/sulfides, chlorides, fluorides, volatile radionuclides or other aqueous components. The FBSR technology can process these wastes into a crystalline ceramic (mineral) waste form. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be comparable to LAW glass, i.e. leaches Tc-99, Re and Na at 6 (the Hanford IDF criteria for Na) in the first few hours. The granular and monolithic waste forms also pass the EPA Toxicity Characteristic Leaching Procedure (TCLP) for all Resource Conservation and Recovery Act (RCRA) components at the Universal Treatment Standards (UTS). Two identical Benchscale Steam Reformers (BSR) were designed and constructed at SRNL, one to treat non-radioactive simulants and the other to treat actual radioactive wastes. The results from the non-radioactive BSR were used to determine the parameters needed to operate the radioactive BSR in order to confirm the findings of non-radioactive FBSR pilot scale and engineering scale tests and to qualify an FBSR LAW waste form for applications at Hanford. Radioactive testing commenced using SRS LAW from Tank 50 chemically trimmed to look like Hanford’s blended LAW known as the Rassat simulant as this simulant composition had been tested in the non-radioactive BSR, the non-radioactive pilot scale FBSR at the Science Applications International Corporation-Science and Technology Applications Research (SAIC-STAR) facility in Idaho Falls, ID and in the TTT Engineering Scale Technology Demonstration (ESTD) at Hazen Research Inc. (HRI) in Denver, CO. This provided a “tie back” between radioactive BSR testing and non-radioactive BSR, pilot scale, and engineering scale testing. Approximately six hundred grams of non-radioactive and radioactive BSR product were made for extensive testing and comparison to the non-radioactive pilot scale tests performed in 2004 at SAIC-STAR and the engineering scale test performed in 2008 at HRI with the Rassat simulant. The same mineral phases and off-gas species were found in the radioactive and non-radioactive testing. The granular ESTD and BSR products (radioactive and non-radioactive) were analyzed for to

Jantzen, C. M.; Crawford, C. L.; Bannochie, C. J.; Burket, P. R.; Cozzi, A. D.; Daniel, W. E.; Hall, H. K.; Miller, D. H.; Missimer, D. M.; Nash, C. A.; Williams, M. F.

2013-08-21T23:59:59.000Z

294

Method for processing aqueous wastes  

DOE Patents (OSTI)

This invention is comprised of a method for treating waste water such as that from an industrial processing facility comprising the separation of the waste water into a dilute waste stream and a concentrated waste stream. The concentrated waste stream is treated chemically to enhance precipitation and then allowed to separate into a sludge and a supernate. The supernate is skimmed or filtered from the sludge and blended with the dilute waste stream to form a second dilute waste stream. The sludge remaining is mixed with cementitious material, rinsed to dissolve soluble components, then pressed to remove excess water and dissolved solids before being allowed to cure. The dilute waste stream is also chemically treated to decompose carbonate complexes and metal ions and then mixed with cationic polymer to cause the precipitated solids to flocculate. Filtration of the flocculant removes sufficient solids to allow the waste water to be discharged to the surface of a stream. The filtered material is added to the sludge of the concentrated waste stream. The method is also applicable to the treatment and removal of soluble uranium from aqueous streams, such that the treated stream may be used as a potable water supply.

Pickett, J.B.; Martin, H.L.; Langton, C.A.; Harley, W.W.

1992-12-31T23:59:59.000Z

295

Method for processing aqueous wastes  

DOE Patents (OSTI)

A method is presented for treating waste water such as that from an industrial processing facility comprising the separation of the waste water into a dilute waste stream and a concentrated waste stream. The concentrated waste stream is treated chemically to enhance precipitation and then allowed to separate into a sludge and a supernate. The supernate is skimmed or filtered from the sludge and blended with the dilute waste stream to form a second dilute waste stream. The sludge remaining is mixed with cementitious material, rinsed to dissolve soluble components, then pressed to remove excess water and dissolved solids before being allowed to cure. The dilute waste stream is also chemically treated to decompose carbonate complexes and metal ions and then mixed with cationic polymer to cause the precipitated solids to flocculate. Filtration of the flocculant removes sufficient solids to allow the waste water to be discharged to the surface of a stream. The filtered material is added to the sludge of the concentrated waste stream. The method is also applicable to the treatment and removal of soluble uranium from aqueous streams, such that the treated stream may be used as a potable water supply. 4 figures.

Pickett, J.B.; Martin, H.L.; Langton, C.A.; Harley, W.W.

1993-12-28T23:59:59.000Z

296

Method for processing aqueous wastes  

DOE Patents (OSTI)

A method for treating waste water such as that from an industrial processing facility comprising the separation of the waste water into a dilute waste stream and a concentrated waste stream. The concentrated waste stream is treated chemically to enhance precipitation and then allowed to separate into a sludge and a supernate. The supernate is skimmed or filtered from the sludge and blended with the dilute waste stream to form a second dilute waste stream. The sludge remaining is mixed with cementitious material, rinsed to dissolve soluble components, then pressed to remove excess water and dissolved solids before being allowed to cure. The dilute waste stream is also chemically treated to decompose carbonate complexes and metal ions and then mixed with cationic polymer to cause the precipitated solids to flocculate. Filtration of the flocculant removes sufficient solids to allow the waste water to be discharged to the surface of a stream. The filtered material is added to the sludge of the concentrated waste stream. The method is also applicable to the treatment and removal of soluble uranium from aqueous streams, such that the treated stream may be used as a potable water supply.

Pickett, John B. (3922 Wood Valley Dr., Aiken, SC 29803); Martin, Hollis L. (Rt. 1, Box 188KB, McCormick, SC 29835); Langton, Christine A. (455 Sumter St. SE., Aiken, SC 29801); Harley, Willie W. (110 Fairchild St., Batesburg, SC 29006)

1993-01-01T23:59:59.000Z

297

Reforming petroleum-based fuels for fuel cell vehicles : composition-performance relationships.  

DOE Green Energy (OSTI)

Onboard reforming of petroleum-based fuels, such as gasoline, may help ease the introduction of fuel cell vehicles to the marketplace. Although gasoline can be reformed, it is optimized to meet the demands of ICEs. This optimization includes blending to increase the octane number and addition of oxygenates and detergents to control emissions. The requirements for a fuel for onboard reforming to hydrogen are quite different than those for combustion. Factors such as octane number and flame speed are not important; however, factors such as hydrogen density, catalyst-fuel interactions, and possible catalyst poisoning become paramount. In order to identify what factors are important in a hydrocarbon fuel for reforming to hydrogen and what factors are detrimental, we have begun a program to test various components of gasoline and blends of components under autothermal reforming conditions. The results indicate that fuel composition can have a large effect on reforming behavior. Components which may be beneficial for ICEs for their octane enhancing value were detrimental to reforming. Fuels with high aromatic and naphthenic content were more difficult to reform. Aromatics were also found to have an impact on the kinetics for reforming of paraffins. The effects of sulfur impurities were dependent on the catalyst. Sulfur was detrimental for Ni, Co, and Ru catalysts. Sulfur was beneficial for reforming with Pt catalysts, however, the effect was dependent on the sulfur concentration.

Kopasz, J. P.; Miller, L. E.; Ahmed, S.; Devlin, P. R.; Pacheco, M.

2001-12-04T23:59:59.000Z

298

Steady-State Simulation of Steam Reforming of INEEL Tank Farm Waste  

SciTech Connect

A steady-state model of the Sodium-Bearing Waste steam reforming process at the Idaho National Engineering and Environmental Laboratory has been performed using the commercial ASPEN Plus process simulator. The preliminary process configuration and its representation in ASPEN are described. As assessment of the capability of the model to mechanistically predict product stream compositions was made, and fidelity gaps and opportunities for model enhancement were identified, resulting in the following conclusions: (1) Appreciable benefit is derived from using an activity coefficient model for electrolyte solution thermodynamics rather than assuming ideality (unity assumed for all activity coefficients). The concentrations of fifteen percent of the species present in the primary output stream were changed by more than 50%, relative to Electrolyte NRTL, when ideality was assumed; (2) The current baseline model provides a good start for estimating mass balances and performing integrated process optimization because it contains several key species, uses a mechanistic electrolyte thermodynamic model, and is based on a reasonable process configuration; and (3) Appreciable improvement to model fidelity can be realized by expanding the species list and the list of chemical and phase transformations. A path forward is proposed focusing on the use of an improved electrolyte thermodynamic property method, addition of chemical and phase transformations for key species currently absent from the model, and the combination of RGibbs and Flash blocks to simulate simultaneous phase and chemical equilibria in the off-gas treatment train.

Nichols, T.T.; Taylor, D.D.; Wood, R.A.; Barnes, C.M.

2002-08-15T23:59:59.000Z

299

Steady-State Simulation of Steam Reforming of INEEL Tank Farm Waste  

SciTech Connect

A steady-state model of the Sodium-Bearing Waste steam reforming process at the Idaho National Engineering and Environmental Laboratory has been performed using the commercial ASPEN Plus process simulator. The preliminary process configuration and its representation in ASPEN are described. As assessment of the capability of the model to mechanistically predict product stream compositions was made, and fidelity gaps and opportunities for model enhancement were identified, resulting in the following conclusions: 1) Appreciable benefit is derived from using an activity coefficient model for electrolyte solution thermodynamics rather than assuming ideality (unity assumed for all activity coefficients). The concentrations of fifteen percent of the species present in the primary output stream were changed by more than 50%, relative to Electrolyte NRTL, when ideality was assumed; 2) The current baseline model provides a good start for estimating mass balances and performing integrated process optimization because it contains several key species, uses a mechanistic electrolyte thermodynamic model, and is based on a reasonable process configuration; and 3) Appreciable improvement to model fidelity can be realized by expanding the species list and the list of chemical and phase transformations. A path forward is proposed focusing on the use of an improved electrolyte thermodynamic property method, addition of chemical and phase transformations for key species currently absent from the model, and the combination of RGibbs and Flash blocks to simulate simultaneous phase and chemical equilibria in the off-gas treatment train.

Nichols, Todd Travis; Taylor, Dean Dalton; Wood, Richard Arthur; Barnes, Charles Marshall

2002-08-01T23:59:59.000Z

300

Process for reducing aqueous nitrate to ammonia  

DOE Patents (OSTI)

Powdered aluminum is added to a nitrate-containing alkaline, aqueous solution to reduce the nitrate and/or nitrite to ammonia and co-produce a sinterable ceramic product.

Mattus, Alfred J. (Oak Ridge, TN)

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Radiation Chemistry of MTBE in Aqueous Solution  

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

Methyl-tert-Butyl Ether (MTBE) in Aqueous Solution Stephen P. Mezyk, Jace Jones, William J. Cooper, Thomas Tobien, Michael G. Nickelsen, J. Wesley Adams, Kevin E. O'Shea, David M....

302

Process for reducing aqueous nitrate to ammonia  

DOE Patents (OSTI)

Powdered aluminum is added to a nitrate-containing alkaline, aqueous solution to reduce the nitrate and/or nitrite to ammonia and co-produce a sinterable ceramic product. 3 figures.

Mattus, A.J.

1993-11-30T23:59:59.000Z

303

Summary of aqueous mobile battery development  

SciTech Connect

Progress at ANL in developing improved aqueous battery technology for use in electric vehicles is briefly described. Research directed at improving the lead-acid, nickel/iron, and nickel/zinc technologies is emphasized. (WHK)

Christianson, C.C.; Yao, N.P.; Rajan, J.; Miller, J.; Lee, J.; Choi, K.

1982-01-01T23:59:59.000Z

304

In situ Gas Conditioning in Fuel Reforming for Hydrogen Generation  

DOE Green Energy (OSTI)

The production of hydrogen for fuel cell applications requires cost and energy efficient technologies. The Absorption Enhanced Reforming (AER), developed at ZSW with industrial partners, is aimed to simplify the process by using a high temperature in situ CO2 absorption. The in situ CO2 removal results in shifting the steam reforming reaction equilibrium towards increased hydrogen concentration (up to 95 vol%). The key part of the process is the high temperature CO2 absorbent. In this contribution results of Thermal Gravimetric Analysis (TGA) investigations on natural minerals, dolomites, silicates and synthetic absorbent materials in regard of their CO2 absorption capacity and absorption/desorption cyclic stability are presented and discussed. It has been found that the inert parts of the absorbent materials have a structure stabilizing effect, leading to an improved cyclic stability of the materials.

Bandi, A.; Specht, M.; Sichler, P.; Nicoloso, N.

2002-09-20T23:59:59.000Z

305

Contract reform: It`s working at Fernald  

SciTech Connect

DOE`s contract reform initiatives at Fernald and the performance-based system DOE is now using to evaluate FERMCO are key elements to the current and future success of DOE and FERMCO at Fernald. Final cleanup of the Fernald site is planned for completion by 2005 per an accelerated 10-year remediation plan which has been approved by DOE and endorsed by the US EPA, Ohio EPA, and the Fernald Citizens Task Force. Required funding of approximately $276 million plus inflation annually for 10 years to accomplish final cleanup is now being considered by US Congress. Contract reform initiatives and modified performance measurement systems, along with best business practices, are clearing the path for the expedited cleanup of Fernald.

Craig, J. [USDOE Fernald Area Office, Cincinnati, OH (United States); Hunt, A. [Fernald Environmental Restoration Management Corp., Cincinnati, OH (United States)

1996-01-25T23:59:59.000Z

306

Reforming with an improved platinum-containing catalyst  

Science Conference Proceedings (OSTI)

A catalyst is disclosed which comprises a physical particle-form mixture of a Component A and a Component B. Said Component A comprises one or more Group VIII noble metals and combined halogen deposed on a refractory inorganic oxide and said Component B comprising a metal from Group IVB or Group VB of the Periodic Table of Elements and a combined halogen deposed on a refrac inorganic oxide. Such catalyst is suitable for use in a hydrocarbon conversion reaction zone. The catalyst can be employed in a process for the reforming of a hydrocarbon stream, which process comprises contacting said stream in a reaction zone under reforming conditions and in the presence hydrogen with said catalyst. The catalyst is not presulfided. A preferred process comprises contacting a hydrocarbon stream that contains a substantial amount of sulfur.

Pellet, R.J.; Bertolacini, R.J.; Lysholm, D.L.

1983-08-30T23:59:59.000Z

307

Reforming with an improved platinum-containing catalyst  

Science Conference Proceedings (OSTI)

There is disclosed a catalyst, which catalyst comprises a physical particle-form mixture of a component A and a component B , said component A comprising one or more group VIII noble metals and a combined halogen deposed on a refractory inorganic oxide and said component B comprising a metal from group IVB or group VB of the periodic table of elements and a combined halogen deposed on a refractory inorganic oxide. Such catalyst is suitable for use in a hydrocarbon conversion reaction zone. The catalyst can be employed in a process for the reforming of a hydrocarbon stream, which process comprises contacting said stream in a reaction zone under reforming conditions and in the presence of hydrogen with said catalyst. The catalyst is not presulfided. A preferred process comprises contacting a hydrocarbon stream that contains a substantial amount of sulfur.

Bertolacini, R.J.; Lysholm, D.L.; Pellet, R.J.

1982-10-12T23:59:59.000Z

308

Making sense of doctoral training reforms in the social sciences:  

E-Print Network (OSTI)

process, occurring through collective reflection and action, whether at the level of the department, institution or the discipline (eg McAlpine et al 2005). Within the UK, this recognition has led the higher education funding council to support a... of this emerging field of academic practice and point to some of the challenges ahead. Within the field of doctoral education, I suggest that these curriculum reforms are often led by senior academic administrators who put their own policy knowledge to good use...

Mills, David

2009-01-01T23:59:59.000Z

309

Fuel cell system with combustor-heated reformer  

DOE Patents (OSTI)

A fuel cell system including a fuel reformer heated by a catalytic combustor fired by anode effluent and/or fuel from a liquid fuel supply providing fuel for the fuel cell. The combustor includes a vaporizer section heated by the combustor exhaust gases for vaporizing the fuel before feeding it into the combustor. Cathode effluent is used as the principle oxidant for the combustor.

Pettit, William Henry (Rochester, NY)

2000-01-01T23:59:59.000Z

310

Power sector reform, private investment and regional co-operation  

E-Print Network (OSTI)

Europe and stimulated FDI in the power sector, and might have similarly stimulative effects in South Asia, quite apart from creating profitable trade opportunities and increasing regional security of supply and greater resilience against external oil... of the Electricity Reforms Act in 1997 setting up the Regulatory Commission. “The state government has directed district administrators and police officials to support the distribution companies for curtailing frauds, theft, etc., but the actual implementation...

Newbery, David

311

AQUEOUS HOMOGENEOUS REACTORTECHNICAL PANEL REPORT  

Science Conference Proceedings (OSTI)

Considerable interest has been expressed for developing a stable U.S. production capacity for medical isotopes and particularly for molybdenum- 99 (99Mo). This is motivated by recent re-ductions in production and supply worldwide. Consistent with U.S. nonproliferation objectives, any new production capability should not use highly enriched uranium fuel or targets. Conse-quently, Aqueous Homogeneous Reactors (AHRs) are under consideration for potential 99Mo production using low-enriched uranium. Although the Nuclear Regulatory Commission (NRC) has guidance to facilitate the licensing process for non-power reactors, that guidance is focused on reactors with fixed, solid fuel and hence, not applicable to an AHR. A panel was convened to study the technical issues associated with normal operation and potential transients and accidents of an AHR that might be designed for isotope production. The panel has produced the requisite AHR licensing guidance for three chapters that exist now for non-power reactor licensing: Reac-tor Description, Reactor Coolant Systems, and Accident Analysis. The guidance is in two parts for each chapter: 1) standard format and content a licensee would use and 2) the standard review plan the NRC staff would use. This guidance takes into account the unique features of an AHR such as the fuel being in solution; the fission product barriers being the vessel and attached systems; the production and release of radiolytic and fission product gases and their impact on operations and their control by a gas management system; and the movement of fuel into and out of the reactor vessel.

Diamond, D.J.; Bajorek, S.; Bakel, A.; Flanagan, G.; Mubayi, V.; Skarda, R.; Staudenmeier, J.; Taiwo, T.; Tonoike, K.; Tripp, C.; Wei, T.; Yarsky, P.

2010-12-03T23:59:59.000Z

312

Steam reforming of low-level mixed waste. Final report  

Science Conference Proceedings (OSTI)

ThermoChem has successfully designed, fabricated and operated a nominal 90 pound per hour Process Development Unit (PDU) on various low-level mixed waste surrogates. The design, construction, and testing of the PDU as well as performance and economic projections for a 300-lb/hr demonstration and commercial system are described. The overall system offers an environmentally safe, non-incinerating, cost-effective, and publicly acceptable method of processing LLMW. The steam-reforming technology was ranked the No. 1 non-incineration technology for destruction of hazardous organic wastes in a study commissioned by the Mixed Waste Focus Area and published in April 1997. The ThermoChem steam-reforming system has been developed over the last 13 years culminating in this successful test campaign on LLMW surrogates. Six surrogates were successfully tested including a 750-hour test on material simulating a PCB- and Uranium-contaminated solid waste found at the Portsmouth Gaseous Diffusion Plant. The test results indicated essentially total (> 99.9999%) destruction of RCRA and TSCA hazardous halogenated organics, significant levels of volume reduction (> 400 to 1), and retention of radionuclides in the volume-reduced solids. Economic evaluations have shown the steam-reforming system to be very cost competitive with more conventional and other emerging technologies.

NONE

1998-06-01T23:59:59.000Z

313

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

314

WHEC 16 / 13-16 June 2006 Lyon France Plasma assisted fuel reforming for on-board hydrogen rich gas production  

E-Print Network (OSTI)

through hydrogen on-board storage. The main reforming technology is catalytic reforming, which has been points are challenges for automotive applications. In parallel with research on catalytic reforming assisted reforming could be used complementary to catalytic reforming to ensure dynamics performance (start

Paris-Sud XI, Université de

315

Electrochemical cell apparatus having an integrated reformer-mixer nozzle-mixer diffuser  

DOE Patents (OSTI)

An electrochemical apparatus is made having a generator section containing electrochemical cells, a fresh gaseous feed fuel inlet, a gaseous feed oxidant inlet, and at least one hot gaseous spent fuel recirculation channel, where the spent fuel recirculation channel, passes from the generator chamber to combine with the fresh feed fuel inlet to form a reformable mixture, where a reforming chamber contains an outer portion containing reforming material, an inner portion preferably containing a mixer nozzle and a mixer-diffuser, and a middle portion for receiving spent fuel, where the mixer nozzle and mixer-diffuser are preferably both within the reforming chamber and substantially exterior to the main portion of the apparatus, where the reformable mixture flows up and then backward before contacting the reforming material, and the mixer nozzle can operate below 400 C. 1 figure.

Shockling, L.A.

1991-09-10T23:59:59.000Z

316

Autothermal reforming of natural gas to synthesis gas:reference: KBR paper #2031.  

DOE Green Energy (OSTI)

This Project Final Report serves to document the project structure and technical results achieved during the 3-year project titled Advanced Autothermal Reformer for US Dept of Energy Office of Industrial Technology. The project was initiated in December 2001 and was completed March 2005. It was a joint effort between Sandia National Laboratories (Livermore, CA), Kellogg Brown & Root LLC (KBR) (Houston, TX) and Sued-Chemie (Louisville, KY). The purpose of the project was to develop an experimental capability that could be used to examine the propensity for soot production in an Autothermal Reformer (ATR) during the production of hydrogen-carbon monoxide synthesis gas intended for Gas-to-Liquids (GTL) applications including ammonia, methanol, and higher hydrocarbons. The project consisted of an initial phase that was focused on developing a laboratory-scale ATR capable of reproducing conditions very similar to a plant scale unit. Due to budget constraints this effort was stopped at the advanced design stages, yielding a careful and detailed design for such a system including ATR vessel design, design of ancillary feed and let down units as well as a PI&D for laboratory installation. The experimental effort was then focused on a series of measurements to evaluate rich, high-pressure burner behavior at pressures as high as 500 psi. The soot formation measurements were based on laser attenuation at a view port downstream of the burner. The results of these experiments and accompanying calculations show that soot formation is primarily dependent on oxidation stoichiometry. However, steam to carbon ratio was found to impact soot production as well as burner stability. The data also showed that raising the operating pressure while holding mass flow rates constant results in considerable soot formation at desirable feed ratios. Elementary reaction modeling designed to illuminate the role of CO{sub 2} in the burner feed showed that the conditions in the burner allow for the direct participation of CO{sub 2} in the oxidation chemistry.

Mann, David (KBR, Houston, TX); Rice, Steven, D.

2007-04-01T23:59:59.000Z

317

Characteristics of Dispersed ZnO-Folic acid Conjugate in Aqueous Medium  

E-Print Network (OSTI)

The focus of this article is based on the aqueous dispersed state properties of inorganic ZnO nanoparticles (average size lessthan or equal to 4 nm), their surface modification and bio-functionalization with folic acid at physiological pH ~ 7.5, suitable for bio-imaging and targeted therapeutic application. While TEM studies of the ZnO nano-crystallites have been performed to estimate their size and morphology in dry state, the band gap properties of the freshly prepared samples, the hydrodynamic size in aqueous solution phase and the wide fluorescence range in visible region have been investigated to establish the fact that the sol is particularly suitable for the bio-medical purpose in the aqueous dispersed state. Key words: ZnO nanoparticle; folic acid; band gap; hydrodynamic size; fluorescence.

Sreetama Dutta; Bichitra Nandi Ganguly

2013-12-04T23:59:59.000Z

318

FLUIDIZED BED STEAM REFORMED MINERAL WASTE FORMS: CHARACTERIZATION AND DURABILITY TESTING  

SciTech Connect

Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium low activity wastes (LAW) such as those existing at the Hanford site, at the Idaho National Laboratory (INL), and the Savannah River Site (SRS). The addition of clay, charcoal, and a catalyst as co-reactants with the waste denitrates the aqueous wastes and forms a granular mineral waste form that can subsequently be made into a monolith for disposal if necessary. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage and ring structures and iron bearing spinel minerals. The mineralization occurs at moderate temperatures between 650-750 C in the presence of superheated steam. The cage and ring structured feldspathoid minerals atomically bond radionuclides like Tc-99 and Cs-137 and anions such as SO{sub 4}, I, F, and Cl. The spinel minerals stabilize Resource Conservation and Recovery Act (RCRA) hazardous species such as Cr and Ni. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium bearing waste (SBW) in pilot scale facilities at the Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The results of the SPFT testing and the activation energies for dissolution are discussed in this study.

Jantzen, C; Troy Lorier, T; John Pareizs, J; James Marra, J

2006-12-06T23:59:59.000Z

319

FLUIDIZED BED STEAM REFORMED MINERAL WASTE FORMS: CHARACTERIZATION AND DURABILITY TESTING  

SciTech Connect

Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium low activity wastes (LAW) such as those existing at the Hanford site, at the Idaho National Laboratory (INL), and the Savannah River Site (SRS). The addition of clay, charcoal, and a catalyst as co-reactants with the waste denitrates the aqueous wastes and forms a granular mineral waste form that can subsequently be made into a monolith for disposal if necessary. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage and ring structures and iron bearing spinel minerals. The mineralization occurs at moderate temperatures between 650-750 C in the presence of superheated steam. The cage and ring structured feldspathoid minerals atomically bond radionuclides like Tc-99 and Cs-137 and anions such as SO4, I, F, and Cl. The spinel minerals stabilize Resource Conservation and Recovery Act (RCRA) hazardous species such as Cr and Ni. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low-activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium bearing waste (SBW) in pilot scale facilities at the Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The results of the SPFT testing and the activation energies for dissolution are discussed in this study.

Jantzen, C; Troy Lorier, T; John Pareizs, J; James Marra, J

2007-03-31T23:59:59.000Z

320

Electrochemical fuel cell generator having an internal and leak tight hydrocarbon fuel reformer  

DOE Patents (OSTI)

An electrochemical fuel cell generator configuration is made having a generator section which contains a plurality of axially elongated fuel cells, each cell containing a fuel electrode, air electrode, and solid oxide electrolyte between the electrodes, in which axially elongated dividers separate portions of the fuel cells from each other, and where at least one divider also reforms a reformable fuel gas mixture prior to electricity generation reactions, the at least one reformer-divider is hollow having a closed end and an open end entrance for a reformable fuel mixture to pass to the closed end of the divider and then reverse flow and pass back along the hollowed walls to be reformed, and then finally to pass as reformed fuel out of the open end of the divider to contact the fuel cells, and further where the reformer-divider is a composite structure having a gas diffusion barrier of metallic foil surrounding the external walls of the reformer-divider except at the entrance to prevent diffusion of the reformable gas mixture through the divider, and further housed in an outer insulating jacket except at the entrance to prevent short-circuiting of the fuel cells by the gas diffusion barrier. 10 figs.

Dederer, J.T.; Hager, C.A.

1998-03-31T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Electrochemical fuel cell generator having an internal and leak tight hydrocarbon fuel reformer  

DOE Patents (OSTI)

An electrochemical fuel cell generator configuration is made having a generator section which contains a plurality of axially elongated fuel cells, each cell containing a fuel electrode, air electrode, and solid oxide electrolyte between the electrodes, in which axially elongated dividers separate portions of the fuel cells from each other, and where at least one divider also reforms a reformable fuel gas mixture prior to electricity generation reactions, the at least one reformer-divider is hollow having a closed end and an open end entrance for a reformable fuel mixture to pass to the closed end of the divider and then reverse flow and pass back along the hollowed walls to be reformed, and then finally to pass as reformed fuel out of the open end of the divider to contact the fuel cells, and further where the reformer-divider is a composite structure having a gas diffusion barrier of metallic foil surrounding the external walls of the reformer-divider except at the entrance to prevent diffusion of the reformable gas mixture through the divider, and further housed in an outer insulating jacket except at the entrance to prevent short-circuiting of the fuel cells by the gas diffusion barrier.

Dederer, Jeffrey T. (Valencia, PA); Hager, Charles A. (Mars, PA)

1998-01-01T23:59:59.000Z

322

Beyond National Uniformity: Diverging Local Economic Governance Under Japan's Decentralization Reforms  

E-Print Network (OSTI)

a Research Agenda for Public-Private Partnerships in thesectors in reforms for public-private partnership. Theunder the banner of public-private partnership. New

Lee, Jung Hwan

2010-01-01T23:59:59.000Z

323

Methodology and Estimation of the Welfare Impact of Energy Reforms on Households in Azerbaijan.  

E-Print Network (OSTI)

??ABSTRACT Title of Dissertation: METHODOLOGY AND ESTIMATION OF THE WELFARE IMPACT OF ENERGY REFORMS ON HOUSEHOLDS IN AZERBAIJAN Irina Klytchnikova, Doctor of Philosophy, 2006 Dissertation… (more)

Klytchnikova, Irina

2006-01-01T23:59:59.000Z

324

Regulatory Reform in the Wake of the Financial Crisis of 2007—2008  

E-Print Network (OSTI)

Purpose – The purpose of this paper is to analyse regulatory reform in the wake of the financial crisis of 2007-2008.

Lo, Andrew W.

325

Microchannel steam-methane reforming under constant and variable surface temperature distributions.  

E-Print Network (OSTI)

??Steam-methane reforming is a well understood industrial process used for generating hydrogen and synthesis gas. The reaction is generally carried out with residence times on… (more)

[No author

2010-01-01T23:59:59.000Z

326

A Mixed-Dimensionality Modeling Approach for Interaction of Heterogeneous Steam Reforming Reactions and Heat Transfer.  

E-Print Network (OSTI)

??Hydrogen is most often produced on an industrial scale by catalytic steam methane reforming, an equilibrium-limited, highly endothermic process requiring the substantial addition of heat… (more)

Valensa, Jeroen

2009-01-01T23:59:59.000Z

327

Fuel-flexible partial oxidation reforming of hydrocarbons for automotive applications.  

DOE Green Energy (OSTI)

Micro-reactor tests indicate that our partial oxidation catalyst is fuel-flexible and can reform conventional (gasoline and diesel) and alternative (ethanol, methanol, natural gas) fuels to hydrogen rich product gases with high hydrogen selectivity. Alcohols are reformed at lower temperatures (< 600 C) while alkanes and unsaturated hydrocarbons require slightly higher temperatures. Cyclic hydrocarbons and aromatics have also been reformed at relatively low temperatures, however, a different mechanism appears to be responsible for their reforming. Complex fuels like gasoline and diesel, which are mixtures of a broad range of hydrocarbons, require temperatures of > 700 C for maximum hydrogen production.

Ahmed, S.; Carter, J. D.; Kopasz, J. P.; Krumpelt, M.; Wilkenhoener, R.

1999-06-07T23:59:59.000Z

328

The Politics of Revenue-Raising Tax Reform in Latin America  

E-Print Network (OSTI)

in the region. These rate increases, along with reforms toby the marginal tax rate increase of 1992. Other causallow despite a small rate increase in 2001—interviews with

Fairfield, Tasha

2010-01-01T23:59:59.000Z

329

Hard or Soft? Institutional Reforms and Infrastructure Spending as Determinants of Foreign Direct Investment in China  

E-Print Network (OSTI)

Soft? Institutional Reforms and Infrastructure Spending aswe examine whether hard infrastructure in the form of moreand railroads or soft infrastructure in the form of more

Fung, K. C.; Garcia-Herrero, Alicia; Iizaka, Hitomi; Siu, Alan

2005-01-01T23:59:59.000Z

330

The Ambiguous Transition: Building State Capacity and Expanding Popular Participation in Venezuela's Agrarian Reform  

E-Print Network (OSTI)

El Universal, Caracas, Venezuela. Bengelsdorf, Carollee.Crisis and Reform in Venezuela. ” Journal of Interamerican2):27-61. Datamonitor. (2004). “Venezuela Country Profile. ”

Page, Tiffany Linton

2011-01-01T23:59:59.000Z

331

Heat Transfer Limitations in Hydrogen Production Via Steam Reformation: The Effect of Reactor Geometry  

E-Print Network (OSTI)

Hydrogen production Reactors, M.S. Thesis, University ofREFORMATION: THE EFFECT OF REACTOR GEOMETRY David, R. ,have been manifest with reactors of different geometries. In

Vernon, David R.; Davieau, David D.; Dudgeon, Bryce A.; Erickson, Paul A.

2006-01-01T23:59:59.000Z

332

Sulfur-tolerant natural gas reforming for fuel-cell applications.  

E-Print Network (OSTI)

??An attractive simplification of PEM-FC systems operated with natural gas would be the use of a sulfur tolerant reforming catalyst, but such a catalyst has… (more)

Hennings, Ulrich

2010-01-01T23:59:59.000Z

333

Phase Stability, Phase Transformations, and Reactive Phase ...  

Science Conference Proceedings (OSTI)

Jul 31, 2012 ... New Phase in Stoichiometric Cu6Sn5 and Effect of Ni Addition on Phase Stabilization in Wide Temperature Range · Optical Properties of ...

334

Phase Diagrams  

Science Conference Proceedings (OSTI)

Mar 7, 2013 ... Computational Thermodynamics and Kinetics: Phase Diagrams ... TMS: Alloy Phases Committee, TMS: Chemistry and Physics of Materials ...

335

Autothermal and partial oxidation reformer-based fuel processor, method for improving catalyst function in autothermal and partial oxidation reformer-based processors  

DOE Patents (OSTI)

The invention provides a fuel processor comprising a linear flow structure having an upstream portion and a downstream portion; a first catalyst supported at the upstream portion; and a second catalyst supported at the downstream portion, wherein the first catalyst is in fluid communication with the second catalyst. Also provided is a method for reforming fuel, the method comprising contacting the fuel to an oxidation catalyst so as to partially oxidize the fuel and generate heat; warming incoming fuel with the heat while simultaneously warming a reforming catalyst with the heat; and reacting the partially oxidized fuel with steam using the reforming catalyst.

Ahmed, Shabbir; Papadias, Dionissios D.; Lee, Sheldon H. D.; Ahluwalia, Rajesh K.

2013-01-08T23:59:59.000Z

336

Atomistic insights into aqueous corrosion of copper.  

SciTech Connect

Corrosion is a fundamental problem in electrochemistry and represents a mode of failure of technologically important materials. Understanding the basic mechanism of aqueous corrosion of metals such as Cu in presence of halide ions is hence essential. Using molecular dynamics simulations incorporating reactive force-field (ReaxFF), the interaction of copper substrates and chlorine under aqueous conditions has been investigated. These simulations incorporate effects of proton transfer in the aqueous media and are suitable for modeling the bond formation and bond breakage phenomenon that is associated with complex aqueous corrosion phenomena. Systematic investigation of the corrosion process has been carried out by simulating different chlorine concentration and solution states. The structural and morphological differences associated with metal dissolution in the presence of chloride ions are evaluated using dynamical correlation functions. The simulated atomic trajectories are used to analyze the charged states, molecular structure and ion density distribution which are utilized to understand the atomic scale mechanism of corrosion of copper substrates under aqueous conditions. Increased concentration of chlorine and higher ambient temperature were found to expedite the corrosion of copper. In order to study the effect of solution states on the corrosion resistance of Cu, partial fractions of proton or hydroxide in water were configured, and higher corrosion rate at partial fraction hydroxide environment was observed. When the Cl{sup -} concentration is low, oxygen or hydroxide ion adsorption onto Cu surface has been confirmed in partial fraction hydroxide environment. Our study provides new atomic scale insights into the early stages of aqueous corrosion of metals such as copper.

Jeon, B.; Sankaranarayanan, S. K. R. S.; van Duin, A. C. T.; Ramanathan, S. (Center for Nanoscale Materials); (Harvard Univ.); (Penn State Univ.)

2011-06-21T23:59:59.000Z

337

Separation of metal ions from aqueous solutions  

DOE Patents (OSTI)

This invention is comprised of a process and apparatus for quantitatively and selectively separating metal ions from mixtures thereof in aqueous solution. The apparatus includes, in combination, a horizontal electrochemical flowing cell containing flowing bulk electrolyte solution and an aqueous, metal ion-containing solution, the cell containing a metal mesh working electrode, a counter electrode positioned downstream from the working electrode, an independent variable power supply/potentiostat positioned outside of the flowing cell and connected to the electrodes, and optionally a detector such as a chromatographic detector, positioned outside the flowing cell. This apparatus and its operation has significant application where trace amounts of metal ions are to be separated.

Almon, A.

1991-12-31T23:59:59.000Z

338

THE TREATMENT OF LOW ACTIVITY AQUEOUS WASTES  

SciTech Connect

The equipment and treatment methods for processing low-activity aqueous wastes at the Latina nuclear power station are discussed. The effluent treatment plant serves two purposes: purification of cooling pond water and decontamination of aqueous wastes from such outlets as regenerant solutions, active laundry and change houses, decontamination center, coffin washing, and charge machine washing. The treatment process consists of chemical precipitation followed by filtration of the sludges thus produced. The process is then followed by ion exchange on a natural inorganic material such as vermiculite and evaporation. This process produces a decontamination factor of l0/sup 3/ to 10/ sup 4/. (N.W.R.)

Cartwright, A.C.

1962-01-01T23:59:59.000Z

339

Regulatory Reform and License Termination Planning in Decommissioning  

SciTech Connect

Decommissioning of commercial nuclear power plants (NPPs) must be safe and cost-effective and consider the needs of a wide range of stakeholders. The creative tension among these objectives has provided opportunities to reform the way these plants are regulated and managed in decommissioning. Enlightened and visionary leaders from the U.S. Nuclear Regulatory Commission (NRC) and industry are seizing these opportunities to create new paradigms for risk-informed regulation; creative stakeholder involvement; and effective, end-state focused, license termination planning.

Michael J. Meisner

2000-06-04T23:59:59.000Z

340

Electricity Reform in Chile: Lessons for Developing Countries  

E-Print Network (OSTI)

% for the country as a whole, but 58% in the central system)7 but as demand increases fossil fuels have become more important (in this it is comparable to Columbia and the south west of Brazil). However Chile is perhaps unusual among developing countries because... of the strength of protection for private property and the stability engendered by the long period of economically disciplined military rule. 2. Chile’s Electricity Reform In 1974 Chile’s electricity utilities were in a mess.8 Inflation, high fuel prices...

Pollitt, Michael G.

2006-03-14T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

SMALL SCALE FUEL CELL AND REFORMER SYSTEMS FOR REMOTE POWER  

DOE Green Energy (OSTI)

New developments in fuel cell technologies offer the promise of clean, reliable affordable power, resulting in reduced environmental impacts and reduced dependence on foreign oil. These developments are of particular interest to the people of Alaska, where many residents live in remote villages, with no roads or electrical grids and a very high cost of energy, where small residential power systems could replace diesel generators. Fuel cells require hydrogen for efficient electrical production, however. Hydrogen purchased through conventional compressed gas suppliers is very expensive and not a viable option for use in remote villages, so hydrogen production is a critical piece of making fuel cells work in these areas. While some have proposed generating hydrogen from renewable resources such as wind, this does not appear to be an economically viable alternative at this time. Hydrogen can also be produced from hydrocarbon feed stocks, in a process known as reforming. This program is interested in testing and evaluating currently available reformers using transportable fuels: methanol, propane, gasoline, and diesel fuels. Of these, diesel fuels are of most interest, since the existing energy infrastructure of rural Alaska is based primarily on diesel fuels, but this is also the most difficult fuel to reform, due to the propensity for coke formation, due to both the high vaporization temperature and to the high sulfur content in these fuels. There are several competing fuel cell technologies being developed in industry today. Prior work at UAF focused on the use of PEM fuel cells and diesel reformers, with significant barriers identified to their use for power in remote areas, including stack lifetime, system efficiency, and cost. Solid Oxide Fuel Cells have demonstrated better stack lifetime and efficiency in demonstrations elsewhere (though cost still remains an issue), and procuring a system for testing was pursued. The primary function of UAF in the fuel cell industry is in the role of third party independent testing. In order for tests to be conducted, hardware must be purchased and delivered. The fuel cell industry is still in a pre-commercial state, however. Commercial products are defined as having a fixed set of specifications, fixed price, fixed delivery date, and a warrantee. Negotiations with fuel cell companies over these issues are often complex, and the results of these discussions often reveal much about the state of development of the technology. This work includes some of the results of these procurement experiments. Fuel cells may one day replace heat engines as the source of electrical power in remote areas. However, the results of this program to date indicate that currently available hardware is not developed sufficiently for these environments, and that significant time and resources will need to be committed for this to occur.

Dennis Witmer

2003-12-01T23:59:59.000Z

342

DEVELOPMENT OF A CATALYST/SORBENT FOR METHANE REFORMING  

DOE Green Energy (OSTI)

This work has led to the initial development of a very promising material that has the potential to greatly simplify hydrocarbon reforming for the production of hydrogen and to improve the overall efficiency and economics of the process. This material, which was derived from an advanced calcium-based sorbent, was composed of core-in-shell pellets such that each pellet consisted of a CaO core and an alumina-based shell. By incorporating a nickel catalyst in the shell, a combined catalyst and sorbent was prepared to facilitate the reaction of hydrocarbons with steam. It was shown that this material not only catalyzes the reactions of methane and propane with steam, it also absorbs CO{sub 2} simultaneously, and thereby separates the principal reaction products, H{sub 2} and CO{sub 2}. Furthermore, the absorption of CO{sub 2} permits the water gas shift reaction to proceed much further towards completion at temperatures where otherwise it would be limited severely by thermodynamic equilibrium. Therefore, an additional water gas shift reaction step would not be required to achieve low concentrations of CO. In a laboratory test of methane reforming at 600 C and 1 atm it was possible to produce a gaseous product containing 96 mole% H{sub 2} (dry basis) while also achieving a H{sub 2} yield of 95%. Methane reforming under these conditions without CO{sub 2} absorption provided a H{sub 2} concentration of 75 mole% and yield of 82%. Similar results were achieved in a test of propane reforming at 560 C and 1 atm which produced a product containing 96 mole% H{sub 2} while CO{sub 2} was being absorbed but which contained only 69 mole% H{sub 2} while CO{sub 2} was not being absorbed. These results were achieved with an improved catalyst support that was developed by replacing a portion of the {alpha}-alumina in the original shell material with {gamma}-alumina having a much greater surface area. This replacement had the unfortunate consequence of reducing the overall compressive strength of the core-in-shell pellets. Therefore, a preliminary study of the factors that control the surface area and compressive strength of the shell material was conducted. The important factors were identified as the relative concentrations and particle size distributions of the {alpha}-alumina, {gamma}-alumina, and limestone particles plus the calcination temperature and time used for sintering the shell material. An optimization of these factors in the future could lead to the development of a material that has both the necessary mechanical strength and catalytic activity.

B.H. Shanks; T.D. Wheelock; Justinus A. Satrio; Timothy Diehl; Brigitte Vollmer

2004-09-27T23:59:59.000Z

343

Cost Analysis of Bio-Derived Liquids Reforming (Presentation)  

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

Analysis of Analysis of Bio-Derived Liquids Reforming Brian James Directed Technologies, Inc. 6 November 2007 This presentation does not contain any proprietary, confidential, or otherwise restricted information Objective * Assess cost of H 2 from bio-derived liquids * Looking at forecourt scale systems: 100-1500kg/day * Emphasis on Ethanol * Looking at both "conventional" and "advanced" systems * Interaction with the Researchers is bi-directional * Researchers help me with catalysts, performance, configurations * I can assist Researchers with system studies, configurations, and system performance estimates * Output of my work will be: * System/Configuration Definition * Performance specification & optimization * Capital cost estimation

344

A flexible computer software package for industrial steam reformers and methanators based on rigorous heterogeneous mathematical models  

Science Conference Proceedings (OSTI)

An advanced software package for industrial steam reformers based upon heterogeneous models for the catalyst tube is developed and successfully checked against a number of top-fired and side-fired industrial reformers. The package is further developed ...

F. M. Alhabdan; M. A. Abashar; S. S. E. Elnashaie

1992-11-01T23:59:59.000Z

345

Novel Catalytic Fuel Reforming Using Micro-Technology with Advanced Separations Technology  

E-Print Network (OSTI)

by the combustion of membrane raffinate for the production of clean hydrogen by steam reforming natural gas primary fuel sources from existing production and distribution networks ­ i.e. natural gas, gasoline gas -- optimize catalyst composition and evaluate reforming conditions. · Hydrogen purification using

346

Evaluation of dissociated and steam-reformed methanol as automotive engine fuels  

SciTech Connect

Dissociated and steam reformed methanol were evaluated as automotive engine fuels. Advantages and disadvantages in using methanol in the reformed rather than liquid state are discussed. Engine dynamometer tests were conducted with a four cylinder, 2.3 liter, spark ignition automotive engine to determine performance and emission characteristics operating on simulated dissociated and steam reformed methanol (2H/sub 2/ + CO and 3H/sub 2/ + CO/sub 2/ respectively), and liquid methanol. Results are presented for engine performance and emissions as functions of equivalence ratio, at various throttle settings and engine speeds. Operation on dissociated and steam reformed methanol was characterized by flashback (violent propagation of a flame into the intake manifold) which limited operation to lower power output than was obtainable using liquid methanol. It was concluded that: an automobile could not be operated solely on dissociated or steam reformed methanol over the entire required power range - a supplementary fuel system or power source would be necessary to attain higher powers; the use of reformed methanol, compared to liquid methanol, may result in a small improvement in thermal efficiency in the low power range; dissociated methanol is a better fuel than steam reformed methanol for use in a spark ignition engine; and use of dissociated or steam reformed methanol may result in lower exhaust emissions compared to liquid methanol. 36 references, 27 figures, 3 tables.

Lalk, T.R.; McCall, D.M.; McCanlies, J.M.

1984-05-01T23:59:59.000Z

347

Performance of Sulfur Tolerant Reforming Catalysts for Production of Hydrogen from Jet Fuel Simulants  

E-Print Network (OSTI)

ReceiVed August 2, 2007 The development of robust desulfurizers and new reforming catalysts for fuel cells: the desulfurization of jet fuel and the development of sulfur-tolerant reforming catalysts/C) ratios. The water gas shift reaction is then used to convert additional CO into CO2. Nickel has been

Azad, Abdul-Majeed

348

Simulation and Optimization of the Stabilizer Tower Operation at Catalytic Reforming of Esfahan Oil Refining Company  

Science Conference Proceedings (OSTI)

Production of gasoline with low RVP specifications have made the operators of the catalytic reforming unit of Esfahan Oil refining company in Iran to apply new operating conditions. RVP is an abbreviation for Reid Vapor Pressure which is the vapor pressure ... Keywords: RVP, platformate, initial boiling point, catalytic reforming, distillation curve

Ali Izadyar; Bahram Hashemi Shahraki; Ahmad Shariati

2010-01-01T23:59:59.000Z

349

Achieving Universal Coverage through Comprehensive Health Reform: The Vermont Experience – Evaluation Results  

E-Print Network (OSTI)

Vermont’s comprehensive health reform law, the Health Care Affordability Acts (HCAA) for Vermonters, was passed in 2006 with the following three goals in mind: 1. To achieve universal access to affordable health insurance for all Vermonters 2. To improve quality of care and contain costs through health system reform

Ronald Deprez; Sherry Glied; Kira Rodriguez; Bill Perry; Brian Robertson; Nina Schwabe

2011-01-01T23:59:59.000Z

350

Catalytic reforming and hydrocracking of organic compounds employing promoted zinc titanate as the catalytic agent  

Science Conference Proceedings (OSTI)

The catalytic reforming of a feedstock which contains at least one reformable organic compound or the hydrocracking of a feedstock which contains at least one hydrocrackable organic compound is carried out in the presence of a catalyst composition comprising zinc, titanium and rhenium.

Drehman, L.E.; Farha, F.E.

1981-04-21T23:59:59.000Z

351

Catalytic reforming and hydrocracking of organic compounds employing zinc titanate as the catalytic agent  

Science Conference Proceedings (OSTI)

The catalytic reforming of a feedstock which contains at least one reformable organic compound or the hydrocracking of a feedstock which contains at least one hydrocrackable organic compound is carried out in the presence of a catalyst composition comprising zinc and titanium.

Drehman, L.E.; Farha, F.E.; Walker, D.W.

1981-04-21T23:59:59.000Z

352

Electricity Markets: Should the Rest of the World Adopt the UK Reforms?  

E-Print Network (OSTI)

PWP-069 Electricity Markets: Should the Rest of the World Adopt the UK Reforms? Catherine D;1 Electricity Markets: Should the Rest of the World Adopt the UK Reforms?1 By Catherine D. Wolfram2 Britain was one of the first countries to liberalize its electricity industry when it restructured and privatized

California at Berkeley. University of

353

Gregory H. Friedman: Provided for The Committee on Oversight and Government Reform U.S. House of Representatives  

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

Gregory H. Friedman: Provided for The Committee on Oversight and Government Reform U.S. House of Representatives

354

Agenda Setting And The Role Of Leadership In National Health Care Reform During The Early 1990s  

E-Print Network (OSTI)

Health care reform was the dominant issue on the political agenda during the early 1990s. Few issues

Kang, Michael S,

2006-01-05T23:59:59.000Z

355

The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate  

Open Energy Info (EERE)

The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate Change Jump to: navigation, search Tool Summary LAUNCH TOOL Name: The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate Change Agency/Company /Organization: International Institute for Sustainable Development (IISD) Topics: Policies/deployment programs Resource Type: Lessons learned/best practices Website: www.iisd.org/pdf/2009/bali_2_copenhagen_dom_policy_lessons.pdf The Lessons of Practice: Domestic Policy Reform as a Way to Address Climate Change Screenshot References: The Lessons of Practice[1] Summary "The objectives of this paper are threefold: to review experience to date with policy reforms that can help mitigate climate change, to review work

356

Federal Onshore Oil and Gas Leasing Reform Act of 1987 (FOOGLRA) | Open  

Open Energy Info (EERE)

Page Page Edit with form History Facebook icon Twitter icon » Federal Onshore Oil and Gas Leasing Reform Act of 1987 (FOOGLRA) Jump to: navigation, search Statute Name Federal Onshore Oil and Gas Leasing Reform Act of 1987 (FOOGLRA) Year 1987 Url FederalOnshore1987.jpg Description Another amendment to the Mineral Leasing Act, The Federal Onshore Oil and Gas Leasing Reform Act of 1987 granted the USDA Forest Service the authority to make decisions and implement regulations concerning the leasing of public domain minerals on National Forest System lands containing oil and gas. References Federal Onshore Oil and Gas Leasing Reform Act of 1987 (FOOGLRA)[1] Federal Onshore Oil and Gas Leasing Reform Act of 1987 (FOOGLRA) (30 U.S.C. § 181 et seq.) - Another amendment to the Mineral Leasing Act, The Federal

357

Update on IT Reform at the Department of Energy | Department of Energy  

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

Update on IT Reform at the Department of Energy Update on IT Reform at the Department of Energy Update on IT Reform at the Department of Energy June 4, 2012 - 2:14pm Addthis The last 18 months have seen great improvements in the Department of Energy's (DOE) information technology and cybersecurity. A major factor in our success is our alignment with the 25 Point Implementation Plan To Reform Federal Information Technology Management to move to a "Cloud First" environment and maximize the use of shared services to reduce costs and improve IT delivery. Cloud-First/Shared Services: In August 2011, we revamped our online presence by launching Energy.gov and delivering a single platform solution through an open-source content management system and cloud hosting environment. Ultimately, the website reform effort aims to save taxpayers more than $10 million per

358

HYDROGEN PRODUCTION FOR FUEL CELLS VIA REFORMING COAL-DERIVED METHANOL  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the tenth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of January 1-March 31, 2006. This quarter saw progress in six areas. These areas are: (1) The effect of catalyst dimension on steam reforming, (2) Transient characteristics of autothermal reforming, (3) Rich and lean autothermal reformation startup, (4) Autothermal reformation degradation with coal derived methanol, (5) Reformate purification system, and (6) Fuel cell system integration. All of the projects are proceeding on or slightly ahead of schedule.

Paul A. Erickson

2006-04-01T23:59:59.000Z

359

Separation of normally gaseous hydrocarbons from a catalytic reforming effluent and recovery of purified hydrogen  

Science Conference Proceedings (OSTI)

A process for the catalytic reforming of a hydrocarbonaceous feedstock, preferably to produce high quality gasoline boiling range products, is disclosed. Relatively impure hydrogen is separated from the reforming zone effluent, compressed, and recontacted with at least a portion of the liquid reformate product to provide relatively pure hydrogen, a portion of which is recycled to the reforming zone. The balance is further compressed and recontacted with at least a portion of the liquid reformate product in a plural stage absorption zone to provide an improved recovery of normally gaseous hydrocarbons as well as an improved recovery of purified hydrogen at a pressure suitable, for example, the relatively high pressure hydrotreating of sulfur-containing feedstocks.

O'brien, D.E.

1982-06-08T23:59:59.000Z

360

Catalytic reforming process using noble metal alkaline zeolites  

Science Conference Proceedings (OSTI)

This patent describes improvement in a process wherein a gasoline boiling range hydrocarbonaceous feedstock is catalytically reformed in the presence of hydrogen in a reforming process unit comprised of serially connected reactors wherein each of the reactors contains a supported noble metal-containing catalyst. The improvement comprises the noble-metal catalyst of at least one reactor being selected from the group consisting of alkaline faujasite zeolite, L zeolite and zeolites isostructural thereto, which catalysts are prepared by a: contacting an alkaline faujasite zeolite, L zeolite, or zeolite isostructural thereto, with a noble metal composition selected from Pt(acetylacetonate){sub 2} or Pd(acetylacetonate){sub 2} for an effective amount of time to form a substantially homogeneous mixture and to incorporate the platinum and/or palladium into the near surface regions of the zeolite, but not to disperse the platinum and/or palladium throughout the entire zeolite; and calcining the so treated zeolite at a temperature from about 250 {degrees} C to about 600 {degrees} C for an effective amount of time.

Schweizer, A.E.

1991-02-12T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Catalytic Reforming Downstream Processing of Fresh Feed Input  

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

Process: Catalytic Reforming Catalytic Cracking Catalytic Hydrocracking Delayed and Fluid Coking Period-Unit: Monthly-Thousand Barrels per Day Annual-Thousand Barrels per Day Process: Catalytic Reforming Catalytic Cracking Catalytic Hydrocracking Delayed and Fluid Coking Period-Unit: Monthly-Thousand Barrels per Day Annual-Thousand Barrels per Day Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes Show Data By: Process Area Apr-13 May-13 Jun-13 Jul-13 Aug-13 Sep-13 View History U.S. 2,563 2,667 2,739 2,807 2,705 2,609 2010-2013 PADD 1 176 178 180 173 156 167 2010-2013 East Coast 166 164 163 161 140 153 2010-2013 Appalachian No. 1 9 14 16 12 15 14 2010-2013 PADD 2 642 638 668 695 677 615 2010-2013 Ind., Ill. and Ky. 426 411 426 460 450 399 2010-2013 Minn., Wis., N. Dak., S. Dak. 67 62 70 72 72 57 2010-2013 Okla., Kans., Mo.

362

[98e]-Catalytic reforming of gasoline and diesel fuel  

DOE Green Energy (OSTI)

Argonne National Laboratory is developing a fuel processor for converting liquid hydrocarbon fuels to a hydrogen-rich product suitable for a polymer electrolyte fuel cell stack. The processor uses an autothermal reformer to convert the feed to a mixture of hydrogen, carbon dioxide, carbon monoxide and water with trace quantities of other components. The carbon monoxide in the product gas is then converted to carbon dioxide in water-gas shift and preferential oxidation reactors. Fuels that have been tested include standard and low-sulfur gasoline and diesel fuel, and Fischer-Tropsch fuels. Iso-octane and n-hexadecane were also examined as surrogates for gasoline and diesel, respectively. Complete conversion of gasoline was achieved at 750 C in a microreactor over a novel catalyst developed at Argonne. Diesel fuel was completely converted at 850 C over this same catalyst. Product streams contained greater than 60% hydrogen on a dry, nitrogen-free basis with iso-octane, gasoline, and n-hexadecane. For a diesel fuel, product streams contained >50% hydrogen on a dry, nitrogen-free basis. The catalyst activity did not significantly decrease over >16 hours operation with the diesel fuel feed. Coke formation was not observed. The carbon monoxide fraction of the product gas could be reduced to as low as 1% on a dry, nitrogen-free basis when the water-gas shift reactors were used in tandem with the reformer.

Pereira, C.; Wilkenhoener, R.; Ahmed, S.; Krumpelt, M.

2000-02-29T23:59:59.000Z

363

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, William A. (Hampton Bays, NY); Healy, Francis E. (Massapequa, NY); Sapienza, Richard S. (Shoreham, NY)

1985-01-01T23:59:59.000Z

364

Corrosion inhibitor for aqueous ammonia absorption system  

DOE Patents (OSTI)

A method of inhibiting corrosion and the formation of hydrogen and thus improving absorption in an ammonia/water absorption refrigeration, air conditioning or heat pump system by maintaining the hydroxyl ion concentration of the aqueous ammonia working fluid within a selected range under anaerobic conditions at temperatures up to 425.degree. F. This hydroxyl ion concentration is maintained by introducing to the aqueous ammonia working fluid an inhibitor in an amount effective to produce a hydroxyl ion concentration corresponding to a normality of the inhibitor relative to the water content ranging from about 0.015 N to about 0.2 N at 25.degree. C. Also, working fluids for inhibiting the corrosion of carbon steel and resulting hydrogen formation and improving absorption in an ammonia/water absorption system under anaerobic conditions at up to 425.degree. F. The working fluids may be aqueous solutions of ammonia and a strong base or aqueous solutions of ammonia, a strong base, and a specified buffer.

Phillips, Benjamin A. (Benton Harbor, MI); Whitlow, Eugene P. (St. Joseph, MI)

1998-09-22T23:59:59.000Z

365

Corrosion inhibitor for aqueous ammonia absorption system  

DOE Patents (OSTI)

A method is described for inhibiting corrosion and the formation of hydrogen and thus improving absorption in an ammonia/water absorption refrigeration, air conditioning or heat pump system by maintaining the hydroxyl ion concentration of the aqueous ammonia working fluid within a selected range under anaerobic conditions at temperatures up to 425 F. This hydroxyl ion concentration is maintained by introducing to the aqueous ammonia working fluid an inhibitor in an amount effective to produce a hydroxyl ion concentration corresponding to a normality of the inhibitor relative to the water content ranging from about 0.015 N to about 0.2 N at 25 C. Also, working fluids for inhibiting the corrosion of carbon steel and resulting hydrogen formation and improving absorption in an ammonia/water absorption system under anaerobic conditions at up to 425 F. The working fluids may be aqueous solutions of ammonia and a strong base or aqueous solutions of ammonia, a strong base, and a specified buffer. 5 figs.

Phillips, B.A.; Whitlow, E.P.

1998-09-22T23:59:59.000Z

366

Water & Aqueous Solutions. Final Progress Report  

SciTech Connect

The Gordon Research Conference (GRC) on Water & Aqueous Solutions was held at Holderness School, New Hampshire, 8/4/02 thru 8/9/02. Emphasis was placed on current unpublished research and discussion of the future target areas in this field.

2002-08-09T23:59:59.000Z

367

Method for aqueous radioactive waste treatment  

DOE Patents (OSTI)

Plutonium, strontium, and cesium found in aqueous waste solutions resulting from nuclear fuel processing are removed by contacting the waste solutions with synthetic zeolite incorporating up to about 5 wt % titanium as sodium titanate in an ion exchange system. More than 99.9% of the plutonium, strontium, and cesium are removed from the waste solutions. 3 figures.

Bray, L.A.; Burger, L.L.

1994-03-29T23:59:59.000Z

368

Method for aqueous radioactive waste treatment  

DOE Patents (OSTI)

Plutonium, strontium, and cesium found in aqueous waste solutions resulting from nuclear fuel processing are removed by contacting the waste solutions with synthetic zeolite incorporating up to about 5 wt % titanium as sodium titanate in an ion exchange system. More than 99.9% of the plutonium, strontium, and cesium are removed from the waste solutions.

Bray, Lane A. (Richland, WA); Burger, Leland L. (Richland, WA)

1994-01-01T23:59:59.000Z

369

Low temperature aqueous desulfurization of coal  

DOE Patents (OSTI)

This invention describes a chemical process for desulfurizing coal, especially adaptable to the treatment of coal-water slurries, at temperatures as low as ambient, comprising treating the coal with aqueous titanous chloride whereby hydrogen sulfide is liberated and the desulfurized coal is separated with the conversion of titanous chloride to titanium oxides.

Slegeir, W.A.; Healy, F.E.; Sapienza, R.S.

1985-04-18T23:59:59.000Z

370

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

371

Phase 6.X Process | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Phase 6.X Process | National Nuclear Security Administration Phase 6.X Process | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Phase 6.X Process Home > Our Mission > Managing the Stockpile > Nuclear Weapons Life Cycle > Phase 6.X Process Phase 6.X Process The Phase 6.x Process is based on the original Joint Nuclear Weapons Life Cycle Process, which includes Phases 1 through 7 and covers all phases of a

372

Phase five  

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

Phase five Phase five 1663 Los Alamos science and technology magazine Latest Issue:November 2013 All Issues » submit Phase five Los Alamos physicists have conclusively demonstrated the existence of a new phase of matter. November 25, 2013 Phase five Scientists still have more to learn about the exotic physics of specialty materials. What makes the cuprates special? How about a new phase of matter. Ceramic metals known as cuprates have mystified physicists for decades. They exhibit a variety of distinct phases of matter, each with its own specific properties, including a phase bearing an exotic type of magnetism, a high-temperature superconducting phase, an ordinary metal phase, a poorly understood and weird metallic phase simply called a strange metal, and an equally poorly understood metallic phase known as the pseudogap. The

373

Stabilization of Nickel Metal Catalysts for Aqueous Processing ...  

Search PNNL. PNNL Home; About; Research; Publications; Jobs; News; Contacts; Stabilization of Nickel Metal Catalysts for Aqueous Processing Systems. ...

374

Aqueous Electrotechnologies: Progress in Theory and Practice - TMS  

Science Conference Proceedings (OSTI)

Aqueous Electrotechnologies: Progress in Theory and Practice ... catalyzed leaching, solvent extraction and ion exchange, and reactor modelling and design .

375

A Novel Slurry-Based Biomass Reforming Process Final Technical Report  

SciTech Connect

This project was focused on developing a catalytic means of producing H2 from raw, ground biomass, such as fast growing poplar trees, willow trees, or switch grass. The use of a renewable, biomass feedstock with minimal processing can enable a carbon neutral means of producing H2 in that the carbon dioxide produced from the process can be used in the environment to produce additional biomass. For economically viable production of H2, the biomass is hydrolyzed and then reformed without any additional purification steps. Any unreacted biomass and other byproduct streams are burned to provide process energy. Thus, the development of a catalyst that can operate in the demanding corrosive environment and presence of potential poisons is vital to this approach. The concept for this project is shown in Figure 1. The initial feed is assumed to be a >5 wt% slurry of ground wood in dilute base, such as potassium carbonate (K2CO3). Base hydrolysis and reforming of the wood is carried out at high but sub-critical pressures and temperatures in the presence of a solid catalyst. A Pd alloy membrane allows the continuous removal of pure , while the retentate, including methane is used as fuel in the plant. The project showed that it is possible to economically produce H2 from woody biomass in a carbon neutral manner. Technoeconomic analyses using HYSYS and the DOE's H2A tool [1] were used to design a 2000 ton day-1 (dry basis) biomass to hydrogen plant with an efficiency of 46% to 56%, depending on the mode of operation and economic assumptions, exceeding the DOE 2012 target of 43%. The cost of producing the hydrogen from such a plant would be in the range of $1/kg H2 to $2/kg H2. By using raw biomass as a feedstock, the cost of producing hydrogen at large biomass consumption rates is more cost effective than steam reforming of hydrocarbons or biomass gasification and can achieve the overall cost goals of the DOE Fuel Cell Technologies Program. The complete conversion of wood to hydrogen, methane, and carbon dioxide was repeatedly demonstrated in batch reactors varying in size from 50 mL to 7.6 L. The different wood sources (e.g., swamp maple, poplar, and commercial wood flour) were converted in the presence of a heterogeneous catalyst and base at relatively low temperatures (e.g., 310 �������°C) at sub-critical pressures sufficient to maintain the liquid phase. Both precious metal and base metal catalysts were found to be active for the liquid phase hydrolysis and reforming of wood. Pt-based catalysts, particularly Pt-Re, were shown to be more selective toward breaking C-C bonds, resulting in a higher selectivity to hydrogen versus methane. Ni-based catalysts were found to prefer breaking C-O bonds, favoring the production of methane. The project showed that increasing the concentration of base (base to wood ratio) in the presence of Raney Ni catalysts resulted in greater selectivity toward hydrogen but at the expense of increasing the production of undesirable organic acids from the wood, lowering the amount of wood converted to gas. It was shown that by modifying Ni-based catalysts with dopants, it was possible to reduce the base concentration while maintaining the selectivity toward hydrogen and increasing wood conversion to gas versus organic acids. The final stage of the project was the construction and testing of a demonstration unit for H2 production. This continuous flow demonstration unit consisted of wood slurry and potassium carbonate feed pump systems, two reactors for hydrolysis and reforming, and a gas-liquid separation system. The technical challenges associated with unreacted wood fines and Raney Ni catalyst retention limited the demonstration unit to using a fixed bed Raney Ni catalyst form. The lower activity of the larger particle Raney Ni in turn limited the residence time and thus the wood mass flow feed rate to 50 g min-1 for a 1 wt% wood slurry. The project demonstrated continuous H2 yields with unmodified, fixed bed Raney Ni, from 63% to 100% with correspond

Sean C. Emerson; Timothy D. Davis; A. Peles; Ying She; Joshua Sheffel; Rhonda R. Willigan; Thomas H. Vanderspurt; Tianli Zhu

2011-09-30T23:59:59.000Z

376

97e Intermediate Temperature Catalytic Reforming of Bio-Oil for Distributed Hydrogen Production  

Science Conference Proceedings (OSTI)

With the world's energy demands rapidly increasing, it is necessary to look to sources other than fossil fuels, preferably those that minimize greenhouse emissions. One such renewable source of energy is biomass, which has the added advantage of being a near-term source of hydrogen. While there are several potential routes to produce hydrogen from biomass thermally, given the near-term technical barriers to hydrogen storage and delivery, distributed technologies such that hydrogen is produced at or near the point of use are attractive. One such route is to first produce bio-oil via fast pyrolysis of biomass close to its source to create a higher energy-density product, then ship this bio-oil to its point of use where it can be reformed to hydrogen and carbon dioxide. This route is especially well suited for smaller-scale reforming plants located at hydrogen distribution sites such as filling stations. There is also the potential for automated operation of the conversion system. A system has been developed for volatilizing bio-oil with manageable carbon deposits using ultrasonic atomization and by modifying bio-oil properties, such as viscosity, by blending or reacting bio-oil with methanol. Non-catalytic partial oxidation of bio-oil is then used to achieve significant conversion to CO with minimal aromatic hydrocarbon formation by keeping the temperature at 650 C or less and oxygen levels low. The non-catalytic reactions occur primarily in the gas phase. However, some nonvolatile components of bio-oil present as aerosols may react heterogeneously. The product gas is passed over a packed bed of precious metal catalyst where further reforming as well as water gas shift reactions are accomplished completing the conversion to hydrogen. The approach described above requires significantly lower catalyst loadings than conventional catalytic steam reforming due to the significant conversion in the non-catalytic step. The goal is to reform and selectively oxidize the bio-oil and catalyze the water gas shift reaction without catalyzing methanation or oxidation of CO and H{sub 2}, thus attaining equilibrium levels of H{sub 2}, CO, H{sub 2}O, and CO{sub 2} at the exit of the catalyst bed. Experimental Bio-oil (mixed with varied amounts of methanol to reduce the viscosity and homogenize the bio-oil) or selected bio-oil components are introduced at a measured flow rate through the top of a vertical quartz reactor which is heated using a five zone furnace. The ultrasonic nozzle used to feed the reactants allows the bio-oil to flow down the center of the reactor at a low, steady flow rate. Additionally, the fine mist created by the nozzle allows for intimate mixing with oxygen and efficient heat transfer, providing optimal conditions to achieve high conversion at relatively low temperatures in the non-catalytic step thus reducing the required catalyst loading. Generation of the fine mist is especially important for providing good contact between non-volatile bio-oil components and oxygen. Oxygen and helium are also delivered at the top of the reactor via mass flow meters with the amount of oxygen being varied to maximize the yields of H{sub 2} and CO and the amount of helium being adjusted such that the gas phase residence time in the hot zone is {approx}0.3 and {approx}0.45 s for bio-oil and methanol experiments, respectively. A catalyst bed can be located at the bottom of the reactor tube. To date, catalyst screening experiments have used Engelhard noble metal catalysts. The catalysts used for these experiments were 0.5 % rhodium, ruthenium, platinum, and palladium (all supported on alumina). Experiments were performed using pure alumina as well. Both the catalyst type and the effect of oxygen and steam on the residual hydrocarbons and accumulated carbon containing particulates were investigated. The residence time before the catalyst is varied to determine the importance of the non-catalytic step and its potential effect on the required catalyst loading. Non-catalytic experiments (primarily homogeneous cracking) use a bed of quartz p

Marda, J. R.; Dean, A. M.; Czernik, S.; Evans, R. J.; French, R.; Ratcliff, M.

2008-01-01T23:59:59.000Z

377

Fundamental kinetic modeling of the catalytic reforming process  

E-Print Network (OSTI)

In this work, a fundamental kinetic model for the catalytic reforming process has been developed. The complex network of elementary steps and molecular reactions occurring in catalytic reforming has been generated through a computer algorithm characterizing the various species by vectors and Boolean relation matrices. The algorithm is based on the fundamental chemistry occurring on both acid and metal sites of the catalyst. Rates are expressed for each of the elementary steps involved in the transformation of the intermediates. The Hougen-Watson approach is used to express the rates of the molecular reactions occurring on the metal sites of the catalyst. The single event approach is used to account for the effect of structure of reactant and activated complex on the rate coefficients of the elementary steps occurring on the acid sites. This approach recognizes that even if the number of elementary steps is very large they belong to a very limited number of types, and therefore it is possible to express the kinetics of elementary steps by a reduced number of parameters. In addition, the single event approach leads to rate coefficients that are independent of the feedstock, due to their fundamental chemical nature. The total number of parameters at isothermal conditions is 45. To estimate these parameters, an objective function based upon the sum of squares of the residuals was minimized through the Marquardt algorithm. Intraparticle mass transport limitations and deactivation of the catalyst by coke formation are considered in the model. Both the Wilke and the Stefan-Maxwell approaches were used to calculate the concentration gradients inside of the particle. The heterogeneous kinetic model was applied in the simulation of the process for typical industrial conditions for both axial and radial flow fixed bed reactors. The influence of the main process variables on the octane number and reformate volume was investigated and optimal conditions were obtained. Additional aspects studied with the kinetic model are the reduction of aromatics, mainly benzene. The results from the simulations agree with the typical performance found in the industrial process.

Sotelo-Boyas, Rogelio

2005-12-01T23:59:59.000Z

378

Radionuclide and contaminant immobilization in the fluidized bed steam reforming waste products  

Science Conference Proceedings (OSTI)

The goal of this chapter is to introduce the reader to the Fluidized Bed Steam Reforming (FBSR) process and resulting waste form. The first section of the chapter gives an overview of the potential need for FBSR processing in nuclear waste remediation followed by an overview of the engineering involved in the process itself. This is followed by a description of waste form production at a chemical level followed by a section describing different process streams that have undergone the FBSR process. The third section describes the resulting mineral product in terms of phases that are present and the ability of the waste form to encapsulate hazardous and radioactive wastes from several sources. Following this description is a presentation of the physical properties of the granular and monolith waste form product including and contaminant release mechanisms. The last section gives a brief summary of this chapter and includes a section on the strengths associated with this waste form and the needs for additional data and remaining questions yet to be answered. The reader is directed elsewhere for more information on other waste forms such as Cast Stone (Lockrem, 2005), Ceramicrete (Singh et al., 1997, Wagh et al., 1999) and geopolymers (Kyritsis et al., 2009; Russell et al., 2006).

Neeway, James J.; Qafoku, Nikolla; Westsik, Joseph H.; Brown, Christopher F.; Jantzen, Carol; Pierce, Eric M.

2012-05-01T23:59:59.000Z

379

ELECTROCHEMISTRY AND ON-CELL REFORMATION MODELING FOR SOLID OXIDE FUEL CELL STACKS  

SciTech Connect

ABSTRACT Providing adequate and efficient cooling schemes for solid-oxide-fuel-cell (SOFC) stacks continues to be a challenge coincident with the development of larger, more powerful stacks. The endothermic steam-methane reformation reaction can provide cooling and improved system efficiency when performed directly on the electrochemically active anode. Rapid kinetics of the endothermic reaction typically causes a localized temperature depression on the anode near the fuel inlet. It is desirable to extend the endothermic effect over more of the cell area and mitigate the associated differences in temperature on the cell to alleviate subsequent thermal stresses. In this study, modeling tools validated for the prediction of fuel use, on-cell methane reforming, and the distribution of temperature within SOFC stacks, are employed to provide direction for modifying the catalytic activity of anode materials to control the methane conversion rate. Improvements in thermal management that can be achieved through on-cell reforming is predicted and discussed. Two operating scenarios are considered: one in which the methane fuel is fully pre-reformed, and another in which a substantial percentage of the methane is reformed on-cell. For the latter, a range of catalytic activity is considered and the predicted thermal effects on the cell are presented. Simulations of the cell electrochemical and thermal performance with and without on-cell reforming, including structural analyses, show a substantial decrease in thermal stresses for an on-cell reforming case with slowed methane conversion.

Recknagle, Kurtis P.; Jarboe, Daniel T.; Johnson, Kenneth I.; Korolev, Alexander; Khaleel, Mohammad A.; Singh, Prabhakar

2007-01-16T23:59:59.000Z

380

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly ({gamma}-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly ({gamma}-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, P.J.; Delhaize, E.; Robinson, N.J.; Unkefer, C.J.; Furlong, C.

1988-08-26T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Aqueous flooding methods for tertiary oil recovery  

DOE Patents (OSTI)

A method of aqueous flooding of subterranean oil bearing formation for tertiary oil recovery involves injecting through a well into the formation a low alkaline pH aqueous sodium bicarbonate flooding solution. The flooding solution's pH ranges from about 8.25 to 9.25 and comprises from 0.25 to 5 weight percent and preferably about 0.75 to 3.0 weight percent of sodium bicarbonate and includes a petroleum recovery surfactant of 0.05 to 1.0 weight percent and between 1 and 20 weight percent of sodium chloride. After flooding, an oil and water mixture is withdrawn from the well and the oil is separated from the oil and water mixture.

Peru, Deborah A. (Bartlesville, OK)

1989-01-01T23:59:59.000Z

382

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat units for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heavy metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (Los Alamos, NM); Delhaize, Emmanuel (Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-01-01T23:59:59.000Z

383

Removal of metal ions from aqueous solution  

DOE Patents (OSTI)

A method of removing heavy metals from aqueous solution, a composition of matter used in effecting said removal, and apparatus used in effecting said removal. One or more of the polypeptides, poly (.gamma.-glutamylcysteinyl)glycines, is immobilized on an inert material in particulate form. Upon contact with an aqueous solution containing heavy metals, the polypeptides sequester the metals, removing them from the solution. There is selectivity of poly (.gamma.-glutamylcysteinyl)glycines having a particular number of monomer repeat unit for particular metals. The polypeptides are easily regenerated by contact with a small amount of an organic acid, so that they can be used again to remove heayv metals from solution. This also results in the removal of the metals from the column in a concentrated form.

Jackson, Paul J. (both Los Alamos, NM); Delhaize, Emmanuel (both Los Alamos, NM); Robinson, Nigel J. (Durham, GB2); Unkefer, Clifford J. (Los Alamos, NM); Furlong, Clement (Seattle, WA)

1990-11-13T23:59:59.000Z

384

Petroleum Refinery Catalytic Reforming -- Cutting High Energy Costs  

E-Print Network (OSTI)

Hydrocarbon reforming involves a variety of chemical reactions at high temperatures and pressures in the presence of suitable catalysts. The conversion of naptha to high octane aromatics requires high energy to initiate and sustain the reaction at temperatures of 850-950oF. Hydrogen - rich off - gases are fired in combinations of process furnaces. Heat is transferred to hydrocarbon fluids by radiation, principally. Feed or return stream temperatures determine the need for convection sections. It is essential that the operation and maintenance of these furnaces be optimized to minimize production costs. This paper describes the performance testing and evaluation of a set of ten refinery furnaces used to thermally drive several reforming reactors and to regenerate catalysts. Firing rates provide an input of 216.2 x 106 Btu/hr. to the furnaces, at $1.90 per 106 Btu. The units are fitted with multiple natural draft burners. There is insufficient turbulence and swirl in the burners. Operators manually set up the burners with excessive airflows for normal, full-load firing. These furnaces represent production limits. Products of combustion exhaust at high thermal levels - the range is from 985-1700oF. The mixed gases flow through a "waste heat" boiler, or they bypass the boiler and enter a single stack. Steam generation at 150 psig averages 38,200 lb/hr. Heat is wasted via the bypass at a rate of 41.1x106 Btu /hr. at 1240oF. When airflows are reduced (to 15% excess air) the loss will be 18.7x106 Btu/hr. at 1180oF. Installation of a second, parallel waste heat boiler will result in a saving of l3.4x106 Btu/hr. Energy savings at this furnace complex will be equivalent to $628,700 per year. Investment costs were estimated to be less than $250,000 for the proposed heat trap addition.

Viar, W. L.

1979-01-01T23:59:59.000Z

385

Five Kilowatt Solid Oxide Fuel Cell/Diesel Reformer  

DOE Green Energy (OSTI)

Reducing fossil fuel consumption both for energy security and for reduction in global greenhouse emissions has been a major goal of energy research in the US for many years. Fuel cells have been proposed as a technology that can address both these issues--as devices that convert the energy of a fuel directly into electrical energy, they offer low emissions and high efficiencies. These advantages are of particular interest to remote power users, where grid connected power is unavailable, and most electrical power comes from diesel electric generators. Diesel fuel is the fuel of choice because it can be easily transported and stored in quantities large enough to supply energy for small communities for extended periods of time. This projected aimed to demonstrate the operation of a solid oxide fuel cell on diesel fuel, and to measure the resulting efficiency. Results from this project have been somewhat encouraging, with a laboratory breadboard integration of a small scale diesel reformer and a Solid Oxide Fuel Cell demonstrated in the first 18 months of the project. This initial demonstration was conducted at INEEL in the spring of 2005 using a small scale diesel reformer provided by SOFCo and a fuel cell provided by Acumentrics. However, attempts to integrate and automate the available technology have not proved successful as yet. This is due both to the lack of movement on the fuel processing side as well as the rather poor stack lifetimes exhibited by the fuel cells. Commercial product is still unavailable, and precommercial devices are both extremely expensive and require extensive field support.

Dennis Witmer; Thomas Johnson

2008-12-31T23:59:59.000Z

386

Chemical Looping Reforming for H2, CO and Syngas Production  

SciTech Connect

We demonstrate that the extension of CLC onto oxidants beyond air opens new, highly efficient pathways for production of ultra-pure hydrogen, activation of CO{sub 2} via reduction to CO, and are currently working on production of syngas using nanocomposite Fe-BHA. CLR hold great potential due to fuel flexibility and CO{sub 2} capture. Chemical Looping Combustion (CLC) is a novel clean combustion technology which offers an elegant and highly efficient route for fossil fuel combustion. In CLC, combustion of a fuel is broken down into two spatially separated steps. In the reducer, the oxygen carrier (typically a metal) supplies the stoichiometric oxygen required for fuel combustion. In the oxidizer, the oxygen-depleted carrier is then re-oxidized with air. After condensation of steam from the effluent of the reducer, a high-pressure, high-purity sequestration-ready CO{sub 2} stream is obtained. In the present study, we apply the CLC principle to the production of high-purity H{sub 2}, CO, and syngas streams by replacing air with steam and/or CO{sub 2} as oxidant, respectively. Using H{sub 2}O as oxidant, pure hydrogen streams can be obtained. Similarly, using CO{sub 2} as oxidant, CO is obtained, thus opening an efficient route for CO{sub 2} utilization. Using steam and CO{sub 2} mixtures for carrier oxidation should thus allow production of syngas with adjustable CO:H{sub 2} ratios. Overall, these processes result in Chemical Looping Reforming (CLR), i.e. the net overall reaction is the steam and/or dry reforming of the respective fuel.

Bhavsar,Saurabh; Najera,Michelle; Solunke,Rahul; Veser,Götz

2001-06-06T23:59:59.000Z

387

Inorganic rechargeable non-aqueous cell  

DOE Patents (OSTI)

A totally inorganic non-aqueous rechargeable cell having an alkali or alkaline earth metal anode such as of lithium, a sulfur dioxide containing electrolyte and a discharging metal halide cathode, such as of CuCl.sub.2, CuBr.sub.2 and the like with said metal halide being substantially totally insoluble in SO.sub.2 and admixed with a conductive carbon material.

Bowden, William L. (Nashua, NH); Dey, Arabinda N. (Needham, MA)

1985-05-07T23:59:59.000Z

388

,"Catalytic Reforming Downstream Processing of Fresh Feed Input"  

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

Catalytic Reforming Downstream Processing of Fresh Feed Input" Catalytic Reforming Downstream Processing of Fresh Feed Input" ,"Click worksheet name or tab at bottom for data" ,"Worksheet Name","Description","# Of Series","Frequency","Latest Data for" ,"Data 1","Catalytic Reforming Downstream Processing of Fresh Feed Input",16,"Monthly","9/2013","1/15/2010" ,"Release Date:","11/27/2013" ,"Next Release Date:","Last Week of December 2013" ,"Excel File Name:","pet_pnp_dwns_a_(na)_ydr_mbblpd_m.xls" ,"Available from Web Page:","http://www.eia.gov/dnav/pet/pet_pnp_dwns_a_(na)_ydr_mbblpd_m.htm" ,"Source:","Energy Information Administration"

389

Investigation of Bio-Ethanol Steam Reforming over Cobalt-based Catalysts (Presentation)  

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

DOE Bio-Derived Liquids to Hydrogen Distributed DOE Bio-Derived Liquids to Hydrogen Distributed Reforming Working Group (BILIWG) Meeting Investigation of Bio-Ethanol Steam Reforming over Cobalt-based Catalysts Hua Song Lingzhi Zhang Umit S. Ozkan* November 6 th , 2007 Heterogeneous Catalysis Research Group Department of Chemical and Biomolecular Engineering The Ohio State University Columbus, OH 43210 *Ozkan.1@osu.edu Biomass to Hydrogen (Environmentally Friendly) Plant cultivation Plant cultivation Saccharification Saccharification / / Fermentation Fermentation Anaerobic digestion Anaerobic digestion Residues of Residues of agroindustries agroindustries and cultivations and cultivations Municipal Solid Waste Municipal Solid Waste (organic fraction) (organic fraction) Distillation Distillation Reformation of ethanol

390

HYDROGEN GENERATION FROM PLASMATRON REFORMERS: A PROMISING TECHNOLOGY FOR NOX ADSORBER REGENERATION AND OTHER AUTOMOTIVE APPLICATIONS  

DOE Green Energy (OSTI)

Plasmatron reformers are being developed at MIT and ArvinMeritor [1]. In these reformers a special low power electrical discharge is used to promote partial oxidation conversion of hydrocarbon fuels into hydrogen and CO. The partial oxidation reaction of this very fuel rich mixture is difficult to initiate. The plasmatron provides continuous enhanced volume initiation. To minimize electrode erosion and electrical power requirements, a low current, high voltage discharge with wide area electrodes is used. The reformers operate at or slightly above atmospheric pressure. Plasmatron reformers provide the advantages of rapid startup and transient response; efficient conversion of the fuel to hydrogen rich gas; compact size; relaxation or elimination of reformer catalyst requirements; and capability to process difficult to reform fuels, such as diesel and bio-oils. These advantages facilitate use of onboard hydrogen-generation technology for diesel exhaust after-treatment. Plasma-enhanced reformer technology can provide substantial conversion even without the use of a catalyst. Recent progress includes a substantial decrease in electrical power consumption (to about 200 W), increased flow rate (above 1 g/s of diesel fuel corresponding to approximately 40 kW of chemical energy), soot suppression and improvements in other operational features.. Plasmatron reformer technology has been evaluated for regeneration of NOx adsorber after-treatment systems. At ArvinMeritor tests were performed on a dual-leg NOx adsorber system using a Cummins 8.3L diesel engine both in a test cell and on a vehicle. A NOx adsorber system was tested using the plasmatron reformer as a regenerator and without the reformer i.e., with straight diesel fuel based regeneration as the baseline case. The plasmatron reformer was shown to improve NOx regeneration significantly compared to the baseline diesel case. The net result of these initial tests was a significant decrease in fuel penalty, roughly 50% at moderate adsorber temperatures. This fuel penalty improvement is accompanied by a dramatic drop in slipped hydrocarbon emissions, which decreased by 90% or more. Significant advantages are demonstrated across a wide range of engine conditions and temperatures. The study also indicated the potential to regenerate NOx adsorbers at low temperatures where diesel fuel based regeneration is not effective, such as those typical of idle conditions. Two vehicles, a bus and a light duty truck, have been equipped for plasmatron reformer NOx adsorber regeneration tests.

Bromberg, L.; Crane, S; Rabinovich, A.; Kong, Y; Cohn, D; Heywood, J; Alexeev, N.; Samokhin, A.

2003-08-24T23:59:59.000Z

391

Modeling of On-Cell Reforming Reaction for Planar SOFC Stacks  

Science Conference Proceedings (OSTI)

Planar Solid Oxide Fuel Cell (SOFC) stack is known to suffer thermal problem from high stack temperature during operation to generate high current. On-Cell Reforming (OCR) phenomenon is often used to reduce stack temperature by an endothermic reaction of steam-methane reforming process. RIST conducted single-cell experiment to validate modeling tool to simulate OCR performance including temperature measurement. 2D modeling is used to check reforming rate during OCR using temperature measurement data, and 3D modeling is used to check overall thermal performance including furnace boundary conditions.

Yang, Choongmo; Lim, Hyung-Tae; Hwang, Soon Cheol; Kim, Dohyung; Lai, Canhai; Koeppel, Brian J.; Recknagle, Kurtis P.; Khaleel, Mohammad A.

2011-05-30T23:59:59.000Z

392

Refiners look at H sub 2 SO sub 4 alkylation and catalytic reforming  

Science Conference Proceedings (OSTI)

Sulfuric acid alkylation and catalytic reforming drew many questions at the most recent National Petroleum Refiners Association (NPRA) question and answer session on refining and petrochemical technology. At this annual meeting, presubmitted questions are answered by a panel of experts. For more information on the meeting's format, see OGJ, Mar. 16, p. 37. This third and final article in the series of excerpts from the 1991 NPRA Q and A Session examines such pertinent alkylation topics as tertiary amyl methyl ether (TAME) raffinate processing and unit operation during acid runaway. Also discussed are skewed platinum/rhenium reforming catalyst and how catalyst life affects reformate aromatics levels.

Not Available

1992-04-27T23:59:59.000Z

393

Catalytic reforming with a platinum group and phosphorus-containing composition  

Science Conference Proceedings (OSTI)

A new catalyst composition for converting hydrocarbons is disclosed. Also disclosed is a method for making the catalyst. The catalyst comprises a platinum group component and a phosphorous component with a porous support material. The catalyst is made by compositing a platinum group component with a porous support material and then contacting that composite with phosphorus or a compound of phosphorus. In a preferred embodiment of the invention a catalyst comprising platinum, phosphorus and chlorine with alumina is utilized in the catalytic reforming of hydrocarbons boiling in the gasoline range to produce a high octane reformate suitable for gasoline blending or a high aromatics content reformate suitable as a petrochemical feedstock.

Antos, G. J.; Chao, T.-H.

1984-11-20T23:59:59.000Z

394

Internal natural gas reformer-dividers for a solid oxide fuel cell generator configuration  

Science Conference Proceedings (OSTI)

This patent describes a fuel cell generator configuration. It comprises electrically connected, axially elongated, fuel cells, each cell having an outer and inner electrode with solid oxide electrolyte therebetween; where elongated dividers separate and are positioned between fuel cells, and where at least one of the elongated dividers is hollow, the hollow divider having solid elongated walls, a reformable fuel mixture entrance, and an exit allowing passage of reformed fuel to the fuel cells, and where the cross-section of the divider contains a catalytic reforming material.

Reichner, P.

1992-01-21T23:59:59.000Z

395

Phase equilibrium studies  

DOE Green Energy (OSTI)

A phase equilibrium model has been developed for the SRC-I process, as well as the other coal liquefaction processes. It is applicable to both vapor/liquid and liquid/liquid equilibria; it also provides an approximate but adequate description of aqueous mixtures where the volatile electrolyte components dissociate to form ionic species. This report completes the description of the model presented in an earlier report (Mathias and Stein, 1983a). Comparisons of the model to previously published data on coal-fluid mixtures are presented. Further, a preliminary analysis of new data on SRC-I coal fluids is presented. Finally, the current capabilities and deficiencies of the model are discussed. 25 references, 17 figures, 30 tables.

Mathias, P.M.; Stein, F.P.

1983-09-01T23:59:59.000Z

396

Sorption of carboxylic acid from carboxylic salt solutions at pHs close to or above the pK[sub a] of the acid, with regeneration with an aqueous solution of ammonia or low-molecular-weight alkylamine  

DOE Patents (OSTI)

Carboxylic acids are sorbed from aqueous feedstocks at pHs close to or above the acids' pH[sub a] into a strongly basic organic liquid phase or onto a basic solid adsorbent or moderately basic ion exchange resin. The acids are freed from the sorbent phase by treating it with aqueous alkylamine or ammonia thus forming an alkylammonium or ammonium carboxylate which dewatered and decomposed to the desired carboxylic acid and the alkylamine or ammonia. 8 figs.

King, C.J.; Tung, L.A.

1992-07-21T23:59:59.000Z

397

An Act to Reform Land Use Planning in the Unorganized Territory (Maine) |  

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

An Act to Reform Land Use Planning in the Unorganized Territory An Act to Reform Land Use Planning in the Unorganized Territory (Maine) An Act to Reform Land Use Planning in the Unorganized Territory (Maine) < Back Eligibility Agricultural Commercial Investor-Owned Utility Local Government Municipal/Public Utility Nonprofit Rural Electric Cooperative Schools Tribal Government Utility Savings Category Wind Buying & Making Electricity Program Info State Maine Program Type Siting and Permitting Provider Conservation An Act to Reform Land Use Planning in the Unorganized Territory alters the makeup and responsibilities of Maine's Land Use Regulation Commission (LURC). It took effect on August 29, 2012 and changed the Commission's name to the Land Use Planning Commission. Under the Act, permitting review for significant projects, such as

398

Incentives in Water Management Reform: Assessing the Effect on Water Use,  

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

Incentives in Water Management Reform: Assessing the Effect on Water Use, Incentives in Water Management Reform: Assessing the Effect on Water Use, Production and Poverty in the Yellow River Basin Speaker(s): Jinixia Wang Date: May 22, 2003 - 12:00pm Location: Bldg. 90 The purpose of this presentation is to better understand water management reform in China's rural communities, focusing on the effect of incentives to water managers on the nation's water resources and the welfare of the rural population. Based on a survey study in the Yellow River Basin, our findings show that Water User Associations and contracting have begun to systematically replace traditional forms of collective management. The analysis demonstrates, however, that it is not a nominal implementation of the reform that matters, but rather it is a creation of new management

399

The risk of reform : privatisation and liberalisation in the Brazilian electric power industry  

E-Print Network (OSTI)

In 1996, when Brazil was well-underway to privatising and liberalising its electric power industry, few would have predicted that within five years the reforms would be a shambles. Like its neighbors Argentina and Chile, ...

Tankha, Sunil, Ph. D. Massachusetts Institute of Technology

2006-01-01T23:59:59.000Z

400

Electricity Sector Reform in Developing Countries: A Survey of Empirical Evidence on Determinants and Performance  

E-Print Network (OSTI)

, patronage, labour opposition to reducing waste, poor collection and other fiscal leakage. Simpler reforms, such as encouraging Independent Power Producers to enter into long-term Power Purchase Agreements with financially fragile counterparts, stored up...

Jamasb, Tooraj; Mota, Raffaella L; Newbery, David; Pollitt, Michael G.

2004-07-09T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

Synthesis and characterization of 1D ceria nanomaterials for CO oxidation and steam reforming of methanol  

Science Conference Proceedings (OSTI)

Novel one-dimensional (1D) ceria nanostructure has been investigated as a promising and practical approach for the reforming of methanol reaction. Size and shape of the ceria nanomaterials are directly involved with the catalytic activities. Several ...

Sujan Chowdhury; Kuen-Song Lin

2011-01-01T23:59:59.000Z

402

Numerical simulation of micro/mini-channel based methane-steam reformer.  

E-Print Network (OSTI)

??Numerical modeling of methane-steam reforming is performed in a micro/mini-channel with heat input through catalytic channel walls. The low-Mach number, variable density Navier-Stokes equations together… (more)

[No author

2010-01-01T23:59:59.000Z

403

Computational heterogeneous catalysis applied to steam methane reforming over nickel and nickel/silver catalysts  

E-Print Network (OSTI)

The steam methane reforming (SMR) reaction is the primary industrial means for producing hydrogen gas. As such, it is a critical support process for applications including petrochemical processing and ammonia synthesis. ...

Blaylock, Donnie Wayne

2011-01-01T23:59:59.000Z

404

"Quality" control in China's reform era : investigating the suzhi discourse in women's work  

E-Print Network (OSTI)

China's reform era has coincided with an emergence of a Chinese Communist Party-State ideological discourse concerning "population quality." Claims and accusations of 'low quality' are particularly targeted at rural migrant ...

Yip, Cheryl

2008-01-01T23:59:59.000Z

405

Deregulating and regulatory reform in the U.S. electric power sector  

E-Print Network (OSTI)

This paper discusses the evolution of wholesale and retail competition in the U.S electricity sector and associated industry restructuring and regulatory reforms. It begins with a discussion of the industry structure and ...

Joskow, Paul L.

2000-01-01T23:59:59.000Z

406

Organizational sense making : responsibilities to the MCAS reform in the Massachusetts public schools  

E-Print Network (OSTI)

Educational reform has become a central concern of public policy debates at both the state and federal level. The policy trend both nationally and locally is towards uniform standards in education, with testing as the ...

Goldman, Janice J., 1953-

2005-01-01T23:59:59.000Z

407

Jews and Catholics in Catholic Poland: A Beleaguered Church in the Post Reformation Era.  

E-Print Network (OSTI)

??Jews and Heretics in Catholic Poland takes issue with historians’ common contention that the Catholic Church triumphed in Counter-reformation Poland. In fact, the Church’s own… (more)

Teter, Magda

2006-01-01T23:59:59.000Z

408

Fuel cell generator with fuel electrodes that control on-cell fuel reformation  

Science Conference Proceedings (OSTI)

A fuel cell for a fuel cell generator including a housing including a gas flow path for receiving a fuel from a fuel source and directing the fuel across the fuel cell. The fuel cell includes an elongate member including opposing first and second ends and defining an interior cathode portion and an exterior anode portion. The interior cathode portion includes an electrode in contact with an oxidant flow path. The exterior anode portion includes an electrode in contact with the fuel in the gas flow path. The anode portion includes a catalyst material for effecting fuel reformation along the fuel cell between the opposing ends. A fuel reformation control layer is applied over the catalyst material for reducing a rate of fuel reformation on the fuel cell. The control layer effects a variable reformation rate along the length of the fuel cell.

Ruka, Roswell J. (Pittsburgh, PA); Basel, Richard A. (Pittsburgh, PA); Zhang, Gong (Murrysville, PA)

2011-10-25T23:59:59.000Z

409

The wholesale market for electricity in England and Wales : recent developments and future reforms  

E-Print Network (OSTI)

The England and Wales wholesale electricity market is about to undergo major reform (NETA). I describe and analyse the proposed arrangements, contrasting them with those currently in operation. I argue that while NETA will ...

Sweeting, Andrew

2000-01-01T23:59:59.000Z

410

Admonition and the academy : installation, video, and performance art in Reform Era China  

E-Print Network (OSTI)

China's Reform Era (1978-present) has seen the reinvigoration of academic, and artistic practice, and a rapprochement between the Chinese Communist Party and the intellectual elite. At its beginnings in the early- to ...

Oen, Karin Grace

2012-01-01T23:59:59.000Z

411

Exposing the seams : the impetus for reforming U.S. counterintelligence .  

E-Print Network (OSTI)

??U.S. counterintelligence is in need of reform. The September 11, 2001 attacks by Al-Qa'ida against America highlight this fact but are not in themselves the… (more)

Gleghorn, Todd E.

2003-01-01T23:59:59.000Z

412

Development of Ni-based Sulfur Resistant Catalyst for Diesel Reforming  

DOE Green Energy (OSTI)

In order for diesel fuel to be used in a solid oxide fuel cell auxiliary power unit, the diesel fuel must be reformed into hydrogen, carbon monoxide and carbon dioxide. One of the major problems facing catalytic reforming is that the level of sulfur found in low sulfur diesel can poison most catalysts. This report shows that a proprietary low cost Ni-based reforming catalyst can be used to reform a 7 and 50 ppm sulfur containing diesel fuel for over 500 hours of operation. Coking, which appears to be route of catalyst deactivation due to metal stripping, can be controlled by catalyst modifications, introduction of turbulence, and/or by application of an electromagnetic field with a frequency from {approx}50 kHz to 13.56 MHz with field strength greater than about 100 V/cm and more preferably greater about 500 V/cm.

Gunther Dieckmann

2006-06-30T23:59:59.000Z

413

Effects of operating conditions, compression ratio, and gasoline reformate on SI engine knock limits  

E-Print Network (OSTI)

A set of experiments was performed to investigate the effects of air-fuel ratio, inlet boost pressure, hydrogen rich fuel reformate, and compression ratio on engine knock behavior. For each condition the effect of spark ...

Gerty, Michael D

2005-01-01T23:59:59.000Z

414

Nonlinear multivariable predictive control of an autothermal reforming reactor for fuel cell applications  

Science Conference Proceedings (OSTI)

In this work, we present a computationally efficient nonlinear multivariable predictive controller (NMPC) for an autothermal reforming (ATR) reactor. The proposed NMPC scheme is based on a fast reduced order nonlinear model and consists of three parts. ...

Yongyou Hu; Donald J. Chmielewski

2009-06-01T23:59:59.000Z

415

Catalytic activation and reforming of methane on supported palladium clusters Aritomo Yamaguchi, Enrique Iglesia *  

E-Print Network (OSTI)

of pollutants, oxygen generation, and intermediate-temperature solid oxide fuel cells, as well as catalytic reforming. Sekine et al.56 investigated four catalytic reactions assisted with an electric field to promote

Iglesia, Enrique

416

Influence of support material on Ni catalysts for propane dry reforming to synthesis gas.  

E-Print Network (OSTI)

??Ni/SiO2 and Ni/Mg(Al)O catalysts with difference metal loadings have been prepared. The activity, selectivity and stability of supported Ni catalysts for propane dry reforming to… (more)

Dai, Xin

2008-01-01T23:59:59.000Z

417

OXIDATION OF FUELS IN THE COOL FLAME REGIME FOR COMBUSTION AND REFORMING FOR FUEL CELLS.  

DOE Green Energy (OSTI)

THE REVIEW INTEGRATES RECENT INVESTIGATIONS ON AUTO OXIDATION OF FUEL OILS AND THEIR REFORMING INTO HYDROGEN RICH GAS THAT COULD SERVE AS A FEED FOR FUEL CELLS AND COMBUSTION SYSTEMS.

NAIDJA,A.; KRISHNA,C.R.; BUTCHER,T.; MAHAJAN,D.

2002-08-01T23:59:59.000Z

418

Earnings Determination and Taxes: Evidence from a Cohort-Based Payroll Tax Reform in Greece  

E-Print Network (OSTI)

pension outcomes i n Greece." British Jour¬ nal ofIndustrialL T A X R E F O R M IN GREECE Emmanuel Saez Manos MatsaganisBased Payroll Tax Reform in Greece Emmanuel Saez, Manos

Saez, Emmanuel; Matsaganis, Manos; Tsakloglou, Panos

2010-01-01T23:59:59.000Z

419

Mechanism of formation of oil by the hot aqueous alkaline digestion of cellulose  

DOE Green Energy (OSTI)

The overall mechanism of cellulose converson in hot aqueous alkali appears to be one of degradation through glucose to low molecular weight saccharinic acids, dihydroxybutyric acid, glycolic acid, and carbonyl products such as acetone, acetaldehyde, formaldehyde, and similar compounds. Although the products identified in the present report were fairly complex furans, carbocyclic ketones, unsaturated hydrocarbons, and aromatic compounds, nevertheless, in most cases, they could have been formed from simple carbonyl compounds through a series of condensations involving carbanion intermediates. It is conceivable that residual alkali in the oil during acetone extraction could have given rise to diacetone alcohol as an artifact. This is refuted by examination of an aqueous residue which was extracted with diethyl ether and which was never exposed to any acetone: Compounds derived from diacetone alcohol (such as mesityl oxide or 4-methyl-3-penten-2-one) were also identified in the diethyl ether extract of the aqueous phase. Other compounds were identified in the oil acetone extract which could not have been derived from acetone or diacetone alcohol, but which could have been formed from other carbonyl compounds by the same mechanism. Hence, diacetone alcohol is a genuine product of cellulose conversion although apparently not an intermediate in further synthesis of other products. The further reaction of the postulated cyclic intermediates, and the route to formation of unsaturated hydrocarbons of high molecular weight is intended to be the next subject of investigation in the current work. The fundamental difference in the mechanism of cellulose conversion to oil by pyrolysis and by aqueous alkaline digestion predicted by theory is therefore confirmed. Pyrolysis products may be explained generally by carbonium ion and free radical reactions (in fact, cellulose decomposition is acid-catalyzed), while in aqueous alkali, nucleophilic carbanion reactions are favored.

Molten, P.M.; Miller, R.K.; Donovan, J.M.; Demmitt, T.F.

1977-01-01T23:59:59.000Z

420

Steam Reforming on Transition-metal Carbides from Density-functional Theory  

Science Conference Proceedings (OSTI)

A screening study of the steam reforming reaction on clean and oxygen covered early transition-metal carbides surfaces is performed by means of density-functional theory calculations. It is found that carbides provide a wide spectrum of reactivities, from too reactive via suitable to too inert. Several molybdenum-based systems are identified as possible steam reforming catalysts. The findings suggest that carbides provide a playground for reactivity tuning, comparable to the one for pure metals.

Vojvodic, Aleksandra

2012-05-11T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

A Methanol Steam Reforming Micro Reactor for Proton Exchange Membrane Micro Fuel Cell System  

DOE Green Energy (OSTI)

The heat, mass and momentum transfer from a fuel reforming packed bed to a surrounding silicon wafer has been simulated. Modeling showed quantitatively reasonable agreement with experimental data for fuel conversion efficiency, hydrogen production rate, outlet methanol mole fraction and outlet steam mole fraction. The variation in fuel conversion efficiency with the micro reformer thermal isolation can be used to optimize fuel-processing conditions for micro PEM fuel cells.

Park, H G; Piggott, W T; Chung, J; Morse, J D; Havstad, M; Grigoropoulos, C P; Greif, R; Benett, W; Sopchak, D; Upadhye, R

2003-07-28T23:59:59.000Z

422

Carbonized material adsorbents for the removal of mercury from aqueous solutions  

SciTech Connect

Although wood has essentially been excluded as a starting material for the production of granular activated carbon because of the poor strength and friability of the products, powdered wood based activated carbons are still being used in water treatment and other liquid phase applications. However, the capability of powdered wood-based charcoal which in itself porous has not been fully known. Few studies have been conducted in harnessing its potential for adsorption purposes especially in water treatment. This study was conducted to investigate the possibility of using wood based carbonized materials from Sugi (Cryptomeria japonica D. Don) as adsorption materials in aqueous solutions of heavy metals like mercury, zinc, lead, cadmium and arsenic. However, of all the heavy metals investigated, mercury is considered to be the most toxic so this paper describes only the adsorption ability of the carbonized materials in adsorbing this metal from aqueous solutions of different concentrations.

Ishihara, S.; Pulido, L.L. [Kyoto Univ. (Japan); Kajimoto, T. [Wakayama Industrial Technology Center (Japan)

1996-12-31T23:59:59.000Z

423

DATA QUALITY OBJECTIVES FOR SELECTING WASTE SAMPLES FOR BENCH-SCALE REFORMER TREATABILITY STUDIES  

SciTech Connect

This document describes the data quality objectives to select archived samples located at the 222-S Laboratory for Bench-Scale Reforming testing. The type, quantity, and quality of the data required to select the samples for Fluid Bed Steam Reformer testing are discussed. In order to maximize the efficiency and minimize the time to treat Hanford tank waste in the Waste Treatment and Immobilization Plant, additional treatment processes may be required. One of the potential treatment processes is the fluidized bed steam reformer. A determination of the adequacy of the fluidized bed steam reformer process to treat Hanford tank waste is required. The initial step in determining the adequacy of the fluidized bed steam reformer process is to select archived waste samples from the 222-S Laboratory that will be used in a bench scale tests. Analyses of the selected samples will be required to confirm the samples meet the shipping requirements and for comparison to the bench scale reformer (BSR) test sample selection requirements.

BANNING DL

2011-02-11T23:59:59.000Z

424

Hydrogen Production for Fuel Cells Via Reforming Coal-Derived Methanol  

DOE Green Energy (OSTI)

Hydrogen can be produced from many feedstocks including coal. The objectives of this project are to establish and prove a hydrogen production pathway from coal-derived methanol for fuel cell applications. This progress report is the eighth report submitted to the DOE reporting on the status and progress made during the course of the project. This report covers the time period of October 1, 2004-September 30, 2005 and includes an entire review of the progress for year 2 of the project. This year saw progress in eight areas. These areas are: (1) steam reformer transient response, (2) steam reformer catalyst degradation, (3) steam reformer degradation tests using bluff bodies, (4) optimization of bluff bodies for steam reformation, (5) heat transfer enhancement, (6) autothermal reforming of coal derived methanol, (7) autothermal catalyst degradation, and (8) autothermal reformation with bluff bodies. The project is on schedule and is now shifting towards the design of an integrated PEM fuel cell system capable of using the coal-derived product. This system includes a membrane clean up unit and a commercially available PEM fuel cell.

Paul A. Erickson

2005-09-30T23:59:59.000Z

425

Removal of uranium from aqueous HF solutions  

DOE Patents (OSTI)

This invention is a simple and effective method for removing uranium from aqueous HF solutions containing trace quantities of the same. The method comprises contacting the solution with particulate calcium fluoride to form uranium-bearing particulates, permitting the particulates to settle, and separting the solution from the settled particulates. The CaF.sub.2 is selected to have a nitrogen surface area in a selected range and is employed in an amount providing a calcium fluoride/uranium weight ratio in a selected range. As applied to dilute HF solutions containing 120 ppm uranium, the method removes at least 92% of the uranium, without introducing contaminants to the product solution.

Pulley, Howard (West Paducah, KY); Seltzer, Steven F. (Paducah, KY)

1980-01-01T23:59:59.000Z

426

NON-AQUEOUS DISSOLUTION OF MASSIVE PLUTONIUM  

DOE Patents (OSTI)

A method is presented for obtaining non-aqueous solutions or plutonium from massive forms of the metal. In the present invention massive plutonium is added to a salt melt consisting of 10 to 40 weight per cent of sodium chloride and the balance zinc chloride. The plutonium reacts at about 800 deg C with the zinc chloride to form a salt bath of plutonium trichloride, sodium chloride, and metallic zinc. The zinc is separated from the salt melt by forcing the molten mixture through a Pyrex filter.

Reavis, J.G.; Leary, J.A.; Walsh, K.A.

1959-05-12T23:59:59.000Z

427

Removal of uranium from aqueous HF solutions  

Science Conference Proceedings (OSTI)

This invention is a simple and effective method for removing uranium from aqueous HF solutions containing trace quantities of the same. The method comprises contacting the solution with particulate calcium fluoride to form uranium-bearing particulates, permitting the particulates to settle, and separating the solution from the settled particulates. The CaF2 is selected to have a nitrogen surface area in a selected range and is employed in an amount providing a calcium fluoride/uranium weight ratio in a selected range. As applied to dilute HF solutions containing 120 ppm uranium, the method removes at least 92% of the uranium without introducing contaminants to the product solution.

Pulley, H.; Seltzer, S.F.

1980-11-18T23:59:59.000Z

428

Functionalized Polymers For Binding To Solutes In Aqueous Solutions  

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

Functionalized Polymers For Binding To Solutes In Aqueous Solutions Functionalized Polymers For Binding To Solutes In Aqueous Solutions Functionalized Polymers For Binding To Solutes In Aqueous Solutions A functionalized polymer for binding a dissolved molecule in an aqueous solution is presented. Available for thumbnail of Feynman Center (505) 665-9090 Email Functionalized Polymers For Binding To Solutes In Aqueous Solutions A functionalized polymer for binding a dissolved molecule in an aqueous solution is presented. The polymer has a backbone polymer to which one or more functional groups are covalently linked. The backbone polymer can be such polymers as polyethylenimine, polyvinylamine, polyallylamine, and polypropylamine. These polymers are generally water-soluble, but can be insoluble when cross-linked. The functional group can be for example diol

429

February 2012Home Production and Social Security Reform  

E-Print Network (OSTI)

This paper incorporates home production into a dynamic general equilibrium model of overlapping generations with endogenous retirement to study Social Security reforms. As such, the model di¤erentiates both consumption goods and labor e¤ort according to their respective roles in home production and market activities. Using a calibrated model, we …nd that eliminating the current pay-asyou-go Social Security system has important implications for both labor supply and consumption decisions and that these decisions are in‡uenced by the presence of a home production technology. Comparing our benchmark economy to one with di¤erentiated goods but no home production, we …nd that eliminating Social Security bene…ts generates larger welfare gains in the presence of home production. This result is due to the self insurance aspects generated by the presence of home production. Comparing our economy to a one-good economy without home production, we show that the welfare gains of eliminating Social Security are magni…ed even further. These policy analyses suggest the importance of modeling home production and distinguishing between both time use and consumption goods depending on whether they are involved in market or home production. JEL Classi…cations: E21, E62, H55

Michael Dotsey; Wenli Li; Michael Dotsey; Wenli Li; Fang Yang

2012-01-01T23:59:59.000Z

430

ESS 2012 Peer Review - New Generation Aqueous Base Redox Flow...  

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

New Generation Aqueous Base Redox Flow Battery Component Development Wei Wang, Qingtao Luo, Xiaoliang Wei, Bin Li, Zimin Nie, Baowei Chen, Yuyan Shao, Vijayakumar Murugesan, Amy...

431

Corrosion problems with aqueous coolants, final report  

DOE Green Energy (OSTI)

The results of a one year program to characterize corrosion of solar collector alloys in aqueous heat-transfer media are summarized. The program involved a literature review and a laboratory investigation of corrosion in uninhibited solutions. It consisted of three separate tasks, as follows: review of the state-of-the-art of solar collector corrosion processes; study of corrosion in multimetallic systems; and determination of interaction between different waters and chemical antifreeze additives. Task 1 involved a comprehensive review of published literature concerning corrosion under solar collector operating conditions. The reivew also incorporated data from related technologies, specifically, from research performed on automotive cooling systems, cooling towers, and heat exchangers. Task 2 consisted of determining the corrosion behavior of candidate alloys of construction for solar collectors in different types of aqueous coolants containing various concentrations of corrosive ionic species. Task 3 involved measuring the degradation rates of glycol-based heat-transfer media, and also evaluating the effects of degradation on the corrosion behavior of metallic collector materials.

Diegle, R B; Beavers, J A; Clifford, J E

1980-04-11T23:59:59.000Z

432

RADIOACTIVE DEMONSTRATION OF MINERALIZED WASTE FORMS MADE FROM HANFORD LOW ACTIVITY WASTE (TANK FARM BLEND) BY FLUIDIZED BED STEAM REFORMATION (FBSR)  

SciTech Connect

The U.S. Department of Energy’s Office of River Protection (ORP) is responsible for the retrieval, treatment, immobilization, and disposal of Hanford’s tank waste. A key aspect of the River Protection Project (RPP) cleanup mission is to construct and operate the Hanford Tank Waste Treatment and Immobilization Plant (WTP). The WTP will separate the tank waste into high-level and low-activity waste (LAW) fractions, both of which will subsequently be vitrified. The projected throughput capacity of the WTP LAW Vitrification Facility is insufficient to complete the RPP mission in the time frame required by the Hanford Federal Facility Agreement and Consent Order, also known as the Tri-Party Agreement (TPA), i.e. December 31, 2047. Supplemental Treatment is likely to be required both to meet the TPA treatment requirements as well as to more cost effectively complete the tank waste treatment mission. The Supplemental Treatment chosen will immobilize that portion of the retrieved LAW that is not sent to the WTP’s LAW Vitrification facility into a solidified waste form. The solidified waste will then be disposed on the Hanford site in the Integrated Disposal Facility (IDF). Fluidized Bed Steam Reforming (FBSR) offers a moderate temperature (700-750°C) continuous method by which LAW can be processed irrespective of whether the waste contain organics, nitrates, sulfates/sulfides, chlorides, fluorides, volatile radionuclides or other aqueous components. The FBSR technology can process these wastes into a crystalline ceramic (mineral) waste form. The mineral waste form that is produced by co-processing waste with kaolin clay in an FBSR process has been shown to be comparable to LAW glass, i.e. leaches Tc-99, Re and Na at <2g/m2 during ASTM C1285 (Product Consistency) durability testing. Monolithing of the granular FBSR product was investigated to prevent dispersion during transport or burial/storage. Monolithing in an inorganic geopolymer binder, which is amorphous, macro-encapsulates the granules, and the monoliths pass ANSI/ANS 16.1 and ASTM C1308 durability testing with Re achieving a Leach Index (LI) of 9 (the Hanford Integrated Disposal Facility, IDF, criteria for Tc-99) after a few days and Na achieving an LI of >6 (the Hanford IDF criteria for Na) in the first few hours. The granular and monolithic waste forms also pass the EPA Toxicity Characteristic Leaching Procedure (TCLP) for all Resource Conservation and Recovery Act (RCRA) components at the Universal Treatment Standards (UTS). Two identical Benchscale Steam Reformers (BSR) were designed and constructed at SRNL, one to treat non-radioactive simulants and the other to treat actual radioactive wastes. The results from the non-radioactive BSR were used to determine the parameters needed to operate the radioactive BSR in order to confirm the findings of non-radioactive FBSR pilot scale and engineering scale tests and to qualify an FBSR LAW waste form for applications at Hanford. Radioactive testing commenced using SRS LAW from Tank 50 chemically trimmed to look like Hanford’s blended LAW known as the Rassat simulant as this simulant composition had been tested in the non-radioactive BSR, the non-radioactive pilot scale FBSR at the Science Applications International Corporation-Science and Technology Applications Research (SAIC-STAR) facility in Idaho Falls, ID and in the TTT Engineering Scale Technology Demonstration (ESTD) at Hazen Research Inc. (HRI) in Denver, CO. This provided a “tie back” between radioactive BSR testing and non-radioactive BSR, pilot scale, and engineering scale testing. Approximately six hundred grams of non-radioactive and radioactive BSR product were made for extensive testing and comparison to the non-radioactive pilot scale tests performed in 2004 at SAIC-STAR and the engineering scale test performed in 2008 at HRI with the Rassat simulant. The same mineral phases and off-gas species were found in the radioactive and non-radioactive testing. The granular ESTD and BSR products (radioactive and non-radioactive) were analyzed for to

Jantzen, C. M.; Crawford, C. L.; Bannochie, C. J.; Burket, P. R.; Cozzi, A. D.; Daniel, W. E.; Hall, H. K.; Miller, D. H.; Missimer, D. M.; Nash, C. A.; Williams, M. F.

2013-08-21T23:59:59.000Z

433

PHASE DETECTOR  

DOE Patents (OSTI)

A phase detector circuit is described for use at very high frequencies of the order of 50 megacycles. The detector circuit includes a pair of rectifiers inverted relative to each other. One voltage to be compared is applied to the two rectifiers in phase opposition and the other voltage to be compared is commonly applied to the two rectifiers. The two result:ng d-c voltages derived from the rectifiers are combined in phase opposition to produce a single d-c voltage having amplitude and polarity characteristics dependent upon the phase relation between the signals to be compared. Principal novelty resides in the employment of a half-wave transmission line to derive the phase opposing signals from the first voltage to be compared for application to the two rectifiers in place of the transformer commonly utilized for such purpose in phase detector circuits for operation at lower frequency.

Kippenhan, D.O.

1959-09-01T23:59:59.000Z

434

Hydrogen production from the steam reforming of Dinethyl Ether and Methanol  

SciTech Connect

This study investigates dimethyl ether (DME) steam reforming for the generation of hydrogen rich fuel cell feeds for fuel cell applications. Methanol has long been considered as a fuel for the generation of hydrogen rich fuel cell feeds due to its high energy density, low reforming temperature, and zero impurity content. However, it has not been accepted as the fuel of choice due its current limited availability, toxicity and corrosiveness. While methanol steam reforming for the generation of hydrogen rich fuel cell feeds has been extensively studied, the steam reforming of DME, CH{sub 3}OCH{sub 3} + 3H{sub 2}O = 2CO{sub 2} + 6H{sub 2}, has had limited research effort. DME is the simplest ether (CH{sub 3}OCH{sub 3}) and is a gas at ambient conditions. DME has physical properties similar to those of LPG fuels (i.e. propane and butane), resulting in similar storage and handling considerations. DME is currently used as an aerosol propellant and has been considercd as a diesel substitute due to the reduced NOx, SOx and particulate emissions. DME is also being considered as a substitute for LPG fuels, which is used extensively in Asia as a fuel for heating and cooking, and naptha, which is used for power generation. The potential advantages of both methanol and DME include low reforming temperature, decreased fuel proccssor startup energy, environmentally benign, visible flame, high heating value, and ease of storage and transportation. In addition, DME has the added advantages of low toxicity and being non-corrosive. Consequently, DME may be an ideal candidate for the generation of hydrogen rich fuel cell feeds for both automotive and portable power applications. The steam reforming of DME has been demonstrated to occur through a pair of reactions in series, where the first reaction is DME hydration followed by MeOH steam reforming to produce a hydrogen rich stream.

Semelsberger, T. A. (Troy A.); Borup, R. L. (Rodney L.)

2004-01-01T23:59:59.000Z

435

SCIENCE TEACHERS' ASSESSMENT PRACTICES AND THEIR PERCEPTIONS OF HOW SCIENCE EDUCATION REFORM AND HIGH STAKES TESTS AFFECT THEIR INSTRUCTIONAL DECISIONS.  

E-Print Network (OSTI)

??Both assessment and reform are prominent topics in education and specifically science education. The purpose of this study was to achieve greater insight into science… (more)

Feitler, Michele

2010-01-01T23:59:59.000Z

436

The Effects of Maternal Welfare Participation on Children’s Developmental Outcomes in the Welfare Reform Era.  

E-Print Network (OSTI)

??Since welfare reform legislation in 1996, Temporary Assistance to Needy Families (TANF) has been implemented. Under TANF, most recipients are required to work. Work requirements… (more)

Lee, Wonik

2010-01-01T23:59:59.000Z

437

A novel technique for on-line coke gasification during propane steam reforming using forced CO2 cycling.  

E-Print Network (OSTI)

??Steam reforming is an important source of synthesis gas production that is used by major petrochemical processes such as ammonia, methanol and the Fisher-Tropsch process.… (more)

Alenazey, Feraih Sheradh

2011-01-01T23:59:59.000Z

438

Adult perceptions of the impact of Kentucky Education Reform Act initiatives on achievement : insights of rural gifted students.  

E-Print Network (OSTI)

??Ph. D. This phenomenological study investigated perceptions regarding the impact of the tenets of the Kentucky Education Reform Act (KERA) on the self-reported achievement and… (more)

Lanham, Jan Kathryn Weaver, 1954-

2010-01-01T23:59:59.000Z

439

Development of an impedance-based sensor for the detection of catalyst coking in fuel-reforming systems.  

E-Print Network (OSTI)

??A novel sensor for detecting the early stages of catalyst coking in fuel reforming systems has been developed. The sensor was manufactured by inkjet printing… (more)

Wheeler, Jeffrey L.

2013-01-01T23:59:59.000Z

440

New silicotitanate molecular sieve and condensed phases  

DOE Patents (OSTI)

This patent application relates to an invention for a new silicotitanate molecular sieve ion exchange material for the capture and immobilization of divalent cations from aqueous and/or hydrocarbon solutions, including elements such as radioactive strontium or industrial RCRA metal cations. The invention also relates to the ability to either recycle the captured metal for future use or to encapsulate the cation through thermal treatment of the molecular sieve to a condensed phase.

Nenoff, Tina M.; Nyman, May D.

2000-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "aqueous phase reforming" 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

FLUIDIZED BED STEAM REFORMER (FBSR) PRODUCT: MONOLITH FORMATION AND CHARACTERIZATION  

SciTech Connect

The most important requirement for Hanford's low activity waste (LAW) form for shallow land disposal is the chemical durability of the product. A secondary, but still essential specification, is the compressive strength of the material with regards to the strength of the material under shallow land disposal conditions, e.g. the weight of soil overburden and potential intrusion by future generations, because the term ''near-surface disposal'' indicates disposal in the uppermost portion, or approximately the top 30 meters, of the earth's surface. The THOR{reg_sign} Treatment Technologies (TTT) mineral waste form for LAW is granular in nature because it is formed by Fluidized Bed Steam Reforming (FBSR). As a granular product it has been shown to be as durable as Hanford's LAW glass during testing with ASTM C-1285-02 known as the Product Consistency Test (PCT) and with the Single Pass Flow Through Test (SPFT). Hanford Envelope A and Envelope C simulants both performed well during PCT and SPFT testing and during subsequent performance assessment modeling. This is partially due to the high aluminosilicate content of the mineral product which provides a natural aluminosilicate buffering mechanism that inhibits leaching and is known to occur in naturally occurring aluminosilicate mineral analogs. In order for the TTT Na-Al-Si (NAS) granular mineral product to meet the compressive strength requirements (ASTM C39) for a Hanford waste form, the granular product needs to be made into a monolith or disposed of in High Integrity Containers (HIC's). Additionally, the Hanford intruder scenario for disposal in the Immobilized Low Activity Waste (ILAW) trench is mitigated as there is reduced intruder exposure when a waste form is in a monolithic form. During the preliminary testing of a monolith binder for TTT's FBSR mineral product, four parameters were monitored: (1) waste loading (not optimized for each waste form tested); (2) density; (3) compressive strength; and (4) durability must not be compromised--binding agent should not react with the NAS product and binding agent should not create an unfavorable pH environment that may cause accelerated leaching. It is the goal of the present study to survey cementitious waste forms based on Ordinary Portland Cement (OPC), Ceramicrete, and hydroceramic binders by correlating waste loading, density and compressive strength and then determine if these binders affect the product performance in terms of the PCT response. This will be done by making a one-to-one comparison of the PCT response measured on granular NAS mineral product (mixed bed and fines products) with the PCT response of the monolithed NAS product in the different binders. Future studies may include, refining the above binders, and examining other binders. It is likely that binders formed from kaolin would be most compatible with the chemistry of the THOR{reg_sign} mineral waste form which is made by steam reforming of kaolin and sodium rich wastes. The economics of production on a large scale have yet to be investigated for any of the binders tested.

Jantzen, C

2006-09-13T23:59:59.000Z

442

Development of a Catalyst/Sorbent for Methane Reforming  

Science Conference Proceedings (OSTI)

This project led to the further development of a combined catalyst and sorbent for improving the process technology required for converting CH{sub 4} and/or CO into H{sub 2} while simultaneously separating the CO{sub 2} byproduct all in a single step. The new material is in the form of core-in-shell pellets such that each pellet consists of a CaO core surrounded by an alumina-based shell capable of supporting a Ni catalyst. The Ni is capable of catalyzing the reactions of steam with CH{sub 4} or CO to produce H{sub 2} and CO{sub 2}, whereas the CaO is capable of absorbing the CO{sub 2} as it is produced. The absorption of CO{sub 2} eliminates the reaction inhibiting effects of CO{sub 2} and provides a means for recovering the CO{sub 2} in a useful form. The present work showed that the lifecycle performance of the sorbent can be improved either by incorporating a specific amount of MgO in the material or by calcining CaO derived from limestone at 1100 C for an extended period. It also showed how to prepare a strong shell material with a large surface area required for supporting an active Ni catalyst. The method combines graded particles of {alpha}-alumina with noncrystalline alumina having a large specific surface area together with a strength promoting additive followed by controlled calcination. Two different additives produced good results: 3 {micro}m limestone and lanthanum nitrate which were converted to their respective oxides upon calcination. The oxides partially reacted with the alumina to form aluminates which probably accounted for the strength enhancing properties of the additives. The use of lanthanum made it possible to calcine the shell material at a lower temperature, which was less detrimental to the surface area, but still capable of producing a strong shell. Core-in-shell pellets made with the improved shell materials and impregnated with a Ni catalyst were used for steam reforming CH{sub 4} at different temperatures and pressures. Under all conditions tested, the CH{sub 4} conversion was large (>80%) and nearly equal to the predicted thermodynamic equilibrium level as long as CO{sub 2} was being rapidly absorbed. Similar results were obtained with both shell material additives. Limited lifecycle tests of the pellets also produced similar results that were not affected by the choice of additive. However, during each lifecycle test the period during which CO{sub 2} was rapidly absorbed declined from cycle to cycle which directly affected the corresponding period when CH{sub 4} was reformed rapidly. Therefore, the results showed a continuing need for improving the lifecycle performance of the sorbent. Core-in-shell pellets with the improved shell materials were also utilized for conducting the water gas shift reaction in a single step. Three different catalyst formulations were tested. The best results were achieved with a Ni catalyst, which proved capable of catalyzing the reaction whether CO{sub 2} was being absorbed or not. The calcined alumina shell material by itself also proved to be a very good catalyst for the reaction as long as CO{sub 2} was being fully absorbed by the core material. However, neither the alumina nor a third formulation containing Fe{sub 2}O{sub 3} were good catalysts for the reaction when CO{sub 2} was not absorbed by the core material. Furthermore, the Fe{sub 2}O{sub 3}-containing catalyst was not as good as the other two catalysts when CO{sub 2} was being absorbed.

B.H. Shans; T.D. Wheelock; Justinus Satrio; Karl Albrecht; Tanya Harris Janine Keeley; Ben Silva; Aaron Shell; Molly Lohry; Zachary Beversdorf

2008-12-31T23:59:59.000Z

443

Development of a comprehensive reporting system for a school reform organization: The Accelerated Schools Project  

E-Print Network (OSTI)

Given the conflicting research results on the effectiveness of whole-school reform models (Nunnery, 1998; Stringfield & Herman, 1997; American Institutes for Research, 1999; U.S. Department of Education, 2004), there is a need to focus on the evaluation procedures of whole-school reform organizations. Because the ultimate goal is to improve school performance, it should also be a goal of each whole-school reform organization to design a comprehensive data collection system to evaluate each schoolÂ?s performance. A comprehensive reporting system was developed for a school reform organization, the Accelerated Schools Project (ASP). Using the steps of the research and development process recommended by Borg and Gall (1989), this study: (a) developed a theoretical framework for the reporting system, (b) identified data that should be collected in the reporting system, (c) performed a field test with an expert panel of educational professionals, (d) developed a preliminary form of the reporting system, (e) performed a main field test with principals and coaches in the ASP network, (f) reported field test results, (g) revised the preliminary reporting system, (h) developed a website for the reporting system, and (i) provided recommendations for the completion, dissemination and implementation of the system in accelerated schools across the nation. This study has important implications for both the ASP community and for the entire whole-school reform community. For the ASP community, the reporting system could be used: (a) to collect data in all accelerated schools across the nation (b) as a longitudinal database of information to monitor data on each ASP school, and (c) to generate school summary reports on ASP schools. These data will assist researchers in measuring the effectiveness of the ASP model on student achievement and other important variables. For the whole-school reform community, the method used in this study could be replicated in other school reform organizations to develop a comprehensive reporting system. By providing consistent data for school reform organizations to evaluate the impact of their models on students and schools, educational researchers will be better equipped to understand each modelÂ?s impact, and thus will better understand the diverse research results on school reform effectiveness.

Stephens, Jennifer Anne

2004-12-01T23:59:59.000Z

444

Nano Res (2010) 3: 452458452 Aqueous Supercapacitors on Conductive Cotton  

E-Print Network (OSTI)

Nano Res (2010) 3: 452­458452 Aqueous Supercapacitors on Conductive Cotton Mauro Pasta1,2 , Fabio the fabrication of wearable supercapacitors using cotton fabric as an essential component. Carbon nanotubes in the supercapacitor. Aqueous lithium sulfate is used as the electrolyte in the devices, because it presents no safety

Cui, Yi

445

Rheological Properties of Aqueous Nanometric Alumina Suspensions  

SciTech Connect

Colloidal processing is an effective and reliable approach in the fabrication of the advanced ceramic products. Successful colloidal processing of fine ceramic powders requires accurate control of the rheological properties. The accurate control relies on the understanding the influences of various colloidal parameters on the rheological properties. Almost all research done on the rheology paid less attention to the interactions of particle and solvent. However, the interactions of the particles are usually built up through the media in which the particles are suspended. Therefore, interactions of the particle with the media, the adsorbed layers on the particle surface, and chemical and physical properties of media themselves must influence the rheology of the suspension, especially for the dense suspensions containing nanosized particles. Relatively little research work has been reported in this area. This thesis addresses the rheological properties of nanometric alumina aqueous suspensions, and paying more attention to the interactions between particle and solvent, which in turn influence the particle-particle interactions. Dense nanometric alumina aqueous suspensions with low viscosity were achieved by environmentally-benign fructose additives. The rheology of nanometric alumina aqueous suspensions and its variation with the particle volume fraction and concentration of fructose were explored by rheometry. The adsorptions of solute (fructose) and solvent (water) on the nanometric alumina particle surfaces were measured and analyzed by TG/DSC, TOC, and NMR techniques. The mobility of water molecules in the suspensions and its variation with particle volume fractions and fructose additive were determined by the {sup 17}O NMR relaxation method. The interactions between the nanometric alumina particles in water and fructose solutions were investigated by AFM. The results indicated that a large number of water layers were physically bound on the particles' surfaces in the aqueous suspension. The viscosity of the suspension increases dramatically when the solid volume fraction exceeds 30 vol.%. The overlap of physically adsorbed water layers at this level causes the sharp increase in viscosity. Fructose molecules can weaken the interactions between the particle surfaces and water molecules, as a consequence, they release some bound water layers from the surfaces to the bulk medium. It is believed that fraction of the water that is bound by the solid surface is reduced hence becoming available for flow. The oxygen-17 relaxation time decreased with the increase of particle volume fractions in the suspension. Fructose addition increased the overall water mobility in the suspension. Only part of the alumina particle surfaces was covered with fructose molecules. This adsorption of fructose molecules on the particle surfaces increased the pH of the suspension with a concomitant decrease in {zeta}-potential of the alumina nanoparticles. The interactions between the nanometric alumina particles in water to a large extent can be explained by the DLVO theory. However, the interactions between particles in fructose solutions cannot be well described by the DLVO theory. The interaction forces (magnitude and range) as well as adhesive force and surface tension between nanometric alumina particles were decreased with the fructose concentration.

Chuanping Li

2004-12-19T23:59:59.000Z

446

Enhanced Oil Recovery: Aqueous Flow Tracer Measurement  

SciTech Connect

A low detection limit analytical method was developed to measure a suite of benzoic acid and fluorinated benzoic acid compounds intended for use as tracers for enhanced oil recovery operations. Although the new high performance liquid chromatography separation successfully measured the tracers in an aqueous matrix at low part per billion levels, the low detection limits could not be achieved in oil field water due to interference problems with the hydrocarbon-saturated water using the system's UV detector. Commercial instrument vendors were contacted in an effort to determine if mass spectrometry could be used as an alternate detection technique. The results of their work demonstrate that low part per billion analysis of the tracer compounds in oil field water could be achieved using ultra performance liquid chromatography mass spectrometry.

Joseph Rovani; John Schabron

2009-02-01T23:59:59.000Z

447

Atomic hydrogen reaction rates in aqueous solution via free-induction decay attenuation  

DOE Green Energy (OSTI)

This new pulsed EPR method is providing data on H-atom reaction rates in water, which are important in radiation chemistry of aqueous solutions, eg, corrosion in reactor cooling systems, H2 production in high-level radioactive waste, and spread of radioactive iodine following the Chernobyl accident. This AECL-Argonne collaborative effort was undertaken to investigate fundamental aqueous H-atom chemistry for the purpose of developing predictive models of iodine transport that will be used by the nuclear power industry to enhance plant safety. Reactions of (H){sub aq} with many representative organic and inorganicmolecules have already been investigated. Radiolysis of aqueous solns with 3-MeV electrons produces H atoms in high yield; in the free induction decay method, a powerful 30 ns microwave pulse is applied immediately following pulse radiolysis, creating a phase coherence of the H-atom electron spins that is detected in the pulsed EPR spectrometer as a damped cosine free induction decay (FID). Natural decay time of the spin coherence is many microseconds, but if a reaction partner for the H atoms is introduced, the FID becomes shorter, revealing the H reaction rate. Results of H atom reaction with benzene, methanol, periodate and periodic acid are discussed briefly.

Bartels, D.M.

1996-02-01T23:59:59.000Z

448

Development of Sulfur and Carbon Tolerant Reforming Alloy Catalysts Aided by Fundamental Atomistics Insights  

SciTech Connect

Current hydrocarbon reforming catalysts suffer from rapid carbon and sulfur poisoning. Even though there is a tremendous incentive to develop more efficient catalysts, these materials are currently formulated using inefficient trial and error experimental approaches. We have utilized a novel hybrid experimental/theoretical approach, combining quantum Density Functional Theory (DFT) calculations and various state-of-the-art experimental tools, to formulate carbon tolerant reforming catalysts. We have employed DFT calculations to develop molecular insights into the elementary chemical transformations that lead to carbon poisoning of Ni catalysts. Based on the obtained molecular insights, we have identified, using DFT quantum calculation, Sn/Ni alloy as a potential carbon tolerant reforming catalyst. Sn/Ni alloy was synthesized and tested in steam reforming of methane, propane, and isooctane. We demonstrated that the alloy catalyst is carbon-tolerant under nearly stoichiometric steam-to-carbon ratios. Under these conditions, monometallic Ni is rapidly poisoned by sp2 carbon deposits. The research approach is distinguished by a few characteristics: (a) Knowledge-based, bottom-up approach, compared to the traditional trial and error approach, allows for a more efficient and systematic discovery of improved catalysts. (b) The focus is on exploring alloy materials which have been largely unexplored as potential reforming catalysts.

Suljo Linic

2006-08-31T23:59:59.000Z

449

Experimental and computational investigations of sulfur-resistant bimetallic catalysts for reforming of biomass gasification products  

DOE Green Energy (OSTI)

A combination of density functional theory (DFT) calculations and experimental studies of supported catalysts was used to identify H{sub 2}S-resistant biomass gasification product reforming catalysts. DFT calculations were used to search for bimetallic, nickel-based (1 1 1) surfaces with lower sulfur adsorption energies and enhanced ethylene adsorption energies. These metrics were used as predictors for H{sub 2}S resistance and activity toward steam reforming of ethylene, respectively. Relative to Ni, DFT studies found that the Ni/Sn surface alloy exhibited enhanced sulfur resistance and the Ni/Ru system exhibited an improved ethylene binding energy with a small increase in sulfur binding energy. A series of supported bimetallic nickel catalysts was prepared and screened under model ethylene reforming conditions and simulated biomass tar reforming conditions. The observed experimental trends in activity were consistent with theoretical predictions, with observed reforming activities in the order Ni/Ru > Ni > Ni/Sn. Interestingly, Ni/Ru showed a high level of resistance to sulfur poisoning compared with Ni. This sulfur resistance can be partly explained by trends in sulfur versus ethylene binding energy at different types of sites across the bimetallic surface.

Rangan, Meghana; Yung, Matthew M.; Medlin, J. William (NREL); (Colorado)

2011-11-17T23:59:59.000Z

450

Development of Sulfur and Carbon Tolerant Reforming Alloy Catalysts Aided Fundamental Atomistic Insights  

SciTech Connect

Current hydrocarbon reforming catalysts suffer from rapid carbon and sulfur poisoning. Even though there is a tremendous incentive to develop more efficient catalysts, these materials are currently formulated using inefficient trial and error experimental approaches. We have utilized a hybrid experimental/theoretical approach, combining quantum Density Functional Theory (DFT) calculations and various state-of-the-art experimental tools, to formulate carbon tolerant reforming catalysts. We have employed DFT calculations to develop molecular insights into the elementary chemical transformations that lead to carbon poisoning of Ni catalysts. Based on the obtained molecular insights, we have identified, using DFT quantum calculation, various Ni alloy catalysts as potential carbon tolerant reforming catalysts. The alloy catalysts were synthesized and tested in steam reforming and partial oxidation of methane, propane, and isooctane. We demonstrated that the alloy catalysts are much more carbon-tolerant than monometallic Ni catalysts under nearly stoichiometric steam-to-carbon ratios. Under these conditions, monometallic Ni is rapidly poisoned by sp2 carbon deposits. The research approach is distinguished by two characteristics: (a) knowledge-based, bottomup approach, compared to the traditional trial and error approach, allows for a more efficient and systematic discovery of improved catalysts. (b) the focus is on exploring alloy materials which have been largely unexplored as potential reforming catalysts.

Suljo Linic

2008-12-31T23:59:59.000Z

451

Development of internal reforming carbonate fuel cell stack technology  

DOE Green Energy (OSTI)

Activities under this contract focused on the development of a coal-fueled carbonate fuel cell system design and the stack technology consistent with the system design. The overall contract effort was divided into three phases. The first phase, completed in January 1988, provided carbonate fuel cell component scale-up from the 1ft{sup 2} size to the commercial 4ft{sup 2} size. The second phase of the program provided the coal-fueled carbonate fuel cell system (CGCFC) conceptual design and carried out initial research and development needs of the CGCFC system. The final phase of the program emphasized stack height scale-up and improvement of stack life. The results of the second and third phases are included in this report. Program activities under Phase 2 and 3 were designed to address several key development areas to prepare the carbonate fuel cell system, particularly the coal-fueled CFC power plant, for commercialization in late 1990's. The issues addressed include: Coal-Gas Related Considerations; Cell and Stack Technology Improvement; Carbonate Fuel Cell Stack Design Development; Stack Tests for Design Verification; Full-Size Stack Design; Test Facility Development; Carbonate Fuel Cell Stack Cost Assessment; and Coal-Fueled Carbonate Fuel Cell System Design. All the major program objectives in each of the topical areas were successfully achieved. This report is organized along the above-mentioned topical areas. Each topical area has been processed separately for inclusion on the data base.

Farooque, M.

1990-10-01T23:59:59.000Z

452

Public Law 108-458-Dec. 17, 2004; Intelligence Reform and Terrorism Prevention Act of 2004  

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

8-458-DEC. 17, 2004 8-458-DEC. 17, 2004 INTELLIGENCE REFORM AND TERRORISM PREVENTION ACT OF 2004 VerDate 11-MAY-2000 13:50 Jan 28, 2005 Jkt 039139 PO 00458 Frm 00001 Fmt 6579 Sfmt 6579 E:\PUBLAW\PUBL458.108 APPS06 PsN: PUBL458 118 STAT. 3638 PUBLIC LAW 108-458-DEC. 17, 2004 Public Law 108-458 108th Congress An Act To reform the intelligence community and the intelligence and intelligence-related activities of the United States Government, and for other purposes. Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. SHORT TITLE; TABLE OF CONTENTS. (a) SHORT TITLE.-This Act may be cited as the ''Intelligence Reform and Terrorism Prevention Act of 2004''. (b) TABLE OF CONTENTS.-The table of contents for this Act is as follows: