Powered by Deep Web Technologies
Note: This page contains sample records for the topic "history catalytic 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.


1

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

2

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

3

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

4

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

5

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

6

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

7

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

8

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

9

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

10

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

11

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

12

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

13

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)

14

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)

15

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)

16

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

17

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

18

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

19

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.

20

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

Note: This page contains sample records for the topic "history catalytic 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

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)

22

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)

23

Catalytic Reforming - Energy Information Administration  

U.S. Energy Information Administration (EIA)

Process: Period: Annual (as of January 1) Download Series History: Definitions, Sources & Notes: Show Data By: Process: Area: 2008 2009 2010 2011 2012 ...

24

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

25

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

26

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

27

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

28

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

29

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

30

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

31

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

32

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

33

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

34

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

35

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

36

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

37

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

38

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

39

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

40

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

Note: This page contains sample records for the topic "history catalytic 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

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

42

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

43

,"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"

44

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

45

GREENHOUSE GAS CATALYTIC REFORMING TO SYNGAS A thesis submitted in partial fulfillment of the requirements for the degree of  

E-Print Network (OSTI)

GREENHOUSE GAS CATALYTIC REFORMING TO SYNGAS A thesis submitted in partial fulfillment've missed over the past two years. #12;4 TABLE OF CONTENTS GREENHOUSE GAS CATALYTIC REFORMING TO SYNGAS 1.083 moles CH4, 0.083 moles CO2, and 0.834 moles Ar which are the inlet conditions for many of the catalytic

Columbia University

46

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.

47

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

48

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

49

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

50

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

51

Recovery of normally gaseous hydrocarbons from net excess hydrogen in a catalytic reforming process  

Science Conference Proceedings (OSTI)

A process is disclosed for the catalytic reforming of hydrocarbons in the presence of hydrogen, preferably to produce high quality gasoline boiling range products. An improved recovery of normally gaseous hydrocarbons from the net excess hydrogen is realized by chilling and contacting said hydrogen with a normally liquid hydrocarbon stream in a plural stage absorption zone at an elevated pressure.

Scheifele, C.A.

1982-06-08T23:59:59.000Z

52

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

53

[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

54

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

55

Catalytic reforming catalyst with modified pore size distribution and a process using the same  

Science Conference Proceedings (OSTI)

This patent describes a catalytic reforming process for conversion of a naptha hydrocarbon at reforming conditions using a catalyst comprising at least one catalytic metal and alumina. The improvement comprises using a catalyst having the following properties in combination: a surface area above about 250 M/sup 2//gram of catalyst; a pore volume above about 0.44 cc/gram of catalyst in pores having diameters of from about 30 angstroms to about 38,000 angstroms; and a pore volume distribution wherein about 70 percent or less of the pore volume is in pores having diameters of from about 30 angstroms to about 400 angstroms. About 30 percent or more pore volume is in pores having diameters of from about 400 angstroms to about 38,000 angstroms.

Unmuth, E.E.; Fleming, B.A.

1987-05-12T23:59:59.000Z

56

A BRIEF HISTORY OF INDUSTRIAL CATALYSIS  

E-Print Network (OSTI)

Naphtha Reforming Catalytic reforming of naphthas serves toalready apparent in catalytic reforming as outlined above,catalysts (e.g. , in catalytic reforming, methanatiom, or

Heinemann, Heinz

2013-01-01T23:59:59.000Z

57

Electro-catalytic oxidation device for removing carbon from a fuel reformate  

SciTech Connect

An electro-catalytic oxidation device (ECOD) for the removal of contaminates, preferably carbonaceous materials, from an influent comprising an ECOD anode, an ECOD cathode, and an ECOD electrolyte. The ECOD anode is at a temperature whereby the contaminate collects on the surface of the ECOD anode as a buildup. The ECOD anode is electrically connected to the ECOD cathode, which consumes the buildup producing electricity and carbon dioxide. The ECOD anode is porous and chemically active to the electro-catalytic oxidation of the contaminate. The ECOD cathode is exposed to oxygen, and made of a material which promotes the electro-chemical reduction of oxygen to oxidized ions. The ECOD electrolyte is non-permeable to gas, electrically insulating and a conductor to oxidized. The ECOD anode is connected to the fuel reformer and the fuel cell. The ECOD electrolyte is between and in ionic contact with the ECOD anode and the ECOD cathode.

Liu, Di-Jia (Naperville, IL)

2010-02-23T23:59:59.000Z

58

Testing of a Catalytic Partial Oxidation Diesel Reformer with a Solid Oxide Fuel Cell System  

DOE Green Energy (OSTI)

Rural Alaska currently uses diesel generator sets to produce much of its power. The high energy content of diesel (i.e. ~140,000 BTU per gallon) makes it the fuel of choice because this reduces the volume of fuel that must be transported, stored, and consumed in generating the power. There is an existing investment in infrastructure for the distribution and use of diesel fuel. Problems do exist, however, in that diesel generators are not very efficient in their use of diesel, maintenance levels can be rather high as systems age, and the environmental issues related to present diesel generators are of concern. The Arctic Energy Technology Development Laboratory at the University of Alaska -- Fairbanks is sponsoring a project to address the issues mentioned above. The project takes two successful systems, a diesel reformer and a tubular solid oxide fuel cell unit, and jointly tests those systems with the objective of producing a for-purpose diesel fueled solid oxide fuel cell system that can be deployed in rural Alaska. The reformer will convert the diesel to a mixture of carbon monoxide and hydrogen that can be used as a fuel by the fuel cell. The high temperature nature of the solid oxide fuel cell (SOFC is capable of using this mixture to generate electricity and provide usable heat with higher efficiency and lower emissions. The high temperature nature of the SOFC is more compatible with the arctic climate than are low temperature technologies such as the proton exchange membrane fuel cells. This paper will look at the interaction of a SOFC system that is designed to internally reform methane and a catalytic partial oxidation (CPOX) diesel reformer. The diesel reformer produces a reformate that is approximately 140 BTU per scf (after removal of much of the reformate water) as compared to a methane based reformate that is over twice that value in BTU content. The project also considers the effect of altitude since the test location will be at 4800 feet with the consequential drop in oxygen content and necessary increases in flow rates.

Lyman Frost; Bob Carrington; Rodger McKain; Dennis Witmer

2005-03-01T23:59:59.000Z

59

Biomass to hydrogen via fast pyrolysis and catalytic steam reforming of the pyrolysis oil or its fractions  

Science Conference Proceedings (OSTI)

Pyrolysis of lignocellulosic biomass and reforming of the pyroligneous oils are being studied as a strategy for producing hydrogen. A process of this nature has the potential to be cost competitive with conventional means of producing hydrogen. The authors propose a regionalized system of hydrogen production, where small- and medium-sized pyrolysis units (catalytic reforming of model compounds to hydrogen using Ni-based catalysts have achieved essentially complete conversion to H{sub 2}. Existing data on the catalytic reforming of oxygenates have been studied to guide catalyst selection. A process diagram for the pyrolysis and reforming operations is discussed, as are initial production cost estimates. A window of opportunity clearly exists if the bio-oil is first refined to yield valuable oxygenates so that only a residual fraction is used for hydrogen production.

Wang, D.; Czernik, S.; Montane, D.; Mann, M. [National Renewable Energy Lab., Golden, CO (United States); Chornet, E. [National Renewable Energy Lab., Golden, CO (United States)]|[Univ. de Sherbrooke, Quebec (Canada)

1997-05-01T23:59:59.000Z

60

Solar reforming of methane in a direct absorption catalytic reactor on a parabolic dish  

DOE Green Energy (OSTI)

The concept of solar driven chemical reactions in a commercial-scale volumetric receiver/reactor on a parabolic concentrator was successfully demonstrated in the CAtalytically Enhanced Solar Absorption Receiver (CAESAR) test. Solar reforming of methane (CH{sub 4}) with carbon dioxide (CO{sub 2}) was achieved in a 64-cm diameter direct absorption reactor on a parabolic dish capable of 150 kW solar power. The reactor was a catalytic volumetric absorber consisting of a multi-layered, porous alumina foam disk coated with rhodium (Rh) catalyst. The system was operated during both steady-state and solar transient (cloud passage) conditions. The total solar power absorbed reached values up to 97 kW and the maximum methane conversion was 70%. Receiver thermal efficiencies ranged up to 85% and chemical efficiencies peaked at 54%. The absorber performed satisfactorily in promoting the reforming reaction during the tests without carbon formation. However, problems of cracking and degradation of the porous matrix, nonuniform dispersion of the Rh through the absorber, and catalyst deactivation due to sintering and possible encapsulation, must be resolved to achieve long-term operation and eventual commercialization. 17 refs., 11 figs., 1 tab.

Muir, J.F.; Hogan, R.E. Jr.; Skocypec, R.D. (Sandia National Labs., Albuquerque, NM (USA)); Buck, R. (Deutsche Forschungsanstalt fuer Luft- und Raumfahrt e.V. (DLR), Stuttgart (Germany, F.R.). Inst. fuer Technische Thermodynamik)

1990-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

Separation and recovery of hydrogen and normally gaseous hydrocarbons from net excess hydrogen from a catalytic reforming process  

Science Conference Proceedings (OSTI)

A process is disclosed for the catalytic reforming of hydrocarbons in the presence of hydrogen, preferably to produce high quality gasoline boiling range products. An improved recovery of normally gaseous hydrocarbons from the net excess hydrogen is realized by chilling and contacting said hydrogen with a normally liquid hydrocarbon stream in a plural stage absorption zone at an elevated pressure.

Scheifele, C.A.

1982-06-08T23:59:59.000Z

62

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

63

Recovery of C/sub 3/. sqrt. hydrocarbon conversion products and net excess hydrogen in a catalytic reforming process  

Science Conference Proceedings (OSTI)

This invention relates to a hydrocarbon conversion process effected in the presence of hydrogen, especially a hydrogenproducing hydrocarbon conversion process. More particularly, this invention relates to the catalytic reforming of a naphtha feedstock, and is especially directed to an improved recovery of the net excess hydrogen, and to an improved recovery of a C/sub 3/..sqrt.. normally gaseous hydrocarbon conversion product and a C/sub 5/..sqrt.. hydrocarbon conversion product boiling in the gasoline range.

Degraff, R.R.; Peters, K.D.

1982-12-21T23:59:59.000Z

64

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

65

Solar reforming of methane in a direct absorption catalytic reactor on a parabolic dish: I-test and analysis  

DOE Green Energy (OSTI)

The concept of solar driven chemical reaction in a commercial-scale volumetric receiver/reactor on a parabolic concentrator was successfully demonstrated in the CAtalytically Enhanced Solar Absorption Receiver (CAESAR) test. Solar reforming of methane (CH[sub 4]) with carbon dioxide (CO[sub 2]) was achieved in a 64 cm diameter direct absorption reactor on a parabolic dish capable of 150 kW solar power. The reactor was a catalytic volumetric absorber consisting of a multilayered, porous alumina foam disk coated with rhodium (Rh) catalyst. The system was operated during both steady-state and solar transient (cloud passage) conditions. The total solar power absorbed reached values up to 97 kW and the maximum methane conversion was 70%. Receiver thermal efficiencies ranged up to 85% and chemical efficiencies peaked at 54%. The absorber performed satisfactorily in promoting the reforming reaction during the tests without carbon formation. However, problems of cracking and degradation of the porous matrix, nonuniform dispersion of the Rh through the absorber, the catalyst deactivation due to sintering and possible encapsulation, must be resolved to achieve long-term operation and eventual commercialization.

Muir, J.F.; Hogan, R.E. Jr.; Skocypec, R.D. (Sandia National Lab., Albuquerque, NM (United States)); Buck, R. (DLR-ITT, Stuttgart (Germany))

1994-06-01T23:59:59.000Z

66

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

Science Conference Proceedings (OSTI)

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

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

2008-07-15T23:59:59.000Z

67

Development of a mathematical description of catalytic reforming taking into account changes of the individual components of the feedstock and catalyst coking  

Science Conference Proceedings (OSTI)

This paper presents an approach for modeling petroleum and petrochemical processing. Based on this approach a mathematical model has been developed for catalytic reforming taking into account changes of individual feedstock components and catalyst coking. Examples are given of calculations and optimization of industrial equipment.

Rabinovich, G.B.; Dynkina, N.E.

1985-12-01T23:59:59.000Z

68

Multiple-stage catalytic reforming with gravity-flowing dissimilar catalyst particles  

Science Conference Proceedings (OSTI)

A multiple-stage catalytic conversion system in which a hydrocarbonaceous charge stock and hydrogen flow serially through a plurality of catalytic reaction zones in each of which the catalyst particles are movable via gravity flow. Dissimilar catalyst particles are utilized in the reactor systems which share a common regenerating tower through which the catalyst particles are downwardly movable via gravity flow and in which the catalyst particles are regenerated in segregated fashion. Dissimilarity of the catalyst particles stems from a difference in activity, stability and selectivity characteristics. In turn, this difference may be attributed either to physical, or chemical distinctions between the two composites, or both.

Sikonia, J. G.; Bennett, R. W.

1985-02-12T23:59:59.000Z

69

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

70

Catalytic Steam Reforming of Gasifier Tars: On-Line Monitoring of Tars with a Transportable Molecular-Beam Mass Spectrometer; Milestone Completion Report  

DOE Green Energy (OSTI)

A method for evaluating catalytic tar decomposition in real time is presented. The effectiveness of two catalysts are compared. A key technical and economic barrier to commercialization of biomass gasification technologies is the removal of tars that are unavoidably formed in this thermochemical process. Tars contain fuel value; however, they are problematic in gas engines (both reciprocating and turbine) because they condense in the fuel delivery system, forming deposits that negatively affect operation and efficiency. These tars also combust with high luminosity, potentially forming soot particles. The conventional technology for tar removal is wet scrubbing. Although this approach has shown some success, there are significant equipment and operating costs associated with it. In order to prevent the generation of toxic wastewater, the tars must be separated and either disposed as hazardous waste or, preferably, combusted in the gasification plant. A conceptually better approach is catalytic steam reforming of the tars to hydrogen and carbon monoxide (CO), effectively increasing the gasification efficiency and eliminating the problems mentioned above. In FY2000, Battelle Columbus Laboratories attempted to demonstrate integrated gasification-gas turbine operation using catalytic steam reforming of tars. NREL participated in those tests using the transportable molecular-beam mass spectrometer (TMBMS) to monitor the catalytic reactor's performance on-line [10]. Unfortunately, the pilot plant tests encountered operational problems that prevented conclusive determination of the efficacy of the selected catalyst (Battelle's DN34). In FY2001, NREL performed on-site tar steam reforming tests using a slip-stream of hot pyrolysis gas from the Thermochemical Process Development Unit (TCPDU), which was directed to a bench-scale fluidized bed reactor system designed expressly for this purpose. Supporting this effort, the TMBMS was employed to provide on-line analysis of the tar conversion. The gas composition changes were monitored by two identical gas chromatographs (GCs), and modified method 5 sampling was performed to obtain gravimetric conversion data. The combination of these analytical techniques provided definitive catalyst performance data, as well as linkage to previous and on-going work elsewhere. Two catalysts were tested: nickel (Ni) on potassium promoted alumina (Sued-Chemie C11-NK), used commercially for naphtha steam reforming, and alumina (Battelle's DN34) claimed to be effective for gasifier tar decomposition. In addition, sand was tested as an inert reference material.

Carpenter, D.; Ratcliff, M.; Dayton, D.

2002-05-01T23:59:59.000Z

71

Plasma Catalytic Conversion of Methane in Ultra Rich Flame using Transient Gliding Arc Combustion Support  

E-Print Network (OSTI)

be carried out in a number of ways: steam reforming, thermo-catalytic reforming, partial oxidation, etc. [1

72

The CAESAR project: Experimental and modeling investigations of methane reforming in a CAtalytically Enhanced Solar Absorption Receiver on a parabolic dish  

DOE Green Energy (OSTI)

A joint US/Federal Republic of Germany (FRG) project has successfully tested a unique solar-driven chemical reactor in the CAtalytically Enhanced Solar Absorption Receiver (CAESAR) experiment. The CAESAR test was a {open_quotes}proof-of-concept{close_quotes} demonstration of carbon-dioxide reforming of methane in a commercial-scale, solar, volumetric receiver/reactor on a parabolic dish concentrator. The CAESAR design; test facility and instrumentation; thermal and chemical tests; and analysis of test results are presented in detail. Numerical models for the absorber and the receiver are developed and predicted performance is compared with test data. Post test analyses to assess the structural condition of the absorber and the effectiveness of the rhodium catalyst are presented. Unresolved technical issues are identified and future development efforts are recommended.

Muir, J.F.; Hogan, R.E. Jr.; Skocypec, R.D. [Sandia National Labs., Albuquerque, NM (US); Buck, R. [Deutsche Forschungsanstalt fuer Luft- und Raumfahrt, Stuttgart (DE). Inst. of Technical Thermodynamics

1993-07-01T23:59:59.000Z

73

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

74

Prepr. Pap.-Am. Chem. Soc., Div. Fuel Chem. 2004, 49 (2), xxxx NON-THERMAL PLASMA CATALYTIC  

E-Print Network (OSTI)

hydrocarbons can be carried out in a number of ways: steam reforming, thermo-catalytic reforming, partial

75

Solar reforming of methane in a direct absorption catalytic reactor on a parabolic dish: 2, Modeling and analysis  

DOE Green Energy (OSTI)

The CAtalytically Enhanced Solar Absorption Receiver (CAESAR) experiment was conducted to determine the thermal, chemical, and mechanical performance of a commercial-scale, dish-mounted, direct catalytic absorption receiver (DCAR) reactor over a range of steady state and transient (cloud) operating conditions. The focus of the experiment is on global performance such as receiver efficiencies and overall methane conversion; it was not intended to provide data for code validation. A numerical model was previously developed to provide guidance in the design of the absorber. The one-dimensional, planar and steady-state model incorporates, the following energy transfer mechanisms: solar and infrared radiation, heterogeneous chemical reaction, conduction in the solid phase, and convection between the fluid and solid phases. A number of upgrades to the model and improved property values are presented here. Model predictions are shown to bound the experimental axial thermocouple data when experimental uncertainties are included. Global predictions are made using a technique in which the incident solar flux distribution is subdivided into flux contour bands. Model predictions for each band are then spatially integrated to provide global predictions such as reactor efficiencies and methane conversions. Global predictions are shown to compare well with experimental data. Reactor predictions for anticipated operating conditions suggest a further decrease in optical density at the front of the absorber inner disk may be beneficial. The need to conduct code-validation experiments is identified as essential to improve the confidence in the capability to predict large-scale reactor operation.

Skocypec, R.D.; Hogan, R.E. Jr.; Muir, J.F.

1991-01-01T23:59:59.000Z

76

Catalytic Properties of Ni-Al Intermetallic Nanoparticle Catalysts for ...  

Science Conference Proceedings (OSTI)

In order to pursue high catalytic performance of Ni-Al intermetallic ... very high catalytic activity for methanol decomposition and methane steam reforming.

77

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

78

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

79

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

80

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

Note: This page contains sample records for the topic "history catalytic 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

Catalytic Reforming - Energy Information Administration  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: Idle refineries ...

82

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.

83

L. van Dyk, L. Lorenzen, S. Miachon, and J.-A. Dalmon, Xylene isomerization in an extractor type Catalytic Membrane Reactor, Catal. Today, 104 (2005) 274. Page 1 / 7  

E-Print Network (OSTI)

. Rabinovich, N. Alexeev, Plasma catalytic reforming of methane, International Journal of Hydrogen Energy, 24

Paris-Sud XI, Université de

84

Catalytic skeletal isomerization  

Science Conference Proceedings (OSTI)

The catalytic reforming of a feedstock which contains a derivative of cyclopentane or which contains organic compounds which are convertible to a derivative of cyclopentane is carried out in the presence of a hydrogrel of zinc titanate and a suitable acidic material. Also, the attrition resistance of zinc titanate is improved by incorporating the zinc titanate into a hydrogel structure.

Aldag, A.W.

1984-05-01T23:59:59.000Z

85

High Activity of Ce1-xNixO2-y for H2 Production through Ethanol Steam Reforming: Tuning Catalytic Performance through Metal-Oxide Interactions  

SciTech Connect

The importance of the oxide: Ce{sub 0.8}Ni{sub 0.2}O{sub 2-y} is an excellent catalyst for ethanol steam reforming. Metal-oxide interactions perturb the electronic properties of the small particles of metallic nickel present in the catalyst under the reaction conditions and thus suppress any methanation activity. The nickel embedded in ceria induces the formation of O vacancies, which facilitate cleavage of the OH bonds in ethanol and water.

G Zhou; L Barrio; S Agnoli; S Senanayake; J Evans; A Kubacka; M Estrella; J Hanson; A Martinez-Arias; et al.

2011-12-31T23:59:59.000Z

86

Catalytic reactor  

DOE Patents (OSTI)

A catalytic reactor is provided with one or more reaction zones each formed of set(s) of reaction tubes containing a catalyst to promote chemical reaction within a feed stream. The reaction tubes are of helical configuration and are arranged in a substantially coaxial relationship to form a coil-like structure. Heat exchangers and steam generators can be formed by similar tube arrangements. In such manner, the reaction zone(s) and hence, the reactor is compact and the pressure drop through components is minimized. The resultant compact form has improved heat transfer characteristics and is far easier to thermally insulate than prior art compact reactor designs. Various chemical reactions are contemplated within such coil-like structures such that as steam methane reforming followed by water-gas shift. The coil-like structures can be housed within annular chambers of a cylindrical housing that also provide flow paths for various heat exchange fluids to heat and cool components.

Aaron, Timothy Mark (East Amherst, NY); Shah, Minish Mahendra (East Amherst, NY); Jibb, Richard John (Amherst, NY)

2009-03-10T23:59:59.000Z

87

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

88

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

89

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

90

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

91

Catalytic decomposition of alcohols over size-selected Pt nanoparticles supported on ZrO2: A study of activity, selectivity, and stability  

E-Print Network (OSTI)

, but do not contribute to steady-state catalytic reforming rates. The high reactivity of Pd surfaces in C

Kik, Pieter

92

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

93

Modelling and Experimental Study of Methane Catalytic Cracking as a Hydrogen Production Technology.  

E-Print Network (OSTI)

??Production of hydrogen is primarily achieved via catalytic steam reforming, partial oxidation,and auto-thermal reforming of natural gas. Although these processes are mature technologies, they are… (more)

Amin, Ashraf Mukhtar Lotfi

2011-01-01T23:59:59.000Z

94

Catalytic Hydrotreating Naphtha/Reformer Feed Downstream ...  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: Idle refineries ...

95

Catalytic Reforming High Pressure Downstream Charge Capacity  

U.S. Energy Information Administration (EIA)

-No Data Reported; --= Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Notes: See Definitions ...

96

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

97

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

98

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

99

Catalytic Distillation  

E-Print Network (OSTI)

Catalytic Distillation' refers to a chemical process which performs both a catalyzed reaction and primary fractionation of the reaction components simultaneously. A structured catalyst which also is an effective distillation component has been patented by Chemical Research & Licensing Co., Houston, Texas, and developed in a joint venture with Neochem Corp., Houston, Texas, and the Department of Energy. The catalytic distillation packing has been commercially demonstrated successfully with nearly three years continuous service for an acid catalyzed reaction in a carbon steel distillation tower.

Smith, L. A., Jr.; Hearn, D.; Wynegar, D. P.

1984-01-01T23:59:59.000Z

100

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

Note: This page contains sample records for the topic "history catalytic 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

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

102

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

103

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

104

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

105

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

106

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

107

Transport in a Microfluidic Catalytic Reactor  

DOE Green Energy (OSTI)

A study of the heat and mass transfer, flow, and thermodynamics of the reacting flow in a catalytic microreactor is presented. Methanol reforming is utilized in the fuel processing system driving a micro-scale proton exchange membrane fuel cell. Understanding the flow and thermal transport phenomena as well as the reaction mechanisms is essential for improving the efficiency of the reforming process as well as the quality of the processed fuel. Numerical studies have been carried out to characterize the transport in a silicon microfabricated reactor system. On the basis of these results, optimized conditions for fuel processing are determined.

Park, H G; Chung, J; Grigoropoulos, C P; Greif, R; Havstad, M; Morse, J D

2003-04-30T23:59:59.000Z

108

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

109

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

110

CATALYTIC BIOMASS LIQUEFACTION  

E-Print Network (OSTI)

LBL-11 019 UC-61 CATALYTIC BIOMASS LIQUEFACTION Sabri Ergun,Catalytic Liquefaction of Biomass,n M, Seth, R. Djafar, G.of California. CATALYTIC BIOMASS LIQUEFACTION QUARTERLY

Ergun, Sabri

2013-01-01T23:59:59.000Z

111

MEMS-based fuel cells with integrated catalytic fuel processor and method thereof  

Science Conference Proceedings (OSTI)

Described herein is a means to incorporate catalytic materials into the fuel flow field structures of MEMS-based fuel cells, which enable catalytic reforming of a hydrocarbon based fuel, such as methane, methanol, or butane. Methods of fabrication are also disclosed.

Jankowski, Alan F. (Livermore, CA); Morse, Jeffrey D. (Martinez, CA); Upadhye, Ravindra S. (Pleasanton, CA); Havstad, Mark A. (Davis, CA)

2011-08-09T23:59:59.000Z

112

Control of Natural Gas Catalytic Partial Oxidation for Hydrogen Generation in Fuel Cell Applications1  

E-Print Network (OSTI)

Control of Natural Gas Catalytic Partial Oxidation for Hydrogen Generation in Fuel Cell Ghosh3 , Huei Peng2 Abstract A fuel processor that reforms natural gas to hydrogen-rich mixture to feed of the hydrogen in the fuel processor is based on catalytic partial oxidation of the methane in the natural gas

Peng, Huei

113

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...

114

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 ...

115

Catalytic cracking. (Latest citations from the Compendex database). Published Search  

Science Conference Proceedings (OSTI)

The bibliography contains citations concerning applications of catalytic cracking processes in fluidized bed systems, moving beds, refineries, vacuum distillations, and reformers. Design aspects, modeling, control systems, and operating procedures are also discussed. (Contains a minimum of 149 citations and includes a subject term index and title list.)

Not Available

1993-07-01T23:59:59.000Z

116

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...

117

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

118

Raney nickel catalytic device  

DOE Patents (OSTI)

A catalytic device for use in a conventional coal gasification process which includes a tubular substrate having secured to its inside surface by expansion a catalytic material. The catalytic device is made by inserting a tubular catalytic element, such as a tubular element of a nickel-aluminum alloy, into a tubular substrate and heat-treating the resulting composite to cause the tubular catalytic element to irreversibly expand against the inside surface of the substrate.

O' Hare, Stephen A. (Vienna, VA)

1978-01-01T23:59:59.000Z

119

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

120

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

Note: This page contains sample records for the topic "history catalytic 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

CATALYTIC LIQUEFACTION OF BIOMASS  

E-Print Network (OSTI)

liquid Fuels from Biomass: "Catalyst Screening and KineticUC-61 (l, RCO osn CDL or BIOMASS CATALYTIC LIQUEFACTION ManuCATALYTIC LIQUEFACTION OF BIOMASS Manu Seth, Roger Djafar,

Seth, Manu

2012-01-01T23:59:59.000Z

122

CATALYTIC BIOMASS LIQUEFACTION  

E-Print Network (OSTI)

Solvent Systems Catalystic Biomass Liquefaction Investigatereactor Product collection Biomass liquefaction process12-13, 1980 CATALYTIC BIOMASS LIQUEFACTION Sabri Ergun,

Ergun, Sabri

2013-01-01T23:59:59.000Z

123

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

124

Hydrogen from Biomass Catalytic Reforming of Pyrolysis Vapors  

E-Print Network (OSTI)

surging, the use of biomass and www.elsevier.com/locate/jaap J. Anal. Appl. Pyrolysis xxx (2006) xxx of the virgin biomass and the development of the microstructure of the char. Structural changes during pyrolysis. Leppamaki, P. Koponen, J. Lavander, E. Tapola, Physical characterization of biomass-based pyrolysis liquids

125

Methanol synthesis gas from catalytic steam reforming of wood  

DOE Green Energy (OSTI)

Laboratory studies were successful in developing catalyst systems and operating conditions for generation of a methanol synthesis gas, a mixture of hydrogen, carbon monoxide and carbon dioxide. Some methane remained in the gas mixture. Wood was reacted with steam at a steam-to-wood weight ratio of about 0.9 and a temperature of 750/sup 0/C (1380/sup 0/F) in the presence of several catalysts. Results are presented for two different catalyst systems.

Mudge, L.K.; Mitchell, D.H.; Robertus, R.J.; Weber, S.L.; Sealock, L.J. Jr.

1981-01-01T23:59:59.000Z

126

Apparatus for catalytic reforming with continuous sulfur removal  

Science Conference Proceedings (OSTI)

An apparatus for continuously removing residual sulfur from a naptha stream has a primary manganous oxide absorber, a secondary parallel manganous oxide absorber and valve and duct means for by-passing the primary absorber and directing the naptha feed stream to the secondary absorber. The apparatus also includes means for removing manganous oxide from the primary absorber and nitrogen purge means for purging the same.

Novak, W. J.

1985-08-13T23:59:59.000Z

127

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

U.S. Energy Information Administration (EIA)

Energy Information Administration - EIA - Official Energy Statistics from the U.S. Government ... solar, wind, geothermal, biomass and ethanol. Nuclear & Uranium.

128

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

129

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

130

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

131

?? /Shigaku / History  

E-Print Network (OSTI)

?? /Shigaku / History Thomas Keirstead Introduction:shigaku as discipline Histories of the historical disciplineedict of 1869 that named history a national priority and

Keirstead, Thomas

2012-01-01T23:59:59.000Z

132

Rich catalytic injection  

SciTech Connect

A gas turbine engine includes a compressor, a rich catalytic injector, a combustor, and a turbine. The rich catalytic injector includes a rich catalytic device, a mixing zone, and an injection assembly. The injection assembly provides an interface between the mixing zone and the combustor. The injection assembly can inject diffusion fuel into the combustor, provides flame aerodynamic stabilization in the combustor, and may include an ignition device.

Veninger, Albert (Coventry, CT)

2008-12-30T23:59:59.000Z

133

Catalytic conversion of biomass.  

E-Print Network (OSTI)

?? Catalytic processes for conversion of biomass to transportation fuels have gained an increasing attention in sustainable energy production. The biomass can be converted to… (more)

Calleja Aguado, Raquel

2013-01-01T23:59:59.000Z

134

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

Science Conference Proceedings (OSTI)

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

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

2006-01-01T23:59:59.000Z

135

Catalytic cracking process  

Science Conference Proceedings (OSTI)

Processes and apparatus for providing improved catalytic cracking, specifically improved recovery of olefins, LPG or hydrogen from catalytic crackers. The improvement is achieved by passing part of the wet gas stream across membranes selective in favor of light hydrocarbons over hydrogen.

Lokhandwala, Kaaeid A. (Union City, CA); Baker, Richard W. (Palo Alto, CA)

2001-01-01T23:59:59.000Z

136

Catalytic distillation structure  

DOE Patents (OSTI)

Catalytic distillation structure for use in reaction distillation columns, a providing reaction sites and distillation structure and consisting of a catalyst component and a resilient component intimately associated therewith. The resilient component has at least about 70 volume % open space and being present with the catalyst component in an amount such that the catalytic distillation structure consist of at least 10 volume % open space.

Smith, Jr., Lawrence A. (Bellaire, TX)

1984-01-01T23:59:59.000Z

137

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

138

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

139

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

140

Beam History  

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

Beam History Print Beamline History Request Form To request a beam current histograph from the ALS storage ring beam histograph database, select the year, month, and day, then...

Note: This page contains sample records for the topic "history catalytic 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

Beam History  

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

Beam Status Beam History Print Beamline History Request Form To request a beam current histograph from the ALS storage ring beam histograph database, select the year, month, and...

142

Catalytic cracking. (Latest citations from the NTIS Bibliographic database). Published Search  

SciTech Connect

The bibliography contains citations concerning applications of catalytic cracking in fluidized beds, moving beds, refineries, vacuum distillation, and reformers. Design criteria, models, controls, and operating procedures are also discussed. (Contains 250 citations and includes a subject term index and title list.)

Not Available

1993-09-01T23:59:59.000Z

143

Catalytic cracking. (Latest citations from the NTIS data base). Published Search  

SciTech Connect

The bibliography contains citations concerning applications of catalytic cracking in fluidized beds, moving beds, refineries, vacuum distillation, and reformers. Design criteria, models, controls, and operating procedures are also discussed. (Contains 250 citations and includes a subject term index and title list.)

Not Available

1992-05-01T23:59:59.000Z

144

Catalytic cracking. (Latest citations from the NTIS bibliographic database). Published Search  

Science Conference Proceedings (OSTI)

The bibliography contains citations concerning applications of catalytic cracking in fluidized beds, moving beds, refineries, vacuum distillation, and reformers. Design criteria, models, controls, and operating procedures are also discussed. (Contains 250 citations and includes a subject term index and title list.)

Not Available

1994-02-01T23:59:59.000Z

145

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

146

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

147

Catalytic distillation process  

DOE Patents (OSTI)

A method for conducting chemical reactions and fractionation of the reaction mixture comprising feeding reactants to a distillation column reactor into a feed zone and concurrently contacting the reactants with a fixed bed catalytic packing to concurrently carry out the reaction and fractionate the reaction mixture. For example, a method for preparing methyl tertiary butyl ether in high purity from a mixed feed stream of isobutene and normal butene comprising feeding the mixed feed stream to a distillation column reactor into a feed zone at the lower end of a distillation reaction zone, and methanol into the upper end of said distillation reaction zone, which is packed with a properly supported cationic ion exchange resin, contacting the C.sub.4 feed and methanol with the catalytic distillation packing to react methanol and isobutene, and concurrently fractionating the ether from the column below the catalytic zone and removing normal butene overhead above the catalytic zone.

Smith, Jr., Lawrence A. (Bellaire, TX)

1982-01-01T23:59:59.000Z

148

Catalytic distillation process  

DOE Patents (OSTI)

A method is described for conducting chemical reactions and fractionation of the reaction mixture comprising feeding reactants to a distillation column reactor into a feed zone and concurrently contacting the reactants with a fixed bed catalytic packing to concurrently carry out the reaction and fractionate the reaction mixture. For example, a method for preparing methyl tertiary butyl ether in high purity from a mixed feed stream of isobutene and normal butene comprising feeding the mixed feed stream to a distillation column reactor into a feed zone at the lower end of a distillation reaction zone, and methanol into the upper end of said distillation reaction zone, which is packed with a properly supported cationic ion exchange resin, contacting the C[sub 4] feed and methanol with the catalytic distillation packing to react methanol and isobutene, and concurrently fractionating the ether from the column below the catalytic zone and removing normal butene overhead above the catalytic zone.

Smith, L.A. Jr.

1982-06-22T23:59:59.000Z

149

Catalytic distillation structure  

DOE Patents (OSTI)

Catalytic distillation structure is described for use in reaction distillation columns, and provides reaction sites and distillation structure consisting of a catalyst component and a resilient component intimately associated therewith. The resilient component has at least about 70 volume % open space and is present with the catalyst component in an amount such that the catalytic distillation structure consists of at least 10 volume % open space. 10 figs.

Smith, L.A. Jr.

1984-04-17T23:59:59.000Z

150

Revolutionary systems for catalytic combustion and diesel catalytic particulate traps.  

DOE Green Energy (OSTI)

This report is a summary of an LDRD project completed for the development of materials and structures conducive to advancing the state of the art for catalyst supports and diesel particulate traps. An ancillary development for bio-medical bone scaffolding was also realized. Traditionally, a low-pressure drop catalyst support, such as a ceramic honeycomb monolith, is used for catalytic reactions that require high flow rates of gases at high-temperatures. A drawback to the traditional honeycomb monoliths under these operating conditions is poor mass transfer to the catalyst surface in the straight-through channels. ''Robocasting'' is a unique process developed at Sandia National Laboratories that can be used to manufacture ceramic monoliths with alternative 3-dimensional geometries, providing tortuous pathways to increase mass transfer while maintaining low-pressure drops. These alternative 3-dimensional geometries may also provide a foundation for the development of self-regenerating supports capable of trapping and combusting soot particles from a diesel engine exhaust stream. This report describes the structures developed and characterizes the improved catalytic performance that can result. The results show that, relative to honeycomb monolith supports, considerable improvement in mass transfer efficiency is observed for robocast samples synthesized using an FCC-like geometry of alternating rods. Also, there is clearly a trade-off between enhanced mass transfer and increased pressure drop, which can be optimized depending on the particular demands of a given application. Practical applications include the combustion of natural gas for power generation, production of syngas, and hydrogen reforming reactions. The robocast lattice structures also show practicality for diesel particulate trapping. Preliminary results for trapping efficiency are reported as well as the development of electrically resistive lattices that can regenerate the structure by combusting the trapped soot. During this project an ancillary bio-medical application was discovered for lattices of hydroxyapatite. These structures show promise as bone scaffolds for the reparation of damaged bone. A case study depicting the manufacture of a customized device that fits into a damaged mandible is described.

Stuecker, John Nicholas; Witze, Peter O.; Ferrizz, Robert Matthew; Cesarano, Joseph, III; Miller, James Edward

2004-12-01T23:59:59.000Z

151

History Publications  

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

List of historical publications available through the Department's History Office, including free PDF versions.

152

Inter-relationship between preparation methods, nickel loading, characteristics and performance in the reforming of crude ethanol over Ni/Al2O3 catalysts: A neural network approach  

Science Conference Proceedings (OSTI)

Artificial neural network (ANN) approach was used to design an optimum Ni/Al"2O"3 catalyst for the production of hydrogen by the catalytic reforming of crude ethanol based on determining the inter-relationships between catalyst-preparation methods, nickel ... Keywords: Artificial neural network, Catalyst characteristics, Crude-ethanol reforming, Hydrogen production, Optimum catalyst design

Shoumin Song; Abayomi J. Akande; Raphael O. Idem; Nader Mahinpey

2007-03-01T23:59:59.000Z

153

Characterization of carbonaceous species formed during reforming of CH{sub 4} with CO{sub 2} over Ni/CaO-Al{sub 2}O{sub 3} catalysts studied by various transient techniques  

Science Conference Proceedings (OSTI)

Catalytic reforming of methane to synthesis gas over wt% Ni/CaO-Al{sub 2}O{sub 3} was studied. Nickel particle morphology and its size distribution is thought to be influenced by the support composition, which in turn controls the origin, the kinetics, and the reactivity of carbon decomposition under reforming reaction conditions. 43 refs., 10 figs., 4 tabs.

Goula, M.A.; Lemonidou, A.A. [Aristotle Univ. of Thessaloniki (Greece); Efstathiou, A.M. [University Campus, Patras (Greece)

1996-07-01T23:59:59.000Z

154

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

155

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 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

156

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...

157

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 ...

158

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

159

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

160

Catalytic Coal Gasification Process  

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

Catalytic Coal Gasification Process Catalytic Coal Gasification Process for the Production of Methane-Rich Syngas Opportunity Research is active on the patent pending technology, titled "Production of Methane-Rich Syngas from Fuels Using Multi-functional Catalyst/Capture Agent." This technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory. Overview Reducing pollution emitted by coal and waste power plants in an economically viable manner and building power plants that co-generate fuels and chemicals during times of low electricity demand are pressing goals for the energy industry. One way to achieve these goals in an economically viable manner is through the use of a catalytic gasifier that

Note: This page contains sample records for the topic "history catalytic 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.


161

Catalytic hydrotreating process  

DOE Patents (OSTI)

Carbonaceous liquids boiling above about 300.degree. C such as tars, petroleum residuals, shale oils and coal-derived liquids are catalytically hydrotreated by introducing the carbonaceous liquid into a reaction zone at a temperature in the range of 300.degree. to 450.degree. C and a pressure in the range of 300 to 4000 psig for effecting contact between the carbonaceous liquid and a catalytic transition metal sulfide in the reaction zone as a layer on a hydrogen permeable transition metal substrate and then introducing hydrogen into the reaction zone by diffusing the hydrogen through the substrate to effect the hydrogenation of the carbonaceous liquid in the presence of the catalytic sulfide layer.

Karr, Jr., Clarence (Morgantown, WV); McCaskill, Kenneth B. (Morgantown, WV)

1978-01-01T23:59:59.000Z

162

Catalytic Solutions Inc CSI | Open Energy Information  

Open Energy Info (EERE)

Developer of the breakthrough catalytic coating technology and the Mixed Phase Catalyst (MPCTM), and also manufacturer of catalytic converters. References Catalytic...

163

HISTORY GALLERY  

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

History Gallery TechLab Virtual Exhibits invisible utility element HISTORY GALLERY The Atomic Age begins The conflict that darkened Europe in the late 1930s at first cast no...

164

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

165

Geopolitics, History, and International Relations  

E-Print Network (OSTI)

for institutional reform in Bosnia and Herzegovina since theReform in Bosnia and Herzegovina”, East European Politics &

Robinson, William I.

2009-01-01T23:59:59.000Z

166

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

167

Catalytic coal hydrogasification process  

SciTech Connect

In Exxon Research and Engineering Co.'s new approach, methane is produced by a thermoneutral process in which finely divided coal or other carbonaceous material is reacted with steam and hydrogen in the presence of an alkali-metal catalyst (1 to 50 wt percent based on carbonaceous material) in a fluidized bed at a temperature of 1200/sup 0/ to 1500/sup 0/F. The hydrogen and reactant steam concentrations are controlled so that the exothermic hydrogasification reactions provide sufficient heat for the endothermic steam reactions, reactant preheat, and reactor heat losses. The overhead gas from the gasifier is steam-reformed in the presence of an alkali-metal catalyst at a temperature of 1300/sup 0/ to 1700/sup 0/F. Acid constituents such as CO/sub 2/ and H/sub 2/S are removed from the reformed gas, which is then cryogenically separated into hydrogen, CO, and methane. The hydrogen is recycled to the hydrogasification zone and the CO used to fire the steam-reformer furnace. The high-purity methane from the cryogenic unit can be employed as a pipeline gas without further treatment.

Kalina, T.; Moore, R.E.

1974-11-12T23:59:59.000Z

168

Catalytic coal liquefaction process  

SciTech Connect

An improved process for catalytic solvent refining or hydroliquefaction of non-anthracitic coal at elevated temperatures under hydrogen pressure in a solvent comprises using as catalyst a mixture of a 1,2- or 1,4-quinone and an alkaline compound, selected from ammonium, alkali metal, and alkaline earth metal oxides, hydroxides or salts of weak acids.

Garg, Diwakar (Macungie, PA); Sunder, Swaminathan (Allentown, PA)

1986-01-01T23:59:59.000Z

169

Catalytic conversion of LPG  

Science Conference Proceedings (OSTI)

The low reactivity of light paraffins has long hindered their utilization as petrochemical feedstocks. Except for their use in ethylene crackers, LPG fractions have traditionally been consumed as fuel. New catalytic processes now being commercialized open new avenues for the utilization of LPG as sources of valuable petrochemical intermediates. This paper discusses processes for the dehydrogenation and aromatization of LPG.

Pujado, P.R.; Vora, B.V.; Mowry, J.R.; Anderson, R.F.

1986-01-01T23:59:59.000Z

170

Catalytic coal liquefaction process  

DOE Patents (OSTI)

An improved process for catalytic solvent refining or hydroliquefaction of non-anthracitic coal at elevated temperatures under hydrogen pressure in a solvent comprises using as catalyst a mixture of a 1,2- or 1,4-quinone and an alkaline compound, selected from ammonium, alkali metal, and alkaline earth metal oxides, hydroxides or salts of weak acids. 1 fig.

Garg, D.; Sunder, S.

1986-12-02T23:59:59.000Z

171

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.

172

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

173

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

174

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...

175

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...

176

Cosmic Growth History and Expansion History  

E-Print Network (OSTI)

LBNL- 58260 Cosmic Growth History andExpansion History Eric V. Linder Physics Division, LawrenceCalifornia. Cosmic Growth History and Expansion History Eric

Linder, Eric V.

2009-01-01T23:59:59.000Z

177

Our History | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

History | National Nuclear Security Administration History | 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 Our History Home > About Us > Our History Our History The NNSA was established by Congress in 2000 as a separately organized agency within the U.S. Department of Energy, responsible for the management and security of the nation's nuclear weapons, nuclear nonproliferation,

178

Our History  

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

Environment Feature Stories Public Reading Room: Environmental Documents, Reports LANL Home Phonebook Calendar Video About Our History aboutassetsimagesicon-70th.jpg...

179

Catalytic thermal barrier coatings  

Science Conference Proceedings (OSTI)

A catalyst element (30) for high temperature applications such as a gas turbine engine. The catalyst element includes a metal substrate such as a tube (32) having a layer of ceramic thermal barrier coating material (34) disposed on the substrate for thermally insulating the metal substrate from a high temperature fuel/air mixture. The ceramic thermal barrier coating material is formed of a crystal structure populated with base elements but with selected sites of the crystal structure being populated by substitute ions selected to allow the ceramic thermal barrier coating material to catalytically react the fuel-air mixture at a higher rate than would the base compound without the ionic substitutions. Precious metal crystallites may be disposed within the crystal structure to allow the ceramic thermal barrier coating material to catalytically react the fuel-air mixture at a lower light-off temperature than would the ceramic thermal barrier coating material without the precious metal crystallites.

Kulkarni, Anand A. (Orlando, FL); Campbell, Christian X. (Orlando, FL); Subramanian, Ramesh (Oviedo, FL)

2009-06-02T23:59:59.000Z

180

Concentric catalytic combustor  

DOE Patents (OSTI)

A catalytic combustor (28) includes a tubular pressure boundary element (90) having a longitudinal flow axis (e.g., 56) separating a first portion (94) of a first fluid flow (e.g., 24) from a second portion (95) of the first fluid flow. The pressure boundary element includes a wall (96) having a plurality of separate longitudinally oriented flow paths (98) annularly disposed within the wall and conducting respective portions (100, 101) of a second fluid flow (e.g., 26) therethrough. A catalytic material (32) is disposed on a surface (e.g., 102, 103) of the pressure boundary element exposed to at least one of the first and second portions of the first fluid flow.

Bruck, Gerald J. (Oviedo, FL); Laster, Walter R. (Oviedo, FL)

2009-03-24T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

CSD: Research: Catalytic Science  

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

Catalytic Science Catalytic Science The DOE Chemical Energy program supports basic research in the area of chemical transformations or conversions which are fundamental to new or existing concepts of energy production and storage. A further goal of the program is to identify and develop environmentally benign approaches to the synthesis of chemicals via routes requiring a minimal consumption of energy. These objectives lead naturally to an emphasis on catalysis. Novel homogeneous and heterogeneous catalysts are constantly being sought to enable the synthesis of desired products from nontraditional reactants, often with the aim of minimizing the production of toxic intermediates or byproducts, or to enable the more efficient production of products via existing reaction pathways. To this end, efforts are undertaken to

182

Advanced turbine systems program conceptual design and product development Task 8.3 - autothermal fuel reformer (ATR). Topical report  

DOE Green Energy (OSTI)

Autothermal fuel reforming (ATR) consists of reacting a hydrocarbon fuel such as natural gas or diesel with steam to produce a hydrogen-rich {open_quotes}reformed{close_quotes} fuel. This work has been designed to investigate the fuel reformation and the product gas combustion under gas turbine conditions. The hydrogen-rich gas has a high flammability with a wide range of combustion stability. Being lighter and more reactive than methane, the hydrogen-rich gas mixes readily with air and can be burned at low fuel/air ratios producing inherently low emissions. The reformed fuel also has a low ignition temperature which makes low temperature catalytic combustion possible. ATR can be designed for use with a variety of alternative fuels including heavy crudes, biomass and coal-derived fuels. When the steam required for fuel reforming is raised by using energy from the gas turbine exhaust, cycle efficiency is improved because of the steam and fuel chemically recuperating. Reformation of natural gas or diesel fuels to a homogeneous hydrogen-rich fuel has been demonstrated. Performance tests on screening various reforming catalysts and operating conditions were conducted on a batch-tube reactor. Producing over 70 percent of hydrogen (on a dry basis) in the product stream was obtained using natural gas as a feedstock. Hydrogen concentration is seen to increase with temperature but less rapidly above 1300{degrees}F. The percent reforming increases as the steam to carbon ratio is increased. Two basic groups of reforming catalysts, nickel - and platinum-basis, have been tested for the reforming activity.

NONE

1996-11-01T23:59:59.000Z

183

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,...

184

Catalytic distillation : design and application of a catalytic distillation column.  

E-Print Network (OSTI)

??Catalytic Distillation (CD) is a hybrid technology that utilizes the dynamics of si- multaneous reaction and separation in a single process unit to achieve a… (more)

Nieuwoudt, Josias Jakobus (Jako)

2005-01-01T23:59:59.000Z

185

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.

186

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

187

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

188

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

189

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 ...

190

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 ...

191

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...

192

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

193

History Images  

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

History Images History Images Los Alamos History in Images Los Alamos has a proud history and heritage of almost 70 years of science and innovation. The people of the Laboratory work on advanced technologies to provide the best scientific and engineering solutions to many of the nation's most crucial security challenges. Click thumbnails to enlarge. Photos arranged by most recent first, horizontal formats before vertical. See Flickr for more sizes and details. Back in the day Back in the day LA bridge in Los Alamos LA bridge in Los Alamos 1945 Army-Navy "E" Award 1945 Army-Navy "E" Award Louis Rosen Louis Rosen Bob Van Ness Robert Kuckuck and Michael Anastasio Bob Van Ness Robert Kuckuck and Michael Anastasio TA-18 TA-18 Elmer Island TU-4 assembly area Elmer Island TU-4 assembly area

194

Catalytic dewaxing of middle distillates  

SciTech Connect

The fractionation and stripping equipment of a middle distillate catalytic dewaxing unit may be eliminated by integrating the catalytic dewaxing unit with a catalytic cracking unit. The light cycle oil sidestream from the cat cracker fractionator, bypasses the sidestream stripper and serves as the feed to the catalytic dewaxing unit. The dewaxed product is separated into a gasoline fraction which is recycled for fractionation in the cat cracker fractionator and a fuel oil fraction which is recycled to the cat cracker sidestream stripper for removal of light materials to produce a low pour fuel oil meeting product specifications.

Antal, M.J.

1982-06-01T23:59:59.000Z

195

Novel Catalytic Membrane Reactors  

DOE Green Energy (OSTI)

There are many industrial catalytic organic reversible reactions with amines or alcohols that have water as one of the products. Many of these reactions are homogeneously catalyzed. In all cases removal of water facilitates the reaction and produces more of the desired chemical product. By shifting the reaction to right we produce more chemical product with little or no additional capital investment. Many of these reactions can also relate to bioprocesses. Given the large number of water-organic compound separations achievable and the ability of the Compact Membrane Systems, Inc. (CMS) perfluoro membranes to withstand these harsh operating conditions, this is an ideal demonstration system for the water-of-reaction removal using a membrane reactor. Enhanced reaction synthesis is consistent with the DOE objective to lower the energy intensity of U.S. industry 25% by 2017 in accord with the Energy Policy Act of 2005 and to improve the United States manufacturing competitiveness. The objective of this program is to develop the platform technology for enhancing homogeneous catalytic chemical syntheses.

Stuart Nemser, PhD

2010-10-01T23:59:59.000Z

196

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

197

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

198

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

199

Cosmic Growth History and Expansion History  

E-Print Network (OSTI)

of the expansion history dark energy equation of state,and growth history constraints on the dark energy equationand growth history constraints on the dark energy equation

Linder, Eric V.

2009-01-01T23:59:59.000Z

200

NETL: History  

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

History History About NETL History Over the past century, fossil energy research and technology development has been advanced by NETL and its predecessor facilities as the energy needs of the Nation have grown and evolved. 1910 - The newly created Bureau of Mines in the U.S. Department of the Interior (DOI) opens the Pittsburgh Experiment Station in Bruceton, Pennsylvania, 12 miles south of Pittsburgh. The station includes an experimental coal mine and offers advanced training for coal operators and miners. Onsite research focuses on developing innovative coal-mining safety equipment and practices. 1918 - Following new discoveries of oil in Oklahoma and Texas, the Petroleum Experiment Station is established in Bartlesville, Oklahoma, as one of 17 DOI Bureau of Mines facilities under Public Law 283 (63rd Congress, 1915). The Station pursues systematic application of engineering and scientific methods to oil drilling, helping the early "boom and bust" oil industry create operating and safety standards.

Note: This page contains sample records for the topic "history catalytic 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

NERSC History  

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

History History NERSC History Powering Scientific Discovery Since 1974 Contact: Jon Bashor, jbashor@lbl.gov, +1 510 486 4236 For more information, read "25 Years of Leadership," a historical perspective written at NERSC's quarter-century mark.⨠Download (PDF, 1.7MB) The oil crisis of 1973 did more than create long lines at the gas pumps - it jumpstarted a supercomputing revolution. The quest for alternative energy sources led to increased funding for the Department of Energy's Magnetic Fusion Energy program, and simulating the behavior of plasma in a fusion reactor required a computer center dedicated to this purpose. Founded in 1974 at Lawrence Livermore National Laboratory, the Controlled Thermonuclear Research Computer Center was the first unclassified supercomputer center and was the model for those that

202

Catalytic Conversion of Bioethanol to Hydrocarbons  

ORNL 2011-G00219/jcn UT-B ID 201002414 08.2011 Catalytic Conversion of Bioethanol to Hydrocarbons Technology Summary A method for catalytically converting an alcohol ...

203

Catalytic Conversion of Bioethanol to Hydrocarbons  

ORNL 2011-G00219/jcn UT-B ID 201002414 08.2011 Catalytic Conversion of Bioethanol to Hydrocarbons Technology Summary A method for catalytically ...

204

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

205

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

206

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

207

ORISE: History  

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

History History The Oak Ridge Institute for Science and Education (ORISE) is a national leader in science education and research, with programs dating back to 1946 and having served as an official U.S. Department of Energy (DOE) institute since 1992. The institute that eventually became what is known today as ORISE was the brainchild of University of Tennessee (UT) physics professor Dr. William G. Pollard. Aware of the valuable assets on hand in Oak Ridge, Tenn., as part of the Manhattan Project, Pollard talked about the possibility of aligning regional universities with the scientific resources and state-of-the-art equipment in Oak Ridge. On Oct. 17, 1946, Pollard's vision became a reality when the Oak Ridge Institute of Nuclear Studies (ORINS) received a charter of incorporation

208

Revision History  

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

Revision History Revision History Rev. 0, August 2012 Original submittal for milestone M3FT-12SN0804032 (Sandia programmatic and classification review) Rev. 1, September 2012 Corrected transposition errors in costing tables; recalculated stainless steel overpacks to be carbon steel; corrected various editorial problems. (SAND2012-7979P) Rev. 2, November 2012 Performed peer review and retitled. Submittal for milestone M2FT-13SN0804031 (formerly milestone M2FT- 12SN0804031) (SAND2012-9737P) Unclassified Unlimited Release Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-AC04-94AL85000.

209

History - Cyclotron  

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

History History Lawrence's original Cyclotron, for which he received a patent and the Nobel Prize. Lawrence's original cyclotron design was limited to energies where relativistic effects were not important. The third generation cyclotron included "sector-focusing" to allow higher energies to be obtained. The 88-Inch Cyclotron was based on Lawrence's design of a sector-focused cyclotron for the MTA project at Livermore. 1500 man-hours of work were necessary to assemble the trim coils which help regulate the strength and shape of the accelerator's magnetic field. Discussing the cyclotron magnet (seen in the background) are Dr. Elmer Kelly, physicist in charge of the 88-Inch Cyclotron and Warren Dexter, electrical coordinator for the cyclotron project.

210

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

211

Reformer assisted lean NO.sub.x catalyst aftertreatment system and method  

DOE Patents (OSTI)

A method and apparatus for catalytically processing a gas stream passing therethrough to reduce the presence of NO.sub.x therein, wherein the apparatus includes a first catalyst composed of a silver-containing alumina that is adapted for catalytically processing the gas stream at a first temperature range, a second catalyst composed of a copper-containing zeolite located downstream from the first catalyst, wherein the second catalyst is adapted for catalytically processing the gas stream at a lower second temperature range relative to the first temperature range, a hydrocarbon compound for injection into the gas stream upstream of the first catalyst to provide a reductant, and a reformer for reforming a portion of the hydrocarbon compound into H.sub.2 and/or oxygenated hydrocarbon for injection into the gas stream upstream of the first catalyst. The second catalyst is adapted to facilitate the reaction of reducing NOx into N.sub.2, whereby the intermediates are produced via the first catalyst reacting with NOx and hydrocarbons.

Kalyanaraman, Mohan (Media, PA); Park, Paul W. (Peoria, IL); Ragle, Christie S. (Havana, IL)

2010-06-29T23:59:59.000Z

212

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

213

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...

214

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

215

Energy Efficiency Improvement and Cost Saving Opportunities for the Petrochemical Industry - An ENERGY STAR(R) Guide for Energy and Plant Managers  

E-Print Network (OSTI)

reformates from catalytic reforming in refineries and steamor aromatic mixtures from catalytic reforming in refineries.and reformates from catalytic reforming in refineries. An

Neelis, Maarten

2008-01-01T23:59:59.000Z

216

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...

217

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...

218

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:...

219

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...

220

Complexity in Big History  

E-Print Network (OSTI)

Spier, Fred. “How Big History Works: Energy Flows and RiseSmil, Vaclav. Energy in World History. Boulder, CO: Westviewkg) Energy and complexity Spier: Complexity in Big History.

Spier, Fred

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

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

222

Cygnus History  

SciTech Connect

The Cygnus Dual Beam Radiographic Facility consists of two identical radiographic sources: Cygnus 1 and Cygnus 2. This Radiographic Facility is located in an underground tunnel test area at the Nevada Test Site. The sources were developed to produce high-resolution images for dynamic plutonium experiments. This work will recount and discuss salient maintenance and operational issues encountered during the history of Cygnus. A brief description of Cygnus systems and rational for design selections will set the stage for this historical narrative. It is intended to highlight the team-derived solutions for technical problems encountered during extended periods of maintenance and operation. While many of the issues are typical to pulsed power systems, some of the solutions are unique. It is hoped that other source teams will benefit from this presentation, as well as other necessary disciplines (e.g., source users, system architects, facility designers and managers, funding managers, and team leaders).

David J. Henderson, Raymond E. Gignac, Douglas E. Good, Mark D. Hansen, Charles V. Mitton; Daniel S. Nelson, Eugene C. Ormond; Steve R. Cordova, Isidro Molina; John R. Smith, Evan A. Rose

2009-07-02T23:59:59.000Z

223

Office of Secure Transportation History | National Nuclear Security  

National Nuclear Security Administration (NNSA)

History | National Nuclear Security History | 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 Office of Secure Transportation History Home > About Us > Our Programs > Defense Programs > Office of Secure Transportation > Office of Secure Transportation History Office of Secure Transportation History Since 1947, NNSA and its predecessor agencies have moved nuclear weapons,

224

Design of Catalytic Materials for Plasma Assisted Catalysis System  

DOE Green Energy (OSTI)

In recent years, the Plasma Assisted Catalysis (PAC) approach for controlling NOx and/or particulate emissions from mobile diesel engines has received a significant amount of attention from researchers. Substantial work has been performed by various researchers to develop an understanding of the reaction mechanisms in a plasma reactor in conjunction with conventional lean-NOx catalyst materials. However, less effort has been devoted to systematically investigating new catalyst materials specifically designed for application in the PAC system. Since it is believed that plasma produces a unique environment for a catalyst bed (i.e. oxidation of NO to NO2 and partial oxidation/reforming of hydrocarbon reductants in the exhaust), new catalytic materials that take advantage of the plasma reactor conditions need to be studied. Optimum catalyst materials will be required in order to develop a PAC system that achieves maximum deNOx performance over the wide range of operating conditions in which the system will be required to operate for application on heavy duty diesel engines. This presentation discusses the issues involved in designing catalytic materials for achieving high NOx conversion in a laboratory test PAC system, and what is required to improve the catalyst materials further for application in an on-engine environment.

Park, Paul W.

2000-08-20T23:59:59.000Z

225

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

226

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.

227

Catalytic hydroprocessing of shale oil to produce distillate fuels  

DOE Green Energy (OSTI)

Results are presented of a Chevron Research Company study sponsored by the Energy Research and Development Administration (ERDA) to demonstrate the feasibility of converting whole shale oil to a synthetic crude resembling a typical petroleum distillate. The synthetic crude thus produced can then be processed, in conventional petroleum-refining facilities, to transportation fuels such as high octane gasoline, diesel, and jet fuel. The raw shale oil feed used is a typical Colorado shale oil produced in a surface retort in the so-called indirectly heated mode. It is shown that whole shale oil can be catalytically hydrodenitrified to reduce the nitrogen to levels as low as one part per million in a single catalytic stage. However, for economic reasons, it appears preferable to denitrify to about 0.05 wt % nitrogen. The resulting synthetic crude resembles a petroleum distillate that can be fractionated and further processed as necessary in conventional petroleum refining facilities. Shale oil contains about 0.6% sulfur. Sulfur is more easily removed by hydrofining than is nitrogen; therefore, only a few parts per million of sulfur remain at a product nitrogen of 0.05 wt %. Oxygen contained in the shale oil is also reduced to low levels during hydrodenitrification. The shale oil contains appreciable quantities of iron and arsenic which are also potential catalyst poisons. These metals are removed by a guard bed placed upstream from the hydrofining catalyst. Based on correlations, the naphthas from the shale oil hydrofiner can readily be upgraded to high octane gasolines by catalytic reforming. The middle distillate fractions may require some additional hydrofining to produce salable diesel or jet fuel. The technology is available, and pilot plant studies are scheduled to verify diesel hydrofiner performance.

Sullivan, R.F.; Stangeland, B.E.

1977-01-01T23:59:59.000Z

228

High temperature catalytic membrane reactors  

DOE Green Energy (OSTI)

Current state-of-the-art inorganic oxide membranes offer the potential of being modified to yield catalytic properties. The resulting modules may be configured to simultaneously induce catalytic reactions with product concentration and separation in a single processing step. Processes utilizing such catalytically active membrane reactors have the potential for dramatically increasing yield reactions which are currently limited by either thermodynamic equilibria, product inhibition, or kinetic selectivity. Examples of commercial interest include hydrogenation, dehydrogenation, partial and selective oxidation, hydrations, hydrocarbon cracking, olefin metathesis, hydroformylation, and olefin polymerization. A large portion of the most significant reactions fall into the category of high temperature, gas phase chemical and petrochemical processes. Microporous oxide membranes are well suited for these applications. A program is proposed to investigate selected model reactions of commercial interest (i.e. dehydrogenation of ethylbenzene to styrene and dehydrogenation of butane to butadiene) using a high temperature catalytic membrane reactor. Membranes will be developed, reaction dynamics characterized, and production processes developed, culminating in laboratory-scale demonstration of technical and economic feasibility. As a result, the anticipated increased yield per reactor pass economic incentives are envisioned. First, a large decrease in the temperature required to obtain high yield should be possible because of the reduced driving force requirement. Significantly higher conversion per pass implies a reduced recycle ratio, as well as reduced reactor size. Both factors result in reduced capital costs, as well as savings in cost of reactants and energy.

Not Available

1990-03-01T23:59:59.000Z

229

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

230

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

231

Thermal and catalytic hydrodehalogenation of halon 1301 ...  

Science Conference Proceedings (OSTI)

... as hydrolysis, steam reforming, dehalogenation, dehydrohalogenation as ... probably be the thermal cleavage of ... of methane-based car,Qon moieties ...

2011-10-04T23:59:59.000Z

232

Superconducting Cuprates on Catalytic Substrates - Energy ...  

Electricity Transmission Superconducting Cuprates on Catalytic Substrates Brookhaven National Laboratory. Contact BNL About This Technology Technology Marketing ...

233

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

234

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

235

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

236

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...

237

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

238

Catalytic conversion of light alkanes, Phase 1. Topical report, January 1990--January 1993  

DOE Green Energy (OSTI)

The authors have found a family of new catalytic materials which, if successfully developed, will be effective in the conversion of light alkanes to alcohols or other oxygenates. Catalysts of this type have the potential to convert natural gas to clean-burning high octane liquid fuels directly without requiring the energy-intensive steam reforming step. In addition they also have the potential to upgrade light hydrocarbons found in natural gas to a variety of high value fuel and chemical products. In order for commercially useful processes to be developed, increases in catalytic life, reaction rate and selectivity are required. Recent progress in the experimental program geared to the further improvement of these catalysts is outlined.

NONE

1993-12-31T23:59:59.000Z

239

Catalytic Hydrocracking - Energy Information Administration  

U.S. Energy Information Administration (EIA)

Process: Period: Annual (as of January 1) Download Series History: Definitions, Sources & Notes: Show Data By: Process: Area: 2008 2009 2010 2011 2012 ...

240

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

Note: This page contains sample records for the topic "history catalytic 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

ENGINEERING SCALE UP OF RENEWABLE HYDROGEN PRODUCTION BY CATALYTIC STEAM REFORMING OF PEANUT  

E-Print Network (OSTI)

resources [1-5]. Well know examples of second generation fuels derived from biomass are pyrolysis oil-ethanol from cellulosic biomass. Fast pyrolysis of lignocellulosic biomass involves heating of the biomass] Bridgwater, A., editor, Fast Pyrolysis of Biomass: A Handbook Volume 3. CPL press: Newbury Berkshire, 2005

242

Catalytic Properties of Ni3Al Foils for Methane Steam Reforming  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, The 8th Pacific Rim International Congress on Advanced Materials and Processing. Symposium, A. Materials for Energy.

243

FEASIBILITY ANALYSIS REPORT (FAR) INTEGRAL CATALYTIC COMBUSTION/FUEL REFORMING FOR GAS TURBINE CYCLES  

E-Print Network (OSTI)

report was prepared as a result of work sponsored by the California Energy Commission (Commission). It does not necessarily represent the views of the Commission, its employees, or the state of California. The Commission, the state of California, its employees, contractors, and subcontractors make no warranty, express or implied, and assume no legal liability for the information in this report; nor does any party represent that the use of this information will not infringe upon privately owned rights. This report has not been approved or disapproved by the Commission nor has the Commission passed upon the accuracy or adequacy of the information in this report. PREFACE The Public Interest Energy Research (PIER) Program supports public interest energy research and development that will help improve the quality of life in California by bringing environmentally safe, affordable and reliable energy services and products to the marketplace. The PIER Program, managed by the California Energy Commission (Commission), annually awards up to $62 million of which $2 million/year is allocated to the Energy Innovation Small Grant (EISG) Program for grants. The EISG Program is administered by the San Diego State

Energy Innovations; Small Grant Program; Eisg Awardee

2000-01-01T23:59:59.000Z

244

Catalysts for steam reforming of Ethanol in a catalytic wall reactor.  

E-Print Network (OSTI)

??La energía se ha convertido en una necesidad vital para garantizar el desarrollo de las sociedades modernas. Entre las diferentes posibles alternativas para producir energía,… (more)

Torres Rivero, José Antonio

2008-01-01T23:59:59.000Z

245

Archives and History Office: Oral History  

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

Oral History Oral History Oral History Oral History interviews with SLAC staff and users have been conducted at SLAC and at other institutions by SLAC Archives and History Office staff and by others interested in the history of physics and computing. Information collected in these interviews supplements original correspondence and other primary source materials collected by the Archives and History Office. SLAC Interviews Interviews have been conducted by SLAC staff on an irregular basis, as resources have permitted. The Archives and History Office staff are currently working on a project to identify all past interview subjects, locate interview tapes and permission forms, and create interview transcripts. Our holdings contain tapes or transcripts of interviews with the following staff members and users:

246

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

247

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

248

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

249

Autothermal Reforming of Renewable Fuels  

DOE Green Energy (OSTI)

The conversion of biomass into energy and chemicals is a major research and technology challenge of this century, comparable to petroleum processing in the last century. Recently we have successfully transformed both volatile liquids and nonvolatile liquids and solids into syngas with no carbon formation in autothermal catalytic reactors with residence times of ~10 milliseconds. In the proposed research program we explore the mechanisms of these processes and their extensions to other biomass sources and applications by examining different feeds, catalysts, flow conditions, and steam addition to maximize production of either syngas or chemicals. We will systematically study the catalytic partial oxidation in millisecond autothermal reactors of solid biomass and the liquid products formed by pyrolysis of solid biomass. We will examine alcohols, polyols, esters, solid carbohydrates, and lignocellulose to try to maximize formation of either hydrogen and syngas or olefins and oxygenated chemicals. We will explore molecules and mixtures of practical interest as well as surrogate molecules that contain the functional groups of biofuels but are simpler to analyze and interpret. We will examine spatial profiles within the catalyst and transient and periodic operation of these reactors at pressures up to 10 atm to obtain data from which to explore more detailed mechanistic models and optimize performance to produce a specific desired product. New experiments will examine the conversion of syngas into biofuels such as methanol and dimethyl ether to explore the entire process of producing biofuels from biomass in small distributed systems. Experiments and modeling will be integrated to probe and understand detailed reaction kinetics and the processes by which solid biomass particles are transformed into syngas and chemicals by reactive flash volatilization.

Schmidt, Lanny D

2009-05-01T23:59:59.000Z

250

What is the History of the NMMSS? | National Nuclear Security  

National Nuclear Security Administration (NNSA)

History of the NMMSS? | National Nuclear Security History of the NMMSS? | 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 What is the History of the NMMSS? Home > About Us > Our Programs > Nuclear Security > Nuclear Materials Management & Safeguards System > NMMSS Information, Reports & Forms > Frequently Asked Questions > What is the History of the NMMSS?

251

Catalytic Device International LLC | Open Energy Information  

Open Energy Info (EERE)

Catalytic Device International LLC Catalytic Device International LLC Jump to: navigation, search Name Catalytic Device International LLC Place Pleasanton, California Product California-based, firm focused on portable, heat-on-demand products. References Catalytic Device International LLC[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Catalytic Device International LLC is a company located in Pleasanton, California . References ↑ "Catalytic Device International LLC" Retrieved from "http://en.openei.org/w/index.php?title=Catalytic_Device_International_LLC&oldid=343285" Categories: Clean Energy Organizations Companies Organizations Stubs What links here Related changes Special pages

252

Endothermic photo-catalytic reactions  

Science Conference Proceedings (OSTI)

The overall objective of this report is to present the results of an investigation to provide guidelines for future experimental work, on solar energy driven endothermic photo-catalytic reactions, and primarily to select candidate synthesis reactions which lead to high $-value products. An intensive literature search was conducted to find properties, market demand, and prices of pertinent chemicals; meeting four criteria: (1) the reaction must be endothermic and favorable; (2) the reaction must be catalytic; (3) the product must be produced from low cost feedstocks; and (4) the product must have a sales price >$1.00/lb. Initial examination of low cost feedstocks to high value products lead to consideration of n-paraffins to aromatics and substituted aromatics. Fifteen candidate endothermic synthesis reactions, meeting the above criteria, are suggested. The ratio of product price by reactant cost indicates {approximately}5--8 for the best possibilities; all can be visualized as starting with low cost paraffin and methanol feedstocks.

Prengle, H.W. Jr.; Wentworth, W.E.; Polonczyk, K.C.; Saghafi, M.; Wilking, J.A.; Kramer, K.S. (Houston Univ., TX (United States))

1992-04-01T23:59:59.000Z

253

NSLS Machine Status & History  

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

Data (Table) Xray and VUV BeamLine: Current Data (Text) Beamline Experimental Floor Layout History One-Week Beam Current History Text Files of Beam Current History Device Readings...

254

History | Department of Energy  

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

History History Aviation Management Green Leases Executive Secretariat Energy Reduction at HQ Real Estate Approvals Documents and Publications Facilities and Infrastructure Federal...

255

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

256

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

257

Role of metal-support interactions on the activity of Pt and Rh catalysts for reforming methane and butane.  

DOE Green Energy (OSTI)

For residential fuel cell systems, reforming of natural gas is one option being considered for providing the H{sub 2} necessary for the fuel cell to operate. Industrially, natural gas is reformed using Ni-based catalysts supported on an alumina substrate, which has been modified to inhibit coke formation. At Argonne National Laboratory, we have developed a new family of catalysts derived from solid oxide fuel cell technology for reforming hydrocarbon fuels to generate H{sub 2}. These catalysts consist of a transition metal supported on an oxide-ion-conducting substrate, such as ceria, that has been doped with a small amount of a non-reducible element, such as gadolinium, samarium, or zirconium. Unlike alumina, the oxide-ion-conducting substrate has been shown to induce strong metal-support interactions. Metal-support interactions are known to play an important role in influencing the catalytic activity of many metals supported on oxide supports. Based on results from temperature-programmed reduction/oxidation and kinetic reaction studies, this paper discusses the role of the metal and the substrate in the metal-support interactions, and how these interactions influence the activity and the selectivity of the catalyst in reforming methane and butane to hydrogen for use in fuel cell power systems.

Rossignol, C.; Krause, T.; Krumpelt, M.

2002-01-11T23:59:59.000Z

258

Method of improving catalytic activity and catalytics produced thereby  

DOE Patents (OSTI)

A process for dissociating H{sub 2}S in a gaseous feed using an improved catalytic material is disclosed in which the feed is contacted at a temperature of at least about 275C with a catalyst of rutile nanocrystalline titania having grain sizes in the range of from about 1 to about 100 manometers. Other transition metal catalysts are disclosed, each of nanocrystalline material with grain sizes in the 1--100 nm range. This invention may have application to vehicle emissions control (three-way catalysts).

Beck, D.D.; Siegel, R.W.

1993-09-23T23:59:59.000Z

259

A Review of Sources of History of Tibet  

E-Print Network (OSTI)

) (Forvols. III-IV). And Ka dampa and dge lugs pa Reformed sect) Amdo - chos 'Byung, the bka gdams portion of the Deb ther sngon po (blue Annals translated by G.N. Roerich) Asiatic Society, Calcutta), Lam Rim bla rna Brgyud pa'Lrnam thar, a History of Ge... .M. 1969) Professor N.C. Sinha: A History and Religion of Tibet published by Ambika Gharan Bosu, (Calcutta, 1975) Professor Ram Rahul The Government and Politics of Tibet (Delhi, Vikas Publications, 1969). We have already referred to H. Richardson...

Ghosh, Bhajagovinda

1996-01-01T23:59:59.000Z

260

Catalytic steam gasification of carbon  

DOE Green Energy (OSTI)

Unsupported carbide powders with high specific surface area, namely {alpha}-WC (35 m{sup 2}/g, hexagonal), {beta}-WC{sub 0.61} (100 m{sup 2}/g, cubic face centered) and {beta}-WC{sub 0.5} (15 m{sup 2}/g, hexagonal) have been prepared. The key element in this preparation is the successful removal of surface polymeric carbon by careful gasification to methane by means of dihydrogen. These tungsten carbide powders have been used in catalytic reactions of oxidation of H{sub 2} and hydrogenolysis of alkanes, such as butane, hexane, and neopentane.

Boudart, M.

1990-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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.


261

Catalytic membranes for fuel cells  

DOE Patents (OSTI)

A fuel cell of the present invention comprises a cathode and an anode, one or both of the anode and the cathode including a catalyst comprising a bundle of longitudinally aligned graphitic carbon nanotubes including a catalytically active transition metal incorporated longitudinally and atomically distributed throughout the graphitic carbon walls of said nanotubes. The nanotubes also include nitrogen atoms and/or ions chemically bonded to the graphitic carbon and to the transition metal. Preferably, the transition metal comprises at least one metal selected from the group consisting of Fe, Co, Ni, Mn, and Cr.

Liu, Di-Jia (Naperville, IL); Yang, Junbing (Bolingbrook, IL); Wang, Xiaoping (Naperville, IL)

2011-04-19T23:59:59.000Z

262

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

263

Fermilab | Women's History Month - The History  

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

Dr. Sandra Hanson, Professor of Sociology, Catholic University of America, titled Gender, Race and Science Education. Click here to RSVP The celebration of Women's History in...

264

Cosmic Growth History and Expansion History  

E-Print Network (OSTI)

The cosmic expansion history tests the dynamics of the global evolution of the universe and its energy density contents, while the cosmic growth history tests the evolution of the inhomogeneous part of the energy density. Precision comparison of the two histories can distinguish the nature of the physics responsible for the accelerating cosmic expansion: an additional smooth component - dark energy - or a modification of the gravitational field equations. With the aid of a new fitting formula for linear perturbation growth accurate to 0.05-0.2%, we separate out the growth dependence on the expansion history and introduce a new growth index parameter \\gamma that quantifies the gravitational modification.

Eric V. Linder

2005-07-11T23:59:59.000Z

265

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

266

Catalytic Combustor for Fuel-Flexible Turbine  

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

Catalytic Lean (RCL TM ) technology, Figure 1, is being developed as an ultra low NOx gas turbine combustor for Integrated Gasification Combined Cycle (IGCC). In this concept,...

267

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

268

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...

269

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

270

Catalytic conversion of light alkanes  

DOE Green Energy (OSTI)

The second Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between April 1, 1992 and June 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products that can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon uwspomdon fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE I).

Lyons, J.E.

1992-06-30T23:59:59.000Z

271

Pemex opts for catalytic dehydrogenation  

SciTech Connect

In the gas-rich areas such as the Middle East, Southeast Asia, Canada, and Mexico, low-cost ethane is the feed of choice for ethylene production. Coproduct production is minimal. Continued growth in demand for propylene, isobutylene, normal butone-1, and butadiene requires that alternate sources of these normally coproduct olefins be developed. Catalytic dehydrogenation, with its high selectivity to the desired olefin, is the logical and economic choice. Mexico is a case in point. It's ethylene production is based on ethane. Demand is rising for propylene and butadiene derivatives, and a potential demand exists for isobutylene to produce octane enhancers to implement an announced lead phase down. Only modest amounts of by-product monoolefin will be available from refining operations. Pemex, the Mexican refining and petrochemical giant, recognized this and started up its first Houdry Catadene /SUP TM/ plant in 1975 at Ciudad Madero to produce 55,000 metric ton/year of butadiene from normal butane. Pemex recently committed to a large (350,000 metric ton/year) propylene-from-propane plant at Morelos based on the Houdry Catofin /SUP TM/ catalytic dehydrogenation process. The plant will supply propylene to a long list of derivative plants (Table 1).

Craig, R.G.; Penny, S.J.; Schwartz, W.A.

1983-07-01T23:59:59.000Z

272

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

273

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

274

Iran in History Iran in History  

E-Print Network (OSTI)

1 Iran in History Iran in History by Bernard Lewis In attempting to attain some perspective on Iran. These events have been variously seen in Iran: by some as a blessing, the advent of the true faith, the end remarkable difference between what happened in Iran and what happened in all the other countries

Mohaghegh, Shahab

275

Advanced power systems featuring a closely coupled catalytic gasification carbonate fuel cell plant  

DOE Green Energy (OSTI)

Pursuing the key national goal of clean and efficient uulization of the abundant domestic coal resources for power generation, a study was conducted with DOE/METC support to evaluate the potential of integrated gasification/carbonate fuel cell power generation systems. By closely coupling the fuel cell with the operation of a catalytic gasifier, the advantages of both the catalytic gasification and the high efficiency fuel cell complement each other, resulting in a power plant system with unsurpassed efficiencies approaching 55% (HHV). Low temperature catalytic gasification producing a high methane fuel gas offers the potential for high gas efficiencies by operating with minimal or no combustion. Heat required for gasification is provided by combination of recycle from the fuel cell and exothermic methanation and shift reactions. Air can be supplemented if required. In combination with internally reforming carbonate fuel cells, low temperature catalytic gasification can achieve very attractive system efficiencies while producing extremely low emissions compared to conventional plants utilizing coal. Three system configurations based on recoverable and disposable gasification catalysts were studied. Experimental tests were conducted to evaluate these gasification catalysts. The recoverable catalyst studied was potassium carbonate, and the disposable catalysts were calcium in the form of limestone and iron in the form of taconite. Reactivities of limestone and iron were lower than that of potassium, but were improved by using the catalyst in solution form. Promising results were obtained in the system evaluations as well as the experimental testing of the gasification catalysts. To realize the potential of these high efficiency power plant systems more effort is required to develop catalytic gasification systems and their integration with carbonate fuel cells.

Steinfeld, G.; Wilson, W.G.

1993-06-01T23:59:59.000Z

276

Advanced power systems featuring a closely coupled catalytic gasification carbonate fuel cell plant  

DOE Green Energy (OSTI)

Pursuing the key national goal of clean and efficient uulization of the abundant domestic coal resources for power generation, a study was conducted with DOE/METC support to evaluate the potential of integrated gasification/carbonate fuel cell power generation systems. By closely coupling the fuel cell with the operation of a catalytic gasifier, the advantages of both the catalytic gasification and the high efficiency fuel cell complement each other, resulting in a power plant system with unsurpassed efficiencies approaching 55% (HHV). Low temperature catalytic gasification producing a high methane fuel gas offers the potential for high gas efficiencies by operating with minimal or no combustion. Heat required for gasification is provided by combination of recycle from the fuel cell and exothermic methanation and shift reactions. Air can be supplemented if required. In combination with internally reforming carbonate fuel cells, low temperature catalytic gasification can achieve very attractive system efficiencies while producing extremely low emissions compared to conventional plants utilizing coal. Three system configurations based on recoverable and disposable gasification catalysts were studied. Experimental tests were conducted to evaluate these gasification catalysts. The recoverable catalyst studied was potassium carbonate, and the disposable catalysts were calcium in the form of limestone and iron in the form of taconite. Reactivities of limestone and iron were lower than that of potassium, but were improved by using the catalyst in solution form. Promising results were obtained in the system evaluations as well as the experimental testing of the gasification catalysts. To realize the potential of these high efficiency power plant systems more effort is required to develop catalytic gasification systems and their integration with carbonate fuel cells.

Steinfeld, G.; Wilson, W.G.

1993-01-01T23:59:59.000Z

277

Texas Inland Downstream Processing of Fresh Feed Input  

U.S. Energy Information Administration (EIA)

Process: Area: 2007 2008 2009 2010 2011 2012 View History; Catalytic Reforming : 133: 125: 131: 2010-2012: Catalytic Cracking: 173: 158: 159: 149: 162: 164: 1987-2012 ...

278

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

279

Year/PAD District Cokers Catalytic Crackers Hydrocrackers Capacity  

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

Cokers Catalytic Crackers Hydrocrackers Capacity Inputs Capacity Inputs Capacity Inputs Table 8. Capacity and Fresh Feed Input to Selected Downstream Units at U.S. Refineries, 2011 - 2013 (Barrels per Calendar Day) Reformers Capacity Inputs 2011 2,396,787 5,794,214 1,687,745 2,093,849 4,952,455 1,466,627 2,570,970 3,346,457 93,700 673,300 41,500 37,932 490,729 18,030 PADD I 188,389 266,950 373,897 1,176,972 254,000 350,063 1,017,616 223,751 PADD II 664,852 812,244 1,318,440 2,933,842 841,285 1,183,318 2,570,348 744,638 PADD III 1,243,427 1,629,967 80,350 185,800 28,200 63,362 158,192 18,214 PADD IV 96,649 120,190 530,400 824,300 522,760 459,175 715,570 461,995 PADD V 377,652 517,106 2012 2,499,293 5,611,191 1,706,540 2,173,336 4,901,284 1,528,708 2,614,571 3,246,874 74,900 489,300 20,000

280

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

Note: This page contains sample records for the topic "history catalytic 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

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

282

Method of fabricating a catalytic structure  

SciTech Connect

A precursor to a catalytic structure comprising zinc oxide and copper oxide. The zinc oxide has a sheet-like morphology or a spherical morphology and the copper oxide comprises particles of copper oxide. The copper oxide is reduced to copper, producing the catalytic structure. The catalytic structure is fabricated by a hydrothermal process. A reaction mixture comprising a zinc salt, a copper salt, a hydroxyl ion source, and a structure-directing agent is formed. The reaction mixture is heated under confined volume conditions to produce the precursor. The copper oxide in the precursor is reduced to copper. A method of hydrogenating a carbon oxide using the catalytic structure is also disclosed, as is a system that includes the catalytic structure.

Rollins, Harry W. (Idaho Falls, ID); Petkovic, Lucia M. (Idaho Falls, ID); Ginosar, Daniel M. (Idaho Falls, ID)

2009-09-22T23:59:59.000Z

283

Catalytic Hydrothermal Gasification of Biomass  

Science Conference Proceedings (OSTI)

A recent development in biomass gasification is the use of a pressurized water processing environment in order that drying of the biomass can be avoided. This paper reviews the research undertaken developing this new option for biomass gasification. This review does not cover wet oxidation or near-atmospheric-pressure steam-gasification of biomass. Laboratory research on hydrothermal gasification of biomass focusing on the use of catalysts is reviewed here, and a companion review focuses on non-catalytic processing. Research includes liquid-phase, sub-critical processing as well as super-critical water processing. The use of heterogeneous catalysts in such a system allows effective operation at lower temperatures, and the issues around the use of catalysts are presented. This review attempts to show the potential of this new processing concept by comparing the various options under development and the results of the research.

Elliott, Douglas C.

2008-05-06T23:59:59.000Z

284

APPARATUS FOR CATALYTICALLY COMBINING GASES  

DOE Patents (OSTI)

A convection type recombiner is described for catalytically recombining hydrogen and oxygen which have been radiolytically decomposed in an aqueous homogeneous nuclear reactor. The device is so designed that the energy of recombination is used to circulate the gas mixture over the catalyst. The device consists of a vertical cylinder having baffles at its lower enda above these coarse screens having platinum and alumina pellets cemented thereon, and an annular passage for the return of recombined, condensed water to the reactor moderator system. This devicea having no moving parts, provides a simple and efficient means of removing the danger of accumulated hot radioactive, explosive gases, and restoring them to the moderator system for reuse.

Busey, H.M.

1958-08-12T23:59:59.000Z

285

Catalytic reactor with improved burner  

DOE Patents (OSTI)

To more uniformly distribute heat to the plurality of catalyst tubes in a catalytic reaction furnace, the burner disposed in the furnace above the tops of the tubes includes concentric primary and secondary annular fuel and air outlets. The fuel-air mixture from the primary outlet is directed towards the tubes adjacent the furnace wall, and the burning secondary fuel-air mixture is directed horizontally from the secondary outlet and a portion thereof is deflected downwardly by a slotted baffle toward the tubes in the center of the furnace while the remaining portion passes through the slotted baffle to another baffle disposed radially outwardly therefrom which deflects it downwardly in the vicinity of the tubes between those in the center and those near the wall of the furnace.

Faitani, Joseph J. (Hartford, CT); Austin, George W. (Glastonbury, CT); Chase, Terry J. (Somers, CT); Suljak, George T. (Vernon, CT); Misage, Robert J. (Manchester,all of, CT)

1981-01-01T23:59:59.000Z

286

HISTORY OF CONSCIOUSNESS HANDBOOK  

E-Print Network (OSTI)

HISTORY OF CONSCIOUSNESS HANDBOOK 2012-2013 #12; 1 HANDBOOK Welcome to graduate study in the History of Consciousness our program's requirements. This handbook is intended as a supplement

California at Santa Cruz, University of

287

National Women's History Month  

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

During Women's History Month, we recall that the pioneering legacy of our grandmothers and great-grandmothers is revealed not only in our museums and history books, but also in the fierce...

288

Family History and Offspring  

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

Family History and Offspring Name: Chad Location: NA Country: NA Date: NA Question: Does a family's history in any way determine the chances of a child being born male or...

289

DOE Solar Decathlon: History  

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

History The history of the U.S. Department of Energy Solar Decathlon dates to the inaugural event in 2002. Since then, the Solar Decathlon has been held biennially in 2005, 2007,...

290

Muon Collider History  

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

Colliders: A Brief History Below is a brief potted history of the muon collider concept. Click here for a one transparency summary. The muon collider concept is an idea dating back...

291

Fermilab | Women's History Month  

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

Women's History Month at Fermilab Fermilab recognized Women's History Month through a series of lab-wide events during March 2010. During the past five decades, women from all...

292

History of AOCS  

Science Conference Proceedings (OSTI)

Dedicated volunteers have helped guide AOCS from a small regional organization into an international society with influence throughout the world. History of AOCS AOCS History and Governance about us aocs committees contact us division council fats

293

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

294

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

295

TCS 2014 Symposium on Thermal and Catalytic Sciences for Biofuels...  

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

TCS 2014 Symposium on Thermal and Catalytic Sciences for Biofuels and Biobased Products TCS 2014 Symposium on Thermal and Catalytic Sciences for Biofuels and Biobased Products...

296

DIESEL REFORMERS FOR LEAN NOX TRAP REGENERATION AND OTHER ON-BOARD HYDROGEN APPLICATIONS  

DOE Green Energy (OSTI)

Many solutions to meeting the 2007 and 2010 diesel emissions requirements have been suggested. On board production of hydrogen for in-cylinder combustion and exhaust after-treatment provide promising opportunities for meeting those requirements. Other benefits may include using syngas to rapidly heat up exhaust after-treatment catalysts during engine startup. HydrogenSource's development of a catalytic partial oxidation reformer for generating hydrogen from ultra-low sulfur diesel fuel is presented. The system can operate on engine exhaust and diesel fuel with no water tank. Test data for hydrogen regeneration of a lean NOx trap is presented showing 90% NOx conversion at temperatures as low as 150 degrees C and 99% conversion at 300 degrees C. Finally, additional efforts required to fully understand the benefits and commercial challenges of this technology are discussed.

Mauss, M; Wnuck, W

2003-08-24T23:59:59.000Z

297

An Inquiry into History, Big History, and Metahistory  

E-Print Network (OSTI)

of Theoretical and Mathematical History Editors’ Column:An Inquiry into History,Big History, and Metahistory David C. Krakauer Santa Fe

Krakauer, David; Gaddis, John L; Pomeranz, Kenneth L

2011-01-01T23:59:59.000Z

298

Minimizing the formation of coke and methane on Co nanoparticles in steam reforming of biomass-derived oxygenates  

SciTech Connect

Fundamental understanding and control of chemical transformations are essential to the development of technically feasible and economically viable catalytic processes for efficient conversion of biomass to fuels and chemicals. Using an integrated experimental and theoretical approach, we report high hydrogen selectivity and catalyst durability of acetone steam reforming (ASR) on inert carbon supported Co nanoparticles. The observed catalytic performance is further elucidated on the basis of comprehensive first-principles calculations. Instead of being considered as an undesired intermediate prone for catalyst deactivation during bioethanol steam reforming (ESR), acetone is suggested as a key and desired intermediate in proposed two-stage ESR process that leads to high hydrogen selectivity and low methane formation on Co-based catalysts. The significance of the present work also sheds a light on controlling the chemical transformations of key intermediates in biomass conversion such as ketones. We gratefully acknowledge the financial support from U. S. Department of Energy (DOE), Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences, and the Laboratory directed research and development (LDRD) project of Pacific Northwest National Laboratory (PNNL). Computing time was granted by the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL). The EMSL is a U.S. DOE national scientific user facility located at PNNL, and sponsored by the U.S. DOE’s Office of Biological and Environmental Research.

Sun, Junming; Mei, Donghai; Karim, Ayman M.; Datye, Abhaya K.; Wang, Yong

2013-06-01T23:59:59.000Z

299

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

E-Print Network (OSTI)

In-situ hydrogen production is carried out by a catalytic reformer kit set up into exhaust gases for a CHP plant based on spark ignition engine running under lean conditions. An overall auto-thermal reforming process is achieved. Hydrogen production is mainly dependent on O2 content in exhaust gases. Experiments are conducted at constant speed at 2 air/fuel ratios and 4 additional natural gas flow rates. H2 content varies in the range 6 % to 10 % in vol. H2 content effect is analyzed with respect to performance and emissions. Comparing with EGR shows an increasing of electrical efficiency of 1 % whilst heat recovery decreases by 1%. NO and HC decrease by 18 % and 12%, but CO increases by 14%, respectively. The results show that: (i) graphite joints were destroyed under effect of H2 and high temperature; (ii) a cold spot appeared in the RGR line, and condensation has as consequence a carbon deposit; and (iii) no back-fire or knock occurred.

O. Le Corre; C. Rahmouni; K. Saikaly; I. Dincer

2013-01-01T23:59:59.000Z

300

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

Note: This page contains sample records for the topic "history catalytic 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

Vacuum-insulated catalytic converter  

DOE Patents (OSTI)

A catalytic converter has an inner canister that contains catalyst-coated substrates and an outer canister that encloses an annular, variable vacuum insulation chamber surrounding the inner canister. An annular tank containing phase-change material for heat storage and release is positioned in the variable vacuum insulation chamber a distance spaced part from the inner canister. A reversible hydrogen getter in the variable vacuum insulation chamber, preferably on a surface of the heat storage tank, releases hydrogen into the variable vacuum insulation chamber to conduct heat when the phase-change material is hot and absorbs the hydrogen to limit heat transfer to radiation when the phase-change material is cool. A porous zeolite trap in the inner canister absorbs and retains hydrocarbons from the exhaust gases when the catalyst-coated substrates and zeolite trap are cold and releases the hydrocarbons for reaction on the catalyst-coated substrate when the zeolite trap and catalyst-coated substrate get hot.

Benson, David K. (Golden, CO)

2001-01-01T23:59:59.000Z

302

Glycoside hydrolases: Catalytic base/nucleophile diversity  

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

Glycoside Glycoside Hydrolases: Catalytic Base/Nucleophile Diversity Thu V. Vuong, David B. Wilson Department of Molecular Biology and Genetics, Cornell University, 458 Biotechnology Building, Ithaca, New York 14850; telephone: 607-255-5706; fax: 607-255-2428; e-mail: dbw3@cornell.edu Received 1 April 2010; revision received 27 May 2010; accepted 2 June 2010 Published online 15 June 2010 in Wiley Online Library (wileyonlinelibrary.com). DOI 10.1002/bit.22838 ABSTRACT: Recent studies have shown that a number of glycoside hydrolase families do not follow the classical catalytic mechanisms, as they lack a typical catalytic base/ nucleophile. A variety of mechanisms are used to replace this function, including substrate-assisted catalysis, a network of several residues, and the use of non-carboxylate residues or exogenous nucleophiles. Removal of the catalytic base/ nucleophile

303

Optimal control of fluid catalytic cracking processes  

Science Conference Proceedings (OSTI)

An investigation was made of the applicability of optimal control theory to the design of control systems for non-linear, multivariable chemical processes. A hypothetical fluid catalytic cracking process was selected as a typical representative of such ...

L. A. Gould; L. B. Evans; H. Kurihara

1970-09-01T23:59:59.000Z

304

History | Department of Energy  

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

About Energy.gov » History About Energy.gov » History History History The Department of Energy has one of the richest and most diverse histories in the Federal Government. Although only in existence since 1977, the Department traces its lineage to the Manhattan Project effort to develop the atomic bomb during World War II and to the various energy-related programs that previously had been dispersed throughout various Federal agencies. The Department has made available to researchers and the general public a rich variety of materials and information: Historical Resources, including published and online histories of the Department and its predecessor agencies and information on records, exhibits, museums, and tours available online and at various locations both within and outside the Department. Major publications and websites can be

305

History | Department of Energy  

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

About Energy.gov » History About Energy.gov » History History History The Department of Energy has one of the richest and most diverse histories in the Federal Government. Although only in existence since 1977, the Department traces its lineage to the Manhattan Project effort to develop the atomic bomb during World War II and to the various energy-related programs that previously had been dispersed throughout various Federal agencies. The Department has made available to researchers and the general public a rich variety of materials and information: Historical Resources, including published and online histories of the Department and its predecessor agencies and information on records, exhibits, museums, and tours available online and at various locations both within and outside the Department. Major publications and websites can be

306

NETL: Albany, Oregon History  

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

Home > About NETL > History > Albany Research Center History Home > About NETL > History > Albany Research Center History About NETL Albany, Oregon History Albany Research Center has a history rich in successful materials research and development. It was on March 17, 1943 that President Franklin D. Roosevelt announced that the U. S. Bureau of Mines had selected a site in Albany, Oregon for the new Northwest Electro-development Laboratory. The original mission of the center was to find methods for using the abundant low-grade resources of the area, and to develop new metallurgical processes using the abundant electrical energy in the area. The name of the center was changed in 1945 to the Albany Metallurgy Research Center and was used through 1977 where the name was shortened to Albany Research Center. One of our first successes was the development

307

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

308

History | ornl.gov  

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

News Careers Work with ORNL About ORNL Fact Sheet Brochure Diversity Leadership Team Organization History Environmental Policy Corporate Giving Research Integrity Who we are,...

309

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

310

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....

311

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

312

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.

313

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 ...

314

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.

315

Final Report for "Investigation of reaction networks and active sites in bio-ethanol steam reforming over Co-based catalysts" with all publications attached.  

DOE Green Energy (OSTI)

This was a university-based research project in support of distributed reforming production technologies for hydrogen. Our objective was to examine the steam reforming of bio-ethanol and other related bio-derived liquids over non-precious metal catalyst systems to enable small-scale distributed hydrogen production technologies from renewable sources. The study targeted development of a catalytic system that does not rely on precious metals and that can be active in the 350-550 C temperature range, with high selectivity and high stability. To this end, we adopted a multi-prong research strategy, that included catalyst formulation and synthesis, detailed catalyst characterization, reaction kinetics and reaction engineering, molecular modeling and economic analysis studies. Our approach was an iterative one, where the knowledge gained in one aspect of the study was utilized to modify and fine-tune catalyst development. The research addressed many fundamental and inter-related phenomena involved in the catalytic steam reforming of ethanol that may not be readily studied in an industrial development setting. The outcome of the project was a catalytic system that was able to meet the DOE targets in hydrogen production, with high H{sub 2} yield, high selectivity and stability that could perform efficiently in the 350-550 C temperature range. In addition, we were able to answer many fundamental questions about the catalytic systems that could easily be translated to other catalytic systems. The study resulted in 14 refereed journal articles, with one more in preparation. The results were also shared broadly at many different national and international forums such as conferences of the American Chemical Society, American Institute of Chemical Engineers, North American Catalysis Society, International Congress on Catalysis and International Conference on Catalysis for Renewable Sources. There were 30 presentations given at various national and international meetings. The P.I. was also invited to give 11 lectures on the findings from this study at many universities and research centers in the USA and other countries. The knowledge base acquired through this study is expected to bring industry closer to designing catalytic systems that can be tailored for the specific hydrogen production applications, especially for distributed hydrogen production strategies.

Umit S. Ozkan

2011-03-31T23:59:59.000Z

316

Molecular surface science of heterogeneous catalysis. History and perspective  

DOE Green Energy (OSTI)

A personal account is given of how the author became involved with modern surface science and how it was employed for studies of the chemistry of surfaces and heterogeneous catalysis. New techniques were developed for studying the properties of the surface monolayers: Auger electron spectroscopy, LEED, XPS, molecular beam surface scattering, etc. An apparatus was developed and used to study hydrocarbon conversion reactions on Pt, CO hydrogenation on Rh and Fe, and NH/sub 3/ synthesis on Fe. A model has been developed for the working Pt reforming catalyst. The three molecular ingredients that control catalytic properties are atomic surface structure, an active carbonaceous deposit, and the proper oxidation state of surface atoms. 40 references, 21 figures. (DLC)

Somorjai, G.A.

1983-08-01T23:59:59.000Z

317

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

318

Microscale acceleration history discriminators  

DOE Patents (OSTI)

A new class of micromechanical acceleration history discriminators is claimed. These discriminators allow the precise differentiation of a wide range of acceleration-time histories, thereby allowing adaptive events to be triggered in response to the severity (or lack thereof) of an external environment. Such devices have applications in airbag activation, and other safety and surety applications.

Polosky, Marc A. (Albuquerque, NM); Plummer, David W. (Albuquerque, NM)

2002-01-01T23:59:59.000Z

319

VOC Destruction by Catalytic Combustion Microturbine  

SciTech Connect

This project concerned the application of a catalytic combustion system that has been married to a micro-turbine device. The catalytic combustion system decomposes the VOC's and transmits these gases to the gas turbine. The turbine has been altered to operate on very low-level BTU fuels equivalent to 1.5% methane in air. The performance of the micro-turbine for VOC elimination has some flexibility with respect to operating conditions, and the system is adaptable to multiple industrial applications. The VOC source that was been chosen for examination was the emissions from coal upgrading operations. The overall goal of the project was to examine the effectiveness of a catalytic combustion based system for elimination of VOCs while simultaneously producing electrical power for local consumption. Project specific objectives included assessment of the feasibility for using a Flex-Microturbine that generates power from natural gas while it consumes VOCs generated from site operations; development of an engineering plan for installation of the Flex-Microturbine system; operation of the micro-turbine through various changes in site and operation conditions; measurement of the VOC destruction quantitatively; and determination of the required improvements for further studies. The micro-turbine with the catalytic bed worked effectively to produce power on levels of fuel much lower than the original turbine design. The ability of the device to add or subtract supplemental fuel to augment the amount of VOC's in the inlet air flow made the device an effective replacement for a traditional flare. Concerns about particulates in the inlet flow and the presence of high sulfur concentrations with the VOC mixtures was identified as a drawback with the current catalytic design. A new microturbine design was developed based on this research that incorporates a thermal oxidizer in place of the catalytic bed for applications where particulates or contamination would limit the lifetime of the catalytic bed.

Tom Barton

2009-03-10T23:59:59.000Z

320

VOC Destruction by Catalytic Combustion Microturbine  

SciTech Connect

This project concerned the application of a catalytic combustion system that has been married to a micro-turbine device. The catalytic combustion system decomposes the VOC's and transmits these gases to the gas turbine. The turbine has been altered to operate on very low-level BTU fuels equivalent to 1.5% methane in air. The performance of the micro-turbine for VOC elimination has some flexibility with respect to operating conditions, and the system is adaptable to multiple industrial applications. The VOC source that was been chosen for examination was the emissions from coal upgrading operations. The overall goal of the project was to examine the effectiveness of a catalytic combustion based system for elimination of VOCs while simultaneously producing electrical power for local consumption. Project specific objectives included assessment of the feasibility for using a Flex-Microturbine that generates power from natural gas while it consumes VOCs generated from site operations; development of an engineering plan for installation of the Flex-Microturbine system; operation of the micro-turbine through various changes in site and operation conditions; measurement of the VOC destruction quantitatively; and determination of the required improvements for further studies. The micro-turbine with the catalytic bed worked effectively to produce power on levels of fuel much lower than the original turbine design. The ability of the device to add or subtract supplemental fuel to augment the amount of VOC's in the inlet air flow made the device an effective replacement for a traditional flare. Concerns about particulates in the inlet flow and the presence of high sulfur concentrations with the VOC mixtures was identified as a drawback with the current catalytic design. A new microturbine design was developed based on this research that incorporates a thermal oxidizer in place of the catalytic bed for applications where particulates or contamination would limit the lifetime of the catalytic bed.

Tom Barton

2009-03-10T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

Mosquito Life Histories  

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

Life Histories Life Histories Nature Bulletin No. 682 June 2, 1962 Forest Preserve District of Cook County John J. Duffy, President David H. Thompson, Senior Naturalist MOSQUITO LIFE HISTORIES Everybody knows that a mosquito is a small, long-legged insect that bites. However, there are many kinds of them each with its own peculiarities of life history and habits. Some are produced in marshes or in flood plains of streams, some in puddles, some in woodlands, and others in cities and towns. Here in the Chicago region, although mosquito-borne diseases are no longer a danger, they become nuisances in many places at certain times in almost every year. In times past and in many countries the mosquitoes which carried malaria, yellow fever and other infections shaped the course of history. Hundreds of scientists have studied them for years but much remains to be learned.

322

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 . . . . . . . . . . . . . . . . . . . . . .

323

Catalytic Combustor for Fuel-Flexible Turbine  

SciTech Connect

Under the sponsorship of the U. S. Department of Energy's National Energy Technology Laboratory, Siemens Westinghouse has conducted a three-year program to develop an ultra low NOx, fuel flexible catalytic combustor for gas turbine application in IGCC. The program is defined in three phases: Phase 1 - Implementation Plan, Phase 2 - Validation Testing and Phase 3 - Field Testing. Both Phase 1 and Phase 2 of the program have been completed. In IGCC power plants, the gas turbine must be capable of operating on syngas as a primary fuel and an available back-up fuel such as natural gas. In this program the Rich Catalytic Lean (RCLTM) technology is being developed as an ultra low NOx combustor. In this concept, ultra low NOx is achieved by stabilizing a lean premix combustion process by using a catalytic reactor to oxidize a portion of the fuel, increasing the temperature of fuel/air mixture prior to the main combustion zone. In Phase 1, the feasibility of the catalytic concept for syngas application has been evaluated and the key technology issues identified. In Phase II the technology necessary for the application of the catalytic concept to IGCC fuels was developed through detailed design and subscale testing. Phase III (currently not funded) will consist of full-scale combustor basket testing on natural gas and syngas.

W. R. Laster; E. Anoshkina

2008-01-31T23:59:59.000Z

324

Catalytic Combustor for Fuel-Flexible Turbine  

SciTech Connect

Under the sponsorship of the U.S. Department of Energy's National Energy Technology Laboratory, Siemens Westinghouse is conducting a three-year program to develop an ultra low NOx, fuel flexible catalytic combustor for gas turbine application in IGCC. The program is defined in three phases: Phase 1-Implementation Plan, Phase 2-Validation Testing and Phase 3-Field Testing. The Phase 1 program has been completed. Phase II was initiated in October 2004. In IGCC power plants, the gas turbine must be capable of operating on syngas as a primary fuel and an available back-up fuel such as natural gas. In this program the Rich Catalytic Lean (RCL{trademark}) technology is being developed as an ultra low NOx combustor. In this concept, ultra low NOx is achieved by stabilizing a lean premix combustion process by using a catalytic reactor to react part of the fuel, increasing the fuel/air mixture temperature. In Phase 1, the feasibility of the catalytic concept for syngas application has been evaluated and the key technology issues identified. In Phase II the catalytic concept will be demonstrated through subscale testing. Phase III will consist of full-scale combustor basket testing on natural gas and syngas.

W. R. Laster; E. Anoshkina; P. Szedlacsek

2006-03-31T23:59:59.000Z

325

Catalytic Combustor for Fuel-Flexible Turbine  

SciTech Connect

Under the sponsorship of the U. S. Department of Energy’s National Energy Technology Laboratory, Siemens Westinghouse has conducted a three-year program to develop an ultra low NOx, fuel flexible catalytic combustor for gas turbine application in IGCC. The program is defined in three phases: Phase 1- Implementation Plan, Phase 2- Validation Testing and Phase 3 – Field Testing. Both Phase 1 and Phase 2 of the program have been completed. In IGCC power plants, the gas turbine must be capable of operating on syngas as a primary fuel and an available back-up fuel such as natural gas. In this program the Rich Catalytic Lean (RCLTM) technology is being developed as an ultra low NOx combustor. In this concept, ultra low NOx is achieved by stabilizing a lean premix combustion process by using a catalytic reactor to oxidize a portion of the fuel, increasing the temperature of fuel/air mixture prior to the main combustion zone. In Phase 1, the feasibility of the catalytic concept for syngas application has been evaluated and the key technology issues identified. In Phase II the technology necessary for the application of the catalytic concept to IGCC fuels was developed through detailed design and subscale testing. Phase III (currently not funded) will consist of full-scale combustor basket testing on natural gas and syngas.

Laster, W. R.; Anoshkina, E.

2008-01-31T23:59:59.000Z

326

Effect of Surface Oxygen Containing Groups on the Catalytic Activity of Multi-walled Carbon Nanotube Supported Pt Catalyst  

Science Conference Proceedings (OSTI)

Multi-walled carbon nanotubes (MWNT) supported platinum catalysts were employed to study the support functionalization on their catalytic performances. The MWNT were subjected to HNO{sub 3} functionalization, in which oxygen-containing-groups (OCGs) were introduced to improve Pt dispersion. The MWNT supports were characterized by nitrogen physisorption and NEXAFS, and the Pt supported on differently functionalized MWNT characterized by X-ray absorption, TEM and both hydrogen and CO chemisorption. Compared to the as received MWNT supports, Pt dispersion is improved on the HNO3 treated MWNT supports, but the turnover frequency (TOF) of aqueous phase reforming decreases by half. The TOF can be recovered by removing the OCGs via high temperature annealing. To further investigate the OCGs effect, different probe reactions, including both steam reforming and liquid phase reforming of hydrocarbon oxygenates and dehydrogenation of alkanes in the liquid and gas phases, have been performed on the MWNT supported catalysts with different OCGs. A comparison of these reaction results suggests that OCGs are only detrimental to reactions in a binary mixture with two components of different hydrophilicity due to their competitive adsorption on the catalyst supports.

X Wang; N Li; J Webb; L Pfefferle; G Haller

2011-12-31T23:59:59.000Z

327

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

328

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

329

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

330

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

331

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

332

Electro Catalytic Oxidation (ECO) Operation  

Science Conference Proceedings (OSTI)

The power industry in the United States is faced with meeting many new regulations to reduce a number of air pollutants including sulfur dioxide, nitrogen oxides, fine particulate matter, and mercury. With over 1,000 power plants in the US, this is a daunting task. In some cases, traditional pollution control technologies such as wet scrubbers and SCRs are not feasible. Powerspan's Electro-Catalytic Oxidation, or ECO{reg_sign} process combines four pollution control devices into a single integrated system that can be installed after a power plant's particulate control device. Besides achieving major reductions in emissions of sulfur dioxide (SO{sub 2}), nitrogen oxides (NOx), fine particulate matter (PM2.5) and mercury (Hg), ECO produces a highly marketable fertilizer, which can help offset the operating costs of the process system. Powerspan has been operating a 50-MW ECO commercial demonstration unit (CDU) at FirstEnergy Corp.'s R.E. Burger Plant near Shadyside, Ohio, since February 2004. In addition to the CDU, a test loop has been constructed beside the CDU to demonstrate higher NOx removal rates and test various scrubber packing types and wet ESP configurations. Furthermore, Powerspan has developed the ECO{reg_sign}{sub 2} technology, a regenerative process that uses a proprietary solvent to capture CO{sub 2} from flue gas. The CO{sub 2} capture takes place after the capture of NOx, SO{sub 2}, mercury, and fine particulate matter. Once the CO{sub 2} is captured, the proprietary solution is regenerated to release CO{sub 2} in a form that is ready for geological storage or beneficial use. Pilot scale testing of ECO{sub 2} began in early 2009 at FirstEnergy's Burger Plant. The ECO{sub 2} pilot unit is designed to process a 1-MW flue gas stream and produce 20 tons of CO{sub 2} per day, achieving a 90% CO{sub 2} capture rate. The ECO{sub 2} pilot program provided the opportunity to confirm process design and cost estimates, and prepare for large scale capture and sequestration projects. The objectives of this project were to prove at a commercial scale that ECO is capable of extended operations over a range of conditions, that it meets the reliability requirements of a typical utility, and that the fertilizer co-product can be consistently generated, providing ECO with an economic advantage over conventional technologies currently available. Further objectives of the project were to show that the ECO system provides flue gas that meets the inlet standards necessary for ECO{sub 2} to operate, and that the outlet CO{sub 2} and other constituents produced by the ECO{sub 2} pilot can meet Kinder-Morgan pipeline standards for purposes of sequestration. All project objectives are consistent with DOE's Pollution Control Innovations for Power Plants program goals.

Morgan Jones

2011-03-31T23:59:59.000Z

333

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

334

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

335

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

336

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,

337

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

338

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

339

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

340

BNL | Our History  

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

Our History Our History A Passion for Discovery, a History of Scientific Achievement Brookhaven National Laboratory was established in 1947 on the eastern end of Long Island at the former site of the U.S. Army's Camp Upton. Originally built out of a post-World War II desire to explore the peaceful applications of atomic energy, the Laboratory now has a broader mission: to perform basic and applied research at the frontiers of science, including nuclear and high-energy physics; physics and chemistry of materials; nanoscience; energy and environmental research; national security and nonproliferation; neurosciences; structural biology; and computational sciences. Over its history, Brookhaven Lab has housed three research reactors, numerous one-of-a-kind particle accelerators, and other

Note: This page contains sample records for the topic "history catalytic 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

Black History Month  

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

During National African American History Month, we pay tribute to the contributions of past generations and reaffirm our commitment to keeping the American dream alive for the next generation.  In...

342

Strategic Planning History  

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

Strategy for Global Change Research Related Federal Climate Efforts Strategic Planning History Print E-mail Below is a timeline of past strategic plans that have guided The U.S....

343

Preprint History at SLAC  

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

and Biased History of Preprint and Database Activities at the SLAC Library, 1962-1994 by L. Addis (with a few updates in Jan 1997, Jun 1999, Apr 2000, Jan 2002) 1962 SLAC Library...

344

Oakes College: An Oral History  

E-Print Network (OSTI)

Oakes College: An Oral History Blake: That’s unfortunate. I’Oakes College: An Oral History Charland: It took awhile toOakes College: An Oral History with: J. Herman Blake Roberto

2011-01-01T23:59:59.000Z

345

Annual Operation of Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

In 2009, many coal-fired generating units equipped with selective catalytic reduction (SCR) systems for nitrogen oxide (NOX) control will convert from seasonal to annual SCR operation. This report provides guidelines on how to prepare for annual operation. It focuses on existing experience with annual operation, catalyst management strategy, equipment reliability, cold weather issues, low load and cycling operation, and risk assessment.

2007-12-18T23:59:59.000Z

346

Fuzzy modeling of fluidized catalytic cracking unit  

Science Conference Proceedings (OSTI)

The paper deals with the fuzzy system identification of reactor-regenerator-stripper-fractionator's (RRSF) section of a fluidized catalytic cracking unit (FCCU). The fuzzy system identification based on the data collected from an operating refinery of ... Keywords: Dynamic fuzzy model, FCCU models, Fuzzy clustering, Fuzzy inference systems, Fuzzy models, Hybrid learning, Mountain clustering, Supervised learning, Unsupervised learning

Mohammad Fazle Azeem; Nesar Ahmad; M. Hanmandlu

2007-01-01T23:59:59.000Z

347

Performance characterization of a hydrogen catalytic heater.  

DOE Green Energy (OSTI)

This report describes the performance of a high efficiency, compact heater that uses the catalytic oxidation of hydrogen to provide heat to the GM Hydrogen Storage Demonstration System. The heater was designed to transfer up to 30 kW of heat from the catalytic reaction to a circulating heat transfer fluid. The fluid then transfers the heat to one or more of the four hydrogen storage modules that make up the Demonstration System to drive off the chemically bound hydrogen. The heater consists of three main parts: (1) the reactor, (2) the gas heat recuperator, and (3) oil and gas flow distribution manifolds. The reactor and recuperator are integrated, compact, finned-plate heat exchangers to maximize heat transfer efficiency and minimize mass and volume. Detailed, three-dimensional, multi-physics computational models were used to design and optimize the system. At full power the heater was able to catalytically combust a 10% hydrogen/air mixture flowing at over 80 cubic feet per minute and transfer 30 kW of heat to a 30 gallon per minute flow of oil over a temperature range from 100 C to 220 C. The total efficiency of the catalytic heater, defined as the heat transferred to the oil divided by the inlet hydrogen chemical energy, was characterized and methods for improvement were investigated.

Johnson, Terry Alan; Kanouff, Michael P.

2010-04-01T23:59:59.000Z

348

Rapid Deployment of Rich Catalytic Combustion  

SciTech Connect

The overall objective of this research under the Turbines Program is the deployment of fuel flexible rich catalytic combustion technology into high-pressure ratio industrial gas turbines. The resulting combustion systems will provide fuel flexibility for gas turbines to burn coal derived synthesis gas or natural gas and achieve NO{sub x} emissions of 2 ppmvd or less (at 15 percent O{sub 2}), cost effectively. This advance will signify a major step towards environmentally friendly electric power generation and coal-based energy independence for the United States. Under Phase 1 of the Program, Pratt & Whitney (P&W) performed a system integration study of rich catalytic combustion in a small high-pressure ratio industrial gas turbine with a silo combustion system that is easily scalable to a larger multi-chamber gas turbine system. An implementation plan for this technology also was studied. The principal achievement of the Phase 1 effort was the sizing of the catalytic module in a manner which allowed a single reactor (rather than multiple reactors) to be used by the combustion system, a conclusion regarding the amount of air that should be allocated to the reaction zone to achieve low emissions, definition of a combustion staging strategy to achieve low emissions, and mechanical integration of a Ceramic Matrix Composite (CMC) combustor liner with the catalytic module.

Richard S. Tuthill

2004-06-10T23:59:59.000Z

349

2001 Workshop on Selective Catalytic Reduction  

Science Conference Proceedings (OSTI)

Approximately 100,000 megawatts of coal-fired capacity in the United States will employ selective catalytic reduction (SCR) for the control of nitrogen oxides (NOx) emissions by 2004. The 2001 Workshop on SCR, held in Baltimore, Maryland, provided a forum for discussion of current SCR issues.

2002-02-04T23:59:59.000Z

350

Archives and History Office: Features  

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

at SLAC and its components The Histories page provides publications that examine SLAC history or particular events, experiments, and equipment. The Nobel Prizes page provides...

351

Ny historia?; A new history?.  

E-Print Network (OSTI)

?? This essay aims to examine how three active history teachers in the upper secondary school interprets the new course plan for history in gy11.… (more)

Axelsson, Christofer

2010-01-01T23:59:59.000Z

352

ARM Orientation: Overview and History  

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

and History Overview and History Mar 2007 ARM Orientation 2 ARM ARM Atmospheric Radiation Measurement Atmospheric Radiation Measurement ARM Chief Scientist Team ARM Chief...

353

Puerto Rico Refinery Catalytic Hydrotreating, Kerosene/Jet Fuel ...  

U.S. Energy Information Administration (EIA)

Puerto Rico Refinery Catalytic Hydrotreating, Kerosene/Jet Fuel Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

354

Puerto Rico Refinery Catalytic Hydrocracking, Gas Oil Downstream ...  

U.S. Energy Information Administration (EIA)

Puerto Rico Refinery Catalytic Hydrocracking, Gas Oil Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

355

Colorado Refinery Catalytic Hydrotreating, Other/Residual Fuel Oil ...  

U.S. Energy Information Administration (EIA)

Colorado Refinery Catalytic Hydrotreating, Other/Residual Fuel Oil Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

356

U.S. Refinery Catalytic Hydrotreating, Heavy Gas Oil ...  

U.S. Energy Information Administration (EIA)

U.S. Refinery Catalytic Hydrotreating, Heavy Gas Oil Downstream Charge Capacity as of January 1 (Barrels per Stream Day)

357

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

358

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

359

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

360

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

Note: This page contains sample records for the topic "history catalytic 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

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

362

History | Department of Energy  

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

History History History On January 7, 2011, the President signed H.R. 6523 (111th), the Ike Skelton National Defense Authorization Act for Fiscal Year 2011 (http://www.govtrack.us/congress/bills/111/hr6523) which became Public Law 111-384. Section 3124 specifically states, "The Secretary of Energy may establish a program to permit the establishment of energy parks on former defense nuclear facilities" (50 U.S.C. 2814). In response, on February 17, 2011, the Department of Energy (DOE) established a Task Force on the ARI to address the legislation in detail. The purpose of the task force was to implement asset revitalization efforts in response to Congressional direction, and to develop recommendations for a continued formalized asset revitalization program. The task force achieved this through facilitating

363

PAFC History and Successes  

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

PAFC History and Successes PAFC History and Successes John Ferro Manager Product Development john.ferro@utcpower.com 2 2 AGENDA Company overview and history System description and applications Failure modes and life analysis Summary 3 3 Research Center Hamilton Sundstrand Pratt & Whitney Sikorsky UTC Power Otis Carrier UTC Fire & Security UNITED TECHNOLOGIES CORPORATION 18 th largest U.S. manufacturer (2009 list, Industry Week) 37 th largest U.S. corporation (2009 list, Fortune) 61 st largest publicly held manufacturer in the world (2009 list, Industry Week) Revenues: $58.7 billion (2008) Commercial & Residential Building Systems, Aerospace & Transportation, Industrial systems 4 UTC POWER Markets Transportation fuel cells Stationary fuel cells Global sales 5 continents 19 countries Space & defense

364

NTS_History.indd  

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

Atmospheric Nuclear Atmospheric Nuclear Weapons Testing 1951 - 1963 Battlefi eld of the Cold War The Nevada Test Site United States Department of Energy Volume I Of related interest: Origins of the Nevada Test Site by Terrence R. Fehner and F. G. Gosling The Manhattan Project: Making the Atomic Bomb * by F. G. Gosling The United States Department of Energy: A Summary History, 1977 - 1994 * by Terrence R. Fehner and Jack M. Holl * Copies available from the U.S. Department of Energy 1000 Independence Ave. S.W., Washington, DC 20585 Attention: Offi ce of History and Heritage Resources Telephone: 301-903-5431 DOE/MA-0003 Terrence R. Fehner & F. G. Gosling Offi ce of History and Heritage Resources Executive Secretariat Offi ce of Management Department of Energy September 2006 Battlefi eld of the Cold War

365

SRS - History Highlights  

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

3 3 SEARCH GO Side Menu Spacer SRS Mission & Vision Where We Are SRS History Fact Sheets Tour SRS Contact SRS SRS Home SRS History Highlights The Savannah River Site was constructed during the early 1950s to produce the basic materials used in the fabrication of nuclear weapons, primarily tritium and plutonium-239, in support of our nation's defense programs. Five reactors were built to produce these materials. Also built were a number of support facilities including two chemical separations plants, a heavy water extraction plant, a nuclear fuel and target fabrication facility, a tritium extraction facility and waste management facilities. If you wish to view an in-depth history (1950-2000), please explore SRS at Fifty, our 50th anniversary book. Browse by Era: 1950s * 1960s * 1970s * 1980s * 1990s * 2000s * 2010s

366

History | Department of Energy  

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

History History History Although they are tiny, atoms have a large amount of energy holding their nuclei together. Certain isotopes of some elements can be split and will release part of their energy as heat. This splitting is called fission. The heat released in fission can be used to help generate electricity in powerplants. Uranium-235 (U-235) is one of the isotopes that fissions easily. During fission, U-235 atoms absorb loose neutrons. This causes U-235 to become unstable and split into two light atoms called fission products. The combined mass of the fission products is less than that of the original U-235. The reduction occurs because some of the matter changes into energy. The energy is released as heat. Two or three neutrons are released along with the heat. These neutrons may hit other

367

Oral Histories: Merril Eisenbud  

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

6 6 HUMAN RADIATION STUDIES: REMEMBERING THE EARLY YEARS Oral History of Merril Eisenbud Conducted January 26, 1995 United States Department of Energy Office of Human Radiation Experiments May 1995 CONTENTS Foreword Short Biography Early Days as an Industrial Hygienist Hired as AEC's First Industrial Hygienist Insuring Atomic Workers Setting up the AEC's Health and Safety Laboratory Worker's Compensation History Contamination and Industrial Worker Education Federal Versus State Responsibility for Materials Production Safety Plant Safety and the Community Monitoring Radioactive Fallout Radiation and Cancer Rates Safety of the Nuclear Industry Use of Children in Research Developing Thyroid Radiation Counters Secrecy, Louis Strauss, and the Bravo Test Nuclear Test Fallout Studies

368

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

369

Management and organizational history: Prospects  

Science Conference Proceedings (OSTI)

We outline the prospects for Management & Organizational History in the form of a 10-point agenda identifying issues that we envisage being addressed in the journal. 1.The 'Historic Turn' in Organization Theory - calls for a more historical orientation ... Keywords: Management history, organizational history, organizational memory, philosophy of history

Charles Booth; Michael Rowlinson

2006-02-01T23:59:59.000Z

370

Catalytic Tri-reforming of Biomass-Derived Syngas to Produce Desired H2:CO Ratios for Fuel Applications.  

E-Print Network (OSTI)

??This study focuses on upgrading biomass derived syngas for the synthesis of liquid fuels using Fischer-Tropsch synthesis (FTS). The process includes novel gasification of biomass… (more)

Walker, Devin Mason

2012-01-01T23:59:59.000Z

371

History of Residential Grounding  

Science Conference Proceedings (OSTI)

This report describes the development of residential electrical service grounding practices in the United States. The report focuses on the history of the National Electrical Code (NEC), which prescribes standards for wiring practices in residences, including grounding of the building electrical service.

2002-09-19T23:59:59.000Z

372

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

373

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,

374

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

375

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

376

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

377

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 ...

378

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...

379

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

380

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

Note: This page contains sample records for the topic "history catalytic 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

An Energy Analysis of the Catalytic Combustion Burner  

E-Print Network (OSTI)

The gas boilers of conventional flame always produce varying degrees of combustion products NOx and CO, which pollute the environment and waste energy. As a new way of combustion, catalytic combustion breaks the flammable limits of conventional flame combustion, and realizes the combustion of ultra-natural gas/air mixture under the flammable limits. Its combustion efficiency is higher, which improves the ratio of energy utilization. Applying the catalytic combustion to gas boilers could solve the gas boilers' lower combustion efficiency, and achieve energy savings. On the basis of the catalytic combustion burner, the catalytic combustion burner was designed according to the catalytic combustion and water heaters. In this paper, we analyzed the heat loss and thermal efficiency of the catalytic combustion burner, and compared it to that of flame combustion boilers. The results showed that catalytic combustion burner ?'s heat loss is not so high as originally considered, and its pollutant emissions are lower.

Dong, Q.; Zhang, S.; Duan, Z.; Zhou, Q.

2006-01-01T23:59:59.000Z

382

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

383

Endothermic photo-catalytic reactions. Final report  

SciTech Connect

The overall objective of this report is to present the results of an investigation to provide guidelines for future experimental work, on solar energy driven endothermic photo-catalytic reactions, and primarily to select candidate synthesis reactions which lead to high $-value products. An intensive literature search was conducted to find properties, market demand, and prices of pertinent chemicals; meeting four criteria: (1) the reaction must be endothermic and favorable; (2) the reaction must be catalytic; (3) the product must be produced from low cost feedstocks; and (4) the product must have a sales price >$1.00/lb. Initial examination of low cost feedstocks to high value products lead to consideration of n-paraffins to aromatics and substituted aromatics. Fifteen candidate endothermic synthesis reactions, meeting the above criteria, are suggested. The ratio of product price by reactant cost indicates {approximately}5--8 for the best possibilities; all can be visualized as starting with low cost paraffin and methanol feedstocks.

Prengle, H.W. Jr.; Wentworth, W.E.; Polonczyk, K.C.; Saghafi, M.; Wilking, J.A.; Kramer, K.S. [Houston Univ., TX (United States)

1992-04-01T23:59:59.000Z

384

Database - Selective Catalytic Reduction Catalyst Deactivation Rates  

Science Conference Proceedings (OSTI)

Selective catalytic reduction (SCR) catalyst deactivation is a critical parameter controlling to a large extent achievable catalyst life, as well as overall SCR system performance. Accurate assessment and prediction of catalyst deactivation is required to adequately manage reactor potential. EPRI has on-going efforts underway aimed at better understanding the factors that affect catalyst deactivation, especially as a function of fuel, boiler design, and boiler operating conditions, in hopes of ...

2013-11-06T23:59:59.000Z

385

2006 Workshop on Selective Catalytic Reduction  

Science Conference Proceedings (OSTI)

EPRI held the 2006 Workshop on Selective Catalytic Reduction (SCR) on October 31 November 2, 2006 at the Dearborn Inn in Dearborn, Michigan and at DTE Energy's Monroe Station. Post-Combustion NOX Control Program members, invited speakers, and EPRI staff participated in this two and a half day event. The workshop agenda was comprised of twenty-seven presentations, two panel discussions, and a plant tour. Operating experience reports on SCR systems at Baldwin, Bowen, Bull Run, Crist, Cumberland, Gaston, Go...

2007-03-07T23:59:59.000Z

386

Preconversion catalytic deoxygenation of phenolic functional groups  

Science Conference Proceedings (OSTI)

The deoxygenation of phenols is a conceptually simple, but unusually difficult chemical transformation to achieve. Aryl carbon-oxygen bond cleavage is a chemical transformation of importance in coal liquefaction and the upgrading of coal liquids as well as in the synthesis of natural products. This proposed research offers the possibility of effecting the selective catalytic deoxygenation of phenolic functional groups using CO. A program of research for the catalytic deoxygenation of phenols, via a low energy mechanistic pathway that is based on the use of the CO/CO{sub 2} couple to remove phenolic oxygen atoms, is underway. We are focusing on systems which have significant promise as catalysts: Ir(triphos)OPh, (Pt(triphos)OPh){sup +} and Rh(triphos)OPh. Our studies of phenol deoxygenation focus on monitoring the reactions for the elementary processes upon which catalytic activity will depend: CO insertion into M-OPh bonds, CO{sub 2} elimination from aryloxy carbonyls {l brace}M-C(O)-O-Ph{r brace}, followed by formation of a coordinated benzyne intermediate.

Kubiak, C.P.

1991-01-01T23:59:59.000Z

387

A revolution in micropower : the catalytic nanodiode.  

DOE Green Energy (OSTI)

Our ability to field useful, nano-enabled microsystems that capitalize on recent advances in sensor technology is severely limited by the energy density of available power sources. The catalytic nanodiode (reported by Somorjai's group at Berkeley in 2005) was potentially an alternative revolutionary source of micropower. Their first reports claimed that a sizable fraction of the chemical energy may be harvested via hot electrons (a 'chemicurrent') that are created by the catalytic chemical reaction. We fabricated and tested Pt/GaN nanodiodes, which eventually produced currents up to several microamps. Our best reaction yields (electrons/CO{sub 2}) were on the order of 10{sup -3}; well below the 75% values first reported by Somorjai (we note they have also been unable to reproduce their early results). Over the course of this Project we have determined that the whole concept of 'chemicurrent', in fact, may be an illusion. Our results conclusively demonstrate that the current measured from our nanodiodes is derived from a thermoelectric voltage; we have found no credible evidence for true chemicurrent. Unfortunately this means that the catalytic nanodiode has no future as a micropower source.

Cross, Karen Charlene; Heller, Edwin J.; Figiel, Jeffrey James; Coker, Eric Nicholas; Creighton, James Randall; Koleske, Daniel David; Bogart, Katherine Huderle Andersen; Coltrin, Michael Elliott; Pawlowski, Roger Patrick; Baucom, Kevin C.

2010-11-01T23:59:59.000Z

388

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

389

VarPetrRef 1 VARIETY AND THE EVOLUTION OF REFINERY PROCESSING  

E-Print Network (OSTI)

. Catalytic reforming followed as a means of upgrading the octane of gasoline range materials principally): Catalytic reforming, Isomerization, Alkylation, Catalytic polymerization, MTBE and Hydrotreating. The last Distillation Visbreaking Hydrotreating Hydrocracking Thermal Reforming Alkylation MTBE Catalytic Reform ing

Paris-Sud XI, Université de

390

Mound History and Information  

Office of Legacy Management (LM)

Mound Site History and Information Mound Site History and Information The Mound site, formerly known as the Mound Plant or Facility, takes its name from a nearby Na- tive American burial mound. The 306 acre facility is sited on a hill in the center of Miamisburg, Ohio. Construction of the Mound Plant began in 1946, and the site became operational in 1949. Mound, the nation's first post-war U.S. Atomic Energy Commission site to be constructed, was established to consolidate and continue the work conducted at the Dayton Units for the Manhattan Project. Much of the work at the Mound Plant during the Cold War involved production of the polonium- beryllium initiators used in early atomic weapons and the manufacture of and research related to ra- dionuclides. In the 1950s, the facility began to

391

About Fermilab - History  

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

What is Fermilab? What is Fermilab? what is Fermilab main page | mission | history | Enrico Fermi History - Wilson Hall Beauvais Cathedral A daring achievement of Gothic architecture, the Saint-Pierre Cathedral of Beauvais, France helped inspire the distinctive design of Wilson Hall. The Cathedral (A.D. 1225-1568) was never completed westward of the choir and transepts, and the site of the proposed nave is partly occupied by the Romanesque church known as the "Basse oeuvre" ("low work"). The roof fell (A.D. 1284); the choir was reconstructed and strengthened by additional piers (A.D. 1337-47), and in the 16th century the transepts were built. The height of the vault (157 ft., 6 ins.) is the loftiest in Europe, and measures about three and a half times its span. One of the most daring

392

BNL | Our History: Accelerators  

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

> See also: Reactors > See also: Reactors A History of Leadership in Particle Accelerator Design Cosmotron Cosmotron (1952-1966) Early in Brookhaven Lab history, the consortium of universities responsible for founding the new research center, decided that Brookhaven should provide leading facilities for high energy physics research. In April 1948, the Atomic Energy Commission approved a plan for a proton synchrotron to be built at Brookhaven. The new machine would accelerate protons to previously unheard of energies-comparable to the cosmic rays showering the earth's outer atmosphere. It would be called the Cosmotron. The Cosmotron was the first accelerator in the world to send particles to energies in the billion electron volt, or GeV, region. The machine reached its full design energy of 3.3 GeV in 1953.

393

RMOTC - About Us - History  

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

History History Teapot Dome Scandal Teapot Dome was the popular name for the scandal during the administration of U.S. President Warren G. Harding. The scandal, which involved the secret leasing of naval oil reserve lands to private companies, was first revealed to the general public in 1924 after findings by a committee of the U.S. Senate. Teapot Rock, From which the famous Teapot Dome derives its name The creation of the Naval Petroleum Reserves originated with the growth of federal conservation policy under presidents Theodore Roosevelt, William Howard Taft, and Woodrow Wilson. The reserves were tracts of public land where oil should be kept in its natural reservoirs for the future use of the Navy. "Teapot Dome" originally acquired its name from a rock nearby

394

Reading Comprehension - Atomic History  

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

Atomic History Atomic History A Greek philosopher named Democritus said that all atoms are small, hard particles. He thought that atoms were made of a single material formed into different shapes and sizes. The word " _________ element compound mixture atom " is derived from the Greek word "atomos" which means "not able to be divided." In 1803, John Dalton, a school teacher, proposed his atomic theory. Dalton's theory states that elements (substances composed of only one type of _________ molecules ions atom ) combine in certain proportions to form _________ compounds atoms mixtures elements . In 1897, a British scientist named J. J. Thomson experimented with a cathode-ray tube which had a positively charged plate. The plate attracted negatively charged particles that we now call _________ protons neutrons

395

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

396

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

397

NERSC Systems History  

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

History of Systems History of Systems History of Systems Established in 1974 at Lawrence Livermore National Laboratory, NERSC was moved to Berkeley Lab in 1996 with a goal of increased interactions with the UC Berkeley campus. NERSC Systems System Name Installed System Type CPU Computational Pool Interconnect Disk (TB) Avg. Power Linpack HPL/ Top Rank Peak GFlops/s Type Speed Nodes SMP Size Total Cores Aggregate Memory (GB) Avg. Memory/ CPU Edison 2013 Cray XC30 Xeon 12-Core 2.3 GHz 5,200 24 124,800 332,800 2.67GB Hopper 2010 Cray XE6 Opteron Hex-Core 2.1 GHz 6,384 24 153,216 216,832 1.3 GB Gemini 2,000 1,054,000 (5) 1,054,000 Carver 2010 IBM iDataPlex Intel Nehalem Quad-Core 2.6 GHz 400 8 3,200 9,600 3 GB 4X QDR InfiniBand NGF 36,856 (322) 42,656

398

Bellona rapport nr. 6 -2002 Bjrnar Kruse Sondre Grinna Cato Buch  

E-Print Network (OSTI)

Distillation High Vacuum Distillation Hydrotreating Isomerisation Catalytic Reforming Alkylation Polymerisation Atmospheric Distillation High Vacuum Distillation Hydrotreating Isomerisation Catalytic Reforming Alkylation

Krothapalli, Anjaneyulu

399

2002 Workshop on Selective Catalytic Reduction  

Science Conference Proceedings (OSTI)

Approximately 100,000 MW of coal-fired generating capacity in the United States will be equipped with selective catalytic reduction (SCR) systems to meet the nitrogen oxides (NOx) limits of the state implementation plan (SIP) call. Approximately 20,000 MW of capacity was expected to go into operation in 2002. Added to early SCR adopters in prior years, about 25 percent of the planned inventory is presently operable. Since 1999, EPRI has organized annual SCR workshops to discuss key issues and development...

2003-01-30T23:59:59.000Z

400

2003 Workshop on Selective Catalytic Reduction  

Science Conference Proceedings (OSTI)

Approximately 105,000 MW of coal-fired generating capacity in the United States will be equipped with selective catalytic reduction (SCR) systems to meet the nitrogen oxide (NOx) limits of the state implementation plan (SIP). Power producers placed approximately 40,000 MW of capacity into operation in 2003. Combined with early SCR adopters from prior years, about 65 percent of the planned inventory is presently operable. Since 1999, EPRI has organized and held annual SCR workshops to discuss key issues a...

2004-02-09T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

Catalytic multi-stage liquefaction (CMSL)  

DOE Green Energy (OSTI)

Under contract with the U.S. Department of Energy, Hydrocarbon Technologies, Inc. has conducted a series of eleven catalytic, multi-stage, liquefaction (CMSL) bench scale runs between February, 1991, and September, 1995. The purpose of these runs was to investigate novel approaches to liquefaction relating to feedstocks, hydrogen source, improved catalysts as well as processing variables, all of which are designed to lower the cost of producing coal-derived liquid products. This report summarizes the technical assessment of these runs, and in particular the evaluation of the economic impact of the results.

Comolli, A.G.; Ganguli, P.; Karolkiewicz, W.F.; Lee, T.L.K.; Pradhan, V.R.; Popper, G.A.; Smith, T.; Stalzer, R.

1996-11-01T23:59:59.000Z

402

Photon: history, mass, charge  

E-Print Network (OSTI)

The talk consists of three parts. ``History'' briefly describes the emergence and evolution of the concept of photon during the first two decades of the 20th century. ``Mass'' gives a short review of the literature on the upper limit of the photon's mass. ``Charge'' is a critical discussion of the existing interpretation of searches for photon charge. Schemes, in which all photons are charged, are grossly inconsistent. A model with three kinds of photons (positive, negative and neutral) seems at first sight to be more consistent, but turns out to have its own serious problems.

L. B. Okun

2006-02-03T23:59:59.000Z

403

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

404

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

405

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

406

CATALYTIC CONVERSION OF SOLVENT REFINED COAL TO LIQUID PRODUCTS  

E-Print Network (OSTI)

and Friedman, S. ,"Conversion of Anthraxylon - Kinetics ofiv- LBL 116807 CATALYTIC CONVERSION OF SOLVENT REFINED COALand Mechanisms of Coal Conversion to Clean Fuel,iI pre-

Tanner, K.I.

2010-01-01T23:59:59.000Z

407

Catalytic conversion of cellulose to liquid hydrocarbon fuels ...  

Catalytic conversion of cellulose to liquid hydrocarbon fuels by progressive removal of oxygen to facilitate separation processes and achieve high selectivities

408

Revealing the rapid isothermal growth of graphene on catalytic...  

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

Materials Synthesis from Atoms to Systems Revealing the rapid isothermal growth of graphene on catalytic substrates July 01, 2013 Optical reflectivity tracks the rapid growth of...

409

Hydrogen-assisted catalytic ignition characteristics of different fuels  

SciTech Connect

Hydrogen-assisted catalytic ignition characteristics of methane (CH{sub 4}), n-butane (n-C{sub 4}H{sub 10}) and dimethyl ether (DME) were studied experimentally in a Pt-coated monolith catalytic reactor. It is concluded that DME has the lowest catalytic ignition temperature and the least required H{sub 2} flow, while CH{sub 4} has the highest catalytic ignition temperature and the highest required H{sub 2} flow among the three fuels. (author)

Zhong, Bei-Jing; Yang, Fan [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Engineering Mechanics, Tsinghua University, Beijing 100084 (China); Yang, Qing-Tao [Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Engineering Mechanics, Tsinghua University, Beijing 100084 (China); China Aerodynamics Research and Development Center, Mianyang 621000 (China)

2010-10-15T23:59:59.000Z

410

Piloted rich-catalytic lean-burn hybrid combustor  

DOE Patents (OSTI)

A catalytic combustor assembly which includes, an air source, a fuel delivery means, a catalytic reactor assembly, a mixing chamber, and a means for igniting a fuel/air mixture. The catalytic reactor assembly is in fluid communication with the air source and fuel delivery means and has a fuel/air plenum which is coated with a catalytic material. The fuel/air plenum has cooling air conduits passing therethrough which have an upstream end. The upstream end of the cooling conduits is in fluid communication with the air source but not the fuel delivery means.

Newburry, Donald Maurice (Orlando, FL)

2002-01-01T23:59:59.000Z

411

Catalytic Acceleration of Carbon Capture via Bio-processes  

Science Conference Proceedings (OSTI)

Recently, transformation of the biomass into fuels such as bioethanol, biodiesel or functional chemicals by means of catalytic and enzymatic conversion has ...

412

Multi-step catalytic hydroprocessing to produce hydrocarbon fuels ...  

Multi-step catalytic hydroprocessing to produce hydrocarbon fuels from biomass pyrolysis bio-oil (PNNL IPID 16665) Pacific Northwest National Laboratory

413

Catalytic distillation for the synthesis of tertiary butyl alcohol.  

E-Print Network (OSTI)

??Catalytic Distillation for the synthesis of tertiary butyl alcohol (TBA) is investigated in this thesis. The solvent, ethylene glycol, is proposed as a means of… (more)

Safinski, Tomasz

2005-01-01T23:59:59.000Z

414

FEEDSTOCK-FLEXIBLE REFORMER SYSTEM (FFRS) FOR SOLID OXIDE FUEL CELL (SOFC)- QUALITY SYNGAS  

DOE Green Energy (OSTI)

The U.S. Department of Energy National Energy Technology Laboratory funded this research collaboration effort between NextEnergy and the University of Michigan, who successfully designed, built, and tested a reformer system, which produced highquality syngas for use in SOFC and other applications, and a novel reactor system, which allowed for facile illumination of photocatalysts. Carbon and raw biomass gasification, sulfur tolerance of non-Platinum Group Metals (PGM) based (Ni/CeZrO2) reforming catalysts, photocatalysis reactions based on TiO2, and mild pyrolysis of biomass in ionic liquids (ILs) were investigated at low and medium temperatures (primarily 450 to 850 C) in an attempt to retain some structural value of the starting biomass. Despite a wide range of processes and feedstock composition, a literature survey showed that, gasifier products had narrow variation in composition, a restriction used to develop operating schemes for syngas cleanup. Three distinct reaction conditions were investigated: equilibrium, autothermal reforming of hydrocarbons, and the addition of O2 and steam to match the final (C/H/O) composition. Initial results showed rapid and significant deactivation of Ni/CeZrO2 catalysts upon introduction of thiophene, but both stable and unstable performance in the presence of sulfur were obtained. The key linkage appeared to be the hydrodesulfurization activity of the Ni reforming catalysts. For feed stoichiometries where high H2 production was thermodynamically favored, stable, albeit lower, H2 and CO production were obtained; but lower thermodynamic H2 concentrations resulted in continued catalyst deactivation and eventual poisoning. High H2 levels resulted in thiophene converting to H2S and S surface desorption, leading to stable performance; low H2 levels resulted in unconverted S and loss in H2 and CO production, as well as loss in thiophene conversion. Bimetallic catalysts did not outperform Ni-only catalysts, and small Ni particles were found to have lower activities under S-free conditions, but did show less effect of S on performance, in this study. Imidazolium-based ILs, choline chloride compounds and low-melting eutectics of metal nitrates were evaluated, and it was found that, ILs have some capacity to dissolve cellulose and show thermal stability to temperatures where pyrolysis begins, have no vapor pressure, (simplifying product recoveries), and can dissolve ionic metal salts, allowing for the potential of catalytic reactions on breakdown intermediates. Clear evidence of photoactive commercial TiO2 was obtained, but in-house synthesis of photoactive TiO2 proved difficult, as did fixed-bed gasification, primarily due to the challenge of removing the condensable products from the reaction zone quickly enough to prevent additional reaction. Further investigation into additional non-PGM catalysts and ILs is recommended as a follow-up to this work.

Kelly Jezierski; Andrew Tadd; Johannes Schwank; Roland Kibler; David McLean; Mahesh Samineni; Ryan Smith; Sameer Parvathikar; Joe Mayne; Tom Westrich; Jerry Mader; F. Michael Faubert

2010-07-30T23:59:59.000Z

415

U.S. Downstream Processing of Fresh Feed Input  

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

2007 2008 2009 2010 2011 2012 View History Catalytic Reforming 2,632 2,571 2,606 2010-2012 Catalytic Cracking 5,250 4,983 4,957 4,873 4,952 4,901 1987-2012 Catalytic Hydrocracking...

416

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

417

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

418

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

419

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

420

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

Note: This page contains sample records for the topic "history catalytic 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

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

422

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

423

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

424

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...

425

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

426

Archives and History Office: Others' Resources  

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

University Historical Photographs Collection Stanford Historical Society (SHS) History of the Stanford Physics Department History of the Ginzton Lab History of science,...

427

Homogeneity Analysis of Event History Data  

E-Print Network (OSTI)

phrases. Correspondence Analysis, Event History Data. JAN DEHOMOGENEITY ANALYSIS OF EVENT HISTORY DATA JAN DE LEEUW,Kreft, Homogeneity Analysis of Event History Data. Methods

Leeuw, Jan de; Heijden, Peter van der; Kreft, Ita

2010-01-01T23:59:59.000Z

428

Homogeneity Analysis of Event History Data  

E-Print Network (OSTI)

phrases. Correspondence Analysis, Event History Data. JAN DEHOMOGENEITY ANALYSIS OF EVENT HISTORY DATA JAN DE LEEUW,Kreft, Homogeneity Analysis of Event History Data. Methods

Jan de Leeuw; Peter van der Heijden; Ita Kreft

2011-01-01T23:59:59.000Z

429

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

430

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

431

History | Argonne National Laboratory  

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

Argonne's Nobelists Argonne's Nobelists Three Argonne physicists have been honored with Nobel Prizes: Enrico Fermi, Argonne's founding director, won the 1938 Nobel Prize in physics for his demonstrations of the existence of new radioactive elements produced by neutron irradiation and for his related discovery of nuclear reactions brought about by slow neutrons. Maria Goeppert Mayer shared the 1963 Nobel Prize in physics. While working at Argonne in 1948, she developed the "nuclear shell model" to explain how neutrons and protons within atomic nuclei are structured. Alexei A. Abrikosov shared the 2003 Nobel Prize in physics for research on condensed-matter physics and superconductivity. Our history sparked the nation's future AVIDAC, Argonne's first digital computer, began operation in January 1953.

432

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

433

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

434

Catalytic cartridge SO.sub.3 decomposer  

DOE Patents (OSTI)

A catalytic cartridge surrounding a heat pipe driven by a heat source is utilized as a SO.sub.3 decomposer for thermochemical hydrogen production. The cartridge has two embodiments, a cross-flow cartridge and an axial flow cartridge. In the cross-flow cartridge, SO.sub.3 gas is flowed through a chamber and incident normally to a catalyst coated tube extending through the chamber, the catalyst coated tube surrounding the heat pipe. In the axial-flow cartridge, SO.sub.3 gas is flowed through the annular space between concentric inner and outer cylindrical walls, the inner cylindrical wall being coated by a catalyst and surrounding the heat pipe. The modular cartridge decomposer provides high thermal efficiency, high conversion efficiency, and increased safety.

Galloway, Terry R. (Berkeley, CA)

1982-01-01T23:59:59.000Z

435

Catalytic carbon membranes for hydrogen production  

DOE Green Energy (OSTI)

Commercial carbon composite microfiltration membranes may be modified for gas separation applications by providing a gas separation layer with pores in the 1- to 10-nm range. Several organic polymeric precursors and techniques for depositing a suitable layer were investigated in this project. The in situ polymerization technique was found to be the most promising, and pure component permeation tests with membrane samples prepared with this technique indicated Knudsen diffusion behavior. The gas separation factors obtained by mixed-gas permeation tests were found to depend strongly on gas temperature and pressure indicating significant viscous flow at high-pressure conditions. The modified membranes were used to carry out simultaneous water gas shift reaction and product hydrogen separation. These tests indicated increasing CO conversions with increasing hydrogen separation. A simple process model was developed to simulate a catalytic membrane reactor. A number of simulations were carried out to identify operating conditions leading to product hydrogen concentrations over 90 percent. (VC)

Damle, A.S.; Gangwal, S.K.

1992-01-01T23:59:59.000Z

436

Catalytic cartridge SO/sub 3/ decomposer  

DOE Patents (OSTI)

A catalytic cartridge surrounding a heat pipe driven by a heat source is utilized as a SO/sub 3/ decomposer for thermochemical hydrogen production. The cartridge has two embodiments, a cross-flow cartridge and an axial flow cartridge. In the cross-flow cartridge, SO/sub 3/ gas is flowed through a chamber and incident normally to a catalyst coated tube extending through the chamber, the catalyst coated tube surrounding the heat pipe. In the axial-flow cartridge, SO/sub 3/ gas is flowed through the annular space between concentric inner and outer cylindrical walls, the inner cylindrical wall being coated by a catalyst and surrounding the heat pipe. The modular cartridge decomposer provides high thermal efficiency, high conversion efficiency, and increased safety. A fusion reactor may be used as the heat source.

Galloway, T.R.

1980-11-18T23:59:59.000Z

437

Contact structure for use in catalytic distillation  

DOE Patents (OSTI)

A method and apparatus for conducting catalytic chemical reactions and fractionation of the reaction mixture, comprising and feeding reactants into a distillation column reactor contracting said reactant in a liquid phase with a fixed bed catalyst in the form of a contact catalyst structure, consisting of closed porous containers containing the catalyst for the reaction and a clip means to hold and support said containers, which are disposed above, i.e., on the distillation trays in the tower. The trays have weir means to provide a liquid level on the trays to substantially cover the containers. In other words, the trays function in their ordinary manner with the addition thereto of the catalyst. The reaction mixture is concurrently fractionated in the column.

Jones, Jr., Edward M. (Friendswood, TX)

1985-01-01T23:59:59.000Z

438

Contact structure for use in catalytic distillation  

DOE Patents (OSTI)

A method is described for conducting catalytic chemical reactions and fractionation of the reaction mixture comprising feeding reactants into a distillation column reactor, contracting said reactant in liquid phase with a fixed bed catalyst in the form of a contact catalyst structure consisting of closed porous containers containing the catalyst for the reaction and a clip means to hold and support said containers, which are disposed above, i.e., on the distillation trays in the tower. The trays have weir means to provide a liquid level on the trays to substantially cover the containers. In other words, the trays function in their ordinary manner with the addition thereto of the catalyst. The reaction mixture is concurrently fractionated in the column. 7 figs.

Jones, E.M. Jr.

1984-03-27T23:59:59.000Z

439

Contact structure for use in catalytic distillation  

DOE Patents (OSTI)

A method for conducting catalytic chemical reactions and fractionation of the reaction mixture comprising feeding reactants into a distillation column reactor contracting said reactant in liquid phase with a fixed bed catalyst in the form of a contact catalyst structure consisting of closed porous containers containing the catatlyst for the reaction and a clip means to hold and support said containers, which are disposed above, i.e., on the distillation trays in the tower. The trays have weir means to provide a liquid level on the trays to substantially cover the containers. In other words, the trays function in their ordinary manner with the addition thereto of the catalyst. The reaction mixture is concurrently fractionated in the column.

Jones, Jr., Edward M. (Friendswood, TX)

1984-01-01T23:59:59.000Z

440

Contact structure for use in catalytic distillation  

DOE Patents (OSTI)

A method and apparatus are disclosed for conducting catalytic chemical reactions and fractionation of the reaction mixture, comprising and feeding reactants into a distillation column reactor contracting said reactant in a liquid phase with a fixed bed catalyst in the form of a contact catalyst structure, consisting of closed porous containers containing the catalyst for the reaction and a clip means to hold and support said containers, which are disposed above, i.e., on the distillation trays in the tower. The trays have weir means to provide a liquid level on the trays to substantially cover the containers. In other words, the trays function in their ordinary manner with the addition thereto of the catalyst. The reaction mixture is concurrently fractionated in the column. 7 figs.

Jones, E.M. Jr.

1985-08-20T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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

Simulation of catalytic oxidation and selective catalytic NOx reduction in lean-exhaust hybrid vehicles  

DOE Green Energy (OSTI)

We utilize physically-based models for diesel exhaust catalytic oxidation and urea-based selective catalytic NOx reduction to study their impact on drive cycle performance of hypothetical light-duty diesel powered hybrid vehicles. The models have been implemented as highly flexible SIMULINK block modules that can be used to study multiple engine-aftertreatment system configurations. The parameters of the NOx reduction model have been adjusted to reflect the characteristics of Cu-zeolite catalysts, which are of widespread current interest. We demonstrate application of these models using the Powertrain System Analysis Toolkit (PSAT) software for vehicle simulations, along with a previously published methodology that accounts for emissions and temperature transients in the engine exhaust. Our results illustrate the potential impact of DOC and SCR interactions for lean hybrid electric and plug-in hybrid electric vehicles.

Gao, Zhiming [ORNL; Daw, C Stuart [ORNL; Chakravarthy, Veerathu K [ORNL

2012-01-01T23:59:59.000Z

442

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

443

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

444

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

445

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

446

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

447

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

448

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

449

Archives and History Office: Credits  

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

Information" portion of the site provided highlights and milestones of SLAC history, information about the Nobel Prizes won for research completed at SLAC, and responses...

450

Archives and History Office: Welcome  

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

photon science, accelerator and particle physics research. SLAC's Archives and History Office is a coordinate archive to the Stanford University Archives. As such, it...

451

Archives and History Office: Resources  

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

Resources Resources Information from the SLAC Archives and History Office can be found using the following tools. Historical Photographs provides an interface to our photograph...

452

Revised History of Fort Watauga.  

E-Print Network (OSTI)

??The history of the Revolutionary War Fort Watauga located in present day Elizabethton, TN has yet to be completed. The critique of several Tennessee historians… (more)

Compton, Brian Patrick

2005-01-01T23:59:59.000Z

453

Archives and History Office: Projects  

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

Archives Prototype (TPAP) Project (2006) Persistent Archives Testbed (PAT) Project (2003-2006) Archives and History Office | Library | InfoMedia Solutions Last Updated: 1017...

454

History | Princeton Plasma Physics Lab  

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

Join Our Mailing List A Collaborative National Center for Fusion & Plasma Research Search form Search Search Home About Overview Learn More Visiting PPPL History...

455

Proposal to Designate an Emission Control Area for Nitrogen Oxides,  

E-Print Network (OSTI)

on a massive scale. These processes include catalytic reforming (to increase the octane number), catalytic

Hanson, Thomas

456

Introduction 1 2BChapter 1. Introduction  

E-Print Network (OSTI)

. These processes include catalytic reforming (to increase the octane number), catalytic cracking (to increase

Groningen, Rijksuniversiteit

457

Nowadays, removal of the sulphur generally takes place prior to the oxygen blowing, as the reduced state of the pig iron promotes the removal of the sulphur.  

E-Print Network (OSTI)

on a massive scale. These processes include catalytic reforming (to increase the octane number), catalytic

Groningen, Rijksuniversiteit

458

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:

459

A BRIEF HISTORY OF INDUSTRIAL CATALYSIS  

E-Print Network (OSTI)

Dealkylation Catalytic Coal Liquefaction and Gasification a)Liquefaction Gasification c) IX Methanation Heterogeneous~IQUEFACTION AND GASIFICATION a) Liquefaction Production of

Heinemann, Heinz

2013-01-01T23:59:59.000Z

460

Our History | Department of Energy  

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

Our History Our History Our History Our History The history of Office of Electricity Delivery and Energy Reliability (OE) begins in August 2003, when the Department created two offices to provide focus in several critical areas: the Office of Electric Transmission and Distribution (TD), which included elements from the DOE Energy Efficiency and Renewable Energy office and the DOE Policy and International Affairs office, to advance the technologies needed to ensure a reliable, robust and modern U.S. electricity grid; and the Office of Energy Assurance (EA), to coordinate Federal response activities within the energy sector during energy disruptions and developed strategies to harden infrastructure against such disruptions. On August 14, 2003, large portions of the Midwest and Northeast United

Note: This page contains sample records for the topic "history catalytic 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.


461

Year/PAD District Distillation Crude Oil Atmospheric Distillation  

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

Distillation Crude Oil Atmospheric Distillation Vacuum Cracking Thermal Catalytic Cracking Fresh Recycled Catalytic Hydro- Cracking Catalytic Reforming Desulfurization...

462

Catalytic Reactor For Oxidizing Mercury Vapor  

DOE Patents (OSTI)

A catalytic reactor (10) for oxidizing elemental mercury contained in flue gas is provided. The catalyst reactor (10) comprises within a flue gas conduit a perforated corona discharge plate (30a, b) having a plurality of through openings (33) and a plurality of projecting corona discharge electrodes (31); a perforated electrode plate (40a, b, c) having a plurality of through openings (43) axially aligned with the through openings (33) of the perforated corona discharge plate (30a, b) displaced from and opposing the tips of the corona discharge electrodes (31); and a catalyst member (60a, b, c, d) overlaying that face of the perforated electrode plate (40a, b, c) opposing the tips of the corona discharge electrodes (31). A uniformly distributed corona discharge plasma (1000) is intermittently generated between the plurality of corona discharge electrode tips (31) and the catalyst member (60a, b, c, d) when a stream of flue gas is passed through the conduit. During those periods when corona discharge (1000) is not being generated, the catalyst molecules of the catalyst member (60a, b, c, d) adsorb mercury vapor contained in the passing flue gas. During those periods when corona discharge (1000) is being generated, ions and active radicals contained in the generated corona discharge plasma (1000) desorb the mercury from the catalyst molecules of the catalyst member (60a, b, c, d), oxidizing the mercury in virtually simultaneous manner. The desorption process regenerates and activates the catalyst member molecules.

Helfritch, Dennis J. (Baltimore, MD)

1998-07-28T23:59:59.000Z

463

Development of high temperature catalytic membrane reactors  

DOE Green Energy (OSTI)

Significant progress was made in 1991 on the development of ceramic membranes as catalytic reactors. Efforts were focused on the design, construction and startup of a reactor system capable of duplicating relevant commercial operating conditions. With this system, yield enhancement was demonstrated for the dehydrogenation of ethylbenzene to styrene in a membrane reactor compared to the standard packed bed configuration. This enhancement came with no loss in styrene selectivity. During operation, coke deposition on the membrane was observed, but this deposition was mitigated by the presence of steam in the reaction mixture and a steady state permeability was achieved for run times in excess of 200 hours. Work began on optimizing the membrane reactor by exploring several parameters including the effect of N{sub 2} diluent in the reaction feed and the effect of a N{sub 2} purge on the permeate side of the membrane. This report details the experimental progress made in 1991. Interactions with the University of Wisconsin on this project are also summarized. Finally, current status of the project and next steps are outlined.

Not Available

1992-02-01T23:59:59.000Z

464

Catalytic oxidative pyrolysis of liquid fuels  

Science Conference Proceedings (OSTI)

The oxidative pyrolysis of n-heptane was investigated with metal oxides Cr/sub 2/O/sub 3/, MnO/sub 2/, Fe/sub 2/O/sub 3/, NiO, Co/sub 3/O/sub 4/, and CuO supported on alumina. Metallic content of the catalyst weight varied from 0.1 to 2.0% with catalytic activity reaching a maximum when the metal content was 1%. The most active catalysts were Co/sub 3/O/sub 4/, MnO/sub 2/, and NiO. Pyrolysis of cyclohexane and toluene was also studied with Co/sub 3/O/sub 4/-Al/sub 2/O/sub 3/ as catalyst. Hydrocarbon stability and coke formation increase with increase of hydrocarbon condensation in the series paraffin < naphthalene < aromatic hydrocarbons. Pyrolysis of the various hydrocarbons at 800/sup 0/C yielded a gas that has an octane number of 90 to 93, and the process was shown to be adaptable to pyrolysis of various commercial fractions such as benzines A-72 and A-76, petroleum fractions, and liquid paraffins to produce gas of about the same octane. (BLM)

Antonova, V.M.; Gorlov, E.G.; Paushkin, Ya.M.

1981-01-01T23:59:59.000Z

465

Catalytic Preparation of Pyrrolidones from Renewable Resources  

SciTech Connect

Use of renewable resources for production of valuable chemical commodities is becoming a topic of great national interest and importance. This objective fits well with the USDOE’s objective of promoting the industrial bio-refinery concept in which a wide array of valuable chemical, fuel, food, nutraceuticals and animal feed products all result from the integrated processing of grains, oil seeds and other bio-mass materials. The bio-refinery thus serves to enhance the overall utility and profitability of the agriculture industry as well as helping to reduce the dependence on petroleum. Pyrrolidones fit well with the bio-refinery concept since they may be produced in a scheme beginning with the fermentation of a portion of the bio-refinery’s sugar product into succinate. Pyrrolidones are a class of industrially important chemicals with a variety of uses including as polymer intermediates, cleaners, and “green solvents” which can replace hazardous chlorinated compounds. Battelle has developed an efficient process for the thermo – catalytic conversion of succinate into pyrrolidones, especially n-methylpyrrolidone. The process uses both novel Rh based catalysts and novel aqueous process conditions and results in high selectivities and yields of pyrrolidone compounds. The process also includes novel methodology for enhancing yields by recycling and converting non-useful side products of the catalysis into additional pyrrolidone. The process has been demonstrated in both batch and continuous reactors. Additionally, stability of the unique Rh-based catalyst has been demonstrated.

Frye, John G.; Zacher, Alan H.; Werpy, Todd A.; Wang, Yong

2005-12-01T23:59:59.000Z

466

Catalytic Preparation of Pyrrolidones from Renewable Resources  

SciTech Connect

Abstract Use of renewable resources for production of valuable chemical commodities is becoming a topic of great national interest and importance. This objective fits well with the U.S. DOE’s objective of promoting the industrial bio-refinery concept in which a wide array of valuable chemical, fuel, food, nutraceuticals, and animal feed products all result from the integrated processing of grains, oil seeds, and other bio-mass materials. The bio-refinery thus serves to enhance the overall utility and profitability of the agriculture industry as well as helping to reduce the USA’s dependence on petroleum. Pyrrolidones fit well into the bio-refinery concept since they may be produced in a scheme beginning with the fermentation of a portion of the bio-refinery’s sugar product into succinate. Pyrrolidones are a class of industrially important chemicals with a variety of uses including polymer intermediates, cleaners, and “green solvents” which can replace hazardous chlorinated compounds. Battelle has developed an efficient process for the thermo-catalytic conversion of succinate into pyrrolidones, especially n-methyl-2-pyrrolidone. The process uses both novel Rh based catalysts and novel aqueous process conditions and results in high selectivities and yields of pyrrolidone compounds. The process also includes novel methodology for enhancing yields by recycling and converting non-useful side products of the catalysis into additional pyrrolidone. The process has been demonstrated in both batch and continuous reactors. Additionally, stability of the unique Rh-based catalyst has been demonstrated.

Frye, John G.; Zacher, Alan H.; Werpy, Todd A.; Wang, Yong

2005-06-01T23:59:59.000Z

467

Catalytic pyrolysis using UZM-39 aluminosilicate zeolite  

Science Conference Proceedings (OSTI)

A new family of coherently grown composites of TUN and IMF zeotypes has been synthesized and show to be effective catalysts for catalytic pyrolysis of biomass. These zeolites are represented by the empirical formula. Na.sub.nM.sub.m.sup.n+R.sub.rQ.sub.qAl.sub1-xE.sub.xSi.sub.yO.s- ub.z where M represents zinc or a metal or metals from Group 1, Group 2, Group 3 or the lanthanide series of the periodic table, R is an A,.OMEGA.-dihalosubstituted paraffin such as 1,4-dibromobutane, Q is a neutral amine containing 5 or fewer carbon atoms such as 1-methylpyrrolidine and E is a framework element such as gallium. The process involves contacting a carbonaceous biomass feedstock with UZM-39 at pyrolysis conditions to produce pyrolysis gases comprising hydrocarbons. The catalyst catalyzes a deoxygenation reaction converting oxygenated hyrdocarbons into hydrocarbons removing the oxygen as carbon oxides and water. A portion of the pyrolysis gases is condensed to produce low oxygen biomass-derived pyrolysis oil.

Nicholas, Christpher P; Boldingh, Edwin P

2013-12-17T23:59:59.000Z

468

Microchannel Reactor System for Catalytic Hydrogenation  

Science Conference Proceedings (OSTI)

We successfully demonstrated a novel process intensification concept enabled by the development of microchannel reactors, for energy efficient catalytic hydrogenation reactions at moderate temperature, and pressure, and low solvent levels. We designed, fabricated, evaluated, and optimized a laboratory-scale microchannel reactor system for hydrogenation of onitroanisole and a proprietary BMS molecule. In the second phase of the program, as a prelude to full-scale commercialization, we designed and developed a fully-automated skid-mounted multichannel microreactor pilot plant system for multiphase reactions. The system is capable of processing 1 – 10 kg/h of liquid substrate, and an industrially relevant immiscible liquid-liquid was successfully demonstrated on the system. Our microreactor-based pilot plant is one-of-akind. We anticipate that this process intensification concept, if successfully demonstrated, will provide a paradigm-changing basis for replacing existing energy inefficient, cost ineffective, environmentally detrimental slurry semi-batch reactor-based manufacturing practiced in the pharmaceutical and fine chemicals industries.

Adeniyi Lawal; Woo Lee; Ron Besser; Donald Kientzler; Luke Achenie

2010-12-22T23:59:59.000Z

469

Catalytic Conversion of Ethanol to Hydrogen Using Combinatorial Shici Duan and Selim Senkan*  

E-Print Network (OSTI)

in this area focused on steam reforming of ethanol at relatively high temperatures (T > 500 °C), where carbon 0.5-5 wt %. Ethanol steam reforming activities and H2 selectivities of these 840 distinct materials reforming. Methane, methanol, and gaso- line, all of which are derived from fossil fuels, have long been

Senkan, Selim M.

470

Revolutionizing history education : using augmented reality games to teach histories  

E-Print Network (OSTI)

In an ever-changing present of multiple truths and reconfigured histories, people need to be critical thinkers. Research has suggested the potential for using augmented reality (AR) games- location-based games that use ...

Schrier, Karen L

2005-01-01T23:59:59.000Z

471

In situ XAS Characterization of Catalytic Nano-Materials with...  

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

XAS Characterization of Catalytic Nano-Materials with Applications to Fuel Cells and Batteries Friday, July 12, 2013 - 11:00am SLAC, Conference Room 137-322 Presented by Qingying...

472

Hydrogen permeable protective coating for a catalytic surface  

DOE Patents (OSTI)

A protective coating for a surface comprising a layer permeable to hydrogen, said coating being deposited on a catalyst layer; wherein the catalytic activity of the catalyst layer is preserved.

Liu, Ping (Irvine, CA); Tracy, C. Edwin (Golen, CO); Pitts, J. Roland (Lakewood, CO); Lee, Se-Hee (Lakewood, CO)

2007-06-19T23:59:59.000Z

473

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

474

NEPA History | Department of Energy  

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

History History NEPA History Selected documents providing historical information on NEPA. June 14, 2012 Federal Register Notices for DOE NEPA Guidelines and Regulations Historical compilation of Federal Register notices for DOE NEPA guidelines and regulations. December 31, 2009 Presidential Proclamation on the 40th Anniversary of the National Environmental Policy Act Proclamation of President Obama to "call upon all executive branch agencies to promote public involvement and transparency in their implementation of the National Environmental Policy Act." July 1, 1999 EPA's Section 309 Review: The Clean Air Act and NEPA This document discusses Section 309 of the Clean Air Act, which authorizes the Environmental Protection Agency to review certain proposed actions of

475

BRS "Symmetry", prehistory and history  

E-Print Network (OSTI)

Prehistory - Starting from 't Hooft's (1971) we have a short look at Taylor's and Slavnov's works (1971-72) and at the lectures given by Rouet and Stora in Lausanne-1973 which determine the transition from pre-history to history. History - We give a brief account of the main analyses and results of the BRS collaboration concerning the renormalized gauge theories, in particular the method of the regularization independent, algebraic renormalization, the algebraic proof of S-matrix unitarity and that of gauge choice independence of the renormalized physics. We conclude this report with a suggestion to the crucial question: what could remain of BRS invariance beyond perturbation theory.

Carlo M. Becchi

2011-07-06T23:59:59.000Z

476

Quantum Histories and Quantum Gravity  

E-Print Network (OSTI)

This paper reviews the histories approach to quantum mechanics. This discussion is then applied to theories of quantum gravity. It is argued that some of the quantum histories must approximate (in a suitable sense) to classical histories, if the correct classical regime is to be recovered. This observation has significance for the formulation of new theories (such as quantum gravity theories) as it puts a constraint on the kinematics, if the quantum/classical correspondence principle is to be preserved. Consequences for quantum gravity, particularly for Lorentz symmetry and the idea of "emergent geometry", are discussed.

Joe Henson

2009-01-26T23:59:59.000Z

477

Catalytic Transformation of Waste Carbon Dioxide into Valuable Products  

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

Catalytic Transformation of Waste Catalytic Transformation of Waste Carbon Dioxide into Valuable Products Background Many industrial processes contribute large amounts of carbon dioxide (CO 2 ) to the earth's atmosphere. In an effort to reduce the amount of CO 2 released to the atmosphere, the U.S. Department of Energy (DOE) is funding efforts to develop CO 2 capture and storage technologies. In addition to permanent storage of CO 2 in underground reservoirs, some

478

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

DOE Green Energy (OSTI)

This technology pathway case investigates the catalytic conversion of solubilized carbohydrate streams to hydrocarbon biofuels, utilizing data from recent efforts within the National Advanced Biofuels Consortium (NABC) in collaboration with Virent, Inc. Technical barriers and key research needs that should be pursued for the catalytic conversion of sugars pathway to be competitive with petroleum-derived gasoline-, diesel-, and jet-range hydrocarbon blendstocks have been identified.

Biddy, M.; Jones, S.

2013-03-01T23:59:59.000Z

479

Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

This document is the 2009 update to Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems, originally published in 2001. The landscape of selective catalytic reduction (SCR) technology has significantly changed since then and promises to continue to change in the coming years. Specifically, the number of SCR applications on coal-fired units has increased considerably beyond the 15 units operating in mid 2001. Approximately 120 GW of capacity are expected to utilize SCR for NOx co...

2009-12-17T23:59:59.000Z

480

Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

Timely and proper execution of operation and maintenance (O&M) activities may be a key factor in ensuring the successful function of selective catalytic reduction (SCR) systems. This report serves as the 2012 update of EPRI’s Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems, originally published in 2001 and updated annually. New and revised content this year includes: 1) recent developments in in situ NOx analyzers, including a ...

2012-12-05T23:59:59.000Z

Note: This page contains sample records for the topic "history catalytic 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.


481

Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

This report is the 2011 update of Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems, originally published in 2001 and updated annually. New and revised content this year includes: (1) an analysis of the performance of the U.S. fleet of selective catalytic reduction (SCR)equipped generating units in 2009, 2010, and 2011; (2) a discussion of experience in mitigating the role of arsenic in catalyst deactivation, including the addition of alkali material to the coal; (3) an updat...

2011-12-16T23:59:59.000Z

482

Making History : : The Role of History in Contemporary Native American Art  

E-Print Network (OSTI)

Michael. Kumeyaay: A History Textbook. El Cajon, CA: Sycuanby Magdalena Zapedowska, History and Theory, no. 45 (2006):Indian and the Problem of History, edited by Calvin Martin,

Cluff, Leah Diane

483

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

484

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

485

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

486

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

487

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

488

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

489

Taking stock of user interface history  

Science Conference Proceedings (OSTI)

The user interface is coming of age and papers adressing UI history have appeared in fair amounts in the last 25 years. Most of them address particular aspects such as an innovative interface paradigm or the contribution of a visionary or a research ... Keywords: HCI history, history of computing, history of technology, user interface history

Anker Helms Jřrgensen

2008-10-01T23:59:59.000Z

490

Integrated Biomass Gasification with Catalytic Partial Oxidation for Selective Tar Conversion  

SciTech Connect

Biomass gasification is a flexible and efficient way of utilizing widely available domestic renewable resources. Syngas from biomass has the potential for biofuels production, which will enhance energy security and environmental benefits. Additionally, with the successful development of low Btu fuel engines (e.g. GE Jenbacher engines), syngas from biomass can be efficiently used for power/heat co-generation. However, biomass gasification has not been widely commercialized because of a number of technical/economic issues related to gasifier design and syngas cleanup. Biomass gasification, due to its scale limitation, cannot afford to use pure oxygen as the gasification agent that used in coal gasification. Because, it uses air instead of oxygen, the biomass gasification temperature is much lower than well-understood coal gasification. The low temperature leads to a lot of tar formation and the tar can gum up the downstream equipment. Thus, the biomass gasification tar removal is a critical technology challenge for all types of biomass gasifiers. This USDA/DOE funded program (award number: DE-FG36-O8GO18085) aims to develop an advanced catalytic tar conversion system that can economically and efficiently convert tar into useful light gases (such as syngas) for downstream fuel synthesis or power generation. This program has been executed by GE Global Research in Irvine, CA, in collaboration with Professor Lanny Schmidt's group at the University of Minnesota (UoMn). Biomass gasification produces a raw syngas stream containing H2, CO, CO2, H2O, CH4 and other hydrocarbons, tars, char, and ash. Tars are defined as organic compounds that are condensable at room temperature and are assumed to be largely aromatic. Downstream units in biomass gasification such as gas engine, turbine or fuel synthesis reactors require stringent control in syngas quality, especially tar content to avoid plugging (gum) of downstream equipment. Tar- and ash-free syngas streams are a critical requirement for commercial deployment of biomass-based power/heat co-generation and biofuels production. There are several commonly used syngas clean-up technologies: (1) Syngas cooling and water scrubbing has been commercially proven but efficiency is low and it is only effective at small scales. This route is accompanied with troublesome wastewater treatment. (2) The tar filtration method requires frequent filter replacement and solid residue treatment, leading to high operation and capital costs. (3) Thermal destruction typically operates at temperatures higher than 1000oC. It has slow kinetics and potential soot formation issues. The system is expensive and materials are not reliable at high temperatures. (4) In-bed cracking catalysts show rapid deactivation, with durability to be demonstrated. (5) External catalytic cracking or steam reforming has low thermal efficiency and is faced with problematic catalyst coking. Under this program, catalytic partial oxidation (CPO) is being evaluated for syngas tar clean-up in biomass gasification. The CPO reaction is exothermic, implying that no external heat is needed and the system is of high thermal efficiency. CPO is capable of processing large gas volume, indicating a very compact catalyst bed and a low reactor cost. Instead of traditional physical removal of tar, the CPO concept converts tar into useful light gases (eg. CO, H2, CH4). This eliminates waste treatment and disposal requirements. All those advantages make the CPO catalytic tar conversion system a viable solution for biomass gasification downstream gas clean-up. This program was conducted from October 1 2008 to February 28 2011 and divided into five major tasks. - Task A: Perform conceptual design and conduct preliminary system and economic analysis (Q1 2009 ~ Q2 2009) - Task B: Biomass gasification tests, product characterization, and CPO tar conversion catalyst preparation. This task will be conducted after completing process design and system economics analysis. Major milestones include identification of syngas cleaning requirements for proposed system

Zhang, Lingzhi; Wei, Wei; Manke, Jeff; Vazquez, Arturo; Thompson, Jeff; Thompson, Mark

2011-05-28T23:59:59.000Z

491

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

492

EM History | Department of Energy  

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

EM History EM History EM History Before (left) and after (right) photos of the Hanford site's F Reactor during operations in 1956 and in 2012, when EM and its contractors completed cleanup there. It was the first reactor area at the 586-square-mile Hanford site to be fully remediated. Before (left) and after (right) photos of the Hanford site's F Reactor during operations in 1956 and in 2012, when EM and its contractors completed cleanup there. It was the first reactor area at the 586-square-mile Hanford site to be fully remediated. EM's HISTORY (1989 - present) Fifty years of nuclear weapons production and energy research generated millions of gallons of liquid radioactive waste, millions of cubic meters of solid radioactive wastes, thousands of tons of spent nuclear fuel and

<