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

Spectroscopic studies on the formation of coke on individual Fluid Catalytic Cracking particles: the effect of poisoning metal compounds.  

E-Print Network (OSTI)

??The formation of coke on individual Fluid Catalytic Cracking (FCC) catalyst particles was studied using UV/Vis microspectroscopy and confocal fluorescence microscopy, with n-hexane cracking as… (more)

Goetze, J.G.

2013-01-01T23:59:59.000Z

2

Fluid catalytic cracking is an important step in producing ...  

U.S. Energy Information Administration (EIA)

... (much as water makes sand into quicksand). Because the catalyst is fluid, it can circulate around the FCC, moving between reactor and regenerator vessels ...

3

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

4

Educating Consumers: New Content on Diesel Vehicles, Diesel Exhaust Fluid, and Selective Catalytic Reduction Technologies on the AFDC (Presentation)  

Science Conference Proceedings (OSTI)

Presentation covers new content available on the Alternative Fuels and Advanced Vehicle Data Center regarding diesel vehicles, diesel exhaust fluid, and selective catalytic reduction technologies.

Brodt-Giles, D.

2008-08-05T23:59:59.000Z

5

Hydrodesulfurization of Fluid Catalytic Cracking Decant Oils for the Production of Low-sulfur Needle Coke Feedstocks.  

E-Print Network (OSTI)

??Needle coke, produced by the delayed coking of fluid catalytic cracking decant oils, is the primary filler used in the production of graphite electrodes. The… (more)

Wincek, Ronald

2013-01-01T23:59:59.000Z

6

Investigation of Coal-biomass Catalytic Gasification using Experiments, Reaction Kinetics, and Computational Fluid Dynamics  

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

Coal-biomass Catalytic Coal-biomass Catalytic Gasification using Experiments, Reaction Kinetics, and Computational Fluid Dynamics Background The U.S. Department of Energy (DOE) supports research and development efforts targeted to improve efficiency and reduce the negative environmental effects of the use of fossil fuels. One way to achieve these goals is to combine coal with biomass to create synthesis gas (syngas) for use in turbines and refineries to produce energy, fuels,

7

Stepwise method determines source of FCC catalyst losses  

Science Conference Proceedings (OSTI)

A set of guidelines for fluid catalytic cracking unit (FCCU) monitoring and a logical, stepwise approach to troubleshooting FCC catalyst losses is discussed. This will help process or operations engineers find the causes of such losses. A thorough understanding of the entire catalyst stem during normal operations establishes the base line data necessary for troubleshooting. A comprehensive, ongoing analysis of catalyst losses include: catalyst balance, fresh catalyst physical properties, equilibrium catalyst properties, fine particle size distribution, pressure surveys, and line and restriction orifice records. The paper goes on to identify each step in monitoring these operations and properties.

Fletcher, R. [Akzo-Nobel Chemicals Inc., Houston, TX (United States)

1995-08-28T23:59:59.000Z

8

FCC LPG olefinicity and branching enhanced by octane catalysts  

SciTech Connect

Refiners are increasingly recognizing the downstream opportunities for fluid catalytic cracking LPG olefins for the production of methyl tertiary butyl ether (MTBE), ethyl tertiary butyl ether (ETBE, if the ethanol subsidy is extended to the production of ETBE), and as petrochemical feedstocks. Some of new gasoline FCC octane-enhancing catalysts can support those opportunities because their low non-framework alumina (low NFA) preserve both LPG olefinicity and promote branching of the LPG streams from the FCCU. The combined effect results in more isobutane for alkylate feed, more propylene in the propane/propylene stream, and more isobutene - which makes the addition of an MTBE unit very enticing.

Keyworth, D.A.; Reid, T.A.; Kreider, K.R.; Yatsu, C.A.

1989-05-29T23:59:59.000Z

9

Catalytic gasification studies in a pressurized fluid-bed unit  

DOE Green Energy (OSTI)

The purpose of the project is to evaluate the technical and economic feasibility of producing specific gas products via the catalytic gasification of biomass. This report presents the results of research conducted from October 1980 to November 1982. In the laboratory scale studis, active catalysts were developed for generation of synthesis gases from wood by steam gasification. A trimetallic catalyst, Ni-Co-Mo on silica-alumina doped with 2 wt % Na, was found to retain activity indefinitely for generation of a methanol synthesis gas from wood at 1380/sup 0/F (750/sup 0/C) and 1 atm (100 kPa) absolute pressure. Catalysts for generation of a methane-rich gas were deactivated rapidly and could not be regenerated as required for economic application. Sodium carbonate and potassium carbonate were effective as catalysts for conversion of wood to synthesis gases and methane-rich gas and should be economically viable. Catalytic gasification conditions were found to be suitable for processing of alternative feedstocks: bagasse, alfalfa, rice hulls, and almond hulls. The PDU was operated successfully at absolute pressures of up to 10 atm (1000 kPa) and temperatures of up to 1380/sup 0/F (750/sup 0/C). Yields of synthesis gases at elevated pressure were greater than those used for previous economic evaluations. A trimetallic catalyst, Ni-Cu-Mo on silica-alumina, did not display a long life as did the doped trimetallic catalyst used in laboratory studies. A computer program for a Radio Shack TRS-80 Model I microcomputer was developed to evaluate rapidly the economics of producing either methane or methanol from wood. The program is based on economic evaluations reported in previous studies. Improved yields from the PDU studies were found to result in a reduction of about 9 cents/gal in methanol cost.

Mudge, L.K.; Baker, E.G.; Mitchell, D.H.; Robertus, R.J.; Brown, M.D.

1983-07-01T23:59:59.000Z

10

Attrition Resistant Fischer-Tropsch Catalysts Based on FCC Supports  

SciTech Connect

Commercial spent fluid catalytic cracking (FCC) catalysts provided by Engelhard and Albemarle were used as supports for Fe-based catalysts with the goal of improving the attrition resistance of typical F-T catalysts. Catalysts with the Ruhrchemie composition (100 Fe/5 Cu/4.2 K/25 spent FCC on mass basis) were prepared by wet impregnation. XRD and XANES analysis showed the presence of Fe{sub 2}O{sub 3} in calcined catalysts. FeC{sub x} and Fe{sub 3}O{sub 4} were present in the activated catalysts. The metal composition of the catalysts was analyzed by ICP-MS. F-T activity of the catalysts activated in situ in CO at the same conditions as used prior to the attrition tests was measured using a fixed bed reactor at T = 573 K, P = 1.38 MPa and H{sub 2}:CO ratio of 0.67. Cu and K promoted Fe supported over Engelhard provided spent FCC catalyst shows relatively good attrition resistance (8.2 wt% fines lost), high CO conversion (81%) and C{sub 5}+ hydrocarbons selectivity (18.3%).

Adeyinka Adeyiga

2010-02-05T23:59:59.000Z

11

Attrition resistant catalysts and sorbents based on heavy metal poisoned FCC catalysts  

DOE Patents (OSTI)

A heavy metal poisoned, spent FCC catalyst is treated by chemically impregnating the poisoned catalyst with a new catalytic metal or metal salt to provide an attrition resistant catalyst or sorbent for a different catalytic or absorption processes, such as catalysts for Fischer-Tropsh Synthesis, and sorbents for removal of sulfur gasses from fuel gases and flue-gases. The heavy metal contaminated FCC catalyst is directly used as a support for preparing catalysts having new catalytic properties and sorbents having new sorbent properties, without removing or "passivating" the heavy metals on the spent FCC catalyst as an intermediate step.

Gangwal, Santosh (Cary, NC); Jothimurugesan, Kandaswamy (Hampton, VA)

1999-01-01T23:59:59.000Z

12

Attrition resistant catalysts and sorbents based on heavy metal poisoned FCC catalysts  

DOE Patents (OSTI)

A heavy metal poisoned, spent FCC catalyst is treated by chemically impregnating the poisoned catalyst with a new catalytic metal or metal salt to provide an attrition resistant catalyst or sorbent for a different catalytic or absorption process, such as catalysts for Fischer-Tropsh Synthesis, and sorbents for removal of sulfur gases from fuel gases and flue-gases. The heavy metal contaminated FCC catalyst is directly used as a support for preparing catalysts having new catalytic properties and sorbents having new sorbent properties, without removing or passivating the heavy metals on the spent FCC catalyst as an intermediate step.

Gangwal, S.; Jothimurugesan, K.

1999-07-27T23:59:59.000Z

13

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

14

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

15

Secretary Chu to Attend FCC Clean Technology Showcase | Department of  

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

to Attend FCC Clean Technology Showcase to Attend FCC Clean Technology Showcase Secretary Chu to Attend FCC Clean Technology Showcase May 18, 2010 - 12:00am Addthis May 18, 2010 Secretary Chu to Attend FCC Clean Technology Showcase Washington DC - Tomorrow, US Energy Steven Chu and Federal Communications Commission Chairman Julius Genachowski will host a Clean Technology Showcase at FCC Headquarters. A number of leading technology companies will exhibit solutions for smarter grids and homes, as well as for sustainable information and communications technologies. The showcase is free and open to the public. Following the showcase Chairman Genachowski and Secretary Chu will give brief remarks. What: Energy Secretary Steven Chu and FCC Chair Julius Genachowski to tour FCC Clean Technology showcase.

16

Secretary Chu to Attend FCC Clean Technology Showcase | Department of  

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

Secretary Chu to Attend FCC Clean Technology Showcase Secretary Chu to Attend FCC Clean Technology Showcase Secretary Chu to Attend FCC Clean Technology Showcase May 18, 2010 - 12:00am Addthis May 18, 2010 Secretary Chu to Attend FCC Clean Technology Showcase Washington DC - Tomorrow, US Energy Steven Chu and Federal Communications Commission Chairman Julius Genachowski will host a Clean Technology Showcase at FCC Headquarters. A number of leading technology companies will exhibit solutions for smarter grids and homes, as well as for sustainable information and communications technologies. The showcase is free and open to the public. Following the showcase Chairman Genachowski and Secretary Chu will give brief remarks. What: Energy Secretary Steven Chu and FCC Chair Julius Genachowski to tour FCC Clean Technology showcase.

17

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

18

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

19

A study of the spray injection Reynolds number effects on gasoline yields of an FCC riser reactor  

SciTech Connect

A computational analysis of the combined effects of feed oil injection parameters in a commercial-scale fluidized catalytic cracking riser reactor was performed using a three-phase, multiple species kinetic cracking computer code. The analysis showed that the injection operating parameters (droplet diameter and injection velocity) had strong impacts on the gasoline yields of the FCC unit. A spray injection Reynolds number combining the two parameters was defined. A correlation between the spray injection Reynolds number and the gasoline product yields for various feed injection conditions was developed. A range of spray injection Reynolds number for the maximum gasoline yield was identified.

Bowman, B. J.; Zhou, C. Q.; Chang, S. L.; Lottes, S. A.

2000-04-03T23:59:59.000Z

20

Broadband over Power Lines (BPL): FCC Emissions Compliance Guidelines  

Science Conference Proceedings (OSTI)

Broadband over power lines (BPL, a.k.a. broadband PLC) has been heralded as an opportunity for electric companies to enhance internal communication and control while delivering broadband service to areas where existing services are unavailable. The Federal Communications Commission (FCC) has published new regulations limiting radio frequency (RF) emissions from BPL equipment. This EPRI Technical Update provides an overview of the "FCC Report & Order 04-245" on BPL and gives guidance and details on the te...

2005-06-21T23:59:59.000Z

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

Cluster expansion of fcc Pd-V intermetallics  

Science Conference Proceedings (OSTI)

A cluster expansion is used to compute fcc ground states from first principles for the Pd-V system. Intermetallic structures are not assumed but derived rigorously by minimizing the configurational energy subject to linear constraints. A large number of concentration-independent interactions are calculated by the method of direct configurational averaging. Agreement with the fcc-based portion of the experimentally-determined Pd-V phase diagram is quite satisfactory. 25 refs., 2 figs.

de Fontaine, D.; Wolverton, C.; Ceder, G. (Lawrence Berkeley Lab., CA (United States)); Dreysse, H. (Nancy-1 Univ., 54 (France). Lab. de Physique du Solide)

1991-06-01T23:59:59.000Z

22

Fluid-Bed Testing of Greatpoint Energy's Direct Oxygen Injection Catalytic Gasification Process for Synthetic Natural Gas and Hydrogen Coproduction Year 6 - Activity 1.14 - Development of a National Center for Hydrogen Technology  

SciTech Connect

The GreatPoint Energy (GPE) concept for producing synthetic natural gas and hydrogen from coal involves the catalytic gasification of coal and carbon. GPE’s technology “refines” coal by employing a novel catalyst to “crack” the carbon bonds and transform the coal into cleanburning methane (natural gas) and hydrogen. The GPE mild “catalytic” gasifier design and operating conditions result in reactor components that are less expensive and produce pipeline-grade methane and relatively high purity hydrogen. The system operates extremely efficiently on very low cost carbon sources such as lignites, subbituminous coals, tar sands, petcoke, and petroleum residual oil. In addition, GPE’s catalytic coal gasification process eliminates troublesome ash removal and slagging problems, reduces maintenance requirements, and increases thermal efficiency, significantly reducing the size of the air separation plant (a system that alone accounts for 20% of the capital cost of most gasification systems) in the catalytic gasification process. Energy & Environmental Research Center (EERC) pilot-scale gasification facilities were used to demonstrate how coal and catalyst are fed into a fluid-bed reactor with pressurized steam and a small amount of oxygen to “fluidize” the mixture and ensure constant contact between the catalyst and the carbon particles. In this environment, the catalyst facilitates multiple chemical reactions between the carbon and the steam on the surface of the coal. These reactions generate a mixture of predominantly methane, hydrogen, and carbon dioxide. Product gases from the process are sent to a gas-cleaning system where CO{sub 2} and other contaminants are removed. In a full-scale system, catalyst would be recovered from the bottom of the gasifier and recycled back into the fluid-bed reactor. The by-products (such as sulfur, nitrogen, and CO{sub 2}) would be captured and could be sold to the chemicals and petroleum industries, resulting in near-zero hazardous air or water pollution. This technology would also be conducive to the efficient coproduction of methane and hydrogen while also generating a relatively pure CO{sub 2} stream suitable for enhanced oil recovery (EOR) or sequestration. Specific results of bench-scale testing in the 4- to 38-lb/hr range in the EERC pilot system demonstrated high methane yields approaching 15 mol%, with high hydrogen yields approaching 50%. This was compared to an existing catalytic gasification model developed by GPE for its process. Long-term operation was demonstrated on both Powder River Basin subbituminous coal and on petcoke feedstocks utilizing oxygen injection without creating significant bed agglomeration. Carbon conversion was greater than 80% while operating at temperatures less than 1400°F, even with the shorter-than-desired reactor height. Initial designs for the GPE gasification concept called for a height that could not be accommodated by the EERC pilot facility. More gas-phase residence time should allow the syngas to be converted even more to methane. Another goal of producing significant quantities of highly concentrated catalyzed char for catalyst recovery and material handling studies was also successful. A Pd–Cu membrane was also successfully tested and demonstrated to produce 2.54 lb/day of hydrogen permeate, exceeding the desired hydrogen permeate production rate of 2.0 lb/day while being tested on actual coal-derived syngas that had been cleaned with advanced warm-gas cleanup systems. The membranes did not appear to suffer any performance degradation after exposure to the cleaned, warm syngas over a nominal 100-hour test.

Swanson, Michael; Henderson, Ann

2012-04-01T23:59:59.000Z

23

State-of-the-art review of computational fluid dynamics modeling for fluid-solids systems  

DOE Green Energy (OSTI)

As the result of 15 years of research (50 staff years of effort) Argonne National Laboratory (ANL), through its involvement in fluidized-bed combustion, magnetohydrodynamics, and a variety of environmental programs, has produced extensive computational fluid dynamics (CFD) software and models to predict the multiphase hydrodynamic and reactive behavior of fluid-solids motions and interactions in complex fluidized-bed reactors (FBRS) and slurry systems. This has resulted in the FLUFIX, IRF, and SLUFIX computer programs. These programs are based on fluid-solids hydrodynamic models and can predict information important to the designer of atmospheric or pressurized bubbling and circulating FBR, fluid catalytic cracking (FCC) and slurry units to guarantee optimum efficiency with minimum release of pollutants into the environment. This latter issue will become of paramount importance with the enactment of the Clean Air Act Amendment (CAAA) of 1995. Solids motion is also the key to understanding erosion processes. Erosion rates in FBRs and pneumatic and slurry components are computed by ANL`s EROSION code to predict the potential metal wastage of FBR walls, intervals, feed distributors, and cyclones. Only the FLUFIX and IRF codes will be reviewed in the paper together with highlights of the validations because of length limitations. It is envisioned that one day, these codes with user-friendly pre and post-processor software and tailored for massively parallel multiprocessor shared memory computational platforms will be used by industry and researchers to assist in reducing and/or eliminating the environmental and economic barriers which limit full consideration of coal, shale and biomass as energy sources, to retain energy security, and to remediate waste and ecological problems.

Lyczkowski, R.W.; Bouillard, J.X.; Ding, J.; Chang, S.L. [Argonne National Lab., IL (United States); Burge, S.W. [Babcock and Wilcox, Alliance, OH (United States). Alliance Research Center

1994-05-12T23:59:59.000Z

24

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

25

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

26

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

27

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

28

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

29

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

30

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

31

The Existence of a Multi-Phase Critical Point in Metastable Fcc ...  

Science Conference Proceedings (OSTI)

Presentation Title, The Existence of a Multi-Phase Critical Point in Metastable Fcc Ordering Phase Diagrams and Its Influence on Phase Diagram Features, ...

32

FURTHER DISCUSSION OF ORIENTATION RELATIONSHIPS, SURFACE RELIEFS AND FCC-BCC TRANSFORMATIONS IN STEELS  

E-Print Network (OSTI)

superposition of a (111) fcc projection (solid circles) anda (110) bee projection (open circles), The three coincidentis illustrated in sional projections of the N-W orientation

Dahmen, U.

2013-01-01T23:59:59.000Z

33

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

34

Increasing Distillate Production at U.S. Refineries – Past ...  

U.S. Energy Information Administration (EIA)

optimization around fluid catalytic cracker (FCC) feeds and operations, hydrocrackers in ... The U.S. Energy Information Administration (EIA) and the U.S.

35

MOLECULAR COMPOSITION OF NEEDLE COKE FEEDSTOCKS AND MESOPHASE DEVELOPMENT DURING CARBONIZATION.  

E-Print Network (OSTI)

??This study investigates the molecular composition of fluid catalytic cracking (FCC) decant oil and its derivatives that are used as feedstocks for delayed coking to… (more)

Wang, Guohua

2005-01-01T23:59:59.000Z

36

The importance of FCC catalyst selection on LPG profitability  

SciTech Connect

Recently the value of LPG in chemical operations downstream of the FCC unit has increased. Such downstream operations utilize propylene not only in alkylate, but also in rapid growth petrochemical applications such as for a raw material in the manufacture of polypropylene and propylene oxide. Isobutane and the butenes (particularly butene-2 in sulfuric acid catalyzed alkylation units) are prized for alkylate feed. The profit potential and incentives to use other LPG components such as isobutene to make MTBE is now increased because of legislative actions and increased octane performance demand; and because of the greater isobutene content in the LPG from the new FCC octane catalysts. A low non-framework alumina (NFA) zeolite studied made a more olefinic LPG with higher iso-to normal C4 ratio than the other zeolites. Pilot plant data has also shown the new low NFA zeolite gave not only outstanding motor octane (MON) performance, but produced an LPG with better propylene to propane ratio, more isobutene, more n-butenes and more C4 branching than other RE promoted zeolite catalysts. Commercial results have verified the improved performance and profitability for the new low-NFA type zeolite catalysts. Three commercial examples are described.

Keyworth, D.A.; Gilman, R.; Pearce, J.R. (AKZO Catalysts, 13000 Bay Park Road, Pasadena, TX (US))

1989-01-01T23:59:59.000Z

37

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

38

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

39

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

40

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

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

Gold-Copper Nanoparticles: Nanostructural Evolution and Bifunctional Catalytic Sites  

Science Conference Proceedings (OSTI)

Understanding of the atomic-scale structure is essential for exploiting the unique catalytic properties of any nanoalloy catalyst. This report describes novel findings of an investigation of the nanoscale alloying of gold-copper (AuCu) nanoparticles and its impact on the surface catalytic functions. Two pathways have been explored for the formation of AuCu nanoparticles of different compositons, including wet chemical synthesis from mixed Au- and Cu-precursor molecules, and nanoscale alloying via an evolution of mixed Au- and Cu-precursor nanoparticles near the nanoscale melting temperatures. For the evolution of mixed precursor nanoparticles, synchrotron x-ray based in-situ real time XRD was used to monitor the structural changes, revealing nanoscale alloying and reshaping towards an fcc-type nanoalloy (particle or cube) via a partial melting–resolidification mechanism. The nanoalloys supported on carbon or silica were characterized by in-situ high-energy XRD/PDFs, revealing an intriguing lattice "expanding-shrinking" phenomenon depending on whether the catalyst is thermochemically processed under oxidative or reductive atmosphere. This type of controllable structural changes is found to play an important role in determining the catalytic activity of the catalysts for carbon monoxide oxidation reaction. The tunable catalytic activities of the nanoalloys under thermochemically oxidative and reductive atmospheres are also discussed in terms of the bifunctional sites and the surface oxygenated metal species for carbon monoxide and oxygen activation.

Yin, Jun; Shan, Shiyao; Yang, Lefu; Mott, Derrick; Malis, Oana; Petkov, Valeri; Cai, Fan; Ng, Mei; Luo, Jin; Chen, Bing H.; Engelhard, Mark H.; Zhong, Chuan-Jian

2012-12-12T23:59:59.000Z

42

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

43

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

44

The selective catalytic cracking of Fischer-Tropsch liquids to high value transportation fuels. Final report  

DOE Green Energy (OSTI)

Amoco Oil Company, investigated a selective catalytic cracking process (FCC) to convert the Fischer-Tropsch (F-T) gasoline and wax fractions to high value transportation fuels. The primary tasks of this contract were to (1) optimize the catalyst and process conditions of the FCC process for maximum conversion of F-T wax into reactive olefins for later production of C{sub 4}{minus}C{sub 8} ethers, and (2) use the olefin-containing light naphtha obtained from FCC processing of the F-T wax as feedstock for the synthesis of ethers. The catalytic cracking of F-T wax feedstocks gave high conversions with low activity catalysts and low process severities. HZSM-5 and beta zeolite catalysts gave higher yields of propylene, isobutylene, and isoamylenes but a lower gasoline yield than Y zeolite catalysts. Catalyst selection and process optimization will depend on product valuation. For a given catalyst and process condition, Sasol and LaPorte waxes gave similar conversions and product selectivities. The contaminant iron F-T catalyst fines in the LaPorte wax caused higher coke and hydrogen yields.

Schwartz, M.M.; Reagon, W.J.; Nicholas, J.J.; Hughes, R.D.

1994-11-01T23:59:59.000Z

45

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

46

Dynamic strain localization in f.c.c. materials: a perturbation approach  

Science Conference Proceedings (OSTI)

In the present work, dynamic strain localization of f.c.c. materials is predicted for strain-rates that range from 0.1 to 1000s?1 and mapped over the ...

47

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

48

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

49

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

50

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

51

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

52

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.

53

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

54

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

55

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

56

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...

57

Refining and upgrading of synfuels from coal and oil shales by advanced catalytic processes. Quarterly report, October--December 1977  

DOE Green Energy (OSTI)

Pilot plant studies have now been completed for the processing of Paraho shale oil. Three processing routes are being evaluated: (1) whole shale oil hydrotreating followed by fluid catalytic cracking (FCC) as the major downstream processing step, (2) whole shale oil hydrotreating followed by hydrocracking as the major processing step, (3) coking of the shale oil followed by hydrotreating of the coker distillate as the major downstream processing step. Pilot plant studies show that all three routes are technically feasible. Analyses of the results and process design studies are being completed. The relative merits and economics of each route will be discussed in the final report. SRC is difficult to process compared to most petroleum feeds and to shale oil. Because of its high melting point, it is necessary to dissolve it in an appropriate solvent before it can be hydrotreated in existing fixed bed pilot plant equipment. The first solvent for SRC in these tests was creosote oil; a 50/50 blend was tested. In the first test, ICR 106 catalyst showed little fouling in 330 hours. About half of the 850/sup 0/F + SRC was converted to 850/sup 0/F - distillate; and the nitrogen content was reduced from 1.5% in the SRC/creosote oil blend to 0.2--0.3% in the product. However, after 330 hours on stream, plugging occurred in the catalyst bed. In a second run, 100 hours of operation were achieved without plugging. However, the catalyst deactivation rate was relatively high. Another solvent being tested is the 350--850/sup 0/F product from the SRC/creosote oil hydroprocessing runs. Plugging problems were again encountered using this solvent.

Sullivan, R.F.; Green, D.C.; Chen, H.C.

1978-01-01T23:59:59.000Z

58

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

59

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

60

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

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

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

62

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

63

Correlation-induced anomalies and extreme sensitivity in fcc-Pu  

Science Conference Proceedings (OSTI)

We have used GGA + U density functional theory to study the effects of correlation on the properties of fcc Pu. We found that the structural and elastic properties of fcc-Pu are highly sensitive to the Hubbard U parameter. Within an interval of 0.05 eV of the U parameter, the equilibrium lattice constants of fcc-Pu can change from 0.42 to 0.47 nm. While the bulk modulus can drop by a factor of 5 to 10. The pressure derivative, dB/dp, of the bulk modulus can rise dramatically from 5 to 15 and then drop to the negative values before recovering to the more normal values. These observations are partially supported by existing experiments and the prediction of a negative dB/dp need to be tested in future experiments.

Chen, Shao-ping [Los Alamos National Laboratory

2008-01-01T23:59:59.000Z

64

SRM -? Fluids  

Science Conference Proceedings (OSTI)

... These reference fluid formulations characterize the behavior of broad ranges of chemically similar fluids; in this way data on propane, for example ...

2012-10-01T23:59:59.000Z

65

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

66

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

67

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

68

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

69

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

70

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

71

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

72

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

73

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 ...

74

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 ...

75

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

76

Puerto Rico Refinery Catalytic Reforming Downstream Charge ...  

U.S. Energy Information Administration (EIA)

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

77

Mississippi Refinery Catalytic Reforming Downstream Charge ...  

U.S. Energy Information Administration (EIA)

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

78

Louisiana Refinery Catalytic Reforming Downstream Charge Capacity ...  

U.S. Energy Information Administration (EIA)

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

79

Fluid turbine  

SciTech Connect

A fluid turbine designed for increased power output includes an annular housing provided with a semi-spherical dome for directing incoming fluid flow to impinge on a plurality of rotor blades within the housing fixed to a vertical output shaft. An angle on the order of between 5 to 85/sup 0/, in the direction of rotation of the shaft, exists between the upper (Leading) and lower (Trailing) edges of each blade. The blades are manufactured from a plurality of aerodynamically-shaped, radially spaced ribs covered with a skin. The leading edge of each rib is curved, while the trailing edge is straight. The straight edge of the ribs in each blade approach a vertical plane through the vertical axis of the housing output shaft as the ribs progress radially inwardly towards the output shaft. The housing has fluid exit passages in its base so that deenergized fluid can be quickly flushed from the housing by the downwardly directed flow in combination with the novel blade configuration, which acts as a screw or force multiplier, to expel deenergized fluid. The airfoil shaped ribs also provide the blades with a contour for increasing the fluid velocity on the underside of the blades adjacent the fluid exit passage to aid in expelling the deenergized air while providing the turbine with both impulse and axial-flow, fluid impingement on the blades, resulting in a force vector of increased magnitude. A downwardly directed, substantially semi-cylindrical deflector frame connected to the housing blocks the path of flow of ambient fluid to create a low pressure area beneath the base to aid in continuously drawing fluid into the housing at high velocity to impinge on the rotor blades. The increased flow velocity and force on the blades along with the enhanced removal of deenergized fluid results in increased power output of the turbine.

Lebost, B.A.

1980-11-18T23:59:59.000Z

80

Cutting Fluids  

Science Conference Proceedings (OSTI)

Table 6   Cutting fluids for aluminum...Table 6 Cutting fluids for aluminum Type of lubricant Principal ingredients Viscosity range Application; maintenance Relative effectiveness Necessary precautions Mineral oils (fatty-additive type preferred) Mineral oil, lard, or neats-foot oil; oleic acid

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

HYDRAULIC FLUIDS  

E-Print Network (OSTI)

This fact sheet answers the most frequently asked health questions (FAQs) about hydraulic fluids. For more information, call the ATSDR Information Center at 1-888-422-8737. This fact sheet is one in a series of summaries about hazardous substances and their health effects. This information is important because this substance may harm you. The effects of exposure to any hazardous substance depend on the dose, the duration, how you are exposed, personal traits and habits, and whether other chemicals are present. HIGHLIGHTS: Exposure to hydraulic fluids occurs mainly in the workplace. Drinking certain types of hydraulic fluids can cause death in humans, and swallowing or inhaling certain types of hydraulic fluids has caused nerve damage in animals. Contact with some types of hydraulic fluids can irritate your skin or eyes. These substances have been found in at least 10 of the 1,428 National Priorities List sites identified by the Environmental Protection Agency (EPA). What are hydraulic fluids? (Pronounced ?????ô????????????) Hydraulic fluids are a large group of liquids made of many kinds of chemicals. They are used in automobile automatic

unknown authors

1997-01-01T23:59:59.000Z

82

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

83

Electronic structure and vibrational entropies of fcc Au-Fe alloys  

SciTech Connect

Phonon density of states (DOS) curves were measured on alloys of face-centered-cubic (fcc) Au-Fe using nuclear resonant inelastic x-ray scattering (NRIXS) and inelastic neutron scattering (INS). The NRIXS and INS results were combined to obtain the total phonon DOS and the partial phonon DOS curves of Au and Fe atoms. The 57Fe partial phonon DOS of the dilute alloy Au0.97 57Fe0.03 shows a localized mode centered 4.3% above the cutoff energy of the phonons in pure Au. The Mannheim model for impurity modes accurately reproduced this partial phonon DOS using the fcc Au phonon DOS with a ratio of host-host to impurity-host force constants of 1.55. First-principles calculations validated the assumption of first-nearest-neighbor forces in the Mannheim model and gave a similar ratio of force constants. The high energy local mode broadens with increasing Fe composition, but this has a small effect on the composition dependence of the vibrational entropy. The main effect on the vibrational entropy of alloying comes from a stiffening of the Au partial phonon DOS with Fe concentration. This stiffening is attributed to two main effects: 1) an increase in electron density in the free-electron-like states, and 2) stronger sd-hybridization. These two effects are comparable in magnitude.

Munoz, Jorge A. [California Institute of Technology, Pasadena] [California Institute of Technology, Pasadena; Lucas, Matthew [United States Air Force Research Laboratory, Wright-Patterson Air Force Base] [United States Air Force Research Laboratory, Wright-Patterson Air Force Base; Mauger, L [California Institute of Technology, W. M. Keck Laboratory, Pasadena] [California Institute of Technology, W. M. Keck Laboratory, Pasadena; Halevy, I [California Institute of Technology, Pasadena] [California Institute of Technology, Pasadena; Horwath, J [United States Air Force Research Laboratory, Wright-Patterson Air Force Base] [United States Air Force Research Laboratory, Wright-Patterson Air Force Base; Semiatin, S L [United States Air Force Research Laboratory, Wright-Patterson Air Force Base] [United States Air Force Research Laboratory, Wright-Patterson Air Force Base; Xiao, Yuming [Carnegie Institution of Washington] [Carnegie Institution of Washington; Stone, Matthew B [ORNL] [ORNL; Abernathy, Douglas L [ORNL] [ORNL; Fultz, B. [California Institute of Technology, Pasadena] [California Institute of Technology, Pasadena

2013-01-01T23:59:59.000Z

84

Imaging the proton concentration and mapping the spatial distribution of the electric field of catalytic micropumps  

E-Print Network (OSTI)

Catalytic engines can use hydrogen peroxide as a chemical fuel in order to drive motion at the microscale. The chemo-mechanical actuation is a complex mechanism based on the interrelation between catalytic reactions and electro-hydrodynamics phenomena. We studied catalytic micropumps using fluorescence confocal microscopy to image the concentration of protons in the liquid. In addition, we measured the motion of particles with different charges in order to map the spatial distributions of the electric field, the electrostatic potential and the fluid flow. The combination of these two techniques allows us to contrast the gradient of the concentration of protons against the spatial variation in the electric field. We present numerical simulations that reproduce the experimental results. Our work sheds light on the interrelation between the different processes at work in the chemo-mechanical actuation of catalytic pumps. Our experimental approach could be used to study other electrochemical systems with heterogeneous electrodes.

A. Afshar Farniya; M. J. Esplandiu; D. Reguera; A. Bachtold

2013-11-13T23:59:59.000Z

85

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

86

Superconducting Cuprates on Catalytic Substrates - Energy ...  

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

87

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

88

R fluids  

E-Print Network (OSTI)

A theory of collisionless fluids is developed in a unified picture, where nonrotating figures with anisotropic random velocity component distributions and rotating figures with isotropic random velocity component distributions, make adjoints configurations to the same system. R fluids are defined and mean and rms angular velocities and mean and rms tangential velocity components are expressed, by weighting on the moment of inertia and the mass, respectively. The definition of figure rotation is extended to R fluids. The generalized tensor virial equations are formulated for R fluids and further attention is devoted to axisymmetric configurations where, for selected coordinate axes, a variation in figure rotation has to be counterbalanced by a variation in anisotropy excess and vice versa. A microscopical analysis of systematic and random motions is performed under a few general hypotheses, by reversing the sign of tangential or axial velocity components of an assigned fraction of particles, leaving the distribution function and other parameters unchanged (Meza 2002). The application of the reversion process to tangential velocity components, implies the conversion of random motion rotation kinetic energy into systematic motion rotation kinetic energy. The application of the reversion process to axial velocity components, implies the conversion of random motion translation kinetic energy into systematic motion translation kinetic energy, and the loss related to a change of reference frame is expressed in terms of systematic (imaginary) motion rotation kinetic energy. A procedure is sketched for deriving the spin parameter distribution (including imaginary rotation) from a sample of observed or simulated large-scale collisionless fluids i.e. galaxies and galaxy clusters.

R. Caimmi

2007-10-20T23:59:59.000Z

89

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

90

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

91

Coal conversion wastewater treatment by catalytic oxidation in supercritical water  

SciTech Connect

Wastewaters from coal-conversion processes contain phenolic compounds in appreciable concentrations. These compounds need to be removed so that the water can be discharged or re-used. Catalytic oxidation in supercritical water is one potential means of treating coal-conversion wastewaters, and this project examined the reactions of phenol over different heterogeneous oxidation catalysts in supercritical water. More specifically, the authors examined the oxidation of phenol over a commercial catalyst and over bulk MnO{sub 2}, bulk TiO{sub 2}, and CuO supported on Al{sub 2}O{sub 3}. They used phenol as the model pollutant because it is ubiquitous in coal-conversion wastewaters and there is a large database for non-catalytic supercritical water oxidation (SCWO) with which they can contrast results from catalytic SCWO. The overall objective of this research project is to obtain the reaction engineering information required to evaluate the utility of catalytic supercritical water oxidation for treating wastes arising from coal conversion processes. All four materials were active for catalytic supercritical water oxidation. Indeed, all four materials produced phenol conversions and CO{sub 2} yields in excess of those obtained from purely homogeneous, uncatalyzed oxidation reactions. The commercial catalyst was so active that the authors could not reliably measure reaction rates that were not limited by pore diffusion. Therefore, they performed experiments with bulk transition metal oxides. The bulk MnO{sub 2} and TiO{sub 2} catalysts enhance both the phenol disappearance and CO{sub 2} formation rates during SCWO. MnO{sub 2} does not affect the selectivity to CO{sub 2}, or to the phenol dimers at a given phenol conversion. However, the selectivities to CO{sub 2} are increased and the selectivities to phenol dimers are decreased in the presence of TiO{sub 2}, which are desirable trends for a catalytic SCWO process. The role of the catalyst appears to be accelerating the rate of formation of phenoxy radicals, which then react in the fluid phase by the same mechanism operative for non-catalytic SCWO of phenol. The rates of phenol disappearance and CO{sub 2} formation are sensitive to the phenol and O{sub 2} concentrations, but independent of the water density. Power-law rate expressions were developed to correlate the catalytic kinetics. The catalytic kinetics were also consistent with a Langmuir-Hinshelwood rate law derived from a dual-site mechanism comprising the following steps: reversible adsorption of phenol on one type of catalytic site, reversible dissociative adsorption of oxygen on a different type of site, and irreversible, rate-determining surface reaction between adsorbed phenol and adsorbed oxygen.

Phillip E. Savage

1999-10-20T23:59:59.000Z

92

COAL CONVERSION WASTEWATER TREATMENT BY CATALYTIC OXIDATION IN SUPERCRITICAL WATER  

SciTech Connect

Wastewaters from coal-conversion processes contain phenolic compounds in appreciable concentrations. These compounds need to be removed so that the water can be discharged or re-used. Catalytic oxidation in supercritical water is one potential means of treating coal-conversion wastewaters, and this project examined the reactions of phenol over different heterogeneous oxidation catalysts in supercritical water. More specifically, we examined the oxidation of phenol over a commercial catalyst and over bulk MnO{sub 2}, bulk TiO{sub 2}, and CuO supported on Al{sub 2} O{sub 3}. We used phenol as the model pollutant because it is ubiquitous in coal-conversion wastewaters and there is a large database for non-catalytic supercritical water oxidation (SCWO) with which we can contrast results from catalytic SCWO. The overall objective of this research project is to obtain the reaction engineering information required to evaluate the utility of catalytic supercritical water oxidation for treating wastes arising from coal conversion processes. All four materials were active for catalytic supercritical water oxidation. Indeed, all four materials produced phenol conversions and CO{sub 2} yields in excess of those obtained from purely homogeneous, uncatalyzed oxidation reactions. The commercial catalyst was so active that we could not reliably measure reaction rates that were not limited by pore diffusion. Therefore, we performed experiments with bulk transition metal oxides. The bulk MnO{sub 2} and TiO{sub 2} catalysts enhance both the phenol disappearance and CO{sub 2} formation rates during SCWO. MnO{sub 2} does not affect the selectivity to CO{sub 2}, or to the phenol dimers at a given phenol conversion. However, the selectivities to CO{sub 2} are increased and the selectivities to phenol dimers are decreased in the presence of TiO{sub 2} , which are desirable trends for a catalytic SCWO process. The role of the catalyst appears to be accelerating the rate of formation of phenoxy radicals, which then react in the fluid phase by the same mechanism operative for non-catalytic SCWO of phenol. The rates of phenol disappearance and CO{sub 2} formation are sensitive to the phenol and O{sub 2} concentrations, but independent of the water density. Power-law rate expressions were developed to correlate the catalytic kinetics. The catalytic kinetics were also consistent with a Langmuir-Hinshelwood rate law derived from a dual-site mechanism comprising the following steps: reversible adsorption of phenol on one type of catalytic site, reversible dissociative adsorption of oxygen on a different type of site, and irreversible, rate-determining surface reaction between adsorbed phenol and adsorbed oxygen.

Phillip E. Savage

1999-10-18T23:59:59.000Z

93

Fluid extraction  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent is described. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated .beta.-diketone. In especially preferred embodiments the extraction solvent is supercritical carbon dioxide, and the chelating agent comprises a fluorinated .beta.-diketone and a trialkyl phosphate, or a fluorinated .beta.-diketone and a trialkylphosphine oxide. Although a trialkyl phosphate can extract lanthanides and actinides from acidic solutions, a binary mixture comprising a fluorinated .beta.-diketone and a trialkyl phosphate or a trialkylphosphine oxide tends to enhance the extraction efficiencies for actinides and lanthanides. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The method is particularly useful for extracting actinides and lanthanides from acidic solutions. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Laintz, Kenneth E. (Los Alamos, NM)

1999-01-01T23:59:59.000Z

94

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

95

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

96

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

97

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

98

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,...

99

Data:7471fc05-fcc9-4e87-a911-e99457471d58 | Open Energy Information  

Open Energy Info (EERE)

fc05-fcc9-4e87-a911-e99457471d58 fc05-fcc9-4e87-a911-e99457471d58 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Howard Greeley Rural P P D Effective date: End date if known: Rate name: Schedule B Three Phase Farm Residential and Commercial Sector: Commercial Description: Source or reference: Ilinois State University Rate binder # 10 Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category: Phase Wiring: << Previous 1 2 3 Next >>

100

Data:35322b46-9203-45b1-910f-cc75aa855986 | Open Energy Information  

Open Energy Info (EERE)

b46-9203-45b1-910f-cc75aa855986 b46-9203-45b1-910f-cc75aa855986 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Three Rivers Electric Coop Effective date: End date if known: Rate name: Residential Sector: Residential Description: Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category: Phase Wiring: << Previous 1 2 3 Next >> << Previous 1 2 3 Next >> Seasonal/Monthly Demand Charge Structures

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101

Data:975d56fc-c153-4c87-84ca-5180277733cb | Open Energy Information  

Open Energy Info (EERE)

d56fc-c153-4c87-84ca-5180277733cb d56fc-c153-4c87-84ca-5180277733cb No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Miami-Cass County Rural E M C Effective date: 2011/10/01 End date if known: Rate name: Security Lights 150 watt high pressure sodium(Non-metered) Sector: Lighting Description: The Miami-Cass County Rural Electric Membership Corporation (REMC) shall charge and collect for security lighting service on the following bases of availability, character of service, monthly rate, and tax adjustment. AVAILABILITY: Available to any member of the REMC for continuous year round service for outdoor lighting where 120 volt service exists ahead of the meter loop.

102

Textured growth of Co film on CoO (fcc) layer; Structural studies using EDXRD beamline at Indus-2  

SciTech Connect

Co film of 13 nm thickness has been deposited on native oxide (CoO) layer using electron beam evaporation technique. CoO (fcc) of 2.3 nm thickness has been prepared by oxidizing surface of 50 nm thick Co (fcc) by thermal annealing. The structure of the sample has been investigated in detail using in-plane and out-of-plane energy dispersive grazing incidence x-ray diffraction (GIXRD) at EDXRD beamline, Indus-2, RRCAT, Indore. It is found that the growth of the Co film takes place with preferential orientation of c-axis perpendicular to the film plane, which results in structure induced magnetic anisotropy with easy axis normal to the film plane.

Kumar, Dileep; Patidar, P.; Sant, T.; Pandey, K. K.; Gupta, A.; Sharma, S. M. [UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore - 452 017 (India); School of Nanotechnology, RGPV, Bhopal-462021 (India); Bhabha Atomic Research Center, Trombay, Mumbai- 400 085 (India); UGC-DAE Consortium for Scientific Research, University Campus, Khandwa Road, Indore - 452 017 (India); Bhabha Atomic Research Center, Trombay, Mumbai- 400 085 (India)

2012-06-05T23:59:59.000Z

103

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

104

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

105

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

106

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

107

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

108

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

109

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...

110

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.

111

Catalytic gasification of bagasse for the production of methanol  

DOE Green Energy (OSTI)

The purpose of the study was to evaluate the technical and economic feasibility of catalytic gasification of bagasse to produce methanol. In previous studies, a catalytic steam gasification process was developed which converted wood to methanol synthesis gas in one step using nickel based catalysts in a fluid-bed gasifier. Tests in a nominal 1 ton/day process development unit (PDU) gasifier with these same catalysts showed bagasse to be a good feedstock for fluid-bed gasifiers, but the catalysts deactivated quite rapidly in the presence of bagasse. Laboratory catalyst screening tests showed K/sub 2/CO/sub 3/ doped on the bagasse to be a promising catalyst for converting bagasse to methanol synthesis gas. PDU tests with 10 wt % K/sub 2/CO/sub 3/ doped on bagasse showed the technical feasibility of this type of catalyst on a larger scale. A high quality synthesis gas was produced and carbon conversion to gas was high. The gasifier was successfully operated without forming agglomerates of catalyst, ash, and char in the gasifier. There was no loss of activity throughout the runs because catalysts is continually added with the bagasse. Laboratory tests showed about 80% of the potassium carbonate could be recovered and recycled with a simple water wash. An economic evaluation of the process for converting bagasse to methanol showed the required selling price of methanol to be significantly higher than the current market price of methanol. Several factors make this current evaluaton using bagasse as a feedstock less favorable: (1) capital costs are higher due to inflation and some extra costs required to use bagasse, (2) smaller plant sizes were considered so economies of scale are lost, and (3) the market price of methanol in the US has fallen 44% in the last six months. 24 refs., 14 figs., 16 tabs.

Baker, E.G.; Brown, M.D.; Robertus, R.J.

1985-10-01T23:59:59.000Z

112

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

113

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

114

Fluid transport container  

DOE Patents (OSTI)

An improved fluid container for the transport, collection, and dispensing of a sample fluid that maintains the fluid integrity relative to the conditions of the location at which it is taken. More specifically, the invention is a fluid sample transport container that utilizes a fitting for both penetrating and sealing a storage container under controlled conditions. Additionally, the invention allows for the periodic withdrawal of portions of the sample fluid without contamination or intermixing from the environment surrounding the sample container. 13 figs.

DeRoos, B.G.; Downing, J.P. Jr.; Neal, M.P.

1995-11-14T23:59:59.000Z

115

Fluid transport container  

DOE Patents (OSTI)

An improved fluid container for the transport, collection, and dispensing of a sample fluid that maintains the fluid integrity relative to the conditions of the location at which it is taken. More specifically, the invention is a fluid sample transport container that utilizes a fitment for both penetrating and sealing a storage container under controlled conditions. Additionally, the invention allows for the periodic withdrawal of portions of the sample fluid without contamination or intermixing from the environment surrounding the sample container.

DeRoos, Bradley G. (41 James St., Sequim, WA 98382); Downing, Jr., John P. (260 Kala Heights Dr., Port Townsand, WA 98368); Neal, Michael P. (921 Amberly Pl., Columbus, OH 43220)

1995-01-01T23:59:59.000Z

116

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

117

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

118

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

119

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

120

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

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

Environmentally safe fluid extractor  

DOE Patents (OSTI)

An environmentally safe fluid extraction device for use in mobile laboratory and industrial settings comprising a pump, compressor, valving system, waste recovery tank, fluid tank, and a exhaust filtering system.

Sungaila, Zenon F. (Orland Park, IL)

1993-01-01T23:59:59.000Z

122

Drilling Fluid Corrosion  

Science Conference Proceedings (OSTI)

Table 8   Drilling fluid corrosion control troubleshooting chart...Table 8 Drilling fluid corrosion control troubleshooting chart Corrosion cause Primary source Identification Major corrosion forms Remedies Oxygen Atmosphere, mud conditioning, equipment, oxidizing

123

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

124

Fluid Suspensions & Emulsions  

Science Conference Proceedings (OSTI)

Fluid Suspensions & Emulsions. Summary: Our primary interest is protein ... protein solutions? 1. Health & Safety. There is ongoing ...

2013-09-29T23:59:59.000Z

125

Spinning fluid cosmology  

E-Print Network (OSTI)

The dynamics of a spinning fluid in a flat cosmological model is investigated. The space-time is itself generated by the spinning fluid which is characterized by an energy-momentum tensor consisting a sum of the usual perfect-fluid energy-momentum tensor and some Belinfante-Rosenfeld tensors. It is shown that the equations of motion admit a solution for which the fluid four-velocity and four-momentum are not co-linear in general. The momentum and spin densities of the fluid are expressed in terms of the scale factor.

Morteza Mohseni

2008-07-22T23:59:59.000Z

126

Spinning fluid cosmology  

E-Print Network (OSTI)

The dynamics of a spinning fluid in a flat cosmological model is investigated. The space-time is itself generated by the spinning fluid which is characterized by an energy-momentum tensor consisting a sum of the usual perfect-fluid energy-momentum tensor and some Belinfante-Rosenfeld tensors. It is shown that the equations of motion admit a solution for which the fluid four-velocity and four-momentum are not co-linear in general. The momentum and spin densities of the fluid are expressed in terms of the scale factor.

Mohseni, Morteza

2008-01-01T23:59:59.000Z

127

Data:2a37681e-f5dd-4fcc-8752-abc9b912fbac | Open Energy Information  

Open Energy Info (EERE)

681e-f5dd-4fcc-8752-abc9b912fbac 681e-f5dd-4fcc-8752-abc9b912fbac No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Tri-County Elec Member Corp Effective date: 2012/01/01 End date if known: Rate name: Church Demand - Single Phase* Sector: Commercial Description: *Applicable for all churches of the Cooperative who do not qualify for or who do not elect to receive service under other church rate schedules offered by the Cooperative. Determination of Billing Demand: The Billing Demand for any delivery point shall be based upon the highest 30-minute kW measurements during the current billing month and the preceding eleven (11) months. For the billing dates June 1 through September 30 and December 1 through February 28, the Billing Demand shall be the greater of: 1. 100% of the metered demand for the current month, or 2. 75% of the highest metered demand occurring in any previous applicable summer billing dates (June 1 - September 30). For all the billing dates of October 1 through November 30 and March 1 through May 31, the Billing Demand shall be the greater of: 1. 85% of the metered demand for the current month, or 2. 75% of the highest metered demand occurring in any previous applicable summer billing dates (June 1 - September 30). In no case shall the Billing Demand be less than the greater of (1) the minimum Billing Demand specified in the contract for service between the Cooperative and the member, or (2) 15 kW.

128

Spinning fluids reactor  

SciTech Connect

A spinning fluids reactor, includes a reactor body (24) having a circular cross-section and a fluid contactor screen (26) within the reactor body (24). The fluid contactor screen (26) having a plurality of apertures and a circular cross-section concentric with the reactor body (24) for a length thus forming an inner volume (28) bound by the fluid contactor screen (26) and an outer volume (30) bound by the reactor body (24) and the fluid contactor screen (26). A primary inlet (20) can be operatively connected to the reactor body (24) and can be configured to produce flow-through first spinning flow of a first fluid within the inner volume (28). A secondary inlet (22) can similarly be operatively connected to the reactor body (24) and can be configured to produce a second flow of a second fluid within the outer volume (30) which is optionally spinning.

Miller, Jan D; Hupka, Jan; Aranowski, Robert

2012-11-20T23:59:59.000Z

129

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

130

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

131

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

132

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

133

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

134

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

135

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)

136

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)

137

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)

138

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)

139

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)

140

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)

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

Microwave fluid flow meter  

DOE Patents (OSTI)

A microwave fluid flow meter is described utilizing two spaced microwave sensors positioned along a fluid flow path. Each sensor includes a microwave cavity having a frequency of resonance dependent upon the static pressure of the fluid at the sensor locations. The resonant response of each cavity with respect to a variation in pressure of the monitored fluid is represented by a corresponding electrical output which can be calibrated into a direct pressure reading. The pressure drop between sensor locations is then correlated as a measure of fluid velocity. In the preferred embodiment the individual sensor cavities are strategically positioned outside the path of fluid flow and are designed to resonate in two distinct frequency modes yielding a measure of temperature as well as pressure. The temperature response can then be used in correcting for pressure responses of the microwave cavity encountered due to temperature fluctuations.

Billeter, Thomas R. (Richland, WA); Philipp, Lee D. (Richland, WA); Schemmel, Richard R. (Lynchburg, VA)

1976-01-01T23:59:59.000Z

142

Complex Fluids Group  

Science Conference Proceedings (OSTI)

... applications in energy, sustainability, electronics and medicine. As these materials are typically in the fluid state during their production or end-use ...

2013-05-14T23:59:59.000Z

143

Working/Functional Fluids  

Science Conference Proceedings (OSTI)

... power cycle except that it uses an organic working fluid instead of water to allow operation at lower temperatures, including geothermal or solar ...

2012-10-05T23:59:59.000Z

144

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

145

Microstructural Characterization of Dislocation Networks During Harper-Dorn Creep of fcc, bcc, and hcp Metals and Alloys  

SciTech Connect

Harper-Dorn (H-D) creep is observed in metals and geological materials exposed to very low stresses at temperatures close to the melting point. It is one of several types of creep processes wherein the steady-state strain rate is proportional to the applied stress, Nabarro-Herring creep and Coble creep being two other important processes. H-D creep can be somewhat insidious because the creep rates are much larger than those expected for Nabarro-Herring or Coble creep. Since the working conditions of structural components of power plants and propulsion systems, as well as the motion of the earth’s mantle all involve very low stresses, an understanding of the factors controlling H-D creep is critical in preventing failures associated with those higher-than-expected creep rates. The purpose of this investigation was to obtain missing microstructural information on the evolution of the dislocation structures during static annealing of materials with fcc, bcc and hcp structure and use obtained results to test predictive capabilities of the dislocation network theory of H-D creep. In our view the evolutionary processes during static annealing and during Harper-Dorn creep are intimately related. The materials used in this study were fcc aluminum, hcp zinc and bcc tin. All characterizations of dislocation structures, densities and dislocation link length distributions were carried out using the etch pit method. To obtain quantitative information on the evolution of the dislocation networks during annealing the pure fcc aluminum samples were pre-deformed by creep at 913 and 620 K and then annealed. The higher deformation temperature was selected to generate starting dislocation networks similar to those forming during Harper-Dorn creep and the lower, to obtain higher dislocation densities suitable for reliable estimates of the parameters of the network growth law. The measured experimental link length distribution were, after scaling, (1) the same for all annealing temperatures, (2) time invariant and (3) identical to the distributions obtained previously for Harper-Dorn creep. This has never been shown before and confirms our theoretical expectations that evolution of the dislocation networks during annealing and H-D creep is governed by the same growth law. Obtained results were also used to predict H-D steady creep rates from annealing kinetics data using equations of the dislocation network theory. For the three considered stresses the theory predicts systematically smaller creep rates by the average factor of 4.5. Considering that the creep rates have been predicted from the annealing data alone and without any adjustable parameters, this results shout be considered as outstanding. In case of hcp zinc the samples were pre-deformed in compression at constant stress of 4 MPa at temperature of 573 K and subsequently annealed at the same temperature. During annealing samples readily recrystallized, but it was possible to obtain information on the link length distributions from several unrecrystallized grains. The results showed that the scaled link length distributions were time invariant and similar to those of the aluminum. The annealing studies on bcc tin were also curtailed by the concurrent recrystallization. It was only possible to obtain link length distribution for samples deformed in compression at constant load of 2 MPa at 423 K after unloading. The link length distribution was also in this case similar to that of the aluminum and zinc. These results suggest that the scaled link length distribution is universal and the same for the three considered crystal structures. This supports theoretical findings of these studies that appropriately scaled dislocation link length distribution should both universal and time invariant. We have also investigated the possibility of using alternative methods of estimating local dislocation densities from etch pits which could give more precise estimates of the dislocation link-lengths. The two most promising method are based on the use of Voronoi diagrams and uniform 3-connected nets

Przystupa, Marek A.

2007-12-13T23:59:59.000Z

146

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

147

Exxon catalytic coal gasification process: predevelopment program. Quarterly technical progress report, July 1--September 30, 1976  

SciTech Connect

Predevelopment Program activities for the Exxon Catalytic Gasification Process include: recommissioning of the existing 20 lbs/hr Fluid Bed Gasifier (FBG); modifications to the FBG data acquisition system including the on-line computer program for the calculation of unit material balances from process variable data; start-up and initial operations of the 1-3 lbs/hr Continuous Gasification Unit (CGU); and computer programs development for CRT display of the CGU operating variables profile and for on-line material balance calculations. Data were obtained in the CGU for the gasification of catalyzed Illinois coal during four continuous and two captive fluid-bed yield periods. Good agreement was obtained with previous fixed bed kinetic data. This project is an ERDA-sponsored extension of previous EXXON results.

Kalina, T.

1976-11-01T23:59:59.000Z

148

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

149

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

150

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

151

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

152

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

153

Supercritical Fluid Extraction  

E-Print Network (OSTI)

In supercritical fluid extraction, many options are available for achieving and controlling the desired selectivity, which is extremely sensitive to variations in pressure, temperature, and choice of solvent. The ability of supercritical fluids to vaporize relatively nonvolatile compounds at moderate temperatures can reduce the energy requirements compared to distillation and liquid extraction.

Johnston, K. P.; Flarsheim, W. M.

1984-01-01T23:59:59.000Z

154

Data:A27f5de2-5942-4365-aaff-608d3fcc54f8 | Open Energy Information  

Open Energy Info (EERE)

f5de2-5942-4365-aaff-608d3fcc54f8 f5de2-5942-4365-aaff-608d3fcc54f8 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Oconto Falls Water & Light Comm Effective date: 2010/10/13 End date if known: Rate name: Gs-1 General Service Three Phase Sector: Commercial Description: Power Cost Adjustment Clause - All metered rates shall be subject to a positive or negative power cost adjustment charge equivalent to the amount by which the current cost of power (per kilowatt-hour of sales) is greater or lesser than the base cost of power purchased (per kilowatt-hour of sales). The base cost of power (U) is $0.0847 per kilowatt-hour.

155

Data:8ee7fcc9-0bdb-4879-acc2-7a4eaff08e41 | Open Energy Information  

Open Energy Info (EERE)

ee7fcc9-0bdb-4879-acc2-7a4eaff08e41 ee7fcc9-0bdb-4879-acc2-7a4eaff08e41 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Perry, Oklahoma (Utility Company) Effective date: End date if known: Rate name: Security Lighting- 175W Metal Halide Sector: Lighting Description: Source or reference: http://www.cityofperryok.com/Files/Codes/City_Code_101211.pdf Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category: Phase Wiring: << Previous

156

Data:B7cbe984-2cf9-4fcc-850a-9d83cfbae672 | Open Energy Information  

Open Energy Info (EERE)

cbe984-2cf9-4fcc-850a-9d83cfbae672 cbe984-2cf9-4fcc-850a-9d83cfbae672 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Sandersville, Georgia (Utility Company) Effective date: 2008/06/01 End date if known: Rate name: Residential Sector: Residential Description: Applicable to all domestic uses of the customer in a separately metered single-family or apartment dwelling unit. Source or reference: Illinois State University Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V):

157

Data:A2d1fc87-ace1-4f40-879a-855431a2fcc7 | Open Energy Information  

Open Energy Info (EERE)

fc87-ace1-4f40-879a-855431a2fcc7 fc87-ace1-4f40-879a-855431a2fcc7 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Delta Electric Power Assn Effective date: 2008/07/01 End date if known: Rate name: 23 Mercury Vapor Yardlight Sector: Lighting Description: Available to consumers for overhead lighting service from lighting equipment provided by the association, subject to the established rules and regulations of the Association. Installation, operation and maintenance of a 175 watt mercury vapor lighting unit by the Association on a suitable pole at a location agreeable both to the consumer and the Association.

158

Data:0cb17933-d5a5-4b7f-bccc-a5fcc855a19e | Open Energy Information  

Open Energy Info (EERE)

7933-d5a5-4b7f-bccc-a5fcc855a19e 7933-d5a5-4b7f-bccc-a5fcc855a19e No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Arrowhead Electric Coop, Inc Effective date: 2012/07/17 End date if known: Rate name: GS Commercial Sector: Commercial Description: This rate is applicable for customers who have General Service. Usage under this rate would be tracked by a 2nd meter. Source or reference: Illinois State University Archives Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V):

159

Data:E6e78ce6-aaba-4fcc-8c35-7a684a841af4 | Open Energy Information  

Open Energy Info (EERE)

ce6-aaba-4fcc-8c35-7a684a841af4 ce6-aaba-4fcc-8c35-7a684a841af4 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Lea County Electric Coop, Inc Effective date: 2009/08/30 End date if known: Rate name: Small Commercial Service - Single Phase Sector: Commercial Description: Available system wide for all single phase service 25 kW or less for all nonresidential use not specified in cooperative's residential schedule. Source or reference: Illinois State University Archive Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh):

160

Data:2fcc37ac-1472-42f2-b13a-15bafb26d773 | Open Energy Information  

Open Energy Info (EERE)

fcc37ac-1472-42f2-b13a-15bafb26d773 fcc37ac-1472-42f2-b13a-15bafb26d773 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Alaska Village Elec Coop, Inc Effective date: 2012/01/06 End date if known: Rate name: Large Power- GS-2: Anvik Village Sector: Industrial Description: Note: The Adjustments entered here is the sum of the "Cost of Fuel" and the "RCC". Source or reference: Rates Binder B Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V):

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161

Data:35b2afea-4bd6-4b97-9d64-009d127fcc95 | Open Energy Information  

Open Energy Info (EERE)

b2afea-4bd6-4b97-9d64-009d127fcc95 b2afea-4bd6-4b97-9d64-009d127fcc95 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Delaware Electric Cooperative Effective date: 2011/02/01 End date if known: Rate name: Lighting Service--Schedule L-1 HP Sodium Vapor Lamp-Post Top Luminaire (100w) Granville Sector: Lighting Description: Available to Members, governments, agencies, public and private organizations desiring Electric Delivery or Electric Supply and Delivery Services through unmetered services for roadway and area lighting. Source or reference: http://www.delaware.coop/my-services/residential/billing/rates

162

Data:F6864d07-f3a6-4fcc-8698-6078926186c5 | Open Energy Information  

Open Energy Info (EERE)

-f3a6-4fcc-8698-6078926186c5 -f3a6-4fcc-8698-6078926186c5 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Paris, Tennessee (Utility Company) Effective date: 2012/10/01 End date if known: Rate name: Outdoor Lighting- LS- Part B (100W HPS) Sector: Lighting Description: Applicable for outdoor lighting for individual customers. Source or reference: ISU Documentation Rate Binder Ted #11 Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service

163

Data:9990e7b9-3215-41c0-873f-cc2f631f6576 | Open Energy Information  

Open Energy Info (EERE)

b9-3215-41c0-873f-cc2f631f6576 b9-3215-41c0-873f-cc2f631f6576 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Butler Public Power District Effective date: End date if known: Rate name: Irrigation Services Rate 40 Wheels only Single Phase Sector: Description: Source or reference: Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category: Phase Wiring: << Previous 1 2 3 Next >> << Previous 1 2 3 Next >> Seasonal/Monthly Demand Charge Structures

164

Data:E0fcc001-4552-41b3-b6d0-77bc872f2062 | Open Energy Information  

Open Energy Info (EERE)

fcc001-4552-41b3-b6d0-77bc872f2062 fcc001-4552-41b3-b6d0-77bc872f2062 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Sacramento Municipal Utility District Effective date: 2012/01/01 End date if known: Rate name: TS_F Sector: Lighting Description: Source or reference: https://www.smud.org/en/residential/customer-service/rate-information/rates-rules-regulations.htm Source Parent: Comments FRA= Solar Surcharge Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category:

165

Data:Fcc58cc4-5fbf-4d98-8180-3d6c39e7644d | Open Energy Information  

Open Energy Info (EERE)

Fcc58cc4-5fbf-4d98-8180-3d6c39e7644d Fcc58cc4-5fbf-4d98-8180-3d6c39e7644d No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Darlington Light & Power Co Effective date: 2008/06/16 End date if known: Rate name: Commercial Sector: Commercial Description: Note: All rates are subject to the energy cost adjustment-tracking procedures, which provide for changes in the cost of purchased power from the Town's wholesale power provider being passed through to customers. Source or reference: http://www.darlingtonindiana.com/electric.html Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW):

166

Data:Da15282e-2d3e-4548-8a18-9fcc341a3de6 | Open Energy Information  

Open Energy Info (EERE)

e-2d3e-4548-8a18-9fcc341a3de6 e-2d3e-4548-8a18-9fcc341a3de6 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Williams - AZ, Arizona (Utility Company) Effective date: End date if known: Rate name: Dusk to Dawn Lighting Service(150 W HPS)-pole Sector: Lighting Description: Where city installs, owns, and operates and maintains lighting facilities. Source or reference: Rate Binder#4 (Illinois State University) Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V):

167

Data:96fcc84b-8497-43d6-981c-ee19252a841f | Open Energy Information  

Open Energy Info (EERE)

fcc84b-8497-43d6-981c-ee19252a841f fcc84b-8497-43d6-981c-ee19252a841f No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of North Little Rock, Arkansas (Utility Company) Effective date: 2012/09/01 End date if known: Rate name: SGS Sector: Industrial Description: Single- or three-phase, 60 hertz, and at one standard delivery voltage required by customer and available at customer's service location where service is delivered and metered at voltages less than 13,800/7,960. Source or reference: http://nlrelectric.com/residential/rates/ Source Parent: Comments Applicability Demand (kW) Minimum (kW):

168

Data:D2066415-4d6c-4fcc-bc93-e3f76843be94 | Open Energy Information  

Open Energy Info (EERE)

5-4d6c-4fcc-bc93-e3f76843be94 5-4d6c-4fcc-bc93-e3f76843be94 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Princeton Public Utils Comm Effective date: 2010/02/01 End date if known: Rate name: 250W High Pressure Sodium Sector: Lighting Description: For year-round illumination for area and security lighting by electric lamps in luminaries supported on wood poles, where the facilities for the service are furnished by the utility. Source or reference: Rates Binder A Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh):

169

Data:65fcc006-4e32-425d-837d-7dce1ad13c67 | Open Energy Information  

Open Energy Info (EERE)

fcc006-4e32-425d-837d-7dce1ad13c67 fcc006-4e32-425d-837d-7dce1ad13c67 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Nashville Electric Service Effective date: 2012/06/01 End date if known: Rate name: Outdoor Lighting Mercury Vapor or Incandescent 250w Sector: Lighting Description: PART B--CHARGES FOR OUTDOOR LIGHTING FOR INDIVIDUAL CUSTOMERS The above charges in this Part B are limited to service from a photoelectrically controlled standard lighting fixture installed on a pole already in place. If the customer wishes to have the fixture installed at a location other than on a pole already in place, Distributor may apply an additional monthly charge.

170

Data:05d8f28f-cc6e-494a-a302-2138f917b84e | Open Energy Information  

Open Energy Info (EERE)

f-cc6e-494a-a302-2138f917b84e f-cc6e-494a-a302-2138f917b84e No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Colquitt Electric Membership Corp Effective date: 1993/06/01 End date if known: Rate name: 100W HPS-Open, OVERHEAD WIRING, Wood Pole (kWh - 20, Consumers Per Light - 2) Sector: Lighting Description: Applicable to street and highway lighting owned by federal, state, or local governments or agencies thereof and to street lighting in residential subdivisions, apartment or condominium complexes, and mobile home parks by ballast operated vapor light fixtures and poles conforming to the Cooperative's specifications.

171

Data:21c51a97-f470-457b-8f85-b65c608fcc4f | Open Energy Information  

Open Energy Info (EERE)

f470-457b-8f85-b65c608fcc4f f470-457b-8f85-b65c608fcc4f No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Butler Public Power District Effective date: 2013/01/01 End date if known: Rate name: Commercial/Industrial Single/Three Phase Rate 06 Sector: Industrial Description: Source or reference: http://www.butlerppd.com/common/New%20Customer%20Packet%20_1.2013.pdf Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V): Character of Service Voltage Category: Phase Wiring:

172

Data:F51a099a-cfc7-44ab-b836-5c0fcc1bdccc | Open Energy Information  

Open Energy Info (EERE)

99a-cfc7-44ab-b836-5c0fcc1bdccc 99a-cfc7-44ab-b836-5c0fcc1bdccc No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Lexington, Tennessee (Utility Company) Effective date: 2012/07/01 End date if known: Rate name: Small Commercial Sector: Commercial Description: Available to the non-residential customer with monthly demand of 50 kW or less. Service under this Schedule shall be used solely by the contracting Customer in a single enterprise, located entirely on a single site. Source or reference: http://www.lexingtonnc.net/modules/showdocument.aspx?documentid=413 Source Parent: Comments

173

Data:696fdf88-ebdf-471f-9fcc-e4a865f3b438 | Open Energy Information  

Open Energy Info (EERE)

fdf88-ebdf-471f-9fcc-e4a865f3b438 fdf88-ebdf-471f-9fcc-e4a865f3b438 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Heartland Rural Elec Coop, Inc Effective date: 2009/08/01 End date if known: Rate name: UNMETERED SECURITY LIGHTING: 175W MV Sector: Lighting Description: AVAILABILITY This schedule is available for unmetered outdoor lighting service to any Customer. Unmetered security lighting shall only be available in locations or installations where, by determination of the Cooperative, it is not feasible and/or practical to install metered security lighting. New or replacement light installations shall be limited to high pressure sodium lights.

174

Data:2306b541-b9e7-4cbf-997f-cc35f2517ba6 | Open Energy Information  

Open Energy Info (EERE)

41-b9e7-4cbf-997f-cc35f2517ba6 41-b9e7-4cbf-997f-cc35f2517ba6 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Colquitt Electric Membership Corp Effective date: 1993/06/01 End date if known: Rate name: 175W Existing MV-Open, OVERHEAD WIRING, Metal or Fiberglass Pole Sector: Lighting Description: Applicable only for dusk to dawn lighting by means of photo-electric controlled, ballast operated vapor lamp luminaries and poles conforming to the Cooperative's specifications. Source or reference: ISU Documentation Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months):

175

MAX Fluid Dynamics facility  

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

MAX Fluid Dynamics facility MAX Fluid Dynamics facility Capabilities Engineering Experimentation Reactor Safety Testing and Analysis Overview Nuclear Reactor Severe Accident Experiments MAX NSTF SNAKE Aerosol Experiments System Components Laser Applications Robots Applications Other Facilities Other Capabilities Work with Argonne Contact us For Employees Site Map Help Join us on Facebook Follow us on Twitter NE on Flickr MAX Fluid Dynamics facility Providing high resolution data for development of computational tools that model fluid flow and heat transfer within complex systems such as the core of a nuclear reactor. 1 2 3 4 5 Hot and cold air jets are mixed within a glass tank while laser-based anemometers and a high-speed infrared camera characterize fluid flow and heat transfer behavior. Click on image to view larger size image.

176

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID...  

Open Energy Info (EERE)

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION GAS CHEMISTRY Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: TRACING...

177

FRACTURING FLUID CHARACTERIZATION FACILITY  

SciTech Connect

Hydraulic fracturing technology has been successfully applied for well stimulation of low and high permeability reservoirs for numerous years. Treatment optimization and improved economics have always been the key to the success and it is more so when the reservoirs under consideration are marginal. Fluids are widely used for the stimulation of wells. The Fracturing Fluid Characterization Facility (FFCF) has been established to provide the accurate prediction of the behavior of complex fracturing fluids under downhole conditions. The primary focus of the facility is to provide valuable insight into the various mechanisms that govern the flow of fracturing fluids and slurries through hydraulically created fractures. During the time between September 30, 1992, and March 31, 2000, the research efforts were devoted to the areas of fluid rheology, proppant transport, proppant flowback, dynamic fluid loss, perforation pressure losses, and frictional pressure losses. In this regard, a unique above-the-ground fracture simulator was designed and constructed at the FFCF, labeled ''The High Pressure Simulator'' (HPS). The FFCF is now available to industry for characterizing and understanding the behavior of complex fluid systems. To better reflect and encompass the broad spectrum of the petroleum industry, the FFCF now operates under a new name of ''The Well Construction Technology Center'' (WCTC). This report documents the summary of the activities performed during 1992-2000 at the FFCF.

Subhash Shah

2000-08-01T23:59:59.000Z

178

Supercritical fluid extraction  

DOE Patents (OSTI)

A method of extracting metalloid and metal species from a solid or liquid material by exposing the material to a supercritical fluid solvent containing a chelating agent. The chelating agent forms chelates that are soluble in the supercritical fluid to allow removal of the species from the material. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is a fluorinated or lipophilic crown ether or fluorinated dithiocarbamate. The method provides an environmentally benign process for removing contaminants from industrial waste without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the contaminant species recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Laintz, Kenneth (Pullman, WA)

1994-01-01T23:59:59.000Z

179

IDENTIFYING FRACTURES AND FLUID TYPES USING FLUID INCLUSION STRATIGRAPHY |  

Open Energy Info (EERE)

IDENTIFYING FRACTURES AND FLUID TYPES USING FLUID INCLUSION STRATIGRAPHY IDENTIFYING FRACTURES AND FLUID TYPES USING FLUID INCLUSION STRATIGRAPHY Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: IDENTIFYING FRACTURES AND FLUID TYPES USING FLUID INCLUSION STRATIGRAPHY Details Activities (1) Areas (1) Regions (0) Abstract: Fluid Inclusion Stratigraphy (FIS) is a method currently being developed for use in geothermal systems to identify fractures and fluid types. This paper is the third in a series of papers on the development of FIS. Fluid inclusion gas chemistry is analyzed and plotted on well log diagrams. The working hypothesis is that select gaseous species and species ratios indicate areas of groundwater and reservoir fluid flow and reservoir seals. Previously we showed that FIS analyses identify fluid types and

180

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

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

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

182

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

183

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

184

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

185

Application of Cutting Fluids  

Science Conference Proceedings (OSTI)

...is transferred to the drill by a rotating gland and is forced directly into the cutting zone. The fluid flowing from the hole assists in chip removal. Oil-hole drills have become very popular in

186

Basic fluid system trainer  

DOE Patents (OSTI)

This invention, a trainer mounted and housed within a mobile console, is used to teach and reinforce fluid principles to students. The system trainer has two centrifugal pumps, each driven by a corresponding two-speed electric motor. The motors are controlled by motor controllers for operating the pumps to circulate the fluid stored within a supply tank through a closed system. The pumps may be connected in series or in parallel. A number of valves are also included within the system to effect different flow paths for the fluid. In addition, temperature and pressure sensing instruments are installed throughout the closed system for measuring the characteristics of the fluid, as it passes through the different valves and pumps. These measurements are indicated on a front panel mounted to the console, as a teaching aid, to allow the students to observe the characteristics of the system.

Semans, J.P.; Johnson, P.G.; LeBoeuf, R.F. Jr.; Kromka, J.A.; Goron, R.H.; Hay, G.D.

1991-04-30T23:59:59.000Z

187

Basic fluid system trainer  

DOE Patents (OSTI)

A trainer, mounted and housed within a mobile console, is used to teach and reinforce fluid principles to students. The system trainer has two centrifugal pumps, each driven by a corresponding two-speed electric motor. The motors are controlled by motor controllers for operating the pumps to circulate the fluid stored within a supply tank through a closed system. The pumps may be connected in series or in parallel. A number of valves are also included within the system to effect different flow paths for the fluid. In addition, temperature and pressure sensing instruments are installed throughout the closed system for measuring the characteristics of the fluid, as it passes through the different valves and pumps. These measurements are indicated on a front panel mounted to the console, as a teaching aid, to allow the students to observe the characteristics of the system.

Semans, Joseph P. (Uniontown, PA); Johnson, Peter G. (Pittsburgh, PA); LeBoeuf, Jr., Robert F. (Clairton, PA); Kromka, Joseph A. (Idaho Falls, ID); Goron, Ronald H. (Connellsville, PA); Hay, George D. (Venetia, PA)

1993-01-01T23:59:59.000Z

188

Phoresis in fluids  

E-Print Network (OSTI)

This paper presents a unified theory of phoretic phenomena in single-component fluids. Simple formulas are given for the phoretic velocities of small inert force-free non-Brownian particles migrating through otherwise ...

Brenner, Howard

189

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

190

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

191

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

192

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

193

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...

194

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

195

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 ...

196

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

197

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

198

MEASUREMENT OF INTERFACIAL TENSION IN FLUID-FLUID SYSTEMS  

E-Print Network (OSTI)

Interfacial tension at fluid-fluid interfaces is a reflection of the excess energy associated with unsaturated in parts per million concentration (27). DYNAMIC INTERFACIAL TENSION MEASUREMENTS In fluid-fluid systems, detergency, foam or froth generation, and stability (3). In these pro- cesses, dynamic interfacial tensions

Loh, Watson

199

GEOTHERMAL FLUID PROPENE AND PROPANE: INDICATORS OF FLUID | Open Energy  

Open Energy Info (EERE)

FLUID PROPENE AND PROPANE: INDICATORS OF FLUID FLUID PROPENE AND PROPANE: INDICATORS OF FLUID Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: GEOTHERMAL FLUID PROPENE AND PROPANE: INDICATORS OF FLUID Details Activities (1) Areas (1) Regions (0) Abstract: The use of fluid inclusion gas analysis propene/propene ratios is investigated. Ratios of these species are affected by geothermal fluid temperature and oxidations state. Our purpose is to determine if analyses of these species in fluid inclusions these species to can be used to interpret fluid type, history, or process. Analyses were performed on drill cuttings at 20ft intervals from four Coso geothermal wells. Two wells are good producers, one has cold-water entrants in the production zone, and the fourth is a non-producer. The ratios show distinct differences between

200

Lecture notes Ideal fluid mechanics  

E-Print Network (OSTI)

involves energy loss--such fluids are known as viscous fluids--we will not consider them here. Some fluids of the basic equations underlying the dynamics of ideal fluids is based on three basic principles (see Chorin. Conservation of energy, energy is neither created nor destroyed. In turn these principles generate the: 1

Malham, Simon J.A.

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

Boiler using combustible fluid  

DOE Patents (OSTI)

A fluid fuel boiler is described comprising a combustion chamber, a cover on the combustion chamber having an opening for introducing a combustion-supporting gaseous fluid through said openings, means to impart rotation to the gaseous fluid about an axis of the combustion chamber, a burner for introducing a fluid fuel into the chamber mixed with the gaseous fluid for combustion thereof, the cover having a generally frustro-conical configuration diverging from the opening toward the interior of the chamber at an angle of between 15/sup 0/ and 55/sup 0/; means defining said combustion chamber having means defining a plurality of axial hot gas flow paths from a downstream portion of the combustion chamber to flow hot gases into an upstream portion of the combustion chamber, and means for diverting some of the hot gas flow along paths in a direction circumferentially of the combustion chamber, with the latter paths being immersed in the water flow path thereby to improve heat transfer and terminating in a gas outlet, the combustion chamber comprising at least one modular element, joined axially to the frustro-conical cover and coaxial therewith. The modular element comprises an inner ring and means of defining the circumferential, radial, and spiral flow paths of the hot gases.

Baumgartner, H.; Meier, J.G.

1974-07-03T23:59:59.000Z

202

Universal fluid droplet ejector  

DOE Patents (OSTI)

A droplet generator comprises a fluid reservoir having a side wall made of glass or quartz, and an end cap made from a silicon plate. The end cap contains a micromachined aperture through which the fluid is ejected. The side wall is thermally fused to the end cap, and no adhesive is necessary. This means that the fluid only comes into contact with the side wall and the end cap, both of which are chemically inert. Amplitudes of drive pulses received by reservoir determine the horizontal displacements of droplets relative to the ejection aperture. The drive pulses are varied such that the dropper generates a two-dimensional array of vertically-falling droplets. Vertical and horizontal interdroplet spacings may be varied in real time. Applications include droplet analysis experiments such as Millikan fractional charge searches and aerosol characterization, as well as material deposition applications.

Lee, Eric R. (Redwood City, CA); Perl, Martin L. (Palo Alto, CA)

1999-08-24T23:59:59.000Z

203

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

204

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

205

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

206

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

207

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

208

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

209

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

210

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

211

FCC Lab Presentation  

Science Conference Proceedings (OSTI)

... May 5, 2009 Julius P. Knapp Chief, Office of Engineering and Technology Federal Communications Commission ... Generator Substation Internet ...

2010-04-28T23:59:59.000Z

212

FCC Lab Presentation  

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

Introduction to Introduction to Spectrum Engineering Julius Knapp, Chief Office of Engineering and Technology U.S. Federal Communications Commission Department of Energy Seminar on Spectrum Policy for the Utility Sector December 8, 2010 Note: The views expressed in this presentation are those of the author and may not necessarily represent the views of the Federal Communications Commission Why We Are Here: Utility Wireless Applications Use Spectrum Voice Dispatcher to Crews Crew to Crew Emergency Call "Talk Around" Interconnect Trunked Operation Mutual Aid/Interoperability Data: System Monitoring and Control, Reports and Status Messaging Telemetry, Protective Relaying SCADA (Supervisory Control and Data Acquisition) Automated Meter Reading Home Automation

213

Novel Fast Pyrolysis/Catalytic Technology for the Production of Stable Upgraded Liquids  

SciTech Connect

The objective of the proposed research is the demonstration and development of a novel biomass pyrolysis technology for the production of a stable bio-oil. The approach is to carry out catalytic hydrodeoxygenation (HDO) and upgrading together with pyrolysis in a single fluidized bed reactor with a unique two-level design that permits the physical separation of the two processes. The hydrogen required for the HDO will be generated in the catalytic section by the water-gas shift reaction employing recycled CO produced from the pyrolysis reaction itself. Thus, the use of a reactive recycle stream is another innovation in this technology. The catalysts will be designed in collaboration with BASF Catalysts LLC (formerly Engelhard Corporation), a leader in the manufacture of attrition-resistant cracking catalysts. The proposed work will include reactor modeling with state-of-the-art computational fluid dynamics in a supercomputer, and advanced kinetic analysis for optimization of bio-oil production. The stability of the bio-oil will be determined by viscosity, oxygen content, and acidity determinations in real and accelerated measurements. A multi-faceted team has been assembled to handle laboratory demonstration studies and computational analysis for optimization and scaleup.

Ted Oyama, Foster Agblevor, Francine Battaglia, Michael Klein

2013-01-18T23:59:59.000Z

214

NETL: C&CBTL - Investigation of Coal-Biomass Catalytic Gasification Using  

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

Coal/Biomass Feed and Gasification Coal/Biomass Feed and Gasification Investigation of Coal-Biomass Catalytic Gasification Using Experiments, Reaction Kinetics and Computational Fluid Dynamics Virginia Polytechnic Institute and State University Project Number: FE0005476 Project Description The objectives of the proposed study are to obtain experimental reactor data and develop kinetic rate expressions for pyrolysis and char gasification for the coal-biomass blends under conditions free from transport limitations, to develop a detailed understanding of the effect of pyrolysis conditions on the porous char structure, to build mathematical models that combine true kinetic rate expressions with transport models for predicting gasification behavior for a broad range of pressures and temperatures, and to investigate the physical and chemical parameters that might lead to synergistic effects in coal-biomass blends gasification.

215

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

216

Data:Dc0982a5-1293-4d9c-b1ae-8fcc073cfa7b | Open Energy Information  

Open Energy Info (EERE)

a5-1293-4d9c-b1ae-8fcc073cfa7b a5-1293-4d9c-b1ae-8fcc073cfa7b No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Princeton, Wisconsin (Utility Company) Effective date: 2006/09/14 End date if known: Rate name: Rg-1 Residential Service Three Phase Sector: Residential Description: Power Cost Adjustment Clause - All metered rates shall be subject to a positive or negative power cost adjustment charge equivalent to the amount by which the current cost of power (per kilowatt-hour of sales) is greater or lesser than the base cost of power purchased (per kilowatt-hour of sales). The base cost of power (U) is $0.0524 per kilowatt-hour.

217

Data:625f2078-2b1f-44cb-bf4f-cc64afa5be8b | Open Energy Information  

Open Energy Info (EERE)

-2b1f-44cb-bf4f-cc64afa5be8b -2b1f-44cb-bf4f-cc64afa5be8b No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Franklin Rural Electric Cooperative Effective date: 2010/05/01 End date if known: Rate name: Single Phase Sector: Commercial Description: Source or reference: https://cas.sharepoint.illinoisstate.edu/grants/Sunshot/Lists/DATA%20ENTRY%20Needs%20V2/Attachments/199/Franklin%20Rural%20Electric%20Coop,%20IA.pdf Source Parent: Comments Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh) Minimum (kWh): Maximum (kWh): History (months): Service Voltage Minimum (V): Maximum (V):

218

Data:8479fcc9-e059-4c39-a251-80242ae5c9e5 | Open Energy Information  

Open Energy Info (EERE)

fcc9-e059-4c39-a251-80242ae5c9e5 fcc9-e059-4c39-a251-80242ae5c9e5 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Kiel, Wisconsin (Utility Company) Effective date: 2011/05/06 End date if known: Rate name: Ms-1 Street Lighting Service Overhead 70 W HPS Sector: Lighting Description: Power Cost Adjustment Clause - All metered rates shall be subject to a positive or negative power cost adjustment charge equivalent to the amount by which the current cost of power (per kilowatt-hour of sales) is greater or lesser than the base cost of power purchased (per kilowatt-hour of sales). The base cost of power (U) is $0.0754 per kilowatt-hour.

219

Data:D977fb50-06f4-4efa-8926-eff5fcc1e050 | Open Energy Information  

Open Energy Info (EERE)

7fb50-06f4-4efa-8926-eff5fcc1e050 7fb50-06f4-4efa-8926-eff5fcc1e050 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Northern Indiana Pub Serv Co Effective date: 2011/12/27 End date if known: Rate name: Dusk to Dawn Light - 100 watt HPS Sector: Lighting Description: TO WHOM AVAILABLE Available for dusk to dawn area lighting service to Customers for Company-owned lighting systems located on electric supply lines of the Company which are suitable and adequate for supplying the service requested, subject to the conditions set forth in this Rate Schedule and the Company Rules. MAINTENANCE Company will repair and/or replace and maintain all equipment owned by Company which may be necessary to provide a continuous supply of electrical Energy to the point of connection of Company's property

220

Data:41be73f5-2b61-4fcc-89f3-7136207d50b6 | Open Energy Information  

Open Energy Info (EERE)

be73f5-2b61-4fcc-89f3-7136207d50b6 be73f5-2b61-4fcc-89f3-7136207d50b6 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Detroit Edison Co Effective date: 2011/12/21 End date if known: Rate name: INTERRUPTIBLE SPACE-CONDITIONING D1.1( RETAIL RESIDENTIAL) Sector: Residential Description: Available on an optional basis to Residential and Commercial customers desiring separately metered interruptible service for central air conditioning and/or central heat pump use. Customers who have more than one heat pump and/or air-conditioning unit which serves their business or home, will not be permitted to have only a portion of their load on the rate, all units will be interrupted upon the signal from the Company. Installations must conform with the Company's specifications. This rate is not available to commercial customers being billed on a demand rate.

Note: This page contains sample records for the topic "fcc fluid catalytic" 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
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221

Data:Badff9c8-b392-400c-8fcc-16f3378c67a8 | Open Energy Information  

Open Energy Info (EERE)

Badff9c8-b392-400c-8fcc-16f3378c67a8 Badff9c8-b392-400c-8fcc-16f3378c67a8 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Two Rivers Water & Light Effective date: 2011/01/01 End date if known: Rate name: General Service- Three-Phase- Time-of-Day- 9am-9pm Sector: Commercial Description: This rate schedule is optional to all Gs-1, General Service customers. Customers that wish to be served on this rate schedule must apply to the utility for service. Once an optional customer begins service on this rate schedule, the customer shall remain on the rate for a minimum of one year. Any customer choosing to be served on this rate schedule waives all rights to billing adjustments arising from a claim that the bill for service would be less on another rate schedule than under this rate schedule.

222

Data:C7ddc3aa-c819-4acc-94bd-eaf4fcc9a06a | Open Energy Information  

Open Energy Info (EERE)

ddc3aa-c819-4acc-94bd-eaf4fcc9a06a ddc3aa-c819-4acc-94bd-eaf4fcc9a06a No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Bangor, Wisconsin (Utility Company) Effective date: 2010/05/19 End date if known: Rate name: Rg-1 Residential Service Single Phase Sector: Residential Description: Application: This rate will be applied to residential single-phase customers for ordinary household purposes. Single-phase motors may not exceed 5 horsepower individual-rated capacity without utility permission. Fixed Monthly Charge includes Commitment to Community Rider: $1.10 per customer per month Source or reference: http://psc.wi.gov/apps40/tariffs/viewfile.aspx?type=electric&id=350

223

Data:A4986fcc-f75a-404f-9fdc-614db53a03f7 | Open Energy Information  

Open Energy Info (EERE)

fcc-f75a-404f-9fdc-614db53a03f7 fcc-f75a-404f-9fdc-614db53a03f7 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Foley Board of Utilities Effective date: 1990/01/01 End date if known: Rate name: Unmetered Outdoor Lighting- 250W Metal Halide, Flood -Without Pole Sector: Lighting Description: Dusk to dawn unmetered service is covered by charges set forth below which also cover initial installation of overhead lines, poles (where applicable), fixture assembly including four foot mounting hardware for standard luminaries and two foot mounting hardware for flood lights, and maintenance including lamp replacements due to burn outs. Such charges do not cover replacement of lamps, luminaries, brackets or overhead lines which are damaged or destroyed due to vandalism or any other cause beyond the Utility's control, such facilities damaged or destroyed under such circumstances to be replaced by the Utility at the Consumer's expense. Lamp renewals and required maintenance will be performed only during regular daytime working hours as soon as practical after notification by the Consumer of the necessity.

224

Data:55fcc527-9fd1-4d65-bcf0-f2e525e03569 | Open Energy Information  

Open Energy Info (EERE)

fcc527-9fd1-4d65-bcf0-f2e525e03569 fcc527-9fd1-4d65-bcf0-f2e525e03569 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Indiana Michigan Power Co (Indiana) Effective date: 2013/04/01 End date if known: Rate name: ECLS - 200 watt HPS - Overhead Circuitry Sector: Lighting Description: Availability of Service. Available for streetlighting service to municipalities, counties, and other governmental subdivisions. The rates are applicable to new streetlights installed after April 6, 1981, and to 50,000 lumen high pressure sodium streetlights installed before that date. Only the lamps set forth below are available for such new service. Service rendered hereunder is predicated upon the execution by the customer of an agreement specifying the type, minimum number, and location of lamps to be served.

225

Data:Da49a4f7-b301-48a0-b0fc-c609e508c65a | Open Energy Information  

Open Energy Info (EERE)

f7-b301-48a0-b0fc-c609e508c65a f7-b301-48a0-b0fc-c609e508c65a No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Clay Electric Cooperative, Inc Effective date: 2011/01/01 End date if known: Rate name: Rate Schedule - RSL(A) Sector: Lighting Description: 6 or more consumers per light with a lamp size of 7000 lumens Source or reference: https://www.clayelectric.com/rates.aspx Source Parent: Comments 6 kWh/month estimate. $1.20 fixed monthly is per customer. Plus current month's Power Cost Adjustment and applicable taxes. Applicability Demand (kW) Minimum (kW): Maximum (kW): History (months): Energy (kWh)

226

Data:8049672c-1cc3-44b8-9ab9-e345633fcc69 | Open Energy Information  

Open Energy Info (EERE)

c-1cc3-44b8-9ab9-e345633fcc69 c-1cc3-44b8-9ab9-e345633fcc69 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: East Central Oklahoma Elec Coop Inc Effective date: 1995/12/01 End date if known: Rate name: Street Lighting - Up to 200 Watts Sector: Lighting Description: Available upon application to all consumers for illumination at desired points in developed areas served by the Cooperative. The monthly rate shall be increased by $2.00 if a steel pole is used for the installation of the light Source or reference: Rate Binder B #4 Source Parent: Comments Rate per month ($5.00) applies to up to 200 Watts of lighting installed on a wooden pole

227

Data:Fcc48f0d-e81c-4ddd-a300-a6b32a436c4d | Open Energy Information  

Open Energy Info (EERE)

Fcc48f0d-e81c-4ddd-a300-a6b32a436c4d Fcc48f0d-e81c-4ddd-a300-a6b32a436c4d No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Duke Energy Ohio Inc Effective date: 2013/05/06 End date if known: Rate name: Rate OL - Outdoor Lighting Service - MH 400 Watts - Flood Sector: Lighting Description: Applicable for outdoor lighting services on private property with Company owned fixtures in the Company's entire service area where secondary distribution lines are adjacent to the premises to be served. Not applicable for lighting public roadways which are dedicated, or anticipated to be dedicated, except to meet the occasional singular need of a customer who has obtained written approval from the proper governmental authority.

228

Experimental Properties of Fluids Group  

Science Conference Proceedings (OSTI)

The Experimental Properties of Fluids Group, Physical and Chemical Properties Division of the Chemical Science and Technology Laboratory, NIST.

2000-07-24T23:59:59.000Z

229

Supercritical fluid reverse micelle systems  

DOE Patents (OSTI)

of 1 ) United States Patent 5,158,704 Fulton ,   et al. October 27, 1992 Supercritical fluid reverse micelle systems

Fulton, John L. (Richland, WA); Smith, Richard D. (Richland, WA)

1992-01-01T23:59:59.000Z

230

Production of MHD fluid  

SciTech Connect

A hot gaseous fluid of low ash content, suitable for use in open-cycle MHD (magnetohydrodynamic) power generation, is produced by means of a three-stage process comprising (1) partial combustion of a fossil fuel to produce a hot gaseous product comprising CO.sub.2 CO, and H.sub.2 O, (2) reformation of the gaseous product from stage (1) by means of a fluidized char bed, whereby CO.sub.2 and H.sub.2 O are converted to CO and H.sub.2, and (3) combustion of CO and H.sub.2 from stage (2) to produce a low ash-content fluid (flue gas) comprising CO.sub.2 and H.sub.2 O and having a temperature of about 4000.degree. to 5000.degree.F.

Lacey, James J. (Library, PA); Kurtzrock, Roy C. (Bethel Park, PA); Bienstock, Daniel (Pittsburgh, PA)

1976-08-24T23:59:59.000Z

231

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

232

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

233

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

234

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

235

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

236

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

237

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

238

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

239

Downhole Fluid Analyzer Development  

SciTech Connect

A novel fiber optic downhole fluid analyzer has been developed for operation in production wells. This device will allow real-time determination of the oil, gas and water fractions of fluids from different zones in a multizone or multilateral completion environment. The device uses near infrared spectroscopy and induced fluorescence measurement to unambiguously determine the oil, water and gas concentrations at all but the highest water cuts. The only downhole components of the system are the fiber optic cable and windows. All of the active components--light sources, sensors, detection electronics and software--will be located at the surface, and will be able to operate multiple downhole probes. Laboratory testing has demonstrated that the sensor can accurately determine oil, water and gas fractions with a less than 5 percent standard error. Once installed in an intelligent completion, this sensor will give the operating company timely information about the fluids arising from various zones or multilaterals in a complex completion pattern, allowing informed decisions to be made on controlling production. The research and development tasks are discussed along with a market analysis.

Bill Turner

2006-11-28T23:59:59.000Z

240

Method for catalytic destruction of organic materials  

DOE Patents (OSTI)

A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250.degree. C. to 500.degree. C. and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials.

Sealock, Jr., L. John (Richland, WA); Baker, Eddie G. (Richland, WA); Elliott, Douglas C. (Richland, WA)

1997-01-01T23:59:59.000Z

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

Method for catalytic destruction of organic materials  

DOE Patents (OSTI)

A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250 to 500 C and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials. 7 figs.

Sealock, L.J. Jr.; Baker, E.G.; Elliott, D.C.

1997-05-20T23:59:59.000Z

242

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...

243

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

244

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

245

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

246

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

247

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

248

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

249

Supercritical fluid reverse micelle separation  

DOE Patents (OSTI)

A method of separating solute material from a polar fluid in a first polar fluid phase is provided. The method comprises combining a polar fluid, a second fluid that is a gas at standard temperature and pressure and has a critical density, and a surfactant. The solute material is dissolved in the polar fluid to define the first polar fluid phase. The combined polar and second fluids, surfactant, and solute material dissolved in the polar fluid is maintained under near critical or supercritical temperature and pressure conditions such that the density of the second fluid exceeds the critical density thereof. In this way, a reverse micelle system defining a reverse micelle solvent is formed which comprises a continuous phase in the second fluid and a plurality of reverse micelles dispersed in the continuous phase. The solute material is dissolved in the polar fluid and is in chemical equilibrium with the reverse micelles. The first polar fluid phase and the continuous phase are immiscible. The reverse micelles each comprise a dynamic aggregate of surfactant molecules surrounding a core of the polar fluid. The reverse micelle solvent has a polar fluid-to-surfactant molar ratio W, which can vary over a range having a maximum ratio W[sub o] that determines the maximum size of the reverse micelles. The maximum ratio W[sub o] of the reverse micelle solvent is then varied, and the solute material from the first polar fluid phase is transported into the reverse micelles in the continuous phase at an extraction efficiency determined by the critical or supercritical conditions. 27 figures.

Fulton, J.L.; Smith, R.D.

1993-11-30T23:59:59.000Z

250

Supercritical fluid reverse micelle separation  

DOE Patents (OSTI)

A method of separating solute material from a polar fluid in a first polar fluid phase is provided. The method comprises combining a polar fluid, a second fluid that is a gas at standard temperature and pressure and has a critical density, and a surfactant. The solute material is dissolved in the polar fluid to define the first polar fluid phase. The combined polar and second fluids, surfactant, and solute material dissolved in the polar fluid is maintained under near critical or supercritical temperature and pressure conditions such that the density of the second fluid exceeds the critical density thereof. In this way, a reverse micelle system defining a reverse micelle solvent is formed which comprises a continuous phase in the second fluid and a plurality of reverse micelles dispersed in the continuous phase. The solute material is dissolved in the polar fluid and is in chemical equilibrium with the reverse micelles. The first polar fluid phase and the continuous phase are immiscible. The reverse micelles each comprise a dynamic aggregate of surfactant molecules surrounding a core of the polar fluid. The reverse micelle solvent has a polar fluid-to-surfactant molar ratio W, which can vary over a range having a maximum ratio W.sub.o that determines the maximum size of the reverse micelles. The maximum ratio W.sub.o of the reverse micelle solvent is then varied, and the solute material from the first polar fluid phase is transported into the reverse micelles in the continuous phase at an extraction efficiency determined by the critical or supercritical conditions.

Fulton, John L. (Richland, WA); Smith, Richard D. (Richland, WA)

1993-01-01T23:59:59.000Z

251

Fluid bed material transfer method  

DOE Patents (OSTI)

A fluidized bed apparatus comprising a pair of separated fluid bed enclosures, each enclosing a fluid bed carried on an air distributor plate supplied with fluidizing air from below the plate. At least one equalizing duct extending through sidewalls of both fluid bed enclosures and flexibly engaged therewith to communicate the fluid beds with each other. The equalizing duct being surrounded by insulation which is in turn encased by an outer duct having expansion means and being fixed between the sidewalls of the fluid bed enclosures.

Pinske, Jr., Edward E. (Akron, OH)

1994-01-01T23:59:59.000Z

252

Non-catalytic steam hydrolysis of fats  

SciTech Connect

Hydrolysis of fats and oils produces fatty acid and glycerol. The catalyzed, liquid phase Colgate-Emry process, state-of-the-art, produces impure products that require extensive energy investment for their purification to commercial grade. Non-catalytic steam hydrolysis may produce products more easily purified. A bench-scale hydrolyzer was designed and constructed to contact descending liquid fat or oil with rising superheated steam. Each of the five stages in the reactor was designed similar to a distillation column stage to promote intimate liquid-gas contact. Degree of hydrolysis achieved in continuous tests using tallow feed were 15% at 280C and 35% at 300C at a tallow-to-steam mass feed ratio of 4.2. At a feed ratio of 9.2, the degree of hydrolysis was 21% at 300C. Decomposition was strongly evident at 325C but not at lower temperatures. Soybean oil rapidly polymerized under reaction conditions. Batch tests at 320C produced degrees of hydrolyses of between 44% and 63% using tallow and palm oil feeds. Over 95% fatty acids were present in a clean, readily separated organic portion of the overhead product from most tests. The test reactor had serious hydraulic resistance to liquid down-flow which limited operation to very long liquid residence times. These times are in excess of those that tallow and palm oil are stable at the reaction temperature. Little glycerol and extensive light organics were produced indicating that unexplained competing reactions to hydrolysis occurred in the experimental system. Further tests using an improved reactor will be required.

Deibert, M.C.

1992-08-28T23:59:59.000Z

253

Acoustic concentration of particles in fluid flow  

DOE Patents (OSTI)

An apparatus for acoustic concentration of particles in a fluid flow includes a substantially acoustically transparent membrane and a vibration generator that define a fluid flow path therebetween. The fluid flow path is in fluid communication with a fluid source and a fluid outlet and the vibration generator is disposed adjacent the fluid flow path and is capable of producing an acoustic field in the fluid flow path. The acoustic field produces at least one pressure minima in the fluid flow path at a predetermined location within the fluid flow path and forces predetermined particles in the fluid flow path to the at least one pressure minima.

Ward, Michael D. (Los Alamos, NM); Kaduchak, Gregory (Los Alamos, NM)

2010-11-23T23:59:59.000Z

254

It's The Fluids SEG Honorary Lecture  

E-Print Network (OSTI)

T.P. Water Butane CO2 #12;Fluid ­ Density 800 1000 1200FluidDensity[kg/m3] Brine CO2 0 2 4 6 8 10 0 200 400 600 Fluid Pressure [MPa] FluidDensity[kg/m Butane CO2 #12;Fluid ­ Modulus 2000 2500 3000 FluidModulus[MPa] Brine 0 2 4 6 8 10 0 500 1000 1500 Fluid Pressure [MPa] FluidModulus[MPa] Butane CO2 #12;GENERAL PHASE

255

Volatiles in hydrothermal fluids- A mass spectrometric study of fluid  

Open Energy Info (EERE)

Volatiles in hydrothermal fluids- A mass spectrometric study of fluid Volatiles in hydrothermal fluids- A mass spectrometric study of fluid inclusions from active geothermal systems Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Report: Volatiles in hydrothermal fluids- A mass spectrometric study of fluid inclusions from active geothermal systems Details Activities (4) Areas (4) Regions (0) Abstract: A system for analysis of inclusion gas contents based upon quadrupole mass spectrometry has been designed, assembled and tested during the first 7 months of funding. The system is currently being tested and calibrated using inclusions with known gas contents from active geothermal systems. Analyses are in progress on inclusions from the Salton Sea, Valles Caldera, Geysers, and Coso geothermal systems. Author(s): Mckibben, M. A.

256

Data:0437a759-bc57-4e39-b9fc-c4db2d15179f | Open Energy Information  

Open Energy Info (EERE)

9-bc57-4e39-b9fc-c4db2d15179f 9-bc57-4e39-b9fc-c4db2d15179f No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Northern Indiana Pub Serv Co Effective date: 2011/12/27 End date if known: Rate name: General Service - Large Sector: Industrial Description: TO WHOM AVAILABLE Available to General Service Customers for electric service who are located on the Company's electric supply lines suitable and adequate for supplying the service requested. CHARACTER OF SERVICE The Company will supply service to the extent of the capacity available from its electric supply lines, at such frequency, phase, regulation and one standard secondary voltage, or the available primary or transmission voltage at the location where service is required. (See Company Rule 3 for the Company's Standard Voltages.) The Customer will supply in accordance with plans and specifications furnished by the Company and at a mutually agreed upon location on the Customer's property, suitable buildings, structures, and foundations to house and support any protecting, switching, relaying, or metering equipment that may be supplied by the Company. For Customers utilizing thermal storage, the Customer must arrange the wiring for the thermal storage equipment to permit the measurement of the demand and energy use of such equipment by suitable metering equipment as specified by the Company. The Company shall, at all times, have the right to inspect such metering to ensure that such service metered is exclusively thermal storage use. The Company shall not supply demands in excess of 25,000 kilowatts under this schedule.

257

Data:56e4009c-31bf-49c8-a6fe-ed7ed4d5fcc4 | Open Energy Information  

Open Energy Info (EERE)

56e4009c-31bf-49c8-a6fe-ed7ed4d5fcc4 56e4009c-31bf-49c8-a6fe-ed7ed4d5fcc4 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: Rochester Gas & Electric Corp Effective date: 2013/11/01 End date if known: Rate name: SERVICE CLASSIFICATION NO. 4 RESIDENTIAL SERVICE - TIME-OF-USE RATE ESS (Retail Access Rate Choice) Schedule I Sector: Residential Description: APPLICABLE TO USE OF SERVICE FOR: All purposes, in Entire Territory, by any customer who would otherwise be served under Service Classification No. 1 of this schedule. The use of this service is voluntary for all customers. This Retail Access choice includes fixed components for RG&E delivery service, a Transition Charge (Non-Bypassable Charge ["NBC"] as described in Section 12.B.), and a Bill Issuance charge. Customers that elect ESS and receive a Consolidated Bill will not be subject to the Bill Issuance Charge. An Energy Service Services Company ("ESCO") provides Electric Power Supply to the customer. RG&E provides the delivery service only. Flat rate Adjustments = SBC+RPS+POR+TCV POR (http://www.rge.com/MediaLibrary/2/5/Content%20Management/RGE/SuppliersPartners/PDFs%20and%20Docs/STAT%20DISC%2019_8%20_2_.pdf)

258

Ultra Low NOx Catalytic Combustion for IGCC Power Plants  

DOE Green Energy (OSTI)

In order to meet DOE's goals of developing low-emissions coal-based power systems, PCI has further developed and adapted it's Rich-Catalytic Lean-burn (RCL{reg_sign}) catalytic reactor to a combustion system operating on syngas as a fuel. The technology offers ultra-low emissions without the cost of exhaust after-treatment, with high efficiency (avoidance of after-treatment losses and reduced diluent requirements), and with catalytically stabilized combustion which extends the lower Btu limit for syngas operation. Tests were performed in PCI's sub-scale high-pressure (10 atm) test rig, using a two-stage (catalytic then gas-phase) combustion process for syngas fuel. In this process, the first stage consists of a fuel-rich mixture reacting on a catalyst with final and excess combustion air used to cool the catalyst. The second stage is a gas-phase combustor, where the air used for cooling the catalyst mixes with the catalytic reactor effluent to provide for final gas-phase burnout and dilution to fuel-lean combustion products. During testing, operating with a simulated Tampa Electric's Polk Power Station syngas, the NOx emissions program goal of less than 0.03 lbs/MMBtu (6 ppm at 15% O{sub 2}) was met. NOx emissions were generally near 0.01 lbs/MMBtu (2 ppm at 15% O{sub 2}) (PCI's target) over a range on engine firing temperatures. In addition, low emissions were shown for alternative fuels including high hydrogen content refinery fuel gas and low BTU content Blast Furnace Gas (BFG). For the refinery fuel gas increased resistance to combustor flashback was achieved through preferential consumption of hydrogen in the catalytic bed. In the case of BFG, stable combustion for fuels as low as 88 BTU/ft{sup 3} was established and maintained without the need for using co-firing. This was achieved based on the upstream catalytic reaction delivering a hotter (and thus more reactive) product to the flame zone. The PCI catalytic reactor was also shown to be active in ammonia reduction in fuel allowing potential reductions in the burner NOx production. These reductions of NOx emissions and expanded alternative fuel capability make the rich catalytic combustor uniquely situated to provide reductions in capital costs through elimination of requirements for SCR, operating costs through reduction in need for NOx abating dilution, SCR operating costs, and need for co-firing fuels allowing use of lower value but more available fuels, and efficiency of an engine through reduction in dilution flows.

Shahrokh Etemad; Benjamin Baird; Sandeep Alavandi; William Pfefferle

2008-03-31T23:59:59.000Z

259

Ultrasonic fluid quality sensor system  

SciTech Connect

A system for determining the composition of a multiple-component fluid and for determining linear flow comprising at least one sing-around circuit that determines the velocity of a signal in the multiple-component fluid and that is correlatable to a database for the multiple-component fluid. A system for determining flow uses two of the inventive circuits, one of which is set at an angle that is not perpendicular to the direction of flow.

Gomm, Tyler J. (Meridian, ID); Kraft, Nancy C. (Idaho Falls, ID); Phelps, Larry D. (Pocatello, ID); Taylor, Steven C. (Idaho Falls, ID)

2002-10-08T23:59:59.000Z

260

Ultrasonic Fluid Quality Sensor System  

DOE Patents (OSTI)

A system for determining the composition of a multiple-component fluid and for determining linear flow comprising at least one sing-around circuit that determines the velocity of a signal in the multiple-component fluid and that is correlatable to a database for the multiple-component fluid. A system for determining flow uses two of the inventive circuits, one of which is set at an angle that is not perpendicular to the direction of flow.

Gomm, Tyler J. (Meridian, ID); Kraft, Nancy C. (Idaho Falls, ID); Phelps, Larry D. (Pocatello, ID); Taylor, Steven C. (Idaho Falls, ID)

2003-10-21T23:59:59.000Z

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

MOLTEN SALT HEAT TRANSFER FLUID  

thermal energy storage tanks Sandia has developed a heat transfer fluid (HTF) for use at elevated temperatures that has a lower freezing point

262

Fracturing Fluid Characterization Facility  

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

Documentation Page Documentation Page 1. Report No. DE - FC 21 - 92MC29077 2. 3. Recipient's Accession No. 5. Report Date August 31, 2000 4. Title and Subtitle Fracturing Fluid Characterization Facility 6. 7. Author(s) The University of Oklahoma 8. Performing Organization Rept. No. 10. Project/Task/Work Unit No. 9. Performing Organization Name and Address The University of Oklahoma Sarkeys Energy Center T301 100 E Boyd St Norman, OK 73019 11. Contract (C) or Grant (G) No. DOE:DE FC21 92 MC29077 13. Type of Report & Period Covered Final Report 09 30 92 - 03 31 00 12. Sponsoring Organization Name and Address US Dept of Energy - FETL 3610 Collins Ferry Road Morgantown, WV 26505 14. 15. Supplementary Notes Several technical papers were prepared and presented at various Society of Petroleum Engineers Conferences and US

263

DOE - Office of Legacy Management -- Catalytic Co - PA 40  

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

Catalytic Co - PA 40 Catalytic Co - PA 40 FUSRAP Considered Sites Site: Catalytic Co. (PA.40 ) Eliminated from further consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: Philadelphia , Pennsylvania PA.40-1 Evaluation Year: 1991 PA.40-1 Site Operations: Prime contractor for construction of the Fernald facility. Records indicate one time shipment of a very small quantity (4 lbs) of uranium metal to this site. PA.40-1 Site Disposition: Eliminated - Construction contractor - Potential for residual contamination from the very small quantity of uranium shipped to this site is considered remote PA.40-2 Radioactive Materials Handled: None - as a construction contractor Primary Radioactive Materials Handled: Uranium Metal - Believed to be a Souvenier. PA.40-1

264

Method for measuring recovery of catalytic elements from fuel cells  

Science Conference Proceedings (OSTI)

A method is provided for measuring the concentration of a catalytic clement in a fuel cell powder. The method includes depositing on a porous substrate at least one layer of a powder mixture comprising the fuel cell powder and an internal standard material, ablating a sample of the powder mixture using a laser, and vaporizing the sample using an inductively coupled plasma. A normalized concentration of catalytic element in the sample is determined by quantifying the intensity of a first signal correlated to the amount of catalytic element in the sample, quantifying the intensity of a second signal correlated to the amount of internal standard material in the sample, and using a ratio of the first signal intensity to the second signal intensity to cancel out the effects of sample size.

Shore, Lawrence (Edison, NJ); Matlin, Ramail (Berkeley, NJ)

2011-03-08T23:59:59.000Z

265

Catalytic Cracking of Gaseous Heavy Hydrocarbons by Ceramic Filters  

DOE Green Energy (OSTI)

The use of syngas from waste or biomass gasification to generate electricity is a way which is attracting increasing attention especially with regard to the demands of regenerable energy consumption and to the reduction of waste disposal. In order to feed the syngas to a gas motor or a gas turbine the gas has to be cleaned. In future also the coupling of biomass gasification with a fuel cell will be applied, which needs a very efficient gas cleaning. The decomposition of tars and the removal of particles from the gas are the key issues of gas cleaning. Up to now these two steps are performed in two separate units. Normally, the tars are decomposed in catalytic beds or honeycomb structures. The catalytic decomposition is achieved at temperatures between 750 C and 900 C depending on the catalyst used. Particles are removed by filtration of the hot gas. Filtration at high temperatures and with high efficiencies is possible when using ceramic filter elements. Ceramic hot gas filters are well established in advanced coal gasification, such as the integrated gasification combined cycle process, as well as in waste and biomass gasification and pyrolysis processes. Since the catalytic reaction requires high temperatures the gas has to be reheated after the particles are removed in the filter or the hot unfiltered gas has to flow through the catalytic unit. If the gas is filtered first, reheating of the gas stream is an additional cost factor. Furthermore, pipes downstream of the filter can be plugged, if the temperature of the gas falls below the condensation temperature of the heavy hydrocarbons. Using the second way of hot unfiltered gas flows through the catalytic unit, there is the problem of deactivation of the catalyst by deposition of dust at higher dust concentrations. At worst the catalytic unit can be plugged by dust deposition.

Heidenreich, S.; Nacken, M.; Walch, A.; Chudzinski, S.

2002-09-19T23:59:59.000Z

266

Optimum catalytic process for alcohol fuels from syngas  

DOE Green Energy (OSTI)

The objectives of this contract are to discover and evaluate the catalytic properties of novel homogeneous, heterogeneous, or combination catalytic systems for the production of alcohol fuel extenders from syngas, to evaluate analytically and on the bench scale novel reactor concepts for use in converting syngas to liquid fuel products, and to develop on the bench scale the best combination of chemistry, reactor, and total process configuration to achieve the minimum product cost for conversion of syngas to liquid fuel products. Methanol production and heterogeneous catalysis utilizing transition elements supported on metal oxides with spinel structure are discussed. 12 figs., 16 tabs.

Not Available

1990-04-28T23:59:59.000Z

267

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

268

Transdisciplinary Fluid Integration Research Center  

E-Print Network (OSTI)

Environment Reality-Coupled Computation Energy Dynamics Integrated Visual Informatics Super-Real-Time Medical of Fluid Science, Tohoku University, in April 2003. The next generation transdisciplinary research Research focus is to advance utilization of Computer Fluid Dynamics (CFD) for solving engineering problems

Obayashi, Shigeru

269

Fracturing fluids -- then and now  

Science Conference Proceedings (OSTI)

Fracturing fluid provides the means by which the hydraulic fracturing process can take place. All applications of well stimulation by fracturing must include selection of fracturing fluid in the initial phases of fracture design and treatment planning. Fracturing fluid has two important purposes: (1) to provide sufficient viscosity to suspend and transport proppant deep into the created fracture system and (2) to decompose, or break, chemically to a low viscosity to allow flowback of a major part of the fluid to the surface for fracture cleanup after the treatment is completed. Because of the importance of its rheological properties and behavior in the fracture under reservoir conditions during (and immediately after) the treatment, service company research laboratories have spent millions of dollars on R and D of fracturing fluids.

Jennings, A.R. Jr. [Enhanced Well Stimulation Inc., Plano, TX (United States)

1996-07-01T23:59:59.000Z

270

Fluid flow monitoring device  

DOE Patents (OSTI)

This invention consists of a flow meter and temperature measuring device comprising a tube with a body centered therein for restricting flow and a sleeve at the upper end of the tube to carry several channels formed longitudinally in the sleeve to the appropriate axial location where they penetrate the tube to allow pressure measurements and temperature measurements with thermocouples. The high pressure measurement is made using a channel penetrating the tube away from the body and the low pressure measurement is made at a location at the widest part of the body. An end plug seals the end of the device and holes at its upper end allow fluid to pass from the interior of the tube into a plenum. The channels are made by cutting grooves in the sleeve, the grooves widened at the surface of the sleeve and then a strip of sleeve material is welded to the grooves closing the channels. Preferably the sleeve is packed with powdered graphite before cutting the grooves and welding the strips.

McKay, M.D.; Sweeney, C.E.

1991-03-05T23:59:59.000Z

271

Fluid sampling system  

DOE Patents (OSTI)

An fluid sampling system allows sampling of radioactive liquid without spillage. A feed tank is connected to a liquid transfer jet powered by a pumping chamber pressurized by compressed air. The liquid is pumped upwardly into a sampling jet of a venturi design having a lumen with an inlet, an outlet, a constricted middle portion, and a port located above the constricted middle portion. The liquid is passed under pressure through the constricted portion causing its velocity to increase and its pressure to decreased, thereby preventing liquid from escaping. A septum sealing the port can be pierced by a two pointed hollow needle leading into a sample bottle also sealed by a pierceable septum affixed to one end. The bottle is evacuated by flow through the sample jet, cyclic variation in the sampler jet pressure periodically leaves the evacuated bottle with lower pressure than that of the port, thus causing solution to pass into the bottle. The remaining solution in the system is returned to the feed tank via a holding tank.

Houck, Edward D. (Idaho Falls, ID)

1994-01-01T23:59:59.000Z

272

Fluid sampling system  

DOE Patents (OSTI)

This invention comprises a fluid sampling system which allows sampling of radioactive liquid without spillage. A feed tank is connected to a liquid transfer jet powered by a pumping chamber pressurized by compressed air. The liquid is pumped up into a sampling jet of venturi design having a lumen with an inlet, an outlet, a constricted middle portion, and a port located above the constricted middle portion. The liquid is passed under pressure through the constricted portion causing its velocity to increase and its pressure to decrease, thereby preventing liquid from escaping. A septum sealing the port can be pierced by a two pointed hollow needle leading into a sample bottle also sealed by a pierceable septum affixed to one end. The bottle is evacuated by flow through the sample jet, cyclic variation in the sampler jet pressure periodicially leaves the evacuated bottle with lower pressure than that of the port, thus causing solution to pass into the bottle. The remaining solution in the system is returned to the feed tank via a holding tank.

Houck, E.D.

1993-12-31T23:59:59.000Z

273

Fluid sampling system  

DOE Patents (OSTI)

An fluid sampling system allows sampling of radioactive liquid without spillage. A feed tank is connected to a liquid transfer jet powered by a pumping chamber pressurized by compressed air. The liquid is pumped upwardly into a sampling jet of a venturi design having a lumen with an inlet, an outlet, a constricted middle portion, and a port located above the constricted middle portion. The liquid is passed under pressure through the constricted portion causing its velocity to increase and its pressure to be decreased, thereby preventing liquid from escaping. A septum sealing the port can be pierced by a two pointed hollow needle leading into a sample bottle also sealed by a pierceable septum affixed to one end. The bottle is evacuated by flow through the sample jet, cyclic variation in the sampler jet pressure periodically leaves the evacuated bottle with lower pressure than that of the port, thus causing solution to pass into the bottle. The remaining solution in the system is returned to the feed tank via a holding tank. 4 figs.

Houck, E.D.

1994-10-11T23:59:59.000Z

274

Tracing Geothermal Fluids  

DOE Green Energy (OSTI)

Geothermal water must be injected back into the reservoir after it has been used for power production. Injection is critical in maximizing the power production and lifetime of the reservoir. To use injectate effectively the direction and velocity of the injected water must be known or inferred. This information can be obtained by using chemical tracers to track the subsurface flow paths of the injected fluid. Tracers are chemical compounds that are added to the water as it is injected back into the reservoir. The hot production water is monitored for the presence of this tracer using the most sensitive analytic methods that are economically feasible. The amount and concentration pattern of the tracer revealed by this monitoring can be used to evaluate how effective the injection strategy is. However, the tracers must have properties that suite the environment that they will be used in. This requires careful consideration and testing of the tracer properties. In previous and parallel investigations we have developed tracers that are suitable from tracing liquid water. In this investigation, we developed tracers that can be used for steam and mixed water/steam environments. This work will improve the efficiency of injection management in geothermal fields, lowering the cost of energy production and increasing the power output of these systems.

Michael C. Adams; Greg Nash

2004-03-01T23:59:59.000Z

275

Development of a catalytic combustion system for the MIT Micro Gas Turbine Engine  

E-Print Network (OSTI)

As part of the MIT micro-gas turbine engine project, the development of a hydrocarbon-fueled catalytic micro-combustion system is presented. A conventionally-machined catalytic flow reactor was built to simulate the ...

Peck, Jhongwoo, 1976-

2003-01-01T23:59:59.000Z

276

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

277

Continued investigations of the catalytic reduction of N? to NH? by molybdenum triamidoamine complexes  

E-Print Network (OSTI)

A study of the effects of employing different solvents and the introduction of dihydrogen during the catalytic reduction of dinitrogen to ammonia with [HIPTN 3N]Mo complexes was completed. During a catalytic reaction, the ...

Hanna, Brian S. (Brian Stewart)

2011-01-01T23:59:59.000Z

278

Pyrolysis Oil Upgrading to Transportation Fuels by Catalytic  

E-Print Network (OSTI)

such as fast- pyrolysis and catalytic fast-pyrolysis for producing liquid fuels from biomass feedstocks biomass to a fast-pyrolysis reactor (Table 3.4), the greatest mass yield of bio-oil can be attributed............................................................................................- 70 - TABLE 2.18. BIOMASS PYROLYSIS TECHNOLOGIES, REACTION CONDITIONS AND PRODUCTS................- 70

Groningen, Rijksuniversiteit

279

Catalytic Esterification of Model Compounds of Biomass Pyrolysis Oil  

Science Conference Proceedings (OSTI)

Biomass pyrolysis oil is a complex mixture containing a wide variety of oxygenated compounds, which results in difficulties in bio-oil upgrading. To gain a clearer understanding of the reaction pathways, seven compounds were chosen to represent biomass ... Keywords: pyrolysis oil, model compounds, catalytic esterification

Zuo-gang Guo; Shu-rong Wang; Ying-ying Zhu

2009-10-01T23:59:59.000Z

280

Homogeneous catalytic hydrogenations of complex carbonaceous substrates. [16 references  

SciTech Connect

Results of homogeneous catalytic hydrogenation of complex unsaturated substrates including coal and coal-derived materials are reported, with organic soluble molecular complexes as catalysts. Among the substrates used were Hvab coal, solvent-refined coal, and COED pyrolysate. The hydrogenations were carried out in an autoclave. The results are summarized in tables.

Cox, J L; Wilcox, W A; Roberts, G L

1976-11-05T23:59:59.000Z

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

Ex-Situ Catalytic Fast Pyrolysis Technology Pathway  

DOE Green Energy (OSTI)

This technology pathway case investigates converting woody biomass using ex-situ catalytic fast pyrolysis followed by upgrading to gasoline-, diesel-, and jet-range hydrocarbon blendstocks. Technical barriers and key research needs that should be pursued for this pathway to be competitive with petroleum-derived blendstocks have been identified.

Biddy, M.; Dutta, A.; Jones, S.; Meyer, A.

2013-03-01T23:59:59.000Z

282

In-Situ Catalytic Fast Pyrolysis Technology Pathway  

DOE Green Energy (OSTI)

This technology pathway case investigates converting woody biomass using in-situ catalytic fast pyrolysis followed by upgrading to gasoline-, diesel-, and jet-range hydrocarbon blendstocks. Technical barriers and key research needs that should be pursued for this pathway to be competitive with petroleum-derived blendstocks have been identified.

Biddy, M.; Dutta, A.; Jones, S.; Meyer, A.

2013-03-01T23:59:59.000Z

283

ULTRA LOW NOx CATALYTIC COMBUSTION FOR IGCC POWER PLANTS  

Science Conference Proceedings (OSTI)

Tests were performed in PCI's sub-scale high-pressure (10 atm) test rig, using PCI's two-stage (catalytic / gas-phase) combustion process for syngas fuel. In this process, the first stage is a Rich-Catalytic Lean-burn (RCL{trademark}) catalytic reactor, wherein a fuel-rich mixture contacts the catalyst and reacts while final and excess combustion air cool the catalyst. The second stage is a gas-phase combustor, wherein the catalyst cooling air mixes with the catalytic reactor effluent to provide for final gas-phase burnout and dilution to fuel-lean combustion products. During the reporting period, PCI successfully achieved NOx = 0.011 lbs/MMBtu at 10 atm pressure (corresponding to 2.0 ppm NOx corrected to 15% O{sub 2} dry) with near-zero CO emissions, surpassing the project goal of baseload conditions corresponding to Tampa Electric's Polk Power Station operation on 100% syngas (no co-firing of natural gas).

Lance L. Smith

2004-03-01T23:59:59.000Z

284

Catalytic pyrolysis of xylan-based hemicellulose over zeolites  

Science Conference Proceedings (OSTI)

Xylan was selected as model compound of hemicellulose to investigate its thermal behavior over zeolites by using TG-FTIR. The chemical structure of xylan and characterization of catalysts were first studied. All the three catalysts, HZSM-5, H-? ... Keywords: TG-FTIR, acids, catalytic pyrolysis, furans, hemicellulose, xylan, zeolites

Xiujuan Guo; Shurong Wang; Yan Zhou; Zhongynag Luo

2011-02-01T23:59:59.000Z

285

Recycling and Disposal of Spent Selective Catalytic Reduction Catalyst  

Science Conference Proceedings (OSTI)

Selective catalytic reduction (SCR) technology has become widespread within the utility industry as a means of controlling emissions of nitrogen oxides (NOx). The technology uses a solid catalyst that deactivates over time; and thus significant volumes of catalyst will need regeneration, recycle, or disposal. This study examined issues related to spent catalyst recycle and disposal.

2003-11-12T23:59:59.000Z

286

Chemical Imaging of Catalytic Solids with Synchrotron Radiation  

Science Conference Proceedings (OSTI)

Heterogeneous catalysis is a term normally used to describe a group of catalytic processes, yet it could equally be employed to describe the catalytic solid itself. A better understanding of the chemical and structural variation within such materials is thus a pre-requisite for the rationalising of structure-function relationships and ultimately to the design of new, more sustainable catalytic processes. The past 20 years has witnessed marked improvements in technologies required for analytical measurements at synchrotron sources, including higher photon brightness, nano-focusing, rapid, high resolution data acquisition and in the handling of large volumes of data. It is now possible to image materials using the entire synchrotron radiative profile, thus heralding a new era of in situ/operando measurements of catalytic solids. In this tutorial review we discuss the recent work in this exciting new research area and finally conclude with a future outlook on what will be possible/challenging to measure in the not-too-distant future.

A Beale; S Jacques; B Weckhuysen

2011-12-31T23:59:59.000Z

287

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

288

Simulation of Hydrogen Production from Biomass Catalytic Gasification  

Science Conference Proceedings (OSTI)

In this study, biomass catalytic gasification process for producing H2-rich gas was presented. The process consists of mainly two fluidized beds—a gasifier and a CaO regenerator. The objective of this research is to develop a computer model of ... Keywords: biomass gasification, hydrogen production, Aspen Plus

Shan Cheng; Qian Wang; Hengsong Ji

2010-12-01T23:59:59.000Z

289

Particle sorter comprising a fluid displacer in a closed-loop fluid circuit  

SciTech Connect

Disclosed herein are methods and devices utilizing a fluid displacer in a closed-loop fluid circuit.

Perroud, Thomas D. (San Jose, CA); Patel, Kamlesh D. (Dublin, CA); Renzi, Ronald F. (Tracy, CA)

2012-04-24T23:59:59.000Z

290

Industrial Gas Turbine Engine Catalytic Pilot Combustor-Prototype Testing  

SciTech Connect

PCI has developed and demonstrated its Rich Catalytic Lean-burn (RCL®) technology for industrial and utility gas turbines to meet DOEâ??s goals of low single digit emissions. The technology offers stable combustion with extended turndown allowing ultra-low emissions without the cost of exhaust after-treatment and further increasing overall efficiency (avoidance of after-treatment losses). The objective of the work was to develop and demonstrate emission benefits of the catalytic technology to meet strict emissions regulations. Two different applications of the RCL® concept were demonstrated: RCL® catalytic pilot and Full RCL®. The RCL® catalytic pilot was designed to replace the existing pilot (a typical source of high NOx production) in the existing Dry Low NOx (DLN) injector, providing benefit of catalytic combustion while minimizing engine modification. This report discusses the development and single injector and engine testing of a set of T70 injectors equipped with RCL® pilots for natural gas applications. The overall (catalytic pilot plus main injector) program NOx target of less than 5 ppm (corrected to 15% oxygen) was achieved in the T70 engine for the complete set of conditions with engine CO emissions less than 10 ppm. Combustor acoustics were low (at or below 0.1 psi RMS) during testing. The RCL® catalytic pilot supported engine startup and shutdown process without major modification of existing engine controls. During high pressure testing, the catalytic pilot showed no incidence of flashback or autoignition while operating over a wide range of flame temperatures. In applications where lower NOx production is required (i.e. less than 3 ppm), in parallel, a Full RCL® combustor was developed that replaces the existing DLN injector providing potential for maximum emissions reduction. This concept was tested at industrial gas turbine conditions in a Solar Turbines, Incorporated high-pressure (17 atm.) combustion rig and in a modified Solar Turbines, Incorporated Saturn engine rig. High pressure single-injector rig and modified engine rig tests demonstrated NOx less than 2 ppm and CO less than 10 ppm over a wide flame temperature operating regime with low combustion noise (<0.15% peak-to-peak). Minimum NOx for the optimized engine retrofit Full RCL® designs was less than 1 ppm with CO emissions less than 10 ppm. Durability testing of the substrate and catalyst material was successfully demonstrated at pressure and temperature showing long term stable performance of the catalytic reactor element. Stable performance of the reactor element was achieved when subjected to durability tests (>5000 hours) at simulated engine conditions (P=15 atm, Tin=400C/750F.). Cyclic tests simulating engine trips was also demonstrated for catalyst reliability. In addition to catalyst tests, substrate oxidation testing was also performed for downselected substrate candidates for over 25,000 hours. At the end of the program, an RCL® catalytic pilot system has been developed and demonstrated to produce NOx emissions of less than 3 ppm (corrected to 15% O2) for 100% and 50% load operation in a production engine operating on natural gas. In addition, a Full RCL® combustor has been designed and demonstrated less than 2 ppm NOx (with potential to achieve 1 ppm) in single injector and modified engine testing. The catalyst/substrate combination has been shown to be stable up to 5500 hrs in simulated engine conditions.

Shahrokh Etemad; Benjamin Baird; Sandeep Alavandi; William Pfefferle

2009-09-30T23:59:59.000Z

291

High Performance Catalytic Heat Exchanger for SOFC Systems - FuelCell Energy  

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

Catalytic Heat Catalytic Heat Exchanger for SOFC Systems-FuelCell Energy Background In a typical solid oxide fuel cell (SOFC) power generation system, hot (~900 °C) effluent gas from a catalytic combustor serves as the heat source within a high-temperature heat exchanger, preheating incoming fresh air for the SOFC's cathode. The catalytic combustor and the cathode air heat exchanger together represent the largest opportunity for cost

292

Component Development to Accelerate Commercial Implementation of Ultra-Low Emissions Catalytic Combustion  

SciTech Connect

This final report describes a 2000-2003 program for the development of components and processes to enhance the commercialization of ultra-low emissions catalytic combustion in industrial gas turbines. The range of project tasks includes: development of more durable, lower-cost catalysts and catalytic combustor components; development and design of a catalytic pre-burner and a catalytic pilot burner for gas turbines, and on-site fuel conversion processing for utilization of liquid fuel.

Jon McCarty, Brian Berry, Kare Lundberg, Orris Anson

2003-03-31T23:59:59.000Z

293

Selective Catalytic Reduction (SCR) Procurement Guideline for Simple- and Combined-Cycle Combustion Turbines  

Science Conference Proceedings (OSTI)

This report is a selective catalytic reduction (SCR) procurement guideline for simple- and combined-cycle combustion turbines.

2008-03-17T23:59:59.000Z

294

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

295

Data:D182d5ba-7914-48b5-b232-8fcc974eaed7 | Open Energy Information  

Open Energy Info (EERE)

d5ba-7914-48b5-b232-8fcc974eaed7 d5ba-7914-48b5-b232-8fcc974eaed7 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Bangor, Wisconsin (Utility Company) Effective date: 2010/05/19 End date if known: Rate name: Cp-2 Large Power Service Transformer Ownership Discount with Parallel Generation(20kW or less) Sector: Industrial Description: Application: This rate will be applied to customers for all types of service if their monthly Maximum Measured Demand is in excess of 200 kilowatts (kW) per month for three or more months in a consecutive 12-month period. Customers billed on this rate shall continue to be billed on this rate until their monthly Maximum Measured Demand is less than 200 kW per month for 12 consecutive months. The utility shall offer customers billed on this rate a one time option to continue to be billed on this rate for another 12 months if their monthly Maximum Measured Demand is less than 200 kW per month. However, this option shall be offered with the provision that the customer waives all rights to billing adjustments arising from a claim that the bill for service would be less on another rate schedule than under this rate schedule. Primary Metering Discount: Customers metered on the primary side of the transformer shall be given a 2.00 percent discount on the monthly energy charge, distribution demand charge, and demand charge. The PCAC and the monthly customer charge will not be eligible for the primary metering discount. Transformer Ownership Discount: Customers who own and maintain their own transformers or substations shall be given a credit of $0.15 per kW of distribution demand. Customer-owned substation equipment shall be operated and maintained by the customer. Support and substation equipment is subject to utility inspection and approval.

296

Short Communication Catalytic coal gasification: use of calcium versus potassium*  

E-Print Network (OSTI)

career on process optimization and control, fluid mechanics, the analysis of coal gasification reactors my earlier work on coal gasification reactors, polymer fiber spinning, and the activated sludge

297

Standardization of Thermo-Fluid Modeling in Modelica.Fluid  

E-Print Network (OSTI)

This article discusses the Modelica.Fluid library that has been included in the Modelica Standard Library 3.1. Modelica.Fluid provides interfaces and basic components for the device-oriented modeling of onedimensional thermo-fluid flow in networks containing vessels, pipes, fluid machines, valves and fittings. A unique feature of Modelica.Fluid is that the component equations and the media models as well as pressure loss and heat transfer correlations are decoupled from each other. All components are implemented such that they can be used for media from the Modelica.Media library. This means that an incompressible or compressible medium, a single or a multiple substance medium with one or more phases might be used with one and the same model as long as the modeling assumptions made hold. Furthermore, trace substances are supported. Modeling assumptions can be configured globally in an outer System object. This covers in particular the initialization, uni- or bi-directional flow, and dynamic or steady-state formulation of mass, energy, and momentum balance. All assumptions can be locally refined for every component. While Modelica.Fluid contains a reasonable set of component models, the goal of the library is not to provide a comprehensive set of models, but rather to provide interfaces and best practices for the treatment of issues such as connector design and implementation of energy, mass and momentum balances. Applications from various domains are presented.

Rüdiger Franke; et al.

2009-01-01T23:59:59.000Z

298

Isotopic Analysis- Fluid | Open Energy Information  

Open Energy Info (EERE)

Isotopic Analysis- Fluid Isotopic Analysis- Fluid Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Isotopic Analysis- Fluid Details Activities (61) Areas (32) Regions (6) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Fluid Lab Analysis Information Provided by Technique Lithology: Water rock interaction Stratigraphic/Structural: Hydrological: Origin of hydrothermal fluids; Mixing of hydrothermal fluids Thermal: Isotopic ratios can be used to characterize and locate subsurface thermal anomalies. Dictionary.png Isotopic Analysis- Fluid: Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in

299

Downhole Fluid Sampling | Open Energy Information  

Open Energy Info (EERE)

Downhole Fluid Sampling Downhole Fluid Sampling Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Downhole Fluid Sampling Details Activities (0) Areas (0) Regions (0) NEPA(0) Exploration Technique Information Exploration Group: Downhole Techniques Exploration Sub Group: Well Testing Techniques Parent Exploration Technique: Well Testing Techniques Information Provided by Technique Lithology: Stratigraphic/Structural: Hydrological: Water composition and source of fluids. Gas composition and source of fluids. Thermal: Water temperature. Distinguish magmatic/mantle heat inputs. Can be used to estimate reservoir fluid temperatures. Dictionary.png Downhole Fluid Sampling: Downhole fluid sampling is done to characterize the chemical, thermal, or hydrological properties of a surface or subsurface aqueous system. Downhole

300

Intelligent Fluid Infrastructure for Embedded Networking  

E-Print Network (OSTI)

mobile element into the networking infrastructure.Our fluid infrastructure design saves significant energy inIntelligent Fluid Infrastructure for Embedded Networks Aman

Kansal, Aman; Somasundara, Arun; Jea, David C; Srivastava, Mani B; Estrin, D

2004-01-01T23:59:59.000Z

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

Intelligent Fluid Infrastructure for Embedded Networks  

E-Print Network (OSTI)

Intelligent Fluid Infrastructure for Embedded Networks Amanto develop a fluid infrastructure: mobile components arebuilt into the system infrastructure for enabling specific

Aman Kansal; Arun Somasundara; David Jea; Mani Srivastava; Deborah Estrin

2004-01-01T23:59:59.000Z

302

Fluid Imaging | Open Energy Information  

Open Energy Info (EERE)

Page Page Edit History Facebook icon Twitter icon » Fluid Imaging Jump to: navigation, search Contents 1 Geothermal Lab Call Projects for Fluid Imaging 2 Geothermal ARRA Funded Projects for Fluid Imaging Geothermal Lab Call Projects for Fluid Imaging Loading map... {"format":"googlemaps3","type":"ROADMAP","types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"limit":200,"offset":0,"link":"all","sort":[""],"order":[],"headers":"show","mainlabel":"","intro":"","outro":"","searchlabel":"\u2026 further results","default":"","geoservice":"google","zoom":14,"width":"600px","height":"350px","centre":false,"layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","icon":"","visitedicon":"","forceshow":true,"showtitle":true,"hidenamespace":false,"template":false,"title":"","label":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"locations":[{"text":"

303

Nonlinear Fluid Dynamics from Gravity  

E-Print Network (OSTI)

Black branes in AdS5 appear in a four parameter family labeled by their velocity and temperature. Promoting these parameters to Goldstone modes or collective coordinate fields -- arbitrary functions of the coordinates on the boundary of AdS5 -- we use Einstein's equations together with regularity requirements and boundary conditions to determine their dynamics. The resultant equations turn out to be those of boundary fluid dynamics, with specific values for fluid parameters. Our analysis is perturbative in the boundary derivative expansion but is valid for arbitrary amplitudes. Our work may be regarded as a derivation of the nonlinear equations of boundary fluid dynamics from gravity. As a concrete application we find an explicit expression for the expansion of this fluid stress tensor including terms up to second order in the derivative expansion.

Sayantani Bhattacharyya; Veronika E Hubeny; Shiraz Minwalla; Mukund Rangamani

2007-12-14T23:59:59.000Z

304

Visually simulating realistic fluid motion  

E-Print Network (OSTI)

In this thesis we investigate various methods for visually simulating fluid flow. The focus is on implementing effective fluid simulation within an interactive animation system. Two implementations have been developed based on derivations and simplifications of the Navier-Stokes' equations. The first implementation is the most accurate and follows the physics of fluid dynamics more closely. However, the high computation times incurred by this implementation make it inappropriate as an interactive method. The second approach is not as accurate as the first one, however it incurs lower computation times. This second method is only able to model a subset of the total fluid behavior. The second method has been integrated into an interactive modeling and animation environment. Several examples are included.

Naithani, Priyanka

2002-01-01T23:59:59.000Z

305

Deferring trust in fluid replication  

Science Conference Proceedings (OSTI)

Mobile nodes rely on external services to provide safety, sharing, and additional resources. Unfortunately, as mobile nodes move through the networking infrastructure, the costs of accessing servers change. Fluid replication allows mobile clients to ...

Brian D. Noble; Ben Fleis; Landon P. Cox

2000-09-01T23:59:59.000Z

306

Bio-inspired fluid locomotion  

E-Print Network (OSTI)

We have developed several novel methods of locomotion at low Reynolds number, for both Newtonian and non-Newtonian fluids: Robosnails 1 and 2, which operate on a lubrication layer, and the three-link swimmer which moves ...

Chan, Brian, 1980-

2009-01-01T23:59:59.000Z

307

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

308

Method for recovering catalytic elements from fuel cell membrane electrode assemblies  

DOE Patents (OSTI)

A method for recovering catalytic elements from a fuel cell membrane electrode assembly is provided. The method includes converting the membrane electrode assembly into a particulate material, wetting the particulate material, forming a slurry comprising the wetted particulate material and an acid leachate adapted to dissolve at least one of the catalytic elements into a soluble catalytic element salt, separating the slurry into a depleted particulate material and a supernatant containing the catalytic element salt, and washing the depleted particulate material to remove any catalytic element salt retained within pores in the depleted particulate material.

Shore, Lawrence (Edison, NJ); Matlin, Ramail (Berkeley Heights, NJ); Heinz, Robert (Ludwigshafen, DE)

2012-06-26T23:59:59.000Z

309

Solar photo-thermal catalytic reactions to produce high value chemicals  

DOE Green Energy (OSTI)

This report presents a summary of the research work accomplished to date on the utilization of solar photo-thermal energy to convert low cost chemical feedstocks into high $-value chemical products. The rationale is that the solar IR-VIS-UV spectrum is unique, supplying endothermic reaction energy as well as VIS-UV for photochemical activation. Chemical market analysis and product price distribution focused attention on speciality chemicals with prices >$1.00/lb, and a synthesis sequence of n-paraffins to aromatics to partial oxidized products. The experimental work has demonstrated that enhanced reaction effects result from VIS-UV irradiation of catalytically active V2O5/SiO2. Experiments of the past year have been on dehydrogenation and dehydrocyclization of n-paraffins to olefins and aromatics with preference for the latter. Recent results using n-hexane produced 95% conversion with 56% benzene; it is speculated that aromatic yield should reach {approximately}70% by further optimization. Pilot- and commercial-scale reactor configurations have been examined; the odds-on-favorite being a shallow fluid-bed of catalyst with incident radiation from the top. Sequencing for maximum cost effectiveness would be day-time endothermic followed by night-time exothermic reactions to produce the products.

Prengle, H.W. Jr.; Wentworth, W.E. [Houston Univ., TX (United States)

1992-04-01T23:59:59.000Z

310

Catalytic destruction of groundwater contaminants in reactive extraction wells  

DOE Green Energy (OSTI)

A system for remediating groundwater contaminated with halogenated solvents, certain metals and other inorganic species based on catalytic reduction reactions within reactive well bores. The groundwater treatment uses dissolved hydrogen as a reducing agent in the presence of a metal catalyst, such a palladium, to reduce halogenated solvents (as well as other substituted organic compounds) to harmless species (e.g., ethane or methane) and immobilize certain metals to low valence states. The reactive wells function by removing water from a contaminated water-bearing zone, treating contaminants with a well bore using catalytic reduction, and then reinjecting the treated effluent into an adjacent water-bearing zone. This system offers the advantages of a compact design with a minimal surface footprint (surface facilities) and the destruction of a broad suite of contaminants without generating secondary waste streams.

McNab, Jr., Walt W. (Concord, CA); Reinhard, Martin (Stanford, CA)

2002-01-01T23:59:59.000Z

311

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

Science Conference Proceedings (OSTI)

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to hydrocarbon fuels to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. 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, Mary J.; Jones, Susanne B.

2013-03-31T23:59:59.000Z

312

Selective dehydrogenation of propane over novel catalytic materials  

Science Conference Proceedings (OSTI)

The conversion of small alkanes into alkenes represents an important chemical processing area; ethylene and propylene are the two most important organic chemicals manufactured in the U.S. These chemicals are currently manufactured by steam cracking of ethane and propane, an extremely energy intensive, nonselective process. The development of catalytic technologies (e.g., selective dehydrogenation) that can be used to produce ethylene and propylene from ethane and propane with greater selectivity and lower energy consumption than steam cracking will have a major impact on the chemical processing industry. This report details a study of two novel catalytic materials for the selective dehydrogenation of propane: Cr supported on hydrous titanium oxide ion-exchangers, and Pt nanoparticles encapsulated in silica and alumina aerogel and xerogel matrices.

Sault, A.G.; Boespflug, E.P.; Martino, A.; Kawola, J.S.

1998-02-01T23:59:59.000Z

313

Selective Dehydrogenation of Propane over Novel Catalytic Materials  

E-Print Network (OSTI)

The conversion of small alkanes into alkenes represents an important chemical processing area; ethylene and propylene are the two most important organic chemicals manufactured in the U.S. These chemicals are currently manufactured by steam cracking of ethane and propane, an extremely energy intensive, nonselective process. The development of catalytic technologies (e.g., selective dehydrogenation) that can be used to produce ethylene and propylene from ethane and propane with greater selectivity and lower energy consumption than steam cracking will have a major impact on the chemical processing industry. This report details a study of two novel catalytic materials for the selective dehydrogenation of propane: Cr supported on hydrous titanium oxide ion-exchangers, and Pt nanoparticles encapsulated in silica and alumina aerogel and xerogel matrices. 4 Acknowledgment The authors thank United Catalysts, Inc. for stimulating technical discussions and for providing samples of commercial ...

Allen Sault Elaine; Elaine P. Boespflug Anthony Martino; Jeffrey S. Kawola

1998-01-01T23:59:59.000Z

314

Size Effect of Ruthenium Nanoparticles in Catalytic Carbon Monoxide Oxidation  

Science Conference Proceedings (OSTI)

Carbon monoxide oxidation over ruthenium catalysts has shown an unusual catalytic behavior. Here we report a particle size effect on CO oxidation over Ru nanoparticle (NP) catalysts. Uniform Ru NPs with a tunable particle size from 2 to 6 nm were synthesized by a polyol reduction of Ru(acac){sub 3} precursor in the presence of poly(vinylpyrrolidone) stabilizer. The measurement of catalytic activity of CO oxidation over two-dimensional Ru NPs arrays under oxidizing reaction conditions (40 Torr CO and 100 Torr O{sub 2}) showed an activity dependence on the Ru NP size. The CO oxidation activity increases with NP size, and the 6 nm Ru NP catalyst shows 8-fold higher activity than the 2 nm catalysts. The results gained from this study will provide the scientific basis for future design of Ru-based oxidation catalysts.

Joo, Sang Hoon; Park, Jeong Y.; Renzas, J. Russell; Butcher, Derek R.; Huang, Wenyu; Somorjai, Gabor A.

2010-04-04T23:59:59.000Z

315

Fluidic Catalytic Cracking Power Recovery Dynamic Computer Simulation  

E-Print Network (OSTI)

Fluidic Cat Crackers (FCC) using the catalyst regeneration cycle are candidates for more power efficient operation by the use of high temperature dirty gas expanders. In a previous paper, a computer simulation was described for the steady state operation of the primary mechanical components, specifically the axial compressor and hot gas expander. The present work expands upon the steady state model to add the dynamic characteristics of these elements as well as the effects of the controlling process valves. In many applications the expander will develop more power than the axial compressor can absorb. A power absorbing source, specifically an electrical generator, converts the mechanical excess power into electrical energy. A review of the mechanical equipment and the electrical generator operating modes and controls is needed so that the process designer and operator will know how the system will respond if process upsets were to occur. The program code developed can simulate these elements for specific processes and demonstrate the logic control scheme proposed by the process designer. This information will therefore allow the process operator, process designer and mechanical equipment supplier an understanding of the interplay of the system control elements and define specific operating limits.

Samurin, N. A.

1980-01-01T23:59:59.000Z

316

Thermochemical Equilibrium Modeling of Selective Catalytic Reduction (SRC) Catalyst Poisons  

Science Conference Proceedings (OSTI)

A previous EPRI publication (1022073) provided a detailed literature review on the propensity of the alkali and alkaline earth metals sodium (Na), potassium (K), calcium (Ca) and the Group (V) elements phosphorus (P) and arsenic (As) to deactivate selective catalytic reduction (SCR) catalysts in commercial flue gas cleaning systems. It also listed the conditions under which such deactivation has been reported. This report extends this earlier work to predict the transformation of SCR catalyst ...

2012-11-01T23:59:59.000Z

317

Selective Catalytic Reduction Mercury Oxidation Data to Support Catalyst Management  

Science Conference Proceedings (OSTI)

Selective catalytic reduction (SCR) mercury oxidation can be pivotal for Mercury and Air Toxics Standards compliance, especially for those units that rely on co-benefits as their primary method of mercury control. Much work has been done historically to understand the mercury behavior across SCRs, especially as a function of operating conditions, and in particular, flue gas composition. The present work seeks to integrate the accumulated knowledge into a practical document that will aid utilities in ...

2013-11-13T23:59:59.000Z

318

Selective Non-Catalytic Reduction (SNCR) Technology Overview  

Science Conference Proceedings (OSTI)

This document provides a technology overview regarding the application and operation of selective non-catalytic reduction (SNCR) to coal-fired electric utility boilers for the incremental reduction of NOx emissions. The document provides a historical perspective of the SNCR technology development, background regarding the reaction chemistry, and process parameters that impact SNCR NOx reduction performance. In addition, a review of reagent choices along with storage and handling requirements is ...

2013-09-12T23:59:59.000Z

319

Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

This document is the 2010 version of Operation and Maintenance Guidelines for Selective Catalytic Reduction Systems, originally published in 2001 and updated annually. New content this year includes: (1) A section on static mixers added in Chapter 3; (2) Substantial expansion of the discussion on inspection of ammonia storage and delivery equipment in Chapter 8; (3) Expanded coverage of unit startup, shutdown, and low-load operation in Chapter 15; (4) a new chapter, Chapter 18, on the means to ensure tha...

2010-11-29T23:59:59.000Z

320

CATALYTIC CONVERSION OF ORGANIC COMPOUNDS USING PENETRATING RADIATION  

DOE Patents (OSTI)

A method of hydrogenating an olefinic hydrocarbon by irradiating a substrate catalyst and increasing its catalytic activity is described. Ferric oxide with about 0.005% by weight of at least one oxide of a metal selected from the group consisting of aluminum, magnesium, nickel, zirconium, and manganese incorporated therein is irradiated. Then an alkane is placed upon the surface of the catalyst and irradiated in an atmosphere of hydrogen. Any olefin produced from this radiolysis becomes hydrogenated. (AEC)

Caffrey, J.M. Jr.

1961-10-01T23:59:59.000Z

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

Equilibrium Characteristics of Selective Catalytic Reduction (SCR) Catalyst Poisons  

Science Conference Proceedings (OSTI)

In Power River Basin (PRB) coal applications, phosphorus (P) is known as the primary catalyst poison. Recent utility experience shows that some units burning PRB coal are deactivating the selective catalytic reduction (SCR) catalyst more rapidly than others. The exact mechanism is not well understood but could be related to boiler type or combustion modifications leading to increased levels of phosphorus vaporization. With increased levels of phosphorus in flue gas, greater quantities of phosphorus would...

2011-12-20T23:59:59.000Z

322

Selective Catalytic Reduction Catalyst Recycle and Re-Use Options  

Science Conference Proceedings (OSTI)

Given the widespread implementation of selective catalytic reduction (SCR) technology, there is a great deal of interest in finding viable recycle/re-use routes for spent catalyst as an alternative to landfilling. The current effort has focused on detailed evaluation of several recycle/re-use processes that were identified in previous EPRI studies. These recycle/re-use technologies include mineral filler applications, incorporation into wet-bottom boiler slag, cement kiln co-processing, and use in iron/s...

2010-12-21T23:59:59.000Z

323

Simulation of ethylbenzene dehydrogenation in microporous 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 of reactions which are currently limited by either thermodynamic equilibria, product inhibition, or kinetic selectivity. Examples of systems 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 of the anticipated increased yield per reactor pass, large 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 reactants and energy. The controlled, defined reaction zone (the membrane interface), will facilitate the reactor design process and permit greater control of reactor dynamics.

Not Available

1989-04-01T23:59:59.000Z

324

Exxon Catalytic Coal Gasification Process Predevelopment Program. Final project report  

SciTech Connect

This report summarizes the results of work conducted on Predevelopment Research for the Exxon Catalytic Coal Gasification Process. The eighteen-month effort (July 1976-December 1977) was a coordinated program which included operation of a continuous fluidized-bed gasifier, parallel bench-scale research, and engineering studies leading to the preparation of a commercial-scale plant study design and economics for producing SNG from Illinois coal.

Kalina, T.; Nahas, N.C.

1978-12-01T23:59:59.000Z

325

Pitch-catch only ultrasonic fluid densitometer  

DOE Patents (OSTI)

The present invention is an ultrasonic fluid densitometer that uses a material wedge and pitch-catch only ultrasonic transducers for transmitting and receiving ultrasonic signals internally reflected within the material wedge. Density of a fluid is determined by immersing the wedge into the fluid and measuring reflection of ultrasound at the wedge-fluid interface.

Greenwood, Margaret S. (Richland, WA); Harris, Robert V. (Pasco, WA)

1999-01-01T23:59:59.000Z

326

Computational fluid dynamic modeling of fluidized-bed polymerization reactors  

SciTech Connect

Polyethylene is one of the most widely used plastics, and over 60 million tons are produced worldwide every year. Polyethylene is obtained by the catalytic polymerization of ethylene in gas and liquid phase reactors. The gas phase processes are more advantageous, and use fluidized-bed reactors for production of polyethylene. Since they operate so close to the melting point of the polymer, agglomeration is an operational concern in all slurry and gas polymerization processes. Electrostatics and hot spot formation are the main factors that contribute to agglomeration in gas-phase processes. Electrostatic charges in gas phase polymerization fluidized bed reactors are known to influence the bed hydrodynamics, particle elutriation, bubble size, bubble shape etc. Accumulation of electrostatic charges in the fluidized-bed can lead to operational issues. In this work a first-principles electrostatic model is developed and coupled with a multi-fluid computational fluid dynamic (CFD) model to understand the effect of electrostatics on the dynamics of a fluidized-bed. The multi-fluid CFD model for gas-particle flow is based on the kinetic theory of granular flows closures. The electrostatic model is developed based on a fixed, size-dependent charge for each type of particle (catalyst, polymer, polymer fines) phase. The combined CFD model is first verified using simple test cases, validated with experiments and applied to a pilot-scale polymerization fluidized-bed reactor. The CFD model reproduced qualitative trends in particle segregation and entrainment due to electrostatic charges observed in experiments. For the scale up of fluidized bed reactor, filtered models are developed and implemented on pilot scale reactor.

Rokkam, Ram [Ames Laboratory

2012-11-02T23:59:59.000Z

327

Ultracentrifuge for separating fluid mixtures  

DOE Patents (OSTI)

1. A centrifuge for the separation of fluid mixtures having light and heavy fractions comprising a cylindrical rotor, disc type end-plugs closing the ends of the rotor, means for mounting said rotor for rotation about its cylindrical axis, a housing member enclosing the rotor, a vacuum chamber in said housing about the central portion of the rotor, a collection chamber at each end of the housing, the innermost side of which is substantially formed by the outer face of the end-plug, means for preventing flow of the fluid from the collection chambers to said vacuum chamber, at least one of said end-plugs having a plurality of holes therethrough communicating between the collection chamber adjacent thereto and the inside of the rotor to induce countercurrent flow of the fluid in the centrifuge, means for feeding fluid to be processed into the centrifuge, means communicating with the collection chambers to extract the light and heavy separated fractions of the fluid, and means for rotating the rotor.

Lowry, Ralph A. (Charlottesville, VA)

1976-01-01T23:59:59.000Z

328

DEVELOPMENT OF NEW DRILLING FLUIDS  

SciTech Connect

The goal of the project has been to develop new types of drill-in fluids (DIFs) and completion fluids (CFs) for use in natural gas reservoirs. Phase 1 of the project was a 24-month study to develop the concept of advanced type of fluids usable in well completions. Phase 1 tested this concept and created a kinetic mathematical model to accurately track the fluid's behavior under downhole conditions. Phase 2 includes tests of the new materials and practices. Work includes the preparation of new materials and the deployment of the new fluids and new practices to the field. The project addresses the special problem of formation damage issues related to the use of CFs and DIFs in open hole horizontal well completions. The concept of a ''removable filtercake'' has, as its basis, a mechanism to initiate or trigger the removal process. Our approach to developing such a mechanism is to identify the components of the filtercake and measure the change in the characteristics of these components when certain cleanup (filtercake removal) techniques are employed.

David B. Burnett

2003-08-01T23:59:59.000Z

329

Fluid Metrology Calibration Services - Gas, Water, or Liquid ...  

Science Conference Proceedings (OSTI)

Fluid Metrology Calibration Services - Gas, Water, Natural Gas, or Liquid Hydrocarbon Flows Special Tests. Fluid Metrology ...

2013-01-25T23:59:59.000Z

330

NETL: Releases & Briefs - MFIX: Particle-fluid flow modeling, fast and free  

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

MFIX: Particle-fluid Flow Modeling, Fast and Free MFIX: Particle-fluid Flow Modeling, Fast and Free Until recently, full solution of the complex set of equations that describe gas-particle flows was nearly impossible. But an open-source code developed by researchers at the National Energy Technology Laboratory (NETL), and designed to run on inexpensive PC (Beowulf) clusters, makes it relatively simple. Called MFIX (Multi-phase Flow with Interphase eXchange), the code incorporates special numerical techniques that provide an efficient solution to the coupled equations, exceeding the capabilities of commercial software. Originally developed at NETL to model fixed, fluidized and bubbling coal gasification technologies, its power has been used in research ranging from catalytic cracking in oil refineries to volcanology. A free, fully-functional version is available at www.mfix.org

331

Fluid dynamics of bacterial turbulence  

E-Print Network (OSTI)

Self-sustained turbulent structures have been observed in a wide range of living fluids, yet no quantitative theory exists to explain their properties. We report experiments on active turbulence in highly concentrated 3D suspensions of Bacillus subtilis and compare them with a minimal fourth-order vector-field theory for incompressible bacterial dynamics. Velocimetry of bacteria and surrounding fluid, determined by imaging cells and tracking colloidal tracers, yields consistent results for velocity statistics and correlations over two orders of magnitude in kinetic energy, revealing a decrease of fluid memory with increasing swimming activity and linear scaling between energy and enstrophy. The best-fit model parameters allow for quantitative agreement with experimental data.

Jörn Dunkel; Sebastian Heidenreich; Knut Drescher; Henricus H. Wensink; Markus Bär; Raymond E. Goldstein

2013-02-21T23:59:59.000Z

332

Wellbottom fluid implosion treatment system  

DOE Patents (OSTI)

A system for inducing implosion shock forces on perforation traversing earth formations with fluid pressure where an implosion tool is selected relative to a shut in well pressure and a tubing pressure to have a large and small area piston relationship in a well tool so that at a predetermined tubing pressure the pistons move a sufficient distance to open an implosion valve which permits a sudden release of well fluid pressure into the tubing string and produces an implosion force on the perforations. A pressure gauge on the well tool records tubing pressure and well pressure as a function of time.

Brieger, Emmet F. (HC 67 Box 58, Nogal, NM 88341)

2001-01-01T23:59:59.000Z

333

Holographic plasma and anyonic fluids  

E-Print Network (OSTI)

We use alternative quantisation of the $D3/D5$ system to explore properties of a strongly coupled charged plasma and strongly coupled anyonic fluids. The $S$-transform of the $D3/D5$ system is used as a model for charged matter interacting with a U(1) gauge field in the large coupling regime, and we compute the dispersion relationship of the propagating electromagnetic modes as the density and temperature are changed. A more general $SL(2,\\mathbb{Z})$ transformation gives a strongly interacting anyonic fluid, and we study its transport properties as we change the statistics of the anyons and the background magnetic field.

Daniel K. Brattan; Gilad Lifschytz

2013-10-09T23:59:59.000Z

334

Directed flow fluid rinse trough  

SciTech Connect

Novel rinse troughs accomplish thorough uniform rinsing. The tanks are suitable for one or more essentially planar items having substantially the same shape. The troughs ensure that each surface is rinsed uniformly. The new troughs also require less rinse fluid to accomplish a thorough rinse than prior art troughs.

Kempka, Steven N. (9504 Lona La., Albuquerque, NM 87111); Walters, Robert N. (11872 LaGrange St., Boise, ID 83709)

1996-01-01T23:59:59.000Z

335

Heat Transfer in Complex Fluids  

SciTech Connect

Amongst the most important constitutive relations in Mechanics, when characterizing the behavior of complex materials, one can identify the stress tensor T, the heat flux vector q (related to heat conduction) and the radiant heating (related to the radiation term in the energy equation). Of course, the expression 'complex materials' is not new. In fact, at least since the publication of the paper by Rivlin & Ericksen (1955), who discussed fluids of complexity (Truesdell & Noll, 1992), to the recently published books (Deshpande et al., 2010), the term complex fluids refers in general to fluid-like materials whose response, namely the stress tensor, is 'non-linear' in some fashion. This non-linearity can manifest itself in variety of forms such as memory effects, yield stress, creep or relaxation, normal-stress differences, etc. The emphasis in this chapter, while focusing on the constitutive modeling of complex fluids, is on granular materials (such as coal) and non-linear fluids (such as coal-slurries). One of the main areas of interest in energy related processes, such as power plants, atomization, alternative fuels, etc., is the use of slurries, specifically coal-water or coal-oil slurries, as the primary fuel. Some studies indicate that the viscosity of coal-water mixtures depends not only on the volume fraction of solids, and the mean size and the size distribution of the coal, but also on the shear rate, since the slurry behaves as shear-rate dependent fluid. There are also studies which indicate that preheating the fuel results in better performance, and as a result of such heating, the viscosity changes. Constitutive modeling of these non-linear fluids, commonly referred to as non-Newtonian fluids, has received much attention. Most of the naturally occurring and synthetic fluids are non-linear fluids, for example, polymer melts, suspensions, blood, coal-water slurries, drilling fluids, mud, etc. It should be noted that sometimes these fluids show Newtonian (linear) behavior for a given range of parameters or geometries; there are many empirical or semi-empirical constitutive equations suggested for these fluids. There have also been many non-linear constitutive relations which have been derived based on the techniques of continuum mechanics. The non-linearities oftentimes appear due to higher gradient terms or time derivatives. When thermal and or chemical effects are also important, the (coupled) momentum and energy equations can give rise to a variety of interesting problems, such as instability, for example the phenomenon of double-diffusive convection in a fluid layer. In Conclusion, we have studied the flow of a compressible (density gradient type) non-linear fluid down an inclined plane, subject to radiation boundary condition. The heat transfer is also considered where a source term, similar to the Arrhenius type reaction, is included. The non-dimensional forms of the equations are solved numerically and the competing effects of conduction, dissipation, heat generation and radiation are discussed. It is observed that the velocity increases rapidly in the region near the inclined surface and is slower in the region near the free surface. Since R{sub 7} is a measure of the heat generation due to chemical reaction, when the reaction is frozen (R{sub 7}=0.0) the temperature distributions would depend only on R{sub 1}, and R{sub 2}, representing the effects of the pressure force developed in the material due to the distribution, R{sub 3} and R{sub 4} viscous dissipation, R{sub 5} the normal stress coefficient, R{sub 6} the measure of the emissivity of the particles to the thermal conductivity, etc. When the flow is not frozen (RP{sub 7} > 0) the temperature inside the flow domain is much higher than those at the inclined and free surfaces. As a result, heat is transferred away from the flow toward both the inclined surface and the free surface with a rate that increases as R{sub 7} increases. For a given temperature, an increase in {zeta} implies that the activation energy is smaller and thus, the reaction ra

Mehrdad Massoudi

2012-01-01T23:59:59.000Z

336

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

337

Fabrication of catalytic electrodes for molten carbonate fuel cells  

DOE Patents (OSTI)

A porous layer of catalyst material suitable for use as an electrode in a molten carbonate fuel cell includes elongated pores substantially extending across the layer thickness. The catalyst layer is prepared by depositing particulate catalyst material into polymeric flocking on a substrate surface by a procedure such as tape casting. The loaded substrate is heated in a series of steps with rising temperatures to set the tape, thermally decompose the substrate with flocking and sinter bond the catalyst particles into a porous catalytic layer with elongated pores across its thickness. Employed as an electrode, the elongated pores provide distribution of reactant gas into contact with catalyst particles wetted by molten electrolyte.

Smith, James L. (Lemont, IL)

1988-01-01T23:59:59.000Z

338

Catalytic steam gasification of bagasse for the production of methanol  

DOE Green Energy (OSTI)

Pacific Northwest Laboratory (PNL) tested the catalytic gasification of bagasse for the production of methanol synthesis gas. The process uses steam, indirect heat, and a catalyst to produce synthesis gas in one step in fluidized bed gasifier. Both laboratory and process development scale (nominal 1 ton/day) gasifiers were used to test two different catalyst systems: (1) supported nickel catalysts and (2) alkali carbonates doped on the bagasse. This paper presents the results of laboratory and process development unit gasification tests and includes an economic evaluation of the process. 20 references, 6 figures, 9 tables.

Baker, E.G.; Brown, M.D.

1983-12-01T23:59:59.000Z

339

Inter-Layer Mixing in Selective Catalytic Reduction Systems  

Science Conference Proceedings (OSTI)

The primary parameter for achieving high NOx reduction and low ammonia (NH3) slip in Selective Catalytic Reduction (SCR) systems on large coal-fired boilers is a uniform NH3/NOx ratio distribution at the catalyst surface. Large non-uniformities yield local NH3/NOx ratios greater than one, leading directly to NH3 slip. Areas of low NH3/NOx ratios have low NOx reduction. Both of these conditions are undesirable. SCR system designers specify a maximum acceptable NH3/NOx non-uniformity at the catalyst inlet....

2005-12-20T23:59:59.000Z

340

Catalytic H2O2 decomposition on palladium surfaces  

E-Print Network (OSTI)

The catalytic decomposition of H?O? at smooth single-crystal and polycrystalline palladium surfaces that had been subjected to various surface modifications has been studied. Monolayer and submonolayer coverages of I, Br and Cl adsorbates were used to pretrial the palladium surfaces. The rate of decomposition was found to be dependent upon the coverage and identity of the halogen adsorbate. Experimental measurements were based upon Auger electron spectroscopy (AES), low-energy electron Diffraction (LEED) and X-ray photoelectron spectroscopy (XPS) for the surface adlayers, redox titration for H?O? concentration determinations, and evolved-O? gas volume measurements for the decomposition rates.

Salinas, S. Adriana

1998-01-01T23:59:59.000Z

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

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

342

Catalytic effects of period iv transition metal in the oxidation of biodiesel.  

E-Print Network (OSTI)

??CATALYTIC EFFECTS OF PERIOD IV TRANSITION METALS IN THE OXIDATION OF BIODIESEL BRADLEY R CLARK December 2011 Advisors: Dr. Steve Salley, Dr. Simon Ng, Dr.… (more)

Clark, Bradley

2012-01-01T23:59:59.000Z

343

Catalytic conversion of C3+ alcohols to hydrocarbon blend-stock  

Catalytic conversion of C3+ alcohols to hydrocarbon blend-stock Note: The technology described above is an early stage opportunity. Licensing rights to this ...

344

Microsoft Word - 41890_PW_Catalytic Combustion_Factsheet_Rev01...  

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

Plan and Integration Study for rich catalytic combustion as applied to industrial gas turbines fired on both natural gas and coal derived synthesis gas. The overall goal is...

345

Experimental investigation and systems modeling of fractional catalytic pyrolysis of pine .  

E-Print Network (OSTI)

??The fractional catalytic pyrolysis of pine was studied both experimentally and through models. A preliminary stage economic analysis was conducted for a wood chip pyrolysis… (more)

Goteti, Anil Chaitanya

2010-01-01T23:59:59.000Z

346

CRITICALITY CURVES FOR PLUTONIUM HYDRAULIC FLUID MIXTURES  

SciTech Connect

This Calculation Note performs and documents MCNP criticality calculations for plutonium (100% {sup 239}Pu) hydraulic fluid mixtures. Spherical geometry was used for these generalized criticality safety calculations and three geometries of neutron reflection are: {sm_bullet}bare, {sm_bullet}1 inch of hydraulic fluid, or {sm_bullet}12 inches of hydraulic fluid. This document shows the critical volume and critical mass for various concentrations of plutonium in hydraulic fluid. Between 1 and 2 gallons of hydraulic fluid were discovered in the bottom of HA-23S. This HA-23S hydraulic fluid was reported by engineering to be Fyrquel 220. The hydraulic fluid in GLovebox HA-23S is Fyrquel 220 which contains phosphorus. Critical spherical geometry in air is calculated with 0 in., 1 in., or 12 inches hydraulic fluid reflection.

WITTEKIND WD

2007-10-03T23:59:59.000Z

347

Environmentally Acceptable Transformer Fluids: An Update  

Science Conference Proceedings (OSTI)

This report offers information about the physical, dielectric, chemical, and environmental properties of transformer fluids and their operational impacts. Companies can use this information to choose environmentally acceptable green fluids.

2010-07-14T23:59:59.000Z

348

Fluid sampling system for a nuclear reactor  

DOE Patents (OSTI)

A system of extracting fluid samples, either liquid or gas, from the interior of a nuclear reactor containment utilizes a jet pump. To extract the sample fluid, a nonradioactive motive fluid is forced through the inlet and discharge ports of a jet pump located outside the containment, creating a suction that draws the sample fluid from the containment through a sample conduit connected to the pump suction port. The mixture of motive fluid and sample fluid is discharged through a return conduit to the interior of the containment. The jet pump and means for removing a portion of the sample fluid from the sample conduit can be located in a shielded sample grab station located next to the containment. A non-nuclear grade active pump can be located outside the grab sampling station and the containment to pump the nonradioactive motive fluid through the jet pump. 1 fig.

Lau, L.K.; Alper, N.I.

1994-11-22T23:59:59.000Z

349

Graphene Compositions And Drilling Fluids Derived Therefrom ...  

Drilling fluids comprising graphenes and nanoplatelet additives and methods for production thereof are disclosed. Graphene includes graphite oxide, graphene oxide ...

350

SUBSIDENCE DUE TO GEOTHERMAL FLUID WITHDRAWAL  

E-Print Network (OSTI)

drilling activity completely ceased. Of these, 65 bores account for about 95 percent of the total fluid

Narasimhan, T.N.

2013-01-01T23:59:59.000Z

351

Fluid Metrology Calibration Services - Water Flow  

Science Conference Proceedings (OSTI)

Fluid Metrology Calibration Services - Water Flow. Water Flow Calibrations 18020C. ... NIST provides calibration services for water flow meters. ...

2011-10-03T23:59:59.000Z

352

Attrition Resistant Catalyst Materials for Fluid Bed ...  

Biomass and Biofuels Attrition Resistant Catalyst Materials for Fluid Bed Applications National Renewable Energy Laboratory. Contact NREL About This ...

353

Ultrasonic fluid densitometer for process control  

DOE Patents (OSTI)

The present invention is an ultrasonic fluid densitometer that uses at least one pair of transducers for transmitting and receiving ultrasonic signals internally reflected within a material wedge. A temperature sensor is provided to monitor the temperature of the wedge material. Density of a fluid is determined by immersing the wedge into the fluid and measuring reflection of ultrasound at the wedge-fluid interface and comparing a transducer voltage and wedge material temperature to a tabulation as a function of density.

Greenwood, Margaret S. (Richland, WA)

2000-01-01T23:59:59.000Z

354

Catalytic combustor for integrated gasification combined cycle power plant  

DOE Patents (OSTI)

A gasification power plant 10 includes a compressor 32 producing a compressed air flow 36, an air separation unit 22 producing a nitrogen flow 44, a gasifier 14 producing a primary fuel flow 28 and a secondary fuel source 60 providing a secondary fuel flow 62 The plant also includes a catalytic combustor 12 combining the nitrogen flow and a combustor portion 38 of the compressed air flow to form a diluted air flow 39 and combining at least one of the primary fuel flow and secondary fuel flow and a mixer portion 78 of the diluted air flow to produce a combustible mixture 80. A catalytic element 64 of the combustor 12 separately receives the combustible mixture and a backside cooling portion 84 of the diluted air flow and allows the mixture and the heated flow to produce a hot combustion gas 46 provided to a turbine 48. When fueled with the secondary fuel flow, nitrogen is not combined with the combustor portion.

Bachovchin, Dennis M. (Mauldin, SC); Lippert, Thomas E. (Murrysville, PA)

2008-12-16T23:59:59.000Z

355

Intensified Fischer-Tropsch Synthesis Process with Microchannel Catalytic Reactors  

SciTech Connect

A microchannel catalytic reactor with improved heat and mass transport has been used for Fischer-Tropsch synthesis to produce fuels and chemicals. This type of novel reactor takes advantages of highly active and selective catalysts with increased site density so that the FT synthesis process can be intensified. It was demonstrated that this microchannel reactor based process can be carried out at gas hourly space velocity (GHSV) as high as 60,000 hr-1 to achieve greater than 60% of one-pass CO conversion while maintaining low methane selectivity (<10%) and high chain growth probability(>0.9). Such superior FT synthesis performance has not ever been reported in the prior open literatures. The overall productivity to heavy hydrocarbons has been significantly improved over the conventional reactor technology. In this study, performance data were obtained in a wide range of pressure (10atm-35atm) and hydrogen to carbon monoxide ratio (1-2.5). The catalytic system was characterized by BET, scanning electron microcopy (SEM), transmission electron microcopy(TEM), and H2 chemisorption. A three dimensional pseudo-homogeneous model were used to simulate temperature profiles in the exothermic reaction system in order to optimize the reactor design and intensify the synthesis process. Intraparticle non-isothermal characteristics are also analyzed for the FT synthesis catalyst.

Cao, Chunshe; Hu, Jianli; Li, Shari; Wilcox, Wayne A.; Wang, Yong

2009-02-28T23:59:59.000Z

356

An Exploration of Catalytic Chemistry on Au/Ni(111)  

Science Conference Proceedings (OSTI)

This project explored the catalytic oxidation chemistry that can be effected on a Au/Ni(111) surface alloy. A Au/Ni(111) surface alloy is a Ni(111) surface on which less than 60% of the Ni atoms are replaced at random positions by Au atoms. The alloy is produced by vapor deposition of a small amount of Au onto Ni single crystals. The Au atoms do not result in an epitaxial Au overlayer or in the condensation of the Au into droplets. Instead, Au atoms displace and then replace Ni atoms on a Ni(111) surface, even though Au is immiscible in bulk Ni. The two dimensional structure of the clean Ni surface is preserved. This alloy is found to stabilize an adsorbed peroxo-like O2 species that is shown to be the critical reactant in the low temperature catalytic oxidation of CO and that is suspected to be the critical reactant in other oxidation reactions. This investigation revealed a new, practically important catalyst for CO oxidation that has since been patented.

Sylvia T. Ceyer

2011-12-09T23:59:59.000Z

357

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

358

Helium measurements of pore-fluids obtained from SAFOD drillcore  

E-Print Network (OSTI)

ionized water (DI) as drilling fluid. This procedure avoidsbeen contaminated with drilling fluids during recovery ofscheduled drilling phases to enable fluid-only sampling.

Ali, S.

2010-01-01T23:59:59.000Z

359

Wavelet Turbulence for Fluid Simulation Theodore Kim  

E-Print Network (OSTI)

in the running time. We instead propose an algorithm that generates small-scale fluid de- tail procedurally. We of the key results of Kolmogorov the- ory is that the energy spectrum of a turbulent fluid approaches a five spectra [Perrier et al. 1995], and the sub- stitution is common in fluid dynamics [Farge et al. 1996

California at Santa Barbara, University of

360

Two Fluid Shear-Free Composites  

E-Print Network (OSTI)

Shear-free composite fluids are constructed from two Letelier rotated unaligned perfect fluids. The component fluid parameters necessary to construct a shear-free composite are investigated. A metric in the Stephani-Barnes solution family and a simple stationary metric are discussed.

J. P. Krisch; E. N. Glass

2013-07-03T23:59:59.000Z

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

Fall 2011 ME 542 Advanced Fluid Mechanics ENG ME 542 Advanced Fluid Mechanics  

E-Print Network (OSTI)

Fall 2011 ME 542 Advanced Fluid Mechanics ENG ME 542 Advanced Fluid Mechanics Instructor: M. S. Howe EMA 218 mshowe@bu.edu This course is intended to consolidate your knowledge of fluid mechanics specialized courses on fluid mechanics, acoustics and aeroacoustics. Outline syllabus: Equations of motion

362

Research on Algae Removal by Electro-flotation/Photo-catalytic Oxidization Combined Process  

Science Conference Proceedings (OSTI)

The lake-type raw water was treated in Photo-catalytic Oxidization reactor. Under the condition of the inflow discharge control in 15L/h, the padding packing compares 2/5, UV lamp 30W, added no chemicals, pH 7.35, use the electro-flotation to treat it ... Keywords: algae, Electro-flotation, photo-catalytic oxidization

Wang Liping; Jiang Weijuan; Gao Naiyun

2011-01-01T23:59:59.000Z

363

==================== !"#$%&'()*+,-+./,0)12 Development of Micro Ejector for Butane Catalytic Combustor  

E-Print Network (OSTI)

==================== !"#$%&'()*+,-+./,0)12 Development of Micro Ejector for Butane Catalytic Combustor ===== ==== !" = !" = = !" A micro ejector for butane catalytic combustor is investigated. Quasi-1 ejector that the volume flow rate of entrained air can reach 43 times the value of butane when the back

Kasagi, Nobuhide

364

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

365

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

366

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

367

Data:67cdf3c6-fcc4-4b0e-ae80-a5d3d1f3e056 | Open Energy Information  

Open Energy Info (EERE)

cdf3c6-fcc4-4b0e-ae80-a5d3d1f3e056 cdf3c6-fcc4-4b0e-ae80-a5d3d1f3e056 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1. Basic Information 2. Demand 3. Energy << Previous 1 2 3 Next >> Basic Information Utility name: City of Clintonville, Wisconsin (Utility Company) Effective date: 2006/05/05 End date if known: Rate name: Gs-2 General Time-of-Day Service Single Phase 8am-8pm Sector: Commercial Description: Power Cost Adjustment Clause - All metered rates shall be subject to a positive or negative power cost adjustment charge equivalent to the amount by which the current cost of power (per kWh of sales) is greater or lesser than the base cost of power purchased (per kWh of sales). The base cost of power is $0.0680 per kWh. See schedule PCAC.

368

Catalytic studies of supported Pd-Au catalysts  

E-Print Network (OSTI)

Although Pd-Au high-surface area catalysts are used in industry to improve activity and selectivity, a thorough understanding of the nature of these enhancements is lacking. A molecular-level understanding of catalytic reactions under actual reaction conditions is the ultimate goal. This thesis is mainly focused on the application of Pd-Au supported catalysts for vinyl acetate synthesis and CO oxidation reactions using highsurface area catalysts. We have attempted to improve the conventional Pd-Au based catalyst by synthesizing novel acetate-based and polymer-based catalysts. The corresponding catalytic reactivity and selectivity were measured and compared to conventional Pd-Au based catalyst systems. Subsequent characterization was performed using characterization techniques, such as, X-ray diffraction (XRD) and transmission electron microscopy (TEM). From our bimetallic catalytic studies, it was evident that the addition of Au to Pd leads to increased reactivity and selectivity. This surface modification is an important factor in the altered reaction kinetics for vinyl acetate (VA) synthesis and CO oxidation reactions. Promoted and unpromoted Pd-Au/SiO2/K+ catalyst were used for VA synthesis and the effect of pre-adsorbed O2, acetic acid and the role of oxygen were explored. The VA reaction rate of novel acetate-based Pd-Au/SiO2 catalyst was 3.5 times higher than conventional Pd-Au catalysts. Also, 100% selectivity was obtained for acetate-based Pd-Au/SiO2 at 130 oC and the VA formation rate was comparable to that of conventional Pd-Au catalysts. Therefore, the acetate-based Pd-Au/SiO2 catalyst seems very promising and can be explored further. Also, Pd(1):Au(4)/SiO2 catalysts demonstrate 100% CO conversion at much lower temperatures (90 oC) compared with other Pd-Au based catalysts. Furthermore, we were successful in obtaining sufficient CO oxidation activity with increased metal loading (5 wt%) and these catalysts did not deactivate under above-ambient reaction temperature conditions, which make 1:4 Pd- Au/SiO2 catalyst a good candidate for further exploration in CO oxidation reactions.

Boopalachandran, Praveenkumar

369

Fluid Inclusion Analysis | Open Energy Information  

Open Energy Info (EERE)

Fluid Inclusion Analysis Fluid Inclusion Analysis Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Fluid Inclusion Analysis Details Activities (20) Areas (11) Regions (1) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Fluid Lab Analysis Information Provided by Technique Lithology: Stratigraphic/Structural: Hydrological: Fluid composition at a point in time and space Thermal: The minimum temperature of fluid inclusion formation Cost Information Low-End Estimate (USD): 17.571,757 centUSD 0.0176 kUSD 1.757e-5 MUSD 1.757e-8 TUSD / sample Median Estimate (USD): 17.571,757 centUSD 0.0176 kUSD 1.757e-5 MUSD 1.757e-8 TUSD / sample High-End Estimate (USD): 26.782,678 centUSD

370

Microsoft Word - 41891_SWPC_Catalytic Combustor_Factsheet_Rev01_04-24.doc  

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

891_SWPC_CATALYTIC COMBUSTOR_FACTSHEET_REV01_04-24.DOC 891_SWPC_CATALYTIC COMBUSTOR_FACTSHEET_REV01_04-24.DOC Facts Sheet: Catalytic Combustor for Fuel Flexible Gas Turbine (DE-FC26-03NT41891) I. PROJECT PARTICIPANTS A. Siemens Westinghouse Power Corporation B. Caterpillar/Solar Turbine C. Penn State University D. Southern Company Services II. PROJECT DESCRIPTION A. Objective: To develop and demonstrate a cost effective, fuel flexible (syngas/natural gas) catalytic combustor that will achieve ultra low NOx emissions (2ppm) at the exit of the gas turbine and without the use of backend cleanup in Integrated Gasification Combined Cycle (IGCC) application. B. Background/Relevancy 1. Background: Catalytic combustion has been shown to achieve lowest emissions in conventional gas turbine application (natural gas only). Available technical data indicate that it can be effective

371

Catalytic carbon membranes for hydrogen production. Final report  

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

372

Catalytic Hydrogenation of Bio-Oil for Chemicals and Fuels  

DOE Green Energy (OSTI)

The scope of work includes optimizing processing conditions and demonstrating catalyst lifetime for catalyst formulations that are readily scaleable to commercial operations. We use a bench-scale, continuous-flow, packed-bed, catalytic, tubular reactor, which can be operated in the range of 100-400 mL/hr., from 50-400 C and up to 20MPa (see Figure 1). With this unit we produce upgraded bio-oil from whole bio-oil or useful bio-oil fractions, specifically pyrolytic lignin. The product oils are fractionated, for example by distillation, for recovery of chemical product streams. Other products from our tests have been used in further testing in petroleum refining technology at UOP and fractionation for product recovery in our own lab. Further scale-up of the technology is envisioned and we will carry out or support process design efforts with industrial partners, such as UOP.

Elliott, Douglas C.

2006-02-14T23:59:59.000Z

373

Catalytic Fast Pyrolysis for the Production of the Hydrocarbon Biofuels  

SciTech Connect

Catalytic fast pyrolysis is a promising technique for conversion of biomass into hydrocarbons for use as transportation fuels. For over 30 years this process has been studied and it has been demonstrated that oils can be produced with high concentrations of hydrocarbons and low levels of oxygen. However, the yields from this type of conversion are typically low and the catalysts, which are often zeolites, are quickly deactivated through coking. In addition, the hydrocarbons produced are primarily aromatic molecules (benzene, toluene, xylene) that not desirable for petroleum refineries and are not well suited for diesel or jet engines. The goals of our research are to develop new multifunction catalysts for the production of gasoline, diesel and jet fuel range molecules and to improve process conditions for higher yields and low coking rates. We are investigating filtration and the use of hydrogen donor molecules to improve catalyst performance.

Nimlos, M. R.; Robichaud, D. J.; Mukaratate, C.; Donohoe, B. S.; Iisa, K.

2013-01-01T23:59:59.000Z

374

Phenol and phenolics from lignocellulosic biomass by catalytic microwave pyrolysis  

Science Conference Proceedings (OSTI)

Catalytic microwave pyrolysis of biomass using activated carbon was investigated to determine the effects of pyrolytic conditions on the yields of phenol and phenolics. The high concentrations of phenol (38.9%) and phenolics (66.9%) were obtained at the temperature of 589 K, catalyst-to-biomass ratio of 3:1 and retention time of 8 min. The increase of phenol and its derivatives compared to pyrolysis without catalysts has a close relationship with the decomposition of lignin under the performance of activated carbon. The concentration of esters was also increased using activated carbon as a catalyst. The high content of phenols obtained in this study can be used either directly as fuel after upgrading or as feedstock of biobased phenols for chemical industry.

Bu, Quan; Lei, Hanwu; Ren, Shoujie; Wang, Lu; Holladay, Johnathan E.; Zhang, Qin; Tang, Juming; Ruan, Roger

2011-07-01T23:59:59.000Z

375

Coal hydrogenation and deashing in ebullated bed catalytic reactor  

SciTech Connect

An improved process for hydrogenation of coal containing ash with agglomeration and removal of ash from an ebullated bed catalytic reactor to produce deashed hydrocarbon liquid and gas products. In the process, a flowable coal-oil slurry is reacted with hydrogen in an ebullated catalyst bed reaction zone at elevated temperature and pressure conditions. The upward velocity and viscosity of the reactor liquid are controlled so that a substantial portion of the ash released from the coal is agglomerated to form larger particles in the upper portion of the reactor above the catalyst bed, from which the agglomerated ash is separately withdrawn along with adhering reaction zone liquid. The resulting hydrogenated hydrocarbon effluent material product is phase separated to remove vapor fractions, after which any ash remaining in the liquid fraction can be removed to produce substantially ash-free coal-derived liquid products.

Huibers, Derk T. A. (Pennington, NJ); Johanson, Edwin S. (Princeton, NJ)

1983-01-01T23:59:59.000Z

376

Ex-Situ Catalytic Fast Pyrolysis Technology Pathway  

SciTech Connect

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to hydrocarbon fuels to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This pathway case investigates converting woody biomass using ex-situ catalytic fast pyrolysis followed by upgrading to gasoline , diesel and jet range blendstocks . Technical barriers and key research needs that should be pursued for this pathway to be competitive with petroleum-derived blendstocks have been identified.

Biddy, Mary J.; Dutta, Abhijit; Jones, Susanne B.; Meyer, Pimphan A.

2013-03-31T23:59:59.000Z

377

In-Situ Catalytic Fast Pyrolysis Technology Pathway  

SciTech Connect

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to hydrocarbon fuels to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This pathway case investigates converting woody biomass using in-situ catalytic fast pyrolysis followed by upgrading to gasoline, diesel, and jet range blendstocks. Technical barriers and key research needs that should be pursued for this pathway to be competitive with petroleum-derived blendstocks have been identified.

Biddy, Mary J.; Dutta, Abhijit; Jones, Susanne B.; Meyer, Pimphan A.

2013-03-31T23:59:59.000Z

378

For stricter emissions needs, try custom catalytic reduction  

Science Conference Proceedings (OSTI)

When O`Brien California Cogen Ltd. was contracted to develop a system to generate steam for an Artesia, Calif., mild producer`s evaporation process, local regulations required NO{sub x} emissions reduced 9 ppm and CO to 10 ppm. Johnson Matthey supplied the solution with a custom system combining an oxidation catalyst to control CSO emissions and a selective catalytic reduction (SCR) system to control NO{sub x}. O`Brien`s cogen operation runs off an aircraft-derivative GE Gas Turbine, model LM2500, with a 22.4-MW output. The catalyst system is installed in the exhaust stream of a heat recovery steam generator (HRSG) form the Henry Vogt Machine Co.

Chambers, A.

1995-08-01T23:59:59.000Z

379

Method For Selective Catalytic Reduction Of Nitrogen Oxides  

DOE Patents (OSTI)

A method for catalytically reducing nitrogen oxide compounds (NO.sub.x, defined as nitric oxide, NO, +nitrogen dioxide, NO.sub.2) in a gas by a material comprising a base metal consisting essentially of CuO and Mn, and oxides of Mn, on an activated metal hydrous metal oxide support, such as HMO:Si. A promoter, such as tungsten oxide or molybdenum oxide, can be added and has been shown to increase conversion efficiency. This method provides good conversion of NO.sub.x to N.sub.2, good selectivity, good durability, resistance to SO.sub.2 aging and low toxicity compared with methods utilizing vanadia-based catalysts.

Mowery-Evans, Deborah L. (Broomfield, CO); Gardner, Timothy J. (Albuquerque, NM); McLaughlin, Linda I. (Albuquerque, NM)

2005-02-15T23:59:59.000Z

380

Method for selective catalytic reduction of nitrogen oxides  

DOE Patents (OSTI)

A method for catalytically reducing nitrogen oxide compounds (NO.sub.x, defined as nitric oxide, NO, +nitrogen dioxide, NO.sub.2) in a gas by a material comprising a base metal consisting essentially of CuO and Mn, and oxides of Mn, on an activated metal hydrous metal oxide support, such as HMO:Si. A promoter, such as tungsten oxide or molybdenum oxide, can be added and has been shown to increase conversion efficiency. This method provides good conversion of NO.sub.x to N.sub.2, good selectivity, good durability, resistance to SO.sub.2 aging and low toxicity compared with methods utilizing vanadia-based catalysts.

Mowery-Evans, Deborah L. (Broomfield, CO); Gardner, Timothy J. (Albuquerque, NM); McLaughlin, Linda I. (Albuquerque, NM)

2005-02-15T23:59:59.000Z

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

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

382

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

383

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

384

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

385

Applications and benefits of catalytic converter thermal management  

DOE Green Energy (OSTI)

A catalytic converter thermal management system (TMS) using variable-conductance vacuum insulation and phase-change thermal storage can maintain the converter temperature above its operating temperature for many hours, allowing most trips to begin with minimal ``cold-start`` emissions. The latest converter TMS prototype was tested on a Ford Taurus (3.0 liter flex-fuel engine) at Southwest Research Institute. Following a 24-hour soak, the FTP-75 emissions were 0.031, 0.13, and 0.066 g/mile for NMHC, CO, and NOx, respectively. Tests were also run using 85% ethanol (E85), resulting in values of 0.005, 0.124, and 0.044 g/mile, and 0.005 g/mile NMOG. Compared to the baseline FTP levels, these values represent reductions of 84% to 96% for NMHC, NMOG, and CO.

Burch, S.D.; Keyser, M.A.; Colucci, C.P.; Potter, T.F.; Benson, D.K.; Biel, J.P.

1996-07-01T23:59:59.000Z

386

Catalytic Synthesis of Oxygenates: Mechanisms, Catalysts and Controlling Characteristics  

DOE Green Energy (OSTI)

This research focused on catalytic synthesis of unsymmetrical ethers as a part of a larger program involving oxygenated products in general, including alcohols, ethers, esters, carboxylic acids and their derivatives that link together environmentally compliant fuels, monomers, and high-value chemicals. The catalysts studied here were solid acids possessing strong Br�������¸nsted acid functionalities. The design of these catalysts involved anchoring the acid groups onto inorganic oxides, e.g. surface-grafted acid groups on zirconia, and a new class of mesoporous solid acids, i.e. propylsulfonic acid-derivatized SBA-15. The former catalysts consisted of a high surface concentration of sulfate groups on stable zirconia catalysts. The latter catalyst consists of high surface area, large pore propylsulfonic acid-derivatized silicas, specifically SBA-15. In both cases, the catalyst design and synthesis yielded high concentrations of acid sites in close proximity to one another. These materials have been well-characterization in terms of physical and chemical properties, as well as in regard to surface and bulk characteristics. Both types of catalysts were shown to exhibit high catalytic performance with respect to both activity and selectivity for the bifunctional coupling of alcohols to form ethers, which proceeds via an efficient SN2 reaction mechanism on the proximal acid sites. This commonality of the dual-site SN2 reaction mechanism over acid catalysts provides for maximum reaction rates and control of selectivity by reaction conditions, i.e. pressure, temperature, and reactant concentrations. This research provides the scientific groundwork for synthesis of ethers for energy applications. The synthesized environmentally acceptable ethers, in part derived from natural gas via alcohol intermediates, exhibit high cetane properties, e.g. methylisobutylether with cetane No. of 53 and dimethylether with cetane No. of 55-60, or high octane properties, e.g. diisopropylether with blending octane No. of 105, and can replace aromatics in liquid fuels.

Kamil Klier; Richard G. Herman

2005-11-30T23:59:59.000Z

387

Immersible solar heater for fluids  

DOE Patents (OSTI)

An immersible solar heater comprising a light-absorbing panel attached to a frame for absorbing heat energy from the light and transferring the absorbed heat energy directly to the fluid in which the heater is immersed. The heater can be used to heat a swimming pool, for example, and is held in position and at a preselected angle by a system of floats, weights and tethers so that the panel can operate efficiently. A skid can be used in one embodiment to prevent lateral movement of the heater along the bottom of the pool. Alternative embodiments include different arrangements of the weights, floats and tethers and methods for making the heater.

Kronberg, James W. (Aiken, SC)

1995-01-01T23:59:59.000Z

388

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

389

Improvement of Sulphur Resistance of a Nickel-modified Catalytic Filter for Tar Removal from Biomass Gasification Gas  

DOE Green Energy (OSTI)

This work focuses on the development of catalytic candle filters for the simultaneous removal of tars and particles from the biomass gasification gas at high temperature. An improvement of sulphur resistance of the nickel-activated catalytic filter was developed by the addition of CaO. The influences of preparation procedure of catalytic filter, the ratio of Ni/CaO and the loading of Ni and CaO on the performance of the catalytic filter were investigated.

Zhang, Y.; Draelants, D.J.; Engelen, K.; Baron, G.V.

2002-09-19T23:59:59.000Z

390

Hydrostatic bearings for a turbine fluid flow metering device  

DOE Patents (OSTI)

A rotor assembly fluid metering device has been improved by development of a hydrostatic bearing fluid system which provides bearing fluid at a common pressure to rotor assembly bearing surfaces. The bearing fluid distribution system produces a uniform film of fluid between bearing surfaces and allows rapid replacement of bearing fluid between bearing surfaces, thereby minimizing bearing wear and corrosion. 3 figs.

Fincke, J.R.

1982-05-04T23:59:59.000Z

391

Hydrostatic bearings for a turbine fluid flow metering device  

DOE Patents (OSTI)

A rotor assembly fluid metering device has been improved by development of a hydrostatic bearing fluid system which provides bearing fluid at a common pressure to rotor assembly bearing surfaces. The bearing fluid distribution system produces a uniform film of fluid between bearing surfaces and allows rapid replacement of bearing fluid between bearing surfaces, thereby minimizing bearing wear and corrosion.

Fincke, James R. (Rigby, ID)

1982-01-01T23:59:59.000Z

392

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

393

Apparatus for unloading pressurized fluid  

DOE Patents (OSTI)

An apparatus is described for unloading fluid, preferably pressurized gas, from containers in a controlled manner that protects the immediate area from exposure to the container contents. The device consists of an unloading housing, which is enclosed within at least one protective structure, for receiving the dispensed contents of the steel container, and a laser light source, located external to the protective structure, for opening the steel container instantaneously. The neck or stem of the fluid container is placed within the sealed interior environment of the unloading housing. The laser light passes through both the protective structure and the unloading housing to instantaneously pierce a small hole within the stem of the container. Both the protective structure and the unloading housing are specially designed to allow laser light passage without compromising the light's energy level. Also, the unloading housing allows controlled flow of the gas once it has been dispensed from the container. The external light source permits remote operation of the unloading device. 2 figures.

Rehberger, K.M.

1994-01-04T23:59:59.000Z

394

Controlling the fluid-fluid mixing-demixing phase transition with electric fields  

E-Print Network (OSTI)

We review recent theoretical advances on controlling the fluid-fluid phase transition with electric fields. Using a mean-field approach, we compare the effects of uniform versus non-uniform electric fields, and show how non-uniform fields are better at altering the phase diagram. Focusing on non-uniform fields, we then discuss the behavior of the fluid concentration profile and the parameters (temperature, fluid concentration, etc.) that control the location of the fluid-fluid interface from both equilibrium and dynamic perspectives.

Jennifer Galanis; Sela Samin; Yoav Tsori

2012-12-06T23:59:59.000Z

395

DWPF CATALYTIC HYDROGEN GENERATION PROGRAM - REVIEW OF CURRENT STATUS  

DOE Green Energy (OSTI)

Significant progress has been made in the past two years in improving the understanding of acid consumption and catalytic hydrogen generation during the Defense Waste Processing Facility (DWPF) processing of waste sludges in the Sludge Receipt and Adjustment Tank (SRAT) and Slurry Mix Evaporator (SME). This report reviews issues listed in prior internal reviews, describes progress with respect to the recommendations made by the December 2006 external review panel, and presents a summary of the current understanding of catalytic hydrogen generation in the DWPF Chemical Process Cell (CPC). Noble metals, such as Pd, Rh, and Ru, are historically known catalysts for the conversion of formic acid into hydrogen and carbon dioxide. Rh, Ru, and Pd are present in the DWPF SRAT feed as by-products of thermal neutron fission of {sup 235}U in the original waste. Rhodium appears to become most active for hydrogen as the nitrite ion concentration becomes low (within a factor of ten of the Rh concentration). Prior to hydrogen generation, Rh is definitely active for nitrite destruction to N{sub 2}O and potentially active for nitrite to NO formation. These reactions are all consistent with the presence of a nitro-Rh complex catalyst, although definite proof for the existence of this complex during Savannah River Site (SRS) waste processing does not exist. Ruthenium does not appear to become active for hydrogen generation until nitrite destruction is nearly complete (perhaps less nitrite than Ru in the system). Catalytic activity of Ru during nitrite destruction is significantly lower than that of either Rh or Pd. Ru appears to start activating as Rh is deactivating from its maximum catalytic activity for hydrogen generation. The slow activation of the Ru, as inferred from the slow rate of increase in hydrogen generation that occurs after initiation, may imply that some species (perhaps Ru itself) has some bound nitrite on it. Ru, rather than Rh, is primarily responsible for the hydrogen generation in the SME cycle when the hydrogen levels are high enough to be noteworthy. Mercury has a role in catalytic hydrogen generation. Two potentially distinct roles have been identified. The most dramatic effect of Hg on hydrogen generation occurs between runs with and without any Hg. When a small amount of Hg is present, it has a major inhibiting effect on Rh-catalyzed H{sub 2} generation. The Rh-Ru-Hg matrix study showed that increasing mercury from 0.5 to 2.5 wt% in the SRAT receipt total solids did not improve the inhibiting effect significantly. The next most readily identified role for Hg is the impact it has on accelerating NO production from nitrite ion. This reaction shifts the time that the ideal concentration of nitrite relative to Rh occurs, and consequently causes the most active nitro-Rh species to form sooner. The potential consequences of this shift in timing are expected to be a function of other factors such as amount of excess acid, Rh concentration, etc. Graphical data from the Rh-Ru-Hg study suggested that Hg might also be responsible for partially inhibiting Ru-catalysis initially, but that the inhibition was not sustained through the SRAT and SME cycles. Continued processing led to a subsequent increase in hydrogen generation that was often abrupt and that frequently more than doubled the hydrogen generation rate. This phenomenon may have been a function of the extent of Hg stripping versus the initial Ru concentration in these tests. Palladium is an active catalyst, and activates during (or prior to) nitrite destruction to promote N{sub 2}O formation followed by a very small amount of hydrogen. Pd then appears to deactivate. Data to date indicate that Pd should not be a species of primary concern relative to Rh and Ru for hydrogen generation. Pd was a very mild catalyst for hydrogen generation compared to Rh and Ru in the simulated waste system. Pd was comparable to Rh in enhancing N{sub 2}O production when present at equal concentration. Pd, however, is almost always present at less than a quarter of the Rh concentration in S

Koopman, D.

2009-07-10T23:59:59.000Z

396

Valve for controlling flow of cryogenic fluid  

DOE Patents (OSTI)

A valve is provided for accurately controlling the flow of cryogenic fluids such as liquid nitrogen. The valve comprises a combination of disc and needle valves affixed to a valve stem in such a manner that the disc and needle are free to rotate about the stem, but are constrained in lateral and vertical movements. This arrangement provides accurate and precise fluid flow control and positive fluid isolation.

Knapp, P.A.

1995-12-31T23:59:59.000Z

397

Definition: Fluid Inclusion Analysis | Open Energy Information  

Open Energy Info (EERE)

or liquid) and occasionally mineral crystals, that are considered to represent the chemical and physical properties of a hydrothermal fluid at a single point in time and...

398

Non-invasive Ultrasonic Fluid Processing Technology ...  

Search PNNL. PNNL Home; About; Research; Publications; Jobs; News; Contacts; Non-invasive Ultrasonic Fluid Processing Technology. Battelle Number(s): ...

399

Shale Gas Development Challenges: Fracture Fluids | Department...  

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

Centers Field Sites Power Marketing Administration Other Agencies You are here Home Shale Gas Development Challenges: Fracture Fluids Shale Gas Development Challenges: Fracture...

400

Universal Fluid Droplet Ejector - Energy Innovation Portal  

... deposition and cell-sorting applications Description A fluid ejector capable of producing micron sized droplets on demand is ... 5,943,075 (USA) ...

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

Universal fluid droplet ejector - Energy Innovation Portal  

A droplet generator comprises a fluid reservoir having a side wall made of glass or quartz, and an end cap made from a silicon plate. The end cap ...

402

Fluid Submersible Sensing Device - Energy Innovation Portal  

The present invention relates to a fluid submersible sensing device and, more particularly, to such a device having sensing structure provided within ...

403

MODELING SUBSIDENCE DUE TO GEOTHERMAL FLUID PRODUCTION  

E-Print Network (OSTI)

compaction, computers, geothermal energy, pore-waternot MODELING SUBSIDENCE DUE T GEOTHERMAL FLUID PRODUCTION Opromise f o r developing geothermal energy i n the United

Lippmann, M.J.

2011-01-01T23:59:59.000Z

404

Theory and Modeling of Fluids Group Homepage  

Science Conference Proceedings (OSTI)

... Modeling of Fluids Group is working in consort with the University of Colorado and the Division's Cryogenics Group on a DARPA funded project to ...

2013-07-23T23:59:59.000Z

405

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

SciTech Connect

The project, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures'', is being conducted jointly by Clark Atlanta University (CAU), the University of Tennessee Space Institute (UTSI) and the Georgia Institute of Technology (GT). The aims of the project are to: identify appropriate eutectic salt mixture catalysts for the gasification of Illinois No.6 coal; evaluate various impregnation or catalyst addition methods to improve catalyst dispersion; evaluate effects of major process variables (e.g., temperature, system pressure, etc.) on coal gasification; evaluate the recovery, regeneration and recycle of the spent catalysts in a bench-scale fixed bed reactor; and conduct thorough analysis and modeling of the gasification process to provide a better understanding of the fundamental mechanisms and kinetics of the process. The eutectic catalysts increased gasification rate significantly. The methods of catalyst preparation and addition had significant effect on the catalytic activity and coal gasification. The incipient wetness method gave more uniform catalyst distribution than that of physical mixing for the soluble catalysts resulting in higher gasification rates for the incipient wetness samples. The catalytic activity increased by varying degrees with catalyst loading. The above results are especially important since the eutectic catalysts (with low melting points) yield significant gasification rates even at low temperatures. Among the ternary eutectic catalysts studied, the system 39% Li{sub 2}CO{sub 3}-38.5% Na{sub 2}CO{sub 3}-22.5% Rb{sub 2}CO{sub 3} showed the best activity and will be used for further bench scale fixed-bed gasification reactor in the next period. Based on the Clark Atlanta University studies in the previous reporting period, the project team selected the 43.5% Li{sub 2}CO{sub 3}-31.5% Na{sub 2}CO{sub 3}-25% K{sub 2}CO{sub 3} ternary eutectic and the 29% Na{sub 2}CO{sub 3}-71% K{sub 2}CO{sub 3} binary eutectic for the fixed-bed studies at UTSI during this reporting period. Temperature was found to have a significant effect on the rate of gasification of coal. The rate of gasification increased up to 1400 F. Pressure did not have much effect on the gasification rates. The catalyst loading increased the gasification rate and approached complete conversion when 10 wt% of catalyst was added to the coal. Upon further increasing the catalyst amount to 20-wt% and above, there was no significant rise in gasification rate. The rate of gasification was lower for a 2:1 steam to char molar ratio (60%) compared to gasification rates at 3.4:1 molar ratio of steam-to-char where the conversion approached 100%. The characterization results of Georgia Tech are very preliminary and inconclusive and will be made available in the next report.

Unknown

1999-04-01T23:59:59.000Z

406

,"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"

407

Immersible solar heater for fluids  

DOE Patents (OSTI)

An immersible solar heater is described comprising a light-absorbing panel attached to a frame for absorbing heat energy from the light and transferring the absorbed heat energy directly to the fluid in which the heater is immersed. The heater can be used to heat a swimming pool, for example, and is held in position and at a preselected angle by a system of floats, weights and tethers so that the panel can operate efficiently. A skid can be used in one embodiment to prevent lateral movement of the heater along the bottom of the pool. Alternative embodiments include different arrangements of the weights, floats and tethers and methods for making the heater. 11 figs.

Kronberg, J.W.

1995-07-11T23:59:59.000Z

408

Immersible solar heater for fluids  

DOE Patents (OSTI)

An immersible solar heater is described comprising a light-absorbing panel attached to a frame for absorbing heat energy from the light and transferring the absorbed heat energy directly to the fluid in which the heater is immersed. The heater can be used to heat a swimming pool, for example, and is held in position and at a preselected angle by a system of floats, weights and tethers so that the panel can operate efficiently. A skid can be used in one embodiment to prevent lateral movement of the heater along the bottom of the pool. Alternative embodiments include different arrangements of the weights, floats and tethers and methods for making the heater.

Hazen, T.C.; Fliermans, C.B.

1994-01-01T23:59:59.000Z

409

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

SciTech Connect

This progress report on the Department of Energy project DE-FG-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures'', covers the period April-September 1998. The specific aims of the project for this period were to identify appropriate eutectic salt mixture catalysts for the gasification of Illinois No.6 coal, evaluate various impregnation or catalyst addition methods to improve catalyst dispersion, and evaluate gasification performance in a bench-scale fixed bed reactor. The project is being conducted jointly by Clark Atlanta University (CAU), the University of Tennessee Space Institute (UTSI) and the Georgia Institute of Technology (Georgia Tech) with CAU as the prime contractor. Several single salt catalysts and binary and ternary eutectic catalysts were investigated at Clark Atlanta University. Physical mixing and incipient wetness methods were investigated as catalyst addition techniques. Gasification was carried out using TGA at CAU and UTSI and with a fixed-bed reactor at UTSI. The results showed better gasification activity in the presence of the catalysts tested. The eutectic salt studies showed clear agreement between the melting points of the prepared eutectics and reported literature values. The order of catalytic activity observed was ternary > binary > single salt. With the soluble single salt catalysts, the incipient wetness method was found to give better results than physical mixing technique. Also, catalyst preparation conditions such as catalyst loading, drying time and temperature were found to influence the gasification rate. Based on the Clark Atlanta University studies on Task 1, the project team selected the 43.5%Li{sub 2}CO{sub 3}-31.5%Na{sub 2}CO{sub 3}-25%K{sub 2}CO{sub 3} ternary eutectic and the 29%Na{sub 2}CO{sub 3}-71%K{sub 2}CO{sub 3} and 2.3% KNO{sub 3}-97.7%K{sub 2}CO{sub 3} binary eutectic for the fixed bed studies at UTSI. The eutectic salts were found to be highly insoluble in aqueous medium. As a result the technique of adding the eutectic to the raw coal was found to be better than using wet methods. Also, addition of the catalyst to the raw coal appeared to give better gasification results than addition to pyrolyzed coal. In addition, eutectic catalysts added to the coal yielded better gasification rates than rates obtained by mixing the individual salts in the eutectic ratio with the coal. These results, especially with the eutectic catalysts are very significant since the use of the low melting eutectics will reduce the severity of gasification processes.

NONE

2000-04-01T23:59:59.000Z

410

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

Science Conference Proceedings (OSTI)

This progress report on the Department of Energy project DE-FG-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures,'' covers the period April-September 1998. The specific aims of the project for this period were to identify appropriate eutectic salt mixture catalysts for the gasification of Illinois No.6 coal, evaluate various impregnation or catalyst addition methods to improve catalyst dispersion, and evaluate gasification performance in a bench-scale fixed bed reactor. The project is being conducted jointly by Clark Atlanta University (CAU), the University of Tennessee Space Institute (UTSI) and the Georgia Institute of Technology (Georgia Tech) with CAU as the prime contractor. Several single salt catalysts and binary and ternary eutectic catalysts were investigated at Clark Atlanta University. Physical mixing and incipient wetness methods were investigated as catalyst addition techniques. Gasification was carried out using TGA at CAU and UTSI and with a fixed-bed reactor at UTSI. The results showed better gasification activity in the presence of the catalysts tested. The eutectic salt studies showed clear agreement between the melting points of the prepared eutectics and reported literature values. The order of catalytic activity observed was ternary > binary > single salt. With the soluble single salt catalysts, the incipient wetness method was found to give better results than physical mixing technique. Also, catalyst preparation conditions such as catalyst loading, drying time and temperature were found to influence the gasification rate. Based on the Clark Atlanta University studies on Task 1, the project team selected the 43.5%Li{sub 2}CO{sub 3}-31.5%Na{sub 2}CO{sub 3}-25%K{sub 2}CO{sub 3} ternary eutectic and the 29%Na{sub 2}CO{sub 3}-71%K{sub 2}CO{sub 3} and 2.3%KNO{sub 3}-97.7%K{sub 2}CO{sub 3} binary eutectic for the fixed bed studies at UTSI. The eutectic salts were found to be highly insoluble in aqueous medium. As a result the technique of adding the eutectic to the raw coal was found to be better than using wet methods. Also, addition of the catalyst to the raw coal appeared to give better gasification results than addition to pyrolyzed coal. In addition, eutectic catalysts added to the coal yielded better gasification rates than rates obtained by mixing the individual salts in the eutectic ratio with the coal. These results, especially with the eutectic catalysts are very significant since the use of the low melting eutectics will reduce the severity of gasification processes.

NONE

1998-10-01T23:59:59.000Z

411

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

412

Hydrostatic bearings for a turbine fluid flow metering device  

DOE Patents (OSTI)

A rotor assembly fluid metering device has been improved by development of a hydrostatic bearing fluid system which provides bearing fluid at a common pressure to rotor assembly bearing surfaces. The bearing fluid distribution system produces a uniform film of fluid distribution system produces a uniform film of fluid between bearing surfaces and allows rapid replacement of bearing fluid between bearing surfaces, thereby minimizing bearing wear and corrosion.

Fincke, J.R.

1980-05-02T23:59:59.000Z

413

A Universe with a Ghost Dark Energy and van der Waals fluid interacting with a Fluid  

E-Print Network (OSTI)

We consider a model of a Universe with Ghost Dark Energy and van der Waals fluid interacting with a fluid which was born as a result of interaction between original fluid and some other fluid existing in Universe. We suppose that Ghost Dark energy has its contribution to the model by an interaction term $Q$ and we suppose that $Q=3Hb(\\rho_{\\small{tot}}-\\rho_{GDe})$.

Martiros Khurshudyan

2013-01-26T23:59:59.000Z

414

Generation of energy by means of a working fluid, and regeneration of a working fluid  

SciTech Connect

A method is provided of optimizing, within limits imposed by a heating medium from the surface of an ocean and a cooling medium from an ocean depth, the energy supply capability of a gaseous working fluid which is expanded from a charged high pressure level to a spent low pressure level to provide available energy, the method comprising expanding the gaseous working fluid to a spent low pressure level where the condensation temperature of the working fluid is below the minimum temperature of the cold water, and regenerating the spent working fluid by, in at least one regeneration stage, absorbing the working fluid being regenerated in an absorption stage by dissolving it in a solvent solution while cooling with the cold water, the solvent solution comprising a solvent having an initial working fluid concentration which is sufficient to provide a solution having a boiling point, after dissolving the working fluid being regenerated, which is above the minimum temperature of the cold water to permit effective absorption of the working fluid being regenerated, increasing the pressure and then evaporating the working fluid being regenerated by heating in an evaporation stage with the available hot water, feeding the evaporated working fluid and the solvent solution to a separator stage for separating the evaporated working fluid and the solvent solution, recovering the evaporated, separated working fluid, and recycling the balance of the solvent solution from the separator stage to constitute the solvent solution for the absorption stage; and an apparatus for carrying out the method.

Kalina, A.I.

1982-08-31T23:59:59.000Z

415

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

416

Mercury Oxidation via Catalytic Barrier Filters Phase II  

SciTech Connect

In 2004, the Department of Energy National Energy Technology Laboratory awarded the University of North Dakota a Phase II University Coal Research grant to explore the feasibility of using barrier filters coated with a catalyst to oxidize elemental mercury in coal combustion flue gas streams. Oxidized mercury is substantially easier to remove than elemental mercury. If successful, this technique has the potential to substantially reduce mercury control costs for those installations that already utilize baghouse barrier filters for particulate removal. Completed in 2004, Phase I of this project successfully met its objectives of screening and assessing the possible feasibility of using catalyst coated barrier filters for the oxidation of vapor phase elemental mercury in coal combustion generated flue gas streams. Completed in September 2007, Phase II of this project successfully met its three objectives. First, an effective coating method for a catalytic barrier filter was found. Second, the effects of a simulated flue gas on the catalysts in a bench-scale reactor were determined. Finally, the performance of the best catalyst was assessed using real flue gas generated by a 19 kW research combustor firing each of three separate coal types.

Wayne Seames; Michael Mann; Darrin Muggli; Jason Hrdlicka; Carol Horabik

2007-09-30T23:59:59.000Z

417

Thermal analysis and testing of a vacuum insulated catalytic converter  

DOE Green Energy (OSTI)

Based on a recent US Environmental Protection Agency (EPA) study, about 95% of all trips start after a cold-soak period of 16 hours or less. By preserving the heat in the catalyst between trips, exhaust gases could be processed without warm-up delay and without the usual cold-start emissions. Vacuum insulation and phase-change thermal storage have been incorporated into a catalytic converter design to enhance its heat-retention time. Laboratory testing of a bench-scale prototype showed that a ``light off`` temperature (above 350 C) could be maintained during a 10-hour cold soak. Design improvements currently being tested should increase this heat-retention time to more than 16 hours. The thermal conductance of the vacuum insulation will be made continuously variable to prevent overheating and excessive thermal cycling. This approach to thermal management may be more durable and less costly than quick-heat methods using electric or fuel-fired preheat catalysts.

Burch, S D; Potter, T F; Keyser, M A; Benson, D K

1994-11-01T23:59:59.000Z

418

Development of a catalytic system for gasification of wet biomass  

DOE Green Energy (OSTI)

A gasification system is under development at Pacific Northwest Laboratory that can be used with high-moisture biomass feedstocks. The system operates at 350 C and 205 atm using a liquid water phase as the processing medium. Since a pressurized system is used, the wet biomass can be fed as a slurry to the reactor without drying. Through the development of catalysts, a useful processing system has been produced. This paper includes assessment of processing test results of different catalysts. Reactor system results including batch, bench-scale continuous, and engineering-scale processing results are presented to demonstrate the applicability of this catalytic gasification system to biomass. The system has utility both for direct conversion of biomass to fuel gas or as a wastewater cleanup system for treatment of unconverted biomass from bioconversion processes. By the use of this system high conversion of biomass to fuel gas can be achieved. Medium-Btu is the primary product. Potential exists for recovery/recycle of some of the unreacted inorganic components from the biomass in the aqueous byproduct stream.

Elliott, D.C.; Sealock, L.J.; Phelps, M.R.; Neuenschwander, G.G.; Hart, T.R.

1993-08-01T23:59:59.000Z

419

Low-temperature catalytic gasification of wet industrial wastes  

DOE Green Energy (OSTI)

Bench-scale reactor tests are in progress at Pacific Northwest Laboratory to develop a low-temperature, catalytic gasification system. The system, licensed under the trade name Thermochemical Environmental Energy System (TEES{reg sign}), is designed for treating a wide variety of feedstocks ranging from dilute organics in water to waste sludges from food processing. This report describes a test program which used a continuous-feed tubular reactor. This test program is an intermediate stage in the process development. The reactor is a laboratory-scale version of the commercial concept as currently envisioned by the process developers. An energy benefit and economic analysis was also completed on the process. Four conceptual commercial installations of the TEES process were evaluated for three food processing applications and one organic chemical manufacturing application. Net energy production (medium-Btu gas) was achieved in all four cases. The organic chemical application was found to be economically attractive in the present situation. Based on sensitivity studies included in the analysis, the three food processing cases will likely become attractive in the near future as waste disposal regulations tighten and disposal costs increase. 21 refs., 2 figs., 9 tabs.

Elliott, D C; Neuenschwander, G G; Baker, E G; Sealock, Jr, L J; Butner, R S

1991-04-01T23:59:59.000Z

420

Cryogenic methane separation/catalytic hydrogasification process analysis. Quarterly report  

Science Conference Proceedings (OSTI)

The objective of this coordinated research program is to obtain the most attractive combinations of acid gas removal, methane separation for the Exxon Catalytic Coal Gasification (CCG) and the Rockwell/Cities Service Hydrogasification processes. The program is divided into nine subtasks with each subtask studying the effect of variation of a key design parameter on the treatment cost of the SNG produced. Progress reports of 8 subtasks are presented. The following are some of the highlights. Subtask 1 - Heat and material balance and equipment sizing was completed for the cryogenic methane separation. The overall material balance is presented in a table. Subtask 2 - Preliminary designs for MEA and DEA gas removal systems were established. Subtasks 3 to 5 - Economic evaluation is in proress. Subtask 6 - The SNG product compressor train was simulated for the case where sufficient SNG fuel is withdrawn from the product compressors to fire the dryer reactivation heater. Subtask 7 - Acid gas removal and cryogenic separation equipment was resized to accommodate Exxon's request for a two-train plant design. Subtask 8 - The Benfield and Selexol systems will be evaluated for acid gas removal.

Klosek, J.

1981-02-13T23:59:59.000Z

Note: This page contains sample records for the topic "fcc fluid catalytic" from the National Library of EnergyBeta (NLEBeta).
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421

Integrating catalytic coal gasifiers with solid oxide fuel cells  

DOE Green Energy (OSTI)

The main advantage of steam gasification of coal to methane and carbon dioxide is that the amount of exergy consumed in the gasifier is small compared to conventional, high temperature, oxygen-blown gasifiers. However, the goal of limiting the amount of exergy destruction in the gasifier has the effect of limiting the rates of chemical reactions. Thus, one of the main advantages of steam gasification leads to one of its main problems: slow reaction kinetics. While conventional entrained-flow, high-temperature gasifiers consume a sizable portion of the available work in the coal oxidation, the consumed exergy speeds up the rates of reactions. And while the rates of steam gasification reactions can be increased through the use of catalysts, only a few catalysts can meet cost requirements because there is often significant deactivation due to chemical reactions between the inorganic species in the coal and the catalyst. Previous research into increasing the kinetics of steam gasification will be reviewed. The goal of this paper is to highlight both the challenges and advantages of integrating catalytic coal gasifiers with SOFCs.

Siefert, N.; Shamsi, A.; Shekhawat, D.; Berry, D.

2010-01-01T23:59:59.000Z

422

Catalytic gasification of wet biomass in supercritical water  

Science Conference Proceedings (OSTI)

Wet biomass (water hyacinth, banana trees, cattails, green algae, kelp, etc.) grows rapidly and abundantly around the world. As a biomass crop, aquatic species are particularly attractive because their cultivation does not compete with land-based agricultural activities designed to produce food for consumption or export. However, wet biomass is not regarded as a promising feed for conventional thermochemical conversion processes because the cost associated with drying it is too high. This research seeks to address this problem by employing water as the gasification medium. Prior work has shown that low concentrations of glucose (a model compound for whole biomass) can be completely gasified in supercritical water at 600{degrees}C and 34.5 Wa after a 30 s reaction time. Higher concentrations of glucose (up to 22% by weight in water) resulted in incomplete conversion under these conditions. The gas contained hydrogen, carbon dioxide, carbon monoxide, methane, ethane, propane, and traces of other hydrocarbons. The carbon monoxide and hydrocarbons are easily converted to hydrogen by commercial technology available in most refineries. This prior work utilized capillary tube reactors with no catalyst. A larger reactor system was fabricated and the heterogeneous catalytic gasification of glucose and wet biomass slurry of higher concentration was studied to attain higher conversions.

Antal, M.J. Jr.; Matsumura, Yukihiko; Xu, Xiaodong [Univ. of Hawaii, Honolulu, HI (United States)] [and others

1995-12-31T23:59:59.000Z

423

Catalytic Hydroprocessing of Chemical Models for Bio-oil  

Science Conference Proceedings (OSTI)

Bio-oil (product liquids from fast pyrolysis of biomass) is a complex mixture of oxygenates derived from the thermal breakdown of the bio-polymers in biomass. In the case of lignocellulosic biomass, the structures of three major components, cellulose, hemicellulose and lignin, are well represented by the bio-oil components. In order to study the chemical mechanisms of catalytic hydroprocessing of bio-oil, three model compounds were chosen to represent those components. Guaiacol represents the large number of mono- and di-methoxy phenols found in bio-oil derived from softwood or hardwood, respectively. Furfural represents a major pyrolysis product group from cellulosics. Acetic acid is a major product from biomass pyrolysis, derived from the hemicellulose, which has important impacts on the further processing of the bio-oil because of the acidic character. These three compounds were processed using palladium or ruthenium catalyst over a temperature range from 150?C to 300?C. The batch reactor was sampled during each test over a period of four hours. The samples were analyzed by gas chromatography with both a mass selective detector and a flame ionization detector. The products were determined and the reaction pathways for their formation are suggested based on these results. Both temperature and catalyst metal have significant effects on the product composition.

Elliott, Douglas C.; Hart, Todd R.

2009-02-20T23:59:59.000Z

424

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

425

Synthesis and catalytic properties of metal and semiconductor nanoclusters  

SciTech Connect

Synthesis of metal or semiconductor nanoclusters in microheterogeneous oil-continuous inverse micelle systems is discussed. We focus on synthesis and catalytic properties of palladium, iron, and iron sulfide nanoclusters. Cluster size-control is achieved by changing the micelle size which is determined by small angle neutron scattering (SANS) and chosen to produce cluster in size range of 1-20 nm. Cluster sizes were determined by either transmission electron microscopy (TEM) or small-angle x-ray scattering (SAXS). Cluster structure was determined by either x-ray or electron diffraction. In the case of Fe nanoclusters the crystal structure depended on the chemical nature of the surfactant micelle used in the synthesis, illustrating the important role of the surfactant during the growth process. Results of in-situ pyrene hydrogenation using size-selected Pd clusters show a significant increase in activity/total surface area as the size decreases. These clusters also proved effective as unsupported catalysts for direct coal hydropyrolysis, even at very low metal concentrations. Synthesis and optical features of a new semiconductor cluster material, FeS{sub 2}, is discussed with regard to its use in photocatalysis. Application of FeS{sub 2} in coal hydrogenolysis reactions has improved yields of short chain hydrocarbons significantly compared to conventional FeS{sub 2} powders.

Wilcoxon, J.P.; Martino, T.; Klavetter, E.; Sylwester, A.P.

1993-08-01T23:59:59.000Z

426

Environmentally advanced refinery nears start-up in Germany  

SciTech Connect

Mitteldeutsche Erdoel-Raffinerie GmbH (Mider), is building a 170,000 b/d, grassroots refinery in Leuna, Germany. The refinery is scheduled to start up in third quarter of this year. At the heart of the new refinery is a new technology called progressive distillation. Other major units include: vacuum distillation, catalytic reforming, alkylation, visbreaking, fluid catalytic cracking (FCC), and hydrodesulfurization (HDS). In addition, an existing partial oxidation (POX)/methanol production unit will be integrated with the new refinery. The paper describes the plant and its major processes.

Rhodes, A.K.

1997-03-17T23:59:59.000Z

427

Electrohydraulic Control Fluid and Elastomer Compatibility Guide  

Science Conference Proceedings (OSTI)

The Electrohydraulic Control Fluid and Elastomer Compatibility Guide provides power plant personnel with current information on the compatibility of turbine-generator electrohydraulic control (EHC) fluids and various elastomers, such as hoses, seals, and gaskets. The information in the guide should assist plant personnel in improving the reliability and performance of the EHC system.

2005-12-22T23:59:59.000Z

428

Joint Distributions for Interacting Fluid Queues  

Science Conference Proceedings (OSTI)

Motivated by recent traffic control models in ATM systems, we analyse three closely related systems of fluid queues, each consisting of two consecutive reservoirs, in which the first reservoir is fed by a two-state (on and off) Markov source. The first ... Keywords: feedback, fluid queue, joint distribution, stationary distribution, tandem queue, traffic shaper

Dirk P. Kroese; Werner R. W. Scheinhardt

2001-03-01T23:59:59.000Z

429

Geek-Up[3.18.2011]: Catalytically Active Material and BELLA | Department of  

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

8.2011]: Catalytically Active Material and BELLA 8.2011]: Catalytically Active Material and BELLA Geek-Up[3.18.2011]: Catalytically Active Material and BELLA March 18, 2011 - 3:54pm Addthis PNNL scientists Grant Johnson and Julia Laskin | Photo Courtesy of the Pacific Northwest National Laboratory PNNL scientists Grant Johnson and Julia Laskin | Photo Courtesy of the Pacific Northwest National Laboratory Niketa Kumar Niketa Kumar Public Affairs Specialist, Office of Public Affairs What are the key facts? PNL researchers produced catalytically active material that may help advance fuel cell and solar energy storage applications. In just one meter a single BELLA stage -- with a "boosted-frame" method -- will accelerate an electron beam to 10 billion electron volts. Thanks to an innovative approach from Pacific Northwest National Laboratory

430

Thermal catalytic conversion of the used isobutyl isoprene rubber into valuable hydrocarbons  

E-Print Network (OSTI)

Jan MR, Mabood F. Catalytic conversion of waste tyres intoJ, Jan MR, Mabood F. Conversion of waste tires into liquidbest method for maximum conversion into useful product, and

Rasul Jan, M.; Jabeen, Farah; Shah, Jasmin; Mabood, Fazal

2010-01-01T23:59:59.000Z

431

Modelling of catalytic aftertreatment of NOx emissions using hydrocarbon as a reductant.  

E-Print Network (OSTI)

??Hydrocarbon selective catalytic reduction (HC-SCR) is emerging as one of the most practical methods for the removal of nitrogen oxides (NOx) from light-duty-diesel engine exhaust… (more)

Sawatmongkhon, Boonlue

2012-01-01T23:59:59.000Z

432

Catalytic and reactive polypeptides and methods for their preparation and use  

DOE Patents (OSTI)

Catalytic and reactive polypeptides include a binding site specific for a reactant or reactive intermediate involved in a chemical reaction of interest. The polypeptides further include at least one active functionality proximate the bi.

Schultz, Peter (Oakland, CA)

1993-01-01T23:59:59.000Z

433

Calibration and performance of a selective catalytic reduction (SCR) bench rig for NOx? emissions control  

E-Print Network (OSTI)

A laboratory test rig was designed and built to easily test SCR (Selective Catalytic Reduction) technology. Equipped with three 6 kW heaters, connections for liquid N2 and an assortment of test gases, and a connection with ...

Castro Galnares, Sebastián (Castro Galnares Wright Paz)

2008-01-01T23:59:59.000Z

434

Reaction mechanisms for catalytic partial oxidation systems : application to ethylene epoxidation  

E-Print Network (OSTI)

With the rapid advances in kinetic modeling, building elementary surface mechanisms have become vital to understand the complex chemistry for catalytic partial oxidation systems. Given that there is selected experimental ...

Anantharaman, Bharthwaj

2005-01-01T23:59:59.000Z

435

Thermal catalytic conversion of the used isobutyl isoprene rubber into valuable hydrocarbons  

E-Print Network (OSTI)

continuous ?ow reactor for thermal degradation of polymers.Qian J. Studies of the thermal degradation of waste rubber.10.1007/s10973-009-0577-3 Thermal catalytic conversion of

Rasul Jan, M.; Jabeen, Farah; Shah, Jasmin; Mabood, Fazal

2010-01-01T23:59:59.000Z

436

Microsoft Word - 41891_SWPC_Catalytic Combustor_Factsheet_Rev01...  

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

COMBUSTORFACTSHEETREV0104-24.DOC Facts Sheet: Catalytic Combustor for Fuel Flexible Gas Turbine (DE-FC26-03NT41891) I. PROJECT PARTICIPANTS A. Siemens Westinghouse Power...

437

Biomass gasification using a horizontal entrained-flow gasifier and catalytic processing of the product gas.  

E-Print Network (OSTI)

??A novel study on biomass-air gasification using a horizontal entrained-flow gasifier and catalytic processing of the product gas has been conducted. The study was designed… (more)

Legonda, Isack Amos

2012-01-01T23:59:59.000Z

438

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

439

Multi-stage selection catalytic reduction of NO{sub x} in lean burn engine exhaust  

DOE Green Energy (OSTI)

Recent studies suggest that the conversion of NO to NO{sub 2} is an important intermediate step in the selective catalytic reduction (SCR) of NO{sub x} to N{sub 2}. These studies have prompted the development of schemes that use an oxidation catalyst to convert NO to NO{sub 2}, followed by a reduction catalyst to convert NO{sub 2} to N{sub 2}. Multi-stage SCR offers high NO{sub x} reduction efficiency from catalysts that, separately, are not very active for reduction of NO, and alleviates the problem of selectivity between NO reduction and hydrocarbon oxidation. A plasma can also be used to oxidize NO to NO{sub 2}. This paper compares the multi-stage catalytic scheme with the plasma-assisted catalytic scheme for reduction of NO{sub x} in lean-bum engine exhausts. The advantages of plasma oxidation over catalytic oxidation are presented.

Penetrante, B.M.; Hsiao, M.O.; Merritt, B.T.; Vogling, E.

1998-01-26T23:59:59.000Z

440

Role of CeO2 Addition on Catalytic Conversion of Plasma Sprayed ...  

Science Conference Proceedings (OSTI)

In the current work, 316L steel substrate is plasma sprayed with CeO2-Al2O3 to achieve a catalytic surface. Microstructural evaluation of plasma-sprayed ...

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

Catalytic Addition of Simple Alkenes to Carbonyl Compounds by Use of Group 10 Metals  

E-Print Network (OSTI)

Recent advances using nickel complexes in the activation of unactivated monosubstituted olefins for catalytic intermolecular carbon-carbon bond-forming reactions with carbonyl compounds, such as simple aldehydes, isocyanates, ...

Ho, Chun-Yu

442

Review of the Literature on Catalytic Biomass Tar Destruction: Milestone Completion Report  

DOE Green Energy (OSTI)

A summary of literature pertaining to catalytic biomass gasification''tar'' destruction, an overview of catalysts studied, and an evaluation of the future potential for this gas cleaning technology.

Dayton, D.

2002-12-01T23:59:59.000Z

443

Experimental and Computational Study of Catalytic Combustion of Methane-Air and Syngas-Air Mixtures.  

E-Print Network (OSTI)

??Catalytic combustion and conversion of methane (CH4) and Syngas (in our case, a gas mixture of H2, CO, CO2 and CH4) is characterized by the… (more)

Pathak, Saurav

2007-01-01T23:59:59.000Z

444

System Study of Rich Catalytic/Lean burn (RCL) Catalytic Combustion for Natural Gas and Coal-Derived Syngas Combustion Turbines  

SciTech Connect

Rich Catalytic/Lean burn (RCL{reg_sign}) technology has been successfully developed to provide improvement in Dry Low Emission gas turbine technology for coal derived syngas and natural gas delivering near zero NOx emissions, improved efficiency, extending component lifetime and the ability to have fuel flexibility. The present report shows substantial net cost saving using RCL{reg_sign} technology as compared to other technologies both for new and retrofit applications, thus eliminating the need for Selective Catalytic Reduction (SCR) in combined or simple cycle for Integrated Gasification Combined Cycle (IGCC) and natural gas fired combustion turbines.

Shahrokh Etemad; Lance Smith; Kevin Burns

2004-12-01T23:59:59.000Z

445

Fluid Lab Analysis | Open Energy Information  

Open Energy Info (EERE)

Page Page Edit with form History Facebook icon Twitter icon » Fluid Lab Analysis Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Fluid Lab Analysis Details Activities (0) Areas (0) Regions (0) NEPA(0) Exploration Technique Information Exploration Group: Lab Analysis Techniques Exploration Sub Group: Fluid Lab Analysis Parent Exploration Technique: Lab Analysis Techniques Information Provided by Technique Lithology: Stratigraphic/Structural: Hydrological: Results can aid in the determination of fluid source regions and circulation pathways, and assist in determining the degree of mixing between different hydrothermal fluids. Thermal: Certain elements exhibit high spatial correlation with high-temperature geothermal systems; Isotopic ratios can be used to characterize and locate subsurface thermal anomalies.

446

Definition: Isotopic Analysis- Fluid | Open Energy Information  

Open Energy Info (EERE)

Definition Definition Edit with form History Facebook icon Twitter icon » Definition: Isotopic Analysis- Fluid Jump to: navigation, search Dictionary.png Isotopic Analysis- Fluid Isotopes are atoms of the same element that have different numbers of neutrons. An isotopic analysis looks at a particular isotopic element(s) in a given system, while the conditions which increase/decrease the number of neutrons are well understood and measurable. Fluid isotopes are used to characterize a fluids origin, age, and/or interaction with rocks or other fluids based on unique isotopic ratios or concentrations.[1] View on Wikipedia Wikipedia Definition Isotope geochemistry is an aspect of geology based upon study of the relative and absolute concentrations of the elements and their isotopes in

447

Definition: Fluid Lab Analysis | Open Energy Information  

Open Energy Info (EERE)

Fluid Lab Analysis Fluid Lab Analysis Jump to: navigation, search Dictionary.png Fluid Lab Analysis Fluid lab analysis encompasses a broad array of techniques used for the analysis of water and gas samples. These analyses are used in a variety of disciplines to quantify the chemical components and properties of groundwater systems. In geothermal exploration and development, fluid analyses often provide a first look into the characteristics of a hydrothermal system, and are routinely used in ongoing monitoring of geothermal reservoirs.[1] View on Wikipedia Wikipedia Definition Water chemistry analyses are carried out to identify and quantify the chemical components and properties of a certain water. This include pH, major cations and anions, trace elements and isotopes. Water chemistry

448

Definition: Downhole Fluid Sampling | Open Energy Information  

Open Energy Info (EERE)

Definition Definition Edit with form History Facebook icon Twitter icon » Definition: Downhole Fluid Sampling Jump to: navigation, search Dictionary.png Downhole Fluid Sampling Downhole fluid sampling is done to characterize the chemical, thermal, or hydrological properties of a surface or subsurface aqueous system. Downhole fluid sampling is typically performed to monitor water quality, study recharge and flow in groundwater systems, and evaluate resource potential of geothermal reservoirs. Analysis of both the liquid and gas fractions of the reservoir fluid allows for detailed characterize the chemical, thermal, or hydrological properties of the subsurface hydrothermal system. View on Wikipedia Wikipedia Definition Ret Like Like You like this.Sign Up to see what your friends like.

449

Radiation stability of biocompatibile magnetic fluid  

E-Print Network (OSTI)

The radiation stability of biocompatibile magnetic fluid used in nanomedicine after electron irradiation was studied. Two types of the water-based magnetic fluids were prepared. The first one was based on the magnetite nanoparticles stabilized by one surfactant natrium oleate. The second one was biocompatibile magnetic fluid stabilized with two surfactants, natrium oleate as a first surfactant and Poly(ethylene glycol) (PEG) as a second surfactant. The magnetization measurements showed that electron irradiation up to 1000Gy caused 50% reduction of saturation magnetization in the case of the first sample with only one surfactant while in the case of the second biocompatibile magnetic fluid, only 25% reduction of saturation magnetization was observed. In the first magnetic fluid the radiation caused the higher sedimentation of the magnetic particles than in the second case, when magnetic particles are covered also with PEG. The obtained results show that PEG behave as a protective element.

Natalia Tomasovicova; Ivan Haysak; Martina Koneracka; Jozef Kovac; Milan Timko; Vlasta Zavisova; Alexander Okunev; Alexander Parlag; Alexey Fradkin; Peter Kopcansky

2010-04-20T23:59:59.000Z

450

Fluid permeability measurement system and method  

DOE Patents (OSTI)

A system for measuring the permeance of a material. The permeability of the material may also be derived. The system provides a liquid or high concentration fluid bath on one side of a material test sample, and a gas flow across the opposing side of the material test sample. The mass flow rate of permeated fluid as a fraction of the combined mass flow rate of gas and permeated fluid is used to calculate the permeance of the material. The material test sample may be a sheet, a tube, or a solid shape. Operational test conditions may be varied, including concentration of the fluid, temperature of the fluid, strain profile of the material test sample, and differential pressure across the material test sample.

Hallman, Jr., Russell Louis (Knoxville, TN); Renner, Michael John (Oak Ridge, TN)

2008-02-05T23:59:59.000Z

451

Catalyst Management Handbook for Coal-Fired Selective Catalytic Reduction NOx Control  

Science Conference Proceedings (OSTI)

This report provides guidelines for operators of coal-fired power plants equipped with selective catalytic reduction (SCR) NOx-control processes. These control processes define when to exchange or replace catalyst, while minimizing power-production cost impacts from SCR process equipment.BackgroundSelective catalytic reduction (SCR) is deployed on most major coal-fired generating units in the United States. Over 225 units, totaling 140 GW of ...

2012-12-14T23:59:59.000Z

452

Heat exchanger with intermediate evaporating and condensing fluid  

DOE Patents (OSTI)

A shell and tube-type heat exchanger, such as a liquid sodium-operated steam generator for use in nuclear reactors, comprises a shell containing a primary fluid tube bundle, a secondary fluid tube bundle at higher elevation, and an intermediate fluid vaporizing at the surface of the primary fluid tubes and condensing at the surface of the secondary fluid tubes.

Fraas, Arthur P. (Knoxville, TN)

1978-01-01T23:59:59.000Z

453

Physics-Based Simulations for Fluid Mixtures Dongwoon Lee  

E-Print Network (OSTI)

experience a chemical reaction which produces a new type of fluid or generates heat energy. When heat energy knowledge of fluids. He helped me to understand dynamics of fluids through his lectures and experiments. I Interaction . . . . . . . . . . . . . . . . . . . . . . . . . . . 8 3 Fluid Models 10 3.1 Fluid Dynamics

Toronto, University of

454

Catalytic multi-stage process for hydroconversion and refining hydrocarbon feeds  

DOE Green Energy (OSTI)

A multi-stage catalytic hydrogenation and hydroconversion process for heavy hydrocarbon feed materials such as coal, heavy petroleum fractions, and plastic waste materials. In the process, the feedstock is reacted in a first-stage, back-mixed catalytic reactor with a highly dispersed iron-based catalyst having a powder, gel or liquid form. The reactor effluent is pressure-reduced, vapors and light distillate fractions are removed overhead, and the heavier liquid fraction is fed to a second stage back-mixed catalytic reactor. The first and second stage catalytic reactors are operated at 700-850.degree. F. temperature, 1000-3500 psig hydrogen partial pressure and 20-80 lb./hr per ft.sup.3 reactor space velocity. The vapor and light distillates liquid fractions removed from both the first and second stage reactor effluent streams are combined and passed to an in-line, fixed-bed catalytic hydrotreater for heteroatom removal and for producing high quality naphtha and mid-distillate or a full-range distillate product. The remaining separator bottoms liquid fractions are distilled at successive atmospheric and vacuum pressures, low and intermediate-boiling hydrocarbon liquid products are withdrawn, and heavier distillate fractions are recycled and further upgraded to provide additional low-boiling hydrocarbon liquid products. This catalytic multistage hydrogenation process provides improved flexibility for hydroprocessing the various carbonaceous feedstocks and adjusting to desired product structures and for improved economy of operations.

Comolli, Alfred G. (Yardley, PA); Lee, Lap-Keung (Cranbury, NJ)

2001-01-01T23:59:59.000Z

455

Coke gasification: the influence and behavior of inherent catalytic mineral matter  

Science Conference Proceedings (OSTI)

Gasification of coke contributes to its degradation in the blast furnace. In this study, the effect of gasification on the inherent catalytic minerals in cokes and their reciprocal influence on gasification are investigated. The catalytic mineral phases identified in the cokes used in this study were metallic iron, iron sulfides, and iron oxides. Metallic iron and pyrrhotite were rapidly oxidized during gasification to iron oxide. The catalysts had a strong influence on the apparent rates at the initial stages of reaction. As gasification proceeds, their effect on the reaction rate diminishes as a result of reducing the surface contact between catalyst and carbon matrix because of carbon consumption around the catalyst particles; with extended burnout the reactivity of the coke becomes increasingly dependent on surface area. The reaction rate in the initial stages was also influenced by the particle size of the catalytic minerals; for a given catalytic iron level, the cokes whose catalytic minerals were more finely dispersed had a higher apparent reaction rate than cokes containing larger catalytic particles. Iron, sodium, and potassium in the amorphous phase did not appear to affect the reaction rate. 40 refs., 16 figs., 6 tabs.

Mihaela Grigore; Richard Sakurovs; David French; Veena Sahajwalla [Commonwealth Scientific and Industrial Research Organisation (CSIRO), Bangor, NSW (Australia)

2009-04-15T23:59:59.000Z

456

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION  

Open Energy Info (EERE)

TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION GAS CHEMISTRY Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: TRACING FLUID SOURCES IN THE COSO GEOTHERMAL SYSTEM USING FLUID-INCLUSION GAS CHEMISTRY Details Activities (1) Areas (1) Regions (0) Abstract: Vein and alteration assemblages from eight Coso wells have been collected and their fluid-inclusion gases analyzed by quadrupole mass spectrometry. Four major types of alteration were sampled: 1) young calcite-hematite-pyrite veins; 2) wairakite or epidote veins and alteration that are spatially associated with deep reservoirs in the main field and eastern wells; 3) older sericite and pyrite wallrock alteration; and 4) stilbite-calcite veins that are common in cooler or marginal portions of

457

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

Science Conference Proceedings (OSTI)

The Gas Research Institute (GRI) estimates that by the year 2010, 40% or more of U.S. gas supply will be provided by supplements including substitute natural gas (SNG) from coal. These supplements must be cost competitive with other energy sources. The first generation technologies for coal gasification e.g. the Lurgi Pressure Gasification Process and the relatively newer technologies e.g. the KBW (Westinghouse) Ash Agglomerating Fluidized-Bed, U-Gas Ash Agglomerating Fluidized-Bed, British Gas Corporation/Lurgi Slagging Gasifier, Texaco Moving-Bed Gasifier, and Dow and Shell Gasification Processes, have several disadvantages. These disadvantages include high severities of gasification conditions, low methane production, high oxygen consumption, inability to handle caking coals, and unattractive economics. Another problem encountered in catalytic coal gasification is deactivation of hydroxide forms of alkali and alkaline earth metal catalysts by oxides of carbon (CO{sub x}). To seek solutions to these problems, a team consisting of Clark Atlanta University (CAU, a Historically Black College and University, HBCU), the University of Tennessee Space Institute (UTSI) and Georgia Institute of Technology (Georgia Tech) proposed to identify suitable low melting eutectic salt mixtures for improved coal gasification. The research objectives of this project were to: Identify appropriate eutectic salt mixture catalysts for coal gasification; Assess agglomeration tendency of catalyzed coal; Evaluate various catalyst impregnation techniques to improve initial catalyst dispersion; Determine catalyst dispersion at high carbon conversion levels; Evaluate effects of major process variables (such as temperature, system pressure, etc.) on coal gasification; Evaluate the recovery, regeneration and recycle of the spent catalysts; and Conduct an analysis and modeling of the gasification process to provide better understanding of the fundamental mechanisms and kinetics of the process.

Dr. Yaw D. Yeboah; Dr. Yong Xu; Dr. Atul Sheth; Dr. Pradeep Agrawal

2001-12-01T23:59:59.000Z

458

Non-catalytic steam hydrolysis of fats. Final report  

SciTech Connect

Hydrolysis of fats and oils produces fatty acid and glycerol. The catalyzed, liquid phase Colgate-Emry process, state-of-the-art, produces impure products that require extensive energy investment for their purification to commercial grade. Non-catalytic steam hydrolysis may produce products more easily purified. A bench-scale hydrolyzer was designed and constructed to contact descending liquid fat or oil with rising superheated steam. Each of the five stages in the reactor was designed similar to a distillation column stage to promote intimate liquid-gas contact. Degree of hydrolysis achieved in continuous tests using tallow feed were 15% at 280C and 35% at 300C at a tallow-to-steam mass feed ratio of 4.2. At a feed ratio of 9.2, the degree of hydrolysis was 21% at 300C. Decomposition was strongly evident at 325C but not at lower temperatures. Soybean oil rapidly polymerized under reaction conditions. Batch tests at 320C produced degrees of hydrolyses of between 44% and 63% using tallow and palm oil feeds. Over 95% fatty acids were present in a clean, readily separated organic portion of the overhead product from most tests. The test reactor had serious hydraulic resistance to liquid down-flow which limited operation to very long liquid residence times. These times are in excess of those that tallow and palm oil are stable at the reaction temperature. Little glycerol and extensive light organics were produced indicating that unexplained competing reactions to hydrolysis occurred in the experimental system. Further tests using an improved reactor will be required.

Deibert, M.C.

1992-08-28T23:59:59.000Z

459

Integrating catalytic coal gasifiers with solid oxide fuel cells  

Science Conference Proceedings (OSTI)

A review was conducted for coal gasification technologies that integrate with solid oxide fuel cells (SOFC) to achieve system efficiencies near 60% while capturing and sequestering >90% of the carbon dioxide [1-2]. The overall system efficiency can reach 60% when a) the coal gasifier produces a syngas with a methane composition of roughly 25% on a dry volume basis, b) the carbon dioxide is separated from the methane-rich synthesis gas, c) the methane-rich syngas is sent to a SOFC, and d) the off-gases from the SOFC are recycled back to coal gasifier. The thermodynamics of this process will be reviewed and compared to conventional processes in order to highlight where available work (i.e. exergy) is lost in entrained-flow, high-temperature gasification, and where exergy is lost in hydrogen oxidation within the SOFC. The main advantage of steam gasification of coal to methane and carbon dioxide is that the amount of exergy consumed in the gasifier is small compared to conventional, high temperature, oxygen-blown gasifiers. However, the goal of limiting the amount of exergy destruction in the gasifier has the effect of limiting the rates of chemical reactions. Thus, one of the main advantages of steam gasification leads to one of its main problems: slow reaction kinetics. While conventional entrained-flow, high-temperature gasifiers consume a sizable portion of the available work in the coal oxidation, the consumed exergy speeds up the rates of reactions. And while the rates of steam gasification reactions can be increased through the use of catalysts, only a few catalysts can meet cost requirements because there is often significant deactivation due to chemical reactions between the inorganic species in the coal and the catalyst. Previous research into increasing the kinetics of steam gasification will be reviewed. The goal of this paper is to highlight both the challenges and advantages of integrating catalytic coal gasifiers with SOFCs.

Siefert, N.; Shamsi, A.; Shekhawat, D.; Berry, D.

2010-01-01T23:59:59.000Z

460

Apparatus And Method For Fluid Analysis  

DOE Patents (OSTI)

The present invention is an apparatus and method for analyzing a fluid used in a machine or in an industrial process line. The apparatus has at least one meter placed proximate the machine or process line and in contact with the machine or process fluid for measuring at least one parameter related to the fluid. The at least one parameter is a standard laboratory analysis parameter. The at least one meter includes but is not limited to viscometer, element meter, optical meter, particulate meter, and combinations thereof.

Wilson, Bary W. (Richland, WA); Peters, Timothy J. (Richland, WA); Shepard, Chester L. (West Richland, WA); Reeves, James H. (Richland, WA)

2003-05-13T23:59:59.000Z

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

Hamiltonian description of the ideal fluid  

SciTech Connect

Fluid mechanics is examined from a Hamiltonian perspective. The Hamiltonian point of view provides a unifying framework; by understanding the Hamiltonian perspective, one knows in advance (within bounds) what answers to expect and what kinds of procedures can be performed. The material is organized into five lectures, on the following topics: rudiments of few-degree-of-freedom Hamiltonian systems illustrated by passive advection in two-dimensional fluids; functional differentiation, two action principles of mechanics, and the action principle and canonical Hamiltonian description of the ideal fluid; noncanonical Hamiltonian dynamics with examples; tutorial on Lie groups and algebras, reduction-realization, and Clebsch variables; and stability and Hamiltonian systems.

Morrison, P.J.

1994-01-01T23:59:59.000Z

462

Fluid Inclusion Stratigraphy: Interpretation of New Wells in...  

Open Energy Info (EERE)

Fluid Inclusion Stratigraphy: Interpretation of New Wells in the Coso Geothermal Field Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: Fluid...

463

Thermal Conductivity Prediction of Nano Fluid Using ANN/GA  

Science Conference Proceedings (OSTI)

Abstract Scope, Thermal conductivities of nano fluid in a two-phase having different compositions of both base fluid as well as nano particles in a closed ...

464

A STOCHASTIC METHOD FOR MODELING FLUID DISPLACEMENT IN PETROLEUM RESERVOIRS  

E-Print Network (OSTI)

FLUID DISPLACEMENT IN PETROLEUM RESERVOIRS C. Anderson andFLUID DISPLACEMENT IN PETROLEUM RESERVOIRS C. Anderson andachieve optimal recovery of petroleum from a reservoir, it

Anderson, C.

2011-01-01T23:59:59.000Z

465

ORGANIC SPECIES IN GEOTHERMAL WATERS IN LIGHT OF FLUID INCLUSION...  

Open Energy Info (EERE)

> 0.001 mol % typically have ethane > ethylene, propane > propylene, and butane > butylene. There are three end member fluid compositions: type 1 fluids in which...

466

FLUID INCLUSION STRATIGRAPHY: NEW METHOD FOR GEOTHERMAL RESERVOIR...  

Open Energy Info (EERE)

(0) Abstract: Fluid Inclusion Stratigraphy (FIS) is a new technique developed for the oil industry in order to map borehole fluids. This method is being studied for application...

467

Water-Miscible (Water-Soluble) Fluids  

Science Conference Proceedings (OSTI)

...the growth of microorganisms such as bacteria, algae, and fungi. If disposal is of no concern, phenolics can be used. The soaps, wetting agents, and couplers used as emulsifiers in water-miscible fluids reduce surface

468

Nanostructured Materials: Symthesis in Supercritical Fluids  

Science Conference Proceedings (OSTI)

This chapter summarizes the recent developent of synthesis and characterization of nanostructured materials synthesized in supercritical fluids. Nanocomposite catalysts such as Pt and Pd on carbon nanotube support have been synthesized and used for fuel cell applications.

Lin, Yuehe; Ye, Xiangrong; Wai, Chien M.

2009-03-24T23:59:59.000Z

469

PULSE RADIOLYSIS IN SUPERCRITICAL RARE GAS FLUIDS  

Science Conference Proceedings (OSTI)

Recently, supercritical fluids have become quite popular in chemical and semiconductor industries for applications in chemical synthesis, extraction, separation processes, and surface cleaning. These applications are based on: the high dissolving power due to density build-up around solute molecules, and the ability to tune the conditions of a supercritical fluid, such as density and temperature, that are most suitable for a particular reaction. The rare gases also possess these properties and have the added advantage of being supercritical at room temperature. Information about the density buildup around both charged and neutral species can be obtained from fundamental studies of volume changes in the reactions of charged species in supercritical fluids. Volume changes are much larger in supercritical fluids than in ordinary solvents because of their higher compressibility. Hopefully basic studies, such as discussed here, of the behavior of charged species in supercritical gases will provide information useful for the utilization of these solvents in industrial applications.

HOLROYD,R.

2007-01-01T23:59:59.000Z

470

Transparent fluids for 157-nm immersion lithography  

E-Print Network (OSTI)

, the latter determined by the thickness of the spacer gaskets. Since the calcium fluoride windows were found that enables the fluid to be reused for many 100 expo- sure fields will be both necessary and possible

French, Roger H.

471

CATALYTIC GASIFICATION OF COAL USING EUTECTIC SALT MIXTURES  

SciTech Connect

This is the progress report for the DOE grant DE-FG26-97FT97263 entitled, ''Catalytic Gasification of Coal Using Eutectic Salt Mixtures'' for the period April 1999 to October 1999. The project is being conducted jointly by Clark Atlanta University, the University of Tennessee Space Institute and Georgia Institute of Technology. The overall objectives of the project are to identify appropriate eutectic salt mixture catalysts for coal gasification; assess agglomeration tendency of catalyzed coal; evaluate various catalyst impregnation techniques to improve initial catalyst dispersion; evaluate effects of major process variables (such as temperature and system pressure) on coal gasification; evaluate the recovery, regeneration and recycle of the spent catalysts; and conduct thorough analysis and modeling of the gasification process to provide better understanding of the fundamental mechanisms and kinetics of the process. During this reporting period, free swelling index measurements of the coal, fixed-bed gasification experiments, kinetic modeling of the catalyzed gasification, and X-ray diffraction analysis of catalyst and gasified char samples were undertaken. The gasification experiments were carried out using two different eutectic salt mixtures of Li{sub 2}CO{sub 3}-Na{sub 2}CO{sub 3}-K{sub 2}CO{sub 3} (LNK) system and Na{sub 2}CO{sub 3}-K{sub 2}CO{sub 3} (NK) system. The gasification process followed a Langmuir-Hinshelwood type model. At 10 wt% of catalyst loading, the activation energy of the ternary catalyst system (LNK) was about half (98kJ/mol) the activation energy of the single catalyst system (K{sub 2}CO{sub 3}), which is about 170 kJ/ mole. The binary catalyst system (NK) showed activation energy of about 201 kJ/mol, which is slightly higher, compared to the K{sub 2}CO{sub 3} catalyst system. The ternary catalyst system was a much better eutectic catalyst system compared to the binary or single catalyst system. In general, a eutectic with a melting point less than the gasification temperature is a better substitute to the single alkali metal salts because they have good catalyst distribution and dispersion in the carbon matrix. The free selling index of the coal was about 1.5 (1 to 2) in comparison to 2.5 (2 to 3) for the coal samples with ternary eutectic. The results for the raw coal were consistent with those from the Penn State Coal Bank. The XRD characterization showed unidentified peaks in the spectra of some of the samples and require further studies to draw any conclusions at the point.

NONE

1999-10-01T23:59:59.000Z

472

Working Fluids Low Global Warming Potential Refrigerants  

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

Working Fluids Low GWP Working Fluids Low GWP Refrigerants - CRADA Ed Vineyard Oak Ridge National Laboratory vineyardea@ornl.gov (865) 574-0576 3 April 2013 2 | Building Technologies Office eere.energy.gov Purpose & Objectives Problem Statement: - High GWP refrigerants increase CO 2 equivalent emissions for HVAC&R equipment - Low GWP alternatives may increase energy consumption, introduce safety risks, require significant modifications to equipment, and have higher costs

473

Control system for fluid heated steam generator  

DOE Patents (OSTI)

A control system for controlling the location of the nucleate-boiling region in a fluid heated steam generator comprises means for measuring the temperature gradient (change in temperature per unit length) of the heating fluid along the steam generator; means for determining a control variable in accordance with a predetermined function of temperature gradients and for generating a control signal in response thereto; and means for adjusting the feedwater flow rate in accordance with the control signal.

Boland, James F. (Bonneville County, ID); Koenig, John F. (Idaho Falls, ID)

1985-01-01T23:59:59.000Z

474

Viscosity of High Energy Nuclear Fluids  

E-Print Network (OSTI)

Relativistic high energy heavy ion collision cross sections have been interpreted in terms of almost ideal liquid dr