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Note: This page contains sample records for the topic "oxide chemical vapor" 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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1

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

Science Conference Proceedings (OSTI)

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

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

1995-10-01T23:59:59.000Z

2

Oxidative chemical vapor deposition of conductive polymers for use in novel photovoltaic device architectures  

E-Print Network (OSTI)

The conductive polymer poly(3,4-ethylenedioxythiophene), (PEDOT), deposited via oxidative chemical vapor deposition (oCVD) has been investigated for use in organic electronic devices. The oCVD process as well as the ...

Howden, Rachel M. (Rachel Mary)

2013-01-01T23:59:59.000Z

3

Aerosol chemical vapor deposition of metal oxide films  

DOE Patents (OSTI)

A process of preparing a film of a multicomponent metal oxide including: forming an aerosol from a solution comprised of a suitable solvent and at least two precursor compounds capable of volatilizing at temperatures lower than the decomposition temperature of said precursor compounds; passing said aerosol in combination with a suitable oxygen-containing carrier gas into a heated zone, said heated zone having a temperature sufficient to evaporate the solvent and volatilize said precursor compounds; and passing said volatilized precursor compounds against the surface of a substrate, said substrate having a sufficient temperature to decompose said volatilized precursor compounds whereby metal atoms contained within said volatilized precursor compounds are deposited as a metal oxide film upon the substrate is disclosed. In addition, a coated article comprising a multicomponent metal oxide film conforming to the surface of a substrate selected from the group consisting of silicon, magnesium oxide, yttrium-stabilized zirconium oxide, sapphire, or lanthanum gallate, said multicomponent metal oxide film characterized as having a substantially uniform thickness upon said substrate, and as having a crystalline orientation defined as predominantly C-axis oriented by x-ray diffraction is disclosed.

Ott, K.C.; Kodas, T.T.

1990-04-16T23:59:59.000Z

4

Plasma enhanced chemical vapor deposition (PECVD) method of forming vanadium oxide films and vanadium oxide thin-films prepared thereby  

DOE Green Energy (OSTI)

A method is disclosed of forming a vanadium oxide film on a substrate utilizing plasma enhanced chemical vapor deposition. The method includes positioning a substrate within a plasma reaction chamber and then forming a precursor gas comprised of a vanadium-containing chloride gas in an inert carrier gas. This precursor gas is then mixed with selected amounts of hydrogen and oxygen and directed into the reaction chamber. The amounts of precursor gas, oxygen and hydrogen are selected to optimize the final properties of the vanadium oxide film An rf plasma is generated within the reaction chamber to chemically react the precursor gas with the hydrogen and the oxygen to cause deposition of a vanadium oxide film on the substrate while the chamber deposition pressure is maintained at about one torr or less. Finally, the byproduct gases are removed from the plasma reaction chamber.

Zhang, Ji-Guang (Golden, CO); Tracy, C. Edwin (Golden, CO); Benson, David K. (Golden, CO); Turner, John A. (Littleton, CO); Liu, Ping (Lakewood, CO)

2000-01-01T23:59:59.000Z

5

On-line coating of glass with tin oxide by atmospheric pressure chemical vapor deposition.  

SciTech Connect

Atmospheric pressure chemical vapor deposition (APCVD) of tin oxide is a very important manufacturing technique used in the production of low-emissivity glass. It is also the primary method used to provide wear-resistant coatings on glass containers. The complexity of these systems, which involve chemical reactions in both the gas phase and on the deposition surface, as well as complex fluid dynamics, makes process optimization and design of new coating reactors a very difficult task. In 2001 the U.S. Dept. of Energy Industrial Technologies Program Glass Industry of the Future Team funded a project to address the need for more accurate data concerning the tin oxide APCVD process. This report presents a case study of on-line APCVD using organometallic precursors, which are the primary reactants used in industrial coating processes. Research staff at Sandia National Laboratories in Livermore, CA, and the PPG Industries Glass Technology Center in Pittsburgh, PA collaborated to produce this work. In this report, we describe a detailed investigation of the factors controlling the growth of tin oxide films. The report begins with a discussion of the basic elements of the deposition chemistry, including gas-phase thermochemistry of tin species and mechanisms of chemical reactions involved in the decomposition of tin precursors. These results provide the basis for experimental investigations in which tin oxide growth rates were measured as a function of all major process variables. The experiments focused on growth from monobutyltintrichloride (MBTC) since this is one of the two primary precursors used industrially. There are almost no reliable growth-rate data available for this precursor. Robust models describing the growth rate as a function of these variables are derived from modeling of these data. Finally, the results are used to conduct computational fluid dynamic simulations of both pilot- and full-scale coating reactors. As a result, general conclusions are reached concerning the factors affecting the growth rate in on-line APCVD reactors. In addition, a substantial body of data was generated that can be used to model many different industrial tin oxide coating processes. These data include the most extensive compilation of thermochemistry for gas-phase tin-containing species as well as kinetic expressions describing tin oxide growth rates over a wide range of temperatures, pressures, and reactant concentrations.

Allendorf, Mark D.; Sopko, J.F. (PPF Industries, Pittsburgh, PA); Houf, William G.; Chae, Yong Kee; McDaniel, Anthony H.; Li, M. (PPF Industries, Pittsburgh, PA); McCamy, J.W. (PPF Industries, Pittsburgh, PA)

2006-11-01T23:59:59.000Z

6

Controlled VLS Growth of Indium, Gallium and Tin Oxide Nanowires via Chemical Vapor Transport  

E-Print Network (OSTI)

technique to synthesize indium oxide, gallium oxide, and tinmaterial systems such as indium oxide, gallium oxide and tinand Characterization A. Indium Oxide Nanowires Indium oxide

Johnson, M.C.; Aloni, S.; McCready, D.E.; Bourret-Courchesne, E.D.

2006-01-01T23:59:59.000Z

7

Chemical vapor deposition sciences  

SciTech Connect

Chemical vapor deposition (CVD) is a widely used method for depositing thin films of a variety of materials. Applications of CVD range from the fabrication of microelectronic devices to the deposition of protective coatings. New CVD processes are increasingly complex, with stringent requirements that make it more difficult to commercialize them in a timely fashion. However, a clear understanding of the fundamental science underlying a CVD process, as expressed through computer models, can substantially shorten the time required for reactor and process development. Research scientists at Sandia use a wide range of experimental and theoretical techniques for investigating the science of CVD. Experimental tools include optical probes for gas-phase and surface processes, a range of surface analytic techniques, molecular beam methods for gas/surface kinetics, flow visualization techniques and state-of-the-art crystal growth reactors. The theoretical strategy uses a structured approach to describe the coupled gas-phase and gas-surface chemistry, fluid dynamics, heat and mass transfer of a CVD process. The software used to describe chemical reaction mechanisms is easily adapted to codes that model a variety of reactor geometries. Carefully chosen experiments provide critical information on the chemical species, gas temperatures and flows that are necessary for model development and validation. This brochure provides basic information on Sandia`s capabilities in the physical and chemical sciences of CVD and related materials processing technologies. It contains a brief description of the major scientific and technical capabilities of the CVD staff and facilities, and a brief discussion of the approach that the staff uses to advance the scientific understanding of CVD processes.

1992-12-31T23:59:59.000Z

8

LOW PRESSURE CHEMICAL VAPOR DEPOSITION OF POLYSILICON  

E-Print Network (OSTI)

THEORY The mass transport processes in low pressure chemical vapor deposition (LPCVD) are similar to those occuring in catalytic reactors

Gieske, R.J.

2011-01-01T23:59:59.000Z

9

Comparison between chemical vapor deposited and physical vapor deposited WSi{sub 2} metal gate for InGaAs n-metal-oxide-semiconductor field-effect transistors  

Science Conference Proceedings (OSTI)

We compare chemical vapor deposition (CVD) and physical vapor deposition (PVD) WSi{sub 2} metal gate process for In{sub 0.53}Ga{sub 0.47}As n-metal-oxide-semiconductor field-effect transistors using 10 and 6.5 nm Al{sub 2}O{sub 3} as dielectric layer. The CVD-processed metal gate device with 6.5 nm Al{sub 2}O{sub 3} shows enhanced transistor performance such as drive current, maximum transconductance and maximum effective mobility. These values are relatively better than the PVD-processed counterpart device with improvement of 51.8%, 46.4%, and 47.8%, respectively. The improvement for the performance of the CVD-processed metal gate device is due to the fluorine passivation at the oxide/semiconductor interface and a nondestructive deposition process.

Ong, B. S.; Pey, K. L. [Advanced Materials for Micro and Nano-Systems, Singapore-MIT Alliance, Singapore 637460 (Singapore); School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Ong, C. Y.; Tan, C. S. [School of Electrical and Electronic Engineering, Nanyang Technological University, Singapore 639798 (Singapore); Antoniadis, D. A. [Advanced Materials for Micro and Nano-Systems, Singapore-MIT Alliance, Singapore 637460 (Singapore); Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Fitzgerald, E. A. [Advanced Materials for Micro and Nano-Systems, Singapore-MIT Alliance, Singapore 637460 (Singapore); Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States)

2011-05-02T23:59:59.000Z

10

Vapor phase modifiers for oxidative coupling  

DOE Patents (OSTI)

Volatilized metal compounds retard vapor phase alkane conversion reactions in oxidative coupling processes that convert lower alkanes to higher hydrocarbons.

Warren, Barbara K. (Charleston, WV)

1991-01-01T23:59:59.000Z

11

Chemical vapor deposition of functionalized isobenzofuran polymers  

E-Print Network (OSTI)

This thesis develops a platform for deposition of polymer thin films that can be further tailored by chemical surface modification. First, we explore chemical vapor deposition of functionalized isobenzofuran films using ...

Olsson, Ylva Kristina

2007-01-01T23:59:59.000Z

12

Vapor phase modifiers for oxidative coupling  

DOE Patents (OSTI)

Volatilized metal compounds are described which are capable of retarding vapor phase alkane conversion reactions in oxidative coupling processes that convert lower alkanes to higher hydrocarbons.

Warren, B.K.

1991-12-17T23:59:59.000Z

13

Aerogel composites using chemical vapor infiltration  

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

Aerogel composites using chemical vapor infiltration Aerogel composites using chemical vapor infiltration Title Aerogel composites using chemical vapor infiltration Publication Type Journal Article Year of Publication 1995 Authors Hunt, Arlon J., Michael R. Ayers, and Wanqing Cao Journal Journal of Non-Crystalline Solids Volume 185 Pagination 227-232 Abstract A new method to produce novel composite materials based on the use of aerogels as a starting material is described. Using chemical vapor infiltration, a variety of solid materials were thermally deposited into the open pore structure of aerogel. The resulting materials possess new and unusual properties including photoluminescence, magnetism and altered optical properties. An important characteristic of this preparation process is the very small size of the deposits that gives rise to new behaviors. Silicon deposits exhibit photoluminescence, indicating quantum confinement. Two or more phases may be deposited simultaneously and one or both chemically or thermally reacted to produce new structures.

14

Chemical vapor depositing of metal fluorides  

Science Conference Proceedings (OSTI)

High Purity BeF2 and BeF2–AlF3glasses have been deposited by the chemical vapor deposition technique using beryllium and aluminum 1

A. Sarhangi; J. M. Power

1992-01-01T23:59:59.000Z

15

Chemical vapor deposition of antimicrobial polymer coatings  

E-Print Network (OSTI)

There is large and growing interest in making a wide variety of materials and surfaces antimicrobial. Initiated chemical vapor deposition (iCVD), a solventless low-temperature process, is used to form thin films of polymers ...

Martin, Tyler Philip, 1977-

2007-01-01T23:59:59.000Z

16

Chemical vapor infiltration using microwave energy  

DOE Patents (OSTI)

This invention is comprised of a method for producing reinforced ceramic composite articles by means of chemical vapor infiltration and deposition in which an inverted temperature gradient is utilized. Microwave energy is the source of heat for the process.

Devlin, D.J.; Currier, R.P.; Laia, J.R.; Barbero, R.S.

1992-12-31T23:59:59.000Z

17

Molecular restrictions for human eye irritation by chemical vapors  

E-Print Network (OSTI)

and reactive airborne chemicals. Pharmacol. Toxicol. 1998;WL. Chemesthesis: The Common Chemical Sense. In: Finger TE,MH. Quantification of chemical vapors in chemosensory

Cometto-Muniz, J. Enrique; Cain, William S.; Abraham, Michael H.

2005-01-01T23:59:59.000Z

18

Chemical vapor deposition of mullite coatings  

DOE Patents (OSTI)

This invention is directed to the creation of crystalline mullite coatings having uniform microstructure by chemical vapor deposition (CVD). The process comprises the steps of establishing a flow of reactants which will yield mullite in a CVD reactor, and depositing a crystalline coating from the reactant flow. The process will yield crystalline coatings which are dense and of uniform thickness.

Sarin, Vinod (Lexington, MA); Mulpuri, Rao (Boston, MA)

1998-01-01T23:59:59.000Z

19

DuPont Chemical Vapor Technical Report  

Science Conference Proceedings (OSTI)

DuPont Safety Resources was tasked with reviewing the current chemical vapor control practices and providing preventive recommendations on best commercial techniques to control worker exposures. The increased focus of the tank closure project to meet the 2024 Tri-Party Agreement (TPA) milestones has surfaced concerns among some CH2MHill employees and other interested parties. CH2MHill is committed to providing a safe working environment for employees and desires to safely manage the tank farm operations using appropriate control measures. To address worker concerns, CH2MHill has chartered a ''Chemical Vapors Project'' to integrate the activities of multiple CH2MHill project teams, and solicit the expertise of external resources, including an independent Industrial Hygiene expert panel, a communications consultant, and DuPont Safety Resources. Over a three-month time period, DuPont worked with CH2MHill ESH&Q, Industrial Hygiene, Engineering, and the independent expert panel to perform the assessment. The process included overview presentations, formal interviews, informal discussions, documentation review, and literature review. DuPont Safety Resources concluded that it is highly unlikely that workers in the tank farms are exposed to chemicals above established standards. Additionally, the conventional and radiological chemistry is understood, the inherent chemical hazards are known, and the risk associated with chemical vapor exposure is properly managed. The assessment highlighted management's commitment to addressing chemical vapor hazards and controlling the associated risks. Additionally, we found the Industrial Hygiene staff to be technically competent and well motivated. The tank characterization data resides in a comprehensive database containing the tank chemical compositions and relevant airborne concentrations.

MOORE, T.L.

2003-10-03T23:59:59.000Z

20

Microwave plasma chemical vapor deposition of nano-composite...  

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

plasma chemical vapor deposition of nano-composite CPt thin-films Title Microwave plasma chemical vapor deposition of nano-composite CPt thin-films Publication Type Journal...

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Microwave Plasma Chemical Vapor Depositon of Nano-Structured...  

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

Plasma Chemical Vapor Depositon of Nano-Structured SnC Composite Thin-Film anodes for Li-ion Battteries Title Microwave Plasma Chemical Vapor Depositon of Nano-Structured SnC...

22

Low Temperature Direct Growth of Graphene Films on Transparent Substrates by Chemical Vapor Deposition  

E-Print Network (OSTI)

and Few- Layer Graphene by Chemical Vapor Deposition",Liu, W. , et al. (2010). "Chemical vapor deposition of large5 1.3.3. Chemical Vapor

Antoine, Geoffrey Sandosh Jeffy

2013-01-01T23:59:59.000Z

23

Gas transport model for chemical vapor infiltration  

Science Conference Proceedings (OSTI)

A node-bond percolation model is presented for the gas permeability and pore surface area of the coarse porosity in woven fiber structures during densification by chemical vapor infiltration (CVI). Model parameters include the number of nodes per unit volume and their spatial distribution, and the node and bond radii and their variability. These parameters relate directly to structural features of the weave. Some uncertainty exists in the proper partition of the porosity between ``node`` and ``bond`` and between intra-tow and inter-tow, although the total is constrained by the known fiber loading in the structure. Applied to cloth layup preforms the model gives good agreement with the limited number of available measurements.

Starr, T.L. [School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0245 (United States)

1995-09-01T23:59:59.000Z

24

Dynamics of nucleation in chemical vapor deposition  

Science Conference Proceedings (OSTI)

We study the evolution of layer morphology during the early stages of metal chemical vapor deposition (CVD) onto Si(100) via pyrolysis of Fe(CO){sub 5} below 250{degrees}C. Scanning tunneling microscopy (STM) shows that nuclei formation is limited by precursor dissociation which occurs on terraces, not at step sites. Also, the average size of clusters formed during CVD is larger than for Fe growth by evaporation (a random deposition process). Based on STM data and Monte Carlo simulations, we conclude that the CVD-growth morphology is affected by preferential dissociation of Fe(CO){sub 5} molecules at existing Fe clusters -- an autocatalytic effect. We demonstrate that nucleation kinetics can be used to control formation of metal nanostructures on chemically tailored surfaces. Reactive sites on Si (001) are first passivated by hydrogen. H atoms are locally removed by electron stimulated desorption using electrons emitted from the STM tip. Subsequent pyrolysis of Fe(CO){sub 5} leads to selective nucleation and growth of Fe films in the areas where H has been removed.

Mayer, T.M.; Adams, D.P.; Swartzentruber, B.S.; Chason, E.

1995-11-01T23:59:59.000Z

25

Chemical oxidizers treat wastewater  

SciTech Connect

Based on the inherent benefits of these original oxidation systems, a second generation of advanced oxidation processes (AOPs) has emerged. These processes combine key features of the first generation technologies with more sophisticated advances in UV technology, such as the new pulsed plasma xenon flash lamp that emits high-energy, high-intensity UV light. Second generation systems can be equipped with a transmittance controller to prevent lamp fouling or scaling. The coupling of the first generation's technology with the new UV sources provides the rapid destruction of chlorinated and nonchlorinated hydrocarbons and humic acids from contaminated water. It also is effective in the treatment of organic laden gases from soil vapor extraction systems. AOPs may promote the oxidation (and subsequent removal) of heavy metals in water, though few data are available to verify the claim. The success of AOPs, including ozonation with UV light, hydrogen peroxide with UV light and advanced photolysis, is linked with their creation of hydroxyl-free radicals (OH[center dot]) that are effective in eliminating contaminants such as formaldehyde, chlorinated hydrocarbons and chlorinated solvents. Hydroxyl free-radicals are consumed in microsecond reactions and exhibit little substrate selectivity with the exception of halogenated alkanes such as chloroform. They can act as chain carriers. Given their power, hydroxyl free-radicals react with virtually all organic solutes more quickly (especially in water) than any other oxidants, except fluorine. There are projects that have found the combination of some AOPs to be the most efficient organic destruction techniques for the job. For example, one project successfully remediated groundwater contaminated with gasoline and Number 2 diesel through successive treatments of ozone and hydrogen peroxide with ultraviolet light, followed by granular activated carbon. 5 refs., 2 tabs.

Stephenson, F.A. (Dames Moore, Phoenix, AZ (United States))

1992-12-01T23:59:59.000Z

26

Worker Protection from Chemical Vapors: Hanford Tank Farms  

Science Conference Proceedings (OSTI)

Chemical vapor emissions from underground hazardous waste storage tanks on the Hanford site in eastern Washington State are a potential concern because workers enter the tank farms on a regular basis for waste retrievals, equipment maintenance, and surveillance. Tank farm contractors are in the process of retrieving all remaining waste from aging single-shell tanks, some of which date to World War II, and transferring it to newer double-shell tanks. During the waste retrieval process, tank farm workers are potentially exposed to fugitive chemical vapors that can escape from tank head-spaces and other emission points. The tanks are known to hold more than 1,500 different species of chemicals, in addition to radionuclides. Exposure assessments have fully characterized the hazards from chemical vapors in half of the tank farms. Extensive sampling and analysis has been done to characterize the chemical properties of hazardous waste and to evaluate potential health hazards of vapors at the ground surface, where workers perform maintenance and waste transfer activities. Worker concerns, risk communication, and exposure assessment are discussed, including evaluation of the potential hazards of complex mixtures of chemical vapors. Concentrations of vapors above occupational exposure limits (OEL) were detected only at exhaust stacks and passive breather filter outlets. Beyond five feet from the sources, vapors disperse rapidly. No vapors have been measured above 50% of their OELs more than five feet from the source. Vapor controls are focused on limited hazard zones around sources. Further evaluations of vapors include analysis of routes of exposure and thorough analysis of nuisance odors. (authors)

Anderson, T.J. [CH2M HILL Hanford Group, Inc. / Environmental Health, Richland, WA (United States)

2007-07-01T23:59:59.000Z

27

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

28

Photoinitiated chemical vapor depostion [sic] : mechanism and applications  

E-Print Network (OSTI)

Photoinitiated chemical vapor deposition (piCVD) is developed as a simple, solventless, and rapid method for the deposition of swellable hydrogels and functional hydrogel copolymers. Mechanistic experiments show that piCVD ...

Baxamusa, Salmaan Husain

2009-01-01T23:59:59.000Z

29

Chemical vapor deposition of organosilicon and sacrificial polymer thin films  

E-Print Network (OSTI)

Chemical vapor deposition (CVD) produced films for a wide array of applications from a variety of organosilicon and organic precursors. The structure and properties of thin films were controlled by varying processing ...

Casserly, Thomas Bryan

2005-01-01T23:59:59.000Z

30

Initiated chemical vapor deposition of functional polyacrylic thin films  

E-Print Network (OSTI)

Initiated chemical vapor deposition (iCVD) was explored as a novel method for synthesis of functional polyacrylic thin films. The process introduces a peroxide initiator, which can be decomposed at low temperatures (<200?C) ...

Mao, Yu, 1975-

2005-01-01T23:59:59.000Z

31

Properties of In-Doped ZnO Films Grown by Metalorganic Chemical Vapor Deposition on GaN(0001) Templates  

E-Print Network (OSTI)

TCO is amor- phous indium tin oxide (ITO), most commonlythe properties of indium-doped zinc oxide layers grown byoxide, doping, n-type, MOCVD, metalorganic chemical vapor deposition, ZnO: In, indium

Ben-Yaacov, Tammy; Ive, Tommy; Walle, Chris G.; Mishra, Umesh K.; Speck, James S.; Denbaars, Steven P.

2010-01-01T23:59:59.000Z

32

Advanced Chemical Heat Pumps Using Liquid-Vapor Reactions  

E-Print Network (OSTI)

Chemical heat pumps utilizing liquid-vapor reactions can be configured in forms analogous to electric drive vapor-compression heat pumps and heat activated absorption heat pumps. Basic thermodynamic considerations eliminate some heat pumps and place restrictive working fluid requirements on others, but two thermodynamically feasible systems have significant potential advantage over conventional technology. An electric drive reactive heat pump can use smaller heat exchangers and compressor than a vapor-compression machine, and have more flexible operating characteristics. A waste heat driven heat pump (temperature amplifier) using liquid-vapor chemical reactions- can operate with higher coefficient of performance and smaller heat exchangers than an absorption temperature amplifying heat pump. Higher temperatures and larger temperature lifts should also be possible.

Kirol, L.

1987-09-01T23:59:59.000Z

33

The Effects of Water Vapor on the Oxidation of Nickel-Base ...  

Science Conference Proceedings (OSTI)

water vapor are compared at temperatures from 700°C to 1100°C. It is shown that water vapor affects the oxidation of such alloys in different ways. Water vapor ...

34

Chemical vapor deposition thin films as biopassivation coatings and directly patternable dielectrics  

E-Print Network (OSTI)

Organosilicon thin films deposited by pulsed plasma-enhanced chemical vapor deposition (PPECVD) and hot-filament chemical vapor deposition (HFCVD) were investigated as potential biopassivation coatings for neural probes. ...

Pryce Lewis, Hilton G. (Hilton Gavin), 1973-

2001-01-01T23:59:59.000Z

35

Method of physical vapor deposition of metal oxides on semiconductors  

DOE Patents (OSTI)

A process for growing a metal oxide thin film upon a semiconductor surface with a physical vapor deposition technique in a high-vacuum environment and a structure formed with the process involves the steps of heating the semiconductor surface and introducing hydrogen gas into the high-vacuum environment to develop conditions at the semiconductor surface which are favorable for growing the desired metal oxide upon the semiconductor surface yet is unfavorable for the formation of any native oxides upon the semiconductor. More specifically, the temperature of the semiconductor surface and the ratio of hydrogen partial pressure to water pressure within the vacuum environment are high enough to render the formation of native oxides on the semiconductor surface thermodynamically unstable yet are not so high that the formation of the desired metal oxide on the semiconductor surface is thermodynamically unstable. Having established these conditions, constituent atoms of the metal oxide to be deposited upon the semiconductor surface are directed toward the surface of the semiconductor by a physical vapor deposition technique so that the atoms come to rest upon the semiconductor surface as a thin film of metal oxide with no native oxide at the semiconductor surface/thin film interface. An example of a structure formed by this method includes an epitaxial thin film of (001)-oriented CeO.sub.2 overlying a substrate of (001) Ge.

Norton, David P. (Knoxville, TN)

2001-01-01T23:59:59.000Z

36

Fabrication of solid oxide fuel cell by electrochemical vapor deposition  

DOE Patents (OSTI)

In a high temperature solid oxide fuel cell (SOFC), the deposition of an impervious high density thin layer of electrically conductive interconnector material, such as magnesium doped lanthanum chromite, and of an electrolyte material, such as yttria stabilized zirconia, onto a porous support/air electrode substrate surface is carried out at high temperatures (approximately 1100.degree.-1300.degree. C.) by a process of electrochemical vapor deposition. In this process, the mixed chlorides of the specific metals involved react in the gaseous state with water vapor resulting in the deposit of an impervious thin oxide layer on the support tube/air electrode substrate of between 20-50 microns in thickness. An internal heater, such as a heat pipe, is placed within the support tube/air electrode substrate and induces a uniform temperature profile therein so as to afford precise and uniform oxide deposition kinetics in an arrangement which is particularly adapted for large scale, commercial fabrication of SOFCs.

Brian, Riley (Willimantic, CT); Szreders, Bernard E. (Oakdale, CT)

1989-01-01T23:59:59.000Z

37

Fabrication of solid oxide fuel cell by electrochemical vapor deposition  

DOE Patents (OSTI)

In a high temperature solid oxide fuel cell (SOFC), the deposition of an impervious high density thin layer of electrically conductive interconnector material, such as magnesium doped lanthanum chromite, and of an electrolyte material, such as yttria stabilized zirconia, onto a porous support/air electrode substrate surface is carried out at high temperatures (/approximately/1100/degree/ /minus/ 1300/degree/C) by a process of electrochemical vapor deposition. In this process, the mixed chlorides of the specific metals involved react in the gaseous state with water vapor resulting in the deposit of an impervious thin oxide layer on the support tube/air electrode substrate of between 20--50 microns in thickness. An internal heater, such as a heat pipe, is placed within the support tube/air electrode substrate and induces a uniform temperature profile therein so as to afford precise and uniform oxide deposition kinetics in an arrangement which is particularly adapted for large scale, commercial fabrication of SOFCs.

Riley, B.; Szreders, B.E.

1988-04-26T23:59:59.000Z

38

Combustion chemical vapor deposited coatings for thermal barrier coating systems  

DOE Green Energy (OSTI)

The new deposition process, combustion chemical vapor deposition, shows a great deal of promise in the area of thermal barrier coating systems. This technique produces dense, adherent coatings, and does not require a reaction chamber. Coatings can therefore be applied in the open atmosphere. The process is potentially suitable for producing high quality CVD coatings for use as interlayers between the bond coat and thermal barrier coating, and/or as overlayers, on top of thermal barrier coatings. In this report, the evaluation of alumina and ceria coatings on a nickel-chromium alloy is described.

Hampikian, J.M.; Carter, W.B. [Georgia Institute of Technology, Atlanta, GA (United States). School of Materials Science and Engineering

1995-12-31T23:59:59.000Z

39

Chemical vapor deposition of amorphous semiconductor films. Final subcontract report  

DOE Green Energy (OSTI)

Chemical vapor deposition (CVD) from higher order silanes has been studied for fabricating amorphous hydrogenated silicon thin-film solar cells. Intrinsic and doped a-Si:H films were deposited in a reduced-pressure, tubular-flow reactor, using disilane feed-gas. Conditions for depositing intrinsic films at growth rates up to 10 A/s were identified. Electrical and optical properties, including dark conductivity, photoconductivity, activation energy, optical absorption, band-gap and sub-band-gap absorption properties of CVD intrinsic material were characterized. Parameter space for depositing intrinsic and doped films, suitable for device analysis, was identified.

Rocheleau, R.E.

1984-12-01T23:59:59.000Z

40

Chemical vapor deposition of hydrogenated amorphous silicon from disilane  

SciTech Connect

The authors describe hydrogenated amorphous silicon (a-Si:H) thin films deposited at growth rates of 1 to 30 A/s by chemical vapor deposition (CVD) from disilane source gas at 24 torr total pressure in a tubular reactor. The effects of substrate temperature and gas holding time (flow rate) on film growth rate and effluent gas composition were measured at temperatures ranging from 360{sup 0} to 485{sup 0}C and gas holding times from 3 to 62s. Effluent gases determined by gas chromatography included silane, disilane and other higher order silanes. A chemical reaction engineering model, based on a silylene (SiH/sub 2/) insertion gas phase reaction network and film growth from both SiH/sub 2/ and high molecular weight silicon species, Si/sub n/H/sub 2n/, was developed. The model predictions were in good agreement with experimentally determined growth rates and effluent gas compositions.

Bogaert, R.J.; Russell, T.W.F.; Klein, M.T. (Delaware Univ., Newark, DE (USA). Dept. of Chemical Engineering); Rocheleau, R.E.; Baron, B.N. (Delaware Univ., Newark, DE (USA). Inst. of Energy Conversion)

1989-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Gas transport model for chemical vapor infiltration. Topical report  

Science Conference Proceedings (OSTI)

A node-bond percolation model is presented for the gas permeability and pore surface area of the coarse porosity in woven fiber structures during densification by chemical vapor infiltration (CVI). Model parameters include the number of nodes per unit volume and their spatial distribution, and the node and bond radii and their variability. These parameters relate directly to structural features of the weave. Some uncertainty exists in the proper partition of the porosity between {open_quotes}node{close_quotes} and{open_quote}bond{close_quotes} and between intra-tow and inter-tow, although the total is constrained by the known fiber loading in the structure. Applied to cloth layup preforms the model gives good agreement with the limited number of available measurements.

Starr, T.L. [Georgia Institute of Technology, Atlanta, GA (United States). School of Materials Science and Engineering

1995-05-01T23:59:59.000Z

42

Measurement of gas transport properties for chemical vapor infiltration  

Science Conference Proceedings (OSTI)

In the chemical vapor infiltration (CVI) process for fabricating ceramic matrix composites (CMCs), transport of gas phase reactant into the fiber preform is a critical step. The transport can be driven by pressure or by concentration. This report describes methods for measuring this for CVI preforms and partially infiltrated composites. Results are presented for Nicalon fiber cloth layup preforms and composites, Nextel fiber braid preforms and composites, and a Nicalon fiber 3-D weave composite. The results are consistent with a percolating network model for gas transport in CVI preforms and composites. This model predicts inherent variability in local pore characteristics and transport properties, and therefore, in local densification during processing; this may lead to production of gastight composites.

Starr, T.L.; Hablutzel, N. [Georgia Inst. of Tech., Atlanta, GA (United States). School of Materials Science and Engineering

1996-12-01T23:59:59.000Z

43

Low Temperature Chemical Vapor Deposition Of Thin Film Magnets  

DOE Patents (OSTI)

A thin-film magnet formed from a gas-phase reaction of tetracyanoetheylene (TCNE) OR (TCNQ), 7,7,8,8-tetracyano-P-quinodimethane, and a vanadium-containing compound such as vanadium hexcarbonyl (V(CO).sub.6) and bis(benzene)vanalium (V(C.sub.6 H.sub.6).sub.2) and a process of forming a magnetic thin film upon at least one substrate by chemical vapor deposition (CVD) at a process temperature not exceeding approximately 90.degree. C. and in the absence of a solvent. The magnetic thin film is particularly suitable for being disposed upon rigid or flexible substrates at temperatures in the range of 40.degree. C. and 70.degree. C. The present invention exhibits air-stable characteristics and qualities and is particularly suitable for providing being disposed upon a wide variety of substrates.

Miller, Joel S. (Salt Lake City, UT); Pokhodnya, Kostyantyn I. (Salt Lake City, UT)

2003-12-09T23:59:59.000Z

44

Iron (III) Chloride doping of large-area chemical vapor deposition graphene  

E-Print Network (OSTI)

Chemical doping is an effective method of reducing the sheet resistance of graphene. This thesis aims to develop an effective method of doping large area Chemical Vapor Deposition (CVD) graphene using Iron (III) Chloride ...

Song, Yi, S.M. Massachusetts Institute of Technology

2013-01-01T23:59:59.000Z

45

Chemical vapor deposition of amorphous silicon films from disilane  

SciTech Connect

Amorphous silicon films for fabrication of solar cells have been deposited by thermal chemical vapor deposition (CVD) from disilane (Si/sub 2/H/sub 6/) using a tubular flow reactor. A mathematical description for the CVD reactor was developed and solved by a numerical procedure. The proposed chemical reaction network for the model is based on silylene (SiH/sub 2/) insertion in the gas phase and film growth from SiH/sub 2/ and silicon polymers (Si/sub n/N/sub 2n/, n approx. 10). Estimates of the rate constants have been obtained for trisilane decomposition, silicon polymer formation, and polymer dehydrogenation. The silane unimolecular decomposition rate constants were corrected for pressure effects. The model behavior is compared to the experimental results over the range of conditions: reactor temperature (360 to 485/sup 0/C), pressures (2 to 48 torr), and gas holding time (1 to 70 s). Within the above range of conditions, film growth rate varies from 0.01 to 30 A/s. Results indicate that silicon polymers are the main film precursors for gas holding times greater than 3 s. Film growth by silylene only becomes important at short holding times, large inert gas dilution, and positions near the beginning of the reactor hot zone.

Bogaert, R.J.

1986-01-01T23:59:59.000Z

46

Synthesis of high-quality monolayer and bilayer graphene on copper using chemical vapor deposition  

E-Print Network (OSTI)

/IG of the Raman spectra (red line in Fig. 6a) taken from the graphene grown on high purity Cu (99.999%) is above 3Synthesis of high-quality monolayer and bilayer graphene on copper using chemical vapor deposition determining the growth of high-quality monolayer and bilayer graphene on Cu using chemical vapor deposition

47

Low temperature photochemical vapor deposition of alloy and mixed metal oxide films  

DOE Patents (OSTI)

Method and apparatus for formation of an alloy thin film, or a mixed metal oxide thin film, on a substrate at relatively low temperatures. Precursor vapor(s) containing the desired thin film constituents is positioned adjacent to the substrate and irradiated by light having wavelengths in a selected wavelength range, to dissociate the gas(es) and provide atoms or molecules containing only the desired constituents. These gases then deposit at relatively low temperatures as a thin film on the substrate. The precursor vapor(s) is formed by vaporization of one or more precursor materials, where the vaporization temperature(s) is selected to control the ratio of concentration of metals present in the precursor vapor(s) and/or the total precursor vapor pressure.

Liu, David K. (San Pablo, CA)

1992-01-01T23:59:59.000Z

48

Chemical vapor deposition growth. Quarterly report No. 3  

DOE Green Energy (OSTI)

The purpose of the contract is to explore the chemical vapor deposition (CVD) method for the growth of Si sheet on inexpensive substrate materials. The work is carried out at the Rockwell Electronics Research Division in Anaheim, and also involves some experimental solar cell fabrication and evaluation by the Photo-electronics Group of Optical Coating Laboratory, Inc. (OCLI), in City of Industry, California. The contract program is composed of six main technical tasks: (1) modification and test of an existing CVD reactor system; (2) identification and/or development of suitable inexpensive substrate materials; (3) experimental investigation of CVD process parameters using various candidate substrate materials; (4) preparation of Si sheet samples for various special studies, including solar cell fabrication; (5) evaluation of the properties of the Si sheet material produced by the CVD process; and (6) fabrication and evaluation of experimental solar cell structures (by OCLI), using standard and near-standard processing techniques. The progress achieved during the fourth quarter is described by task, followed by a summary of conclusions and recommendations and an outline of the work planned for the next three months. The manpower and funding expenditures to date are summarized in Appendix A, and the Updated Technical Program Plan is included as Appendix B.

Ruth, R.P.; Manasevit, H.M.; Johnson, R.D.; Moudy, L.A..; Simpson, W.I.; Yang, J.J.

1977-01-01T23:59:59.000Z

49

Effect of gas feeding methods on optical properties of GaN grown by rapid thermal chemical vapor deposition reactor  

Science Conference Proceedings (OSTI)

Keywords: Ga vacancies, GaN growth, gas feeding method, optical property, rapid thermal chemical vapor deposition (RTCVD), yellow luminescence

Sun Jung Kim; Young Hun Seo; Kee Suk Nahm; Yun Bong Hahn; Hyun Wook Shim; Eun-Kyung Suh; Kee Young Lim; Hyung Jae Lee

1999-08-01T23:59:59.000Z

50

Metal film deposition by laser breakdown chemical vapor deposition  

Science Conference Proceedings (OSTI)

Dielectric breakdown of gas mixtures can be used to deposit homogeneous thin films by chemical vapor deposition with appropriate control of flow and pressure conditions to suppress gas phase nucleation and particle formation. Using a pulsed CO/sub 2/ laser operating at 10.6 microns where there is no significant resonant absorption in any of the source gases, we have succeeded in depositing homogeneous films from several gas phase precursors by gas phase laser pyrolysis. Nickel and molybdenum from the respective carbonyls and tungsten from the hexafluoride have been examined to date. In each case the gas precursor is buffered to reduce the partial pressure of the reactants and to induce breakdown. The films are spectrally reflective and uniform over a large area. Films have been characterized by Auger electron spectroscopy, x-ray diffraction, pull tests, and resistivity measurements. The highest quality films have resulted from the nickel depositions. Detailed x-ray diffraction analysis of these films yields a very small domain size (approx. 50 A) consistent with rapid quenching from the gas phase reaction zone. This analysis also shows nickel carbide formation consistent with the temperature of the reaction zone and the Auger electron spectroscopy results which show some carbon and oxygen incorporation (8% and 1% respectively). Gas phase transport and condensation of the molybdenum carbonyl results in substantial carbon and oxygen contamination of the molybdenum films requiring heated substrates, a requirement not consistent with the goals of the program to maximize the quench rate of the deposition. Results from tungsten deposition experiments representing a reduction chemistry instead of the decomposition chemistry involved in the carbonyl experiments are also reported.

Jervis, T.R.

1985-01-01T23:59:59.000Z

51

Initiated chemical vapor deposition of polymeric thin films : mechanism and applications  

E-Print Network (OSTI)

Initiated chemical vapor deposition (iCVD) is a novel technique for depositing polymeric thin films. It is able to deposit thin films of application-specific polymers in one step without using any solvents. Its uniqueness ...

Chan, Kelvin, Ph. D. Massachusetts Institute of Technology

2005-01-01T23:59:59.000Z

52

Single- and few-layer graphene by ambient pressure chemical vapor deposition on nickel  

E-Print Network (OSTI)

An ambient pressure chemical vapor deposition (APCVD) process is used to fabricate graphene based films consisting of one to several graphene layers across their area. Polycrystalline Ni thin films are used and the graphene ...

Reina Ceeco, Alfonso

2010-01-01T23:59:59.000Z

53

Optimal design of a high pressure organometallic chemical vapor deposition reactor  

Science Conference Proceedings (OSTI)

A team composed of material scientists, physicists, and applied mathematicians have used computer simulations as a fundamental design tool in developing a new prototype High Pressure Organometallic Chemical Vapor Deposition (HPOMCVD) reactor for use ...

K. J. Bachmann; H. T. Banks; C. Höpfner; G. M. Kepler; S. Lesure; S. D. Mccall; J. S. Scroggs

1999-04-01T23:59:59.000Z

54

Chemical Vapor Deposition of Fluoroalkylsilane Monolayer Films for Adhesion Control in Microelectromechanical Systems  

SciTech Connect

We have developed a new process for applying a hydrophobic, low adhesion energy coating to microelectromechanical (MEMS) devices. Monolayer films are synthesized from tridecafluoro-1,1,2,2-tetrahydrooctyltrichlorosilane (FOTS) and water vapor in a low-pressure chemical vapor deposition process at room temperature. Film thickness is self-limiting by virtue of the inability of precursors to stick to the fluorocarbon surface of the film once it has formed. We have measured film densities of {approx}3 molecules nm{sup 2} and film thickness of {approx}1 nm. Films are hydrophobic, with a water contact angle >110{sup o}. We have also incorporated an in-situ downstream microwave plasma cleaning process, which provides a clean, reproducible oxide surface prior to film deposition. Adhesion tests on coated and uncoated MEMS test structures demonstrate superior performance of the FOTS coatings. Cleaned, uncoated cantilever beam structures exhibit high adhesion energies in a high humidity environment. An adhesion energy of 100 mJ m{sup -2} is observed after exposure to >90% relative humidity. Fluoroalkylsilane coated beams exhibit negligible adhesion at low humidity and {<=} 20 {micro}J m{sup -2} adhesion energy at >90% relative humidity. No obvious film degradation was observed for films exposed to >90% relative humidity at room temperature for >24 hr.

MAYER,THOMAS M.; DE BOER,MAARTEN P.; SHINN,NEAL D.; CLEWS,PEGGY J.; MICHALSKE,TERRY A.

2000-01-26T23:59:59.000Z

55

Micro Chemical Vapor Deposition for the Synthesis of Nanomaterials  

E-Print Network (OSTI)

delivery," Current Opinion in Chemical Biology, vol. 9, pp.Journal of the American Chemical Society, vol. 126, pp.Park and R. S. Ruoff, "Chemical methods for the production

Zhou, Qin

2011-01-01T23:59:59.000Z

56

Verification of the O-Si-N complex in plasma-enhanced chemical vapor deposition silicon oxynitride films  

SciTech Connect

Silicon oxynitride films were deposited using a plasma-enhanced chemical vapor deposition process. The bond configurations of the constituent atoms in the deposited film were analyzed using x-ray photoelectron spectroscopy. Analysis of the Si 2p spectra showed the presence of nonstoichiometric silicon oxide and silicon oxynitride. Analysis of the binding energy shifts induced by Si-O and Si-N bond formation indicated an O-Si-N complex was present in the film matrix. Component balance analysis indicated that second-nearest-neighbor bond interactions were not the cause of these energy shifts and supported the presence of an O-Si-N complex.

Naskar, Sudipto; Wolter, Scott D.; Bower, Christopher A.; Stoner, Brian R.; Glass, Jeffrey T. [Center for Materials and Electronics Technologies, RTI-International, Research Triangle Park, North Carolina 27709 and Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27705 (United States); Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27705 (United States); Center for Materials and Electronics Technologies, RTI-International, Research Triangle Park, North Carolina 27709 (United States); Center for Materials and Electronics Technologies, RTI-International, Research Triangle Park, North Carolina 27709 and Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27705 (United States); Department of Electrical and Computer Engineering, Duke University, Durham, North Carolina 27705 (United States)

2005-12-26T23:59:59.000Z

57

Hot Wire Chemical Vapor Deposition with Carbide Filaments ...  

Many of the current industry cells in production have come through NREL, ... One deposition technology utilized at NREL deals with hot wire chemical ...

58

AlGaN/GaN high electron mobility transistors based on InGaN/GaN multi-quantum-well structures with photo-chemical vapor deposition of SiO2 dielectrics  

Science Conference Proceedings (OSTI)

AlGaN/GaN metal-oxide-semiconductor high electron mobility transistor (MOS-HEMT) based on InGaN/GaN multi-quantum-well (MQW) structure has been fabricated with SiO"2 dielectric deposited via photo-chemical vapor deposition (PHCVD) using a deuterium lamp ... Keywords: GaN, HEMT, MQW, Photo-chemical vapor deposition, SiO 2

Kai-Hsuan Lee; Ping-Chuan Chang; Shoou-Jinn Chang

2013-04-01T23:59:59.000Z

59

Solar-induced chemical vapor deposition of diamond-type carbon films  

DOE Patents (OSTI)

An improved chemical vapor deposition method for depositing transparent continuous coatings of sp[sup 3]-bonded diamond-type carbon films, comprises: (a) providing a volatile hydrocarbon gas/H[sub 2] reactant mixture in a cold wall vacuum/chemical vapor deposition chamber containing a suitable substrate for said films, at pressure of about 1 to 50 Torr; and (b) directing a concentrated solar flux of from about 40 to about 60 watts/cm[sup 2] through said reactant mixture to produce substrate temperatures of about 750 C to about 950 C to activate deposition of the film on said substrate. 11 figs.

Pitts, J.R.; Tracy, C.E.; King, D.E.; Stanley, J.T.

1994-09-13T23:59:59.000Z

60

Solar-induced chemical vapor deposition of diamond-type carbon films  

DOE Patents (OSTI)

An improved chemical vapor deposition method for depositing transparent continuous coatings of sp.sup.3 -bonded diamond-type carbon films, comprising: a) providing a volatile hydrocarbon gas/H.sub.2 reactant mixture in a cold wall vacuum/chemical vapor deposition chamber containing a suitable substrate for said films, at pressure of about 1 to 50 Torr; and b) directing a concentrated solar flux of from about 40 to about 60 watts/cm.sup.2 through said reactant mixture to produce substrate temperatures of about 750.degree. C. to about 950.degree. C. to activate deposition of the film on said substrate.

Pitts, J. Roland (Lakewood, CO); Tracy, C. Edwin (Golden, CO); King, David E. (Lakewood, CO); Stanley, James T. (Beaverton, OR)

1994-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Evaluation of Chemical Warfare Agent Percutaneous Vapor Toxicity: Derivation of Toxicity Guidelines for Assessing Chemical Protective Ensembles.  

SciTech Connect

Percutaneous vapor toxicity guidelines are provided for assessment and selection of chemical protective ensembles (CPEs) to be used by civilian and military first responders operating in a chemical warfare agent vapor environment. The agents evaluated include the G-series and VX nerve agents, the vesicant sulfur mustard (agent HD) and, to a lesser extent, the vesicant Lewisite (agent L). The focus of this evaluation is percutaneous vapor permeation of CPEs and the resulting skin absorption, as inhalation and ocular exposures are assumed to be largely eliminated through use of SCBA and full-face protective masks. Selection of appropriately protective CPE designs and materials incorporates a variety of test parameters to ensure operability, practicality, and adequacy. One aspect of adequacy assessment should be based on systems tests, which focus on effective protection of the most vulnerable body regions (e.g., the groin area), as identified in this analysis. The toxicity range of agent-specific cumulative exposures (Cts) derived in this analysis can be used as decision guidelines for CPE acceptance, in conjunction with weighting consideration towards more susceptible body regions. This toxicity range is bounded by the percutaneous vapor estimated minimal effect (EME{sub pv}) Ct (as the lower end) and the 1% population threshold effect (ECt{sub 01}) estimate. Assumptions of exposure duration used in CPE certification should consider that each agent-specific percutaneous vapor cumulative exposure Ct for a given endpoint is a constant for exposure durations between 30 min and 2 hours.

Watson, A.P.

2003-07-24T23:59:59.000Z

62

Effects of Water Vapor on Oxidation Behavior of Ferritic Stainless Steels Under Solid Oxide Fuel Cell Interconnect Exposure Conditions  

Science Conference Proceedings (OSTI)

The oxidation of ferritic stainless steels has been studied under solid oxide fuel cell (SOFC) interconnect ''dual'' exposure conditions, i.e. simultaneous exposure to air on one side of the sample, and fuel (hydrogen) on the other. It was found that, under the dual exposures, the oxidation behavior of the stainless steels at the airside differed significantly from that observed during exposure to air at both sides. Increased water vapor partial pressure in the air at the airside further accelerated the anomalous oxidation, resulting in nucleation and growth of hematite in the scale that led to a localized attack. The accelerated oxidation and growth of the hematite nodules was a result of combined effects of hydrogen transport from the fuel side to the airside and the presence of increased water vapor.

Yang, Z Gary; Xia, Gordon; Singh, Prabhakar; Stevenson, Jeffry W.

2005-08-01T23:59:59.000Z

63

Initiated chemical vapor deposition of fluoropolymer coatings for the surface modification of complex geometries  

E-Print Network (OSTI)

Initiated chemical vapor deposition (iCVD) is a one-step, soventless process that can be used to produce polymeric thin films. The iCVD technique has been used to polymerize a wide variety of vinyl monomers such as glycidyl ...

Gupta, Malancha, 1980-

2007-01-01T23:59:59.000Z

64

All-Hot-Wire Chemical Vapor Deposition a-Si:H Solar Cells  

DOE Green Energy (OSTI)

Efficient hydrogenated amorphous silicon (a-Si:H) nip solar cells have been fabricated with all doped and undoped a-Si:H layers deposited by hot-wire chemical vapor deposition (HWCVD). The total deposition time of all layers, except the top ITO-contact, is less than 4 minutes.

Iwaniczko, E.; Wang, Q.; Xu, Y.; Nelson, B. P.; Mahan, A. H.; Crandall, R. S.; Branz, H. M.

2000-01-01T23:59:59.000Z

65

Demonstration of spatially programmable chemical vapor deposition: Model-based uniformity/nonuniformity control  

E-Print Network (OSTI)

Demonstration of spatially programmable chemical vapor deposition: Model-based uniformity of deposition experiments to develop a model relating precursor concentration to film thickness in each segment region. As a demonstration of spatial programmability, the system was reprogramed using this model

Rubloff, Gary W.

66

Chemical vapor deposition of W-Si-N and W-B-N  

DOE Patents (OSTI)

A method of depositing a ternary, refractory based thin film on a substrate by chemical vapor deposition employing precursor sources of tungsten comprising WF.sub.6, either silicon or boron, and nitrogen. The result is a W--Si--N or W--B--N thin film useful for diffusion barrier and micromachining applications.

Fleming, James G. (Albuquerque, NM); Roherty-Osmun, Elizabeth Lynn (Albuquerque, NM); Smith, Paul M. (Albuquerque, NM); Custer, Jonathan S. (Albuquerque, NM); Jones, Ronald V. (Albuquerque, NM); Nicolet, Marc-A. (Pasadena, CA); Madar, Roland (Eybens, FR); Bernard, Claude (Brie et Angonnes, FR)

1999-01-01T23:59:59.000Z

67

Atomic-scale Chemical Quantification of Oxide Interfaces Using ...  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, Materials Science & Technology 2013. Symposium, Multifunctional Oxides. Presentation Title, Atomic-scale Chemical ...

68

Application of Thermochemical Modeling to Chemical Vapor Deposition  

Science Conference Proceedings (OSTI)

Thermochemical modeling of a CVD process is relatively easy as compared to developing a full computational fluid dynamics description coupled with reaction kinetics for a geometrically complex system. As such, a thermochemical computational study should be performed before embarking on the development of any new CVD process or material. The results of this kind of analysis can provide important information about whether the phases of interest are thermochemically allowed to form from a proposed precursor system. It can also indicate whether secondary phases can form, and give some idea as to the maximum theoretical efficiency of the process. All of this information is predicated on reaching chemical equilibrium in a system, which is the fundamental assumption of thermochemical analysis. Yet, the presumption of chemical equilibrium is not realistic given the relatively short residence time of precursors in CVD reactors. However, reactions will proceed toward equilibrium to a sufficient extent that it is a reasonable assumption for gaining process insights. In addition, it is possible to constrain equilibrium calculations to provide a more realistic result, for example, by eliminating a phase from consideration when it is known that kinetic or steric conditions will prevent its formation even when it is thermochemically permitted.

Besmann, Theodore M [ORNL

2009-01-01T23:59:59.000Z

69

Plasma enhanced chemical vapor deposition vanadium oxide thin ...  

... exhibits a high discharge capacity, a high energy density, and a negligible capacity fade fiom its second cycle to at least 2,900 cycles, ...

70

Proposed Occupational Exposure Limits for Non-Carcinogenic Hanford Waste Tank Vapor Chemicals  

SciTech Connect

A large number of volatile chemicals have been identified in the headspaces of tanks used to store mixed chemical and radioactive waste at the U.S. Department of Energy (DOE) Hanford Site, and there is concern that vapor releases from the tanks may be hazardous to workers. Contractually established occupational exposure limits (OELs) established by the Occupational Safety and Health Administration (OSHA) and American Conference of Governmental Industrial Hygienists (ACGIH) do not exist for all chemicals of interest. To address the need for worker exposure guidelines for those chemicals that lack OSHA or ACGIH OELs, a procedure for assigning Acceptable Occupational Exposure Limits (AOELs) for Hanford Site tank farm workers has been developed and applied to a selected group of 57 headspace chemicals.

Poet, Torka S.; Timchalk, Chuck

2006-03-24T23:59:59.000Z

71

Development of Single Crystal Chemical Vapor Deposition Diamonds for Detector Applications  

Science Conference Proceedings (OSTI)

Diamond was studied as a possible radiation hard technology for use in future high radiation environments. With the commissioning of the LHC expected in 2010, and the LHC upgrades expected in 2015, all LHC experiments are planning for detector upgrades which require radiation hard technologies. Chemical Vapor Deposition (CVD) diamond has now been used extensively in beam conditions monitors as the innermost detectors in the highest radiation areas of BaBar, Belle and CDF and is installed and operational in all LHC experiments. As a result, this material is now being discussed as an alternative sensor material for tracking very close to the interaction region of the super-LHC where the most extreme radiation conditions will exist. Our work addressed the further development of the new material, single-crystal Chemical Vapor Deposition diamond, towards reliable industrial production of large pieces and new geometries needed for detector applications.

Rainer Wallny

2012-10-15T23:59:59.000Z

72

Metal organic chemical vapor deposition of 111-v compounds on silicon  

DOE Patents (OSTI)

Expitaxial composite comprising thin films of a Group III-V compound semiconductor such as gallium arsenide (GaAs) or gallium aluminum arsenide (GaAlAs) on single crystal silicon substrates are disclosed. Also disclosed is a process for manufacturing, by chemical deposition from the vapor phase, epitaxial composites as above described, and to semiconductor devices based on such epitaxial composites. The composites have particular utility for use in making light sensitive solid state solar cells.

Vernon, Stanley M. (Wellesley, MA)

1986-01-01T23:59:59.000Z

73

Monolayer Graphene Growth on Ni(111) by Low Temperature Chemical Vapor Deposition  

Science Conference Proceedings (OSTI)

In contrast to the commonly employed high temperature chemical vapor deposition growth that leads to multilayer graphene formation by carbon segregation from the bulk, we demonstrate that below 600 C graphene can be grown in a self-limiting monolayer growth process. Optimum growth is achieved at {approx}550 C. Above this temperature, carbon diffusion into the bulk is limiting the surface growth rate, while at temperatures below {approx}500 C a competing surface carbide phase impedes graphene formation.

Batzill, M.; Sutter, P.; Addou, R.; Dahal, A.

2012-01-09T23:59:59.000Z

74

High rate chemical vapor deposition of carbon films using fluorinated gases  

DOE Patents (OSTI)

A high rate, low temperature deposition of amorphous carbon films is produced by PE-CVD in the presence of a fluorinated or other halide gas. The deposition can be 5 performed at less than 100C, including ambient room temperature, with a radio frequency plasma assisted chemical vapor deposition process. With less than 6.5 at% fluorine incorporated into the amorphous carbon film, the characteristics of the carbon film, including index of 10 refraction, mass density, optical clarity, and chemical resistance are within 15% of those characteristics for pure amorphous carbon films, but the deposition rates are high.

Stafford, B.L.; Tracy, C.E.; Benson, D.K.; Nelson, A.J.

1991-03-15T23:59:59.000Z

75

High rate chemical vapor deposition of carbon films using fluorinated gases  

DOE Patents (OSTI)

A high rate, low-temperature deposition of amorphous carbon films is produced by PE-CVD in the presence of a fluorinated or other halide gas. The deposition can be performed at less than 100.degree. C., including ambient room temperature, with a radio frequency plasma assisted chemical vapor deposition process. With less than 6.5 atomic percent fluorine incorporated into the amorphous carbon film, the characteristics of the carbon film, including index of refraction, mass density, optical clarity, and chemical resistance are within fifteen percent (15%) of those characteristics for pure amorphous carbon films, but the deposition rates are high.

Stafford, Byron L. (Arvada, CO); Tracy, C. Edwin (Golden, CO); Benson, David K. (Golden, CO); Nelson, Arthur J. (Longmont, CO)

1993-01-01T23:59:59.000Z

76

Epitaxial Thin Film Silicon Solar Cells Fabricated by Hot Wire Chemical Vapor Deposition Below 750 ..deg..C: Preprint  

Science Conference Proceedings (OSTI)

We report on fabricating film c-Si solar cells on Si wafer templates by hot-wire chemical vapor deposition. These devices, grown at glass-compatible temperatures 500 mV and efficiencies > 5%.

Alberi, K.; Martin, I. T.; Shub, M.; Teplin, C. W.; Iwaniczko, E.; Xu, Y.; duda, A.; Stradin, P.; Johnston, S. W.; Romero, M. J.; Branz, H. M.; Young, D. L.

2009-06-01T23:59:59.000Z

77

Self-catalyzed chemical vapor deposition method for the growth of device-quality metal thin films  

Science Conference Proceedings (OSTI)

Deposition of metals and alloys was demonstrated using thermal chemical vapor deposition starting from commercially available precursors in the absence of molecular hydrogen. The adopted chemical strategy relies solely on the selective reactivity of ... Keywords: CVD of metals, Chemical reduction, Direct liquid injection, Pulsed spray evaporation

N. Bahlawane; P. Antony Premkumar; K. Onwuka; G. Reiss; K. Kohse-Höinghaus

2007-11-01T23:59:59.000Z

78

Chemical vapor deposition of ZrC in small bore carbon-composite tubes  

SciTech Connect

Process conditions are described for the chemical vapor deposition of ZrC from ZrCl/sub 4/--CH/sub 4/--HCl--H/sub 2/--Ar vapor over the temperature range 1320 to 1775 deg K. From an analysis of the process conditions (initial composition of coating gas, axial temperature profile along the tubes, total pressure, and length of deposition time), the subsequent ZrC coat thickness profiles and thermodynamic data, an equation expressing the variation of the axial rate of ZrC deposition is derived. This expression can be used for the estimation of process conditions required to yield a specified ZrC coat profile. Variations of the chlorine and oxygen contents, lattice pararmeter, microstructure of the ZrC deposit and thermal expansion coefficient as a function of deposition temperature are described. (11 figures, 3 tables) (auth)

Wallace, T.C.

1973-01-01T23:59:59.000Z

79

Continuous growth of single-wall carbon nanotubes using chemical vapor deposition  

DOE Patents (OSTI)

The invention relates to a chemical vapor deposition process for the continuous growth of a carbon single-wall nanotube where a carbon-containing gas composition is contacted with a porous membrane and decomposed in the presence of a catalyst to grow single-wall carbon nanotube material. A pressure differential exists across the porous membrane such that the pressure on one side of the membrane is less than that on the other side of the membrane. The single-wall carbon nanotube growth may occur predominately on the low-pressure side of the membrane or, in a different embodiment of the invention, may occur predominately in between the catalyst and the membrane. The invention also relates to an apparatus used with the carbon vapor deposition process.

Grigorian, Leonid (Raymond, OH); Hornyak, Louis (Evergreen, CO); Dillon, Anne C (Boulder, CO); Heben, Michael J (Denver, CO)

2008-10-07T23:59:59.000Z

80

Method of making AlInSb by metal-organic chemical vapor deposition  

DOE Patents (OSTI)

A method for producing aluminum-indium-antimony materials by metal-organic chemical vapor deposition (MOCVD). This invention provides a method of producing Al.sub.X In.sub.1-x Sb crystalline materials by MOCVD wherein an Al source material, an In source material and an Sb source material are supplied as a gas to a heated substrate in a chamber, said Al source material, In source material, and Sb source material decomposing at least partially below 525.degree. C. to produce Al.sub.x In.sub.1-x Sb crystalline materials wherein x is greater than 0.002 and less than one.

Biefeld, Robert M. (Albuquerque, NM); Allerman, Andrew A. (Albuquerque, NM); Baucom, Kevin C. (Albuquerque, NM)

2000-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Photoluminescence in Chemical Vapor Deposited ZnS: insight into electronic defects  

SciTech Connect

Photoluminescence spectra taken from chemical vapor deposited (CVD) ZnS are shown to exhibit sub-band-gap emission bands characteristic of isoelectronic oxygen defects. The emission spectra vary spatially with position and orientation with respect to the major axis of CVD growth. These data suggest that a complex set of defects exist in the band gap of CVD ZnS whose structural nature is highly dependent upon local deposition and growth conditions, contributing to inherent heterogeneity in optical behavior throughout the material.

McCloy, John S.; Potter, B.g.

2013-08-09T23:59:59.000Z

82

Improved process for the preparation of fiber-reinforced ceramic composites by chemical vapor deposition  

DOE Patents (OSTI)

A specially designed apparatus provides a steep thermal gradient across the thickness of fibrous preform. A flow of gaseous ceramic matrix material is directed into the fibrous preform at the cold surface. The deposition of the matrix occurs progressively from the hot surface of the fibrous preform toward the cold surface. Such deposition prevents the surface of the fibrous preform from becoming plugged. As a result thereof, the flow of reactant matrix gases into the uninfiltrated (undeposited) portion of the fibrous preform occurs throughout the deposition process. The progressive and continuous deposition of ceramic matrix within the fibrous preform provides for a significant reduction in process time over known chemical vapor deposition processes.

Lackey, W.J. Jr.; Caputo, A.J.

1984-09-07T23:59:59.000Z

83

Chemical vapor deposition techniques and related methods for manufacturing microminiature thermionic converters  

DOE Patents (OSTI)

Methods of manufacturing microminiature thermionic converters (MTCs) having high energy-conversion efficiencies and variable operating temperatures using MEMS manufacturing techniques including chemical vapor deposition. The MTCs made using the methods of the invention incorporate cathode to anode spacing of about 1 micron or less and use cathode and anode materials having work functions ranging from about 1 eV to about 3 eV. The MTCs also exhibit maximum efficiencies of just under 30%, and thousands of the devices can be fabricated at modest costs.

King, Donald B. (Albuquerque, NM); Sadwick, Laurence P. (Salt Lake City, UT); Wernsman, Bernard R. (Clairton, PA)

2002-06-25T23:59:59.000Z

84

Low temperature metal-organic chemical vapor deposition growth processes for high-efficiency solar cells  

DOE Green Energy (OSTI)

This report describes the results of a program to develop a more complete understanding of the physical and chemical processes involved in low-temperature growth of III-V compounds by metal-organic chemical vapor deposition (MOCVD) and to develop a low-temperature process that is suitable for the growth of high-efficiency solar cells. The program was structured to develop a better understanding of the chemical reactions involved in MOCVD growth, to develop a model of the processes occurring in the gas phase, to understand the physical kinetics and reactions operative on the surface of the growing crystal, and to develop an understanding of the means by which these processes may be altered to reduce the temperature of growth and the utilization of toxic hydrides. The basic approach was to develop the required information about the chemical and physical kinetics operative in the gas phase and on the surface by the direct physical measurement of the processes whenever possible. The program included five tasks: (1) MOCVD growth process characterization, (2) photoenhanced MOCVD studies, (3) materials characterization, (4) device fabrication and characterization, and (5) photovoltaic training. Most of the goals of the program were met and significant progress was made in defining an approach that would allow both high throughput and high uniformity growth of compound semiconductors at low temperatures. The technical activity was focused on determining the rates of thermal decomposition of trimethyl gallium, exploring alternate arsenic sources for use MOCVD, and empirical studies of atomic layer epitaxy as an approach.

Dapkus, P.D. (University of Southern California, Los Angeles, CA (United States))

1993-02-01T23:59:59.000Z

85

Finite-volume model for chemical vapor infiltration incorporating radiant heat transfer. Interim report  

SciTech Connect

Most finite-volume thermal models account for the diffusion and convection of heat and may include volume heating. However, for certain simulation geometries, a large percentage of heat flux is due to thermal radiation. In this paper a finite-volume computational procedure for the simulation of heat transfer by conduction, convection and radiation in three dimensional complex enclosures is developed. The radiant heat transfer is included as a source term in each volume element which is derived by Monte Carlo ray tracing from all possible radiating and absorbing faces. The importance of radiative heat transfer is illustrated in the modeling of chemical vapor infiltration (CVI) of tubes. The temperature profile through the tube preform matches experimental measurements only when radiation is included. An alternative, empirical approach using an {open_quotes}effective{close_quotes} thermal conductivity for the gas space can match the initial temperature profile but does not match temperature changes that occur during preform densification.

Smith, A.W.; Starr, T.L. [Georgia Institute of Technology, Atlanta, GA (United States). School of Materials Science and Engineering

1995-05-01T23:59:59.000Z

86

Chemical Vapor Deposition of Silicon Carbide Epitaxial Films and their Characterization  

DOE Green Energy (OSTI)

A chemical vapor deposition (CVD) system was designed and fabricated in our laboratory and SiC homo-epitaxial layers were grown in the CVD process using silicon tetrachloride and propane precursors with hydrogen as a carrier gas. The temperature field was generated using numerical modeling. Gas flow rates, temperature field, and the gradients are found to influence the growth rates of the epitaxial layers. Growth rates were found to increase as the temperature increased at high carrier gas flow rate, while at lower carrier gas flow rate, growth rates were observed to decrease as the temperature increased. Based on the equilibrium model, 'thermodynamically controlled growth' accounts for the growth rate reduction. The grown epitaxial layers were characterized using various techniques. Reduction in the threading screw dislocation (SD) density in the epilayers was observed. Suitable models were developed for explaining the reduction in the SD density as well as the conversion of basal plane dislocations (BPDs) into threading edge dislocations (TEDs).

Dhanaraj,G.; Chen, Y.; Dudley, M.; Cai, D.; Zhang, H.

2007-01-01T23:59:59.000Z

87

Fabrication of commercial-scale fiber-reinforced hot-gas filters by chemical vapor deposition  

SciTech Connect

Goal was to fabricate a filter for removing particulates from hot gases; principal applications would be in advanced utility processes such as pressurized fluidized bed combustion or coal gasification combined cycle systems. Filters were made in two steps: make a ceramic fiber preform and coat it with SiC by chemical vapor infiltration (CVD). The most promising construction was felt/filament wound. Light, tough ceramic composite filters can be made; reinforcement by continuous fibers is needed to avoid brittleness. Direct metal to filter contact does not damage the top which simplifies installation. However, much of the filter surface of felt/filament wound structures is closed over by the CVD coating, and the surface is rough and subject to delamination. Recommendations are given for improving the filters.

White, L.R. [Minnesota Mining and Mfg. Co., St. Paul, MN (United States). New Products Dept.

1992-11-01T23:59:59.000Z

88

Epitaxial Thin Film Silicon Solar Cells Fabricated by Hot Wire Chemical Vapor Deposition Below 750 ..deg..C: Preprint  

SciTech Connect

We report on fabricating film c-Si solar cells on Si wafer templates by hot-wire chemical vapor deposition. These devices, grown at glass-compatible temperatures < 750..deg..C, demonstrate open-circuit voltages > 500 mV and efficiencies > 5%.

Alberi, K.; Martin, I. T.; Shub, M.; Teplin, C. W.; Iwaniczko, E.; Xu, Y.; duda, A.; Stradin, P.; Johnston, S. W.; Romero, M. J.; Branz, H. M.; Young, D. L.

2009-06-01T23:59:59.000Z

89

A comparison of diamond growth rate using in-liquid and conventional plasma chemical vapor deposition methods  

Science Conference Proceedings (OSTI)

In order to make high-speed deposition of diamond effective, diamond growth rates for gas-phase microwave plasma chemical vapor deposition and in-liquid microwave plasma chemical vapor deposition are compared. A mixed gas of methane and hydrogen is used as the source gas for the gas-phase deposition, and a methanol solution of ethanol is used as the source liquid for the in-liquid deposition. The experimental system pressure is in the range of 60-150 kPa. While the growth rate of diamond increases as the pressure increases, the amount of input microwave energy per unit volume of diamond is 1 kW h/mm{sup 3} regardless of the method used. Since the in-liquid deposition method provides a superior cooling effect through the evaporation of the liquid itself, a higher electric input power can be applied to the electrodes under higher pressure environments. The growth rate of in-liquid microwave plasma chemical vapor deposition process is found to be greater than conventional gas-phase microwave plasma chemical vapor deposition process under the same pressure conditions.

Takahashi, Yoshiyuki; Toyota, Hiromichi; Nomura, Shinfuku; Mukasa, Shinobu [Graduate School of Science and Engineering, Ehime University, 3 Bunkyo-cho, Matsuyama 790-8577 (Japan); Inoue, Toru [Geodynamics Research Center, Ehime University, 2-5 Bunkyo-cho, Matsuyama 790-8577 (Japan)

2009-06-01T23:59:59.000Z

90

Characteristics of Gd2-xLaxO3 high-k films by metal-organic chemical vapor deposition  

Science Conference Proceedings (OSTI)

Gd"2"-"xLa"xO"3 high-k films were deposited on (100) Si substrates by low-pressure metal-organic chemical vapor deposition (MOCVD). The metal-organic precursors we used were Gd and La @b-diketonates. The structure, band gap, composition and electrical ... Keywords: Gd2-xLaxO3, High- k, MOCVD

Liu-Ying Huang; Ai-Dong Li; Ying-Ying Fu; Wen-Qi Zhang; Xiao-Jie Liu; Di Wu

2012-06-01T23:59:59.000Z

91

Chemical reduction of refractory oxides by atomic hydrogen  

DOE Green Energy (OSTI)

The chemical reduction of UO/sub 2/ and Al/sub 2/O/sub 3/ by atomic hydrogen was studied. Results of the UO/sub 2//H investigation indicates that reduction of UO/sub 2/ by atomic hydrogen proceeds by the production of water vapor and hypostoichiometric urania. Water vapor and aluminum metal are formed in the Al/sub 2/O/sub 3//H system. The relative ease which UO/sub 2/ is reduced by atomic hydrogen compared with Al/sub 2/O/sub 3/ is due to two factors. The first is related to the thermochemistry of the reactions. The second factor which favors efficient reduction of UO/sub 2/ but not of Al/sub 2/O/sub 3/ is the oxygen diffusivity. (LK)

Dooley, D.; Balooch, M.; Olander, D.R.

1978-11-01T23:59:59.000Z

92

Oxidation of zirconium alloys in 2.5 kPa water vapor for tritium readiness.  

DOE Green Energy (OSTI)

A more reactive liner material is needed for use as liner and cruciform material in tritium producing burnable absorber rods (TPBAR) in commercial light water nuclear reactors (CLWR). The function of these components is to convert any water that is released from the Li-6 enriched lithium aluminate breeder material to oxide and hydrogen that can be gettered, thus minimizing the permeation of tritium into the reactor coolant. Fourteen zirconium alloys were exposed to 2.5 kPa water vapor in a helium stream at 300 C over a period of up to 35 days. Experimental alloys with aluminum, yttrium, vanadium, titanium, and scandium, some of which also included ternaries with nickel, were included along with a high nitrogen impurity alloy and the commercial alloy Zircaloy-2. They displayed a reactivity range of almost 500, with Zircaloy-2 being the least reactive.

Mills, Bernice E.

2007-11-01T23:59:59.000Z

93

Chemically homogeneous and thermally reversible oxidation of epitaxial graphene  

Science Conference Proceedings (OSTI)

With its exceptional charge mobility, graphene holds great promise for applications in next-generation electronics. In an effort to tailor its properties and interfacial characteristics, the chemical functionalization of graphene is being actively pursued. The oxidation of graphene via the Hummers method is most widely used in current studies, although the chemical inhomogeneity and irreversibility of the resulting graphene oxide compromises its use in high-performance devices. Here, we present an alternative approach for oxidizing epitaxial graphene using atomic oxygen in ultrahigh vacuum. Atomic-resolution characterization with scanning tunnelling microscopy is quantitatively compared to density functional theory, showing that ultrahigh-vacuum oxidization results in uniform epoxy functionalization. Furthermore, this oxidation is shown to be fully reversible at temperatures as low as 260 8C using scanning tunnelling microscopy and spectroscopic techniques. In this manner, ultrahigh-vacuum oxidation overcomes the limitations of Hummers-method graphene oxide, thus creating new opportunities for the study and application of chemically functionalized graphene.

Hossain, Md. Zakir [Northwestern University, Evanston; Johns, James E. [Northwestern University, Evanston; Bevan, Kirk H [ORNL; Karmel, Hunter J. [Northwestern University, Evanston; Liang, Yu Teng [Northwestern University, Evanston; Yoshimoto, Shinya [University of Tokyo, Tokyo, Japan; Mukai, Kozo [University of Tokyo, Tokyo, Japan; Koitaya, Tatanori [University of Tokyo, Tokyo, Japan; Yoshinobu, Jun [University of Tokyo, Tokyo, Japan; Kawai, Maki [University of Tokyo, Tokyo, Japan; Lear, Amanda M. [Indiana University; Kesmodel, Larry L. [Indiana University; Tait, Steven L. [Indiana University; Hersam, Mark C. [Northwestern University, Evanston

2012-01-01T23:59:59.000Z

94

Measurement of gas transport through fiber preforms and densified composites for chemical vapor infiltration  

Science Conference Proceedings (OSTI)

Gas transport via pressure-driven permeation or via concentration-driven diffusion is a key step in the chemical vapor infiltration (CVI) process. This paper describes methods for the measurement of these properties for CVI preforms and partially infiltrated composites. Results are presented for Nicalon-fiber cloth layup preforms and composites, Nextel-fiber braid preforms and composites, and a Nicalon-fiber three-dimensional (3-D) weave composite. The permeability of Nicalon cloth layup preforms is strongly dependent on the packing density over the range of 29--40 vol% but is only weakly dependent on the orientation of the alternating cloth layers. The permeability of Nextel braid preforms is dependent on the thread count and the weight for cloths with similar construction and packing density. The gas permeability of the finer wave (6.3 tows/cm (16 tows/in.)) is approximately one-half that of the coarser weave (3.5 tows/cm (9 tows/in.)). Results are reported for a small number of infiltrated composites with Nextel fiber reinforcement. Attempts to mount a Nicalon-fiber 3-D weave preform specimen have been unsuccessful. Results for a small number of composite specimens with 3-D weave reinforcement are reported.

Starr, T.L.; Hablutzel, N. [Georgia Inst. of Tech., Atlanta, GA (United States). School of Materials Science and Engineering

1998-05-01T23:59:59.000Z

95

Atmospheric-Pressure Chemical Vapor Deposition of Iron Pyrite Thin Films  

Science Conference Proceedings (OSTI)

Iron pyrite (cubic FeS{sub 2}) is a promising candidate absorber material for earth-abundant thin-film solar cells. In this report, single-phase, large-grain, and uniform polycrystalline pyrite thin films are fabricated on glass and molybdenum-coated glass substrates by atmospheric-pressure chemical vapor deposition (AP-CVD) using the reaction of iron(III) acetylacetonate and tert-butyl disulfide in argon at 300 C, followed by sulfur annealing at 500--550 C to convert marcasite impurities to pyrite. The pyrite-marcasite phase composition depends strongly on the concentration of sodium in the growth substrate and the sulfur partial pressure during annealing. Phase and elemental composition of the films are characterized by X-ray diffraction, Raman spectroscopy, Auger electron spectroscopy, secondary ion mass spectrometry, Rutherford backscattering spectrometry, and X-ray photoelectron spectroscopy. The in-plane electrical properties are surprisingly insensitive to phase and elemental impurities, with all films showing p-type, thermally activated transport with a small activation energy ({approx}30 meV), a room- temperature resistivity of {approx}1 {Omega} cm, and low mobility. These ubiquitous electrical properties may result from robust surface effects. These CVD pyrite thin films are well suited to fundamental electrical studies and the fabrication of pyrite photovoltaic device stacks.

Berry, Nicholas; Cheng, Ming; Perkins, Craig L.; Limpinsel, Moritz; Hemminger, John C.; Law, Matt (NREL); (UCI)

2012-10-23T23:59:59.000Z

96

Growth of homo-epitaxial silicon at low temperatures using hot wire chemical vapor deposition  

DOE Green Energy (OSTI)

The authors report on the first known growth of high-quality epitaxial Si via the hot wire chemical vapor deposition (HWCVD) method. This method yields device-quality epitaxial Si at the comparatively low temperatures of 195 to 450 C, and relatively high growth rates of 3 to 20 {angstrom}/sec. Layers up to 4,500-{angstrom} thick have been grown. These epitaxial layers have been characterized by transmission electron microscopy (TEM), indicating large regions of nearly perfect atomic registration. Electron channeling patterns (ECPs) generated on a scanning electron microscope (SEM) have been used to characterize as well as optimize the growth process. Electron beam induced current (EBIC) characterization has also been performed, indicating defect densities as low as 5 x 104/cm{sup 2}. Secondary ion beam mass spectrometry (SIMS) data shows that these layers have reasonable impurity levels within the constraints of the current deposition system. Both n and p-type layers were grown, and p/n diodes have been fabricated.

Thiesen, J.; Jones, K.M.; Matson, R.; Reedy, R.; Crandall, R.; Iwaniczko, E.; Mahan, H.

1999-12-13T23:59:59.000Z

97

Aspects of nitrogen surface chemistry relevant to TiN chemical vapor deposition  

Science Conference Proceedings (OSTI)

NH{sub 3} is an important component of many chemical vapor deposition (CVD) processes for TiN films, which are used for diffusion barriers and other applications in microelectronic circuits. In this study, the interaction of NH{sub 3} with TiN surfaces is examined with temperature programmed desorption (TPD) and Auger electron spectroscopy. NH{sub 3} has two adsorption states on TiN: a chemisorbed state and a multilayer state. A new method for analyzing TPD spectra in systems with slow pumping speeds yields activation energies for desorption for the two states of 24 kcal/mol and 7.3 kcal/mol, respectively. The sticking probability into the chemisorption state is {approximately}0.06. These results are discussed in the context of TiN CVD. In addition, the high temperature stability of TiN is investigated. TiN decomposes to its elements only after heating to 1300 K, showing that decomposition is unlikely to occur under CVD conditions.

Schulberg, M.T.; Allendorf, M.D.; Outka, D.A.

1996-08-01T23:59:59.000Z

98

Hydrogenated amorphous silicon films produced by chemical vapor deposition: Final report  

SciTech Connect

Hydrogenated amorphous silicon (a-Si:H) is a technologically important semiconductor, well-suited for solar photovoltaic energy conversion and thin film device applications. While the glow discharge technique is widely used for the deposition of a-Si:H films, this work is focused on the use of the chemical vapor deposition (CVD) technique, i.e., the thermal decomposition of disilane and higher silanes, for the deposition of a-Si:H films. A simple technique for the preparation of disilane and higher silanes by using an electric discharge in monosilane under atmospheric pressure has been developed, and the discharge product can be used directly for the deposition process. The important parameters of the CVD process including the substrate temperature, the composition and flow rate of the reaction mixture, and the nature of the diluent gas for disilane, have also been investigated. The deposition rate of a-Si:H films in a helium atmosphere is considerably higher than that in a hydrogen atmosphere, and the CVD process in a helium atmosphere is well-suited for the deposition of thick a-Si:H films. The a-Si:H films deposited under various conditions have been characterized by the photoconductivity, dissolution rate, optical absorption, mechanical stress, gap state density, minority carrier diffusion length, and stability measurements. On the basis of these measurements, a-Si:H films deposited by the thermal decomposition of disilane in a helium atmosphere exhibit better structural and electronic properties than those deposited in a hydrogen atmosphere.

Not Available

1987-04-01T23:59:59.000Z

99

Gas-phase reaction study of disilane pyrolysis: Applications to low pressure chemical vapor deposition  

SciTech Connect

The gas-phase thermal reactions during disilane decomposition at low pressure chemical vapor deposition conditions were studied from 300 to 1,000 K using resonance enhanced multiphoton ionization (REMPI) and multiphoton ionization (MPI). REMPI of gas-phase Si, mass 28, was detected from 640 to 840 K and 1 to 10 Torr, with a maximum signal intensity between 700 to 720 K. During disilane decomposition, no SiH (427.8 nm), SiH[sub 2] (494-515 nm), or SiH[sub 3] (419.0 nm) was detected. MPI of higher silanes, silenes, and silylenes were detected through mass fragments 2, 32, and 60; these species reached a maximum signal intensity 20 degrees prior to the mass-28 maximum. Modeling studies that included a detailed low pressure gas-phase kinetic scheme predict relative gas-phase partial pressures generated during disilane pyrolysis. The model predicted experimental trends in the Si partial pressure and the higher silane, silene, and silylene partial pressures.

Johannes, J.E.; Ekerdt, J.G. (Univ. of Texas, Austin, TX (United States). Dept. of Chemical Engineering)

1994-08-01T23:59:59.000Z

100

Chemical vapor deposition of amorphous semiconductor films. Semiannual report, 1 May 1984-31 October 1984  

DOE Green Energy (OSTI)

This report describes the results of research done by the Institute of Energy Conversion for the Solar Energy Research Institute in 1984 on high-efficiency, stable, amorphous silicon solar cells, fabricated by chemical vapor deposition (CVD) from disilane at high growth rates. The kinetics of CVD with higher order silanes were modelled for a tubular reactor with static substrates. A gas-phase reaction network was adopted, based on published silylene insertion and decomposition pathways. Mass balances for hydrogen and all saturated silanes through octasilane were derived. Boron-doped a-Si:H p-layers were deposited by CVD at 200/sup 0/ to 250/sup 0/C. Band gap and conductivity depended strongly on the diborane fraction in the feed gas, independent of substrate temperature. The effects of intrinsic layer deposition temperature and growth rate on material properties and device performance were studied. Cell parameters of p-i-n cells were correlated with i-layer deposition temperature and growth rate. Fill factor and short-circuit current depended on deposition conditions, while open-circuit voltage did not. Effects of diborane additions to the feed gas during i-layer deposition were studied. Experimental evidence and calculations indicate high resistance at the back contact.

Baron, B.N.; Rocheleau, R.E.; Hegedus, S.S.

1985-06-01T23:59:59.000Z

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


101

Effect of e-beam irradiation on graphene layer grown by chemical vapor deposition  

Science Conference Proceedings (OSTI)

We have grown graphene by chemical vapor deposition (CVD) and transferred it onto Si/SiO{sub 2} substrates to make tens of micron scale devices for Raman spectroscopy study. The effect of electron beam (e-beam) irradiation of various doses (600 to 12 000 {mu}C/cm{sup 2}) on CVD grown graphene has been examined by using Raman spectroscopy. It is found that the radiation exposures result in the appearance of the strong disorder D band attributed the damage to the lattice. The evolution of peak frequencies, intensities, and widths of the main Raman bands of CVD graphene is analyzed as a function of defect created by e-beam irradiation. Especially, the D and G peak evolution with increasing radiation dose follows the amorphization trajectory, which suggests transformation of graphene to the nanocrystalline and then to amorphous form. We have also estimated the strain induced by e-beam irradiation in CVD graphene. These results obtained for CVD graphene are in line with previous findings reported for the mechanically exfoliated graphene [D. Teweldebrhan and A. A. Balandin, Appl. Phys. Lett. 94, 013101 (2009)]. The results have important implications for CVD graphene characterization and device fabrication, which rely on the electron microscopy.

Iqbal, M. Z.; Kumar Singh, Arun; Iqbal, M. W.; Seo, Sunae; Eom, Jonghwa [Department of Physics and Graphene Research Institute, Sejong University, Seoul 143-747 (Korea, Republic of)

2012-04-15T23:59:59.000Z

102

Impact of hydrogen and oxygen defects on the lattice parameter of chemical vapor deposited zinc sulfide  

SciTech Connect

The lattice parameter of cubic chemical vapor deposited (CVD) ZnS with measured oxygen concentrations < 0.6 at.% and hydrogen impurities of < 0.015 at.% have been measured and found to vary between -0.10% and +0.09% relative to the reference lattice parameter (5.4093 Ĺ) of oxygen-free cubic ZnS as reported in the literature. Defects other than substitutional O must be invoked to explain these observed volume changes. The structure and thermodynamic stability of a wide range of native and impurity induced defects in ZnS have been determined by Ab initio calculations. Lattice contraction is caused by S-vacancies, substitutional O on S sites, Zn vacancies, H in S vacancies, peroxy defects, and dissociated water in S-vacancies. The lattice is expanded by interstitial H, H in Zn vacancies, dihydroxy defects, interstitial oxygen, Zn and [ZnHn] complexes (n=1,…,4), interstitial Zn, and S2 dumbbells. Oxygen, though present, likely forms substitutional defects for sulfur resulting in lattice contraction rather than as interstitial oxygen resulting in lattice expansion. It is concluded based on measurement and calculations that excess zinc atoms either at anti-sites (i.e. Zn atoms on S-sites) or possibly as interstitial Zn are responsible for the relative increase of the lattice parameter of commercially produced CVD ZnS.

McCloy, John S.; Wolf, Walter; Wimmer, Erich; Zelinski, Brian

2013-01-09T23:59:59.000Z

103

Electrical conductivity of. gamma. -irradiated and chemically oxidized wool  

SciTech Connect

Examples of wool fibers were irradiated with gamma rays and chemically oxidized with H/sub 2/O/sub 2/ to study the effect on their electrical conductivity. In both cases, electrical conductivity increased whereas the activation cnergy decreased with increases in diameter, moisture content and intrensic ash content of the wool samples.

Moharram, M.A. (Tanta Univ., Cairo, Egypt); Abou Sekkina, M.M.; Rabie, S.M.

1981-08-01T23:59:59.000Z

104

Structure and properties of braided sleeve preforms for chemical vapor infiltration  

Science Conference Proceedings (OSTI)

In all composites the properties and structure of the reinforcement strongly influence the performance of the material. For some composites, however, the reinforcement also affects the fabrication process itself exerting an additional, second order influence on performance. This is the case for the chemical vapor infiltration (CVI) process for fabrication of ceramic matrix composites. In this process the matrix forms progressively as a solid deposit, first onto the fiber surfaces, then onto the previous layer of deposit, ultimately growing to fill the inter-fiber porosity. The transport of reactants to the surfaces and the evolved morphology of the matrix depend on the initial reinforcement structure. This structure can vary greatly and is controlled by such factors as fiber size and cross-section, the number of filaments and amount of twist per tow or yarn, and the weave or braid architecture. Often the choice of reinforcement is based on mechanical performance analysis or on the cost and availability of the material or on the temperature stability of the fiber. Given this choice, the composite densification process--CVI--must be optimized to attain a successful material. Ceramic fiber in the form of cylindrical braided sleeve is an attractive choice for fabrication of tube-form ceramic matrix composites. Multiple, concentric layers of sleeve can be placed over a tubular mandrel, compressed and fixed with a binder to form a freestanding tube preform. This fiber architecture is different than that created by layup of plain weave cloth--the material used in most previous CVI development. This report presents the results of the investigation of CVI densification of braided sleeve preforms and the evolution of their structure and transport properties during processing.

Starr, T.L.; Fiadzo, O.G.; Hablutzel, N. [Georgia Inst. of Tech., Atlanta, GA (United States). School of Materials Science and Technology

1998-04-01T23:59:59.000Z

105

Low Temperature Chemical Vapor Deposition of Zirconium Nitride in a Fluidized Bed  

E-Print Network (OSTI)

The objective of this research was to design, assemble, and demonstrate the initial performance of a fluidized bed chemical vapor deposition (FB-CVD) system capable of producing thin, uniform zirconium nitride (ZrN) coatings (1 to 10 micrometers thick) on uranium-molybdenum (UMo) particulate fuel. Plate-type fuel with U-xMo (x = 3 to 10 wt.%) particle fuel dispersed in an aluminum matrix is under development at Idaho National Laboratory (INL) for the Reduced Enrichment for Research and Test Reactors (RERTR) program. Initial irradiation tests performed at INL in the Advanced Test Reactor (ATR) indicate an interaction layer forms between the fuel microspheres and the matrix at relatively high power levels. These power levels induce higher temperatures which enables uranium diffusion into the aluminum during irradiation, eventually causing fuel plate failure. The objective of this work was to create a process to mitigate the fuel/matrix interaction by forming a thin barrier coating on the surface of the U-xMo microspheres before incorporation into the dispersion fuel plate matrix. One of the main challenges in performance of the FB-CVD system was the effective fluidization of a powder whose physical characteristics (size, density) are continuously changing. To address this, two types of fluidized bed reaction vessels were designed and improved over the course of this research: a spouted fluidized bed and an inverted fluidized bed. Both reaction vessels utilized tetrakis(dimethylamino)zirconium (TDMAZ) and ammonia gas as precursors at atmospheric pressure. Tungsten wires and zirconia-silica (ZrO2-SiO2) microspheres were used as the substrates for the coating experiments. The substrate temperature and precursor gas flow were manipulated as the process variables. The FB-CVD system was successful in forming zirconium based coatings on surrogate microspheres with elevated levels of chemical impurities. At atmospheric pressure, coatings of thicknesses ranging from 0.5 micrometers to 1.5 micrometers were produced between temperatures of 250 degrees C and 350 degrees C. The deposited coatings were characterized using scanning electron microscopy, energy dispersive spectroscopy and wavelength dispersive spectroscopy.

Arrieta, Marie

2012-08-01T23:59:59.000Z

106

Towards improved spinnability of chemical vapor deposition generated multi-walled carbon nanotubes  

E-Print Network (OSTI)

and Dresselhaus G. 1997 From Carbon Fibers to Nanotubes inV VGCF Vapor Grown Carbon Fiber X XRD X-ray Diffraction ixgraphite whiskers, carbon fibers, and carbon nanotubes, each

McKee, Gregg Sturdivant Burke

2008-01-01T23:59:59.000Z

107

Electrolytic photodissociation of chemical compounds by iron oxide photochemical diodes  

DOE Patents (OSTI)

Chemical compounds can be dissociated by contacting the same with a p/n type semi-conductor photochemical diode having visible light as its sole source of energy. The photochemical diode consists of low cost, readily available materials, specifically polycrystalline iron oxide doped with silicon in the case of the n-type semi-conductor electrode, and polycrystalline iron oxide doped with magnesium in the case of the p-type electrode. So long as the light source has an energy greater than 2.2 electron volts, no added energy source is needed to achieve dissociation.

Somorjai, Gabor A. (Berkeley, CA); Leygraf, Christofer H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

108

Electrolytic photodissociation of chemical compounds by iron oxide electrodes  

DOE Patents (OSTI)

Chemical compounds can be dissociated by contacting the same with a p/n type semi-conductor diode having visible light as its sole source of energy. The diode consists of low cost, readily available materials, specifically polycrystalline iron oxide doped with silicon in the case of the n-type semi-conductor electrode, and polycrystalline iron oxide doped with magnesium in the case of the p-type electrode. So long as the light source has an energy greater than 2.2 electron volts, no added energy source is needed to achieve dissociation.

Somorjai, Gabor A. (Berkeley, CA); Leygraf, Christofer H. (Berkeley, CA)

1984-01-01T23:59:59.000Z

109

Plasma Enhanced Chemical Vapor Deposition on Living Substrates: Development, Characterization, and Biological Applications  

E-Print Network (OSTI)

This dissertation proposed the idea of “plasma-enhanced chemical vapor deposition on living substrates (PECVD on living substrates)” to bridge the gap between the thin film deposition technology and the biological and living substrates. This study focuses on the establishment of the knowledge and techniques necessary to perform “PECVD on living substrates” and contains three main aspects: development, characterization, and biological applications. First, a PECVD tool which can operate in ambient air and at low temperature was developed using a helium dielectric barrier discharge jet (DBD jet). It was demonstrated that various materials, such as polymeric, metallic, and composite films, can be readily synthesized through this technique. Second, the PMMA and copper films deposited using DBD jets were characterized. High-rate (22 nm/s), low-temperature (39 şC) PMMA deposition was achieved and the film surface morphology can be tailored by altering the discharge power. Conductive copper films with an electrical resistivity lower than 1×10-7 ohm-m were obtained through hydrogen reduction. Both PMMA and copper films can be grown on temperature-sensitive substrates, such as plastics, pork skin, and even fingernail. The electrical, optical, and imaging characterization of the DBD jets was also conducted and several new findings were reported. Multiple short-duration current pulses instead of only one broad pulse per half voltage cycle were observed when a dielectric substrate was employed. Each short-duration current pulse is induced by a leading ionization wave followed by the formation of a plasma channel. Precursor addition further changed the temporal sequence of the pulses. An increase in the power led to a mode change from a diffuse DBD jet to a concentrated one. This mode change showed significant dependence on the precursor type, tube size, and electrode configuration. These findings regarding the discharge characteristics can thus facilitate the development of DBD-jet operation strategies to improve the deposition efficacy. Finally, this technique was used to grow PMMA films onto agar to demonstrate one of its potential biological applications: sterile bandage deposition. The DBD jet with the film depositing ability enabled the surface to be not only efficiently sanitized but also protected by a coating from being reached by bacteria.

Tsai, Tsung-Chan 1982-

2012-12-01T23:59:59.000Z

110

Atomic-level investigation of the growth of Si/Ge by ultrahigh vacuum chemical vapor deposition  

SciTech Connect

Si and Ge films can be prepared under ultrahigh vacuum conditions by chemical vapor deposition using disilane and digermane as source gases. These gases offer a high sticking probability, and are suitable for atomic layer epitaxy. Using synchrotron radiation photoemission spectroscopy and scanning tunneling microscopy, we have examined the surface processes associated with the heteroepitaxial growth of Ge/Si. The measured surface-induced shifts and chemical shifts of the Si 2p and Ge 3d core levels allow us to identify the surface species and to determine the surface chemical composition, and this information is correlated with the atomic features observed by scanning tunneling microscopy. Issues related to precursor dissociation, attachment to dangling bonds, diffusion, surface segregation, growth morphology, and pyrolytic reaction pathways will be discussed. {copyright} {ital 1997 American Vacuum Society.}

Lin, D. [Institute of Physics, National Chiao-Tung University, Hsinchu, Taiwan, Republic of (China)] [Institute of Physics, National Chiao-Tung University, Hsinchu, Taiwan, Republic of (China); Miller, T.; Chiang, T. [Department of Physics and Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801 (United States)] [Department of Physics and Materials Research Laboratory, University of Illinois, Urbana, Illinois 61801 (United States)

1997-05-01T23:59:59.000Z

111

Use of Optical Microscopy to Examine Crystallite Nucleation and Growth in Thermally Annealed Plasma Enhanced Chemical Vapor Deposition and Hot Wire Chemical Vapor Deposition a-Si:H Films  

DOE Green Energy (OSTI)

We report a simple method to investigate crystallite nucleation and growth in stepwise, thermally annealed plasma enhanced chemical vapor deposition and hot wire chemical vapor deposition a-Si:H films. By confining film thicknesses to the range 500-4000 {angstrom}, optical microscopy in the reflection mode can be used to readily detect crystallites in the thermally annealed a-Si:H lattice. Measurements of the crystallite density versus annealing time for identically prepared films of different thickness show that the crystallite nucleation rate is smaller for thinner films, suggesting that crystallite nucleation is homogeneous, in agreement with previous results. A comparison of film nucleation rates with those obtained by other methods on identically prepared films shows excellent agreement, thus establishing the validity of the current technique. The potential effect of impurity (oxygen) incorporation during the stepwise annealing in air is shown not to affect crystallite nucleation and growth, in that SIMS oxygen profiles for stepwise versus continuous annealing show not only similar impurity profiles but also similar bulk impurity densities.

Mahan, A. H.; Dabney, M. S.; Reedy, Jr R. C.; Molina, D.; Ginley, D. S.

2012-05-15T23:59:59.000Z

112

Detailed chemical kinetic oxidation mechanism for a biodiesel surrogate  

DOE Green Energy (OSTI)

A detailed chemical kinetic mechanism has been developed and used to study the oxidation of methyl decanoate, a surrogate for biodiesel fuels. This model has been built by following the rules established by Curran et al. for the oxidation of n-heptane and it includes all the reactions known to be pertinent to both low and high temperatures. Computed results have been compared with methyl decanoate experiments in an engine and oxidation of rapeseed oil methyl esters in a jet stirred reactor. An important feature of this mechanism is its ability to reproduce the early formation of carbon dioxide that is unique to biofuels and due to the presence of the ester group in the reactant. The model also predicts ignition delay times and OH profiles very close to observed values in shock tube experiments fueled by n-decane. These model capabilities indicate that large n-alkanes can be good surrogates for large methyl esters and biodiesel fuels to predict overall reactivity, but some kinetic details, including early CO2 production from biodiesel fuels, can be predicted only by a detailed kinetic mechanism for a true methyl ester fuel. The present methyl decanoate mechanism provides a realistic kinetic tool for simulation of biodiesel fuels.

Herbinet, O; Pitz, W J; Westbrook, C K

2007-09-17T23:59:59.000Z

113

Detailed chemical kinetic oxidation mechanism for a biodiesel surrogate  

DOE Green Energy (OSTI)

A detailed chemical kinetic mechanism has been developed and used to study the oxidation of methyl decanoate, a surrogate for biodiesel fuels. This model has been built by following the rules established by Curran et al. for the oxidation of n-heptane and it includes all the reactions known to be pertinent to both low and high temperatures. Computed results have been compared with methyl decanoate experiments in an engine and oxidation of rapeseed oil methyl esters in a jet stirred reactor. An important feature of this mechanism is its ability to reproduce the early formation of carbon dioxide that is unique to biofuels and due to the presence of the ester group in the reactant. The model also predicts ignition delay times and OH profiles very close to observed values in shock tube experiments fueled by n-decane. These model capabilities indicate that large n-alkanes can be good surrogates for large methyl esters and biodiesel fuels to predict overall reactivity, but some kinetic details, including early CO{sub 2} production from biodiesel fuels, can be predicted only by a detailed kinetic mechanism for a true methyl ester fuel. The present methyl decanoate mechanism provides a realistic kinetic tool for simulation of biodiesel fuels.

Herbinet, O; Pitz, W J; Westbrook, C K

2007-09-20T23:59:59.000Z

114

Calibrated vapor generator source  

DOE Patents (OSTI)

A portable vapor generator is disclosed that can provide a controlled source of chemical vapors, such as, narcotic or explosive vapors. This source can be used to test and calibrate various types of vapor detection systems by providing a known amount of vapors to the system. The vapor generator is calibrated using a reference ion mobility spectrometer. A method of providing this vapor is described, as follows: explosive or narcotic is deposited on quartz wool, placed in a chamber that can be heated or cooled (depending on the vapor pressure of the material) to control the concentration of vapors in the reservoir. A controlled flow of air is pulsed over the quartz wool releasing a preset quantity of vapors at the outlet.

Davies, John P. (Idaho Falls, ID); Larson, Ronald A. (Idaho Falls, ID); Goodrich, Lorenzo D. (Shelley, ID); Hall, Harold J. (Idaho Falls, ID); Stoddard, Billy D. (Idaho Falls, ID); Davis, Sean G. (Idaho Falls, ID); Kaser, Timothy G. (Idaho Falls, ID); Conrad, Frank J. (Albuquerque, NM)

1995-01-01T23:59:59.000Z

115

Calibrated vapor generator source  

DOE Patents (OSTI)

A portable vapor generator is disclosed that can provide a controlled source of chemical vapors, such as, narcotic or explosive vapors. This source can be used to test and calibrate various types of vapor detection systems by providing a known amount of vapors to the system. The vapor generator is calibrated using a reference ion mobility spectrometer. A method of providing this vapor is described, as follows: explosive or narcotic is deposited on quartz wool, placed in a chamber that can be heated or cooled (depending on the vapor pressure of the material) to control the concentration of vapors in the reservoir. A controlled flow of air is pulsed over the quartz wool releasing a preset quantity of vapors at the outlet. 10 figs.

Davies, J.P.; Larson, R.A.; Goodrich, L.D.; Hall, H.J.; Stoddard, B.D.; Davis, S.G.; Kaser, T.G.; Conrad, F.J.

1995-09-26T23:59:59.000Z

116

High temperature step-flow growth of gallium phosphide by molecular beam epitaxy and metalorganic chemical vapor deposition  

Science Conference Proceedings (OSTI)

Post-growth surface morphologies of high-temperature homoepitaxial GaP films grown by molecular beam epitaxy (MBE) and metalorganic chemical vapor deposition (MOCVD) have been studied. Smooth, stepped surface morphologies of MBE-grown layers, measured by atomic force microscopy, were found for a wide range of substrate temperatures and P{sub 2}:Ga flux ratios. A MOCVD-based growth study performed under similar conditions to MBE-grown samples shows a nearly identical smooth, step-flow surface morphology, presenting a convergence of growth conditions for the two different methods. The additional understanding of GaP epitaxy gained from this study will impact its use in applications that include GaP-based device technologies, III-V metamorphic buffers, and III-V materials integration with silicon.

Ratcliff, C. [Department of Electrical and Computer Engineering, Ohio State University, Columbus, Ohio 43210 (United States); Grassman, T. J.; Ringel, S. A. [Department of Electrical and Computer Engineering, Ohio State University, Columbus, Ohio 43210 (United States); Institute for Materials Research, Ohio State University, Columbus, Ohio 43210 (United States); Carlin, J. A. [Institute for Materials Research, Ohio State University, Columbus, Ohio 43210 (United States)

2011-10-03T23:59:59.000Z

117

Nitrogen actinometry for measurement of nitrogen radical spatial distribution in large-area plasma-enhanced chemical vapor deposition  

Science Conference Proceedings (OSTI)

Density distributions of radicals in the large-area silicon nitride (Si{sub 3}N{sub 4}) plasma-enhanced chemical vapor deposition (PECVD) process were measured using a spatially resolvable optical emission spectrometer (SROES). To determine the qualitative distribution of a target radical, the authors used optical actinometry with nitrogen (N{sub 2}) gas as an actinometer. To compare the SROES data and process results, the thickness of the deposited Si{sub 3}N{sub 4} thin films using an ellipsometer was measured. By introducing nitrogen-based optical actinometry, the authors obtained very good agreement between the experimental results of the distributions of atomic nitrogen radical and the deposited thicknesses of Si{sub 3}N{sub 4} thin films. Based on these experimental results, the uniformity of the process plasma in the PECVD process at different applied radio frequency powers was analyzed.

Oh, Changhoon; Kang, Minwook; Hahn, Jae W. [Nano Photonics Laboratory, School of Mechanical Engineering, Yonsei University, 50 Yonesi-ro, Seodaemun-gu, Seoul 120-749 (Korea, Republic of); Nam, Seungsuk [Based Technology of Equipment Team, LG Display, Paju-City, Gyeonggi-do 413-811 (Korea, Republic of)

2013-05-15T23:59:59.000Z

118

ZnO light-emitting diode grown by plasma-assisted metal organic chemical vapor deposition  

SciTech Connect

We report a breakthrough in fabricating ZnO homojunction light-emitting diode by metal organic chemical vapor deposition. Using NO plasma, we are able to grow p-type ZnO thin films on n-type bulk ZnO substrates. The as-grown films on glass substrates show hole concentration of 10{sup 16}-10{sup 17} cm{sup -3} and mobility of 1-10 cm{sup 2} V{sup -1} s{sup -1}. Room-temperature photoluminescence spectra reveal nitrogen-related emissions. A typical ZnO homojunction shows rectifying behavior with a turn-on voltage of about 2.3 V. Electroluminescence at room temperature has been demonstrated with band-to-band emission at I=40 mA and defect-related emissions in the blue-yellow spectrum range.

Xu, W.Z.; Ye, Z.Z.; Zeng, Y.J.; Zhu, L.P.; Zhao, B.H.; Jiang, L.; Lu, J.G.; He, H.P.; Zhang, S.B. [State Key Laboratory of Silicon Materials, Zhejiang University, Hangzhou 310027 (China); National Renewable Energy Laboratory, Golden, Colorado 80401 (United States)

2006-04-24T23:59:59.000Z

119

Model-based dummy feature placement for oxide chemical-mechanical polishing manufacturability  

Science Conference Proceedings (OSTI)

Chemical-mechanical polishing (CMP) is an enabling technique used in deep-submicron VLSI manufacturing to achieve uniformity in long range oxide planarization [1]. Post-CMP oxide topography is highly related to local spatial pattern density in layout. ...

Ruiqi Tian; D. F. Wong; Robert Boone

2000-06-01T23:59:59.000Z

120

Carotenoids & Retinoids; Molecular Aspects and Health IssuesChapter 4 Chemical and Metabolic Oxidation of Carotenoids  

Science Conference Proceedings (OSTI)

Carotenoids & Retinoids; Molecular Aspects and Health Issues Chapter 4 Chemical and Metabolic Oxidation of Carotenoids Health Nutrition Biochemistry eChapters Health - Nutrition - Biochemistry Press   Downlo

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121

In-Situ Chemical Oxidation of Soil Contaminated by Benzene ... - TMS  

Science Conference Proceedings (OSTI)

May 1, 2007 ... In-Situ Chemical Oxidation of Soil Contaminated by Benzene, Lead and Cadmium by Marcia Bragato and Jorge Alberto Soares Tenorio ...

122

Silicon nucleation and film evolution on silicon dioxide using disilane: Rapid thermal chemical vapor deposition of very smooth silicon at high deposition rates  

SciTech Connect

An investigation of Si{sub 2}H{sub 6} and H{sub 2} for rapid thermal chemical vapor deposition (RTCVD) of silicon on SiO{sub 2} has been performed at temperatures ranging from 590 to 900 C and pressures ranging from 0.1 to 1.5 Torr. Deposition at 590 C yields amorphous silicon films with the corresponding ultrasmooth surface with a deposition rate of 68 nm/min. Cross-sectional transmission electron microscopy of a sample deposited at 625 C and 1 Torr reveals a bilayer structure which is amorphous at the growth surface and crystallized at the oxide interface. Higher temperatures yield polycrystalline films where the surface roughness depends strongly on both deposition pressure and temperature. Silane-based amorphous silicon deposition in conventional systems yields the expected ultrasmooth surfaces, but at greatly reduced deposition rates unsuitable for single-wafer processing. However, disilane, over the process window considered here, yields growth rates high enough to be appropriate for single-wafer manufacturing, thus providing a viable means for deposition of very smooth silicon films on SiO{sub 2} in a single-wafer environment.

Violette, K.E.; Oeztuerk, M.C.; Christensen, K.N.; Maher, D.M. [North Carolina State Univ., Raleigh, NC (United States)

1996-02-01T23:59:59.000Z

123

Chemically Modified Metal Oxide Nanostructure for Photoelectrochemical Water Splitting  

E-Print Network (OSTI)

nanoparticle seeded indium-tin oxide (ITO) substrate usingarrays were grown on an indium-tin oxide substrate followedof a double-sided indium-tin-oxide (ITO) glass substrate

Wang, Gongming

2013-01-01T23:59:59.000Z

124

Thermal Stability and Substitutional Carbon Incorporation far above Solid-Solubility in Si1-xCx and Si1-x-yGexCy Layers Grown by Chemical Vapor Deposition  

E-Print Network (OSTI)

Cx and Si1-x-yGexCy Layers Grown by Chemical Vapor Deposition using Disilane M. S. Carroll*, J. C. Sturm on (100) silicon substrates by rapid thermal chemical vapor deposition (RTCVD) with disilane source gas and disilane is known to produce higher silicon epitaxial growth rates for similar partial

125

Data for First Responder Use of Photoionization Detectors for Vapor Chemical Constituents  

SciTech Connect

First responders need appropriate measurement technologies for evaluating incident scenes. This report provides information about photoionization detectors (PIDs), obtained from manufacturers and independent laboratory tests, and the use of PIDs by first responders, obtained from incident commanders in the United States and Canada. PIDs are valued for their relatively low cost, light weight, rapid detection response, and ease of use. However, it is clear that further efforts are needed to provide suitable instruments and decision tools to incident commanders and first responders for assessing potential hazardous chemical releases. Information provided in this report indicates that PIDs should always be part of a decision-making context in which other qualitative and more definitive tests and instruments are used to confirm a finding. Possible amelioratory actions ranging from quick and relatively easy fixes to those requiring significant additional effort are outlined in the report.

Keith A. Daum; Matthew G. Watrous; M. Dean Neptune; Daniel I. Michael; Kevin J. Hull; Joseph D. Evans

2006-11-01T23:59:59.000Z

126

Chemical vapor deposition of amorphous semiconductor films. Semiannual report, 1 May 1983-31 October 1984  

DOE Green Energy (OSTI)

This report presents an analysis of intrinsic and phosphorus-doped n-type amorphous silicon films deposited by LPCVD from disilane in a laminar flow tubular reactor. These films were analyzed using SIMs, ESR measurements, optical absorption, and conductivity in light and dark. CVD deposited i layers were used to make platinum Schottky barrier devices and hybrid cells utilizing glow discharge deposited layers in both the ITO/nip/Mo and ITO/pin/Mo configurations. The highest efficiency of hybrid cells with the ITO/ni(CVD)/p(GD)/Mo structure was approximately 1.5%. The highest efficiencies were obtained with thin i layers. The highest efficiency for the ITO/p(GD)/in(CVD)/Mo configuration was 4.0%. A chemical model was developed describing the gas phase reactions and film growth; the model quantitatively describes the effluent composition when the measured growth rate is input. Kinetic rate expressions and constants for growth from higher silanes are being determined for a wide range of reaction conditions.

Not Available

1984-03-01T23:59:59.000Z

127

Real-time optical diagnostics of graphene growth induced by pulsed chemical vapor deposition  

Science Conference Proceedings (OSTI)

The kinetics and mechanisms of graphene growth on Ni films at 720 -880 C have been measured using fast pulses of acetylene and real-time optical diagnostics. In situ UV-Raman spectroscopy was used to unambiguously detect isothermal graphene growth at high temperatures, measure the growth kinetics with ~ 1s temporal resolution, and estimate the fractional precipitation upon cooldown for the first time. Optical reflectivity and videography provided much faster temporal resolution. Both the growth kinetics and the fractional isothermal precipitation were found to be governed by the C2H2 partial pressure in the CVD pulse for a given film thickness and temperature, with up to ~ 94% of graphene growth occurring isothermally within 1 second at 800 C at high partial pressures. At lower partial pressures, isothermal graphene growth is shown to continue 10 seconds after the gas pulse. These flux-dependent growth kinetics are described in the context of a dissolution/precipitation model, where carbon rapidly dissolves into the Ni film and later precipitates driven by gradients in the chemical potential. The combination of pulsed-CVD and real-time optical diagnostics opens new opportunities to understand and control the fast, sub-second growth of graphene on various substrates at high temperatures.

Puretzky, Alexander A [ORNL; Geohegan, David B [ORNL; Pannala, Sreekanth [ORNL; Rouleau, Christopher M [ORNL; Regmi, Murari [Oak Ridge National Laboratory (ORNL); Thonnard, Norbert [ORNL; Eres, Gyula [ORNL

2013-01-01T23:59:59.000Z

128

The Effect of High Temperature Annealing on the Grain Characteristics of a Thin Chemical Vapor Deposition Silicon Carbide Layer.  

SciTech Connect

The unique combination of thermo-mechanical and physiochemical properties of silicon carbide (SiC) provides interest and opportunity for its use in nuclear applications. One of the applications of SiC is as a very thin layer in the TRi-ISOtropic (TRISO) coated fuel particles for high temperature gas reactors (HTGRs). This SiC layer, produced by chemical vapor deposition (CVD), is designed to withstand the pressures of fission and transmutation product gases in a high temperature, radiation environment. Various researchers have demonstrated that macroscopic properties can be affected by changes in the distribution of grain boundary plane orientations and misorientations [1 - 3]. Additionally, various researchers have attributed the release behavior of Ag through the SiC layer as a grain boundary diffusion phenomenon [4 - 6]; further highlighting the importance of understanding the actual grain characteristics of the SiC layer. Both historic HTGR fission product release studies and recent experiments at Idaho National Laboratory (INL) [7] have shown that the release of Ag-110m is strongly temperature dependent. Although the maximum normal operating fuel temperature of a HTGR design is in the range of 1000-1250°C, the temperature may reach 1600°C under postulated accident conditions. The aim of this specific study is therefore to determine the magnitude of temperature dependence on SiC grain characteristics, expanding upon initial studies by Van Rooyen et al, [8; 9].

Isabella J van Rooyen; Philippus M van Rooyen; Mary Lou Dunzik-Gougar

2013-08-01T23:59:59.000Z

129

Laser-induced fluorescence measurements and kinetic analysis of Si atom formation in a rotating disk chemical vapor deposition reactor  

SciTech Connect

An extensive set of laser-induced fluorescence (LIF) measurements of Si atoms during the chemical vapor deposition (CVD) of silicon from silane and disilane in a research rotating disk reactor are presented. The experimental results are compared in detail with predictions from a numerical model of CVD from silane and disilane that treats the fluid flow coupled to gas-phase and gas-surface chemistry. The comparisons showed that the unimolecular decomposition of SiH[sub 2] could not account for the observed gas-phase Si atom density profiles. The H[sub 3]SiSiH [leftrightarrow] Si + SiH[sub 4] and H[sub 3]SiSiH + SiH[sub 2] [leftrightarrow] Si + Si[sub 2]H[sub 6] reactions are proposed as the primary Si atom production routes. The model is in good agreement with the measured shapes of the Si atom profiles and the trends in Si atom density with susceptor temperature, pressure, and reactant gas mixture. 33 refs., 12 figs., 3 tabs.

Ho, P.; Coltrin, M.E.; Breiland, W.G. (Sandia National Lab., Albuquerque, NM (United States))

1994-10-06T23:59:59.000Z

130

Use of SiBN and SiBON films prepared by plasma enhanced chemical vapor deposition from borazine as interconnection dielectrics  

SciTech Connect

Thin films of silicon boron nitride (SiBN) of typical composition Si{sub 0.09}B{sub 0.39}N{sub 0.51} and silicon boron oxynitride (SiBON) of typical composition Si{sub 0.16}B{sub 0.29}O{sub 0.41}N{sub 0.14} were prepared by plasma enhanced chemical vapor deposition and the properties of these films were evaluated with respect to their suitability as interconnection dielectrics in microelectronic fabrication. Films were deposited on 125 mm silicon substrates in a parallel-plate reactor at a substrate temperature of 400 C and a plasma power of 0.5 W/cm{sup 2}. Boron nitride, for comparison of electrical properties, was deposited from borazine (B{sub 3}N{sub 3}H{sub 6}); silicon boron nitride was deposited from borazine, disilane (Si{sub 2}H{sub 6}), and ammonia (NH{sub 3}); silicon boron oxynitride was deposited from borazine, disilane, ammonia, and nitrous oxide (N{sub 2}O). Metal-insulator-metal capacitors were fabricated and electrical measurements indicated that all three films had excellent dielectric properties with dielectric constants of 4.1, 4.7, and 3.9 for BN, SiBN, and SiBON, respectively. Tests of conformality indicated that deposition into trenches with an aspect ratio of 4:1 gave conformality greater than 70%. Silicon boron oxynitride was shown to be an excellent barrier to the diffusion of copper. A planar, single level metal-insulator structure was constructed using a SiBN/SiBON insulator with copper metallization.

Kane, W.F.; Cohen, S.A.; Hummel, J.P.; Luther, B. [IBM Research Div., Yorktown Heights, NY (United States). T.J. Watson Research Center; Beach, D.B. [Oak Ridge National Lab., TN (United States). Chemical and Analytical Sciences Div.

1997-02-01T23:59:59.000Z

131

Oxidative and initiated chemical vapor deposition for application to organic electronics  

E-Print Network (OSTI)

Since the first discovery of polymeric conductors in 1977, the research area of "organic electronics" has grown dramatically. However, methods for forming thin films comprised solely of conductive polymers are limited by ...

Im, Sung Gap

2009-01-01T23:59:59.000Z

132

Fundamental studies of the chemical vapor deposition of diamond. Final technical report, April 1, 1988--December 31, 1994  

SciTech Connect

We submit here a final technical report for the research program entitled: Fundamental Studies of the Chemical Vapor Deposition of Diamond, DOE Grant No. DE-FG05-88ER45345-M006. This research program was initiated in 1988 under the direction of the late Professor David A. Stevenson and was renewed in 1992. Unfortunately, at the end of 1992, just as the last phase of this work was getting underway, Professor Stevenson learned that he had developed mesothelioma, a form of cancer based on asbestos. Professor Stevenson died from that disease in February of 1994. Professor William D. Nix, the Chairman of the Materials Science department at Stanford was named the Principal Investigator. Professor Nix has assembled this final technical report. Much of the work of this grant was conducted by Mr. Paul Dennig, a graduate student who will receive his Ph.D. degree from Stanford in a few months. His research findings are described in the chapters of this report and in the papers published over the past few years. The main discovery of this work was that surface topology plays a crucial role in the nucleation of diamond on silicon. Dennig and his collaborators demonstrated this by showing that diamond nucleates preferentially at the tips of asperities on a silicon surface rather than in the re-entrant comers at the base of such asperities. Some of the possible reasons for this effect are described in this report. The published papers listed on the next page of this report also describe this research. Interested persons can obtain copies of these papers from Professor Nix at Stanford. A full account of all of the research results obtained in this work is given in the regular chapters that follow this brief introduction. In addition, interested readers will want to consult Mr. Dennig`s Ph.D. dissertation when it is made available later this year.

Nix, W.D.

1995-05-01T23:59:59.000Z

133

TEOS-based SiO{sub 2} chemical vapor deposition: Reaction kinetics and related surface chemistry  

Science Conference Proceedings (OSTI)

We have developed a comprehensive understanding of thermal TEOS (tetracthylorthosificate, Si(OCH{sub 2}CH{sub 3}){sub 4}) surface chemistry at CVD (chemical vapor deposition) temperatures and pressures. This was accomplished by examining how TEOS reaction rate are influenced by factors critical to the heterogeneous reaction. This includes determining the TEOS pressure dependence, testing if reaction by-products inhibit TEOS decomposition, identifying reaction sites on the surface, and establishing the reaction sites coverage dependencies. We evaluated the pressure dependencies and by-product inhibition with GCMS. The experiments in a cold-wall research reactor revealed that the TEOS surface reaction at 1000K (1) was first-order with respect to TEOS pressure (0.10 to 1.50Torr) and (2) was not inhibited by surface reaction by-products (ethylene, ethanol, and water). Reactivities of surface sites and their coverage dependencies were compared with FTIR. Our experiments demonstrated that two-membered siloxane ((Si-O){sub 2}) rings on the SiO{sub 2} surface were consumed almost instantaneously when exposed to TEOS. Our FTIR experiments also revealed that TEOS decomposition was zero-order with respect to coverages of hydroxyl groups and (by indirect evidence) three-membered siloxane ((Si-O){sub 3}) rings. This type of site-independent reactivity is consistent with TEOS reacting with hydroxyl groups and (Si-O){sub 3} rings via a common rate-determining step at 1000K. With respect to deposition uniformity, our results predict that deposition rates will be insensitive to the relative coverages of (Si-O){sub 3} rings and hydroxyls on SiO{sub 2} as well as the re-adsorbed by-products of the surface reaction. Therefore, it is likely that nonuniform SiO{sub 2} depositions from TEOS reactions are due to depletion of TEOS in the gas-phase and/or thermal gradients.

Bartram, M.E.; Moffat, H.K.

1995-11-01T23:59:59.000Z

134

Performance and analysis of amorphous silicon p-i-n solar cells made by chemical-vapor deposition from disilane  

SciTech Connect

The photovoltaic performance of amorphous silicon p-i-n solar cells made by chemical-vapor deposition (CVD) from disilane is reported and analyzed. Intrinsic layers were deposited at rates from 0.2 to 50 A/s at temperatures from 380 to 460 /sup 0/C with and without boron doping. Device performance was insensitive to substantial differences in disilane purity. A cell efficiency of 4% was achieved. The primary limitation to higher efficiency was low fill factor (<50%) due to high series resistance (>18 ..cap omega.. cm/sup 2/). Analysis of the series resistance indicated a contact-related resistance of 4--12 ..cap omega.. cm/sup 2/ and a photoconductive resistance composed of intrinsic layer thickness-independent (10 ..cap omega.. cm/sup 2/) and thickness-dependent terms. Analysis of the voltage dependence of the current collection indicated a fill factor of 60% would be expected in the absence of series resistance. The maximum short-circuit current of 12.5 mA/cm/sup 2/ (normalized to 100 mW/cm/sup 2/) resulted with a boron-doped i layer deposited at 440 /sup 0/C at 3.3 A/s. Modeling of the collection efficiency indicated collection widths up to 0.33 ..mu..m for boron-doped and 0.24 ..mu..m for undoped p-i-n devices. In order to achieve high-efficiency cells using CVD from disilane, the limitations imposed by low photoconductivity, a high density of states, and restricted cell design imposed by the high deposition temperatures would have to be overcome.

Hegedus, S.S.; Rocheleau, R.E.; Buchanan, W.; Baron, B.N.

1987-01-01T23:59:59.000Z

135

Occupational Exposure Evaluation of Complex Vapor Mixtures at the Hanford Nuclear Waste Site, Washington Work-site Vapor Characterization  

SciTech Connect

Extensive sampling and analysis has been done over the years to characterize the radioactive and chemical properties of hazardous waste stored in 177 underground tanks at the Hanford site in eastern Washington State. The purpose of these analyses was to evaluate safety and environmental concerns related to tank stability. More recently, characterization studies have broadened to evaluate potential health hazards of chemical vapors at the ground surface, where workers perform maintenance and waste transfer activities. Chemical vapor emissions from underground hazardous waste storage tanks on the Hanford site are a potential concern because workers enter the tank farms on a regular basis for waste retrievals, equipment maintenance, and surveillance. The extensive sampling done during this campaign evaluated vapor concentrations of more than 100 different chemical at 70 sites in and around one section of the tank farms. Sampling identified only four vapors (ammonia, nitrous oxide, nitrosodimethylamine, and nitrosomethylethylamine) that were present above occupational exposure limits. These elevated concentrations were detected only at exhaust stacks and passive breather filter outlets. Beyond five feet from the sources, vapors disperse rapidly. No vapors were measured above 10% of their OELs more than five feet from the source. This suggests that vapor controls can be focused on limited hazard zones around sources. (authors)

Anderson, T. J. [CH2M HILL Hanford Group, Inc. / Environmental Health, P.O. Box 1000, S7-70, Richland, WA 99352 (United States)

2006-07-01T23:59:59.000Z

136

Environmentally focused patterning and processing of polymer thin films by initiated chemical vapor deposition (iCVD) and oxidative chemical vapor deposition (oCVD)  

E-Print Network (OSTI)

The new millennium has brought fourth many technological innovations made possible by the advancement of high speed integrated circuits. The materials and energy requirements for a microchip is orders of magnitude higher ...

Trujillo, Nathan J. (Nathan Jeffrey)

2010-01-01T23:59:59.000Z

137

Application of chemical structure and bonding of actinide oxide materials for forensic science  

SciTech Connect

We are interested in applying our understanding of actinide chemical structure and bonding to broaden the suite of analytical tools available for nuclear forensic analyses. Uranium- and plutonium-oxide systems form under a variety of conditions, and these chemical species exhibit some of the most complex behavior of metal oxide systems known. No less intriguing is the ability of AnO{sub 2} (An: U, Pu) to form non-stoichiometric species described as AnO{sub 2+x}. Environmental studies have shown the value of utilizing the chemical signatures of these actinide oxide materials to understand transport following release into the environment. Chemical speciation of actinide-oxide samples may also provide clues as to the age, source, or process history of the material. The scientific challenge is to identify, measure and understand those aspects of speciation of actinide analytes that carry information about material origin and history most relevant to forensics. Here, we will describe our efforts in material synthesis and analytical methods development that we will use to provide the fundamental science to characterize actinide oxide molecular structures for forensic science. Structural properties and initial results to measure structural variability of uranium oxide samples using synchrotron-based X-ray Absorption Fine Structure will be discussed.

Wilkerson, Marianne Perry [Los Alamos National Laboratory

2010-01-01T23:59:59.000Z

138

Use of amine oxide surfactants for chemical flooding EOR (enhanced oil recovery)  

Science Conference Proceedings (OSTI)

The use of amine oxides with and without alcohols as cosolvents, and in combination with other surfactants as mixed micellar formulations for enhanced oil recovery by surfactant flooding was investigated. Amine oxides are a salt-tolerant class of surfactants that produce low interfacial tension and can develop viscosity without the addition of polymers. These salt-tolerant formulations generate three-phase regions with hydrocarbons over a broad salinity range, develop moderate solubilization, and produce low interfacial tensions, however oil recovery from amine oxide-alcohol phase behavior optimized formulations was directly dependent upon the quantity of surfactant injected. The large pore volume and high concentration of surfactant required prohibits their economic use as the primary surfactant in chemical flooding EOR. Dimethylalkylamine oxides are useful as cosurfactants and viscosifiers in formulations with other surfactants for chemical flooding EOR but the use of ethoxylated and propoxylated amine oxides should be avoided due to the decomposition of these amine oxides under reservoir conditions. Phase behavior, phase inversion temperatures, and viscosity scans have been correlated with surfactant structures to provide a guide for amine oxide applications in chemical flooding. 36 refs., 5 figs., 6 tabs.

Olsen, D.K.

1989-11-01T23:59:59.000Z

139

Low-pressure chemical vapor deposition of amorphous silicon photovoltaic devices. Annual technical progress report, 1 May 1984-30 April 1985  

DOE Green Energy (OSTI)

Intrinsic and doped a-Si:H films were deposited by low pressure chemical vapor deposition (CVD) for disilane. Intrinsic layers were deposited at growth rates as high as 50 A/s. A chemical reaction engineering model that quantitatively describes the CVD reactor behavior has been developed. CVD intrinsic material was characterized by measurements of impurities, optical band gap, photoconductivity, activation energy, diffusion length, and density of states. Photovoltaic cells of the p-i-n type with efficiencies of 4% and 3.6% were fabricated using CVD intrinsic layers deposited at 1 A/s and 9 A/s, respectively. A maximum short-circuit current of 11 mA/cm/sup 2/ under 87.5 MW/cm/sup 2/ ELH illumination was obtained with boron-compensated CVD intrinsic material. Efficiency-limiting mechanisms in CVD cells were quantitatively analyzed and related to fundamental properties.

Baron, B.N.; Rocheleau, R.E.; Hegedus, S.S.

1986-02-01T23:59:59.000Z

140

A field-scale test of in situ chemical oxidation through recirculation  

Science Conference Proceedings (OSTI)

In situ chemical oxidation is a developing class of remediation technologies in which organic contaminants are degraded in place by powerful oxidants. Successful implementation of this technology requires an effective means for dispersing the oxidant to contaminated regions in the subsurface. An oxidant delivery technique has been developed wherein the treatment solution is made by adding an oxidant to extracted groundwater. The oxidant-laden groundwater is then injected and recirculated into a contaminated aquifer through multiple horizontal and/or vertical wells. This technique, referred to as in situ chemical oxidation through recirculation (ISCOR), can be applied to saturated and hydraulically conductive formations and used with relatively stable oxidants such as potassium permanganate (KMnO{sub 4}). A field-scale test of ISCOR was conducted at a site (Portsmouth Gaseous Diffusion Plant) where groundwater in a 5-ft thick silty gravel aquifer is contaminated with trichloroethylene (TCE) at levels that indicate the presence of residual dense non-aqueous phase liquids (DNAPLs). The field test was implemented using a pair of parallel horizontal wells with 200-ft screened sections. For approximately one month, groundwater was extracted from one horizontal well, dosed with crystalline KMnO{sub 4}, and re-injected into the other horizontal well 90 ft away. Post-treatment characterization showed that ISCOR was effective at removing TCE in the saturated region. Lateral and vertical heterogeneities within the treatment zone impacted the uniform delivery of the oxidant solution. However, TCE was not detected in groundwater samples collected from monitoring wells and soil samples from borings in locations where the oxidant had permeated.

West, O.R.; Cline, S.R.; Holden, W.L.; Gardner, F.G.; Schlosser, B.M. [Oak Ridge National Lab., TN (United States); Siegrist, R.L. [Colorado School of Mines, Golden, CO (United States); Houk, T.C. [Bechtel-Jacobs, Piketon, OH (United States). Portsmouth Gaseous Diffusion Plant

1998-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" from the National Library of EnergyBeta (NLEBeta).
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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

Screening values for Non-Carcinogenic Hanford Waste Tank Vapor Chemicals that Lack Established Occupational Exposure Limits  

SciTech Connect

Over 1,500 different volatile chemicals have been reported in the headspaces of tanks used to store high-level radioactive waste at the U.S. Department of Energy's Hanford Site. Concern about potential exposure of tank farm workers to these chemicals has prompted efforts to evaluate their toxicity, identify chemicals that pose the greatest risk, and incorporate that information into the tank farms industrial hygiene worker protection program. Established occupation exposure limits for individual chemicals and petroleum hydrocarbon mixtures have been used elsewhere to evaluate about 900 of the chemicals. In this report headspace concentration screening values were established for the remaining 600 chemicals using available industrial hygiene and toxicological data. Screening values were intended to be more than an order of magnitude below concentrations that may cause adverse health effects in workers, assuming a 40-hour/week occupational exposure. Screening values were compared to the maximum reported headspace concentrations.

Poet, Torka S.; Mast, Terryl J.; Huckaby, James L.

2006-02-06T23:59:59.000Z

142

Low temperature metal-organic chemical vapor deposition growth processes for high-efficiency solar cells. Final technical report, 1 September 1985--30 November 1989  

DOE Green Energy (OSTI)

This report describes the results of a program to develop a more complete understanding of the physical and chemical processes involved in low-temperature growth of III-V compounds by metal-organic chemical vapor deposition (MOCVD) and to develop a low-temperature process that is suitable for the growth of high-efficiency solar cells. The program was structured to develop a better understanding of the chemical reactions involved in MOCVD growth, to develop a model of the processes occurring in the gas phase, to understand the physical kinetics and reactions operative on the surface of the growing crystal, and to develop an understanding of the means by which these processes may be altered to reduce the temperature of growth and the utilization of toxic hydrides. The basic approach was to develop the required information about the chemical and physical kinetics operative in the gas phase and on the surface by the direct physical measurement of the processes whenever possible. The program included five tasks: (1) MOCVD growth process characterization, (2) photoenhanced MOCVD studies, (3) materials characterization, (4) device fabrication and characterization, and (5) photovoltaic training. Most of the goals of the program were met and significant progress was made in defining an approach that would allow both high throughput and high uniformity growth of compound semiconductors at low temperatures. The technical activity was focused on determining the rates of thermal decomposition of trimethyl gallium, exploring alternate arsenic sources for use MOCVD, and empirical studies of atomic layer epitaxy as an approach.

Dapkus, P.D. [University of Southern California, Los Angeles, CA (United States)

1993-02-01T23:59:59.000Z

143

Oxidative weathering chemical migration under variably saturated conditions and supergene copper enrichment  

Science Conference Proceedings (OSTI)

Transport of oxygen gas from the land surface through an unsaturated zone has a strong influence on oxidative weathering processes. Oxidation of sulfide minerals such as pyrite (FeS{sub 2}), one of the most common naturally occurring minerals, is the primary source of acid drainage from mines and waste rock piles. Here we present a detailed numerical model of supergene copper enrichment that involves the oxidative weathering of pyrite (FeS{sub 2}) and chalcopyrite (CuFeS{sub 2}), and acidification that causes mobilization of metals in the unsaturated zone, with subsequent formation of enriched ore deposits of chalcocite (CuS) and covellite (Cu{sub 2}S) in the reducing conditions below the water table. We examine and identify some significant conceptual and computational issues regarding the oxidative weathering processes through the modeling tool. The dissolution of gaseous oxygen induced by the oxidation reduces oxygen partial pressure, as well as the total pressure of the gas phase. As a result, the gas flow is modified, then the liquid phase flow. Results indicate that this reaction effect on the fluid flow may not be important under ambient conditions, and gas diffusion can be a more important mechanism for oxygen supply than gas or liquid advection. Acidification, mobilization of metals, and alteration of primary minerals mostly take place in unsaturated zone (oxidizing), while precipitation of secondary minerals mainly occurs in saturated zone (reducing). The water table may be considered as an interface between oxidizing and reducing zones. Moving water table due to change of infiltration results in moving oxidizing zone and redistributing aqueous chemical constitutes and secondary mineral deposits. The oxidative weathering processes are difficult to model numerically, because concentrations of redox sensitive chemical species such as O{sub 2}(aq), SO{sub 4}{sup 2-} and HS{sup -} may change over tens of orders of magnitude between oxidizing and reducing conditions. In order to simulate substantial reaction progress over geologic time, one can benefit from the quasi-stationary state (QSS) approximation. A significant saving of computing time using QSS is demonstrated through the example. In addition, changes in porosity and permeability due to mineral dissolution and precipitation are also addressed in some degree. Even though oxidative weathering is sensitive to many factors, this work demonstrates that our model provides a comprehensive suite of process modeling capabilities, which could serve as a prototype for oxidative weathering processes with broad significance for geoscientific, engineering, and environmental applications.

Xu, Tianfu; Pruess, K.; Brimhall, G.

1999-04-01T23:59:59.000Z

144

The relationship between structural evolution and electrical percolation of the initial stages of tungsten chemical vapor deposition on polycrystalline TiN  

SciTech Connect

This paper presents experimental results and a geometric model of the evolution of sheet resistance and surface morphology during the transition from nucleation to percolation of tungsten chemical vapor deposition over ultrathin polycrystalline titanium nitride (TiN). We observed two mechanisms of reduction in sheet resistance. At deposition temperatures higher than 310 deg. C, percolation effect is formed at {approx}35% of surface coverage, {theta}, and characterized with a sharp drop in resistance. At temperature below 310 deg. C, a reduction in resistance occurs in two steps. The first step occurs when {theta} = 35% and the second step at {theta} = 85%. We suggest a geometric model in which the electrical percolation pass is modulated by the thickness threshold of the islands at the instant of collision.

Rozenblat, A. [Micron Semiconductors Israel Ltd., Qiryat-Gat 82109 (Israel); Department of Physical Electronics, Electrical Engineering, Tel Aviv University, Tel Aviv 69978 (Israel); Haimson, S. [Material Science Program, Tel Aviv University, Tel Aviv 69978 (Israel); Shacham-Diamand, Y. [Department of Physical Electronics, Electrical Engineering, Tel Aviv University, Tel Aviv 69978 (Israel); Horvitz, D. [Micron Semiconductors Israel Ltd., Qiryat-Gat 82109 (Israel)

2012-01-16T23:59:59.000Z

145

Atmospheric Pressure Chemical Vapor Deposition of High Silica SiO2-TiO2 Antireflective Thin Films for Glass Based Solar Panels  

SciTech Connect

The atmospheric pressure chemical vapor deposition (APCVD) of SiO2-TiO2 thin films employing [[(tBuO)3Si]2O-Ti(OiPr)2], which can be prepared from commercially available materials, results in antireflective thin films on float glass under industrially relevant manufacturing conditions. It was found that while the deposition temperature had an effect on the SiO2:TiO2 ratio, the thickness was dependent on the time of deposition. This study shows that it is possible to use APCVD employing a single source precursor containing titanium and silicon to produce thin films on float glass with high SiO2:TiO2 ratios.

Klobukowski, Erik R [ORNL; Tenhaeff, Wyatt E [ORNL; McCamy, James [PPG; Harris, Caroline [PPG; Narula, Chaitanya Kumar [ORNL

2013-01-01T23:59:59.000Z

146

The use of electron channeling patterns for process optimization of low-temperature epitaxial silicon using hot-wire chemical vapor deposition  

DOE Green Energy (OSTI)

The authors demonstrate the first reported use of electron channeling patterns (ECPs) as a response for a statistical design of experiments process-optimization for epitaxial silicon. In an effort to fully characterize the new hot-wire chemical vapor deposition (HWCVD) method of epitaxial growth recently discovered at NREL, a large number of parameters with widely varying values needed to be considered. To accomplish this, they used the statistical design of experiments method. This technique allows one to limit the number of sample points necessary to evaluate a given parameter space. In this work they demonstrate how ECPs can effectively be used to optimize the process space as well as to quickly and economically provide the process engineer with absolutely key information.

Matson, R.; Thiesen, J.; Jones, K.M.; Crandall, R.; Iwaniczko, E.; Mahan, H.

1999-10-25T23:59:59.000Z

147

Amorphous silicon photovoltaic devices prepared by chemical and photochemical vapor deposition of higher order silanes. Annual subcontract progress report, 1 September 1984-31 August 1985  

DOE Green Energy (OSTI)

This report describes the preparation of hydrogenated amorphous silicon (a-Si:H) films and photovoltaic devices by chemical vapor deposition (CVD) from higher order silanes and the properties of such films and devices. The research explored new deposition techniques that could produce a-Si:H superior to that achieved by the glow-discharge method. For example, the improvement could stem from ease of deposition (lower cost and/or better reproducibility), from material improvement (higher efficiency and/or better stability under illumination), or from innovative materials that improve device performance. Research focused on photo-CVD techniques; thermal CVD deemphasized. This report presents results for deposition by mercury-sensitized decomposition of disilane. These results indicate that this technique is a very promising alternative to the glow-discharge method.

Delahoy, A.E.; Ellis, F.B. Jr.

1985-11-01T23:59:59.000Z

148

Amorphous silicon photovoltaic devices prepared by chemical and photochemical vapor deposition of higher order silanes. Technical progress report, 1 September 1984-28 February 1985  

DOE Green Energy (OSTI)

This report describes the preparation of hydrogenated amorphous silicon (a-Si:H) films and photovoltaic devices by chemical vapor deposition (CVD) from higher order silanes, and the properties of such films and devices. The research is directed at exploring new, improved deposition techniques to produce a-Si:H. The improvement could stem from ease of deposition (lower cost and/or better reproducibility), from material improvement (higher efficiency and/or better stability under illumination), or from innovative materials that improve device performance. Research efforts have focused, therefore, on photo-CVD techniques; thermal CVD has been emphasized. This report summarizes the properties of the experimental thermal CVD films and the reasons for terminating the research in this area. In addition, the results for deposition by mercury-sensitized decomposition of disilane are presented. These results indicate that this technique is a very promising alternative to the glow-discharge method.

Delahoy, A.E.; Ellis, F.B. Jr.

1985-05-01T23:59:59.000Z

149

Direct growth of few-layer graphene on 6H-SiC and 3C-SiC/Si via propane chemical vapor deposition  

Science Conference Proceedings (OSTI)

We propose to grow graphene on SiC by a direct carbon feeding through propane flow in a chemical vapor deposition reactor. X-ray photoemission and low energy electron diffraction show that propane allows to grow few-layer graphene (FLG) on 6H-SiC(0001). Surprisingly, FLG grown on (0001) face presents a rotational disorder similar to that observed for FLG obtained by annealing on (000-1) face. Thanks to a reduced growth temperature with respect to the classical SiC annealing method, we have also grown FLG/3C-SiC/Si(111) in a single growth sequence. This opens the way for large-scale production of graphene-based devices on silicon substrate.

Michon, A.; Vezian, S.; Portail, M. [CNRS-CRHEA, Rue Bernard Gregory, 06560 Valbonne (France); Ouerghi, A. [CNRS-LPN, Route de Nozay, 91460 Marcoussis (France); Zielinski, M.; Chassagne, T. [NOVASiC, Savoie Technolac, Arche Bat 4, BP267, 73375 Le Bourget du Lac (France)

2010-10-25T23:59:59.000Z

150

The Effect of Growth Parameters on the Intrinsic Properties of Large-Area Single Layer Graphene Grown by Chemical Vapor Deposition on Cu  

SciTech Connect

We present a comprehensive study of the parameter space for single layer graphene growth by chemical vapor deposition on Cu. The temperature is the most widely recognized parameter in single layer graphene growth. We show that the methane-to-hydrogen ratio and the growth pressure also are critical parameters that affect the structural perfection and the cleanliness of graphene. The optimal conditions for suppressing double and multilayer graphene growth occur near 1000 C, 1:20 methane-to-hydrogen ratio, and a total pressure in the range from 0.5 to 1 Torr. Raman mapping of a 40x30 m2 area shows single layer domains with 5-10 m linear dimensions. Atomic resolution imaging of suspended graphene by aberration corrected scanning transmission electron microscopy shows that the cleanest single layer graphene consists of areas of 10-15 nm linear dimensions and smaller patches of residual contamination that was undetected by other characterization methods.

Regmi, Murari [ORNL; Chisholm, Matthew F [ORNL; Eres, Gyula [ORNL

2012-01-01T23:59:59.000Z

151

Comparison of Short-Term Oxidation Behavior of Model and Commercial Chromia-Forming Ferritic Stainless Steels in Air with Water Vapor  

Science Conference Proceedings (OSTI)

A high-purity Fe-20Cr and commercial type 430 ferritic stainless steel were exposed at 700 and 800 C in dry air and air with 10% water vapor (wet air) and characterized by SEM, XRD, STEM, SIMS, and EPMA. The Fe-20Cr alloy formed a fast growing Fe-rich oxide scale at 700 C in wet air after 24 h exposure, but formed a thin chromia scale at 700 C in dry air and at 800 C in both dry air and wet air. In contrast, thin spinel + chromia base scales with a discontinuous silica subscale were formed on 430 stainless steel under all conditions studied. Extensive void formation was observed at the alloy-oxide interface for the Fe-20Cr in both dry and wet conditions, but not for the 430 stainless steel. The Fe-20Cr alloy was found to exhibit a greater relative extent of subsurface Cr depletion than the 430 stainless steel, despite the former's higher Cr content. Depletion of Cr in the Fe-20Cr after 24 h exposure was also greater at 700 C than 800 C. The relative differences in oxidation behavior are discussed in terms of the coarse alloy grain size of the high-purity Fe-20Cr material, and the effects of Mn, Si, and C on the oxide scale formed on the 430 stainless steel.

Brady, Michael P [ORNL; Keiser, James R [ORNL; More, Karren Leslie [ORNL; Fayek, Mostafa [University of Manitoba, Canada; Walker, Larry R [ORNL; Meisner, Roberta Ann [ORNL; Anovitz, Lawrence {Larry} M [ORNL; Wesolowski, David J [ORNL; Cole, David R [ORNL

2012-01-01T23:59:59.000Z

152

Process Optimization for High Efficiency Heterojunction c-Si Solar Cells Fabrication Using Hot-Wire Chemical Vapor Deposition: Preprint  

SciTech Connect

The researchers extensively studied the effects of annealing or thermal history of cell process on the minority carrier lifetimes of FZ n-type c-Si wafers with various i-layer thicknesses from 5 to 60 nm, substrate temperatures from 100 to 350 degrees C, doped layers both p- and n-types, and transparent conducting oxide (TCO).

Ai, Y.; Yuan, H. C.; Page, M.; Nemeth, W.; Roybal, L.; Wang, Q.

2012-06-01T23:59:59.000Z

153

Characterization of photoluminescent (Y{sub 1{minus}x}Eu{sub x}){sub 2}O{sub 3} thin-films prepared by metallorganic chemical vapor deposition  

SciTech Connect

Europium doped yttrium oxide, (Y{sub 1{minus}x}Eu{sub x}){sub 2}O{sub 3}, thin-films were deposited on silicon and sapphire substrates by metallorganic chemical vapor deposition (MOCVD). The films were grown in a MOCVD chamber reacting yttrium and europium tris(2,2,6,6-tetramethyl-3,5,-heptanedionates) precursors in an oxygen atmosphere at low pressures (5 Torr) and low substrate temperatures (500--700 C). The films deposited at 500 C were flat and composed of nanocrystalline regions of cubic Y{sub 2}O{sub 3}, grown in a textured [100] or [110] orientation to the substrate surface. Films deposited at 600 C developed from the flat, nanocrystalline morphology into a plate-like growth morphology oriented in the [111] with increasing deposition time. Monoclinic Y{sub 2}O{sub 3}:Eu{sup 3+} was observed in x-ray diffraction for deposition temperatures {ge}600 C on both (111) Si and (001) sapphire substrates. This was also confirmed by the photoluminescent emission spectra.

McKittrick, J.; Bacalski, C.F.; Hirata, G.A. [Univ. of California, San Diego, La Jolla, CA (United States); Hubbard, K.M.; Pattillo, S.G.; Salazar, K.V.; Trkula, M. [Los Alamos National Lab., NM (United States). Materials Science and Technology Div.

1998-12-01T23:59:59.000Z

154

Development of a polysilicon process based on chemical vapor deposition (Phase 1). First quarterly progress report, 6 October-31 December 1979  

DOE Green Energy (OSTI)

The goal of this program is to demonstrate that a dichlorosilane based reductive chemical vapor deposition (CVD) process is capable of producing, at low cost, high quality polycrystalline silicon. Physical form and purity of this material will be consistent with LSA material requirements for use in the manufacture of high efficiency solar cells. Chemical processes involved in achieving the objective are reviewed with emphasis placed on advantages of this process when compared with existing polycrystalline silicon production technology. Installation of a CVD reactor with associated analytical instrumentation is described. Preliminary reactor data has been favorable demonstrating the anticipated increased deposition rate and conversion efficiency when dichlorosilane decomposition is compared with trichlorosilane decomposition. No serious problems have been encountered which might limit dichlorosilane use as a reactor feed material. Design considerations for a process development unit (PDU) for dichlorosilane synthesis are reviewed. A design which effectively suppresses monochlorosilane during the redistribution of trichlorosilane was decided upon and its implementation is described. The PDU will be used to collect data on optimization of the redistribution process as well as to determine product quality. Based on experimental data collected during the first quarter along with already available data on the redistribution and hydrogenation processes, a preliminary mass balance is established.

McCormick, J. R.; Arvidson, A.; Plahutnik, F.; Sawyer, D.; Sharp, K.

1980-01-01T23:59:59.000Z

155

Vapor Degreasing  

Science Conference Proceedings (OSTI)

Table 6   Applications of vapor degreasing by vapor-spray-vapor systems...hardware Brass 2270 5000 Buffing compound; rouge Lacquer spray Racked work on continuous monorail Acoustic ceiling tile Steel 2720 6000 Light oil (stamping lubricant) Painting Monorail conveyor Gas meters Terneplate 4540 10,000 Light oil Painting Monorail conveyor Continuous strip, 0.25â??4.1 mm...

156

Vapor Characterization  

Science Conference Proceedings (OSTI)

... thermodynamics (that is, vapor liquid equilibrium) as ... of solids and low volatility liquids is extraordinarily ... such situations is the gas saturation method ...

2013-12-10T23:59:59.000Z

157

Investigation of forced and isothermal chemical vapor infiltrated SiC/SiC ceramic matrix composites. Final report  

Science Conference Proceedings (OSTI)

Mechanical properties of two different layups for each of the forced CVI (41 specimens) and isothermal CVI (36 specimens) materials were investigated in air at room temperature (RT), 1000C, and at room temperature after thermal shock (RT/TS) and exposure to oxidation (RT/OX). The FCVI specimens had a nominal interfacial coating thickness of 0.3 {mu}m of pyrolytic carbon, while CVI specimens had a coating thickness of 0.1 {mu}m. Effect of reinforcement and interfacial bond on mechanical properties of composite were investigated. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were employed to analyze the fiber-matrix interface and the toughening mechanisms in this ceramic composite system.

Sankar, J.; Kelkar, A.D.; Vaidyanathan, R. [North Carolina Agricultural and Technical State Univ., Greensboro, NC (United States). Dept. of Mechanical Engineering

1993-09-01T23:59:59.000Z

158

VAPOR PRESSURES AND HEATS OF VAPORIZATION OF PRIMARY COAL TARS  

DOE Green Energy (OSTI)

This project had as its main focus the determination of vapor pressures of coal pyrolysis tars. It involved performing measurements of these vapor pressures and from them, developing vapor pressure correlations suitable for use in advanced pyrolysis models (those models which explicitly account for mass transport limitations). This report is divided into five main chapters. Each chapter is a relatively stand-alone section. Chapter A reviews the general nature of coal tars and gives a summary of existing vapor pressure correlations for coal tars and model compounds. Chapter B summarizes the main experimental approaches for coal tar preparation and characterization which have been used throughout the project. Chapter C is concerned with the selection of the model compounds for coal pyrolysis tars and reviews the data available to us on the vapor pressures of high boiling point aromatic compounds. This chapter also deals with the question of identifying factors that govern the vapor pressures of coal tar model materials and their mixtures. Chapter D covers the vapor pressures and heats of vaporization of primary cellulose tars. Chapter E discusses the results of the main focus of this study. In summary, this work provides improved understanding of the volatility of coal and cellulose pyrolysis tars. It has resulted in new experimentally verified vapor pressure correlations for use in pyrolysis models. Further research on this topic should aim at developing general vapor pressure correlations for all coal tars, based on their molecular weight together with certain specific chemical characteristics i.e. hydroxyl group content.

Eric M. Suuberg; Vahur Oja

1997-07-01T23:59:59.000Z

159

The destruction of hazardous chemical waste by oxidation in supercritical water  

SciTech Connect

The chemistry of oxidation in supercritical water is being investigated for development into a practical destruction process for hazardous chemical waste. In principle, a wide variety of waste streams might be treated by this technology, including those that are unsuitable for incineration because of high water content. To establish a basis for extrapolation of kinetic measurements to a variety of compounds, a mechanism is being developed for oxidation in supercritical water on the basis of conventional free-radical reactions, with modifications for high pressures and high concentrations of water. Global rate expressions for oxidation of methane and methanol in supercritical water have been determined. A base mechanism and modifications to the mechanism to account for the roles of hydrogen bonding and water dimer formation have been investigated for CO. On this limited basis, reasonable agreement between model and experimental results has been obtained. Further verification of the model with experimental results will provide insight into the roles of hydrogen bonding and water dimer formation in oxidation in supercritical water. 30 refs., 3 tabs.

Rofer, C.K.; Streit, G.E.

1989-01-01T23:59:59.000Z

160

Detailed chemical kinetic mechanism for the oxidation of biodiesel fuels blend surrogate.  

DOE Green Energy (OSTI)

Detailed chemical kinetic mechanisms were developed and used to study the oxidation of two large unsaturated esters: methyl-5-decenoate and methyl-9-decenoate. These models were built from a previous methyl decanoate mechanism and were compared with rapeseed oil methyl esters oxidation experiments in a jet stirred reactor. A comparative study of the reactivity of these three oxygenated compounds was performed and the differences in the distribution of the products of the reaction were highlighted showing the influence of the presence and the position of a double bond in the chain. Blend surrogates, containing methyl decanoate, methyl-5-decenoate, methyl-9-decenoate and n-alkanes, were tested against rapeseed oil methyl esters and methyl palmitate/n-decane experiments. These surrogate models are realistic kinetic tools allowing the study of the combustion of biodiesel fuels in diesel and homogeneous charge compression ignition engines.

Herbinet, O; Pitz, W J; Westbrook, C K

2009-07-21T23:59:59.000Z

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


161

Effects of pressure, temperature, and hydrogen during graphene growth on SiC(0001) using propane-hydrogen chemical vapor deposition  

SciTech Connect

Graphene growth from a propane flow in a hydrogen environment (propane-hydrogen chemical vapor deposition (CVD)) on SiC differentiates from other growth methods in that it offers the possibility to obtain various graphene structures on the Si-face depending on growth conditions. The different structures include the (6{radical}3 Multiplication-Sign 6{radical}3)-R30 Degree-Sign reconstruction of the graphene/SiC interface, which is commonly observed on the Si-face, but also the rotational disorder which is generally observed on the C-face. In this work, growth mechanisms leading to the formation of the different structures are studied and discussed. For that purpose, we have grown graphene on SiC(0001) (Si-face) using propane-hydrogen CVD at various pressure and temperature and studied these samples extensively by means of low energy electron diffraction and atomic force microscopy. Pressure and temperature conditions leading to the formation of the different structures are identified and plotted in a pressure-temperature diagram. This diagram, together with other characterizations (X-ray photoemission and scanning tunneling microscopy), is the basis of further discussions on the carbon supply mechanisms and on the kinetics effects. The entire work underlines the important role of hydrogen during growth and its effects on the final graphene structure.

Michon, A.; Vezian, S.; Roudon, E.; Lefebvre, D.; Portail, M. [CNRS-CRHEA, Rue Bernard Gregory, 06560 Valbonne (France)] [CNRS-CRHEA, Rue Bernard Gregory, 06560 Valbonne (France); Zielinski, M.; Chassagne, T. [NOVASiC, Savoie Technolac, Arche Bat 4, BP267, 73375 Le Bourget du Lac (France)] [NOVASiC, Savoie Technolac, Arche Bat 4, BP267, 73375 Le Bourget du Lac (France)

2013-05-28T23:59:59.000Z

162

Development of a polysilicon process based on chemical vapor deposition. Phase 1. Fourth quarterly progress report, 1 July-30 September 1980  

DOE Green Energy (OSTI)

The goal of this program is to demonstrate that a dichlorosilane-based reductive chemical vapor deposition (CVD) process is capable of producing, at low cost, high quality polycrystalline silicon for use in the manufacture of high efficiency solar cells. The feasibility of silicon generation from dichlorosilane (DCS) has been well established. The feasibility and optimization portions of the experimental reactor program have been completed, with a number of runs having been conducted over a broad range of conditions in an experimental CVD reactor. Activities relating to feed of commercially purchased DCS to an intermediate sized reactor and to construction of a Process Development Unit (PDU) to generate and feed DCS to one or more production scale reactors were suspended during the previous quarter because of the receipt of new safety-related information about DCS from Hazards Research Corp. Experimental data generated by Hazards Research Corp. indicate that DCS/air mixtures possess about four times the explosive severity potential as hydrogen/air mixtures, and that DCS/air mixtures are very readily ignited. As a consequence of this new information, designs and procedures for the intermediate reactor feed and PDU tasks were deemed inadequate and new designs incorporating new safety-related elements are being formulated. A preliminary economic evaluation of the Hemlock Semiconductor process has been completed. The analysis for a plant to generate 1000 metric tonne of silicon indicates a plant investment of $21.9 M, and a product selling price of $19.85/kg.

Sharp, K.; Arvidson, A.; Sawyer, D.

1980-12-01T23:59:59.000Z

163

As-grown deep-level defects in n-GaN grown by metal-organic chemical vapor deposition on freestanding GaN  

SciTech Connect

Traps of energy levels E{sub c}-0.26 and E{sub c}-0.61 eV have been identified as as-grown traps in n-GaN grown by metal-organic chemical vapor deposition by using deep level transient spectroscopy of the Schottky contacts fabricated by resistive evaporation. The additional traps of E{sub c}-0.13 and E{sub c}-0.65 eV have been observed in samples whose contacts are deposited by electron-beam evaporation. An increase in concentration of the E{sub c}-0.13 and E{sub c}-0.65 eV traps when approaching the interface between the contact and the GaN film supports our argument that these traps are induced by electron-beam irradiation. Conversely, the depth profiles of as-grown traps show different profiles between several samples with increased or uniform distribution in the near surface below 50 nm. Similar profiles are observed in GaN grown on a sapphire substrate. We conclude that the growth process causes these large concentrations of as-grown traps in the near-surface region. It is speculated that the finishing step in the growth process should be an essential issue in the investigation of the surface state of GaN.

Chen Shang; Ishikawa, Kenji; Hori, Masaru [Nagoya University, Chikusa, Nagoya 464-8603 (Japan); Honda, Unhi; Shibata, Tatsunari; Matsumura, Toshiya; Tokuda, Yutaka [Aichi Institute of Technology, Yakusa, Toyota 470-0392 (Japan); Ueda, Hiroyuki; Uesugi, Tsutomu; Kachi, Tetsu [Toyota Central R and D Laboratories, Inc., Yokomichi, Nagakute 480-1192 (Japan)

2012-09-01T23:59:59.000Z

164

Photoconduction efficiencies and dynamics in GaN nanowires grown by chemical vapor deposition and molecular beam epitaxy: A comparison study  

Science Conference Proceedings (OSTI)

The normalized gains, which determines the intrinsic photoconduction (PC) efficiencies, have been defined and compared for the gallium nitride (GaN) nanowires (NWs) grown by chemical vapor deposition (CVD) and molecular beam epitaxy (MBE). By excluding the contributions of experimental parameters and under the same light intensity, the CVD-grown GaN NWs exhibit the normalized gain which is near two orders of magnitude higher than that of the MBE-ones. The temperature-dependent time-resolved photocurrent measurement further indicates that the higher photoconduction efficiency in the CVD-GaN NWs is originated from the longer carrier lifetime induced by the higher barrier height ({phi}{sub B} = 160 {+-} 30 mV) of surface band bending. In addition, the experimentally estimated barrier height at 20 {+-} 2 mV for the MBE-GaN NWs, which is much lower than the theoretical value, is inferred to be resulted from the lower density of charged surface states on the non-polar side walls.

Chen, R. S. [Graduate Institute of Applied Science and Technology, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Tsai, H. Y. [Graduate Institute of Electro-Optical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Huang, Y. S. [Graduate Institute of Electro-Optical Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Department of Electronic Engineering, National Taiwan University of Science and Technology, Taipei 10607, Taiwan (China); Chen, Y. T. [Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan (China); Chen, L. C. [Center for Condensed Matter Sciences, National Taiwan University, Taipei 10617, Taiwan (China); Chen, K. H. [Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 10617, Taiwan (China); Center for Condensed Matter Sciences, National Taiwan University, Taipei 10617, Taiwan (China)

2012-09-10T23:59:59.000Z

165

Chemical Synthesis of Nano-Sized particles of Lead Oxide and their Characterization Studies  

E-Print Network (OSTI)

The quantum dots of semiconductor display novel and interesting phenomena that have not been in the bulk material. The color tunability is one of the most attractive characteristics in II-VI semiconductor nanoparticles such as CdS, ZnS, CdSe, ZnSe and PbO. In this work, the semiconductor lead oxide nanoparticles are prepared by chemical method. The average particle size, specific surface area, crystallinity index are estimated from XRD analysis. The structural, functional groups and optical characters are analyzed with using of SEM, FTIR and UV- Visible techniques. The optical band gap value has also been determined.

M. Alagar; T. Theivasanthi; A. Kubera Raja

2012-04-04T23:59:59.000Z

166

Published on Web 08/16/2003 Vapor Phase Synthesis of Tungsten Nanowires  

E-Print Network (OSTI)

Vapor phase methods for synthesizing metal nanowires directly without the help of templates have not been studied extensively. Even though there have been few reports with one dating back to 1877 on metal whisker synthesis from the vapor phase, the inconclusive growth mechanism did not lead to any serious developments for nanowires. 1 Recently, there are also two reports with one using hydrogen on tungsten oxide for tungsten nanowires, and another using decomposition of tungsten complexed organic precursors for amorphous carbon sheathed, polycrystalline tungsten nanowires. 2 In this context, we report a novel method in which nucleation and growth of metal oxides at temperatures higher than the oxide decomposition temperatures lead to the respective metal nanowires. Specifically, we demonstrate this concept with the bulk synthesis of tungsten nanowires. The chemical vapor transport of tungsten in the presence of oxygen onto substrates kept at temperatures

Sreeram Vaddiraju; Hari Ch; Mahendra K. Sunkara

2003-01-01T23:59:59.000Z

167

Evaluation of reaction mechanism of coal-metal oxide interactions in chemical-looping combustion  

SciTech Connect

The knowledge of reaction mechanism is very important in designing reactors for chemical-looping combustion (CLC) of coal. Recent CLC studies have considered the more technically difficult problem of reactions between abundant solid fuels (i.e. coal and waste streams) and solid metal oxides. A definitive reaction mechanism has not been reported for CLC reaction of solid fuels. It has often been assumed that the solid/solid reaction is slow and therefore requires that reactions be conducted at temperatures high enough to gasify the solid fuel, or decompose the metal oxide. In contrast, data presented in this paper demonstrates that solid/solid reactions can be completed at much lower temperatures, with rates that are technically useful as long as adequate fuel/metal oxide contact is achieved. Density functional theory (DFT) simulations as well as experimental techniques such as thermo-gravimetric analysis (TGA), flow reactor studies, in situ X-ray photo electron spectroscopy (XPS), in situ X-ray diffraction (XRD) and scanning electron microscopy (SEM) are used to evaluate how the proximal interaction between solid phases proceeds. The data indicate that carbon induces the Cu-O bond breaking process to initiate the combustion of carbon at temperatures significantly lower than the spontaneous decomposition temperature of CuO, and the type of reducing medium in the vicinity of the metal oxide influences the temperature at which the oxygen release from the metal oxide takes place. Surface melting of Cu and wetting of carbon may contribute to the solid-solid contacts necessary for the reaction. (author)

Siriwardane, Ranjani; Richards, George; Poston, James [US Department of Energy, National Energy Technology Laboratory, 3610 Collins Ferry Road, P.O. Box 880, Morgantown, WV 26507-0880 (United States); Tian, Hanjing; Miller, Duane; Simonyi, Thomas [US Department of Energy, National Energy Technology Laboratory, 3610 Collins Ferry Road, P.O. Box 880, Morgantown, WV 26507-0880 (United States); URS, 3610 Collins Ferry Road, Morgantown, WV 26505 (United States)

2010-11-15T23:59:59.000Z

168

Development of hybrid organic-inorganic light emitting diodes using conducting polymers deposited by oxidative chemical vapor deposition process  

E-Print Network (OSTI)

Difficulties with traditional methods of synthesis and film formation for conducting polymers, many of which are insoluble, motivate the development of CVD methods. Indeed, conjugated polymers with rigid linear backbones ...

Chelawat, Hitesh

2010-01-01T23:59:59.000Z

169

Evaluation of Solvent Processes for Chemical Cleaning of Supercritical Waterwalls and Removal of Duplex Oxides Formed by High-Temper ature In Situ Oxidation of Ferritic Steels  

Science Conference Proceedings (OSTI)

Electric Power Research Institute (EPRI) report 1003994, Guidelines for Chemical Cleaning of Conventional Fossil Plant Equipment, published in 2001, provides information pertinent to the chemical cleaning of boiler water and steam touched surfaces. The guidelines consider the needs of both drum type and once-through boilers. After the publication of these guidelines, the presence of in situ duplex oxides was identified on the internal diameter of liquid-like touched surfaces of supercritical waterwalls i...

2010-04-30T23:59:59.000Z

170

The Progress on Low-Cost, High-Quality, High-Temperature Superconducting Tapes Deposited by the Combustion Chemical Vapor Deposition Process  

Science Conference Proceedings (OSTI)

The innovative Combustion Chemical Vapor Deposition (CCVD) process is a non-vacuum technique that is being investigated to enable next generation products in several application areas including high-temperature superconductors (HTS). In combination with the Rolling Assisted Biaxially Textured Substrate (RABiTS) technology, the CCVD process has significant promise to provide low-cost, high-quality lengths of YBCO coated conductor. Over 100 meter lengths of both Ni and Ni-W (3 at. Wt.%) substrates with a surface roughness of 12-18 nm were produced. The CCVD technology has been used to deposit both buffer layer coatings as well as YBCO superconducting layers. Buffer layer architecture of strontium titanate (SrTiO{sub 3}) and ceria (CeO{sub 2}) have been deposited by CCVD on textured nickel substrates and optimized to appropriate thicknesses and microstructures to provide templates for growing PLD YBCO with a J{sub c} of 1.1 MA/cm{sup 2} at 77 K and self-field. The CCVD buffer layers have been scaled to meter plus lengths with good epitaxial uniformity along the length. A short sample cut from one of the lengths enabled high critical current density PLD YBCO. Films of CCVD YBCO superconductors have been grown on single crystal substrates with critical current densities over 1 MA/cm{sup 2}. In addition, superconducting YBCO films with an I{sub c} of 60 A/cm-width (J{sub c} = 1.5 MA/cm{sup 2}) were grown on ORNL RABiTS (CeO{sub 2}/YSZ/Y{sub 2}O{sub 3}/Ni/Ni-3W) using CCVD process.

Shoup, S.S.; White, M.K.; Krebs, S.L.; Darnell, N.; King, A.C.; Mattox, D.S.; Campbell, I.H.; Marken, K.R.; Hong, S.; Czabaj, B.; Paranthaman, M.; Christen, H.M.; Zhai, H.-Y. Specht, E.

2008-06-24T23:59:59.000Z

171

Bench Scale Study of Integrated Chemical Oxidation and Enhanced Bio-Stabilization of Manufactured Gas Plant SoilsBench Scale Study of Integrated Chemical Oxidation and Enhanced Bio-Stabilization of Manufactured Gas Plant Soils  

Science Conference Proceedings (OSTI)

A bench-scale study was conducted to investigate a new remedial approach to treat constituents of concern (COC) that were present in soil from a former manufactured gas plant (MGP) site. The approach combines in situ chemical oxidation, in situ stabilization, and enhanced biodegradation to provide overall degradation/stabilization of COCs that would not be possible using any of the three technologies alone. Sodium persulfate was chosen as the oxidant because it can be activated by ...

2013-07-18T23:59:59.000Z

172

Study of plasma enhanced chemical vapor deposition of boron-doped hydrogenated amorphous silicon thin films and the application to p-channel thin film transistor  

E-Print Network (OSTI)

The material and process characteristics of boron doped hydrogenated amorphous silicon (a-Si:H) thin film deposited by plasma enhanced chemical vapor deposition technique (PECVD) have been studied. The goal is to apply the high quality films deposited at low substrate temperature for devices such as thin film transistors (TFTs). The effect of the deposition parameters such as doping gas concentration, substrate temperature, hydrogen dilution, helium dilution, power density, and pressure at 50 kHz rf frequency on the films' characteristics were analyzed. The films' electrical property was characterized by its dark resistivity. The chemical composition and bonding characteristics were discussed. p-channel TFTs were fabricated with these optimized films. Three different levels of dopant concentrations in the channel were used to detect the dopant effect on the TFT properties. Doping resulted in the increase of film deposition rate. The low film deposition rate at the high temperature deposition corresponds to a dense structured film. The increase of gas phase H? concentration could increase H? etching of the weak bonds in the film, which is consistent with the decrease of the deposition rate. Film's dark conductivity is determined by the atomic B concentration in the film, the substrate temperature, the ion bombardment effect, the surface morphology, and the gas phase and film hydrogen concentration. At high power density and high pressure plasma condition, film with a high deposition rate shows a high conductivity. However, excessive ion bombardment effect, e.g. in powdery plasma region, limits the further increase of the conductivity. Film deposited with He dilution demonstrates a higher conductivity compared to the H? dilution counterpart. This might be attributed to a more effective ion bombardment effect of the former. Powder generation in the plasma significantly affects the conductivity of He diluted film compared to the H? diluted ones, which might be due to the less H? etching effect at the He dilution deposition. The output and transfer characteristics show the normal p-channel TFTs behavior. TFT characteristics, such as mobility, threshold voltage, and on-off current ratio were affected by the doping gas concentration in the channel layer and the deposition process.

Nominanda, Helinda

2004-01-01T23:59:59.000Z

173

Principles of Chemical Vapor Deposition  

Science Conference Proceedings (OSTI)

...as well as the fluid dynamic aspects of the reactor system, to improve process efficiency. Many computational

174

Standard test methods for chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide (Gd2O3) powder  

E-Print Network (OSTI)

1.1 These test methods cover procedures for the chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide powders to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Carbon by Direct CombustionThermal Conductivity C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Total Chlorine and Fluorine by Pyrohydrolysis Ion Selective Electrode C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Loss of Weight on Ignition 7-13 Sulfur by CombustionIodometric Titration Impurity Elements by a Spark-Source Mass Spectrographic C761 Test Methods for Chemical, Mass Spectrometric, Spectrochemical,Nuclear, and Radiochemical Analysis of Uranium Hexafluoride C1287 Test Method for Determination of Impurities In Uranium Dioxide By Inductively Coupled Plasma Mass Spectrometry Gadolinium Content in Gadolinium Oxid...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

175

Chemical kinetic modeling of high pressure propane oxidation and comparison to experimental results. Revision 1  

SciTech Connect

A pressure dependent kinetic mechanism for propane oxidation is developed and compared to experimental data from a high pressure flow reactor. Experimental conditions range from 10--15 atm, 650--800 K, and a residence time of 198 ms for propane-air mixtures at an equivalence ratio of 0.4. The experimental results clearly indicate a negative temperature coefficient (NTC) behavior. The chemistry describing this phenomena is critical in understanding automotive engine knock and cool flame oscillations. Results of the numerical model are compared to a spectrum of stable species profiles sampled from the flow reactor. Rate constants and product channels for the reaction of propyl radicals, hydroperoxy-propyl radicals and important isomers (radicals) with O{sub 2} were estimated using thermodynamic properties, with multifrequency quantum Kassel Theory for k(E) coupled with modified strong collision analysis for fall-off. Results of the chemical kinetic model show an NTC region over nearly the same temperature regime as observed in the experiments. Sensitivity analysis identified the key reaction steps that control the rate of oxidation in the NTC region. The model reasonably simulates the profiles for many of the major and minor species observed in the experiments.

Koert, D.N. [Wichita State Univ., KS (United States). Mechanical Engineering Dept.; Pitz, W.J. [Lawrence Livermore National Lab., CA (United States); Bozzelli, J.W. [New Jersey Inst. of Tech., Newark, NJ (United States). Chemistry and Chemical Engineering Dept.; Cernansky, N.P. [Drexel Univ., Philadelphia, PA (United States). Dept. of Mechanical Engineering and Mechanics

1996-02-01T23:59:59.000Z

176

Chemical Bonding, Interfaces and Defects in Hafnium Oxide/Germanium Oxynitride Gate Stacks on Ge (100)  

SciTech Connect

Correlations among interface properties and chemical bonding characteristics in HfO{sub 2}/GeO{sub x}N{sub y}/Ge MIS stacks were investigated using in-situ remote nitridation of the Ge (100) surface prior to HfO{sub 2} atomic layer deposition (ALD). Ultra thin ({approx}1.1 nm), thermally stable and aqueous etch-resistant GeO{sub x}N{sub y} interfaces layers that exhibited Ge core level photoelectron spectra (PES) similar to stoichiometric Ge{sub 3}N{sub 4} were synthesized. To evaluate GeO{sub x}N{sub y}/Ge interface defects, the density of interface states (D{sub it}) was extracted by the conductance method across the band gap. Forming gas annealed (FGA) samples exhibited substantially lower D{sub it} ({approx} 1 x 10{sup 12} cm{sup -2} eV{sup -1}) than did high vacuum annealed (HVA) and inert gas anneal (IGA) samples ({approx} 1x 10{sup 13} cm{sup -2} eV{sup -1}). Germanium core level photoelectron spectra from similar FGA-treated samples detected out-diffusion of germanium oxide to the HfO{sub 2} film surface and apparent modification of chemical bonding at the GeO{sub x}N{sub y}/Ge interface, which is related to the reduced D{sub it}.

Oshima, Yasuhiro; /Stanford U., Materials Sci. Dept.; Sun, Yun; /SLAC, SSRL; Kuzum, Duygu; /Stanford U.; Sugawara, Takuya; Saraswat, Krishna C.; Pianetta, Piero; /SLAC, SSRL; McIntyre, Paul C.; /Stanford U., Materials Sci. Dept.

2008-10-31T23:59:59.000Z

177

Chemical kinetic modeling of high pressure propane oxidation and comparison to experimental results  

SciTech Connect

A pressure dependent kinetic mechanism for propane oxidation is developed and compared to experimental data from a high pressure flow reactor. The experiment conditions range from 10--15 atm, 650--800 K, and were performed at a residence time of 200 {micro}s for propane-air mixtures at an equivalence ratio of 0.4. The experimental results include data on negative temperature coefficient (NTC) behavior, where the chemistry describing this phenomena is considered critical in understanding automotive engine knock and cool flame oscillations. Results of the numerical model are compared to a spectrum of stable species profiles sampled from the flow reactor. Rate constants and product channels for the reaction of propyl radicals, hydroperoxy-propyl radicals and important isomers with O{sub 2} were estimated using thermodynamic properties, with multifrequency quantum Kassel Theory for k(E) coupled with modified strong collision analysis for fall-off. Results of the chemical kinetic model show an NTC region over nearly the same temperature regime as observed in the experiments. The model simulates properly the production of many of the major and minor species observed in the experiments. Numerical simulations show many of the key reactions involving propylperoxy radicals are in partial equilibrium at 10--15 atm. This indicates that their relative concentrations are controlled by a combination of thermochemistry and rate of minor reaction channels (bleed reactions) rather than primary reaction rates. This suggests that thermodynamic parameters of the oxygenated species, which govern equilibrium concentrations, are important. The modeling results show propyl radical and hydroperoxy-propyl radicals reaction with O{sub 2} proceeds, primarily, through thermalized adducts, not chemically activated channels.

Koert, D.N. [Wichita State Univ., KS (United States). Mechanical Engineering Dept.; Pitz, W.J. [Lawrence Livermore National Lab., CA (United States); Bozzelli, J.W. [New Jersey Inst. of Tech., Newark, NJ (United States). Chemistry and Chemical Engineering Dept.; Cernansky, N.P. [Drexel Univ., Philadelphia, PA (United States). Dept. of Mechanical Engineering and Mechanics

1995-11-08T23:59:59.000Z

178

The Statistical Evolution of Multiple Generations of Oxidation Products in the Photochemical Aging of Chemically Reduced Organic Aerosol  

Science Conference Proceedings (OSTI)

The heterogeneous reaction of hydroxyl radicals (OH) with squalane and bis(2-ethylhexyl) sebacate (BES) particles are used as model systems to examine how distributions of reactionproducts evolve during the oxidation of chemically reduced organic aerosol. A kinetic model of multigenerational chemistry, which is compared to previously measured (squalane) and new(BES) experimental data, reveals that it is the statistical mixtures of different generations of oxidation products that control the average particle mass and elemental composition during thereaction. The model suggests that more highly oxidized reaction products, although initially formed with low probability, play a large role in the production of gas phase reaction products.In general, these results highlight the importance of considering atmospheric oxidation as a statistical process, further suggesting that the underlying distribution of molecules could playimportant roles in aerosol formation as well as in the evolution of key physicochemical properties such as volatility and hygroscopicity.

Wilson, Kevin R.; Smith, Jared D.; Kessler, Sean; Kroll, Jesse H.

2011-10-03T23:59:59.000Z

179

Chemical kinetic study of the oxidation of toluene and related cyclic compounds  

SciTech Connect

Chemical kinetic models of hydrocarbons found in transportation fuels are needed to simulate combustion in engines and to improve engine performance. The study of the combustion of practical fuels, however, has to deal with their complex compositions, which generally involve hundreds of compounds. To provide a simplified approach for practical fuels, surrogate fuels including few relevant components are used instead of including all components. Among those components, toluene, the simplest of the alkyl benzenes, is one of the most prevalent aromatic compounds in gasoline in the U.S. (up to 30%) and is a promising candidate for formulating gasoline surrogates. Unfortunately, even though the combustion of aromatics been studied for a long time, the oxidation processes relevant to this class of compounds are still matter of discussion. In this work, the combustion of toluene is systematically approached through the analysis of the kinetics of some important intermediates contained in its kinetic submechanism. After discussing the combustion chemistry of cyclopentadiene, benzene, phenol and, finally, of toluene, the model is validated against literature experimental data over a wide range of operating conditions.

Mehl, M; Frassoldati, A; Fietzek, R; Faravelli, T; Pitz, W; Ranzi, E

2009-10-01T23:59:59.000Z

180

Effect of temperature and iron-oxide nano-particle inclusions on the ultrasound vaporization pressure of perfluorocarbon droplets for disease detection and therapy  

E-Print Network (OSTI)

Temperature and Iron-Oxide Nano-particle inclusions on the22 1.9.1 Why Iron-Oxide NanoTemperature and Iron-Oxide Nano-particle inclusions on the

Amirriazi, Seyed Saleh

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Chemical and Radiochemical Composition of Thermally Stabilized Plutonium Oxide from the Plutonium Finishing Plant Considered as Alternate Feedstock for the Mixed Oxide Fuel Fabrication Facility  

Science Conference Proceedings (OSTI)

Eighteen plutonium oxide samples originating from the Plutonium Finishing Plant (PFP) on the Hanford Site were analyzed to provide additional data on the suitability of PFP thermally stabilized plutonium oxides and Rocky Flats oxides as alternate feedstock to the Mixed Oxide Fuel Fabrication Facility (MFFF). Radiochemical and chemical analyses were performed on fusions, acid leaches, and water leaches of these 18 samples. The results from these destructive analyses were compared with nondestructive analyses (NDA) performed at PFP and the acceptance criteria for the alternate feedstock. The plutonium oxide materials considered as alternate feedstock at Hanford originated from several different sources including Rocky Flats oxide, scrap from the Remote Mechanical C-Line (RMC) and the Plutonium Reclamation Facility (PRF), and materials from other plutonium conversion processes at Hanford. These materials were received at PFP as metals, oxides, and solutions. All of the material considered as alternate feedstock was converted to PuO2 and thermally stabilized by heating the PuO2 powder at 950 C in an oxidizing environment. The two samples from solutions were converted to PuO2 by precipitation with Mg(OH)2. The 18 plutonium oxide samples were grouped into four categories based on their origin. The Rocky Flats oxide was divided into two categories, low- and high-chloride Rocky Flats oxides. The other two categories were PRF/RMC scrap oxides, which included scrap from both process lines and oxides produced from solutions. The two solution samples came from samples that were being tested at Pacific Northwest National Laboratory because all of the plutonium oxide from solutions at PFP had already been processed and placed in 3013 containers. These samples originated at the PFP and are from plutonium nitrate product and double-pass filtrate solutions after they had been thermally stabilized. The other 16 samples originated from thermal stabilization batches before canning at PFP. Samples varied in appearance depending on the original source of material. Rocky Flats items were mostly dark olive green with clumps that crushed easily with a mortar and pestle. PRF/RMC items showed more variability. These items were mostly rust colored. One sample contained white particles that were difficult to crush, and another sample was a dark grey with a mixture of fines and large, hard fragments. The appearance and feel of the fragments indicated they might be an alloy. The color of the solution samples was indicative of the impurities in the sample. The double-pass filtrate solution was a brown color indicative of the iron impurities in the sample. The other solution sample was light gray in color. Radiochemical analyses, including thermal ionization mass spectrometry (TIMS), alpha and gamma energy analysis (AEA and GEA), and kinetic phosphorescence analysis (KPA), indicate that these materials are all weapons-grade plutonium with consistent plutonium isotopics. A small amount of uranium (Rocky Flats materials was Cl-, but the PRF/RMC samples had significant quantities of all of the primary anions observed. Prompt gamma measurements provide a representative analysis of the Cl- concentration in the bulk material. The primary anions observed in the solution samples were NO3-, and PO43-. The concentration of these anions did not exceed the mixed oxide (MOX) specification limits. Cations that exceeded the MOX specification limits included Cr, Fe, Ni, Al, Cu, and Si. All of the samples exceeded at least the 75% specification limit in one element.

Tingey, Joel M.; Jones, Susan A.

2005-07-01T23:59:59.000Z

182

Chemical and Radiochemical Composition of Thermally Stabilized Plutonium Oxide from the Plutonium Finishing Plant Considered as Alternate Feedstock for the Mixed Oxide Fuel Fabrication Facility  

SciTech Connect

Eighteen plutonium oxide samples originating from the Plutonium Finishing Plant (PFP) on the Hanford Site were analyzed to provide additional data on the suitability of PFP thermally stabilized plutonium oxides and Rocky Flats oxides as alternate feedstock to the Mixed Oxide Fuel Fabrication Facility (MFFF). Radiochemical and chemical analyses were performed on fusions, acid leaches, and water leaches of these 18 samples. The results from these destructive analyses were compared with nondestructive analyses (NDA) performed at PFP and the acceptance criteria for the alternate feedstock. The plutonium oxide materials considered as alternate feedstock at Hanford originated from several different sources including Rocky Flats oxide, scrap from the Remote Mechanical C-Line (RMC) and the Plutonium Reclamation Facility (PRF), and materials from other plutonium conversion processes at Hanford. These materials were received at PFP as metals, oxides, and solutions. All of the material considered as alternate feedstock was converted to PuO2 and thermally stabilized by heating the PuO2 powder at 950 C in an oxidizing environment. The two samples from solutions were converted to PuO2 by precipitation with Mg(OH)2. The 18 plutonium oxide samples were grouped into four categories based on their origin. The Rocky Flats oxide was divided into two categories, low- and high-chloride Rocky Flats oxides. The other two categories were PRF/RMC scrap oxides, which included scrap from both process lines and oxides produced from solutions. The two solution samples came from samples that were being tested at Pacific Northwest National Laboratory because all of the plutonium oxide from solutions at PFP had already been processed and placed in 3013 containers. These samples originated at the PFP and are from plutonium nitrate product and double-pass filtrate solutions after they had been thermally stabilized. The other 16 samples originated from thermal stabilization batches before canning at PFP. Samples varied in appearance depending on the original source of material. Rocky Flats items were mostly dark olive green with clumps that crushed easily with a mortar and pestle. PRF/RMC items showed more variability. These items were mostly rust colored. One sample contained white particles that were difficult to crush, and another sample was a dark grey with a mixture of fines and large, hard fragments. The appearance and feel of the fragments indicated they might be an alloy. The color of the solution samples was indicative of the impurities in the sample. The double-pass filtrate solution was a brown color indicative of the iron impurities in the sample. The other solution sample was light gray in color. Radiochemical analyses, including thermal ionization mass spectrometry (TIMS), alpha and gamma energy analysis (AEA and GEA), and kinetic phosphorescence analysis (KPA), indicate that these materials are all weapons-grade plutonium with consistent plutonium isotopics. A small amount of uranium (<0.14 wt%) is also present in these samples. The isotopic composition of the uranium varied widely but was consistent among each category of material. The primary water-soluble anions in these samples were Cl-, NO3-, SO42-, and PO43-. The only major anion observed in the Rocky Flats materials was Cl-, but the PRF/RMC samples had significant quantities of all of the primary anions observed. Prompt gamma measurements provide a representative analysis of the Cl- concentration in the bulk material. The primary anions observed in the solution samples were NO3-, and PO43-. The concentration of these anions did not exceed the mixed oxide (MOX) specification limits. Cations that exceeded the MOX specification limits included Cr, Fe, Ni, Al, Cu, and Si. All of the samples exceeded at least the 75% specification limit in one element.

Tingey, Joel M.; Jones, Susan A.

2005-07-01T23:59:59.000Z

183

Selective Chemical Vapor Deposition of Heavily Boron Doped Silicon-Germanium Films from Disilane, Germane and Chlorine for Source/ Drain Junctions of Nanoscale CMOS.  

E-Print Network (OSTI)

??As metal-oxide semiconductor field effect transistors (MOSFETs) are scaled for higher speed and reduced power, new challenges are imposed on the source/drain junctions and their… (more)

Pesovic, Nemanja

2002-01-01T23:59:59.000Z

184

Low-band-gap, amorphous-silicon-based alloys by chemical vapor deposition: Annual subcontract report, 1 October 1985-31 January 1986  

DOE Green Energy (OSTI)

This research was conducted to determine the potential of photochemical vapor deposition (photo-CVD) for producing high-quality, low-band-gap amorphous silicon germanium alloys for use in high-efficiency, multijunction, thin-film photovoltaic solar cells. A photo-CVD reactor for mercury-sensitized photolysis of silane-germane and disilane-germane mixtures was developed. Alloy thin films of undoped a-Si/sub 1-x/Ge/sub x/:H were deposited using mercury vapor mixed with SiH/sub 4/ or Si/sub 2/H/sub 6/, GeH/sub 4/, and diluent gas of Ar, He, or H/sub 2/. Materials properties were characterized by measurements of Ge content, optical transmission and reflection, and dark and photo-conductivity. Opto-electronic properties of photo-CVD a-Si/sub 1-x/Ge/sub x/:H were found to be comparable to glow discharge and sputtered materials. Moreover, p-i-n solar cells with low-band-gap i-layers were able to be fabricated by photo-CVD.

Baron, B.N.; Jackson, S.C.

1986-12-01T23:59:59.000Z

185

Fluorine compounds for doping conductive oxide thin films  

DOE Patents (OSTI)

Methods of forming a conductive fluorine-doped metal oxide layer on a substrate by chemical vapor deposition are described. The methods may include heating the substrate in a processing chamber, and introducing a metal-containing precursor and a fluorine-containing precursor to the processing chamber. The methods may also include adding an oxygen-containing precursor to the processing chamber. The precursors are reacted to deposit the fluorine-doped metal oxide layer on the substrate. Methods may also include forming the conductive fluorine-doped metal oxide layer by plasma-assisted chemical vapor deposition. These methods may include providing the substrate in a processing chamber, and introducing a metal-containing precursor, and a fluorine-containing precursor to the processing chamber. A plasma may be formed that includes species from the metal-containing precursor and the fluorine-containing precursor. The species may react to deposit the fluorine-doped metal oxide layer on the substrate.

Gessert, Tim; Li, Xiaonan; Barnes, Teresa M; Torres, Jr., Robert; Wyse, Carrie L

2013-04-23T23:59:59.000Z

186

Solar Thermo-Chemical Splitting of Carbon Dioxide by Metal Oxide ...  

Science Conference Proceedings (OSTI)

Presentation Title, Solar Thermo-Chemical Splitting of Carbon Dioxide by Metal ... which can split carbon dioxide as well as water molecules by abstracting ...

187

Continuum and Quantum-Chemical Modeling of Oxygen Reduction on the Cathode in a Solid Oxide Fuel Cell  

DOE Green Energy (OSTI)

Solid oxide fuel cells (SOFCs) have several advantages over other types of fuels cells such as high-energy efficiency and excellent fuel flexibility. To be economically competitive, however, new materials with extraordinary transport and catalytic properties must be developed to dramatically improve the performance while reducing the cost. This article reviews recent advancements in understanding oxygen reduction on various cathode materials using phenomenological and quantum chemical approaches in order to develop novel cathode materials with high catalytic activity toward oxygen reduction. We summarize a variety of results relevant to understanding the interactions between O2 and cathode materials at the molecular level as predicted using quantum-chemical cal-culations and probed using in situ surface vibrational spectroscopy. It is hoped that this in-depth understanding may provide useful insights into the design of novel cath-ode materials for a new generation of SOFCs.

Choi, Yongman; Mebane, David S.; Wang, Jeng-Han; Liu, Meilin

2009-10-08T23:59:59.000Z

188

The aging of organic aerosol in the atmosphere : chemical transformations by heterogeneous oxidation  

E-Print Network (OSTI)

The immense chemical complexity of atmospheric organic particulate matter ("aerosol") has left the general field of condensed-phase atmospheric organic chemistry relatively under-developed when compared with either gas-phase ...

Kessler, Sean Herbert

2013-01-01T23:59:59.000Z

189

Physicochemical Characterization of Capstone Depleted Uranium Aerosols III: Morphologic and Chemical Oxide Analyses  

Science Conference Proceedings (OSTI)

The impact of depleted uranium (DU) penetrators against an armored target causes erosion and fragmentation of the penetrators, the extent of which is dependent on the thickness and material composition of the target. Vigorous oxidation of the DU particles and fragments creates an aerosol of DU oxide particles and DU particle agglomerations combined with target materials. Aerosols from the Capstone DU aerosol study, in which vehicles were perforated by DU penetrators, were evaluated for their oxidation states using X-ray diffraction (XRD) and particle morphologies using scanning electron microscopy/energy dispersive spectrometry (SEM/EDS). The oxidation state of a DU aerosol is important as it offers a clue to its solubility in lung fluids. The XRD analysis showed that the aerosols evaluated were a combination primarily of U3O8 (insoluble) and UO3 (relatively more soluble) phases, though intermediate phases resembling U4O9 and other oxides were prominent in some samples. Analysis of particle residues in the micrometer-size range by SEM/EDS provided microstructural information such as phase composition and distribution, fracture morphology, size distribution, and material homogeneity. Observations from SEM analysis show a wide variability in the shapes of the DU particles. Some of the larger particles appear to have been fractured (perhaps as a result of abrasion and comminution); others were spherical, occasionally with dendritic or lobed surface structures. Amorphous conglomerates containing metals other than uranium were also common, especially with the smallest particle sizes. A few samples seemed to contain small chunks of nearly pure uranium metal, which were verified by EDS to have a higher uranium content exceeding that expected for uranium oxides. Results of the XRD and SEM/EDS analyses were used in other studies described in this issue of The Journal of Health Physics to interpret the results of lung solubility studies and in selecting input parameters for dose assessments.

Krupka, Kenneth M.; Parkhurst, MaryAnn; Gold, Kenneth; Arey, Bruce W.; Jenson, Evan D.; Guilmette, Raymond A.

2009-03-01T23:59:59.000Z

190

A full-scale demonstration of in situ chemical oxidation through recirculation at the X-701B site  

Science Conference Proceedings (OSTI)

In 1996, researchers at Oak Ridge National Laboratory (ORNL) proposed an oxidant delivery technique involving injection and recirculation of the oxidant solution into a contaminated aquifer through multiple horizontal and vertical wells. This technique would be applicable to saturated, hydraulically conductive formations. In the spring of 1997, the Department of Energy (DOE) at the Portsmouth Gaseous Diffusion Plant (PORTS) agreed to collaborate with the DOE`s Subsurface Contaminants Focus Area to conduct a field-scale treatability study using in situ chemical oxidation through recirculation (ISCOR). PORTS agreed to support the demonstration at the X-701B site where the technology can potentially be used to remediate TCE-contaminated groundwater and sediments. The ISCOR field demonstration took advantage of existing infrastructure and extensive site characterization data generated from previous field demonstrations at X-701B. The field test was implemented using a pair of previously installed horizontal wells that transect an area of DNAPL contamination. Groundwater was extracted from one horizontal well, pumped to an existing pump and treat facility, dosed with KMnO{sub 4}, and re-injected into a parallel horizontal well approximately 90 ft away. The field demonstration lasted approximately one month. Treatment effectiveness was determined by comparing contaminant levels in pre-treatment, during, and post-treatment groundwater samples and pre- and post-treatment soil samples.

West, O.R.; Cline, S.R.; Holden, W.L.; Gardner, F.G.; Schlosser, B.M.; Thate, J.E.; Pickering, D.A. [Oak Ridge National Lab., TN (United States); Houk, T.C. [Lockheed Martin Energy Systems Technology Applications, Piketon, OH (United States)

1997-12-01T23:59:59.000Z

191

New manganese catalyst for light alkane oxidation  

DOE Patents (OSTI)

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

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

1994-01-01T23:59:59.000Z

192

Synthesis of graphene nanosheets via oxalic acid-induced chemical reduction of exfoliated graphite oxide  

SciTech Connect

Preparing high-quality graphene through reduction of graphene oxide (GO) by oxalic acid is demonstrated in this paper. Transmission electron microscopy, scanning electron microscopy, Fourier transform infrared spectrometry, X-ray diffraction and Raman spectrometry were taken to confirm the reduction of GO and the formation of graphene under these mild conditions. Thermogravimetric analysis and conductivity measurements further testify the excellent thermal stability and conductivity of the obtained graphene. A possible mechanism for the reduction process was also proposed. Furthermore, a Pt-graphene composite was fabricated on a glassy carbon electrode and excellent electrocatalytic activity towards methanol oxidation was observed. With advantages of low toxicity, simple purification process and high quality of the product, oxalic acid provides a feasible route to prepare graphene from GO under mild conditions, thus facilitating the use of graphene-based materials for large-scale applications.

Song, Peng; Zhang, Xiao-Yan; Sun, Mingxun; Cui, Xiao-Li; Lin, Yuehe

2012-02-01T23:59:59.000Z

193

LNG fire and vapor control system technologies  

SciTech Connect

This report provides a review of fire and vapor control practices used in the liquefied natural gas (LNG) industry. Specific objectives of this effort were to summarize the state-of-the-art of LNG fire and vapor control; define representative LNG facilities and their associated fire and vapor control systems; and develop an approach for a quantitative effectiveness evaluation of LNG fire and vapor control systems. In this report a brief summary of LNG physical properties is given. This is followed by a discussion of basic fire and vapor control design philosophy and detailed reviews of fire and vapor control practices. The operating characteristics and typical applications and application limitations of leak detectors, fire detectors, dikes, coatings, closed circuit television, communication systems, dry chemicals, water, high expansion foam, carbon dioxide and halogenated hydrocarbons are described. Summary descriptions of a representative LNG peakshaving facility and import terminal are included in this report together with typical fire and vapor control systems and their locations in these types of facilities. This state-of-the-art review identifies large differences in the application of fire and vapor control systems throughout the LNG industry.

Konzek, G.J.; Yasutake, K.M.; Franklin, A.L.

1982-06-01T23:59:59.000Z

194

Mercury Vapor Pressure Correlation  

Science Conference Proceedings (OSTI)

An apparent difference between the historical mercury vapor concentration equations used by the mercury atmospheric measurement community ...

2012-10-09T23:59:59.000Z

195

A Pilot Scale Evaluation of Surfactant-Enhanced In Situ Chemical Oxidation (S-ISCO) Technology: A Field Application at a Former Manu factured Gas Plant  

Science Conference Proceedings (OSTI)

Former manufactured gas plant (MGP) sites commonly contain areas where coal tar has been released, potentially existing in several phases including non-aqueous phase liquid (NAPL) in portions of the subsurface site soils. This report describes a field-based pilot scale study of an in situ oxidation technology called Surfactant-Enhanced In Situ Chemical Oxidation (S-ISCO), which was developed by VeruTEK Technologies, Inc.BackgroundCoal tar can remain as ...

2013-10-29T23:59:59.000Z

196

Synthesis and characterization of chloride doped polyaniline by bulk oxidative chemical polymerization.Doping effect on electrical conductivity  

E-Print Network (OSTI)

Conductive polymers or "organic metals" are highly engineered nanostructured materials made from organic building blocks. They are candidates as molecular wires for nanotechnology applications in molecular electronics. The conduction in these polymers is due to the presence of delocalized molecular orbitals. In this work, we present the synthesis of chloride doped polyaniline by bulk oxidative chemical polymerization using a solid aniline salt as a monomer instead of liquid aniline to diminish toxic hazards. The FTIR and UV-visible spectra confirmed the expected structure of the polymer. The electrical conductivity measured using a four-probe method was 1.7 S/cm. The dependence of impedance modulus on frequency was measured using an HP impedance analyzer in the range 10 kHz-13 MHz. The influence of doping and the preparation temperature on the electrical conductivity were also investigated.

Yomen Atassi; Mohammad Tally; Mazen Ismail

2008-09-21T23:59:59.000Z

197

Subscriber access provided by STANFORD UNIV GREEN LIBR Nano Letters is published by the American Chemical Society. 1155 Sixteenth  

E-Print Network (OSTI)

) was grown by hot wire chemical vapor deposition (HWCVD) on an indium-tin-oxide (ITO) coated glass substrate 94305, and National Renewable Energy Laboratory, 1617 Cole BouleVard., Golden, Colorado 80401 Received, Stanford University. National Renewable Energy Laboratory. NANO LETTERS 2009 Vol. 9, No. 1 279-282 10

Fan, Shanhui

198

Subscriber access provided by STANFORD UNIV GREEN LIBR Nano Letters is published by the American Chemical Society. 1155 Sixteenth  

E-Print Network (OSTI)

(Figure 1a) was grown by hot wire chemical vapor deposition (HWCVD) on an indium-tin-oxide (ITO) coated of Chemistry, Stanford UniVersity, Stanford, California 94305, and National Renewable Energy Laboratory, 1617, Stanford University. | Department of Chemistry, Stanford University. National Renewable Energy Laboratory

Cui, Yi

199

Final Technical Report - High-Performance, Oxide-Dispersion-Strengthened Tubes for Production of Ethylene adn Other Industrial Chemicals  

SciTech Connect

This project was undertaken by Michigan Technological University and Special Metals Corporation to develop creep-resistant, coking-resistant oxide-dispersion-strengthened (ODS) tubes for use in industrial-scale ethylene pyrolysis and steam methane reforming operations. Ethylene pyrolysis tubes are exposed to some of the most severe service conditions for metallic materials found anywhere in the chemical process industries, including elevated temperatures, oxidizing atmospheres and high carbon potentials. During service, hard deposits of carbon (coke) build up on the inner wall of the tube, reducing heat transfer and restricting the flow of the hydrocarbon feedstocks. About every 20 to 60 days, the reactor must be taken off-line and decoked by burning out the accumulated carbon. This decoking costs on the order of $9 million per year per ethylene plant, accelerates tube degradation, and requires that tubes be replaced about every 5 years. The technology developed under this program seeks to reduce the energy and economic cost of coking by creating novel bimetallic tubes offering a combination of improved coking resistance, creep resistance and fabricability not available in current single-alloy tubes. The inner core of this tube consists of Incoloy(R) MA956, a commercial ferritic Fe-Cr-Al alloy offering a 50% reduction in coke buildup combined with improved carburization resistance. The outer sheath consists of a new material - oxide dispersion strengthened (ODS) Alloy 803(R) developed under the program. This new alloy retains the good fireside environmental resistance of Alloy 803, a commercial wrought alloy currently used for ethylene production, and provides an austenitic casing to alleviate the inherently-limited fabricability of the ferritic Incoloy(R) MA956 core. To provide mechanical compatibility between the two alloys and maximize creep resistance of the bimetallic tube, both the inner Incoloy(R) MA956 and the outer ODS Alloy 803 are oxide dispersion strengthened materials produced using mechanical alloying technology. To minimize cost, the bimetallic tube is produced by direct powder co-extrusion. This technology has potential for domestic energy savings of up to 4.1 trillion BTU/year (4.3 x 1015J/year) and a reduction of 370,000 tons (340,000 tonnes) of CO2 emissions in short-residence-time ethylene furnaces. This represents an energy savings and CO2 emissions reduction of about 3.3%. If the technology is also applied to other types of ethylene pyrolysis furnaces, total energy savings and CO2 emissions reductions could increase by up to five times. The work involved: Developing powder and consolidation processing protocols to produce an oxide-dispersion strengthened variant of Alloy 803 exhibiting creep strength comparable to Incoloy? Alloy MA956, Developing a direct powder co-extrusion protocol for fabricating co-extruded bimetallic Incoloy? Alloy MA956 / ODS Alloy 803 tubes, Characterizing the properties of the ODS Alloy 803 material, the welding characteristics of the bimetallic tubes, and the coking characteristics of the Incoloy? MA956 alloy, and Documenting the potential energy savings and user requirements for these bimetallic pyrolysis furnace tubes. The project demonstrated that oxide dispersion strengthened Alloy 803 can be produced successfully using conventional mechanical alloying technology. The oxide dispersion strengthened bimetallic radiant coil technology explored under this program has significant potential for energy savings and productivity improvements for domestic ethylene producers. In today's competitive market, however, domestic furnace manufacturers and ethylene producers appear reluctant to pay any cost premium for higher-performance coil materials offering either higher temperature capabilities or longer service life. Interest in oxide dispersion strengthened radiant coils is likely to increase if furnace and ethylene producers begin to focus more on increasing tube wall temperatures to improve productivity.

McKimpson, Marvin G.

2006-04-06T23:59:59.000Z

200

Adsorption of TiCl[sub 4], SiH[sub 4], and HCl on Si(100): Application to TiSi[sub 2] chemical vapor deposition and Si etching  

SciTech Connect

The interactions of TiCl[sub 4], SiH[sub 4], and HCl with Si(100) have been investigated by temperature programmed desorption (TPD) with the goal of better understanding the initial stages of TiSi[sub 2] chemical vapor deposition for circuit metallization and wafer etching with HCl/H[sub 2]. Coadsorption experiments with TiCl[sub 4] and SiH[sub 4] show that under most conditions H[sub 2] and SiCl[sub 2] are the main desorption products, with Ti being left behind on the surface. HCl is a minor product. However, at sufficiently low exposures of either TiCl[sub 4] or SiH[sub 4], the desorption of SiCl[sub 2] or H[sub 2], respectively, is inhibited in favor of HCl. A kinetic model involving formation of an HCl complex at defects has been formulated which explains the results quantitatively. HCl adsorption gives rise to the principal desorption products SiCl[sub 2] and H[sub 2], with HCl as a minor product. The kinetic behavior can also be explained quantitatively with the proposed model. Implications for TiSi[sub 2] growth are discussed with reference to possible growth temperatures and source gas pressures. The mechanism for etching by HCl is further elucidated.

Mendicino, M.A.; Seebauer, E.G. (Univ. of Illinois, Urbana, IL (United States). Dept. of Chemical Engineering)

1993-06-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Microwave Plasma Chemical Vapor Deposition of Carbon Coatings on LiNi1/3Co1/3Mn1/3O2 for Li-Ion Battery Composite Cathodes  

DOE Green Energy (OSTI)

In this paper, we report results of a novel synthesis method of thin film conductive carbon coatings on LiNi{sub 1/3}Co{sub 1/3}Mn{sub 1/3}O{sub 2} cathode active material powders for lithium-ion batteries. Thin layers of graphitic carbon were produced from a solid organic precursor, anthracene, by a one-step microwave plasma chemical vapor deposition (MPCVD) method. The structure and morphology of the carbon coatings were examined using SEM, TEM, and Raman spectroscopy. The composite LiNi{sub 1/3}Co{sub 1/3}Mn{sub 1/3}O{sub 2} electrodes were electrochemically tested in lithium half coin cells. The composite cathodes made of the carbon-coated LiNi{sub 1/3}Co{sub 1/3}Mn{sub 1/3}O{sub 2} powder showed superior electrochemical performance and increased capacity compared to standard composite LiNi{sub 1/3}Co{sub 1/3}Mn{sub 1/3}O{sub 2} electrodes.

Doeff, M.M.; Kostecki, R.; Marcinek, M.; Wilcoc, J.D.

2008-12-10T23:59:59.000Z

202

Compliant alkali silicate sealing glass for solid oxide fuel cell applications: thermal cycle stability and chemical compatibility  

Science Conference Proceedings (OSTI)

An alkali silicate glass (SCN-1) is currently being evaluated as a candidate sealing glass for solid oxide fuel (SOFC) applications. The glass containing ~17 mole% alkalis (K2O and Na2O) remains vitreous and compliant during SOFC operation, unlike conventional SOFC sealing glasses, which experience substantial devitrification after the sealing process. The non-crystallizing compliant sealing glass has lower glass transition and softening temperatures since the microstructure remains glassy without significant crystallite formation, and hence can relieve or reduce residual stresses and also has the potential for crack healing. Sealing approaches based on compliant glass will also need to satisfy all the mechanical, thermal, chemical, physical, and electrical requirements for SOFC applications, not only in bulk properties but also at sealing interfaces. In this first of a series of papers we will report the thermal cycle stability of the glass when sealed between two SOFC components, i.e., a NiO/YSZ anode supported YSZ bilayer and a coated ferritic stainless steel interconnect material. High temperature leak rates were monitored versus thermal cycles between 700-850oC using back pressures ranging from 0.2 psi to 1.0 psi. Isothermal stability was also evaluated in a dual environment consisting of flowing dilute H2 fuel versus ambient air. In addition, chemical compatibility at the alumina and YSZ interfaces was examined with scanning electron microscopy and energy dispersive spectroscopy. The results shed new light on the topic of SOFC glass seal development.

Chou, Y. S.; Thomsen, Edwin C.; Williams, Riley T.; Choi, Jung-Pyung; Canfield, Nathan L.; Bonnett, Jeff F.; Stevenson, Jeffry W.; Shyam, Amit; Lara-Curzio, E.

2011-03-01T23:59:59.000Z

203

EVALUATION OF PLUTONIUM OXIDE DESTRUCTIVE CHEMICAL ANALYSES FOR VALIDITY OF ORIGINAL 3013 CONTAINER BINNING  

SciTech Connect

The surveillance program for 3013 containers is based, in part, on the separation of containers into various bins related to potential container failure mechanisms. The containers are assigned to bins based on moisture content and pre-storage estimates of content chemistry. While moisture content is measured during the packaging of each container, chemistry estimates are made by using a combination of process knowledge, packaging data and prompt gamma analyses to establish the moisture and chloride/fluoride content of the materials. Packages with high moisture and chloride/fluoride contents receive more detailed surveillances than packages with less chloride/fluoride and/or moisture. Moisture verification measurements and chemical analyses performed during the surveillance program provided an opportunity to validate the binning process. Validation results demonstrated that the binning effort was generally successful in placing the containers in the appropriate bin for surveillance and analysis.

Mcclard, J.; Kessinger, G.

2010-02-01T23:59:59.000Z

204

Hybrid deposition of thin film solid oxide fuel cells and electrolyzers  

DOE Patents (OSTI)

The use of vapor deposition techniques enables synthesis of the basic components of a solid oxide fuel cell (SOFC); namely, the electrolyte layer, the two electrodes, and the electrolyte-electrode interfaces. Such vapor deposition techniques provide solutions to each of the three critical steps of material synthesis to produce a thin film solid oxide fuel cell (TFSOFC). The electrolyte is formed by reactive deposition of essentially any ion conducting oxide, such as defect free, yttria stabilized zirconia (YSZ) by planar magnetron sputtering. The electrodes are formed from ceramic powders sputter coated with an appropriate metal and sintered to a porous compact. The electrolyte-electrode interface is formed by chemical vapor deposition of zirconia compounds onto the porous electrodes to provide a dense, smooth surface on which to continue the growth of the defect-free electrolyte, whereby a single fuel cell or multiple cells may be fabricated. 8 figs.

Jankowski, A.F.; Makowiecki, D.M.; Rambach, G.D.; Randich, E.

1998-05-19T23:59:59.000Z

205

Hybrid deposition of thin film solid oxide fuel cells and electrolyzers  

DOE Patents (OSTI)

The use of vapor deposition techniques enables synthesis of the basic components of a solid oxide fuel cell (SOFC); namely, the electrolyte layer, the two electrodes, and the electrolyte-electrode interfaces. Such vapor deposition techniques provide solutions to each of the three critical steps of material synthesis to produce a thin film solid oxide fuel cell (TFSOFC). The electrolyte is formed by reactive deposition of essentially any ion conducting oxide, such as defect free, yttria stabilized zirconia (YSZ) by planar magnetron sputtering. The electrodes are formed from ceramic powders sputter coated with an appropriate metal and sintered to a porous compact. The electrolyte-electrode interface is formed by chemical vapor deposition of zirconia compounds onto the porous electrodes to provide a dense, smooth surface on which to continue the growth of the defect-free electrolyte, whereby a single fuel cell or multiple cells may be fabricated.

Jankowski, Alan F. (Livermore, CA); Makowiecki, Daniel M. (Livermore, CA); Rambach, Glenn D. (Livermore, CA); Randich, Erik (Endinboro, PA)

1999-01-01T23:59:59.000Z

206

Hybrid deposition of thin film solid oxide fuel cells and electrolyzers  

DOE Patents (OSTI)

The use of vapor deposition techniques enables synthesis of the basic components of a solid oxide fuel cell (SOFC); namely, the electrolyte layer, the two electrodes, and the electrolyte-electrode interfaces. Such vapor deposition techniques provide solutions to each of the three critical steps of material synthesis to produce a thin film solid oxide fuel cell (TFSOFC). The electrolyte is formed by reactive deposition of essentially any ion conducting oxide, such as defect free, yttria stabilized zirconia (YSZ) by planar magnetron sputtering. The electrodes are formed from ceramic powders sputter coated with an appropriate metal and sintered to a porous compact. The electrolyte-electrode interface is formed by chemical vapor deposition of zirconia compounds onto the porous electrodes to provide a dense, smooth surface on which to continue the growth of the defect-free electrolyte, whereby a single fuel cell or multiple cells may be fabricated.

Jankowski, Alan F. (Livermore, CA); Makowiecki, Daniel M. (Livermore, CA); Rambach, Glenn D. (Livermore, CA); Randich, Erik (Endinboro, PA)

1998-01-01T23:59:59.000Z

207

Evaluation of a sulfur oxide chemical heat storage process for a steam solar electric plant  

DOE Green Energy (OSTI)

The purpose of this study was to develop and evaluate technically feasible process configurations for the use of the sulfur oxide system, 2 SO/sub 3/ reversible 2 SO/sub 2/ + O/sub 2/, in energy storage. The storage system is coupled with a conventional steam-cycle power plant. Heat for both the power plant and the storage system is supplied during sunlit hours by a field of heliostats focussed on a central solar receiver. When sunlight is not available, the storage system supplies the heat to operate the power plant. A technically feasible, relatively efficient configuration is proposed for incorporating this type of energy storage system into a solar power plant. Complete material and energy balances are presented for a base case that represents a middle range of expected operating conditions. Equipment sizes and costs were estimated for the base case to obtain an approximate value for the cost of the electricity that would be produced from such an installation. In addition, the sensitivity of the efficiency of the system to variations in design and operating conditions was determined for the most important parameters and design details. In the base case the solar tower receives heat at a net rate of 230 MW(t) for a period of eight hours. Daytime electricity is about 30 MW(e). Nighttime generation is at a rate of about 15 MW(e) for a period of sixteen hours. The overall efficiency of converting heat into electricity is about 26%. The total capital cost for the base case is estimated at about $68 million, of which about 67% is for the tower and heliostats, 11% is for the daytime power plant, and 22% is for the storage system. The average cost of the electricity produced for the base case is estimated to be about 11 cents/kW(e)-hr.

Dayan, J.; Lynn, S.; Foss, A.

1979-07-01T23:59:59.000Z

208

Vapor spill monitoring method  

DOE Patents (OSTI)

Method for continuous sampling of liquified natural gas effluent from a spill pipe, vaporizing the cold liquified natural gas, and feeding the vaporized gas into an infrared detector to measure the gas composition. The apparatus utilizes a probe having an inner channel for receiving samples of liquified natural gas and a surrounding water jacket through which warm water is flowed to flash vaporize the liquified natural gas.

Bianchini, Gregory M. (Livermore, CA); McRae, Thomas G. (Livermore, CA)

1985-01-01T23:59:59.000Z

209

Chemically capping copper with cobalt  

Science Conference Proceedings (OSTI)

Amorphous cobalt-phosphorus alloy is grown on SiO"2 and Cu by chemical vapor deposition from dicobaltoctacarbonyl and trimethylphosphine at 250^oC, 300^oC, and 350^oC. Film properties most relevant to adoption into back-end chip fabrication have been ... Keywords: Chemical vapor deposition, Cobalt alloys, Selective deposition

Lucas B. Henderson; John G. Ekerdt

2010-04-01T23:59:59.000Z

210

Chemical vapor deposition growth. Annual report  

DOE Green Energy (OSTI)

The formal objective of the contract is development of CVD techniques for producing large areas of Si sheet on inexpensive substrate materials, with sheet properties suitable for fabricating solar cells. The techniques developed are to be directed toward (1) minimum-cost processing, (2) production of sheet having properties adequate to result in cells with terrestrial array efficiency of 10 percent or more, and (3) eventual scale-up to large-quantity production. (WDM)

Ruth, R.P.; Manasevit, H.M.; Johnson, R.E.; Kenty, J.L.; Moudy, L.A.; Simpson, W.I.; Yang, J.J.

1976-10-01T23:59:59.000Z

211

Microwave plasma chemical vapor deposition of nano ...  

radiation was also applied for rapid heating of solutions ... of the system was designed to generate Ar ... model JEOL 200CX), and scanning electron ...

212

Urania vapor composition at very high temperatures  

SciTech Connect

Due to the chemically unstable nature of uranium dioxide its vapor composition at very high temperatures is, presently, not sufficiently studied though more experimental knowledge is needed for risk assessment of nuclear reactors. We used laser vaporization coupled to mass spectrometry of the produced vapor to study urania vapor composition at temperatures in the vicinity of its melting point and higher. The very good agreement between measured melting and freezing temperatures and between partial pressures measured on the temperature increase and decrease indicated that the change in stoichiometry during laser heating was very limited. The evolutions with temperature (in the range 2800-3400 K) of the partial pressures of the main vapor species (UO{sub 2}, UO{sub 3}, and UO{sub 2}{sup +}) were compared with theoretically predicted evolutions for equilibrium noncongruent gas-liquid and gas-solid phase coexistences and showed very good agreement. The measured main relative partial pressure ratios around 3300 K all agree with calculated values for total equilibrium between condensed and vapor phases. It is the first time the three main partial pressure ratios above stoichiometric liquid urania have been measured at the same temperature under conditions close to equilibrium noncongruent gas-liquid phase coexistence.

Pflieger, Rachel [Institute for Transuranium Elements, Joint Research Centre, European Commission, P.O. Box 2340, 76125 Karlsruhe (Germany); Marcoule Institute for Separation Chemistry (ICSM), UMR 5257, CEA-CNRS-UMII-ENSCM, Bagnols sur Ceze Cedex (France); Colle, Jean-Yves [Institute for Transuranium Elements, Joint Research Centre, European Commission, P.O. Box 2340, 76125 Karlsruhe (Germany); Iosilevskiy, Igor [Joint Institute for High Temperature, Russian Academy of Science, 125412 Moscow (Russian Federation); Moscow Institute of Physics and Technology, State University, 141700 Moscow (Russian Federation); Extreme Matter Institute (EMMI), 64291 Darmstadt (Germany); Sheindlin, Michael [Institute for Transuranium Elements, Joint Research Centre, European Commission, P.O. Box 2340, 76125 Karlsruhe (Germany); Joint Institute for High Temperature, Russian Academy of Science, 125412 Moscow (Russian Federation)

2011-02-01T23:59:59.000Z

213

Quantum cascade laser investigations of CH{sub 4} and C{sub 2}H{sub 2} interconversion in hydrocarbon/H{sub 2} gas mixtures during microwave plasma enhanced chemical vapor deposition of diamond  

Science Conference Proceedings (OSTI)

CH{sub 4} and C{sub 2}H{sub 2} molecules (and their interconversion) in hydrocarbon/rare gas/H{sub 2} gas mixtures in a microwave reactor used for plasma enhanced diamond chemical vapor deposition (CVD) have been investigated by line-of-sight infrared absorption spectroscopy in the wavenumber range of 1276.5-1273.1 cm{sup -1} using a quantum cascade laser spectrometer. Parameters explored include process conditions [pressure, input power, source hydrocarbon, rare gas (Ar or Ne), input gas mixing ratio], height (z) above the substrate, and time (t) after addition of hydrocarbon to a pre-existing Ar/H{sub 2} plasma. The line integrated absorptions so obtained have been converted to species number densities by reference to the companion two-dimensional (r,z) modeling of the CVD reactor described in Mankelevich et al. [J. Appl. Phys. 104, 113304 (2008)]. The gas temperature distribution within the reactor ensures that the measured absorptions are dominated by CH{sub 4} and C{sub 2}H{sub 2} molecules in the cool periphery of the reactor. Nonetheless, the measurements prove to be of enormous value in testing, tensioning, and confirming the model predictions. Under standard process conditions, the study confirms that all hydrocarbon source gases investigated (methane, acetylene, ethane, propyne, propane, and butane) are converted into a mixture dominated by CH{sub 4} and C{sub 2}H{sub 2}. The interconversion between these two species is highly dependent on the local gas temperature and the H atom number density, and thus on position within the reactor. CH{sub 4}->C{sub 2}H{sub 2} conversion occurs most efficiently in an annular shell around the central plasma (characterized by 1400CH{sub 4} is favored in the more distant regions where T{sub gas}C{sub 2}H{sub 2} conversion, whereas the reverse C{sub 2}H{sub 2}->CH{sub 4} process only requires H atoms to drive the reactions; H atoms are not consumed by the overall conversion.

Ma Jie; Cheesman, Andrew; Ashfold, Michael N. R. [School of Chemistry, University of Bristol, Bristol BS8 1TS (United Kingdom); Hay, Kenneth G.; Wright, Stephen; Langford, Nigel; Duxbury, Geoffrey [Department of Physics, University of Strathclyde, John Anderson Building, 107 Rottenrow, Glasgow G4 0NG (United Kingdom); Mankelevich, Yuri A. [Skobel'tsyn Institute of Nuclear Physics, Moscow State University, Leninskie Gory, Moscow 119991 (Russian Federation)

2009-08-01T23:59:59.000Z

214

Standoff Detection of Chemicals Using Rydberg Fingerprint ...  

applied for non-intrusive detection of combustion intermediates. The technique can be applied to detection of chemical vapors as well as residues on ...

215

Chemical microsensors  

DOE Patents (OSTI)

An article of manufacture is provided including a substrate having an oxide surface layer and a selective thin film of a cyclodextrin derivative chemically bound upon said substrate, said film is adapted for the inclusion of a selected organic compound therewith. Such an article can be either a chemical sensor capable of detecting a resultant mass change from inclusion of the selected organic compound or a chemical separator capable of reversibly selectively separating a selected organic compound.

Li, DeQuan (Los Alamos, NM); Swanson, Basil I. (Los Alamos, NM)

1995-01-01T23:59:59.000Z

216

High-temperature oxidation of an alumina-coated Ni-base alloy  

Science Conference Proceedings (OSTI)

Alumina coatings were applied to Ni-20Cr (wt%) using combustion chemical vapor deposition (combustion CVD). Combustion CVD is an open air deposition technique performed in a flame. The oxidation kinetics of coated and uncoated specimens were measured by isothermal oxidation tests carried out in pure flowing air at temperatures of 800, 900, 1,000 and 1,100 C. The alumina coatings reduced the oxidation kinetics at all temperatures. The morphologies and compositions of the alumina coatings were characterized by transmission and scanning electron microscopy, energy dispersive x-ray spectroscopy and x-ray photoelectron spectroscopy.

Hendrick, M.R.; Hampikian, J.M.; Carter, W.B.

1996-06-01T23:59:59.000Z

217

Safety Topic Chemical Hood General purpose: prevent exposure to toxic, irritating, or noxious chemical  

E-Print Network (OSTI)

Safety Topic ­ Chemical Hood General purpose: prevent exposure to toxic, irritating, or noxious chemical vapors and gases. A face velocity of 100 feet per minute (fpm) provides efficient vapor capture the better. (T) (F) A chemical hood can be used for storage of volatile, flammable, or odiferous materials

Cohen, Robert E.

218

Electrolyte vapor condenser  

DOE Patents (OSTI)

A system is disclosed for removing electrolyte from a fuel cell gas stream. The gas stream containing electrolyte vapor is supercooled utilizing conventional heat exchangers and the thus supercooled gas stream is passed over high surface area passive condensers. The condensed electrolyte is then drained from the condenser and the remainder of the gas stream passed on. The system is particularly useful for electrolytes such as phosphoric acid and molten carbonate, but can be used for other electrolyte cells and simple vapor separation as well. 3 figs.

Sederquist, R.A.; Szydlowski, D.F.; Sawyer, R.D.

1983-02-08T23:59:59.000Z

219

Electrolyte vapor condenser  

DOE Patents (OSTI)

A system is disclosed for removing electrolyte from a fuel cell gas stream. The gas stream containing electrolyte vapor is supercooled utilizing conventional heat exchangers and the thus supercooled gas stream is passed over high surface area passive condensers. The condensed electrolyte is then drained from the condenser and the remainder of the gas stream passed on. The system is particularly useful for electrolytes such as phosphoric acid and molten carbonate, but can be used for other electrolyte cells and simple vapor separation as well.

Sederquist, Richard A. (Newington, CT); Szydlowski, Donald F. (East Hartford, CT); Sawyer, Richard D. (Canton, CT)

1983-01-01T23:59:59.000Z

220

Vapor concentration monitor  

DOE Patents (OSTI)

An apparatus for monitoring the concentration of a vapor, such as heavy water, having at least one narrow bandwidth in its absorption spectrum, in a sample gas such as air. The air is drawn into a chamber in which the vapor content is measured by means of its radiation absorption spectrum. High sensitivity is obtained by modulating the wavelength at a relatively high frequency without changing its optical path, while high stability against zero drift is obtained by the low frequency interchange of the sample gas to be monitored and of a reference sample. The variable HDO background due to natural humidity is automatically corrected.

Bayly, John G. (Deep River, CA); Booth, Ronald J. (Deep River, CA)

1977-01-01T23:59:59.000Z

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


221

Method for the generation of variable density metal vapors which bypasses the liquidus phase  

DOE Patents (OSTI)

The present invention provides a method for producing a metal vapor that includes the steps of combining a metal and graphite in a vessel to form a mixture; heating the mixture to a first temperature in an argon gas atmosphere to form a metal carbide; maintaining the first temperature for a period of time; heating the metal carbide to a second temperature to form a metal vapor; withdrawing the metal vapor and the argon gas from the vessel; and separating the metal vapor from the argon gas. Metal vapors made using this method can be used to produce uniform powders of the metal oxide that have narrow size distribution and high purity.

Kunnmann, Walter (Stony Brook, NY); Larese, John Z. (Rocky Point, NY)

2001-01-01T23:59:59.000Z

222

Industrial Heat Pumps Using Solid/Vapor Working Fluids  

E-Print Network (OSTI)

Industrial heat pumps have the potential to reduce the operating costs of chemical and heat treating processes in the chemical, petroleum, paper, dairy, and many other industries. The cost development of fossil fuel and other prime energy require excellent efficiency/cost ratios and hardware designs adaptable to specific process needs, in order to compete with vapor re-compression recovery systems. The state-of-the-art heat pump equipment employing liquid/vapor working fluids fulfills the requirements only in some applications. The employment of solid/vapor complex compounds leads to more cost effective heat recovery, which is due to simple hardware with no moving parts, extraordinary low maintenance effort, excellent temperature lifts avoiding the need of two-stage systems, and low first cost. This paper describes the advantages and disadvantages of solid/vapor working media.

Rockenfeller, U.

1986-06-01T23:59:59.000Z

223

On the Theory of Oxidation-Reduction Reactions Involving Electron Transfer. V. Comparison and Properties of Electrochemical and Chemical Rate Constants  

DOE R&D Accomplishments (OSTI)

Using a theory of electron transfers which takes cognizance of reorganization of the medium outside the inner coordination shell and of changes of bond lengths inside it, relations between electrochemical and related chemical rate constants are deduced and compared with the experimental data. A correlation is found, without the use of arbitrary parameters. Effects of weak complexes with added electrolytes are included under specified conditions. The deductions offer a way of coordinating a variety of data in the two fields, internally as well as with each those in another. For example, the rate of oxidation or reduction of a series of related reactants by one reagent is correlated with that of another and with that of the corresponding electrochemical oxidation-reduction reaction, under certain specified conditions. These correlations may also provide a test for distinguishing an electron from an atom transfer mechanism. (auth)

Marcus, R. A.

1962-00-00T23:59:59.000Z

224

Definition: Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor Jump to: navigation, search Dictionary.png Mercury Vapor Mercury is discharged as a highly volatile vapor during hydrothermal activity and high concentrations in...

225

Organic vapor jet printing system  

DOE Patents (OSTI)

An organic vapor jet printing system includes a pump for increasing the pressure of an organic flux.

Forrest, Stephen R

2012-10-23T23:59:59.000Z

226

Mercury Vapor | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor Mercury Vapor Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Technique: Mercury Vapor Details Activities (23) Areas (23) Regions (0) 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: Anomalously high concentrations can indicate high permeability or conduit for fluid flow Hydrological: Field wide soil sampling can generate a geometrical approximation of fluid circulation Thermal: High concentration in soils can be indicative of active hydrothermal activity Dictionary.png Mercury Vapor: Mercury is discharged as a highly volatile vapor during hydrothermal

227

Stratified vapor generator  

DOE Patents (OSTI)

A stratified vapor generator (110) comprises a first heating section (H.sub.1) and a second heating section (H.sub.2). The first and second heating sections (H.sub.1, H.sub.2) are arranged so that the inlet of the second heating section (H.sub.2) is operatively associated with the outlet of the first heating section (H.sub.1). A moisture separator (126) having a vapor outlet (164) and a liquid outlet (144) is operatively associated with the outlet (124) of the second heating section (H.sub.2). A cooling section (C.sub.1) is operatively associated with the liquid outlet (144) of the moisture separator (126) and includes an outlet that is operatively associated with the inlet of the second heating section (H.sub.2).

Bharathan, Desikan (Lakewood, CO); Hassani, Vahab (Golden, CO)

2008-05-20T23:59:59.000Z

228

Fuel vapor canister  

SciTech Connect

This paper discusses an improved fuel vapor storage canister for use in a vehicle emission system of the type utilizing an enclosure with an interior communicated with a source of fuel vapor. The improved canister comprises: the enclosure having a mixture including particles of activated charcoal and many pieces of foam rubber, the pieces of foam rubber in the mixture being randomly and substantially evenly dispersed whereby substantially all the charcoal particles are spaced relatively closely to at least one foam rubber piece; the mixture being packed into the enclosure under pressure so that the pieces of foam rubber are compressed enough to tightly secure the charcoal particles one against another to prevent a griding action therebetween.

Moskaitis, R.J.; Ciuffetelli, L.A.

1991-03-26T23:59:59.000Z

229

A Detailed Chemical Kinetic Reaction Mechanism for Oxidation of Four Small Alkyl Esters in Laminar Premixed Flames  

Science Conference Proceedings (OSTI)

A detailed chemical kinetic reaction mechanism has been developed for a group of four small alkyl ester fuels, consisting of methyl formate, methyl acetate, ethyl formate and ethyl acetate. This mechanism is validated by comparisons between computed results and recently measured intermediate species mole fractions in fuel-rich, low pressure, premixed laminar flames. The model development employs a principle of similarity of functional groups in constraining the H atom abstraction and unimolecular decomposition reactions in each of these fuels. As a result, the reaction mechanism and formalism for mechanism development are suitable for extension to larger oxygenated hydrocarbon fuels, together with an improved kinetic understanding of the structure and chemical kinetics of alkyl ester fuels that can be extended to biodiesel fuels. Variations in concentrations of intermediate species levels in these flames are traced to differences in the molecular structure of the fuel molecules.

Westbrook, C K; Pitz, W J; Westmoreland, P R; Dryer, F L; Chaos, M; Osswald, P; Kohse-Hoinghaus, K; Cool, T A; Wang, J; Yang, B; Hansen, N; Kasper, T

2008-02-08T23:59:59.000Z

230

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

Science Conference Proceedings (OSTI)

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

2004-03-31T23:59:59.000Z

231

Fighting Against the Invisible: The new weapons against chemical warfare  

E-Print Network (OSTI)

chemicalwarfare.html (accessed Sandia National Laboratories.Sandia’s portable vapor detection system being preparednumer- ous chemicals (Sandia Lab 2000). Further analysis of

Nguyen, Leana

2009-01-01T23:59:59.000Z

232

Vapor spill pipe monitor  

DOE Patents (OSTI)

The invention is a method and apparatus for continually monitoring the composition of liquefied natural gas flowing from a spill pipe during a spill test by continually removing a sample of the LNG by means of a probe, gasifying the LNG in the probe, and sending the vaporized LNG to a remote ir gas detector for analysis. The probe comprises three spaced concentric tubes surrounded by a water jacket which communicates with a flow channel defined between the inner and middle, and middle and outer tubes. The inner tube is connected to a pump for providing suction, and the probe is positioned in the LNG flow below the spill pipe with the tip oriented partly downward so that LNG is continuously drawn into the inner tube through a small orifice. The probe is made of a high thermal conductivity metal. Hot water is flowed through the water jacket and through the flow channel between the three tubes to provide the necessary heat transfer to flash vaporize the LNG passing through the inner channel of the probe. The gasified LNG is transported through a connected hose or tubing extending from the probe to a remote ir sensor which measures the gas composition.

Bianchini, G.M.; McRae, T.G.

1983-06-23T23:59:59.000Z

233

Assessment of materials for use in a solar ceramic receiver for chemical process heat  

DOE Green Energy (OSTI)

Candidate ceramic matrials were evaluated on the basis of two potential temperature operating regimes: 600 to 1300/sup 0/C (1100 to 2400/sup 0/F) and 1300 to 2200/sup 0/C (2400 to 4000/sup 0/F). Discussion of properties important to the proposed application includes thermal shock resistance, tensile strength, creep resistance, oxidation resistance, vaporization rate, chemical inertness to process reactants and products, cost, and fabricability. Many ceramic materials were considered for the 600 to 1300/sup 0/C operating regime. On the basis of a significant data base on tensile strength, thermal expansion, thermal conductivity, fabricability, and stability, the leading candidates were identified, in decreasing order of preference, as (1) silicon carbide, (2) magnesium oxide, (3) cordierite (2MgO.2Al/sub 2/O/sub 3/.5SiO/sub 2/) known as MAS (4) aluminum oxide, (5) silicon nitride, (6) silicon aluminum oxynitrides (Si/sub w/Al/sub x/N/sub y/O/sub z/) known as sialons, and (7) beryllium oxide. Selection of candidate materials for the 1300 to 2200/sup 0/C regime was restricted because of the insufficient property data and operational experience on key performance parameters. Leading candidates were identified, in decreasing ordr of preference, as (1) zirconium oxide (Y/sub 2/O/sub 3/) stabilized), (2) magnesium oxide, (3) cerium oxide, (4) beryllium oxide, (5) calcium oxide, and (6) thorium and uranium oxide.

Tennery, V.J.; Weber, G.W.

1979-02-01T23:59:59.000Z

234

The Chemical Behavior and Degradation Mitigation Effect of Cerium Oxide Nanoparticles in Perfluorosulfonic Acid Polymer Electrolyte Membranes  

Science Conference Proceedings (OSTI)

Perfluorosulfonic acid membranes, the polymer of choice for polymer electrolyte hydrogen fuel cells, are susceptible to degradation due to attacks on polymer chains from radicals. Mitigation of this attack by cerium-based radical scavengers is an approach that has shown promise. In this work, two formulations of single-crystal cerium oxide nanoparticles, with an order of magnitude difference in particle size, are incorporated into said membranes and subjected to proton conductivity measurements and ex-situ durability tests. We found that ceria is reduced to Ce(III) ions in the acidic environment of a heated, humidified membrane which negatively impacts proton conductivity. In liquid and gas Fenton testing, fluoride emission is reduced by an order of magnitude, drastically increasing membrane longevity. Side-product analysis demonstrated that in the liquid Fenton test, the main point of attack are weak polymer end groups, while in the gas Fenton test, there is additional side-chain attack. Both mechanisms are mitigated by the addition of the ceria nanoparticles, whereby the extent of the durability improvement is found to be independent of particle size.

Pearman, Benjamin P [ORNL; Mohajeri, Nahid [ORNL; Slattery, Darlene [Florida Solar Energy Center (FSEC); Hampton, Michael [University of Florida; Seal, Sudipta [University of Central Florida; Cullen, David A [ORNL

2013-01-01T23:59:59.000Z

235

Comprehensive chemical kinetic modeling of the oxidation of C8 and larger n-alkanes and 2-methylalkanes  

DOE Green Energy (OSTI)

Conventional petroleum jet and diesel fuels, as well as alternative Fischer-Tropsch (FT) fuels and hydrotreated renewable jet (HRJ) fuels, contain high molecular weight lightly branched alkanes (i.e., methylalkanes) and straight chain alkanes (n-alkanes). Improving the combustion of these fuels in practical applications requires a fundamental understanding of large hydrocarbon combustion chemistry. This research project presents a detailed and reduced chemical kinetic mechanism for singly methylated iso-alkanes (i.e., 2-methylalkanes) ranging from C{sub 8} to C{sub 20}. The mechanism also includes an updated version of our previously published C{sub 8} to C{sub 16} n-alkanes model. The complete detailed mechanism contains approximately 7,200 species 31,400 reactions. The proposed model is validated against new experimental data from a variety of fundamental combustion devices including premixed and nonpremixed flames, perfectly stirred reactors and shock tubes. This new model is used to show how the presence of a methyl branch affects important combustion properties such as laminar flame propagation, ignition, and species formation.

Sarathy, S M; Westbrook, C K; Pitz, W J; Mehl, M; Togbe, C; Dagaut, P; Wang, H; Oehlschlaeger, M; NIemann, U; Seshadri, K; Veloo, P S; Ji, C; Egolfopoulos, F; Lu, T

2011-03-16T23:59:59.000Z

236

VAPOR SHIELD FOR INDUCTION FURNACE  

DOE Patents (OSTI)

This patent relates to a water-cooled vapor shield for an inductlon furnace that will condense metallic vapors arising from the crucible and thus prevent their condensation on or near the induction coils, thereby eliminating possible corrosion or shorting out of the coils. This is accomplished by placing, about the top, of the crucible a disk, apron, and cooling jacket that separates the area of the coils from the interior of the cruclbIe and provides a cooled surface upon whlch the vapors may condense.

Reese, S.L.; Samoriga, S.A.

1958-03-11T23:59:59.000Z

237

Vapor adsorption process  

SciTech Connect

The removal of undesirable acid components from sour natural gas is often accomplished by a vapor adsorption process wherein a bed of solid adsorbent material is contacted with an inlet gas stream so that desired components contained in the gas stream are adsorbed on the bed, then regenerated by contact with a heated regeneration gas stream. Adsorbed components are desorbed from the bed and the bed is cooled preparatory to again being contacted with the inlet gas stream. By this process, the bed is contacted, during the regeneration cycle, with a selected adsorbable material. This material has the property of being displaced from the bed by the desired components and has a heat of desorption equal to or greater than the heat of adsorption of the desired components. When the bed is contacted with the inlet gas stream, the selected adsorbable material is displaced by the desired components resulting in the temperature of the bed remaining relatively constant, thereby allowing the utilization of the maximum bed adsorption capacity. (4 claims)

Snyder, C.F.; Casad, B.M.

1973-04-24T23:59:59.000Z

238

Oxidation, volatilization, and redistribution of molybdenum from TZM alloy in air  

Science Conference Proceedings (OSTI)

The excellent high temperature strength and thermal conductivity of molybdenum-base alloys provide attractive features for components in advanced magnetic and inertial fusion devices. Refractory metal alloys react readily with oxygen and other gases. Oxidized molybdenum in turn is susceptible to losses from volatile molybdenum trioxide species, MoO{sub 3}(m), in air and the hydroxide, MoO{sub 2}(OH){sub 2}, formed from water vapor. Transport of radioactivity by the volatilization, migration, and re-deposition of these volatile species during a potential accident involving a loss of vacuum or inert environment represents a safety issue. In this report the authors present experimental results on the oxidation, volatilization and re-deposition of molybdenum from TZM in flowing air between 400 and 800 C. These results are compared with calculations obtained from a vaporization mass transfer model using chemical thermodynamic data for vapor pressures of MoO{sub 3}(g) over pure solid MoO{sub 3} and an expression for the vapor pressures of MoO{sub 2}(OH){sub 2} from the literature. Calculations correlate well with experimental data.

Smolik, G.R.; Petti, D.A.; McCarthy, K.A.; Schuetz, S.T.

2000-01-01T23:59:59.000Z

239

Oxidation, Volatilization, and Redistribution of Molybdenum from TZM Alloy in Air  

Science Conference Proceedings (OSTI)

The excellent high temperature strength and thermal conductivity of molybdenum-base alloys provide attractive features for components in advanced magnetic and inertial fusion devices. Refractory metal alloys react readily with oxygen and other gases. Oxidized molybdenum in turn is susceptible to losses from volatile molybdenum trioxide species, (MoO3)m, in air and the hydroxide, MoO2(OH)2, formed from water vapor. Transport of radioactivity by the volatilization, migration, and re-deposition of these volatile species during a potential accident involving a loss of vacuum or inert environment represents a safety issue. In this report we present experimental results on the oxidation, volatilization and re-deposition of molybdenum from TZM in flowing air between 400 and 800°C. These results are compared with calculations obtained from a vaporization mass transfer model using chemical thermodynamic data for vapor pressures of MoO3(g) over pure solid MoO3 and an expression for the vapor pressures of MoO2(OH)2 from the literature. Calculations correlate well with experimental data.

Smolik, Galen Richard; Petti, David Andrew; Mccarthy, Kathryn Ann; Schuetz, Stanley Thomas

2000-01-01T23:59:59.000Z

240

Atmospheric Water Vapor over China  

Science Conference Proceedings (OSTI)

Chinese radiosonde data from 1970 to 1990 are relatively homogeneous in time and are used to examine the climatology, trends, and variability of China’s atmospheric water vapor content. The climatological distribution of precipitable water (PW) ...

Panmao Zhai; Robert E. Eskridge

1997-10-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Vapor deposition of hardened niobium  

DOE Patents (OSTI)

A method of coating ceramic nuclear fuel particles containing a major amount of an actinide ceramic in which the particles are placed in a fluidized bed maintained at ca. 800.degree. to ca. 900.degree. C., and niobium pentachloride vapor and carbon tetrachloride vapor are led into the bed, whereby niobium metal is deposited on the particles and carbon is deposited interstitially within the niobium. Coating apparatus used in the method is also disclosed.

Blocher, Jr., John M. (Columbus, OH); Veigel, Neil D. (Columbus, OH); Landrigan, Richard B. (Columbus, OH)

1983-04-19T23:59:59.000Z

242

Complex defects in the oxidation of uranium  

Science Conference Proceedings (OSTI)

We are reporting EPR results obtained with uranium powder samples fully oxidized in dry air, water vapor, and air/water vapor mixtures. The results reported previously are confirmed and additional paramagnetic centers, associated with chemisorbed species, have been identified. The temperature dependence of the g-value for these centers from room temperature to 10K is also reported.

MacCrone, R.K.; Sankaran, S.; Shatynski, S.R.; Colmenares, C.A.

1986-06-10T23:59:59.000Z

243

Chemical Sensing for Buried Landmines - Fundamental Processes Influencing Trace Chemical Detection  

SciTech Connect

Mine detection dogs have a demonstrated capability to locate hidden objects by trace chemical detection. Because of this capability, demining activities frequently employ mine detection dogs to locate individual buried landmines or for area reduction. The conditions appropriate for use of mine detection dogs are only beginning to emerge through diligent research that combines dog selection/training, the environmental conditions that impact landmine signature chemical vapors, and vapor sensing performance capability and reliability. This report seeks to address the fundamental soil-chemical interactions, driven by local weather history, that influence the availability of chemical for trace chemical detection. The processes evaluated include: landmine chemical emissions to the soil, chemical distribution in soils, chemical degradation in soils, and weather and chemical transport in soils. Simulation modeling is presented as a method to evaluate the complex interdependencies among these various processes and to establish conditions appropriate for trace chemical detection. Results from chemical analyses on soil samples obtained adjacent to landmines are presented and demonstrate the ultra-trace nature of these residues. Lastly, initial measurements of the vapor sensing performance of mine detection dogs demonstrates the extreme sensitivity of dogs in sensing landmine signature chemicals; however, reliability at these ultra-trace vapor concentrations still needs to be determined. Through this compilation, additional work is suggested that will fill in data gaps to improve the utility of trace chemical detection.

PHELAN, JAMES M.

2002-05-01T23:59:59.000Z

244

Effect of higher water vapor content on TBC performance  

Science Conference Proceedings (OSTI)

Coal gasification, or IGCC (integrated gasification combined cycle), is one pathway toward cleaner use of coal for power generation with lower emissions. However, when coal-derived synthesis gas (i.e., syngas) is burned in turbines designed for natural gas, turbine manufacturers recommend 'derating,' or lowering the maximum temperature, which lowers the efficiency of the turbine, making electricity from IGCC more expensive. One possible reason for the derating is the higher water vapor contents in the exhaust gas. Water vapor has a detrimental effect on many oxidation-resistant high-temperature materials. In a turbine hot section, Ni-base superalloys are coated with a thermal barrier coating (TBC) allowing the gas temperature to be higher than the superalloy solidus temperature. TBCs have a low thermal conductivity ceramic top coating (typically Y{sub 2}O{sub 3}-stabilized ZrO{sub 2}, or YSZ) and an oxidation-resistant metallic bond coating. For land-based gas turbines, the industry standard is air plasma sprayed (APS) YSZ and high velocity oxygen fuel (HVOF) sprayed NiCoCrAlY bond coatings. To investigate the role of higher water vapor content on TBC performance and possible mitigation strategies, furnace cycling experiments were conducted in dry O{sub 2} and air with 10% (typical with natural gas or jet fuel) or 50 vol% water vapor. Cycle frequency and temperature were accelerated to one hour at 1100 C (with 10 minute cooling to {approx}30 C between each thermal cycle) to induce early failures in coatings that are expected to operate for several years with a metal temperature of {approx}900 C. Coupons (16 mm diameter x 2 mm thick) of commercial second-generation single crystal superalloy CMSX4 were HVOF coated on both sides with {approx}125 {micro}m of Ni-22wt%Co-17Cr-12Al either with 0.7Y or 0.7Y-0.3Hf-0.4Si. One side was then coated with 190-240 {micro}m of APS YSZ. Coatings were cycled until the YSZ top coating spalled. Figure 2 shows the results of the initial phase of experiments. Compared to dry O{sub 2}, the addition of 10% water vapor decreased the lifetime of MCrAlY by {approx}30% for the conventional CMSX4 substrates. Higher average lifetimes were observed with Hf in the bond coating, but a similar decrease in lifetime was observed when water vapor was added. The addition of Y and La to the superalloy substrate did not change the YSZ lifetime with 10% water vapor. However, increasing water vapor content from 10 to 50% did not further decrease the lifetime of either bond coating with the doped superalloy substrate. Thus, these results suggest that higher water vapor contents cannot explain the derating of syngas-fired turbines, and other factors such as sulfur and ash from imperfect syngas cleanup (or upset conditions) need to be explored. Researchers continue to study effects of water vapor on thermally grown alumina scale adhesion and growth rate, and are looking for bond coating compositions more resistant to oxidation in the presence of water vapor.

Pint, Bruce A [ORNL; Haynes, James A [ORNL

2012-01-01T23:59:59.000Z

245

Kinetics of Chromium(III) Oxidation by Manganese(IV) Oxides Using  

E-Print Network (OSTI)

. This represents the first study to determine the chemical kinetics of Cr(III) oxidation on Mn-oxides. The results focusing on the "chemical" kinetics of Cr(III) oxidation on manganese oxides, i.e., the initial rates of Obtaining and Analyzing Kinetic Data. In Rates of Soil Chemical Processes, Sparks, D. L., Suarez, D. L., Eds

Sparks, Donald L.

246

Image Storage in Hot Vapors  

E-Print Network (OSTI)

We theoretically investigate image propagation and storage in hot atomic vapor. A $4f$ system is adopted for imaging and an atomic vapor cell is placed over the transform plane. The Fraunhofer diffraction pattern of an object in the object plane can thus be transformed into atomic Raman coherence according to the idea of ``light storage''. We investigate how the stored diffraction pattern evolves under diffusion. Our result indicates, under appropriate conditions, that an image can be reconstructed with high fidelity. The main reason for this procedure to work is the fact that diffusion of opposite-phase components of the diffraction pattern interfere destructively.

Zhao, L; Xiao, Y; Yelin, S F

2007-01-01T23:59:59.000Z

247

Image Storage in Hot Vapors  

E-Print Network (OSTI)

We theoretically investigate image propagation and storage in hot atomic vapor. A $4f$ system is adopted for imaging and an atomic vapor cell is placed over the transform plane. The Fraunhofer diffraction pattern of an object in the object plane can thus be transformed into atomic Raman coherence according to the idea of ``light storage''. We investigate how the stored diffraction pattern evolves under diffusion. Our result indicates, under appropriate conditions, that an image can be reconstructed with high fidelity. The main reason for this procedure to work is the fact that diffusion of opposite-phase components of the diffraction pattern interfere destructively.

L. Zhao; T. Wang; Y. Xiao; S. F. Yelin

2007-10-22T23:59:59.000Z

248

Reference Handbook for Site-Specific Assessment of Subsurface Vapor Intrusion to Indoor Air  

Science Conference Proceedings (OSTI)

Subsurface vapor intrusion is only one of several possible sources for volatile and semi-volatile chemicals in indoor air. This report provides guidance on the site-specific assessment of the significance of subsurface vapor intrusion into indoor air. Topics covered include theoretical considerations, sampling and analysis considerations, recommended strategies and procedures, interpretive tools, mitigation measures, and suggestions for future research. This document reflects a comprehensive understandin...

2005-03-28T23:59:59.000Z

249

Results of Field-Based Soil Vapor Intrusion (SVI) Research at Two MGP Sites and Implications for SVI Assessment  

Science Conference Proceedings (OSTI)

Soil vapor intrusion (SVI; also known simply as vapor intrusion, or VI) is the migration of volatile or semi-volatile chemicals from subsurface contaminated soil or groundwater to indoor air in an overlying building. In the past decade, SVI has emerged as a major environmental issue. This report presents previously unpublished results of a three-year study of two former manufactured gas plant (MGP) sites to determine the potential for subsurface chemicals to migrate into buildings.

2011-12-30T23:59:59.000Z

250

Oxidation Kinetics Modeling Applying Phase Field Approach  

Science Conference Proceedings (OSTI)

Presentation Title, Oxidation Kinetics Modeling Applying Phase Field Approach ... chemical reaction rates will increase exponentially and environmental attack ...

251

Atomic vapor laser isotope separation process  

DOE Patents (OSTI)

A laser spectroscopy system is utilized in an atomic vapor laser isotope separation process. The system determines spectral components of an atomic vapor utilizing a laser heterodyne technique. 23 figs.

Wyeth, R.W.; Paisner, J.A.; Story, T.

1990-08-21T23:59:59.000Z

252

Distribution of Tropical Tropospheric Water Vapor  

Science Conference Proceedings (OSTI)

Utilizing a conceptual model for tropical convection and observational data for water vapor, the maintenance of the vertical distribution of the tropical tropospheric water vapor is discussed. While deep convection induces large-scale subsidence ...

De-Zheng Sun; Richard S. Lindzen

1993-06-01T23:59:59.000Z

253

Atmospheric Water Vapor Characteristics at 70°N  

Science Conference Proceedings (OSTI)

Using an extensive rawinsonde archive, characteristics of Arctic water vapor and its transports at 70°N are examined for the period 1974–1991. Monthly-mean profiles and vertically integrated values of specific humidity and meridional vapor fluxes ...

Mark C. Serreze; Roger G. Barry; John E. Walsh

1995-04-01T23:59:59.000Z

254

Vapor Pressure Measurement of Supercooled Water  

Science Conference Proceedings (OSTI)

A new dewpoint hygrometer was developed for subfreezing temperature application. Vapor pressure of supercooled water was determined by measuring temperatures at the dew-forming surface and the vapor source ice under the flux density balance, and ...

N. Fukuta; C. M. Gramada

2003-08-01T23:59:59.000Z

255

Chemical nature of the passivation layer depending on the oxidizing agent in Gd2O3/GeO2/Ge stacks grown by molecular beam deposition  

Science Conference Proceedings (OSTI)

In Ge-based metal oxide semiconductor technology, the insertion of a passivation layer seems to be crucial in unpinning the Fermi level at the interface and in reducing the amount of interface defects. GeO"2 was obtained by atomic oxygen (AO), molecular ... Keywords: Gadolinium oxide, Germanium, Molecular beam deposition, Passivation layer, Time-of-flight secondary ion mass spectrometry

A. Lamperti; S. Baldovino; A. Molle; M. Fanciulli

2011-04-01T23:59:59.000Z

256

Lipid Oxidation and Quality Division of AOCS  

Science Conference Proceedings (OSTI)

For professionals in lipid oxidation with a major focus in food applications including flavor, instrumentation, chemical analyses, biological oxidation, antioxidants, nutraceuticals, processing and mechanisms Lipid Oxidation and Quality Division of AOCS ...

257

Vapor Pressures and Heats of Vaporization of Primary Coal Tars  

Office of Scientific and Technical Information (OSTI)

/ PC92544-18 / PC92544-18 VAPOR PRESSURES AND HEATS OF VAPORIZATION OF PRIMARY COAL TARS FINAL REPORT Grant Dates: August, 1992 - November, 1996 Principal Authors: Eric M. Suuberg (PI) and Vahur Oja Report Submitted: April, 1997 Revised: July, 1997 Grant Number: DE-FG22-92PC92544 Report Submitted by: ERIC M. SUUBERG DIVISION OF ENGINEERING BROWN UNIVERSITY PROVIDENCE, RI 02912 TEL. (401) 863-1420 Prepared For: U. S. DEPT. OF ENERGY FEDERAL ENERGY TECHNOLOGY CENTER P.O. BOX 10940 PITTSBURGH, PA 15236 DR. KAMALENDU DAS, FETC, MORGANTOWN , WV TECHNICAL PROJECT OFFICER "US/DOE Patent Clearance is not required prior to the publication of this document" ii United States Government Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any

258

Formation of amorphous metal alloys by chemical vapor deposition  

SciTech Connect

Amorphous alloys are deposited by a process of thermal dissociation of mixtures or organometallic compounds and metalloid hydrides, e.g., transition metal carbonyl such as nickel carbonyl, and diborane. Various sizes and shapes of deposits can be achieved, including near-net-shape free standing articles, multilayer deposits, and the like. Manipulation or absence of a magnetic field affects the nature and the structure of the deposit.

Mullendore, Arthur W. (Sandia Park, NM)

1990-01-01T23:59:59.000Z

259

Modeling the Gas By-products of Metalorganic Chemical Vapor ...  

Science Conference Proceedings (OSTI)

The fiber then proceeds through an inert gas seal, inlet cross, hot-wall reactor, ... The effluent flows through a burn box (heated to greater than 500°C) before ... involve transport-kinetic modeling that describes the fluid flow, heat transfer, and  ...

260

Chemical vapor deposition growth. Quarterly report No. 1  

DOE Green Energy (OSTI)

The activities of the first quarter of the contract, which began December 29, 1975, are described. An existing laboratory-type CVD reactor system with a vertical deposition chamber has been used for growth of the Si films studied to date. Extensive modifications of this system, involving mass flow controllers and automatic timing of reactant gas flows by means of solenoid-activated air-operated bellows valves, will be completed early in the second quarter. (WDM)

Ruth, R.P.; Manasevit, H.M.; Kenty, J.L.; Moudy, L.A.; Simpson, W.I.; Yang, J.J.

1976-03-31T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Chemical vapor deposition growth. Quarterly report No. 2  

DOE Green Energy (OSTI)

The objective of the program is the development of CVD techniques for producing large areas of Si sheet on inexpensive substrate materials, with sheet properties suitable for fabricating solar cells meeting the technical goals of the Low Cost Silicon Solar Array Project (LCSSAP). The techniques developed are to be directed toward (1) minimum-cost processing, (2) production of sheet having properties adequate to result in cells with terrestrial array efficiency of 10 percent or more, and (3) eventual scale-up to large-quantity production. (WDM)

Ruth, R.P.; Manasevit, H.M.; Kenty, J.L.; Mondy, L.A.; Simpson, W.I.; Yang, J.J.

1976-07-01T23:59:59.000Z

262

Organic lateral heterojunction devices for vapor-phase chemical detection  

E-Print Network (OSTI)

As the U.S. is engaged in battle overseas, there is an urgent need for the development of sensors for early warning and protection of military forces against potential attacks. On the battlefields, improvised explosive ...

Ho, John C., 1980-

2009-01-01T23:59:59.000Z

263

Micro Chemical Vapor Deposition for the Synthesis of Nanomaterials  

E-Print Network (OSTI)

distribution when the heat conduction through 1-?m-thick gasdistribution when heat conduction through the 1-?m-thick gaslarge area and the heat conduction through the gases is

Zhou, Qin

2011-01-01T23:59:59.000Z

264

Chemical vapor deposition growth. Quarterly report No. 4  

DOE Green Energy (OSTI)

The contract activities during the quarter were concentrated in the following areas: (1) preparation of polished substrates of three new experimental glasses received in raw billet form from the manufacturer; (2) exploratory Si CVD growth on two experimental glazes (on aluminas), at temperatures below and above the softening points; (3) evaluation of several different surface cleaning procedures for glass substrates, with a procedure involving an acid-cleaning step being adopted as standard; (4) determination of Si film crystallographic properties on glasses (and sapphire) as a function of deposition temperature and thickness in three different thickness ranges; (5) determination of the effect of HCl additions to SiH/sub 4/ on the net growth rates and the properties of Si films grown by a two-step process at two different deposition temperatures; (6) investigation of the reproducibility of Si film growth rates when the SiH/sub 4/ flow rate is controlled by a) the mass-flow controller and b) the conventional rotameter; (7) determination of further carrier density vs added dopant concentration data for B-doped Si films grown in He at low temperatures (approximately 850/sup 0/C); (8) preparation of p-type B-doped Si films in a range of carrier densities on substrates of single-crystal Si, sapphire, and several glasses for fabrication of experimental solar cell structures; (9) preparation of p/p/sup +/ films on substrates of sapphire and single-crystal Si for solar cell fabrication; (10) evaluation of the electrical properties of the various films prepared; and (11) fabrication and characterization of experimental cells made by P diffusion into the p-type and the p/p/sup +/ CVD layers.

Ruth, R.P.; Manasevit, H.M.; Campbell, A.G.; Johnson, R.E.; Moudy, L.A.; Shaw, G.L.; Simpson, W.I.

1977-04-01T23:59:59.000Z

265

Graphene growth with giant domains using chemical vapor deposition  

E-Print Network (OSTI)

N. Martensson, Controlling graphene corrugation on lattice-in patterned epitaxial graphene, Science, 2006, 312(5777), 92009, 4(6), 17 A. K. Geim, Graphene: Status and Prospects,

Yong, Virginia; Hahn, H. Thomas

2011-01-01T23:59:59.000Z

266

A detailed chemical kinetic reaction mechanism for the oxidation of iso-octane and n-heptane over an extended temperature range and its application to analysis of engine knock  

SciTech Connect

A detailed chemical kinetic reaction is developed to describe the oxidation of n-heptane, iso-octane, and their mixtures over a wide range of operating conditions. In addition to a high temperature submechanism, reaction paths are included to describe the lower temperature regimes in which the rate and intermediate products of oxidation are controlled by addition of molecular oxygen to alkyl and isomerized alkylperoxy radicals, internal H atom abstractions, and reactions involving O-heterocyclic species. The mechanism is then used to study the influence of fuel composition on knocking in internal combustion engines. Autoignition of mixtures of iso-octane and n-heptane is examined. The computations reproduce the variations of autoignition delay time with octane number and these variations are interpreted in terms of detailed differences in the structure of the two primary reference fuels. Sensitivity analyses of the computations are also presented. 30 refs., 2 figs.

Westbrook, C.K.; Warnatz, J.; Pitz, W.J.

1988-01-11T23:59:59.000Z

267

Means and method for vapor generation  

DOE Patents (OSTI)

A liquid, in heat transfer contact with a surface heated to a temperature well above the vaporization temperature of the liquid, will undergo a multiphase (liquid-vapor) transformation from 0% vapor to 100% vapor. During this transition, the temperature driving force or heat flux and the coefficients of heat transfer across the fluid-solid interface, and the vapor percentage influence the type of heating of the fluid--starting as "feedwater" heating where no vapors are present, progressing to "nucleate" heating where vaporization begins and some vapors are present, and concluding with "film" heating where only vapors are present. Unstable heating between nucleate and film heating can occur, accompanied by possibly large and rapid temperature shifts in the structures. This invention provides for injecting into the region of potential unstable heating and proximate the heated surface superheated vapors in sufficient quantities operable to rapidly increase the vapor percentage of the multiphase mixture by perhaps 10-30% and thereby effectively shift the multiphase mixture beyond the unstable heating region and up to the stable film heating region.

Carlson, Larry W. (Oswego, IL)

1984-01-01T23:59:59.000Z

268

Chemical Looping | Open Energy Information  

Open Energy Info (EERE)

Looping Looping Jump to: navigation, search Contents 1 Introduction 2 Process Description 3 Benefits 4 Oxygen Carriers 5 Multimedia 6 Patents 7 References 8 External Links Introduction Chemical looping or chemical looping combustion (CLC) is a novel technology that could provide the means to convert fossil fuels to electricity and provide carbon capture without significant efficiency or cost penalties. Chemical looping combustion is very similar to oxy-fuel combustion where there is no direct contact between air and fuel.[1] Oxygen is extracted from air, then the oxygen is reacted with the hydrocarbon fuel producing an exhaust gas composed of carbon dioxide and water vapor.[2] The water vapor is condensed out of the gas resulting in near 100% carbon dioxide stream that could be sequestered in the ground.

269

Oxide Dispersion Strengthened Iron Aluminide by CVD Coated Powders  

SciTech Connect

This I &I Category2 program developed chemical vapor deposition (CVD) of iron, aluminum and aluminum oxide coated iron powders and the availability of high temperature oxidation, corrosion and erosion resistant coating for future power generation equipment and can be used for retrofitting existing fossil-fired power plant equipment. This coating will provide enhanced life and performance of Coal-Fired Boilers components such as fire side corrosion on the outer diameter (OD) of the water wall and superheater tubing as well as on the inner diameter (ID) and OD of larger diameter headers. The program also developed a manufacturing route for readily available thermal spray powders for iron aluminide coating and fabrication of net shape component by powder metallurgy route using this CVD coated powders. This coating can also be applid on jet engine compressor blade and housing, industrial heat treating furnace fixtures, magnetic electronic parts, heating element, piping and tubing for fossil energy application and automotive application, chemical processing equipment , heat exchanger, and structural member of aircraft. The program also resulted in developing a new fabrication route of thermal spray coating and oxide dispersion strengthened (ODS) iron aluminide composites enabling more precise control over material microstructures.

Asit Biswas Andrew J. Sherman

2006-09-25T23:59:59.000Z

270

Molecules and materials for the optical detection of explosives and toxic chemicals  

E-Print Network (OSTI)

Optical chemosensing, especially using amplifying fluorescent polymers, can allow for the highly sensitive and selective vapor-phase detection of both explosives and highly toxic chemicals, including chemical warfare agents. ...

Thomas, Samuel William, III

2006-01-01T23:59:59.000Z

271

Chemical leukoderma  

E-Print Network (OSTI)

the first report, to date, of chemical leukoderma that wasreview on biological, chemical and clinical aspects. Pigment4. Briganti S, et al. Chemical and instrumental approaches

O'Reilly, Kathryn E; Patel, Utpal; Chu, Julie; Patel, Rishi; Machler, Brian C

2011-01-01T23:59:59.000Z

272

Oxidative Tritium Decontamination System  

DOE Patents (OSTI)

The Oxidative Tritium Decontamination System, OTDS, provides a method and apparatus for reduction of tritium surface contamination on various items. The OTDS employs ozone gas as oxidizing agent to convert elemental tritium to tritium oxide. Tritium oxide vapor and excess ozone gas is purged from the OTDS, for discharge to atmosphere or transport to further process. An effluent stream is subjected to a catalytic process for the decomposition of excess ozone to diatomic oxygen. One of two configurations of the OTDS is employed: dynamic apparatus equipped with agitation mechanism and large volumetric capacity for decontamination of light items, or static apparatus equipped with pressurization and evacuation capability for decontamination of heavier, delicate, and/or valuable items.

Gentile, Charles A. (Plainsboro, NJ), Guttadora, Gregory L. (Highland Park, NJ), Parker, John J. (Medford, NJ)

2006-02-07T23:59:59.000Z

273

Determination of Mercury in Coal by Isotope Dilution Cold-Vapor Generation Inductively  

E-Print Network (OSTI)

Articles Determination of Mercury in Coal by Isotope Dilution Cold-Vapor Generation Inductively developed for high-accuracy determinations of mer- cury in bituminous and sub-bituminous coals. A closed- system digestion process employing a Carius tube is used to completely oxidize the coal matrix

274

Mutual separation of rare earths using chemically modified chitosan ...  

Science Conference Proceedings (OSTI)

Calcium Reductants – A historical review. Chemical ... Electrochemistry for Nd electrowinning from fluoride-oxide molten salts · Electrodeposition of Zinc from ...

275

Vapor phase heat transport systems  

DOE Green Energy (OSTI)

Vapor phase heat-transport systems are being tested in two of the passive test cells at Los Alamos. The systems consist of an active fin-and-tube solar collector and a condenser inside a water storage tank. The refrigerant, R-11, can be returned to the collector by a pump or by a self-pumping scheme. In one of the test cells the liquid was self-pumped to the roof-mounted collector 17 ft above the condenser. A mechanical valve was designed and tested that showed that the system could operate in a completely passive mode. Performance comparisons have been made with a passive water wall test cell.

Hedstrom, J.C.

1984-01-01T23:59:59.000Z

276

Chemical Science  

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

Chemical Science Chemical Science Compton double ionization of helium in the region of the cross-section maximum B. Krässig, R.W. Dunford, D.S. Gemmell, S. Hasegawa, E.P. Kanter, H. Schmidt-Böcking, W. Schmitt, S.H. Southworth, Th. Weber, and L. Young Crystal structure analysis of microporous Na16Nb12.8Ti3.2O44.8(OH)3.2l8H2O and Na/Nb/Zr/O/H2O phases A. Tripathi, J. Parise, M. Nyman, T.M. Nenoff, and W. Harrison Double K-photoionization of heavy atoms R.W. Dunford, D.S. Gemmell, E.P. Kanter, B. Krässig, and S.H. Southworth Forward-backward asymmetries of atomic photoelectrons S.H. Southworth, B. Krässig, E.P. Kanter, J.C. Bilheux, R.W. Dunford, D.S. Gemmell, S. Hasegawa, and L. Young In situreduction of various iron oxides to form high-surface-area Fe-metal catalysts as studied by high-resolution powder diffraction

277

Coupling apparatus for a metal vapor laser  

DOE Patents (OSTI)

Coupling apparatus for a large bore metal vapor laser is disclosed. The coupling apparatus provides for coupling high voltage pulses (approximately 40 KV) to a metal vapor laser with a high repetition rate (approximately 5 KHz). The coupling apparatus utilizes existing thyratron circuits and provides suitable power input to a large bore metal vapor laser while maintaining satisfactory operating lifetimes for the existing thyratron circuits.

Ball, D.G.; Miller, J.L.

1993-02-23T23:59:59.000Z

278

METAL OXIDE NANOPARTICLES  

SciTech Connect

This chapter covers the fundamental science, synthesis, characterization, physicochemical properties and applications of oxide nanomaterials. Explains fundamental aspects that determine the growth and behavior of these systems, briefly examines synthetic procedures using bottom-up and top-down fabrication technologies, discusses the sophisticated experimental techniques and state of the art theory results used to characterize the physico-chemical properties of oxide solids and describe the current knowledge concerning key oxide materials with important technological applications.

FERNANDEZ-GARCIA,M.; RODGRIGUEZ, J.A.

2007-10-01T23:59:59.000Z

279

Mercury Vapor (Kooten, 1987) | Open Energy Information  

Open Energy Info (EERE)

Mercury Vapor (Kooten, 1987) Mercury Vapor (Kooten, 1987) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor (Kooten, 1987) Exploration Activity Details Location Unspecified Exploration Technique Mercury Vapor Activity Date Usefulness useful DOE-funding Unknown Notes Surface soil-mercury surveys are an inexpensive and useful exploration tool for geothermal resources. ---- Surface geochemical surveys for mercury were conducted in 16 areas in 1979-1981 by ARCO Oil and Gas Company as part of its geothermal evaluation program. Three techniques used together have proved satisfactory in evaluating surface mercury data. These are contouring, histograms and cumulative frequency plots of the data. Contouring geochemical data and constructing histograms are standard

280

Thermoplastic Composite with Vapor Grown Carbon Fiber.  

E-Print Network (OSTI)

??Vapor grown carbon fiber (VGCF) is a new class of highly graphitic carbon nanofiber and offers advantages of economy and simpler processing over continuous-fiber composites.… (more)

Lee, Jaewoo

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Moisture Durability of Vapor Permeable Insulating Sheathing ...  

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

Existing Homes, Building Technologies Office (BTO) In this project, Building America team Building Science Corporation researched some of the ramifications of using exterior, vapor...

282

Water Vapor Fields Deduced from METEOSAT-1 Water Vapor Channel Data  

Science Conference Proceedings (OSTI)

A quasi-operational process for the determination of water vapor fields from METEPSAT-1 water vapor channel data is described. Each count of the WV picture is replaced by the corresponding mean relative humidity value using both the calibration ...

M. M. Poc; M. Roulleau

1983-09-01T23:59:59.000Z

283

Useful and Undesirable Chemical Reactions during Detonation ...  

Science Conference Proceedings (OSTI)

In our work, we consider chemical changes in the sprayed materials induced by reducing or oxidizing species in the detonation products and interactions ...

284

Physical vapor deposition and patterning of calcium fluoride films  

Science Conference Proceedings (OSTI)

Physical vapor deposition of calcium fluoride (CaF{sub 2}) thin films was performed via electron beam evaporation, resistive/thermal evaporation, and nonreactive radio frequency sputtering. Patterning of the resultant ''usable'' thin films was then also attempted in several ways, including by shadow mask deposition, liftoff, and direct chemical etching. Resistive evaporation produced the most stable films, having polycrystalline morphology with a moderately strong preference to the 331 orientation. The cleanest patterning results were obtained via a polymer/metal liftoff. The results and implications of each of the various deposition and patterning techniques are discussed.

Pinol, L.; Rebello, K.; Caruso, K.; Francomacaro, A. S.; Coles, G. L. [Applied Physics Laboratory, Johns Hopkins University, Laurel, Maryland 20723 (United States)

2011-03-15T23:59:59.000Z

285

Dosimeter for monitoring vapors and aerosols of organic compounds  

DOE Patents (OSTI)

A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique.

Vo-Dinh, Tuan (625 Gulfwood Rd., Knoxville, TN 37923)

1987-01-01T23:59:59.000Z

286

Dosimeter for monitoring vapors and aerosols of organic compounds  

DOE Patents (OSTI)

A dosimeter is provided for collecting and detecting vapors and aerosols of organic compounds. The dosimeter comprises a lightweight, passive device that can be conveniently worn by a person as a badge or placed at a stationary location. The dosimeter includes a sample collector comprising a porous web treated with a chemical for inducing molecular displacement and enhancing phosphorescence. Compounds are collected onto the web by molecular diffusion. The web also serves as the sample medium for detecting the compounds by a room temperature phosphorescence technique. 7 figs.

Vo-Dinh, T.

1987-07-14T23:59:59.000Z

287

Near real time vapor detection and enhancement using aerosol adsorption  

DOE Patents (OSTI)

A vapor sample detection method where the vapor sample contains vapor and ambient air and surrounding natural background particles. The vapor sample detection method includes the steps of generating a supply of aerosol that have a particular effective median particle size, mixing the aerosol with the vapor sample forming aerosol and adsorbed vapor suspended in an air stream, impacting the suspended aerosol and adsorbed vapor upon a reflecting element, alternatively directing infrared light to the impacted aerosol and adsorbed vapor, detecting and analyzing the alternatively directed infrared light in essentially real time using a spectrometer and a microcomputer and identifying the vapor sample.

Novick, Vincent J.; Johnson, Stanley A.

1997-12-01T23:59:59.000Z

288

G-Band Vapor Radiometer Precipitable Water Vapor (GVRPWV) Value-Added Product  

SciTech Connect

The G-Band Vapor Radiometer Precipitable Water Vapor (GVRPWV) value-added product (VAP) computes precipitable water vapor using neural network techniques from data measured by the GVR. The GVR reports time-series measurements of brightness temperatures for four channels located at 183.3 ± 1, 3, 7, and 14 GHz.

Koontz, A; Cadeddu, M

2012-12-05T23:59:59.000Z

289

PREPARATION OF REFRACTORY OXIDE CRYSTALS  

DOE Patents (OSTI)

A method is given for preparing uranium dioxide, thorium oxide, and beryllium oxide in the form of enlarged individual crystals. The surface of a fused alkali metal halide melt containing dissolved uranium, thorium, or beryllium values is contacted with a water-vapor-bearing inert gas stream at a rate of 5 to 10 cubic centimeters per minute per square centimeter of melt surface area. Growth of individual crystals is obtained by prolonged contact. Beryllium oxide-coated uranium dioxide crystals are prepared by disposing uranium dioxide crystals 5 to 20 microns in diameter in a beryllium-containing melt and contacting the melt with a water-vapor-bearing inert gas stream in the same manner. (AEC)

Grimes, W.R.; Shaffer, J.H.; Watson, G.M.

1962-11-13T23:59:59.000Z

290

Quantitative organic vapor-particle sampler  

DOE Patents (OSTI)

A quantitative organic vapor-particle sampler for sampling semi-volatile organic gases and particulate components. A semi-volatile organic reversible gas sorbent macroreticular resin agglomerates of randomly packed microspheres with the continuous porous structure of particles ranging in size between 0.05-10 .mu.m for use in an integrated diffusion vapor-particle sampler.

Gundel, Lara (Berkeley, CA); Daisey, Joan M. (Walnut Creek, CA); Stevens, Robert K. (Cary, NC)

1998-01-01T23:59:59.000Z

291

A New Global Water Vapor Dataset  

Science Conference Proceedings (OSTI)

A comprehensive and accurate global water vapor dataset is critical to the adequate understanding of water vapor's role in the earth's climate system. To begin to satisfy this need, the authors have produced a blended dataset made up of global, 5-...

David L. Randel; Thomas J. Greenwald; Thomas H. Vonder Haar; Graeme L. Stephens; Mark A. Ringerud; Cynthia L. Combs

1996-06-01T23:59:59.000Z

292

Atomic vapor laser isotope separation  

SciTech Connect

Atomic vapor laser isotope separation (AVLIS) is a general and powerful technique. A major present application to the enrichment of uranium for light-water power reactor fuel has been under development for over 10 years. In June 1985 the Department of Energy announced the selection of AVLIS as the technology to meet the nation's future need for the internationally competitive production of uranium separative work. The economic basis for this decision is considered, with an indicated of the constraints placed on the process figures of merit and the process laser system. We then trace an atom through a generic AVLIS separator and give examples of the physical steps encountered, the models used to describe the process physics, the fundamental parameters involved, and the role of diagnostic laser measurements.

Stern, R.C.; Paisner, J.A.

1985-11-08T23:59:59.000Z

293

Stacked vapor fed amtec modules  

DOE Patents (OSTI)

The present invention pertains to a stacked AMTEC module. The invention includes a tubular member which has an interior. The member is comprised of a ion conductor that substantially conducts ions relative to electrons, preferably a beta"-alumina solid electrolyte, positioned about the interior. A porous electrode for conducting electrons and allowing sodium ions to pass therethrough, and wherein electrons and sodium ions recombine to form sodium is positioned about the beta"-alumina solid electrolyte. The electrode is operated at a temperature and a pressure that allows the recombined sodium to vaporize. Additionally, an outer current collector grid for distributing electrons throughout the porous electrode is positioned about and contacts the porous electrode. Also included in the invention is transporting means for transporting liquid sodium to the beta"-alumina solid electrolyte of the tubular member. A transition piece is positioned about the interior of the member and contacts the transporting means. The transition piece divides the member into a first cell and a second cell such that each first and second cell has a beta"-alumina solid electrolyte, a first and second porous electrode and a grid. The transition piece conducts electrons from the interior of the tubular member. There is supply means for supplying sodium to the transporting means. Preferably the supply means is a shell which surrounds the tubular member and is operated at a temperature such that the vaporized sodium condenses thereon. Returning means for returning the condensed sodium from the shell to the transporting means provides a continuous supply of liquid sodium to the transporting means. Also, there are first conducting means for conducting electric current from the transition piece which extends through the shell, and second conducting means for conducting electric current to the grid of the first cell which extends through the shell.

Sievers, Robert K. (North Huntingdon, PA)

1989-01-01T23:59:59.000Z

294

ARM - Field Campaign - Water Vapor IOP  

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

govCampaignsWater Vapor IOP govCampaignsWater Vapor IOP Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Campaign : Water Vapor IOP 2000.09.18 - 2000.10.08 Lead Scientist : Henry Revercomb Data Availability Yes For data sets, see below. Description Scientific hypothesis: 1. Microwave radiometer (MWR) observations of the 22 GHz water vapor line can accurately constrain the total column amount of water vapor (assuming a calibration accuracy of 0.5 degC or better, which translates into 0.35 mm PWV). 2. Continuous profiling by Raman lidar provides a stable reference for handling sampling problems and observes a fixed column directly above the site only requiring a single height- independent calibration factor. 3. Agreement between the salt-bath calibrated in-situ probes, chilled

295

Hydrogen production from the steam-iron process with direct reduction of iron oxide by chemical looping combustion of coal char  

SciTech Connect

Experimental results performed with a fluidized-bed reactor supported the feasibility of the three processes including direct reduction of iron oxide by char, H{sub 2} production by the steam-iron process, and the oxidation of Fe{sub 3}O{sub 4} resulting from the steam-iron process to the original Fe{sub 2}O{sub 3} by air. Chars resulting from a Chinese lignite loaded with K{sub 2}CO{sub 3} were used successfully as a reducing material, leading to the reduction of Fe{sub 2}O{sub 3} to FeO and Fe for the steam-iron process, which was confirmed by both the off-gases concentrations and X-ray diffractometer analysis. The reduction of Fe{sub 2}O{sub 3} by K-10-char at 1073 K is desirable from the perspective of the carbon conversion rate and high concentration of CO{sub 2}. The carbon in char was completely converted to CO{sub 2} when the mass ratio of Fe{sub 2}O{sub 3}/K-10-char was increased to 10/0.3. The oxidation rate of K-10-char by Fe{sub 2}O{sub 3} without a gasifying agent was comparable to the K-10-char steam gasification rate. The fractions of FeO and Fe in the reduced residue were 43 and 57%, respectively, in the case of 3 g of Fe{sub 2}O{sub 3} and 0.5 g of K-10-char, which was verified by the total H{sub 2} yield equaling 1000 mL/g K-10-char from the steam-iron process. The time that it took to achieve complete oxidation of Fe{sub 3}O{sub 4} to Fe{sub 2}O{sub 3} by air with an 8.7% O{sub 2} concentration at 1073 K was about 15 min. 53 refs., 19 figs., 5 tabs.

Jing-biao Yang; Ning-sheng Cai; Zhen-shan Li [Tsinghua University, Beijing (China). Key Laboratory of Thermal Science and Power Engineering of Ministry of Education

2008-07-15T23:59:59.000Z

296

Observed Increase of TTL Temperature and Water Vapor in Polluted Couds over Asia  

Science Conference Proceedings (OSTI)

Aerosols can affect cloud particle size and lifetime, which impacts precipitation, radiation and climate. Previous studies1-4 suggested that reduced ice cloud particle size and fall speed due to the influence of aerosols may increase evaporation of ice crystals and/or cloud radiative heating in the tropical tropopause layer (TTL), leading to higher water vapor abundance in air entering the stratosphere. Observational substantiation of such processes is still lacking. Here, we analyze new observations from multiple NASA satellites to show the imprint of pollution influence on stratospheric water vapor. We focus our analysis on the highly-polluted South and East Asia region during boreal summer. We find that "polluted" ice clouds have smaller ice effective radius than "clean" clouds. In the TTL, the polluted clouds are associated with warmer temperature and higher specific humidity than the clean clouds. The water vapor difference between the polluted and clean clouds cannot be explained by other meteorological factors, such as updraft and detrainment strength. Therefore, the observed higher water vapor entry value into the stratosphere in the polluted clouds than in the clean clouds is likely a manifestation of aerosol pollution influence on stratospheric water vapor. Given the radiative and chemical importance of stratospheric water vapor, the increasing emission of aerosols over Asia may have profound impacts on stratospheric chemistry and global energy balance and water cycle.

Su, Hui; Jiang, Jonathan; Liu, Xiaohong; Penner, J.; Read, William G.; Massie, Steven T.; Schoeberl, Mark R.; Colarco, Peter; Livesey, Nathaniel J.; Santee, Michelle L.

2011-06-01T23:59:59.000Z

297

Chemical heat pump  

DOE Patents (OSTI)

A chemical heat pump system is disclosed for use in heating and cooling structures such as residences or commercial buildings. The system is particularly adapted to utilizing solar energy, but also increases the efficiency of other forms of thermal energy when solar energy is not available. When solar energy is not available for relatively short periods of time, the heat storage capacity of the chemical heat pump is utilized to heat the structure, as during nighttime hours. The design also permits home heating from solar energy when the sun is shining. The entire system may be conveniently rooftop located. In order to faciliate installation on existing structures, the absorber and vaporizer portions of the system may each be designed as flat, thin wall, thin pan vessels which materially increase the surface area available for heat transfer. In addition, this thin, flat configuration of the absorber and its thin walled (and therefore relatively flexible) construction permits substantial expansion and contraction of the absorber material during vaporization and absorption without generating voids which would interfere with heat transfer.

Greiner, Leonard (2853-A Hickory Pl., Costa Mesa, CA 92626)

1984-01-01T23:59:59.000Z

298

Chemical heat pump  

DOE Patents (OSTI)

A chemical heat pump system is disclosed for use in heating and cooling structures such as residences or commercial buildings. The system is particularly adapted to utilizing solar energy, but also increases the efficiency of other forms of thermal energy when solar energy is not available. When solar energy is not available for relatively short periods of time, the heat storage capacity of the chemical heat pump is utilized to heat the structure, as during nighttime hours. The design also permits home heating from solar energy when the sun is shining. The entire system may be conveniently rooftop located. In order to facilitate intallation on existing structures, the absorber and vaporizer portions of the system may each be designed as flat, thin wall, thin pan vessels which materially increase the surface area available for heat transfer. In addition, this thin, flat configuration of the absorber and its thin walled (and therefore relatively flexible) construction permits substantial expansion and contraction of the absorber material during vaporization and absorption without generating voids which would interfere with heat transfer.

Greiner, Leonard (2853-A Hickory Pl., Costa Mesa, CA 92626)

1984-01-01T23:59:59.000Z

299

Chemical heat pump  

DOE Patents (OSTI)

A chemical heat pump system is disclosed for use in heating and cooling structures such as residences or commercial buildings. The system is particularly adapted to utilizing solar energy, but also increases the efficiency of other forms of thermal energy when solar energy is not available. When solar energy is not available for relatively short periods of time, the heat storage capacity of the chemical heat pump is utilized to heat the structure, as during nighttime hours. The design also permits home heating from solar energy when the sun is shining. The entire system may be conveniently rooftop located. In order to facilitate installation on existing structures, the absorber and vaporizer portions of the system may each be designed as flat, thin wall, thin pan vessels which materially increase the surface area available for heat transfer. In addition, this thin, flat configuration of the absorber and its thin walled (and therefore relatively flexible) construction permits substantial expansion and contraction of the absorber material during vaporization and absorption without generating voids which would interfere with heat transfer.

Greiner, Leonard (2853-A Hickory Pl., Costa Mesa, CA 92626)

1981-01-01T23:59:59.000Z

300

Chemical heat pump  

DOE Patents (OSTI)

A chemical heat pump system is disclosed for use in heating and cooling structures such as residences or commercial buildings. The system is particularly adapted to utilizing solar energy, but also increases the efficiency of other forms of thermal energy when solar energy is not available. When solar energy is not available for relatively short periods of time, the heat storage capacity of the chemical heat pump is utilized to heat the structure, as during nighttime hours. The design also permits home heating from solar energy when the sun is shining. The entire system may be conveniently rooftop located. In order to facilitate installation on existing structures, the absorber and vaporizer portions of the system may each be designed as flat, thin wall, thin pan vessels which materially increase the surface area available for heat transfer. In addition, this thin, flat configuration of the absorber and its thin walled (and therefore relatively flexible) construction permits substantial expansion and contraction of the absorber material during vaporization and absorption without generating voids which would interfere with heat transfer.

Greiner, Leonard (2853-A Hickory Pl., Costa Mesa, CA 92626)

1984-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Vapor-Particle Separation Using Microporous Metallic Membrane in Crossflow Filtration  

SciTech Connect

Simultaneous separation of vapor and particles in industrial processes could be a key step toward manufacturing of high-quality goods. The separation is critical for successful measurement of volatile or semi-volatile aerosol particles, which no reliable technique exists. We have developed a technique for separation of vapor and particles simultaneously using a specialty microporous metallic membrane. The separator allows the thermally denuded particles traverse straight through the membrane tube, while the vapor molecules permeate through the membrane, separate from the particles and are removed subsequently. The separation technique virtually eliminates the possibility of contamination by vapor re- condensation. We tested the prototype of the vapor-particle separator (VPS) using aerosols prepared from sodium chloride to represent non-volatile aerosols. Chemical like dioctyl phthalate was chosen to represent volatile particles. The test aerosol particles were generated by an atomizer followed by a tandem differential mobility analyser to produce a stream of monodisperse particles in the size range of 10 to 100 nm. In real world particles, we tested the VPS using diesel engine particles that is a mixture of complex chemical composition. Number concentration of the nonvolatile particles reduced as the temperature increased, but the mode diameter of the aerosol population remained unchanged. Number concentration of the volatile particles was also reduced as the temperature increased, but their mode diameters became smaller as particles shrunk in diameter. Differences in the thermal behaviour of the particles were attributed to its transition energy barrier and evaporation rate. Mass balance analysis suggests the separation of vapor and test particles was reasonably complete. Thus, we conclude the VPS could provide an effective means for quantitative characterization of aerosol volatility and separation of vapors from particles.

Cheng, Mengdawn [ORNL

2013-01-01T23:59:59.000Z

302

The combustion chemistry of a fuel tracer: Measured flame speeds and ignition delays and a detailed chemical kinetic model for the oxidation of acetone  

SciTech Connect

Acetone ignition delay and stretch-free laminar flame speed measurements have been carried out and a kinetic model has been developed to simulate these and literature data for acetone and for ketene, which was found to be an important intermediate in its oxidation. The mechanism has been based on one originally devised for dimethyl ether and modified through validation of the hydrogen, carbon monoxide and methane sub-mechanisms. Acetone oxidation in argon was studied behind reflected shock waves in the temperature range 1340-1930 K, at 1 atm and at equivalence ratios of 0.5, 1 and 2; it is also shown that the addition of up to 15% acetone to a stoichiometric n-heptane mixture has no effect on the measured ignition delay times. Flame speeds at 298 K and 1 atm of pure acetone in air were measured in a spherical bomb; a maximum flame speed of {proportional_to}35 cm s{sup -1} at {phi}=1.15 is indicated. (author)

Pichon, S.; Black, G.; Simmie, J.M.; Curran, H.J. [Combustion Chemistry Centre, National University of Ireland, Galway (Ireland); Chaumeix, N.; Yahyaoui, M. [Institut de Combustion Aerothermique Reactivite et Environnement, CNRS, Orleans (France); Donohue, R. [Information Technology, National University of Ireland, Galway (Ireland)

2009-02-15T23:59:59.000Z

303

Chemical Storage-Overview  

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

Storage - Storage - Overview Ali T-Raissi, FSEC Hydrogen Storage Workshop Argonne National Laboratory, Argonne, Illinois August 14-15, 2002 Hydrogen Fuel - Attributes * H 2 +½ O 2 → H 2 O (1.23 V) * High gravimetric energy density: 27.1 Ah/g, based on LHV of 119.93 kJ/g * 1 wt % = 189.6 Wh/kg (0.7 V; i.e. η FC = 57%) * Li ion cells: 130-150 Wh/kg Chemical Hydrides - Definition * They are considered secondary storage methods in which the storage medium is expended - primary storage methods include reversible systems (e.g. MHs & C-nanostructures), GH 2 & LH 2 storage Chemical Hydrides - Definition (cont.) * The usual chemical hydride system is reaction of a reactant containing H in the "-1" oxidation state (hydride) with a reactant containing H in the "+1" oxidation

304

Mercury Vapor At Desert Peak Area (Varekamp & Buseck, 1983) ...  

Open Energy Info (EERE)

Mercury Vapor At Desert Peak Area (Varekamp & Buseck, 1983) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Desert Peak Area...

305

Mercury Vapor At Socorro Mountain Area (Kooten, 1987) | Open...  

Open Energy Info (EERE)

Mercury Vapor At Socorro Mountain Area (Kooten, 1987) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Socorro Mountain Area...

306

Abstract: Apparatus for Measuring Vapor-Liquid Equilibrium ...  

Science Conference Proceedings (OSTI)

... Measurements of the vapor pressures and saturated liquid densities of ethanol and the vapor pressure of an ethanol water mixture (ethanol=0.6743 ...

307

Mercury Vapor At Mccoy Geothermal Area (DOE GTP) | Open Energy...  

Open Energy Info (EERE)

Mercury Vapor At Mccoy Geothermal Area (DOE GTP) Exploration Activity Details Location Mccoy Geothermal Area Exploration Technique Mercury Vapor Activity Date Usefulness not...

308

CORRELATIONS BETWEEN VAPOR SATURATION, FLUID COMPOSITION, AND WELL DECLINE IN LARDERELLO  

Science Conference Proceedings (OSTI)

A large body of field data from Larderello shows striking temporal correlations between decline of well flow-rate, produced gas/steam ratio, chloride concentration and produced vapor fraction. The latter is inferred from measured concentrations of non-condensible gases in samples of well fluid, using chemical phase equilibrium principles. Observed temporal changes in the vapor fractions can be interpreted in term of a ''multiple source'' model, as suggested by D'Amore and Truesdell (1979). This provides clues to the dynamics of reservoir depletion, and to the evaluation of well productivity and longevity.

D'Amore, F.; Pruess, K.

1985-01-22T23:59:59.000Z

309

Water vapor retrieval over many surface types  

SciTech Connect

In this paper we present a study of of the water vapor retrieval for many natural surface types which would be valuable for multi-spectral instruments using the existing Continuum Interpolated Band Ratio (CIBR) for the 940 nm water vapor absorption feature. An atmospheric code (6S) and 562 spectra were used to compute the top of the atmosphere radiance near the 940 nm water vapor absorption feature in steps of 2.5 nm as a function of precipitable water (PW). We derive a novel technique called ``Atmospheric Pre-corrected Differential Absorption`` (APDA) and show that APDA performs better than the CIBR over many surface types.

Borel, C.C.; Clodius, W.C.; Johnson, J.

1996-04-01T23:59:59.000Z

310

Modeling engine oil vaporization and transport of the oil vapor in the piston ring pack on internal combustion engines.  

E-Print Network (OSTI)

??A model was developed to study engine oil vaporization and oil vapor transport in the piston ring pack of internal combustion engines. With the assumption… (more)

Cho, Yeunwoo, 1973-

2004-01-01T23:59:59.000Z

311

Analysis of binary vapor turbines  

DOE Green Energy (OSTI)

The effect the binary mixture has on the turbine is examined in terms of design and cost. Several flow theories for turbines and turbine blading are reviewed. The similarity method, which uses dimensionless parameters, is used in determining rotative speeds and diameters for a variety of inlet temperatures and exit pressures. It is shown that the ratio of exit to inlet specific volume for each component in the mixture is the same for each specie. The specific volume ratio constraints are combined with the temperature equalities, the condenser pressure, and the total inlet entropy to form the constraints necessary to determine the exit state uniquely in an isentropic expansion. The non-isentropic exit state is found in a similar manner. The expansion process is examined for several cases and compared with the expansion of a single component vapor. Finally, in order to maintain high efficiency and to meet the criteria which makes the similarity method valid at high inlet temperatures, turbine multistaging is examined and a sample case is given for a two stage turbine.

Bliss, R.W.; Boehm, R.F.; Jacobs, H.R.

1976-12-01T23:59:59.000Z

312

Perfluorocarbon vapor tagging of blasting cap detonators  

DOE Patents (OSTI)

A plug for a blasting cap is made of an elastomer in which is dissolved a perfluorocarbon. The perfluorocarbon is released as a vapor into the ambient over a long period of time to serve as a detectable taggant.

Dietz, Russell N. (Shoreham, NY); Senum, Gunnar I. (Patchogue, NY)

1981-01-01T23:59:59.000Z

313

Perfluorocarbon vapor tagging of blasting cap detonators  

SciTech Connect

A plug for a blasting cap is made of an elastomer in which is dissolved a perfluorocarbon. The perfluorocarbon is released as a vapor into the ambient over a long period of time to serve as a detectable taggant.

Dietz, R.N.; Senum, G.I.

1981-03-17T23:59:59.000Z

314

Tropospheric Water Vapor and Climate Sensitivity  

Science Conference Proceedings (OSTI)

Estimates are made of the effect of changes in tropospheric water vapor on the climate sensitivity to doubled carbon dioxide (CO2), using a coarse resolution atmospheric general circulation model coupled to a slab mixed layer ocean. The ...

Edwin K. Schneider; Ben P. Kirtman; Richard S. Lindzen

1999-06-01T23:59:59.000Z

315

Forced Dispersion of Liquefied Natural Gas Vapor Clouds with Water Spray Curtain Application  

E-Print Network (OSTI)

There has been, and will continue to be, tremendous growth in the use and distribution of liquefied natural gas (LNG). As LNG poses the hazard of flammable vapor cloud formation from a release, which may result in a massive fire, increased public concerns have been expressed regarding the safety of this fuel. In addition, regulatory authorities in the U.S. as well as all over the world expect the implementation of consequence mitigation measures for LNG spills. For the effective and safer use any safety measure to prevent and mitigate an accidental release of LNG, it is critical to understand thoroughly the action mechanisms. Water spray curtains are generally used by petro-chemical industries to prevent and mitigate heavier-than-air toxic or flammable vapors. It is also used to cool and protect equipment from heat radiation of fuel fires. Currently, water spray curtains are recognized as one of the economic and promising techniques to enhance the dispersion of the LNG vapor cloud formed from a spill. Usually, water curtains are considered to absorb, dilute, disperse and warm a heavier-than-air vapor cloud. Dispersion of cryogenic LNG vapor behaves differently from other dense gases because of low molecular weight and extremely low temperature. So the interaction between water curtain and LNG vapor is different than other heavier vapor clouds. Only two major experimental investigations with water curtains in dispersing LNG vapor clouds were undertaken during the 1970s and 1980s. Studies showed that water spray curtains enhanced LNG vapor dispersion from small spills. However, the dominant phenomena to apply the water curtain most effectively in controlling LNG vapor were not clearly demonstrated. The main objective of this research is to investigate the effectiveness of water spray curtains in controlling the LNG vapor clouds from outdoor experiments. A research methodology has been developed to study the dispersion phenomena of LNG vapor by the action of different water curtains experimentally. This dissertation details the research and experiment development. Small scale outdoor LNG spill experiments have been performed at the Brayton Fire Training Field at Texas A&M University. Field test results regarding important phenomena are presented and discussed. Results have determined that the water curtains are able to reduce the concentration of the LNG vapor cloud, push the vapor cloud upward and transfer heat to the cloud. These are being identified due to the water curtain mechanisms of entrainment of air, dilution of vapor with entrained air, transfer of momentum and heat to the gas cloud. Some of the dominant actions required to control and disperse LNG vapor cloud are also identified from the experimental tests. The gaps are presented as the future work and recommendation on how to improve the experiments in the future. This will benefit LNG industries to enhance its safety system and to make LNG facilities safer.

Rana, Morshed A.

2009-12-01T23:59:59.000Z

316

Multicomponent fuel vaporization at high pressures.  

DOE Green Energy (OSTI)

We extend our multicomponent fuel model to high pressures using a Peng-Robinson equation of state, and implement the model into KIVA-3V. Phase equilibrium is achieved by equating liquid and vapor fugacities. The latent heat of vaporization and fuel enthalpies are also corrected for at high pressures. Numerical simulations of multicomponent evaporation are performed for single droplets for a diesel fuel surrogate at different pressures.

Torres, D. J. (David J.); O'Rourke, P. J. (Peter J.)

2002-01-01T23:59:59.000Z

317

Vehicle exhaust gas chemical sensors using acoustic wave resonators  

DOE Green Energy (OSTI)

Under Sandia`s Laboratory Directed Research and Development (LDRD) program, novel acoustic wave-based sensors were explored for detecting gaseous chemical species in vehicle exhaust streams. The need exists for on-line, real-time monitors to continuously analyze the toxic exhaust gases -- nitrogen oxides (NOx), carbon monoxide (CO), and hydrocarbons (HC) -- for determining catalytic converter efficiency, documenting compliance to emission regulations, and optimizing engine performance through feedback control. In this project, the authors adapted existing acoustic wave chemical sensor technology to the high temperature environment and investigated new robust sensor materials for improving gas detection sensitivity and selectivity. This report describes one new sensor that has potential use as an exhaust stream residual hydrocarbon monitor. The sensor consists of a thickness shear mode (TSM) quartz resonator coated with a thin mesoporous silica layer ion-exchanged with palladium ions. When operated at temperatures above 300 C, the high surface area film catalyzes the combustion of the hydrocarbon vapors in the presence of oxygen. The sensor acts as a calorimeter as the exothermic reaction slightly increases the temperature, stressing the sensor surface, and producing a measurable deviation in the resonator frequency. Sensitivities as high as 0.44 (ppm-{Delta}f) and (ppm-gas) have been measured for propylene gas, with minimum detectable signals of < 50 ppm of propylene at 500 C.

Cernosek, R.W.; Small, J.H.; Sawyer, P.S.; Bigbie, J.R. [Sandia National Labs., Albuquerque, NM (United States); Anderson, M.T. [3M Industrial and Consumer Sector Research Lab., St. Paul, MN (United States)

1998-03-01T23:59:59.000Z

318

Metal atom oxidation laser  

DOE Patents (OSTI)

A chemical laser which operates by formation of metal or carbon atoms and reaction of such atoms with a gaseous oxidizer in an optical resonant cavity is described. The lasing species are diatomic or polyatomic in nature and are readily produced by exchange or other abstraction reactions between the metal or carbon atoms and the oxidizer. The lasing molecules may be metal or carbon monohalides or monoxides. (auth)

Jensen, R.J.; Rice, W.W.; Beattie, W.H.

1975-10-28T23:59:59.000Z

319

Metal atom oxidation laser  

DOE Patents (OSTI)

A chemical laser which operates by formation of metal or carbon atoms and reaction of such atoms with a gaseous oxidizer in an optical resonant cavity is described. The lasing species are diatomic or polyatomic in nature and are readily produced by exchange or other abstraction reactions between the metal or carbon atoms and the oxidizer. The lasing molecules may be metal or carbon monohalides or monoxides.

Jensen, R.J.; Rice, W.W.; Beattie, W.H.

1975-10-28T23:59:59.000Z

320

Combustion chamber and thermal vapor stream producing apparatus and method  

DOE Patents (OSTI)

A new and improved method and apparatus for burning a hydrocarbon fuel for producing a high pressure thermal vapor stream comprising steam and combustion gases for injecting into a subterranean formation for the recovery of liquefiable minerals therefrom, wherein a high pressure combustion chamber having multiple refractory lined combustion zones of varying diameters is provided for burning a hydrocarbon fuel and pressurized air in predetermined ratios injected into the chamber for producing hot combustion gases essentially free of oxidizing components and solid carbonaceous particles. The combustion zones are formed by zones of increasing diameters up a final zone of decreasing diameter to provide expansion zones which cause turbulence through controlled thorough mixing of the air and fuel to facilitate complete combustion. The high pressure air and fuel is injected into the first of the multiple zones where ignition occurs with a portion of the air injected at or near the point of ignition to further provide turbulence and more complete combustion.

Sperry, John S. (Houston, TX); Krajicek, Richard W. (Sugar Land, TX); Cradeur, Robert R. (Spring, TX)

1978-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Chemically assisted mechanical refrigeration process  

DOE Patents (OSTI)

There is provided a chemically assisted mechanical refrigeration process including the steps of: mechanically compressing a refrigerant stream which includes vaporized refrigerant; contacting the refrigerant with a solvent in a mixer at a pressure sufficient to promote substantial dissolving of the refrigerant in the solvent in the mixer to form a refrigerant-solvent solution while concurrently placing the solution in heat exchange relation with a working medium to transfer energy to the working medium, said refrigerant-solvent solution exhibiting a negative deviation from Raoult's Law; reducing the pressure over the refrigerant-solvent solution in an evaporator to allow the refrigerant to vaporize and substantially separate from the solvent while concurrently placing the evolving refrigerant-solvent solution in heat exchange relation with a working medium to remove energy from the working medium to thereby form a refrigerant stream and a solvent stream; and passing the solvent and refrigerant stream from the evaporator. 5 figs.

Vobach, A.R.

1987-11-24T23:59:59.000Z

322

Chemically assisted mechanical refrigeration process  

DOE Patents (OSTI)

There is provided a chemically assisted mechanical refrigeration process including the steps of: mechanically compressing a refrigerant stream which includes vaporized refrigerant; contacting the refrigerant with a solvent in a mixer (11) at a pressure sufficient to promote substantial dissolving of the refrigerant in the solvent in the mixer (11) to form a refrigerant-solvent solution while concurrently placing the solution in heat exchange relation with a working medium to transfer energy to the working medium, said refrigerant-solvent solution exhibiting a negative deviation from Raoult's Law; reducing the pressure over the refrigerant-solvent solution in an evaporator (10) to allow the refrigerant to vaporize and substantially separate from the solvent while concurrently placing he evolving refrigerant-solvent solution in heat exchange relation with a working medium to remove energy from the working medium to thereby form a refrigerant stream and a solvent stream; and passing the solvent and refrigerant stream from the evaporator.

Vobach, Arnold R. (6006 Allentown Dr., Spring, TX 77379)

1987-01-01T23:59:59.000Z

323

Chemically assisted mechanical refrigeration process  

DOE Patents (OSTI)

There is provided a chemically assisted mechanical refrigeration process including the steps of: mechanically compressing a refrigerant stream which includes vaporized refrigerant; contacting the refrigerant with a solvent in a mixer (11) at a pressure sufficient to promote substantial dissolving of the refrigerant in the solvent in the mixer (11) to form a refrigerant-solvent solution while concurrently placing the solution in heat exchange relation with a working medium to transfer energy to the working medium, said refrigerant-solvent solution exhibiting a negative deviation from Raoult's Law; reducing the pressure over the refrigerant-solvent solution in an evaporator (10) to allow the refrigerant to vaporize and substantially separate from the solvent while concurrently placing the evolving refrigerant-solvent solution in heat exchange relation with a working medium to remove energy from the working medium to thereby form a refrigerant stream and a solvent stream; and passing the solvent and refrigerant stream from the evaporator.

Vobach, Arnold R. (6006 Allentown Dr., Spring, TX 77389)

1987-01-01T23:59:59.000Z

324

Chemically assisted mechanical refrigeration process  

DOE Patents (OSTI)

There is provided a chemically assisted mechanical refrigeration process including the steps of: mechanically compressing a refrigerant stream which includes vaporized refrigerant; contacting the refrigerant with a solvent in a mixer at a pressure sufficient to promote substantial dissolving of the refrigerant in the solvent in the mixer to form a refrigerant-solvent solution while concurrently placing the solution in heat exchange relation with a working medium to transfer energy to the working medium, said refrigerant-solvent solution exhibiting a negative deviation from Raoult's Law; reducing the pressure over the refrigerant-solvent solution in an evaporator to allow the refrigerant to vaporize and substantially separate from the solvent while concurrently placing the evolving refrigerant-solvent solution in heat exchange relation with a working medium to remove energy from the working medium to thereby form a refrigerant stream and a solvent stream; and passing the solvent and refrigerant stream from the evaporator. 5 figs.

Vobach, A.R.

1987-06-23T23:59:59.000Z

325

Evaluation of selected chemical processes for production of low-cost silicon (Phase II). Silicon Material Task Low-Cost Silicon Solar Array Project. Eighth quarterly progress report, July 1, 1977--September 30, 1977. [Zinc vapor reduction of silicon tetrachloride in fluidized bed of seed particles  

DOE Green Energy (OSTI)

Progress is reported in the design of a large experimental facility for the preparation of high-purity silicon by the zinc vapor reduction of silicon tetrachloride in a fluidized bed of seed particles to form a free-flowing granular product. As of July 25, 1977, the capacity goal for the experimental facility was raised from 25 to 50 MT Si/year. Process flow diagrams and materials/energy flow sheets have been revised to conform to the higher capacity and a plant layout has been developed for locating the facility within an available structure. A unit-by-unit review of instrumentation and other requirements has been made, with the inclusion of those items in the flow diagrams and flow sheets. Alternative designs are presented for a silicon carbide-coated carbon-lined fluidized-bed reactor contained in hot-wall stainless steel, including alternative designs for zinc vaporizers based on detailed heat-transfer calculations. Conditions and equipment for the conversion of by-product chlorine to hypochlorite for use in the treatment of sewage effluent locally were defined. The logistics of 19 percent NaOH delivery and pick-up of 14 percent NaOCL was worked out and equipment suppliers were identified. Heat dissipation requirements for the fluidized bed, Zn/ZnCl/sub 2/ condenser, and SiCl/sub 4/ waste disposal sections were established. Resistivity and purity data were obtained for DuPont's silicon prepared by batchwise zinc reduction of SiCl/sub 4/. A preliminary safety review was made of the experimental facility. During the report period, the miniplant was operated to (1) provide 2.2 kg of product for JPL evaluation, (2) evaluate methods of product withdrawal, and (3) test three zinc vaporizer concepts. Results of the zinc vaporizer tests were consistent with concurrent heat-transfer calculations. An average value of approximately 450 Btu hr/sup -1/ ft/sup -2/ F/sup -1/ for heat transfer from graphite to boiling zinc (1 atm) was determined.

Blocher, J.M. Jr.; Browning, M.F.; Wilson, W.J.; Carmichael, D.C.

1977-10-20T23:59:59.000Z

326

Next Generation Non-particulate Dry Nonwoven Pad for Chemical Warfare Agent Decontamination  

SciTech Connect

New, non-particulate decontamination materials promise to reduce both military and civilian casualties by enabling individuals to decontaminate themselves and their equipment within minutes of exposure to chemical warfare agents or other toxic materials. One of the most promising new materials has been developed using a needlepunching nonwoven process to construct a novel and non-particulate composite fabric of multiple layers, including an inner layer of activated carbon fabric, which is well-suited for the decontamination of both personnel and equipment. This paper describes the development of a composite nonwoven pad and compares efficacy test results for this pad with results from testing other decontamination systems. The efficacy of the dry nonwoven fabric pad was demonstrated specifically for decontamination of the chemical warfare blister agent bis(2-chloroethyl)sulfide (H or sulfur mustard). GC/MS results indicate that the composite fabric was capable of significantly reducing the vapor hazard from mustard liquid absorbed into the nonwoven dry fabric pad. The mustard adsorption efficiency of the nonwoven pad was significantly higher than particulate activated carbon (p=0.041) and was similar to the currently fielded US military M291 kit (p=0.952). The nonwoven pad has several advantages over other materials, especially its non-particulate, yet flexible, construction. This composite fabric was also shown to be chemically compatible with potential toxic and hazardous liquids, which span a range of hydrophilic and hydrophobic chemicals, including a concentrated acid, an organic solvent and a mild oxidant, bleach.

Ramkumar, S S; Love, A; Sata, U R; Koester, C J; Smith, W J; Keating, G A; Hobbs, L; Cox, S B; Lagna, W M; Kendall, R J

2008-05-01T23:59:59.000Z

327

High ethylene to ethane processes for oxidative coupling  

DOE Patents (OSTI)

Oxidative coupling of lower alkane to higher hydrocarbon is conducted using a catalyst comprising barium and/or strontium component and a metal oxide combustion promoter in the presence of vapor phase halogen component. High ethylene to ethane mole ratios in the product can be obtained over extended operating periods.

Chafin, R.B.; Warren, B.K.

1991-12-17T23:59:59.000Z

328

Chemical Science  

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

reactor concept for deep space exploration Research directions Weapons chemistry and nuclear performance Radiological, nuclear, and chemical signatures Energy production,...

329

Chemical heat pump  

DOE Patents (OSTI)

A chemical heat pump system is disclosed for use in heating and cooling structures such as residences or commercial buildings. The system is particularly adapted to utilizing solar energy, but also increases the efficiency of other forms of thermal energy when solar energy is not available. When solar energy is not available for relatively short periods of time, the heat storage capacity of the chemical heat pump is utilized to heat the structure as during nighttime hours. The design also permits home heating from solar energy when the sun is shining. The entire system may be conveniently rooftop located. In order to facilitate installation on existing structures, the absorber and vaporizer portions of the system may each be designed as flat, thin wall, thin pan vessels which materially increase the surface area available for heat transfer. In addition, this thin, flat configuration of the absorber and its thin walled (and therefore relatively flexible) construction permits substantial expansion and contraction of the absorber material during vaporization and absorption without generating voids which would interfere with heat transfer. The heat pump part of the system heats or cools a house or other structure through a combination of evaporation and absorption or, conversely, condensation and desorption, in a pair of containers. A set of automatic controls change the system for operation during winter and summer months and for daytime and nighttime operation to satisfactorily heat and cool a house during an entire year. The absorber chamber is subjected to solar heating during regeneration cycles and is covered by one or more layers of glass or other transparent material. Daytime home air used for heating the home is passed at appropriate flow rates between the absorber container and the first transparent cover layer in heat transfer relationship in a manner that greatly reduce eddies and resultant heat loss from the absorbant surface to ambient atmosphere.

Greiner, Leonard (2750-C Segerstrom Ave., Santa Ana, CA 92704)

1980-01-01T23:59:59.000Z

330

Oxidative Degradation of Monoethanolamine  

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

Oxidative Degradation of Monoethanolamine Oxidative Degradation of Monoethanolamine Susan Chi Gary T. Rochelle* (gtr@che.utexas.edu, 512-471-7230) The University of Texas at Austin Department of Chemical Engineering Austin, Texas 78712 Prepared for presentation at the First National Conference on Carbon Sequestration, Washington, DC, May 14-17, 2001 Abstract Oxidative degradation of monoethanolamine (MEA) was studied under typical absorber condition of 55°C. The rate of evolution of NH 3 , which was indicative of the overall rate of degradation, was measured continuously in a batch system sparged with air. Dissolved iron from 0.0001 mM to 1 mM yields oxidation rates from 0.37 to 2 mM/hr in MEA solutions loaded with 0.4 mole CO 2 / mole MEA. Ethylenediaminetetraacetic acid (EDTA) and N,N-bis(2- hydroxyethyl)glycine effectively decrease the rate of oxidation in the presence of iron by 40 to

331

Vapor scavenging by atmospheric aerosol particles  

Science Conference Proceedings (OSTI)

Particle growth due to vapor scavenging was studied using both experimental and computational techniques. Vapor scavenging by particles is an important physical process in the atmosphere because it can result in changes to particle properties (e.g., size, shape, composition, and activity) and, thus, influence atmospheric phenomena in which particles play a role, such as cloud formation and long range transport. The influence of organic vapor on the evolution of a particle mass size distribution was investigated using a modified version of MAEROS (a multicomponent aerosol dynamics code). The modeling study attempted to identify the sources of organic aerosol observed by Novakov and Penner (1993) in a field study in Puerto Rico. Experimentally, vapor scavenging and particle growth were investigated using two techniques. The influence of the presence of organic vapor on the particle`s hydroscopicity was investigated using an electrodynamic balance. The charge on a particle was investigated theoretically and experimentally. A prototype apparatus--the refractive index thermal diffusion chamber (RITDC)--was developed to study multiple particles in the same environment at the same time.

Andrews, E.

1996-05-01T23:59:59.000Z

332

Effects of adsorbed water vapor on the Wheeler kinetic rate constant and kinetic adsorption capacity for activated carbon adsorbents  

SciTech Connect

Activated carbon plays a key role reducing organic vapor emissions to the environment from synthetic chemical manufacturing, pesticide manufacturing, in odor control, for removal of contaminant vapors during remediation of hazardous waste sites, and as an adsorption matrix for collection of organic vapors from ambient air in occupational and environmental settings to assess exposure. The Wheeler dynamic adsorption model has been evaluated under laboratory conditions and has shown potential for predicting activated carbon bed penetration. Water vapor is a normal constituent of ambient air that is present at concentrations 1-2 orders of magnitude greater than the concentrations of potentially toxic air contaminants. Many investigations have shown that adsorbed water vapor can reduce the breakthrough-time of activated charcoal beds. The effect of adsorbed water vapor on the predictive power of the Wheeler model has not been evaluated. The research evaluated the effect of water vapor adsorbed on activated charcoal on the subsequent adsorption of four air contaminants, carbon tetrachloride, 1,1,1-trichloroethane, 1,1,2-trichloroethylene, and 1-propanol. The adsorbent used in this research had a large surface area, 1200 m[sup 2]/g and that 95% of the surface area was associated with micropores (pores with diameters less than 2 micrometers). Kinetic adsorption capacities for all four adsorbates were not affected by the presence of water vapor except for some observed enhancement. The kinetic trial data suggest that the primary effect of adsorbed water vapor was to reduce the effective pore radius of the smaller mesopores thus restricting pore diffusion. This results in an increase in the critical bed capacity with shorter breakthrough times for adsorbent beds.

Hall, T.A.

1992-01-01T23:59:59.000Z

333

atmospheric water vapor | OpenEI  

Open Energy Info (EERE)

atmospheric water vapor atmospheric water vapor Dataset Summary Description (Abstract): Monthly Average Solar Resource for 2-axis tracking concentrating collectors for Mexico, Central America, and the Caribbean Islands. (Purpose): Provide information on the solar resource potential for the data domain. The insolation values represent the average solar energy available to a concentrating collector, such as a dish collector, which tracks the sun continuously. Source NREL Date Released July 31st, 2006 (8 years ago) Date Updated October 30th, 2007 (7 years ago) Keywords atmospheric water vapor Carribean Islands Central America DNI GIS Mexico NREL GEF solar SWERA UNEP Data application/zip icon Download Shapefile (zip, 247.8 KiB) text/csv icon Download Data (csv, 370.6 KiB) Quality Metrics Level of Review Some Review

334

ARM - Field Campaign - Water Vapor IOP  

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

govCampaignsWater Vapor IOP govCampaignsWater Vapor IOP Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Campaign : Water Vapor IOP 1996.09.10 - 1996.09.30 Lead Scientist : Henry Revercomb For data sets, see below. Summary SCHEDULE This IOP will be conducted from September 10 - 30, 1996 (coincident with the Fall ARM-UAV IOP). Instruments that do not require supervision will be operated continuously during this period. Instruments that do require supervision are presently planned to be operated for 8-hour periods each day. Because it is necessary to cover as broad a range of environmental conditions as possible, the daily 8-hour period will be shifted across the diurnal cycle as deemed appropriate during the IOP (but will be maintained as a contiguous 8-hour block).

335

atmoshperic water vapor | OpenEI  

Open Energy Info (EERE)

atmoshperic water vapor atmoshperic water vapor Dataset Summary Description (Abstract): Monthly Average Solar Resource for flat-plate collectors tilted at latitude for China. Source NREL Date Released April 12th, 2005 (9 years ago) Date Updated October 30th, 2007 (7 years ago) Keywords atmoshperic water vapor China GEF GIS NREL solar SWERA TILT UNEP Data application/zip icon Download Shapefile (zip, 625.6 KiB) text/csv icon Download Data (csv, 704.1 KiB) Quality Metrics Level of Review Some Review Comment Temporal and Spatial Coverage Frequency Time Period 01/01/1985 - 12/31/1991 License License Open Data Commons Public Domain Dedication and Licence (PDDL) Comment Rate this dataset Usefulness of the metadata Average vote Your vote Usefulness of the dataset Average vote Your vote Ease of access

336

Thermal electric vapor trap arrangement and method  

DOE Patents (OSTI)

A technique for trapping vapor within a section of a tube is disclosed herein. This technique utilizes a conventional, readily providable thermal electric device having a hot side and a cold side and means for powering the device to accomplish this. The cold side of this device is positioned sufficiently close to a predetermined section of the tube and is made sufficiently cold so that any condensable vapor passing through the predetermined tube section is condensed and trapped, preferably within the predetermined tube section itself.

Alger, Terry (Tracy, CA)

1988-01-01T23:59:59.000Z

337

Adsorption of water vapor on reservoir rocks  

DOE Green Energy (OSTI)

Progress is reported on: adsorption of water vapor on reservoir rocks; theoretical investigation of adsorption; estimation of adsorption parameters from transient experiments; transient adsorption experiment -- salinity and noncondensible gas effects; the physics of injection of water into, transport and storage of fluids within, and production of vapor from geothermal reservoirs; injection optimization at the Geysers Geothermal Field; a model to test multiwell data interpretation for heterogeneous reservoirs; earth tide effects on downhole pressure measurements; and a finite-difference model for free surface gravity drainage well test analysis.

Not Available

1993-07-01T23:59:59.000Z

338

Method and Apparatus for Concentrating Vapors for Analysis  

DOE Patents (OSTI)

An apparatus and method are disclosed for pre-concentrating gaseous vapors for analysis. The invention finds application in conjunction with, e.g., analytical instruments where low detection limits for gaseous vapors are desirable. Vapors sorbed and concentrated within the bed of the apparatus can be thermally desorbed achieving at least partial separation of vapor mixtures. The apparatus is suitable, e.g., for preconcentration and sample injection, and provides greater resolution of peaks for vapors within vapor mixtures, yielding detection levels that are 10-10,000 times better than for direct sampling and analysis systems. Features are particularly useful for continuous unattended monitoring applications.

Grate, Jay W. (West Richland, WA); Baldwin, David L. (Kennewick, WA); Anheier, Jr., Norman C. (Richland, WA)

2008-10-07T23:59:59.000Z

339

Development of a chemical vision spectrometer to detect chemical agents.  

DOE Green Energy (OSTI)

This paper describes initial work in developing a no-moving-parts hyperspectral-imaging camera that provides both a thermal image and specific identification of chemical agents, even in the presence of nontoxic plumes. The camera uses enhanced stand-off chemical agent detector (ESCAD) technology based on a conventional thermal-imaging camera interfaced with an acousto-optical tunable filter (AOTF). The AOTF is programmed to allow selected spectral frequencies to reach the two dimensional array detector. These frequencies are combined to produce a spectrum that is used for identification. If a chemical agent is detected, pixels containing the agent-absorbing bands are given a colored hue to indicate the presence of the agent. In test runs, two thermal-imaging cameras were used with a specially designed vaporizer capable of controlled low-level (low ppm-m) dynamic chemical releases. The objective was to obtain baseline information about detection levels. Dynamic releases allowed for realistic detection scenarios such as low sky, grass, and wall structures, in addition to reproducible laboratory releases. Chemical releases consisted of dimethylmethylphosphonate (DMMP) and methanol. Initial results show that the combination of AOTF and thermal imaging will produce a chemical image of a plume that can be detected in the presence of interfering substances.

Demirgian, J.

1999-02-23T23:59:59.000Z

340

Investigation of gasification chemical looping combustion combined cycle performance  

SciTech Connect

A novel combined cycle based on coal gasification and chemical looping combustion (CLC) offers a possibility of both high net power efficiency and separation of the greenhouse gas CO{sub 2}. The technique involves the use of a metal oxide as an oxygen carrier, which transfers oxygen from the combustion air to the fuel, and the avoidance of direct contact between fuel and combustion air. The fuel gas is oxidized by an oxygen carrier, an oxygen-containing compound, in the fuel reactor. The oxygen carrier in this study is NiO. The reduced oxygen carrier, Ni, in the fuel reactor is regenerated by the air in the air reactor. In this way, fuel and air are never mixed, and the fuel oxidation products CO{sub 2} and water vapor leave the system undiluted by air. All that is needed to get an almost pure CO{sub 2} product is to condense the water vapor and to remove the liquid water. When the technique is combined with gas turbine and heat recovery steam generation technology, a new type of combined cycle is formed which gives a possibility of obtaining high net power efficiency and CO{sub 2} separation. The performance of the combined cycle is simulated using the ASPEN software tool in this paper. The influence of the water/coal ratio on the gasification and the influence of the CLC process parameters such as the air reactor temperature, the turbine inlet supplementary firing, and the pressure ratio of the compressor on the system performance are discussed. Results show that, assuming an air reactor temperature of 1200{sup o}C, a gasification temperature of 1100 {sup o}C, and a turbine inlet temperature after supplementary firing of 1350{sup o}C, the system has the potential to achieve a thermal efficiency of 44.4% (low heating value), and the CO{sub 2} emission is 70.1 g/(kW h), 90.1% of the CO{sub 2} captured. 22 refs., 7 figs., 6 tabs.

Wenguo Xiang; Sha Wang; Tengteng Di [Southeast University, Nanjing (China). Key Laboratory of Clean Coal Power Generation and Combustion Technology of the Ministry of Education

2008-03-15T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

The speciation and morphology of chromium oxide nanoparticles in a diffusion flame  

E-Print Network (OSTI)

along the centerline of a flame from the 7.5 mm ID nozzle,Oxide Nanoparticles in a Diffusion Flame Bing Guo and Ian M.in a hydrogen diffusion flame seeded with Cr(CO) 6 vapor.

Guo, B; Kennedy, Ian M

2004-01-01T23:59:59.000Z

342

Profiling Atmospheric Water Vapor by Microwave Radiometry  

Science Conference Proceedings (OSTI)

High-altitude microwave radiometric observations at frequencies near 92 and 183.3 GHz were used to study the potential of retrieving atmospheric water vapor profiles over both land and water. An algorithm based on an extended Kaiman-Bucy filter ...

J. R. Wang; J. L. King; T. T. Wilheit; G. Szejwach; L. H. Gesell; R. A. Nieman; D. S. Niver; B. M. Krupp; J. A. Gagliano

1983-05-01T23:59:59.000Z

343

Polynomial Fits to Saturation Vapor Pressure  

Science Conference Proceedings (OSTI)

The authors describe eighth- and sixth-order polynomial fits to Wexler's and Hyland-Wexler's saturation-vapor-pressure expressions. Fits are provided in both least-squares and relative-error norms. Error analysis is presented. The authors show ...

Piotr J. Flatau; Robert L. Walko; William R. Cotton

1992-12-01T23:59:59.000Z

344

Vaporization of synthetic fuels. Final report. [Thesis  

DOE Green Energy (OSTI)

The problem of transient droplet vaporization in a hot convective environment is examined. The main objective of the present study is to develop an algorithm for the droplet vaporization which is simple enough to be feasibly incorporated into a complete spray combustion analysis and yet will also account for the important physics such as liquid-phase internal circulation, unsteady droplet heating and axisymmetric gas-phase convection. A simplified liquid-phase model has been obtained based on the assumption of the existence of a Hill's spherical vortex inside the droplet together with some approximations made in the governing diffusion equation. The use of the simplified model in a spray situation has also been examined. It has been found that droplet heating and vaporization are essentially unsteady and droplet temperature is nonuniform for a significant portion of its lifetime. It has also been found that the droplet vaporization characteristic can be quite sensitive to the particular liquid-phase and gas-phase models. The results of the various models are compared with the existing experimental data. Due to large scattering in the experimental measurements, particularly the droplet diameter, no definite conclusion can be drawn based on the experimental data. Finally, certain research problems which are related to the present study are suggested for future studies.

Sirignano, W.A.; Yao, S.C.; Tong, A.Y.; Talley, D.

1983-01-01T23:59:59.000Z

345

A Water Vapor Index from Satellite Measurements  

Science Conference Proceedings (OSTI)

A method for deriving a water vapor index is presented. An important feature of the index is the fact that it does not rely on radiosondes. Thus, it is not influenced by problems associated with radiosondes and the extent to which the horizontal ...

Larry M. McMillin; David S. Crosby; Mitchell D. Goldberg

1995-07-01T23:59:59.000Z

346

Bi-based Piezoelectric Thin Films via Chemical Solution Deposition  

Science Conference Proceedings (OSTI)

BNT-BKT-BMgT thin films showed very promising piezoelectric response with ... Chemical Quantification of Oxide Interfaces Using Energy-dispersive X-ray ...

347

The Homogeneous Forcing of Mercury Oxidation to Provide Low-Cost Capture  

DOE Green Energy (OSTI)

Oxidized mercury formed in combustors (e.g., HgCl{sub 2}) is much more easily captured in existing pollution control equipment (e.g., wet scrubbers for SO{sub 2}) than elemental mercury. This is principally due to the high solubility of the oxidized form in water. Work over the last several years in our laboratory and elsewhere has identified the general outlines of the homogeneous chemistry of oxidation. The goal of the work reported here is to make use of this knowledge of the oxidation mechanism to devise simple and inexpensive ways to promote the oxidation. The hypothesis is that simple fuels such as hydrogen or CO can promote oxidation via the free radicals they generate during their decomposition. These free radicals then promote the formation of Cl from HCl via reactions such as OH+HCl {yields} H{sub 2}O+Cl. The Cl (and Cl{sub 2} derived from Cl recombination) are considered the principal oxidizing species. In our studies, mercury vapor is exposed to HCl under isothermal conditions in a gas containing N{sub 2}, O{sub 2}, and H{sub 2}O. The experiments systematically explore the influence of reaction temperature, HCl concentration, and H{sub 2}O concentration. These baseline conditions are then perturbed by the addition of varying amounts of H{sub 2}, CO, and H{sub 2}/CO added jointly. The following report presents the results of a literature review associated with the dissertation of the student supported by the program. This outlines the state-of-the-art in mercury behavior. It then describes the experimental facilities and the results of tests involving the promotion of the oxidation reaction by H{sub 2}, CO, and H{sub 2}/CO combinations. These results indicate a substantial enhancement of oxidation under isothermal conditions at 900-1000 K, while the additives inhibit oxidation at 1200 K. The next step is to determine whether the existing chemical kinetic models of mercury oxidation are capable of reproducing this behavior. These models can then be used to extrapolate the findings to nonisothermal conditions typical of boiler environments. This would provide guidance on where to inject the oxidation promoters in a practical boiler, and how much promoter is required.

John C. Kramlich; Linda Castiglone

2006-04-01T23:59:59.000Z

348

Oxidation of coal-water slurry feed to hydrogasifier  

DOE Patents (OSTI)

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

Lee, Bernard S. (Lincolnwood, IL)

1976-01-01T23:59:59.000Z

349

Chemical technology division: Annual technical report 1987  

DOE Green Energy (OSTI)

Highlights of the Chemical Technology (CMT) Division's activities during 1987 are presented. In this period, CMT conducted research and development in the following areas: (1) high-performance batteries--mainly lithium-alloy/metal sulfide and sodium/sulfur; (2) aqueous batteries (lead-acid, nickel/iron, etc.); (3) advanced fuel cells with molten carbonate or solid oxide electrolytes; (4) coal utilization, including the heat and seed recovery technology for coal-fired magnetohydrodynamics plants and the technology for fluidized-bed combustion; (5) methods for the electromagnetic continuous casting of steel sheet and for the purification of ferrous scrap; (6) methods for recovery of energy from municipal waste and techniques for treatment of hazardous organic waste; (7) nuclear technology related to a process for separating and recovering transuranic elements from nuclear waste, the recovery processes for discharged fuel and the uranium blanket in a sodium-cooled fast reactor, and waste management; and (8) physical chemistry of selected materials in environments simulating those of fission and fusion energy systems. The Division also has a program in basic chemistry research in the areas of fluid catalysis for converting small molecules to desired products; materials chemistry for liquids and vapors at high temperatures; interfacial processes of importance to corrosion science, high-temperature superconductivity, and catalysis; the thermochemistry of various minerals; and the geochemical processes responsible for trace-element migration within the earth's crust. The Division continued to be the major user of the technical support provided by the Analytical Chemistry Laboratory at ANL. 54 figs., 9 tabs.

Not Available

1988-05-01T23:59:59.000Z

350

The Effect of vapor subcooling on film condensation of metals  

E-Print Network (OSTI)

This work presents an analysis of the interfacial "vapor-condensate" temperature distribution, which includes the effect of subcooling (supersaturation) in the vapor. Experimental data from previous investigators for ...

Fedorovich, Eugene D.

1968-01-01T23:59:59.000Z

351

Waste tank headspace gas and vapor characterization reference guide  

SciTech Connect

This document is to serve as a reference guide for gas and vapor sample results presented in tank characterization reports. It describes sampling equipment, devices, and protocols, and sample collection and analysis methods common to all vapor samples.

Huckaby, J.L.

1995-06-01T23:59:59.000Z

352

Atmospheric Solar Heating Rate in the Water Vapor Bands  

Science Conference Proceedings (OSTI)

The total absorption of solar radiation by water vapor in clear atmosphere is parameterized as a simple function of the scaled water vapor amount. For applications to cloudy and hazy atmospheres, the flux-weighted k-distribution functions are ...

Ming-Dah Chou

1986-11-01T23:59:59.000Z

353

Estimating the Atmospheric Water Vapor Content from Sun Photometer Measurements  

Science Conference Proceedings (OSTI)

The differential absorption technique for estimating columnar water vapor values from the analysis of sunphotometric measurements with wide- and narrowband interferential filters centered near 0.94 ?m is discussed and adapted. Water vapor line ...

Artemio Plana-Fattori; Michel Legrand; Didier Tanré; Claude Devaux; Anne Vermeulen; Philippe Dubuisson

1998-08-01T23:59:59.000Z

354

Moisture Durability of Vapor Permeable Insulating Sheathing (Fact Sheet)  

SciTech Connect

In this project, Building America team Building Science Corporation researched some of the ramifications of using exterior, vapor permeable insulation on retrofit walls with vapor permeable cavity insulation. Retrofit strategies are a key factor in reducing exterior building stock consumption.

Not Available

2013-10-01T23:59:59.000Z

355

Improved Retrieval of Integrated Water Vapor from Water Vapor Radiometer Measurements Using Numerical Weather Prediction Models  

Science Conference Proceedings (OSTI)

Water vapor radiometer (WVR) retrieval algorithms require a priori information on atmospheric conditions along the line of sight of the radiometer in order to derive opacities from observed brightness temperatures. This paper's focus is the mean ...

Steven R. Chiswell; Steven Businger; Michael Bevis; Fredrick Solheim; Christian Rocken; Randolph Ware

1994-10-01T23:59:59.000Z

356

Effects of capillarity and vapor adsorption in the depletion of vapor-dominated geothermal reservoirs  

DOE Green Energy (OSTI)

Vapor-dominated geothermal reservoirs in natural (undisturbed) conditions contain water as both vapor and liquid phases. The most compelling evidence for the presence of distributed liquid water is the observation that vapor pressures in these systems are close to saturated vapor pressure for measured reservoir temperatures (White et al., 1971; Truesdell and White, 1973). Analysis of natural heat flow conditions provides additional, indirect evidence for the ubiquitous presence of liquid. From an analysis of the heat pipe process (vapor-liquid counterflow) Preuss (1985) inferred that effective vertical permeability to liquid phase in vapor-dominated reservoirs is approximately 10{sup 17} m{sup 2}, for a heat flux of 1 W/m{sup 2}. This value appears to be at the high end of matrix permeabilities of unfractured rocks at The Geysers, suggesting that at least the smaller fractures contribute to liquid permeability. For liquid to be mobile in fractures, the rock matrix must be essentially completely liquid-saturated, because otherwise liquid phase would be sucked from the fractures into the matrix by capillary force. Large water saturation in the matrix, well above the irreducible saturation of perhaps 30%, has been shown to be compatible with production of superheated steam (Pruess and Narasimhan, 1982). In response to fluid production the liquid phase will boil, with heat of vaporization supplied by the reservoir rocks. As reservoir temperatures decline reservoir pressures will decline also. For depletion of ''bulk'' liquid, the pressure would decline along the saturated vapor pressure curve, while for liquid held by capillary and adsorptive forces inside porous media, an additional decline will arise from ''vapor pressure lowering''. Capillary pressure and vapor adsorption effects, and associated vapor pressure lowering phenomena, have received considerable attention in the geothermal literature, and also in studies related to geologic disposal of heat generating nuclear wastes, and in the drying of porous materials. Geothermally oriented studies were presented by Chicoine et al. (1977), Hsieh and Ramey (1978, 1981), Herkelrath et al. (1983), and Nghiem and Ramey (1991). Nuclear waste-related work includes papers by Herkelrath and O'Neal (1985), Pollock (1986), Eaton and Bixler (1987), Pruess et al. (1990), Nitao (1990), and Doughty and E'ruess (1991). Applications to industrial drying of porous materials have been discussed by Hamiathy (1969) arid Whitaker (1977). This paper is primarily concerned with evaluating the impact of vapor pressure lowering (VPL) effects on the depletion behavior of vapor-dominated reservoirs. We have examined experimental data on vapor adsorption and capillary pressures in an effort to identify constitutive relationships that would be applicable to the tight matrix rocks of vapor-dominated systems. Numerical simulations have been performed to evaluate the impact of these effects on the depletion of vapor-dominated reservoirs.

Pruess, Karsten; O'Sullivan, Michael

1992-01-01T23:59:59.000Z

357

Chemical sensors  

DOE Patents (OSTI)

Sensors responsive to small changes in the concentration of chemical species are disclosed, comprising (a) a mechanochemically responsive polymeric film capable of expansion or contraction in response to a change in its chemical environment, operatively coupled to (b) a transducer capable of directly converting said expansion or contraction to a measurable electrical response.

Lowell, Jr., James R. (Bend, OR); Edlund, David J. (Bend, OR); Friesen, Dwayne T. (Bend, OR); Rayfield, George W. (Bend, OR)

1991-01-01T23:59:59.000Z

358

Chemical preconcentrator  

DOE Patents (OSTI)

A chemical preconcentrator is disclosed with applications to chemical sensing and analysis. The preconcentrator can be formed by depositing a resistive heating element (e.g. platinum) over a membrane (e.g. silicon nitride) suspended above a substrate. A coating of a sorptive material (e.g. a microporous hydrophobic sol-gel coating or a polymer coating) is formed on the suspended membrane proximate to the heating element to selective sorb one or more chemical species of interest over a time period, thereby concentrating the chemical species in the sorptive material. Upon heating the sorptive material with the resistive heating element, the sorbed chemical species are released for detection and analysis in a relatively high concentration and over a relatively short time period. The sorptive material can be made to selectively sorb particular chemical species of interest while not substantially sorbing other chemical species not of interest. The present invention has applications for use in forming high-sensitivity, rapid-response miniaturized chemical analysis systems (e.g. a "chem lab on a chip").

Manginell, Ronald P. (Albuquerque, NM); Frye-Mason, Gregory C. (Cedar Crest, NM)

2001-01-01T23:59:59.000Z

359

Modeling engine oil vaporization and transport of the oil vapor in the piston ring pack on internal combustion engines  

E-Print Network (OSTI)

A model was developed to study engine oil vaporization and oil vapor transport in the piston ring pack of internal combustion engines. With the assumption that the multi-grade oil can be modeled as a compound of several ...

Cho, Yeunwoo, 1973-

2004-01-01T23:59:59.000Z

360

Evaluation of Catalysts from Different Origin for Vapor Phase Upgrading in Biomass Pyrolysis  

SciTech Connect

Liquid fuels and chemicals from biomass resources arouse much interests in research and development. Fast pyrolysis of biomass has the potential to effectively change solid biomass materials into liquid products. However, bio-oil from traditional pyrolysis processes is difficult to apply in industry, because of its complicated composition, high oxygen content, low stability, etc. Upgrading or refining of the bio-oil should be performed for industrial application of biomass pyrolysis. Often, the process would be done in a separate reactor downstream of the pyrolysis process. In this paper, a laboratory scale micro test facility was constructed, wherein the pyrolysis of pine and catalytic upgrading of the resulting vapors were closely coupled in one reactor. The composition of vapor effluent was monitored with a molecular beam mass spectrometer (MBMS) for the online evaluation of the catalyst performance. Catalysts from different origin were tested and compared for the effectiveness of pyrolysis vapor upgrading, namely commercial zeolites, Ni based steam reforming catalyst, CaO, MgO, and several laboratory-made catalysts. The reaction temperature for catalytic upgrading varied between 400 and 600 centigrade, and the gaseous residence time ranged from 0.1 second to above 2 second, to simulate the conditions in industrial application. It is revealed that some catalysts are active in transform most of primary biomass pyrolysis vapors into hydrocarbons, resulting in nonoxygenated products, which is beneficial for downstream utilization. Others are not as effective, results in minor improvement compared with blank test results.

Zhang, X.; Mukarakate, C.; Zheng, Z.; Nimlos, M.

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

CHEMICAL ENGINEERING AND MANUFACTURING CHEMICAL ENGINEERING  

E-Print Network (OSTI)

CHEMICAL ENGINEERING AND MANUFACTURING CHEMICAL ENGINEERING Objective Chemical Engineers of chemicals. This lesson introduces students to one component of chemical engineering: food processing, and a chemical engineer 2. How chemical engineers are involved in food production 3. That chemical engineers need

Provancher, William

362

Chemical heat pump and chemical energy storage system  

DOE Patents (OSTI)

A chemical heat pump and storage system employs sulfuric acid and water. In one form, the system includes a generator and condenser, an evaporator and absorber, aqueous acid solution storage and water storage. During a charging cycle, heat is provided to the generator from a heat source to concentrate the acid solution while heat is removed from the condenser to condense the water vapor produced in the generator. Water is then stored in the storage tank. Heat is thus stored in the form of chemical energy in the concentrated acid. The heat removed from the water vapor can be supplied to a heat load of proper temperature or can be rejected. During a discharge cycle, water in the evaporator is supplied with heat to generate water vapor, which is transmitted to the absorber where it is condensed and absorbed into the concentrated acid. Both heats of dilution and condensation of water are removed from the thus diluted acid. During the discharge cycle the system functions as a heat pump in which heat is added to the system at a low temperature and removed from the system at a high temperature. The diluted acid is stored in an acid storage tank or is routed directly to the generator for reconcentration. The generator, condenser, evaporator, and absorber all are operated under pressure conditions specified by the desired temperature levels for a given application. The storage tanks, however, can be maintained at or near ambient pressure conditions. In another form, the heat pump system is employed to provide usable heat from waste process heat by upgrading the temperature of the waste heat.

Clark, Edward C. (Woodinville, WA); Huxtable, Douglas D. (Bothell, WA)

1985-08-06T23:59:59.000Z

363

Thermodynamic properties of some metal oxide-zirconia systems  

SciTech Connect

Metal oxide-zirconia systems are a potential class of materials for use as structural materials at temperatures above 1900 K. These materials must have no destructive phase changes and low vapor pressures. Both alkaline earth oxide (MgO, CaO, SrO, and BaO)-zirconia and some rare earth oxide (Y2O3, Sc2O3, La2O3, CeO2, Sm2O3, Gd2O3, Yb2O3, Dy2O3, Ho2O3, and Er2O3)-zirconia system are examined. For each system, the phase diagram is discussed and the vapor pressure for each vapor species is calculated via a free energy minimization procedure. The available thermodynamic literature on each system is also surveyed. Some of the systems look promising for high temperature structural materials.

Jacobson, N.S.

1989-12-01T23:59:59.000Z

364

Lateral steam flow revealed by a pressure build-up test at the Matsukawa vapor-dominated geothermal field, Japan  

Science Conference Proceedings (OSTI)

Results and discussion of a pressure build-up test at the Matsukawa vapor-dominated geothermal field in north-east Japan are reported. Pressure build-up behavior of three dry steam wells was monitored at the wellhead in October 1986. The observed pressure gradient clearly shows the existence of a lateral steam flow from south-west to north-east in the reservoir. This result suggests that the vapor-dominated reservoir extends further south-west than it is currently being developed. These conclusions are supported by production records and chemical data.

Hanano, M. Sakagawa, Y. (Japan Metals and Chemicals Co. Ltd., 24-Ukai, Takizawa-mura, Iwate 020-01 (JP))

1990-01-01T23:59:59.000Z

365

Advanced Membrane Systems: Recovering Wasteful and Hazardous Fuel Vapors at the Gasoline Tank  

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

Case study covering Compact Membrane Systems, Inc. and its membrane vapor processor that recovers fuel vapors from gasoline refueling.

366

Vapor-pressure lowering in geothermal systems  

SciTech Connect

The water vapor-pressure lowering phenomenon in porous media was investigated for a range of temperatures by measuring vapor pressure vs. mass of water adsorbed in consolidated sandstone cores and unconsolidated silica sands. Experimental results showed that the mass of water adsorbed on the rock surface is much more than the amount of pore steam. Results also revealed that the water adsorption is caused mainly by micropores in the porous medium. Measurement of the mass of methane and ethane adsorbed on dry rocks showed that the amount of adsorption is not great in comparison with the pore gas. It was found that adsorption data for water/sandstone core studies could be normalized with respect to temperature. Although this appears not to have been reported previously, it does agree in principle with findings for solid powders with micropores. Another interesting result was that reanalysis of previous studies of capillarity in sandstones indicates that experimental data probably were influenced mostly by adsorption.

Hsieh, C.H.; Ramey, H.J. Jr.

1983-02-01T23:59:59.000Z

367

Hydrocarbon pool and vapor fire data analysis  

SciTech Connect

The flame geometry and thermal radiation data from a series of large scale experiments involving liquefied petroleum gas (LPG) and gasoline spills on water were analyzed. The experiments were conducted at the Naval Weapons Center, China Lake, California. Two types of fires have been studied; namely, pool fires and vapor fires. The spill quantity varied from 4 m/sup 3/ to approximately 6 m/sup 3/. The LPG pool fire flame height to diameter ratio were between 3.5 and 4.5. The gasoline flame height was about 2. The flame emissive powers for LPG pool fires ranged from 78 kW/m/sup 2/ to 115 kW/m/sup 2/. The average surface emissive power for gasoline pool fire was 40 kW/m/sup 2/. The LPG vapor fire emissive power ranged from 159 to 269 kW/m/sup 2/. 63 figures, 13 tables.

Mudan, K.S.

1984-10-01T23:59:59.000Z

368

Chemical Activation  

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

Chemical Activation of Single-walled Carbon Nanotubes for Hydrogen Adsorption Milton R. Smith, Jr., 1 Edward W. Bittner, 1 Wei Shi, 1, 2 J. Karl Johnson, 1, 2 and Bradley C....

369

Chemical deposition methods using supercritical fluid solutions  

DOE Patents (OSTI)

A method for depositing a film of a desired material on a substrate comprises dissolving at least one reagent in a supercritical fluid comprising at least one solvent. Either the reagent is capable of reacting with or is a precursor of a compound capable of reacting with the solvent to form the desired product, or at least one additional reagent is included in the supercritical solution and is capable of reacting with or is a precursor of a compound capable of reacting with the first reagent or with a compound derived from the first reagent to form the desired material. The supercritical solution is expanded to produce a vapor or aerosol and a chemical reaction is induced in the vapor or aerosol so that a film of the desired material resulting from the chemical reaction is deposited on the substrate surface. In an alternate embodiment, the supercritical solution containing at least one reagent is expanded to produce a vapor or aerosol which is then mixed with a gas containing at least one additional reagent. A chemical reaction is induced in the resulting mixture so that a film of the desired material is deposited.

Sievers, Robert E. (Boulder, CO); Hansen, Brian N. (Boulder, CO)

1990-01-01T23:59:59.000Z

370

Copper vapor laser modular packaging assembly  

DOE Patents (OSTI)

A modularized packaging arrangement for one or more copper vapor lasers and associated equipment is disclosed herein. This arrangement includes a single housing which contains the laser or lasers and all their associated equipment except power, water and neon, and means for bringing power, water, and neon which are necessary to the operation of the lasers into the container for use by the laser or lasers and their associated equipment.

Alger, Terry W. (Tracy, CA); Ault, Earl R. (Dublin, CA); Moses, Edward I. (Castro Valley, CA)

1992-01-01T23:59:59.000Z

371

Copper vapor laser modular packaging assembly  

DOE Patents (OSTI)

A modularized packaging arrangement for one or more copper vapor lasers and associated equipment is disclosed herein. This arrangement includes a single housing which contains the laser or lasers and all their associated equipment except power, water and neon, and means for bringing power, water, and neon which are necessary to the operation of the lasers into the container for use by the laser or lasers and their associated equipment. 2 figs.

Alger, T.W.; Ault, E.R.; Moses, E.I.

1992-12-01T23:59:59.000Z

372

OPERATIONAL TESTS OF EBWR VAPOR RECOVERY SYSTEM  

SciTech Connect

A description of the Experimental Boiling Water Reactor vapor-recovery system is given. The seal air operating pressures, temperatures, and moisture content were measured. Air flow through the seals was measured and seal wear was assessed. Assuming direct-cycle D/sub 2/ operation, the seals were evaluated relative to the amount of D/sub 2/ leakage that would be controlled (C.J.G.)

Gariboldi, R.J.; Jacobson, D.R.

1960-08-01T23:59:59.000Z

373

Transport properties of fission product vapors  

DOE Green Energy (OSTI)

Kinetic theory of gases is used to calculate the transport properties of fission product vapors in a steam and hydrogen environment. Provided in tabular form is diffusivity of steam and hydrogen, viscosity and thermal conductivity of the gaseous mixture, and diffusivity of cesium iodide, cesium hydroxide, diatomic tellurium and tellurium dioxide. These transport properties are required in determining the thermal-hydraulics of and fission product transport in light water reactors.

Im, K.H.; Ahluwalia, R.K.

1983-07-01T23:59:59.000Z

374

Apparatus and method for photochemical vapor deposition  

DOE Patents (OSTI)

A photochemical vapor deposition apparatus includes a reactor housing having a window in one wall above a reaction chamber in the housing. A transparent curtain divides the reaction chamber into a reaction zone and a flush zone. At least one substrate is mounted in the reaction zone in light communication with the window so that ultraviolet radiation may penetrate through the window into the reaction zone. The window is kept clear by a gas flowing through the flush zone.

Jackson, Scott C. (Wilmington, DE); Rocheleau, Richard E. (Wilmington, DE)

1987-03-31T23:59:59.000Z

375

Passive vapor transport solar heating systems  

DOE Green Energy (OSTI)

In the systems under consideration, refrigerant is evaporated in a solar collector and condensed in thermal storage for space or water heating located within the building at a level below that of the collector. Condensed liquid is lifted to an accumulator above the collector by the vapor pressure generated in the collector. Tests of two systems are described, and it is concluded that one of these systems offers distinct advantages.

Hedstrom, J.C.; Neeper, D.A.

1985-01-01T23:59:59.000Z

376

Chemical sensors  

DOE Patents (OSTI)

Sensors responsive to small changes in the concentration of chemical species are disclosed, comprising a mechanicochemically responsive polymeric film capable of expansion or contraction in response to a change in its chemical environment, either operatively coupled to a transducer capable of directly converting the expansion or contraction to a measurable electrical or optical response, or adhered to a second inert polymeric strip, or doped with a conductive material. 12 figs.

Lowell, J.R. Jr.; Edlund, D.J.; Friesen, D.T.; Rayfield, G.W.

1992-06-09T23:59:59.000Z

377

Chemical sensors  

DOE Patents (OSTI)

Sensors responsive to small changes in the concentration of chemical species are disclosed, comprising a mechanicochemically responsive polymeric film capable of expansion or contraction in response to a change in its chemical environment, either operatively coupled to a transducer capable of directly converting the expansion or contraction to a measurable electrical or optical response, or adhered to a second inert polymeric strip, or doped with a conductive material.

Lowell, Jr., James R. (Bend, OR); Edlund, David J. (Bend, OR); Friesen, Dwayne T. (Bend, OR); Rayfield, George W. (Eugene, OR)

1992-01-01T23:59:59.000Z

378

A molecular view of vapor deposited glasses  

SciTech Connect

Recently, novel organic glassy materials that exhibit remarkable stability have been prepared by vapor deposition. The thermophysical properties of these new ''stable'' glasses are equivalent to those that common glasses would exhibit after aging over periods lasting thousands of years. The origin of such enhanced stability has been elusive; in the absence of detailed models, past studies have discussed the formation of new polyamorphs or that of nanocrystals to explain the observed behavior. In this work, an atomistic molecular model of trehalose, a disaccharide of glucose, is used to examine the properties of vapor-deposited stable glasses. Consistent with experiment, the model predicts the formation of stable glasses having a higher density, a lower enthalpy, and higher onset temperatures than those of the corresponding ''ordinary'' glass formed by quenching the bulk liquid. Simulations reveal that newly formed layers of the growing vapor-deposited film exhibit greater mobility than the remainder of the material, thereby enabling a reorganization of the film as it is grown. They also reveal that ''stable'' glasses exhibit a distinct layered structure in the direction normal to the substrate that is responsible for their unusual properties.

Singh, Sadanand; Pablo, Juan J. de [Department of Chemical and Biological Engineering, University of Wisconsin, Madison Wisconsin 53706 (United States)

2011-05-21T23:59:59.000Z

379

Boiler Tube Internal Oxide Scale Thickness Measurement: Best Practices  

Science Conference Proceedings (OSTI)

Long-term high-temperature exposure of reheater and superheater tubes in fossil-fired steam boilers results in the growth of iron oxide scale (magnetite) on the inner tube surface. This internal oxide layer on the water side of the tube acts as a thermal insulator, reducing heat transfer through the tube wall into the internal water vapor. Over time, this insulating effect limits heat transmission into the water vapor inside the tube, which, in turn, causes chronic overheating of the tube wall. The ...

2013-12-20T23:59:59.000Z

380

The Homogeneus Forcing of Mercury Oxidation to provide Low-Cost Capture  

DOE Green Energy (OSTI)

Trace amounts of mercury are found in all coals. During combustion, or during thermal treatment in advanced coal processes, this mercury is vaporized and can be released to the atmosphere with the ultimate combustion products. This has been a cause for concern for a number of years, and has resulted in a determination by the EPA to regulate and control these emissions. Present technology does not, however, provide inexpensive ways to capture or remove mercury. Mercury that exits the furnace in the oxidized form (HgCl{sub 2}) is known to much more easily captured in existing pollution control equipment (e.g., wet scrubbers for SO{sub 2}), principally due to its high solubility in water. Work funded by DOE has helped understand the chemical kinetic processes that lead to mercury oxidation in furnaces. The scenario is as follows. In the flame the mercury is quantitatively vaporized as elemental mercury. Also, the chlorine in the fuel is released as HCl. The direct reaction Hg+HCl is, however, far too slow to be of practical consequence in oxidation. The high temperature region does supports a small concentration of atomic chlorine. As the gases cool (either in the furnace convective passes, in the quench prior to cold gas cleanup, or within a sample probe), the decay in Cl atom is constrained by the slowness of the principal recombination reaction, Cl+Cl+M{yields}Cl{sub 2}+M. This allows chlorine atom to hold a temporary, local superequilibrium concentration . Once the gases drop below about 550 C, the mercury equilibrium shifts to favor HgCl{sub 2} over Hg, and this superequilibrium chlorine atom promotes oxidation via the fast reactions Hg+Cl+M{yields}HgCl+M, HgCl+Cl+M{yields}HgCl{sub 2}+M, and HgCl+Cl{sub 2}{yields}HgCl{sub 2}+Cl. Thus, the high temperature region provides the Cl needed for the reaction, while the quench region allows the Cl to persist and oxidize the mercury in the absence of decomposition reactions that would destroy the HgCl{sub 2}. Promoting mercury oxidation is one means of getting moderate-efficiency, 'free' mercury capture when wet gas cleanup systems are already in place. The chemical kinetic model we developed to describe the oxidation process suggests that in fuel lean gases, the introduction of trace amounts of H{sub 2} within the quench region leads to higher Cl concentrations via chain branching. The amount of additive, and the temperature at the addition point are critical. We investigated this process in a high-temperature quartz flow reactor. The results do indicate a substantial amount of promotion of oxidation with the introduction of relatively small amounts of hydrogen at around 1000 K ({approx}100 ppm relative to the furnace gas). In practical systems the source of this hydrogen is likely to be a small natural gas steam reformer. This would also produce CO, so co-injection of CO was also tested. The CO did not provide any additional promotion, and in some cases led to a reduction in oxidation. We also examined the influence of NO and SO{sub 2} on the promotion process. We did not see any influence under the conditions examined. The present results were for a 0.5 s, isothermal plug flow environment. The next step should be to determine the appropriate injection point for the hydrogen and the performance under realistic temperature quench conditions. This could be accomplished first by chemical kinetic modeling, and then by tunnel flow experiment.

John Kramlich; Linda Castiglone

2007-06-30T23:59:59.000Z

Note: This page contains sample records for the topic "oxide chemical vapor" 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

FIRST DETECTION OF WATER VAPOR IN A PRE-STELLAR CORE  

Science Conference Proceedings (OSTI)

Water is a crucial molecule in molecular astrophysics as it controls much of the gas/grain chemistry, including the formation and evolution of more complex organic molecules in ices. Pre-stellar cores provide the original reservoir of material from which future planetary systems are built, but few observational constraints exist on the formation of water and its partitioning between gas and ice in the densest cores. Thanks to the high sensitivity of the Herschel Space Observatory, we report on the first detection of water vapor at high spectral resolution toward a dense cloud on the verge of star formation, the pre-stellar core L1544. The line shows an inverse P-Cygni profile, characteristic of gravitational contraction. To reproduce the observations, water vapor has to be present in the cold and dense central few thousand AU of L1544, where species heavier than helium are expected to freeze out onto dust grains, and the ortho:para H{sub 2} ratio has to be around 1:1 or larger. The observed amount of water vapor within the core (about 1.5 Multiplication-Sign 10{sup -6} M{sub Sun }) can be maintained by far-UV photons locally produced by the impact of galactic cosmic rays with H{sub 2} molecules. Such FUV photons irradiate the icy mantles, liberating water vapor in the core center. Our Herschel data, combined with radiative transfer and chemical/dynamical models, shed light on the interplay between gas and solids in dense interstellar clouds and provide the first measurement of the water vapor abundance profile across the parent cloud of a future solar-type star and its potential planetary system.

Caselli, Paola; Douglas, Thomas [School of Physics and Astronomy, University of Leeds, Leeds LS2 9JT (United Kingdom); Keto, Eric [Harvard-Smithsonian Center for Astrophysics, 60 Garden Street, Cambridge, MA 02138 (United States); Bergin, Edwin A. [Department of Astronomy, The University of Michigan, 500 Church Street, Ann Arbor, MI 48109-1042 (United States); Tafalla, Mario [Observatorio Astronomico Nacional (IGN), Calle Alfonso XII, 3, E-28014 Madrid (Spain); Aikawa, Yuri [Department of Earth and Planetary Sciences, Kobe University, Nada, 657-8501 Kobe (Japan); Pagani, Laurent [LERMA and UMR 8112 du CNRS, Observatoire de Paris, 61 Av. de l'Observatoire, F-75014 Paris (France); Yildiz, Umut A.; Kristensen, Lars E.; Van Dishoeck, Ewine F. [Leiden Observatory, Leiden University, P.O. Box 9513, 2300 RA Leiden (Netherlands); Van der Tak, Floris F. S. [SRON Netherlands Institute for Space Research, P.O. Box 800, 9700 AV, Groningen (Netherlands); Walmsley, C. Malcolm; Codella, Claudio [INAF-Osservatorio Astrofisico di Arcetri, Largo E. Fermi 5, I-50125 Firenze (Italy); Nisini, Brunella, E-mail: p.caselli@leeds.ac.uk [INAF-Osservatorio Astronomico di Roma, I-00040 Monte Porzio Catone (Italy)

2012-11-10T23:59:59.000Z

382

Thermal Design of an Ultrahigh Temperature Vapor Core Reactor Combined Cycle Nuclear Power Plant  

SciTech Connect

Current work modeling high temperature compact heat exchangers may demonstrate the design feasibility of a Vapor Core Reactor (VCR) driven combined cycle power plant. For solid nuclear fuel designs, the cycle efficiency is typically limited by a metallurgical temperature limit which is dictated by fuel and structural melting points. In a vapor core, the gas/vapor phase nuclear fuel is uniformly mixed with the topping cycle working fluid. Heat is generated homogeneously throughout the working fluid thus extending the metallurgical temperature limit. Because of the high temperature, magnetohydrodynamic (MHD) generation is employed for topping cycle power extraction. MHD rejected heat is transported via compact heat exchanger to a conventional Brayton gas turbine bottoming cycle. High bottoming cycle mass flow rates are required to remove the waste heat because of low heat capacities for the bottoming cycle gas. High mass flow is also necessary to balance the high Uranium Tetrafluoride (UF{sub 4}) mass flow rate in the topping cycle. Heat exchanger design is critical due to the high temperatures and corrosive influence of fluoride compounds and fission products existing in VCR/MHD exhaust. Working fluid compositions for the topping cycle include variations of Uranium Tetrafluoride, Helium and various electrical conductivity seeds for the MHD. Bottoming cycle working fluid compositions include variations of Helium and Xenon. Some thought has been given to include liquid metal vapor in the bottoming cycle for a Cheng or evaporative cooled design enhancement. The NASA Glenn Lewis Research Center code Chemical Equilibrium with Applications (CEA) is utilized for evaluating chemical species existing in the gas stream. Work being conducted demonstrates the compact heat exchanger design, utilization of the CEA code, and assessment of different topping and bottoming working fluid compositions. (authors)

Bays, Samuel E.; Anghaie, Samim; Smith, Blair; Knight, Travis [Innovative Space Power and Propulsion Institute, University of Florida, 202 Nuclear Science Building, Gainesville, FL 32611 (United States)

2004-07-01T23:59:59.000Z

383

Chemical Scientist Hendrik Bluhm Receives Bessel Research Award  

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

Chemical Scientist Hendrik Bluhm Chemical Scientist Hendrik Bluhm Receives Bessel Research Award Chemical Scientist Hendrik Bluhm Receives Bessel Research Award Print Friday, 24 May 2013 00:00 Hendrik Bluhm of the Lab's Chemical Sciences Division is the recipient of the Friedrich Wilhelm Bessel Research award, bestowed by Germany's Alexander von Humboldt Foundation. Award winners are honored for their outstanding research record and invited to spend a period of up to one year cooperating on a long-term research project with specialist colleagues at a research institution in Germany. Bluhm works on beamline 11.0.2 at the Advanced Light Source, investigating solid/vapor and liquid/vapor interfaces under realistic conditions of pressure and temperature, using photoelectron spectroscopy and scanning probe microscopy

384

Multifunctional Oxides  

Science Conference Proceedings (OSTI)

3) Electric, ferroelectric, magnetic and photonic properties of oxides 4) Theoretical modeling of epitaxial growth, interfaces and microstructures 5) Composition ...

385

Mechanical Stability of Solid Oxide Fuel Cell (SOFC) Materials  

Science Conference Proceedings (OSTI)

Abstract Scope, Solid oxide fuel cells (SOFCs) are devices that convert chemical energy into electricity with high efficiency and low pollutant emissions. In case ...

386

Thermal conversion of biomass to valuable fuels, chemical feedstocks and chemicals  

DOE Patents (OSTI)

A continuous process for the conversion of biomass to form a chemical feedstock is described. The biomass and an exogenous metal oxide, preferably calcium oxide, or metal oxide precursor are continuously fed into a reaction chamber that is operated at a temperature of at least 1400.degree. C. to form reaction products including metal carbide. The metal oxide or metal oxide precursor is capable of forming a hydrolizable metal carbide. The reaction products are quenched to a temperature of 800.degree. C. or less. The resulting metal carbide is separated from the reaction products or, alternatively, when quenched with water, hydolyzed to provide a recoverable hydrocarbon gas feedstock.

Peters, William A. (Lexington, MA); Howard, Jack B. (Winchester, MA); Modestino, Anthony J. (Hanson, MA); Vogel, Fredreric (Villigen PSI, CH); Steffin, Carsten R. (Herne, DE)

2009-02-24T23:59:59.000Z

387

Chemical Evolution  

E-Print Network (OSTI)

In this series of lectures we first describe the basic ingredients of galactic chemical evolution and discuss both analytical and numerical models. Then we compare model results for the Milky Way, Dwarf Irregulars, Quasars and the Intra-Cluster- Medium with abundances derived from emission lines. These comparisons allow us to put strong constraints on the stellar nucleosynthesis and the mechanisms of galaxy formation.

Francesca Matteucci

2007-04-05T23:59:59.000Z

388

Vapor port and groundwater sampling well  

DOE Patents (OSTI)

A method and apparatus have been developed for combining groundwater monitoring wells with unsaturated-zone vapor sampling ports. The apparatus allows concurrent monitoring of both the unsaturated and the saturated zone from the same well at contaminated areas. The innovative well design allows for concurrent sampling of groundwater and volatile organic compounds (VOCs) in the vadose (unsaturated) zone from a single well, saving considerable time and money. The sample tubes are banded to the outer well casing during installation of the well casing. 10 figs.

Hubbell, J.M.; Wylie, A.H.

1996-01-09T23:59:59.000Z

389

Vapor port and groundwater sampling well  

DOE Patents (OSTI)

A method and apparatus has been developed for combining groundwater monitoring wells with unsaturated-zone vapor sampling ports. The apparatus allows concurrent monitoring of both the unsaturated and the saturated zone from the same well at contaminated areas. The innovative well design allows for concurrent sampling of groundwater and volatile organic compounds (VOCs) in the vadose (unsaturated) zone from a single well, saving considerable time and money. The sample tubes are banded to the outer well casing during installation of the well casing.

Hubbell, Joel M. (Idaho Falls, ID); Wylie, Allan H. (Idaho Falls, ID)

1996-01-01T23:59:59.000Z

390

Copper vapor laser acoustic thermometry system  

DOE Patents (OSTI)

A copper vapor laser (CVL) acoustic thermometry system is disclosed. The invention couples an acoustic pulse a predetermined distance into a laser tube by means of a transducer and an alumina rod such that an echo pulse is returned along the alumina rod to the point of entry. The time differential between the point of entry of the acoustic pulse into the laser tube and the exit of the echo pulse is related to the temperature at the predetermined distance within the laser tube. This information is processed and can provide an accurate indication of the average temperature within the laser tube.

Galkowski, J.J.

1986-08-27T23:59:59.000Z

391

Photochemical studies of alkali halide vapors  

SciTech Connect

Thesis. An apparatus has been constructed for studying the photodissociation of alkali halides to produce excited alkali metal atoms. The key component is a low pressure H/sub 2/ arc continuum uv source. Radiation from this source, modulated by a chopping wheel and analyzed by a monochromator, enters a cell containing the alkali halide vapor. In the appropriate wavelength range, photodissociation occurs to produce the alkali atom in an excited /sup 2/p state, the flourescence from which is detected by a photomultiplier-lock-in amplifier combination. (auth)

Earl, B.L.

1973-08-01T23:59:59.000Z

392

ARM - Field Campaign - Fall 1997 Water Vapor IOP  

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

Water Vapor IOP Water Vapor IOP Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Campaign : Fall 1997 Water Vapor IOP 1997.09.15 - 1997.10.05 Lead Scientist : Henry Revercomb For data sets, see below. Summary The Water Vapor IOP was conducted as a follow-up to a predecessor IOP on water vapor held in September 1996. This IOP relied heavily on both ground-based guest and CART instrumentation and in-situ aircraft and tethered sonde/kite measurements. Primary operational hours were from 6 p.m. Central until at least midnight, with aircraft support normally from about 9 p.m. until midnight when available. However, many daytime measurements were made to support this IOP. The first Water Vapor IOP primarily concentrated on the atmosphere's lowest

393

Analysis of the transient compressible vapor flow in heat pipe  

SciTech Connect

The transient compressible one-dimensional vapor flow dynamics in a heat pipe is modeled. The numerical results are obtained by using the implicit non-iterative Beam-Warming finite difference method. The model is tested for simulated heat pipe vapor flow and actual vapor flow in cylindrical heat pipes. A good comparison of the present transient results for the simulated heat pipe vapor flow with the previous results of a two-dimensional numerical model is achieved and the steady state results are in agreement with the existing experimental data. The transient behavior of the vapor flow under subsonic, sonic, and supersonic speeds and high mass flow rates are successfully predicted. The one-dimensional model also describes the vapor flow dynamics in cylindrical heat pipes at high temperatures.

Jang, J.H.; Faghri, A. [Wright State Univ., Dayton, OH (United States); Chang, W.S. [Wright Research and Development Center, Wright-Patterson, OH (United States)

1989-07-01T23:59:59.000Z

394

Method and apparatus for concentrating vapors for analysis  

DOE Patents (OSTI)

A pre-concentration device and a method are disclosed for concentrating gaseous vapors for analysis. Vapors sorbed and concentrated within the bed of the pre-concentration device are thermally desorbed, achieving at least partial separation of the vapor mixtures. The pre-concentration device is suitable, e.g., for pre-concentration and sample injection, and provides greater resolution of peaks for vapors within vapor mixtures, yielding detection levels that are 10-10,000 times better than direct sampling and analysis systems. Features are particularly useful for continuous unattended monitoring applications. The invention finds application in conjunction with, e.g., analytical instruments where low detection limits for gaseous vapors are desirable.

Grate, Jay W. (West Richland, WA); Baldwin, David L. (Kennewick, WA); Anheier, Jr., Norman C. (Richland, WA)

2012-06-05T23:59:59.000Z

395

Interfacial instability induced by lateral vapor pressure fluctuation in bounded thin liquid-vapor layers  

E-Print Network (OSTI)

We study an instability of thin liquid-vapor layers bounded by rigid parallel walls from both below and above. In this system, the interfacial instability is induced by lateral vapor pressure fluctuation, which is in turn attributed to the effect of phase change: evaporation occurs at the hotter portion of the interface and condensation at the colder one. The high vapor pressure drives the liquid away and the low one pulls it up. A set of equations describing the temporal evolution of the interface of the liquid-vapor layers is derived. This model neglects the effect of mass loss or gain at the interface and guarantees the mass conservation of the liquid layer. The result of linear stability analysis of the model shows that the presence of the pressure dependence of the local saturation temperature suppresses the growth of long-wave disturbances. We find the stability criterion, which suggests that only slight temperature gradients are sufficient to overcome the stabilizing gravitational effect for a water an...

Kanatani, Kentaro

2008-01-01T23:59:59.000Z

396

Method for controlling corrosion in thermal vapor injection gases  

DOE Patents (OSTI)

An improvement in the method for producing high pressure thermal vapor streams from combustion gases for injection into subterranean oil producing formations to stimulate the production of viscous minerals is described. The improvement involves controlling corrosion in such thermal vapor gases by injecting water near the flame in the combustion zone and injecting ammonia into a vapor producing vessel to contact the combustion gases exiting the combustion chamber.

Sperry, John S. (Houston, TX); Krajicek, Richard W. (Houston, TX)

1981-01-01T23:59:59.000Z

397

Effect of aluminizing of Cr-containing ferritic alloys on the seal strength of a novel high-temperature solid oxide fuel cell sealing glass  

Science Conference Proceedings (OSTI)

A novel high-temperature alkaline-earth silicate sealing glass was developed for solid oxide fuel cell (SOFC) applications. The glass was used to join two metallic coupons of Cr-containing ferritic stainless steel for seal strength evaluation. In previous work, SrCrO4 was found to form along the glass/steel interface, which led to severe strength degradation. In the present study, aluminization of the steel surface was investigated as a remedy to minimize or prevent the strontium chromate formation. Three different processes for aluminization were evaluated with Crofer22APU stainless steel: pack cementation, vapor phase deposition, and aerosol spraying. It was found that pack cementation resulted in a rough surface with occasional cracks in the Al-diffused region. Vapor phase deposition yielded a smoother surface, but the resulting high Al content increased the coefficient of thermal expansion (CTE), resulting in failure of joined coupons. Aerosol spraying of an Al-containing salt resulted in formation of a thin aluminum oxide layer without any surface damage. The room temperature seal strength was evaluated in the as-fired state and in environmentally aged conditions. In contrast to earlier results with uncoated Crofer22APU, the aluminized samples showed no strength degradation even for samples aged in air. Interfacial and chemical compatibility was also investigated. The results showed aluminization to be a viable candidate approach to minimize undesirable chromate formation between alkaline earth silicate sealing glass and Cr-containing interconnect alloys for SOFC applications.

Chou, Y. S.; Stevenson, Jeffry W.; Singh, Prabhakar

2008-12-01T23:59:59.000Z

398

Decontamination of metals using chemical etching  

DOE Patents (OSTI)

The invention relates to chemical etching process for reclaiming contaminated equipment wherein a reduction-oxidation system is included in a solution of nitric acid to contact the metal to be decontaminated and effect reduction of the reduction-oxidation system, and includes disposing a pair of electrodes in the reduced solution to permit passage of an electrical current between said electrodes and effect oxidation of the reduction-oxidation system to thereby regenerate the solution and provide decontaminated equipment that is essentially radioactive contamination-free.

Lerch, Ronald E. (Kennewick, WA); Partridge, Jerry A. (Richland, WA)

1980-01-01T23:59:59.000Z

399

Mercury Vapor At Lassen Volcanic National Park Area (Varekamp...  

Open Energy Info (EERE)

Community Login | Sign Up Search Page Edit History Facebook icon Twitter icon Mercury Vapor At Lassen Volcanic National Park Area (Varekamp & Buseck, 1983) Jump to:...

400

Mercury Vapor At Mickey Hot Springs Area (Varekamp & Buseck,...  

Open Energy Info (EERE)

Community Login | Sign Up Search Page Edit History Facebook icon Twitter icon Mercury Vapor At Mickey Hot Springs Area (Varekamp & Buseck, 1983) Jump to: navigation,...

Note: This page contains sample records for the topic "oxide chemical vapor" 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

Mercury Vapor At Breitenbush Hot Springs Area (Varekamp & Buseck...  

Open Energy Info (EERE)

Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Breitenbush Hot Springs Area (Varekamp & Buseck, 1983) Exploration Activity...

402

Mercury Vapor At Vale Hot Springs Area (Varekamp & Buseck, 1983...  

Open Energy Info (EERE)

Community Login | Sign Up Search Page Edit History Facebook icon Twitter icon Mercury Vapor At Vale Hot Springs Area (Varekamp & Buseck, 1983) Jump to: navigation, search...

403

Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) | Open Energy  

Open Energy Info (EERE)

Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Exploration Activity: Mercury Vapor At Haleakala Volcano Area (Thomas, 1986) Exploration Activity Details Location Haleakala Volcano Area Exploration Technique Mercury Vapor Activity Date Usefulness not indicated DOE-funding Unknown Notes The field survey program on the northwest rift zone consisted of soil mercury and radon emanometry surveys, groundwater temperature and chemistry studies, Schlumberger resistivity soundings and self-potential profiles. Geophysical and geochemical surveys along this rift (southwest) were limited by difficult field conditions and access limitations. The geophysical program consisted of one Schlumberger sounding, one

404

Measurements of Vapor Pressures and PVT Properties for n ...  

Science Conference Proceedings (OSTI)

Page 1. Measurements of Vapor Pressures and PVT Properties for n-Butane from 280 to 440 K at Pressures to 200 MPa ...

2006-07-20T23:59:59.000Z

405

Interaction of sodium vapor and graphite studied by ...  

Science Conference Proceedings (OSTI)

The kinetics of the reaction between graphite and sodium vapor is analyzed with support ... High temperature compression test to determine the anode paste ...

406

Optimal Control of Vapor Extraction of Heavy Oil.  

E-Print Network (OSTI)

??Vapor extraction (Vapex) process is an emerging technology for viscous oil recovery that has gained much attention in the oil industry. However, the oil production… (more)

Muhamad, Hameed

2012-01-01T23:59:59.000Z

407

ARM - Field Campaign - ARM-FIRE Water Vapor Experiment  

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

Order Data Browell, Edward LASE Order Data Gutman, Seth GPS Order Data Richardson, Scott Chilled Mirror Order Data Sachse, G. Water Vapor Order Data Schmidlin, Francis CM Sondes...

408

Raman Lidar Measurements of Aerosols and Water Vapor During the...  

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

Raman Lidar Measurements of Aerosols and Water Vapor During the May 2003 Aerosol IOP R. A. Ferrare National Aeronautics and Space Administration Langley Research Center Hampton,...

409

Cesium vapor cycle for an advanced LMFBR  

SciTech Connect

A review indicates that a cesium vapor topping cycle appears attractive for use in the intermediate fluid circuit of an advanced LMFBR designed for a reactor outlet temperature of 1250$sup 0$F or more and would have the following advantages: (1) it would increase the thermal efficiency by about 5 to 10 points (from approximately 40 percent to approximately 45 to 50 percent) thus reducing the amount of waste heat rejected to the environment by 15 to 30 percent. (2) the higher thermal efficiency should reduce the overall capital cost of the reactor plant in dollars per kilowatt. (3) the cesium can be distilled out of the intermediate fluid circuit to leave it bone-dry, thus greatly reducing the time and cost of maintenance work (particularly for the steam generator). (4) the large volume and low pressure of the cesium vapor region in the cesium condenser-steam generator greatly reduces the magnitude of pressure fluctuations that might occur in the event of a leak in a steam generator tube, and the characteristics inherent in a condenser make it easy to design for rapid concentration of any noncondensibles that may form as a consequence of a steam leak into the cesium region so that a steam leak can be detected easily in the very early stages of its development. (auth)

Fraas, A.P.

1975-01-01T23:59:59.000Z

410

Reactions of atmospheric vapors with lunar soil  

SciTech Connect

Detailed experimental data have been acquired for the hydration of the surfaces of lunar fines. Inert vapor adsorption has been employed to measure the surface properties (surface energy, surface area, porosity, etc.) and changes wrought in the hydration-dehydration processes. Plausible mechanisms have been considered and the predominant process involves hydration of the metamict metallosilicate surfaces to form a hydrated laminar structure akin to terrestrial clays. Additional credence for this interpretation is obtained by comparison to existing geochemical literature concerning terrestrial weathering of primary metallosilicates. The surface properties of the hydrated lunar fines are compared favorably to those of terrestrial clay minerals. In addition, experimental results are given to show that fresh disordered surfaces of volcanic sand react with water vapor in a manner virtually identical to the majority of the lunar fines. The results show that ion track etching and/or grain boundary attack are minor contributions in the weathering of lunar fines in the realm of our microgravimetric experimental conditions. 14 references. (auth)

Fuller, E.L. Jr.; Agron, P.A.

1976-03-01T23:59:59.000Z

411

Ethanol production by vapor compression distillation  

DOE Green Energy (OSTI)

The goal of this project is to develop and demonstrate a one gallon per hour vapor compression distillation unit for fuel ethanol production that can be profitably manufactured and economically operated by individual family units. Vapor compression distillation is already an industrially accepted process and this project's goal is to demonstrate that it can be done economically on a small scale. Theoretically, the process is independent of absolute pressure. It is only necessary that the condenser be at higher pressure than the evaporator. By reducing the entire process to a pressure of approximately 0.1 atmosphere, the evaporation and condensation can occur at near ambient temperature. Even though this approach requires a vacuum pump, and thus will not represent the final cost effective design, it does not require preheaters, high temperature materials, or as much insulation as if it were to operate a near ambient pressure. Therefore, the operation of the ambient temperature unit constitutes the first phase of this project. Presently, the ambient temperature unit is fully assembled and has begun testing. So far it has successfully separated ethanol from a nine to one diluted input solution. However the production rate has been very low.

Ellis, G.S.

1981-01-01T23:59:59.000Z

412

Porous iron and ferric oxide pellets for hydrogen storage: texture and transport characteristics  

Science Conference Proceedings (OSTI)

Materials for hydrogen storage based on the recovery reduction of Fe3O4 to iron and back iron oxidation to Fe3O4 by water vapor were studied. The preparation conditions for cylindrical pellets from ferric oxide/aluminium ... Keywords: hydrogen storage, inverse gas chromatography, steam iron process, transport parameters

Karel Soukup; Jan Rogut; Jacek Grabowski; Marian Wiatowski; Magdalena Ludwik-Parda?a; Petr Schneider; Olga Šolcová

2010-11-01T23:59:59.000Z

413

About Chemical Hazards  

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

Chemical Hazards What Is a Chemical Hazard? chemical hazards.jpg A chemical hazard is any substance that can cause harm, primarily to people. Chemicals of all kinds are stored in...

414

Integration of Global Positioning System and Scanning Water Vapor Radiometers for Precipitable Water Vapor and Cloud Liquid Path Estimates  

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

Integration of Global Positioning System and Scanning Integration of Global Positioning System and Scanning Water Vapor Radiometers for Precipitable Water Vapor and Cloud Liquid Path Estimates V. Mattioli and P. Basili Department of Electronic and Information Engineering University of Perugia Perugia, Italy E. R. Westwater Cooperative Institute for Research in Environmental Sciences University of Colorado National Oceanic and Atmospheric Administration Environmental Technology Laboratory Boulder, Colorado Introduction In recent years the Global Positioning System (GPS) has proved to be a reliable instrument for measuring precipitable water vapor (PWV) (Bevis et al. 1992), offering an independent source of information on water vapor when compared with microwave radiometers (MWRs), and/or radiosonde

415

Vapor and gas sampling of Single-Shell Tank 241-A-101 using the Vapor Sampling System  

Science Conference Proceedings (OSTI)

This document presents sampling data resulting from the June 8, 1995, sampling of SST 241-A-101 using the Vapor Sampling System.

Caprio, G.S.

1995-11-01T23:59:59.000Z

416

Vapor and gas sampling of single-shell tank 241-SX-106 using the vapor sampling system  

SciTech Connect

This document presents sampling data resulting from the March 24, 1995, sampling of SST 241-SX-106 using the vapor sampling system.

Caprio, G.S.

1995-09-20T23:59:59.000Z

417

Economic and Technical Tradeoffs Between Open and Closed Cycle Vapor Compression Evaporators  

E-Print Network (OSTI)

Evaporators are used extensively in the chemical, pulp and paper, food and beverage, and related industries. Mechanical vapor recompression (MVR) evaporators are a type using an open heat pump cycle with steam as the working fluid. The technology is widely used and time-proven. Closed cycle vapor compression is an emerging technology. A secondary working fluid such as a halocarbon is used in a closed heat pump cycle to transfer heat from the steam condenser to the hottest surface. Advantages of closed cycle evaporation include flexibility in working fluid selection, potential savings in compressor first cost, and isolation of the compressor from potentially corrosive or troublesome gases and liquid droplets in the suction vapor. A major disadvantage of closed cycle evaporation is that the driving force developed by the compressor (temperature difference) must be shared between two heat transfer surfaces, vs. one in the open cycle design. This paper explores the advantages and disadvantages of open and closed cycle evaporators. Factors considered include working fluid physical properties and thermodynamics, compressor operating limits and cost, and surface area sizing and cost.

Timm, M. L.

1986-06-01T23:59:59.000Z

418

Chemical Looping for Combustion and Hydrogen Production  

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

ChemiCal looping for Combustion and ChemiCal looping for Combustion and hydrogen produCtion Objective The objective of this project is to determine the benefits of chemical looping technology used with coal to reduce CO 2 emissions. Background Chemical looping is a new method to convert coal or gasified coal to energy. In chemical looping, there is no direct contact between air and fuel. The chemical looping process utilizes oxygen from metal oxide oxygen carrier for fuel combustion, or for making hydrogen by "reducing" water. In combustion applications, the products of chemical looping are CO 2 and H 2 O. Thus, once the steam is condensed, a relatively pure stream of CO 2 is produced ready for sequestration. The production of a sequestration ready CO 2 stream does not require any additional separation units

419

Mechanisms and controlling characteristics of the catalytic oxidation of methane  

DOE Green Energy (OSTI)

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

Klier, K.

1990-01-01T23:59:59.000Z

420

RESONANT FARADAY ROTATION IN A HOT LITHIUM VAPOR  

E-Print Network (OSTI)

RESONANT FARADAY ROTATION IN A HOT LITHIUM VAPOR By SCOTT RUSSELL WAITUKAITIS A Thesis Submitted: #12;Abstract I describe a study of Faraday rotation in a hot lithium vapor. I begin by dis- cussing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 2.3 The Lithium Oven and Solenoid . . . . . . . . . . . . . . . . . 7 3 Theoretical Framework

Cronin, Alex D.

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


421

New Regenerative Cycle for Vapor Compression Refrigeration  

Office of Scientific and Technical Information (OSTI)

SCIENTIFIC REPORT SCIENTIFIC REPORT Title Page Project Title: New Regenerative Cycle for Vapor Compression Refrigeration DOE Award Number: DE-FG36-04GO14327 Document Title: Final Scientific Report Period Covered by Report: September 30, 2004 to September 30, 2005 Name and Address of Recipient Organization: Magnetic Development, Inc., 68 Winterhill Road, Madison, CT 06443, phone: 203-214-7247, fax: 203-421-7948, e-mail: mjb1000@aol.com Contact Information: Mark J. Bergander, Ph.D., P.E., Principal Investigator, phone: 203-214-7247, fax: 203-421-7948, e-mail: mjb1000@aol.com Project Objective (as stated in the proposal): The main objective of this project is to confirm on a well-instrumented prototype the theoretically derived claims of higher efficiency and coefficient

422

FLAMMABILITY CHARACTERISTICS OF COMBUSTIBLE GASES AND VAPORS  

Office of Scientific and Technical Information (OSTI)

Bulletin 627 Bulletin 627 BUREAU o b MINES FLAMMABILITY CHARACTERISTICS OF COMBUSTIBLE GASES AND VAPORS By Michael G. Zabetakis DISCLAIMER This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency Thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement,

423

How solvent vapors can improve steam floods  

Science Conference Proceedings (OSTI)

Thermal recovery methods depend for their success on the viscosity reduction of heavy crude oils at high temperatures. The viscosity of a heavy oil can also be reduced if it is diluted with a low-viscosity solvent, such as one of the lighter hydrocarbons. It is not surprising that there has been considerable interest in combining the two methods. The process of injecting vaporized solvent with the steam for a gravity drainage type recovery is described here along with a description of the particular phase behavior of steam/solvent mixtures which is beneficial to the process. And computer simulations which compare steam-only and steam/solvent floods under Athabasca-type conditions are overviewed.

Vogel, J. [Vogel, (Jack), Seabrook, TX (United States)

1996-11-01T23:59:59.000Z

424

Destruction of organic wastes with molten oxidizers  

DOE Patents (OSTI)

A process for destruction of biologically hazardous organic chemical wastes by using liquefied strongly oxidizing inorganic salts, such as the alkali metal nitrates, at high temperatures and atmospheric pressure, to yield inorganic salts, carbon dioxide, and water. The oxidizing salts are regenerated and recycled.

Bradshaw, R.W.; Holmes, J.T.; Tyner, C.E.

1990-12-31T23:59:59.000Z

425

Destruction of organic wastes with molten oxidizers  

DOE Patents (OSTI)

A process for destruction of biologically hazardous organic chemical wastes by using liquefied strongly oxidizing inorganic salts, such as the alkali metal nitrates, at high temperatures and atmospheric pressure, to yield inorganic salts, carbon dioxide, and water. The oxidizing salts are regenerated and recycled.

Bradshaw, R.W.; Holmes, J.T.; Tyner, C.E.

1990-01-01T23:59:59.000Z

426

Hybrid Vapor Compression Adsorption System: Thermal Storage Using Hybrid Vapor Compression Adsorption System  

SciTech Connect

HEATS Project: UTRC is developing a new climate-control system for EVs that uses a hybrid vapor compression adsorption system with thermal energy storage. The targeted, closed system will use energy during the battery-charging step to recharge the thermal storage, and it will use minimal power to provide cooling or heating to the cabin during a drive cycle. The team will use a unique approach of absorbing a refrigerant on a metal salt, which will create a lightweight, high-energy-density refrigerant. This unique working pair can operate indefinitely as a traditional vapor compression heat pump using electrical energy, if desired. The project will deliver a hot-and-cold battery that provides comfort to the passengers using minimal power, substantially extending the driving range of EVs.

None

2012-01-04T23:59:59.000Z

427

Water Vapor Flux Measurements from Ground-Based Vertically Pointed Water Vapor Differential Absorption and Doppler Lidars  

Science Conference Proceedings (OSTI)

For the first time, two lidar systems were used to measure the vertical water vapor flux in a convective boundary layer by means of eddy correlation. This was achieved by combining a water vapor differential absorption lidar and a heterodyne wind ...

Andreas Giez; Gerhard Ehret; Ronald L. Schwiesow; Kenneth J. Davis; Donald H. Lenschow

1999-02-01T23:59:59.000Z

428

Excursions in Chemical Dynamics  

E-Print Network (OSTI)

2009). [118] F. A. Cotton, Chemical Applications of GroupExcursions in Chemical Dynamics by Shervin Fatehi AFall 2010 Excursions in Chemical Dynamics Copyright 2010 by

Fatehi, Shervin

2010-01-01T23:59:59.000Z

429

Oil shale oxidation at subretorting temperatures  

SciTech Connect

Green River oil shale was air oxidized at subretorting temperatures. Off gases consisting of nitrogen, oxygen, carbon monoxide, carbon dioxide, and water were monitored and quantitatively determined. A mathematical model of the oxidation reactions based on a shrinking core model has been developed. This model incorporates the chemical reaction of oxygen and the organic material in the oil shale as well as the diffusivity of the oxygen into the shale particle. Diffusivity appears to be rate limiting for the oxidation. Arrhenius type equations, which include a term for oil shale grade, have been derived for both the chemical reaction and the diffusivity.

Jacobson, I.A. Jr.

1980-06-01T23:59:59.000Z

430

Mercury Vapor At Silver Peak Area (Henkle, Et Al., 2005) | Open...  

Open Energy Info (EERE)

Mercury Vapor At Silver Peak Area (Henkle, Et Al., 2005) Exploration Activity Details Location Silver Peak Area Exploration Technique Mercury Vapor Activity Date Usefulness useful...

431

EA-0881: Tank 241-c-103 Organic Vapor and Liquid Characterization...  

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

881: Tank 241-c-103 Organic Vapor and Liquid Characterization and Supporting Activities, Hanford Site, Richland, Washington EA-0881: Tank 241-c-103 Organic Vapor and Liquid...

432

Does EIA report water vapor emissions data? - FAQ - U.S. Energy ...  

U.S. Energy Information Administration (EIA)

Does EIA report water vapor emissions data? No. Water vapor is the most abundant greenhouse gas, but most scientists believe that human activity has a very small ...

433

Light-extraction enhancement in GaN-based light-emitting diodes using grade-refractive-index amorphous titanium oxide films with porous structures  

SciTech Connect

Amorphous titanium oxide (a-TiO{sub x}:OH) films prepared by plasma-enhanced chemical-vapor deposition at 200 and 25 deg. C are in turn deposited onto the GaN-based light-emitting diode (LED) to enhance the associated light extraction efficiency. The refractive index, porosity, and photocatalytic effect of the deposited films are correlated strongly with the deposition temperatures. The efficiency is enhanced by a factor of {approx}1.31 over that of the uncoated LEDs and exhibited an excellent photocatalytic property after an external UV light irradiation. The increase in the light extraction is related to the reduction in the Fresnel transmission loss and the enhancement of the light scattering into the escape cone by using the graded-refractive-index a-TiO{sub x}:OH film with porous structures.

Liu, D.-S.; Lin, T.-W.; Huang, B.-W.; Juang, F.-S.; Lei, P.-H. [Institute of Electro-Optical and Materials Science, National Formosa University, Huwei 63201, Taiwan (China); Hu, C.-Z. [Chilin Technology Co. Ltd., Tainan County 71758, Taiwan (China)

2009-04-06T23:59:59.000Z

434

Dual-environment effects on the oxidation of metallic interconnects  

DOE Green Energy (OSTI)

Metallic interconnects in solid oxide fuel cells are exposed to a dual environment: fuel on one side (i.e., H2 gas) and oxidizer on the other side (i.e., air). It has been observed that the oxidation behavior of thin stainless steel sheet in air is changed by the presence of H2 on the other side of the sheet. The resulting dual-environment scales are flaky and more friable than the single-environment scales. The H2 disrupts the scale on the air side. A model to explain some of the effects of a dual environment is presented where hydrogen diffusing through the stainless steel sheet reacts with oxygen diffusing through the scale to form water vapor, which has sufficient vapor pressure to mechanically disrupt the scale. Experiments on preoxidized 316L stainless steel tubing exposed to air-air, H2-air, and H2-Ar environments are reported in support of the model.

Holcomb, G.R.; Ziomek-Moroz, M.; Covino, B.S., Jr.; Bullard, S.J.

2006-08-01T23:59:59.000Z

435

New Regenerative Cycle for Vapor Compression Refrigeration  

SciTech Connect

The main objective of this project is to confirm on a well-instrumented prototype the theoretically derived claims of higher efficiency and coefficient of performance for geothermal heat pumps based on a new regenerative thermodynamic cycle as comparing to existing technology. In order to demonstrate the improved performance of the prototype, it will be compared to published parameters of commercially available geothermal heat pumps manufactured by US and foreign companies. Other objectives are to optimize the design parameters and to determine the economic viability of the new technology. Background (as stated in the proposal): The proposed technology closely relates to EERE mission by improving energy efficiency, bringing clean, reliable and affordable heating and cooling to the residential and commercial buildings and reducing greenhouse gases emission. It can provide the same amount of heating and cooling with considerably less use of electrical energy and consequently has a potential of reducing our nations dependence on foreign oil. The theoretical basis for the proposed thermodynamic cycle was previously developed and was originally called a dynamic equilibrium method. This theory considers the dynamic equations of state of the working fluid and proposes the methods for modification of T-S trajectories of adiabatic transformation by changing dynamic properties of gas, such as flow rate, speed and acceleration. The substance of this proposal is a thermodynamic cycle characterized by the regenerative use of the potential energy of two-phase flow expansion, which in traditional systems is lost in expansion valves. The essential new features of the process are: (1) The application of two-step throttling of the working fluid and two-step compression of its vapor phase. (2) Use of a compressor as the initial step compression and a jet device as a second step, where throttling and compression are combined. (3) Controlled ratio of a working fluid at the first and second step of compression. In the proposed system, the compressor compresses the vapor only to 50-60% of the final pressure, while the additional compression is provided by a jet device using internal potential energy of the working fluid flow. Therefore, the amount of mechanical energy required by a compressor is significantly reduced, resulting in the increase of efficiency (either COP or EER). The novelty of the cycle is in the equipment and in the way the multi-staging is accomplished. The anticipated result will be a new refrigeration system that requires less energy to accomplish a cooling task. The application of this technology will be for more efficient designs of: (1) Industrial chillers, (2) Refrigeration plants, (3) Heat pumps, (4) Gas Liquefaction plants, (5) Cryogenic systems.

Mark J. Bergander

2005-08-29T23:59:59.000Z

436

Enhanced Attenuation Technologies: Passive Soil Vapor Extraction  

SciTech Connect

Passive soil vapor extraction (PSVE) is an enhanced attenuation (EA) approach that removes volatile contaminants from soil. The extraction is driven by natural pressure gradients between the subsurface and atmosphere (Barometric Pumping), or by renewable sources of energy such as wind or solar power (Assisted PSVE). The technology is applicable for remediating sites with low levels of contamination and for transitioning sites from active source technologies such as active soil vapor extraction (ASVE) to natural attenuation. PSVE systems are simple to design and operate and are more cost effective than active systems in many scenarios. Thus, PSVE is often appropriate as an interim-remedial or polishing strategy. Over the past decade, PSVE has been demonstrated in the U.S. and in Europe. These demonstrations provide practical information to assist in selecting, designing and implementing the technology. These demonstrations indicate that the technology can be effective in achieving remedial objectives in a timely fashion. The keys to success include: (1) Application at sites where the residual source quantities, and associated fluxes to groundwater, are relatively low; (2) Selection of the appropriate passive energy source - barometric pumping in cases with a deep vadose zone and barrier (e.g., clay) layers that separate the subsurface from the atmosphere and renewable energy assisted PSVE in other settings and where higher flow rates are required. (3) Provision of sufficient access to the contaminated vadose zones through the spacing and number of extraction wells. This PSVE technology report provides a summary of the relevant technical background, real-world case study performance, key design and cost considerations, and a scenario-based cost evaluation. The key design and cost considerations are organized into a flowchart that dovetails with the Enhanced Attenuation: Chlorinated Organics Guidance of the Interstate Technology and Regulatory Council (ITRC). The PSVE flowchart provides a structured process to determine if the technology is, or is not, reasonable and defensible for a particular site. The central basis for that decision is the expected performance of PSVE under the site specific conditions. Will PSVE have sufficient mass removal rates to reduce the release, or flux, of contamination into the underlying groundwater so that the site can meet it overall remedial objectives? The summary technical information, case study experiences, and structured decision process provided in this 'user guide' should assist environmental decision-makers, regulators, and engineers in selecting and successfully implementing PSVE at appropriate sites.

Vangelas, K.; Looney, B.; Kamath, R.; Adamson, D.; Newell, C.

2010-03-15T23:59:59.000Z

437

Desalination Using Vapor-Compression Distillation  

E-Print Network (OSTI)

The ability to produce potable water economically is the primary purpose of seawater desalination research. Reverse osmosis (RO) and multi-stage flash (MSF) cost more than potable water produced from fresh water resources. As an alternative to RO and MSF, this research investigates a high-efficiency mechanical vapor-compression distillation system that employs an improved water flow arrangement. The incoming salt concentration was 0.15% salt for brackish water and 3.5% salt for seawater, whereas the outgoing salt concentration was 1.5% and 7%, respectively. Distillation was performed at 439 K (331oF) and 722 kPa (105 psia) for both brackish water feed and seawater feed. Water costs of the various conditions were calculated for brackish water and seawater feeds using optimum conditions considered as 25 and 20 stages, respectively. For brackish water at a temperature difference of 0.96 K (1.73oF), the energy requirement is 2.0 kWh/m3 (7.53 kWh/kgal). At this condition, the estimated water cost is $0.39/m3 ($1.48/kgal) achieved with 10,000,000 gal/day distillate, 30-year bond, 5% interest rate, and $0.05/kWh electricity. For seawater at a temperature difference of 0.44 K (0.80oF), the energy requirement is 3.97 kWh/m3 (15.0 kWh/kgal) and the estimated water cost is $0.61/m3 ($2.31/kgal). Greater efficiency of the vapor compression system is achieved by connecting multiple evaporators in series, rather than the traditional parallel arrangement. The efficiency results from the gradual increase of salinity in each stage of the series arrangement in comparison to parallel. Calculations using various temperature differences between boiling brine and condensing steam show the series arrangement has the greatest improvement at lower temperature differences. The following table shows the improvement of a series flow arrangement compared to parallel: ?T (K) Improvement (%)*1.111 2.222 3.333 15.21 10.80 8.37 * Incoming salt concentration: 3.5% Outgoing salt concentration: 7% Temperature: 450 K (350oF) Pressure: 928 kPa (120 psig) Stages: 4

Lubis, Mirna R.

2009-05-01T23:59:59.000Z

438

Growth of gadolinium oxide films for advanced MOS structure  

Science Conference Proceedings (OSTI)

We have investigated properties of insulating gadolinium oxide (Gd"2O"3) films in connection with the replacement of silicon oxide (SiO"2) gate dielectrics in new generation of CMOS devices. The Gd"2O"3 layers were grown using metal organic chemical ... Keywords: Gadolinium oxide, High-? dielectric, MOCVD, MOS structure

R. Lupták; K. Fröhlich; A. Rosová; K. Hušeková; M. apajna; D. Machajd?k; M. Jergel; J. P. Espinós; C. Mansilla

2005-06-01T23:59:59.000Z

439

Boiler Chemical Cleaning Waste Management Manual  

Science Conference Proceedings (OSTI)

Chemical cleaning to remove tube deposits/oxides that occur during unit operation or scale during unit commissioning from conventional fossil plants and combined cycle plants with heat recovery steam generators (HRSGs) will result in the generation of a waste solution. The waste contains residual solvent and elevated levels of heavy metals (primarily iron and copper) in addition to rinse and passivation solutions. An earlier manual, Boiler Chemical Cleaning Wastes Management Manual (EPRI ...

2013-12-20T23:59:59.000Z

440

Numerical simulation of water injection into vapor-dominated reservoirs  

DOE Green Energy (OSTI)

Water injection into vapor-dominated reservoirs is a means of condensate disposal, as well as a reservoir management tool for enhancing energy recovery and reservoir life. We review different approaches to modeling the complex fluid and heat flow processes during injection into vapor-dominated systems. Vapor pressure lowering, grid orientation effects, and physical dispersion of injection plumes from reservoir heterogeneity are important considerations for a realistic modeling of injection effects. An example of detailed three-dimensional modeling of injection experiments at The Geysers is given.

Pruess, K.

1995-01-01T23:59:59.000Z

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441

Controlling the vapor pressure of a mercury lamp  

DOE Patents (OSTI)

The invention described herein discloses a method and apparatus for controlling the Hg vapor pressure within a lamp. This is done by establishing and controlling two temperature zones within the lamp. One zone is colder than the other zone. The first zone is called the cold spot. By controlling the temperature of the cold spot, the Hg vapor pressure within the lamp is controlled. Likewise, by controlling the Hg vapor pressure of the lamp, the intensity and linewidth of the radiation emitted from the lamp is controlled.

Grossman, Mark W. (Belmont, MA); George, William A. (Rockport, MA)

1988-01-01T23:59:59.000Z

442

Controlling the vapor pressure of a mercury lamp  

DOE Patents (OSTI)

The invention described herein discloses a method and apparatus for controlling the Hg vapor pressure within a lamp. This is done by establishing and controlling two temperature zones within the lamp. One zone is colder than the other zone. The first zone is called the cold spot. By controlling the temperature of the cold spot, the Hg vapor pressure within the lamp is controlled. Likewise, by controlling the Hg vapor pressure of the lamp, the intensity and linewidth of the radiation emitted from the lamp is controlled. 2 figs.

Grossman, M.W.; George, W.A.

1988-05-24T23:59:59.000Z

443

Simple microwave field imaging technique using hot atomic vapor cells  

E-Print Network (OSTI)

We demonstrate a simple technique for microwave field imaging using alkali atoms in a vapor cell. The microwave field to be measured drives Rabi oscillations on atomic hyperfine transitions, which are detected in a spatially resolved way using a laser beam and a CCD camera. Our vapor cell geometry enables single-shot recording of two-dimensional microwave field images with 350 {\\mu}m spatial resolution. Using microfabricated vapor cell arrays, a resolution of a few micrometers seems feasible. All vector components of the microwave magnetic field can be imaged. Our apparatus is simple and compact and does not require cryogenics or ultra-high vacuum.

Böhi, Pascal

2012-01-01T23:59:59.000Z

444

Simple microwave field imaging technique using hot atomic vapor cells  

E-Print Network (OSTI)

We demonstrate a simple technique for microwave field imaging using alkali atoms in a vapor cell. The microwave field to be measured drives Rabi oscillations on atomic hyperfine transitions, which are detected in a spatially resolved way using a laser beam and a camera. Our vapor cell geometry enables single-shot recording of two-dimensional microwave field images with 350 {\\mu}m spatial resolution. Using microfabricated vapor</