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


1

Hydridable material for the negative electrode in a nickel-metal hydride storage battery  

DOE Patents [OSTI]

A monophase hydridable material for the negative electrode of a nickel-metal hydride storage battery with a "Lave's phase" structure of hexagonal C14 type (MgZn.sub.2) has the general formula: Zr.sub.1-x Ti.sub.x Ni.sub.a Mn.sub.b Al.sub.c Co.sub.d V.sub.e where ##EQU1##

Knosp, Bernard (Neuilly-sur-Seine, FR); Bouet, Jacques (Paris, FR); Jordy, Christian (Dourdan, FR); Mimoun, Michel (Neuilly-sur-Marne, FR); Gicquel, Daniel (Lanorville, FR)

1997-01-01T23:59:59.000Z

2

Hydrogen, lithium, and lithium hydride production  

DOE Patents [OSTI]

A method of producing high purity lithium metal is provided, where gaseous-phase lithium metal is extracted from lithium hydride and condensed to form solid high purity lithium metal. The high purity lithium metal may be hydrided to provide high purity lithium hydride.

Brown, Sam W; Spencer, Larry S; Phillips, Michael R; Powell, G. Louis; Campbell, Peggy J

2014-03-25T23:59:59.000Z

3

Identification of a new pseudo-binary hydroxide during calendar corrosion of (La, Mg)2Ni7-type hydrogen storage alloys for Nickel-Metal Hydride batteries  

E-Print Network [OSTI]

hydrogen storage alloys for Nickel-Metal Hydride batteries J. Monnier 1 , H. Chen 1 , S. Joiret2,3 , J-MH batteries have been extensively studied during calendar storage and cycling [6-8]. In these alloys To improve the performances of Nickel-Metal Hydride batteries, an important step is the understanding

Boyer, Edmond

4

Hydrogen Outgassing from Lithium Hydride  

SciTech Connect (OSTI)

Lithium hydride is a nuclear material with a great affinity for moisture. As a result of exposure to water vapor during machining, transportation, storage and assembly, a corrosion layer (oxide and/or hydroxide) always forms on the surface of lithium hydride resulting in the release of hydrogen gas. Thermodynamically, lithium hydride, lithium oxide and lithium hydroxide are all stable. However, lithium hydroxides formed near the lithium hydride substrate (interface hydroxide) and near the sample/vacuum interface (surface hydroxide) are much less thermally stable than their bulk counterpart. In a dry environment, the interface/surface hydroxides slowly degenerate over many years/decades at room temperature into lithium oxide, releasing water vapor and ultimately hydrogen gas through reaction of the water vapor with the lithium hydride substrate. This outgassing can potentially cause metal hydriding and/or compatibility issues elsewhere in the device. In this chapter, the morphology and the chemistry of the corrosion layer grown on lithium hydride (and in some cases, its isotopic cousin, lithium deuteride) as a result of exposure to moisture are investigated. The hydrogen outgassing processes associated with the formation and subsequent degeneration of this corrosion layer are described. Experimental techniques to measure the hydrogen outgassing kinetics from lithium hydride and methods employing the measured kinetics to predict hydrogen outgassing as a function of time and temperature are presented. Finally, practical procedures to mitigate the problem of hydrogen outgassing from lithium hydride are discussed.

Dinh, L N; Schildbach, M A; Smith, R A; Balazs1, B; McLean II, W

2006-04-20T23:59:59.000Z

5

Current status of environmental, health, and safety issues of nickel metal-hydride batteries for electric vehicles  

SciTech Connect (OSTI)

This report identifies important environment, health, and safety issues associated with nickel metal-hydride (Ni-MH) batteries and assesses the need for further testing and analysis. Among the issues discussed are cell and battery safety, workplace health and safety, shipping requirements, and in-vehicle safety. The manufacture and recycling of Ni-MH batteries are also examined. This report also overviews the ``FH&S`` issues associated with other nickel-based electric vehicle batteries; it examines venting characteristics, toxicity of battery materials, and the status of spent batteries as a hazardous waste.

Corbus, D.; Hammel, C.J.; Mark, J.

1993-08-01T23:59:59.000Z

6

Advanced nickel-metal hydride cell development. Final report, September 1993--March 1996  

SciTech Connect (OSTI)

Inert gas atomization using metal hydride alloys for a Ni/MH{sub x}cell was studied. Atomization of the alloys was demonstrated on a small production scale up to batch size of several kg. Relative performance of the atomized and nonatomized alloys was investigated for the electrode material in a Ni/MH{sub x} cell. The study included effects of charge-discharge rates, temperature, and particle size on cell voltage (polarization) and specific capacity. Results show that the specific capacity of the present atomized alloys was apprecialy smaller than that of the nonatomized powder, especially for initial cycles. Full activation of the atomized alloys oftentook several hundreds of cycles. However, no appreciable difference in discharge rate capability was observed with R10 and R12 alloys. Chemical compositions were indistinguishable, although the oxygen contents of the atomized alloys were always higher. Effects of Ni and Cu coating on alloy performance were studied after electroless coating; the coatings noticeably improved the electrode rate capability for all the alloys. The electrode polarization was esecially improved, but not the cycle life. Further studies are needed.

Lim, Hong S.

1996-03-01T23:59:59.000Z

7

Development of encapsulated lithium hydride thermal energy storage for space power systems  

SciTech Connect (OSTI)

Inclusion of thermal energy storage in a pulsed space power supply will reduce the mass of the heat rejection system. In this mode, waste heat generated during the brief high-power burst operation is placed in the thermal store; later, the heat in the store is dissipated to space via the radiator over the much longer nonoperational period of the orbit. Thus, the radiator required is of significantly smaller capacity. Scoping analysis indicates that use of lithium hydride as the thermal storage medium results in system mass reduction benefits for burst periods as long as 800 s. A candidate design for the thermal energy storage component utilizes lithium hydride encapsulated in either 304L stainless steel or molybdenum in a packed-bed configuration with a lithium or sodium-potassium (NaK) heat transport fluid. Key issues associated with the system design include phase-change induced stresses in the shell, lithium hydride and shell compatibility, lithium hydride dissociation and hydrogen loss from the system, void presence and movement associated with the melt-freeze process, and heat transfer limitations on obtaining the desired energy storage density. 58 refs., 40 figs., 11 tabs.

Morris, D.G.; Foote, J.P.; Olszewski, M.

1987-12-01T23:59:59.000Z

8

A mechanistic study of aryl halide reactions with lithium aluminum hydride  

E-Print Network [OSTI]

A M:"CHA~JISTIC STUDv OF ARYL HALID RHAC IC~JS ' ITH LITHIUM ALUM 'J"M HYDRIDE A Thesis FU-FAJJ CHUI'JG Submitted to the Graduate College of Texas ARM University in nartial fulfillment of the reauirement for the degree of MASTER OF SCI- JC... of this stud!y :a to investigate possibility o f a. fr ee r a . 1 ca machina=--. by;;h:ch ". thium alum'num hydride may reduce organic ccmnounds. evzcus results have irdicated that thc reductior of o-allylcxy- 'oenzene diazonium icn by . ributyltin hydrioe...

Chung, Fu-Fan

1980-01-01T23:59:59.000Z

9

Measurements of Ionic Structure in Shock Compressed Lithium Hydride from Ultrafast X-Ray Thomson Scattering  

SciTech Connect (OSTI)

We present the first ultrafast temporally, spectrally, and angularly resolved x-ray scattering measurements from shock-compressed matter. The experimental spectra yield the absolute elastic and inelastic scattering intensities from the measured density of free electrons. Laser-compressed lithium-hydride samples are well characterized by inelastic Compton and plasmon scattering of a K-alpha x-ray probe providing independent measurements of temperature and density. The data show excellent agreement with the total intensity and structure when using the two-species form factor and accounting for the screening of ion-ion interactions.

Kritcher, A. L. [L-399, Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, California 94551 (United States); Department of Nuclear Engineering, University of California Berkeley, Berkeley, California 94709 (United States); Neumayer, P.; Doeppner, T.; Landen, O. L.; Glenzer, S. H. [L-399, Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, California 94551 (United States); Brown, C. R. D. [Department of Physics, Imperial College, London SW7 2AZ (United Kingdom); AWE plc., Aldermaston, Reading, RG7 4PR (United Kingdom); Davis, P. [L-399, Lawrence Livermore National Laboratory, P.O. Box 808, Livermore, California 94551 (United States); Department of Physics, University of California Berkeley, Berkeley, California 94709 (United States); Falcone, R. W.; Lee, H. J. [Department of Physics, University of California Berkeley, Berkeley, California 94709 (United States); Gericke, D. O.; Vorberger, J.; Wuensch, K. [CFSA, Department of Physics, University of Warwick, Coventry CV4 7AL (United Kingdom); Gregori, G. [Department of Physics, Oxford University, Oxford OX1 3PU (United Kingdom); Holst, B.; Redmer, R. [Universitaet Rostock, Institut fuer Physik, D-18051 Rostock (Germany); Morse, E. C. [Department of Nuclear Engineering, University of California Berkeley, Berkeley, California 94709 (United States); Pelka, A.; Roth, M. [Institut fuer Kernphysik, Technische Universitaet Darmstadt, Darmstadt (Germany)

2009-12-11T23:59:59.000Z

10

Steps to Commercialization: Nickel Metal Hydride Batteries | Department of  

Energy Savers [EERE]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankCombustion |Energy UsageAUDITVehicles »ExchangeDepartmentResolveFuture |Energy Steps to

11

Revêtements métalliques : Dépôts électrolytiques de nickel Metallic coatings : Electrodeposited coatings of nickel  

E-Print Network [OSTI]

Revêtements métalliques : Dépôts électrolytiques de nickel Metallic coatings : Electrodeposited coatings of nickel

International Organization for Standardization. Geneva

2002-01-01T23:59:59.000Z

12

Raman Spectroscopy of Lithium Hydride Corrosion: Selection of an Appropriate Excitation Wavelength to Minimize Fluorescence  

SciTech Connect (OSTI)

The recent interest in a hydrogen-based fuel economy has renewed research into metal hydride chemistry. Many of these compounds react readily with water to release hydrogen gas and form a caustic. Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFT) has been used to study the hydrolysis reaction. The LiOH stretch appears at 3670 cm{sup -1}. Raman spectroscopy is a complementary technique that employs monochromatic excitation (laser) allowing access to the low energy region of the vibrational spectrum (<600 cm{sup -1}). Weak scattering and fluorescence typically prevent Raman from being used for many compounds. The role of Li{sub 2}O in the moisture reaction has not been fully studied for LiH. Li{sub 2}O can be observed by Raman while being hidden in the Infrared spectrum.

Stowe, A. C.; Smyrl, N. R.

2011-05-26T23:59:59.000Z

13

Development of a metal hydride electrode waste treatment process  

SciTech Connect (OSTI)

Manufacturing residues of metal hydride electrodes for nickel - metal hydride batteries were chemically processed to recover the metal part and heat treated for the organic part. Chemical recovery yielded Ni-Co alloy after electrolysis of the solution and hydroxides of other metal, mainly rare earths. The organic part, pyrolyzed at 700 C, led to separation between carbon and fluorinated matter. Infrared coupling at the output of the pyrolysis furnace was used to identify the pyrolysis gases.

Bianco, J.C.; Martin, D.; Ansart, F.; Castillo, S.

1999-12-01T23:59:59.000Z

14

Inhalation carcinogenicity study with nickel metal powder in Wistar rats  

SciTech Connect (OSTI)

Epidemiological studies of nickel refinery workers have demonstrated an association between increased respiratory cancer risk and exposure to certain nickel compounds (later confirmed in animal studies). However, the lack of an association found in epidemiological analyses for nickel metal remained unconfirmed for lack of robust animal inhalation studies. In the present study, Wistar rats were exposed by whole-body inhalation to 0, 0.1, 0.4, and 1.0 mg Ni/m{sup 3} nickel metal powder (MMAD = 1.8 {mu}m, GSD = 2.4 {mu}m) for 6 h/day, 5 days/week for up to 24 months. A subsequent six-month period without exposures preceded the final euthanasia. High mortality among rats exposed to 1.0 mg Ni/m{sup 3} nickel metal resulted in the earlier termination of exposures in this group. The exposure level of 0.4 mg Ni/m{sup 3} was established as the MTD for the study. Lung alterations associated with nickel metal exposure included alveolar proteinosis, alveolar histiocytosis, chronic inflammation, and bronchiolar-alveolar hyperplasia. No increased incidence of neoplasm of the respiratory tract was observed. Adrenal gland pheochromocytomas (benign and malignant) in males and combined cortical adenomas/carcinomas in females were induced in a dose-dependent manner by the nickel metal exposure. The incidence of pheochromocytomas was statistically increased in the 0.4 mg Ni/m{sup 3} male group. Pheochromocytomas appear to be secondary to the lung toxicity associated with the exposure rather than being related to a direct nickel effect on the adrenal glands. The incidence of cortical tumors among 0.4 mg Ni/m{sup 3} females, although statistically higher compared to the concurrent controls, falls within the historical control range; therefore, in the present study, this tumor is of uncertain relationship to nickel metal exposure. The lack of respiratory tumors in the present animal study is consistent with the findings of the epidemiological studies.

Oller, Adriana R. [NiPERA, 2605 Meridian Parkway, Suite 200, Durham, NC 27713 (United States)], E-mail: aoller@nipera.org; Kirkpatrick, Daniel T.; Radovsky, Ann [WIL Research Laboratories, LLC, 1407 George Road, Ashland, OH 44805 8946 (United States); Bates, Hudson K. [NiPERA, 2605 Meridian Parkway, Suite 200, Durham, NC 27713 (United States)

2008-12-01T23:59:59.000Z

15

A Lattice Energy Calculation for LiH Lithium hydride is a white crystalline solid with the face-centered cubic crystal structure. The model for LiH(s)  

E-Print Network [OSTI]

operators for each of the electrons, and an electron-electron potential energy operator. HLi 1 2 r1 - 2 r1 r 2 - 1 r1 - 1 r2 - 1 r12 += When the trial wavefunction and the appropriate energy operator is usedA Lattice Energy Calculation for LiH Lithium hydride is a white crystalline solid with the face

Rioux, Frank

16

CRADA (AL-C-2009-02) Final Report: Phase I. Lanthanum-based Start Materials for Hydride Batteries  

SciTech Connect (OSTI)

The purpose of Phase I of this work is to focus on developing a La-based start material for making nickel-metal (lanthanum)-hydride batteries based on our carbothermic-silicon process. The goal is to develop a protocol for the manufacture of (La{sub 1-x}R{sub x})(Ni{sub 1-y}M{sub y})(Si{sub z}), where R is a rare earth metal and M is a non-rare earth metal, to be utilized as the negative electrode in nickel-metal hydride (NiMH) rechargeable batteries.

Gschneidner, Jr., Karl [Ames Laboratory; Schmidt, Frederick [Ames Laboratory] [Ames Laboratory; Frerichs, A.E. [Ames Laboratory] [Ames Laboratory; Ament, Katherine A. [Ames Laboratory] [Ames Laboratory

2013-05-01T23:59:59.000Z

17

Recycling Programs | Department of Energy  

Office of Environmental Management (EM)

Germantown Paperclips Supply Stores. Batteries accepted for recycling are: Alkaline, Lithium Ion, Nickel Cadmium (Ni-Cd), Nickel-Iron, and Nickel Metal Hydride (NiMH). Toner...

18

Improving nickel metal hydride batteries through research in negative electrode corrosion control and novel electrode materials  

E-Print Network [OSTI]

electrode materials. In order to fully understand the processes involved in the corrosion study, tests were carried at Brookhaven National Laboratory using X-ray Absorption Near Edge Spectroscopy. These tests showed that Zn prevented the corrosion of Ni-a...

Alexander, Michael Scott

1997-01-01T23:59:59.000Z

19

Method Of Charging Maintenance-Free Nickel Metal Hydride Storage Cells  

DOE Patents [OSTI]

A method of charging an industrial maintenance-free Ni-MH storage cell, the method comprising in combination a first stage at a constant current I.sub.1 lying in the range I.sub.c /10 to I.sub.c /2, and a second stage at a constant current I.sub.2 lying in the range I.sub.c /50 to I.sub.c /10, the changeover from the first stage to the second stage taking place when the time derivative of the temperature reaches a threshold value which varies as a function of the temperature at the time of the changeover.

Berlureau, Thierry (Bordeaux, FR); Liska, Jean-Louis (Bordeaux, FR)

1999-11-16T23:59:59.000Z

20

New sealed rechargeable batteries and supercapacitors  

SciTech Connect (OSTI)

This conference was divided into the following sections: supercapacitors; nickel-metal hydride batteries; lithium polymer batteries; lithium/carbon batteries; cathode materials; and lithium batteries. Separate abstracts were prepared for the 46 papers of this conference.

Barnett, B.M. (ed.) (Arthur D. Little, Inc., Cambridge, MA (United States)); Dowgiallo, E. (ed.) (Dept. of Energy, Washington, DC (United States)); Halpert, G. (ed.) (Jet Propulsion Lab., Pasadena, CA (United States)); Matsuda, Y. (ed.) (Yamagushi Univ., Ube (Japan)); Takehara, Z.I. (ed.) (Kyoto Univ. (Japan))

1993-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Mathematical model of a NiOOH/metal hydride cell. Final report, September 15, 1993--November 14, 1996  

SciTech Connect (OSTI)

One of the objectives of work on the nickel/metal hydride cell has been to develop a mathematical model of the performance of the cell. This is a summary of work to date and is meant to be a Final Report of the BES project. Mathematical model of the nickel/metal hydride cell depends on the kinetics, thermodynamics, and transport properties of the metal hydride electrode. Consequently, investigations were carried out to determine: (1) the exchange current density and the equilibrium potential as a function of hydrogen content in the electrode; (2) the hydrogen diffusion coefficient in the bulk of the alloy; (3) the hydrogen reaction rate order; (4) the symmetry factor for hydrogen evolution reaction and (5) to determine the reaction mechanisms of the hydrogen charge and discharge processes including overcharge and overdischarge mechanism.

White, R.E.; Popov, B.N.

1996-12-31T23:59:59.000Z

22

Hydride compositions  

DOE Patents [OSTI]

Disclosed are a composition for use in storing hydrogen and a method for making the composition. The composition comprises a mixture of two or more hydrides, each hydride having a different series of hydrogen sorption isotherms that contribute to the overall isotherms of the mixture. The hydrides are chosen so that the isotherms of the mixture have regions wherein the H equilibrium pressure increases with increasing hydrogen, preferably linearly. The isotherms of the mixture can be adjusted by selecting hydrides with different isotherms and by varying the amounts of the individual hydrides, or both. Preferably, the mixture is made up of hydrides that have isotherms with substantially flat plateaus and in nearly equimolar amounts. The composition is activated by degassing, exposing to H, and then heating below the softening temperature of any of the constituents. When the composition is used to store hydrogen, its hydrogen content can be found simply by measuring P{sub H}{sub 2} and determining H/M from the isothermic function of the composition.

Lee, Myung, W.

1994-01-01T23:59:59.000Z

23

Technological assessment and evaluation of high power batteries and their commercial values  

E-Print Network [OSTI]

Lithium Ion (Li-ion) battery technology has the potential to compete with the more matured Nickel Metal Hydride (NiMH) battery technology in the Hybrid Electric Vehicle (HEV) energy storage market as it has higher specific ...

Teo, Seh Kiat

2006-01-01T23:59:59.000Z

24

Are batteries ready for plug-in hybrid buyers?  

E-Print Network [OSTI]

Of the battery chemistries discussed, only Li-ion shows the2008) battery researchers continue to develop Li-ionbattery chemistries: nickel-metal hydride (NiMH) and lithium-ion (Li-

Axsen, Jonn; Kurani, Kenneth S.; Burke, Andrew

2008-01-01T23:59:59.000Z

25

Are Batteries Ready for Plug-in Hybrid Buyers?  

E-Print Network [OSTI]

Of the battery chemistries discussed, only Li-ion shows the2008) battery researchers continue to develop Li-ionbattery chemistries: nickel- metal hydride (NiMH) and lithium-ion (Li-

Axsen, Jonn; Burke, Andy; Kurani, Kenneth S

2010-01-01T23:59:59.000Z

26

Are Batteries Ready for Plug-in Hybrid Buyers?  

E-Print Network [OSTI]

Of the battery chemistries discussed, only Li-ion shows the2008) battery researchers continue to develop Li-ionbattery chemistries: nickel-metal hydride (NiMH) and lithium-ion (Li-

Axsen, Jonn; Kurani, Kenneth S; Burke, Andy

2009-01-01T23:59:59.000Z

27

Recent advances in metal hydrides for clean energy applications  

SciTech Connect (OSTI)

Metal hydrides are a fascinating class of materials that can be utilized for a surprising variety of clean energy applications, including smart solar collectors, smart windows, sensors, thermal energy storage, and batteries, in addition to their traditional application for hydrogen storage. Over the past decade, research on metal hydrides for hydrogen storage increased due to global governmental incentives and an increased focus on hydrogen storage research for polymer electrolyte membrane fuel cell operation. Tremendous progress has been made in so-called complex metal hydrides for hydrogen storage applications with the discovery of many new hydrides containing covalently bound complex anions. Many of these materials have applications beyond hydrogen storage and are being investigated for lithium-ion battery separator and anode materials. In this issue of MRS Bulletin , we present the state of the art of key evolving metal-hydride-based clean energy technologies with an outlook toward future needs.

Ronnebro, Ewa; Majzoub, Eric H.

2013-06-01T23:59:59.000Z

28

Advanced Hydride Laboratory  

SciTech Connect (OSTI)

Metal hydrides have been used at the Savannah River Tritium Facilities since 1984. However, the most extensive application of metal hydride technology at the Savannah River Site is being planned for the Replacement Tritium Facility, a $140 million facility schedules for completion in 1990 and startup in 1991. In the new facility, metal hydride technology will be used to store, separate, isotopically purify, pump, and compress hydrogen isotopes. In support of the Replacement Tritium Facility, a $3.2 million, cold,'' process demonstration facility, the Advanced Hydride Laboratory began operation in November of 1987. The purpose of the Advanced Hydride Laboratory is to demonstrate the Replacement Tritium Facility's metal hydride technology by integrating the various unit operations into an overall process. This paper will describe the Advanced Hydride Laboratory, its role and its impact on the application of metal hydride technology to tritium handling.

Motyka, T.

1989-01-01T23:59:59.000Z

29

Advanced Hydride Laboratory  

SciTech Connect (OSTI)

Metal hydrides have been used at the Savannah River Tritium Facilities since 1984. However, the most extensive application of metal hydride technology at the Savannah River Site is being planned for the Replacement Tritium Facility, a $140 million facility schedules for completion in 1990 and startup in 1991. In the new facility, metal hydride technology will be used to store, separate, isotopically purify, pump, and compress hydrogen isotopes. In support of the Replacement Tritium Facility, a $3.2 million, ``cold,`` process demonstration facility, the Advanced Hydride Laboratory began operation in November of 1987. The purpose of the Advanced Hydride Laboratory is to demonstrate the Replacement Tritium Facility`s metal hydride technology by integrating the various unit operations into an overall process. This paper will describe the Advanced Hydride Laboratory, its role and its impact on the application of metal hydride technology to tritium handling.

Motyka, T.

1989-12-31T23:59:59.000Z

30

Recycle Batteries CSM recycles a variety of battery types including automotive, sealed lead acid, nickel  

E-Print Network [OSTI]

metal hydride and lithium ion batteries. The use of these batteries is increasing as a green, nickel metal hydride and lithium ion batteries. Please contact EHS if you need an accumulation containerRecycle Batteries CSM recycles a variety of battery types including automotive, sealed lead acid

31

Metal Hydrides - Science Needs  

Broader source: Energy.gov (indexed) [DOE]

with traditions in metal hydride research Metal and Ceramic Sciences Condensed Matter Physics Materials Chemistry Chemical and Biological Sciences Located on campus of Tier...

32

Carbon effects on corrosion of lithium hydride.  

SciTech Connect (OSTI)

{sm_bullet}Corrosion layer growth in LiH can be monitored by RBS; alpha beams affect the LiH material, causing enhanced corrosion in irradiated regions. {sm_bullet} O and C chemistries show wide variation across the LiH powder compacts studied. {sm_bullet} The O growth for a LiH reaction with H{sub 2}O (with or without C) shows an initial rise, followed by a linear rate which is likely diffusion controlled by a Li{sub 2}O layer thickness.

Haertling, C. L. (Carol L.); Tesmer, Joseph R.; Wetteland, C. J. (Christopher, J.); Phillips, J. (Jonathan); Mooday, R. (Rick); Kelly, D. (Daniel); Hanrahan, R. J. (Robert J.)

2002-01-01T23:59:59.000Z

33

Chemical Hydride Slurry for Hydrogen Production and Storage  

SciTech Connect (OSTI)

The purpose of this project was to investigate and evaluate the attractiveness of using a magnesium chemical hydride slurry as a hydrogen storage, delivery, and production medium for automobiles. To fully evaluate the potential for magnesium hydride slurry to act as a carrier of hydrogen, potential slurry compositions, potential hydrogen release techniques, and the processes (and their costs) that will be used to recycle the byproducts back to a high hydrogen content slurry were evaluated. A 75% MgH2 slurry was demonstrated, which was just short of the 76% goal. This slurry is pumpable and storable for months at a time at room temperature and pressure conditions and it has the consistency of paint. Two techniques were demonstrated for reacting the slurry with water to release hydrogen. The first technique was a continuous mixing process that was tested for several hours at a time and demonstrated operation without external heat addition. Further work will be required to reduce this design to a reliable, robust system. The second technique was a semi-continuous process. It was demonstrated on a 2 kWh scale. This system operated continuously and reliably for hours at a time, including starts and stops. This process could be readily reduced to practice for commercial applications. The processes and costs associated with recycling the byproducts of the water/slurry reaction were also evaluated. This included recovering and recycling the oils of the slurry, reforming the magnesium hydroxide and magnesium oxide byproduct to magnesium metal, hydriding the magnesium metal with hydrogen to form magnesium hydride, and preparing the slurry. We found that the SOM process, under development by Boston University, offers the lowest cost alternative for producing and recycling the slurry. Using the H2A framework, a total cost of production, delivery, and distribution of $4.50/kg of hydrogen delivered or $4.50/gge was determined. Experiments performed at Boston University have demonstrated the technical viability of the process and have provided data for the cost analyses that have been performed. We also concluded that a carbothermic process could also produce magnesium at acceptable costs. The use of slurry as a medium to carry chemical hydrides has been shown during this project to offer significant advantages for storing, delivering, and distributing hydrogen: • Magnesium hydride slurry is stable for months and pumpable. • The oils of the slurry minimize the contact of oxygen and moisture in the air with the metal hydride in the slurry. Thus reactive chemicals, such as lithium hydride, can be handled safely in the air when encased in the oils of the slurry. • Though magnesium hydride offers an additional safety feature of not reacting readily with water at room temperatures, it does react readily with water at temperatures above the boiling point of water. Thus when hydrogen is needed, the slurry and water are heated until the reaction begins, then the reaction energy provides heat for more slurry and water to be heated. • The reaction system can be relatively small and light and the slurry can be stored in conventional liquid fuel tanks. When transported and stored, the conventional liquid fuel infrastructure can be used. • The particular metal hydride of interest in this project, magnesium hydride, forms benign byproducts, magnesium hydroxide (“Milk of Magnesia”) and magnesium oxide. • We have estimated that a magnesium hydride slurry system (including the mixer device and tanks) could meet the DOE 2010 energy density goals. ? During the investigation of hydriding techniques, we learned that magnesium hydride in a slurry can also be cycled in a rechargeable fashion. Thus, magnesium hydride slurry can act either as a chemical hydride storage medium or as a rechargeable hydride storage system. Hydrogen can be stored and delivered and then stored again thus significantly reducing the cost of storing and delivering hydrogen. Further evaluation and development of this concept will be performed as follow-on work under a

McClaine, Andrew W.

2008-09-30T23:59:59.000Z

34

Metal Hydride Hydrogen Storage R and D | Department of Energy  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Metal Hydride Hydrogen Storage R and D Metal Hydride Hydrogen Storage R and D DOE's research on complex metal hydrides targets the development of advanced metal hydride materials...

35

CHEMICAL WASTE RECYCLING PROGRAM All types of batteries are collected by Chemical Waste Services (CWS) for recycling. These include  

E-Print Network [OSTI]

Services (CWS) for recycling. These include alkaline, lithium, rechargeable, coin batteries, lead-cadmium (ni-cads), nickel metal hydride, lithium, etc. They are individually bagged and placed phones, drills, computers, cameras, PDAs, toys and games. It is also used as a corrosion resistant

Baker, Chris I.

36

Highly Reversible Open Framework Nanoscale Electrodes for Divalent Ion Batteries  

E-Print Network [OSTI]

Blue family of open framework materials, such as nickel hexacyanoferrate, allow for the reversible of protons and lithium ions into solid materials has led to the success of nickel metal hydride and lithium materials have been studied extensively.15,16,18,20-23 Electrodeposited PB thin films have demonstrated

Cui, Yi

37

Method for preparing porous metal hydride compacts  

DOE Patents [OSTI]

A method for preparing porous metallic-matrix hydride compacts which can be repeatedly hydrided and dehydrided without disintegration. A mixture of a finely divided metal hydride and a finely divided matrix metal is contacted with a poison which prevents the metal hydride from dehydriding at room temperature and atmospheric pressure. The mixture of matrix metal and poisoned metal hydride is then compacted under pressure at room temperature to form porous metallic-matrix hydride compacts.

Ron, M.; Gruen, D.M.; Mendelsohn, M.H.; Sheft, I.

1980-01-21T23:59:59.000Z

38

Method for preparing porous metal hydride compacts  

DOE Patents [OSTI]

A method for preparing porous metallic-matrix hydride compacts which can be repeatedly hydrided and dehydrided without disintegration. A mixture of a finely divided metal hydride and a finely divided matrix metal is contacted with a poison which prevents the metal hydride from dehydriding at room temperature and atmospheric pressure. The mixture of matrix metal and poisoned metal hydride is then compacted under pressure at room temperature to form porous metallic-matrix hydride compacts.

Ron, Moshe (Haifa, IL); Gruen, Dieter M. (Downers Grove, IL); Mendelsohn, Marshall H. (Woodridge, IL); Sheft, Irving (Oak Park, IL)

1981-01-01T23:59:59.000Z

39

Manufacturing of Protected Lithium Electrodes for Advanced Lithium...  

Broader source: Energy.gov (indexed) [DOE]

Lithium Electrodes for Advanced Lithium-Air, Lithium-Water, and Lithium-Sulfur Batteries, April 2013 Manufacturing of Protected Lithium Electrodes for Advanced Lithium-Air,...

40

Erbium hydride decomposition kinetics.  

SciTech Connect (OSTI)

Thermal desorption spectroscopy (TDS) is used to study the decomposition kinetics of erbium hydride thin films. The TDS results presented in this report are analyzed quantitatively using Redhead's method to yield kinetic parameters (E{sub A} {approx} 54.2 kcal/mol), which are then utilized to predict hydrogen outgassing in vacuum for a variety of thermal treatments. Interestingly, it was found that the activation energy for desorption can vary by more than 7 kcal/mol (0.30 eV) for seemingly similar samples. In addition, small amounts of less-stable hydrogen were observed for all erbium dihydride films. A detailed explanation of several approaches for analyzing thermal desorption spectra to obtain kinetic information is included as an appendix.

Ferrizz, Robert Matthew

2006-11-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Complex Hydrides for Hydrogen Storage  

SciTech Connect (OSTI)

This report describes research into the use of complex hydrides for hydrogen storage. The synthesis of a number of alanates, (AIH4) compounds, was investigated. Both wet chemical and mechano-chemical methods were studied.

Slattery, Darlene; Hampton, Michael

2003-03-10T23:59:59.000Z

42

Modeling of a Nickel-Hydrogen Cell Phase Reactions in the Nickel Active Material  

E-Print Network [OSTI]

submitted July 6, 2000; revised manuscript received February 18, 2001. The nickel-hydrogen battery has been the primary energy storage device in aerospace applications for more than two decades. Com- pared to the newly developed high-energy-density batteries, e.g., the nickel-metal hydride battery and the lithium-ion battery

43

Regeneration of Aluminum Hydride - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

hydride is an attractive alternative to the traditional metal hydrides for the storage of hydrogen for its use as an energy source. Alanes use as the primary source of hydrogen has...

44

E-Print Network 3.0 - alkali metal hydrides Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hf for selected alkali metal hydrides, alkaline earth metal hydrides, transition metal hydrides... of binary hydrides based on alkali metals, alkaline earth ... Source:...

45

Vanadium hydride deuterium-tritium generator  

DOE Patents [OSTI]

A pressure controlled vanadium hydride gas generator to provide deuterium-tritium gas in a series of pressure increments. A high pressure chamber filled with vanadium-deuterium-tritium hydride is surrounded by a heater which controls the hydride temperature. The heater is actuated by a power controller which responds to the difference signal between the actual pressure signal and a programmed pressure signal.

Christensen, Leslie D. (Livermore, CA)

1982-01-01T23:59:59.000Z

46

Interaction of Lithium Hydride and Ammonia Borane in THF . | EMSL  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: Vegetation ProposedUsingFunInfrared Land SurfaceVirus-InfectedIntelligentCO2 with Oxygen

47

Vanadium hydride deuterium-tritium generator  

DOE Patents [OSTI]

A pressure controlled vanadium hydride gas generator was designed to provide deuterium-tritium gas in a series of pressure increments. A high pressure chamber filled with vanadium-deuterium-tritium hydride is surrounded by a heater which controls the hydride temperature. The heater is actuated by a power controller which responds to the difference signal between the actual pressure signal and a programmed pressure signal.

Christensen, L.D.

1980-03-13T23:59:59.000Z

48

Igniter containing titanium hydride and potassium perchlorate  

DOE Patents [OSTI]

An explosive device is described which employs a particular titanium hydride-potassium perchlorate composition directly ignitible by an electrical bridgewire.

Dietzel, Russel W. (Albuquerque, NM); Leslie, William B. (Albuquerque, NM)

1976-01-01T23:59:59.000Z

49

Comprehensive Thermodynamics of Nickel Hydride Bis(Diphosphine...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Thermodynamics of Nickel Hydride Bis(Diphosphine) Complexes: A Predictive Model through Computations. Comprehensive Thermodynamics of Nickel Hydride Bis(Diphosphine) Complexes: A...

50

Proposed Virtual Center for Excellence for Metal Hydride Development  

Broader source: Energy.gov (indexed) [DOE]

& Engineering Sciences Center Atoms to Continuum Proposed Virtual Center of Excellence Proposed Virtual Center of Excellence for Metal Hydride Development for Metal Hydride...

51

Neutron Irradiation of Hydrided Cladding Material in HFIR Summary...  

Broader source: Energy.gov (indexed) [DOE]

Neutron Irradiation of Hydrided Cladding Material in HFIR Summary of Initial Activities Neutron Irradiation of Hydrided Cladding Material in HFIR Summary of Initial Activities...

52

argon hydrides: Topics by E-print Network  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

authors 2 Geoneutrino and Hydridic Earth model CERN Preprints Summary: Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic...

53

aluminium hydrides: Topics by E-print Network  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Norman A. 3 Geoneutrino and Hydridic Earth model CERN Preprints Summary: Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic...

54

automated hydride generation-cryotrapping-atomic: Topics by E...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Mohammad 3 Geoneutrino and Hydridic Earth model CERN Preprints Summary: Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic...

55

Incorporation of Hydride Nuclear Fuels in Commercial Light Water Reactors  

E-Print Network [OSTI]

of hydride fueled BWRs. Nuclear Engineering and Design, 239:Fueled PWR Cores. Nuclear Engineering and Design, 239:1489–Hydride Fueled LWRs. Nuclear Engineering and Design, 239:

Terrani, Kurt Amir

2010-01-01T23:59:59.000Z

56

Method to predict relative hydriding within a group of zirconium alloys under nuclear irradiation  

DOE Patents [OSTI]

An out-of-reactor method for screening to predict relative in-reactor hydriding behavior of zirconium-based materials is disclosed. Samples of zirconium-based materials having different compositions and/or fabrication methods are autoclaved in a relatively concentrated (0.3 to 1.0M) aqueous lithium hydroxide solution at constant temperatures within the water reactor coolant temperature range (280 to 316 C). Samples tested by this out-of-reactor procedure, when compared on the basis of the ratio of hydrogen weight gain to oxide weight gain, accurately predict the relative rate of hydriding for the same materials when subject to in-reactor (irradiated) corrosion. 1 figure.

Johnson, A.B. Jr.; Levy, I.S.; Trimble, D.J.; Lanning, D.D.; Gerber, F.S.

1990-04-10T23:59:59.000Z

57

Direct synthesis of catalyzed hydride compounds  

DOE Patents [OSTI]

A method is disclosed for directly preparing alkali metal aluminum hydrides such as NaAlH.sub.4 and Na.sub.3 AlH.sub.6 from either the alkali metal or its hydride, and aluminum. The hydride thus prepared is doped with a small portion of a transition metal catalyst compound, such as TiCl.sub.3, TiF.sub.3, or a mixture of these materials, in order to render them reversibly hydridable. The process provides for mechanically mixing the dry reagents under an inert atmosphere followed by charging the mixed materials with high pressure hydrogen while heating the mixture to about 125.degree. C. The method is relatively simple and inexpensive and provides reversible hydride compounds which are free of the usual contamination introduced by prior art wet chemical methods.

Gross, Karl J.; Majzoub, Eric

2004-09-21T23:59:59.000Z

58

Wire Wrapped Hexagonal Pin Arrays for Hydride Fueled PWRs  

E-Print Network [OSTI]

This work contributes to the Hydride Fuels Project, a collaborative effort between UC Berkeley and MIT

Diller, Peter

59

Activated aluminum hydride hydrogen storage compositions and uses thereof  

DOE Patents [OSTI]

In one aspect, the invention relates to activated aluminum hydride hydrogen storage compositions containing aluminum hydride in the presence of, or absence of, hydrogen desorption stimulants. The invention particularly relates to such compositions having one or more hydrogen desorption stimulants selected from metal hydrides and metal aluminum hydrides. In another aspect, the invention relates to methods for generating hydrogen from such hydrogen storage compositions.

Sandrock, Gary (Ringwood, NJ); Reilly, James (Bellport, NY); Graetz, Jason (Mastic, NY); Wegrzyn, James E. (Brookhaven, NY)

2010-11-23T23:59:59.000Z

60

Hydrogen-storing hydride complexes  

DOE Patents [OSTI]

A ternary hydrogen storage system having a constant stoichiometric molar ratio of LiNH.sub.2:MgH.sub.2:LiBH.sub.4 of 2:1:1. It was found that the incorporation of MgH.sub.2 particles of approximately 10 nm to 20 nm exhibit a lower initial hydrogen release temperature of 150.degree. C. Furthermore, it is observed that the particle size of LiBNH quaternary hydride has a significant effect on the hydrogen sorption concentration with an optimum size of 28 nm. The as-synthesized hydrides exhibit two main hydrogen release temperatures, one around 160.degree. C. and the other around 300.degree. C., with the main hydrogen release temperature reduced from 310.degree. C. to 270.degree. C., while hydrogen is first reversibly released at temperatures as low as 150.degree. C. with a total hydrogen capacity of 6 wt. % to 8 wt. %. Detailed thermal, capacity, structural and microstructural properties have been demonstrated and correlated with the activation energies of these materials.

Srinivasan, Sesha S. (Tampa, FL); Niemann, Michael U. (Venice, FL); Goswami, D. Yogi (Tampa, FL); Stefanakos, Elias K. (Tampa, FL)

2012-04-10T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Liquid suspensions of reversible metal hydrides  

DOE Patents [OSTI]

The reversibility of the process M + x/2 H/sub 2/ ..-->.. MH/sub x/, where M is a metal hydride former that forms a hydride MH/sub x/ in the presence of H/sub 2/, generally used to store and recall H/sub 2/, is found to proceed under a liquid, thereby to reduce contamination, provide better temperature control and provide in situ mobility of the reactants. Thus, a slurry of particles of a metal hydride former with an inert solvent is subjected to temperature and pressure controlled atmosphere containing H/sub 2/, to store hydrogen (at high pressures) and to release (at low pressures) previously stored hydrogen. The direction of the flow of the H/sub 2/ through the liquid is dependent upon the H/sub 2/ pressure in the gas phase at a given temperature. When the former is above the equilibrium absorption pressure of the respective hydride the reaction proceeds to the right, i.e., the metal hydride is formed and hydrogen is stored in the solid particle. When the H/sub 2/ pressure in the gas phase is below the equilibrium dissociation pressure of the respective hydride the reaction proceeds to the left, the metal hydride is decomposed and hydrogen is released into the gas phase.

Reilly, J.J.; Grohse, E.W.; Winsche, W.E.

1983-12-08T23:59:59.000Z

62

Lithium Local Pseudopotential Using  

E-Print Network [OSTI]

Lithium Local Pseudopotential Using DFT Sergio Orozco Student Advisor: Chen Huang Faculty Mentor Lithium LPS Test Lithium LPS #12;Density Functional Theory (DFT) Successful quantum mechanical approach (1979) #12;Building LPS for Lithium Create a LPS using NLPS density for Lithium Test LPS by comparing

Petta, Jason

63

Thermal hydraulic analysis of hydride fuels in BWR's  

E-Print Network [OSTI]

This thesis contributes to the hydride nuclear fuel project being completed by UC Berkeley and MIT to assess the possible benefits of using hydride fuel in light water nuclear reactors (LWR's). More specifically, this ...

Creighton, John Everett

2005-01-01T23:59:59.000Z

64

Optimization of hydride fueled pressurized water reactor cores  

E-Print Network [OSTI]

This thesis contributes to the Hydride Fuels Project, a collaborative effort between UC Berkeley and MIT aimed at investigating the potential benefits of hydride fuel use in light water reactors (LWRs). This pursuit involves ...

Shuffler, Carter Alexander

2004-01-01T23:59:59.000Z

65

americium hydrides: Topics by E-print Network  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

2012-01-01 3 Geoneutrino and Hydridic Earth model CERN Preprints Summary: Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic...

66

Geoneutrino and Hydridic Earth model. Version 2  

E-Print Network [OSTI]

Uranium, Thorium and Potassium-40 abundances in the Earth were calculated in the frame of Hydridic Earth model. Terrestrial heat producton from U, Th and K40 decays was calculated also. We must admit the existance of Earth expansion process to understand the obtained large value of terrestrial heat producton. The geoneutrino detector with volume more than 5 kT (LENA type) must be constructed to definitely separate between Bulk Silicat Earth model and Hydridic Earth model. In second version of the article we assume that K40 concentration distributes in the Earth uniformly.

Leonid Bezrukov

2014-02-12T23:59:59.000Z

67

Encapsulated Metal Hydride for Hydrogen Separation  

E-Print Network [OSTI]

concentration feed stock, not for low concentration ­ Hydrogen economy will need hydrogen recovery from lowEncapsulated Metal Hydride for Hydrogen Separation (Formerly Separation Membrane Development) DOE Hydrogen Program 2003 Merit Review and Peer Evaluation L. Kit Heung, Jim Congdon Savannah River Technology

68

Metal hydride fuel storage and method thereof  

DOE Patents [OSTI]

Disclosed herein is a metal hydride fuel storage cartridge having integrated resistive heaters that can be used in conjunction with fuel cells such as MEMS-based fuel cells. The cartridge is fabricated using micromachining methods and thin/thick film materials synthesis techniques.

Morse, Jeffrey D. (Martinez, CA); Jankowski, Alan F. (Livermore, CA); Yu, Conrad (Antioch, CA)

2006-10-17T23:59:59.000Z

69

Metal hydride fuel storage and method thereof  

DOE Patents [OSTI]

Disclosed herein is a metal hydride fuel storage cartridge having integrated resistive heaters that can be used in conjunction with fuel cells such as MEMS-based fuel cells. The cartridge is fabricated using micromachining methods and thin/thick film materials synthesis techniques.

Morse, Jeffrey D [Martinez, CA; Jankowski, Alan F [Livermore, CA; Yu, Conrad [Antioch, CA

2009-05-05T23:59:59.000Z

70

Molten salt lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell (10) which may be operated at temperatures between about 100.degree.-170.degree. C. Cell (10) comprises an electrolyte (16), which preferably includes lithium nitrate, and a lithium or lithium alloy electrode (12).

Raistrick, Ian D. (Menlo Park, CA); Poris, Jaime (Portola Valley, CA); Huggins, Robert A. (Stanford, CA)

1982-02-09T23:59:59.000Z

71

Molten salt lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell (10) which may be operated at temperatures between about 100.degree.-170.degree. C. Cell (10) comprises an electrolyte (16), which preferably includes lithium nitrate, and a lithium or lithium alloy electrode (12).

Raistrick, Ian D. (Menlo Park, CA); Poris, Jaime (Portola Valley, CA); Huggins, Robert A. (Stanford, CA)

1983-01-01T23:59:59.000Z

72

Molten salt lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and light weight. One type of lithium-based cell utilizes a molten salt electrolyte and is operated in the temperature range of about 400 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems and a substantial amount of energy is lost through heat transfer. The present invention provides an electrochemical cell which may be operated at temperatures between about 100 to 170/sup 0/C. The cell is comprised of an electrolyte, which preferably includes lithium nitrate, and a lithium or lithium alloy electrode.

Raistrick, I.D.; Poris, J.; Huggins, R.A.

1980-07-18T23:59:59.000Z

73

Ductility Evaluation of As-Hydrided and Hydride Reoriented Zircaloy-4 Cladding under Simulated Dry-Storage Condition  

SciTech Connect (OSTI)

Pre-storage drying-transfer operations and early stage storage expose cladding to higher temperatures and much higher pressure-induced tensile hoop stresses relative to normal operation in-reactor and pool storage under these conditions. Radial hydrides could precipitate during slow cooling and provide an additional embrittlement mechanism as the cladding temperature decreases below the ductile-to-brittle transition temperature. As a means of simulating this behavior, unirradiated hydrided Zircaloy-4 samples were fabricated by a gas charging method to levels that encompass the range of hydrogen concentrations observed in current used fuel. Mechanical testing was carried out by the ring compression test (RCT) method at various temperatures to evaluate the sample s ductility for both as-hydrided and post-hydride reorientation treated specimens. As-hydrided samples with higher hydrogen concentration (>800 ppm) resulted in lower strain before fracture and reduced maximum load. Increasing RCT temperatures resulted in increased ductility of the as-hydrided cladding. A systematic radial hydride treatment was conducted at various pressures and temperatures for the hydrided samples with H content around 200 ppm. Following the radial hydride treatment, RCTs on the hydride reoriented samples were conducted and exhibited lower ductility compared to as-hydrided samples.

Yan, Yong [ORNL] [ORNL; Plummer, Lee K [ORNL] [ORNL; Ray, Holly B [ORNL] [ORNL; Cook, Tyler S [ORNL] [ORNL; Bilheux, Hassina Z [ORNL] [ORNL

2014-01-01T23:59:59.000Z

74

Lithium Ion Production NDE  

E-Print Network [OSTI]

Lithium Ion Electrode Production NDE and QC Considerations David Wood, Debasish Mohanty, Jianlin Li, and Claus Daniel 12/9/13 EERE Quality Control Workshop #12;2 Presentation name Lithium Ion Electrode to be meaningful and provide electrode and cell QC. #12;3 Presentation name New Directions in Lithium Ion Electrode

75

Lithium ion sources  

E-Print Network [OSTI]

HIFAN 1866 Lithium ion sources by Prabir K. Roy, Wayne G.No. DE-AC02-05CH11231. Lithium ion sources Prabir K. RoyUSA Abstract A 10.9 cm diameter lithium alumino-silicate ion

Roy, Prabir K.

2014-01-01T23:59:59.000Z

76

Proposed Virtual Center for Excellence for Metal Hydride Development...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Virtual Center for Excellence for Metal Hydride Development Presentation from the Hydrogen Storage Pre-Solicitation Meeting held June 19, 2003 in Washington, DC....

77

Mathematical modelling of a metal hydride hydrogen storage system.  

E-Print Network [OSTI]

??In order for metal hydride hydrogen storage systems to compete with existing energy storage technology, such as gasoline tanks and batteries, it is important to… (more)

MacDonald, Brendan David

2009-01-01T23:59:59.000Z

78

Final Report for the DOE Metal Hydride Center of Excellence  

Broader source: Energy.gov (indexed) [DOE]

Figure 9. Organometallic approach to incorporation of metal hydrides into C aerogels. ...42 Figure 10. Comparison of H 2 evolution from bulk-like ball milled...

79

Project Profile: Engineering a Novel High Temperature Metal Hydride...  

Office of Environmental Management (EM)

ELEMENTS) funding program, is developing a concept for high energy density thermochemical energy storage for concentrating solar power (CSP) using metal hydrides. These materials...

80

METAL HYDRIDE HYDROGEN COMPRESSORS: A REVIEW  

SciTech Connect (OSTI)

Metal hydride (MH) thermal sorption compression is an efficient and reliable method allowing a conversion of energy from heat into a compressed hydrogen gas. The most important component of such a thermal engine the metal hydride material itself should possess several material features in order to achieve an efficient performance in the hydrogen compression. Apart from the hydrogen storage characteristics important for every solid H storage material (e.g. gravimetric and volumetric efficiency of H storage, hydrogen sorption kinetics and effective thermal conductivity), the thermodynamics of the metal-hydrogen systems is of primary importance resulting in a temperature dependence of the absorption/desorption pressures). Several specific features should be optimized to govern the performance of the MH-compressors including synchronisation of the pressure plateaus for multi-stage compressors, reduction of slope of the isotherms and hysteresis, increase of cycling stability and life time, together with challenges in system design associated with volume expansion of the metal matrix during the hydrogenation. The present review summarises numerous papers and patent literature dealing with MH hydrogen compression technology. The review considers (a) fundamental aspects of materials development with a focus on structure and phase equilibria in the metal-hydrogen systems suitable for the hydrogen compression; and (b) applied aspects, including their consideration from the applied thermodynamic viewpoint, system design features and performances of the metal hydride compressors and major applications.

Bowman Jr, Robert C [ORNL] [ORNL; Yartys, Dr. Volodymyr A. [Institute for Energy Technology (IFE)] [Institute for Energy Technology (IFE); Lototskyy, Dr. Michael V [University of the Western Cape, South Africa] [University of the Western Cape, South Africa; Pollet, Dr. B.G. [University of the Western Cape, South Africa

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

LANL/PNNL Virtual Center for Chemical Hydrides and New Concepts...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

LANLPNNL Virtual Center for Chemical Hydrides and New Concepts for Hydrogen Storage LANLPNNL Virtual Center for Chemical Hydrides and New Concepts for Hydrogen Storage...

82

E-Print Network 3.0 - antimony hydrides Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

and Sb(V) were the only hydride-forming species found... WATERS BY HYDRIDE GENERATION ATOMIC ABSORPTION SPECTROMETRY Water-Resources Investigations Report 03... Prior to the...

83

Argonne, Western Lithium to develop lithium carbonate for multiple...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Laboratory as a step toward the commercialization of lithium carbonate from the Company's Kings Valley Lithium Project located in Humboldt County, Nevada, USA. Under the agreement,...

84

Metal Hydride Thermal Storage: Reversible Metal Hydride Thermal Storage for High-Temperature Power Generation Systems  

SciTech Connect (OSTI)

HEATS Project: PNNL is developing a thermal energy storage system based on a Reversible Metal Hydride Thermochemical (RMHT) system, which uses metal hydride as a heat storage material. Heat storage materials are critical to the energy storage process. In solar thermal storage systems, heat can be stored in these materials during the day and released at night—when the sun is not out—to drive a turbine and produce electricity. In nuclear storage systems, heat can be stored in these materials at night and released to produce electricity during daytime peak-demand hours. PNNL’s metal hydride material can reversibly store heat as hydrogen cycles in and out of the material. In a RHMT system, metal hydrides remain stable in high temperatures (600- 800°C). A high-temperature tank in PNNL’s storage system releases heat as hydrogen is absorbed, and a low-temperature tank stores the heat until it is needed. The low-cost material and simplicity of PNNL’s thermal energy storage system is expected to keep costs down. The system has the potential to significantly increase energy density.

None

2011-12-05T23:59:59.000Z

85

Method of making crack-free zirconium hydride  

DOE Patents [OSTI]

Crack-free hydrides of zirconium and zirconium-uranium alloys are produced by alloying the zirconium or zirconium-uranium alloy with beryllium, or nickel, or beryllium and scandium, or nickel and scandium, or beryllium and nickel, or beryllium, nickel and scandium and thereafter hydriding.

Sullivan, Richard W. (Denver, CO)

1980-01-01T23:59:59.000Z

86

Separation Membrane Development (Separation Using Encapsulated Metal Hydride)  

E-Print Network [OSTI]

Separation Membrane Development (Separation Using Encapsulated Metal Hydride) L. Kit Heung Savannah: The first is to produce a sol-gel encapsulated metal hydride packing material that will a) absorbs hydrogen may be that hydrogen must come from multiple sources. These sources will include renewable (solar

87

A novel plating process for microencapsulating metal hydrides  

SciTech Connect (OSTI)

One approach to increasing the lifetime of the metal hydride electrode has been the use of conventional electroless plating to produce a coating of copper or nickel on the surface of the metal hydride powders. In this paper, a novel method for microencapsulating the active electrode powders is presented. This new plating technique takes advantage of the reducing power of hydrogen already stored inside the metal hydride to plate a variety of metals onto metal hydride materials. This method greatly simplifies electroless plating for these powders, eliminating the need for stabilizers and additives typically required for conventional electroless plating solutions. Metals that can be electrolessly plated with stored hydrogen have been identified based on thermodynamic considerations. Experimentally, micrometers thick coatings of copper, silver, and nickel have been plated on several metal hydrides.

Law, H.H.; Vyas, B.; Zahurak, S.M.; Kammlott, G.W. [AT and T Bell Labs., Murray Hill, NJ (United States)

1996-08-01T23:59:59.000Z

88

Porous metal hydride composite and preparation and uses thereof  

DOE Patents [OSTI]

A composite formed from large pieces of aggregate formed from (1) metal hydride (or hydride-former) powder and (2) either metal powder or plastic powder or both is prepared. The composite has large macroscopic interconnected pores (much larger than the sizes of the powders which are used) and will have a very fast heat transfer rate and low windage loss. It will be useful, for example, in heat engines, hydrogen storage devices, and refrigerator components which depend for their utility upon both a fast rate of hydriding and dehydriding. Additionally, a method of preparing the composite and a method of increasing the rates of hydriding and dehydriding of metal hydrides are also given.

Steyert, William A. (Los Alamos, NM); Olsen, Clayton E. (Los Alamos, NM)

1982-01-01T23:59:59.000Z

89

Porous metal hydride composite and preparation and uses thereof  

DOE Patents [OSTI]

A composite formed from large pieces of aggregate formed from (1) metal hydride (or hydride-former) powder and (2) either metal powder or plastic powder or both is prepared. The composite has large macroscopic interconnected pores (much larger than the sizes of the powders which are used) and will have a very fast heat transfer rate and low windage loss. It will be useful, for example, in heat engines, hydrogen storage devices, and refrigerator components which depend for their utility upon both a fast rate of hydriding and dehydriding. Additionally, a method of preparing the composite and a method of increasing the rates of hydriding and dehydriding of metal hydrides are also given.

Steyert, W.A.; Olsen, C.E.

1980-03-12T23:59:59.000Z

90

Lithium purification technique  

DOE Patents [OSTI]

A method for purifying liquid lithium to remove unwanted quantities of nitrogen or aluminum. The method involves precipitation of aluminum nitride by adding a reagent to the liquid lithium. The reagent will be either nitrogen or aluminum in a quantity adequate to react with the unwanted quantity of the impurity to form insoluble aluminum nitride. The aluminum nitride can be mechanically separated from the molten liquid lithium.

Keough, Robert F. (Richland, WA); Meadows, George E. (Richland, WA)

1985-01-01T23:59:59.000Z

91

Modular hydride beds for mobile applications  

SciTech Connect (OSTI)

Design, construction, initial testing and simple thermal modeling of modular, metal hydride beds have been completed. Originally designed for supplying hydrogen to a fuel cell on a mobile vehicle, the complete bed design consists of 8 modules and is intended for use on the Palm Desert Vehicle (PDV) under development at the Schatz Energy Center, Humbolt State University. Each module contains approximately 2 kg of a commercially available, low temperature, hydride-forming metal alloy. Waste heat from the fuel cell in the form of heated water is used to desorb hydrogen from the alloy for supplying feed hydrogen to the fuel cell. In order to help determine the performance of such a modular bed system, six modules were constructed and tested. The design and construction of the modules is described in detail. Initial testing of the modules both individually and as a group showed that each module can store {approximately} 30 g of hydrogen (at 165 PSIA fill pressure, 17 C), could be filled with hydrogen in 6 minutes at a nominal, 75 standard liters/min (slm) fueling rate, and could supply hydrogen during desorption at rates of 25 slm, the maximum anticipated hydrogen fuel cell input requirement. Tests made of 5 modules as a group indicated that the behavior of the group run in parallel both in fueling and gas delivery could be directly predicted from the corresponding, single module characteristics by using an appropriate scaling factor. Simple thermal modeling of a module as an array of cylindrical, hydride-filled tubes was performed. The predictions of the model are in good agreement with experimental data.

Malinowski, M.E.; Stewart, K.D.

1997-08-01T23:59:59.000Z

92

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

facing rechargeable lithium batteries. Nature, 2001. 414(of rechargeable lithium batteries, I. Lithium manganeseof rechargeable lithium batteries, II. Lithium ion

Wilcox, James D.

2010-01-01T23:59:59.000Z

93

Results of NDE Technique Evaluation of Clad Hydrides  

SciTech Connect (OSTI)

This report fulfills the M4 milestone, M4FT-14IN0805023, Results of NDE Technique Evaluation of Clad Hydrides, under Work Package Number FT-14IN080502. During service, zirconium alloy fuel cladding will degrade via corrosion/oxidation. Hydrogen, a byproduct of the oxidation process, will be absorbed into the cladding and eventually form hydrides due to low hydrogen solubility limits. The hydride phase is detrimental to the mechanical properties of the cladding and therefore it is important to be able to detect and characterize the presence of this constituent within the cladding. Presently, hydrides are evaluated using destructive examination. If nondestructive evaluation techniques can be used to detect and characterize the hydrides, the potential exists to significantly increase test sample coverage while reducing evaluation time and cost. To demonstrate the viability this approach, an initial evaluation of eddy current and ultrasonic techniques were performed to demonstrate the basic ability to these techniques to detect hydrides or their effects on the microstructure. Conventional continuous wave eddy current techniques were applied to zirconium based cladding test samples thermally processed with hydrogen gas to promote the absorption of hydrogen and subsequent formation of hydrides. The results of the evaluation demonstrate that eddy current inspection approaches have the potential to detect both the physical damage induced by hydrides, e.g. blisters and cracking, as well as the combined effects of absorbed hydrogen and hydride precipitates on the electrical properties of the zirconium alloy. Similarly, measurements of ultrasonic wave velocities indicate changes in the elastic properties resulting from the combined effects of absorbed hydrogen and hydride precipitates as well as changes in geometry in regions of severe degradation. However, for both approaches, the signal responses intended to make the desired measurement incorporate a number of contributing parameters. These contributing factors need to be recognized and a means to control them or separate their contributions will be required to obtain the desired information.

Dennis C. Kunerth

2014-09-01T23:59:59.000Z

94

Metal hydride fuel storage and method thereof  

DOE Patents [OSTI]

An apparatus having a first substrate having (1) a cavity, (2) one or more resistive heaters, and (3) one or more coatings forming a diffusion barrier to hydrogen; a second substrate having (1) an outlet valve comprising a pressure relief structure and (2) one or more coatings forming a diffusion barrier to hydrogen, wherein said second substrate is coupled to said first substrate forming a sealed volume in said cavity; a metal hydride material contained within said cavity; and a gas distribution system formed by coupling a microfluidic interconnect to said pressure relief structure. Additional apparatuses and methods are also disclosed.

Morse, Jeffrey D. (Martinez, CA); Jankowski, Alan F. (Livermore, CA); Yu, Conrad (Antioch, CA)

2010-08-10T23:59:59.000Z

95

Highly Concentrated Palladium Hydrides/Deuterides; Theory  

SciTech Connect (OSTI)

Accomplishments are reported in these areas: tight-binding molecular dynamics study of palladium; First-principles calculations and tight-binding molecular dynamics simulations of the palladium-hydrogen system; tight-binding studies of bulk properties and hydrogen vacancies in KBH{sub 4}; tight-binding study of boron structures; development of angular dependent potentials for Pd-H; and density functional and tight-binding calculations for the light-hydrides NaAlH4 and NaBH4

Papaconstantopoulos, Dimitrios

2013-11-26T23:59:59.000Z

96

Lithium Hexamethyldisilazide: A View of Lithium Ion Solvation  

E-Print Network [OSTI]

Lithium Hexamethyldisilazide: A View of Lithium Ion Solvation through a Glass-Bottom Boat BRETT L and reactivities, we were drawn to lithium hexamethyldisilazide (LiHMDS; (Me3Si)2NLi) by its promi- nence principles of lithium ion coordination chemistry.2 Understanding how solvation influences organolithium

Collum, David B.

97

Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis  

E-Print Network [OSTI]

Lithium Diisopropylamide-Mediated Ortholithiations: Lithium Chloride Catalysis Lekha Gupta, 2008 Ortholithiations of a range of arenes mediated by lithium diisopropylamide (LDA) in THF at -78 °C protocols with unpurified commercial samples of n-butyl- lithium to prepare LDA or commercially available

Collum, David B.

98

Synthesis and Hydride Transfer Reactions of Cobalt and Nickel Hydride Complexes to BX3 Compounds  

SciTech Connect (OSTI)

Hydrides of numerous transition metal complexes can be generated by the heterolytic cleavage of H{sub 2} gas such that they offer alternatives to using main group hydrides in the regeneration of ammonia borane, a compound that has been intensely studied for hydrogen storage applications. Previously, we reported that HRh(dmpe){sub 2}, dmpe = 1,2-bis(dimethylphosphinoethane) was capable of reducing a variety of BX{sub 3} compounds having hydride affinity (HA) greater than or equal to HA of BEt{sub 3}. This study examines the reactivity of less expensive cobalt and nickel hydride complexes, (HCo(dmpe){sub 2} and [HNi(dmpe){sub 2}]{sup +}), to form B-H bonds. The hydride donor abilities ({Delta}G{sub H{sup -}}{sup o}) of HCo(dmpe){sub 2} and [HNi(dmpe){sub 2}]{sup +} were positioned on a previously established scale in acetonitrile that is cross-referenced with calculated HAs of BX{sub 3} compounds. The collective data guided our selection of BX{sub 3} compounds to investigate and aided our analysis of factors that determine favorability of hydride transfer. HCo(dmpe){sub 2} was observed to transfer H{sup -} to BX{sub 3} compounds with X = H, OC{sub 6}F{sub 5} and SPh. The reaction with B(SPh){sub 3} is accompanied by formation of (BH{sub 3}){sub 2}-dmpe and (BH{sub 2}SPh){sub 2}-dmpe products that follow from reduction of multiple BSPh bonds and loss of a dmpe ligand from Co. Reactions between HCo(dmpe){sub 2} and B(SPh){sub 3} in the presence of triethylamine result in formation of Et{sub 3}N-BH{sub 2}SPh and Et{sub 3}N-BH{sub 3} with no loss of dmpe ligand. Reactions of the cationic complex [HNi(dmpe){sub 2}]{sup +} with B(SPh){sub 3} under analogous conditions give Et{sub 3}N-BH{sub 2}SPh as the final product along with the nickel-thiolate complex [Ni(dmpe){sub 2}(SPh)]{sup +}. The synthesis and characterization of HCo(dedpe){sub 2} (dedpe = diethyldiphenyl(phosphino)ethane) from H{sub 2} and a base is also discussed; including the formation of an uncommon trans dihydride species, trans-[(H{sub 2})Co(dedpe){sub 2}][BF{sub 4}].

Mock, Michael T.; Potter, Robert G.; O'Hagan, Molly J.; Camaioni, Donald M.; Dougherty, William G.; Kassel, W. S.; DuBois, Daniel L.

2011-12-05T23:59:59.000Z

99

Cathode material for lithium batteries  

DOE Patents [OSTI]

A method of manufacture an article of a cathode (positive electrode) material for lithium batteries. The cathode material is a lithium molybdenum composite transition metal oxide material and is prepared by mixing in a solid state an intermediate molybdenum composite transition metal oxide and a lithium source. The mixture is thermally treated to obtain the lithium molybdenum composite transition metal oxide cathode material.

Park, Sang-Ho; Amine, Khalil

2013-07-23T23:59:59.000Z

100

Lithium Insertion Chemistry of Some Iron Vanadates  

E-Print Network [OSTI]

in A. Nazri, G.Pistoia (Eds. ), Lithium batteries, Science &structure materials in lithium cells, for a lower limitLithium Insertion Chemistry of Some Iron Vanadates Sébastien

Patoux, Sebastien; Richardson, Thomas J.

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

J. -P. Gabano, Ed. , Lithium Batteries, Academic Press, Newfor Rechargeable Lithium Batteries," J. Electrochem.for Rechargeable Lithium Batteries," J. Electroclzern.

Doyle, C.M.

2010-01-01T23:59:59.000Z

102

Lithium Insertion Chemistry of Some Iron Vanadates  

E-Print Network [OSTI]

G.Pistoia (Eds. ), Lithium batteries, Science & Technology,Keywords: Lithium batteries, iron vanadates, insertionelectrode materials for lithium batteries, (mostly layered

Patoux, Sebastien; Richardson, Thomas J.

2008-01-01T23:59:59.000Z

103

Ionic liquids for rechargeable lithium batteries  

E-Print Network [OSTI]

for rechargeable lithium batteries (Preliminary report,applications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

Salminen, Justin; Papaiconomou, Nicolas; Kerr, John; Prausnitz, John; Newman, John

2008-01-01T23:59:59.000Z

104

Side Reactions in Lithium-Ion Batteries  

E-Print Network [OSTI]

for rechargeable lithium batteries. Advanced Materials 10,Protection of Secondary Lithium Batteries. Journal of thein Rechargeable Lithium Batteries for Overcharge Protection.

Tang, Maureen Han-Mei

2012-01-01T23:59:59.000Z

105

Advances in lithium-ion batteries  

E-Print Network [OSTI]

Advances in Lithium-Ion Batteries Edited by Walter A. vanpuzzling mysteries of lithium ion batteries. The book beginssuch importance to lithium ion batteries one is amazed that

Kerr, John B.

2003-01-01T23:59:59.000Z

106

Block copolymer electrolytes for lithium batteries  

E-Print Network [OSTI]

polymer electrolytes for lithium batteries. Nature 394, 456-facing rechargeable lithium batteries. Nature 414, 359-367 (vanadium oxides for lithium batteries. Journal of Materials

Hudson, William Rodgers

2011-01-01T23:59:59.000Z

107

Lithium metal oxide electrodes for lithium batteries  

DOE Patents [OSTI]

An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.x<1 and .delta. is less than 0.2, and in which M is a non-lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

Thackeray, Michael M. (Naperville, IL); Kim, Jeom-Soo (Naperville, IL); Johnson, Christopher S. (Naperville, IL)

2008-01-01T23:59:59.000Z

108

ENVIRONMENTAL REACTIVITY OF SOLID STATE HYDRIDE MATERIALS  

SciTech Connect (OSTI)

In searching for high gravimetric and volumetric density hydrogen storage systems, it is inevitable that higher energy density materials will be used. In order to make safe and commercially acceptable condensed phase hydrogen storage systems, it is important to understand quantitatively the risks involved in using and handling these materials and to develop appropriate mitigation strategies to handle potential material exposure events. A crucial aspect of the development of risk identification and mitigation strategies is the development of rigorous environmental reactivity testing standards and procedures. This will allow for the identification of potential risks and implementation of risk mitigation strategies. Modified testing procedures for shipping air and/or water sensitive materials, as codified by the United Nations, have been used to evaluate two potential hydrogen storage materials, 2LiBH{sub 4} {center_dot} MgH{sub 2} and NH{sub 3}BH{sub 3}. The modified U.N. procedures include identification of self-reactive substances, pyrophoric substances, and gas-emitting substances with water contact. The results of these tests for air and water contact sensitivity will be compared to the pure material components where appropriate (e.g. LiBH{sub 4} and MgH{sub 2}). The water contact tests are divided into two scenarios dependent on the hydride to water mole ratio and heat transport characteristics. Air contact tests were run to determine whether a substance will spontaneously react with air in a packed or dispersed form. In the case of the 2LiBH{sub 4} {center_dot} MgH{sub 2} material, the results from the hydride mixture compared to the pure materials results showed the MgH{sub 2} to be the least reactive component and LiBH{sub 4} the more reactive. The combined 2LiBH{sub 4} {center_dot} MgH{sub 2} resulted in a material having environmental reactivity between these two materials. Relative to 2LiBH{sub 4} {center_dot} MgH{sub 2}, the chemical hydride NH{sub 3}BH{sub 3} was observed to be less environmentally reactive.

Gray, J; Donald Anton, D

2009-04-23T23:59:59.000Z

109

Process for production of a metal hydride  

DOE Patents [OSTI]

A process for production of a metal hydride compound MH.sub.x, wherein x is one or two and M is an alkali metal, Be or Mg. The process comprises combining a compound of formula (R.sup.1O).sub.xM with aluminum, hydrogen and at least one metal selected from among titanium, zirconium, hafnium, niobium, vanadium, tantalum and iron to produce a compound of formula MH.sub.x. R.sup.1 is phenyl or phenyl substituted by at least one alkyl or alkoxy group. A mole ratio of aluminum to (R.sup.1O).sub.xM is from 0.1:1 to 1:1. The catalyst is present at a level of at least 200 ppm based on weight of aluminum.

Allen, Nathan Tait; Butterick, III, Robert; Chin, Arthur Achhing; Millar, Dean Michael; Molzahn, David Craig

2014-08-12T23:59:59.000Z

110

High capacity stabilized complex hydrides for hydrogen storage  

DOE Patents [OSTI]

Complex hydrides based on Al(BH.sub.4).sub.3 are stabilized by the presence of one or more additional metal elements or organic adducts to provide high capacity hydrogen storage material.

Zidan, Ragaiy; Mohtadi, Rana F; Fewox, Christopher; Sivasubramanian, Premkumar

2014-11-11T23:59:59.000Z

111

Transient analysis of hydride fueled pressurized water reactor cores  

E-Print Network [OSTI]

This thesis contributes to the hydride nuclear fuel project led by U. C. Berkeley for which MIT is to perform the thermal hydraulic and economic analyses. A parametric study has been performed to determine the optimum ...

Trant, Jarrod Michael

2004-01-01T23:59:59.000Z

112

Metal Hydride Chemical Heat Pumps for Industrial Use  

E-Print Network [OSTI]

Hydriding alloys are intermetallic absorbent compounds which have the remarkable quality of absorbing very large quantities of hydrogen gas per unit volume of metallic powder. The absorption and desorption of hydrogen are exothermic and endothermic...

Ally, M. R.; Rebello, W. J.; Rosso, M. J., Jr.

1984-01-01T23:59:59.000Z

113

Lithium metal oxide electrodes for lithium batteries  

DOE Patents [OSTI]

An uncycled preconditioned electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula xLi2-yHyO.xM'O2.(1-x)Li1-zHzMO2 in which 0lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. The xLi2-yHy.xM'O2.(1-x)Li1-zHzMO2 material is prepared by preconditioning a precursor lithium metal oxide (i.e., xLi2M'O3.(1-x)LiMO2) with a proton-containing medium with a pH<7.0 containing an inorganic acid. Methods of preparing the electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kang, Sun-Ho

2010-06-08T23:59:59.000Z

114

Optimization of Hydride Rim Formation in Unirradiated Zr 4 Cladding  

SciTech Connect (OSTI)

The purpose of this work is to build on the results reported in the M2 milestone M2FT 13PN0805051, document number FCRD-USED-2013-000151 (Hanson, 2013). In that work, it was demonstrated that unirradiated samples of zircaloy-4 cladding could be pre-hydrided at temperatures below 400°C in pure hydrogen gas and that the growth of hydrides on the surface could be controlled by changing the surface condition of the samples and form a desired hydride rim on the outside diameter of the cladding. The work performed at Pacific Northwest National Laboratory since the issuing of the M2 milestone has focused its efforts to optimize the formation of a hydride rim on available zircaloy-4 cladding samples by controlling temperature variation and gas flow control during pre-hydriding treatments. Surface conditioning of the outside surface was also examined as a variable. The results of test indicate that much of the variability in the hydride thickness is due to temperature variation occurring in the furnaces as well as how hydrogen gas flows across the sample surface. Efforts to examine other alloys, gas concentrations, and different surface conditioning plan to be pursed in the next FY as more cladding samples become available

Shimskey, Rick W.; Hanson, Brady D.; MacFarlan, Paul J.

2013-09-30T23:59:59.000Z

115

Electrocatalysts for Nonaqueous Lithium–Air Batteries:...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrocatalysts for Nonaqueous Lithium–Air Batteries: Status, Challenges, and Perspective. Electrocatalysts for Nonaqueous Lithium–Air Batteries: Status, Challenges,...

116

OBSERVATIONS IN REACTIVITY BETWEEN BH CONTAINING COMPOUNDS AND ORGANOMETALLIC REAGENTS: SYNTHESIS OF BORONIC ACIDS, BORONIC ESTERS, AND MAGNESIUM HYDRIDES  

E-Print Network [OSTI]

Reaction of BH 3 :THF with magnesium hydride byproduct. A.It was also observed that magnesium hydride can partiallyACIDS, BORONIC ESTERS, AND MAGNESIUM HYDRIDES A dissertation

Clary, Jacob William

2012-01-01T23:59:59.000Z

117

Lithium battery management system  

DOE Patents [OSTI]

Provided is a system for managing a lithium battery system having a plurality of cells. The battery system comprises a variable-resistance element electrically connected to a cell and located proximate a portion of the cell; and a device for determining, utilizing the variable-resistance element, whether the temperature of the cell has exceeded a predetermined threshold. A method of managing the temperature of a lithium battery system is also included.

Dougherty, Thomas J. (Waukesha, WI)

2012-05-08T23:59:59.000Z

118

Solid-state lithium battery  

DOE Patents [OSTI]

The present invention is directed to a higher power, thin film lithium-ion electrolyte on a metallic substrate, enabling mass-produced solid-state lithium batteries. High-temperature thermodynamic equilibrium processing enables co-firing of oxides and base metals, providing a means to integrate the crystalline, lithium-stable, fast lithium-ion conductor lanthanum lithium tantalate (La.sub.1/3-xLi.sub.3xTaO.sub.3) directly with a thin metal foil current collector appropriate for a lithium-free solid-state battery.

Ihlefeld, Jon; Clem, Paul G; Edney, Cynthia; Ingersoll, David; Nagasubramanian, Ganesan; Fenton, Kyle Ross

2014-11-04T23:59:59.000Z

119

Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes Inexpensive, Nonfluorinated Anions for Lithium Salts and Ionic Liquids for Lithium Battery Electrolytes...

120

Six-Membered-Ring Malonatoborate-Based Lithium Salts as Electrolytes for Lithium Ion Batteries  

E-Print Network [OSTI]

References 1. Lithium Ion Batteries: Fundamentals andProgram for Lithium Ion Batteries, U.S. Department ofas Electrolytes for Lithium Ion Batteries Li Yang a , Hanjun

Yang, Li

2014-01-01T23:59:59.000Z

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


121

Influence of uranium hydride oxidation on uranium metal behaviour  

SciTech Connect (OSTI)

This work addresses concerns that the rapid, exothermic oxidation of active uranium hydride in air could stimulate an exothermic reaction (burning) involving any adjacent uranium metal, so as to increase the potential hazard arising from a hydride reaction. The effect of the thermal reaction of active uranium hydride, especially in contact with uranium metal, does not increase in proportion with hydride mass, particularly when considering large quantities of hydride. Whether uranium metal continues to burn in the long term is a function of the uranium metal and its surroundings. The source of the initial heat input to the uranium, if sufficient to cause ignition, is not important. Sustained burning of uranium requires the rate of heat generation to be sufficient to offset the total rate of heat loss so as to maintain an elevated temperature. For dense uranium, this is very difficult to achieve in naturally occurring circumstances. Areas of the uranium surface can lose heat but not generate heat. Heat can be lost by conduction, through contact with other materials, and by convection and radiation, e.g. from areas where the uranium surface is covered with a layer of oxidised material, such as burned-out hydride or from fuel cladding. These rates of heat loss are highly significant in relation to the rate of heat generation by sustained oxidation of uranium in air. Finite volume modelling has been used to examine the behaviour of a magnesium-clad uranium metal fuel element within a bottle surrounded by other un-bottled fuel elements. In the event that the bottle is breached, suddenly, in air, it can be concluded that the bulk uranium metal oxidation reaction will not reach a self-sustaining level and the mass of uranium oxidised will likely to be small in relation to mass of uranium hydride oxidised. (authors)

Patel, N.; Hambley, D. [National Nuclear Laboratory (United Kingdom); Clarke, S.A. [Sellafield Ltd (United Kingdom); Simpson, K.

2013-07-01T23:59:59.000Z

122

Characterization and High Throughput Analysis of Metal Hydrides for Hydrogen Storage  

E-Print Network [OSTI]

Metal Hydrides for Hydrogen Storage by Steven James BarceloMetal Hydrides for Hydrogen Storage by Steven James BarceloCo-chair Efficient hydrogen storage is required for fuel

Barcelo, Steven James

2009-01-01T23:59:59.000Z

123

PREPRINT submitted to Journal of Physics B Electronic structure of the Magnesium hydride  

E-Print Network [OSTI]

PREPRINT submitted to Journal of Physics B Electronic structure of the Magnesium hydride molecular: 31.15.AR,31.15.Ct,31.50.Be,31.50.Df #12; Electronic structure of the Magnesium hydride molecular ion

Recanati, Catherine

124

Opening of a Post Doctoral Position Complex hydrides for hydrogen storage applications  

E-Print Network [OSTI]

Opening of a Post Doctoral Position Complex hydrides for hydrogen storage applications on complex hydrides for hydrogen storage applications in connection with the « Fast, reliable and cost effective boron hydride based high capacity solid state hydrogen storage materials» project co

125

Phenomenological theory of a single domain wall in uniaxial trigonal ferroelectrics: Lithium niobate and lithium tantalate  

E-Print Network [OSTI]

Phenomenological theory of a single domain wall in uniaxial trigonal ferroelectrics: Lithium niobate and lithium tantalate David A. Scrymgeour and Venkatraman Gopalan Department of Materials Science, lithium niobate and lithium tantalate. The contributions to the domain- wall energy from polarization

Gopalan, Venkatraman

126

Composite Materials for Hazard Mitigation of Reactive Metal Hydrides.  

SciTech Connect (OSTI)

In an attempt to mitigate the hazards associated with storing large quantities of reactive metal hydrides, polymer composite materials were synthesized and tested under simulated usage and accident conditions. The composites were made by polymerizing vinyl monomers using free-radical polymerization chemistry, in the presence of the metal hydride. Composites with vinyl-containing siloxane oligomers were also polymerized with and without added styrene and divinyl benzene. Hydrogen capacity measurements revealed that addition of the polymer to the metal hydride reduced the inherent hydrogen storage capacity of the material. The composites were found to be initially effective at reducing the amount of heat released during oxidation. However, upon cycling the composites, the mitigating behavior was lost. While the polymer composites we investigated have mitigating potential and are physically robust, they undergo a chemical change upon cycling that makes them subsequently ineffective at mitigating heat release upon oxidation of the metal hydride. Acknowledgements The authors would like to thank the following people who participated in this project: Ned Stetson (U.S. Department of Energy) for sponsorship and support of the project. Ken Stewart (Sandia) for building the flow-through calorimeter and cycling test stations. Isidro Ruvalcaba, Jr. (Sandia) for qualitative experiments on the interaction of sodium alanate with water. Terry Johnson (Sandia) for sharing his expertise and knowledge of metal hydrides, and sodium alanate in particular. Marcina Moreno (Sandia) for programmatic assistance. John Khalil (United Technologies Research Corp) for insight into the hazards of reactive metal hydrides and real-world accident scenario experiments. Summary In an attempt to mitigate and/or manage hazards associated with storing bulk quantities of reactive metal hydrides, polymer composite materials (a mixture of a mitigating polymer and a metal hydride) were synthesized and tested under simulated usage and accident conditions. Mitigating the hazards associated with reactive metal hydrides during an accident while finding a way to keep the original capability of the active material intact during normal use has been the focus of this work. These composites were made by polymerizing vinyl monomers using free-radical polymerization chemistry, in the presence of the metal hydride, in this case a prepared sodium alanate (chosen as a representative reactive metal hydride). It was found that the polymerization of styrene and divinyl benzene could be initiated using AIBN in toluene at 70 degC. The resulting composite materials can be either hard or brittle solids depending on the cross-linking density. Thermal decomposition of these styrene-based composite materials is lower than neat polystyrene indicating that the chemical nature of the polymer is affected by the formation of the composite. The char-forming nature of cross-linked polystyrene is low and therefore, not an ideal polymer for hazard mitigation. To obtain composite materials containing a polymer with higher char-forming potential, siloxane-based monomers were investigated. Four vinyl-containing siloxane oligomers were polymerized with and without added styrene and divinyl benzene. Like the styrene materials, these composite materials exhibited thermal decomposition behavior significantly different than the neat polymers. Specifically, the thermal decomposition temperature was shifted approximately 100 degC lower than the neat polymer signifying a major chemical change to the polymer network. Thermal analysis of the cycled samples was performed on the siloxane-based composite materials. It was found that after 30 cycles the siloxane-containing polymer composite material has similar TGA/DSC-MS traces as the virgin composite material indicating that the polymer is physically intact upon cycling. Hydrogen capacity measurements revealed that addition of the polymer to the metal hydride in the form of a composite material reduced the inherent hydrogen storage capacity of the material. This

Pratt, Joseph William; Cordaro, Joseph Gabriel; Sartor, George B.; Dedrick, Daniel E.; Reeder, Craig L.

2012-02-01T23:59:59.000Z

127

Models for Metal Hydride Particle Shape, Packing, and Heat Transfer  

E-Print Network [OSTI]

A multiphysics modeling approach for heat conduction in metal hydride powders is presented, including particle shape distribution, size distribution, granular packing structure, and effective thermal conductivity. A statistical geometric model is presented that replicates features of particle size and shape distributions observed experimentally that result from cyclic hydride decreptitation. The quasi-static dense packing of a sample set of these particles is simulated via energy-based structural optimization methods. These particles jam (i.e., solidify) at a density (solid volume fraction) of 0.665+/-0.015 - higher than prior experimental estimates. Effective thermal conductivity of the jammed system is simulated and found to follow the behavior predicted by granular effective medium theory. Finally, a theory is presented that links the properties of bi-porous cohesive powders to the present systems based on recent experimental observations of jammed packings of fine powder. This theory produces quantitative experimental agreement with metal hydride powders of various compositions.

Kyle C. Smith; Timothy S. Fisher

2012-05-04T23:59:59.000Z

128

High-Spin Cobalt Hydrides for Catalysis  

SciTech Connect (OSTI)

Organometallic chemists have traditionally used catalysts with strong-field ligands that give low-spin complexes. However, complexes with a weak ligand field have weaker bonds and lower barriers to geometric changes, suggesting that they may lead to more rapid catalytic reactions. Developing our understanding of high-spin complexes requires the use of a broader range of spectroscopic techniques, but has the promise of changing the mechanism and/or selectivity of known catalytic reactions. These changes may enable the more efficient utilization of chemical resources. A special advantage of cobalt and iron catalysts is that the metals are more abundant and cheaper than those currently used for major industrial processes that convert unsaturated organic molecules and biofeedstocks into useful chemicals. This project specifically evaluated the potential of high-spin cobalt complexes for small-molecule reactions for bond rearrangement and cleavage reactions relevant to hydrocarbon transformations. We have learned that many of these reactions proceed through crossing to different spin states: for example, high-spin complexes can flip one electron spin to access a lower-energy reaction pathway for beta-hydride elimination. This reaction enables new, selective olefin isomerization catalysis. The high-spin cobalt complexes also cleave the C-O bond of CO2 and the C-F bonds of fluoroarenes. In each case, the detailed mechanism of the reaction has been determined. Importantly, we have discovered that the cobalt catalysts described here give distinctive selectivities that are better than known catalysts. These selectivities come from a synergy between supporting ligand design and electronic control of the spin-state crossing in the reactions.

Holland, Patrick L. [Yale University] [Yale University

2013-08-29T23:59:59.000Z

129

Photoelectron spectroscopy of boron aluminum hydride cluster anions  

SciTech Connect (OSTI)

Boron aluminum hydride clusters are studied through a synergetic combination of anion photoelectron spectroscopy and density functional theory based calculations. Boron aluminum hydride cluster anions, B{sub x}Al{sub y}H{sub z}{sup ?}, were generated in a pulsed arc cluster ionization source and identified by time-of-flight mass spectrometry. After mass selection, their photoelectron spectra were measured by a magnetic bottle-type electron energy analyzer. The resultant photoelectron spectra as well as calculations on a selected series of stoichiometries reveal significant geometrical changes upon substitution of aluminum atoms by boron atoms.

Wang, Haopeng; Zhang, Xinxing; Ko, Yeon Jae; Gantefoer, Gerd; Bowen, Kit H., E-mail: kbowen@jhu.edu, E-mail: kiran@mcneese.edu [Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218 (United States); Li, Xiang [Center for Space Science and Technology, University of Maryland–Baltimore County, Baltimore, Maryland 21250 (United States)] [Center for Space Science and Technology, University of Maryland–Baltimore County, Baltimore, Maryland 21250 (United States); Kiran, Boggavarapu, E-mail: kbowen@jhu.edu, E-mail: kiran@mcneese.edu [Department of Chemistry and Physics, McNeese State University, Lake Charles, Louisiana 70609 (United States)] [Department of Chemistry and Physics, McNeese State University, Lake Charles, Louisiana 70609 (United States); Kandalam, Anil K. [Department of Physics, West Chester University, West Chester, Pennsylvania 19383 (United States)] [Department of Physics, West Chester University, West Chester, Pennsylvania 19383 (United States)

2014-04-28T23:59:59.000Z

130

Micro-and nanoscale domain engineering in lithium niobate and lithium tantalate  

E-Print Network [OSTI]

Micro- and nanoscale domain engineering in lithium niobate and lithium tantalate Vladimir Ya. Shur investigation of the domain evolution in lithium niobate and lithium tantalate during backswitched electric sources based on quasi-phase matching.11 Lithium niobate LiNbO3 (LN) and lithium tantalate LiTaO3 (LT

Byer, Robert L.

131

Lithium ion conducting electrolytes  

DOE Patents [OSTI]

A liquid, predominantly lithium-conducting, ionic electrolyte is described having exceptionally high conductivity at temperatures of 100 C or lower, including room temperature, and comprising the lithium salts selected from the group consisting of the thiocyanate, iodide, bromide, chloride, perchlorate, acetate, tetrafluoroborate, perfluoromethane sulfonate, perfluoromethane sulfonamide, tetrahaloaluminate, and heptahaloaluminate salts of lithium, with or without a magnesium-salt selected from the group consisting of the perchlorate and acetate salts of magnesium. Certain of the latter embodiments may also contain molecular additives from the group of acetonitrile (CH{sub 3}CN), succinnonitrile (CH{sub 2}CN){sub 2}, and tetraglyme (CH{sub 3}--O--CH{sub 2}--CH{sub 2}--O--){sub 2} (or like solvents) solvated to a Mg{sup +2} cation to lower the freezing point of the electrolyte below room temperature. Other particularly useful embodiments contain up to about 40, but preferably not more than about 25, mol percent of a long chain polyether polymer dissolved in the lithium salts to provide an elastic or rubbery solid electrolyte of high ambient temperature conductivity and exceptional 100 C conductivity. Another embodiment contains up to about but not more than 10 mol percent of a molecular solvent such as acetone. 2 figs.

Angell, C.A.; Liu, C.

1996-04-09T23:59:59.000Z

132

Lithium ion conducting electrolytes  

DOE Patents [OSTI]

A liquid, predominantly lithium-conducting, ionic electrolyte having exceptionally high conductivity at temperatures of 100.degree. C. or lower, including room temperature, and comprising the lithium salts selected from the group consisting of the thiocyanate, iodide, bromide, chloride, perchlorate, acetate, tetrafluoroborate, perfluoromethane sulfonate, perfluoromethane sulfonamide, tetrahaloaluminate, and heptahaloaluminate salts of lithium, with or without a magnesium-salt selected from the group consisting of the perchlorate and acetate salts of magnesium. Certain of the latter embodiments may also contain molecular additives from the group of acetonitrile (CH.sub.3 CN) succinnonitrile (CH.sub.2 CN).sub.2, and tetraglyme (CH.sub.3 --O--CH.sub.2 --CH.sub.2 --O--).sub.2 (or like solvents) solvated to a Mg.sup.+2 cation to lower the freezing point of the electrolyte below room temperature. Other particularly useful embodiments contain up to about 40, but preferably not more than about 25, mol percent of a long chain polyether polymer dissolved in the lithium salts to provide an elastic or rubbery solid electrolyte of high ambient temperature conductivity and exceptional 100.degree. C. conductivity. Another embodiment contains up to about but not more than 10 mol percent of a molecular solvent such as acetone.

Angell, C. Austen (Tempe, AZ); Liu, Changle (Tempe, AZ)

1996-01-01T23:59:59.000Z

133

Hydride generation from the Exide load-leveling cells  

SciTech Connect (OSTI)

Stibine and arsine evolution from lead-acid cells in a 36-kWh Exide load-leveling module was measured as this module approached 1900 cycles of operation. A gas-collection apparatus enabled us to determine the maximum and average rates for evolution of both toxic hydrides. Hydride generation began once the cell voltage exceeded 2.4 V. The maximum rate for arsine occurred just above 2.5 V and consistently preceded the peak rate for stibine for each sampled cell. The average rates of hydride generation were found to be 175 ..mu..g/min for stibine and 12.6 ..mu..g/min for arsine. The former rate proved to be the critical value in determining safe ventilation requirements for cell off-gases. The minimum airflow requirement was calculated to be 340 L/min per cell. Projections for a hypothetical 1-MWh Exide battery without an abatement system indicated that the normal ventilation capacity in the Battery Energy Storage Test facility provides nearly five times the airflow needed for safe hydride removal.

Marr, J.J.; Smaga, J.A.

1987-05-01T23:59:59.000Z

134

HYDROGEN STORAGE USINGHYDROGEN STORAGE USING COMPLEX HYDRIDESCOMPLEX HYDRIDES  

E-Print Network [OSTI]

, Michael D. HamptonDarlene K. Slattery, Michael D. Hampton FL Solar Energy Center, U. of Central FLFL Solar Energy Center, U. of Central FL #12;Objective · Identify a hydrogen storage system that meets the DOEHYDROGEN STORAGE USINGHYDROGEN STORAGE USING COMPLEX HYDRIDESCOMPLEX HYDRIDES Darlene K. Slattery

135

Sputter deposition of lithium silicate - lithium phosphate amorphous electrolytes  

SciTech Connect (OSTI)

Thin films of an amorphous lithium-conducting electrolyte were deposited by rf magnetron sputtering of ceramic targets containing Li{sub 4}SiO{sub 4} and Li{sub 3}PO{sub 4}. The lithium content of the films was found to depend more strongly on the nature and composition of the targets than on many other sputtering parameters. For targets containing Li{sub 4}SiO{sub 4}, most of the lithium was found to segregate away from the sputtered area of the target. Codeposition using two sputter sources achieves a high lithium content in a controlled and reproducible film growth. 10 refs., 4 figs.

Dudney, N.J.; Bates, J.B.; Luck, C.F. (Oak Ridge National Lab., TN (USA)); Robertson, J.D. (Kentucky Univ., Lexington, KY (USA). Dept. of Chemistry)

1991-01-01T23:59:59.000Z

136

EERE Partner Testimonials - Phil Roberts, California Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Phil Roberts, California Lithium Battery (CalBattery) EERE Partner Testimonials - Phil Roberts, California Lithium Battery (CalBattery) Addthis Text Version The words "Office of...

137

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

Gabano, Ed. , Lithium Batteries, Academic Press, New York,K. V. Kordesch, "Primary Batteries 1951-1976," J. Elec- n ~.Rechargeable Lithium Batteries," J. Electrochem. Soc. , [20

Doyle, C.M.

2010-01-01T23:59:59.000Z

138

Washington: Graphene Nanostructures for Lithium Batteries Recieves...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Washington: Graphene Nanostructures for Lithium Batteries Recieves 2012 R&D 100 Award Washington: Graphene Nanostructures for Lithium Batteries Recieves 2012 R&D 100 Award February...

139

Lithium-based electrochromic mirrors  

E-Print Network [OSTI]

LITHIUM-BASED ELECTROCHROMIC MIRRORS Thomas J. Richardson*with pure antimony films. Electrochromic cycling speed andand silver. INTRODUCTION Electrochromic devices that exhibit

Richardson, Thomas J.; Slack, Jonathan L.

2003-01-01T23:59:59.000Z

140

Effect of Gaseous Impurities on Long-Term Thermal Cycling and Aging Properties of Complex Hydrides for Hydrogen Storage  

SciTech Connect (OSTI)

This program was dedicated to understanding the effect of impurities on Long-Term Thermal Cycling and aging properties of Complex Hydrides for Hydrogen Storage. At the start of the program we found reversibility between Li2NH+LiH ? LiH+LiNH2 (yielding ~5.8 wt.%H capacity). Then we tested the effect of impurity in H2 gas by pressure cycling at 255oC; first with industrial gas containing ppm levels of O2 and H2O as major impurities. Both these impurities had a significant impact on the reversibility and decreased the capacity by 2.65 wt.%H. Further increase in number of cycles from 500 to 1100 showed only a 0.2 wt%H more weight loss, showing some capacity is still maintained after a significant number of cycles. The loss of capacity is attributed to the formation of ~55 wt% LiH and ~30% Li2O, as major contaminant phases, along with the hydride Li2NH phase; suggesting loss of nitrogen during cycling. The effect of 100 ppm H2O in H2 also showed a decrease of ~2.5 wt.%H (after 560 cycles), and 100ppm O2 in H2; a loss of ~4.1 wt.%. Methane impurity (100 ppm, 100cycles), showed a very small capacity loss of 0.9 wt.%H under similar conditions. However, when Li3N was pressure cycled with 100ppmN2-H2 there were beneficial effects were observed (255oC); the reversible capacity increased to 8.4wt.%H after 853 cycles. Furthermore, with 20 mol.%N2-H2 capacity increased to ~10 wt.%H after 516 cycles. We attribute this enhancement to the reaction of nitrogen with liquid lithium during cycling as the Gibbs free energy of formation of Li3N (?Go = -98.7 kJ/mol) is more negative than that of LiH (?Go = -50.3 kJ/mol). We propose that the mitigation of hydrogen capacity losses is due to the destabilization of the LiH phase that tends to accumulate during cycling. Also more Li2NH phase was found in the cycled product. Mixed Alanates (3LiNH2:Li3AlH6) showed that 7 wt% hydrogen desorbed under dynamic vacuum. Equilibrium experiments (maximum 12 bar H2) showed up to 4wt% hydrogen reversibly stored in the material after the first desorption. The activation energy was found to be 51 kJ/mol, as compared to 81 kJ/mol for pure lithium alanate. It is proposed that based on the data obtained and CALPHAD modeling that the improvement in cycling is due to the formation of pure lithium (liquid at 255oC), which is able to react with nitrogen specifically forming Li3N. The presence of nitrogen in the 80/20 molar mixtures in a hydride bed along with hydrogen causes Li to form Li3N rather than LiH, and subsequently regenerates the Li2NH phase and yields a ~10 wt.%H reversibly.

Chandra, Dhanesh (Primary Contact); Lamb, Joshua; Chien, Wen-Ming; Talekar, Anjali; and Pal, Narendra.

2011-03-28T23:59:59.000Z

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


141

FEASIBILITY OF RECYCLING PLUTONIUM AND MINOR ACTINIDES IN LIGHT WATER REACTORS USING HYDRIDE FUEL  

SciTech Connect (OSTI)

The objective of this DOE NERI program sponsored project was to assess the feasibility of improving the plutonium (Pu) and minor actinide (MA) recycling capabilities of pressurized water reactors (PWRs) by using hydride instead of oxide fuels. There are four general parts to this assessment: 1) Identifying promising hydride fuel assembly designs for recycling Pu and MAs in PWRs 2) Performing a comprehensive systems analysis that compares the fuel cycle characteristics of Pu and MA recycling in PWRs using the promising hydride fuel assembly designs identified in Part 1 versus using oxide fuel assembly designs 3) Conducting a safety analysis to assess the likelihood of licensing hydride fuel assembly designs 4) Assessing the compatibility of hydride fuel with cladding materials and water under typical PWR operating conditions Hydride fuel was found to offer promising transmutation characteristics and is recommended for further examination as a possible preferred option for recycling plutonium in PWRs.

Greenspan, Ehud; Todreas, Neil; Taiwo, Temitope

2009-03-10T23:59:59.000Z

142

Lithium Research Status and PlansLithium Research Status and Plans Charles H. Skinner, PPPL  

E-Print Network [OSTI]

Lithium Research Status and PlansLithium Research Status and Plans Charles H. Skinner, PPPL Robert February 3-5, 2010 #12;NSTX PAC-27 ­ Lithium Research Status and Plans 2/15February 3-5, 2010 NSTX lithium research is an integral part of a program to develop lithium as a PFC concept for magnetic fusion NSTX w

Princeton Plasma Physics Laboratory

143

Solid lithium-ion electrolyte  

DOE Patents [OSTI]

The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li{sub 2}O--CeO{sub 2}--SiO{sub 2} system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications. 12 figs.

Zhang, J.G.; Benson, D.K.; Tracy, C.E.

1998-02-10T23:59:59.000Z

144

Solid lithium-ion electrolyte  

DOE Patents [OSTI]

The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li.sub.2 O--CeO.sub.2 --SiO.sub.2 system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications.

Zhang, Ji-Guang (Golden, CO); Benson, David K. (Golden, CO); Tracy, C. Edwin (Golden, CO)

1998-01-01T23:59:59.000Z

145

Hydriding and dehydriding characteristics of LiBH{sub 4} and transition metals-added magnesium hydride  

SciTech Connect (OSTI)

Graphical abstract: Hydriding reaction curves under 12 bar H{sub 2}, and dehydriding reaction curves under 1.0 bar H{sub 2}, at 593 K at the 1st cycle for MgH{sub 2}–10Ni–2LiBH{sub 4}–2Ti and MgH{sub 2}. Highlights: ? Addition of Ni, LiBH{sub 4}, and Ti to MgH{sub 2} to increase reaction rates. ? Sample preparation by reactive mechanical grinding. ? At n = 2, the sample absorbed 4.05 wt% H for 60 min at 593 K under 12 bar H{sub 2}. ? Analysis of rate-controlling step for dehydriding of the sample at n = 3. - Abstract: In this study, MgH{sub 2} was used as a starting material instead of Mg. Ni, Ti, and LiBH{sub 4} with a high hydrogen-storage capacity of 18.4 wt% were added. A sample with a composition of MgH{sub 2}–10Ni–2LiBH{sub 4}–2Ti was prepared by reactive mechanical grinding. The activation of MgH{sub 2}–10Ni–2LiBH{sub 4}–2Ti was completed after the first hydriding–dehydrding cycle. The hydriding rate decreases as the temperature increases due to the decrease in the driving force for the hydriding reaction. At the 1st cycle, the sample desorbs 1.45 wt% H for 10 min, 2.54 wt% H for 20 min, 3.13 wt% H for 30 min, and 3.40 wt% H for 60 min at 593 K under 1.0 bar H{sub 2}. At the 2nd cycle, the sample absorbs 3.84 wt% H for 5 min, 3.96 wt% H for 10 min, and 4.05 wt% H for 60 min at 593 K under 12 bar H{sub 2}. MgH{sub 2}–10Ni–2LiBH{sub 4}–2Ti after reactive mechanical grinding contained MgH{sub 2}, Mg, Ni, TiH{sub 1.924}, and MgO phases. The reactive mechanical grinding of Mg with Ni, LiBH{sub 4}, and Ti is considered to create defects on the surface and in the interior of Mg (to facilitate nucleation), and to reduce the particle size of Mg (to shorten diffusion distances of hydrogen atoms). The formation of Mg{sub 2}Ni during hydriding–dehydriding cycling increases the hydriding and dehydriding rates of the sample.

Song, Myoung Youp, E-mail: songmy@jbnu.ac.kr [Division of Advanced Materials Engineering, Hydrogen and Fuel Cell Research Center, Engineering Research Institute, Chonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju, 561-756 (Korea, Republic of); Kwak, Young Jun; Lee, Seong Ho [Department of Materials Engineering, Graduate School, Chonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju, 561-756 (Korea, Republic of); Park, Hye Ryoung [Faculty of Applied Chemical Engineering, Chonnam National University, 300 Yongbongdong, Bukgu, Gwangju, 500-757 (Korea, Republic of)

2013-07-15T23:59:59.000Z

146

Preparation and X-Ray diffraction studies of curium hydrides  

SciTech Connect (OSTI)

Curium hydrides were prepared by reaction of curium-248 metal with hydrogen and characterized by X-ray powder diffraction. Several of the syntheses resulted in a hexagonal compound with average lattice parameters of a/sub 0/ = 0.3769(8) nm and c/sub 0/ = 0.6732(12) nm. These products are considere to be CmH/sub 3//sup -//sub 8/ by analogy with the behavior of lanthanide-hydrogen and lighter actinide-hydrogen systems. Face-centered cubic products with an average lattice parameter of a/sub 0/ = 0.5322(4) nm were obtained from other curium hydride preparations. This parameter is slightly smaller than that reported previously for cubic curium dihydride, CmH /SUB 2-x/ (B.M. Bansal and D. Damien. Inorg. Nucl. Chem. Lett. 6 603, 1970). The present results established a continuation of typical heavy trivalent lanthanidelike behavior of the transuranium actinide-hydrogen systems through curium.

Gibson, J.K.; Maire, R.G.

1985-10-01T23:59:59.000Z

147

ALUMINUM HYDRIDE: A REVERSIBLE STORAGE MATERIAL FOR HYDROGEN STORAGE  

SciTech Connect (OSTI)

One of the challenges of implementing the hydrogen economy is finding a suitable solid H{sub 2} storage material. Aluminium (alane, AlH{sub 3}) hydride has been examined as a potential hydrogen storage material because of its high weight capacity, low discharge temperature, and volumetric density. Recycling the dehydride material has however precluded AlH{sub 3} from being implemented due to the large pressures required (>10{sup 5} bar H{sub 2} at 25 C) and the thermodynamic expense of chemical synthesis. A reversible cycle to form alane electrochemically using NaAlH{sub 4} in THF been successfully demonstrated. Alane is isolated as the triethylamine (TEA) adduct and converted to unsolvated alane by heating under vacuum. To complete the cycle, the starting alanate can be regenerated by direct hydrogenation of the dehydrided alane and the alkali hydride (NaH) This novel reversible cycle opens the door for alane to fuel the hydrogen economy.

Zidan, R; Christopher Fewox, C; Brenda Garcia-Diaz, B; Joshua Gray, J

2009-01-09T23:59:59.000Z

148

Thermodynamic Studies and Hydride Transfer Reactions from a Rhodium Complex to BX3 Compounds  

SciTech Connect (OSTI)

This study examines the use of transition-metal hydride complexes that can be generated by the heterolytic cleavage of H2 gas to form B–H bonds. Specifically, these studies are focused on providing a reliable and quantitative method for determining when hydride transfer from transition-metal hydrides to three-coordinate BX3 compounds will be favorable. This involves both experimental and theoretical determinations of hydride transfer abilities. Thermodynamic hydride donor abilities (?G°H-) were determined for HRh(dmpe)2 and HRh(depe)2, where dmpe = 1,2-bis(dimethylphosphinoethane) and depe = 1,2-bis(diethylphosphinoethane), on a previously established scale in acetonitrile. This hydride donor ability was used to determine the hydride donor ability of [HBEt3]? on this scale. Isodesmic reactions between [HBEt3]? and various BX3 complexes to form BEt3 and [HBX3]? were examined computationally to determine the relative hydride affinities of various BX3 compounds. The use of these scales of hydride donor abilities and hydride affinities for transition-metal hydrides and BX3 compounds is illustrated with a few selected reactions relevant to the regeneration of ammonia borane. Our findings indicate that it is possible to form B?H bonds from B?X bonds, and the extent to which BX3 compounds are reduced by transition-metal hydride complexes forming species containing multiple B?H bonds depends on the heterolytic B?X bond energy. An example is the reduction of B(SPh)3 using HRh(dmpe)2 in the presence of triethylamine to form Et3N-BH3 in high yields. Pacific Northwest National Laboratory is operated by Battelle for the US Department of Energy.

Mock, Michael T.; Potter, Robert G.; Camaioni, Donald M.; Li, Jun; Dougherty, William G.; Kassel, W. S.; Twamley, Brendan; DuBois, Daniel L.

2009-10-14T23:59:59.000Z

149

Thermomechanics of hydrogen storage in metallic hydrides: modeling and analysis  

E-Print Network [OSTI]

A thermodynamically consistent mathematical model for hydrogen adsorption in metal hydrides is proposed. Beside hydrogen diffusion, the model accounts for phase transformation accompanied by hysteresis, swelling, temperature and heat transfer, strain, and stress. We prove existence of solutions of the ensuing system of partial differential equations by a carefully-designed, semi-implicit approximation scheme. A generalization for a drift-diffusion of multi-component ionized "gas" is outlined, too.

Tomas Roubicek; Giuseppe Tomassetti

2013-09-12T23:59:59.000Z

150

Effects of Carbonate Solvents and Lithium Salts on Morphology...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Carbonate Solvents and Lithium Salts on Morphology and Coulombic Efficiency of Lithium Electrode. Effects of Carbonate Solvents and Lithium Salts on Morphology and Coulombic...

151

ELLIPSOMETRY OF SURFACE LAYERS ON LEAD AND LITHIUM  

E-Print Network [OSTI]

Surface Layers on Lead and Lithium By Richard Dudley Peterssulfuric acid and and lithium to water, Acid concentrationsbeen observed in the reaction of lithium with water vapor. i

Peters, Richard Dudley

2011-01-01T23:59:59.000Z

152

ELLIPSOMETRY OF SURFACE LAYERS ON LEAD AND LITHIUM  

E-Print Network [OSTI]

rate. The corrosion reaction between lithium and water vaporOpen Circuit Corrosion Bo Lithium, , L A~ueous Electrolytecalculated representing corrosion of lithium in water vapor,

Peters, Richard Dudley

2011-01-01T23:59:59.000Z

153

Redox shuttle additives for overcharge protection in lithium batteries  

E-Print Network [OSTI]

Protection in Lithium Batteries”, T. J. Richardson* and P.OVERCHARGE PROTECTION IN LITHIUM BATTERIES T. J. Richardson*improve the safety of lithium batteries. ACKNOWLEDGEMENT

Richardson, Thomas J.; Ross Jr., P.N.

1999-01-01T23:59:59.000Z

154

Visualization of Charge Distribution in a Lithium Battery Electrode  

E-Print Network [OSTI]

for Rechargeable Lithium Batteries. J. Electrochem. Soc.Calculations for Lithium Batteries. J. Electrostatics 1995,Modeling of Lithium Polymer Batteries. J. Power Sources

Liu, Jun

2010-01-01T23:59:59.000Z

155

The UC Davis Emerging Lithium Battery Test Project  

E-Print Network [OSTI]

for rechargeable lithium batteries, Journal of Powerand iron phosphate lithium batteries will be satisfactoryapplications. The cost of lithium batteries remains high ($

Burke, Andy; Miller, Marshall

2009-01-01T23:59:59.000Z

156

Grafted polyelectrolyte membranes for lithium batteries and fuel cells  

E-Print Network [OSTI]

MEMBRANES FOR LITHIUM BATTERIES AND FUEL CELLS. John Kerralso be discussed. Lithium Batteries for Transportation andpolymer membrane for lithium batteries. This paper will give

Kerr, John B.

2003-01-01T23:59:59.000Z

157

Coated Silicon Nanowires as Anodes in Lithium Ion Batteries  

E-Print Network [OSTI]

for rechargeable lithium batteries. J. Power Sources 139,for advanced lithium-ion batteries. J. Power Sources 174,nano-anodes for lithium rechargeable batteries. Angew. Chem.

Watts, David James

2014-01-01T23:59:59.000Z

158

Synthesis, Characterization and Performance of Cathodes for Lithium Ion Batteries  

E-Print Network [OSTI]

0 lithium batteries. J. Electrochem. Soc.for rechargeable lithium batteries. Advanced Materials 1998,for rechargeable lithium batteries. J. Electrochem. Soc.

Zhu, Jianxin

2014-01-01T23:59:59.000Z

159

LANL/PNNL Virtual Center for Chemical Hydrides and New Concepts...  

Broader source: Energy.gov (indexed) [DOE]

LANLPNNL Virtual Center for Chemical Hydrides and New Concepts for Hydrogen Storage * Thermodynamics * Kinetics * Recycle * WeightVolume Capacity * Durability Investigate...

160

E-Print Network 3.0 - arsenic hydrides Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

(2002) 1080-703902.50 Summary: for arsenic species using hydride generation and atomic absorption spectroscopy. The detec- tion limit for As... by ASP Estimation of...

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

E-Print Network 3.0 - aluminum hydride phases Sample Search Results  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

The nonlinear coupled dierential equations... enhancement by the aluminum sheets and the optimization of the operation of hydride bed are examined... It consists of a quantity...

162

Diffusional exchange of isotopes in a metal hydride sphere.  

SciTech Connect (OSTI)

This report describes the Spherical Particle Exchange Model (SPEM), which simulates exchange of one hydrogen isotope by another hydrogen isotope in a spherical metal hydride particle. This is one of the fundamental physical processes during isotope exchange in a bed of spherical metal particles and is thus one of the key components in any comprehensive physics-based model of exchange. There are two important physical processes in the model. One is the entropy of mixing between the two isotopes; the entropy of mixing is increased by having both isotopes randomly placed at interstitial sites on the lattice and thus impedes the exchange process. The other physical process is the elastic interaction between isotope atoms on the lattice. The elastic interaction is the cause for {beta}-phase formation and is independent of the isotope species. In this report the coupled diffusion equations for two isotopes in the {beta}-phase hydride are solved. A key concept is that the diffusion of one isotope depends not only on its concentration gradient, but also on the concentration gradient of the other isotope. Diffusion rate constants and the chemical potentials for deuterium and hydrogen in the {beta}-phase hydride are reviewed because these quantities are essential for an accurate model of the diffusion process. Finally, a summary of some of the predictions from the SPEM model are provided.

Wolfer, Wilhelm G.; Hamilton, John C.; James, Scott Carlton

2011-04-01T23:59:59.000Z

163

Lithium niobate explosion monitor  

DOE Patents [OSTI]

Monitoring explosive devices is accomplished with a substantially z-cut lithium niobate crystal in abutment with the explosive device. Upon impact by a shock wave from detonation of the explosive device, the crystal emits a current pulse prior to destruction of the crystal. The current pulse is detected by a current viewing transformer and recorded as a function of time in nanoseconds. In order to self-check the crystal, the crystal has a chromium film resistor deposited thereon which may be heated by a current pulse prior to detonation. This generates a charge which is detected by a charge amplifier. 8 figs.

Bundy, C.H.; Graham, R.A.; Kuehn, S.F.; Precit, R.R.; Rogers, M.S.

1990-01-09T23:59:59.000Z

164

Lithium niobate explosion monitor  

DOE Patents [OSTI]

Monitoring explosive devices is accomplished with a substantially z-cut lithium niobate crystal in abutment with the explosive device. Upon impact by a shock wave from detonation of the explosive device, the crystal emits a current pulse prior to destruction of the crystal. The current pulse is detected by a current viewing transformer and recorded as a function of time in nanoseconds. In order to self-check the crystal, the crystal has a chromium film resistor deposited thereon which may be heated by a current pulse prior to detonation. This generates a charge which is detected by a charge amplifier.

Bundy, Charles H. (Clearwater, FL); Graham, Robert A. (Los Lunas, NM); Kuehn, Stephen F. (Albuquerque, NM); Precit, Richard R. (Albuquerque, NM); Rogers, Michael S. (Albuquerque, NM)

1990-01-01T23:59:59.000Z

165

Lithium ion conducting ionic electrolytes  

DOE Patents [OSTI]

A liquid, predominantly lithium-conducting, ionic electrolyte is described which has exceptionally high conductivity at temperatures of 100.degree. C. or lower, including room temperature. It comprises molten lithium salts or salt mixtures in which a small amount of an anionic polymer lithium salt is dissolved to stabilize the liquid against recrystallization. Further, a liquid ionic electrolyte which has been rubberized by addition of an extra proportion of anionic polymer, and which has good chemical and electrochemical stability, is described. This presents an attractive alternative to conventional salt-in-polymer electrolytes which are not cationic conductors.

Angell, C. Austen (Mesa, AZ); Xu, Kang (Tempe, AZ); Liu, Changle (Tulsa, OK)

1996-01-01T23:59:59.000Z

166

Anodes for rechargeable lithium batteries  

DOE Patents [OSTI]

A negative electrode (12) for a non-aqueous electrochemical cell (10) with an intermetallic host structure containing two or more elements selected from the metal elements and silicon, capable of accommodating lithium within its crystallographic host structure such that when the host structure is lithiated it transforms to a lithiated zinc-blende-type structure. Both active elements (alloying with lithium) and inactive elements (non-alloying with lithium) are disclosed. Electrochemical cells and batteries as well as methods of making the negative electrode are disclosed.

Thackeray, Michael M. (Naperville, IL); Kepler, Keith D. (Mountain View, CA); Vaughey, John T. (Elmhurst, IL)

2003-01-01T23:59:59.000Z

167

Lithium Reagents DOI: 10.1002/anie.200603038  

E-Print Network [OSTI]

Lithium Reagents DOI: 10.1002/anie.200603038 Lithium Diisopropylamide: Solution Kinetics Keywords: kinetics · lithium diisopropylamide · metalation · solvent effects · synthesis design D. B: lithium diiso- propylamide (LDA). LDA has played a profound role in organic synthesis, serving as the base

Collum, David B.

168

Electromagnetically Restrained Lithium Blanket APEX Interim Report November, 1999  

E-Print Network [OSTI]

to avoid corrosion or fire. Lithium's high electrical conductivity may possibly permit efficient, compactElectromagnetically Restrained Lithium Blanket APEX Interim Report November, 1999 6-1 CHAPTER 6: ELECTROMAGNETICALLY RESTRAINED LITHIUM BLANKET Contributors Robert Woolley #12;Electromagnetically Restrained Lithium

California at Los Angeles, University of

169

A Lithium Superionic Sulfide Cathode for Lithium-Sulfur Batteries  

SciTech Connect (OSTI)

This work presents a facile synthesis approach for core-shell structured Li2S nanoparticles, which have Li2S as the core and Li3PS4 as the shell. This material functions as lithium superionic sulfide (LSS) cathode for long-lasting, energy-efficient lithium-sulfur (Li-S) batteries. The LSS has an ionic conductivity of 10-7 S cm-1 at 25 oC, which is 6 orders of magnitude higher than that of bulk Li2S (~10-13 S cm-1). The high lithium-ion conductivity of LSS imparts an excellent cycling performance to all-solid Li-S batteries, which also promises safe cycling of high-energy batteries with metallic lithium anodes.

Lin, Zhan [ORNL] [ORNL; Liu, Zengcai [ORNL] [ORNL; Dudney, Nancy J [ORNL] [ORNL; Liang, Chengdu [ORNL] [ORNL

2013-01-01T23:59:59.000Z

170

Combined on-board hydride slurry storage and reactor system and process for hydrogen-powered vehicles and devices  

DOE Patents [OSTI]

An on-board hydride storage system and process are described. The system includes a slurry storage system that includes a slurry reactor and a variable concentration slurry. In one preferred configuration, the storage system stores a slurry containing a hydride storage material in a carrier fluid at a first concentration of hydride solids. The slurry reactor receives the slurry containing a second concentration of the hydride storage material and releases hydrogen as a fuel to hydrogen-power devices and vehicles.

Brooks, Kriston P; Holladay, Jamelyn D; Simmons, Kevin L; Herling, Darrell R

2014-11-18T23:59:59.000Z

171

Cyanoethylated compounds as additives in lithium/lithium batteries  

DOE Patents [OSTI]

The power loss of lithium/lithium ion battery cells is significantly reduced, especially at low temperatures, when about 1% by weight of an additive is incorporated in the electrolyte layer of the cells. The usable additives are organic solvent soluble cyanoethylated polysaccharides and poly(vinyl alcohol). The power loss decrease results primarily from the decrease in the charge transfer resistance at the interface between the electrolyte and the cathode.

Nagasubramanian, Ganesan (Albuquerque, NM)

1999-01-01T23:59:59.000Z

172

Solid-State Gadolinium-Magnesium Hydride Optical Switch R. Armitage  

E-Print Network [OSTI]

-state electrochromic device. With positive polarization of the hydride electrode, the visible reflectance approaches 35 and reflecting states. Keywords: gadolinium-magnesium; electrochromic hydride; optical switching device. 2 #12;A conventional electrochromics5 . Optical switching has also been demonstrated by varying the H content

173

Hydrogen storage material and process using graphite additive with metal-doped complex hydrides  

DOE Patents [OSTI]

A hydrogen storage material having improved hydrogen absorbtion and desorption kinetics is provided by adding graphite to a complex hydride such as a metal-doped alanate, i.e., NaAlH.sub.4. The incorporation of graphite into the complex hydride significantly enhances the rate of hydrogen absorbtion and desorption and lowers the desorption temperature needed to release stored hydrogen.

Zidan, Ragaiy (Aiken, SC); Ritter, James A. (Lexington, SC); Ebner, Armin D. (Lexington, SC); Wang, Jun (Columbia, SC); Holland, Charles E. (Cayce, SC)

2008-06-10T23:59:59.000Z

174

Hydride production in zircaloy-4 as a function of time and temperature  

E-Print Network [OSTI]

..................................................................................................... 40 Figure 15 Formation of zirconium hydride as a function of temperature................ 44 Figure 16 Time dependence of hydrogen pickup with Avrami correlation............. 50 Figure 17 Time dependence of hydrogen pickup with parabolic... rate study....................................................... 43 Table 8 Results of rate study using Avrami equation .......................................... 50 Table 9 Constants for parabolic hydride rate...

Parkison, Adam Joseph

2009-05-15T23:59:59.000Z

175

Rotational Mixing and Lithium Depletion  

E-Print Network [OSTI]

I review basic observational features in Population I stars which strongly implicate rotation as a mixing agent; these include dispersion at fixed temperature in coeval populations and main sequence lithium depletion for a range of masses at a rate which decays with time. New developments related to the possible suppression of mixing at late ages, close binary mergers and their lithium signature, and an alternate origin for dispersion in young cool stars tied to radius anomalies observed in active young stars are discussed. I highlight uncertainties in models of Population II lithium depletion and dispersion related to the treatment of angular momentum loss. Finally, the origins of rotation are tied to conditions in the pre-main sequence, and there is thus some evidence that enviroment and planet formation could impact stellar rotational properties. This may be related to recent observational evidence for cluster to cluster variations in lithium depletion and a connection between the presence of planets and s...

Pinsonneault, M H

2010-01-01T23:59:59.000Z

176

Getting metal-hydrides to do what you want them to  

SciTech Connect (OSTI)

With the discovery of AB/sub 5/ compounds, intermetallic hydrides with unusual properties began to be developed (H dissociation pressures of one to several atmospheres, extremely rapid and reversible adsorption/desorption very large amounts of H adsorbed). This paper reviews the factors that must be controlled in order to modify these hydrides to make them useful. The system LaNi/sub 5/ + H/sub 2/ is used as example. Use of AB/sub 5/ hydrides to construct a chemical heat pumps is discussed. Results of a systematic study substituting Al for Ni are reported; the HYCSOS pump is described briefly. Use of hydrides as hydrogen getters (substituted ZrV/sub 2/) is also discussed. Finally, possible developments in intermetallic hydride research in the 1980's and the hydrogen economy are discussed. 10 figures. (DLC)

Gruen, D.M.

1981-01-01T23:59:59.000Z

177

Air breathing lithium power cells  

DOE Patents [OSTI]

A cell suitable for use in a battery according to one embodiment includes a catalytic oxygen cathode; a stabilized zirconia electrolyte for selective oxygen anion transport; a molten salt electrolyte; and a lithium-based anode. A cell suitable for use in a battery according to another embodiment includes a catalytic oxygen cathode; an electrolyte; a membrane selective to molecular oxygen; and a lithium-based anode.

Farmer, Joseph C.

2014-07-15T23:59:59.000Z

178

Development of Lithium Deposition Techniques for TFTR  

SciTech Connect (OSTI)

The ability to increase the quantity of lithium deposition into TFTR beyond that of the Pellet Injector while minimizing perturbations to the plasma provides interesting experimental and operational options. Two additional lithium deposition tools were developed for possible application during the 1996 Experimental Schedule: a solid lithium target probe for real-time deposition, and a lithium effusion oven for deposition between discharges. The lithium effusion oven was operated in TFTR to deposit lithium on the Inner Limiter in the absence of plasma. This resulted in the third highest power TFTR discharge.

Gorman, J.; Johnson, D.; Kugel, H.W.; Labik, G.; Lemunyan, G.; et al

1997-10-01T23:59:59.000Z

179

Development of lithium deposition techniques for TFTR  

SciTech Connect (OSTI)

The ability to increase the quantity of lithium deposition into TFTR beyond that of the Pellet Injector while minimizing perturbations to the plasma provides interesting experimental and operational options. Two additional lithium deposition tools were developed for possible application during the 1996 Experimental Schedule: a solid lithium target probe for real-time deposition, and a lithium effusion oven for deposition between discharges. The lithium effusion oven was operated in TFTR to deposit lithium on the Inner Limiter in the absence of plasma. This resulted in the third highest power TFTR discharge.

Kugel, H.W.; Gorman, J.; Johnson, D.; Labik, G.; Lemunyan, G.; Mansfield, D.; Timberlake, J.; Vocaturo, M.

1997-10-01T23:59:59.000Z

180

ALUMINUM HYDRIDE: A REVERSIBLE MATERIAL FOR HYDROGEN STORAGE  

SciTech Connect (OSTI)

Hydrogen storage is one of the greatest challenges for implementing the ever sought hydrogen economy. Here we report a novel cycle to reversibly form high density hydrogen storage materials such as aluminium hydride. Aluminium hydride (AlH{sub 3}, alane) has a hydrogen storage capacity of 10.1 wt% H{sub 2}, 149 kg H{sub 2}/m{sup 3} volumetric density and can be discharged at low temperatures (< 100 C). However, alane has been precluded from use in hydrogen storage systems because of the lack of practical regeneration methods; the direct hydrogenation of aluminium to form AlH{sub 3} requires over 10{sup 5} bars of hydrogen pressure at room temperature and there are no cost effective synthetic means. Here we show an unprecedented reversible cycle to form alane electrochemically, using alkali alanates (e.g. NaAlH{sub 4}, LiAlH{sub 4}) in aprotic solvents. To complete the cycle, the starting alanates can be regenerated by direct hydrogenation of the dehydrided alane and the alkali hydride being the other compound formed in the electrochemical cell. The process of forming NaAlH{sub 4} from NaH and Al is well established in both solid state and solution reactions. The use of adducting Lewis bases is an essential part of this cycle, in the isolation of alane from the mixtures of the electrochemical cell. Alane is isolated as the triethylamine (TEA) adduct and converted to pure, unsolvated alane by heating under vacuum.

Fewox, C; Ragaiy Zidan, R; Brenda Garcia-Diaz, B

2008-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

ALUMINUM HYDRIDE: A REVERSIBLE MATERIAL FOR HYDROGEN STORAGE  

SciTech Connect (OSTI)

Hydrogen storage is one of the challenges to be overcome for implementing the ever sought hydrogen economy. Here we report a novel cycle to reversibly form high density hydrogen storage materials such as aluminium hydride. Aluminium hydride (AlH{sub 3}, alane) has a hydrogen storage capacity of 10.1 wt% H{sub 2}, 149 kg H{sub 2}/m{sup 3} volumetric density and can be discharged at low temperatures (< 100 C). However, alane has been precluded from use in hydrogen storage systems because of the lack of practical regeneration methods. The direct hydrogenation of aluminium to form AlH{sub 3} requires over 10{sup 5} bars of hydrogen pressure at room temperature and there are no cost effective synthetic means. Here we show an unprecedented reversible cycle to form alane electrochemically, using alkali metal alanates (e.g. NaAlH{sub 4}, LiAlH{sub 4}) in aprotic solvents. To complete the cycle, the starting alanates can be regenerated by direct hydrogenation of the dehydrided alane and the alkali hydride being the other compound formed in the electrochemical cell. The process of forming NaAlH{sub 4} from NaH and Al is well established in both solid state and solution reactions. The use of adducting Lewis bases is an essential part of this cycle, in the isolation of alane from the mixtures of the electrochemical cell. Alane is isolated as the triethylamine (TEA) adduct and converted to pure, unsolvated alane by heating under vacuum.

Zidan, R; Christopher Fewox, C; Brenda Garcia-Diaz, B; Joshua Gray, J

2009-01-09T23:59:59.000Z

182

Chemical Hydrides for Hydrogen Storage in Fuel Cell Applications  

SciTech Connect (OSTI)

Due to its high hydrogen storage capacity (up to 19.6% by weight for the release of 2.5 molar equivalents of hydrogen gas) and its stability under typical ambient conditions, ammonia borane (AB) is a promising material for chemical hydrogen storage for fuel cell applications in transportation sector. Several systems models for chemical hydride materials such as solid AB, liquid AB and alane were developed and evaluated at PNNL to determine an optimal configuration that would meet the 2010 and future DOE targets for hydrogen storage. This paper presents an overview of those systems models and discusses the simulation results for various transient drive cycle scenarios.

Devarakonda, Maruthi N.; Brooks, Kriston P.; Ronnebro, Ewa; Rassat, Scot D.; Holladay, Jamelyn D.

2012-04-16T23:59:59.000Z

183

Electrochemical process and production of novel complex hydrides  

DOE Patents [OSTI]

A process of using an electrochemical cell to generate aluminum hydride (AlH.sub.3) is provided. The electrolytic cell uses a polar solvent to solubilize NaAlH.sub.4. The resulting electrochemical process results in the formation of AlH.sub.3. The AlH.sub.3 can be recovered and used as a source of hydrogen for the automotive industry. The resulting spent aluminum can be regenerated into NaAlH.sub.4 as part of a closed loop process of AlH.sub.3 generation.

Zidan, Ragaiy

2013-06-25T23:59:59.000Z

184

Working with SRNL - Our Facilities - Metal Hydride Laboratories  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear SecurityTensile Strain Switched FerromagnetismWaste and MaterialsWenjun1 Table 1.14Working WithGloveboxMetal Hydride

185

Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide (LiHMDS)  

E-Print Network [OSTI]

Lithium Ion Solvation: Amine and Unsaturated Hydrocarbon Solvates of Lithium Hexamethyldisilazide, and 13C NMR spectroscopic studies of 6Li-15N labeled lithium hexamethyldisilazide ([6Li,15N]- Li ligand structure and lithium amide aggregation state is a complex and sensitive function of amine alkyl

Collum, David B.

186

SOLID STATE NMR STUDY SUPPORTING THE LITHIUM VACANCY DEFECT MODEL IN CONGRUENT LITHIUM  

E-Print Network [OSTI]

@ Pergamon SOLID STATE NMR STUDY SUPPORTING THE LITHIUM VACANCY DEFECT MODEL IN CONGRUENT LITHIUM performed on powdered and single crystal lithium niobate of defectivecongruent composition (48.4%LirO;51.6% NbrOr) using a magnetic field strength of 7.05 Tesla with the aim to distinguish between a lithium

Bluemel, Janet

187

Synthesis and Electrochemical Performance of a Lithium Titanium Phosphate Anode for Aqueous Lithium-Ion Batteries  

E-Print Network [OSTI]

on larger scales. Im- provement of the safety of lithium-ion batteries must occur if they are to be utilized in aqueous cells. However, the choice of a suitable anode material for an aqueous lithium-ion battery is moreSynthesis and Electrochemical Performance of a Lithium Titanium Phosphate Anode for Aqueous Lithium

Cui, Yi

188

Protective lithium ion conducting ceramic coating for lithium metal anodes and associate method  

DOE Patents [OSTI]

A battery structure including a cathode, a lithium metal anode and an electrolyte disposed between the lithium anode and the cathode utilizes a thin-film layer of lithium phosphorus oxynitride overlying so as to coat the lithium anode and thereby separate the lithium anode from the electrolyte. If desired, a preliminary layer of lithium nitride may be coated upon the lithium anode before the lithium phosphorous oxynitride is, in turn, coated upon the lithium anode so that the separation of the anode and the electrolyte is further enhanced. By coating the lithium anode with this material lay-up, the life of the battery is lengthened and the performance of the battery is enhanced.

Bates, John B. (Oak Ridge, TN)

1994-01-01T23:59:59.000Z

189

Khalil Amine on Lithium-air Batteries  

ScienceCinema (OSTI)

Khalil Amine, materials scientist at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries.

Khalil Amine

2010-01-08T23:59:59.000Z

190

Michael Thackery on Lithium-air Batteries  

ScienceCinema (OSTI)

Michael Thackery, Distinguished Fellow at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries.

Michael Thackery

2010-01-08T23:59:59.000Z

191

(Lithium and lead-lithium corrosion and chemistry)  

SciTech Connect (OSTI)

Presentations on Mass Transport Processes in Li/Fe-12Cr-1MoVW Steel,'' A Lower Temperature Lithium Purification Process Incorporating Warm Trapping','' and Kinetic Analysis of Corrosion in Pb-17 at. % Li and Comparison to Pure Lithium'' were given by the traveler at the 1989 European Workshop on Lithium and Lead-Lithium Corrosion and Chemistry in Vienna, Austria. The European effort in lead-lithium appeared to be continuing unabated with a future focus on deposition and surface products reactions that can lead to corrosion control. The temperature gain realized from the use of ferritic/martensitic steels instead of austenitic steels in Pb-17 at. % Li appears to be 25--50{degrees}C. The traveler also visited the European Community's Joint Research Centre at Ispra to discuss Fe-Mn-Cr steels. He presented a seminar on Recent ORNL Results on the Development of Fe-Mn-Cr Steels,'' and toured the liquid metal laboratories. Our developmental Fe-Mn-Cr steels, which are compositionally tailored for shallow land burial, would not qualify as low activation'' materials per European standards. Because of both this and the poor sensitization resistance of these steels, our alloy development strategy for reduced activation materials should be critically reviewed.

Tortorelli, P.F.

1989-10-09T23:59:59.000Z

192

GAS-PHASE REACTIONS OF HYDRIDE ANION, H{sup -}  

SciTech Connect (OSTI)

Rate constants were measured at 300 K for the reactions of the hydride anion, H{sup -}, with neutral molecules C{sub 2}H{sub 2}, H{sub 2}O, CH{sub 3}CN, CH{sub 3}OH, (CH{sub 3}){sub 2}CO, CH{sub 3}CHO, N{sub 2}O, CO{sub 2}, O{sub 2}, CO, CH{sub 3}Cl, (CH{sub 3}){sub 3}CCl, (CH{sub 3}CH{sub 2}){sub 2}O, C{sub 6}H{sub 6}, and D{sub 2} using a flowing-afterglow instrument. Experimental work was supplemented by ab initio calculations to provide insight into the viability of reaction pathways. Our reported rate constants should prove useful to models of astrophysical environments where conditions prevail for the existence of both H{sup -} and neutral species. The variety of neutral reactants studied includes representative species from prototypical chemical groups, effectively mapping reactivity trends for the hydride anion.

Martinez, Oscar; Yang Zhibo; Demarais, Nicholas J.; Bierbaum, Veronica M. [Department of Chemistry and Biochemistry, 215 UCB, University of Colorado, Boulder, CO 80309-0215 (United States); Snow, Theodore P., E-mail: Oscar.Martinez@colorado.ed, E-mail: Zhibo.Yang@colorado.ed, E-mail: Nicholas.Demarais@colorado.ed, E-mail: Veronica.Bierbaum@colorado.ed, E-mail: Theodore.Snow@colorado.ed [Department of Astrophysical and Planetary Sciences, 391 UCB, University of Colorado, Boulder, CO 80309-0391 (United States)

2010-09-01T23:59:59.000Z

193

Method of generating hydrogen-storing hydride complexes  

DOE Patents [OSTI]

A ternary hydrogen storage system having a constant stoichiometric molar ratio of LiNH.sub.2:MgH.sub.2:LiBH.sub.4 of 2:1:1. It was found that the incorporation of MgH.sub.2 particles of approximately 10 nm to 20 nm exhibit a lower initial hydrogen release temperature of 150.degree. C. Furthermore, it is observed that the particle size of LiBNH quaternary hydride has a significant effect on the hydrogen sorption concentration with an optimum size of 28 nm. The as-synthesized hydrides exhibit two main hydrogen release temperatures, one around 160.degree. C. and the other around 300.degree. C., with the main hydrogen release temperature reduced from 310.degree. C. to 270.degree. C., while hydrogen is first reversibly released at temperatures as low as 150.degree. C. with a total hydrogen capacity of 6 wt. % to 8 wt. %. Detailed thermal, capacity, structural and microstructural properties have been demonstrated and correlated with the activation energies of these materials.

Srinivasan, Sesha S; Niemann, Michael U; Goswami, D. Yogi; Stefanakos, Elias K

2013-05-14T23:59:59.000Z

194

Novel Electrolytes for Lithium Ion Batteries  

SciTech Connect (OSTI)

We have been investigating three primary areas related to lithium ion battery electrolytes. First, we have been investigating the thermal stability of novel electrolytes for lithium ion batteries, in particular borate based salts. Second, we have been investigating novel additives to improve the calendar life of lithium ion batteries. Third, we have been investigating the thermal decomposition reactions of electrolytes for lithium-oxygen batteries.

Lucht, Brett L

2014-12-12T23:59:59.000Z

195

Multi-layered, chemically bonded lithium-ion and lithium/air batteries  

SciTech Connect (OSTI)

Disclosed are multilayer, porous, thin-layered lithium-ion batteries that include an inorganic separator as a thin layer that is chemically bonded to surfaces of positive and negative electrode layers. Thus, in such disclosed lithium-ion batteries, the electrodes and separator are made to form non-discrete (i.e., integral) thin layers. Also disclosed are methods of fabricating integrally connected, thin, multilayer lithium batteries including lithium-ion and lithium/air batteries.

Narula, Chaitanya Kumar; Nanda, Jagjit; Bischoff, Brian L; Bhave, Ramesh R

2014-05-13T23:59:59.000Z

196

Conductive lithium storage electrode  

DOE Patents [OSTI]

A compound comprising a composition A.sub.x(M'.sub.1-aM''.sub.a).sub.y(XD.sub.4).sub.z, A.sub.x(M'.sub.1-aM''.sub.a).sub.y(DXD.sub.4).sub.z, or A.sub.x(M'.sub.1-aM''.sub.a).sub.y(X.sub.2D.sub.7).sub.z, and have values such that x, plus y(1-a) times a formal valence or valences of M', plus ya times a formal valence or valence of M'', is equal to z times a formal valence of the XD.sub.4, X.sub.2D.sub.7, or DXD.sub.4 group; or a compound comprising a composition (A.sub.1-aM''.sub.a).sub.xM'.sub.y(XD.sub.4).sub.z, (A.sub.1-aM''.sub.a).sub.xM'.sub.y(DXD.sub.4).sub.z(A.sub.1-aM''.sub.a).s- ub.xM'.sub.y(X.sub.2D.sub.7).sub.z and have values such that (1-a).sub.x plus the quantity ax times the formal valence or valences of M'' plus y times the formal valence or valences of M' is equal to z times the formal valence of the XD.sub.4, X.sub.2D.sub.7 or DXD.sub.4 group. In the compound, A is at least one of an alkali metal and hydrogen, M' is a first-row transition metal, X is at least one of phosphorus, sulfur, arsenic, molybdenum, and tungsten, M'' any of a Group IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB, IVB, VB, and VIB metal, D is at least one of oxygen, nitrogen, carbon, or a halogen, 0.0001lithium phosphate that can intercalate lithium or hydrogen. The compound can be used in an electrochemical device including electrodes and storage batteries and can have a gravimetric capacity of at least about 80 mAh/g while being charged/discharged at greater than about C rate of the compound.

Chiang, Yet-Ming (Framingham, MA); Chung, Sung-Yoon (Seoul, KR); Bloking, Jason T. (Cambridge, MA); Andersson, Anna M. (Uppsala, SE)

2008-03-18T23:59:59.000Z

197

Conductive lithium storage electrode  

DOE Patents [OSTI]

A compound comprising a composition A.sub.x(M'.sub.1-aM''.sub.a).sub.y(XD.sub.4).sub.z, A.sub.x(M'.sub.1-aM''.sub.a).sub.y(DXD.sub.4).sub.z, or A.sub.x(M'.sub.1-aM''.sub.a).sub.y(X.sub.2D.sub.7).sub.z, and have values such that x, plus y(1-a) times a formal valence or valences of M', plus ya times a formal valence or valence of M'', is equal to z times a formal valence of the XD.sub.4, X.sub.2D.sub.7, or DXD.sub.4 group; or a compound comprising a composition (A.sub.1-aM''.sub.a).sub.xM'.sub.y(XD.sub.4).sub.z, (A.sub.1-aM''.sub.a).sub.xM'.sub.y(DXD.sub.4).sub.z (A.sub.1-aM''.sub.a).sub.xM'.sub.y(X.sub.2D.sub.7).sub.z and have values such that (1-a).sub.x plus the quantity ax times the formal valence or valences of M'' plus y times the formal valence or valences of M' is equal to z times the formal valence of the XD.sub.4, X.sub.2D.sub.7 or DXD.sub.4 group. In the compound, A is at least one of an alkali metal and hydrogen, M' is a first-row transition metal, X is at least one of phosphorus, sulfur, arsenic, molybdenum, and tungsten, M'' any of a Group IIA, IIIA, IVA, VA, VIA, VIIA, VIIIA, IB, IIB, IIIB, IVB, VB, and VIB metal, D is at least one of oxygen, nitrogen, carbon, or a halogen, 0.0001lithium phosphate that can intercalate lithium or hydrogen. The compound can be used in an electrochemical device including electrodes and storage batteries and can have a gravimetric capacity of at least about 80 mAh/g while being charged/discharged at greater than about C rate of the compound.

Chiang, Yet-Ming (Framingham, MA); Chung, Sung-Yoon (Incheon, KR); Bloking, Jason T. (Mountain View, CA); Andersson, Anna M. (Vasteras, SE)

2012-04-03T23:59:59.000Z

198

Magnetism in Lithium–Oxygen Discharge Product  

SciTech Connect (OSTI)

Nonaqueous lithium–oxygen batteries have a much superior theoretical gravimetric energy density compared to conventional lithium-ion batteries, and thus could render long-range electric vehicles a reality. A molecular-level understanding of the reversible formation of lithium peroxide in these batteries, the properties of major/minor discharge products, and the stability of the nonaqueous electrolytes is required to achieve successful lithium–oxygen batteries. We demonstrate that the major discharge product formed in the lithium–oxygen cell, lithium peroxide, exhibits a magnetic moment. These results are based on dc-magnetization measurements and a lithium– oxygen cell containing an ether-based electrolyte. The results are unexpected because bulk lithium peroxide has a significant band gap. Density functional calculations predict that superoxide- type surface oxygen groups with unpaired electrons exist on stoichiometric lithium peroxide crystalline surfaces and on nanoparticle surfaces; these computational results are consistent with the magnetic measurement of the discharged lithium peroxide product as well as EPR measurements on commercial lithium peroxide. The presence of superoxide-type surface oxygen groups with spin can play a role in the reversible formation and decomposition of lithium peroxide as well as the reversible formation and decomposition of electrolyte molecules.

Lu, Jun; Jung, Hun-Ji; Lau, Kah Chun; Zhang, Zhengcheng; Schlueter, John A.; Du, Peng; Assary, Rajeev S.; Greeley, Jeffrey P.; Ferguson, Glen A.; Wang, Hsien-Hau; Hassoun, Jusef; Iddir, Hakim; Zhou, Jigang; Zuin, Lucia; Hu, Yongfeng; Sun, Yang-Kook; Scrosati, Bruno; Curtiss, Larry A.; Amine, Khalil

2013-05-13T23:59:59.000Z

199

Heterogeneous lithium niobate photonics on silicon substrates  

E-Print Network [OSTI]

Heterogeneous lithium niobate photonics on silicon substrates Payam Rabiei,1,* Jichi Ma,1 Saeed-confined lithium niobate photonic devices and circuits on silicon substrates is reported based on wafer bonding high- performance lithium niobate microring optical resonators and Mach- Zehnder optical modulators

Fathpour, Sasan

200

COSMOLOGICAL LITHIUM PROBLEM: A DIFFERENT APPROACH  

E-Print Network [OSTI]

LITHIUM 7Li sources BBN cosmic-ray interactions (ingredients: shock waves, magnetic field, chargedCOSMOLOGICAL LITHIUM PROBLEM: A DIFFERENT APPROACH Tijana Prodanovi, University of Novi Sad Tamara Observations - boxes 4He ­ OK D ­ right on! 7Li ­ problem! Factor of 3-4 discrepancy! LITHIUM PROBLEM

?umer, Slobodan

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Solid composite electrolytes for lithium batteries  

DOE Patents [OSTI]

Solid composite electrolytes are provided for use in lithium batteries which exhibit moderate to high ionic conductivity at ambient temperatures and low activation energies. In one embodiment, a ceramic-ceramic composite electrolyte is provided containing lithium nitride and lithium phosphate. The ceramic-ceramic composite is also preferably annealed and exhibits an activation energy of about 0.1 eV.

Kumar, Binod (Dayton, OH); Scanlon, Jr., Lawrence G. (Fairborn, OH)

2000-01-01T23:59:59.000Z

202

Anode materials for lithium-ion batteries  

DOE Patents [OSTI]

An anode material for lithium-ion batteries is provided that comprises an elongated core structure capable of forming an alloy with lithium; and a plurality of nanostructures placed on a surface of the core structure, with each nanostructure being capable of forming an alloy with lithium and spaced at a predetermined distance from adjacent nanostructures.

Sunkara, Mahendra Kumar; Meduri, Praveen; Sumanasekera, Gamini

2014-12-30T23:59:59.000Z

203

Lithium metal oxide electrodes for lithium cells and batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Downers Grove, IL); Kim, Jaekook (Naperville, IL)

2004-01-13T23:59:59.000Z

204

The Primordial Lithium Problem  

E-Print Network [OSTI]

Big-bang nucleosynthesis (BBN) theory, together with the precise WMAP cosmic baryon density, makes tight predictions for the abundances of the lightest elements. Deuterium and 4He measurements agree well with expectations, but 7Li observations lie a factor 3-4 below the BBN+WMAP prediction. This 4-5\\sigma\\ mismatch constitutes the cosmic "lithium problem," with disparate solutions possible. (1) Astrophysical systematics in the observations could exist but are increasingly constrained. (2) Nuclear physics experiments provide a wealth of well-measured cross-section data, but 7Be destruction could be enhanced by unknown or poorly-measured resonances, such as 7Be + 3He -> 10C^* -> p + 9B. (3) Physics beyond the Standard Model can alter the 7Li abundance, though D and 4He must remain unperturbed; we discuss such scenarios, highlighting decaying Supersymmetric particles and time-varying fundamental constants. Present and planned experiments could reveal which (if any) of these is the solution to the problem.

Brian D. Fields

2012-03-15T23:59:59.000Z

205

Spatial periphery of lithium isotopes  

SciTech Connect (OSTI)

The spatial structure of lithium isotopes is studied with the aid of the charge-exchange and (t, p) reactions on lithium nuclei. It is shown that an excited isobaric-analog state of {sup 6}Li (0{sup +}, 3.56MeV) has a halo structure formed by a proton and a neutron, that, in the {sup 9}Li nucleus, there is virtually no neutron halo, and that {sup 11}Li is a Borromean nucleus formed by a {sup 9}Li core and a two-neutron halo manifesting itself in cigar-like and dineutron configurations.

Galanina, L. I., E-mail: galan_lidiya@mail.ru; Zelenskaja, N. S. [Moscow State University, Skobeltsyn Institute of Nuclear Physics (Russian Federation)

2013-12-15T23:59:59.000Z

206

Liquid Lithium Experiments in CDX-U  

SciTech Connect (OSTI)

The initial results of experiments involving the use of liquid lithium as a plasma facing component in the Current Drive Experiment-Upgrade (CDX-U) are reported. Studies of the interaction of a steady-state plasma with liquid lithium in the Plasma Interaction with Surface and Components Experimental Simulator (PISCES-B) are also summarized. In CDX-U a solid or liquid lithium covered rail limiter was introduced as the primary limiting surface for spherical torus discharges. Deuterium recycling was observed to be reduced, but so far not eliminated, for glow discharge-cleaned lithium surfaces. Some lithium influx was observed during tokamak operation. The PISCES-B results indicate that the rates of plasma erosion of lithium can exceed predictions by an order of magnitude at elevated temperatures. Plans to extend the CDX-U experiments to large area liquid lithium toroidal belt limiters are also described.

R. Majeski; R. Doerner; R. Kaita; G. Antar; J. Timberlake; et al

2000-11-15T23:59:59.000Z

207

Solid solution lithium alloy cermet anodes  

DOE Patents [OSTI]

A metal-ceramic composite ("cermet") has been produced by a chemical reaction between a lithium compound and another metal. The cermet has advantageous physical properties, high surface area relative to lithium metal or its alloys, and is easily formed into a desired shape. An example is the formation of a lithium-magnesium nitride cermet by reaction of lithium nitride with magnesium. The reaction results in magnesium nitride grains coated with a layer of lithium. The nitride is inert when used in a battery. It supports the metal in a high surface area form, while stabilizing the electrode with respect to dendrite formation. By using an excess of magnesium metal in the reaction process, a cermet of magnesium nitride is produced, coated with a lithium-magnesium alloy of any desired composition. This alloy inhibits dendrite formation by causing lithium deposited on its surface to diffuse under a chemical potential into the bulk of the alloy.

Richardson, Thomas J.

2013-07-09T23:59:59.000Z

208

Final report for the DOE Metal Hydride Center of Excellence.  

SciTech Connect (OSTI)

This report summarizes the R&D activities within the U.S. Department of Energy Metal Hydride Center of Excellence (MHCoE) from March 2005 to June 2010. The purpose of the MHCoE has been to conduct highly collaborative and multi-disciplinary applied R&D to develop new reversible hydrogen storage materials that meet or exceed DOE 2010 and 2015 system goals for hydrogen storage materials. The MHCoE combines three broad areas: mechanisms and modeling (which provide a theoretically driven basis for pursuing new materials), materials development (in which new materials are synthesized and characterized) and system design and engineering (which allow these new materials to be realized as practical automotive hydrogen storage systems). This Final Report summarizes the organization and execution of the 5-year research program to develop practical hydrogen storage materials for light duty vehicles. Major results from the MHCoE are summarized, along with suggestions for future research areas.

Keller, Jay O.; Klebanoff, Leonard E.

2012-01-01T23:59:59.000Z

209

LITHIUM--1997 46.1 By Joyce A. Ober  

E-Print Network [OSTI]

LITHIUM--1997 46.1 LITHIUM By Joyce A. Ober After decades as the world's leading producer of lithium and its compounds, the United States was surpassed in 1997 when Chile became the world's largest lithium carbonate producer. Both lithium carbonate operations at the Salar de Atacama produced during

210

Photogeneration of Hydride Donors and Their Use Toward CO2 Reduction  

SciTech Connect (OSTI)

Despite substantial effort, no one has succeeded in efficiently producing methanol from CO2 using homogeneous photocatalytic systems. We are pursuing reaction schemes based on a sequence of hydride-ion transfers to carry out stepwise reduction of CO2 to methanol. We are using hydride-ion transfer from photoproduced C-H bonds in metal complexes with bio-inspired ligands (i.e., NADH-like ligands) that are known to store one proton and two electrons.

Fujita,E.; Muckerman, J.T.; Polyansky, D.E.

2009-06-07T23:59:59.000Z

211

Advanced Metal-Hydrides-Based Thermal Battery: A New Generation of High Density Thermal Battery Based on Advanced Metal Hydrides  

SciTech Connect (OSTI)

HEATS Project: The University of Utah is developing a compact hot-and-cold thermal battery using advanced metal hydrides that could offer efficient climate control system for EVs. The team’s innovative designs of heating and cooling systems for EVs with high energy density, low-cost thermal batteries could significantly reduce the weight and eliminate the space constraint in automobiles. The thermal battery can be charged by plugging it into an electrical outlet while charging the electric battery and it produces heat and cold through a heat exchanger when discharging. The ultimate goal of the project is a climate-controlling thermal battery that can last up to 5,000 charge and discharge cycles while substantially increasing the driving range of EVs, thus reducing the drain on electric batteries.

None

2011-12-01T23:59:59.000Z

212

First-principles calculations of niobium hydride formation in superconducting radio-frequency cavities  

SciTech Connect (OSTI)

Niobium hydride is suspected to be a major contributor to degradation of the quality factor of niobium superconducting radio-frequency (SRF) cavities. In this study, we connect the fundamental properties of hydrogen in niobium to SRF cavity performance and processing. We modeled several of the niobium hydride phases relevant to SRF cavities and present their thermodynamic, electronic, and geometric properties determined from calculations based on density-functional theory. We find that the absorption of hydrogen from the gas phase into niobium is exothermic and hydrogen becomes somewhat anionic. The absorption of hydrogen by niobium lattice vacancies is strongly preferred over absorption into interstitial sites. A single vacancy can accommodate six hydrogen atoms in the symmetrically equivalent lowest-energy sites and additional hydrogen in the nearby interstitial sites affected by the strain field: this indicates that a vacancy can serve as a nucleation center for hydride phase formation. Small hydride precipitates may then occur near lattice vacancies upon cooling. Vacancy clusters and extended defects should also be enriched in hydrogen, potentially resulting in extended hydride phase regions upon cooling. We also assess the phase changes in the niobium-hydrogen system based on charge transfer between niobium and hydrogen, the strain field associated with interstitial hydrogen, and the geometry of the hydride phases. The results of this study stress the importance of not only the hydrogen content in niobium, but also the recovery state of niobium for the performance of SRF cavities.

Ford, Denise C.; Cooley, Lance D.; Seidman, David N.

2013-09-01T23:59:59.000Z

213

Lithium Ephedrate-Mediated Addition of a Lithium Acetylide to a Ketone: Solution Structures and Relative Reactivities of Mixed  

E-Print Network [OSTI]

Lithium Ephedrate-Mediated Addition of a Lithium Acetylide to a Ketone: Solution Structures-1301 ReceiVed April 30, 1997. ReVised Manuscript ReceiVed NoVember 26, 1997 Abstract: Addition of lithiumLi and 13C NMR spectroscopies reveal lithium cyclopropylacetylide in THF to be a dimer

Collum, David B.

214

Anode material for lithium batteries  

DOE Patents [OSTI]

Primary and secondary Li-ion and lithium-metal based electrochemical cell systems. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plasticized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

Belharouak, Ilias (Westmont, IL); Amine, Khalil (Downers Grove, IL)

2012-01-31T23:59:59.000Z

215

Anode material for lithium batteries  

DOE Patents [OSTI]

Primary and secondary Li-ion and lithium-metal based electrochemical cell system. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plastized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

Belharouak, Ilias (Bolingbrook, IL); Amine, Khalil (Downers Grove, IL)

2008-06-24T23:59:59.000Z

216

Lithium-loaded liquid scintillators  

DOE Patents [OSTI]

The invention is directed to a liquid scintillating composition containing (i) one or more non-polar organic solvents; (ii) (lithium-6)-containing nanoparticles having a size of up to 10 nm and surface-capped by hydrophobic molecules; and (iii) one or more fluorophores. The invention is also directed to a liquid scintillator containing the above composition.

Dai, Sheng (Knoxville, TN); Kesanli, Banu (Mersin, TR); Neal, John S. (Knoxville, TN)

2012-05-15T23:59:59.000Z

217

Anode material for lithium batteries  

DOE Patents [OSTI]

Primary and secondary Li-ion and lithium-metal based electrochemical cell systems. The suppression of gas generation is achieved through the addition of an additive or additives to the electrolyte system of respective cell, or to the cell itself whether it be a liquid, a solid- or plasticized polymer electrolyte system. The gas suppression additives are primarily based on unsaturated hydrocarbons.

Belharouak, Ilias (Bolingbrook, IL); Amine, Khalil (Oak Brook, IL)

2011-04-05T23:59:59.000Z

218

1. MOST SIGNIFICANT RESEARCH ACCOMPLISHMENTS IN POWER SOURCES Currently, Dr. Popov is professor at USC and Director of the Center for  

E-Print Network [OSTI]

Research Novel high performance anode materials were developed for Nickel-Metal Hydride (Ni-MH) batteries and corrosion resistance. From this research one step electroless process was discovered for deposition of Ni

Popov, Branko N.

219

Comparison of various battery technologies for electric vehicles  

E-Print Network [OSTI]

four technologies; Lead-Acid, Nickel-Cadmium, Nickel-Metal Hydride and Zinc-Bromide. A standard set of testing procedures for electric vehicle batteries, based on industry accepted testing procedures, and any tests which were specific to individual...

Dickinson, Blake Edward

1993-01-01T23:59:59.000Z

220

Abstract--This paper outlines the design of an autonomous flying vehicle (AFV) for use in researching formation  

E-Print Network [OSTI]

with a full suite of integrated peripherals. Today, Nickel- Metal Hydride (NiMH) batteries can source more predators and efficiently forage for food [6]. Both the Air Force and NASA have identified autonomous

Sukhatme, Gaurav S.

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Effects of outgassing of loader chamber walls on hydriding of thin films for commercial applications  

SciTech Connect (OSTI)

An important aspect of understanding industrial processing is to know the characteristics of the materials used in such processes. A study was performed to determine the effects of hydriding chamber material on the degree of hydriding for the commercial production of thin film hydride targets for various research universities, commercial companies, and government national laboratories. The goal was to increase the degree of hydriding of various thin film hydrides and to study the vacuum environment during air-exposure hydriding. For this purpose, dynamic residual gas analysis during deuterium gas hydride processing was utilized with erbium thin films, employing a special set-up for direct dynamic hydride gas sampling during processing at elevated temperature and full loading gas pressure. Complete process data for (1) a copper–(1.83?wt.?%)beryllium wet hydrogen fired passivated (600?°C–1?h) externally heated pipe hydriding chamber are reported. Dynamic residual gas analysis comparisons during hydriding are presented for hydriding chambers made from (2) alumina (99.8 wt.?%), (3) copper (with an interior aluminum coating ?10 k Å thick, and (4) for a stainless-steel air-fired passivated (900?°C–1?h) chamber. Dynamic data with deuterium gas in the chamber at the hydriding temperature (450?°C) showed the presence and growth of water vapor (D{sub 2}O) and related mixed ion species(H{sub 2}O{sup +}, HDO{sup +}, D{sub 2}O{sup +}, and OD{sup +}) from hydrogen isotope exchange reactions during the 1?h process time. Peaks at mass-to-charge ratios (i.e., m/e) of 12(C{sup +}), 16(CD{sub 2}{sup +}), 17(CHD{sub 2}{sup +}), and 18(CD{sub 3}{sup +}, OD{sup +}) increased for approximately the first half hour of a 1?h hydriding process and then approach steady state. Mass-to-charge peaks at 19(HDO{sup +}) and 20(D{sub 2}O{sup +}) continue to increase throughout the process cycle. Using the m/e?=?20 (D{sub 2}O{sup +}) peak intensity from chamber (1)–Cu(1.83 wt.?%)Be as a standard, the peak intensity from chamber (4)—stainless-steel (air-fired) was 7.1× higher, indicating that the surface of stainless-steel had a larger concentration of reactive oxygen and/or water than hydrogen. The (D{sub 2}O{sup +}) peak intensity from chamber (3)—Cu (interior Al coating) was 1.55× larger and chamber (2)—alumina(99.8%) was 1.33× higher than Cu(1.83 wt.?%)Be. Thus copper–(1.83 wt.?%)beryllium was the best hydriding chamber material studied followed closely by the alumina (99.8 wt.?%) chamber. Gas take-up by Er occluder targets processed in Cu(1.83?wt.?%)Be hydriding chambers (i.e., gas/metal atomic ratios) correlate with the dynamic RGA data.

Provo, James L., E-mail: jlprovo@verizon.net [Consultant, J.L. Provo Consulting, Trinity, Florida 34655-7179 (United States)

2014-07-01T23:59:59.000Z

222

Development of a lithium hydride powered hydrogen generator for use in long life, low power PEM fuel cell power supplies  

E-Print Network [OSTI]

This thesis studies a hybrid PEM fuel cell system for use in low power, long life sensor networks. PEM fuel cells offer high efficiency and environmental friendliness but have not been widely adopted due to cost, reliability, ...

Strawser, Daniel DeWitt

2012-01-01T23:59:59.000Z

223

Lithium Diisopropylamide: Oligomer Structures at Low Ligand Concentrations  

E-Print Network [OSTI]

Lithium Diisopropylamide: Oligomer Structures at Low Ligand Concentrations Jennifer L. Rutherford-dimensional 6Li and 15N NMR spectroscopic studies of lithium diisopropylamide (LDA) solvated ligand concentrations are discussed. Introduction Spectroscopic studies of lithium amides at low ligand

Collum, David B.

224

A Better Anode Design to Improve Lithium-Ion Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

A Better Anode Design to Improve Lithium-Ion Batteries A Better Anode Design to Improve Lithium-Ion Batteries Print Friday, 23 March 2012 13:53 Lithium-ion batteries are in smart...

225

Model Reformulation and Design of Lithium-ion Batteries  

E-Print Network [OSTI]

987 94 Model Reformulation and Design of Lithium-ion Batteries V.R. Subramanian1,*, V. Boovaragavan Prediction......................................997 Optimal Design of Lithium-ion Batteries Lithium-ion batteries, product design, Bayesian estimation, Markov Chain Monte Carlo simulation

Subramanian, Venkat

226

Ab initio screening of lithium diffusion rates in transition metal oxide cathodes for lithium ion batteries  

E-Print Network [OSTI]

A screening metric for diffusion limitations in lithium ion battery cathodes is derived using transition state theory and common materials properties. The metric relies on net activation barrier for lithium diffusion. ...

Moore, Charles J. (Charles Jacob)

2012-01-01T23:59:59.000Z

227

Complex Hydride Compounds with Enhanced Hydrogen Storage Capacity  

SciTech Connect (OSTI)

The United Technologies Research Center (UTRC), in collaboration with major partners Albemarle Corporation (Albemarle) and the Savannah River National Laboratory (SRNL), conducted research to discover new hydride materials for the storage of hydrogen having on-board reversibility and a target gravimetric capacity of ? 7.5 weight percent (wt %). When integrated into a system with a reasonable efficiency of 60% (mass of hydride / total mass), this target material would produce a system gravimetric capacity of ? 4.5 wt %, consistent with the DOE 2007 target. The approach established for the project combined first principles modeling (FPM - UTRC) with multiple synthesis methods: Solid State Processing (SSP - UTRC), Solution Based Processing (SBP - Albemarle) and Molten State Processing (MSP - SRNL). In the search for novel compounds, each of these methods has advantages and disadvantages; by combining them, the potential for success was increased. During the project, UTRC refined its FPM framework which includes ground state (0 Kelvin) structural determinations, elevated temperature thermodynamic predictions and thermodynamic / phase diagram calculations. This modeling was used both to precede synthesis in a virtual search for new compounds and after initial synthesis to examine reaction details and options for modifications including co-reactant additions. The SSP synthesis method involved high energy ball milling which was simple, efficient for small batches and has proven effective for other storage material compositions. The SBP method produced very homogeneous chemical reactions, some of which cannot be performed via solid state routes, and would be the preferred approach for large scale production. The MSP technique is similar to the SSP method, but involves higher temperature and hydrogen pressure conditions to achieve greater species mobility. During the initial phases of the project, the focus was on higher order alanate complexes in the phase space between alkaline metal hydrides (AmH), Alkaline earth metal hydrides (AeH2), alane (AlH3), transition metal (Tm) hydrides (TmHz, where z=1-3) and molecular hydrogen (H2). The effort started first with variations of known alanates and subsequently extended the search to unknown compounds. In this stage, the FPM techniques were developed and validated on known alanate materials such as NaAlH4 and Na2LiAlH6. The coupled predictive methodologies were used to survey over 200 proposed phases in six quaternary spaces, formed from various combinations of Na, Li Mg and/or Ti with Al and H. A wide range of alanate compounds was examined using SSP having additions of Ti, Cr, Co, Ni and Fe. A number of compositions and reaction paths were identified having H weight fractions up to 5.6 wt %, but none meeting the 7.5 wt%H reversible goal. Similarly, MSP of alanates produced a number of interesting compounds and general conclusions regarding reaction behavior of mixtures during processing, but no alanate based candidates meeting the 7.5 wt% goal. A novel alanate, LiMg(AlH4)3, was synthesized using SBP that demonstrated a 7.0 wt% capacity with a desorption temperature of 150°C. The deuteride form was synthesized and characterized by the Institute for Energy (IFE) in Norway to determine its crystalline structure for related FPM studies. However, the reaction exhibited exothermicity and therefore was not reversible under acceptable hydrogen gas pressures for on-board recharging. After the extensive studies of alanates, the material class of emphasis was shifted to borohydrides. Through SBP, several ligand-stabilized Mg(BH4)2 complexes were synthesized. The Mg(BH4)2*2NH3 complex was found to change behavior with slightly different synthesis conditions and/or aging. One of the two mechanisms was an amine-borane (NH3BH3) like dissociation reaction which released up to 16 wt %H and more conservatively 9 wt%H when not including H2 released from the NH3. From FPM, the stability of the Mg(BH4)2*2NH3 compound was found to increase with the inclusion of NH3 groups in the inner-Mg coordination

Mosher, Daniel A.; Opalka, Susanne M.; Tang, Xia; Laube, Bruce L.; Brown, Ronald J.; Vanderspurt, Thomas H.; Arsenault, Sarah; Wu, Robert; Strickler, Jamie; Anton, Donald L.; Zidan, Ragaiy; Berseth, Polly

2008-02-18T23:59:59.000Z

228

Documentation of Hybrid Hydride Model for Incorporation into Moose-Bison and Validation Strategy  

SciTech Connect (OSTI)

This report documents the development, demonstration and validation of a mesoscale, microstructural evolution model for simulation of zirconium hydride ?-ZrH1.5 precipitation in the cladding of used nuclear fuels that may occur during long-term dry storage. While the Zr-based claddings are manufactured free of any hydrogen, they absorb hydrogen during service, in the reactor by a process commonly termed ‘hydrogen pick-up’. The precipitation and growth of zirconium hydrides during dry storage is one of the most likely fuel rod integrity failure mechanisms either by embrittlement or delayed hydride cracking of the cladding (Hanson et al., 2011). While the phenomenon is well documented and identified as a potential key failure mechanism during long-term dry storage (Birk et al., 2012 and NUREG/CR-7116), the ability to actually predict the formation of hydrides is poor. The model being documented in this work is a computational capability for the prediction of hydride formation in different claddings of used nuclear fuels. This work supports the Used Fuel Disposition Research and Development Campaign in assessing the structural engineering performance of the cladding during and after long-term dry storage. In this work, a model to numerically simulate hydride precipitation at the microstructural scale, in a wide variety of Zr-based claddings, under dry-storage conditions is being developed. It will be used to aid in the evaluation of the mechanical integrity of used fuel rods during dry storage and transportation by providing the structural conditions from the microstructural scale to the continuum scale to engineering component scale models to predict if the used fuel rods will perform without failure under normal and off-normal conditions. The microstructure, especially, the hydride structure is thought to be a primary determinant of cladding failure, thus this component of UFD’s storage and transportation analysis program is critical. The model development, application and validation of the model are documented and the limitations of the current model are discussed. The model has been shown to simulate hydride precipitation in Zircaloy-4 cladding with correct morphology, thermodynamics and kinetics. An unexpected insight obtained from simulations hydride formation in Zircaloy-4 is that small (sub-micron) precipitates need to order themselves to form the larger hydrides typically described as radially-reoriented precipitates. A limitation of this model is that it does not currently solve the stress state that forms dynamically in the precipitate or matrix surrounding the precipitate. A method to overcome the limitations is suggested and described in detail. The necessary experiments to provide key materials physics and to validate the model are also recommended.

Veena Tikare; Philippe Weck; Peter Schultz; Blythe Clark; John Mitchell; Michael Glazoff; Eric Homer

2014-10-01T23:59:59.000Z

229

Lithium borate cluster salts as novel redox shuttles for overcharge protection of lithium-ion cells.  

SciTech Connect (OSTI)

Redox shuttle is a promising mechanism for intrinsic overcharge protection in lithium-ion cells and batteries. Two lithium borate cluster salts are reported to function as both the main salt for a nonaqueous electrolyte and the redox shuttle for overcharge protection. Lithium borate cluster salts with a tunable redox potential are promising candidates for overcharge protection for most positive electrodes in state-of-the-art lithium-ion cells.

Chen, Z.; Liu, J.; Jansen, A. N.; Casteel, B.; Amine, K.; GirishKumar, G.; Air Products and Chemicals, Inc.

2010-01-01T23:59:59.000Z

230

Lithium metal oxide electrodes for lithium cells and batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO2.(1-x)Li2M'O3 in which 0

Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

2006-11-14T23:59:59.000Z

231

Lithium Metal Oxide Electrodes For Lithium Cells And Batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Downers Grove, IL); Kim, Jaekook (Naperville, IL)

2004-01-20T23:59:59.000Z

232

Lithium metal oxide electrodes for lithium cells and batteries  

DOE Patents [OSTI]

A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Amine, Khalil (Oakbrook, IL)

2008-12-23T23:59:59.000Z

233

ENDOR study of Cr3 centers substituting for lithium in lithium niobate  

E-Print Network [OSTI]

ENDOR study of Cr3¿ centers substituting for lithium in lithium niobate G. Malovichko,1, * V centers in lithium niobate crystals were investigated with the help of electron nuclear double resonance and the parameters of hyperfine and quadrupole interactions were determined. It is found that Cr3 substitutes for Li

Malovichko, Galina

234

Real-time observation of lithium fibers growth inside a nanoscale lithium-ion battery  

E-Print Network [OSTI]

to observe the real-time nucleation and growth of the lithium fibers inside a nanoscale Li-ion battery. Our needed for safe and high power Li-ion batteries. VC 2011 American Institute of Physics. [doi:10Real-time observation of lithium fibers growth inside a nanoscale lithium-ion battery Hessam

Endres. William J.

235

Development of Large Format Lithium Ion Cells with Higher Energy...  

Broader source: Energy.gov (indexed) [DOE]

Large Format Lithium Ion Cells with Higher Energy Density Development of Large Format Lithium Ion Cells with Higher Energy Density 2013 DOE Hydrogen and Fuel Cells Program and...

236

ALS Technique Gives Novel View of Lithium Battery Dendrite Growth  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

ALS Technique Gives Novel View of Lithium Battery Dendrite Growth Print Lithium-ion batteries, popular in today's electronic devices and electric vehicles, could gain significant...

237

Secretary Chu Celebrates Expansion of Lithium-Ion Battery Production...  

Office of Environmental Management (EM)

Celebrates Expansion of Lithium-Ion Battery Production in North Carolina Secretary Chu Celebrates Expansion of Lithium-Ion Battery Production in North Carolina July 26, 2011 -...

238

Interface Modifications by Anion Acceptors for High Energy Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Modifications by Anion Acceptors for High Energy Lithium Ion Batteries. Interface Modifications by Anion Acceptors for High Energy Lithium Ion Batteries. Abstract: Li-rich, Mn-rich...

239

EV Everywhere Batteries Workshop - Next Generation Lithium Ion...  

Energy Savers [EERE]

Next Generation Lithium Ion Batteries Breakout Session Report EV Everywhere Batteries Workshop - Next Generation Lithium Ion Batteries Breakout Session Report Breakout session...

240

Linking Ion Solvation and Lithium Battery Electrolyte Properties...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Linking Ion Solvation and Lithium Battery Electrolyte Properties Linking Ion Solvation and Lithium Battery Electrolyte Properties 2010 DOE Vehicle Technologies and Hydrogen...

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Molecular Structure and Stability of Dissolved Lithium Polysulfide...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Stability of Dissolved Lithium Polysulfide Species. Molecular Structure and Stability of Dissolved Lithium Polysulfide Species. Abstract: Ability to predict the solubility and...

242

Designing Silicon Nanostructures for High Energy Lithium Ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Designing Silicon Nanostructures for High Energy Lithium Ion Battery Anodes Designing Silicon Nanostructures for High Energy Lithium Ion Battery Anodes 2012 DOE Hydrogen and Fuel...

243

Celgard US Manufacturing Facilities Initiative for Lithium-ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Celgard US Manufacturing Facilities Initiative for Lithium-ion Battery Separator Celgard US Manufacturing Facilities Initiative for Lithium-ion...

244

New lithium-based ionic liquid electrolytes that resist salt...  

Energy Savers [EERE]

lithium-based ionic liquid electrolytes that resist salt concentration polarization New lithium-based ionic liquid electrolytes that resist salt concentration polarization...

245

EV Everywhere Batteries Workshop - Beyond Lithium Ion Breakout...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Beyond Lithium Ion Breakout Session Report EV Everywhere Batteries Workshop - Beyond Lithium Ion Breakout Session Report Breakout session presentation for the EV Everywhere Grand...

246

Examining Hysteresis in Lithium- and Manganese-Rich Composite...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Hysteresis in Lithium- and Manganese-Rich Composite Cathode Materials Examining Hysteresis in Lithium- and Manganese-Rich Composite Cathode Materials 2013 DOE Hydrogen and Fuel...

247

Addressing the Voltage Fade Issue with Lithium-Manganese-Rich...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials 2013 DOE...

248

Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

15eswise2012p.pdf More Documents & Publications Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production Expansion of Novolyte Capacity for Lithium Ion Electrolyte...

249

Manipulating the Surface Reactions in Lithium Sulfur Batteries...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode Structures. Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode...

250

Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

15eswise2011p.pdf More Documents & Publications Expansion of Novolyte Capacity for Lithium Ion Electrolyte Production Expansion of Novolyte Capacity for Lithium Ion Electrolyte...

251

Addressing the Voltage Fade Issue with Lithium-Manganese-Rich...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials Addressing the Voltage Fade Issue with Lithium-Manganese-Rich Oxide Cathode Materials 2012 DOE Hydrogen and...

252

Diagnostic Studies on Lithium Battery Cells and Cell Components...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Studies on Lithium Battery Cells and Cell Components Diagnostic Studies on Lithium Battery Cells and Cell Components 2012 DOE Hydrogen and Fuel Cells Program and Vehicle...

253

Development of High Energy Lithium Batteries for Electric Vehicles...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Lithium Batteries for Electric Vehicles Development of High Energy Lithium Batteries for Electric Vehicles 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program...

254

Vehicle Technologies Office Merit Review 2014: High Energy Lithium...  

Broader source: Energy.gov (indexed) [DOE]

High Energy Lithium Batteries for PHEV Applications Vehicle Technologies Office Merit Review 2014: High Energy Lithium Batteries for PHEV Applications Presentation given by...

255

Additives and Cathode Materials for High-Energy Lithium Sulfur...  

Broader source: Energy.gov (indexed) [DOE]

Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries 2013 DOE Hydrogen and Fuel Cells...

256

Development of Polymer Electrolytes for Advanced Lithium Batteries...  

Broader source: Energy.gov (indexed) [DOE]

Development of Polymer Electrolytes for Advanced Lithium Batteries Development of Polymer Electrolytes for Advanced Lithium Batteries 2013 DOE Hydrogen and Fuel Cells Program and...

257

Thermodynamic Investigations of Lithium- and Manganese-Rich Transition...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Thermodynamic Investigations of Lithium- and Manganese-Rich Transition Metal Oxides Thermodynamic Investigations of Lithium- and Manganese-Rich Transition Metal Oxides 2013 DOE...

258

Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage...  

Energy Savers [EERE]

Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage (October 2012) Fact Sheet: Lithium-Ion Batteries for Stationary Energy Storage (October 2012) DOE's Energy Storage...

259

Optimization of mesoporous carbon structures for lithium&ndash...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

mesoporous carbon structures for lithium–sulfur battery applications. Optimization of mesoporous carbon structures for lithium–sulfur battery applications. Abstract:...

260

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Hierarchically Porous Graphene as a Lithium-Air Battery Electrode. Abstract: Functionalized graphene sheets (FGS)...

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Exploring the interaction between lithium ion and defective graphene...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Exploring the interaction between lithium ion and defective graphene surface using dispersion corrected DFT studies. Exploring the interaction between lithium ion and defective...

262

Electrode materials and lithium battery systems  

DOE Patents [OSTI]

A material comprising a lithium titanate comprising a plurality of primary particles and secondary particles, wherein the average primary particle size is about 1 nm to about 500 nm and the average secondary particle size is about 1 .mu.m to about 4 .mu.m. In some embodiments the lithium titanate is carbon-coated. Also provided are methods of preparing lithium titanates, and devices using such materials.

Amine, Khalil (Downers Grove, IL); Belharouak, Ilias (Westmont, IL); Liu, Jun (Naperville, IL)

2011-06-28T23:59:59.000Z

263

Lithium Metal Anodes for Rechargeable Batteries  

SciTech Connect (OSTI)

Rechargeable lithium metal batteries have much higher energy density than those of lithium ion batteries using graphite anode. Unfortunately, uncontrollable dendritic lithium growth inherent in these batteries (upon repeated charge/discharge cycling) and limited Coulombic efficiency during lithium deposition/striping has prevented their practical application over the past 40 years. With the emerging of post Li-ion batteries, safe and efficient operation of lithium metal anode has become an enabling technology which may determine the fate of several promising candidates for the next generation of energy storage systems, including rechargeable Li-air battery, Li-S battery, and Li metal battery which utilize lithium intercalation compounds as cathode. In this work, various factors which affect the morphology and Coulombic efficiency of lithium anode will be analyzed. Technologies used to characterize the morphology of lithium deposition and the results obtained by modeling of lithium dendrite growth will also be reviewed. At last, recent development in this filed and urgent need in this field will also be discussed.

Xu, Wu; Wang, Jiulin; Ding, Fei; Chen, Xilin; Nasybulin, Eduard N.; Zhang, Yaohui; Zhang, Jiguang

2014-02-28T23:59:59.000Z

264

ORNL microscopy directly images problematic lithium dendrites...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

865.574.7308 ORNL microscopy directly images problematic lithium dendrites in batteries ORNL electron microscopy captured the first real-time nanoscale images of the nucleation and...

265

Block copolymer electrolytes for lithium batteries  

E-Print Network [OSTI]

connecting to the solid-state lithium battery. c. An opticalbattery (discounting packaging, tabs, etc. ) demonstrate the advantage of the solid-state

Hudson, William Rodgers

2011-01-01T23:59:59.000Z

266

Ternary compound electrode for lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and of light weight. One type of lithium-based cell utilizes a molten salt electrolyte and normally is operated in the temperature range of about 350.degree.-500.degree. C. Such high temperature operation accelerates corrosion problems. The present invention provides an electrochemical cell in which lithium is the electroactive species. The cell has a positive electrode which includes a ternary compound generally represented as Li-M-O, wherein M is a transition metal. Corrosion of the inventive cell is considerably reduced.

Raistrick, Ian D. (Menlo Park, CA); Godshall, Ned A. (Stanford, CA); Huggins, Robert A. (Stanford, CA)

1982-01-01T23:59:59.000Z

267

Ternary compound electrode for lithium cells  

DOE Patents [OSTI]

Lithium-based cells are promising for applications such as electric vehicles and load-leveling for power plants since lithium is very electropositive and of light weight. One type of lithium-based cell utilizes a molten salt electrolyte and normally is operated in the temperature range of about 350 to 500/sup 0/C. Such high temperature operation accelerates corrosion problems. The present invention provides an electrochemical cell in which lithium is the electroactive species. The cell has a positive electrode which includes a ternary compound generally represented as Li-M-O, wherein M is a transition metal. Corrosion of the inventive cell is considerably reduced.

Raistrick, I.D.; Godshall, N.A.; Huggins, R.A.

1980-07-30T23:59:59.000Z

268

Categorical Exclusion 4577: Lithium Isotope Separation & Enrichment...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

This is entirely a paper study. The scope of this Cooperative Rssearch and development (CRADA) is to: 1) systematically review existing potential lithium enrichment processes, 2)...

269

High-capacity hydrogen storage in lithium and sodium amidoboranes...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Ir-based catalysts or ionic liquids.4-6 Some work has focused on modifying the thermodynamics of ‘stable’ hydrides with additives that stabilize the dehydrogenated...

270

Electrolytes for lithium ion batteries  

DOE Patents [OSTI]

A family of electrolytes for use in a lithium ion battery. The genus of electrolytes includes ketone-based solvents, such as, 2,4-dimethyl-3-pentanone; 3,3-dimethyl 2-butanone(pinacolone) and 2-butanone. These solvents can be used in combination with non-Lewis Acid salts, such as Li.sub.2[B.sub.12F.sub.12] and LiBOB.

Vaughey, John; Jansen, Andrew N.; Dees, Dennis W.

2014-08-05T23:59:59.000Z

271

Solid polymer electrolyte lithium batteries  

DOE Patents [OSTI]

This invention pertains to Lithium batteries using Li ion (Li[sup +]) conductive solid polymer electrolytes composed of solvates of Li salts immobilized in a solid organic polymer matrix. In particular, this invention relates to Li batteries using solid polymer electrolytes derived by immobilizing solvates formed between a Li salt and an aprotic organic solvent (or mixture of such solvents) in poly(vinyl chloride). 3 figures.

Alamgir, M.; Abraham, K.M.

1993-10-12T23:59:59.000Z

272

Solid polymer electrolyte lithium batteries  

DOE Patents [OSTI]

This invention pertains to Lithium batteries using Li ion (Li.sup.+) conductive solid polymer electrolytes composed of solvates of Li salts immobilized in a solid organic polymer matrix. In particular, this invention relates to Li batteries using solid polymer electrolytes derived by immobilizing solvates formed between a Li salt and an aprotic organic solvent (or mixture of such solvents) in poly(vinyl chloride).

Alamgir, Mohamed (Dedham, MA); Abraham, Kuzhikalail M. (Needham, MA)

1993-01-01T23:59:59.000Z

273

Materials Down-selection Decisions Made within the DOE Metal Hydride Center of Excellence (MHCoE) - September-October 2007  

Fuel Cell Technologies Publication and Product Library (EERE)

Reports on which hydrogen storage materials offer potential for further research as decided by DOE's Metal Hydride Center of Excellence.

274

XPS analysis of lithium surface and modification of surface state for uniform deposition of lithium  

SciTech Connect (OSTI)

The surface modification of lithium deposited at various current densities in propylene carbonate containing 1.0 ml dm{sup {minus}3} LiClO{sub 4} was performed by addition of various amounts of HF into the electrolyte, in order to investigate the effect of the HF addition on the surface reaction of lithium. XPS and SEM analyses showed that the surface state of lithium was influenced by the concentration of HF and the electrodeposition current. These two parameters are related to the chemical reaction rate of the lithium surface with HF and the electrodeposition rate of lithium, respectively. The surface modification was highly effective in suppressing lithium dendrite formation when the chemical reaction rate with HF was greater than the electrochemical deposition rate of lithium.

Kanamura, K.; Shiraishi, S.; Takehara, Z. [Kyoto Univ. (Japan)

1995-12-31T23:59:59.000Z

275

URANIUM METAL POWDER PRODUCTION, PARTICLE DISTRIBUTION ANALYSIS, AND REACTION RATE STUDIES OF A HYDRIDE-DEHYDRIDE PROCESS  

E-Print Network [OSTI]

atmosphere to reduce sample oxidation .................................................................................................. 13 12 Aluminum oxide crucible located at the bottom of the hydride-dehydride rig. ... 14 13 Furnace and furnace... at 60 minutes, 5psig, 250?C hydride, 325?C dehydride ................................................................................................... 30 27 Rotary kiln designed at ORNL for use in voloxidation...

Sames, William

2011-08-08T23:59:59.000Z

276

Lithium electric dipole polarizability M. Puchalski  

E-Print Network [OSTI]

Lithium electric dipole polarizability M. Puchalski Faculty of Chemistry, Adam Mickiewicz, 00-681 Warsaw, Poland The electric dipole polarizability of the lithium atom in the ground state phenomena, such as van der Waals interactions in ultra-cold collisions [1­3] and Bose- Einstein condensation

Pachucki, Krzysztof

277

Jeff Chamberlain on Lithium-air batteries  

ScienceCinema (OSTI)

Jeff Chamberlain, technology transfer expert at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries. More information at http://www.anl.gov/Media_Center/News/2009/batteries090915.html

Chamberlain, Jeff

2013-04-19T23:59:59.000Z

278

Jeff Chamberlain on Lithium-air batteries  

SciTech Connect (OSTI)

Jeff Chamberlain, technology transfer expert at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries. More information at http://www.anl.gov/Media_Center/News/2009/batteries090915.html

Chamberlain, Jeff

2009-01-01T23:59:59.000Z

279

Michael Thackeray on Lithium-air Batteries  

ScienceCinema (OSTI)

Michael Thackeray, Distinguished Fellow at Argonne National Laboratory, speaks on the new technology Lithium-air batteries, which could potentially increase energy density by 5-10 times over lithium-ion batteries. More information at http://www.anl.gov/Media_Center/News/2009/batteries090915.html

Thackeray, Michael

2013-04-19T23:59:59.000Z

280

Bimetallic Cathode Materials for Lithium Based Batteries  

E-Print Network [OSTI]

Bimetallic Cathode Materials for Lithium Based Batteries Frontiers in Materials Science Seminar / Chemistryg g g g g y University at Buffalo ­ The State University of New York (SUNY) Abstract Batteries for implantable cardiac defibrillators (ICDs) are based on the Lithium/Silver vanadium oxide (SVO, Ag2V4O11

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Titanium tritide radioisotope heat source development : palladium-coated titanium hydriding kinetics and tritium loading tests.  

SciTech Connect (OSTI)

We have found that a 180 nm palladium coating enables titanium to be loaded with hydrogen isotopes without the typical 400-500 C vacuum activation step. The hydriding kinetics of Pd coated Ti can be described by the Mintz-Bloch adherent film model, where the rate of hydrogen absorption is controlled by diffusion through an adherent metal-hydride layer. Hydriding rate constants of Pd coated and vacuum activated Ti were found to be very similar. In addition, deuterium/tritium loading experiments were done on stacks of Pd coated Ti foil in a representative-size radioisotope heat source vessel. The experiments demonstrated that such a vessel could be loaded completely, at temperatures below 300 C, in less than 10 hours, using existing department-of-energy tritium handling infrastructure.

Van Blarigan, Peter; Shugard, Andrew D.; Walters, R. Tom (Savannah River National Labs, Aiken, SC)

2012-01-01T23:59:59.000Z

282

High Density Hydrogen Storage System Demonstration Using NaAlH4 Based Complex Compound Hydrides  

SciTech Connect (OSTI)

This final report describes the motivations, activities and results of the hydrogen storage independent project "High Density Hydrogen Storage System Demonstration Using NaAlH4 Based Complex Compound Hydrides" performed by the United Technologies Research Center under the Department of Energy Hydrogen Program, contract # DE-FC36-02AL67610. The objectives of the project were to identify and address the key systems technologies associated with applying complex hydride materials, particularly ones which differ from those for conventional metal hydride based storage. This involved the design, fabrication and testing of two prototype systems based on the hydrogen storage material NaAlH4. Safety testing, catalysis studies, heat exchanger optimization, reaction kinetics modeling, thermochemical finite element analysis, powder densification development and material neutralization were elements included in the effort.

Daniel A. Mosher; Xia Tang; Ronald J. Brown; Sarah Arsenault; Salvatore Saitta; Bruce L. Laube; Robert H. Dold; Donald L. Anton

2007-07-27T23:59:59.000Z

283

NSTX Liquid Lithium Divertor (LLD) Design Status and Plans  

E-Print Network [OSTI]

NSTX Liquid Lithium Divertor (LLD) Design Status and Plans Office of Science H. W. Kugel, PPPL Design Status and Plans (Kugel) 2July 28, 2008 Motivation for NSTX Lithium Research · NSTX research with solid lithium is aimed initially towards using liquid lithium to control density, edge collisionality

Princeton Plasma Physics Laboratory

284

Intense Lithium Streams in Tokamaks 1 Leonid E. Zakharov,  

E-Print Network [OSTI]

Intense Lithium Streams in Tokamaks 1 Leonid E. Zakharov, Princeton University, Princeton Plasma. Temperature of the streams. 2. Lithium jets. 3. Injection into vacuum chamber. 4. Propulsion inside the vacuum chamber. 5. Stability of the lithium streams. 6. Expulsion of the lithium. 7. Summary. PRINCETON PLASMA

Zakharov, Leonid E.

285

Impact of Lithium Availability on Vehicle Electrification (Presentation)  

SciTech Connect (OSTI)

This presentation discusses the relationship between electric drive vehicles and the availability of lithium.

Neubauer, J.

2011-07-01T23:59:59.000Z

286

Lithium Iron Phosphate Composites for Lithium Batteries | Argonne National  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: VegetationEquipment Surfaces and Interfaces Sample6, 2011Liisa O'NeillFuelsLaboratory Lithium Iron

287

Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure. Dendrite-Free Lithium Deposition with Self-Aligned Nanorod Structure. Abstract: Suppressing lithium (Li)...

288

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

the lithium- transition metal electrostatic interaction. Thecation electrostatic interactions. 1 Lithium ions occupy theinteractions or by inhibiting the complete removal of lithium

Wilcox, James D.

2010-01-01T23:59:59.000Z

289

Design Principles for the Use of Electroactive Polymers for Overcharge Protection of Lithium-Ion Batteries  

E-Print Network [OSTI]

Modeling of Lithium Batteries. Kluwer Academic Publishers,of interest for lithium batteries. Therefore, we can use y =and J. Newman, Advances in Lithium-Ion Batteries, ch.

Thomas-Alyea, Karen E.; Newman, John; Chen, Guoying; Richardson, Thomas J.

2005-01-01T23:59:59.000Z

290

Studies of ionic liquids in lithium-ion battery test systems  

E-Print Network [OSTI]

are not useful for lithium batteries. We are therefore nowapplications using lithium batteries, we must be sure thattemperature range. For lithium batteries in hybrid vehicles,

Salminen, Justin; Prausnitz, John M.; Newman, John

2006-01-01T23:59:59.000Z

291

Characterization of an Electroactive Polymer for Overcharge Protection in Secondary Lithium Batteries  

E-Print Network [OSTI]

Protection in Secondary Lithium Batteries Guoying Chen,protection agents in lithium batteries is relatively new,in rechargeable lithium batteries with a variety of

Chen, Guoying; Thomas-Alyea, Karen E.; Newman, John; Richardson, Thomas J.

2005-01-01T23:59:59.000Z

292

Performance Characteristics of Lithium-ion Batteries of Various Chemistries for Plug-in Hybrid Vehicles  

E-Print Network [OSTI]

the manufacture of lithium batteries (References 2 and 3).Characteristics of Lithium-ion Batteries of VariousAdvisor utilizing lithium-ion batteries of the different

Burke, Andrew; Miller, Marshall

2009-01-01T23:59:59.000Z

293

Synthesis and Characterization of Simultaneous Electronic and Ionic Conducting Block Copolymers for Lithium Battery Electrodes  

E-Print Network [OSTI]

Protection in Secondary Lithium Batteries. Electrochim. ActaFacing Rechargeable Lithium Batteries. Nature 2001, 414,for Rechargeable Lithium Batteries Using Electroactive

Patel, Shrayesh

2013-01-01T23:59:59.000Z

294

A Failure and Structural Analysis of Block Copolymer Electrolytes for Rechargeable Lithium Metal Batteries  

E-Print Network [OSTI]

for Rechargeable Lithium Metal Batteries By Gregory Michaelfor Rechargeable Lithium Metal Batteries by Gregory Michaelin rechargeable lithium metal batteries. The block copolymer

Stone, Gregory Michael

2012-01-01T23:59:59.000Z

295

Surface reconstruction and chemical evolution of stoichiometric layered cathode materials for lithium-ion batteries  

E-Print Network [OSTI]

Layered Oxides for Lithium Batteries. Nano Lett. 13, 3857–O 2 Cathode Material in Lithium Ion Batteries. Adv. Energydecomposition in lithium ion batteries: first-principles

Lin, Feng

2014-01-01T23:59:59.000Z

296

Layered manganese oxide intergrowth electrodes for rechargeable lithium batteries: Part 1-substitution with Co or Ni  

E-Print Network [OSTI]

Cathode Materials for Lithium Batteries, 2003, Massachusettsfor Rechargeable Lithium Batteries: Part 1-Substitution withelectrode materials for lithium batteries because of their

Dolle, Mickael; Patoux, Sebastien; Doeff, Marca M.

2004-01-01T23:59:59.000Z

297

Performance, Charging, and Second-use Considerations for Lithium Batteries for Plug-in Electric Vehicles  

E-Print Network [OSTI]

Considerations for Lithium Batteries for Plug-in Electricfast charging of the lithium batteries should be possiblefast charging of the lithium batteries will be is possible

Burke, Andrew

2009-01-01T23:59:59.000Z

298

Overcharge Protection for 4 V Lithium Batteries at High Rates and Low Temperature  

E-Print Network [OSTI]

Protection for 4 V Lithium Batteries at High Rates and LowIntroduction Rechargeable lithium batteries are known forfor rechargeable lithium batteries. When impregnated into a

Chen, Guoying

2010-01-01T23:59:59.000Z

299

Cu2Sb thin film electrodes prepared by pulsed laser deposition f or lithium batteries  

E-Print Network [OSTI]

Laser Deposition for Lithium Batteries Seung-Wan Song, a, *in rechargeable lithium batteries. Introduction Sb-in rechargeable lithium batteries. Two advantages of

Song, Seung-Wan; Reade, Ronald P.; Cairns, Elton J.; Vaughey, Jack T.; Thackeray, Michael M.; Striebel, Kathryn A.

2003-01-01T23:59:59.000Z

300

Method and composition in which metal hydride particles are embedded in a silica network  

DOE Patents [OSTI]

A silica embedded metal hydride composition and a method for making such a composition. The composition is made via the following process: A quantity of fumed silica is blended with water to make a paste. After adding metal hydride particles, the paste is dried to form a solid. According to one embodiment of the invention, the solid is ground into granules for use of the product in hydrogen storage. Alternatively, the paste can be molded into plates or cylinders and then dried for use of the product as a hydrogen filter. Where mechanical strength is required, the paste can be impregnated in a porous substrate or wire network.

Heung, Leung K. (Aiken, SC)

1999-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides  

E-Print Network [OSTI]

J. Am. Chem. SOC.1991, 113,9575-9585 9575 Mixed Aggregation of Lithium Enolates and Lithium Halides with Lithium 2,2,6,6-Tetramethylpiperidide(LiTMP) Patricia L. Hall, James H. Gilchrist, Aidan T. Harrison]-lithiumdi-tert-butylamide and conformationally locked [6Li]-lithium2,2,4,6,6-pentamethylpiperidide shed further light

Collum, David B.

302

Phostech Lithium | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth'sOklahoma/GeothermalOrangePeru: Energy ResourcesPhilippines:SanPhostech Lithium

303

Lithium abundances in exoplanet-hosts stars  

E-Print Network [OSTI]

Exoplanet-host stars (EHS) are known to present surface chemical abundances different from those of stars without any detected planet (NEHS). EHS are, on the average, overmetallic compared to the Sun. The observations also show that, for cool stars, lithium is more depleted in EHS than in NEHS. The overmetallicity of EHS may be studied in the framework of two different scenarii. We have computed main sequence stellar models with various masses, metallicities and accretion rates. The results show different profiles for the lithium destruction according to the scenario. We compare these results to the spectroscopic observations of lithium.

M. Castro; S. Vauclair; O. Richard; N. C. Santos

2008-03-20T23:59:59.000Z

304

Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl Carbamates: Role of  

E-Print Network [OSTI]

Lithium Diisopropylamide-Mediated Ortholithiation and Anionic Fries Rearrangement of Aryl of the lithium diisopropylamide (LDA)-mediated anionic Fries rearrangements of aryl carbamates are described, an LDA-lithium phenolate mixed dimer, and homoaggregated lithium phenolates. The highly insoluble

Collum, David B.

305

Mathematical Modelling of a Metal Hydride Hydrogen Storage System Brendan David MacDonald  

E-Print Network [OSTI]

Mathematical Modelling of a Metal Hydride Hydrogen Storage System by Brendan David MacDonald B of MASTER OF APPLIED SCIENCE in the Department of Mechanical Engineering © Brendan David MacDonald, 2006 Hydrogen Storage System by Brendan David MacDonald B.A.Sc., University of Waterloo, 2004 Supervisory

Victoria, University of

306

A non-isothermal model of a nickelmetal hydride cell , M. Mohammedb  

E-Print Network [OSTI]

) to avoid oxygen gas generation during over discharge and has extra capacity to avoid hydrogen gas generation during over- charge. Since the metal hydride material gradually loses capacity through usage due. The side reaction at the positive electrode is oxygen evolu- tion and at the negative electrode oxygen

307

Friction Stir Welding of Hydrided Titanium Alloys Mark Taylor, D.P. Field  

E-Print Network [OSTI]

Friction Stir Welding of Hydrided Titanium Alloys Mark Taylor, D.P. Field Multi-Scale Engineering for Undergraduates program under grant number EEC-0754370 During Friction Stir Welding (FSW), a non-consumable tool-state welding process, much frictional heating and force is required of the tool. This steep demand on the tool

Collins, Gary S.

308

A PROTOTYPE FOUR INCH SHORT HYDRIDE (FISH) BED AS A REPLACEMENT TRITIUM STORAGE BED  

SciTech Connect (OSTI)

The Savannah River Site (SRS) tritium facilities have used 1st generation (Gen1) metal hydride storage bed assemblies with process vessels (PVs) fabricated from 3 inch nominal pipe size (NPS) pipe to hold up to 12.6 kg of LaNi{sub 4.25}Al{sub 0.75} metal hydride for tritium gas absorption, storage, and desorption for over 15 years. The 2nd generation (Gen2) of the bed design used the same NPS for the PV, but the added internal components produced a bed nominally 1.2 m long, and presented a significant challenge for heater cartridge replacement in a footprint limited glove-box. A prototype 3rd generation (Gen3) metal hydride storage bed has been designed and fabricated as a replacement candidate for the Gen2 storage bed. The prototype Gen3 bed uses a PV pipe diameter of 4 inch NPS so the bed length can be reduced below 0.7 m to facilitate heater cartridge replacement. For the Gen3 prototype bed, modeling results show increased absorption rates when using hydrides with lower absorption pressures. To improve absorption performance compared to the Gen2 beds, a LaNi{sub 4.15}Al{sub 0.85} material was procured and processed to obtain the desired pressure-composition-temperature (PCT) properties. Other bed design improvements are also presented.

Klein, J.; Estochen, E.; Shanahan, K.; Heung, L.

2011-02-23T23:59:59.000Z

309

Hydrogen Internal Combustion Engine Two Wheeler with on-board Metal Hydride Storage  

E-Print Network [OSTI]

be obtained from sources such as electrolysis using low cost electricity, hydrogen as a by of cost- effective hydrogen in India (which we chose as a test case) is not a barrier. Thus, in the nearHydrogen Internal Combustion Engine Two Wheeler with on-board Metal Hydride Storage K. Sapru*, S

310

The influence of hydride blisters on the fracture of Zircaloy-4 O.N. Pierron a  

E-Print Network [OSTI]

.elsevier.com/locate/jnucmat Journal of Nuclear Materials 322 (2003) 21­35 #12;hydrogen embrittlement [15]. Such an effect becomes, and radiation damage [1]. As the cladding undergoes oxidation with the associated hydrogen pickup, the total amount of hydrogen increases, and hydride precipitates form pref- erentially near the outer (cooler

Motta, Arthur T.

311

X-ray Absorption Spectroscopy of Transition Metal-Magnesium Hydride Thin Films  

E-Print Network [OSTI]

X-ray Absorption Spectroscopy of Transition Metal-Magnesium Hydride Thin Films T. J. Richardsona@lbl.gov Abstract Mixed metal thin films containing magnesium and a first-row transition element exhibit very large and coordination of the magnesium and transition metal atoms during hydrogen absorption were studied using dynamic

312

Observations of proton beam enhancement due to erbium hydride on gold foil targets  

SciTech Connect (OSTI)

Recent theoretical work suggests that the conversion efficiency from laser to protons in laser irradiated thin foil experiments increases if the atomic mass of nonhydrogen atoms on the foil rear surface increases. Experiments were performed at the Lawrence Livermore National Laboratory Jupiter Laser Facility to observe the effect of thin foils coated with erbium hydride on the conversion efficiency from laser to protons. Gold foils with and without the rear surface coated with ErH{sub 3} were irradiated using the ultrashort pulse, 40 TW Callisto laser. An argon-ion etching system was used to remove naturally occurring nanometer thick surface layer contaminants from the hydride. With the etcher, gold with ErH{sub 3} showed a 25% increase in the conversion efficiency to protons above 3.4 MeV relative to contaminants, where C{sup +4} and H{sup +} were the dominant ion species. No difference in the ion signal was observed without first cleaning the hydrides. Simulations using the hybrid PIC code, LSP, revealed that the increase due to erbium hydride versus contaminants is 37% for protons above 3 MeV.

Offermann, D. T.; Van Woerkom, L. D. [Department of Physics, Ohio State University, Columbus, Ohio 43210 (United States); Freeman, R. R. [Department of Physics, Ohio State University, Columbus, Ohio 43210 (United States); Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, California 92093 (United States); Department of Applied Science, University of California Davis, Livermore, California 94550 (United States); Foord, M. E.; Hey, D.; Key, M. H.; Mackinnon, A. J.; MacPhee, A. G.; Patel, P. K.; Ping, Y.; Sanchez, J. J.; Shen, N. [Lawrence Livermore National Laboratory, Livermore, California 94550 (United States); Bartal, T.; Beg, F. N. [Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, California 92093 (United States); Espada, L. [Sandia National Laboratory, Albuquerque, New Mexico 87185 (United States); Chen, C. D. [Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States)

2009-09-15T23:59:59.000Z

313

Evaluation of Protected Metal Hydride Slurries in a H2 Mini-  

E-Print Network [OSTI]

Evaluation of Protected Metal Hydride Slurries in a H2 Mini- Grid TIAX, LLC Acorn Park Cambridge_MERIT_REVIEW_MAY2003 2 Introduction Hydrogen Mini-Grid Concept Distributed FCPS utilizing a H2 Mini-Grid can provide waste heat can be used for hot water or space heating in buildings (i.e. "cogen") Distributed FCPS

314

First Principles Studies of Phase Stability and Reaction Dynamics in Complex Metal Hydrides  

SciTech Connect (OSTI)

Complex metal hydrides are believed to be one of the most promising materials for developing hydrogen storage systems that can operate under desirable conditions. At the same time, these are also a class of materials that exhibit intriguing properties. We have used state-of-the-art computational techniques to study the fundamental properties of these materials.

Chou, Mei-Yin

2014-09-29T23:59:59.000Z

315

Complex Hydrides for Hydrogen Storage Darlene K. Slattery and Michael D. Hampton  

E-Print Network [OSTI]

at a temperature of less than 100 o C in order to be compatible with fuel cells and must have an installed hydrogen have reported the discovery of a number of catalysts that improve the reversing of the hydrogen release the hydrogenation/dehydrogenation of sodium aluminum hydride. Mechanical incorporation of the catalyst

316

Effect of gold-nickel metallization microstructure on fluxless soldering  

SciTech Connect (OSTI)

Gold plating is used in the microelectronics industry to maintain the wettability of metal substrates. The nature of wetting during soldering of gold plated metals is discussed, and the results of experiments on the fluxless wettability and oxidation of gold plated nickel are described. The results suggest that electrodeposition of a thin gold plate (0.14 [mu]m) and the concurrent reduction of nickel oxide produce a gold-nickel system which will wet without flux. Oxidation of nickel was observed to occur via nickel out-diffusion and by direct exposure of the substrate through pinhole plating defects. Auger chemical analysis indicates that pinholes do not produce oxidation of the surrounding substrate area. 20 refs., 10 figs.

Cinque, R.B.; Morris, J.W. Jr. (Lawrence Berkeley Lab., CA (United States) Univ. of California, Berkeley, CA (United States))

1994-06-01T23:59:59.000Z

317

Stabilization of Nickel Metal Catalysts for Aqueous Processing Systems -  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administrationcontroller systemsBiSiteNeutron Scattering4 By I. Tudosa,SpreadingStabilityEnergy

318

Finding Room for Improvement in Transition Metal Oxides Cathodes for Lithium-ion Batteries  

E-Print Network [OSTI]

Oxides Cathodes for Lithium-ion Batteries Kinson C. Kam andusing rechargeable lithium-ion batteries has become an

Kam, Kinson

2012-01-01T23:59:59.000Z

319

Lithium-cation conductivity and crystal structure of lithium diphosphate  

SciTech Connect (OSTI)

The electrical conductivity of lithium diphosphate Li{sub 4}P{sub 2}O{sub 7} has been measured and jump-like increasing of ionic conductivity at 913 K has been found. The crystal structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction at 300–1050 K. At 913 K low temperature triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one, space group P2{sub 1}/n, a=8.8261(4) Å, b=5.2028(4) Å, c=13.3119(2) Å, ?=104.372(6)°. The migration maps of Li{sup +} cations based on experimental data implemented into program package TOPOS have been explored. It was found that lithium cations in both low- and high temperature forms of Li{sub 4}P{sub 2}O{sub 7} migrate in three dimensions. Cross sections of the migrations channels extend as the temperature rises, but at the phase transition point have a sharp growth showing a strong “crystal structure – ion conductivity” correlation. -- Graphical abstract: Crystal structure of Li{sub 4}P{sub 2}O{sub 7} at 950 K. Red balls represent oxygen atoms; black lines show Li{sup +} ion migration channels in the layers perpendicular to [001] direction. Highlights: • Structure of Li{sub 4}P{sub 2}O{sub 7} has been refined using high temperature neutron diffraction. • At 913 K triclinic form of Li{sub 4}P{sub 2}O{sub 7} transforms into high temperature monoclinic one. • The migration maps of Li{sup +} implemented into program package TOPOS have been explored. • Cross sections of the migrations channels at the phase transition have a sharp growth.

Voronin, V.I., E-mail: voronin@imp.uran.ru [Institute of Metal Physics Urals Branch RAS, S.Kovalevskoy Street 18, 620041 Ekaterinburg (Russian Federation); Sherstobitova, E.A. [Institute of Metal Physics Urals Branch RAS, S.Kovalevskoy Street 18, 620041 Ekaterinburg (Russian Federation); Blatov, V.A., E-mail: blatov@samsu.ru [Samara Center for Theoretical Materials Science (SCTMS), Samara State University, Ac.Pavlov Street 1, 443011 Samara (Russian Federation); Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah 21589 (Saudi Arabia); Shekhtman, G.Sh., E-mail: shekhtman@ihte.uran.ru [Institute of High Temperature Electrochemistry Urals Branch RAS, Akademicheskaya 20, 620990 Ekaterinburg (Russian Federation)

2014-03-15T23:59:59.000Z

320

Threat of Hydride Re-orientation to Spent Fuel Integrity During Transportation Accidents: Myth or Reality?  

SciTech Connect (OSTI)

The source-term study conducted by Sandia National Laboratories nearly two decades ago for the spent fuel inventory known at the time, which was in the low-to-medium burnup range ({approx}35 GWd/MTU), showed that the effects of transportation accidents on spent fuel failures, and consequential radioactivity release to the environment, were relatively benign. However, with today's discharged fuel burnups routinely greater than 45 GWd/MTU, potential hydride reorientation during interim dry storage, and its effects on cladding properties, has become one of the primary concerns for spent fuel transportation. Laboratory tests of un-irradiated cladding specimens subjected to heat treatments promoting hydride dissolution followed by re-precipitation in the radial direction have shown that relatively moderate concentrations ({approx}70 ppm) of radial hydrides can significantly degrade cladding ductility, at least at room temperature. The absence of specific data that are relevant to high-burnup spent fuel under dry storage conditions have led to the conjecture, deduced from those tests, that massive cladding failures, possibly resulting in fuel reconfiguration, can be expected during cask drop events. Such conclusions are not borne out by the findings in this paper. The analysis results indicate that cladding failure is bi-modal: a state of failure initiation at the cladding ID remaining as part-wall damage with less than 2% probability of occurrence, and a through-wall failure at a probability of 1 E-5. These results indicate that spent fuel conditions that could promote the formation of radial hydrides during dry storage are not sufficient to produce radial hydrides concentrations of significant levels to cause major threat to spent fuel integrity. It is important to note in this regard that the through-wall cladding failure probability of 1 E-5 is of the same order of magnitude as calculated in the cited Sandia study for low burnup fuel. (authors)

Rashid, Joe [ANATECH, 5435 Oberlin Drive, San Diego, CA 92121 (United States); Machiels, Albert [EPRI, 3420 Hillview Avenue, Palo Alto, CA 94304 (United States)

2007-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Lithium ion battery with improved safety  

DOE Patents [OSTI]

A lithium battery with improved safety that utilizes one or more additives in the battery electrolyte solution wherein a lithium salt is dissolved in an organic solvent, which may contain propylene, carbonate. For example, a blend of 2 wt % triphenyl phosphate (TPP), 1 wt % diphenyl monobutyl phosphate (DMP) and 2 wt % vinyl ethylene carbonate additives has been found to significantly enhance the safety and performance of Li-ion batteries using a LiPF6 salt in EC/DEC electrolyte solvent. The invention relates to both the use of individual additives and to blends of additives such as that shown in the above example at concentrations of 1 to 4-wt % in the lithium battery electrolyte. This invention relates to additives that suppress gas evolution in the cell, passivate graphite electrode and protect it from exfoliating in the presence of propylene carbonate solvents in the electrolyte, and retard flames in the lithium batteries.

Chen, Chun-hua; Hyung, Yoo Eup; Vissers, Donald R.; Amine, Khalil

2006-04-11T23:59:59.000Z

322

Solid State Thin Film Lithium Microbatteries  

E-Print Network [OSTI]

Solid state thin film lithium microbatteries fabricated by pulsed-laser deposition (PLD) are suggested. During deposition the following process parameters must be considered, which are laser energy and fluence, laser pulse ...

Shi, Z.

323

NSTX Plasma Response to Lithium Coated Divertor  

SciTech Connect (OSTI)

NSTX experiments have explored lithium evaporated on a graphite divertor and other plasma facing components in both L- and H- mode confinement regimes heated by high-power neutral beams. Improvements in plasma performance have followed these lithium depositions, including a reduction and eventual elimination of the HeGDC time between discharges, reduced edge neutral density, reduced plasma density, particularly in the edge and the SOL, increased pedestal electron and ion temperature, improved energy confinement and the suppression of ELMs in the H-mode. However, with improvements in confinement and suppression of ELMs, there was a significant secular increase in the effective ion charge Zeff and the radiated power in H-mode plasmas as a result of increases in the carbon and medium-Z metallic impurities. Lithium itself remained at a very low level in the plasma core, <0.1%. Initial results are reported from operation with a Liquid Lithium Divertor (LLD) recently installed.

H.W. Kugel, M.G. Bell, J.P. Allain, R.E. Bell, S. Ding, S.P. Gerhardt, M.A. Jaworski, R. Kaita, J. Kallman, S.M. Kaye, B.P. LeBlanc, R. Maingi, R. Majeski, R. Maqueda, D.K. Mansfield, D. Mueller, R. Nygren, S.F. Paul, R. Raman, A.L. Roquemore, S.A. Sabbagh, H. Schneider, C.H. Skinner, V.A. Soukhanovskii, C.N. Taylor, J.R. Timberlak, W.R. Wampler, L.E. Zakharov, S.J. Zweben, and the NSTX Research Team

2011-01-21T23:59:59.000Z

324

Layered electrodes for lithium cells and batteries  

DOE Patents [OSTI]

Lithium metal oxide compounds of nominal formula Li.sub.2MO.sub.2, in which M represents two or more positively charged metal ions, selected predominantly and preferably from the first row of transition metals are disclosed herein. The Li.sub.2MO.sub.2 compounds have a layered-type structure, which can be used as positive electrodes for lithium electrochemical cells, or as a precursor for the in-situ electrochemical fabrication of LiMO.sub.2 electrodes. The Li.sub.2MO.sub.2 compounds of the invention may have additional functions in lithium cells, for example, as end-of-discharge indicators, or as negative electrodes for lithium cells.

Johnson, Christopher S. (Naperville, IL); Thackeray, Michael M. (Naperville, IL); Vaughey, John T. (Elmhurst, IL); Kahaian, Arthur J. (Chicago, IL); Kim, Jeom-Soo (Naperville, IL)

2008-04-15T23:59:59.000Z

325

Design and Simulation of Lithium Rechargeable Batteries  

E-Print Network [OSTI]

A New Rechargeable Plastic Li-Ion Battery," Lithium Batteryion battery developed at Bellcore in Red Bank, NJ.1-6 The experimental prototYpe cell has the configuration: Li

Doyle, C.M.

2010-01-01T23:59:59.000Z

326

Lithium Circuit Test Section Design and Fabrication  

SciTech Connect (OSTI)

The Early Flight Fission -- Test Facilities (EFF-TF) team has designed and built an actively pumped lithium flow circuit. Modifications were made to a circuit originally designed for NaK to enable the use of lithium that included application specific instrumentation and hardware. Component scale freeze/thaw tests were conducted to both gain experience with handling and behavior of lithium in solid and liquid form and to supply anchor data for a Generalized Fluid System Simulation Program (GFSSP) model that was modified to include the physics for freeze/thaw transitions. Void formation was investigated. The basic circuit components include: reactor segment, lithium to gas heat exchanger, electromagnetic (EM) liquid metal pump, load/drain reservoir, expansion reservoir, instrumentation, and trace heaters. This paper discusses the overall system design and build and the component testing findings.

Godfroy, Thomas; Garber, Anne; Martin, James [NASA Marshall Space Flight Center, Nuclear Systems Engineering Analysis, Huntsville, Alabama 35812 (United States)

2006-01-20T23:59:59.000Z

327

Electrode for a lithium cell  

DOE Patents [OSTI]

This invention relates to a positive electrode for an electrochemical cell or battery, and to an electrochemical cell or battery; the invention relates more specifically to a positive electrode for a non-aqueous lithium cell or battery when the electrode is used therein. The positive electrode includes a composite metal oxide containing AgV.sub.3O.sub.8 as one component and one or more other components consisting of LiV.sub.3O.sub.8, Ag.sub.2V.sub.4O.sub.11, MnO.sub.2, CF.sub.x, AgF or Ag.sub.2O to increase the energy density of the cell, optionally in the presence of silver powder and/or silver foil to assist in current collection at the electrode and to improve the power capability of the cell or battery.

Thackeray, Michael M. (Naperville, IL); Vaughey, John T. (Elmhurst, IL); Dees, Dennis W. (Downers Grove, IL)

2008-10-14T23:59:59.000Z

328

Predissociation dynamics of lithium iodide  

E-Print Network [OSTI]

The predissociation dynamics of lithium iodide (LiI) in the first excited A-state is investigated for molecules in the gas phase and embedded in helium nanodroplets, using femtosecond pump-probe photoionization spectroscopy. In the gas phase, the transient Li+ and LiI+ ion signals feature damped oscillations due to the excitation and decay of a vibrational wave packet. Based on high-level ab initio calculations of the electronic structure of LiI and simulations of the wave packet dynamics, the exponential signal decay is found to result from predissociation predominantly at the lowest avoided X-A potential curve crossing, for which we infer a coupling constant V=650(20) reciprocal cm. The lack of a pump-probe delay dependence for the case of LiI embedded in helium nanodroplets indicates fast droplet-induced relaxation of the vibrational excitation.

Schmidt, H; Stienkemeier, F; Bogomolov, A S; Baklanov, A V; Reich, D M; Skomorowski, W; Koch, C P; Mudrich, M

2015-01-01T23:59:59.000Z

329

Glass for sealing lithium cells  

DOE Patents [OSTI]

Glass compositions resistant to corrosion by lithium cell electrolyte and having an expansion coefficient of 45 to 85 x 10/sup -70/C/sup -1/ have been made with SiO/sub 2/, 25 to 55% by weight; B/sub 2/O/sub 3/, 5 to 12%; Al/sub 2/O/sub 3/, 12 to 35%; CaO, 5 to 15%; MgO, 5 to 15%; SrO, 0 to 10%; and La/sub 2/O/sub 3/, 0 to 5%. Preferred compositions within that range contain 3 to 8% SrO and 0.5 to 2.5% La/sub 2/O/sub 3/.

Leedecke, C.J.

1981-08-28T23:59:59.000Z

330

Rechargeable lithium-ion cell  

DOE Patents [OSTI]

The invention relates to a rechargeable lithium-ion cell, a method for its manufacture, and its application. The cell is distinguished by the fact that it has a metallic housing (21) which is electrically insulated internally by two half shells (15), which cover electrode plates (8) and main output tabs (7) and are composed of a non-conductive material, where the metallic housing is electrically insulated externally by means of an insulation coating. The cell also has a bursting membrane (4) which, in its normal position, is located above the electrolyte level of the cell (1). In addition, the cell has a twisting protection (6) which extends over the entire surface of the cover (2) and provides centering and assembly functions for the electrode package, which comprises the electrode plates (8).

Bechtold, Dieter (Bad Vilbel, DE); Bartke, Dietrich (Kelkheim, DE); Kramer, Peter (Konigstein, DE); Kretzschmar, Reiner (Kelkheim, DE); Vollbert, Jurgen (Hattersheim, DE)

1999-01-01T23:59:59.000Z

331

Nanostructured material for advanced energy storage : magnesium battery cathode development.  

SciTech Connect (OSTI)

Magnesium batteries are alternatives to the use of lithium ion and nickel metal hydride secondary batteries due to magnesium's abundance, safety of operation, and lower toxicity of disposal. The divalency of the magnesium ion and its chemistry poses some difficulties for its general and industrial use. This work developed a continuous and fibrous nanoscale network of the cathode material through the use of electrospinning with the goal of enhancing performance and reactivity of the battery. The system was characterized and preliminary tests were performed on the constructed battery cells. We were successful in building and testing a series of electrochemical systems that demonstrated good cyclability maintaining 60-70% of discharge capacity after more than 50 charge-discharge cycles.

Sigmund, Wolfgang M. (University of Florida, Gainesville, FL); Woan, Karran V. (University of Florida, Gainesville, FL); Bell, Nelson Simmons

2010-11-01T23:59:59.000Z

332

Thermal analysis of uranium zirconium hydride fuel using a lead-bismuth gap at LWR operating temperatures  

E-Print Network [OSTI]

Next generation nuclear technology calls for more advanced fuels to maximize the effectiveness of new designs. A fuel currently being studied for use in advanced light water reactors (LWRs) is uranium zirconium hydride ...

Ensor, Brendan M. (Brendan Melvin)

2012-01-01T23:59:59.000Z

333

Deproto-metallation using mixed lithium-zinc and lithium-copper bases and computed CH acidity of 2-substituted quinolines  

E-Print Network [OSTI]

Deproto-metallation using mixed lithium-zinc and lithium-copper bases and computed CH acidity of 2 corresponding iodo derivatives or 2-chlorophenyl ketones using the lithium-zinc or the lithium using the lithium-zinc base. With 3-pyridyl, 2-furyl and 2-thienyl substituents, the reaction took place

Boyer, Edmond

334

(Data in metric tons of contained lithium, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world, followed by China,  

E-Print Network [OSTI]

, but growing through the recycling of lithium batteries. Import Sources (1994-97): Chile, 96%; and other, 4 lithium salts from battery recycling and lithium hydroxide monohydrate from former Department of Energy102 LITHIUM (Data in metric tons of contained lithium, unless otherwise noted) Domestic Production

335

Mitigating Performance Degradation of High-Energy Lithium-Ion...  

Broader source: Energy.gov (indexed) [DOE]

Mitigating Performance Degradation of High-Energy Lithium-Ion Cells Mitigating Performance Degradation of High-Energy Lithium-Ion Cells 2013 DOE Hydrogen and Fuel Cells Program and...

336

Two Studies Reveal Details of Lithium-Battery Function  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Two Studies Reveal Details of Lithium-Battery Function Two Studies Reveal Details of Lithium-Battery Function Print Wednesday, 27 February 2013 00:00 Our way of life is deeply...

337

Novel Lithium Ion Anode Structures: Overview of New DOE BATT...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Lithium Ion Anode Structures: Overview of New DOE BATT Anode Projects Novel Lithium Ion Anode Structures: Overview of New DOE BATT Anode Projects 2011 DOE Hydrogen and Fuel Cells...

338

Molecular Structures of Polymer/Sulfur Composites for Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long Cycle Life. Molecular Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long...

339

Development of Large Format Lithium Ion Cells with Higher Energy...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Large Format Lithium Ion Cells with Higher Energy Density Exceeding 500WhL Development of Large Format Lithium Ion Cells with Higher Energy Density Exceeding 500WhL 2012 DOE...

340

Lithium-based inorganic-organic framework materials  

E-Print Network [OSTI]

This dissertation describes research into lithium-based inorganic-organic frameworks, which has led to an increased understanding of the structural diversity and properties of these materials. The crystal structures of 11 new forms of lithium...

Yeung, Hamish Hei-Man

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Shell Model for Atomistic Simulation of Lithium Diffusion in...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Shell Model for Atomistic Simulation of Lithium Diffusion in Mixed MnTi Oxides. Shell Model for Atomistic Simulation of Lithium Diffusion in Mixed MnTi Oxides. Abstract: Mixed...

342

Lithium-ion batteries having conformal solid electrolyte layers  

DOE Patents [OSTI]

Hybrid solid-liquid electrolyte lithium-ion battery devices are disclosed. Certain devices comprise anodes and cathodes conformally coated with an electron insulating and lithium ion conductive solid electrolyte layer.

Kim, Gi-Heon; Jung, Yoon Seok

2014-05-27T23:59:59.000Z

343

Direct Evidence of Lithium-Induced Atomic Ordering in Amorphous...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Evidence of Lithium-Induced Atomic Ordering in Amorphous TiO2 Nanotubes . Direct Evidence of Lithium-Induced Atomic Ordering in Amorphous TiO2 Nanotubes . Abstract: In this paper,...

344

Celgard US Manufacturing Facilities Initiative for Lithium-ion...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Initiative for Lithium-ion Battery Separator Celgard US Manufacturing Facilities Initiative for Lithium-ion Battery Separator FY 2012 Annual Progress Report for Energy Storage R&D...

345

Design of novel lithium storage materials with a polyanionic framework  

E-Print Network [OSTI]

Lithium ion batteries for large-scale applications demand a strict safety standard from a cathode material during operating cycles. Lithium manganese borate (LiMnBO?) that crystallizes into a hexagonal or monoclinic framework ...

Kim, Jae Chul, Ph. D. Massachusetts Institute of Technology

2014-01-01T23:59:59.000Z

346

Electrochemical Isotope Effect and Lithium Isotope Separation Jay R. Black,  

E-Print Network [OSTI]

results showing a large lithium isotope separation due to electrodeposition. The fractionation is tunable lithium were plated from solutions of 1 M LiClO4 in propylene carbonate (PC) on planar nickel electrodes

Mcdonough, William F.

347

LITHIUM--2002 46.1 By Joyce A. Ober  

E-Print Network [OSTI]

domestic producer of lithium carbonate from brine is Chemetall Foote's operation in Nevada. Nevada brines enriched in lithium chloride, which averaged about 300 parts per million (ppm) when Foote Mineral Co. (the

348

Lithium based electrochemical cell systems having a degassing agent  

DOE Patents [OSTI]

A lithium based electrochemical cell system includes a positive electrode; a negative electrode; an electrolyte; and a degassing agent.

Hyung, Yoo-Eup (Naperville, IL); Vissers, Donald R. (Naperville, IL); Amine, Khalil (Downers Grove, IL)

2012-05-01T23:59:59.000Z

349

Methods for making lithium vanadium oxide electrode materials  

DOE Patents [OSTI]

A method of making vanadium oxide formulations is presented. In one method of preparing lithium vanadium oxide for use as an electrode material, the method involves: admixing a particulate form of a lithium compound and a particulate form of a vanadium compound; jet milling the particulate admixture of the lithium and vanadium compounds; and heating the jet milled particulate admixture at a temperature below the melting temperature of the admixture to form lithium vanadium oxide.

Schutts, Scott M. (Menomonie, WI); Kinney, Robert J. (Woodbury, MN)

2000-01-01T23:59:59.000Z

350

Use of Solid Hydride Fuel for Improved long-Life LWR Core Designs  

SciTech Connect (OSTI)

The primary objective of this project was to assess the feasibility of improving the performance of PWR and BWR cores by using solid hydride fuels instead of the commonly used oxide fuel. The primary measure of performance considered is the bus-bar cost of electricity (COE). Additional performance measures considered are safety, fuel bundle design simplicity – in particular for BWR’s, and plutonium incineration capability. It was found that hydride fuel can safely operate in PWR’s and BWR’s without restricting the linear heat generation rate of these reactors relative to that attainable with oxide fuel. A couple of promising applications of hydride fuel in PWR’s and BWR’s were identified: (1) Eliminating dedicated water moderator volumes in BWR cores thus enabling to significantly increase the cooled fuel rods surface area as well as the coolant flow cross section area in a given volume fuel bundle while significantly reducing the heterogeneity of BWR fuel bundles thus achieving flatter pin-by-pin power distribution. The net result is a possibility to significantly increase the core power density – on the order of 30% and, possibly, more, while greatly simplifying the fuel bundle design. Implementation of the above modifications is, though, not straightforward; it requires a design of completely different control system that could probably be implemented only in newly designed plants. It also requires increasing the coolant pressure drop across the core. (2) Recycling plutonium in PWR’s more effectively than is possible with oxide fuel by virtue of a couple of unique features of hydride fuel – reduced inventory of U-238 and increased inventory of hydrogen. As a result, the hydride fuelled core achieves nearly double the average discharge burnup and the fraction of the loaded Pu it incinerates in one pass is double that of the MOX fuel. The fissile fraction of the Pu in the discharged hydride fuel is only ~2/3 that of the MOX fuel and the discharged hydride fuel is more proliferation resistant. Preliminary feasibility assessment indicates that by replacing some of the ZrH1.6 by ThH2 it will be possible to further improve the plutonium incineration capability of PWR’s. Other possibly promising applications of hydride fuel were identified but not evaluated in this work. A number of promising oxide fueled PWR core designs were also found as spin-offs of this study: (1) The optimal oxide fueled PWR core design features smaller fuel rod diameter of D=6.5 mm and a larger pitch-to-diameter ratio of P/D=1.39 than presently practiced by industry – 9.5mm and 1.326. This optimal design can provide a 30% increase in the power density and a 24% reduction in the cost of electricity (COE) provided the PWR could be designed to have the coolant pressure drop across the core increased from the reference 29 psia to 60 psia. (2) Using wire wrapped oxide fuel rods in hexagonal fuel assemblies it is possible to design PWR cores to operate at 54% higher power density than the reference PWR design that uses grid spacers and a square lattice, provided 60 psia coolant pressure drop across the core could be accommodated. Uprating existing PWR’s to use such cores could result in 40% reduction in the COE. The optimal lattice geometry is D = 8.08 mm and P/D = 1.41. The most notable advantages of wire wraps over grid spacers are their significant lower pressure drop, higher critical heat flux and improved vibrations characteristics.

Greenspan, E

2006-04-30T23:59:59.000Z

351

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.

352

Proposal on Lithium Wall Experiment (LWX) on PBXM 1  

E-Print Network [OSTI]

Proposal on Lithium Wall Experiment (LWX) on PBX­M 1 Leonid E. Zakharov, Princeton University; OUTLINE 1. Mini­conference on Lithium walls and low recycling regime. 2. PBX­M Capabilities. 3. Motivation "Lithium covered walls and low recycling regimes in toka­ maks". APS meeting, October 23­27, 2000, Quebec

Zakharov, Leonid E.

353

Lithium-Mediated Benzene Adsorption on Graphene and Graphene Nanoribbons  

E-Print Network [OSTI]

Lithium-Mediated Benzene Adsorption on Graphene and Graphene Nanoribbons Dana Krepel and Oded Hod on lithium adsorption sites at the surface of graphene and nanoribbons thereof are investigated. The effects, bare lithium adsorption turns armchair graphene nanoribbons metallic and their zigzag counterparts half

Hod, Oded

354

Lithium Diisopropylamide Solvated by Hexamethylphosphoramide: Substrate-Dependent  

E-Print Network [OSTI]

Lithium Diisopropylamide Solvated by Hexamethylphosphoramide: Substrate-Dependent Mechanisms-1301 Received February 9, 2006; E-mail: dbc6@cornell.edu Abstract: Lithium diisopropylamide of lithium-ion solvation at a molecular level of resolution.5 Our interest in HMPA stems from studies

Collum, David B.

355

Lithium acetate transformation of yeast Maitreya Dunham August 2004  

E-Print Network [OSTI]

Lithium acetate transformation of yeast Maitreya Dunham August 2004 Original protocol from Katja until the OD600 is around 0.7-0.8 (~7 hours). Spin down the cells. Resuspend in 5 ml lithium acetate mix. Spin. Resuspend in 0.5 ml lithium acetate mix. Transfer to an eppendorf tube. Incubate 60 minutes

Dunham, Maitreya

356

Lithium Diisopropylamide-Mediated Enolization: Catalysis by Hemilabile Ligands  

E-Print Network [OSTI]

Lithium Diisopropylamide-Mediated Enolization: Catalysis by Hemilabile Ligands Antonio Ramirez of a lithium diisopropylamide (LDA)-mediated ester enolization. Hemilabile amino ether MeOCH2CH2NMe2, binding-based catalysis are thwarted by the occlusion of the catalyst on the lithium salt products and byproducts (eq 1

Collum, David B.

357

Use of Lithium Hexafluoroisopropoxide as a Mild Base for  

E-Print Network [OSTI]

Use of Lithium Hexafluoroisopropoxide as a Mild Base for Horner-Wadsworth-Emmons Olefination The weak base lithium 1,1,1,3,3,3-hexafluoroisopropoxide (LiHFI) is shown to be highly effective of base-sensitive substrates, leading to the discovery that lithium 1,1,1,3,3,3-hexafluoroisopropoxide (Li

358

Description: Lithium batteries are used daily in our work  

E-Print Network [OSTI]

Description: Lithium batteries are used daily in our work activities from flashlights, cell phones containing one SureFire 3-volt non-rechargeable 123 lithium battery and one Interstate 3-volt non-rechargeable 123 lithium battery. A Garage Mechanic had the SureFire flashlight in his shirt pocket with the lens

359

The Lithium-Ion Cell: Model, State Of Charge Estimation  

E-Print Network [OSTI]

The Lithium-Ion Cell: Model, State Of Charge Estimation and Battery Management System Tutor degradation mechanisms of a Li-ion cell based on LiCoO2", Journal of Power Sources #12;Lithium ions and e and Y. Fuentes. Computer simulations of a lithium-ion polymer battery and implications for higher

Schenato, Luca

360

Liquid Lithium Wall Experiments in CDX-U R. Majeski,  

E-Print Network [OSTI]

Liquid Lithium Wall Experiments in CDX-U R. Kaita, a R. Majeski, a S. Luckhardt, b R. Doerner, b M ABSTRACT The concept of a flowing lithium first wall for a fusion reactor may lead to a significant advance is intensely heated and well diagnosed, and an extensive liquid lithium plasma-facing surface will be used

California at Los Angeles, University of

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Stabilization of tokamak plasma by lithium streams L. E. Zakharov,  

E-Print Network [OSTI]

a stabilization mechanism independent of the plasma properties. 2. Interaction of lithium streams with externalStabilization of tokamak plasma by lithium streams L. E. Zakharov, Princeton Plasma Physics-boundary magnetohydrodynamic instabilities in tokamaks by liquid lithium streams driven by magnetic propulsion is formulated

362

Stabilization of tokamak plasma by lithium streams L. E. Zakharov,  

E-Print Network [OSTI]

a stabilization mechanism independent of the plasma properties. 2 Interaction of lithium streams with externalStabilization of tokamak plasma by lithium streams L. E. Zakharov, Princeton Plasma Physics-boundary magnetohydrodynamic instabilities in tokamaks by liquid lithium streams driven by magnetic propulsion is formulated

Zakharov, Leonid E.

363

Author's personal copy Reactivity of lithium exposed graphite surface  

E-Print Network [OSTI]

on the surface [18]. Hence the effect of lithium on plasma­wall interactions is expected to dependAuthor's personal copy Reactivity of lithium exposed graphite surface S.S. Harilal a, *, J in fusion devices [1­5]. For example, wall conditioning with thin lithium layers gives rise to low hydrogen

Harilal, S. S.

364

Lithium Isotope History of Cenozoic Seawater: Changes in Silicate Weathering  

E-Print Network [OSTI]

Lithium Isotope History of Cenozoic Seawater: Changes in Silicate Weathering and Reverse Weathering 70 Ma · Overview of the Marine Lithium Cycle · Analytical Challenges · 68 Million Year Seawater Lithium Isotope Record (Forams) · Interpretation Standard: NIST L-SVEC Li (SRM 8545) #12;100 Ma Climate

Paytan, Adina

365

Microstructural Modeling and Design of Rechargeable Lithium-Ion Batteries  

E-Print Network [OSTI]

Microstructural Modeling and Design of Rechargeable Lithium-Ion Batteries R. Edwin Garci´a,a, *,z microstructure. Experi- mental measurements are reproduced. Early models for lithium-ion batteries were developed Institute of Technology, Cambridge, Massachusetts 01239-4307, USA The properties of rechargeable lithium

García, R. Edwin

366

Response of Lithium Polymer Batteries to Mechanical Loading  

E-Print Network [OSTI]

Response of Lithium Polymer Batteries to Mechanical Loading Karl Suabedissen1, Christina Peabody2 · Lithium polymer batteries are everywhere. · Efforts to create flexible batteries. · Restrictive battery performance. #12;Lithium Polymer Battery Structure · Al cathode coated with LiCoO2. · Cu anode coated

Petta, Jason

367

Mechanical Properties of Lithium-Ion Battery Separator Materials  

E-Print Network [OSTI]

Mechanical Properties of Lithium-Ion Battery Separator Materials Patrick Sinko B.S. Materials Science and Engineering 2013, Virginia Tech John Cannarella PhD. Candidate Mechanical and Aerospace and motivation ­ Why study lithium-ion batteries? ­ Lithium-ion battery fundamentals ­ Why study the mechanical

Petta, Jason

368

LITHIUM--2003 45.1 By Joyce A. Ober  

E-Print Network [OSTI]

.S. operations. The single U.S. lithium carbonate producer, Chemetall Foote Corp. (a subsidiary of the German). Chemetall Foote produced lithium carbonate from brines near Silver Peak, NV. The company's other U for further processing. The only domestic producer of lithium carbonate from brine is Chemetall Foote

369

Evaporated Lithium Surface Coatings in NSTX  

SciTech Connect (OSTI)

Two lithium evaporators were used to evaporate more than 100 g of lithium on to the NSTX lower divertor region. Prior to each discharge, the evaporators were withdrawn behind shutters, where they also remained during the subsequent HeGDC applied for periods up to 9.5 min. After the HeGDC, the shutters were opened and the LITERs were reinserted to deposit lithium on the lower divertor target for 10 min, at rates of 10-70 mg/min, prior to the next discharge. The major improvements in plasma performance from these lithium depositions include: 1) plasma density reduction as a result of lithium deposition; 2) suppression of ELMs; 3) improvement of energy confinement in a low-triangularity shape; 4) improvement in plasma performance for standard, high-triangularity discharges; 5) reduction of the required HeGDC time between discharges; 6) increased pedestal electron and ion temperature; 7) reduced SOL plasma density; and 8) reduced edge neutral density.

Kugel, H. W.; Mansfield, D.; Maingi, R.; Bel, M. G.; Bell, R. E.; Allain, J. P.; Gates, D.; Gerhardt, S.; Kaita, R.; Kallman, J.; Kaye, S.; LeBlanc, B.; Majeski, R.; Menard, J.; Mueller, D.; Ono, M.

2009-04-09T23:59:59.000Z

370

OPTIMIZATION OF INTERNAL HEAT EXCHANGERS FOR HYDROGEN STORAGE TANKS UTILIZING METAL HYDRIDES  

SciTech Connect (OSTI)

Two detailed, unit-cell models, a transverse fin design and a longitudinal fin design, of a combined hydride bed and heat exchanger are developed in COMSOL{reg_sign} Multiphysics incorporating and accounting for heat transfer and reaction kinetic limitations. MatLab{reg_sign} scripts for autonomous model generation are developed and incorporated into (1) a grid-based and (2) a systematic optimization routine based on the Nelder-Mead downhill simplex method to determine the geometrical parameters that lead to the optimal structure for each fin design that maximizes the hydrogen stored within the hydride. The optimal designs for both the transverse and longitudinal fin designs point toward closely-spaced, small cooling fluid tubes. Under the hydrogen feed conditions studied (50 bar), a 25 times improvement or better in the hydrogen storage kinetics will be required to simultaneously meet the Department of Energy technical targets for gravimetric capacity and fill time. These models and methodology can be rapidly applied to other hydrogen storage materials, such as other metal hydrides or to cryoadsorbents, in future work.

Garrison, S.; Tamburello, D.; Hardy, B.; Anton, D.; Gorbounov, M.; Cognale, C.; van Hassel, B.; Mosher, D.

2011-07-14T23:59:59.000Z

371

Systems Modeling, Simulation and Material Operating Requirements for Chemical Hydride Based Hydrogen Storage  

SciTech Connect (OSTI)

Research on ammonia borane (AB, NH3BH3) has shown it to be a promising material for chemical hydride based hydrogen storage. AB was selected by DOE's Hydrogen Storage Engineering Center of Excellence (HSECoE) as the initial chemical hydride of study because of its high hydrogen storage capacity (up to 19.6% by weight for the release of {approx}2.5 molar equivalents of hydrogen gas) and its stability under typical ambient conditions. A new systems concept based on augers, ballast tank, hydrogen heat exchanger and H2 burner was designed and implemented in simulation. In this design, the chemical hydride material was assumed to produce H2 on the augers itself, thus minimizing the size of ballast tank and reactor. One dimensional models based on conservation of mass, species and energy were used to predict important state variables such as reactant and product concentrations, temperatures of various components, flow rates, along with pressure, in various components of the storage system. Various subsystem components in the models were coded as C language S-functions and implemented in Matlab/Simulink environment. The control variable AB (or alane) flow rate was determined through a simple expression based on the ballast tank pressure, H2 demand from the fuel cell and hydrogen production from AB (or alane) in the reactor. System simulation results for solid AB, liquid AB and alane for both steady state and transient drive cycle cases indicate the usefulness of the model for further analysis and prototype development.

Devarakonda, Maruthi N.; Brooks, Kriston P.; Ronnebro, Ewa; Rassat, Scot D.

2012-02-01T23:59:59.000Z

372

Empirical and physics based mathematical models of uranium hydride decomposition kinetics with quantified uncertainties.  

SciTech Connect (OSTI)

Metal particle beds have recently become a major technique for hydrogen storage. In order to extract hydrogen from such beds, it is crucial to understand the decomposition kinetics of the metal hydride. We are interested in obtaining a a better understanding of the uranium hydride (UH3) decomposition kinetics. We first developed an empirical model by fitting data compiled from different experimental studies in the literature and quantified the uncertainty resulting from the scattered data. We found that the decomposition time range predicted by the obtained kinetics was in a good agreement with published experimental results. Secondly, we developed a physics based mathematical model to simulate the rate of hydrogen diffusion in a hydride particle during the decomposition. We used this model to simulate the decomposition of the particles for temperatures ranging from 300K to 1000K while propagating parametric uncertainty and evaluated the kinetics from the results. We compared the kinetics parameters derived from the empirical and physics based models and found that the uncertainty in the kinetics predicted by the physics based model covers the scattered experimental data. Finally, we used the physics-based kinetics parameters to simulate the effects of boundary resistances and powder morphological changes during decomposition in a continuum level model. We found that the species change within the bed occurring during the decomposition accelerates the hydrogen flow by increasing the bed permeability, while the pressure buildup and the thermal barrier forming at the wall significantly impede the hydrogen extraction.

Salloum, Maher N.; Gharagozloo, Patricia E.

2013-10-01T23:59:59.000Z

373

Simulations of Plug-in Hybrid Vehicles Using Advanced Lithium Batteries and Ultracapacitors on Various Driving Cycles  

E-Print Network [OSTI]

using Advanced Lithium Batteries and Ultracapacitors onusing advanced lithium batteries having energy densities ofA number of lithium batteries and ultracapacitors have been

Burke, Andy; Zhao, Hengbing

2010-01-01T23:59:59.000Z

374

The development of low cost LiFePO4-based high power lithium-ion batteries  

E-Print Network [OSTI]

study of rechargeable lithium batteries for application inin consumer-size lithium batteries, such as the synthetic4 -BASED HIGH POWER LITHIUM-ION BATTERIES Joongpyo Shim,

Shim, Joongpyo; Sierra, Azucena; Striebel, Kathryn A.

2003-01-01T23:59:59.000Z

375

Deuterium Retention in NSTX with Lithium Conditioning  

SciTech Connect (OSTI)

High (? 90%) deuterium retention was observed in NSTX gas balance measurements both withand without lithiumization of the carbon plasma facing components. The gas retained in ohmic discharges was measured by comparing the vessel pressure rise after a discharge to that of a gasonly pulse with the pumping valves closed. For neutral beam heated discharges the gas input and gas pumped by the NB cryopanels were tracked. The discharges were followed by outgassing of deuterium that reduced the retention. The relationship between retention and surface chemistry was explored with a new plasma-material interface probe connected to an in-vacuo surface science station that exposed four material samples to the plasma. XPS and TDS analysis showed that the binding of D atoms is fundamentally changed by lithium - in particular atoms are weakly bonded in regions near lithium atoms bound to either oxygen or the carbon matrix.

C.H. Skinner, J.P. Allain, W. Blanchard, H.W. Kugel, R. Maingi, L. Roquemore, V. Soukhanovskii, C.N. Taylor

2010-06-02T23:59:59.000Z

376

Lithium metal reduction of plutonium oxide to produce plutonium metal  

DOE Patents [OSTI]

A method is described for the chemical reduction of plutonium oxides to plutonium metal by the use of pure lithium metal. Lithium metal is used to reduce plutonium oxide to alpha plutonium metal (alpha-Pu). The lithium oxide by-product is reclaimed by sublimation and converted to the chloride salt, and after electrolysis, is removed as lithium metal. Zinc may be used as a solvent metal to improve thermodynamics of the reduction reaction at lower temperatures. Lithium metal reduction enables plutonium oxide reduction without the production of huge quantities of CaO--CaCl.sub.2 residues normally produced in conventional direct oxide reduction processes.

Coops, Melvin S. (Livermore, CA)

1992-01-01T23:59:59.000Z

377

Lithium/water interactions: Experiments and analysis  

SciTech Connect (OSTI)

The interaction of molten-lithium droplets with water is studied experimentally. In one set of experiments, droplets of [approximately]10- to 15-mm diameter are injected into a vessel filled with water. The reaction is filmed, and pressure measurements are made. The initial metal and water temperatures range from 200 to 500[degrees]C and 20 to 70[degrees]C, respectively. It is found that when reactant temperatures are high, an explosive reaction often occurs. When the initial lithium temperature is >400[degrees]C and the water is >30[degrees]C, the explosive reactions become much more probable, with pressure peaks as high as 4 MPa. The reaction is modeled to explain the temperature threshold for this metal-ignition phenomena. Results with the model support the hypothesis that explosive reactions occur when the lithium droplet surface reaches its saturation temperature while the hydrogen film surrounding the drop is relatively thin. A second set of experiments measures the reaction rate of nonexplosive lithium-water reactions. The test geometry parallels that of the previous experiments, and the reactant temperature combinations are deliberately kept below the observed ignition threshold. Two separate methods are used to determine the reaction rate in each test: One uses a three-color pyrometer to measure the drop temperature as the lithium rises through the water, while the other consists of a photographic technique that measures the amount of hydrogen generated. Measured reaction rates range from [approximately]10 to 50 mol/s[center dot]m[sup 2] with good agreement between the two measurement techniques. The data do not show any significant variation in the reaction rate as a function of either the initial water or initial lithium temperature. 17 refs., 15 figs.

Lomperski, S.; Corradini, M.L. (Univ. of Wisconsin, Madison, WI (United States))

1993-08-01T23:59:59.000Z

378

Draft of M2 Report on Integration of the Hybrid Hydride Model into INL’s MBM Framework for Review  

SciTech Connect (OSTI)

This report documents the development, demonstration and validation of a mesoscale, microstructural evolution model for simulation of zirconium hydride {delta}-ZrH{sub 1.5} precipitation in the cladding of used nuclear fuels that may occur during long-term dry storage. While the Zr-based claddings are manufactured free of any hydrogen, they absorb hydrogen during service, in the reactor by a process commonly termed ‘hydrogen pick-up’. The precipitation and growth of zirconium hydrides during dry storage is one of the most likely fuel rod integrity failure mechanisms either by embrittlement or delayed hydride cracking of the cladding (Hanson et al., 2011). While the phenomenon is well documented and identified as a potential key failure mechanism during long-term dry storage (Birk et al., 2012 and NUREG/CR-7116), the ability to actually predict the formation of hydrides is poor. The model being documented in this work is a computational capability for the prediction of hydride formation in different claddings of used nuclear fuels. This work supports the Used Fuel Disposition Research and Development Campaign in assessing the structural engineering performance of the cladding during and after long-term dry storage. This document demonstrates a basic hydride precipitation model that is built on a recently developed hybrid Potts-phase field model that combines elements of Potts-Monte Carlo and the phase-field models (Homer et al., 2013; Tikare and Schultz, 2012). The model capabilities are demonstrated along with the incorporation of the starting microstructure, thermodynamics of the Zr-H system and the hydride formation mechanism.

Tikare, Veena; Weck, Philippe F.; Schultz, Peter A.; Clark, Blythe; Michael Glazoff; Eric Homer

2014-07-01T23:59:59.000Z

379

Electrolytic orthoborate salts for lithium batteries  

DOE Patents [OSTI]

Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

Angell, Charles Austen [Mesa, AZ; Xu, Wu [Tempe, AZ

2009-05-05T23:59:59.000Z

380

Electrolytic orthoborate salts for lithium batteries  

DOE Patents [OSTI]

Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

Angell, Charles Austen (Mesa, AZ); Xu, Wu (Tempe, AZ)

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Properties of lead-lithium solutions  

SciTech Connect (OSTI)

Lead-lithium solutions are of interest to liquid metal wall ICF reactor designers because Pb may be present to some extent in both heavy ion beam and laser-driven ICF targets; therefore, Pb will be present as an impurity in a flowing lithium wall. In addition, Pb-Li solutions containing approx. 80 a/o Pb are a strong candidate for a heavy ion beam driven HYLIFE converter and a viable alternative to a pure Li wall for a laser driven converter. The properties of Pb-Li solutions including the effect of hydrogen impurities are reviewed, and the reactor design implications are discussed.

Hoffman, N.J.; Darnell, A.; Blink, J.A.

1980-10-01T23:59:59.000Z

382

Corrosion Resistance of Niobium Alloys in Lithium  

SciTech Connect (OSTI)

NbP1-1 niobium and NV-7, NTsU, and 5VMTs alloys, the chemical composition of which and the experimental method for were presented earlier, were investigated. The specimens were heat treated after which they were held in lithium. It was shown that in long holds of niobium alloys in lithium at temperatures below 1050/sup 0/C, the increase in their corrosion resistance is obtained not by combining the oxygen in oxides, but by the increase in the equilibrium concentration of oxygen in the investigated material by solid solution alloying of it with a metal more active toward oxygen.

Ignativ, M.I.

1986-03-01T23:59:59.000Z

383

Solid composite electrolytes for lithium batteries  

DOE Patents [OSTI]

Solid composite electrolytes are provided for use in lithium batteries which exhibit moderate to high ionic conductivity at ambient temperatures and low activation energies. In one embodiment, a polymer-ceramic composite electrolyte containing poly(ethylene oxide), lithium tetrafluoroborate and titanium dioxide is provided in the form of an annealed film having a room temperature conductivity of from 10.sup.-5 S cm.sup.-1 to 10.sup.-3 S cm.sup.-1 and an activation energy of about 0.5 eV.

Kumar, Binod (Dayton, OH); Scanlon, Jr., Lawrence G. (Fairborn, OH)

2001-01-01T23:59:59.000Z

384

Lithium-Ion Battery Teacher Workshop  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: VegetationEquipment Surfaces and Interfaces Sample6, 2011Liisa O'NeillFuelsLaboratoryLithiumLithium

385

Lithium Surface Coatings for Improved Plasma Performance in NSTX  

SciTech Connect (OSTI)

NSTX high-power divertor plasma experiments have shown, for the first time, significant and frequent benefits from lithium coatings applied to plasma facing components. Lithium pellet injection on NSTX introduced lithium pellets with masses 1 to 5 mg via He discharges. Lithium coatings have also been applied with an oven that directed a collimated stream of lithium vapor toward the graphite tiles of the lower center stack and divertor. Lithium depositions from a few mg to 1 g have been applied between discharges. Benefits from the lithium coating were sometimes, but not always seen. These improvements sometimes included decreases plasma density, inductive flux consumption, and ELM frequency, and increases in electron temperature, ion temperature, energy confinement and periods of MHD quiescence. In addition, reductions in lower divertor D, C, and O luminosity were measured.

Kugel, H W; Ahn, J -W; Allain, J P; Bell, R; Boedo, J; Bush, C; Gates, D; Gray, T; Kaye, S; Kaita, R; LeBlanc, B; Maingi, R; Majeski, R; Mansfield, D; Menard, J; Mueller, D; Ono, M; Paul, S; Raman, R; Roquemore, A L; Ross, P W; Sabbagh, S; Schneider, H; Skinner, C H; Soukhanovskii, V; Stevenson, T; Timberlake, J; Wampler, W R

2008-02-19T23:59:59.000Z

386

Corrosion behaviour of materials selected for FMIT lithium system  

SciTech Connect (OSTI)

The corrosion behavior of selected materials in a liquid lithium environment was studied in support of system and component designs for the Fusion Materials Irradiation Test (FMIT) Facility. Testing conditions ranged from about 3700 to about6500 hours of exposure to flowing lithium at temperatures from 230/sup 0/ to 270/sup 0/C and static lithium at temperatures from 200/sup 0/ to 500/sup 0/C. Principal areas of investigation included lithium corrosion/erosion effects on FMIT lithium system baseline and candidate materials. Material coupons and full-size prototypic components were evaluated to determine corrosion rates, fatigue crack growth rates, structural compatibility, and component acceptability for the lithium system. Based on the results of these studies, concerns regarding system materials and component designs were satisfactorily resolved to support a 20-year design life requirement for the FMIT lithium system.

Bazinet, G.D.; Brehm, W.F.

1983-09-01T23:59:59.000Z

387

Lithium pellet production (LiPP): A device for the production of small spheres of lithium  

SciTech Connect (OSTI)

With lithium as a fusion material gaining popularity, a method for producing lithium pellets relatively quickly has been developed for NSTX. The Lithium Pellet Production device is based on an injector with a sub-millimeter diameter orifice and relies on a jet of liquid lithium breaking apart into small spheres via the Plateau-Rayleigh instability. A prototype device is presented in this paper and for a pressure difference of {Delta}P= 5 Torr, spheres with diameters between 0.91 < D < 1.37 mm have been produced with an average diameter of D= 1.14 mm, which agrees with the developed theory. Successive tests performed at Princeton Plasma Physics Laboratory with Wood's metal have confirmed the dependence of sphere diameter on pressure difference as predicted.

Fiflis, P.; Andrucyzk, D.; McGuire, M.; Curreli, D.; Ruzic, D. N. [Center for Plasma Material Interactions, Department of Nuclear, Plasma, and Radiological Engineering, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801 (United States); Roquemore, A. L. [Princeton Plasma Physics Laboratory, Princeton, New Jersey 08540 (United States)

2013-06-15T23:59:59.000Z

388

Nanostructured lithium-aluminum alloy electrodes for lithium-ion batteries.  

SciTech Connect (OSTI)

Electrodeposited aluminum films and template-synthesized aluminum nanorods are examined as negative electrodes for lithium-ion batteries. The lithium-aluminum alloying reaction is observed electrochemically with cyclic voltammetry and galvanostatic cycling in lithium half-cells. The electrodeposition reaction is shown to have high faradaic efficiency, and electrodeposited aluminum films reach theoretical capacity for the formation of LiAl (1 Ah/g). The performance of electrodeposited aluminum films is dependent on film thickness, with thicker films exhibiting better cycling behavior. The same trend is shown for electron-beam deposited aluminum films, suggesting that aluminum film thickness is the major determinant in electrochemical performance regardless of deposition technique. Synthesis of aluminum nanorod arrays on stainless steel substrates is demonstrated using electrodeposition into anodic aluminum oxide templates followed by template dissolution. Unlike nanostructures of other lithium-alloying materials, the electrochemical performance of these aluminum nanorod arrays is worse than that of bulk aluminum.

Hudak, Nicholas S.; Huber, Dale L.

2010-12-01T23:59:59.000Z

389

Lithium Polysulfidophosphates: A Family of Lithium-Conducting Sulfur-Rich Compounds for Lithium-Sulfur Batteries  

SciTech Connect (OSTI)

Given the great potential for improving the energy density of state-of-the-art lithium-ion batteries by a factor of 5, a breakthrough in lithium-sulfur (Li-S) batteries will have a dramatic impact in a broad scope of energy related fields. Conventional Li-S batteries that use liquid electrolytes are intrinsically short-lived with low energy efficiency. The challenges stem from the poor electronic and ionic conductivities of elemental sulfur and its discharge products. We report herein lithium polysulfidophosphates (LPSP), a family of sulfur-rich compounds, as the enabler of long-lasting and energy-efficient Li-S batteries. LPSP have ionic conductivities of 3.0 10-5 S cm-1 at 25 oC, which is 8 orders of magnitude higher than that of Li2S (~10-13 S cm-1). The high Li-ion conductivity of LPSP is the salient characteristic of these compounds that impart the excellent cycling performance to Li-S batteries. In addition, the batteries are configured in an all-solid state that promises the safe cycling of high-energy batteries with metallic lithium anodes.

Lin, Zhan [ORNL] [ORNL; Liu, Zengcai [ORNL] [ORNL; Fu, Wujun [ORNL] [ORNL; Dudney, Nancy J [ORNL] [ORNL; Liang, Chengdu [ORNL] [ORNL

2013-01-01T23:59:59.000Z

390

NMR Spectroscopic Investigations of Mixed Aggregates Underlying Highly Enantioselective 1,2-Additions of Lithium  

E-Print Network [OSTI]

,2-Additions of Lithium Cyclopropylacetylide to Quinazolinones Rodney L. Parsons, Jr.,*, Joseph M. Fortunak Abstract: The solution structures of mixed aggregates derived from lithium alkoxides and lithium acetylides that mixtures of lithium cyclopropylacetylide (RCCLi), a (+)-carene-derived amino alkoxide (R*OLi), and lithium

Collum, David B.

391

Paper-Based Lithium-Ion Battery Nojan Aliahmad, Mangilal Agarwal, Sudhir Shrestha, and Kody Varahramyan  

E-Print Network [OSTI]

Paper-Based Lithium-Ion Battery Nojan Aliahmad, Mangilal Agarwal, Sudhir Shrestha, and Kody Indianapolis (IUPUI), Indianapolis, IN 46202 Lithium-ion batteries have a wide range of applications including devices. Lithium titanium oxide (Li4Ti5O12), lithium magnesium oxide (LiMn2O4) and lithium cobalt oxide

Zhou, Yaoqi

392

Lithium in LP 944-20  

E-Print Network [OSTI]

We present a new estimate of the lithium abundance in the atmosphere of the brown dwarf LP 944-20. Our analysis is based on a self-consistent analysis of low, intermediate and high resolution optical and near-infrared spectra. We obtain log N(Li) = 3.25 +/-0.25 using fits of our synthetic spectra to the Li I resonance line doublet profiles observed with VLT/UVES and AAT/SPIRAL. This lithium abundance is over two orders of magnitude larger than previous estimates in the literature. In order to obtain good fits of the resonance lines of K I and Rb I and better fits to the TiO molecular absorption around the Li I resonance line, we invoke a semi-empirical model atmosphere with the dusty clouds located above the photosphere. The lithium abundance, however, is not changed by the effects of the dusty clouds. We discuss the implications of our estimate of the lithium abundance in LP 944-20 for the understanding of the properties of this benchmark brown dwarf.

Ya. V. Pavlenko; H. R. A. Jones; E. L. Martin; E. Guenther; M. A. Kenworthy; M. R. Zapatero Osorio

2007-07-14T23:59:59.000Z

393

Rechargeable thin-film lithium batteries  

SciTech Connect (OSTI)

Rechargeable thin-film batteries consisting of lithium metal anodes, an amorphous inorganic electrolyte, and cathodes of lithium intercalation compounds have been fabricated and characterized. These include Li-TiS{sub 2}, Li-V{sub 2}O{sub 5}, and Li-Li{sub x}Mn{sub 2}O{sub 4} cells with open circuit voltages at full charge of about 2.5 V, 3.7 V, and 4.2 V, respectively. The realization of these robust cells, which can be cycled thousands of times, was possible because of the stability of the amorphous lithium electrolyte, lithium phosphorus oxynitride. This material has a typical composition of Li{sub 2.9}PO{sub 3.3}N{sub 0.46}and a conductivity at 25 C of 2 {mu}S/cm. The thin-film cells have been cycled at 100% depth of discharge using current densities of 5 to 100 {mu}A/cm{sup 2}. Over most of the charge-discharge range, the internal resistance appears to be dominated by the cathode, and the major source of the resistance is the diffusion of Li{sup +} ions from the electrolyte into the cathode. Chemical diffusion coefficients were determined from ac impedance measurements.

Bates, J.B.; Gruzalski, G.R.; Dudney, N.J.; Luck, C.F.; Yu, X.

1993-09-01T23:59:59.000Z

394

ReaxFFMgH Reactive Force Field for Magnesium Hydride Systems Sam Cheung, Wei-Qiao Deng, Adri C. T. van Duin, and William A. Goddard III*  

E-Print Network [OSTI]

ReaxFFMgH Reactive Force Field for Magnesium Hydride Systems Sam Cheung, Wei-Qiao Deng, Adri C. TFFMgH) for magnesium and magnesium hydride systems. The parameters for this force field were derived from fitting to quantum chemical (QM) data on magnesium clusters and on the equations of states for condensed phases

van Duin, Adri

395

Implications of NSTX Lithium Results for Magnetic Fusion Research  

SciTech Connect (OSTI)

Lithium wall coating techniques have been experimentally explored on NSTX for the last five years. The lithium experimentation on NSTX started with a few milligrams of lithium injected into the plasma as pellets and it has evolved to a lithium evaporation system which can evaporate up to ~ 100 g of lithium onto the lower divertor plates between lithium reloadings. The unique feature of the lithium research program on NSTX is that it can investigate the effects of lithium in H-mode divertor plasmas. This lithium evaporation system thus far has produced many intriguing and potentially important results; the latest of these are summarized in a companion paper by H. Kugel. In this paper, we suggest possible implications and applications of the NSTX lithium results on the magnetic fusion research which include electron and global energy confinement improvements, MHD stability enhancement at high beta, ELM control, H-mode power threshold reduction, improvements in radio frequency heating and non-inductive plasma start-up performance, innovative divertor solutions and improved operational efficiency.

M. Ono, M.G. Bell, R.E. Bell, R. Kaita, H.W. Kugel, B.P. LeBlanc, J.M. Canik, S. Diem, S.P.. Gerhardt, J. Hosea, S. Kaye, D. Mansfield, R. Maingi, J. Menard, S. F. Paul, R. Raman, S.A. Sabbagh, C.H. Skinner, V. Soukhanovskii, G. Taylor, and the NSTX Research Team

2010-01-14T23:59:59.000Z

396

Lithium Depletion of Nearby Young Stellar Associations  

E-Print Network [OSTI]

We estimate cluster ages from lithium depletion in five pre-main-sequence groups found within 100 pc of the Sun: TW Hydrae Association, Eta Chamaeleontis Cluster, Beta Pictoris Moving Group, Tucanae-Horologium Association and AB Doradus Moving Group. We determine surface gravities, effective temperatures and lithium abundances for over 900 spectra through least squares fitting to model-atmosphere spectra. For each group, we compare the dependence of lithium abundance on temperature with isochrones from pre-main-sequence evolutionary tracks to obtain model dependent ages. We find that the Eta Chamaelontis Cluster and the TW Hydrae Association are the youngest, with ages of 12+/-6 Myr and 12+/-8 Myr, respectively, followed by the Beta Pictoris Moving Group at 21+/-9 Myr, the Tucanae-Horologium Association at 27+/-11 Myr, and the AB Doradus Moving Group at an age of at least 45 Myr (where we can only set a lower limit since the models -- unlike real stars -- do not show much lithium depletion beyond this age). Here, the ordering is robust, but the precise ages depend on our choice of both atmospheric and evolutionary models. As a result, while our ages are consistent with estimates based on Hertzsprung-Russell isochrone fitting and dynamical expansion, they are not yet more precise. Our observations do show that with improved models, much stronger constraints should be feasible: the intrinsic uncertainties, as measured from the scatter between measurements from different spectra of the same star, are very low: around 10 K in effective temperature, 0.05 dex in surface gravity, and 0.03 dex in lithium abundance.

Erin Mentuch; Alexis Brandeker; Marten H. van Kerkwijk; Ray Jayawardhana; Peter H. Hauschildt

2008-08-26T23:59:59.000Z

397

Lithium Diisopropylamide-Mediated Ortholithiation of 2Fluoropyridines: Rates, Mechanisms, and the Role of Autocatalysis  

E-Print Network [OSTI]

Lithium Diisopropylamide-Mediated Ortholithiation of 2Fluoropyridines: Rates, Mechanisms, Ithaca, New York 14853-1301, United States *S Supporting Information ABSTRACT: Lithium diisopropylamide herein mechanistic studies of the lithium diisopropylamide (LDA)-mediated ortholithiation of 2-fluoro

Collum, David B.

398

Solid state thin film battery having a high temperature lithium alloy anode  

DOE Patents [OSTI]

An improved rechargeable thin-film lithium battery involves the provision of a higher melting temperature lithium anode. Lithium is alloyed with a suitable solute element to elevate the melting point of the anode to withstand moderately elevated temperatures.

Hobson, David O. (Oak Ridge, TN)

1998-01-01T23:59:59.000Z

399

Overcharge Protection for 4 V Lithium Batteries at High Rates and Low Temperature  

E-Print Network [OSTI]

Protection for 4 V Lithium Batteries at High Rates and LowRechargeable lithium batteries are known for their highBecause lithium ion batteries are especially susceptible to

Chen, Guoying

2010-01-01T23:59:59.000Z

400

STUDIES ON TWO CLASSES OF POSITIVE ELECTRODE MATERIALS FOR LITHIUM-ION BATTERIES  

E-Print Network [OSTI]

Linden, D. , Handbook of Batteries. 2nd ed. 1995, New York:rechargeable lithium batteries. Nature, 2001. 414(6861): p.of rechargeable lithium batteries, I. Lithium manganese

Wilcox, James D.

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries using Synchrotron Radiation Techniques  

E-Print Network [OSTI]

Alternatives to Current Lithium-Ion Batteries. Adv. EnergyMaterials for Lithium Ion Batteries. Materials Matters. 7 4.to the Study of Lithium Ion Batteries. J. Solid State

Doeff, Marca M.

2013-01-01T23:59:59.000Z

402

Failure modes in high-power lithium-ion batteries for use in hybrid electric vehicles  

E-Print Network [OSTI]

MODES IN HIGH-POWER LITHIUM-ION BATTERIES FOR USE IN HYBRIDof high-power lithium-ion batteries for hybrid electricthe development of lithium-ion batteries for hybrid electric

2001-01-01T23:59:59.000Z

403

Metal hydride/chemical heat-pump development project. Phase I. Final report  

SciTech Connect (OSTI)

The metal hydride/chemical heat pump (MHHP) is a chemical heat pump containing two hydrides for the storage and/or recovery of thermal energy. It utilizes the heat of reaction of hydrogen with specific metal alloys. The MHHP design can be tailored to provide heating and/or cooling or temperature upgrading over a wide range of input and ambient temperatures. The system can thus be used with a variety of heat sources including waste heat, solar energy or a fossil fuel. The conceptual design of the MHHP was developed. A national market survey including a study of applications and market sectors was conducted. The technical tasks including conceptual development, thermal and mechanical design, laboratory verification of design and material performance, cost analysis and the detailed design of the Engineering Development Test Unit (EDTU) were performed. As a result of the market study, the temperature upgrade cycle of the MHHP was chosen for development. Operating temperature ranges for the upgrader were selected to be from 70 to 110/sup 0/C (160 to 230/sup 0/F) for the source heat and 140 to 190/sup 0/C (280 to 375/sup 0/F) for the product heat. These ranges are applicable to many processes in industries such as food, textile, paper and pulp, and chemical. The hydride pair well suited for these temperatures is LaNi/sub 5//LaNi/sub 4/ /sub 5/Al/sub 0/ /sub 5/. The EDTU was designed for the upgrade cycle. It is a compact finned tube arrangement enclosed in a pressure vessel. This design incorporates high heat transfer and low thermal mass in a system which maximizes the coefficient of performance (COP). It will be constructed in Phase II. Continuation of this effort is recommended.

Argabright, T.A.

1982-02-01T23:59:59.000Z

404

Method and apparatus for storing hydrogen isotopes. [stored as uranium hydride in a block of copper  

DOE Patents [OSTI]

An improved method and apparatus for storing isotopes of hydrogen (especially tritium) are provided. The hydrogen gas is stored as hydrides of material (for example uranium) within boreholes in a block of copper. The mass of the block is critically important to the operation, as is the selection of copper, because no cooling pipes are used. Because no cooling pipes are used, there can be no failure due to cooling pipes. And because copper is used instead of stainless steel, a significantly higher temperature can be reached before the eutectic formation of uranium with copper occurs, (the eutectic of uranium with the iron in stainless steel forms at a significantly lower temperature).

McMullen, J.W.; Wheeler, M.G.; Cullingford, H.S.; Sherman, R.H.

1982-08-10T23:59:59.000Z

405

Metal hydrides as electrode/catalyst materials for oxygen evolution/reduction in electrochemical devices  

DOE Patents [OSTI]

An at least ternary metal alloy of the formula, AB.sub.(5-Y)X(.sub.y), is claimed. In this formula, A is selected from the rare earth elements, B is selected from the elements of groups 8, 9, and 10 of the periodic table of the elements, and X includes at least one of the following: antimony, arsenic, and bismuth. Ternary or higher-order substitutions, to the base AB.sub.5 alloys, that form strong kinetic interactions with the predominant metals in the base metal hydride are used to form metal alloys with high structural integrity after multiple cycles of hydrogen sorption.

Bugga, Ratnakumar V. (Arcadia, CA); Halpert, Gerald (Pasadena, CA); Fultz, Brent (Pasadena, CA); Witham, Charles K. (Pasadena, CA); Bowman, Robert C. (La Mesa, CA); Hightower, Adrian (Whittier, CA)

1997-01-01T23:59:59.000Z

406

(Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine in the United States was a brine  

E-Print Network [OSTI]

94 LITHIUM (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine in the United States was a brine operation in Nevada. The mine's production capacity was expanded in 2012, and a new lithium hydroxide plant opened in North

407

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

100 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

408

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

98 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

409

Lithium Polymer (LiPo) Battery Usage Lithium polymer batteries are now being widely used in hobby and UAV applications. They work  

E-Print Network [OSTI]

Lithium Polymer (LiPo) Battery Usage 1 Lithium polymer batteries are now being widely used in hobby only LiPo Chargers with Error Detection - It is always recommended that you charge your lithium polymer batteries with a battery charger specifically designed for lithium polymer batteries. As an example, you

Langendoen, Koen

410

Lithium 2,2,6,6-Tetramethylpiperidide and Lithium 2,2,4,6,6-Pentamethylpiperidide: Influence of TMEDA and Related  

E-Print Network [OSTI]

Lithium 2,2,6,6-Tetramethylpiperidide and Lithium 2,2,4,6,6-Pentamethylpiperidide: Influence,2,6,6-tetramethylpiperidide (LiTMP) and the conformationally locked (but otherwise isostructural) lithium 2 and conformational preferences of lithium 2,2,6,6-tetramethylpiperidide (LiTMP) in the solid state studied by Lappert

Collum, David B.

411

(Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China,  

E-Print Network [OSTI]

96 LITHIUM (Data in metric tons of lithium content, unless otherwise noted) Domestic Production and Use: Chile was the largest lithium chemical producer in the world; Argentina, China, Russia, and the United States were large producers also. Australia, Canada, and Zimbabwe were major producers of lithium

412

(Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine operating in the United States was a  

E-Print Network [OSTI]

94 LITHIUM (Data in metric tons of lithium content unless otherwise noted) Domestic Production and Use: The only commercially active lithium mine operating in the United States was a brine operation in Nevada. Two companies produced a large array of downstream lithium compounds in the United States from

413

Theory of Hydride-Proton Transfer (HPT) Carbonyl Reduction by [Os(III)(tpy)(Cl)(NH=CHCH3)(NSAr)  

SciTech Connect (OSTI)

Quantum mechanical analysis reveals that carbonyl reduction of aldehydes and ketones by the imine-based reductant cis-[Os{sup III}(tpy)(Cl)(NH?CHCH{sub 3})(NSAr)] (2), which is accessible by reduction of the analogous nitrile, occurs by hydride-proton transfer (HPT) involving both the imine and sulfilimido ligands. In carbonyl reduction, water or alcohol is necessary to significantly lower the barrier for proton shuttling between ligands. The ?N(H)SAr group activates the carbonyl group through hydrogen bonding while the ?NC(H)CH{sub 3} ligand delivers the hydride.

Ess, Daniel H.; Schauer, Cynthia; Meyer, Thomas J.

2010-01-01T23:59:59.000Z

414

Effects of Cesium Cations in Lithium Deposition via Self-Healing...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Cesium Cations in Lithium Deposition via Self-Healing Electrostatic Shield Mechanism. Effects of Cesium Cations in Lithium Deposition via Self-Healing Electrostatic Shield...

415

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Documents & Publications CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries Additives and Cathode Materials for High-Energy Lithium Sulfur...

416

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium...

417

ELECTROCHEMICAL STUDIES OF THE FILM FORMATION ON LITHIUM IN PROPYLENE CARBONATE SOLUTIONS UNDER OPEN CIRCUIT CONDITIONS  

E-Print Network [OSTI]

for film growth and lithium corrosion. The increase in LiCl0drastically decreases the lithium corrosion and reduces the

Geronov, Y.

2014-01-01T23:59:59.000Z

418

Innovative Manufacturing and Materials for Low-Cost Lithium-Ion...  

Broader source: Energy.gov (indexed) [DOE]

Merit Review 2014: Innovative Manufacturing and Materials for Low-Cost Lithium-Ion Batteries Innovative Manufacturing and Materials for Low-Cost Lithium-Ion Batteries...

419

au-implanted lithium niobate: Topics by E-print Network  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

based on silicon-on-lithium-niobate photonics JEFF. By transferring large areas of thin, monocrystalline silicon to bulk lithium niobate (LiNbO3) substrates difference...

420

E-Print Network 3.0 - accumulateurs au lithium Sample Search...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

au lithium Search Powered by Explorit Topic List Advanced Search Sample search results for: accumulateurs au lithium Page: << < 1 2 3 4 5 > >> 1 ACCUMULATEUR LECTRIQUE...

Note: This page contains sample records for the topic "nickel-metal hydride lithium" 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

Solid lithium ion conducting electrolytes and methods of preparation  

DOE Patents [OSTI]

A composition comprised of nanoparticles of lithium ion conducting solid oxide material, wherein the solid oxide material is comprised of lithium ions, and at least one type of metal ion selected from pentavalent metal ions and trivalent lanthanide metal ions. Solution methods useful for synthesizing these solid oxide materials, as well as precursor solutions and components thereof, are also described. The solid oxide materials are incorporated as electrolytes into lithium ion batteries.

Narula, Chaitanya K; Daniel, Claus

2013-05-28T23:59:59.000Z

422

Lithium: Measurement of Young's Modulus and Yield Strength  

SciTech Connect (OSTI)

The Lithium Collection Lens is used for anti-proton collection. In analyzing the structural behavior during operation, various material properties of lithium are often needed. properties such as density, coefficient of thermal expansion, thermal conductivity, specific heat, compressability, etc.; are well known. However, to the authors knowledge there is only one published source for Young's Modulus. This paper reviews the results from the testing of Young's Modulus and the yield strength of lithium at room temperature.

Ryan P Schultz

2002-11-07T23:59:59.000Z

423

Overcoming Processing Cost Barriers of High-Performance Lithium...  

Broader source: Energy.gov (indexed) [DOE]

Office Merit Review 2014: Overcoming Processing Cost Barriers of High-Performance Lithium-Ion Battery Electrodes Vehicle Technologies Office Merit Review 2014:...

424

Lithium In Tufas Of The Great Basin- Exploration Implications...  

Open Energy Info (EERE)

Tufas Of The Great Basin- Exploration Implications For Geothermal Energy And Lithium Resources Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper:...

425

Overcoming Processing Cost Barriers of High-Performance Lithium...  

Broader source: Energy.gov (indexed) [DOE]

methods - Tailored Aqueous Colloids for Lithium-Ion Electrodes (TACLE) B.L. Armstrong et al., U.S. Patent Application No. 13651,270. - Surface charge measurement,...

426

Development of High Energy Lithium Batteries for Electric Vehicles...  

Broader source: Energy.gov (indexed) [DOE]

Kasei * Focused on High Capacity Manganese Rich (HCMR TM ) cathodes & Silicon-Carbon composite anodes for Lithium ion batteries * Envia's high energy Li-ion battery materials...

427

Studies on Lithium Manganese Rich MNC Composite Cathodes  

Broader source: Energy.gov (indexed) [DOE]

America Inc. 3 Presentation name Project Objectives - Relevance Undertake advanced materials research in the area of high energy (capacity) electrode materials for lithium-ion...

428

Electrolytes - R&D for Advanced Lithium Batteries. Interfacial...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

es089kerr2011o.pdf More Documents & Publications Electrolytes - R&D for Advanced Lithium Batteries. Interfacial Behavior of Electrolytes Interfacial Behavior of Electrolytes...

429

Lithium Ion Battery Performance of Silicon Nanowires With Carbon...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Ion Battery Performance of Silicon Nanowires With Carbon Skin . Lithium Ion Battery Performance of Silicon Nanowires With Carbon Skin . Abstract: Silicon (Si) nanomaterials have...

430

Development of Novel Electrolytes for Use in High Energy Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Development of Novel Electrolytes for Use in High Energy Lithium-Ion Batteries with Wide Operating Temperature Range Development of Novel Electrolytes...

431

Advanced Cathode Material Development for PHEV Lithium Ion Batteries...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Advanced Cathode Material Development for PHEV Lithium Ion Batteries High Energy Novel Cathode Alloy Automotive Cell Develop & evaluate...

432

Novel Redox Shuttles for Overcharge Protection of Lithium-Ion...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Redox Shuttles for Overcharge Protection of Lithium-Ion Batteries Technology available for licensing: Electrolytes containing novel redox shuttles (electron transporters) for...

433

Sandia National Laboratories: Solid-State Lithium Batteries  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lithium Batteries ARPAe: Innovation Activities On November 25, 2013, in Technology Showcase Nominees Partnering with Sandia Research Facilities Current Projects Technology Showcase...

434

Two Studies Reveal Details of Lithium-Battery Function  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Two Studies Reveal Details of Lithium-Battery Function Print Our way of life is deeply intertwined with battery technologies that have enabled a mobile revolution powering cell...

435

Intermetallic Electrodes Improve Safety and Performance in Lithium...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Intermetallic Electrodes Improve Safety and Performance in Lithium-Ion Batteries Technology available for licensing: A new class of intermetallic material that can be used as a...

436

Edge Turbulence Velocity Changes with Lithium Coating on NSTX  

SciTech Connect (OSTI)

Lithium coating improves energy confinement and eliminates edge localized modes in NSTX, but the mechanism of this improvement is not yet well understood. We used the gas-puff-imaging (GPI) diagnostic on NSTX to measure the changes in edge turbulence which occurred during a scan with variable lithium wall coating, in order to help understand the reason for the confinement improvement with lithium. There was a small increase in the edge turbulence poloidal velocity and a decrease in the poloidal velocity fluctuation level with increased lithium. The possible effect of varying edge neutral density on turbulence damping was evaluated for these cases in NSTX. __________________________________________________

Cao, A.; Zweben, S. J.; Stotler, D. P.; Bell, M.; Diallo, A.; Kaye, S. M.; LeBlanc, B.

2012-08-10T23:59:59.000Z

437

Electrode Materials for Rechargeable Lithium-Ion Batteries: A...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Electrode Materials for Rechargeable Lithium-Ion Batteries: A New Synthetic Approach Technology available for licensing: New high-energy cathode materials for use in rechargeable...

438

Electrolytes - R&D for Advanced Lithium Batteries. Interfacial...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

- Interfacial and Bulk Properties and Stability Electrolytes - R&D for Advanced Lithium Batteries. Interfacial Behavior of Electrolytes Interfacial Behavior of Electrolytes...

439

Correlation of Lithium-Ion Battery Performance with Structural...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Correlation of Lithium-Ion Battery Performance with Structural and Chemical Transformations Wednesday, April 30, 2014 Chemical evolution and structural transformations in a...

440

Advanced Cathode Material Development for PHEV Lithium Ion Batteries...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

More Documents & Publications Advanced Cathode Material Development for PHEV Lithium Ion Batteries Vehicle Technologies Office Merit Review 2014: High Energy Novel...

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


441

Fundamental Studies of Lithium-Sulfur Cell Chemistry  

Broader source: Energy.gov (indexed) [DOE]

Studies of Lithium-Sulfur Cell Chemistry PI: Nitash Balsara LBNL June 17, 2014 Project ID ESS224 This presentation does not contain any proprietary, confidential, or otherwise...

442

Lower Cost Lithium Ion Batteries From Aluminum Substituted Cathode...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Lower Cost Lithium Ion Batteries From Aluminum Substituted Cathode Materials Lawrence Berkeley National Laboratory Contact LBL About This Technology Technology Marketing...

443

Visualization of Charge Distribution in a Lithium Battery Electrode  

E-Print Network [OSTI]

Distribution in Thin-Film Batteries. J. Electrochem. Soc.of Lithium Polymer Batteries. J. Power Sources 2002, 110,for Rechargeable Li Batteries. Chem. Mater. 2010, 15. Padhi,

Liu, Jun

2010-01-01T23:59:59.000Z

444

California: Geothermal Plant to Help Meet High Lithium Demand...  

Energy Savers [EERE]

of 2009, EERE's Geothermal Technologies Office is working with California's Simbol Materials to develop technologies that extract battery materials like lithium, manganese, and...

445

Lithium Ion Electrode Production NDE and QC Considerations |...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

QC Considerations Lithium Ion Electrode Production NDE and QC Considerations Review of Oak Ridge process and QC activities by David Wood, Oak Ridge National Laboratory, at the...

446

Negative Electrodes Improve Safety in Lithium Cells and Batteries...  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

Negative Electrodes Improve Safety in Lithium Cells and Batteries Technology available for licensing: Enhanced stability at a lower cost Lowers cost for enhanced stability...

447

JCESR: Moving Beyond Lithium-Ion | Argonne National Laboratory  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

JCESR: Moving Beyond Lithium-Ion Share Topic Energy Energy usage Energy storage Batteries Browse By - Any - Energy -Energy efficiency --Vehicles ---Alternative fuels ---Automotive...

448

Expanded North Carolina Lithium Facility Opens, Boosting U.S...  

Broader source: Energy.gov (indexed) [DOE]

plug-in hybrids and other advanced clean energy technologies grows worldwide, rare earth elements and other critical materials, including lithium, are facing increasing global...

449

Development of Electrolytes for Lithium-ion Batteries  

Broader source: Energy.gov (indexed) [DOE]

Battaglia & J. Kerr (LBNL) * M. Payne (Novolyte) * F. Puglia & B. Ravdel (Yardney) * G. Smith & O. Borodin (U. Utah) 3 3 Develop novel electrolytes for lithium ion batteries that...

450

Overcoming Processing Cost Barriers of High-Performance Lithium...  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

Cost Barriers of High-Performance Lithium-Ion Battery Electrodes 2012 DOE Hydrogen and Fuel Cells Program and Vehicle Technologies Program Annual Merit Review and Peer...

451

Development of Large Format Lithium Ion Cells with Higher Energy...  

Broader source: Energy.gov (indexed) [DOE]

Overall Project Goal: To research, develop and demonstrate large format lithium ion cells with energy density > 500 WhL Barriers addressed: - Low energy density - Cost -...

452

Rapid hydrogen gas generation using reactive thermal decomposition of uranium hydride.  

SciTech Connect (OSTI)

Oxygen gas injection has been studied as one method for rapidly generating hydrogen gas from a uranium hydride storage system. Small scale reactors, 2.9 g UH{sub 3}, were used to study the process experimentally. Complimentary numerical simulations were used to better characterize and understand the strongly coupled chemical and thermal transport processes controlling hydrogen gas liberation. The results indicate that UH{sub 3} and O{sub 2} are sufficiently reactive to enable a well designed system to release gram quantities of hydrogen in {approx} 2 seconds over a broad temperature range. The major system-design challenge appears to be heat management. In addition to the oxidation tests, H/D isotope exchange experiments were performed. The rate limiting step in the overall gas-to-particle exchange process was found to be hydrogen diffusion in the {approx}0.5 {mu}m hydride particles. The experiments generated a set of high quality experimental data; from which effective intra-particle diffusion coefficients can be inferred.

Kanouff, Michael P.; Van Blarigan, Peter; Robinson, David B.; Shugard, Andrew D.; Gharagozloo, Patricia E.; Buffleben, George M.; James, Scott Carlton; Mills, Bernice E.

2011-09-01T23:59:59.000Z

453

Mechanical Behavior Studies of Depleted Uranium in the Presence of Hydrides  

SciTech Connect (OSTI)

This project addresses critical issues related to aging in the presence of hydrides (UH{sub 3}) in DU and the subsequent effect on mechanical behavior. Rolled DU specimens with three different hydrogen concentrations and the as-rolled condition were studied. The texture measurements indicate that the hydrogen charging is affecting the initial as-rolled DU microstructure/texture. The macroscopic mechanical behavior suggests the existence of a threshold between the 0 wpmm H and 0.3 wppm H conditions. A VPSC simulation of the macroscopic strain-stress behavior, when taking into account only a texture effect, shows no agreement with the experiment. This suggests that the macroscopic mechanical behavior observed is indeed due to the presence of hydrogen/hydrides in the DU bulk. From the lattice strain variation it can be concluded that the hydrogen is affecting the magnitude and/or the nature of CRSS. The metallography indicates the specimens that underwent the hydrogen charging process, developed large grains and twinning, which were enhanced by the presence of hydrogen. Further studies using electron microscopy and modeling will be conducted to learn about the deformation mechanisms responsible for the observed behavior.

Garlea, E.; Morrell, J. S.; Bridges, R. L.; Powell, G. L.; Brown, d. W.; Sisneros, T. A.; Tome, C. N.; Vogel, S. C.

2011-02-14T23:59:59.000Z

454

THERMAL ENHANCEMENT CARTRIDGE HEATER MODIFIED TECH MOD TRITIUM HYDRIDE BED DEVELOPMENT PART I DESIGN AND FABRICATION  

SciTech Connect (OSTI)

The Savannah River Site (SRS) tritium facilities have used 1{sup st} generation (Gen1) LaNi{sub 4.25}Al{sub 0.75} (LANA0.75) metal hydride storage beds for tritium absorption, storage, and desorption. The Gen1 design utilizes hot and cold nitrogen supplies to thermally cycle these beds. Second and 3{sup rd} generation (Gen2 and Gen3) storage bed designs include heat conducting foam and divider plates to spatially fix the hydride within the bed. For thermal cycling, the Gen2 and Gen 3 beds utilize internal electric heaters and glovebox atmosphere flow over the bed inside the bed external jacket for cooling. The currently installed Gen1 beds require replacement due to tritium aging effects on the LANA0.75 material, and cannot be replaced with Gen2 or Gen3 beds due to different designs of these beds. At the end of service life, Gen1 bed desorption efficiencies are limited by the upper temperature of hot nitrogen supply. To increase end-of-life desorption efficiency, the Gen1 bed design was modified, and a Thermal Enhancement Cartridge Heater Modified (TECH Mod) bed was developed. Internal electric cartridge heaters in the new design to improve end-of-life desorption, and also permit in-bed tritium accountability (IBA) calibration measurements to be made without the use of process tritium. Additional enhancements implemented into the TECH Mod design are also discussed.

Klein, J.; Estochen, E.

2014-03-06T23:59:59.000Z

455

A Novel Zr-1Nb Alloy and a New Look at Hydriding  

SciTech Connect (OSTI)

A novel Zr-1Nb has begun development based on a working model that takes into account the hydrogen permeabilities for zirconium and niobium metals. The beta-Nb secondary phase particles (SPPs) in Zr-1Nb are believed to promote more rapid hydrogen dynamics in the alloy in comparison to other zirconium alloys. Furthermore, some hydrogen release is expected at the lower temperatures corresponding to outages when the partial pressure of H2 in the coolant is less. These characteristics lessen the negative synergism between corrosion and hydriding that is otherwise observed in cladding alloys without niobium. In accord with the working model, development of nanoscale precursors was initiated to enhance the performance of existing Zr-1Nb alloys. Their characteristics and properties can be compared to oxide-dispersion strengthened alloys, and material additions have been proposed to zirconium-based LWR cladding to guard further against hydriding and to fix the size of the SPPs for microstructure stability enhancements. A preparative route is being investigated that does not require mechanical alloying, and 10 nanometer molybdenum particles have been prepared which are part of the nanoscale precursors. If successful, the approach has implications for long term dry storage of used fuel and for new routes to nanoferritic and ODS alloys.

Robert D. Mariani; James I. Cole; Assel Aitkaliyeva

2013-09-01T23:59:59.000Z

456

Solid polymeric electrolytes for lithium batteries  

DOE Patents [OSTI]

Novel conductive polyanionic polymers and methods for their preparion are provided. The polyanionic polymers comprise repeating units of weakly-coordinating anionic groups chemically linked to polymer chains. The polymer chains in turn comprise repeating spacer groups. Spacer groups can be chosen to be of length and structure to impart desired electrochemical and physical properties to the polymers. Preferred embodiments are prepared from precursor polymers comprising the Lewis acid borate tri-coordinated to a selected ligand and repeating spacer groups to form repeating polymer chain units. These precursor polymers are reacted with a chosen Lewis base to form a polyanionic polymer comprising weakly coordinating anionic groups spaced at chosen intervals along the polymer chain. The polyanionic polymers exhibit high conductivity and physical properties which make them suitable as solid polymeric electrolytes in lithium batteries, especially secondary lithium batteries.

Angell, Charles A.; Xu, Wu; Sun, Xiaoguang

2006-03-14T23:59:59.000Z

457

Manganese oxide composite electrodes for lithium batteries  

DOE Patents [OSTI]

An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor of a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Li, Naichao (Croton on Hudson, NY)

2007-12-04T23:59:59.000Z

458

Manganese oxide composite electrodes for lithium batteries  

DOE Patents [OSTI]

An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor thereof a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0.5lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

Johnson, Christopher S. (Naperville, IL); Kang, Sun-Ho (Naperville, IL); Thackeray, Michael M. (Naperville, IL)

2009-12-22T23:59:59.000Z

459

Lithium-Polysulfide Flow Battery Demonstration  

ScienceCinema (OSTI)

In this video, Stanford graduate student Wesley Zheng demonstrates the new low-cost, long-lived flow battery he helped create. The researchers created this miniature system using simple glassware. Adding a lithium polysulfide solution to the flask immediately produces electricity that lights an LED. A utility version of the new battery would be scaled up to store many megawatt-hours of energy.

Zheng, Wesley

2014-07-16T23:59:59.000Z

460

Conductive polymeric compositions for lithium batteries  

DOE Patents [OSTI]

Novel chain polymers comprising weakly basic anionic moieties chemically bound into a polyether backbone at controllable anionic separations are presented. Preferred polymers comprise orthoborate anions capped with dibasic acid residues, preferably oxalato or malonato acid residues. The conductivity of these polymers is found to be high relative to that of most conventional salt-in-polymer electrolytes. The conductivity at high temperatures and wide electrochemical window make these materials especially suitable as electrolytes for rechargeable lithium batteries.

Angell, Charles A. (Mesa, AZ); Xu, Wu (Tempe, AZ)

2009-03-17T23:59:59.000Z

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


461

High expansion, lithium corrosion resistant sealing glasses  

DOE Patents [OSTI]

Glass compositions containing CaO, Al.sub.2 O.sub.3, B.sub.2 O.sub.3, SrO and BaO in various combinations of mole % are provided. These compositions are capable of forming stable glass-to-metal seals with pin materials of 446 Stainless Steel and Alloy-52 rather than molybdenum, for use in harsh chemical environments, specifically in lithium batteries.

Brow, Richard K. (Albuquerque, NM); Watkins, Randall D. (Albuquerque, NM)

1991-01-01T23:59:59.000Z

462

High-discharge-rate lithium ion battery  

SciTech Connect (OSTI)

The present invention provides for a lithium ion battery and process for creating such, comprising higher binder to carbon conductor ratios than presently used in the industry. The battery is characterized by much lower interfacial resistances at the anode and cathode as a result of initially mixing a carbon conductor with a binder, then with the active material. Further improvements in cycleability can also be realized by first mixing the carbon conductor with the active material first and then adding the binder.

Liu, Gao; Battaglia, Vincent S; Zheng, Honghe

2014-04-22T23:59:59.000Z

463

Lithium-Polysulfide Flow Battery Demonstration  

SciTech Connect (OSTI)

In this video, Stanford graduate student Wesley Zheng demonstrates the new low-cost, long-lived flow battery he helped create. The researchers created this miniature system using simple glassware. Adding a lithium polysulfide solution to the flask immediately produces electricity that lights an LED. A utility version of the new battery would be scaled up to store many megawatt-hours of energy.

Zheng, Wesley

2014-06-30T23:59:59.000Z

464

High expansion, lithium corrosion resistant sealing glasses  

DOE Patents [OSTI]

Glass compositions containing CaO, Al[sub 2]O[sub 3], B[sub 2]O[sub 3], SrO and BaO in various combinations of mole % are provided. These compositions are capable of forming stable glass-to-metal seals with pin materials of 446 Stainless Steel and Alloy-52 rather than molybdenum, for use in harsh chemical environments, specifically in lithium batteries.

Brow, R.K.; Watkins, R.D.

1991-06-04T23:59:59.000Z

465

Aluminum-lithium alloys -- the next generation  

SciTech Connect (OSTI)

The advantages of aluminum-lithium (Al-Li) alloys, such as low density and high modulus, have been well documented in the last 15 years, but their impact on the aerospace market has fallen short of initial expectations. However, vacuum refining processes have now been developed at Comalco Aluminium Ltd., Melbourne, Australia, that provide improved mechanical properties. In addition, the patented technology allows higher levels of lithium, which results in higher stiffness and lower densities. For example, alloys with 3.3% lithium and very low amounts of hydrogen and alkali metal impurities demonstrate good mechanical properties. It also exhibits good weldability, as shown in results of varestraint'' testing, which evaluates the tendency to crack during welding. The high purity of these VacLite alloys ensures that grain boundary fracture is minimized, and cleavage fracture is reduced almost to the limit of detectability. Furthermore, advanced vacuum techniques using electron beam melting at 10[sup [minus]5] torr may eventually reduce impurities to a level at which fracture occurs only in a ductile, transgranular manner.

Webster, D. (Advanced Material Development, Saratoga, CA (United States))

1994-05-01T23:59:59.000Z

466

Recovery of lithium and cobalt from waste lithium ion batteries of mobile phone  

SciTech Connect (OSTI)

Graphical abstract: Recovery of valuable metals from scrap batteries of mobile phone. - Highlights: • Recovery of Co and Li from spent LIBs was performed by hydrometallurgical route. • Under the optimum condition, 99.1% of lithium and 70.0% of cobalt were leached. • The mechanism of the dissolution of lithium and cobalt was studied. • Activation energy for lithium and cobalt were found to be 32.4 kJ/mol and 59.81 kJ/mol, respectively. • After metal recovery, residue was washed before disposal to the environment. - Abstract: In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2 M sulfuric acid with the addition of 5% H{sub 2}O{sub 2} (v/v) at a pulp density of 100 g/L and 75 °C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H{sub 2}O{sub 2} in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1 ? (1 ? X){sup 1/3} = k{sub c}t. Leaching kinetics of cobalt fitted well to the model ‘ash diffusion control dense constant sizes spherical particles’ i.e. 1 ? 3(1 ? X){sup 2/3} + 2(1 ? X) = k{sub c}t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

Jha, Manis Kumar, E-mail: mkjha@nmlindia.org; Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

2013-09-15T23:59:59.000Z

467

Chemical overcharge protection of lithium and lithium-ion secondary batteries  

DOE Patents [OSTI]

This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn{sub 2}O{sub 4} positive electrode (cathode). 8 figs.

Abraham, K.M.; Rohan, J.F.; Foo, C.C.; Pasquariello, D.M.

1999-01-12T23:59:59.000Z

468

Chemical overcharge protection of lithium and lithium-ion secondary batteries  

DOE Patents [OSTI]

This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn.sub.2 O.sub.4 positive electrode (cathode).

Abraham, Kuzhikalail M. (Needham, MA); Rohan, James F. (Cork City, IE); Foo, Conrad C. (Dedham, MA); Pasquariello, David M. (Pawtucket, RI)

1999-01-01T23:59:59.000Z

469

Verification and Validation Strategy for Implementation of Hybrid Potts-Phase Field Hydride Modeling Capability in MBM  

SciTech Connect (OSTI)

The Used Fuel Disposition (UFD) program has initiated a project to develop a hydride formation modeling tool using a hybrid Potts­phase field approach. The Potts model is incorporated in the SPPARKS code from Sandia National Laboratories. The phase field model is provided through MARMOT from Idaho National Laboratory.

Jason D. Hales; Veena Tikare

2014-04-01T23:59:59.000Z

470

OBSERVATIONS IN REACTIVITY BETWEEN BH CONTAINING COMPOUNDS AND ORGANOMETALLIC REAGENTS: SYNTHESIS OF BORONIC ACIDS, BORONIC ESTERS, AND MAGNESIUM HYDRIDES  

E-Print Network [OSTI]

aryl bromides and H 2 BN(iPr) 2 Scheme 2.7. Hydroboration oftransfer hydride to BH 2 -N(iPr) 2 Scheme 2.10. Conversionchloride with BH 2 -N(iPr) 2 Scheme 3; Aqueous quench of p-

Clary, Jacob William

2012-01-01T23:59:59.000Z

471

Room-Temperature Metal-Hydride Discharge Source, with Observations on NiH and FeH Raphael Vallon,  

E-Print Network [OSTI]

Room-Temperature Metal-Hydride Discharge Source, with Observations on NiH and FeH Raphae¨l Vallon laser excitation and dispersed fluorescence spectra of NiH have also been recorded. The source has been are strong enough to record dispersed fluorescence from NiH by Fourier transform interferometry in magnetic

Ashworth, Stephen H.

472

Thin film method of conducting lithium-ions  

DOE Patents [OSTI]

The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li.sub.2 O--CeO.sub.2 --SiO.sub.2 system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications.

Zhang, Ji-Guang (Golden, CO); Benson, David K. (Golden, CO); Tracy, C. Edwin (Golden, CO)

1998-11-10T23:59:59.000Z

473

Thin film method of conducting lithium-ions  

DOE Patents [OSTI]

The present invention relates to the composition of a solid lithium-ion electrolyte based on the Li{sub 2}O-CeO{sub 2}-SiO{sub 2} system having good transparent characteristics and high ion conductivity suitable for uses in lithium batteries, electrochromic devices and other electrochemical applications. 12 figs.

Zhang, J.G.; Benson, D.K.; Tracy, C.E.

1998-11-10T23:59:59.000Z

474

Integration of Arsenic Trisulfide and Titanium Diffused Lithium Niobate Waveguides  

E-Print Network [OSTI]

A chalcogenide glass (arsenic-trisulfide, As2S3) optical waveguide is vertically integrated onto titanium-diffused lithium-niobate (Ti:LiNbO3) waveguides to add optical feedback paths and to create more compact optical circuits. Lithium...

Solmaz, Mehmet E.

2011-08-08T23:59:59.000Z

475

Liquid surface skimmer apparatus for molten lithium and method  

DOE Patents [OSTI]

This invention relates to an apparatus for separating two fluids having different specific gravities. The invention also relates to a method for using the separating apparatus of the present invention. This invention particularly relates to the skimming of molten lithium metal from the surface of a fused salt electrolyte in the electrolytic production of lithium metal from a mixed fused salt.

Robinson, Samuel C. (Knoxville, TN); Pollard, Roy E. (Maryville, TN); Thompson, William F. (Oak Ridge, TN); Stark, Marshall W. (Gastonia, NC); Currin, Jr., Robert T. (Salisbury, NC)

1995-01-01T23:59:59.000Z

476

Cubic Lithium Nitride Amy Lazicki1,2  

E-Print Network [OSTI]

Cubic Lithium Nitride to 200 GPa Amy Lazicki1,2 Choong-Shik Yoo1, Warren Pickett2, Richard electrolyte material for lithium-based batteries · possible hydrogen storage material Thrust of this research ­ differences between the XRS and PDOS are indications of the presence of core-hole interactions (excitons

Islam, M. Saif

477

Lithium Lorentz Force Accelerator Thruster (LiLFA)  

E-Print Network [OSTI]

Argon Flow Copper Water Flow Piston/Lithium Feeding System Lithium Flow Pipes Heaters Heaters MAI Li procedure · Fire the thruster! #12;Previous Firing #12;Conclusions · Heaters and Thermocouples · Water Vacuum Pumps Thrust Stand Main Tank Water Line In Water Line Out Power Lines Computer Data Acquisition

Petta, Jason

478

Development of Regenerable High Capacity Boron Nitrogen Hydrides as Hydrogen Storage Materials  

SciTech Connect (OSTI)

The objective of this three-phase project is to develop synthesis and hydrogen extraction processes for nitrogen/boron hydride compounds that will permit exploitation of the high hydrogen content of these materials. The primary compound of interest in this project is ammonia-borane (NH{sub 3}BH{sub 3}), a white solid, stable at ambient conditions, containing 19.6% of its weight as hydrogen. With a low-pressure on-board storage and an efficient heating system to release hydrogen, ammonia-borane has a potential to meet DOE's year 2015 specific energy and energy density targets. If the ammonia-borane synthesis process could use the ammonia-borane decomposition products as the starting raw material, an efficient recycle loop could be set up for converting the decomposition products back into the starting boron-nitrogen hydride. This project is addressing two key challenges facing the exploitation of the boron/nitrogen hydrides (ammonia-borane), as hydrogen storage material: (1) Development of a simple, efficient, and controllable system for extracting most of the available hydrogen, realizing the high hydrogen density on a system weight/volume basis, and (2) Development of a large-capacity, inexpensive, ammonia-borane regeneration process starting from its decomposition products (BNHx) for recycle. During Phase I of the program both catalytic and non-catalytic decomposition of ammonia borane are being investigated to determine optimum decomposition conditions in terms of temperature for decomposition, rate of hydrogen release, purity of hydrogen produced, thermal efficiency of decomposition, and regenerability of the decomposition products. The non-catalytic studies provide a base-line performance to evaluate catalytic decomposition. Utilization of solid phase catalysts mixed with ammonia-borane was explored for its potential to lower the decomposition temperature, to increase the rate of hydrogen release at a given temperature, to lead to decomposition products amenable for regeneration, and direct catalytic hydrogenation of the decomposition products. Two different approaches of heating ammonia-borane are being investigated: (a) 'heat to material approach' in which a fixed compartmentalized ammonia-borane is heated by a carefully controlled heating pattern, and (b) 'material to heat approach' in which a small amount of ammonia-borane is dispensed at a time in a fixed hot zone. All stages of AB decomposition are exothermic which should allow the small 'hot zone' used in the second approach for heating to be self-sustaining. During the past year hydrogen release efforts focused on the second approach determining the amount of hydrogen released, kinetics of hydrogen release, and the amounts of impurities released as a function of AB decomposition temperature in the 'hot zone.'

Damle, A.

2010-02-03T23:59:59.000Z

479

Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural carbonates  

E-Print Network [OSTI]

Measurement of lithium isotope ratios by quadrupole-ICP-MS: application to seawater and natural method for lithium isotope ratio (7 Li/6 Li) determinations with low total lithium consumption ( lithium from all matrix elements using small volume resin (2 ml/3.4 meq AG 50W-X8) and low volume elution

Weston, Ken

480

Kinetics of Initial Lithiation of Crystalline Silicon Electrodes of Lithium-Ion Batteries  

E-Print Network [OSTI]

Kinetics of Initial Lithiation of Crystalline Silicon Electrodes of Lithium-Ion Batteries Matt phase. KEYWORDS: Lithium-ion batteries, silicon, kinetics, plasticity Lithium-ion batteries already at the electrolyte/lithiated silicon interface, diffusion of lithium through the lithiated phase, and the chemical

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


481

Analysis of the October 5, 1979 lithium spill and fire in the Lithium Processing Test Loop  

SciTech Connect (OSTI)

On October 5, 1979, the Lithium Processing Test Loop (LPTL) developed a lithium leak in the electromagnetic (EM) pump channel, which damaged the pump, its surrounding support structure, and the underlying floor pan. A thorough analysis of the causes and consequences of the pump failure was conducted by personnel from CEN and several other ANL divisions. Metallurgical analyses of the elliptical pump channel and adjacent piping revealed that there was a significant buildup of iron-rich crystallites and other solid material in the region of the current-carrying bus bars (region of high magnetic field), which may have resulted in a flow restriction that contributed to the deterioration of the channel walls. The location of the failure was in a region of high residual stress (due to cold work produced during channel fabrication); this failure is typical of other cold work/stress-related failures encountered in components operated in forced-circulation lithium loops. Another important result was the isolation of crystals of a compound characterized as Li/sub x/CrN/sub y/. Compounds of this type are believed to be responsible for much of the Fe, Cr, and Ni mass transfer encountered in lithium loops constructed of stainless steel. The importance of nitrogen in the mass-transfer mechanism has long been suspected, but the existence of stable ternary Li-M-N compounds (M = Fe, Cr, Ni) had not previously been verified.

Maroni, V.A.; Beatty, R.A.; Brown, H.L.; Coleman, L.F.; Foose, R.M.; McPheeters, C.C.; Slawecki, M.; Smith, D.L.; Van Deventer, E.H.; Weston, J.R.

1981-12-01T23:59:59.000Z

482

Factors influencing the discharge characteristics of Na0.44MnO2-based positive electrode materials for rechargeable lithium batteries  

E-Print Network [OSTI]

for Rechargeable Lithium Batteries Marca M. Doeff, Kwang-For Rechargeable Lithium Batteries Marca M. Doefr*, Kwang-FOR RECHARGEABLE LITHIUM BATTERIES Marca M. Doeff * , Kwang-

Doeff, M.M.

2011-01-01T23:59:59.000Z

483

The Impact Of Lithium Wall Coatings On NSTX Discharges And The Engineering Of The Lithium Tokamak eXperiment (LTX)  

SciTech Connect (OSTI)

Recent experiments on the National Spherical Torus eXperiment (NSTX) have shown the benefits of solid lithium coatings on carbon PFC's to diverted plasma performance, in both Land H- mode confinement regimes. Better particle control, with decreased inductive flux consumption, and increased electron temperature, ion temperature, energy confinement time, and DD neutron rate were observed. Successive increases in lithium coverage resulted in the complete suppression of ELM activity in H-mode discharges. A liquid lithium divertor (LLD), which will employ the porous molybdenum surface developed for the LTX shell, is being installed on NSTX for the 2010 run period, and will provide comparisons between liquid walls in the Lithium Tokamak eXperiment (LTX) and liquid divertor targets in NSTX. LTX, which recently began operations at the Princeton Plasma Physics Laboratory, is the world's first confinement experiment with full liquid metal plasma-facing components (PFCs). All materials and construction techniques in LTX are compatible with liquid lithium. LTX employs an inner, heated, stainless steel-faced liner or shell, which will be lithium-coated. In order to ensure that lithium adheres to the shell, it is designed to operate at up to 500 - 600 oC to promote wetting of the stainless by the lithium, providing the first hot wall in a tokamak to operate at reactor-relevant temperatures. The engineering of LTX will be discussed.

R. Majeski, H. Kugel and R. Kaita

2010-03-18T23:59:59.000Z

484

A New Method for Quantitative Marking of Deposited Lithium via Chemical Treatment on Graphite Anodes in Lithium-Ion Cells  

E-Print Network [OSTI]

A New Method for Quantitative Marking of Deposited Lithium via Chemical Treatment on Graphite*[e] and Thomas Schleid[f] Abstract: A novel approach for the marking of deposited lithium on graphite anodes from of the electrochemical stability window of the electrolyte components.[3] Therefore, changes on the electrode

Schmidt, Volker

485

Deposition of lithium on a plasma edge probe in TFTR -- Behavior of lithium-painted walls interacting with edge plasmas  

SciTech Connect (OSTI)

Recent observations have indicated that lithium pellet injection wall conditioning plays an important role in achieving the enhanced supershot regime in TFTR. However, little is understood about the behavior of lithium-coated limiter walls, interacting with edge plasmas. In the final campaign of TFTR, a cylindrical carbon fiber composite probe was inserted into the boundary plasma region and exposed to ohmically-heated deuterium discharges with lithium pellet injection. The ion-drift side probe surface exhibits a sign of codeposition of lithium, carbon, oxygen, and deuterium, whereas the electron side essentially indicates high-temperature erosion. It is found that lithium is incorporated in these codeposits in the form of oxide at the concentration of a few percent. In the electron side, lithium has been found to penetrate deeply into the probe material, presumably via rapid diffusion through interplane spaces in the graphite crystalline. Though it is not conclusive, materials mixing in the carbon and lithium system appears to be a key process in successful lithium wall conditioning.

Hirooka, Y. [Univ. of California, San Diego, La Jolla, CA (United States); Ashida, K. [Toyama Univ. (Japan); Kugel, H. [Princeton Univ., NJ (United States)] [and others

1998-05-01T23:59:59.000Z

486

A comparative study of the corrosion resistance of an austenitic steel in lithium and the eutectic lead-lithium alloy  

SciTech Connect (OSTI)

In a number of designs of thermonuclear reactors, besides liquid lithium, the use of lead-lithium alloy of the eutectic composition (Pb/sub 83/ Li/sub 17/) is envisaged for tritium breeding, heat transfer, and protecting the primary wall. The interaction of this alloy with water and air is less vigorous as compared to lithium, and the (n, 2n) type reactions involving lead atoms can ensure a tritium-breeding factor exceeding unity in the blanket at a relatively low concentration of lithium in the alloy. Tests are carried out on the 18-10 steel in convective currents of lithium and the Pb-17Li alloy in order to compare their corrosive action on the austenitic chromiumnickel steels that are promising materials for the primary wall and the blanket. Based on the obtained results, the high corrosive activity of the lead-lithium alloy as compared to pure lithium can be explained in the following way: the increased solubility of iron in lead as compared to that in lithium alone cannot ensure the observed rate of mass transfer of the steel by the lead base alloy.

Gryaznov, G.M.; Evtikhin, V.A.; Kosukhin, A.Y.; Zavyal'skii, L.P.

1986-05-01T23:59:59.000Z

487

Electronic transport in Lithium Nickel Manganese Oxide, a high-voltage cathode material for Lithium-Ion batteries  

E-Print Network [OSTI]

Potential routes by which the energy densities of lithium-ion batteries may be improved abound. However, the introduction of Lithium Nickel Manganese Oxide (LixNi1i/2Mn3/2O4, or LNMO) as a positive electrode material appears ...

Ransil, Alan Patrick Adams

2013-01-01T23:59:59.000Z

488

Metal Hydrides  

Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

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489

Startup and Operation of a Metal Hydride Based Isotope Separation Process  

SciTech Connect (OSTI)

Production scale separation of tritium from other hydrogen isotopes at the Savannah River Site (SRS) in Aiken, SC, has been accomplished by several methods. These methods include thermal diffusion (1957--1986), fractional absorption (1964--1968), and cryogenic distillation (1967-present). Most recently, the Thermal Cycling Absorption Process (TCAP), a metal hydride based hydrogen isotope separation system, began production in the Replacement Tritium Facility (RTF) on April 9, 1994. TCAP has been in development at the Savannah River Technology Center since 1980. The production startup of this semi-continuous gas chromatographic separation process is a significant accomplishment for the Savannah River Site and was achieved after years of design, development, and testing.

Scogin, J.H.; Poore, A.S.

1995-02-27T23:59:59.000Z

490

Quantum Simulation of Helium Hydride in a Solid-State Spin Register  

E-Print Network [OSTI]

\\emph{Ab initio} computation of molecular properties is one of the most promising applications of quantum computing. While this problem is widely believed to be intractable for classical computers, efficient quantum algorithms exist which have the potential to vastly accelerate research throughput in fields ranging from material science to drug discovery. Using a solid-state quantum register realized in a nitrogen-vacancy (NV) defect in diamond, we compute the bond dissociation curve of the minimal basis helium hydride cation, HeH$^+$. Moreover, we report an energy uncertainty (given our model basis) of the order of $10^{-14}$ Hartree, which is ten orders of magnitude below desired chemical precision. As NV centers in diamond provide a robust and straightforward platform for quantum information processing, our work provides several important steps towards a fully scalable solid state implementation of a quantum chemistry simulator.

Ya Wang; Florian Dolde; Jacob Biamonte; Ryan Babbush; Ville Bergholm; Sen Yang; Ingmar Jakobi; Philipp Neumann; Alán Aspuru-Guzik; James D. Whitfield; Jörg Wrachtrup

2014-05-12T23:59:59.000Z

491

Mechanistic Insights into Hydride Transfer for Catalytic Hydrogenation of CO2 with Cobalt Complexes  

SciTech Connect (OSTI)

The catalytic hydrogenation of CO2 to formate by Co(dmpe)2H can proceeds via direct hydride transfer or via CO2 coordination to Co followed by reductive elimination of formate. Both pathways have activation barriers consistent with experiment (~17.5 kcal/mol). Controlling the basicity of Co by ligand design is key to improve catalysis. The research by N.K., D.M.C. and A.M.A. was supported by the US Department of Energy, Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. The research by S.R. and M.D. was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for the DOE by Battelle.

Kumar, Neeraj; Camaioni, Donald M.; Dupuis, Michel; Raugei, Simone; Appel, Aaron M.

2014-08-21T23:59:59.000Z

492

LaNi{sub 5}-based metal hydride electrode in Ni-MH rechargeable cells  

DOE Patents [OSTI]

An at least ternary metal alloy of the formula AB{sub (Z-Y)}X{sub (Y)} is disclosed. In this formula, A is selected from the rare earth elements, B is selected from the elements of Groups 8, 9, and 10 of the Periodic Table of the Elements, and X includes at least one of the following: antimony, arsenic, germanium, tin or bismuth. Z is greater than or equal to 4.8 and less than or equal to 6.0. Y is greater than 0 and less than 1. Ternary or higher-order substitutions to the base AB{sub 5} alloys that form strong kinetic interactions with the predominant metals in the base metal hydride are used to form metal alloys with high structural integrity after multiple cycles of hydrogen sorption. 16 figs.

Bugga, R.V.; Fultz, B.; Bowman, R.; Surampudi, S.R.; Witham, C.K.; Hightower, A.

1999-03-30T23:59:59.000Z

493

Production of Hydrogen by Electrocatalysis: Making the H-H Bond by Combining Protons and Hydrides  

SciTech Connect (OSTI)

Generation of hydrogen by reduction of two protons by two electrons can be catalysed by molecular electrocatalysts. Determination of the thermodynamic driving force for elimination of H2 from molecular complexes is important for the rational design of molecular electrocatalysts, and allows the design of metal complexes of abundant, inexpensive metals rather than precious metals (“Cheap Metals for Noble Tasks”). The rate of H2 evolution can be dramatically accelerated by incorporating pendant amines into diphosphine ligands. These pendant amines in the second coordination sphere function as protons relays, accelerating intramolecular and intermolecular proton transfer reactions. The thermodynamics of hydride transfer from metal hydrides and the acidity of protonated pendant amines (pKa of N-H) contribute to the thermodynamics of elimination of H2; both of the hydricity and acidity can be systematically varied by changing the substituents on the ligands. A series of Ni(II) electrocatalysts with pendant amines have been developed. In addition to the thermochemical considerations, the catalytic rate is strongly influenced by the ability to deliver protons to the correct location of the pendant amine. Protonation of the amine endo to the metal leads to the N-H being positioned appropriately to favor rapid heterocoupling with the M-H. Designing ligands that include proton relays that are properly positioned and thermodynamically tuned is a key principle for molecular electrocatalysts for H2 production as well as for other multi-proton, multi-electron reactions important for energy conversions. The research was supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences. Pacific Northwest National Laboratory is operated by Battelle for DOE.

Bullock, R. Morris; Appel, Aaron M.; Helm, Monte L.

2014-03-25T23:59:59.000Z

494

Electric quadrupole transition probabilities for atomic lithium  

SciTech Connect (OSTI)

Electric quadrupole transition probabilities for atomic lithium have been calculated using the weakest bound electron potential model theory (WBEPMT). We have employed numerical non-relativistic Hartree–Fock wavefunctions for expectation values of radii and the necessary energy values have been taken from the compilation at NIST. The results obtained with the present method agree very well with the Coulomb approximation results given by Caves (1975). Moreover, electric quadrupole transition probability values not existing in the literature for some highly excited levels have been obtained using the WBEPMT.

Çelik, Gültekin, E-mail: gultekin@selcuk.edu.tr [Department of Physics, Faculty of Science, Selçuk University, Campus 42049 Konya (Turkey); Gökçe, Yasin; Y?ld?z, Murat [Department of Physics, Faculty of Science, Karamanoglu Mehmetbey University, Karaman (Turkey)

2014-05-15T23:59:59.000Z

495

Long life lithium batteries with stabilized electrodes  

DOE Patents [OSTI]

The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In some embodiments the additives include a substituted or unsubstituted cyclic or spirocyclic hydrocarbon containing at least one oxygen atom and at least one alkenyl or alkynyl group. When used in electrochemical devices with, e.g., lithium manganese oxide spinel electrodes or olivine or carbon-coated olivine electrodes, the new electrolytes provide batteries with improved calendar and cycle life.

Amine, Khalil (Downers Grove, IL); Liu, Jun (Naperville, IL); Vissers, Donald R. (Naperville, IL); Lu, Wenquan (Darien, IL)

2009-03-24T23:59:59.000Z

496

Lithium Metal Anodes for Rechargeable Batteries. | EMSL  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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497

Lithium-Ion Batteries - Energy Innovation Portal  

Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: VegetationEquipment Surfaces and Interfaces Sample6, 2011Liisa O'NeillFuelsLaboratoryLithium

498

American Lithium Energy Corp | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 NoPublic Utilities Address: 160 East 300Algoil JumpAltergy SystemsAmerican Energy Systems Inc Place:Fork,Lithium

499

Testing of Liquid Lithium Limiters in CDX-U  

SciTech Connect (OSTI)

Part of the development of liquid metals as a first wall or divertor for reactor applications must involve the investigation of plasma-liquid metal interactions in a functioning tokamak. Most of the interest in liquid-metal walls has focused on lithium. Experiments with lithium limiters have now been conducted in the Current Drive Experiment-Upgrade (CDX-U) device at the Princeton Plasma Physics Laboratory. Initial experiments used a liquid-lithium rail limiter (L3) built by the University of California at San Diego. Spectroscopic measurements showed some reduction of impurities in CDX-U plasmas with the L3, compared to discharges with a boron carbide limiter. While no reduction in recycling was observed with the L3, which had a plasma-wet area of approximately 40 cm2, subsequent experiments with a larger area fully toroidal lithium limiter demonstrated significant reductions in both recycling and in impurity levels. Two series of experiments with the toroidal limiter have now be en performed. In each series, the area of exposed, clean lithium was increased, until in the latest experiments the liquid-lithium plasma-facing area was increased to 2000 cm2. Under these conditions, the reduction in recycling required a factor of eight increase in gas fueling in order to maintain the plasma density. The loop voltage required to sustain the plasma current was reduced from 2 V to 0.5 V. This paper summarizes the technical preparations for lithium experiments and the conditioning required to prepare the lithium surface for plasma operations. The mechanical response of the liquid metal to induced currents, especially through contact with the plasma, is discussed. The effect of the lithium-filled toroidal limiter on plasma performance is also briefly described.

R. Majeski; R. Kaita; M. Boaz; P. Efthimion; T. Gray; B. Jones; D. Hoffman; H. Kugel; J. Menard; T. Munsat; A. Post-Zwicker; V. Soukhanovskii; J. Spaleta; G. Taylor; J. Timberlake; R. Woolley; L. Zakharov; M. Finkenthal; D. Stutman; G. Antar; R. Doerner; S. Luckhardt; R. Seraydarian; R. Maingi; M. Maiorano; S. Smith; D. Rodgers

2004-07-30T23:59:59.000Z

500

Novel carbonaceous materials for lithium secondary batteries  

SciTech Connect (OSTI)

Carbonaceous materials have been synthesized using pillared clays (PILCs) as templates. The PILC was loaded with organic materials such as pyrene in the liquid and vapor phase, styrene in the vapor phase, trioxane, ethylene and propylene. The samples were then pyrolyzed at 700 C in an inert atmosphere, followed by dissolution of the inorganic template by conventional demineralization methods. X-ray powder diffraction of the carbons showed broad d{sub 002} peaks in the diffraction pattern, indicative of a disordered or turbostratic system. N{sub 2} BET surface areas of the carbonaceous materials range from 10 to 100 m{sup 2}/g. There is some microporosity (r < 1 nm) in the highest surface area carbons. Most of the surface area, however, comes from a mixture of micro and mesopores with radii of 2--5 nm. Electrochemical studies were performed on these carbons. Button cells were fabricated with capacity- limiting carbon pellets electrodes as the cathode a/nd metallic lithium foil as the anode. Large reversible capacities (up to 850 mAh/g) were achieved for most of the samples. The irreversible capacity loss was less than 180 mAh/g after the first cycle, suggesting that these types of carbon materials are very stable to lithium insertion and de-insertion reactions.

Sandi, G.; Winans, R.E.; Carrado, K.A.; Johnson, C.S.

1997-07-01T23:59:59.000Z