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Sample records for electrolyte non-pyrolytically produced

  1. Autogenous electrolyte, non-pyrolytically produced solid capacitor structure

    DOEpatents

    Sharp, D.J.; Armstrong, P.S.; Panitz, J.K.G.

    1998-03-17

    A solid electrolytic capacitor is described having a solid electrolyte comprising manganese dioxide dispersed in an aromatic polyamide capable of further cure to form polyimide linkages, the solid electrolyte being disposed between a first electrode made of valve metal covered by an anodic oxide film and a second electrode opposite the first electrode. The electrolyte autogenously produces water, oxygen, and hydroxyl groups which act as healing substances and is not itself produced pyrolytically. Reduction of the manganese dioxide and the water molecules released by formation of imide linkages result in substantially improved self-healing of anodic dielectric layer defects. 2 figs.

  2. Autogenous electrolyte, non-pyrolytically produced solid capacitor structure

    DOEpatents

    Sharp, Donald J.; Armstrong, Pamela S.; Panitz, Janda Kirk G.

    1998-01-01

    A solid electrolytic capacitor having a solid electrolyte comprising manganese dioxide dispersed in an aromatic polyamide capable of further cure to form polyimide linkages, the solid electrolyte being disposed between a first electrode made of valve metal covered by an anodic oxide film and a second electrode opposite the first electrode. The electrolyte autogenously produces water, oxygen, and hydroxyl groups which act as healing substances and is not itself produced pyrolytically. Reduction of the manganese dioxide and the water molecules released by formation of imide linkages result in substantially improved self-healing of anodic dielectric layer defects.

  3. Autogenous electrolyte, non-pyrolytically produced solid capacitor structure

    SciTech Connect

    Sharp, D.J.; Armstrong, P.S.; Paintz, J.K.G.

    1998-04-01

    This report discusses the design of a solid electrolytic capacitor having a solid electrolyte comprised of manganese dioxide dispersed in an aromatic polyamide capable of to forming polyimide linkages. This solid electrolyte being disposed between a first electrode made of valve metal covered by an anodic oxide film and a second electrode opposite the first electrode. The electrolyte autogenously produces water, oxygen, and hydroxyl groups which act as healing substances and is not itself produced pyrolytically. Reduction of the manganese dioxide and the water molecules released by formation of imide linkages result in substantially improved self-healing of anodic dielectric layer defects.

  4. Cathode for aluminum producing electrolytic cell

    DOEpatents

    Brown, Craig W.

    2004-04-13

    A method of producing aluminum in an electrolytic cell comprising the steps of providing an anode in a cell, preferably a non-reactive anode, and also providing a cathode in the cell, the cathode comprised of a base material having low electrical conductivity reactive with molten aluminum to provide a highly electrically conductive layer on the base material. Electric current is passed from the anode to the cathode and alumina is reduced and aluminum is deposited at the cathode. The cathode base material is selected from boron carbide, and zirconium oxide.

  5. Electric current-producing device having sulfone-based electrolyte

    SciTech Connect

    Angell, Charles Austen; Sun, Xiao-Guang

    2010-11-16

    Electrolytic solvents and applications of such solvents including electric current-producing devices. For example, a solvent can include a sulfone compound of R1--SO2--R2, with R1 being an alkyl group and R2 a partially oxygenated alkyl group, to exhibit high chemical and thermal stability and high oxidation resistance. For another example, a battery can include, between an anode and a cathode, an electrolyte which includes ionic electrolyte salts and a non-aqueous electrolyte solvent which includes a non-symmetrical, non-cyclic sulfone. The sulfone has a formula of R1--SO2--R2, wherein R1 is a linear or branched alkyl or partially or fully fluorinated linear or branched alkyl group having 1 to 7 carbon atoms, and R2 is a linear or branched or partially or fully fluorinated linear or branched oxygen containing alkyl group having 1 to 7 carbon atoms. The electrolyte can include an electrolyte co-solvent and an electrolyte additive for protective layer formation.

  6. Cu--Ni--Fe anode for use in aluminum producing electrolytic cell

    DOEpatents

    Bergsma, S. Craig; Brown, Craig W.; Bradford, Donald R; Barnett, Robert J.; Mezner, Michael B.

    2006-07-18

    A method of producing aluminum in an electrolytic cell containing alumina dissolved in an electrolyte, the method comprising the steps of providing a molten salt electrolyte at a temperature of less than 900.degree. C. having alumina dissolved therein in an electrolytic cell having a liner for containing the electrolyte, the liner having a bottom and walls extending upwardly from said bottom. A plurality of non-consumable Cu--Ni--Fe anodes and cathodes are disposed in a vertical direction in the electrolyte, the cathodes having a plate configuration and the anodes having a flat configuration to compliment the cathodes. The anodes contain apertures therethrough to permit flow of electrolyte through the apertures to provide alumina-enriched electrolyte between the anodes and the cathodes. Electrical current is passed through the anodes and through the electrolyte to the cathodes, depositing aluminum at the cathodes and producing gas at the anodes.

  7. Maintaining molten salt electrolyte concentration in aluminum-producing electrolytic cell

    DOEpatents

    Barnett, Robert J.; Mezner, Michael B.; Bradford, Donald R

    2005-01-04

    A method of maintaining molten salt concentration in a low temperature electrolytic cell used for production of aluminum from alumina dissolved in a molten salt electrolyte contained in a cell free of frozen crust wherein volatile material is vented from the cell and contacted and captured on alumina being added to the cell. The captured volatile material is returned with alumina to cell to maintain the concentration of the molten salt.

  8. Electrolytes

    MedlinePlus

    ... body fluids that carry an electric charge. Electrolytes affect how your body functions in many ways, including: The amount of water in your body The acidity of your blood (pH) Your muscle function Other important processes You lose ...

  9. Cathode for a hall-heroult type electrolytic cell for producing aluminum

    DOEpatents

    Brown, Craig W.

    2004-04-13

    A method of producing aluminum from alumina in an electrolytic cell including using a cathode comprised of a base material having low electrical conductivity and wettable with molten aluminum to form a reaction layer having a high electrical conductivity on said base layer and a cathode bar extending from said reaction layer through said base material to conduct electrical current from said reaction layer.

  10. Underwater microdischarge in arranged microbubbles produced by electrolysis in electrolyte solution using fabric-type electrode

    SciTech Connect

    Sakai, Osamu; Kimura, Masaru; Tachibana, Kunihide; Shirafuji, Tatsuru

    2008-12-08

    Pulsed microdischarge was generated in microbubbles produced by electrolysis in an electrolyte solution without external gas feed by using a fabric-type electrode. The electrode structure not only allowed low-voltage ignition of the atmospheric-pressure discharge in hydrogen or oxygen containing microbubbles but also worked effectively in producing and holding the bubbles on its surface. The generation of reactive species was verified by optical emissions from the produced microplasmas, and their transport into the solution was monitored by the change in hydrogen concentration.

  11. Cathodes for secondary electrochemical power-producing cells. [layers of porous substrates impregnated with S alternate with layers containing electrolyte

    DOEpatents

    Cairns, E.J.; Kyle, M.; Shimotake, H.

    1973-02-13

    A secondary electrochemical power-producing cell includes an anode containing lithium, an electrolyte containing lithium ions, and a cathode containing sulfur. The cathode comprises plates of a porous substrate material impregnated with sulfur alternating with layers (which may also comprise porous substrate plates) containing electrolyte.

  12. Electrolytic process to produce sodium hypochlorite using sodium ion conductive ceramic membranes

    SciTech Connect

    Balagopal, Shekar; Malhotra, Vinod; Pendleton, Justin; Reid, Kathy Jo

    2012-09-18

    An electrochemical process for the production of sodium hypochlorite is disclosed. The process may potentially be used to produce sodium hypochlorite from seawater or low purity un-softened or NaCl-based salt solutions. The process utilizes a sodium ion conductive ceramic membrane, such as membranes based on NASICON-type materials, in an electrolytic cell. In the process, water is reduced at a cathode to form hydroxyl ions and hydrogen gas. Chloride ions from a sodium chloride solution are oxidized in the anolyte compartment to produce chlorine gas which reacts with water to produce hypochlorous and hydrochloric acid. Sodium ions are transported from the anolyte compartment to the catholyte compartment across the sodium ion conductive ceramic membrane. Sodium hydroxide is transported from the catholyte compartment to the anolyte compartment to produce sodium hypochlorite within the anolyte compartment.

  13. Influence of pyrolytic and non-pyrolytic rice and castor straws on the immobilization of Pb and Cu in contaminated soil.

    PubMed

    Rizwan, Muhammad Shahid; Imtiaz, Muhammad; Chhajro, Muhammad Afzal; Huang, Guoyong; Fu, Qingling; Zhu, Jun; Aziz, Omar; Hu, Hongqing

    2016-11-01

    Soil contamination with heavy metals has become a global environmental health concern. In the present study, European Community Bureau of Reference (BCR) sequential extraction and toxicity characteristic leaching procedure (TCLP) techniques were used to evaluate the Pb and Cu subsequent transformations, immobilizing impact of pyrolytic and non-pyrolytic rice and castor straws and their efficiency to reduce the metals mobility and leachability in the polluted soil. Obtained results highlight the potential of biochar over non-pyrolytic residues to enhance the immobilization of Pb and Cu in the soil. Castor leaves-derived biochar (CLB), castor stem-derived biochar (CSB), and rice straw-derived biochar (RSB) prominently decreased the mobility (acid-soluble fraction) of Pb 49.8%, 31.1%, and 31.9%, respectively, while Cu decreased 15.8%, 11.5%, and 12%, respectively, as compare to control. Sequential extraction showed that biochar treatments prominently modified the proportioning of Pb and Cu from acid soluble to a less bioavailable fraction and increased the geochemical stability in the polluted soil as compared to relative feedstocks as well as the controlled soil. Additionally, the soil pH increased markedly after the addition of biochar. Compared with control, the TCLP-extractable Pb and Cu were reduced to 29.2-41.4% and 5.7-22.8% from the soil respectively by the application of CLB. The immobilization and reduction in leachability of Pb and Cu were correlated with the soil pH. The biochar effect on the Pb immobilization was much better as compared to Cu in co-contaminated soil. Overall addition of CLB offered the best results and could be effective in both Pb and Cu immobilization thereby reducing their mobility and bioavailability in the co-contaminated soil. PMID:26934087

  14. Method of producing ceramic distribution members for solid state electrolyte cells

    NASA Technical Reports Server (NTRS)

    Clark, Douglas J. (Inventor); Galica, Leo M. (Inventor); Losey, Robert W. (Inventor); Suitor, Jerry W. (Inventor)

    1995-01-01

    A solid state electrolyte cells apparatus and method of producing is disclosed. The apparatus can be used for separating oxygen from an oxygen-containing feedstock or as a fuel cell for reacting fluids. Cells can be stacked so that fluids can be introduced and removed from the apparatus through ceramic distribution members having ports designed for distributing the fluids in parallel flow to and from each cell. The distribution members can also serve as electrodes to membranes or as membrane members between electrodes, The distribution member design does not contain any horizontal internal ports which allows the member to be thin. A method of tape casting in combination with an embossing method allows intricate radial ribs and bosses to be formed on each distribution member. The bosses serve as seals for the ports and allow the distribution members to be made without any horizontal internal ports.

  15. Ceramic distribution members for solid state electrolyte cells and method of producing

    NASA Technical Reports Server (NTRS)

    Clark, Douglas J. (Inventor); Galica, Leo M. (Inventor); Losey, Robert W. (Inventor); Suitor, Jerry W. (Inventor)

    1993-01-01

    A solid state electrolyte cells apparatus and method of producing is disclosed. The apparatus can be used for separating oxygen from an oxygen-containing feedstock or as a fuel cell for reacting fluids. Cells can be stacked so that fluids can be introduced and removed from the apparatus through ceramic distribution members having ports designed for distributing the fluids in parallel flow to and from each cell. The distribution members can also serve as electrodes to membranes or as membrane members between electrodes. The distribution member design does not contain any horizontal internal ports which allows the member to be thin. A method of tape casting in combination with an embossing method allows intricate radial ribs and bosses to be formed on each distribution member. The bosses serve as seals for the ports and allow the distribution members to be made without any horizontal internal ports.

  16. Effect of the graphite electrode material on the characteristics of molten salt electrolytically produced carbon nanomaterials

    SciTech Connect

    Kamali, Ali Reza Schwandt, Carsten; Fray, Derek J.

    2011-10-15

    The electrochemical erosion of a graphite cathode during the electrolysis of molten lithium chloride salt may be used for the preparation of nano-structured carbon materials. It has been found that the structures and morphologies of these carbon nanomaterials are dependent on those of the graphite cathodes employed. A combination of tubular and spherical carbon nanostructures has been produced from a graphite with a microstructure of predominantly planar micro-sized grains and a minor fraction of more irregular nano-sized grains, whilst only spherical carbon nanostructures have been produced from a graphite with a microstructure of primarily nano-sized grains. Based on the experimental results, a best-fit regression equation is proposed that relates the crystalline domain size of the graphite reactants and the carbon products. The carbon nanomaterials prepared possess a fairly uniform mesoporosity with a sharp peak in pore size distribution at around 4 nm. The results are of crucial importance to the production of carbon nanomaterials by way of the molten salt electrolytic method. - Highlights: {yields} Carbon nanomaterials are synthesised by LiCl electrolysis with graphite electrodes. {yields} The degree of crystallinity of graphite reactant and carbon product are related. {yields} A graphite reactant is identified that enables the preparation of carbon nanotubes. {yields} The carbon products possess uniform mesoporosity with narrow pore size distribution.

  17. Microstructure and Mechanical Properties of AA1235 Aluminum Foil Stocks Produced Directly from Electrolytic Aluminum Melt

    NASA Astrophysics Data System (ADS)

    Xiong, Hanqing; Yu, Kun; Wen, Li; Yao, Sujuan; Dai, Yilong; Wang, Zhifeng

    2016-02-01

    A new process is developed to obtain high-quality AA1235 aluminum foil stocks and to replace the traditional manufacture process. During the new manufacture process, AA1235 aluminum sheets are twin-roll casted directly through electrolytic aluminum melt (EAM), and subsequently the sheets are processed into aluminum foil stocks by cold rolling and annealing. Microstructure and mechanical properties of the AA1235 aluminum sheets produced through such new process are investigated in each state by optimal microscope, scanning electron microscopy, X-ray diffraction, orientation imaging microscopy, transmission electron microscopy, etc. The results show that compared with the traditional AA1235 aluminum foil stocks produced through re-melted aluminum melt (RAM), the amount of impurities is decreased in the EAM aluminum foil stocks. The EAM aluminum foil stock obtains less β-FeSiAl5 phases, but more α-Fe2SiAl8 phases. The elongation of EAM aluminum foil stocks is improved significantly owing to more cubic orientation. Especially, the elongation value of the EAM aluminum foil stocks is approximately 25 pct higher than that of the RAM aluminum foil stocks. As a result, the EAM aluminum foil stocks are at an advantage in increasing the processing performance for the aluminum foils during subsequent processes.

  18. Method for producing electricity from a fuel cell having solid-oxide ionic electrolyte

    DOEpatents

    Mason, David M.

    1984-01-01

    Stabilized quadrivalent cation oxide electrolytes are employed in fuel cells at elevated temperatures with a carbon and/or hydrogen containing fuel anode and an oxygen cathode. The fuel cell is operated at elevated temperatures with conductive metallic coatings as electrodes and desirably having the electrolyte surface blackened. Of particular interest as the quadrivalent oxide is zirconia.

  19. Characteristics and in vitro response of thin hydroxyapatite–titania films produced by plasma electrolytic oxidation of Ti alloys in electrolytes with particle additions

    PubMed Central

    Yeung, W. K.; Sukhorukova, I. V.; Shtansky, D. V.; Levashov, E. A.; Zhitnyak, I. Y.; Gloushankova, N. A.; Kiryukhantsev-Korneev, P. V.; Petrzhik, M. I.; Matthews, A.

    2016-01-01

    The enhancement of the biological properties of Ti by surface doping with hydroxyapatite (HA) is of great significance, especially for orthodontic applications. This study addressed the effects of HA particle size in the electrolyte suspension on the characteristics and biological properties of thin titania-based coatings produced on Ti–6Al–4V alloy by plasma electrolytic oxidation (PEO). Detailed morphological investigation of the coatings formed by a single-stage PEO process with two-step control of the electrical parameters was performed using the Minkowski functionals approach. The surface chemistry was studied by glow discharge optical emission spectroscopy and Fourier transform infrared spectroscopy, whereas mechanical properties were evaluated using scratch tests. The biological assessment included in vitro evaluation of the coating bioactivity in simulated body fluid (SBF) as well as studies of spreading, proliferation and osteoblastic differentiation of MC3T3-E1 cells. The results demonstrated that both HA micro- and nanoparticles were successfully incorporated in the coatings but had different effects on their surface morphology and elemental distributions. The micro-particles formed an irregular surface morphology featuring interpenetrated networks of fine pores and coating material, whereas the nanoparticles penetrated deeper into the coating matrix which retained major morphological features of the porous TiO2 coating. All coatings suffered cohesive failure in scratch tests, but no adhesive failure was observed; moreover doping with HA increased the coating scratch resistance. In vitro tests in SBF revealed enhanced bioactivity of both HA-doped PEO coatings; furthermore, the cell proliferation/morphometric tests showed their good biocompatibility. Fluorescence microscopy revealed a well-organised actin cytoskeleton and focal adhesions in MC3T3-E1 cells cultivated on these substrates. The cell alkaline phosphatase activity in the presence of

  20. [Russian oxygen generation system "Elektron-VM": hydrogen content in electrolytically produced oxygen for breathing by International Space Station crews].

    PubMed

    Proshkin, V Yu; Kurmazenko, E A

    2014-01-01

    The article presents the particulars of hydrogen content in electrolysis oxygen produced aboard the ISS Russian segment by oxygen generator "Elektron-VM" (SGK) for crew breathing. Hydrogen content was estimated as in the course of SGK operation in the ISS RS, so during the ground life tests. According to the investigation of hydrogen sources, the primary path of H2 appearance in oxygen is its diffusion through the porous diaphragm separating the electrolytic-cell cathode and anode chambers. Effectiveness of hydrogen oxidation in the SGK reheating unit was evaluated.

  1. [Russian oxygen generation system "Elektron-VM": hydrogen content in electrolytically produced oxygen for breathing by International Space Station crews].

    PubMed

    Proshkin, V Yu; Kurmazenko, E A

    2014-01-01

    The article presents the particulars of hydrogen content in electrolysis oxygen produced aboard the ISS Russian segment by oxygen generator "Elektron-VM" (SGK) for crew breathing. Hydrogen content was estimated as in the course of SGK operation in the ISS RS, so during the ground life tests. According to the investigation of hydrogen sources, the primary path of H2 appearance in oxygen is its diffusion through the porous diaphragm separating the electrolytic-cell cathode and anode chambers. Effectiveness of hydrogen oxidation in the SGK reheating unit was evaluated. PMID:25035898

  2. S-N Fatigue Behavior of Anodized 7050-T7451 Produced in Different Electrolytes

    NASA Astrophysics Data System (ADS)

    Lee, Eungyeong; Jeong, Yooin; Kim, Sangshik

    2012-06-01

    The effect of anodizing layers processed in different electrolytes of chromic acid (chromic acid anodizing [CAA]), sulfuric acid (sulfuric acid anodizing [SAA]), and tartaric acid (tartaric acid anodizing [TAA]) on the S-N fatigue behavior of the 7050-T7451 specimen was examined. The fatigue tests were conducted at an R ratio of 0.1 and at three different stress levels of 200, 220, and 270 MPa. Some specimens were exposed to continuous salt spraying of 5 pct NaCl solution for 336 hours and subsequently fatigue tested at an applied stress of 200 MPa. The detrimental effect of anodizing on the S-N fatigue resistance of 7050-T7451 was observed. The fatigue resistance varied with different anodizing electrolytes particularly at low stress with the greatest resistance for the TAA followed by CAA and SAA. The fractographic and micrographic observations showed the morphological difference in each anodized layer, which seemed to determine the ease of crack initiation and the resistance to S-N fatigue. The resistance to S-N fatigue of anodized 7050-T7451 specimens was, for example, affected strongly by the nature of preanodized layer with different acid-pickling processes. The pits found in the pre-CAA specimens seemed to be slightly irregular and deeper than those in the pre-TAA counterparts, reducing the fatigue resistance of the 7050-T7451 specimens. The CAA, SAA, and TAA specimens showed similar resistance to corrosion plus fatigue.

  3. High-performance dye-sensitized solar cells based on solvent-free electrolytes produced from eutectic melts.

    PubMed

    Bai, Yu; Cao, Yiming; Zhang, Jing; Wang, Mingkui; Li, Renzhi; Wang, Peng; Zakeeruddin, Shaik M; Grätzel, Michael

    2008-08-01

    Low-cost excitonic solar cells based on organic optoelectronic materials are receiving an ever-increasing amount of attention as potential alternatives to traditional inorganic photovoltaic devices. In this rapidly developing field, the dye-sensitized solar cell (DSC) has achieved so far the highest validated efficiency of 11.1% (ref. 2) and remarkable stability. However, the cells with the best performance use volatile solvents in their electrolytes, which may be prohibitive for outdoor solar panels in view of the need for robust encapsulation. Solvent-free room-temperature ionic liquids have been pursued as an attractive solution to this dilemma, and device efficiencies of over 7% were achieved by using some low-viscosity formulations containing 1-ethyl-3-methylimidazolium thiocyanate, selenocyanate, tricyanomethide or tetracyanoborate. Unfortunately, apart from tetracyanoborate, all of these low-viscosity melts proved to be unstable under prolonged thermal stress and light soaking. Here, we introduce the concept of using eutectic melts to produce solvent-free liquid redox electrolytes. Using a ternary melt in conjunction with a nanocrystalline titania film and the amphiphilic heteroleptic ruthenium complex Z907Na (ref. 10) as a sensitizer, we reach excellent stability and an unprecedented efficiency of 8.2% under air-mass 1.5 global illumination. Our results are of importance to realize large-scale outdoor applications of mesoscopic DSCs.

  4. High-performance dye-sensitized solar cells based on solvent-free electrolytes produced from eutectic melts.

    PubMed

    Bai, Yu; Cao, Yiming; Zhang, Jing; Wang, Mingkui; Li, Renzhi; Wang, Peng; Zakeeruddin, Shaik M; Grätzel, Michael

    2008-08-01

    Low-cost excitonic solar cells based on organic optoelectronic materials are receiving an ever-increasing amount of attention as potential alternatives to traditional inorganic photovoltaic devices. In this rapidly developing field, the dye-sensitized solar cell (DSC) has achieved so far the highest validated efficiency of 11.1% (ref. 2) and remarkable stability. However, the cells with the best performance use volatile solvents in their electrolytes, which may be prohibitive for outdoor solar panels in view of the need for robust encapsulation. Solvent-free room-temperature ionic liquids have been pursued as an attractive solution to this dilemma, and device efficiencies of over 7% were achieved by using some low-viscosity formulations containing 1-ethyl-3-methylimidazolium thiocyanate, selenocyanate, tricyanomethide or tetracyanoborate. Unfortunately, apart from tetracyanoborate, all of these low-viscosity melts proved to be unstable under prolonged thermal stress and light soaking. Here, we introduce the concept of using eutectic melts to produce solvent-free liquid redox electrolytes. Using a ternary melt in conjunction with a nanocrystalline titania film and the amphiphilic heteroleptic ruthenium complex Z907Na (ref. 10) as a sensitizer, we reach excellent stability and an unprecedented efficiency of 8.2% under air-mass 1.5 global illumination. Our results are of importance to realize large-scale outdoor applications of mesoscopic DSCs. PMID:18587401

  5. Fluoride ions as modifiers of the oxide layer produced by plasma electrolytic oxidation on AZ91D magnesium alloy

    NASA Astrophysics Data System (ADS)

    Kazanski, Barbara; Kossenko, Alexey; Zinigrad, Michael; Lugovskoy, Alex

    2013-12-01

    Plasma electrolytic oxidation (PEO) is a powerful technique allowing hardening and corrosion protection of valve metals due to formation of an oxide layer on the metal surface. PEO produces much thicker oxide layers as compared to anodizing, which is of critical importance for many technological applications. The present research investigated the influence of the fluoride ion concentration on the composition, structure and morphology of PEO layers on the magnesium alloy AZ91D. The obtained oxide layers were characterized with XRD, SEM, EDS and tested for corrosion resistance by linear sweep voltammetry in 3.5% NaCl medium. During this investigation it was found that KF addition produces significant changes in the structure and properties of the oxide layers. Fluorine was detected as an amorphous phase in the vicinity of the base metal for both alloys and plausible mechanism was suggested to explain these phenomena. Fluoride ions have pronounced catalytic activity and their presence considerably increases the thickness of the oxide layer. Depending on the process parameters, significant improvement of the corrosion stability of AZ91D alloy is achieved by the use of PEO.

  6. Stabilization of the high-temperature phases in ceramic coatings on zirconium alloy produced by plasma electrolytic oxidation

    NASA Astrophysics Data System (ADS)

    Apelfeld, A. V.; Betsofen, S. Y.; Borisov, A. M.; Vladimirov, B. V.; Savushkina, S. V.; Knyazev, E. V.

    2016-09-01

    The composition and structure of ceramic coatings obtained on Zr-1%Nb alloy by plasma electrolytic oxidation (PEO) in aqueous electrolyte comprising 2 g/L KOH, 6 g/L NaAlO2 and 2 g/L Na2SiO3 with addition of yttria nanopowder, have been studied. The PEO coatings of thickness ∼⃒20 μm were studied using scanning electron microscopy, X-ray microanalysis and X-ray phase analysis. Additives in the electrolyte of yttria nanopowder allowed stabilizing the high-temperature tetragonal and cubic zirconia in the coating.

  7. Effect of Nano-crystalline Ceramic Coats Produced by Plasma Electrolytic Oxidation on Corrosion Behavior of AA5083 Aluminum Alloy

    NASA Astrophysics Data System (ADS)

    Thayananth, T.; Muthupandi, V.; Rao, S. R. Koteswara

    2010-10-01

    High specific strength offered by aluminum and magnesium alloys makes them desirable in modern transportation industries. Often the restrictions imposed on the usage of these alloys are due to their poor tribological and corrosion properties. However, their corrosion properties can be further enhanced by synthesizing ceramic coating on the substrate through Plasma Electrolytic Oxidation (PEO) process. In this study, nano-crystalline alumina coatings were formed on the surface of AA5083 aluminum alloy test coupons using PEO process in aqueous alkali-silicate electrolyte with and without addition of sodium aluminate. X-ray diffraction (XRD) studies showed that the crystallite size varied between 38 and 46 nm and α- and γ- alumina were the dominant phases present in the coatings. Corrosion studies by potentiodynamic polarization tests in 3.5% NaCl revealed that the electrolyte composition has an influence on the corrosion resistance of nano-crystalline oxide layer formed.

  8. Electrolytes Test

    MedlinePlus

    ... include other tests such as BUN , creatinine , and glucose . Electrolyte measurements may be used to help investigate conditions that cause electrolyte imbalances such as dehydration , kidney disease , lung diseases , or heart conditions . Repeat testing may then ...

  9. Influence of the Ti microstructure on anodic self-organized TiO2 nanotube layers produced in ethylene glycol electrolytes

    NASA Astrophysics Data System (ADS)

    Macak, J. M.; Jarosova, M.; Jäger, A.; Sopha, H.; Klementová, M.

    2016-05-01

    The relationship between the microstructure of Ti substrates and the anodic growth of self-organized TiO2 nanotube layers obtained upon their anodization in the ethylene glycol based electrolytes on these substrates is reported for the first time. Polished Ti sheets with mirror-like surface as well as unpolished Ti foils were considered in this work. Grains with a wide range of crystallographic orientations and sizes were revealed by Electron Backscatter Diffraction (EBSD) and correlated with nanotube growth on both types of substrates. A preferred grain orientation with [0 0 0 1] axis perpendicular to the surface was observed on all substrates. Surfaces of all substrates were anodized for 18 h in ethylene glycol electrolytes containing 88 mM NH4F and 1.5% water and thoroughly inspected by SEM. By a precise comparison of Ti substrates before and after anodization, the uniformity of produced self-organized TiO2 nanotube layers was evaluated in regard to the specific orientation of individual grains. Grains with [0 0 0 1] axis perpendicular to the surface turned out to be the most growth-promoting orientation on polished substrates. No orientation was found to be strictly growth-retarding, but sufficient anodization time (24 h) was needed to obtain uniform nanotube layers on all grains without remnant porous initial oxide. In contrast with polished Ti sheets, no specific orientation was found to significantly promote or retard the nanotube growth in the case of unpolished Ti foils. Finally, the difference between the average nanotube diameters of nanotubes grown on various grains was investigated showing non-negligible differences in the diameter for different grain orientations and substrates.

  10. Some preliminary evaluations of black coating on aluminium AA2219 alloy produced by plasma electrolytic oxidation (PEO) process for space applications

    NASA Astrophysics Data System (ADS)

    Shrestha, S.; Merstallinger, A.; Sickert, D.; Dunn, B. D.

    2003-09-01

    This paper describes the results of a study of a black coating produced on aluminium AA2219 alloy using a process that involves creation of a hard ceramic oxide layer on the surface of the alloy by plasma electrolytic oxidation (PEO) known as the 'KERONITE®' process. Coating microstructure has been examined and the coating characteristics such as porosity, hardness, adhesion and phase composition were measured. The thermo-optical properties such as solar absorptance 'as' and normal infrared emittance 'en-IR' of the coating were measured in the 'as-prepared' condition and after environmental exposures to humidity, thermal cycling and UV-radiation in vacuum and to thermal shock. Comparison was made with alternative coatings produced using standard black anodising processes. The study also looked at the cold welding and friction behaviours of the coated alloy in vacuum and in an ambient laboratory environment. Standard spacecraft materials tests were conducted on the coated disc against an AISI 52100 steel ball and also against a coated pin using a pin-on-disc apparatus. Parameters such as friction coefficient and wear depth were measured and the cold welding behaviours were investigated. Test results were compared with the data generated for NiCr plated and anodised coatings. Corrosion performance was assessed using a salt spray exposure test and using an accelerated electrochemical test method. In addition, the study looked at the effect of post coating sealing with a sol-gel solution.

  11. Electrolytic cell

    NASA Astrophysics Data System (ADS)

    Bullock, J. S.; Hale, B. D.

    1984-09-01

    An apparatus is described for the separation of the anolyte and the catholyte during electrolysis. The electrolyte flows through an electrolytic cell between the oppositely charged electrodes. The cell is equipped with a wedge-shaped device, the tapered end is located between the electrodes on the effluent side of the cell. The wedge diverts the flow of the electrolyte to either side of the wedge, substantially separating the anolyte and the catholyte.

  12. Electrolytic dissolver

    DOEpatents

    Wheelwright, E.J.; Fox, R.D.

    1975-08-26

    This patent related to an electrolytic dissolver wherein dissolution occurs by solution contact including a vessel of electrically insulative material, a fixed first electrode, a movable second electrode, means for insulating the electrodes from the material to be dissolved while permitting a free flow of electrolyte therebetween, means for passing a direct current between the electrodes and means for circulating electrolyte through the dissolver. (auth)

  13. ELECTROLYTIC PROCESS FOR PRODUCING METALS

    DOEpatents

    Kopelman, B.; Holden, R.B.

    1961-06-01

    A method is described for reducing beryllium halides to beryllium. The beryllfum halide fs placed in an eutectic mixture of alkali halides and alkaline earth halides. The constituents of this eutectic bath are so chosen that it has a melting point less than the boiling point of mercury, which acts as a cathode for the system. The beryllium metal is then deposited in the mercury upon electrolysis.

  14. Thin film polymeric gel electrolytes

    DOEpatents

    Derzon, Dora K.; Arnold, Jr., Charles; Delnick, Frank M.

    1996-01-01

    Novel hybrid thin film electrolyte, based on an organonitrile solvent system, which are compositionally stable, environmentally safe, can be produced efficiently in large quantity and which, because of their high conductivities .apprxeq.10.sup.-3 .OMEGA..sup.-1 cm.sup.-1 are useful as electrolytes for rechargeable lithium batteries.

  15. Thin film polymeric gel electrolytes

    DOEpatents

    Derzon, D.K.; Arnold, C. Jr.; Delnick, F.M.

    1996-12-31

    Novel hybrid thin film electrolytes, based on an organonitrile solvent system, which are compositionally stable, environmentally safe, can be produced efficiently in large quantity and which, because of their high conductivities {approx_equal}10{sup {minus}3}{Omega}{sup {minus}1} cm{sup {minus}1} are useful as electrolytes for rechargeable lithium batteries. 1 fig.

  16. Electrolyte Racers

    ERIC Educational Resources Information Center

    Kellie, Shawn; Kellie, Tonya; Corbin-Tipton, Elizabeth

    2006-01-01

    A fast way to teach investigative skills in science is to tie them to NASCAR using Hot Wheels Formula Fuelers Race Cars. These inexpensive toy cars travel different distances based on the strength of the "electrolyte" (a substance that conducts electricity when dissolved in water) in their "fuel" tanks. Advertisements for these race cars urge kids…

  17. Solid electrolytes

    DOEpatents

    Abraham, Kuzhikalail M.; Alamgir, Mohamed

    1993-06-15

    This invention pertains to Li ion (Li.sup.+) conductive solid polymer electrolytes composed of solvates of Li salts immobilized (encapsulated) in a solid organic polymer matrix. In particular, this invention relates to solid polymer electrolytes derived by immobilizing complexes (solvates) formed between a Li salt such as LiAsF.sub.6, LiCF.sub.3 SO.sub.3 or LiClO.sub.4 and a mixture of aprotic organic solvents having high dielectric constants such as ethylene carbonate (EC) (dielectric constant=89.6) and propylene carbonate (PC) (dielectric constant=64.4) in a polymer matrix such as polyacrylonitrile, poly(tetraethylene glycol diacrylate), or poly(vinyl pyrrolidinone).

  18. Electrolyte salts for nonaqueous electrolytes

    DOEpatents

    Amine, Khalil; Zhang, Zhengcheng; Chen, Zonghai

    2012-10-09

    Metal complex salts may be used in lithium ion batteries. Such metal complex salts not only perform as an electrolyte salt in a lithium ion batteries with high solubility and conductivity, but also can act as redox shuttles that provide overcharge protection of individual cells in a battery pack and/or as electrolyte additives to provide other mechanisms to provide overcharge protection to lithium ion batteries. The metal complex salts have at least one aromatic ring. The aromatic moiety may be reversibly oxidized/reduced at a potential slightly higher than the working potential of the positive electrode in the lithium ion battery. The metal complex salts may also be known as overcharge protection salts.

  19. Fabrication of large ceramic electrolyte disks

    NASA Technical Reports Server (NTRS)

    Ring, S. A.

    1972-01-01

    Process for sintering compressed ceramic powders produces large ceramic disks for use as electrolytes in high-temperature electrolytic cells. Thin, strain-free uniformly dense disks as large as 30 cm squared have been fabricated by slicing ceramic slugs produced by this technique.

  20. Electrolytic fixer.

    PubMed

    Stevens

    1982-12-01

    Interest in the recovery of silver from radiographic film generates a need to understand the operating procedures of recovery units utilizing the electrolytic fixer principle. Tailing or terminal units and recirculation units using electrolysis are evaluated. Difficulties encountered in the number of Coulombs applied to a specific amount of fixer are discussed. Reduction of sulfiding as a result of electrolysis and variations in film volumes are noted. The quantity and quality of silver collected can be improved by being aware of alterations in chemical activity used in a silver recovery program.

  1. Solid-oxide fuel cell electrolyte

    SciTech Connect

    Bloom, I.D.; Hash, M.C.; Krumpelt, M.

    1991-12-31

    This invention is comprised of a solid-oxide electrolyte operable at between 600{degrees}C and 800{degrees}C and a method of producing the solid-oxide electrolyte. The solid-oxide electrolyte comprises a combination of a compound having a weak metal-oxygen interactions with a compound having stronger metal-oxygen interactions whereby the resulting combination has both strong and weak metal-oxygen interaction properties.

  2. Solid-oxide fuel cell electrolyte

    DOEpatents

    Bloom, Ira D.; Hash, Mark C.; Krumpelt, Michael

    1993-01-01

    A solid-oxide electrolyte operable at between 600.degree. C. and 800.degree. C. and a method of producing the solid-oxide electrolyte are provided. The solid-oxide electrolyte comprises a combination of a compound having weak metal-oxygen interactions with a compound having stronger metal-oxygen interactions whereby the resulting combination has both strong and weak metal-oxygen interaction properties.

  3. Mechanical properties of Ti(C 0.7N 0.3) film produced by plasma electrolytic carbonitriding of Ti6Al4V alloy

    NASA Astrophysics Data System (ADS)

    Li, Xin-Mei; Han, Yong

    2008-08-01

    Porous nanocrystalline Ti(C 0.7N 0.3) film on Ti6Al4V substrate was prepared by plasma electrolytic carbonitriding (PECN). The film was characterized and analyzed by using a variety of analytical techniques, such as XRD, SEM, EDX, TEM, FESEM, Rockwell C indenter, scratch tester, Vickers microhardness tester and ring-on-block tribometer. The results showed that the film was about 15 μm thick and its hardness was Hv 2369 at a load of 0.2 N. The adhesion of the film was characterized by Lc and Pc value, and was found to be about 42 N and more than 800 N, respectively. The friction coefficients and wear volume loss of the PECN-treated samples sliding against a steel counterpart were much less than those of the untreated Ti6Al4V. The film possessed a good wear-resistance and antifriction under oil-lubricated condition due to its high hardness, adhesion and fracture toughness. Also, the porous surface morphology of the Ti(C 0.7N 0.3) film contributed to the enhanced tribological resistance by promoting the formation of lubricant film and entrapping wear debris.

  4. Electrolytic process for preparing uranium metal

    DOEpatents

    Haas, Paul A.

    1990-01-01

    An electrolytic process for making uranium from uranium oxide using Cl.sub.2 anode product from an electrolytic cell to react with UO.sub.2 to form uranium chlorides. The chlorides are used in low concentrations in a melt comprising fluorides and chlorides of potassium, sodium and barium in the electrolytic cell. The electrolysis produces Cl.sub.2 at the anode that reacts with UO.sub.2 in the feed reactor to form soluble UCl.sub.4, available for a continuous process in the electrolytic cell, rather than having insoluble UO.sub.2 fouling the cell.

  5. Electrolytic Cell For Production Of Aluminum Employing Planar Anodes.

    DOEpatents

    Barnett, Robert J.; Mezner, Michael B.; Bradford, Donald R

    2004-10-05

    A method of producing aluminum in an electrolytic cell containing alumina dissolved in an electrolyte, the method comprising providing a molten salt electrolyte having alumina dissolved therein in an electrolytic cell. A plurality of anodes and cathodes having planar surfaces are disposed in a generally vertical orientation in the electrolyte, the anodes and cathodes arranged in alternating or interleaving relationship to provide anode planar surfaces disposed opposite cathode planar surfaces, the anode comprised of carbon. Electric current is passed through anodes and through the electrolyte to the cathodes depositing aluminum at the cathodes and forming carbon containing gas at the anodes.

  6. Recovery of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, Mark W.; George, William A.

    1989-01-01

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

  7. Recovery of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, Mark W.; George, William A.

    1988-01-01

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

  8. Recovery of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, M.W.; George, W.A.

    1991-06-18

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg[sub 2]Cl[sub 2] employing as the electrolyte solution a mixture of HCl and H[sub 2]O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H[sub 2]O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds. 3 figures.

  9. Recovery of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, M.W.; George, W.A.

    1989-11-07

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg[sub 2]Cl[sub 2] employing as the electrolyte solution a mixture of HCl and H[sub 2]O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H[sub 2]O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds. 3 figs.

  10. Recovery of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, Mark W.; George, William A.

    1991-01-01

    A process for electrolytically recovering mercury from mercury compounds is provided. In one embodiment, Hg is recovered from Hg.sub.2 Cl.sub.2 employing as the electrolyte solution a mixture of HCl and H.sub.2 O. In another embodiment, Hg is electrolytically recovered from HgO wherein the electrolyte solution is comprised of glacial acetic acid and H.sub.2 O. Also provided is an apparatus for producing isotopically enriched mercury compounds in a reactor and then transporting the dissolved compounds into an electrolytic cell where mercury ions are electrolytically reduced and elemental mercury recovered from the mercury compounds.

  11. Electrolytic pretreatment of urine

    NASA Technical Reports Server (NTRS)

    1977-01-01

    Electrolysis has been under evaluation for several years as a process to pretreat urine for ultimate recovery of potable water in manned spacecraft applications. The conclusions that were drawn from this investigation are the following: (1) A platinum alloy containing 10 percent rhodium has been shown to be an effective, corrosion-resistant anode material for the electrolytic pretreatment of urine. Black platinum has been found to be suitable as a cathode material. (2) The mechanism of the reactions occurring during the electrolysis of urine is two-stage: (a) a total Kjeldahl nitrogen and total organic carbon (TOC) removal in the first stage is the result of electrochemical oxidation of urea to CO2, H2O, and ammonia followed by chloride interaction to produce N2 from ammonia, (b) after the urea has been essentially removed and the chloride ions have no more ammonia to interact with, the chloride ions start to oxidize to higher valence states, thus producing perchlorates. (3) Formation of perchlorates can be suppressed by high/low current operation, elevated temperature, and pH adjustment. (4) UV-radiation showed promise in assisting electrolytic TOC removal in beaker tests, but was not substantiated in limited single cell testing. This may have been due to non-optimum configurations of the single cell test rig and the light source.

  12. Glass electrolytes

    SciTech Connect

    Not Available

    1984-06-25

    The objective of this research is a glass electrolyte for use in sodium/sulfur batteries that has a low resistivity (100 ohm-cm at 300/sup 0/C) and is stable in the cell environment. Experiments in this program are focussed on glasses in the quaternary system: soda, alumina, zirconia and silica. The FY 1983 research on glass analogs of NASICON, parallel thermodynamic calculations, and a review of the literature in the areas of glass conductivity and corrosion resistance led to selection of this system for more detailed investigation. The main program elements are: (1) conductivity measurements at 300 to 500/sup 0/C; (2) differential thermal analysis for determination of glass-transition and crystallization temperatures; (3) static corrosion tests at 400/sup 0/C using Na, Na/sub 2/S/sub 4/, and S; (4) mechanical strength and fracture toughness measurements; and (5) sodium/sulfur cell tests at 350/sup 0/C. Elements (1) and (2) are nearly completed; element (3) is being initiated using the glasses prepared for (1) and (2), and elements (4) and (5) will begin in the first and second quarters of FY 1985, respectively. Fourteen quaternary glasses having a broad range of compositions have been made. The resistivities of these glasses at 300/sup 0/C extended from 130 to 3704 ohm-cm; the activation energies for conduction extended from 0.488 to 0.684 eV, and the glass transition temperatures extended from 397 to 685/sup 0/C. Through a multiple linear regression analysis of these data response surfaces were generated for resistivity, activation energy for conduction, and glass transition temperature over the composition region within the quaternary system that is bounded by SiO/sub 2/, Na/sub 2/O/sub 3/, Na/sub 2/AlO/sub 4/ and Na/sub 2/ZrO/sub 3/. These response surfaces indicated a new region of high conductivity and high glass transition temperature in the neighborhood of 42% soda, 31% silica and 27% alumina plus zirconia.

  13. Fuel cell having electrolyte

    DOEpatents

    Wright, Maynard K.

    1989-01-01

    A fuel cell having an electrolyte control volume includes a pair of porous opposed electrodes. A maxtrix is positioned between the pair of electrodes for containing an electrolyte. A first layer of backing paper is positioned adjacent to one of the electrodes. A portion of the paper is substantially previous to the acceptance of the electrolyte so as to absorb electrolyte when there is an excess in the matrix and to desorb electrolyte when there is a shortage in the matrix. A second layer of backing paper is positioned adjacent to the first layer of paper and is substantially impervious to the acceptance of electrolyte.

  14. A simple synthesis method to produce metal oxide loaded carbon paper using bacterial cellulose gel and characterization of its electrochemical behavior in an aqueous electrolyte

    NASA Astrophysics Data System (ADS)

    Miyajima, Naoya; Jinguji, Ken; Matsumura, Taiyu; Matsubara, Toshihiro; Sakane, Hideto; Akatsu, Takashi; Tanaike, Osamu

    2016-04-01

    A simple synthetic chemical process to produce metal oxide loaded carbon papers was developed using bacterial cellulose gel, which consisted of nanometer-sized fibrous cellulose and water. Metal ions were successfully impregnated into the gel via aqueous solution media before drying and carbonization methods resulting in metal oxide contents that were easy to control through variations in the concentration of aqueous solutions. The papers loaded by molybdenum oxides were characterized as pseudocapacitor electrodes preliminary, and the large redox capacitance of the oxides was followed by a conductive fibrous carbon substrate, suggesting that a binder and carbon black additive-free electrode consisting of metal oxides and carbon paper was formed.

  15. Process for producing silicon

    DOEpatents

    Olson, J.M.; Carleton, K.L.

    1982-06-10

    A process of producing silicon includes forming an alloy of copper and silicon and positioning the alloy in a dried, molten salt electrolyte to form a solid anode structure therein. An electrically conductive cathode is placed in the electrolyte for plating silicon thereon. The electrolyte is then purified to remove dissolved oxides. Finally, an electrical potential is applied between the anode and cathode in an amount sufficient to form substantially pure silicon on the cathode in the form of substantially dense, coherent deposits.

  16. Electrolytic production of neodymium without perfluorinated carbon compounds on the offgases

    DOEpatents

    Keller, Rudolf; Larimer, Kirk T.

    1998-01-01

    A method of producing neodymium in an electrolytic cell without formation of perfluorinated carbon gases (PFCs), the method comprising the steps of providing an electrolyte in the electrolytic cell and providing an anode in an anode region of the electrolyte and providing a cathode in a cathode region of the electrolytic cell. Dissolving an oxygen-containing neodymium compound in the electrolyte in the anode region and maintaining a more intense electrolyte circulation in the anode region than in the cathode region. Passing an electrolytic current between said anode and said cathode and depositing neodymium metal at the cathode, preventing the formation of perfluorinated carbon gases by limiting anode over voltage.

  17. Molten salt electrolyte separator

    DOEpatents

    Kaun, Thomas D.

    1996-01-01

    A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

  18. Electrolyte materials containing highly dissociated metal ion salts

    SciTech Connect

    Lee, Hung-Sui; Geng, Lin; Skotheim, Terje A.

    1996-07-23

    The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy of dissociation and may be dissolved in a suitable polymer to produce a polymer solid electrolyte or in a polar aprotic liquid solvent to produce a liquid electrolyte. The anion of the salts may be covalently attached to polymer backbones to produce polymer solid electrolytes with exclusive cation conductivity.

  19. Electrolyte materials containing highly dissociated metal ion salts

    SciTech Connect

    Lee, H.S.; Geng, L.; Skotheim, T.A.

    1996-07-23

    The present invention relates to metal ion salts which can be used in electrolytes for producing electrochemical devices, including both primary and secondary batteries, photoelectrochemical cells and electrochromic displays. The salts have a low energy of dissociation and may be dissolved in a suitable polymer to produce a polymer solid electrolyte or in a polar aprotic liquid solvent to produce a liquid electrolyte. The anion of the salts may be covalently attached to polymer backbones to produce polymer solid electrolytes with exclusive cation conductivity. 2 figs.

  20. Solid polymer electrolyte compositions

    DOEpatents

    Garbe, James E.; Atanasoski, Radoslav; Hamrock, Steven J.; Le, Dinh Ba

    2001-01-01

    An electrolyte composition is featured that includes a solid, ionically conductive polymer, organically modified oxide particles that include organic groups covalently bonded to the oxide particles, and an alkali metal salt. The electrolyte composition is free of lithiated zeolite. The invention also features cells that incorporate the electrolyte composition.

  1. Lithium ion conducting electrolytes

    DOEpatents

    Angell, Charles Austen; Liu, Changle; Xu, Kang; Skotheim, Terje A.

    1999-01-01

    The present invention relates generally to highly conductive alkali-metal ion non-crystalline electrolyte systems, and more particularly to novel and unique molten (liquid), rubbery, and solid electrolyte systems which are especially well suited for use with high current density electrolytic cells such as primary and secondary batteries.

  2. Nanoporous polymer electrolyte

    DOEpatents

    Elliott, Brian; Nguyen, Vinh

    2012-04-24

    A nanoporous polymer electrolyte and methods for making the polymer electrolyte are disclosed. The polymer electrolyte comprises a crosslinked self-assembly of a polymerizable salt surfactant, wherein the crosslinked self-assembly includes nanopores and wherein the crosslinked self-assembly has a conductivity of at least 1.0.times.10.sup.-6 S/cm at 25.degree. C. The method of making a polymer electrolyte comprises providing a polymerizable salt surfactant. The method further comprises crosslinking the polymerizable salt surfactant to form a nanoporous polymer electrolyte.

  3. Electrolyte vapor condenser

    DOEpatents

    Sederquist, Richard A.; Szydlowski, Donald F.; Sawyer, Richard D.

    1983-01-01

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

  4. Electrolyte vapor condenser

    DOEpatents

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

    1983-02-08

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

  5. Apparatus for the electrolytic production of metals

    DOEpatents

    Sadoway, Donald R.

    1993-01-01

    Improved electrolytic cells for producing metals by the electrolytic reduction of a compound dissolved in a molten electrolyte are disclosed. In the improved cells, at least one electrode includes a protective layer comprising an oxide of the cell product metal formed upon an alloy of the cell product metal and a more noble metal. In the case of an aluminum reduction cell, the electrode can comprise an alloy of aluminum with copper, nickel, iron, or combinations thereof, upon which is formed an aluminum oxide protective layer.

  6. Portable electrophoresis apparatus using minimum electrolyte

    NASA Technical Reports Server (NTRS)

    Stevens, M. R.; Vickers, J. M. (Inventor)

    1976-01-01

    An electrophoresis unit for use in conducting electrophoretic analysis of specimens is described. The unit includes a sealable container in which a substrate mounted specimen is suspended in an electrolytic vapor. A heating unit is employed to heat a supply of electrolyte to produce the vapor. The substrate is suspended within the container by being attached between a pair of clips which also serve as electrodes to which a direct current power source may be connected.

  7. Ceramic electrolyte coating methods

    DOEpatents

    Seabaugh, Matthew M.; Swartz, Scott L.; Dawson, William J.; McCormick, Buddy E.

    2004-10-12

    Processes for preparing aqueous suspensions of a nanoscale ceramic electrolyte material such as yttrium-stabilized zirconia. The invention also includes a process for preparing an aqueous coating slurry of a nanoscale ceramic electrolyte material. The invention further includes a process for depositing an aqueous spray coating slurry including a ceramic electrolyte material on pre-sintered, partially sintered, and unsintered ceramic substrates and products made by this process.

  8. Electrolytic purification of metals

    DOEpatents

    Bowman, Kenneth A.

    1980-01-01

    A method of electrolytically separating metal from impurities comprises providing the metal and impurities in a molten state in a container having a porous membrane therein, the membrane having a thickness in the range of about 0.01 to 0.1 inch, being capable of containing the molten metal in the container, and being permeable by a molten electrolyte. The metal is electrolytically transferred through the membrane to a cathode in the presence of the electrolyte for purposes of separating or removing impurities from the metal.

  9. Molten salt electrolyte separator

    DOEpatents

    Kaun, T.D.

    1996-07-09

    The patent describes a molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication. 5 figs.

  10. Solid electrolyte oxygen regeneration system

    NASA Technical Reports Server (NTRS)

    Shumar, J. W.; See, G. G.; Schubert, F. H.; Powell, J. D.

    1976-01-01

    A program to design, develop, fabricate and assemble a one-man, self-contained, solid electrolyte oxygen regeneration system (SX-1) incorporating solid electrolyte electrolyzer drums was completed. The SX-1 is a preprototype engineering model designed to produce 0.952 kg (2.1 lb)/day of breathable oxygen (O2) from the electrolysis of metabolic carbon dioxide (CO2) and water vapor. The CO2 supply rate was established based on the metabolic CO2 generation rate for one man of 0.998 kg (2.2 lb)/day. The water supply rate (0.254 kg (0.56 lb)/day) was designed to be sufficient to make up the difference between the 0.952 kg (2.1 lb)/day O2 generation specification and the O2 available through CO2 electrolysis, 0.726 kg (1.6 lb)/day. The SX-1 was successfully designed, fabricated and assembled. Design verification tests (DVT) or the CO Disproportionators, H2 separators, control instrumentation, monitor instrumentation, water feed mechanism were successfully completed. The erratic occurrence of electrolyzer drum leakage prevented the completion of the CO2 electrolyzer module and water electrolyzer module DVT's and also prevented the performance of SX-1 integrated testing. Further development work is required to improve the solid electrolyte cell high temperature seals.

  11. Electrolytic cell stack with molten electrolyte migration control

    DOEpatents

    Kunz, H.R.; Guthrie, R.J.; Katz, M.

    1987-03-17

    An electrolytic cell stack includes inactive electrolyte reservoirs at the upper and lower end portions thereof. The reservoirs are separated from the stack of the complete cells by impermeable, electrically conductive separators. Reservoirs at the negative end are initially low in electrolyte and the reservoirs at the positive end are high in electrolyte fill. During stack operation electrolyte migration from the positive to the negative end will be offset by the inactive reservoir capacity. In combination with the inactive reservoirs, a sealing member of high porosity and low electrolyte retention is employed to limit the electrolyte migration rate. 5 figs.

  12. Electrolytic cell stack with molten electrolyte migration control

    DOEpatents

    Kunz, H. Russell; Guthrie, Robin J.; Katz, Murray

    1988-08-02

    An electrolytic cell stack includes inactive electrolyte reservoirs at the upper and lower end portions thereof. The reservoirs are separated from the stack of the complete cells by impermeable, electrically conductive separators. Reservoirs at the negative end are initially low in electrolyte and the reservoirs at the positive end are high in electrolyte fill. During stack operation electrolyte migration from the positive to the negative end will be offset by the inactive reservoir capacity. In combination with the inactive reservoirs, a sealing member of high porosity and low electrolyte retention is employed to limit the electrolyte migration rate.

  13. Electrochemically stable electrolytes

    DOEpatents

    Angell, Charles Austen; Zhang, Sheng-Shui; Xu, Kang

    1999-01-01

    This invention relates generally to inorganic ionic liquids which function as electrolytes and do not crystallize at ambient temperature. More specifically, this invention is directed to quasi-salt inorganic ionic liquids which comprise the reaction product of a strong Lewis acid with an inorganic halide-donating molecule. This invention is further directed to quasi-salt inorganic ionic liquid mixtures which comprise combinations of electrolyte additives and quasi-salt inorganic ionic liquids. These quasi-salt inorganic ionic liquid mixtures are useful electrolytes.

  14. Electrochemically stable electrolytes

    DOEpatents

    Angell, C.A.; Zhang, S.S.; Xu, K.

    1999-01-05

    This invention relates generally to inorganic ionic liquids which function as electrolytes and do not crystallize at ambient temperature. More specifically, this invention is directed to quasi-salt inorganic ionic liquids which comprise the reaction product of a strong Lewis acid with an inorganic halide-donating molecule. This invention is further directed to quasi-salt inorganic ionic liquid mixtures which comprise combinations of electrolyte additives and quasi-salt inorganic ionic liquids. These quasi-salt inorganic ionic liquid mixtures are useful electrolytes. 16 figs.

  15. New Solid Polymer Electrolytes for Improved Lithium Batteries

    NASA Technical Reports Server (NTRS)

    Hehemann, David G.

    2002-01-01

    The objective of this work was to identify, synthesize and incorporate into a working prototype, next-generation solid polymer electrolytes, that allow our pre-existing solid-state lithium battery to function better under extreme conditions. We have synthesized polymer electrolytes in which emphasis was placed on the temperature-dependent performance of these candidate electrolytes. This project was designed to produce and integrate novel polymer electrolytes into a lightweight thin-film battery that could easily be scaled up for mass production and adapted to different applications.

  16. Method of preparing thin film polymeric gel electrolytes

    DOEpatents

    Derzon, D.K.; Arnold, C. Jr.

    1997-11-25

    Novel hybrid thin film electrolyte is described, based on an organonitrile solvent system, which are compositionally stable, environmentally safe, can be produced efficiently in large quantity and which, because of their high conductivities {approx_equal}10{sup {minus}3}{Omega}{sup {minus}1}cm{sup {minus}1} are useful as electrolytes for rechargeable lithium batteries. 1 fig.

  17. Method of preparing thin film polymeric gel electrolytes

    DOEpatents

    Derzon, Dora K.; Arnold, Jr., Charles

    1997-01-01

    Novel hybrid thin film electrolyte, based on an organonitrile solvent system, which are compositionally stable, environmentally safe, can be produced efficiently in large quantity and which, because of their high conductivities .apprxeq.10.sup.-3 .OMEGA..sup.-1 cm.sup.-1 are useful as electrolytes for rechargeable lithium batteries.

  18. Electrolytic oxidation of anthracite

    USGS Publications Warehouse

    Senftle, F.E.; Patton, K.M.; Heard, I.

    1981-01-01

    An anthracite slurry can be oxidized only with difficulty by electrolytic methods in which aqueous electrolytes are used if the slurry is confined to the region of the anode by a porous pot or diaphragm. However, it can be easily oxidized if the anthracite itself is used as the anode. No porous pot or diaphragm is needed. Oxidative consumption of the coal to alkali-soluble compounds is found to proceed preferentially at the edges of the aromatic planes. An oxidation model is proposed in which the chief oxidants are molecular and radical species formed by the electrolytic decomposition of water at the coal surface-electrolyte interface. The oxidation reactions proposed account for the opening of the aromatic rings and the subsequent formation of carboxylic acids. The model also explains the observed anisotropic oxidation and the need for the porous pot or diaphragm used in previous studies of the oxidation of coal slurries. ?? 1981.

  19. Anion exchange polymer electrolytes

    SciTech Connect

    Kim, Yu Seung; Kim, Dae Sik

    2015-06-02

    Anion exchange polymer electrolytes that include guanidinium functionalized polymers may be used as membranes and binders for electrocatalysts in preparation of anodes for electrochemical cells such as solid alkaline fuel cells.

  20. Solid electrolyte cell

    NASA Technical Reports Server (NTRS)

    Richter, R. (Inventor)

    1982-01-01

    A solid electrolyte cell including a body of solid ionized gas-conductive electrolyte having mutually spaced surfaces and on which is deposited a multiplicity of mutually spaced electrodes is described. Strips and of bare substances are interposed between electrodes, so that currents of ionic gas may be established between the electrodes via the bare strips, whereby electrical resistance for the cells is lowered and the gas conductivity is enhanced.

  1. Apparatus and method for the electrolytic production of metals

    DOEpatents

    Sadoway, Donald R.

    1991-01-01

    Improved electrolytic cells and methods for producing metals by electrolytic reduction of a compound dissolved in a molten electrolyte are disclosed. In the improved cells and methods, a protective surface layer is formed upon at least one electrode in the electrolytic reduction cell and, optionally, upon the lining of the cell. This protective surface layer comprises a material that, at the operating conditions of the cell: (a) is not substantially reduced by the metal product; (b) is not substantially reactive with the cell electrolyte to form materials that are reactive with the metal product; and, (c) has an electrochemical potential that is more electronegative than that of the compound undergoing electrolysis to produce the metal product of the cell. The protective surface layer can be formed upon an electrode metal layer comprising a material, the oxide of which also satisfies the protective layer selection criteria. The protective layer material can also be used on the surface of a cell lining.

  2. Plasma electrolytic oxidation of AMCs

    NASA Astrophysics Data System (ADS)

    Morgenstern, R.; Sieber, M.; Lampke, T.

    2016-03-01

    Aluminum Matrix Composites (AMCs) consisting of high-strength alloys and ceramic reinforcement phases exhibit a high potential for security relevant lightweight components due to their high specific mechanical properties. However, their application as tribologically stressed components is limited because of their susceptibility against fatigue wear and delamination wear. Oxide ceramic protective coatings produced by plasma electrolytic oxidation (PEO) can solve these problems and extend the possible applications of AMCs. The substrate material was powder metallurgically processed using alloy EN AW 2017 and SiC or Al2O3 particles. The influence of material properties like particle type, size and volume fraction on coating characteristics is clarified within this work. An alkaline silicate electrolyte was used to produce PEO coatings with technically relevant thicknesses under bipolar-pulsed current conditions. Coating properties were evaluated with regard to morphology, chemical composition, hardness and wear resistance. The particle type proved to have the most significant effect on the coating properties. Whereas compactness and thickness are not deteriorated by the incorporation of thermodynamically stable alumina particles, the decomposition of silica particles during the PEO processes causes an increase of the porosity. The higher silica particle content decreases also the coating thickness and hardness, which leads in particular to reduction of the wear resistance of the PEO coatings. Finally, different approaches for the reduction of the coating porosity of silica reinforced AMCs are discussed.

  3. Method of fabrication of electrodes and electrolytes

    DOEpatents

    Jankowski, Alan F.; Morse, Jeffrey D.

    2004-01-06

    Fuel cell stacks contain an electrolyte layer surrounded on top and bottom by an electrode layer. Porous electrodes are prepared which enable fuel and oxidant to easily flow to the respective electrode-electrolyte interface without the need for high temperatures or pressures to assist the flow. Rigid, inert microspheres in combination with thin-film metal deposition techniques are used to fabricate porous anodes, cathodes, and electrolytes. Microshperes contained in a liquid are randomly dispersed onto a host structure and dried such that the microsperes remain in position. A thin-film deposition technique is subsequently employed to deposit a metal layer onto the microsperes. After such metal layer deposition, the microspheres are removed leaving voids, i.e. pores, in the metal layer, thus forming a porous electrode. Successive repetitions of the fabrication process result in the formation of a continuous fuel cell stack. Such stacks may produce power outputs ranging from about 0.1 Watt to about 50 Watts.

  4. Electrolytes in the Aging

    PubMed Central

    Schlanger, Lynn E.; Bailey, James Lynch; Sands, Jeff M.

    2010-01-01

    The elderly population in the United States continues to grow and is expected to double by 2050. With aging there are degenerative changes in many organs and the kidney is no exception. After age forty there is an increase in cortical glomerulosclerosis and a decline in both glomerular filtration rate and renal plasma flow. These changes may be associated with an inability to excrete a concentrated or a dilute urine, ammonium, sodium, or potassium. Hypernatremia and hyponatremia are the most common electrolyte abnormalities found in the elderly and both are associated with a high mortality. Under normal conditions the elderly are able to maintain water and electrolyte balance but this may be jeopardized by an illness, a decline in cognitive ability, and with certain medications. Therefore, it is important to be aware of the potential electrolyte abnormalities in the elderly that can arise under these various conditions in order to prevent adverse outcomes. PMID:20610358

  5. Solid electrolyte battery

    SciTech Connect

    Cipriano, R.A.; Snelgrove, R.V.; McCullough, F.P. Jr.

    1990-08-28

    This patent describes a primary rechargeable electrical storage device, a housing, at least one cell position in the housing, each cell comprising an anode consisting of a metal selected from the group consisting of alkaline earth metal, alkaline earth metal alloy, alkali metal, alkali metal alloy and alkali metal eutectic mixtures, a separator surrounding the anode. The separator being capable of transporting or passing ionic species and electrically isolating the anode, a cathode, and an electrolyte associated with the cathode. The electrolyte comprising a membrane of a non-porous solid polymeric material containing a sulfonic acid group.

  6. Improved electrolytes for fuel cells

    SciTech Connect

    Gard, G.L.; Roe, D.K.

    1991-06-01

    Present day fuel cells based upon hydrogen and oxygen have limited performance due to the use of phosphoric acid as an electrolyte. Improved performance is desirable in electrolyte conductivity, electrolyte management, oxygen solubility, and the kinetics of the reduction of oxygen. Attention has turned to fluorosulfonic acids as additives or substitute electrolytes to improve fuel cell performance. The purpose of this project is to synthesize and electrochemically evaluate new fluorosulfonic acids as superior alternatives to phosphoric acid in fuel cells. (VC)

  7. Batteries using molten salt electrolyte

    DOEpatents

    Guidotti, Ronald A.

    2003-04-08

    An electrolyte system suitable for a molten salt electrolyte battery is described where the electrolyte system is a molten nitrate compound, an organic compound containing dissolved lithium salts, or a 1-ethyl-3-methlyimidazolium salt with a melting temperature between approximately room temperature and approximately 250.degree. C. With a compatible anode and cathode, the electrolyte system is utilized in a battery as a power source suitable for oil/gas borehole applications and in heat sensors.

  8. Electrolytic production of neodymium without perfluorinated carbon compounds on the offgases

    DOEpatents

    Keller, R.; Larimer, K.T.

    1998-09-22

    A method is described for producing neodymium in an electrolytic cell without formation of perfluorinated carbon gases (PFCs), the method comprising the steps of providing an electrolyte in the electrolytic cell and providing an anode in an anode region of the electrolyte and providing a cathode in a cathode region of the electrolytic cell. Dissolving an oxygen-containing neodymium compound in the electrolyte in the anode region and maintaining a more intense electrolyte circulation in the anode region than in the cathode region. Passing an electrolytic current between said anode and said cathode and depositing neodymium metal at the cathode, preventing the formation of perfluorinated carbon gases by limiting anode over voltage. 4 figs.

  9. Fluid and Electrolyte Balance

    MedlinePlus

    ... the foods you eat and the fluids you drink. Levels of electrolytes in your body can become too low or too high. That can happen when the amount of water in your body changes, causing dehydration or overhydration. Causes include some medicines, vomiting, diarrhea, ...

  10. Spin coating of electrolytes

    DOEpatents

    Stetter, Joseph R.; Maclay, G. Jordan

    1989-01-01

    Methods for spin coating electrolytic materials onto substrates are disclosed. More particularly, methods for depositing solid coatings of ion-conducting material onto planar substrates and onto electrodes are disclosed. These spin coating methods are employed to fabricate electrochemical sensors for use in measuring, detecting and quantifying gases and liquids.

  11. Solid electrolyte structure

    DOEpatents

    Fraioli, Anthony V.

    1984-01-01

    A solid electrolyte structure for fuel cells and other electrochemical devices providing oxygen ion transfer by a multiplicity of exposed internal surfaces made of a composition containing an oxide of a multivalent transition metal and forming small pore-like passages sized to permit oxygen ion transfer while limiting the transfer of oxygen gas.

  12. MultiLayer solid electrolyte for lithium thin film batteries

    DOEpatents

    Lee, Se -Hee; Tracy, C. Edwin; Pitts, John Roland; Liu, Ping

    2015-07-28

    A lithium metal thin-film battery composite structure is provided that includes a combination of a thin, stable, solid electrolyte layer [18] such as Lipon, designed in use to be in contact with a lithium metal anode layer; and a rapid-deposit solid electrolyte layer [16] such as LiAlF.sub.4 in contact with the thin, stable, solid electrolyte layer [18]. Batteries made up of or containing these structures are more efficient to produce than other lithium metal batteries that use only a single solid electrolyte. They are also more resistant to stress and strain than batteries made using layers of only the stable, solid electrolyte materials. Furthermore, lithium anode batteries as disclosed herein are useful as rechargeable batteries.

  13. Crystallographic texture of light tinplate coatings made in various electrolytes

    NASA Astrophysics Data System (ADS)

    Gburík, R.; Černík, M.; Leggat, R.; Vranec, P.

    2015-04-01

    Two electrolytic tinplating processes are currently used in Europe: PSA (based on phenolsulfonic acid) and MSA (based on methanesulfonic acid). The Halogen Process is used in other parts of the world. The electrolyte composition and process parameters affect the electrodeposit and ultimately the tinplate appearance and performance. In order to better understand the impact of electrolyte composition on the crystallographic texture of tin coating tinplate, light tin coatings on single reduced, continuously annealed (CA) tinplate produced in three electrolytes: Halogen, PSA and MSA were analyzed. The crystallographic texture of thin tin coating (<2.8gm-2) was analyzed by X-ray Diffraction and Electron Backscatter Diffraction. The effect of reflow (melting of the tin followed by rapid solidification) and ironing during drawn and wall ironed (DWI) can forming on the tin crystallography were evaluated. Both texture analysis by XRD and EBSD confirmed that all un-melted tin coatings, made in three different electrolytes, contain texture fibers. The effect of steel sheet crystallographic texture was investigated by comparing the tin crystallographic orientation on continuously annealed steel substrate (with α and γ fiber texture) versus batch annealed (BA) steel with a strong γ fiber texture. The main electrolytic parameters, current density and line speed, did not affect the texture formation of tin coating produced in MSA-based electrolyte within the commercial ranges. Un-melted tin coatings produced in the MSA-based electrolyte showed sharper texture than those produced in PSA and Halogen electrolytes. The FeSn2 alloy structure was not observed in un-melted tin coatings; however, it was detected after ironing in the DWI process.

  14. A review of electrolyte materials and compositions for electrochemical supercapacitors.

    PubMed

    Zhong, Cheng; Deng, Yida; Hu, Wenbin; Qiao, Jinli; Zhang, Lei; Zhang, Jiujun

    2015-11-01

    Electrolytes have been identified as some of the most influential components in the performance of electrochemical supercapacitors (ESs), which include: electrical double-layer capacitors, pseudocapacitors and hybrid supercapacitors. This paper reviews recent progress in the research and development of ES electrolytes. The electrolytes are classified into several categories, including: aqueous, organic, ionic liquids, solid-state or quasi-solid-state, as well as redox-active electrolytes. Effects of electrolyte properties on ES performance are discussed in detail. The principles and methods of designing and optimizing electrolytes for ES performance and application are highlighted through a comprehensive analysis of the literature. Interaction among the electrolytes, electro-active materials and inactive components (current collectors, binders, and separators) is discussed. The challenges in producing high-performing electrolytes are analyzed. Several possible research directions to overcome these challenges are proposed for future efforts, with the main aim of improving ESs' energy density without sacrificing existing advantages (e.g., a high power density and a long cycle-life) (507 references). PMID:26050756

  15. A review of electrolyte materials and compositions for electrochemical supercapacitors.

    PubMed

    Zhong, Cheng; Deng, Yida; Hu, Wenbin; Qiao, Jinli; Zhang, Lei; Zhang, Jiujun

    2015-11-01

    Electrolytes have been identified as some of the most influential components in the performance of electrochemical supercapacitors (ESs), which include: electrical double-layer capacitors, pseudocapacitors and hybrid supercapacitors. This paper reviews recent progress in the research and development of ES electrolytes. The electrolytes are classified into several categories, including: aqueous, organic, ionic liquids, solid-state or quasi-solid-state, as well as redox-active electrolytes. Effects of electrolyte properties on ES performance are discussed in detail. The principles and methods of designing and optimizing electrolytes for ES performance and application are highlighted through a comprehensive analysis of the literature. Interaction among the electrolytes, electro-active materials and inactive components (current collectors, binders, and separators) is discussed. The challenges in producing high-performing electrolytes are analyzed. Several possible research directions to overcome these challenges are proposed for future efforts, with the main aim of improving ESs' energy density without sacrificing existing advantages (e.g., a high power density and a long cycle-life) (507 references).

  16. Gel polymer electrolytes for batteries

    DOEpatents

    Balsara, Nitash Pervez; Eitouni, Hany Basam; Gur, Ilan; Singh, Mohit; Hudson, William

    2014-11-18

    Nanostructured gel polymer electrolytes that have both high ionic conductivity and high mechanical strength are disclosed. The electrolytes have at least two domains--one domain contains an ionically-conductive gel polymer and the other domain contains a rigid polymer that provides structure for the electrolyte. The domains are formed by block copolymers. The first block provides a polymer matrix that may or may not be conductive on by itself, but that can soak up a liquid electrolyte, thereby making a gel. An exemplary nanostructured gel polymer electrolyte has an ionic conductivity of at least 1.times.10.sup.-4 S cm.sup.-1 at 25.degree. C.

  17. Reference electrode for electrolytic cell

    DOEpatents

    Kessie, R.W.

    1988-07-28

    A reference electrode device is provided for a high temperature electrolytic cell used to electrolytically recover uranium from spent reactor fuel dissolved in an anode pool, the device having a glass tube to enclose the electrode and electrolyte and serve as a conductive membrane with the cell electrolyte, and an outer metal tube about the glass tube to serve as a shield and basket for any glass sections broken by handling of the tube to prevent their contact with the anode pool, the metal tube having perforations to provide access between the bulk of the cell electrolyte and glass membrane. 4 figs.

  18. Electrolytic cell with reference electrode

    DOEpatents

    Kessie, Robert W.

    1989-01-01

    A reference electrode device is provided for a high temperature electrolytic cell used to electrolytically recover uranium from spent reactor fuel dissolved in an anode pool, the device having a glass tube to enclose the electrode and electrolyte and serve as a conductive membrane with the cell electrolyte, and an outer metal tube about the glass tube to serve as a shield and basket for any glass sections broken by handling of the tube to prevent their contact with the anode pool, the metal tube having perforations to provide access between the bulk of the cell electrolyte and glass membrane.

  19. Recovering copper using a combination of electrolytic cells

    NASA Astrophysics Data System (ADS)

    Wang, Shijie

    2002-06-01

    Electrolytic winning (or electrowinning), the most widely used pure metal production technique, permits the recovery of metal values from a greater variety of ever-decreasing grades of feedstock and compliance with increasingly stringent environmental regulations. Over the past decades, the metallurgical industry has made tremendous progress in recovering metals from tankhouse electrolytes, purified leaching solutions, and industrial wastewater. Improved solutionpurification and electrowinning techniques produce metal products swiftly and return or discharge environmentally compliant spent solutions immediately. This paper presents a new process for combining electrolytic cells to make a typical electrowinning process more practical, efficient, and economical.

  20. Ice electrode electrolytic cell

    SciTech Connect

    Glenn, D.F.; Suciu, D.F.; Harris, T.L.; Ingram, J.C.

    1992-12-31

    This invention relates to a method and apparatus for removing heavy metals from waste water, soils, or process streams by electrolytic cell means. The method includes cooling a cell cathode to form an ice layer over the cathode and then applying an electric current to deposit a layer of the heavy metal over the ice. The metal is then easily removed after melting the ice. In a second embodiment, the same ice-covered electrode can be employed to form powdered metals.

  1. Electrolyte Concentrates Treat Dehydration

    NASA Technical Reports Server (NTRS)

    2009-01-01

    Wellness Brands Inc. of Boulder, Colorado, exclusively licensed a unique electrolyte concentrate formula developed by Ames Research Center to treat and prevent dehydration in astronauts returning to Earth. Marketed as The Right Stuff, the company's NASA-derived formula is an ideal measure for athletes looking to combat dehydration and boost performance. Wellness Brands also plans to expand with products that make use of the formula's effective hydration properties to help treat conditions including heat stroke, altitude sickness, jet lag, and disease.

  2. Solid polymer electrolytes

    DOEpatents

    Abraham, K.M.; Alamgir, M.; Choe, H.S.

    1995-12-12

    This invention relates to Li ion (Li{sup +}) conductive solid polymer electrolytes composed of poly(vinyl sulfone) and lithium salts, and their use in all-solid-state rechargeable lithium ion batteries. The lithium salts comprise low lattice energy lithium salts such as LiN(CF{sub 3}SO{sub 2}){sub 2}, LiAsF{sub 6}, and LiClO{sub 4}. 2 figs.

  3. Ice electrode electrolytic cell

    DOEpatents

    Glenn, David F.; Suciu, Dan F.; Harris, Taryl L.; Ingram, Jani C.

    1993-01-01

    This invention relates to a method and apparatus for removing heavy metals from waste water, soils, or process streams by electrolytic cell means. The method includes cooling a cell cathode to form an ice layer over the cathode and then applying an electric current to deposit a layer of the heavy metal over the ice. The metal is then easily removed after melting the ice. In a second embodiment, the same ice-covered electrode can be employed to form powdered metals.

  4. Ice electrode electrolytic cell

    DOEpatents

    Glenn, D.F.; Suciu, D.F.; Harris, T.L.; Ingram, J.C.

    1993-04-06

    This invention relates to a method and apparatus for removing heavy metals from waste water, soils, or process streams by electrolytic cell means. The method includes cooling a cell cathode to form an ice layer over the cathode and then applying an electric current to deposit a layer of the heavy metal over the ice. The metal is then easily removed after melting the ice. In a second embodiment, the same ice-covered electrode can be employed to form powdered metals.

  5. Solid polymer electrolytes

    DOEpatents

    Abraham, Kuzhikalail M.; Alamgir, Mohamed; Choe, Hyoun S.

    1995-01-01

    This invention relates to Li ion (Li.sup.+) conductive solid polymer electrolytes composed of poly(vinyl sulfone) and lithium salts, and their use in all-solid-state rechargeable lithium ion batteries. The lithium salts comprise low lattice energy lithium salts such as LiN(CF.sub.3 SO.sub.2).sub.2, LiAsF.sub.6, and LiClO.sub.4.

  6. Dedicated nuclear facilities for electrolytic hydrogen production

    NASA Technical Reports Server (NTRS)

    Foh, S. E.; Escher, W. J. D.; Donakowski, T. D.

    1979-01-01

    An advanced technology, fully dedicated nuclear-electrolytic hydrogen production facility is presented. This plant will produce hydrogen and oxygen only and no electrical power will be generated for off-plant use. The conceptual design was based on hydrogen production to fill a pipeline at 1000 psi and a 3000 MW nuclear base, and the base-line facility nuclear-to-shaftpower and shaftpower-to-electricity subsystems, the water treatment subsystem, electricity-to-hydrogen subsystem, hydrogen compression, efficiency, and hydrogen production cost are discussed. The final conceptual design integrates a 3000 MWth high-temperature gas-cooled reactor operating at 980 C helium reactor-out temperature, direct dc electricity generation via acyclic generators, and high-current density, high-pressure electrolyzers based on the solid polymer electrolyte approach. All subsystems are close-coupled and optimally interfaced and pipeline hydrogen is produced at 1000 psi. Hydrogen costs were about half of the conventional nuclear electrolysis process.

  7. Lithium ion conducting electrolytes

    DOEpatents

    Angell, C. Austen; Liu, Changle

    1996-01-01

    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.

  8. Lithium ion conducting electrolytes

    DOEpatents

    Angell, C.A.; Liu, C.

    1996-04-09

    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.

  9. Polarization of ferroelectric films through electrolyte.

    PubMed

    Toss, Henrik; Sani, Negar; Fabiano, Simone; Simon, Daniel T; Forchheimer, Robert; Berggren, Magnus

    2016-03-16

    A simplified model is developed to understand the field and potential distribution through devices based on a ferroelectric film in direct contact with an electrolyte. Devices based on the ferroelectric polymer polyvinylidenefluoride-trifluoroethylene (PVDF-TrFE) were produced--in metal-ferroelectric-metal, metal-ferroelectric-dielectric-metal, and metal-ferroelectric-electrolyte-metal architectures--and used to test the model, and simulations based on the model and these fabricated devices were performed. From these simulations we find indication of progressive polarization of the films. Furthermore, the model implies that there is a relation between the separation of charge within the devices and the observed open circuit voltage. This relation is confirmed experimentally. The ability to polarize ferroelectric polymer films through aqueous electrolytes, combined with the strong correlation between the properties of the electrolyte double layer and the device potential, opens the door to a variety of new applications for ferroelectric technologies, e.g. regulation of cell culture growth and release, steering molecular self-assembly, or other large area applications requiring aqueous environments.

  10. Polarization of ferroelectric films through electrolyte.

    PubMed

    Toss, Henrik; Sani, Negar; Fabiano, Simone; Simon, Daniel T; Forchheimer, Robert; Berggren, Magnus

    2016-03-16

    A simplified model is developed to understand the field and potential distribution through devices based on a ferroelectric film in direct contact with an electrolyte. Devices based on the ferroelectric polymer polyvinylidenefluoride-trifluoroethylene (PVDF-TrFE) were produced--in metal-ferroelectric-metal, metal-ferroelectric-dielectric-metal, and metal-ferroelectric-electrolyte-metal architectures--and used to test the model, and simulations based on the model and these fabricated devices were performed. From these simulations we find indication of progressive polarization of the films. Furthermore, the model implies that there is a relation between the separation of charge within the devices and the observed open circuit voltage. This relation is confirmed experimentally. The ability to polarize ferroelectric polymer films through aqueous electrolytes, combined with the strong correlation between the properties of the electrolyte double layer and the device potential, opens the door to a variety of new applications for ferroelectric technologies, e.g. regulation of cell culture growth and release, steering molecular self-assembly, or other large area applications requiring aqueous environments. PMID:26885704

  11. Electrolytic method to make alkali alcoholates using ion conducting alkali electrolyte/separator

    SciTech Connect

    Joshi, Ashok V.; Balagopal, Shekar; Pendelton, Justin

    2011-12-13

    Alkali alcoholates, also called alkali alkoxides, are produced from alkali metal salt solutions and alcohol using a three-compartment electrolytic cell. The electrolytic cell includes an anolyte compartment configured with an anode, a buffer compartment, and a catholyte compartment configured with a cathode. An alkali ion conducting solid electrolyte configured to selectively transport alkali ions is positioned between the anolyte compartment and the buffer compartment. An alkali ion permeable separator is positioned between the buffer compartment and the catholyte compartment. The catholyte solution may include an alkali alcoholate and alcohol. The anolyte solution may include at least one alkali salt. The buffer compartment solution may include a soluble alkali salt and an alkali alcoholate in alcohol.

  12. Electrolyte materials - Issues and challenges

    SciTech Connect

    Balbuena, Perla B.

    2014-06-16

    Electrolytes are vital components of an electrochemical energy storage device. They are usually composed of a solvent or mixture of solvents and a salt or a mixture of salts which provide the appropriate environment for ionic conduction. One of the main issues associated with the selection of a proper electrolyte is that its electronic properties have to be such that allow a wide electrochemical window - defined as the voltage range in which the electrolyte is not oxidized or reduced - suitable to the battery operating voltage. In addition, electrolytes must have high ionic conductivity and negligible electronic conductivity, be chemically stable with respect to the other battery components, have low flammability, and low cost. Weak stability of the electrolyte against oxidation or reduction leads to the formation of a solid-electrolyte interphase (SEI) layer at the surface of the cathode and anode respectively. Depending on the materials of the electrolyte and those of the electrode, the SEI layer may be composed by combinations of organic and inorganic species, and it may exert a passivating role. In this paper we discuss the current status of knowledge about electrolyte materials, including non-aqueous liquids, ionic liquids, solid ceramic and polymer electrolytes. We also review the basic knowledge about the SEI layer formation, and challenges for a rational design of stable electrolytes.

  13. Note: Electrochemical etching of cylindrical nanoprobes using a vibrating electrolyte

    SciTech Connect

    Wang, Yufeng; Zeng, Yongbin Qu, Ningsong; Zhu, Di

    2015-07-15

    An electrochemical etching process using a vibrating electrolyte of potassium hydroxide to prepare tungsten cylindrical nanotips is developed. The vibrating electrolyte eases the effects of a diffusion layer and extends the etching area, which aid in the production of cylindrical nanotips. Larger amplitudes and a vibration frequency of 35 Hz are recommended for producing cylindrical nanotips. Nanotips with a tip radius of approximately 43 nm and a conical angle of arctan 0.0216 are obtained.

  14. Evaluation of an NH4VO3 derived electrolyte for the vanadium-redox flow battery

    NASA Astrophysics Data System (ADS)

    Menictas, C.; Cheng, M.; Skyllas-Kazascos, M.

    1993-05-01

    The electrolyte used in the vanadium-redox flow battery provides an energy storage system that produces no waste products. Initially, the electrolyte was derived from VOSO4 and significant cost of reductions were obtained by using an electrolyte derived from V2O5. The use of NH4VO3 as the starting material for electrolyte production offers further possible cost reductions. A Coulombic efficiency of 98%, a voltage efficiency of 94%, and an overall energy efficiency of 91.8% are obtained at a constant charging and discharging current density of 14.5 mA/sq cm for a test vanadium-redox flow cell that employs an electrolyte derived from NH4VO3. The electrolyte has been further treated to examine the possibility of ammonium removal. Cell-resistance measurements and cyclic voltammetry studies are reported for the treated and untreated NH4VO3 electrolyte.

  15. Ceramic electrolyte coating and methods

    SciTech Connect

    Seabaugh, Matthew M.; Swartz, Scott L.; Dawson, William J.; McCormick, Buddy E.

    2007-08-28

    Aqueous coating slurries useful in depositing a dense coating of a ceramic electrolyte material (e.g., yttrium-stabilized zirconia) onto a porous substrate of a ceramic electrode material (e.g., lanthanum strontium manganite or nickel/zirconia) and processes for preparing an aqueous suspension of a ceramic electrolyte material and an aqueous spray coating slurry including a ceramic electrolyte material. The invention also includes processes for depositing an aqueous spray coating slurry including a ceramic electrolyte material onto pre-sintered, partially sintered, and unsintered ceramic substrates and products made by this process.

  16. Solid state electrolyte systems

    SciTech Connect

    Pederson, L.R.; Armstrong, B.L.; Armstrong, T.R.

    1997-12-01

    Lanthanum gallates are a new family of solid electrolytes that exhibit high ionic conductivity and are stable to high temperatures. Compositions have been developed that are as much as a factor of two more conductive than yttria-stabilized zirconia at a given temperature, through partial replacement of lanthanum by calcium, strontium, and/or barium and through partial replacement of gallium by magnesium. Oxide powders were prepared using combustion synthesis techniques developed in this laboratory; these were sintered to >95% of theoretical density and consisted of a single crystalline phase. Electrical conductivities, electron and ion transference numbers, thermal expansion, and phase behavior were evaluated as a function of temperature and oxygen partial pressure. A key advantage of the use of lanthanum gallate electrolytes in solid oxide fuel cells is that the temperature of operation may be lowered to perhaps 800 C, yet provide approximately the same power density as zirconia-based cells operating at 1000 C. Ceramic electrolytes that conduct both oxygen ions and electrons are potentially useful to passively separate pure oxygen from an air source at low cost. In such materials, an oxygen ion flux in one direction is charge-compensated by an opposing electron flux. The authors have examined a wide range of mixed ion and electron conducting perovskite ceramics in the system La{sub 1{minus}x}M{sub x}Co{sub 1{minus}y{minus}z}Fe{sub y}N{sub z}O{sub 3{minus}{delta}}, where M = Sr, Ca, and Ba, and N = Pr, Mn, Ni, Cu, Ti, and Al, as well as mixed conducting brownmillerite ceramics, and have characterized oxygen permeation behavior, defect chemistry, structural and phase stability, and performance as cathodes.

  17. Glass electrolyte composition

    DOEpatents

    Kucera, Gene H.; Roche, Michael F.

    1985-01-01

    An ionically conductive glass is disclosed for use as electrolyte in a high temperature electrochemical cell, particularly a cell with sodium anode and sulfur cathode. The glass includes the constituents Na.sub.2 O, ZrO.sub.2, Al.sub.2 O.sub.3 and SiO.sub.2 in selected proportions to be a single phase solid solution substantially free of crystalline regions and undissolved constituents. Other advantageous properties are an ionic conductivity in excess of 2.times.10.sup.-3 (ohm-cm).sup.-1 at 300.degree. C. and a glass transition temperature in excess of 500.degree. C.

  18. Electrolytic oxide reduction system

    DOEpatents

    Wiedmeyer, Stanley G; Barnes, Laurel A; Williamson, Mark A; Willit, James L; Berger, John F

    2015-04-28

    An electrolytic oxide reduction system according to a non-limiting embodiment of the present invention may include a plurality of anode assemblies, a plurality of cathode assemblies, and a lift system configured to engage the anode and cathode assemblies. The cathode assemblies may be alternately arranged with the anode assemblies such that each cathode assembly is flanked by two anode assemblies. The lift system may be configured to selectively engage the anode and cathode assemblies so as to allow the simultaneous lifting of any combination of the anode and cathode assemblies (whether adjacent or non-adjacent).

  19. Glass electrolyte composition

    DOEpatents

    Kucera, G.H.; Roche, M.F.

    1985-01-08

    An ionically conductive glass is disclosed for use as electrolyte in a high temperature electrochemical cell, particularly a cell with sodium anode and sulfur cathode. The glass includes the constituents Na/sub 2/O, ZrO/sub 2/, Al/sub 2/O/sub 3/ and SiO/sub 2/ in selected proportions to be a single phase solid solution substantially free of crystalline regions and undissolved constituents. Other advantageous properties are an ionic conductivity in excess of 2 x 10/sup -3/ (ohm-cm)/sup -1/ at 300/sup 0/C and a glass transition temperature in excess of 500/sup 0/C.

  20. LOW TEMPERATURE CATHODE SUPPORTED ELECTROLYTES

    SciTech Connect

    Harlan U. Anderson

    2000-03-31

    This project has three main goals: Thin Films Studies, Preparation of Graded Porous Substrates and Basic Electrical Characterization and Testing of Planar Single Cells. During this time period substantial progress has been made in developing low temperature deposition techniques to produce dense, nanocrystalline yttrium-stabilized zirconia films on both dense oxide and polymer substrates. Progress has been made in the preparation and characterization of thin electrolytes and porous LSM substrates. Both of these tasks are essentially on or ahead of schedule. In our proposal, we suggested that the ZrO{sub 2}/Sc system needed to be considered as a candidate as a thin electrolyte. This was because microcrystalline ZrO{sub 2}/Sc has a significantly higher ionic conductivity than YSZ, particularly at the lower temperatures. As a result, some 0.5 micron thick film of ZrO{sub 2}/16% Sc on an alumina substrate (grain size 20nm) was prepared and the electrical conductivity measured as a function of temperature and oxygen activity. The Sc doped ZrO{sub 2} certainly has a higher conductivity that either 20nm or 2400nm YSZ, however, electronic conductivity dominates the conductivity for oxygen activities below 10{sup -15}. Whereas for YSZ, electronic conductivity is not a problem until the oxygen activity decreases below 10{sup -25}. These initial results show that the ionic conductivity of 20nm YSZ and 20nm ZrO{sub 2}/16% Sc are essentially the same and the enhanced conductivity which is observed for Sc doping in microcrystalline specimens is not observed for the same composition when it is nanocrystalline. In addition they show that the electronic conductivity of Sc doped ZrO{sub 2} is at least two orders of magnitude higher than that observed for YSZ. The conclusion one reaches is that for 0.5 to 1 micron thick nanocrystalline films, Sc doping of ZrO{sub 2} has no benefits compared to YSZ. As a result, electrolyte films of ZrO{sub 2}/Sc should not be considered as candidates

  1. Electrolyte creepage barrier for liquid electrolyte fuel cells

    DOEpatents

    Li, Jian; Farooque, Mohammad; Yuh, Chao-Yi

    2008-01-22

    A dielectric assembly for electrically insulating a manifold or other component from a liquid electrolyte fuel cell stack wherein the dielectric assembly includes a substantially impermeable dielectric member over which electrolyte is able to flow and a barrier adjacent the dielectric member and having a porosity of less than 50% and greater than 10% so that the barrier is able to measurably absorb and chemically react with the liquid electrolyte flowing on the dielectric member to form solid products which are stable in the liquid electrolyte. In this way, the barrier inhibits flow or creepage of electrolyte from the dielectric member to the manifold or component to be electrically insulated from the fuel cell stack by the dielectric assembly.

  2. Electrolytic production of high purity aluminum using inert anodes

    DOEpatents

    Ray, Siba P.; Liu, Xinghua; Weirauch, Jr., Douglas A.

    2001-01-01

    A method of producing commercial purity aluminum in an electrolytic reduction cell comprising inert anodes is disclosed. The method produces aluminum having acceptable levels of Fe, Cu and Ni impurities. The inert anodes used in the process preferably comprise a cermet material comprising ceramic oxide phase portions and metal phase portions.

  3. Electrolytic production of high purity aluminum using ceramic inert anodes

    DOEpatents

    Ray, Siba P.; Liu, Xinghua; Weirauch, Douglas A.; DiMilia, Robert A.; Dynys, Joseph M.; Phelps, Frankie E.; LaCamera, Alfred F.

    2002-01-01

    A method of producing commercial purity aluminum in an electrolytic reduction cell comprising ceramic inert anodes is disclosed. The method produces aluminum having acceptable levels of Fe, Cu and Ni impurities. The ceramic inert anodes used in the process may comprise oxides containing Fe and Ni, as well as other oxides, metals and/or dopants.

  4. Electrolytes - Technology review

    SciTech Connect

    Meutzner, Falk; Ureña de Vivanco, Mateo

    2014-06-16

    Safety, lifetime, energy density, and costs are the key factors for battery development. This generates the need for improved cell chemistries and new, advanced battery materials. The components of an electrolyte are the solvent, in which a conducting salt and additives are dissolved. Each of them plays a specific role in the overall mechanism of a cell: the solvent provides the host medium for ionic conductivity, which originates in the conductive salt. Furthermore, additives can be used to optimize safety, performance, and cyclability. By understanding the tasks of the individual components and their optimum conditions of operation, the functionality of cells can be improved from a holistic point of view. This paper will present the most important technological features and requirements for electrolytes in lithium-ion batteries. The state-of-the-art chemistry of each component is presented, as well as different approaches for their modification. Finally, a comparison of Li-cells with lithium-based technologies currently under development is conducted.

  5. Low electrolytic conductivity standards

    SciTech Connect

    Wu, Y.C.; Berezansky, P.A.

    1995-09-01

    The monitoring and control of the quality of feedwater and boiler water are necessary for power plants. The generation of steam at high temperature and pressure requires that contaminants be strictly limited to very low levels to prevent corrosion and scaling. Standards of low electrolytic conductivity were developed to satisfy the demands of the US Navy and American industry for the measurement of high quality water. The criteria for the selection of appropriate solvent and solutes, based on the principles of equivalent conductivity and Onsager`s limiting law, are described. Dilute solutions of potassium chloride and benzoic acid in 30% n-propanol-water have been chosen as standards. The electrolytic conductivity of both sets of these solutions as a function of molality was determined. Solutions of potassium chloride and of benzoic acid are recommended for use as 5, 10, 15, 20, and 25 {micro}S/cm conductivity standards. Solutions prepared from potassium chloride in 30% n-propanol-water have been certified as Standard Reference Materials (SRMs). SRM 3198 and SRM 3199 are certified nominally at 5 and 15 {micro}S/cm, respectively, at 25.000 C.

  6. Application of Organic Solid Electrolytes

    NASA Technical Reports Server (NTRS)

    Sekido, S.

    1982-01-01

    If ions are considered to be solid material which transport electric charges, polymer materials can then be considered as organic solid electrolytes. The role of these electrolytes is discussed for (1) ion concentration sensors; (2) batteries using lithium as the cathode and a charge complex of organic material and iodine in the anode; and (3) elements applying electrical double layer capability.

  7. Electrolyte treatment for aluminum reduction

    DOEpatents

    Brown, Craig W.; Brooks, Richard J.; Frizzle, Patrick B.; Juric, Drago D.

    2002-01-01

    A method of treating an electrolyte for use in the electrolytic reduction of alumina to aluminum employing an anode and a cathode, the alumina dissolved in the electrolyte, the treating improving wetting of the cathode with molten aluminum during electrolysis. The method comprises the steps of providing a molten electrolyte comprised of ALF.sub.3 and at least one salt selected from the group consisting of NaF, KF and LiF, and treating the electrolyte by providing therein 0.004 to 0.2 wt. % of a transition metal or transition metal compound for improved wettability of the cathode with molten aluminum during subsequent electrolysis to reduce alumina to aluminum.

  8. Polymeric electrolytic hygrometer

    NASA Technical Reports Server (NTRS)

    Lawson, D. D. (Inventor)

    1978-01-01

    An improved flow-through electrolytic hygrometer is described which utilizes a long lasting oxidation-resistant, hollow fiber formed from persulfonic acid substituted polytetrafluoroethylene having closely spaced noble metal electrodes in contact with the inner and outer surfaces of the fiber. The fiber is disposed within a chamber so that the moisture-bearing gas passes in contact with at least one surface of the fiber. The electrodes are connected in series to a dc voltage supply and an ammeter. As the gas passes through the chamber, moisture absorbed into the wall of the fiber is electrolyzed to hydrogen and oxygen by the closely spaced electrodes. The amount of electricity required for electrolysis is proportional to the absorbed moisture and is observed on the ammeter.

  9. Electrolytes and thermoregulation

    NASA Technical Reports Server (NTRS)

    Nielsen, B.; Greenleaf, J. E.

    1977-01-01

    The influence of ions on temperature is studied for cases where the changes in ionic concentrations are induced by direct infusion or injection of electrolyte solutions into the cerebral ventricles or into specific areas of brain tissue; intravenous infusion or injection; eating food or drinking solutions of different ionic composition; and heat or exercise dehydration. It is shown that introduction of Na(+) and Ca(++) into the cerebral ventricles or into the venous system affects temperature regulation. It appears that the specific action of these ions is different from their osmotic effects. It is unlikely that their action is localized to the thermoregulatory centers in the brain. The infusion experiments demonstrate that the changes in sodium balance occurring during exercise and heat stress are large enough to affect sweat gland function and vasomotor activity.

  10. LOW TEMPERATURE CATHODE SUPPORTED ELECTROLYTES

    SciTech Connect

    Harlan U. Anderson; Fatih Dogan; Vladimir Petrovsky

    2003-03-31

    This report represents a summary of the work carried out on this project which started October 1999 and ended March 2003. A list of the publications resulting from the work are contained in Appendix A. The most significant achievements are: (1) Dense nanocrystalline zirconia and ceria films were obtained at temperatures < 400 C. (2) Nanocrystalline films of both ceria and zirconia were characterized. (3) We showed that under anodic conditions 0.5 to 1 micron thick nanocrystalline films of Sc doped zirconia have sufficient electronic conductivity to prevent them from being useful as an electrolyte. (4) We have developed a process by which dense 0.5 to 5 micron thick dense films of either YSZ or ceria can be deposited on sintered porous substrates which serve as either the cathode or anode at temperatures as low as 400 C. (5) The program has provided the research to produce two PhD thesis for students, one is now working in the solid oxide fuel cell field. (6) The results of the research have resulted in 69 papers published, 3 papers submitted or being prepared for publication, 50 oral presentations and 3 patent disclosures.

  11. Organic electrolytes for sodium batteries

    NASA Astrophysics Data System (ADS)

    Vestergaard, B.

    1992-09-01

    A summary of earlier given status reports in connection with the project on organic electrolytes for sodium batteries is presented. The aim of the investigations was to develop new room temperature molten salts electrolytes mainly with radical substituted heterocyclic organic chlorides mixed with aluminum chloride. The new electrolytes should have an ionic conductivity comparable with MEIC1:AlCl3 or better. A computer model program MOPAC (Molecular Orbital Package) was to be included to calculate theoretically reduction potentials for a variety of organic cations. Furthermore, MOPAC could be utilized to predict the electron densities, and then give a prediction of the stability of the organic cation.

  12. Electrolyte composition for electrochemical cell

    DOEpatents

    Vissers, Donald R.; Tomczuk, Zygmunt; Anderson, Karl E.; Roche, Michael F.

    1979-01-01

    A high-temperature, secondary electrochemical cell that employs FeS as the positive electrode reactant and lithium or lithium alloy as the negative electrode reactant includes an improved electrolyte composition. The electrolyte comprises about 60-70 mole percent LiCl and 30-40 percent mole percent KCl which includes LiCl in excess of the eutectic composition. The use of this electrolyte suppresses formation of the J phase and thereby improves the utilization of positive electrode active material during cell cycling.

  13. Lithium ion conducting ionic electrolytes

    DOEpatents

    Angell, C. Austen; Xu, Kang; Liu, Changle

    1996-01-01

    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.

  14. Lithium ion conducting ionic electrolytes

    DOEpatents

    Angell, C.A.; Xu, K.; Liu, C.

    1996-01-16

    A liquid, predominantly lithium-conducting, ionic electrolyte is described which has exceptionally high conductivity at temperatures of 100 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. 4 figs.

  15. Adaption of kinetics to solid electrolyte interphase layer formation and application to electrolyte-soluble reaction products

    NASA Astrophysics Data System (ADS)

    Gourdin, Gerald; Zheng, Dong; Qu, Deyang

    2015-12-01

    During the electrochemical lithiation of a carbon electrode, carbonate-based electrolytes react with the electrode surface and undergo reductive decomposition to form a solid electrolyte interphase (SEI) layer that passivates the surface of the carbon electrode. In addition, reduction of the electrolyte also results in the generation of electrolyte-soluble products. Structural similarities between the soluble and insoluble products provide an opportunity to examine the formation kinetics of the SEI layer through an analysis of the kinetic behavior of the soluble products. In this work, the electrolyte-soluble products generated by reductive decomposition of a baseline electrolyte were analyzed at different stages and at different hold times during the initial lithiation of an amorphous carbon electrode. A statistical regression analysis of that data was used to produce a representative lithiation experiment from which was calculated the potential-dependent formation rates for the soluble decomposition products. The predicted formation rate data was fitted using an adapted rate equation that accounts for the effect of the SEI layer to obtain estimated formation rate constants and redox potentials.

  16. Cured composite materials for reactive metal battery electrolytes

    DOEpatents

    Harrup, Mason K.; Stewart, Frederick F.; Peterson, Eric S.

    2006-03-07

    A solid molecular composite polymer-based electrolyte is made for batteries, wherein silicate compositing produces a electrolytic polymer with a semi-rigid silicate condensate framework, and then mechanical-stabilization by radiation of the outer surface of the composited material is done to form a durable and non-tacky texture on the electrolyte. The preferred ultraviolet radiation produces this desirable outer surface by creating a thin, shallow skin of crosslinked polymer on the composite material. Preferably, a short-duration of low-medium range ultraviolet radiation is used to crosslink the polymers only a short distance into the polymer, so that the properties of the bulk of the polymer and the bulk of the molecular composite material remain unchanged, but the tough and stable skin formed on the outer surface lends durability and processability to the entire composite material product.

  17. Non-aqueous electrolytes for electrochemical cells

    DOEpatents

    Zhang, Zhengcheng; Dong, Jian; Amine, Khalil

    2016-06-14

    An electrolyte electrochemical device includes an anodic material and an electrolyte, the electrolyte including an organosilicon solvent, a salt, and a hybrid additiving having a first and a second compound, the hybrid additive configured to form a solid electrolyte interphase film on the anodic material upon application of a potential to the electrochemical device.

  18. The contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using diamond anodes.

    PubMed

    Bensalah, Nasr; Dbira, Sondos; Bedoui, Ahmed

    2016-07-01

    In this work, the contribution of mediated oxidation mechanisms in the electrolytic degradation of cyanuric acid using boron-doped diamond (BDD) anodes was investigated in different electrolytes. A complete mineralization of cyanuric acid was obtained in NaCl; however lower degrees of mineralization of 70% and 40% were obtained in Na2SO4 and NaClO4, respectively. This can be explained by the nature of the oxidants electrogenerated in each electrolyte. It is clear that the contribution of active chlorine (Cl2, HClO, ClO(-)) electrogenerated from oxidation of chlorides on BDD is much more important in the electrolytic degradation of cyanuric acid than the persulfate and hydroxyl radicals produced by electro-oxidation of sulfate and water on BDD anodes. This could be explained by the high affinity of active chlorine towards nitrogen compounds. No organic intermediates were detected during the electrolytic degradation of cyanuric acid in any the electrolytes, which can be explained by their immediate depletion by hydroxyl radicals produced on the BDD surface. Nitrates and ammonium were the final products of electrolytic degradation of cyanuric acid on BDD anodes in all electrolytes. In addition, small amounts of chloramines were formed in the chloride medium. Low current density (≤10mA/cm(2)) and neutral medium (pH in the range 6-9) should be used for high efficiency electrolytic degradation and negligible formation of hazardous chlorate and perchlorate. PMID:27372125

  19. Composite Solid Electrolyte For Lithium Cells

    NASA Technical Reports Server (NTRS)

    Peled, Emmanuel; Nagasubramanian, Ganesan; Halpert, Gerald; Attia, Alan I.

    1994-01-01

    Composite solid electrolyte material consists of very small particles, each coated with thin layer of Lil, bonded together with polymer electrolyte or other organic binder. Material offers significant advantages over other solid electrolytes in lithium cells and batteries. Features include high ionic conductivity and strength. Composite solid electrolyte expected to exhibit flexibility of polymeric electrolytes. Polymer in composite solid electrolyte serves two purposes: used as binder alone, conduction taking place only in AI2O3 particles coated with solid Lil; or used as both binder and polymeric electrolyte, providing ionic conductivity between solid particles that it binds together.

  20. Electrolyte salts for power sources

    DOEpatents

    Doddapaneni, N.; Ingersoll, D.

    1995-11-28

    Electrolyte salts are disclosed for power sources comprising salts of phenyl polysulfonic acids and phenyl polyphosphonic acids. The preferred salts are alkali and alkaline earth metal salts, most preferably lithium salts. 2 figs.

  1. Composite solid polymer electrolyte membranes

    DOEpatents

    Formato, Richard M.; Kovar, Robert F.; Osenar, Paul; Landrau, Nelson; Rubin, Leslie S.

    2001-06-19

    The present invention relates to composite solid polymer electrolyte membranes (SPEMs) which include a porous polymer substrate interpenetrated with an ion-conducting material. SPEMs of the present invention are useful in electrochemical applications, including fuel cells and electrodialysis.

  2. Electrolyte salts for power sources

    DOEpatents

    Doddapaneni, Narayan; Ingersoll, David

    1995-01-01

    Electrolyte salts for power sources comprising salts of phenyl polysulfonic acids and phenyl polyphosphonic acids. The preferred salts are alkali and alkaline earth metal salts, most preferably lithium salts.

  3. Solid polymer electrolyte lithium batteries

    DOEpatents

    Alamgir, Mohamed; Abraham, Kuzhikalail M.

    1993-01-01

    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).

  4. Solid polymer electrolyte lithium batteries

    DOEpatents

    Alamgir, M.; Abraham, K.M.

    1993-10-12

    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.

  5. High cation transport polymer electrolyte

    SciTech Connect

    Gerald, II, Rex E.; Rathke, Jerome W.; Klingler, Robert J.

    2007-06-05

    A solid state ion conducting electrolyte and a battery incorporating same. The electrolyte includes a polymer matrix with an alkali metal salt dissolved therein, the salt having an anion with a long or branched chain having not less than 5 carbon or silicon atoms therein. The polymer is preferably a polyether and the salt anion is preferably an alkyl or silyl moiety of from 5 to about 150 carbon/silicon atoms.

  6. Electrolytes for lithium ion batteries

    SciTech Connect

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

    2014-08-05

    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.

  7. [Iatrogenic electrolyte disorders].

    PubMed

    Kettritz, R; Luft, F C

    2015-07-01

    The maintenance of water and electrolyte homeostasis is of enormous importance for the functioning of cells and tissues. A number of therapeutic procedures intentionally or unintentionally influence important regulatory mechanisms of these interdependent balanced systems. Excessive salt intake doesn't only expand the extracellular volume; it can also cause a considerable increase in tonicity. Owing to its insulin-dependent duality of action, glucose can represent an effective or an ineffective osmolyte. This fact has to be considered in patients with diabetic ketoacidosis. Diuretics reduce the volume expansion via renal excretion of sodium (and water); however, in addition to hypokalemia, diuretics can also cause severe alkalosis. Nowadays, hemodialysis is a routine procedure-but even routine procedures can deliver undesirable surprises. Can dialysis cause an increase in calcium levels, or does the procedure remove therapeutically administered radioactive iodine? The current article presents a series of cases we have come across in recent years. These case reports illustrate common, but also rare iatrogenic situations. The discussion of these cases is aimed at raising awareness of the issues involved in a pathophysiological approach to clinical problems. PMID:26036655

  8. Fluid and Electrolyte Nutrition

    NASA Technical Reports Server (NTRS)

    Lane, Helen W.; Smith, Scott M.; Leach, Carolyn S.; Rice, Barbara L.

    1999-01-01

    Studies of fluid and electrolyte homeostasis have been completed since the early human space flight programs, with comprehensive research completed on the Spacelab Life Sciences missions SLS-1 and SLS-2 flights, and more recently on the Mir 18 mission. This work documented the known shifts in fluids, the decrease in total blood volume, and indications of reduced thirst. Data from these flights was used to evaluate the nutritional needs for water, sodium, and potassium. Interpretations of the data are confounded by the inadequate energy intakes routinely observed during space flight. This in turn results in reduced fluid intake, as food provides approximately 70% water intake. Subsequently, body weight, lean body mass, total body water, and total body potassium may decrease. Given these issues, there is evidence to support a minimum required water intake of 2 L per day. Data from previous Shuttle flights indicated that water intake is 2285 +/- 715 ml/day (mean +/- SD, n=26). There are no indications that sodium intake or homeostasis is compromised during space flight. The normal or low aldosterone and urinary sodium levels suggest adequate sodium intake (4047 +/- 902 mg/day, n=26). Because excessive sodium intake is associated with hypercalciuria, the recommended maximum amount of sodium intake during flight is 3500 mg/day (i.e., similar to the Recommended Dietary Allowance, RDA). Potassium metabolism appears to be more complex. Data indicate loss of body potassium related to muscle atrophy and low dietary intake (2407 +/- 548 mg/day, n=26). Although possibly related to measurement error, the elevations in blood potassium suggest alterations in potassium homeostasis. The space RDA for minimum potassium intake is 3500 mg/day. With the documented inadequate intakes, efforts are being made to increase dietary consumption of potassium.

  9. Vanadium Electrolyte Studies for the Vanadium Redox Battery-A Review.

    PubMed

    Skyllas-Kazacos, Maria; Cao, Liuyue; Kazacos, Michael; Kausar, Nadeem; Mousa, Asem

    2016-07-01

    The electrolyte is one of the most important components of the vanadium redox flow battery and its properties will affect cell performance and behavior in addition to the overall battery cost. Vanadium exists in several oxidation states with significantly different half-cell potentials that can produce practical cell voltages. It is thus possible to use the same element in both half-cells and thereby eliminate problems of cross-contamination inherent in all other flow battery chemistries. Electrolyte properties vary with supporting electrolyte composition, state-of-charge, and temperature and this will impact on the characteristics, behavior, and performance of the vanadium battery in practical applications. This Review provides a broad overview of the physical properties and characteristics of the vanadium battery electrolyte under different conditions, together with a description of some of the processing methods that have been developed to produce vanadium electrolytes for vanadium redox flow battery applications. PMID:27295523

  10. Vanadium Electrolyte Studies for the Vanadium Redox Battery-A Review.

    PubMed

    Skyllas-Kazacos, Maria; Cao, Liuyue; Kazacos, Michael; Kausar, Nadeem; Mousa, Asem

    2016-07-01

    The electrolyte is one of the most important components of the vanadium redox flow battery and its properties will affect cell performance and behavior in addition to the overall battery cost. Vanadium exists in several oxidation states with significantly different half-cell potentials that can produce practical cell voltages. It is thus possible to use the same element in both half-cells and thereby eliminate problems of cross-contamination inherent in all other flow battery chemistries. Electrolyte properties vary with supporting electrolyte composition, state-of-charge, and temperature and this will impact on the characteristics, behavior, and performance of the vanadium battery in practical applications. This Review provides a broad overview of the physical properties and characteristics of the vanadium battery electrolyte under different conditions, together with a description of some of the processing methods that have been developed to produce vanadium electrolytes for vanadium redox flow battery applications.

  11. The Light Attracting Effect of Pyridine Derivatives Based Quasi-Solid Electrolyte in Dye-Sensitized Solar Cell.

    PubMed

    Cai, Molang; Bell, John; Dai, Songyuan

    2016-06-01

    The pyridine derivatives are added into acetonitrile based electrolyte to establish framework, then form the quasi solid electrolyte. The ion diffusion of cetylpyridinium chloride and cetylpyridinium bromide based electrolytes is enhanced comparing with the ion diffusion of reference acetonitrile electrolyte. The ordered structure of cetylpyridinuium chloride quasi solid electrolyte has been observed by SEM images. Light scattering effect of cetylpyridinuium chloride quasi solid electrolyte is evidenced by the larger resulted by transmitted and scattered spectra. The light harvesting efficiency of device based on C16Cl is much higher than acetonitrile based device. The cell efficiency of C16Cl and C16Br based device are 5.72% and 6.02%, which are 41% and 48% higher than acetonitrile liquid electrolyte based device. The C16l based device produces low cell efficiency 2.06%, which is 49% decrease compare to the blank device due to the limitation of iodide-triodide transportation in the iodide framework. PMID:27427629

  12. Electrolytic cell and methods combining electrowinning and electrochemical reactions employing a membrane or diaphragm

    SciTech Connect

    Smith, G.R.; Thompson, W.R.

    1986-12-09

    A process is described for combining at compatible cell geometries and current densities the electrowinning of a free metal element on a cathode in a catholytic electrolyte in a cell in which there is an anode with an anolytic electrolyte with a cationic permselective membrane between the catholytic electrolyte and anolytic electrolyte thereby forming a catholytic half-cell compartment and an anolytic half-cell compartment. The voltage for the combined catholytic half-cell and anolytic half-cell is reduced greater than 50% as compared to the sum of the cell voltages of two independently operating nonmembrane cells using an electrolyte selected from the catholytic electrolyte or the anolytic electrolyte and with water electrolysis at the anode. The process consists of (a) introducing a metal sulfate salt into the catholytic electrolyte in the half-cell catholytic compartment (b) introducing an alkali metal chlorate and an alkali metal perchlorate into the anolytic electrolyte in the half-cell anolytic compartment; and (c) applying an electromotive force across the cathode and anode whereby an oxidation electrochemical reaction occurs at the anode to produce a perchlorate while the free metal element of the metal salt is deposited at the cathode.

  13. Apparatus and process for the electrolytic reduction of uranium and plutonium oxides

    DOEpatents

    Poa, David S.; Burris, Leslie; Steunenberg, Robert K.; Tomczuk, Zygmunt

    1991-01-01

    An apparatus and process for reducing uranium and/or plutonium oxides to produce a solid, high-purity metal. The apparatus is an electrolyte cell consisting of a first container, and a smaller second container within the first container. An electrolyte fills both containers, the level of the electrolyte in the first container being above the top of the second container so that the electrolyte can be circulated between the containers. The anode is positioned in the first container while the cathode is located in the second container. Means are provided for passing an inert gas into the electrolyte near the lower end of the anode to sparge the electrolyte and to remove gases which form on the anode during the reduction operation. Means are also provided for mixing and stirring the electrolyte in the first container to solubilize the metal oxide in the electrolyte and to transport the electrolyte containing dissolved oxide into contact with the cathode in the second container. The cell is operated at a temperature below the melting temperature of the metal product so that the metal forms as a solid on the cathode.

  14. Internal electrolyte supply system for reliable transport throughout fuel cell stacks

    DOEpatents

    Wright, Maynard K.; Downs, Robert E.; King, Robert B.

    1988-01-01

    An improved internal electrolyte supply system in a fuel cell stack employs a variety of arrangements of grooves and passages in bipolar plates of the multiplicity of repeating fuel cells to route gravity-assisted flowing electrolyte throughout the stack. The grooves route electrolyte flow along series of first paths which extend horizontally through the cells between the plates thereof. The passages route electrolyte flow along series of second paths which extend vertically through the stack so as to supply electrolyte to the first paths in order to expose the electrolyte to the matrices of the cells. Five different embodiments of the supply system are disclosed. Some embodiments employ wicks in the grooves for facilitating transfer of the electrolyte to the matrices as well as providing support for the matrices. Additionally, the passages of some embodiments by-pass certain of the grooves and supply electrolyte directly to other of the grooves. Some embodiments employ single grooves and others have dual grooves. Finally, in some embodiments the passages are connected to the grooves by a step which produces a cascading electrolyte flow.

  15. Anion exchange polymer electrolytes

    DOEpatents

    Kim, Yu Seung; Kim, Dae Sik; Lee, Kwan-Soo

    2013-07-23

    Solid anion exchange polymer electrolytes and compositions comprising chemical compounds comprising a polymeric core, a spacer A, and a guanidine base, wherein said chemical compound is uniformly dispersed in a suitable solvent and has the structure: ##STR00001## wherein: i) A is a spacer having the structure O, S, SO.sub.2, --NH--, --N(CH.sub.2).sub.n, wherein n=1-10, --(CH.sub.2).sub.n--CH.sub.3--, wherein n=1-10, SO.sub.2-Ph, CO-Ph, ##STR00002## wherein R.sub.5, R.sub.6, R.sub.7 and R.sub.8 each are independently --H, --NH.sub.2, F, Cl, Br, CN, or a C.sub.1-C.sub.6 alkyl group, or any combination of thereof; ii) R.sub.9, R.sub.10, R.sub.11, R.sub.12, or R.sub.13 each independently are --H, --CH.sub.3, --NH.sub.2, --NO, --CH.sub.nCH.sub.3 where n=1-6, HC.dbd.O--, NH.sub.2C.dbd.O--, --CH.sub.nCOOH where n=1-6, --(CH.sub.2).sub.n--C(NH.sub.2)--COOH where n=1-6, --CH--(COOH)--CH.sub.2--COOH, --CH.sub.2--CH(O--CH.sub.2CH.sub.3).sub.2, --(C.dbd.S)--NH.sub.2, --(C.dbd.NH)--N--(CH.sub.2).sub.nCH.sub.3, where n=0-6, --NH--(C.dbd.S)--SH, --CH.sub.2--(C.dbd.O)--O--C(CH.sub.3).sub.3, --O--(CH.sub.2).sub.n--CH--(NH.sub.2)--COOH, where n=1-6, --(CH.sub.2).sub.n--CH.dbd.CH wherein n=1-6, --(CH.sub.2).sub.n--CH--CN wherein n=1-6, an aromatic group such as a phenyl, benzyl, phenoxy, methylbenzyl, nitrogen-substituted benzyl or phenyl groups, a halide, or halide-substituted methyl groups; and iii) wherein the composition is suitable for use in a membrane electrode assembly.

  16. Thermal effects of asymmetric electrolytes in electric double layer capacitors

    NASA Astrophysics Data System (ADS)

    d'Entremont, Anna L.; Pilon, Laurent

    2015-01-01

    This study presents a thermal model, derived from first principles, for electric double layer capacitors (EDLCs) with multiple ion species and/or asymmetric electrolytes. It accounts for both irreversible and reversible heat generation rates resulting from the transient electrodiffusion of ions within the electrolyte. Detailed numerical simulations of EDLCs with planar electrodes and binary and asymmetric electrolytes were performed under galvanostatic cycling. The irreversible Joule heating decreased with increasing valency and/or diffusion coefficient of either ion. The local reversible heat generation rate near a given electrode was determined by the properties of the counterion. It increased with increasing counterion valency and/or decreasing counterion diameter. As a result, the electrode with the counterion of smaller diameter and/or larger valency experienced significantly larger temperature oscillations during galvanostatic cycling than the opposite electrode. In general, EDLC electrolytes featuring ions with large valency and/or small diameter produce large capacitance but also large reversible heating. The present study suggests that EDLC electrolytes should feature large bulk ion concentrations and at least one ion with a large diffusion coefficient to minimize both irreversible and reversible heating.

  17. High elastic modulus polymer electrolytes

    DOEpatents

    Balsara, Nitash Pervez; Singh, Mohit; Eitouni, Hany Basam; Gomez, Enrique Daniel

    2013-10-22

    A polymer that combines high ionic conductivity with the structural properties required for Li electrode stability is useful as a solid phase electrolyte for high energy density, high cycle life batteries that do not suffer from failures due to side reactions and dendrite growth on the Li electrodes, and other potential applications. The polymer electrolyte includes a linear block copolymer having a conductive linear polymer block with a molecular weight of at least 5000 Daltons, a structural linear polymer block with an elastic modulus in excess of 1.times.10.sup.7 Pa and an ionic conductivity of at least 1.times.10.sup.-5 Scm.sup.-1. The electrolyte is made under dry conditions to achieve the noted characteristics.

  18. Towards Prognostics of Electrolytic Capacitors

    NASA Technical Reports Server (NTRS)

    Celaya, Jose R.; Kulkarni, Chetan; Biswas, Gautam; Goegel, Kai

    2011-01-01

    A remaining useful life prediction algorithm and degradation model for electrolytic capacitors is presented. Electrolytic capacitors are used in several applications ranging from power supplies on critical avionics equipment to power drivers for electro-mechanical actuators. These devices are known for their low reliability and given their criticality in electronics subsystems they are a good candidate for component level prognostics and health management research. Prognostics provides a way to assess remaining useful life of a capacitor based on its current state of health and its anticipated future usage and operational conditions. In particular, experimental results of an accelerated aging test under electrical stresses are presented. The capacitors used in this test form the basis for a remaining life prediction algorithm where a model of the degradation process is suggested. This preliminary remaining life prediction algorithm serves as a demonstration of how prognostics methodologies could be used for electrolytic capacitors.

  19. Diabetes mellitus and electrolyte disorders

    PubMed Central

    Liamis, George; Liberopoulos, Evangelos; Barkas, Fotios; Elisaf, Moses

    2014-01-01

    Diabetic patients frequently develop a constellation of electrolyte disorders. These disturbances are particularly common in decompensated diabetics, especially in the context of diabetic ketoacidosis or nonketotic hyperglycemic hyperosmolar syndrome. These patients are markedly potassium-, magnesium- and phosphate-depleted. Diabetes mellitus (DM) is linked to both hypo- and hyper-natremia reflecting the coexistence of hyperglycemia-related mechanisms, which tend to change serum sodium to opposite directions. The most important causal factor of chronic hyperkalemia in diabetic individuals is the syndrome of hyporeninemic hypoaldosteronism. Impaired renal function, potassium-sparing drugs, hypertonicity and insulin deficiency are also involved in the development of hyperkalemia. This article provides an overview of the electrolyte disturbances occurring in DM and describes the underlying mechanisms. This insight should pave the way for pathophysiology-directed therapy, thus contributing to the avoidance of the several deleterious effects associated with electrolyte disorders and their treatment. PMID:25325058

  20. Water and electrolyte absorption by the colon in tropical sprue.

    PubMed Central

    Ramakrishna, B S; Mathan, V I

    1982-01-01

    A defect in colonic absorption of electrolytes and water was demonstrated in patients with tropical sprue by perfusing the colon with normal saline containing a non-absorbable marker. Colonic water absorption correlated negatively with stool weight and was abnormal in patients with steatorrhoea. The possible mechanisms producing this defect are discussed. This defect may be related to colonocyte damage produced by unabsorbed unsaturated fatty acids in patients with steatorrhoea. PMID:7117904

  1. Magnesium Battery Electrolytes in Ionic Liquids

    NASA Astrophysics Data System (ADS)

    Watkins, Tylan Strike

    A lack of adequate energy storage technologies is arguably the greatest hindrance to a modern sustainable energy infrastructure. Chemical energy storage, in the form of batteries, is an obvious solution to the problem. Unfortunately, today's state of the art battery technologies fail to meet the desired metrics for full scale electric grid and/or electric vehicle role out. Considerable effort from scientists and engineers has gone into the pursuit of battery chemistries theoretically capable of far outperforming leading technologies like Li-ion cells. For instance, an anode of the relatively abundant and cheap metal, magnesium, would boost the specific energy by over 4.6 times that of the current Li-ion anode (LiC6). The work presented here explores the compatibility of magnesium electrolytes in TFSI---based ionic liquids with a Mg anode (TFSI = bis(trifluoromethylsulfonyl)imide). Correlations are made between the Mg2+ speciation conditions in bulk solutions (as determined via Raman spectroscopy) and the corresponding electrochemical behavior of the electrolytes. It was found that by creating specific chelating conditions, with an appropriate Mg salt, the desired electrochemical behavior could be obtained, i.e. reversible electrodeposition and dissolution. Removal of TFSI -- contact ion pairs from the Mg2+ solvation shell was found to be essential for reversible electrodeposition. Ionic liquids with polyethylene glycol chains pendent from a parent pyrrolidinium cation were synthesized and used to create the necessary complexes with Mg 2+, from Mg(BH4)2, so that reversible electrodeposition from a purely ionic liquid medium was achieved. The following document discusses findings from several electrochemical experiments on magnesium electrolytes in ionic liquids. Explanations for the failure of many of these systems to produce reversible Mg electrodeposition are provided. The key characteristics of ionic liquid systems that are capable of achieving reversible Mg

  2. Thermoelectricity in Confined Liquid Electrolytes.

    PubMed

    Dietzel, Mathias; Hardt, Steffen

    2016-06-01

    The electric field in an extended phase of a liquid electrolyte exposed to a temperature gradient is attributed to different thermophoretic mobilities of the ion species. As shown herein, such Soret-type ion thermodiffusion is not required to induce thermoelectricity even in the simplest electrolyte if it is confined between charged walls. The space charge of the electric double layer leads to selective ion diffusion driven by a temperature-dependent electrophoretic ion mobility, which-for narrow channels-may cause thermovoltages larger in magnitude than for the classical Soret equilibrium. PMID:27314730

  3. LOWER TEMPERATURE ELECTROLYTE AND ELECTRODE MATERIALS

    SciTech Connect

    Keqin Huang

    2003-04-30

    A thorough literature survey on low-temperature electrolyte and electrode materials for SOFC is given in this report. Thermodynamic stability of selected electrolyte and its chemical compatibility with cathode substrate were evaluated. Preliminary electrochemical characterizations were conducted on symmetrical cells consisting of the selected electrolyte and various electrode materials. Feasibility of plasma spraying new electrolyte material thin-film on cathode substrate was explored.

  4. Solid lithium-ion electrolyte

    SciTech Connect

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

    1998-02-10

    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.

  5. Solid polymer electrolyte photovoltaic cell

    SciTech Connect

    Skotheim, T.; Lundstrom, I.

    1982-04-01

    Solid photoelectrochemical cells are described based on PEO-KI/I/sub 2/ electrolytes, n-Si/Pt/PPy photoanodes, and conductive tin-oxide glass counter electrodes. The performance of the present devices is limited by a high series resistance in the polymer film. 22 refs.

  6. Solid lithium-ion electrolyte

    DOEpatents

    Zhang, Ji-Guang; Benson, David K.; Tracy, C. Edwin

    1998-01-01

    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.

  7. Rechargeable solid polymer electrolyte battery cell

    DOEpatents

    Skotheim, Terji

    1985-01-01

    A rechargeable battery cell comprising first and second electrodes sandwiching a solid polymer electrolyte comprising a layer of a polymer blend of a highly conductive polymer and a solid polymer electrolyte adjacent said polymer blend and a layer of dry solid polymer electrolyte adjacent said layer of polymer blend and said second electrode.

  8. Lithium Polymer Electrolytes and Solid State NMR

    NASA Technical Reports Server (NTRS)

    Berkeley, Emily R.

    2004-01-01

    participation on a variety of other projects, including aero-gels and carbon graphite mat en als. The goals of the polymer electrolyte research are to improve the physical properties of the polymers. This includes improving conductivity, durability, and expanding the temperature range over which it is effective. Currently, good conductivity is only present at high temperatures. My goals are to experiment with different arrangements of rods and coils to achieve these desirable properties. Some of my experiments include changing the number of repeat units in the polymer, the size of the diamines, and the types of coil. Analysis of these new polymers indicates improvement in some properties, such as lower glass transition temperature; however, they are not as flexible as desired. With further research we hope to produce polymers that encompass all of these properties to a high degree.

  9. Electrolyte measurement device and measurement procedure

    DOEpatents

    Cooper, Kevin R.; Scribner, Louie L.

    2010-01-26

    A method and apparatus for measuring the through-thickness resistance or conductance of a thin electrolyte is provided. The method and apparatus includes positioning a first source electrode on a first side of an electrolyte to be tested, positioning a second source electrode on a second side of the electrolyte, positioning a first sense electrode on the second side of the electrolyte, and positioning a second sense electrode on the first side of the electrolyte. current is then passed between the first and second source electrodes and the voltage between the first and second sense electrodes is measured.

  10. Fuel cell with electrolyte feed system

    DOEpatents

    Feigenbaum, Haim

    1984-01-01

    A fuel cell having a pair of electrodes at the sites of electrochemical reactions of hydrogen and oxygen and a phosphoric acid electrolyte provided with an electrolyte supporting structure in the form of a laminated matrix assembly disposed between the electrodes. The matrix assembly is formed of a central layer disposed between two outer layers, each being permeable to the flow of the electrolyte. The central layer is provided with relatively large pores while the outer layers are provided with relatively small pores. An external reservoir supplies electrolyte via a feed means to the central layer to compensate for changes in electrolyte volume in the matrix assembly during the operation of fuel cell.

  11. Reactivity of nonaqueous organic electrolytes towards lithium

    NASA Technical Reports Server (NTRS)

    Shen, D. H.; Subbarao, S.; Deligiannis, F.; Huang, C.-K.; Halpert, G.

    1990-01-01

    The successful operation of an ambient temperature secondary lithium cell is primarily dependent on the stability of the electrolyte towards lithium. The lithium electrode on open circuit must be inert towards the electrolyte to achieve a long shelf life. The reactivity of tetrahydrofuran and 2-methyltetrahydrofuran based electrolytes with additives such as 2-methylfuran, ethylene carbonate, propylene carbonate, and 3-methylsulfolane was investigated by microcalorimetry and ac impedance spectroscopy techniques. Also the stability of electrolytes by open circuit stand tests was studied. Addition of ethylene carbonate and 2-methylfuran additives was found to improve the stability of tetrahydrofuran and 2-methyltetrahydrofuran based electrolytes. Long term microcalorimetry and ac impedance data clearly confirmed the higher stability of ethylene carbonate/2-methyltetrahydrofuran electrolyte compared to the 2-methyltetrahydrofuran and propylene carbonate/2-methyltetrahydrofuran electrolytes.

  12. An investigation into magnetic electrolytic abrasive turning

    NASA Astrophysics Data System (ADS)

    Mahdy, M. A. M.; Ismaeial, A. L.; Aly, F. F.

    2013-07-01

    The magnetic electrolytic abrasive turning (MEAT) process as a non-traditional machining is used to obtain surface finishing like mirror. MEAT provides one of the best alternatives for producing complex shapes with good finish in advanced materials used in aircraft and aerospace industries. The improvement of machining accuracy of MEAT continues to be a major challenge for modern industry. MEAT is a hybrid machining which combines two or more processes to remove material. The present research focuses on the development of precision electrochemical turning (ECT) under the effects of magnetic field and abrasives. The effect of magnetic flux density, electrochemical conditions and abrasive parameters on finishing efficiency and surface roughness are investigated. An empirical relationship is deduced.

  13. Insulated electrocardiographic electrodes. [without paste electrolyte

    NASA Technical Reports Server (NTRS)

    David, R. M.; Portnoy, W. A. (Inventor)

    1975-01-01

    An integrated system is disclosed including an insulated electrode and an impedance transformer which can be assembled in a small plastic housing and used for the acquisition of electrocardiographic data. The electrode may be employed without a paste electrolyte and may be attached to the body for extended usage without producing skin reaction. The electrode comprises a thin layer of suitable nontoxic dielectric material preferably deposited by radio frequency sputtering onto a conductive substrate. The impedance transformer preferably comprises an operational amplifier having an FET input stage connected in the unity gain configuration which provides a very low lower cut-off frequency, a high input impedance with a very small input bias current, a low output impedance, and a high signal-to-noise ratio.

  14. Electrolytic production of neodymium metal from a molten chloride electrolyte

    SciTech Connect

    Chambers, M.F.; Murphy, J.E.

    1991-01-01

    This paper reports that the U.S. Bureau of Mines conducted experiments on electrowinning of neodymium metal by using a molten-metal cathode at 650{degrees} C and an electrolyte of 50 mol pet NdCl, (neodymium chloride) and 50 mol pet KCl (potassium chloride). The molten-metal cathodes were alloys of magnesium and zinc or magnesium and cadmium. Current efficiencies were 90 pct with a Mg-Zn cathode and 80 pct with a Mg-Cd cathode. The Mg-Cd cathode was easily separated from the electrolyte. In contrast, the Mg-Zn cathode tended to mix with the electrolyte, making separation difficult. The cathode metals were separated from the neodymium by distillation at 1,100{degrees} C under a vacuum of 10{sup {minus}4} torr. Neodymium metal of 99.9 + purity was recovered from the Mg-Cd alloy cathode after 30 min distillation time. The neodymium recovered from the Mg-Zn system contained almost 2 pct Zn after vacuum distillation. Continuous operation using the Mg-Cd alloy cathode was demonstrated.

  15. Characterization of calcium containing plasma electrolytic oxidation coatings on AM50 magnesium alloy

    NASA Astrophysics Data System (ADS)

    Srinivasan, P. Bala; Liang, J.; Blawert, C.; Störmer, M.; Dietzel, W.

    2010-04-01

    An attempt was made to produce calcium containing plasma electrolytic oxidation (PEO) coatings on AM50 magnesium alloy using an alkaline electrolyte. This study was performed in three alkaline electrolytes containing calcium hydroxide and sodium phosphate with three different mass ratios viz., 1:2.5, 1:5 and 1:7.5. All the three coatings produced were found to contain Ca and P in appreciable amounts. The concentration of P was found to be higher in the coatings obtained in the electrolytes with higher concentration of phosphate ions. Even though all the three coatings were found to be constituted with magnesium oxide and magnesium phosphate phases, X-ray diffraction analyses revealed that the phase composition was influenced by the phosphate ion concentration/conductivity of the electrolyte. Further, the PEO coating obtained in the 1:7.5 ratio electrolyte was found to contain di-calcium phosphate (monetite) and calcium peroxide phases, which were absent in the other two coatings. Potentiodynamic polarization studies performed in 0.1 M NaCl solution showed that the coatings obtained from the 1:5 ratio electrolyte possessed a superior corrosion resistance, which is attributed to the combined effect of thickness, compactness and phase/chemical composition of this coating.

  16. Electrochromic Device with Polymer Electrolyte

    NASA Astrophysics Data System (ADS)

    Solovyev, Andrey A.; Zakharov, Alexander N.; Rabotkin, Sergey V.; Kovsharov, Nikolay F.

    2016-08-01

    In this study a solid-state electrochromic device (ECD) comprised of a WO3 and Prussian blue (Fe4[Fe(CN)6]3) thin film couple with a Li+-conducting solid polymer electrolyte is discussed. WO3 was deposited on K-Glass substrate by magnetron sputtering method, while Prussian blue layer was formed on the same substrate by electrodeposition method. The parameters of the electrochromic device K-Glass/WO3/Li+-electrolyte/PB/K-Glass, such as change of transmittance, response time and stability were successfully tested using coupled optoelectrochemical methods. The device was colored or bleached by the application of +2 V or -2 V, respectively. Light modulation with transmittance variation of up to 59% and coloration efficiency of 43 cm2/C at a wavelength of 550 nm were obtained. Numerous switching of the ECD over 1200 cycles without the observation of significant degradation has been demonstrated.

  17. Monolithic solid electrolyte oxygen pump

    DOEpatents

    Fee, Darrell C.; Poeppel, Roger B.; Easler, Timothy E.; Dees, Dennis W.

    1989-01-01

    A multi-layer oxygen pump having a one-piece, monolithic ceramic structure affords high oxygen production per unit weight and volume and is thus particularly adapted for use as a portable oxygen supply. The oxygen pump is comprised of a large number of small cells on the order of 1-2 millimeters in diameter which form the walls of the pump and which are comprised of thin, i.e., 25-50 micrometers, ceramic layers of cell components. The cell components include an air electrode, an oxygen electrode, an electrolyte and interconnection materials. The cell walls form the passages for input air and for exhausting the oxygen which is transferred from a relatively dilute gaseous mixture to a higher concentration by applying a DC voltage across the electrodes so as to ionize the oxygen at the air electrode, whereupon the ionized oxygen travels through the electrolyte and is converted to oxygen gas at the oxygen electrode.

  18. New Polymer Electrolyte Cell Systems

    NASA Technical Reports Server (NTRS)

    Smyrl, William H.; Owens, Boone B.; Mann, Kent; Pappenfus, T.; Henderson, W.

    2004-01-01

    PAPERS PUBLISHED: 1. Pappenfus, Ted M.; Henderson, Wesley A.; Owens, Boone B.; Mann, Kent R.; Smyrl, William H. Complexes of Lithium Imide Salts with Tetraglyme and Their Polyelectrolyte Composite Materials. Journal of the Electrochemical Society (2004), 15 1 (2), A209-A2 15. 2. Pappenfus, Ted M.; Henderson, Wesley A.; Owens, Boone B.; Mann, Kent R.; Smyrl, William H. Ionic-liquidlpolymer electrolyte composite materials for electrochemical device applications. Polymeric Materials Science and Engineering (2003), 88 302. 3. Pappenfus, Ted R.; Henderson, Wesley A.; Owens, Boone B.; Mann, Kent R.; and Smyrl, William H. Ionic Conductivity of a poly(vinylpyridinium)/Silver Iodide Solid Polymer Electrolyte System. Solid State Ionics (in press 2004). 4. Pappenfus Ted M.; Mann, Kent R; Smyrl, William H. Polyelectrolyte Composite Materials with LiPFs and Tetraglyme. Electrochemical and Solid State Letters, (2004), 7(8), A254.

  19. Improved Electrolytic Hydrogen Peroxide Generator

    NASA Technical Reports Server (NTRS)

    James, Patrick I.

    2005-01-01

    An improved apparatus for the electrolytic generation of hydrogen peroxide dissolved in water has been developed. The apparatus is a prototype of H2O2 generators for the safe and effective sterilization of water, sterilization of equipment in contact with water, and other applications in which there is need for hydrogen peroxide at low concentration as an oxidant. Potential applications for electrolytic H2O2 generators include purification of water for drinking and for use in industrial processes, sanitation for hospitals and biotechnological industries, inhibition and removal of biofouling in heat exchangers, cooling towers, filtration units, and the treatment of wastewater by use of advanced oxidation processes that are promoted by H2O2.

  20. Composite electrode/electrolyte structure

    DOEpatents

    Visco, Steven J.; Jacobson, Craig P.; DeJonghe, Lutgard C.

    2004-01-27

    Provided is an electrode fabricated from highly electronically conductive materials such as metals, metal alloys, or electronically conductive ceramics. The electronic conductivity of the electrode substrate is maximized. Onto this electrode in the green state, a green ionic (e.g., electrolyte) film is deposited and the assembly is co-fired at a temperature suitable to fully densify the film while the substrate retains porosity. Subsequently, a catalytic material is added to the electrode structure by infiltration of a metal salt and subsequent low temperature firing. The invention allows for an electrode with high electronic conductivity and sufficient catalytic activity to achieve high power density in ionic (electrochemical) devices such as fuel cells and electrolytic gas separation systems.

  1. Cerium ion conducting solid electrolyte

    NASA Astrophysics Data System (ADS)

    Hasegawa, Yasunori; Imanaka, Nobuhito; Adachi, Gin-ya

    2003-02-01

    A cerium ion conducting solid electrolyte, (Ce xZr 1- x) 4/4- xNb(PO 4) 3, was successfully realized with the NASICON-type structure which possesses a three-dimensional network, especially suitable for bulky ion migration. The cerium ion conductivity exceeds approximately one order of magnitude in comparison to that of the rare-earth ion conducting R2(WO 4) 3 and R1/3Zr 2(PO 4) 3 ( R=Sc, Y, Eu-Lu) series and the value is in the range between typical oxide anion conductors of yttria stabilized zirconia (YSZ) and calcia stabilized zirconia (CSZ). Since cerium ion has been demonstrated to be another migrating ion species in solid electrolyte field, a promising application for various functional materials is greatly expected.

  2. Anion Solvation in Carbonate Electrolytes

    SciTech Connect

    Zhang, Zhengcheng

    2015-11-16

    With the correlation between Li+ solvation and interphasial chemistry on anodes firmly established in Li-ion batteries, the effect of cation–solvent interaction has gone beyond bulk thermodynamic and transport properties and become an essential element that determines the reversibility of electrochemistry and kinetics of Li-ion intercalation chemistries. As of now, most studies are dedicated to the solvation of Li+, and the solvation of anions in carbonate-based electrolytes and its possible effect on the electrochemical stability of such electrolytes remains little understood. As a mirror effort to prior Li+ solvation studies, this work focuses on the interactions between carbonate-based solvents and two anions (hexafluorophosphate, PF6–, and tetrafluoroborate, BF4–) that are most frequently used in Li-ion batteries. The possible correlation between such interaction and the interphasial chemistry on cathode surface is also explored.

  3. Electrochemical method of producing eutectic uranium alloy and apparatus

    DOEpatents

    Horton, James A.; Hayden, H. Wayne

    1995-01-01

    An apparatus and method for continuous production of liquid uranium alloys through the electrolytic reduction of uranium chlorides. The apparatus includes an electrochemical cell formed from an anode shaped to form an electrolyte reservoir, a cathode comprising a metal, such as iron, capable of forming a eutectic uranium alloy having a melting point less than the melting point of pure uranium, and molten electrolyte in the reservoir comprising a chlorine or fluorine containing salt and uranium chloride. The method of the invention produces an eutectic uranium alloy by creating an electrolyte reservoir defined by a container comprising an anode, placing an electrolyte in the reservoir, the electrolyte comprising a chlorine or fluorine containing salt and uranium chloride in molten form, positioning a cathode in the reservoir where the cathode comprises a metal capable of forming an uranium alloy having a melting point less than the melting point of pure uranium, and applying a current between the cathode and the anode.

  4. Perovskite solid electrolytes for SOFC

    SciTech Connect

    Sammells, A.F.

    1992-09-01

    Selected perovskite solid electrolytes incorporated into research size fuel cells have shown stability for > 4000 hours at 600{degrees}C. Perovskite lattice requirements which favor low E{sub a} for ionic conduction include (i) that the perovskite lattice possess a moderate enthalpy of formation, (ii) perovskite lattice possess large free volumes, (iii) that the lattice minimally polarizes the mobile ion and (iv) that the crystallographic saddle point r{sub c} for ionic conduction is {approx_equal} 1.

  5. Perovskite solid electrolytes for SOFC

    SciTech Connect

    Sammells, A.F.

    1992-01-01

    Selected perovskite solid electrolytes incorporated into research size fuel cells have shown stability for > 4000 hours at 600{degrees}C. Perovskite lattice requirements which favor low E{sub a} for ionic conduction include (i) that the perovskite lattice possess a moderate enthalpy of formation, (ii) perovskite lattice possess large free volumes, (iii) that the lattice minimally polarizes the mobile ion and (iv) that the crystallographic saddle point r{sub c} for ionic conduction is {approx equal} 1.

  6. Low hydrostatic head electrolyte addition to fuel cell stacks

    DOEpatents

    Kothmann, Richard E.

    1983-01-01

    A fuel cell and system for supply electrolyte, as well as fuel and an oxidant to a fuel cell stack having at least two fuel cells, each of the cells having a pair of spaced electrodes and a matrix sandwiched therebetween, fuel and oxidant paths associated with a bipolar plate separating each pair of adjacent fuel cells and an electrolyte fill path for adding electrolyte to the cells and wetting said matrices. Electrolyte is flowed through the fuel cell stack in a back and forth fashion in a path in each cell substantially parallel to one face of opposite faces of the bipolar plate exposed to one of the electrodes and the matrices to produce an overall head uniformly between cells due to frictional pressure drop in the path for each cell free of a large hydrostatic head to thereby avoid flooding of the electrodes. The bipolar plate is provided with channels forming paths for the flow of the fuel and oxidant on opposite faces thereof, and the fuel and the oxidant are flowed along a first side of the bipolar plate and a second side of the bipolar plate through channels formed into the opposite faces of the bipolar plate, the fuel flowing through channels formed into one of the opposite faces and the oxidant flowing through channels formed into the other of the opposite faces.

  7. Transpassive electrodissolution of depleted uranium in alkaline electrolytes

    SciTech Connect

    Weisbrod, K.R.; Schake, A.R.; Morgan, A.N.; Purdy, G.M.; Martinez, H.E.; Nelson, T.O.

    1998-03-01

    To aid in removal of oralloy from the nuclear weapons stockpile, scientists at the Los Alamos National Laboratory Plutonium Facility are decontaminating oralloy parts by electrodissolution in neutral to alkaline electrolytes composed of sodium nitrate and sodium sulfate. To improve the process, electrodissolution experiments were performed with depleted uranium to understand the effects of various operating parameters. Sufficient precipitate was also produced to evaluate the feasibility of using ultrafiltration to separate the uranium oxide precipitates from the electrolyte before it enters the decontamination fixture. In preparation for the experiments, a potential-pH diagram for uranium was constructed from thermodynamic data for fully hydrated species. Electrodissolution in unstirred solutions showed that uranium dissolution forms two layers, an acidic bottom layer rich in uranium and an alkaline upper layer. Under stirred conditions results are consistent with the formation of a yellow precipitate of composition UO{sub 3}{center_dot}2H{sub 2}O, a six electron process. Amperometric experiments showed that current efficiency remained near 100% over a wide range of electrolytes, electrolyte concentrations, pH, and stirring conditions.

  8. Flecainide cardiotoxicity precipitated by electrolyte imbalance. Caution with thiazide diuretics

    PubMed Central

    Khavandi, A; Walker, P R

    2007-01-01

    A man presented with recurrent syncope, weakness and fatigue. His ECG showed marked QRS widening and he had gross hyponatraemia and hypokalaemia. His medications included bendroflumethiazide (long term) and flecainide (started 2 months previously). This presentation was consistent with flacainide cardiotoxicity exacerbated by electrolyte disturbance. The syncopal episodes probably represented life‐threatening arrhythmias. The ECG and symptoms resolved completely once the electrolytes were corrected. Increased cardiotoxicity with hypokalaemia is documented, but not widely recognised. Hyponatraemia‐induced flecainide cardiotoxicity has not been documented. The clinical effects of flecainide are due to use‐dependent block of sodium channels. There are reports that support the use of hypertonic sodium salts to reverse flecainide toxicity via antagonism at the receptor. By this rationale, hyponatraemia would lead to Flecainide toxicity. Flecainide has been shown to reduce salt absorption in animal bowel. It is possible that in combination with bendroflumethiazide it acted synergistically to produce profound electrolyte disturbance. Flecainide cardiotoxicity has a significant mortality and can present non‐specifically. Thus, early recognition is essential. This case demonstrates the importance of strict electrolyte control in patients who are on flecainide. We would discourage concomitant use of flecainide and bendroflumethiazide. PMID:17452686

  9. Electrical pulse fabrication of graphene nanopores in electrolyte solution

    SciTech Connect

    Kuan, Aaron T.; Szalay, Tamas; Lu, Bo; Xie, Ping; Golovchenko, Jene A.

    2015-05-18

    Nanopores in graphene membranes can potentially offer unprecedented spatial resolution for single molecule sensing, but their fabrication has thus far been difficult, poorly scalable, and prone to contamination. We demonstrate an in-situ fabrication method that nucleates and controllably enlarges nanopores in electrolyte solution by applying ultra-short, high-voltage pulses across the graphene membrane. This method can be used to rapidly produce graphene nanopores with subnanometer size accuracy in an apparatus free of nanoscale beams or tips.

  10. Electrical pulse fabrication of graphene nanopores in electrolyte solution

    PubMed Central

    Kuan, Aaron T.; Lu, Bo; Xie, Ping; Szalay, Tamas; Golovchenko, Jene A.

    2015-01-01

    Nanopores in graphene membranes can potentially offer unprecedented spatial resolution for single molecule sensing, but their fabrication has thus far been difficult, poorly scalable, and prone to contamination. We demonstrate an in-situ fabrication method that nucleates and controllably enlarges nanopores in electrolyte solution by applying ultra-short, high-voltage pulses across the graphene membrane. This method can be used to rapidly produce graphene nanopores with subnanometer size accuracy in an apparatus free of nanoscale beams or tips. PMID:26045626

  11. LOW TEMPERATURE CATHODE SUPPORTED ELECTROLYTES

    SciTech Connect

    Harlan U. Anderson; Wayne Huebner; Igor Kosacki

    2001-09-30

    This project has three main goals: Thin Films Studies, Preparation of Graded Porous Substrates and Basic Electrical Characterization and testing of Planar Single Cells. In this portion of study we have focused on producing YSZ films on porous LSM substrates. When using the polymer precursor there are a number of obstacles to overcome in order to form dense electrolyte layers on porous substrates (cathode or anode). Probably the most difficult problems are: (1) Extreme penetration of the polymer into the substrate must be prevented. (2) Shrinkage cracking must be avoided. (3) Film thickness in the 1 to 5{micro}m range must be achieved. We have demonstrated that cracking due to shrinkage involved during the elimination of solvents and organic matter and densification of the remaining oxide is not a problem as long as the resulting oxide film is < {approx} 0.15 {micro}m in thickness. We have also shown that we can make thicker films by making multiple depositions if the substrate is smooth (roughness {le} 0.1 {micro}m) and contains no surface pores > 0.2 {micro}m. The penetration of the polymer into the porous substrate can be minimized by increasing the viscosity of the polymer and reducing the largest pore at the surface of the substrate to {le} 0.2 {micro}m. We have shown that this can be done, but we have also shown that it is difficult to make dense films that are defect free with areas > 1 cm{sup 2}. This is because of the roughness of the substrate and the difficulty in making a substrate which does not have surface voids > 0.2 {micro}m. Thus the process works well for dense, smooth substrates for films < 1 {micro}m thick, but is difficult to apply to rough, porous surfaces and to make film thickness > 1 {micro}m. As a result of these problems, we have been addressing the issue of how to make dense films in the thickness range of 1 to 5 {micro}m on sintered porous substrates without introducing cracks and holes due to shrinkage and surface voids? These

  12. Nanocomposite polymer electrolyte for rechargeable magnesium batteries

    SciTech Connect

    Shao, Yuyan; Rajput, Nav Nidhi; Hu, Jian Z.; Hu, Mary Y.; Liu, Tianbiao L.; Wei, Zhehao; Gu, Meng; Deng, Xuchu; Xu, Suochang; Han, Kee Sung; Wang, Jiulin; Nie, Zimin; Li, Guosheng; Zavadil, K.; Xiao, Jie; Wang, Chong M.; Henderson, Wesley A.; Zhang, Jiguang; Wang, Yong; Mueller, Karl T.; Persson, Kristin A.; Liu, Jun

    2014-12-28

    Nanocomposite polymer electrolytes present new opportunities for rechargeable magnesium batteries. However, few polymer electrolytes have demonstrated reversible Mg deposition/dissolution and those that have still contain volatile liquids such as tetrahydrofuran (THF). In this work, we report a nanocomposite polymer electrolyte based on poly(ethylene oxide) (PEO), Mg(BH4)2 and MgO nanoparticles for rechargeable Mg batteries. Cells with this electrolyte have a high coulombic efficiency of 98% for Mg plating/stripping and a high cycling stability. Through combined experiment-modeling investigations, a correlation between improved solvation of the salt and solvent chain length, chelation and oxygen denticity is established. Following the same trend, the nanocomposite polymer electrolyte is inferred to enhance the dissociation of the salt Mg(BH4)2 and thus improve the electrochemical performance. The insights and design metrics thus obtained may be used in nanocomposite electrolytes for other multivalent systems.

  13. Metal-gas cell with electrolyte reservoir

    SciTech Connect

    Miller, L.E.; Carr, D.D.

    1984-10-16

    A metal-gas electrochemical cell is disclosed wherein electrolyte is progressively supplied from a reservoir into the electrode or cell stack as needed, so as to maintain each stack component with adequate electrolyte, as the plates ''grow'' and absorb electrolyte with repeated cycling. The reservoir preferably is a compressible bladder positioned between on end of the plate stack and a retaining plate. As the plate stack ''grows'' with repeated cycling, the bladder is slowly compressed, forcing electrolyte from the bladder through an electrolyte distribution tube located within the plate stack. One end of the electrolyte distribution tube is fixed to an end plate of the plate stack and the second end of the distribution tube may be connected to a Belleville washer or other spring which acts through the distribution tube to compress the plate stack. The elasticity of the spring permits the stack to expand as the electrodes grow.

  14. Safeguard monitoring of direct electrolytic reduction

    NASA Astrophysics Data System (ADS)

    Jurovitzki, Abraham L.

    Nuclear power is regaining global prominence as a sustainable energy source as the world faces the consequences of depending on limited fossil based, CO2 emitting fuels. A key component to achieving this sustainability is to implement a closed nuclear fuel cycle. Without achieving this goal, a relatively small fraction of the energy value in nuclear fuel is actually utilized. This involves recycling of spent nuclear fuel (SNF)---separating fissile actinides from waste products and using them to fabricate fresh fuel. Pyroprocessing is a viable option being developed for this purpose with a host of benefits compared to other recycling options, such as PUREX. Notably, pyroprocessing is ill suited to separate pure plutonium from spent fuel and thus has non-proliferation benefits. Pyroprocessing involves high temperature electrochemical and chemical processing of SNF in a molten salt electrolyte. During this batch process, several intermediate and final streams are produced that contain radioactive material. While pyroprocessing is ineffective at separating pure plutonium, there are various process misuse scenarios that could result in diversion of impure plutonium into one or more of these streams. This is a proliferation risk that should be addressed with innovative safeguards technology. One approach to meeting this challenge is to develop real time monitoring techniques that can be implemented in the hot cells and coupled with the various unit operations involved with pyroprocessing. Current state of the art monitoring techniques involve external chemical assaying which requires sample removal from these unit operations. These methods do not meet International Atomic Energy Agency's (IAEA) timeliness requirements. In this work, a number of monitoring techniques were assessed for their viability as online monitoring tools. A hypothetical diversion scenario for the direct electrolytic reduction process was experimentally verified (using Nd2O3 as a surrogate for PuO2

  15. Investigation of electrolyte electric discharge characteristics

    NASA Astrophysics Data System (ADS)

    Kirko, D. L.; Savjolov, A. S.

    2016-09-01

    The most important electrical characteristics of electrolyte electric discharge were investigated. The electric burning discharge was obtained with the help of different electrolytes. The spectral composition of the electric discharge electromagnetic radiation was determined, the plasma temperature was determined. The spectrum of the electric discharge high-frequency oscillations was calculated in the region v=10 kHz-80 MHz. The most appropriate modes of the electric burning discharge in different electrolytes were proposed.

  16. Fuel cell assembly with electrolyte transport

    DOEpatents

    Chi, Chang V.

    1983-01-01

    A fuel cell assembly wherein electrolyte for filling the fuel cell matrix is carried via a transport system comprising a first passage means for conveying electrolyte through a first plate and communicating with a groove in a second plate at a first point, the first and second plates together sandwiching the matrix, and second passage means acting to carry electrolyte exclusively through the second plate and communicating with the groove at a second point exclusive of the first point.

  17. Novel Electrolytes for Lithium Ion Batteries

    SciTech Connect

    Lucht, Brett L.

    2014-12-12

    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.

  18. Polymeric electrolytes based on hydrosilyation reactions

    DOEpatents

    Kerr, John Borland; Wang, Shanger; Hou, Jun; Sloop, Steven Edward; Han, Yong Bong; Liu, Gao

    2006-09-05

    New polymer electrolytes were prepared by in situ cross-linking of allyl functional polymers based on hydrosilation reaction using a multifunctional silane cross-linker and an organoplatinum catalyst. The new cross-linked electrolytes are insoluble in organic solvent and show much better mechanical strength. In addition, the processability of the polymer electrolyte is maintained since the casting is finished well before the gel formation.

  19. Electrolytic cell. [For separating anolyte and catholyte

    DOEpatents

    Bullock, J.S.; Hale, B.D.

    1984-09-14

    An apparatus is described for the separation of the anolyte and the catholyte during electrolysis. The electrolyte flows through an electrolytic cell between the oppositely charged electrodes. The cell is equipped with a wedge-shaped device, the tapered end being located between the electrodes on the effluent side of the cell. The wedge diverts the flow of the electrolyte to either side of the wedge, substantially separating the anolyte and the catholyte.

  20. Polymer gel electrolytes for lithium batteries

    NASA Astrophysics Data System (ADS)

    Baskakova, Yu V.; Yarmolenko, Ol'ga V.; Efimov, Oleg N.

    2012-04-01

    The data on the most promising polymer gel electrolytes for lithium batteries published in the past decade are surveyed and described systematically. Gel electrolytes with matrices of polyethylene oxide, poly(vinylidene fluoride) and its copolymer with hexafluoropropylene, poly(methyl methacrylate), polyacrylonitrile, poly(vinyl chloride) and polyacrylates are discussed. A special section is devoted to gel electrolytes with ionic liquids as the solvents. The bibliography includes 160 references.

  1. Conductivity of electrolytes for rechargeable lithium batteries

    NASA Astrophysics Data System (ADS)

    Dudley, J. T.; Wilkinson, D. P.; Thomas, G.; Levae, R.; Woo, S.

    1991-06-01

    The conductivity of 150 nonaqueous electrolytes for rechargeable Li batteries between -60 and 80 C is reported. A wide range of solvents including esters, ethers, aromatics, chlorinated solvents, etc., and mixtures thereof, were studied. Results for five electrolyte salts which have some promise for rechargeable Li cells are presented. Several of the trends in the data are discussed, and the importance of solvent viscosity in determining electrolyte conductivity is shown.

  2. Electrochemical cell with high conductivity glass electrolyte

    DOEpatents

    Nelson, Paul A.; Bloom, Ira D.; Roche, Michael F.

    1987-01-01

    A secondary electrochemical cell with sodium-sulfur or other molten reactants is provided with a ionically conductive glass electrolyte. The cell is contained within an electrically conductive housing with a first portion at negative potential and a second portion insulated therefrom at positive electrode potential. The glass electrolyte is formed into a plurality of elongated tubes and placed lengthwise within the housing. The positive electrode material, for instance sulfur, is sealed into the glass electrolyte tubes and is provided with an elongated axial current collector. The glass electrolyte tubes are protected by shield tubes or sheets that also define narrow annuli for wicking of the molten negative electrode material.

  3. Electrochemical cell with high conductivity glass electrolyte

    DOEpatents

    Nelson, P.A.; Bloom, I.D.; Roche, M.F.

    1986-04-17

    A secondary electrochemical cell with sodium-sulfur or other molten reactants is provided with an ionically conductive glass electrolyte. The cell is contained within an electrically conductive housing with a first portion at negative potential and a second portion insulated therefrom at positive electrode potential. The glass electrolyte is formed into a plurality of elongated tubes and placed lengthwise within the housing. The positive electrode material, for instance sulfur, is sealed into the glass electrolyte tubes and is provided with an elongated axial current collector. The glass electrolyte tubes are protected by shield tubes or sheets that also define narrow annuli for wicking of the molten negative electrode material.

  4. Electrochemical cell with high conductivity glass electrolyte

    DOEpatents

    Nelson, P.A.; Bloom, I.D.; Roche, M.F.

    1987-04-21

    A secondary electrochemical cell with sodium-sulfur or other molten reactants is provided with a ionically conductive glass electrolyte. The cell is contained within an electrically conductive housing with a first portion at negative potential and a second portion insulated therefrom at positive electrode potential. The glass electrolyte is formed into a plurality of elongated tubes and placed lengthwise within the housing. The positive electrode material, for instance sulfur, is sealed into the glass electrolyte tubes and is provided with an elongated axial current collector. The glass electrolyte tubes are protected by shield tubes or sheets that also define narrow annuli for wicking of the molten negative electrode material. 6 figs.

  5. Rebalancing electrolytes in redox flow battery systems

    SciTech Connect

    Chang, On Kok; Pham, Ai Quoc

    2014-12-23

    Embodiments of redox flow battery rebalancing systems include a system for reacting an unbalanced flow battery electrolyte with a rebalance electrolyte in a first reaction cell. In some embodiments, the rebalance electrolyte may contain ferrous iron (Fe.sup.2+) which may be oxidized to ferric iron (Fe.sup.3+) in the first reaction cell. The reducing ability of the rebalance reactant may be restored in a second rebalance cell that is configured to reduce the ferric iron in the rebalance electrolyte back into ferrous iron through a reaction with metallic iron.

  6. Photocured Gelled Electrolytes For Secondary Li Cells

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, Ganesan

    1994-01-01

    Class of photocured polymers exhibiting lithium-ion conductivities greater than those of well-studied polymers based on polyethylene oxide (PEO) show promise as polymeric electrolytes in rechargeable lithium cells. Increase in conductivity occasioned by use of electrolytes, coupled with amenability of electrolytes to formation into uniform thin (less than 25 micrometers thick), wide films, expected to result in cells with power densities greater than 100 W h/kg and charge/discharge rates exceeding currents equal, in amperes, to ampere-hour ratings. All-solid-state lithium batteries containing these electrolytes used as high-power, high-rate rechargeable power sources in commercial and aerospace applications.

  7. Interfacial behavior of polymer electrolytes

    SciTech Connect

    Kerr, John; Kerr, John B.; Han, Yong Bong; Liu, Gao; Reeder, Craig; Xie, Jiangbing; Sun, Xiaoguang

    2003-06-03

    Evidence is presented concerning the effect of surfaces on the segmental motion of PEO-based polymer electrolytes in lithium batteries. For dry systems with no moisture the effect of surfaces of nano-particle fillers is to inhibit the segmental motion and to reduce the lithium ion transport. These effects also occur at the surfaces in composite electrodes that contain considerable quantities of carbon black nano-particles for electronic connection. The problem of reduced polymer mobility is compounded by the generation of salt concentration gradients within the composite electrode. Highly concentrated polymer electrolytes have reduced transport properties due to the increased ionic cross-linking. Combined with the interfacial interactions this leads to the generation of low mobility electrolyte layers within the electrode and to loss of capacity and power capability. It is shown that even with planar lithium metal electrodes the concentration gradients can significantly impact the interfacial impedance. The interfacial impedance of lithium/PEO-LiTFSI cells varies depending upon the time elapsed since current was turned off after polarization. The behavior is consistent with relaxation of the salt concentration gradients and indicates that a portion of the interfacial impedance usually attributed to the SEI layer is due to concentrated salt solutions next to the electrode surfaces that are very resistive. These resistive layers may undergo actual phase changes in a non-uniform manner and the possible role of the reduced mobility polymer layers in dendrite initiation and growth is also explored. It is concluded that PEO and ethylene oxide-based polymers are less than ideal with respect to this interfacial behavior.

  8. High performance electrolytes for MCFC

    DOEpatents

    Kaun, T.D.; Roche, M.F.

    1999-08-24

    A carbonate electrolyte of the Li/Na or CaBaLiNa system is described. The Li/Na carbonate has a composition displaced from the eutectic composition to diminish segregation effects in a molten carbonate fuel cell. The CaBaLiNa system includes relatively small amounts of Ca{sub 2}CO{sub 3} and BaCO{sub 3}, and preferably of equimolar amounts. The presence of both Ca and BaCO{sub 3} enables lower temperature fuel cell operation. 15 figs.

  9. High performance electrolytes for MCFC

    DOEpatents

    Kaun, Thomas D.; Roche, Michael F.

    1999-01-01

    A carbonate electrolyte of the Li/Na or CaBaLiNa system. The Li/Na carbonate has a composition displaced from the eutectic composition to diminish segregation effects in a molten carbonate fuel cell. The CaBaLiNa system includes relatively small amounts of Ca.sub.2 CO.sub.3 and BaCO.sub.3, and preferably of equimolar amounts. The presence of both Ca and BaCO.sub.3 enables lower temperature fuel cell operation.

  10. ELECTROLYTIC PRODUCTION OF URANIUM TETRAFLUORIDE

    DOEpatents

    Lofthouse, E.

    1954-08-31

    This patent relates to electrolytic methods for the production of uranium tetrafluoride. According to the present invention a process for the production of uranium tetrafluoride comprises submitting to electrolysis an aqueous solution of uranyl fluoride containing free hydrofluoric acid. Advantageously the aqueous solution of uranyl fluoride is obtained by dissolving uranium hexafluoride in water. On electrolysis, the uranyl ions are reduced to uranous tons at the cathode and immediately combine with the fluoride ions in solution to form the insoluble uranium tetrafluoride which is precipitated.

  11. Thin-Film Solid Oxide Fuel Cell Based on Doped LaGaO3 Electrolyte

    NASA Astrophysics Data System (ADS)

    Wan, Jen-Hau; Goodenough, John B.

    2003-03-01

    Losses in a solid oxide fuel cell (SOFC) arise from the resistance to O2--ion conduction across the electrolyte and from the rate of reactant dissociative chemisorption and migration across the electrode/electrolyte interfaces. Efforts made to reduce the electrolyte thickness have increased the power density that can be withdrawn from the fuel cell. Whereas a SOFC based on a thin layer of yittria-stablized zirconia (YSZ) as the electrolyte has been under development for several years, a similar thin-electrolyte SOFC with La0.8Sr0.2Ga0.83Mg0.17O2.815 (LSGM) has received little attention. A SOFC with a thin layer of LSGM deposited on a porous YSZ substrate that was subsequently impregnated with Ni has been reported to give a power density of 850 mW/cm2 at 800¢XC with H2 as fuel. In our group, different methods have been used to fabricate a thin LSGM membrane on a composite anode, these methods include screen-printing, colloidal deposition, impregnation, and dry-pressing methods. Because of the reaction between LSGM and a Ni anode during fabrication, a layer of La0.4Ce0.6O1.8 (LDC) must be put between the LSGM electrolyte and a NiO+LDC composite anode. The thin-film SOFC made by screen-printing technique produced an anode-supported fuel cell with a 50 mm thick electrolyte+LDC layer. However because the screen-printing method did not produce an air-tight dense electrolyte membrane, the open-circuit voltage dropped to 0.7V instead of the theoretical 1.1V when running on humid hydrogen as fuel. The power density of this cell reaches 700 mW/cm2 at 850¢XC and 520mW/cm2 at 800¢XC. The dry-pressing method allows co-sintering of anode/electrolyte, which lowers the interfacial overpotentials and guarantees an air-tight, dense electrolyte layer. A SOFC power density of 1400 mW/cm2 at 800¢XC with a 200 mm thick LSGM electrolyte will be compared with the result for a thin-film electrolyte.

  12. Electrolyte optimization and electrode material evaluation for the vanadium redox battery

    NASA Astrophysics Data System (ADS)

    Kazacos, Michael

    1990-05-01

    The preparation of the electrolyte for the all vanadium redox flow battery was investigated using both chemical and electrolytic reduction of V2O5 powder. Oxalic acid and SO2 reduction were found to be unsuitable as only the V(IV) state could be produced directly. With suspended powder hydrolysis, however, vanadium sulphate of any oxidation state, in this case 50 percent V(IV) plus 50 percent V(III) in sulphuric acid can readily be prepared from V2O5 powder, thus allowing a significant reduction in the cost of the vanadium battery electrolyte. Results from conductivity and electrolyte stability tests at elevated temperature have led to modification of the electrolyte composition for the vanadium redox cell, from the 2 M V plus 2 M H2SO4, originally employed, to the use of 3 M H2SO4, much higher energy efficiencies and greater electrolyte stability was demonstrated with the 3 M H2SO4 supporting electrolyte. Spectroscopy and electrolyte conductivity were demonstrated as suitable techniques for state-of-charge monitoring. A number of electrode materials were also evaluated and a Toray graphite bonded to a carbon plastic electrode was selected for further prototype development. Energy efficiencies of between 83 and 86 percent obtained for a current density of 30 mA/sq cm for a temperature range of 5 to 45 C, and between 0 and 100 percent state-of-charge. A wide range of construction materials was tested for long term stability in the vanadium redox electrolyte.

  13. Exploring zinc coordination in novel zinc battery electrolytes.

    PubMed

    Kar, Mega; Winther-Jensen, Bjorn; Forsyth, Maria; MacFarlane, Douglas R

    2014-06-14

    The coordination of zinc ions by tetraglyme has been investigated here to support the development of novel electrolytes for rechargeable zinc batteries. Zn(2+) reduction is electrochemically reversible from tetraglyme. The spectroscopic data, molar conductivity and thermal behavior as a function of zinc composition, between mole ratios [80 : 20] and [50 : 50] [tetraglyme : zinc chloride], all suggest that strong interactions take place between chloro-zinc complexes and tetraglyme. Varying the concentration of zinc chloride produces a range of zinc-chloro species (ZnClx)(2-x) in solution, which hinder full interaction between the zinc ion and tetraglyme. Both the [70 : 30] and [50 : 50] mixtures are promising electrolyte candidates for reversible zinc batteries, such as the zinc-air device.

  14. Exploring zinc coordination in novel zinc battery electrolytes.

    PubMed

    Kar, Mega; Winther-Jensen, Bjorn; Forsyth, Maria; MacFarlane, Douglas R

    2014-06-14

    The coordination of zinc ions by tetraglyme has been investigated here to support the development of novel electrolytes for rechargeable zinc batteries. Zn(2+) reduction is electrochemically reversible from tetraglyme. The spectroscopic data, molar conductivity and thermal behavior as a function of zinc composition, between mole ratios [80 : 20] and [50 : 50] [tetraglyme : zinc chloride], all suggest that strong interactions take place between chloro-zinc complexes and tetraglyme. Varying the concentration of zinc chloride produces a range of zinc-chloro species (ZnClx)(2-x) in solution, which hinder full interaction between the zinc ion and tetraglyme. Both the [70 : 30] and [50 : 50] mixtures are promising electrolyte candidates for reversible zinc batteries, such as the zinc-air device. PMID:24760367

  15. Electrochromic cells with lutetium diphthalocyanine and semisolid polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Pizzarello, F. A.; Nicholson, M. M.

    1987-11-01

    Cyclic voltammograms were obtained for lutetium diphthalocyanine films in contact with plasticized poly(ethylene oxide) (PEO) electrolytes or solvent-swollen 2-acrylamido-2-methylpropane- sulfonic acid (AMPS) polymer electrolytes. Cells containing PEO-salt combinations plasticized with propylene glycol (PG) or acetonitrile resulted in slow, nonuniform color changes due to high interfacial resistance. The AMPS cell fabrication was simplified by starting with a commercial AMPS polymer product in the form of a transparent sheet containing water and other additives. This material, when further swollen in a PG-HC1 solution, produced the full range of uniform colors, accompanied by well defined voltammograms. It maintained good contact with the dye from -5 to 40 C.

  16. Formation of a Spinel Coating on AZ31 Magnesium Alloy by Plasma Electrolytic Oxidation

    NASA Astrophysics Data System (ADS)

    Sieber, Maximilian; Simchen, Frank; Scharf, Ingolf; Lampke, Thomas

    2016-03-01

    Plasma electrolytic oxidation (PEO) is a common means for the surface modification of light metals. However, PEO of magnesium substrates in dilute electrolytes generally leads to the formation of coatings consisting of unfavorable MgO magnesium oxide. By incorporation of electrolyte components, the phase constitution of the oxide coatings can be modified. Coatings consisting exclusively of MgAl2O4 magnesium-aluminum spinel are produced by PEO in an electrolyte containing hydroxide, aluminate, and phosphate anions. The hardness of the coatings is 3.5 GPa on Martens scale on average. Compared to the bare substrate, the coatings reduce the corrosion current density in dilute sodium chloride solution by approx. one order of magnitude and slightly shift the corrosion potential toward more noble values.

  17. Fundamental Aspects of Ion Transport in Solid Electrolytes

    NASA Technical Reports Server (NTRS)

    Ratnakumar, B. V.; Narayanan, S. R.

    1994-01-01

    Solid electrolytes (also termed as superionic solids or fast ion conductors) are characterized by high electrical conductivity, comparable to concentrated liquid electrolytes or even molten salt electrolytes, made possible by rapid transport of ions in the crystalline lattice.

  18. Evaluation of Electrochemical Methods for Electrolyte Characterization

    NASA Technical Reports Server (NTRS)

    Heidersbach, Robert H.

    2001-01-01

    This report documents summer research efforts in an attempt to develop an electrochemical method of characterizing electrolytes. The ultimate objective of the characterization would be to determine the composition and corrosivity of Martian soil. Results are presented using potentiodynamic scans, Tafel extrapolations, and resistivity tests in a variety of water-based electrolytes.

  19. Colloidal Electrolytes and the Critical Micelle Concentration

    ERIC Educational Resources Information Center

    Knowlton, L. G.

    1970-01-01

    Describes methods for determining the Critical Micelle Concentration of Colloidal Electrolytes; methods described are: (1) methods based on Colligative Properties, (2) methods based on the Electrical Conductivity of Colloidal Electrolytic Solutions, (3) Dye Method, (4) Dye Solubilization Method, and (5) Surface Tension Method. (BR)

  20. Polymeric electrolytes for ambient temperature lithium batteries

    NASA Astrophysics Data System (ADS)

    Farrington, G. C.

    1987-09-01

    During this reporting period a number of novel solid polymer electrolytes formed by salts of multivalent cations and polyethylene oxide (PEO) have been prepared and characterized. These materials are of interest not only because of their potential ionic conductivities, but also because some of them may have electronic conductivity and oxidizing power which would be useful for novel electrode materials in all-solid-state batteries. Two broad classes of materials were investigated: PEO solutions of Zn(2), Cd(2), and Pb(2), all of which are potential electrolytes for solid-state batteries, and PEO solutions of transition metal salts, which are of interest as possible cathode materials. Mixed compositions containing both divalent cations and lithium ions were also prepared. Electrolytes formed with small, highly-polarizing ions, such as Mg(2) and Ca(2), are essentially pure anion conductors. Electrolytes containing Zn(2) behave similarly, unless they are hydrated, in which case the Zn(2) ions are quite mobile. Electrolytes formed with larger, more polarizable cations, such as Pb(2) and Cd(2), conduct both anions and cations. Solutions of salts of transition metal cations form a third group of electrolytes. Of the electrolytes investigated so far, those formed with Ni(++) salts are the most unusual. It appears as if the transport number of Ni(2) and the electrolyte conductivity can be greatly enhanced by controlling the hydration and dehydration of the polymer.

  1. Solid composite electrolytes for lithium batteries

    DOEpatents

    Kumar, Binod; Scanlon, Jr., Lawrence G.

    2000-01-01

    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.

  2. Anion selective membrane. [ion exchange resins and ion exchange membrane electrolytes for electrolytic cells

    NASA Technical Reports Server (NTRS)

    Alexander, S. S.; Geoffroy, R. R.; Hodgdon, R. B.

    1975-01-01

    Experimental anion permselective membranes were prepared and tested for their suitability as cell separators in a chemical redox power storage system being developed at NASA-Lewis Research Center. The goals of long-term (1000 hr) oxidative and thermal stability at 80 C in FeCl3 and CrCl3 electrolytes were met by most of the weak base and strong base amino exchange groups considered in the program. Good stability is exhibited by several of the membrane substrate resins. These are 'styrene' divinylbenzene copolymer and PVC film. At least four membrane systems produce strong flexible films with electrochemical properties (resistivity, cation transfer) superior to those of the 103QZL, the most promising commercial membrane. The physical and chemical properties of the resins are listed.

  3. Design of an efficient electrolyte circulation system for the lead-acid battery

    NASA Astrophysics Data System (ADS)

    Thuerk, D.

    The design and operation of an electrolyte circulation system are described. Application of lead acid batteries to electric vehicle and other repetitive deep cycle services produces a nondesirable state in the battery cells, electrolyte stratification. This stratification is the result of acid and water generation at the electrodes during cycling. With continued cycling, the extent of the stratification increases and prevents complete charging with low percentages of overcharge. Ultimately this results in extremely short life for the battery system. The stratification problem was overcome by substantially overcharging the battery. This abusive overcharge produces gassing rates sufficient to mix the electrolyte during the end portion of the charge. Overcharge, even though it is required to eliminate stratification, produces the undesirable results related to high voltage and gassing rates.

  4. Engineering the Electrode-Electrolyte Interface: From Electrode Architecture to Zinc Redox in Ionic Liquid Electrolytes

    NASA Astrophysics Data System (ADS)

    Engstrom, Erika

    2011-12-01

    The electrode-electrolyte interface in electrochemical environments involves the understanding of complex processes relevant for all electrochemical applications. Some of these processes include electronic structure, charge storage, charge transfer, solvent dynamics and structure and surface adsorption. In order to engineer electrochemical systems, no matter the function, requires fundamental intuition of all the processes at the interface. The following work presents different systems in which the electrode-electrolyte interface is highly important. The first is a charge storage electrode utilizing percolation theory to develop an electrode architecture producing high capacities. This is followed by Zn deposition in an ionic liquid in which the deposition morphology is highly dependant on the charge transfer and surface adsorption at the interface. Electrode Architecture: A three-dimensional manganese oxide supercapacitor electrode architecture is synthesized by leveraging percolation theory to develop a hierarchically designed tri-continuous percolated network. The three percolated phases include a faradaically-active material, electrically conductive material and pore-former templated void space. The micropores create pathways for ionic conductivity, while the nanoscale electrically conducting phase provides both bulk conductivity and local electron transfer with the electrochemically active phase. Zn Electrodeposition: Zn redox in air and water stable N-ethyl-N-methylmorpholinium bis(trifluoromethanesulfonyl)imide, [C2nmm][NTf2] is presented. Under various conditions, characterization of overpotential, kinetics and diffusion of Zn species and morphological evolution as a function of overpotential and Zn concentration are analyzed. The surface stress evolution during Zn deposition is examined where grain size and texturing play significant rolls in compressive stress generation. Morphological repeatability in the ILs led to a novel study of purity in ionic

  5. Solid polymer electrolyte from phosphorylated chitosan

    SciTech Connect

    Fauzi, Iqbal Arcana, I Made

    2014-03-24

    Recently, the need of secondary battery application continues to increase. The secondary battery which using a liquid electrolyte was indicated had some weakness. A solid polymer electrolyte is an alternative electrolytes membrane which developed in order to replace the liquid electrolyte type. In the present study, the effect of phosphorylation on to polymer electrolyte membrane which synthesized from chitosan and lithium perchlorate salts was investigated. The effect of the component’s composition respectively on the properties of polymer electrolyte, was carried out by analyzed of it’s characterization such as functional groups, ion conductivity, and thermal properties. The mechanical properties i.e tensile resistance and the morphology structure of membrane surface were determined. The phosphorylation processing of polymer electrolyte membrane of chitosan and lithium perchlorate was conducted by immersing with phosphoric acid for 2 hours, and then irradiated on a microwave for 60 seconds. The degree of deacetylation of chitosan derived from shrimp shells was obtained around 75.4%. Relative molecular mass of chitosan was obtained by viscometry method is 796,792 g/mol. The ionic conductivity of chitosan membrane was increase from 6.33 × 10{sup −6} S/cm up to 6.01 × 10{sup −4} S/cm after adding by 15 % solution of lithium perchlorate. After phosphorylation, the ionic conductivity of phosphorylated lithium chitosan membrane was observed 1.37 × 10{sup −3} S/cm, while the tensile resistance of 40.2 MPa with a better thermal resistance. On the strength of electrolyte membrane properties, this polymer electrolyte membrane was suggested had one potential used for polymer electrolyte in field of lithium battery applications.

  6. Electrolyte for an electrochemical cell

    DOEpatents

    Bates, J.B.; Dudney, N.J.

    1997-01-28

    Described is a thin-film battery, especially a thin-film microbattery, and a method for making the same having application as a backup or primary integrated power source for electronic devices. The battery includes a novel electrolyte amorphous lithium phosphorus oxynitride which is electrochemically stable and does not react with the lithium anode and a novel vanadium oxide cathode Configured as a microbattery, the battery can be fabricated directly onto a semiconductor chip, onto the semiconductor die or onto any portion of the chip carrier. The battery can be fabricated to any specified size or shape to meet the requirements of a particular application. The battery is fabricated of solid state materials and is capable of operation between {minus}15 C and 150 C. 9 figs.

  7. Electrolytes near structured dielectric interfaces

    NASA Astrophysics Data System (ADS)

    Wu, Huanxin; Jing, Yufei; Solis, Francisco; Olvera de La Cruz, Monica; Luijten, Erik

    2015-03-01

    The ion distribution in an electrolyte near a dielectric interface has important consequences for numerous applications. To date, most studies have focused on planar interfaces, where, e.g., simulations can take advantage of the image-charge method. However, for surfaces that display structure on the nanoscale, dielectric effects may be significantly different. Here, we investigate such interfaces via a combination of computer simulations and Poisson-Boltzmann theory. We demonstrate how, even for systems with piecewise uniform dielectric constant, surface structure affects the induced polarization charge as well as the ion distribution near the interface, in particular for asymmetric salts. We explore the role of ion concentration, dielectric mismatch and characteristic length scale of the surface structure.

  8. Electrolyte for an electrochemical cell

    DOEpatents

    Bates, John B.; Dudney, Nancy J.

    1997-01-01

    Described is a thin-film battery, especially a thin-film microbattery, and a method for making same having application as a backup or primary integrated power source for electronic devices. The battery includes a novel electrolyte amorphous lithium phosphorus oxynitride which is electrochemically stable and does not react with the lithium anode and a novel vanadium oxide cathode Configured as a microbattery, the battery can be fabricated directly onto a semiconductor chip, onto the semiconductor die or onto any portion of the chip carrier. The battery can be fabricated to any specified size or shape to meet the requirements of a particular application. The battery is fabricated of solid state materials and is capable of operation between -15.degree. C. and 150.degree. C.

  9. Stretching short DNAs in electrolytes.

    PubMed

    Wang, Jizeng; Fan, Xiaojun; Gao, Huajian

    2006-03-01

    This paper is aimed at a combined theoretical and numerical study of the force-extension relation of a short DNA molecule stretched in an electrolyte. A theoretical formula based on a recent discrete wormlike chain (WLC) model of Kierfeld et al. (Eur Phys. J. E, Vol. 14, pp.17-34, 2004) and the classical OSF mean-field theory on electrostatic stiffening of a charged polymer is numerically verified by a set of Brownian dynamics simulations based on a generalized bead-rod (GBR) model incorporating long-ranged electrostatic interactions via the Debye-Hueckel potential (DH). The analysis indicates that the stretching of a short DNA can be well described as a WLC with a constant effective persistent length. This contrasts the behavior of long DNA chains that are known to exhibit variable persistent lengths depending on the ion concentration levels and force magnitudes. PMID:16711068

  10. Design of an efficient electrolyte circulation system for the lead-acid battery

    SciTech Connect

    Thuerk, D.

    1982-01-01

    Application of lead-acid batteries to electric vehicle and other repetitive deep-cycle services produces a non-desirable state in the battery cells, electrolyte stratification. This stratification is the result of acid and water generation at the electrodes during cycling. Water, which is generated during discharge, rises to the electrolyte surface due to gravity differences, whereas the concentrated sulfuric acid generated during charge falls to the bottom of the container. With continued cycling, the extent of the stratification increases and prevents complete charging with low percentages of overcharge. Ultimately this results in extremely short life for the battery system. The industry presently overcomes the stratification problem by substantially overcharging the battery. This abusive overcharge produces gassing rates sufficient to mix the electrolyte during the end portion of the charge. The amount of recharge typically used to mix the electrolyte ranges from 120% to 140% of the prior discharge. Overcharge, even though it is required to eliminate stratification, produces the undesirable results related to high voltage and gassing rates. The design and operation of an electrolyte circulation system are described. (WHK)

  11. New electrolytes and electrolyte additives to improve the low temperature performance of lithium-ion batteries

    SciTech Connect

    Yang, Xiao-Qing

    2008-08-31

    In this program, two different approaches were undertaken to improve the role of electrolyte at low temperature performance - through the improvement in (i) ionic conductivity and (ii) interfacial behavior. Several different types of electrolytes were prepared to examine the feasibil.ity of using these new electrolytes in rechargeable lithium-ion cells in the temperature range of +40°C to -40°C. The feasibility studies include (a) conductivity measurements of the electrolytes, (b) impedance measurements of lithium-ion cells using the screened electrolytes with di.fferent electrochemical history such as [(i) fresh cells prior to formation cycles, (ii) after first charge, and (iii) after first discharge], (c) electrical performance of the cells at room temperatures, and (d) charge discharge behavior at various low temperatures. Among the different types of electrolytes investigated in Phase I and Phase II of this SBIR project, carbonate-based LiPF6 electrolytes with the proposed additives and the low viscous ester as a third component to the carbonate-based LiPF6 electrolytes show promising results at low temperatures. The latter electrolytes deliver over 80% of room temperature capacity at -20{degrees}C when the lithium-ion cells containing these electrolytes were charged at -20 °C. Also, there was no lithium plating when the lithium­-ion cells using C-C composite anode and LiPF{sub 6} in EC/EMC/MP electrolyte were charged at -20{degrees}C at C/5 rate. The studies of ionic conductivity and AC impedance of these new electrolytes, as well as the charge discharge characteristics of lithium-ion cells using these new electrolytes at various low temperatures provide new findings: The reduced capacity and power capability, as well as the problem of lithium plating at low temperatures charging of lithium-ion cells are primarily due to slow the lithium-ion intercalation/de-intercalation kinetics in the carbon structure.

  12. An electrolytic process for magnesium and its alloys production

    SciTech Connect

    Sharma, R.

    1996-10-01

    The largest amount of magnesium is used for aluminum-magnesium alloy production. The second largest use is in desulfurization of steel. A magnesium {minus}10 weight percent (w/o) aluminum alloy can also be used in both the above processes. Pure magnesium metal is not of much use for structural purposes. However, a magnesium {minus}10 w/o aluminum alloy melt which is also suitable for structural applications, can be produced as a bottom layer in an electrolytic magnesium production cell using a potassium chloride-magnesium chloride electrolyte at {approximately} 750 C. In this situation, the magnesium production process and the cell can be similar to the aluminum production process and its cell. The magnesium-aluminum alloys can be produced by electrolysis at far less cost than these alloys produced from the respective metals. The process can also be used to produce other magnesium alloys for use in the auto industry at comparatively far less cost. The largest increase in the magnesium usage in the future is going to be only in the magnesium alloys sector.

  13. Rechargable molten-electrolyte lithium batteries

    NASA Astrophysics Data System (ADS)

    Kaun, T. D.

    1989-10-01

    Lithium-alloy/metal sulfide cells with on molten-halide electrolytes, which are operated in a temperature range of 375 to 474 C, have undergone many improvements in recent years. Cycle life now exceeds 1000 cycles. The Li-alloy/LiCl-LiBr-KBr eutectic (25:37:38 mol percent)/upper-plateau (U.P.) FeS2 cell operated at 400 C has shown excellence performance prospects: 200 Wh/kg specific energy and 200-W/kg specific power. Electrolyte composition has played a dominant role in attaining long-term stable electrochemical performance. A modified LiCl-LiBr-KBr composition (34:32.5:33.5 mol percent) was found to exhibit 25 percent increased ionic conductivity over that of the eutectic. This higher-conductivity electrolyte approximately compensates for the reduced electrolyte content of the electrolyte-starved FeS2 cell. Such a cell has attained of 95 percent utilization of U.P. FeS2 electrode capacity at a comparable cell impedance (0.8 to 1.0 ohm sq cm) to that of an electrolyte-flooded cell. Advancements in cell design and materials application have reduced materials costs and increased battery durability. Both FeS and FeS2 cell tests have demonstrated overcharge tolerance (3 to 5 mA/sq cm) for electrolyte-starved operation with MgO powder separators.

  14. A study of electrolytes for lithium batteries

    NASA Astrophysics Data System (ADS)

    Perron, Gerald; Desnoyers, J. E.; Rheault, F.; Gagnon, R.; Quirion, F.; Camire, C.; Ledoux, J.

    1989-05-01

    The main objective of the work described here was to develop a fast and efficient method to optimize the electrolytic medium in primary and secondary high density Li/SO2 batteries over a wide range of temperatures. Mixed aprotic solvents are frequently used in batteries to optimize their performance. In the work described here, combinations of five solvents (acetonitrile, gamma butyrolacetone, 1,3- dimethoxyethane, 1,3- dioxolane and sulfolane), three electrolytes (LiBr, LiClO4, and LiAsF6), and SO2 were studied. The liquid-solid phase diagrams at 25 C were correlated with the viscosity, conductivity, density, and in some cases heat capacity of the mixture. Five types of material combinations were analyzed. These combinations included: (1) aprotic solvents + aprotic solvents, (2) electrolytes + aprotic solvents, (3) electrolytes + mixtures of aprotic solvents, (4) aprotic solvents + SO2, and (5) electrolytes + solvents + SO2. Mixed solvent plus electrolyte conductivities were up to 50 percent greater than the best conductivity observed when a single solvent was combined with an electrolyte. In addition the conductivity of the lithium salts in mixtures of aprotic solvents with SO2 at minus 15 C were measured. In this case, the specific conductivity maximized in the region corresponding to the SO2 rich eutectic for all mixtures studied. The study showed a correlation between the liquid solids equilibrium properties for the mixtures and their physico-chemical properties in solution, even at temperatures far above the solid liquid equilibrium point.

  15. Solid biopolymer electrolytes came from renewable biopolymer

    NASA Astrophysics Data System (ADS)

    Wang, Ning; Zhang, Xingxiang; Qiao, Zhijun; Liu, Haihui

    2009-07-01

    Solid polymer electrolytes (SPEs) have attracted many attentions as solid state ionic conductors, because of their advantages such as high energy density, electrochemical stability, and easy processing. SPEs obtained from starch have attracted many attentions in recent years because of its abundant, renewable, low price, biodegradable and biocompatible. In addition, the efficient utilization of biodegradable polymers came from renewable sources is becoming increasingly important due to diminishing resources of fossil fuels as well as white pollution caused by undegradable plastics based on petroleum. So N, N-dimethylacetamide (DMAc) with certain concentration ranges of lithium chloride (LiCl) is used as plasticizers of cornstarch. Li+ can complexes with the carbonyl atoms of DMAc molecules to produce a macro-cation and leave the Cl- free to hydrogen bond with the hydroxyl or carbonyl of starch. This competitive hydrogen bond formation serves to disrupt the intra- and intermolecular hydrogen bonding existed in starch. Therefore, melt extrusion process conditions are used to prepare conductive thermoplastic starch (TPS). The improvements of LiCl concentration increase the water absorption and conductance of TPS. The conductance of TPS containing 0.14 mol LiCl achieve to 10-0.5 S cm-1 with 18 wt% water content.

  16. Electrolytic production and dispensing of hydrogen

    SciTech Connect

    Thomas, C.E.; Kuhn, I.F. Jr.

    1995-09-01

    The fuel cell electric vehicle (FCEV) is undoubtedly the only option that can meet both the California zero emission vehicle (ZEV) standard and the President`s goal of tripling automobile efficiency without sacrificing performance in a standard 5-passenger vehicle. The three major automobile companies are designing and developing FCEVs powered directly by hydrogen under cost-shared contracts with the Department of Energy. Once developed, these vehicles will need a reliable and inexpensive source of hydrogen. Steam reforming of natural gas would produce the least expensive hydrogen, but funding may not be sufficient initially to build both large steam reforming plants and the transportation infrastructure necessary to deliver that hydrogen to geographically scattered FCEV fleets or individual drivers. This analysis evaluates the economic feasibility of using small scale water electrolysis to provide widely dispersed but cost-effective hydrogen for early FCEV demonstrations. We estimate the cost of manufacturing a complete electrolysis system in large quantities, including compression and storage, and show that electrolytic hydrogen could be cost competitive with fully taxed gasoline, using existing residential off-peak electricity rates.

  17. Role of the electrolyte in cathodic lead dioxide reduction

    SciTech Connect

    Lyamina, L.I.; Gorbunova, K.M.; Tarasova, N.I.

    1985-09-01

    The electrolyte composition and particularly the anions are thought to be important in cathodic lead dioxide reduction. Data are reported for the process in 0.1 M Na/sub 2/B/sub 4/O/sub 7/, Na/sub 2/HPO/sub 4/, KOH, and KC1 solution and in 0.3 M K/sub 2/SO/sub 4/ solution. Deposits of alpha-PbO/sub 2/ were produced electrolytically on nickel. The potentials are reported on the hydrogen scale. The electrochemical behavior of lead dioxide in said solutions was evaluated from charging curves and from potentiodynamic curves obtained with a P-5848 potentiostat. The first stage of lead dioxide reduction in all solutions results in the formation of an intermediate oxide having the composition of PbO/sub 1/ /sub 43/ to PbO/sub 1/ /sub 24/. The second stage (reduction of the intermediate oxide to metallic lead) depends on the nature of the electrolyte. An examination of the results obtained action of lead dioxide with the electrophilic component increases in the order of KOH yields KC1 yields Na/sub 2/B/sub 4/O/sub 7/ yields Na/sub 2/HPO/sub 4/ yields K/sub 2/SO/sub 4/.

  18. Electrolytic orthoborate salts for lithium batteries

    DOEpatents

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

    2009-05-05

    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.

  19. Electrolytic orthoborate salts for lithium batteries

    DOEpatents

    Angell, Charles Austen; Xu, Wu

    2008-01-01

    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.

  20. New Polymer and Liquid Electrolytes for Lithium Batteries

    SciTech Connect

    McBreen, J.; Lee, H. S.; Yang, X. Q.; Sun, X.

    1999-03-29

    All non-aqueous lithium battery electrolytes are Lewis bases that interact with cations. Unlike water, they don't interact with anions. The result is a high degree of ion pairing and the formation of triplets and higher aggregates. This decreases the conductivity and the lithium ion transference and results in polarization losses in batteries. Approaches that have been used to increase ion dissociation in PEO based electrolytes are the use of salts with low lattice energy, the addition of polar plasticizers to the polymer, and the addition of cation completing agents such as crown ethers or cryptands. Complexing of the anions is a more promising approach since it should increase both ion dissociation and the lithium transference. At Brookhaven National Laboratory (BNL) we have synthesized two new families of neutral anion completing agents, each based on Lewis acid centers. One is based on electron deficient nitrogen sites on substituted aza-ethers, wherein the hydrogen on the nitrogen is replaced by electron withdrawing groups such as CF{sub 3}SO{sub 3{sup -}}. The other is based on electron deficient boron sites on borane or borate compounds with various fluorinated aryl or alkyl groups. Some of the borane based anion receptors can promote the dissolution of LiF in several solvents. Several of these compounds, when added in equivalent amounts, produce 1.2M LiF solutions in DME, an increase in volubility of LiF by six orders of magnitude. Some of these LiF electrolytes have conductivities as high as 6 x 10{sup -3} Scm{sup -1}. The LiF electrolytes with borane anion acceptors in PC:EC:DEC solvents have excellent electrochemical stability. This has been demonstrated in small Li/LiMn{sub 2}O{sub 4} cells.

  1. Inorganic-organic electrolyte materials for energy applications

    NASA Astrophysics Data System (ADS)

    Fei, Shih-To

    emphasizes the flammability studies. Chapter 4 expands the application of the ethyleneoxy phosphazene system to dye sensitized solar cell systems, and uses this material as a model for the study of electrode-electrolyte interfaces. We report here the results of our study on polymer electrolyte infiltration and its effect on dye-sensitized solar cells. In-depth studies have been made to compare the effects of different cell assembly procedures on the electrochemical properties as well as infiltration of electrolytes into various electrode designs. The first part of the study is based on the use of thermoplastic phosphazene electrolytes and how the overall fabrication procedure affects electrochemical performance, and the second is the use of cross-section microscopy to characterize the degree of electrolyte infiltration into various nanostructured titanium dioxide electrode surfaces. The results of this study should eventually improve the efficiency and longevity of thermally stable polymer dye solar cell systems. In Chapter 5 the effect of pendant polymer design on methanol fuel cell membrane performance was investigated. A synthetic method is described to produce a proton conductive polymer membrane with a polynorbornane backbone and inorganic-organic cyclic phosphazene pendent groups that bear sulfonic acid units. This hybrid polymer combines the inherent hydrophobicity and flexibility of the organic polymer with the tuning advantages of the cyclic phosphazene to produce a membrane with high proton conductivity and low methanol crossover at room temperature. The ion exchange capacity (IEC), the water swelling behavior of the polymer, and the effect of gamma radiation crosslinking were studied, together with the proton conductivity and methanol permeability of these materials. A typical membrane had an IEC of 0.329 mmolg-1 and had water swelling of 50 wt%. The maximum proton conductivity of 1.13x10 -4 Scm-1 at room temperature is less than values reported for some

  2. Electrolyte and Cathode Degradation Mechanisms in Lithium Ion Batteries

    NASA Astrophysics Data System (ADS)

    Tebbe, Jonathon

    Lithium ion battery technologies suffer from limitations in performance, such as capacity fading, due in part to degradation of the cathode and electrolyte materials. Quantum chemical simulations were employed to investigate the reactions leading to degradation of LiCoO2 cathodes and the electrolyte molecules. Formation of HF in the electrolyte resulting from reaction between PF5 and H2O impurities was first investigated. This research predicts HF is produced as a result of PF5 complexing with H2O, then reacting through ligand exchange to form HF and PF4OH with an activation barrier of 1.18 eV and reaction enthalpy of 0.15 eV. HF undergoes dissociative adsorption at that the (101¯4) surface of LiCoO2 without a barrier, leading to formation of LiF-Li+ precipitates and H 2O on the surface with a reaction energy of -2.41 eV. The formation of H2O is of particular concern because H2O drives further formation of HF in the electrolyte, resulting in an autocatalytic cycle of degradation. These findings indicate that HF initially occurs in low concentrations rapidly increases due to H2O generation upon HF attack. Reduction in capacity fading is observed in alumina ALD coated LiCoO2 cathodes and we have investigated a monolayer alumina coating on the LiCoO2 (101¯4) surface to identify the mechanism by which the alumina coating protects the cathode surface. We have found that HF will preferentially dissociate at the alumina coating with a reaction energy of -2.84 eV and without any resolvable barrier to dissociation. Additionally, our calculations predict that H2O does not form as a result of HF dissociation at the alumina monolayer; instead HF dissociation produces neighboring hydroxyl sites on the alumina surface. Consequently, the alumina coating prevents the autocatalytic degradation of the cathode by sequestering HF impurities in the alumina film. Finally, we found that Lewis acid-base complexation between ethylene carbonate (EC) electrolyte molecules and PF5 or the Li

  3. High conductivity electrolyte solutions and rechargeable cells incorporating such solutions

    DOEpatents

    Angell, Charles Austen; Zhang, Sheng-Shui; Xu, Kang

    1998-01-01

    This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents.

  4. High conductivity electrolyte solutions and rechargeable cells incorporating such solutions

    DOEpatents

    Angell, C.A.; Zhang, S.S.; Xu, K.

    1998-10-20

    This invention relates generally to electrolyte solvents for use in liquid or rubbery polymer electrolyte solutions as are used, for example, in electrochemical devices. More specifically, this invention relates to sulfonyl/phospho-compound electrolyte solvents and sulfonyl/phospho-compound electrolyte solutions incorporating such solvents. 9 figs.

  5. Electrolytic exfoliation of graphite in water with multifunctional electrolytes: en route towards high quality, oxide-free graphene flakes.

    PubMed

    Munuera, J M; Paredes, J I; Villar-Rodil, S; Ayán-Varela, M; Martínez-Alonso, A; Tascón, J M D

    2016-02-01

    Electrolytic--usually referred to as electrochemical--exfoliation of graphite in water under anodic potential holds enormous promise as a simple, green and high-yield method for the mass production of graphene, but currently suffers from several drawbacks that hinder its widespread adoption, one of the most critical being the oxidation and subsequent structural degradation of the carbon lattice that is usually associated with such a production process. To overcome this and other limitations, we introduce and implement the concept of multifunctional electrolytes. The latter are amphiphilic anions (mostly polyaromatic hydrocarbons appended with sulfonate groups) that play different relevant roles as (1) an intercalating electrolyte to trigger exfoliation of graphite into graphene flakes, (2) a dispersant to afford stable aqueous colloidal suspensions of the flakes suitable for further use, (3) a sacrificial agent to prevent graphene oxidation during exfoliation and (4) a linker to promote nanoparticle anchoring on the graphene flakes, yielding functional hybrids. The implementation of this strategy with some selected amphiphiles even furnishes anodically exfoliated graphenes of a quality similar to that of flakes produced by direct, ultrasound- or shear-induced exfoliation of graphite in the liquid phase (i.e., almost oxide- and defect-free). These high quality materials were used for the preparation of catalytically efficient graphene-Pt nanoparticle hybrids, as demonstrated by model reactions (reduction of nitroarenes). The multifunctional performance of these electrolytes is also discussed and rationalized, and a mechanistic picture of their oxidation-preventing ability is proposed. Overall, the present results open the prospect of anodic exfoliation as a competitive method for the production of very high quality graphene flakes.

  6. Electrolytic exfoliation of graphite in water with multifunctional electrolytes: en route towards high quality, oxide-free graphene flakes

    NASA Astrophysics Data System (ADS)

    Munuera, J. M.; Paredes, J. I.; Villar-Rodil, S.; Ayán-Varela, M.; Martínez-Alonso, A.; Tascón, J. M. D.

    2016-01-01

    Electrolytic - usually referred to as electrochemical - exfoliation of graphite in water under anodic potential holds enormous promise as a simple, green and high-yield method for the mass production of graphene, but currently suffers from several drawbacks that hinder its widespread adoption, one of the most critical being the oxidation and subsequent structural degradation of the carbon lattice that is usually associated with such a production process. To overcome this and other limitations, we introduce and implement the concept of multifunctional electrolytes. The latter are amphiphilic anions (mostly polyaromatic hydrocarbons appended with sulfonate groups) that play different relevant roles as (1) an intercalating electrolyte to trigger exfoliation of graphite into graphene flakes, (2) a dispersant to afford stable aqueous colloidal suspensions of the flakes suitable for further use, (3) a sacrificial agent to prevent graphene oxidation during exfoliation and (4) a linker to promote nanoparticle anchoring on the graphene flakes, yielding functional hybrids. The implementation of this strategy with some selected amphiphiles even furnishes anodically exfoliated graphenes of a quality similar to that of flakes produced by direct, ultrasound- or shear-induced exfoliation of graphite in the liquid phase (i.e., almost oxide- and defect-free). These high quality materials were used for the preparation of catalytically efficient graphene-Pt nanoparticle hybrids, as demonstrated by model reactions (reduction of nitroarenes). The multifunctional performance of these electrolytes is also discussed and rationalized, and a mechanistic picture of their oxidation-preventing ability is proposed. Overall, the present results open the prospect of anodic exfoliation as a competitive method for the production of very high quality graphene flakes.Electrolytic - usually referred to as electrochemical - exfoliation of graphite in water under anodic potential holds enormous promise

  7. Electrolytic silver ion cell sterilizes water supply

    NASA Technical Reports Server (NTRS)

    Albright, C. F.; Gillerman, J. B.

    1968-01-01

    Electrolytic water sterilizer controls microbial contamination in manned spacecraft. Individual sterilizer cells are self-contained and require no external power or control. The sterilizer generates silver ions which do not impart an unpleasant taste to water.

  8. Self-doped molecular composite battery electrolytes

    DOEpatents

    Harrup, Mason K.; Wertsching, Alan K.; Stewart, Frederick F.

    2003-04-08

    This invention is in solid polymer-based electrolytes for battery applications. It uses molecular composite technology, coupled with unique preparation techniques to render a self-doped, stabilized electrolyte material suitable for inclusion in both primary and secondary batteries. In particular, a salt is incorporated in a nano-composite material formed by the in situ catalyzed condensation of a ceramic precursor in the presence of a solvated polymer material, utilizing a condensation agent comprised of at least one cation amenable to SPE applications. As such, the counterion in the condensation agent used in the formation of the molecular composite is already present as the electrolyte matrix develops. This procedure effectively decouples the cation loading levels required for maximum ionic conductivity from electrolyte physical properties associated with condensation agent loading levels by utilizing the inverse relationship discovered between condensation agent loading and the time domain of the aging step.

  9. Galvanic cell with tin fluoborate electrolyte

    SciTech Connect

    Ruben, S.

    1984-12-11

    The invention is the utilization of an aqueous solution of tin fluoborate as the electrolyte in galvanic cells. It is particularly useful in primary galvanic cells employing permanganate depolarizers.

  10. Molten salt bath circulation design for an electrolytic cell

    DOEpatents

    Dawless, R.K.; LaCamera, A.F.; Troup, R.L.; Ray, S.P.; Hosler, R.B.

    1999-08-17

    An electrolytic cell for reduction of a metal oxide to a metal and oxygen has an inert anode and an upwardly angled roof covering the inert mode. The angled roof diverts oxygen bubbles into an upcomer channel, thereby agitating a molten salt bath in the upcomer channel and improving dissolution of a metal oxide in the molten salt bath. The molten salt bath has a lower velocity adjacent the inert anode in order to minimize corrosion by substances in the bath. A particularly preferred cell produces aluminum by electrolysis of alumina in a molten salt bath containing aluminum fluoride and sodium fluoride. 4 figs.

  11. Molten salt bath circulation design for an electrolytic cell

    DOEpatents

    Dawless, Robert K.; LaCamera, Alfred F.; Troup, R. Lee; Ray, Siba P.; Hosler, Robert B.

    1999-01-01

    An electrolytic cell for reduction of a metal oxide to a metal and oxygen has an inert anode and an upwardly angled roof covering the inert mode. The angled roof diverts oxygen bubbles into an upcomer channel, thereby agitating a molten salt bath in the upcomer channel and improving dissolution of a metal oxide in the molten salt bath. The molten salt bath has a lower velocity adjacent the inert anode in order to minimize corrosion by substances in the bath. A particularly preferred cell produces aluminum by electrolysis of alumina in a molten salt bath containing aluminum fluoride and sodium fluoride.

  12. Operating mechanisms of electrolytes in magnesium ion batteries: chemical equilibrium, magnesium deposition, and electrolyte oxidation.

    PubMed

    Kim, Dong Young; Lim, Younhee; Roy, Basab; Ryu, Young-Gyoon; Lee, Seok-Soo

    2014-12-21

    Since the early nineties there have been a number of reports on the experimental development of Mg electrolytes based on organo/amide-magnesium chlorides and their transmetalations. However, there are no theoretical papers describing the underlying operating mechanisms of Mg electrolytes, and there is no clear understanding of these mechanisms. We have therefore attempted to clarify the operating mechanisms of Mg electrolytes by studying the characteristics of Mg complexes, solvation, chemical equilibrium, Mg-deposition processes, electrolyte-oxidation processes, and oxidative degradation mechanism of RMgCl-based electrolytes, using ab initio calculations. The formation and solvation energies of Mg complexes highly depend on the characteristics of R groups. Thus, changes in R groups of RMgCl lead to changes in the equilibrium position and the electrochemical reduction and oxidation pathways and energies. We first provide a methodological scheme for calculating Mg reduction potential values in non-aqueous electrolytes and electrochemical windows. We also describe a strategy for designing Mg electrolytes to maximize the electrochemical windows and oxidative stabilities. These results will be useful not only for designing improved Mg electrolytes, but also for developing new electrolytes in the future.

  13. Improving sulfolane-based electrolyte for high voltage Li-ion cells with electrolyte additives

    NASA Astrophysics Data System (ADS)

    Xia, Jian; Dahn, J. R.

    2016-08-01

    An electrolyte mixture containing 1 M LiPF6 in sulfolane:ethylmethyl carbonate 3:7 with vinylene carbonate and other electrolyte additives exhibited promising cycling and storage performance in high voltage Li(Ni0·4Mn0·4Co0.2)O2/graphite pouch type Li-ion cells tested to 4.5 V. Voltage drop during storage, coulombic efficiency, charge endpoint capacity slippage during ultra high precision cycling, charge-transfer resistance after storage or cycling, gas evolution during storage and cycling as well as capacity retention during long-term cycling were examined. The results for cells with sulfolane-based electrolytes were compared with those for cells with ethylene carbonate-based electrolytes containing state-of-the-art electrolyte additives. This survey showed that the combination of vinylene carbonate and triallyl phosphate as electrolyte additives in sulfolane:ethylmethyl carbonate electrolyte yielded cells capable of better performance during tests to 4.5 V than cells with ethylene carbonate-based electrolytes. These results suggest that sulfolane-based electrolytes may be promising for high voltage Li-ion cells.

  14. Highly Quantitative Electrochemical Characterization of Non-Aqueous Electrolytes & Solid Electrolyte Interphases

    SciTech Connect

    Sergiy V. Sazhin; Kevin L. Gering; Mason K. Harrup; Harry W. Rollins

    2012-10-01

    The methods to measure solid electrolyte interphase (SEI) electrochemical properties and SEI formation capability of non-aqueous electrolyte solutions are not adequately addressed in the literature. And yet, there is a strong demand in new electrolyte generations that promote stabilized SEIs and have an influence to resolve safety, calendar life and other limitations of Li-ion batteries. To fill this gap, in situ electrochemical approach with new descriptive criteria for highly quantitative characterization of SEI and electrolytes is proposed. These criteria are: SEI formation capacity, SEI corrosion rate, SEI maintenance rate, and SEI kinetic stability. These criteria are associated with battery parameters like irreversible capacity, self-discharge, shelf-life, power, etc. Therefore, they are especially useful for electrolyte development and standard fast screening, allowing a skillful approach to narrow down the search for the best electrolyte. The characterization protocol also allows retrieving information on interfacial resistance for SEI layers and the electrochemical window of electrolytes, the other important metrics of characterization. The method validation was done on electrolyte blends containing phosphazenes, developed at Idaho National Laboratory, as 1.2M LiPF6 [80 % EC-MEC (2:8) (v/v) + 20% Phosphazene variety] (v/v), which were targeted for safer electrolyte variations.

  15. Improving sulfolane-based electrolyte for high voltage Li-ion cells with electrolyte additives

    NASA Astrophysics Data System (ADS)

    Xia, Jian; Dahn, J. R.

    2016-08-01

    An electrolyte mixture containing 1 M LiPF6 in sulfolane:ethylmethyl carbonate 3:7 with vinylene carbonate and other electrolyte additives exhibited promising cycling and storage performance in high voltage Li(Ni0·4Mn0·4Co0.2)O2/graphite pouch type Li-ion cells tested to 4.5 V. Voltage drop during storage, coulombic efficiency, charge endpoint capacity slippage during ultra high precision cycling, charge-transfer resistance after storage or cycling, gas evolution during storage and cycling as well as capacity retention during long-term cycling were examined. The results for cells with sulfolane-based electrolytes were compared with those for cells with ethylene carbonate-based electrolytes containing state-of-the-art electrolyte additives. This survey showed that the combination of vinylene carbonate and triallyl phosphate as electrolyte additives in sulfolane:ethylmethyl carbonate electrolyte yielded cells capable of better performance during tests to 4.5 V than cells with ethylene carbonate-based electrolytes. These results suggest that sulfolane-based electrolytes may be promising for high voltage Li-ion cells.

  16. Ionic conduction in polymer composite electrolytes

    NASA Astrophysics Data System (ADS)

    Dam, Tapabrata; Tripathy, Satya N.; Paluch, M.; Jena, S.; Pradhan, D. K.

    2016-05-01

    Conductivity and structural relaxation has been explored from modulus and dielectric loss formalisms respectively for a series of polymer composite electrolytes with zirconia as filler. The temperature dependence of conductivity followed Vogel-Tamman-Fulcher (VTF) behavior, which suggested a close correlation between conductivity and the segmental relaxation process in polymer electrolytes. Vogel temperature (T0) plays significant role in ion conduction process in these kind of materials.

  17. Fuel cell with electrolyte matrix assembly

    DOEpatents

    Kaufman, Arthur; Pudick, Sheldon; Wang, Chiu L.

    1988-01-01

    This invention is directed to a fuel cell employing a substantially immobilized electrolyte imbedded therein and having a laminated matrix assembly disposed between the electrodes of the cell for holding and distributing the electrolyte. The matrix assembly comprises a non-conducting fibrous material such as silicon carbide whiskers having a relatively large void-fraction and a layer of material having a relatively small void-fraction.

  18. Regulation of body fluid volume and electrolyte concentrations in spaceflight

    NASA Technical Reports Server (NTRS)

    Smith, S. M.; Krauhs, J. M.; Leach, C. S.

    1997-01-01

    rhythms. Atrial natriuretic peptide does not seem to play an important role in the control of natriuresis during spaceflight. Inflight activity of the sympathetic nervous system, assessed by measuring catecholamines and their metabolites and precursors in body fluids, generally seems to be no greater than on Earth, but this system is usually activated at landing. Collaborative experiments on the Mir and the International Space Station should provide more of the data needed from long-term flights, and perhaps help to resolve some of the discrepancies between U.S. and Russian data. The use of alternative methods that are easier to execute during spaceflight, such as collection of saliva instead of blood and urine, should permit more thorough study of circadian rhythms and rapid hormone changes in weightlessness. More investigations of dietary intake of fluid and electrolytes must be performed to understand regulatory processes. Additional hormones that may participate in these processes, such as other natriuretic hormones, should be determined during and after spaceflight. Alterations in body fluid volume and blood electrolyte concentrations during spaceflight have important consequences for readaptation to the 1-G environment. The current assessment of fluid and electrolyte status during weightlessness and at landing and our still incomplete understanding of the processes of adaptation to weightlessness and readaptation to Earth's gravity have resulted in the development of countermeasures that are only partly successful in reducing the postflight orthostatic intolerance experienced by astronauts and cosmonauts. More complete knowledge of these processes can be expected to produce countermeasures that are even more successful, as well as expand our comprehension of the range of adaptability of human physiologic processes.

  19. Regulation of body fluid volume and electrolyte concentrations in spaceflight.

    PubMed

    Smith, S M; Krauhs, J M; Leach, C S

    1997-01-01

    rhythms. Atrial natriuretic peptide does not seem to play an important role in the control of natriuresis during spaceflight. Inflight activity of the sympathetic nervous system, assessed by measuring catecholamines and their metabolites and precursors in body fluids, generally seems to be no greater than on Earth, but this system is usually activated at landing. Collaborative experiments on the Mir and the International Space Station should provide more of the data needed from long-term flights, and perhaps help to resolve some of the discrepancies between U.S. and Russian data. The use of alternative methods that are easier to execute during spaceflight, such as collection of saliva instead of blood and urine, should permit more thorough study of circadian rhythms and rapid hormone changes in weightlessness. More investigations of dietary intake of fluid and electrolytes must be performed to understand regulatory processes. Additional hormones that may participate in these processes, such as other natriuretic hormones, should be determined during and after spaceflight. Alterations in body fluid volume and blood electrolyte concentrations during spaceflight have important consequences for readaptation to the 1-G environment. The current assessment of fluid and electrolyte status during weightlessness and at landing and our still incomplete understanding of the processes of adaptation to weightlessness and readaptation to Earth's gravity have resulted in the development of countermeasures that are only partly successful in reducing the postflight orthostatic intolerance experienced by astronauts and cosmonauts. More complete knowledge of these processes can be expected to produce countermeasures that are even more successful, as well as expand our comprehension of the range of adaptability of human physiologic processes. PMID:9048137

  20. [Extreme results in electrolyte determination].

    PubMed

    Vogt, W; Oesterle, B

    1992-01-01

    Besides statistical quality control, quality control based on patient specimens is an important tool for quality enhancement and thus for an increased diagnostic certainty in laboratory medicine. One of three possibilities of plausibility judgement is the control of extreme results, that is alert and absurd value check. The aim of our study was to look for extremely high or low findings of the most frequently examined clinical-chemical parameters, to scrutinize their validity according to clearly defined criteria and to find out the underlying actual clinical situations and diseases. In this publication only the results for the electrolytes are discussed. Retrospectively the most extreme values of all results for serum sodium, potassium and chloride concentrations of a 21-month interval were extracted in a large university hospital. The clinical situation was then evaluated by reading the medical reports of these patients. The validity of the findings was judged by previously defined criteria and rated as confirmed, questionable and not confirmed. In all cases the survival time was determined. The most extreme confirmed results were for sodium 191 and 100 mmol/l, for potassium 9.0 and 1.3 mmol/l and for chloride 138 and 65 mmol/l. All these findings were compatible with life, at least for several hours. Even if it is probably impossible to give generally valid extreme ranges. Nevertheless our results should certainly have practical importance in absurd and alert value check. PMID:1502820

  1. Electrolytic recovery of reactor metal fuel

    DOEpatents

    Miller, W.E.; Tomczuk, Z.

    1994-09-20

    A new electrolytic process and apparatus are provided using sodium, cerium or a similar metal in alloy or within a sodium beta or beta[double prime]-alumina sodium ion conductor to electrolytically displace each of the spent fuel metals except for cesium and strontium on a selective basis from the electrolyte to an inert metal cathode. Each of the metals can be deposited separately. An electrolytic transfer of spent fuel into the electrolyte includes a sodium or cerium salt in the electrolyte with sodium or cerium alloy being deposited on the cathode during the transfer of the metals from the spent fuel. The cathode with the deposit of sodium or cerium alloy is then shunted to an anode and the reverse transfer is carried out on a selective basis with each metal being deposited separately at the cathode. The result is that the sodium or cerium needed for the process is regenerated in the first step and no additional source of these reactants is required. 2 figs.

  2. Electrolytic recovery of reactor metal fuel

    DOEpatents

    Miller, William E.; Tomczuk, Zygmunt

    1994-01-01

    A new electrolytic process and apparatus are provided using sodium, cerium or a similar metal in alloy or within a sodium beta or beta"-alumina sodium ion conductor to electrolytically displace each of the spent fuel metals except for cesium and strontium on a selective basis from the electrolyte to an inert metal cathode. Each of the metals can be deposited separately. An electrolytic transfer of spent fuel into the electrolyte includes a sodium or cerium salt in the electrolyte with sodium or cerium alloy being deposited on the cathode during the transfer of the metals from the spent fuel. The cathode with the deposit of sodium or cerium alloy is then chanted to an anode and the reverse transfer is carried out on a selective basis with each metal being deposited separately at the cathode. The result is that the sodium or cerium needed for the process is regenerated in the first step and no additional source of these reactants is required.

  3. Nonaqueous electrolyte for electrical storage devices

    DOEpatents

    McEwen, Alan B.; Yair, Ein-Eli

    1999-01-01

    Improved nonaqueous electrolytes for application in electrical storage devices such as electrochemical capacitors or batteries are disclosed. The electrolytes of the invention contain salts consisting of alkyl substituted, cyclic delocalized aromatic cations, and their perfluoro derivatives, and certain polyatomic anions having a van der Waals volume less than or equal to 100 .ANG..sup.3, preferably inorganic perfluoride anions and most preferably PF.sub.6.sup.-, the salts being dissolved in organic liquids, and preferably alkyl carbonate solvents, or liquid sulfur dioxide or combinations thereof, at a concentration of greater than 0.5M and preferably greater than 1.0M. Exemplary electrolytes comprise 1-ethyl-3-methylimidazolium hexafluorophosphate dissolved in a cyclic or acylic alkyl carbonate, or methyl formate, or a combination therof. These improved electrolytes have useful characteristics such as higher conductivity, higher concentration, higher energy storage capabilities, and higher power characteristics compared to prior art electrolytes. Stacked capacitor cells using electrolytes of the invention permit high energy, high voltage storage.

  4. Electrolytic recovery of reactor metal fuel

    DOEpatents

    Miller, W.E.; Tomczuk, Z.

    1993-02-03

    This invention is comprised of a new electrolytic process and apparatus using sodium, cerium or a similar metal in an alloy or within a sodium beta or beta-alumina sodium ion conductor to electrolytically displace each of the spent fuel metals except for Cesium and strontium on a selective basis from the electrolyte to an inert metal cathode. Each of the metals can be deposited separately. An electrolytic transfer of spent fuel into the electrolyte includes a sodium or cerium salt in the electrolyte with sodium or cerium alloy being deposited on the cathode during the transfer of the metals from the spent fuel. The cathode with the deposit of sodium or cerium alloy is then changed to an anode and the reverse transfer is carried out on a selective basis with each metal being deposited separately at the cathode. The result is that the sodium or cerium needed for the process is regenerated in the first step and no additional source of these reactants is required.

  5. Safer Electrolytes for Lithium-Ion Cells

    NASA Technical Reports Server (NTRS)

    Kejha, Joe; Smith, Novis; McCloseky, Joel

    2004-01-01

    A number of nonvolatile, low-flammability liquid oligomers and polymers based on aliphatic organic carbonate molecular structures have been found to be suitable to be blended with ethylene carbonate to make electrolytes for lithium-ion electrochemical cells. Heretofore, such electrolytes have often been made by blending ethylene carbonate with volatile, flammable organic carbonates. The present nonvolatile electrolytes have been found to have adequate conductivity (about 2 mS/cm) for lithium ions and to remain liquid at temperatures down to -5 C. At normal charge and discharge rates, lithiumion cells containing these nonvolatile electrolytes but otherwise of standard design have been found to operate at current and energy densities comparable to those of cells now in common use. They do not perform well at high charge and discharge rates -- an effect probably attributable to electrolyte viscosity. Cells containing the nonvolatile electrolytes have also been found to be, variously, nonflammable or at least self-extinguishing. Hence, there appears to be a basis for the development of safer high-performance lithium-ion cells.

  6. Charge regulation at semiconductor-electrolyte interfaces.

    PubMed

    Fleharty, Mark E; van Swol, Frank; Petsev, Dimiter N

    2015-07-01

    The interface between a semiconductor material and an electrolyte solution has interesting and complex electrostatic properties. Its behavior will depend on the density of mobile charge carriers that are present in both phases as well as on the surface chemistry at the interface through local charge regulation. The latter is driven by chemical equilibria involving the immobile surface groups and the potential determining ions in the electrolyte solution. All these lead to an electrostatic potential distribution that propagate such that the electrolyte and the semiconductor are dependent on each other. Hence, any variation in the charge density in one phase will lead to a response in the other. This has significant implications on the physical properties of single semiconductor-electrolyte interfaces and on the electrostatic interactions between semiconductor particles suspended in electrolyte solutions. The present paper expands on our previous publication (Fleharty et al., 2014) and offers new results on the electrostatics of single semiconductor interfaces as well as on the interaction of charged semiconductor colloids suspended in electrolyte solution.

  7. All fluorine-free lithium battery electrolytes

    NASA Astrophysics Data System (ADS)

    Scheers, Johan; Lim, Du-Hyun; Kim, Jae-Kwang; Paillard, Elie; Henderson, Wesley A.; Johansson, Patrik; Ahn, Jou-Hyeon; Jacobsson, Per

    2014-04-01

    Fluorine-free lithium battery electrolytes have been prepared from lithium salts with nitrile based anions, LiB(CN)4 or LiDCTA, dissolved in PEGDME or PC. After soaked into electrospun PAN membranes the resulting electrolytes were tested for physical and electrochemical properties and compared with reference PAN electrolytes containing LiPF6 or LiTFSI. The fluorine-free electrolytes were successfully cycled in Li/LiFePO4 cells at room temperature with up to 98% Coulombic efficiency. Small and qualitatively different effects were observed with the addition of Al2O3 particles to the PAN membranes, which could be of importance for long-term performance. However, for fluorine-free electrolytes to be truly competitive, the relatively low anodic stability and elevated temperature performance must first of all be improved by a change of solvent - or addition of co-solvents. Further work in this direction is encouraged by the strong influence of the solvent (PC or PEGDME) on the properties of the LiDCTA electrolytes demonstrated in this work.

  8. Lithium-Air Batteries with Hybrid Electrolytes.

    PubMed

    He, Ping; Zhang, Tao; Jiang, Jie; Zhou, Haoshen

    2016-04-01

    During the past decade, Li-air batteries with hybrid electrolytes have attracted a great deal of attention because of their exceptionally high capacity. Introducing aqueous solutions and ceramic lithium superionic conductors to Li-air batteries can circumvent some of the drawbacks of conventional Li-O2 batteries such as decomposition of organic electrolytes, corrosion of Li metal from humidity, and insoluble discharge product blocking the air electrode. The performance of this smart design battery depends essentially on the property and structure of the cell components (i.e., hybrid electrolyte, Li anode, and air cathode). In recent years, extensive efforts toward aqueous electrolyte-based Li-air batteries have been dedicated to developing the high catalytic activity of the cathode as well as enhancing the conductivity and stability of the hybrid electrolyte. Herein, the progress of all aspects of Li-air batteries with hybrid electrolytes is reviewed. Moreover, some suggestions and concepts for tailored design that are expected to promote research in this field are provided. PMID:26977713

  9. Polymer electrolytes for lithium-ion batteries.

    PubMed

    Meyer, W H

    1998-04-01

    The motivation for lithium battery development and a discussion of ion conducting polymers as separators begin this review, which includes a short history of polymer electrolyte research, a summary of the major parameters that determine lithium ion transport in polymer matrices, and consequences for solid polymer electrolyte development. Two major strategies for the application of ion conducting polymers as separators in lithium batteries are identified: One is the development of highly conductive materials via the crosslinking of mobile chains to form networks, which are then swollen by lithium salt solutions ("gel electrolytes"). The other is the construction of solid polymer electrolytes (SPEs) with supramolecular architectures, which intrinsically give rise to much enhanced mechanical strength. These materials as yet exhibit relatively common conductivity levels but may be applied as very thin films. Molecular composites based on poly(p-phenylene)- (PPP)-reinforced SPEs are a striking example of this direction. Neither strategy has as yet led to a "breakthrough" with respect to technical application, at least not for electrically powered vehicles. Before being used as separators, the gel electrolytes must be strengthened, while the molecularly reinforced solid polymer electrolytes must demonstrate improved conductivity.

  10. Lithium-Air Batteries with Hybrid Electrolytes.

    PubMed

    He, Ping; Zhang, Tao; Jiang, Jie; Zhou, Haoshen

    2016-04-01

    During the past decade, Li-air batteries with hybrid electrolytes have attracted a great deal of attention because of their exceptionally high capacity. Introducing aqueous solutions and ceramic lithium superionic conductors to Li-air batteries can circumvent some of the drawbacks of conventional Li-O2 batteries such as decomposition of organic electrolytes, corrosion of Li metal from humidity, and insoluble discharge product blocking the air electrode. The performance of this smart design battery depends essentially on the property and structure of the cell components (i.e., hybrid electrolyte, Li anode, and air cathode). In recent years, extensive efforts toward aqueous electrolyte-based Li-air batteries have been dedicated to developing the high catalytic activity of the cathode as well as enhancing the conductivity and stability of the hybrid electrolyte. Herein, the progress of all aspects of Li-air batteries with hybrid electrolytes is reviewed. Moreover, some suggestions and concepts for tailored design that are expected to promote research in this field are provided.

  11. Self-doped microphase separated block copolymer electrolyte

    DOEpatents

    Mayes, Anne M.; Sadoway, Donald R.; Banerjee, Pallab; Soo, Philip; Huang, Biying

    2002-01-01

    A polymer electrolyte includes a self-doped microphase separated block copolymer including at least one ionically conductive block and at least one second block that is immiscible in the ionically conductive block, an anion immobilized on the polymer electrolyte and a cationic species. The ionically conductive block provides a continuous ionically conductive pathway through the electrolyte. The electrolyte may be used as an electrolyte in an electrochemical cell.

  12. Polymer Electrolytes:. Problems, Prospects, and Promises

    NASA Astrophysics Data System (ADS)

    Nagasubramanian, G.; Doughty, D. H.

    2002-12-01

    In 1975 P. V. Wright observed ionic conduction at elevated temperatures in polyethylene oxide (PEO) thin film electrolyte containing sodium salt. This seminal research generated wide spread interest in all-solid-state rechargeable lithium batteries. Armand took the cue from this observation and demonstrated the use of PEO/salt complex as electrolyte in lithium batteries. Soon after this a number of researchers have followed suit and studied the physical, electrical and transport properties of thin film PEO electrolyte. These studies have clearly identified the limitations of the PEO electrolyte. Chief among the limitations are a low cation transport number (t+), high glass transition temperature (Tg), and segmental motion of the polymer chain, which carries the cation through the bulk electrolyte. While low t+ leads to cell polarization and increase in cell resistance high Tg reduces conductivity at and around room temperature. For example, the conductivity of PEO electrolyte containing lithium salt is ~10-8 S/cm at room temperature. Attempts have been made to reduce Tg of PEO polymer by attaching PEO macromolecules to polyphosphazene (N=P) inorganic backbone, which is very flexible. Another material that has been investigated as a backbone material consists of Si-O chain. These two polymers exhibit a lower Tg and higher room temperature conductivity than the unmodified PEO. For example, the room temperature conductivity of the two polymers is around 10-5 S/cm - a 3 orders of magnitude increase in conductivity compared to unmodified PEO at around room temperature. Although this approach has yielded polymers with lower Tg, the t+ is still very low - ~0.25 - for lithium ion. Nano-ceramic particles of Al2O3, TiO2 etc. mechanically mixed with PEO electrolyte seem to increase t+. This approach also has inherent limitations regarding phase separation. The latest approach appears to involve integrating nano domains of inorganic moieties such as Si-O as part of the polymer

  13. The Role of Polymer Electrolytes in Drug Delivery

    NASA Astrophysics Data System (ADS)

    Latham, R. J.; Linford, R. G.; Schlindwein, W. S.

    2002-12-01

    30 years ago Michel Armand, who was working on intercalation cathode materials in high energy power sources, identified the need to develop flexible, ionically conducting, electronically insulating electrolyte materials to accommodate the gross dimensional changes that occur on charge and discharge. In 1973, Peter Wright produced the first such materials designed for this purpose. His "polymer electrolytes" consisted of thin films of sodium or potassium salts dissolved in poly (ethylene oxide) PEO. Many polymer electrolytes had been developed in the ensuing years. Those for power source use have focussed on Lithium as the conducting species whereas complementary materials have been utilised for sensor and other applications. It is well known that the flexible matrix, a heteropolymer usually modified by additives such as plasticisers and/or inert fillers, provides a facile conducting pathway for ions. It is a significant disadvantage of many early polymer electrolytes that both the electrochemically active cations and the charge-compensating anions were mobile. Classic methods of drug delivery have embraced a number of routes into the site of pharmacological action, including ingestion into the lung, the digestive tract or the colon; injection into muscle tissue; and intravenous delivery through a catheter (a "drip"). Modern preference, wherever possible, is for a non-invasive route to minimise the chance of cross infection, especially of the AIDS virus. The skin, which is the largest organ in the human body, is a particularly appealing route as, in the absence of wounds and blemishes, it offers a natural, high-integrity, barrier to the outside world. Skin patches containing active drug that is allowed to diffuse across the external skin barrier into the bloodstream now enjoy wide application but a problem is that the rate of egress is often slow. Transport can be enhanced by artificially dilating the skin pores and/or by opening up additional pores by the

  14. Electrochemical power-producing cell. [Li/Se

    DOEpatents

    Cairns, E.J.; Chilenskas, A.A.; Steunenberg, R.K.; Shimotake, H.

    1972-05-30

    An electrochemical power-producing cell including a molten lithium metal anode, a molten selenium metal cathode, a paste electrolyte separating the anode from the cathode, an anode current collector, and a single layer of niobium expanded metal formed in corrugated shape as cathode current collector is described. In addition, means are provided for sealing the anode and the cathode from loss of lithium and selenium, respectively, and an insulator is provided between the anode housing and the paste electrolyte disk.

  15. 66 FR 1950 - Electrolytic Manganese Dioxide From Greece: Preliminary Results of Antidumping Duty...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2001-01-10

    ... Register (54 FR 15243) the antidumping duty order on electrolytic manganese dioxide (EMD) from Greece. On... (65 FR 19736). Tosoh Hellas A.I.C. (Tosoh), a Greek producer, requested a review on April 27, 2000. In... 2, 2000, in accordance with 19 CFR 351.213(b) (65 FR 35320. The Department is conducting...

  16. Reduced temperature aluminum production in an electrolytic cell having an inert anode

    SciTech Connect

    Dawless, R.K.; Ray, S.P.; Hosler, R.B.; Kozarek, R.L.; LaCamera, A.F.

    2000-02-29

    Aluminum is produced by electrolytic reduction of alumina in a cell having a cathode, an inert anode and a molten salt bath containing metal fluorides and alumina. The inert anode preferably contains copper, silver and oxides of iron and nickel. Reducing the molten salt bath temperature to about 900--950 C lowers corrosion on the inert anode constituents.

  17. Reduced temperature aluminum production in an electrolytic cell having an inert anode

    SciTech Connect

    Dawless, Robert K.; Ray, Siba P.; Hosler, Robert B.; Kozarek, Robert L.; LaCamera, Alfred F.

    2000-01-01

    Aluminum is produced by electrolytic reduction of alumina in a cell having a cathode, an inert anode and a molten salt bath containing metal fluorides and alumina. The inert anode preferably contains copper, silver and oxides of iron and nickel. Reducing the molten salt bath temperature to about 900-950.degree. C. lowers corrosion on the inert anode constituents.

  18. 78 FR 54269 - Electrolytic Manganese Dioxide From Australia and China; Institution of Five-Year Reviews

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-09-03

    ... electrolytic manganese dioxide from Australia and China (73 FR 58537-58539). The Commission is conducting...) (19 CFR 201.15(b)), 73 FR 24609 (May 5, 2008). This advice was developed in consultation with the.... producers of the Domestic Like Product. Identify any known related parties and the nature of...

  19. Theoretical analysis of solid oxide fuel cells with two-layer, composite electrolytes - Electrolyte stability

    NASA Astrophysics Data System (ADS)

    Virkar, Anil V.

    1991-05-01

    Theoretical analysis of solid oxide fuel cells (SOFCs) using two-layer, composite electrolytes consisting of a solid electrolyte of a significantly higher conductivity compared to zirconia (such as ceria or bismuth oxide) with a thin layer of zirconia or thoria on the fuel side is presented. Electrochemical transport in the two-layer composite electrolytes is examined by taking both ionic and electronic fluxes into account. Similar to most electrochemical transport phenomena, it is assumed that local equilibrium prevails. An equivalent circuit approach is used to estimate the partial pressure of oxygen at the interface. It is shown that thermodynamic stability of the electrolyte (ceria or bismuth oxide) depends upon the transport characteristics of the composite electrolyte, in particular the electronic conductivity of the air-side part of the electrolyte. The analysis shows that it would be advantageous to use composite electrolytes instead of all-zirconia electrolytes, thus making low-temperature (about 600-800 C) SOFCs feasible. Implications of the analysis from the standpoint of the desired characteristics of SOFC components are discussed.

  20. Inorganic-organic composite solid polymer electrolytes

    SciTech Connect

    Abraham, K.M.; Koch, V.R.; Blakley, T.J.

    2000-04-01

    Inorganic-organic composite solid polymer electrolytes (CSPEs) have been prepared from the poly(ethylene oxide) (PEO)-like electrolytes of the general formula polyvinylidene fluoride-hexafluoropropylene (PVdF-HFP)-PEO{sub n}-LiX and Li{sup +}-conducting ceramic powders. In the PEO-like electrolytes, PVdF-HFP is the copolymer of PVdF and HFP, PEO{sub n} is a nonvolatile oligomeric polyethylene oxide of {approximately}400 g/mol molecular weight, and LiX is lithium bis(trifluoroethylsulfonyl)imide. Two types of inorganic oxide ceramic powders were used: a highly Li{sup +}-conducting material of the composition 14 mol % Li{sub 2}O-9Al{sub 2}O{sub 3}-38TiO{sub 2}-39P{sub 2}O{sub 5}, and the poorly Li{sup +}-conducting Li-silicates Li{sub 4{minus}x}M{sub x}SiO{sub 4} where M is Ca or Mg and x is 0 or 0.05. The composite electrolytes can be prepared as thin membranes in which the Li{sup +} conductivity and good mechanical strength of the Li{sup +}-conducting inorganic ceramics are complemented by the structural flexibility and high conductivity of organic polymer electrolytes. Excellent electrochemical and thermal stabilities have been demonstrated for the electrolyte films. Li//composite electrolyte//LiCoO{sub 2} rechargeable cells have been fabricated and cycled at room temperature and 50 C.

  1. Direct electrowinning of lead from suspension galena concentrate anode in different electrolytes

    NASA Astrophysics Data System (ADS)

    Paramguru, R. K.; Küzeci, E.; Kammel, R.

    1988-02-01

    Electrochemical extraction of lead from galena by suspension electrolysis has been examined. Galvanostatic studies with slurry electrode as well as voltametric studies with carbon paste electrode in various electrolytes have been made in order to evaluate bath performance. Sodium hydroxide has been found to result in poor dissolution whereas ionic conduction through the electrolyte as well as oxide formation at the anode hinders lead dissolution in perchlorate media. Acetate bath results in substantial amount of oxide formation at anode even though solid bed conduction dominates. Sodium chloride bath has been found to have good prospects for producing lead ions and elemental sulfur with good current efficiencies.

  2. [Synthesis and Characterization of a Sugar Based Electrolyte for Thin-film Polymer Batteries

    NASA Technical Reports Server (NTRS)

    1998-01-01

    The work performed during the current renewal period, March 1,1998 focused primarily on the synthesis and characterization of a sugar based electrolyte for thin-film polymer batteries. The initial phase of the project involved developing a suitable sugar to use as the monomer in the polymeric electrolyte synthesis. The monomer has been synthesized and characterized completely. Overall the yield of this material is high and it can be produced in relatively large quantity easily and in high purity. The scheme used for the preparation of the monomer is outlined along with pertinent yields.

  3. Highly conductive electrolyte composites containing glass and ceramic, and method of manufacture

    DOEpatents

    Hash, M.C.; Bloom, I.D.

    1992-10-13

    An electrolyte composite is manufactured by pressurizing a mixture of sodium ion conductive glass and an ionically conductive compound at between 12,000 and 24,000 pounds per square inch to produce a pellet. The resulting pellet is then sintered at relatively lower temperatures (800--1200 C), for example 1000 C, than are typically required (1400 C) when fabricating single constituent ceramic electrolytes. The resultant composite is 100 percent conductive at 250 C with conductivity values of 2.5 to 4[times]10[sup [minus]2](ohm-cm)[sup [minus]1]. The matrix exhibits chemical stability against sodium for 100 hours at 250 to 300 C. 1 figure.

  4. Novel Nonflammable Electrolytes for Secondary Magnesium Batteries and High Voltage Electrolytes for Electrochemcial Supercapacitors

    SciTech Connect

    Dixon, Brian

    2008-12-30

    Magnesium has been used successfully in primary batteries, but its use in rechargeable cells has been stymied by the lack of suitable non-aqueous electrolyte that can conduct Mg+2 species, combined with poor stripping and plating properties. The development of a suitable cathode material for rechargeable magnesium batteries has also been a roadblock, but a nonflammable electrolyte is key. Likewise, the development of safe high voltage electrochemical supercapaitors has been stymied by the use of flammable solvents in the liquid electrolyte; to wit, acetonitrile. The purpose of the research conducted in this effort was to identify useful compositions of magnesium salts and polyphosphate solvents that would enable magnesium ions to be cycled within a secondary battery design. The polyphosphate solvents would provide the solvent for the magnesium salts while preventing the electrolyte from being flammable. This would enable these novel electrolytes to be considered as an alternative to THF-based electrolytes. In addition, we explored several of these solvents together with lithium slats for use as high voltage electrolytes for carbon-based electrochemical supercapacitors. The research was successful in that: 1) Magnesium imide dissolved in a phosphate ester solvent that contains a halogented phosphate ester appears to be the preferred electrolyte for a rechargeable Mg cell. 2) A combination of B-doped CNTs and vanadium phosphate appear to be the cathode of choice for a rechargeable Mg cell by virtue of higher voltage and better reversibility. 3) Magnesium alloys appear to perform better than pure magnesium when used in combination with the novel polyphosphate electrolytes. Also, this effort has established that Phoenix Innovation's family of phosphonate/phosphate electrolytes together with specific lithium slats can be used in supercapacitor systems at voltages of greater than 10V.

  5. Acute Symptomatic Seizures Caused by Electrolyte Disturbances

    PubMed Central

    Nardone, Raffaele; Brigo, Francesco

    2016-01-01

    In this narrative review we focus on acute symptomatic seizures occurring in subjects with electrolyte disturbances. Quite surprisingly, despite its clinical relevance, this issue has received very little attention in the scientific literature. Electrolyte abnormalities are commonly encountered in clinical daily practice, and their diagnosis relies on routine laboratory findings. Acute and severe electrolyte imbalances can manifest with seizures, which may be the sole presenting symptom. Seizures are more frequently observed in patients with sodium disorders (especially hyponatremia), hypocalcemia, and hypomagnesemia. They do not entail a diagnosis of epilepsy, but are classified as acute symptomatic seizures. EEG has little specificity in differentiating between various electrolyte disturbances. The prominent EEG feature is slowing of the normal background activity, although other EEG findings, including various epileptiform abnormalities may occur. An accurate and prompt diagnosis should be established for a successful management of seizures, as rapid identification and correction of the underlying electrolyte disturbance (rather than an antiepileptic treatment) are of crucial importance in the control of seizures and prevention of permanent brain damage. PMID:26754778

  6. The buffer effect in neutral electrolyte supercapacitors

    NASA Astrophysics Data System (ADS)

    Vindt, Steffen T.; Skou, Eivind M.

    2016-02-01

    The observation that double-layer capacitors based on neutral aqueous electrolytes can have significantly wider usable potential windows than those based on acidic or alkaline electrolytes is studied. This effect is explained by a local pH change taking place at the electrode surfaces, leading to a change in the redox potential of water in opposite directions on the two electrodes, resulting in the wider stability window. The magnitude of this effect is suggested to be dependent on the buffer capacity, rather than the intrinsic pH value of the electrolyte. This is confirmed by studying the impact of addition of a buffer to such systems. It is shown that a 56 % higher dynamic storage capacity may be achieved, simply by controlling the buffer capacity of the electrolyte. The model system used, is based on a well-known commercial activated carbon (NORIT™ A SUPRA) as the electrode material, aqueous potassium nitrate as the electrolyte and potassium phosphates as the buffer system.

  7. Acute Symptomatic Seizures Caused by Electrolyte Disturbances.

    PubMed

    Nardone, Raffaele; Brigo, Francesco; Trinka, Eugen

    2016-01-01

    In this narrative review we focus on acute symptomatic seizures occurring in subjects with electrolyte disturbances. Quite surprisingly, despite its clinical relevance, this issue has received very little attention in the scientific literature. Electrolyte abnormalities are commonly encountered in clinical daily practice, and their diagnosis relies on routine laboratory findings. Acute and severe electrolyte imbalances can manifest with seizures, which may be the sole presenting symptom. Seizures are more frequently observed in patients with sodium disorders (especially hyponatremia), hypocalcemia, and hypomagnesemia. They do not entail a diagnosis of epilepsy, but are classified as acute symptomatic seizures. EEG has little specificity in differentiating between various electrolyte disturbances. The prominent EEG feature is slowing of the normal background activity, although other EEG findings, including various epileptiform abnormalities may occur. An accurate and prompt diagnosis should be established for a successful management of seizures, as rapid identification and correction of the underlying electrolyte disturbance (rather than an antiepileptic treatment) are of crucial importance in the control of seizures and prevention of permanent brain damage. PMID:26754778

  8. Combination for electrolytic reduction of alumina

    DOEpatents

    Brown, Craig W.; Brooks, Richard J.; Frizzle, Patrick B.; Juric, Drago D.

    2002-04-30

    An electrolytic bath for use during the electrolytic reduction of alumina to aluminum. The bath comprises molten electrolyte having the following ingredients: AlF.sub.3 and at least one salt selected from the group consisting of NaF, KF, and LiF; and about 0.004 wt. % to about 0.2 wt. %, based on total weight of the molten electrolyte, of at least one transition metal or at least one compound of the metal or both. The compound is, a fluoride; oxide, or carbonate. The metal is nickel, iron, copper, cobalt, or molybdenum. The bath is employed in a combination including a vessel for containing the bath and at least one non-consumable anode and at least one dimensionally stable cathode in the bath. Employing the instant bath during electrolytic reduction of alumina to aluminum improves the wetting of aluminum on a cathode by reducing or eliminating the formation of non-metallic deposits on the cathode.

  9. Theoretical and experimental study of mixed solvent electrolytes. Final report

    SciTech Connect

    P.T. Cummings; J.P. O'Connell

    1995-01-31

    The goals of the research program evolved into six areas: Molecular simulation of phase equilibria in aqueous and mixed solvent electrolyte solutions. Molecular simulation of solvation and structure in supercritical aqueous systems. Extension of experimental database on mixed solvent electrolytes. Analysis of the thermodynamic properties of mixed solvent electrolyte solutions and mixed electrolyte solutions using fluctuation solution theory. Development of analytic expressions for thermodynamic properties of mixed solvent electrolyte solutions using analytically solved integral equation approximations. Fundamental modeling of mixed solvent electrolytes using numerically solved integral equation approximation theories.

  10. Effects of adding ethanol to KOH electrolyte on electrochemical performance of titanium carbide-derived carbon

    NASA Astrophysics Data System (ADS)

    Xu, Jiang; Zhang, Ruijun; Chen, Peng; Ge, Shanhai

    2014-01-01

    Porous carbide-derived carbons (CDCs) are synthesized from TiC at different chlorination temperatures as electrode materials for electrochemical capacitors. It is found that the microstructure of the produced CDCs has significant influence on both the hydrophilicity in aqueous KOH electrolyte and the resultant electrochemical performance. Because the TiC-CDC synthesized at higher temperature (e.g. 1000 °C) contains well-ordered graphite ribbons, it shows lower hydrophilicity and specific capacitance. It is also found that addition of a small amount of ethanol to KOH electrolyte effectively improves the wettability of the CDCs synthesized at higher temperature and the corresponding specific capacitance. Compared with the CDC synthesized at 600 °C, the CDC synthesized at 1000 °C shows fast ion transport and excellent capacitive behavior in KOH electrolyte with addition of ethanol because of the existences of mesopores and high specific surface area.

  11. Electrokinetic behavior of melamine-formaldehyde latex particles at moderate electrolyte concentration.

    PubMed

    Dahlsten, Per; Próchniak, Piotr; Kosmulski, Marek; Rosenholm, Jarl B

    2009-11-15

    The electrokinetic behavior of micrometer-sized melamine-formaldehyde latex particles in 10(-3)-10(-1)M monovalent electrolyte dispersions was investigated by electrophoresis and electroacoustics. Specific adsorption of the electrolytes was identified as a shift of the isoelectric point (pH(iep)) with an increased ionic strength. All salts had an equal dependence on the ionic strength. The pH(iep) was correlated with the anion sequence predicted by the hard-soft acid-base (HSAB) principle, Hofmeister series, and Born charging. The Born and the Hofmeister anion scale were successful in producing a systematic dependency of the isoelectric point (pH(iep)), particularly in high (10(-1)M) and low (10(-3)M) MF electrolyte dispersions. No clear trend could be found for the pH(iep) dependence on the anion HSAB scale.

  12. Basic investigation into the production of oxygen in a solid electrolyte process

    NASA Technical Reports Server (NTRS)

    Richter, R.

    1981-01-01

    Mission analyses indicated that by extracting oxygen from the Martian atmosphere, which consists primarily of carbon dioxide, the launch mass of a spacecraft can be reduced by such an amount that samples from the planet can be returned to earth. The solid electrolyte process for producing O2 from CO2 was investigated. A model of the thermodynamic and electrochemical processes in the electrolyte cell was postulated, thereby establishing the parameters influencing the effectiveness and efficiency of an in situ O2 production system. The major operating parameters were investigated over a wide range of temperature and pressure. Operating limits imposed by the solid electrolyte material, 8% yttria stabilized zirconia, were determined as a function of the operating temperature.

  13. Combination of an electrolytic pretreatment unit with secondary water reclamation processes

    NASA Technical Reports Server (NTRS)

    Wells, G. W.; Bonura, M. S.

    1973-01-01

    The design and fabrication of a flight concept prototype electrolytic pretreatment unit (EPU) and of a contractor-furnished air evaporation unit (AEU) are described. The integrated EPU and AEU potable water recovery system is referred to as the Electrovap and is capable of processing the urine and flush water of a six-man crew. Results of a five-day performance verification test of the Electrovap system are presented and plans are included for the extended testing of the Electrovap to produce data applicable to the combination of electrolytic pretreatment with most final potable water recovery systems. Plans are also presented for a program to define the design requirements for combining the electrolytic pretreatment unit with a reverse osmosis final processing unit.

  14. Modeling mechanical degradation in lithium ion batteries during cycling: Solid electrolyte interphase fracture

    NASA Astrophysics Data System (ADS)

    Laresgoiti, Izaro; Käbitz, Stefan; Ecker, Madeleine; Sauer, Dirk Uwe

    2015-12-01

    During cycling, mechanical stresses can occur in the composite electrode, inside the active material, but also in the solid electrolyte interphase layer. A mechanical model is proposed based on a system made of a spherical graphite particle surrounded by the solid electrolyte interphase layer. During lithium intercalation or de-intercalation, stresses in the graphite are produced, governed by the diffusion induced stress phenomena and in the solid electrolyte interphase, driven by the graphite expansion. The stresses in both materials were simulated and a sensitivity analysis was performed to clarify the influence of principal parameters on both processes. Finally, assuming that the solid electrolyte interphase is the weakest material and therefore more prone to fracture than graphite, the experimental capacity fade during cycling was modeled based on its break and repair effect rather than on the fracture of the active material. The mechanical model of the solid electrolyte interphase was implemented in a single particle lithium ion battery model in order to reproduce capacity fade during battery lifetime. The model results were compared against cycle life aging experimental data, reproducing accurately the influence of the depth of discharge as well as the average state of charge on the capacity fade.

  15. Investigations of sound waves generated by the Hall effect in electrolytes.

    PubMed

    Campanella, Angelo J

    2002-05-01

    Electrolyte ions moving in a magnetic field produce a velocity component transverse to the electric and magnetic fields. This phenomenon can be alternatively termed as the Hall effect, a magnetohydrodynamic transducer, or a liquid-state electromagnetic transducer. In electrolytes, the viscous drag of the electrolyte fluid is dominant, so the ion deflection soon reaches a terminal velocity dependent only on the electric field strength. The alternating velocity component transverse to the electric and magnetic fields produces a pressure wave due to the viscous drag of the fluid on the ions. Acoustic waves of very high frequencies can be produced since the mass of an ion is very small. Theory for this method of generating sound waves by ultrahigh frequency (UHF) electromagnetic wave impinging on a conducting medium in a magnetic field, causing a conduction current to flow near the surface (skin effect), is presented. Experiments were performed in an electrolyte at frequencies from 8 kHz to 1 MHz to study the effects of electrode size, ionic mobility, and ionic concentration. In the reciprocal effect, ions moving en masse with the particle velocity of a passing acoustic wave induce an alternating voltage between a pair of electrodes in a transverse magnetic field.

  16. Communication: Nanoscale ion fluctuations in Nafion polymer electrolyte

    SciTech Connect

    Rumberger, Brant; Bennett, Mackenzie; Zhang, Jingyun; Israeloff, N. E.; Dura, J. A.

    2014-08-21

    Ion conduction mechanisms and the nanostructure of ion conduction networks remain poorly understood in polymer electrolytes which are used as proton-exchange-membranes (PEM) in fuel cell applications. Here we study nanoscale surface-potential fluctuations produced by Brownian ion dynamics in thin films of low-hydration Nafion™, the prototype PEM. Images and power spectra of the fluctuations are used to derive the local conductivity-relaxation spectrum, in order to compare with bulk behavior and hopping-conductivity models. Conductivity relaxation-times ranged from hours to milliseconds, depending on hydration and temperature, demonstrating that the observed fluctuations are produced by water-facilitated hydrogen-ion hopping within the ion-channel network. Due to the small number of ions probed, non-Gaussian statistics of the fluctuations can be used to constrain ion conduction parameters and mechanisms.

  17. Hydroxyl radical production in plasma electrolysis with KOH electrolyte solution

    NASA Astrophysics Data System (ADS)

    Saksono, Nelson; Febiyanti, Irine Ayu; Utami, Nissa; Ibrahim

    2015-12-01

    Plasma electrolysis is an effective technology for producing hydroxyl radical (•OH). This method can be used for waste degradation process. This study was conducted to obtain the influence of applied voltage, electrolyte concentration, and anode depth in the plasma electrolysis system for producing hydroxyl radical. The materials of anode and cathode, respectively, were made from tungsten and stainless steel. KOH solution was used as the solution. Determination of hydroxyl radical production was done by measuring H2O2 amount formed in plasma system using an iodometric titration method, while the electrical energy consumed was obtained by measuring the electrical current throughout the process. The highest hydroxyl radical production was 3.51 mmol reached with 237 kJ energy consumption in the power supply voltage 600 V, 0.02 M KOH, and 0.5 cm depth of anode.

  18. Hydroxyl radical production in plasma electrolysis with KOH electrolyte solution

    SciTech Connect

    Saksono, Nelson; Febiyanti, Irine Ayu Utami, Nissa; Ibrahim

    2015-12-29

    Plasma electrolysis is an effective technology for producing hydroxyl radical (•OH). This method can be used for waste degradation process. This study was conducted to obtain the influence of applied voltage, electrolyte concentration, and anode depth in the plasma electrolysis system for producing hydroxyl radical. The materials of anode and cathode, respectively, were made from tungsten and stainless steel. KOH solution was used as the solution. Determination of hydroxyl radical production was done by measuring H{sub 2}O{sub 2} amount formed in plasma system using an iodometric titration method, while the electrical energy consumed was obtained by measuring the electrical current throughout the process. The highest hydroxyl radical production was 3.51 mmol reached with 237 kJ energy consumption in the power supply voltage 600 V, 0.02 M KOH, and 0.5 cm depth of anode.

  19. Composite Solid Electrolyte Containing Li+- Conducting Fibers

    NASA Technical Reports Server (NTRS)

    Appleby, A. John; Wang, Chunsheng; Zhang, Xiangwu

    2006-01-01

    Improved composite solid polymer electrolytes (CSPEs) are being developed for use in lithium-ion power cells. The matrix components of these composites, like those of some prior CSPEs, are high-molecular-weight dielectric polymers [generally based on polyethylene oxide (PEO)]. The filler components of these composites are continuous, highly-Li(+)-conductive, inorganic fibers. PEO-based polymers alone would be suitable for use as solid electrolytes, were it not for the fact that their room-temperature Li(+)-ion conductivities lie in the range between 10(exp -6) and 10(exp -8) S/cm, too low for practical applications. In a prior approach to formulating a CSPE, one utilizes nonconductive nanoscale inorganic filler particles to increase the interfacial stability of the conductive phase. The filler particles also trap some electrolyte impurities. The achievable increase in conductivity is limited by the nonconductive nature of the filler particles.

  20. Alkylated imidazolium salt electrolyte for lithium cells

    NASA Astrophysics Data System (ADS)

    Hayashi, Katsuya; Nemoto, Yasue; Akuto, Keiji; Sakurai, Yoji

    The use of a nonflammable electrolyte in a lithium secondary battery will greatly improve battery safety. Therefore, we focused on the nonflammability of ionic liquids and investigated these liquids as possible electrolyte solvents. In this study, we synthesized 1,2-diethyl-3,4(5)-dimethyl imidazolium (DEDMI) cations with imido anions. DEDMI cations with bis(trifluoromethylsulfonyl)imido anions (DEDMI-TFSI) showed a lower solidification point of -35 °C, and higher specific conductivity than DEDMI cations with BF4 -. We prepared an electrolyte consisting of DEDMI-TFSI with LiTFSI, and applied it to a Li/LiCoO 2 cell. The cell was capable of charge-discharge cycling with LiCoO 2 cathode material showing a specific capacity of about 100 mAh g-1.

  1. High-Energy-Density Electrolytic Capacitors

    NASA Technical Reports Server (NTRS)

    Yen, Shiao-Ping S.; Lewis, Carol R.

    1993-01-01

    Reductions in weight and volume make new application possible. Supercapacitors and improved ultracapacitors advanced electrolytic capacitors developed for use as electric-load-leveling devices in such applications as electric vehicle propulsion systems, portable power tools, and low-voltage pulsed power supplies. One primary advantage: offer power densities much higher than storage batteries. Capacitors used in pulse mode, with short charge and discharge times. Derived from commercially available ultracapacitors. Made of lightweight materials; incorporate electrode/electrolyte material systems capable of operation at voltages higher than previous electrode/electrolyte systems. By use of innovative designs and manufacturing processes, made in wide range of rated capacitances and in rated operating potentials ranging from few to several hundred volts.

  2. Secondary calcium solid electrolyte high temperature battery

    NASA Astrophysics Data System (ADS)

    Sammells, A. F.; Schumacher, B.

    1986-01-01

    The application of polycrystalline Ca(2+) conducting beta-double prime alumina solid electrolytes to a new type of high temperature battery is investigated, experimentally. The negative electrode in the battery consisted of a calcium-silicon alloy whose redox electrochemistry was mediated by the solid electrolyte via molten salt eutectic CaCl2 (51.4 m/o), and CaI2 (mp 550 C). The molten salt and the calcium alloy material were separated from the positive active material via the Ca2 Ca(2+) conducting polycrystalline electrolyte. The positive electrode consisted of a solid-state matrix having related crystallographic structure. The electrochemical reversibility of the cells was measured at 580 C. The charge-discharge characteristics of the cells are plotted vs. time in a graph.

  3. Polyethylene imine-metal salt solid electrolyte

    NASA Astrophysics Data System (ADS)

    Davis, G. T.; Chiang, C. K.; Takahashi, T.

    1985-02-01

    This research pertains to the development of new solid battery electrolytes. An object of this invention is to provide polymeric electrolytes using a wider variety of metal salts. These and other objects of this invention are accomplished by providing: (1) a solid polymer electrolyte comprising: a matrix of linear poly(ethylene amine) having the formula (-CH2CH2NH-)n; and (2) a metal salt which is LiI, LiClO4, NaI, NaBr, KI, CsSCN, AgNO3, CuCl1, CoCl2, or Mg(ClO4)2, wherein the salt is dissolved in and distributed throughout the poly(ethylene amine) matrix and from more than zero to 0.10 moles of salt are used per mole of monomer repeat unit, (-CH2CH2NH-).

  4. Barrier anodic coatings formed on 6061-T6 aluminum alloy in electrolytes containing different ethanol to water ratios

    SciTech Connect

    Panitz, J.K.G.; Sharp, D.J.; Martinez, F.E.; Merrill, R.M.; Ward, K.J.

    1988-12-01

    We have studied barrier anodic film formation on 6061-T6 aluminum alloy substrates as a function of electrolyte composition for five mixtures of ammonium tartrate dissolved in water and diluted with different amounts of ethanol. The effects of electrolyte temperatures within the range of 18/degree/C to 38/degree/C were explored. The results of this study indicate that the best dielectric coatings and the shortest processing times occur for the 100% water-ammonium tartrate electrolyte. The second best coatings and processing times occur in conjunction with the use of 98% ethanol, 2% water plus ammonium tartrate electrolyte. In general, visibly flawed coatings, scintillation events at cell voltages in excess of approximately 750-800 volts and/or abnormally long processing times occur in conjunction with the use of electrolyte mixtures containing 20%, 60%, and 90% water. We analysed samples of electrolyte as a function of usage, and evaluated the composition of the coatings using Fourier Transform Infrared Analysis to better understand the mechanisms which contribute to anodic coating growth that result in the observed variations in the dielectric properties. All of the coatings exhibited similar compositions except with regard to the amount of CO2 that was physisorbed in the coatings. The dielectrically inferior coatings that were typically produced by the electrolytes containing ethanol contain substantially more CO2 than the coatings grown in the 100% water-based electrolyte. These results strongly suggest that the ethanol in the electrolyte oxidizes and forms CO2 which is incorporated in the coatings and results in inferior dielectric properties. 8 refs., 7 figs.

  5. Quasi-solid electrolyte with polyamidoamine dendron modified-talc applied to dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Andrade, Marcos A. S.; Nogueira, Ana F.; Miettunen, Kati; Tiihonen, Armi; Lund, Peter D.; Pastore, Heloise O.

    2016-09-01

    A sequence of generations of polyamidoamine dendron modified-talc, PAMAM-talc-Gn (n = 1, 3, 5 and 7), is proposed as additive in a composite gel electrolyte for dye-sensitized solar cells. Polyiodides are intercalated into the organotalc interlamellar space by adsorption of iodine vapor, producing triiodide and polyiodides. We investigate the effect of organotalc content on the charge transport in the electrolyte and solar cell performance and optimize the organotalc content. Without the previous adsorption of iodine molecules, the organotalcs appear to remove iodine from the electrolyte solution decreasing device's performance significantly. Instead, the samples with additional iodide had higher Jsc and efficiency approaching the values of the reference cells containing liquid, which suggests that this kind of gelling method would be suitable for dye solar cells. Charge transport in the gel electrolyte is investigated with electrochemical impedance spectroscopy and cyclic voltammetry analyses using symmetrical CE-CE electrochemical cells.

  6. Theory of electrohydrodynamic instabilities in electrolytic cells

    NASA Technical Reports Server (NTRS)

    Bruinsma, R.; Alexander, S.

    1990-01-01

    The paper develops the theory of the hydrodynamic stability of an electrolytic cell as a function of the imposed electric current. A new electrohydrodynamic instability is encountered when the current is forced to exceed the Nernst limit. The convection is driven by the volume force exerted by the electric field on space charges in the electrolyte. This intrinsic instability is found to be easily masked by extrinsic convection sources such as gravity or stirring. A linear stability analysis is performed and a dimensionless number Le is derived whose value determines the convection pattern.

  7. Solid electrolytes strengthened by metal dispersions

    DOEpatents

    Lauf, Robert J.; Morgan, Chester S.

    1983-01-01

    An improvement in solid electrolytes of advanced secondary batteries of the sodium-sulfur, sodium-halogen, and like combinations is achieved by providing said battery with a cermet electrolyte containing a metal dispersion ranging from 0.1 to 10.0 vol. % of a substantially nonreactive metal selected from the group consisting essentially of Pt, Cr, Fe, Co, Ni, Nb, their alloys, and their physical mixtures in the elemental or uncombined state, the remainder of said cermet being an ion-conductive ceramic material.

  8. Solid electrolytes strengthened by metal dispersions

    DOEpatents

    Lauf, R.J.; Morgan, C.S.

    1981-10-05

    An improvement in solid electrolytes of advanced secondary batteries of the sodium-sulfur, sodium-halogen, and like combinations is achieved by providing said battery with a cermet electrolyte containing a metal dispersion ranging from 0.1 to 10.0 vol. % of a substantially nonreactive metal selected from the group consisting essentially of Pt, Cr, Fe, Co, Ni, Nb, their alloys, and their physical mixtures in the elemental or uncombined state, the remainder of said cermet being an ion-conductive ceramic material.

  9. Small domain-size multiblock copolymer electrolytes

    DOEpatents

    Pistorino, Jonathan; Eitouni, Hany Basam

    2016-09-20

    New block polymer electrolytes have been developed which have higher conductivities than previously reported for other block copolymer electrolytes. The new materials are constructed of multiple blocks (>5) of relatively low domain size. The small domain size provides greater protection against formation of dendrites during cycling against lithium in an electrochemical cell, while the large total molecular weight insures poor long range alignment, which leads to higher conductivity. In addition to higher conductivity, these materials can be more easily synthesized because of reduced requirements on the purity level of the reagents.

  10. Solid composite electrolytes for lithium batteries

    DOEpatents

    Kumar, Binod; Scanlon, Jr., Lawrence G.

    2001-01-01

    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.

  11. Effect of cycling on the lithium/electrolyte interface in organic electrolytes

    NASA Technical Reports Server (NTRS)

    Surampudi, S.; Shen, D. H.; Huang, C.-K.; Narayanan, S. R.; Attia, A.; Halpert, G.; Peled, E.

    1993-01-01

    Nondestructive methods such as ac impedance spectroscopy and microcalorimetry are used to study the effect of cell cycling on the lithium/electrolyte interface. The reactivity of both uncycled and cycled lithium towards various electrolytes is examined by measuring the heat evolved from the cells under open-circuit conditions at 25 C by microcalorimetry. Cycled cells at the end of charge/discharge exhibited considerably higher heat output compared with the uncycled cells. After 30 d of storage, the heat output of the cycled cells is similar to that of the uncycled cells. The cell internal resistance increases with cycling, and this is attributed to the degradation of the electrolyte with cycling.

  12. Lithium-ion batteries having conformal solid electrolyte layers

    DOEpatents

    Kim, Gi-Heon; Jung, Yoon Seok

    2014-05-27

    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.

  13. Electrolytes: transport properties and non-equilibrium thermodynamics

    SciTech Connect

    Miller, D.G.

    1980-12-01

    This paper presents a review on the application of non-equilibrium thermodynamics to transport in electrolyte solutions, and some recent experimental work and results for mutual diffusion in electrolyte solutions.

  14. Novel reversible and switchable electrolytes based on magneto-rheology

    PubMed Central

    Ding, Jie; Peng, Gangrou; Shu, Kewei; Wang, Caiyun; Tian, Tongfei; Yang, Wenrong; Zhang, Yuanchao; Wallace, Gordon G.; Li, Weihua

    2015-01-01

    Replacing organic liquid electrolytes with solid electrolytes has led to a new perspective on batteries, enabling high-energy battery chemistry with intrinsically safe cell designs. However, most solid/gel electrolytes are easily deformed; under extreme deformation, leakage and/or short-circuiting can occur. Here, we report a novel magneto-rheological electrolyte (MR electrolyte) that responds to changes in an external magnetic field; the electrolyte exhibits low viscosity in the absence of a magnetic field and increased viscosity or a solid-like phase in the presence of a magnetic field. This change from a liquid to solid does not significantly change the conductivity of the MR electrolyte. This work introduces a new class of magnetically sensitive solid electrolytes that can enhance impact resistance and prevent leakage from electronic devices through reversible active switching of their mechanical properties. PMID:26493967

  15. Polyethylene glycol-electrolyte solution (PEG-ES)

    MedlinePlus

    Polyethylene glycol-electrolyte solution (PEG-ES) is used to empty the colon (large intestine, bowel) before a ... Polyethylene glycol-electrolyte solution (PEG-ES) comes as a powder to mix with water and take by ...

  16. Performance comparison: Aluminum electrolytic and solid tantalum capacitor

    NASA Technical Reports Server (NTRS)

    Hawthornthwaite, B. G.; Piper, J.; Holland, H. W.

    1981-01-01

    Several key electrical and environmental parameters of latest technology aluminum electrolytic and solid tantalum capacitors were evaluated in terms of price fluctuations of tantalum metal. Performance differences between solid tantalums and aluminum electrolytics are examined.

  17. Wide electrochemical window solvents for use in electrochemical devices and electrolyte solutions incorporating such solvents

    DOEpatents

    Angell, Charles Austen; Zhang, Sheng-Shui; Xu, Kang

    1998-01-01

    The present invention relates to electrolyte solvents for use in liquid or rubbery electrolyte solutions. Specifically, this invention is directed to boron-containing electrolyte solvents and boron-containing electrolyte solutions.

  18. Electrocatalysis of fuel cell reactions: Investigation of alternate electrolytes

    NASA Technical Reports Server (NTRS)

    Chin, D. T.; Hsueh, K. L.; Chang, H. H.

    1983-01-01

    Oxygen reduction and transport properties of the electrolyte in the phosphoric acid fuel cell are studied. A theoretical expression for the rotating ring-disk electrode technique; the intermediate reaction rate constants for oxygen reduction on platinum in phosphoric acid electrolyte; oxygen reduction mechanism in trifluoromethanesulfonic acid (TFMSA), considered as an alternate electrolyte for the acid fuel cells; and transport properties of the phosphoric acid electrolyte at high concentrations and temperatures are covered.

  19. Protective interlayer for high temperature solid electrolyte electrochemical cells

    DOEpatents

    Isenberg, Arnold O.; Ruka, Roswell J.; Zymboly, Gregory E.

    1985-01-01

    A high temperature, solid electrolyte electrochemical cell is made, having a first and second electrode with solid electrolyte between them, where the electrolyte is formed by hot chemical vapor deposition, where a solid, interlayer material, which is electrically conductive, oxygen permeable, and protective of electrode material from hot metal halide vapor attack, is placed between the first electrode and the electrolyte, to protect the first electrode from the hot metal halide vapors during vapor deposition.

  20. Protective interlayer for high temperature solid electrolyte electrochemical cells

    DOEpatents

    Isenberg, Arnold O.; Ruka, Roswell J.

    1986-01-01

    A high temperature, solid electrolyte electrochemical cell is made, having a first and second electrode with solid electrolyte between them, where the electrolyte is formed by hot chemical vapor deposition, where a solid, interlayer material, which is electrically conductive, oxygen permeable, and protective of electrode material from hot metal halide vapor attack, is placed between the first electrode and the electrolyte, to protect the first electrode from the hot metal halide vapors during vapor deposition.

  1. Protective interlayer for high temperature solid electrolyte electrochemical cells

    DOEpatents

    Isenberg, Arnold O.; Ruka, Roswell J.

    1987-01-01

    A high temperature, solid electrolyte electrochemical cell is made, having a first and second electrode with solid electrolyte between them, where the electrolyte is formed by hot chemical vapor deposition, where a solid, interlayer material, which is electrically conductive, oxygen permeable, and protective of electrode material from hot metal halide vapor attack, is placed between the first electrode and the electrolyte, to protect the first electrode from the hot metal halide vapors during vapor deposition.

  2. Project Produce

    ERIC Educational Resources Information Center

    Wolfinger, Donna M.

    2005-01-01

    The grocery store produce section used to be a familiar but rather dull place. There were bananas next to the oranges next to the limes. Broccoli was next to corn and lettuce. Apples and pears, radishes and onions, eggplants and zucchinis all lay in their appropriate bins. Those days are over. Now, broccoli may be next to bok choy, potatoes beside…

  3. High performance polymer electrolytes for new types of lithium batteries

    SciTech Connect

    Scrosati, B.; Appetecchi, G.B.

    1998-07-01

    Long-life, environmentally friendly, low-cost reliable batteries are today urgently required to meet some crucial demands of modern society, which include the need of a large diffusion of electric cars in urban areas and the request of reliable and safe power sources for a large variety of portable consumer electronic devices. Batteries based on the combination of a lithium metal (or of a lithiated carbon) anode and a lithium intercalation cathode, have in principle the requisites to meet these requirements. Indeed, a first generation of lithium batteries using the rocking chair concept and generally called lithium ion batteries is already a commercial success. Lithium ion batteries are presently produced at a rate of several millions units per month and they are rapidly replacing the bulkier and less energetic nickel-cadmium and nickel-metal hydride batteries in popular devices, such as cellular phones and computers. In addition, lithium ion batteries are also scaled-up in view of their use in electric vehicles. The next important step in lithium battery technology would be the passage from the conventional, liquid-like structure to an advanced, plastic-like configuration. This innovation may indeed assure modularity in design and reduced production cost. Many attempts to reach this goal are presently underway. One of the main requirements for a successful result is the availability of polymer electrolyte membranes having lithium ion conductivity approaching that of common liquid electrolytes. In the attempt of developing materials capable of meeting this requirement the authors have carried out in recent years a systematic investigation on ionically conducting polymer membrane.. In particular, they have synthesized and characterized various classes of electrolyte membranes formed by the gelification of liquid organic solutions in a polymer matrix. The most relevant properties of these gel-type electrolyte membranes are the high ionic conductivity and the wide

  4. Electrolytic hydrogen production infrastructure options evaluation. Final subcontract report

    SciTech Connect

    Thomas, C.E.; Kuhn, I.F. Jr.

    1995-09-01

    Fuel-cell electric vehicles have the potential to provide the range, acceleration, rapid refueling times, and other creature comforts associated with gasoline-powered vehicles, but with virtually no environmental degradation. To achieve this potential, society will have to develop the necessary infrastructure to supply hydrogen to the fuel-cell vehicles. Hydrogen could be stored directly on the vehicle, or it could be derived from methanol or other hydrocarbon fuels by on-board chemical reformation. This infrastructure analysis assumes high-pressure (5,000 psi) hydrogen on-board storage. This study evaluates one approach to providing hydrogen fuel: the electrolysis of water using off-peak electricity. Other contractors at Princeton University and Oak Ridge National Laboratory are investigating the feasibility of producing hydrogen by steam reforming natural gas, probably the least expensive hydrogen infrastructure alternative for large markets. Electrolytic hydrogen is a possible short-term transition strategy to provide relatively inexpensive hydrogen before there are enough fuel-cell vehicles to justify building large natural gas reforming facilities. In this study, the authors estimate the necessary price of off-peak electricity that would make electrolytic hydrogen costs competitive with gasoline on a per-mile basis, assuming that the electrolyzer systems are manufactured in relatively high volumes compared to current production. They then compare this off-peak electricity price goal with actual current utility residential prices across the US.

  5. Electrolytic smelting of lunar rock for oxygen, iron, and silicon

    NASA Technical Reports Server (NTRS)

    Haskin, Larry A.; Colson, Russell O.; Lindstrom, David J.; Lewis, Robert H.; Semkow, Krystyna W.

    1992-01-01

    Preliminary studies of the electrochemical properties of silicate melts such as those available from heating of lunar mare soils indicate that conductivities are high enough for design of a practical electrolytic cell. The nature and kinetics of the electrode reactions, which involve reduction of Fe(++) and Si(IV) and oxidation of silicate anions as the primary, product-forming reactions, are also satisfactory. A survey of the efficiencies for production (amount of product for a given current) of O2, Fe(sup 0), and Si(sup 0) as functions of potential and of electrolyte composition indicate that conditions can be chosen to yield high production efficiencies. We also conclude that electronic conductivity does not occur to a significant extent. Based on these data, a cell with electrodes of 30 sq m in area operating between 1 and 5V with a current between 1.6 and 3.5(10)(exp 5) A for a mean power requirement of 0.54 MW and total energy use of approximately 13 MWhr per 24-hr day would produce 1 ton of O2, 0.81 ton of Fe(sup 0), 0.65 ton of Si(sup 0) (as Fe(sup 0)-Si(sup 0) alloy), and about 3.5 tons of silicate melt of altered composition per 24 hr. Adjustable distance between electrodes could offer flexibility with respect to feedstock and power source.

  6. Composite Solid Electrolyte for Li Battery Applications

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, G.; Attia, A. I.; Halpert, G.; Peled, E.

    1993-01-01

    The electrochemical, bulk and interfacial properties of the polyethylene oxide (PEO) based composite solid electrolyte (CSE) comprising LiI, PEO, and Al2O3 have been evaluated for Li battery applications. The bulk interfacial and transport properties of the CSEs seem to strongly depend on the alumina particle size. For the CSE films with 0.05 micron alumina while the bulk conductivity is around 10(exp -4) (mho/cm) at 103 C, the Li ion transport number seems to be close to unity at the same temperature. Compared to the PEO electrolyte this polymer composite electrolyte seems to exhibit robust mechanical and interfacial properties. We have studied three different films with three different alumina sizes in the range 0.01-0.3 micron. Effects of Al2O3 particle size on the electrochemical performance of polymer composite electrolyte is discussed. With TiS2 as cathode a 10 mAh small capacity cell was charged and discharged at C/40 and C/20 rates respectively.

  7. Ionic liquid electrolytes for reversible magnesium electrochemistry.

    PubMed

    Kar, Mega; Ma, Zheng; Azofra, Luis Miguel; Chen, Kun; Forsyth, Maria; MacFarlane, Douglas R

    2016-03-14

    Mg has great potential as the basis for a safe, low cost energy storage technology, however, cycling of magnesium is difficult to achieve in most electrolytes. We demonstrate cycling of Mg from a novel alkoxyammonium ionic liquid. DFT calculations highlight the role that Mg coordination with [BH4](-) ions plays in the mechanism.

  8. Ultrasonic hydrometer. [Specific gravity of electrolyte

    DOEpatents

    Swoboda, C.A.

    1982-03-09

    The disclosed ultrasonic hydrometer determines the specific gravity (density) of the electrolyte of a wet battery, such as a lead-acid battery. The hydrometer utilizes a transducer that when excited emits an ultrasonic impulse that traverses through the electrolyte back and forth between spaced sonic surfaces. The transducer detects the returning impulse, and means measures the time t between the initial and returning impulses. Considering the distance d between the spaced sonic surfaces and the measured time t, the sonic velocity V is calculated with the equation V = 2d/t. The hydrometer also utilizes a thermocouple to measure the electrolyte temperature. A hydrometer database correlates three variable parameters including sonic velocity in and temperature and specific gravity of the electrolyte, for temperature values between 0 and 40/sup 0/C and for specific gravity values between 1.05 and 1.30. Upon knowing two parameters (the calculated sonic velocity and the measured temperature), the third parameter (specific gravity) can be uniquely found in the database. The hydrometer utilizes a microprocessor for data storage and manipulation.

  9. LOWER TEMPERATURE ELECTROLYTE AND ELECTRODE MATERIALS

    SciTech Connect

    Keqin Huang

    2001-04-30

    A thorough literature survey on low-temperature electrolyte and electrode materials for solid oxide fuel cells (SOFC) is presented. Preliminary results of co-sintering LaGaO{sub 3} (LSGM) film on the cathode substrate were also reported. The chemical stability of LSGM in various SOFC environments was thermodynamically assessed and verified by the molten-salt technique.

  10. EFFECT OF LITHIUM ON SERUM ELECTROLYTES

    PubMed Central

    Geetha, P.R.; Channabasavanna, S.M.; Rama Rao, B.S. Sridhara

    1983-01-01

    SUMMARY 26 patients diagnosed as manic depressive psychosis were treated with lithium for three months and serum levels of calcium, magnesium, phosphates and proteins were estimated repeatedly. There were no significant changes in the levels of these electrolytes and proteins during the three months of study period. PMID:21847255

  11. Macroscopic Modeling of Polymer-Electrolyte Membranes

    SciTech Connect

    Weber, A.Z.; Newman, J.

    2007-04-01

    In this chapter, the various approaches for the macroscopic modeling of transport phenomena in polymer-electrolyte membranes are discussed. This includes general background and modeling methodologies, as well as exploration of the governing equations and some membrane-related topic of interest.

  12. Properties of polypyrrole-electrolyte-polypyrrole cells

    NASA Astrophysics Data System (ADS)

    Mohammadi, A.; Inganas, O.; Lundstrom, I.

    1986-05-01

    The charging and discharging characteristics of polypyrrole-electrolyte-polypyrrole cells were studied. It was found that 'secondary' batteries could be formed in this way with rather large coulombic efficiencies, but poor charge-retention properties. The coulombic capacity varied strongly with the total charge used during the production of the polypyrrole films, probably due to the morphology of the films.

  13. Anhydrous hydrogen fluoride electrolyte battery. [Patent application

    DOEpatents

    Not Available

    1972-06-26

    It is an object of the invention to provide a primary cell or battery using ammonium fluoride--anhydrous hydrogen fluoride electrolyte having improved current and power production capabilities at low temperatures. It is operable at temperatures substantially above the boiling point of hydrogen fluoride. (GRA)

  14. Miniaturized Amperometric Solid Electrolyte Carbon Dioxide Sensors

    NASA Technical Reports Server (NTRS)

    Hunter, G. W.; Xu, J. C.; Liu, C. C.; Hammond, J. W.; Ward, B.; Lukco, D.; Lampard, P.; Artale, M.; Androjna, D.

    2006-01-01

    A miniaturized electrochemical carbon dioxide (CO2) sensor using Na3Z r2Si2PO12 (NASICON) as a solid electrolyte has been fabricated and de monstrated. Microfabrication techniques were used for sensor fabricat ion to yield a sensing area around 1.0 mm x 1.1 mm. The NASICON solid electrolyte and the Na2CO3/BaCO3 (1:1.7 molar ratio) auxiliary elect rolyte were deposited by sputtering in between and on top of the inte rdigitated finger-shaped platinum electrodes. This structure maximize s the length of the three-phase boundary (electrode, solid electrolyt e, and auxiliary electrolyte), which is critical for gas sensing. The robust CO2 sensor operated up to 600 C in an amperometric mode and a ttempts were made to optimize sensor operating parameters. Concentrat ions of CO2 between 0.02% and 4% were detected and the overall sensor performance was evaluated. Linear response of sensor current output to ln[CO2 concentration] ranging from 0.02% to 1% was achieved.

  15. Secondary calcium solid electrolyte high temperature battery

    SciTech Connect

    Sammells, A.F.; Schumacher, B.

    1986-01-01

    The authors report on recent work directed towards determining the viability of polycrystalline Ca/sup 2 +/ conducting ..beta..''-alumina solid electrolytes as the basis for a new type of high temperature battery. In this battery system the negative electrode consisted of a calcium-silicon alloy whose redox electro-chemistry was mediated to the calcium conducting solid electrolyte via the use of the molten salt eutectic CaCl/sub 2/ (51.4/sup M//0), CaI/sub 2/ (mp 550/sup 0/C). Both the molten salt and the calcium-alloy negative active material were separated from the positive active material via the Ca/sup 2 +/ conducting polycrystalline solid electrolyte. The positive electrode consisted of a solid-state matrix having a somewhat related crystallographic structure to Ca/sup 2 +/ ..beta..''-alumina, but where a significant fraction of the A1/sup 3 +/ sites located within this solid electrolyte's spinel block were replaced by immobile transition metal species. These species were available for participating in solid-state redox electrochemistry upon electrochemical cell cycling.

  16. Energetics of the Semiconductor-Electrolyte Interface.

    ERIC Educational Resources Information Center

    Turner, John A.

    1983-01-01

    The use of semiconductors as electrodes for electrochemistry requires an understanding of both solid-state physics and electrochemistry, since phenomena associated with both disciplines are seen in semiconductor/electrolyte systems. The interfacial energetics of these systems are discussed. (JN)

  17. Polymeric Electrolytic Hygrometer For Harsh Environments

    NASA Technical Reports Server (NTRS)

    Lawson, Daniel D.; Shakkottai, Parthasarathy; Venkateshan, Shakkottai P.

    1989-01-01

    Design of polymeric electrolytic hygrometer improved to meet need for reliable measurements of relative humidity in harsh environments of pulpmills and papermills. Redesigned sensor head features shorter, more-rigidly-held sensing element, less vulnerable than previous version to swell and loss of electrical contact. Useful for control of batch dryers in food and pharmaceutical industries.

  18. Polarization of ferroelectric films through electrolyte

    NASA Astrophysics Data System (ADS)

    Toss, Henrik; Sani, Negar; Fabiano, Simone; Simon, Daniel T.; Forchheimer, Robert; Berggren, Magnus

    2016-03-01

    A simplified model is developed to understand the field and potential distribution through devices based on a ferroelectric film in direct contact with an electrolyte. Devices based on the ferroelectric polymer polyvinylidenefluoride-trifluoroethylene (PVDF-TrFE) were produced—in metal-ferroelectric-metal, metal-ferroelectric-dielectric-metal, and metal-ferroelectric-electrolyte-metal architectures—and used to test the model, and simulations based on the model and these fabricated devices were performed. From these simulations we find indication of progressive polarization of the films. Furthermore, the model implies that there is a relation between the separation of charge within the devices and the observed open circuit voltage. This relation is confirmed experimentally. The ability to polarize ferroelectric polymer films through aqueous electrolytes, combined with the strong correlation between the properties of the electrolyte double layer and the device potential, opens the door to a variety of new applications for ferroelectric technologies, e.g. regulation of cell culture growth and release, steering molecular self-assembly, or other large area applications requiring aqueous environments.

  19. Physical properties of molten carbonate electrolyte

    SciTech Connect

    Kojima, T.; Yanagida, M.; Tanimoto, K.

    1996-12-31

    Recently many kinds of compositions of molten carbonate electrolyte have been applied to molten carbonate fuel cell in order to avoid the several problems such as corrosion of separator plate and NiO cathode dissolution. Many researchers recognize that the addition of alkaline earth (Ca, Sr, and Ba) carbonate to Li{sub 2}CO{sub 3}-Na{sub 2}CO{sub 3} and Li{sub 2}CO{sub 3}-K{sub 2}CO{sub 3} eutectic electrolytes is effective to avoid these problems. On the other hand, one of the corrosion products, CrO{sub 4}{sup 2-} ion is found to dissolve into electrolyte and accumulated during the long-term MCFC operations. This would affect the performance of MCFC. There, however, are little known data of physical properties of molten carbonate containing alkaline earth carbonates and CrO{sub 4}{sup 2-}. We report the measured and accumulated data for these molten carbonate of electrical conductivity and surface tension to select favorable composition of molten carbonate electrolytes.

  20. Process for electrolytically preparing uranium metal

    DOEpatents

    Haas, Paul A.

    1989-01-01

    A process for making uranium metal from uranium oxide by first fluorinating uranium oxide to form uranium tetrafluoride and next electrolytically reducing the uranium tetrafluoride with a carbon anode to form uranium metal and CF.sub.4. The CF.sub.4 is reused in the fluorination reaction rather than being disposed of as a hazardous waste.

  1. Process for electrolytically preparing uranium metal

    DOEpatents

    Haas, Paul A.

    1989-08-01

    A process for making uranium metal from uranium oxide by first fluorinating uranium oxide to form uranium tetrafluoride and next electrolytically reducing the uranium tetrafluoride with a carbon anode to form uranium metal and CF.sub.4. The CF.sub.4 is reused in the fluorination reaction rather than being disposed of as a hazardous waste.

  2. Fuel cell electrolyte membrane with basic polymer

    DOEpatents

    Larson, James M.; Pham, Phat T.; Frey, Matthew H.; Hamrock, Steven J.; Haugen, Gregory M.; Lamanna, William M.

    2012-12-04

    The present invention is an electrolyte membrane comprising an acid and a basic polymer, where the acid is a low-volatile acid that is fluorinated and is either oligomeric or non-polymeric, and where the basic polymer is protonated by the acid and is stable to hydrolysis.

  3. Fuel cell electrolyte membrane with basic polymer

    DOEpatents

    Larson, James M.; Pham, Phat T.; Frey, Matthew H.; Hamrock, Steven J.; Haugen, Gregory M.; Lamanna, William M.

    2010-11-23

    The present invention is an electrolyte membrane comprising an acid and a basic polymer, where the acid is a low-volatile acid that is fluorinated and is either oligomeric or non-polymeric, and where the basic polymer is protonated by the acid and is stable to hydrolysis.

  4. Ionometry in the analysis of electrolyte solutions (review)

    SciTech Connect

    Petrukhin, O.M.; Rogatinskaya, S.L.; Shipulo, E.V.

    1995-04-01

    The potential usefulness of ionometry in the analytical control of plating electrolytes, etching solutions, and waste effluents has been considered. Complete ionometric analysis of plating electrolytes and determination of metal cyanide complexes have been presented as examples. Ion-selective field-effect transistors (IEFT), semiconductor electrodes, and ISE pairs have been shown to have potential usefulness for the potentiometric titration of plating electrolytes.

  5. Electrolytes for Wide Operating Temperature Lithium-Ion Cells

    NASA Technical Reports Server (NTRS)

    Smart, Marshall C. (Inventor); Bugga, Ratnakumar V. (Inventor)

    2016-01-01

    Provided herein are electrolytes for lithium-ion electrochemical cells, electrochemical cells employing the electrolytes, methods of making the electrochemical cells and methods of using the electrochemical cells over a wide temperature range. Included are electrolyte compositions comprising a lithium salt, a cyclic carbonate, a non-cyclic carbonate, and a linear ester and optionally comprising one or more additives.

  6. Electrode electrolyte interlayers containing cerium oxide for electrochemical fuel cells

    DOEpatents

    Borglum, Brian P.; Bessette, Norman F.

    2000-01-01

    An electrochemical cell is made having a porous fuel electrode (16) and a porous air electrode (13), with solid oxide electrolyte (15) therebetween, where the air electrode surface opposing the electrolyte has a separate, attached, dense, continuous layer (14) of a material containing cerium oxide, and where electrolyte (16) contacts the continuous oxide layer (14), without contacting the air electrode (13).

  7. Battery electrolytes. Citations from the NTIS data base

    NASA Astrophysics Data System (ADS)

    Young, C. G.

    1980-05-01

    Many types of solid, liquid and gaseous battery electrolytes are described and analyzed in the cited abstracts. Battery design, construction, and use, employing the listed electrolytes, are discussed. Battery design, construction, and use, employing the listed electrolytes, are discussed. Battery life, efficiency, and maintenance characteristics are also delineated. Included are 196 citations.

  8. Superacid-Based Lithium Salts For Polymer Electrolytes

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, Ganesan; Prakash, Surya; Shen, David H.; Surampudi, Subbarao; Olah, George

    1995-01-01

    Solid polymer electrolytes exhibiting high lithium-ion conductivities made by incorporating salts of superacids into thin films of polyethylene oxide (PEO). These and other solid-polymer electrolytes candidates for use in rechargeable lithium-based electrochemical cells. Increases in room-temperature lithium-ion conductivities of solid electrolytes desirable because they increase achievable power and energy densities.

  9. Effect of electrolyte conductance on current distribution in porous zinc electrode in KOH electrolyte

    SciTech Connect

    Liu, M.B.; Cook, G.M.; Yao, N.P.

    1981-01-01

    An analysis of the current distributions in porous zinc electrodes is presented which indicates that the current distributions are indeed controlled by the conductivity of the electrolyte within the porous structure. (WHK)

  10. Atrial natriuretic peptide: water and electrolyte homeostasis.

    PubMed

    Kenyon, C J; Jardine, A G

    1989-08-01

    In the few years since its identification, a clear role for ANP in the regulation of water and electrolyte balance has emerged (Figure 3). The peptide is released in response to blood volume expansion, both acutely and gradually during changes in dietary sodium intake. Similarly, plasma levels are elevated in pathophysiological conditions such as cardiac and renal failure. It has become apparent that ANP has natriuretic, diuretic and vasorelaxant properties. Many of the original studies employed what we now know to be pharmacological doses of the peptide. However, recent reports have confirmed that small, sustained elevations in plasma ANP within or marginally above the 'normal' physiological range produce similar effects. A number of recent studies have tried to specifically address the physiological relevance of ANP. Although undoubtedly release by atrial distension and effective when infused to similar concentrations, atrial distension also has other effects via neural pathways. Thus, the demonstration that excretion of saline is impaired by atrial appendectomy (Benjamin et al, 1988) does not imply that this is only due to the absence of an atrial hormone. Goetz et al (1986) demonstrated that in the denervated heart, although ANP is still released, the excretion of a saline load is impaired. Similarly, in man, Richards et al (1988a) needed to infuse ANP to much higher plasma levels than those achieved by a saline load in order to reproduce the natriuresis. Although these experiments can be criticized, they confirm that ANP is not the sole mechanism for excreting a volume load, or for the natriuresis following atrial distension, but that these effects are likely to reflect the balance between ANP, AVP, the renin-angiotensin and autonomic nervous systems. In rats immunized against ANP (Greenwald et al, 1988), although the ability to excrete an acute saline load was impaired, long-term sodium balance was normal, suggesting that the rats were able to compensate for

  11. Obtaining accurate amounts of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, M.W.; George, W.A.

    1987-07-07

    A process is described for obtaining pre-determined, accurate rate amounts of mercury. In one embodiment, predetermined, precise amounts of Hg are separated from HgO and plated onto a cathode wire. The method for doing this involves dissolving a precise amount of HgO which corresponds to a pre-determined amount of Hg desired in an electrolyte solution comprised of glacial acetic acid and H[sub 2]O. The mercuric ions are then electrolytically reduced and plated onto a cathode producing the required pre-determined quantity of Hg. In another embodiment, pre-determined, precise amounts of Hg are obtained from Hg[sub 2]Cl[sub 2]. The method for doing this involves dissolving a precise amount of Hg[sub 2]Cl[sub 2] in an electrolyte solution comprised of concentrated HCl and H[sub 2]O. The mercurous ions in solution are then electrolytically reduced and plated onto a cathode wire producing the required, pre-determined quantity of Hg. 1 fig.

  12. Obtaining accurate amounts of mercury from mercury compounds via electrolytic methods

    DOEpatents

    Grossman, Mark W.; George, William A.

    1987-01-01

    A process for obtaining pre-determined, accurate rate amounts of mercury. In one embodiment, predetermined, precise amounts of Hg are separated from HgO and plated onto a cathode wire. The method for doing this involves dissolving a precise amount of HgO which corresponds to a pre-determined amount of Hg desired in an electrolyte solution comprised of glacial acetic acid and H.sub.2 O. The mercuric ions are then electrolytically reduced and plated onto a cathode producing the required pre-determined quantity of Hg. In another embodiment, pre-determined, precise amounts of Hg are obtained from Hg.sub.2 Cl.sub.2. The method for doing this involves dissolving a precise amount of Hg.sub.2 Cl.sub.2 in an electrolyte solution comprised of concentrated HCl and H.sub.2 O. The mercurous ions in solution are then electrolytically reduced and plated onto a cathode wire producing the required, pre-determined quantity of Hg.

  13. Preliminary Evaluations of Polymer-based Lithium Battery Electrolytes Under Development for the Polymer Electrolyte Rechargeable Systems Program

    NASA Technical Reports Server (NTRS)

    Manzo, Michelle A.; Bennett, William R.

    2003-01-01

    A component screening facility has been established at The NASA Glenn Research Center (GRC) to evaluate candidate materials for next generation, lithium-based, polymer electrolyte batteries for aerospace applications. Procedures have been implemented to provide standardized measurements of critical electrolyte properties. These include ionic conductivity, electronic resistivity, electrochemical stability window, cation transference number, salt diffusion coefficient and lithium plating efficiency. Preliminary results for poly(ethy1ene oxide)-based polymer electrolyte and commercial liquid electrolyte are presented.

  14. Supersaturated Electrolyte Solutions: Theory and Experiment

    NASA Technical Reports Server (NTRS)

    Izmailov, Alexander F.; Myerson, Allan S.; Na, Han-Soo

    1995-01-01

    Highly supersaturated electrolyte solutions can be prepared and studied employing an electrodynamic levitator trap (ELT) technique. The ELT technique involves containerless suspension of a microdroplet thus eliminating dust, dirt, and container walls which normally cause heterogeneous nucleation. This allows very high supersaturations to be achieved. A theoretical study of the experimental results obtained for the water activity in microdroplets of various electrolyte solutions is based on the development of the Cahn-Hilliard formalism for electrolyte solutions. In the approach suggested the metastable state for electrolyte solutions is described in terms of the conserved order parameter omega(r,t) associated with fluctuations of the mean solute concentration n(sub 0). Parameters of the corresponding Ginzburg-Landau free energy functional which defines the dynamics of metastable state relaxation are determined and expressed through the experimentally measured quantities. A correspondence of 96-99 % between theory and experiment for all solutions studied was achieved and allowed the determination of an analytical expression for the spinodal concentration n(sub spin), and its calculation for various electrolyte solutions at 298 K. The assumption that subcritical solute clusters consist of the electrically neutral Bjerrum pairs has allowed both analytical and numerical investigation of the number-size N(sub c) of nucleation monomers (aggregates of the Bjerrum pairs) which are elementary units of the solute critical clusters. This has also allowed estimations for the surface tension Alpha, and equilibrium bulk energy Beta per solute molecule in the nucleation monomers. The dependence of these properties on the temperature T and on the solute concentration n(sub 0) through the entire metastable zone (from saturation concentration n(sub sat) to spinodal n(sub spin) is examined. It has been demonstrated that there are the following asymptotics: N(sub c), = I at spinodal

  15. Plasma electrolytic oxidation of Titanium Aluminides

    NASA Astrophysics Data System (ADS)

    Morgenstern, R.; Sieber, M.; Grund, T.; Lampke, T.; Wielage, B.

    2016-03-01

    Due to their outstanding specific mechanical and high-temperature properties, titanium aluminides exhibit a high potential for lightweight components exposed to high temperatures. However, their application is limited through their low wear resistance and the increasing high-temperature oxidation starting from about 750 °C. By the use of oxide ceramic coatings, these constraints can be set aside and the possible applications of titanium aluminides can be extended. The plasma electrolytic oxidation (PEO) represents a process for the generation of oxide ceramic conversion coatings with high thickness. The current work aims at the clarification of different electrolyte components’ influences on the oxide layer evolution on alloy TNM-B1 (Ti43.5Al4Nb1Mo0.1B) and the creation of compact and wear resistant coatings. Model experiments were applied using a ramp-wise increase of the anodic potential in order to show the influence of electrolyte components on the discharge initiation and the early stage of the oxide layer growth. The production of PEO layers with technically relevant thicknesses close to 100 μm was conducted in alkaline electrolytes with varying amounts of Na2SiO3·5H2O and K4P2O7 under symmetrically pulsed current conditions. Coating properties were evaluated with regard to morphology, chemical composition, hardness and wear resistance. The addition of phosphates and silicates leads to an increasing substrate passivation and the growth of compact oxide layers with higher thicknesses. Optimal electrolyte compositions for maximum coating hardness and thickness were identified by statistical analysis. Under these conditions, a homogeneous inner layer with low porosity can be achieved. The frictional wear behavior of the compact coating layer is superior to a hard anodized layer on aluminum.

  16. LOW TEMPERATURE CATHODE SUPPORTED ELECTROLYTES

    SciTech Connect

    Harlan U. Anderson; Wayne Huebner; Igor Kosacki

    2001-03-31

    This project has three main goals: Thin Films Studies, Preparation of Graded Porous Substrates and Basic Electrical Characterization and testing of Planar Single Cells. Substantial progress has been made on both characterizing thin films as well as developing methods to produce films on nanoporous substrates. The results of electrical conductivity measurements on ZrO{sub 2}:16%Sc nanocrystalline thin films under controlled oxygen partial pressure and temperature are presented. The experimental data have been interpreted using a defect model, which describes the interaction between Sc and oxygen vacancies resulting in the formation of donor - (Sc{sub Zr} - V{sub o} - e){sup x} and acceptor - (Sc{sub Zr}-h){sup x} levels. From this the electronic and ionic contribution to the electrical transport has been determined and correlated with the band structure. These results suggest that ZrO{sub 2}:16%Sc possesses higher electronic conductivity than ZrO{sub 2}:16%Y, which dominates the total conductivity in reducing atmospheres. This is an important result since it indicates that Sc-YSZ maybe useful in the anode regions of the cell. We have made important breakthroughs on depositing dense Ceria films on to porous LSM substrates. In previous studies we have found that in order to produce a surface which is smooth enough to coat with dense polymer precursor derived films, the required thickness of the colloidal film layer is determined by the maximum surface roughness. That is, if we wish to make 2 micron thick colloidal oxide layers, the roughness of the LSM surface can not exceed 2 microns. Currently, we are producing the composite CeO{sub 2}/LSM structures that can be coated with polymer precursor to produce 0.5 to 1.5 micron thickness dense YSZ films. In the next quarter, we will be testing SOFC's using these structures. YSZ/CeO{sub 2}/LSM composites have been formed by annealing at 800 C. Our studies show that the YSZ films are very dense with a 20 nm grain size. SOFC

  17. Effect upon biocompatibility and biocorrosion properties of plasma electrolytic oxidation in trisodium phosphate electrolytes.

    PubMed

    Kim, Yu-Kyoung; Park, Il-Song; Lee, Kwang-Bok; Bae, Tae-Sung; Jang, Yong-Seok; Oh, Young-Min; Lee, Min-Ho

    2016-03-01

    Surface modification to improve the corrosion resistance and biocompatibility of the Mg-Al-Zn-Ca alloy was conducted via plasma electrolytic oxidation (PEO) in an electrolyte that included phosphate. Calcium phosphate can be easily induced on the surface of a PEO coating that includes phosphate in a physiological environment because Ca(2+) ions in body fluids can be combined with PO4 (3-). Cytotoxicity of the PEO coating formed in electrolytes with various amounts of Na3PO4 was identified. In particular, the effects that PEO films have upon oxidative stress and differentiation of osteoblast activity were studied. As the concentration of Na3PO4 in the electrolyte increased, the oxide layer was found to become thicker, which increased corrosion resistance. However, the PEO coating formed in electrolytes with over 0.2 M of added Na3PO4 exhibited more microcracks and larger pores than those formed in smaller Na3PO4 concentrations owing to a large spark discharge. A nonuniform oxide film that included more phosphate caused more cytotoxicity and oxidative stress, and overabundant phosphate content in the oxide layer interrupted the differentiation of osteoblasts. The corrosion resistance of the magnesium alloy and the thickness of the oxide layer were increased by the addition of Na3PO4 in the electrolyte for PEO treatment. However, excessive phosphate content in the oxide layer led to oxidative stress, which resulted in reduced cell viability and activity. PMID:26829967

  18. Effect upon biocompatibility and biocorrosion properties of plasma electrolytic oxidation in trisodium phosphate electrolytes.

    PubMed

    Kim, Yu-Kyoung; Park, Il-Song; Lee, Kwang-Bok; Bae, Tae-Sung; Jang, Yong-Seok; Oh, Young-Min; Lee, Min-Ho

    2016-03-01

    Surface modification to improve the corrosion resistance and biocompatibility of the Mg-Al-Zn-Ca alloy was conducted via plasma electrolytic oxidation (PEO) in an electrolyte that included phosphate. Calcium phosphate can be easily induced on the surface of a PEO coating that includes phosphate in a physiological environment because Ca(2+) ions in body fluids can be combined with PO4 (3-). Cytotoxicity of the PEO coating formed in electrolytes with various amounts of Na3PO4 was identified. In particular, the effects that PEO films have upon oxidative stress and differentiation of osteoblast activity were studied. As the concentration of Na3PO4 in the electrolyte increased, the oxide layer was found to become thicker, which increased corrosion resistance. However, the PEO coating formed in electrolytes with over 0.2 M of added Na3PO4 exhibited more microcracks and larger pores than those formed in smaller Na3PO4 concentrations owing to a large spark discharge. A nonuniform oxide film that included more phosphate caused more cytotoxicity and oxidative stress, and overabundant phosphate content in the oxide layer interrupted the differentiation of osteoblasts. The corrosion resistance of the magnesium alloy and the thickness of the oxide layer were increased by the addition of Na3PO4 in the electrolyte for PEO treatment. However, excessive phosphate content in the oxide layer led to oxidative stress, which resulted in reduced cell viability and activity.

  19. Self-consistent modeling of electrochemical strain microscopy of solid electrolytes

    DOE PAGES

    Tselev, Alexander; Morozovska, Anna N.; Udod, Alexei; Eliseev, Eugene A.; Kalinin, Sergei V.

    2014-10-10

    Electrochemical strain microscopy (ESM) employs a strong electromechanical coupling in solid ionic conductors to map ionic transport and electrochemical processes with nanometer-scale spatial resolution. To elucidate the mechanisms of the ESM image formation, we performed self-consistent numerical modeling of the electromechanical response in solid electrolytes under the probe tip in a linear, small-signal regime using the Boltzmann–Planck–Nernst–Einstein theory and Vegard's law while taking account of the electromigration and diffusion. We identified the characteristic time scales involved in the formation of the ESM response and found that the dynamics of the charge carriers in the tip-electrolyte system with blocking interfaces canmore » be described as charging of the diffuse layer at the tip-electrolyte interface through the tip contact spreading resistance. At the high frequencies used in the detection regime, the distribution of the charge carriers under the tip is governed by evanescent concentration waves generated at the tip-electrolyte interface. The ion drift length in the electric field produced by the tip determines the ESM response at high frequencies, which follows a 1/f asymptotic law. The electronic conductivity, as well as the electron transport through the electrode-electrolyte interface, do not have a significant effect on the ESM signal in the detection regime. The results indicate, however, that for typical solid electrolytes at room temperature, the ESM response originates at and contains information about the very surface layer of a sample, and the properties of the one-unit-cell-thick surface layer may significantly contribute to the ESM response, implying a high surface sensitivity and a high lateral resolution of the technique. On the other hand, it follows that a rigorous analysis of the ESM signals requires techniques that account for the discrete nature of a solid.« less

  20. Self-consistent modeling of electrochemical strain microscopy of solid electrolytes

    SciTech Connect

    Tselev, Alexander; Morozovska, Anna N.; Udod, Alexei; Eliseev, Eugene A.; Kalinin, Sergei V.

    2014-10-10

    Electrochemical strain microscopy (ESM) employs a strong electromechanical coupling in solid ionic conductors to map ionic transport and electrochemical processes with nanometer-scale spatial resolution. To elucidate the mechanisms of the ESM image formation, we performed self-consistent numerical modeling of the electromechanical response in solid electrolytes under the probe tip in a linear, small-signal regime using the Boltzmann–Planck–Nernst–Einstein theory and Vegard's law while taking account of the electromigration and diffusion. We identified the characteristic time scales involved in the formation of the ESM response and found that the dynamics of the charge carriers in the tip-electrolyte system with blocking interfaces can be described as charging of the diffuse layer at the tip-electrolyte interface through the tip contact spreading resistance. At the high frequencies used in the detection regime, the distribution of the charge carriers under the tip is governed by evanescent concentration waves generated at the tip-electrolyte interface. The ion drift length in the electric field produced by the tip determines the ESM response at high frequencies, which follows a 1/f asymptotic law. The electronic conductivity, as well as the electron transport through the electrode-electrolyte interface, do not have a significant effect on the ESM signal in the detection regime. The results indicate, however, that for typical solid electrolytes at room temperature, the ESM response originates at and contains information about the very surface layer of a sample, and the properties of the one-unit-cell-thick surface layer may significantly contribute to the ESM response, implying a high surface sensitivity and a high lateral resolution of the technique. On the other hand, it follows that a rigorous analysis of the ESM signals requires techniques that account for the discrete nature of a solid.

  1. An Insoluble Titanium-Lead Anode for Sulfate Electrolytes

    SciTech Connect

    Ferdman, Alla

    2005-05-11

    The project is devoted to the development of novel insoluble anodes for copper electrowinning and electrolytic manganese dioxide (EMD) production. The anodes are made of titanium-lead composite material produced by techniques of powder metallurgy, compaction of titanium powder, sintering and subsequent lead infiltration. The titanium-lead anode combines beneficial electrochemical behavior of a lead anode with high mechanical properties and corrosion resistance of a titanium anode. In the titanium-lead anode, the titanium stabilizes the lead, preventing it from spalling, and the lead sheathes the titanium, protecting it from passivation. Interconnections between manufacturing process, structure, composition and properties of the titanium-lead composite material were investigated. The material containing 20-30 vol.% of lead had optimal combination of mechanical and electrochemical properties. Optimal process parameters to manufacture the anodes were identified. Prototypes having optimized composition and structure were produced for testing in operating conditions of copper electrowinning and EMD production. Bench-scale, mini-pilot scale and pilot scale tests were performed. The test anodes were of both a plate design and a flow-through cylindrical design. The cylindrical anodes were composed of cylinders containing titanium inner rods and fitting over titanium-lead bushings. The cylindrical design allows the electrolyte to flow through the anode, which enhances diffusion of the electrolyte reactants. The cylindrical anodes demonstrate higher mass transport capabilities and increased electrical efficiency compared to the plate anodes. Copper electrowinning represents the primary target market for the titanium-lead anode. A full-size cylindrical anode performance in copper electrowinning conditions was monitored over a year. The test anode to cathode voltage was stable in the 1.8 to 2.0 volt range. Copper cathode morphology was very smooth and uniform. There was no

  2. Non-aqueous electrolytes for lithium ion batteries

    SciTech Connect

    Chen, Zonghai; Amine, Khalil

    2015-11-12

    The present invention is generally related to electrolytes containing anion receptor additives to enhance the power capability of lithium-ion batteries. The anion receptor of the present invention is a Lewis acid that can help to dissolve LiF in the passivation films of lithium-ion batteries. Accordingly, one aspect the invention provides electrolytes comprising a lithium salt; a polar aprotic solvent; and an anion receptor additive; and wherein the electrolyte solution is substantially non-aqueous. Further there are provided electrochemical devices employing the electrolyte and methods of making the electrolyte.

  3. Ceramic and polymeric solid electrolytes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Fergus, Jeffrey W.

    Lithium-ion batteries are important for energy storage in a wide variety of applications including consumer electronics, transportation and large-scale energy production. The performance of lithium-ion batteries depends on the materials used. One critical component is the electrolyte, which is the focus of this paper. In particular, inorganic ceramic and organic polymer solid-electrolyte materials are reviewed. Solid electrolytes provide advantages in terms of simplicity of design and operational safety, but typically have conductivities that are lower than those of organic liquid electrolytes. This paper provides a comparison of the conductivities of solid-electrolyte materials being used or developed for use in lithium-ion batteries.

  4. Tunable optical properties of colloidal quantum dots in electrolytic environments.

    PubMed

    Ramadurai, D; Kohanpour, B; Alexson, D; Shi, P; Sethuraman, A; Li, Y; Saini, V; Dutta, M; Stroscio, M A

    2004-12-01

    The absorption spectra of colloidal cadmium sulfide quantum dots in electrolytic solutions are found to manifest a shift in the absorption threshold as the concentration of the electrolyte is varied. These results are consistent with a shift in the absorption threshold that would be caused by electrolytic screening of the field caused by the intrinsic spontaneous polarisation of these würtzite structured quantum dots. These electrolyte-dependent absorption properties provide a potential means of gaining insights on the variable extracellular and intracellular electrolytic concentrations that are present in biological systems.

  5. Terahertz characteristics of electrolytes in aqueous Luria-Bertani media

    NASA Astrophysics Data System (ADS)

    Oh, Seung Jae; Son, Joo-Hiuk; Yoo, Ocki; Lee, Dong-Hee

    2007-10-01

    We measured the optical constants of aqueous biomaterial mixtures with various electrolyte concentrations using terahertz time-domain spectroscopy. The mixtures were divided into water and other electrolyte parts in mass fractions for analysis. The optical constants of the electrolyte, excluding water, were obtained by applying the ideal mixture equation, and the power absorption of the electrolyte was observed to be larger than that of water above 1THz. Data from the measurement were fitted with the modified double Debye model, and the reorientation and hydrogen-bond formation decomposition times were found to decrease as the electrolyte concentration increased.

  6. Method and apparatus for storage battery electrolyte circulation

    DOEpatents

    Inkmann, Mark S.

    1980-09-09

    An electrolyte reservoir in fluid communication with the cell of a storage battery is intermittently pressurized with a pulse of compressed gas to cause a flow of electrolyte from the reservoir to the upper region of less dense electrolyte in the cell. Upon termination of the pressure pulse, more dense electrolyte is forced into the reservoir from the lower region of the cell by the differential pressure head between the cell and reservoir electrolyte levels. The compressed gas pulse is controlled to prevent the entry of gas from the reservoir into the cell.

  7. DNA based electrolyte/separator for lithium battery application

    NASA Astrophysics Data System (ADS)

    Kumar, Jitendra; Ouchen, Fahima; Smarra, Devin A.; Subramanyam, Guru; Grote, James G.

    2015-09-01

    In this study, we demonstrated the use of DNA-CTMA (DC) in combination with PolyVinylidene Fluoride (PVDF) as a host matrix or separator for Lithium based electrolyte to form solid polymer/gel like electrolyte for potential application in Li-ion batteries. The addition of DC provided a better thermal stability of the composite electrolyte as shown by the thermos-gravimetric analysis (TGA). The AC conductivity measurements suggest that the addition of DC to the gel electrolyte had no effect on the overall ionic conductivity of the composite. The obtained films are flexible with high mechanical stretch-ability as compared to the gel type electrolytes only.

  8. A Comparative Study of Electrolyte Flow and Slime Particle Transport in a Newly Designed Copper Electrolytic Cell and a Laboratory-Scale Conventional Electrolytic Cell

    NASA Astrophysics Data System (ADS)

    Zeng, Weizhi; Wang, Shijie; Free, Michael L.

    2016-08-01

    An innovative copper electrolytic cell was designed with its inlet at the cell top and its outlet near the cell bottom, in opposite to conventional electrolytic cells. It was modeled in COMSOL Multiphysics to simulate copper electrorefining process. Unlike conventional electrorefining cells, downward electrolyte flows are more dominant in the fluid flow field in this cell, which leads to faster settlement of slime particles and less contamination to the cathode. Copper concentration profiles, electrolyte flow velocity field, slime particle movements, and slime particle distributions were obtained as simulation results, which were compared with those in a laboratory-scale conventional electrolytic cell. Advantages of the newly designed electrolytic cell were found: copper ions are distributed more uniformly in the cell with a thinner diffusion layer near the cathode; stronger convection exists in the inter-electrode domain with dominant downward flows; and slime particles have larger possibilities to settle down and are less likely to reach the cathode.

  9. Electrowinning process with electrode compartment to avoid contamination of electrolyte

    SciTech Connect

    Poa, D.S.; Pierce, R.D.; Mulcahey, T.P.; Johnson, G.K.

    1993-07-06

    A process is described of electrolytically recovering a metal from an oxide of the metal comprising the steps of: (a) providing an electrolytic cell including a molten salt electrolyte containing the metal oxide and one or more halide salts of the metal, a pair of spaced apart electrodes in the electrolyte, and a source of electrical voltage to the electrodes, one of the electrodes being an anode and a source of particulate carbon contamination of the electrolyte during operation of the cell, (b) operating the cell to recover the metal as an element at the other electrode while confining the contaminant to a zone in the electrolyte about the one electrode, and (c) periodically removing the contaminant from the electrolyte zone while interrupting operation of the cell.

  10. Fuel cell and system for supplying electrolyte thereto

    DOEpatents

    Adlhart, Otto J.; Feigenbaum, Haim

    1984-01-01

    An electrolyte distribution and supply system for use with a fuel cell having means for drawing electrolyte therein is formed by a set of containers of electrolyte joined to respective fuel cells in a stack of such cells. The electrolyte is separately stored so as to provide for electrical isolation between electrolytes of the individual cells of the stack. Individual storage compartments are coupled by capillary tubes to the respective fuel cells. Hydrostatic pressure is maintained individually for each of the fuel cells by separately elevating each compartment of the storing means to a specific height above the corresponding fuel cell which is to be fed from that compartment of the storing means. The individual compartments are filled with electrolyte by allowing the compartments to overflow thereby maintaining the requisite depth of electrolyte in each of the storage compartments.

  11. Primary certification of reference material for electrolytic conductivity of bioethanol

    NASA Astrophysics Data System (ADS)

    da Silva, L. F.; Gomes, M. R. F.; Cassini, G. C.; Faria, A. C. V.; Fraga, I. C. S.

    2016-07-01

    Nowadays the preservation of the planet is spreading into the international scene with the use of renewable energy sources such as bioethanol. The challenge is to guarantee the quality of produced bioethanol, and the electrolytic conductivity (EC) is one of the specified parameters for this purpose. However, is necessary to demonstrate the metrological traceability of the measurement results for EC in this matrix. This study presents the certification of a reference material for EC in bioethanol by using only primary measurements. The value of primary certified reference material (CRM) is (0.77 ± 0.06) µS.cm-1, and its use will provide the metrological traceability needed for measurement results in laboratories.

  12. Porous matrix structures for alkaline electrolyte fuel cells

    NASA Technical Reports Server (NTRS)

    Vine, R. W.; Narsavage, S. T.

    1975-01-01

    A number of advancements have been realized by a continuing research program to develop higher chemically stable porous matrix structures with high bubble pressure (crossover resistance) for use as separators in potassium hydroxide electrolyte fuel cells. More uniform, higher-bubble-pressure asbestos matrices were produced by reconstituting Johns-Manville asbestos paper; Fybex potassium titanate which was found compatible with 42% KOH at 250 F for up to 3000 hr; good agreement was found between bubble pressures predicted by an analytical study and those measured with filtered structures; Teflon-bonded Fybex matrices with bubble pressures greater than 30 psi were obtained by filtering a water slurry of the mixture directly onto fuel cell electrodes; and PBI fibers have satisfactory compatibility with 42% KOH at 250 F.

  13. Development of solid electrolytes for water electrolysis at higher temperature

    SciTech Connect

    Linkous, C.A.

    1996-10-01

    This report describes efforts in developing new solid polymer electrolytes that will enable operation of proton exchange membrane electrolyzers at higher temperatures than are currently possible. Several ionomers have been prepared from polyetheretherketone (PEEK), polyethersulfone (PES), and polyphenylquinoxaline (PPQ) by employing various sulfonation procedures. By controlling the extent of sulfonation, a range of proton conductivities could be achieved, whose upper limit actually exceeded that of commercially available perfluoralkyl sulfonates. Thermoconductimetric analysis of samples at various degrees of sulfonation showed an inverse relationship between conductivity and maximum operating temperature. This was attributed to the dual effect of adding sulfonate groups to the polymer: more acid groups produce more protons for increased conductivity, but they also increase water uptake, which mechanically weakens the membrane. This situation was exacerbated by the limited acidity of the aromatic sulfonic acids (pK{sub A} {approx} 2-3). The possibility of using partial fluorination to raise the acid dissociation constant is discussed.

  14. Method and apparatus for spatially uniform electropolishing and electrolytic etching

    DOEpatents

    Mayer, Steven T.; Contolini, Robert J.; Bernhardt, Anthony F.

    1992-01-01

    In an electropolishing or electrolytic etching apparatus the anode is separated from the cathode to prevent bubble transport to the anode and to produce a uniform current distribution at the anode by means of a solid nonconducting anode-cathode barrier. The anode extends into the top of the barrier and the cathode is outside the barrier. A virtual cathode hole formed in the bottom of the barrier below the level of the cathode permits current flow while preventing bubble transport. The anode is rotatable and oriented horizontally facing down. An extended anode is formed by mounting the workpiece in a holder which extends the electropolishing or etching area beyond the edge of the workpiece to reduce edge effects at the workpiece. A reference electrode controls cell voltage. Endpoint detection and current shut-off stop polishing. Spatially uniform polishing or etching can be rapidly performed.

  15. Method and apparatus for spatially uniform electropolishing and electrolytic etching

    DOEpatents

    Mayer, S.T.; Contolini, R.J.; Bernhardt, A.F.

    1992-03-17

    In an electropolishing or electrolytic etching apparatus the anode is separated from the cathode to prevent bubble transport to the anode and to produce a uniform current distribution at the anode by means of a solid nonconducting anode-cathode barrier. The anode extends into the top of the barrier and the cathode is outside the barrier. A virtual cathode hole formed in the bottom of the barrier below the level of the cathode permits current flow while preventing bubble transport. The anode is rotatable and oriented horizontally facing down. An extended anode is formed by mounting the workpiece in a holder which extends the electropolishing or etching area beyond the edge of the workpiece to reduce edge effects at the workpiece. A reference electrode controls cell voltage. Endpoint detection and current shut-off stop polishing. Spatially uniform polishing or etching can be rapidly performed. 6 figs.

  16. Electrochemical method of producing eutectic uranium alloy and apparatus

    DOEpatents

    Horton, J.A.; Hayden, H.W.

    1995-01-10

    An apparatus and method are disclosed for continuous production of liquid uranium alloys through the electrolytic reduction of uranium chlorides. The apparatus includes an electrochemical cell formed from an anode shaped to form an electrolyte reservoir, a cathode comprising a metal, such as iron, capable of forming a eutectic uranium alloy having a melting point less than the melting point of pure uranium, and molten electrolyte in the reservoir comprising a chlorine or fluorine containing salt and uranium chloride. The method of the invention produces an eutectic uranium alloy by creating an electrolyte reservoir defined by a container comprising an anode, placing an electrolyte in the reservoir, the electrolyte comprising a chlorine or fluorine containing salt and uranium chloride in molten form, positioning a cathode in the reservoir where the cathode comprises a metal capable of forming an uranium alloy having a melting point less than the melting point of pure uranium, and applying a current between the cathode and the anode. 2 figures.

  17. Studies on the thermal breakdown of common Li-ion battery electrolyte components

    SciTech Connect

    Lamb, Joshua; Orendorff, Christopher J.; Roth, Emanuel Peter; Langendorf, Jill Louise

    2015-08-06

    While much attention is paid to the impact of the active materials on the catastrophic failure of lithium ion batteries, much of the severity of a battery failure is also governed by the electrolytes used, which are typically flammable themselves and can decompose during battery failure. The use of LiPF6 salt can be problematic as well, not only catalyzing electrolyte decomposition, but also providing a mechanism for HF production. This work evaluates the safety performance of the common components ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) in the context of the gasses produced during thermal decomposition, looking at both the quantity and composition of the vapor produced. EC and DEC were found to be the largest contributors to gas production, both producing upwards of 1.5 moles of gas/mole of electrolyte. DMC was found to be relatively stable, producing very little gas regardless of the presence of LiPF6. EMC was stable on its own, but the addition of LiPF6 catalyzed decomposition of the solvent. As a result, while gas analysis did not show evidence of significant quantities of any acutely toxic materials, the gasses themselves all contained enough flammable components to potentially ignite in air.

  18. Frequency of Electrolyte Derangement after Transurethral Resection of Prostate: Need for Postoperative Electrolyte Monitoring

    PubMed Central

    Aziz, Wajahat; Ather, M. Hammad

    2015-01-01

    Objective. To determine the electrolyte derangement following transurethral resection of prostate (TURP). Methods. All patients undergoing TURP from June 2012 to April 2013 were included. Preoperative electrolytes were performed within a week of procedures. Monopolar TURP using 1.5% glycine was performed. Serum Na+ and K+ were assessed within 1 hour postoperatively and subsequently if clinically indicated. Results. The study included 280 patients. Sixty-six patients (23.6%) had electrolyte derangement after TURP. Patients with deranged electrolytes were older (mean age of 73.41 ± 4.08 yrs. versus 68.93 yrs. ± 10.34) and had a longer mean resection time (42.5 ± 20.04 min versus 28.34 ± 14.64 min). Mean weight of tissue resected (41.49 ± 34.46 g versus 15.33 ± 9.74 g) and volume of irrigant used (23.55 ± 15.20 L versus 12.81 ± 7.57 L) were also significantly higher in patients with deranged electrolytes (all p = 0.00). On multivariate logistic regression analysis preoperative sodium level was found to be a significant predictor of postoperative electrolyte derangement (odds ratio 0.267, S.E. = 0.376, and p value = 0.00). Conclusion. Electrolyte derangement occurs in older patients, with larger amount of tissue and longer time of resection and higher volume of irrigant, and in those with lower serum preoperative sodium levels. PMID:26089874

  19. Self-organized pattern formation of an atmospheric-pressure, ac glow discharge with an electrolyte electrode

    NASA Astrophysics Data System (ADS)

    Zheng, Peichao; Wang, Xiaomeng; Wang, Jinmei; Yu, Bin; Liu, Hongdi; Zhang, Bin; Yang, Rui

    2015-02-01

    An atmospheric-pressure plasma sustained by an ac power supply was generated using electrolyte solution as one of the electrodes. By altering the power supply, ring-like patterns, double-ring patterns and plasma-spot patterns were observed at the electrolyte-electrode surface. Synchronous current-voltage characteristics and time-resolved images were measured. Important factors for the self-organized patterns, including the electrode gap, power, frequency and electrolyte concentration, were explored. The optical spectrum characteristics of the device were investigated. The pH of the solution after discharge was also explored and the results show that the pH of the solution is evidently reduced after the discharge, implying that acidic components are produced in the solution. This study provides an alternative discharge method for producing patterns on a water surface.

  20. STABLE HIGH CONDUCTIVITY BILAYERED ELECTROLYTES FOR LOW TEMPERATURE SOLID OXIDE FUEL CELLS

    SciTech Connect

    Eric D. Wachsman; Keith L. Duncan

    2002-03-31

    Solid oxide fuel cells (SOFCs) are the future of energy production in America. They offer great promise as a clean and efficient process for directly converting chemical energy to electricity while providing significant environmental benefits (they produce negligible hydrocarbons, CO, or NO{sub x} and, as a result of their high efficiency, produce about one-third less CO{sub 2} per kilowatt hour than internal combustion engines). Unfortunately, the current SOFC technology, based on a stabilized zirconia electrolyte, must operate in the region of 1000 C to avoid unacceptably high ohmic losses. These high temperatures demand (a) specialized (expensive) materials for the fuel cell interconnects and insulation, (b) time to heat up to the operating temperature and (c) energy input to arrive at the operating temperature. Therefore, if fuel cells could be designed to give a reasonable power output at low to intermediate temperatures tremendous benefits may be accrued. At low temperatures, in particular, it becomes feasible to use ferritic steel for interconnects instead of expensive and brittle ceramic materials such as those based on LaCrO{sub 3}. In addition, sealing the fuel cell becomes easier and more reliable; rapid startup is facilitated; thermal stresses (e.g., those caused by thermal expansion mismatches) are reduced; radiative losses ({approx}T{sup 4}) become minimal; electrode sintering becomes negligible and (due to a smaller thermodynamic penalty) the SOFC operating cycle (heating from ambient) would be more efficient. Combined, all these improvements further result in reduced initial and operating costs. The problem is, at lower temperatures the conductivity of the conventional stabilized zirconia electrolyte decreases to the point where it cannot supply electrical current efficiently to an external load. The primary objectives of the proposed research is to develop a stable high conductivity (> 0.05 S cm{sup -1} at {le} 550 C) electrolyte for lower

  1. Non-Newtonian stress in an electrolyte.

    PubMed

    Sherwood, J D

    2011-02-10

    Analogies are drawn between the dynamics of electrolyte solutions and those of dilute suspensions of charged colloidal particles. The viscosity of both electrolytes and suspensions is a function of the ionic concentration c and of the Peclet number Pe characterizing the ratio of applied shear rate that tends to deform the ionic charge clouds, to diffusion that allows them to relax back to equilibrium. In particular, previously published results on the rheology of colloidal suspensions ( Lever , D. A. J. Fluid Mech. 1979 , 92 , 421 - 433 ) imply not only that the Falkenhagen O(c(1/2)) electrical contribution to viscosity is shear thinning, as shown by H. Wada ( J. Stat. Mech.: Theory Exp. 2005 , P01001 ), but also that this contribution to the stress is elastic, with normal stress differences appearing at O(Pe(2)). In practice, the shear rates required for substantial departure from a Newtonian rheology are large, typically 10(9) s(-1).

  2. Glasslike behavior in aqueous electrolyte solutions.

    PubMed

    Turton, David A; Hunger, Johannes; Hefter, Glenn; Buchner, Richard; Wynne, Klaas

    2008-04-28

    When salts are added to water, generally the viscosity increases, suggesting that the ions increase the strength of the water's hydrogen-bond network. However, infrared pump-probe measurements on electrolyte solutions have found that ions have no influence on the rotational dynamics of water molecules, implying no enhancement or breakdown of the hydrogen-bond network. Here, we report optical Kerr effect and dielectric relaxation spectroscopic measurements, which have enabled us to separate the effects of rotational and transitional motions of the water molecules. These data show that electrolyte solutions behave like a supercooled liquid approaching a glass transition in which rotational and translational molecular motions are decoupled. It is now possible to understand previously conflicting viscosity data, nuclear magnetic resonance relaxation, and ultrafast infrared spectroscopy in a single unified picture.

  3. Electrolyte compositions for lithium ion batteries

    DOEpatents

    Sun, Xiao-Guang; Dai, Sheng; Liao, Chen

    2016-03-29

    The invention is directed in a first aspect to an ionic liquid of the general formula Y.sup.+Z.sup.-, wherein Y.sup.+ is a positively-charged component of the ionic liquid and Z.sup.- is a negatively-charged component of the ionic liquid, wherein Z.sup.- is a boron-containing anion of the following formula: ##STR00001## The invention is also directed to electrolyte compositions in which the boron-containing ionic liquid Y.sup.+Z.sup.- is incorporated into a lithium ion battery electrolyte, with or without admixture with another ionic liquid Y.sup.+X.sup.- and/or non-ionic solvent and/or non-ionic solvent additive.

  4. Functional electrolyte for lithium-ion batteries

    SciTech Connect

    Zhang, Lu; Zhang, Zhengcheng; Amine, Khalil

    2015-04-14

    Functional electrolyte solvents include compounds having at least one aromatic ring with 2, 3, 4 or 5 substituents, at least one of which is a substituted or unsubstituted methoxy group, at least one of which is a tert-butyl group and at least one of which is a substituted or unsubstituted polyether or poly(ethylene oxide) (PEO) group bonded through oxygen to the aromatic ring, are provided.

  5. Solid acids as fuel cell electrolytes.

    PubMed

    Haile, S M; Boysen, D A; Chisholm, C R; Merle, R B

    2001-04-19

    Fuel cells are attractive alternatives to combustion engines for electrical power generation because of their very high efficiencies and low pollution levels. Polymer electrolyte membrane fuel cells are generally considered to be the most viable approach for mobile applications. However, these membranes require humid operating conditions, which limit the temperature of operation to less than 100 degrees C; they are also permeable to methanol and hydrogen, which lowers fuel efficiency. Solid, inorganic, acid compounds (or simply, solid acids) such as CsHSO4 and Rb3H(SeO4)2 have been widely studied because of their high proton conductivities and phase-transition behaviour. For fuel-cell applications they offer the advantages of anhydrous proton transport and high-temperature stability (up to 250 degrees C). Until now, however, solid acids have not been considered viable fuel-cell electrolyte alternatives owing to their solubility in water and extreme ductility at raised temperatures (above approximately 125 degrees C). Here we show that a cell made of a CsHSO4 electrolyte membrane (about 1.5 mm thick) operating at 150-160 degrees C in a H2/O2 configuration exhibits promising electrochemical performances: open circuit voltages of 1.11 V and current densities of 44 mA cm-2 at short circuit. Moreover, the solid-acid properties were not affected by exposure to humid atmospheres. Although these initial results show promise for applications, the use of solid acids in fuel cells will require the development of fabrication techniques to reduce electrolyte thickness, and an assessment of possible sulphur reduction following prolonged exposure to hydrogen.

  6. Fluid and Electrolyte Balance model (FEB)

    NASA Technical Reports Server (NTRS)

    Fitzjerrell, D. G.

    1973-01-01

    The effects of various oral input water loads on solute and water distribution throughout the body are presented in the form of a model. The model was a three compartment model; the three compartments being plasma, interstitial fluid and cellular fluid. Sodium, potassium, chloride and urea were the only major solutes considered explicitly. The control of body water and electrolyte distribution was affected via drinking and hormone levels.

  7. Grain Boundary Effects in Solid Oxide Electrolytes

    NASA Astrophysics Data System (ADS)

    Ng, Mai

    Ion conducting ceramics are essential in applications such as solid oxide fuel cells and oxygen sensors. Traditional 8 mol% yttria-stabilized zirconia (8YSZ) solid oxide electrolytes operate at high temperatures (850°C-1000°C) to achieve high ionic conductivity (> 0.1 Scm-1 at 1000°C) by oxygen ion diffusion via vacancies. Operation at such temperatures requires high temperature electrode materials and shortens device lifetime due to interdiffusion and reactions at electrode/electrolyte interfaces. These concerns drive research in current systems and alternative materials to improve ionic conductivity at reduced operating temperatures. This research considers how grain size and grain boundary phases affect three electrolyte materials with different ion diffusion mechanisms. First, the conductivity of ultra-fine grained two-step sintered and large grained conventional sintered 8YSZ are compared to determine if enhanced ionic conductivity occurs supporting the theory that ion blocking impurities in grain boundaries are diluted with decreasing grain size. Second, apatite-type lanthanide silicates (Ln9.33(SiO4)6O2) which exhibit anisotropic interstitial oxygen diffusion at intermediate temperatures (400°C-800°C) are studied to determine whether grain boundaries detrimentally affect conductivity. Lastly, proton conducting La-monazite (LaPO4) is evaluated to determine the role of Sr-doping (up to 10% substitution of La with Sr) on grain size and conductivity as well as the effect of sintering in air or water vapor on the formation of intergranular phases rich in Sr and P. This research investigates grain boundary effects in three solid oxide electrolyte materials with the goal of understanding how grain boundaries affect ionic conductivity and the atomistic behavior governing these different diffusion mechanisms.

  8. Improved Liquid-Electrode/Solid-Electrolyte Cell

    NASA Technical Reports Server (NTRS)

    Bugga, Ratnakumar V.; Distefano, Salvador; Williams, Roger M.; Bankston, Clyde P.

    1990-01-01

    Organic liquid in cathode extends working life. Rechargeable solid-electrolyte electrochemical cell includes novel mixture of organic and inorganic materials in liquid cathode. Operates at temperature about 120 to 170 degrees C lower than sodium/sulfur cells. Offers energy density comparable to that of sodium/sulfur cells - about 10 Wh/kg - and suited to such applications as military systems and electric vehicles.

  9. ELECTROLYTIC CLADDING OF ZIRCONIUM ON URANIUM

    DOEpatents

    Wick, J.J.

    1959-09-22

    A method is presented for coating uranium with zircoalum by rendering the uranium surface smooth and oxidefree, immersing it in a molten electrolytic bath in NaCI, K/sub 2/ZrF/sub 6/, KF, and ZrO/sub 2/, and before the article reaches temperature equilibrium with the bath, applying an electrolyzing current of 60 amperes per square dectmeter at approximately 3 volts to form a layer of zirconium metal on the uranium.

  10. Electrolyte reservoir for carbonate fuel cells

    DOEpatents

    Iacovangelo, C.D.; Shores, D.A.

    1984-05-23

    An electrode for a carbonate fuel cell and method of making same are described wherein a substantially uniform mixture of an electrode-active powder and porous ceramic particles suitable for a carbonate fuel cell are formed into an electrode with the porous ceramic particles having pores in the range of from about 1 micron to about 3 microns, and a carbonate electrolyte is in the pores of the ceramic particles.

  11. Electrolyte reservoir for carbonate fuel cells

    DOEpatents

    Iacovangelo, Charles D.; Shores, David A.

    1985-01-01

    An electrode for a carbonate fuel cell and method of making same wherein a substantially uniform mixture of an electrode-active powder and porous ceramic particles suitable for a carbonate fuel cell are formed into an electrode with the porous ceramic particles having pores in the range of from about 1 micron to about 3 microns, and a carbonate electrolyte is in the pores of the ceramic particles.

  12. Anti-perovskite solid electrolyte compositions

    SciTech Connect

    Zhao, Yusheng; Daemen, Luc Louis

    2015-12-26

    Solid electrolyte antiperovskite compositions for batteries, capacitors, and other electrochemical devices have chemical formula Li.sub.3OA, Li.sub.(3-x)M.sub.x/2OA, Li.sub.(3-x)N.sub.x/3OA, or LiCOX.sub.zY.sub.(1-z), wherein M and N are divalent and trivalent metals respectively and wherein A is a halide or mixture of halides, and X and Y are halides.

  13. Correlations Between Electrolyte Concentration and Solid Electrolyte Interphase Composition in Electrodeposited Lithium.

    PubMed

    Jeong, Soon-Ki; Kim, Jin Hee; Jeong, Yoon-Taek; Kim, Yang Soo

    2016-03-01

    This study examined the electrochemical deposition and dissolution of lithium on nickel electrodes in propylene carbonate (PC) electrolytes containing different concentrations of lithium salts, including LiN(SO2C2F5)2 or LiPF6. The electrode reactions were significantly affected by the electrolyte concentration. The cyclability of the electrodes was considerably improved by increasing the electrolyte concentration. X-ray photoelectron spectroscopy (XPS) showed that the composition of the solid electrolyte interphase (SEI) was also affected by the electrolyte concentration. The SEI formed in the 1st cycle consisted mainly of LiF in 1 and 2.15 M LiN(SO2C2F5)2/PC solutions. After the 30th cycle in the former solution, there was a large decrease in the amount of LiF and a large increase in the amount of LiOH. On the other hand, in the latter solution there was a smaller decrease and a smaller increase in the amount of LiF and LiOH, respectively, as compared to the former solution after the 30th cycle. PMID:27455758

  14. Ionic Conduction Mechanism of Polymer Gel Electrolytes

    NASA Astrophysics Data System (ADS)

    Saito, Yuria; Kataoka, Hiroshi

    2002-12-01

    Carrier migration mechanism of polymer gel electrolyte for lithium secondary batteries was investigated through the dynamic behavior of diffusion coefficient and conductivity. The gel prepared with PEO showed a homogeneous structure with any fraction of the electrolyte solution. The diffusion coefficient of the ionic species decreased with the increase in the polymer fraction in the gel. Cation migration is closely associated with the polymer, showing the reduced activation energy for diffusion with polymer in contrast to the increasing feature of the activation energy of the anion diffusion. The PVDF-gel electrolytes have a solid solubility limit due to the swelling saturation. The excess solution was then trapped in the cavities of the swollen polymer network. As a result, the diffusion showed two components. One is the fast migration of the carriers similar to that in the solution and the other is the relatively slow migration in the swollen region. The latter was influenced by the polymer due to the physical blocking and chemical interactive effects.

  15. A new perturbation theory for electrolyte solutions

    NASA Astrophysics Data System (ADS)

    Drunsel, F.; Zmpitas, W.; Gross, J.

    2014-08-01

    Developing physically based equations of state for electrolyte solutions is demanding due to the long range behaviour of the Coulombic interaction potentials. In this work, we present a new perturbation approach for nonprimitive model electrolyte solutions consisting of hard spheres with a positive or negative point charge or with point dipoles. We overcome the problem of diverging correlation integrals by separating the interaction potentials into short ranged parts and a long ranged contribution. For the point charges, the division is done like in most implementations of the Ewald sum. The perturbation expansion to 3rd order is formulated using the short ranged part of the potentials only, which results in converging correlation integrals for which we provide simple analytical expressions. The long range contribution to the Helmholtz energy is taken into account by a analytical term that has recently been presented by Rodgers and Weeks [J. M. Rodgers and J. D. Weeks, J. Chem. Phys. 131, 244108 (2009)]. In order to assess the proposed theory, we present molecular simulation data for Helmholtz energies of the same model electrolyte solutions. Predictions for the Helmholtz energy from the new theory are found to be in very good agreement with results from the molecular simulations for all state points we regarded.

  16. Hindered Glymes for Graphite-Compatible Electrolytes.

    PubMed

    Shanmukaraj, Devaraj; Grugeon, Sylvie; Laruelle, Stephane; Armand, Michel

    2015-08-24

    Organic carbonate mixtures are used almost exclusively as lithium battery electrolyte solvents. The linear compounds (dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate) act mainly as thinner for the more viscous and high-melting ethylene carbonate but are the least stable component and have low flash points; these are serious handicaps for lifetime and safety. Polyethers (glymes) are useful co-solvents, but all formerly known representatives solvate Li(+) strongly enough to co-intercalate in the graphite negative electrode and exfoliate it. We have put forward a new electrolyte composition comprising a polyether to which a bulky tert-butyl group is attached ("hindered glyme"), thus completely preventing co-intercalation while maintaining good conductivity. This alkyl-carbonate-free electrolyte shows remarkable cycle efficiency of the graphite electrode, not only at room temperature, but also at 50 and 70 °C in the presence of lithium bis(fluorosulfonimide). The two-ethylene-bridge hindered glyme has a high boiling point and a flash point of 80 °C, a considerable advantage for safety.

  17. Hindered Glymes for Graphite-Compatible Electrolytes.

    PubMed

    Shanmukaraj, Devaraj; Grugeon, Sylvie; Laruelle, Stephane; Armand, Michel

    2015-08-24

    Organic carbonate mixtures are used almost exclusively as lithium battery electrolyte solvents. The linear compounds (dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate) act mainly as thinner for the more viscous and high-melting ethylene carbonate but are the least stable component and have low flash points; these are serious handicaps for lifetime and safety. Polyethers (glymes) are useful co-solvents, but all formerly known representatives solvate Li(+) strongly enough to co-intercalate in the graphite negative electrode and exfoliate it. We have put forward a new electrolyte composition comprising a polyether to which a bulky tert-butyl group is attached ("hindered glyme"), thus completely preventing co-intercalation while maintaining good conductivity. This alkyl-carbonate-free electrolyte shows remarkable cycle efficiency of the graphite electrode, not only at room temperature, but also at 50 and 70 °C in the presence of lithium bis(fluorosulfonimide). The two-ethylene-bridge hindered glyme has a high boiling point and a flash point of 80 °C, a considerable advantage for safety. PMID:26212607

  18. Direct Lorentz force compensation flowmeter for electrolytes

    SciTech Connect

    Vasilyan, S. Froehlich, Th.

    2014-12-01

    A simplified method of contactless Lorentz force (LF) measurements for flow meters on electrolytes is described and realized. Modification and comparative representation are discussed against recently well-developed methods. Based on the catapult effect, that current carrying conductor experiences a repulsive force in a magnetic field, we demonstrate force measurement method of LF velocimetry applications by commonly known “electromagnetic force” compensation principle. Measurement approach through zero point stability is considered to minimize mechanical influences and avoid gravimetric uncertainties. Here, the current carrying wires are static fixed in the vicinity of magnet system at zero point stable position, while occurring deflection of magnets by electrolyte flow is compensated by external applied current within wires. Measurements performed by developed servo-system which drives control loop by means of optical position sensor for simplified (i) single wire and (ii) coil-like extended compensation schemes. Guided by experiments on electrolyte flow, we demonstrate the applicability of adopted principle for conductivities ranging from 2 to 20 S/m. Further improvements are discussed in agreement with the parameters of demonstration setup, straightforward theory, and experimental results. We argue that this method is potentially suitable for: (a) applications with higher conductivity like molten metal (order of 10{sup 6 }S/m) assuming spatial configuration of setup and (b) for lower range of conductivity (below 1 S/m) while this is strongly subject to stiffness of system and noise mainly mechanical and thermal radiations.

  19. Electrolytic pretreatment unit gaseous effluent conditioning

    NASA Technical Reports Server (NTRS)

    Colombo, G. V.; Putnam, D. F.

    1976-01-01

    The electrolytic pretreatment of urine is an advanced process that eliminates the need for handling and storing the highly corrosive chemicals that are normally used in water reclamation systems. The electrolytic pretreatment process also converts the organic materials in urine to gases (N2 and O2) that can be used to replenish those lost to space by leakage, venting, and air lock operations. The electrolytic process is more than a pretreatment, since it decreases the urine solids content by approximately one third, thus reducing the load and eventual solids storage requirements of the urine processing system. The evolved gases from the pretreatment step cannot, however, be returned directly to the atmosphere of a spacecraft without first removing several impurities including hydrogen, chlorine, and certain organic compounds. A treatment concept was developed that would decrease the impurities in the gas stream that emanates from an electrolysis unit to levels sufficiently low to allow the conditioned gas stream to be safely discharged to a spacecraft atmosphere. Two methods were experimentally demonstrated that can accomplish the desired cleanup. The bases of the two methods are, repectively: (1) raw urine scrubbing and (2) silica gel sorption.

  20. Direct Lorentz force compensation flowmeter for electrolytes

    NASA Astrophysics Data System (ADS)

    Vasilyan, S.; Froehlich, Th.

    2014-12-01

    A simplified method of contactless Lorentz force (LF) measurements for flow meters on electrolytes is described and realized. Modification and comparative representation are discussed against recently well-developed methods. Based on the catapult effect, that current carrying conductor experiences a repulsive force in a magnetic field, we demonstrate force measurement method of LF velocimetry applications by commonly known "electromagnetic force" compensation principle. Measurement approach through zero point stability is considered to minimize mechanical influences and avoid gravimetric uncertainties. Here, the current carrying wires are static fixed in the vicinity of magnet system at zero point stable position, while occurring deflection of magnets by electrolyte flow is compensated by external applied current within wires. Measurements performed by developed servo-system which drives control loop by means of optical position sensor for simplified (i) single wire and (ii) coil-like extended compensation schemes. Guided by experiments on electrolyte flow, we demonstrate the applicability of adopted principle for conductivities ranging from 2 to 20 S/m. Further improvements are discussed in agreement with the parameters of demonstration setup, straightforward theory, and experimental results. We argue that this method is potentially suitable for: (a) applications with higher conductivity like molten metal (order of 106 S/m) assuming spatial configuration of setup and (b) for lower range of conductivity (below 1 S/m) while this is strongly subject to stiffness of system and noise mainly mechanical and thermal radiations.

  1. Electrochemical capacitor of magnetite in aqueous electrolytes

    NASA Astrophysics Data System (ADS)

    Wu, Nae-Lih; Wang, Shi-Yu; Han, Chih-Yu; Wu, Dien-Shi; Shiue, Lih-Ren

    The capacitive behaviours of magnetite nanocrystallites, along with conductive carbon black additive, in aqueous electrolytes, including sodium sulphite, sulphate, chloride, and phosphate, and potassium hydroxide, have been characterised by means of cyclic voltammetry and chrono-potentiometry. The behaviour can be categorised into three groups. Sodium sulphate and chloride electrolytes give capacitances (˜5 F/g-Fe 3O 4) close to the space-charge capacitance of the oxide. Potassium hydroxide and sodium phosphate gave rise to a higher capacitance (˜7 F/g) which can in part be attributed to a surface redox reaction which involves hydroxide ions. Sodium sulphite results in the highest capacitances, which depend heavily on the dispersion of magnetite crystallites on the conductive matrix and range from ˜30 to 510 F/g-Fe 3O 4 with an operation voltage range of 1.2 V. Correlation between rest potential and anion-concentration gives strong indication of potential-determining process which involve either OH under extremely alkaline conditions (pOH<3) or SO 32- in the sulphite electrolyte.

  2. STABLE HIGH CONDUCTIVITY BILAYERED ELECTROLYTES FOR LOW TEMPERATURE SOLID OXIDE FUEL CELLS

    SciTech Connect

    Eric D. Wachsman; Keith L. Duncan

    2001-09-30

    Solid oxide fuel cells (SOFCs) are the future of energy production in America. They offer great promise as a clean and efficient process for directly converting chemical energy to electricity while providing significant environmental benefits (they produce negligible hydrocarbons, CO, or NO{sub x} and, as a result of their high efficiency, produce about one-third less CO{sub 2} per kilowatt hour than internal combustion engines). Unfortunately, the current SOFC technology, based on a stabilized zirconia electrolyte, must operate in the region of 1000 C to avoid unacceptably high ohmic losses. These high temperatures demand (a) specialized (expensive) materials for the fuel cell interconnects and insulation, (b) time to heat up to the operating temperature and (c) energy input to arrive at the operating temperature. Therefore, if fuel cells could be designed to give a reasonable power output at low to intermediate1 temperatures tremendous benefits may be accrued. At low temperatures, in particular, it becomes feasible to use ferritic steel for interconnects instead of expensive and brittle ceramic materials such as those based on LaCrO{sub 3}. In addition, sealing the fuel cell becomes easier and more reliable; rapid start-up is facilitated; thermal stresses (e.g., those caused by thermal expansion mismatches) are reduced; radiative losses ({approx}T{sup 4}) become minimal; electrode sintering becomes negligible and (due to a smaller thermodynamic penalty) the SOFC operating cycle (heating from ambient) would be more efficient. Combined, all these improvements further result in reduced initial and operating costs. The problem is, at lower temperatures the conductivity of the conventional stabilized zirconia electrolyte decreases to the point where it cannot supply electrical current efficiently to an external load. The primary objectives of the proposed research are to develop a stable high conductivity (> 0.05 S cm{sup -1} at {le} 550 C) electrolyte for lower

  3. High voltage electric double layer capacitor using a novel solid-state polymer electrolyte

    NASA Astrophysics Data System (ADS)

    Sato, Takaya; Marukane, Shoko; Morinaga, Takashi; Kamijo, Toshio; Arafune, Hiroyuki; Tsujii, Yoshinobu

    2015-11-01

    We designed and fabricated a bipolar-type electric double layer capacitor (EDLC) with a maximum 7.5 V operating voltage using a new concept in solid electrolytes. A cell having a high operating voltage, that is free from liquid leakage and is non-flammable is achieved by a bipolar design utilizing a solid polymer electrolyte made up of particles in a three-dimensional array, such as crystals composed of 75 wt% of hybrid particles decorated with a concentrated ionic liquid polymer brush (PSiP) and 25wt% of an ionic liquid (IL). The resulting solid film had sufficient physical strength and a high enough ionic conductivity to function as an electrolyte. Solidification as well as ionic conduction is due to the regular array of PSiPs, thereby producing a high ion-conductivity from a networked path between cores containing an appropriate amount of IL as a plasticizer. The demonstration cell shows a relatively good cycle durability and rate properties up to a 10C discharge process. It also has a very small leakage current in continuous charging and better self-discharge properties, even at 60 °C, compared with conventional cells. This paper demonstrates the first successful fabrication of a bipolar EDLC in a simple structure using this novel polymer solid electrolyte.

  4. Study of triallyl phosphate as an electrolyte additive for high voltage lithium-ion cells

    NASA Astrophysics Data System (ADS)

    Xia, J.; Madec, L.; Ma, L.; Ellis, L. D.; Qiu, W.; Nelson, K. J.; Lu, Z.; Dahn, J. R.

    2015-11-01

    The role of triallyl phosphate as an electrolyte additive in Li(Ni0.42Mn0.42Co0.16)O2/graphite pouch cells was studied using ex-situ gas measurements, ultra high precision coulometry, automated storage experiments, electrochemical impedance spectroscopy, long-term cycling and X-ray photoelectron spectroscopy. Cells containing triallyl phosphate produced less gas during formation, cycling and storage than control cells. The use of triallyl phosphate led to higher coulombic efficiency and smaller charge endpoint capacity slippage during ultra high precision charger testing. Cells containing triallyl phosphate showed smaller potential drop during 500 h storage at 40 °C and 60 °C and the voltage drop decreased as the triallyl phosphate content in the electrolyte increased. However, large amounts of triallyl phosphate (>3% by weight in the electrolyte) led to large impedance after cycling and storage. Symmetric cell studies showed large amounts of triallyl phosphate (5% or more) led to significant impedance increase at both negative and positive electrodes. X-ray photoelectron spectroscopy studies suggested that the high impedance came from the polymerization of triallyl phosphate molecules which formed thick solid electrolyte interphase films at the surfaces of both negative and positive electrodes. An optimal amount of 2%-3% triallyl phosphate led to better capacity retention during long term cycling.

  5. The reduction of nickelzirconia cermet anodes and the effects on supported thin electrolytes

    NASA Astrophysics Data System (ADS)

    Cassidy, M.; Lindsay, G.; Kendall, K.

    An important objective in the development of solid oxide fuel cells (SOFC) is to produce thin stabilized zirconia electrolytes that are supported upon the nickelzirconia cermet anode. Although this will reduce some of the problems associated with SOFCs by permitting lower temperature operation, this design may encounter problems during the cell start-up. The first step in a start-up involves the reduction of nickel oxide in the anode to metallic nickel and the volume change associated with this may damage the supported electrolyte. In this work, the effects of this reduction both on the anode and the supported electrolyte have been investigated. The findings show that the initial reduction does not seem to damage the cell, although an increase in volume with respect to the initial volume upon reoxidation of the anode cracks the electrolyte and will fracture the cell when constrained in an operational environment. The reason for this increase appears to be linked to the sintoring of the nickel while in its reduced state.

  6. Electrolytic method for the production of lithium using a lithium-amalgam electrode

    DOEpatents

    Cooper, John F.; Krikorian, Oscar H.; Homsy, Robert V.

    1979-01-01

    A method for recovering lithium from its molten amalgam by electrolysis of the amalgam in an electrolytic cell containing as a molten electrolyte a fused-salt consisting essentially of a mixture of two or more alkali metal halides, preferably alkali metal halides selected from lithium iodide, lithium chloride, potassium iodide and potassium chloride. A particularly suitable molten electrolyte is a fused-salt consisting essentially of a mixture of at least three components obtained by modifying an eutectic mixture of LiI-KI by the addition of a minor amount of one or more alkali metal halides. The lithium-amalgam fused-salt cell may be used in an electrolytic system for recovering lithium from an aqueous solution of a lithium compound, wherein electrolysis of the aqueous solution in an aqueous cell in the presence of a mercury cathode produces a lithium amalgam. The present method is particularly useful for the regeneration of lithium from the aqueous reaction products of a lithium-water-air battery.

  7. All-Polymer Electrolytic Tilt Sensor with Conductive Poly(dimethylsiloxane) Electrodes

    NASA Astrophysics Data System (ADS)

    Lee, June Kyoo; Choi, Ju Chan; Kong, Seong Ho

    2013-06-01

    In this study, an all-polymer electrolytic tilt sensor with conductive and corrosion-resistant poly(dimethylsiloxane) (PDMS) electrodes was designed and its performances were characterized. A PDMS cavity in the sensor for holding an electrolyte was fabricated by soft lithography using an ultraviolet-sensitive polymer. A conductive PDMS composite (gPDMS) with graphite powder was used for the electrode to measure the inclination angle of the electrolyte. A gPDMS composite with a graphite concentration above 40 wt % was able to function as a conductive polymer. The fabricated all-polymer tilt sensor exhibited a detectable inclination range of ± 60° and showed a relatively linear output signal compared with those exhibited by conventional micromachined tilt sensors with axis asymmetrical cavities. The maximum hysteresis of the output signal was approximately 0.1 V\\text{rms when the sensor repeatedly tilted and leveled off. In addition to the fundamental characterization of the sensor, various characteristics of the all-polymer tilt sensor, such as time-dependent and electrolyte-volume-dependent variations in the output signal, were investigated in this study. While the performance of the proposed sensor was comparable to that of conventional silicon-micromachined tilt sensors, the sensor could be produced at a fraction of the cost required to fabricate the conventional sensors.

  8. Novel poly(ethylene glycol) gel electrolytes prepared using self-assembled 1,3:2,4-dibenzylidene-D-sorbitol.

    PubMed

    Lai, Wei-Chi; Chen, Chien-Chu

    2014-01-14

    Gel electrolytes have usually been prepared by adding gelators or polymers to the liquid organic solvent-based electrolytes. In this study, we proposed a method to prepare gel electrolytes using gelators in liquid (low molecular weight) polymer-based electrolytes. Inexpensive 1,3:2,4-dibenzylidene-D-sorbitol (DBS) was chosen as a gelator for poly(ethylene glycol) (PEG)-based electrolytes at relatively low DBS concentrations. A series of gel electrolytes was produced by varying the DBS amounts, PEG molecular weights and PEG end groups. First, we found that DBS molecules self-assembled into 3-D networks consisting of nanofibrils that were approximately 10 nm in diameter, as measured by transmission electron microscopy; they exhibited spherulite-like morphologies under polarizing optical microscopy. Second, the dynamic rheological measurements demonstrated that the elastic modulus and the dissolution temperature of DBS-PEG gels increased with the increasing DBS content. The thermal degradation temperature of these gels also increased when the DBS concentration increased, as determined by thermogravimetric analysis. In addition, adding DBS may help to facilitate the dissolution of iodide and iodine in PEG due to its ether groups. Furthermore, the conductivity of the prepared DBS-PEG gel electrolytes was similar to that of the liquid PEG electrolytes (without DBS). When used in dye-sensitized solar cells (DSSC), the PEG-based electrolytes having inactive methyl end groups achieved the highest energy conversion efficiency among the tested cells. The efficiency of DSSC filled with our gel electrolytes remained basically the same over a one-month period, implying that the materials were relatively stable.

  9. Computer model for characterizing, screening, and optimizing electrolyte systems

    SciTech Connect

    Gering, Kevin L.

    2015-06-15

    Electrolyte systems in contemporary batteries are tasked with operating under increasing performance requirements. All battery operation is in some way tied to the electrolyte and how it interacts with various regions within the cell environment. Seeing the electrolyte plays a crucial role in battery performance and longevity, it is imperative that accurate, physics-based models be developed that will characterize key electrolyte properties while keeping pace with the increasing complexity of these liquid systems. Advanced models are needed since laboratory measurements require significant resources to carry out for even a modest experimental matrix. The Advanced Electrolyte Model (AEM) developed at the INL is a proven capability designed to explore molecular-to-macroscale level aspects of electrolyte behavior, and can be used to drastically reduce the time required to characterize and optimize electrolytes. Although it is applied most frequently to lithium-ion battery systems, it is general in its theory and can be used toward numerous other targets and intended applications. This capability is unique, powerful, relevant to present and future electrolyte development, and without peer. It redefines electrolyte modeling for highly-complex contemporary systems, wherein significant steps have been taken to capture the reality of electrolyte behavior in the electrochemical cell environment. This capability can have a very positive impact on accelerating domestic battery development to support aggressive vehicle and energy goals in the 21st century.

  10. Computer model for characterizing, screening, and optimizing electrolyte systems

    2015-06-15

    Electrolyte systems in contemporary batteries are tasked with operating under increasing performance requirements. All battery operation is in some way tied to the electrolyte and how it interacts with various regions within the cell environment. Seeing the electrolyte plays a crucial role in battery performance and longevity, it is imperative that accurate, physics-based models be developed that will characterize key electrolyte properties while keeping pace with the increasing complexity of these liquid systems. Advanced modelsmore » are needed since laboratory measurements require significant resources to carry out for even a modest experimental matrix. The Advanced Electrolyte Model (AEM) developed at the INL is a proven capability designed to explore molecular-to-macroscale level aspects of electrolyte behavior, and can be used to drastically reduce the time required to characterize and optimize electrolytes. Although it is applied most frequently to lithium-ion battery systems, it is general in its theory and can be used toward numerous other targets and intended applications. This capability is unique, powerful, relevant to present and future electrolyte development, and without peer. It redefines electrolyte modeling for highly-complex contemporary systems, wherein significant steps have been taken to capture the reality of electrolyte behavior in the electrochemical cell environment. This capability can have a very positive impact on accelerating domestic battery development to support aggressive vehicle and energy goals in the 21st century.« less

  11. LOW TEMPERATURE CATHODE SUPPORTED ELECTROLYTES

    SciTech Connect

    Harlan U. Anderson; Wayne Huebner; Igor Kosacki

    2000-09-30

    This project has three main goals: Thin Films Studies, Preparation of Graded Porous Substrates and Basic Electrical Characterization and testing of Planar Single Cells. During this time period substantial progress has been made in developing low temperature deposition techniques to produce dense, nanocrystalline yttrium-stabilized zirconia films on both dense oxide and polymer substrates. Microstructural changes in unsupported nanocrystalline yttrium stabilized zirconia (ZrO{sub 2}:16%Y, or YSZ) thin films were examined as a function of temperature and annealing time in order to determine the grain growth exponent and the mechanisms of pinhole formation. Grain growth and pinhole formation were measured using high resolution transmission electron microscopy (HRTEM), normal imaging mode transmission electron microscopy (TEM), electron diffraction, and energy dispersive X-ray microanalysis (EDS). Grain growth was found to vary with a time exponent of about one half before pinhole formation and about one third after. Pinhole formation in 70 nm thick films occurred at temperatures near 600 C, corresponding to a grain size of about 15 nm, or a grain size to film thickness ration of approximately 0.25. The deposition of films on porous substrates is hampered by the penetration of the polymer precursor solution into the substrate whose pores as > 0.2 {micro}m, therefore much attention has to be paid to the development of porous colloidal oxide films onto surfaces. Thus during this line period we have been studying these films. Optical properties have proven to be an excellent way to study the quality of these nanoporous films. The influence of porosity and densification on optical properties of films on sapphire substrates that were prepared from water colloidal suspensions of small ({approx}5nm) particles of ceria was investigated. The colloidal ceria films have initially very porous structure (porosity about 50%) and densification starts at about 600 C accompanied by

  12. Studies on the thermal breakdown of common Li-ion battery electrolyte components

    DOE PAGES

    Lamb, Joshua; Orendorff, Christopher J.; Roth, Emanuel Peter; Langendorf, Jill Louise

    2015-08-06

    While much attention is paid to the impact of the active materials on the catastrophic failure of lithium ion batteries, much of the severity of a battery failure is also governed by the electrolytes used, which are typically flammable themselves and can decompose during battery failure. The use of LiPF6 salt can be problematic as well, not only catalyzing electrolyte decomposition, but also providing a mechanism for HF production. This work evaluates the safety performance of the common components ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) in the context of the gasses producedmore » during thermal decomposition, looking at both the quantity and composition of the vapor produced. EC and DEC were found to be the largest contributors to gas production, both producing upwards of 1.5 moles of gas/mole of electrolyte. DMC was found to be relatively stable, producing very little gas regardless of the presence of LiPF6. EMC was stable on its own, but the addition of LiPF6 catalyzed decomposition of the solvent. As a result, while gas analysis did not show evidence of significant quantities of any acutely toxic materials, the gasses themselves all contained enough flammable components to potentially ignite in air.« less

  13. Microbial Electrolytic Carbon Capture for Carbon Negative and Energy Positive Wastewater Treatment.

    PubMed

    Lu, Lu; Huang, Zhe; Rau, Greg H; Ren, Zhiyong Jason

    2015-07-01

    Energy and carbon neutral wastewater management is a major goal for environmental sustainability, but current progress has only reduced emission rather than using wastewater for active CO2 capture and utilization. We present here a new microbial electrolytic carbon capture (MECC) approach to potentially transform wastewater treatment to a carbon negative and energy positive process. Wastewater was used as an electrolyte for microbially assisted electrolytic production of H2 and OH(-) at the cathode and protons at the anode. The acidity dissolved silicate and liberated metal ions that balanced OH(-), producing metal hydroxide, which transformed CO2 in situ into (bi)carbonate. Results using both artificial and industrial wastewater show 80-93% of the CO2 was recovered from both CO2 derived from organic oxidation and additional CO2 injected into the headspace, making the process carbon-negative. High rates and yields of H2 were produced with 91-95% recovery efficiency, resulting in a net energy gain of 57-62 kJ/mol-CO2 captured. The pH remained stable without buffer addition and no toxic chlorine-containing compounds were detected. The produced (bi)carbonate alkalinity is valuable for wastewater treatment and long-term carbon storage in the ocean. Preliminary evaluation shows promising economic and environmental benefits for different industries.

  14. Microbial Electrolytic Carbon Capture for Carbon Negative and Energy Positive Wastewater Treatment.

    PubMed

    Lu, Lu; Huang, Zhe; Rau, Greg H; Ren, Zhiyong Jason

    2015-07-01

    Energy and carbon neutral wastewater management is a major goal for environmental sustainability, but current progress has only reduced emission rather than using wastewater for active CO2 capture and utilization. We present here a new microbial electrolytic carbon capture (MECC) approach to potentially transform wastewater treatment to a carbon negative and energy positive process. Wastewater was used as an electrolyte for microbially assisted electrolytic production of H2 and OH(-) at the cathode and protons at the anode. The acidity dissolved silicate and liberated metal ions that balanced OH(-), producing metal hydroxide, which transformed CO2 in situ into (bi)carbonate. Results using both artificial and industrial wastewater show 80-93% of the CO2 was recovered from both CO2 derived from organic oxidation and additional CO2 injected into the headspace, making the process carbon-negative. High rates and yields of H2 were produced with 91-95% recovery efficiency, resulting in a net energy gain of 57-62 kJ/mol-CO2 captured. The pH remained stable without buffer addition and no toxic chlorine-containing compounds were detected. The produced (bi)carbonate alkalinity is valuable for wastewater treatment and long-term carbon storage in the ocean. Preliminary evaluation shows promising economic and environmental benefits for different industries. PMID:26076212

  15. Mixed organic compound-ionic liquid electrolytes for lithium battery electrolyte systems

    NASA Astrophysics Data System (ADS)

    Montanino, M.; Moreno, M.; Carewska, M.; Maresca, G.; Simonetti, E.; Lo Presti, R.; Alessandrini, F.; Appetecchi, G. B.

    2014-12-01

    The thermal, transport, rheological and flammability properties of electrolyte mixtures, proposed for safer lithium-ion battery systems, were investigated as a function of the mole composition. The blends were composed of a lithium salt (LiTFSI), organic solvents (namely EC, DEC) and an ionic liquid (PYR13TFSI). The main goal is to combine the fast ion transport properties of the organic compounds with the safe issues of the non-flammable and non-volatile ionic liquids. Preliminary tests in batteries have evidenced cycling performance approaching that observed in commercial organic electrolytes.

  16. Solid electrolyte for solid-state batteries: Have lithium-ion batteries reached their technical limit?

    NASA Astrophysics Data System (ADS)

    Kartini, Evvy; Manawan, Maykel

    2016-02-01

    , promise the potential to replace organic liquid electrolytes and thereby improve the safety of next-generation high-energy batteries. Li3PO4 has been proved to be a good candidate for solid electrolyte, due to its easy in preparation, low cost, high melting temperature and good compatibility with the electrode materials. In the present work, Li3PO4 has been prepared by wet chemical reaction, a simple method with the advantage of recycling a waste product H3PO4. The crystal structure has been characterized by both neutron and x-ray diffraction. The use of neutron scattering plays important role on observing the light atoms such as lithium ion. The x-ray diffraction results showed the crystal structure of orthorhombic phase P m n 21 (31), that belongs to the β-Li3PO4, with the lattice parameters are a = 6.123872, b = 5.250211, c = 4.876378. The conductivity of β-Li3PO4 was around 10-8 S/cm. Furthermore, the future application of the solid electrolyte layer in lithium ion battery will also be considered. It is concluded that the used of local resources on producing the solid electrolyte Li3PO4 for lithium ion battery will give more added values to the researches and national industry.

  17. Safer lithium ion batteries based on nonflammable electrolyte

    NASA Astrophysics Data System (ADS)

    Zeng, Ziqi; Wu, Bingbin; Xiao, Lifen; Jiang, Xiaoyu; Chen, Yao; Ai, Xinping; Yang, Hanxi; Cao, Yuliang

    2015-04-01

    The safety of lithium ion batteries has long been a critical obstacle for their high-power and large-scale applications because of the flammable nature of their carbon anode and organic carbonate electrolytes. To eliminate the potential safety hazards, lithium ion batteries should be built up with thermal-stable electrodes and nonflammable electrolytes. Here we report safer lithium ion batteries using nonflammable phosphonate electrolyte, thermal-stable LiFePO4 cathode and alloy anodes. Benefiting from the electrochemical compatibility and strong fire-retardancy of the phosphonate electrolyte, the cathode and anode materials in the nonflammable phosphonate electrolyte demonstrate similar charge-discharge performances with those in the conventional carbonate electrolyte, showing a great prospect for large-scale applications in electric vehicles and grid-scale electric energy storage.

  18. Theoretical and experimental study of mixed solvent electrolytes

    SciTech Connect

    Cummings, P.T.; O'Connell, J.P.

    1991-07-01

    The goals of the research program have evolved into the following: Molecular simulation of phase equilibria in aqueous and mixed solvent electrolyte solutions; molecular simulation of solvation and structure in supercritical aqueous systems; extension of experimental database on mixed solvent electrolytes; analysis of the thermodynamic properties of mixed solvent electrolyte solutions and mixed electrolyte solutions using fluctuation solution theory; development of analytic expressions for thermodynamic properties of mixed solvent electrolyte solutions using analytically solved integral equation approximations; and fundamental modeling of mixed solvent electrolytes using numerically solved integral equation approximation theories. We report and evaluate our progress during the period of the grant in light of these six goals in detail in this paper.

  19. Electrolyte matrix in a molten carbonate fuel cell stack

    DOEpatents

    Reiser, Carl A.; Maricle, Donald L.

    1987-04-21

    A fuel cell stack is disclosed with modified electrolyte matrices for limiting the electrolytic pumping and electrolyte migration along the stack external surfaces. Each of the matrices includes marginal portions at the stack face of substantially greater pore size than that of the central body of the matrix. Consequently, these marginal portions have insufficient electrolyte fill to support pumping or wicking of electrolyte from the center of the stack of the face surfaces in contact with the vertical seals. Various configurations of the marginal portions include a complete perimeter, opposite edge portions corresponding to the air plenums and tab size portions corresponding to the manifold seal locations. These margins will substantially limit the migration of electrolyte to and along the porous manifold seals during operation of the electrochemical cell stack.

  20. Electrolyte matrix in a molten carbonate fuel cell stack

    DOEpatents

    Reiser, C.A.; Maricle, D.L.

    1987-04-21

    A fuel cell stack is disclosed with modified electrolyte matrices for limiting the electrolytic pumping and electrolyte migration along the stack external surfaces. Each of the matrices includes marginal portions at the stack face of substantially greater pore size than that of the central body of the matrix. Consequently, these marginal portions have insufficient electrolyte fill to support pumping or wicking of electrolyte from the center of the stack of the face surfaces in contact with the vertical seals. Various configurations of the marginal portions include a complete perimeter, opposite edge portions corresponding to the air plenums and tab size portions corresponding to the manifold seal locations. These margins will substantially limit the migration of electrolyte to and along the porous manifold seals during operation of the electrochemical cell stack. 6 figs.

  1. Pharmacologic Approaches to Electrolyte Abnormalities in Heart Failure.

    PubMed

    Grodin, Justin L

    2016-08-01

    Electrolyte abnormalities are common in heart failure and can arise from a variety of etiologies. Neurohormonal activation from ventricular dysfunction, renal dysfunction, and heart failure medications can perturb electrolyte homeostasis which impact both heart failure-related morbidity and mortality. These include disturbances in serum sodium, chloride, acid-base, and potassium homeostasis. Pharmacological treatments differ for each electrolyte abnormality and vary from older, established treatments like the vaptans or acetazolamide, to experimental or theoretical treatments like hypertonic saline or urea, or to newer, novel agents like the potassium binders: patiromer and zirconium cyclosilicate. Pharmacologic approaches range from limiting electrolyte intake or directly repleting the electrolyte, to blocking or promoting their resorption, and to neurohormonal antagonism. Because of the prevalence and clinical impact of electrolyte abnormalities, understanding both the older and newer therapeutic options is and will continue to be necessity for the management of heart failure. PMID:27278221

  2. Boron compounds as anion binding agents for nonaqueous battery electrolytes

    DOEpatents

    Lee, Hung Sui; Yang, Xia-Oing; McBreen, James; Xiang, Caili

    2000-02-08

    Novel fluorinated boron-based compounds which act as anion receptors in non-aqueous battery electrolytes are provided. When added to non-aqueous battery electrolytes, the fluorinated boron-based compounds of the invention enhance ionic conductivity and cation transference number of non-aqueous electrolytes. The fluorinated boron-based anion receptors include borane and borate compounds bearing different fluorinated alkyl and aryl groups.

  3. Characterization of the Cathode Electrolyte Interface in Lithium Ion Batteries by Desorption Electrospray Ionization Mass Spectrometry.

    PubMed

    Liu, Yao-Min; G Nicolau, Bruno; Esbenshade, Jennifer L; Gewirth, Andrew A

    2016-07-19

    The solid electrolyte interface (SEI) formed via electrolyte decomposition on the anode of lithium ion batteries is largely responsible for the stable cycling of conventional lithium ion batteries. Similarly, there is a lesser-known analogous layer on the cathode side of a lithium ion battery, termed the cathode electrolyte interface (CEI), whose composition and role are debated. To confirm the existence and composition of the CEI, desorption electrospray ionization mass spectrometry (DESI-MS) is applied to study common lithium ion battery cathodes. We observe CEI formation on the LiMn2O4 cathode material after cycling between 3.5 and 4.5 V vs Li/Li(+) in electrolyte solution containing 1 M LiPF6 or LiClO4 in 1:1 (v/v) ethylene carbonate (EC) and dimethyl carbonate (DMC). Intact poly(ethylene glycol) dimethyl ether is identified as the electrolyte degradation product on the cathode surface by the high mass-resolution Orbitrap mass spectrometer. When EC is paired with ethyl methyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether, and poly(ethylene glycol) are found on the surface simultaneously. The presence of ethoxy and methoxy end groups indicates both methoxide and ethoxide are produced and involved in the process of oligomerization. Au surfaces cycled under different electrochemical windows as model systems for Li-ion battery anodes are also examined. Interestingly, the identical oligomeric species to those found in the CEI are found on Au surfaces after running five cycles between 2.0 and 0.1 V vs Li/Li(+) in half-cells. These results show that DESI-MS provides intact molecular information on battery electrodes, enabling deeper understanding of the SEI or CEI composition.

  4. Mechanism of hydrofluoric acid formation in ethylene carbonate electrolytes with fluorine salt additives

    NASA Astrophysics Data System (ADS)

    Tebbe, Jonathon L.; Fuerst, Thomas F.; Musgrave, Charles B.

    2015-11-01

    We utilized density functional theory to examine HF generation in lithium-ion battery electrolytes from reactions between H2O and the decomposition products of three electrolyte additives: LiPF6, LiPOF4, and LiAsF6. Decomposition of these additives produces PF5, AsF5, and POF3 along with LiF precipitates. We found PF5 and AsF5 react with H2O in two sequential steps to form two HF molecules and POF3 and AsOF3, respectively. PF5 (or AsF5) complexes with H2O and undergoes ligand exchange to form HF and PF4OH (AsF4OH) with an activation barrier of 114.2 (30.5) kJ mol-1 and reaction enthalpy of 14.6 (-11.3) kJ mol-1. The ethylene carbonate (EC) electrolyte forms a Lewis acid-base complex with the PF4OH (AsF4OH) product, reducing the barrier to HF formation. Reactions of POF3 were examined and are not characterized by complexation of POF3 with H2O or EC, while PF5 and AsF5 complex favorably with H2O and EC. HF formation from POF3 occurs with a reaction enthalpy of -3.8 kJ mol-1 and a 157.7 kJ mol-1 barrier, 43.5 kJ mol-1 higher than forming HF from PF5. HF generation in electrolytes employing LiPOF4 should be significantly lower than those using LiPF6 or LiAsF6 and LiPOF4 should be further investigated as an alternative electrolyte additive.

  5. Characterization of the Cathode Electrolyte Interface in Lithium Ion Batteries by Desorption Electrospray Ionization Mass Spectrometry.

    PubMed

    Liu, Yao-Min; G Nicolau, Bruno; Esbenshade, Jennifer L; Gewirth, Andrew A

    2016-07-19

    The solid electrolyte interface (SEI) formed via electrolyte decomposition on the anode of lithium ion batteries is largely responsible for the stable cycling of conventional lithium ion batteries. Similarly, there is a lesser-known analogous layer on the cathode side of a lithium ion battery, termed the cathode electrolyte interface (CEI), whose composition and role are debated. To confirm the existence and composition of the CEI, desorption electrospray ionization mass spectrometry (DESI-MS) is applied to study common lithium ion battery cathodes. We observe CEI formation on the LiMn2O4 cathode material after cycling between 3.5 and 4.5 V vs Li/Li(+) in electrolyte solution containing 1 M LiPF6 or LiClO4 in 1:1 (v/v) ethylene carbonate (EC) and dimethyl carbonate (DMC). Intact poly(ethylene glycol) dimethyl ether is identified as the electrolyte degradation product on the cathode surface by the high mass-resolution Orbitrap mass spectrometer. When EC is paired with ethyl methyl carbonate (EMC), poly(ethylene glycol) dimethyl ether, poly(ethylene glycol) ethyl methyl ether, and poly(ethylene glycol) are found on the surface simultaneously. The presence of ethoxy and methoxy end groups indicates both methoxide and ethoxide are produced and involved in the process of oligomerization. Au surfaces cycled under different electrochemical windows as model systems for Li-ion battery anodes are also examined. Interestingly, the identical oligomeric species to those found in the CEI are found on Au surfaces after running five cycles between 2.0 and 0.1 V vs Li/Li(+) in half-cells. These results show that DESI-MS provides intact molecular information on battery electrodes, enabling deeper understanding of the SEI or CEI composition. PMID:27346184

  6. An amino acid-electrolyte beverage may increase cellular rehydration relative to carbohydrate-electrolyte and flavored water beverages

    PubMed Central

    2014-01-01

    Background In cases of dehydration exceeding a 2% loss of body weight, athletic performance can be significantly compromised. Carbohydrate and/or electrolyte containing beverages have been effective for rehydration and recovery of performance, yet amino acid containing beverages remain unexamined. Therefore, the purpose of this study is to compare the rehydration capabilities of an electrolyte-carbohydrate (EC), electrolyte-branched chain amino acid (EA), and flavored water (FW) beverages. Methods Twenty men (n = 10; 26.7 ± 4.8 years; 174.3 ± 6.4 cm; 74.2 ± 10.9 kg) and women (n = 10; 27.1 ± 4.7 years; 175.3 ± 7.9 cm; 71.0 ± 6.5 kg) participated in this crossover study. For each trial, subjects were dehydrated, provided one of three random beverages, and monitored for the following three hours. Measurements were collected prior to and immediately after dehydration and 4 hours after dehydration (3 hours after rehydration) (AE = −2.5 ± 0.55%; CE = −2.2 ± 0.43%; FW = −2.5 ± 0.62%). Measurements collected at each time point were urine volume, urine specific gravity, drink volume, and fluid retention. Results No significant differences (p > 0.05) existed between beverages for urine volume, drink volume, or fluid retention for any time-point. Treatment x time interactions existed for urine specific gravity (USG) (p < 0.05). Post hoc analysis revealed differences occurred between the FW and EA beverages (p = 0.003) and between the EC and EA beverages (p = 0.007) at 4 hours after rehydration. Wherein, EA USG returned to baseline at 4 hours post-dehydration (mean difference from pre to 4 hours post-dehydration = -0.0002; p > 0.05) while both EC (-0.0067) and FW (-0.0051) continued to produce dilute urine and failed to return to baseline at the same time-point (p < 0.05). Conclusion Because no differences existed for fluid retention, urine or drink volume at any time point, yet USG returned to

  7. Method of synthesizing polymers from a solid electrolyte

    DOEpatents

    Skotheim, T.A.

    1984-10-19

    A method of synthesizing electrically conductive polymers from a solvent-free solid polymer electrolyte is disclosed. An assembly of a substrate having an electrode thereon, a thin coating of solid electrolyte including a solution of PEO complexed with an alkali salt, and a thin transparent noble metal electrode are disposed in an evacuated chamber into which a selected monomer vapor is introduced while an electric potential is applied across the solid electrolyte to hold the thin transparent electrode at a positive potential relative to the electrode on the substrate, whereby a highly conductive polymer film is grown on the transparent electrode between it and the solid electrolyte.

  8. Discharge Characteristics of Low Molecular Weight Solid Polymer Electrolyte

    NASA Astrophysics Data System (ADS)

    Kumar, P. Naveen; Sasikala, U.; Sekhar, P. Chandra; Achari, V. B. S.; Rao, V. V. R. N.; Sharma, A. K.

    2011-07-01

    Solid polymer electrolytes based on polyethylene glycol (PEG) complexed with sodium chloride (NaCl) at different weight percent ratios were prepared using solution cast technique. Measurement of DC conductivity in the temperature range 303-373 K shows that the conductivity increases with increase in concentration of salt and with increase in temperature. Transference number measurent has been employed to investigate the charge transport in the polymer electrolyte system. This data has shown that the charge transport in the polymer electrolyte system is predominantly due to ions. Using this polymer electrolyte, solid state electrochemical cells have been fabricated. Various cell parameters associated with these cells were evaluated and reported.

  9. Electrocatalysis of fuel cell reactions: Investigation of alternate electrolytes

    NASA Technical Reports Server (NTRS)

    Chin, D. T.; Hsueh, K. L.; Chang, H. H.

    1984-01-01

    Oxygen reduction and transport properties of the electrolyte in the phosphoric acid fuel cell are studied. The areas covered were: (1) development of a theoretical expression for the rotating ring disk electrode technique; (2) determination of the intermediate reaction rate constants for oxygen reduction on platinum in phosphoric acid electrolyte; (3) determination of oxygen reduction mechanism in trifluoreomethanesulfonic acid (TFMSA) which was considered as an alternate electrolyte for the acid fuel cells; and (4) the measurement of transport properties of the phosphoric acid electrolyte at high concentrations and temperatures.

  10. Short protection device for stack of electrolytic cells

    DOEpatents

    Katz, M.; Schroll, C.R.

    1984-11-29

    The present invention relates to a device for preventing the electrical shorting of a stack of electrolytic cells during an extended period of operation. The device has application to fuel cell and other electrolytic cell stacks operating in low or high temperature corrosive environments. It is of particular importance for use in a stack of fuel cells operating with molten metal carbonate electrolyte for the production of electric power. Also, the device may have application in similar technology involving stacks of electrolytic cells for electrolysis to decompose chemical compounds.

  11. Zinc halogen battery electrolyte composition with lead additive

    DOEpatents

    Henriksen, Gary L.

    1981-01-01

    This disclosure relates to a zinc halogen battery electrolyte composition containing an additive providing improved zinc-on-zinc recyclability. The improved electrolyte composition involves the use of a lead additive to inhibit undesirable irregular plating and reduce nodular or dendritic growth on the electrode surface. The lead-containing electrolyte composition of the present invention appears to influence not only the morphology of the base plate zinc, but also the morphology of the zinc-on-zinc replate. In addition, such lead-containing electrolyte compositions appear to reduce hydrogen formation.

  12. Carbonate fuel cell endurance: Hardware corrosion and electrolyte management status

    SciTech Connect

    Yuh, C.; Johnsen, R.; Farooque, M.; Maru, H.

    1993-05-01

    Endurance tests of carbonate fuel cell stacks (up to 10,000 hours) have shown that hardware corrosion and electrolyte losses can be reasonably controlled by proper material selection and cell design. Corrosion of stainless steel current collector hardware, nickel clad bipolar plate and aluminized wet seal show rates within acceptable limits. Electrolyte loss rate to current collector surface has been minimized by reducing exposed current collector surface area. Electrolyte evaporation loss appears tolerable. Electrolyte redistribution has been restrained by proper design of manifold seals.

  13. Carbonate fuel cell endurance: Hardware corrosion and electrolyte management status

    SciTech Connect

    Yuh, C.; Johnsen, R.; Farooque, M.; Maru, H.

    1993-01-01

    Endurance tests of carbonate fuel cell stacks (up to 10,000 hours) have shown that hardware corrosion and electrolyte losses can be reasonably controlled by proper material selection and cell design. Corrosion of stainless steel current collector hardware, nickel clad bipolar plate and aluminized wet seal show rates within acceptable limits. Electrolyte loss rate to current collector surface has been minimized by reducing exposed current collector surface area. Electrolyte evaporation loss appears tolerable. Electrolyte redistribution has been restrained by proper design of manifold seals.

  14. Method of synthesizing polymers from a solid electrolyte

    DOEpatents

    Skotheim, Terje A.

    1985-01-01

    A method of synthesizing electrically conductive polymers from a solvent-free solid polymer electrolyte wherein an assembly of a substrate having an electrode thereon, a thin coating of solid electrolyte including a solution of PEO complexed with an alkali salt, and a thin transparent noble metal electrode are disposed in an evacuated chamber into which a selected monomer vapor is introduced while an electric potential is applied across the solid electrolyte to hold the thin transparent electrode at a positive potential relative to the electrode on the substrate, whereby a highly conductive polymer film is grown on the transparent electrode between it and the solid electrolyte.

  15. Monitoring electrolyte concentrations in redox flow battery systems

    DOEpatents

    Chang, On Kok; Sopchak, David Andrew; Pham, Ai Quoc; Kinoshita, Kimio

    2015-03-17

    Methods, systems and structures for monitoring, managing electrolyte concentrations in redox flow batteries are provided by introducing a first quantity of a liquid electrolyte into a first chamber of a test cell and introducing a second quantity of the liquid electrolyte into a second chamber of the test cell. The method further provides for measuring a voltage of the test cell, measuring an elapsed time from the test cell reaching a first voltage until the test cell reaches a second voltage; and determining a degree of imbalance of the liquid electrolyte based on the elapsed time.

  16. Non-aqueous electrolyte for high voltage rechargeable magnesium batteries

    DOEpatents

    Doe, Robert Ellis; Lane, George Hamilton; Jilek, Robert E; Hwang, Jaehee

    2015-02-10

    An electrolyte for use in electrochemical cells is provided. The properties of the electrolyte include high conductivity, high Coulombic efficiency, and an electrochemical window that can exceed 3.5 V vs. Mg/Mg.sup.+2. The use of the electrolyte promotes the electrochemical deposition and dissolution of Mg without the use of any Grignard reagents, other organometallic materials, tetraphenyl borate, or tetrachloroaluminate derived anions. Other Mg-containing electrolyte systems that are expected to be suitable for use in secondary batteries are also described.

  17. Theoretical and experimental study of mixed solvent electrolytes

    SciTech Connect

    Cummings, P.T.; O'Connell, J.P.

    1990-01-01

    In the original proposal to study mixed solvent electrolyte solutions, four major goals were formulated: fundamental modeling of mixed solvent electrolytes using numerically solved integral equation approximation theories; evaluation of intermolecular pair potential models by computer simulation of selected systems for comparison with experiment and the numerical integral equation studies; development of fundamentally based correlations for the thermodynamic properties of mixed solvent electrolyte solutions using analytically solvable statistical mechanical models; and extension of experimental database on mixed solvent electrolytes by performing vapor-liquid equilibrium measurements on selected systems. This paper discusses the progress on these goals.

  18. Characteristics of aluminium solid electrolytic capacitors using a conducting polymer

    NASA Astrophysics Data System (ADS)

    Yamamoto, Hideo; Oshima, Masashi; Fukuda, Minoru; Isa, Isao; Yoshino, Katsumi

    In order to form an electrochemically polymerized polypyrrole film on an electrically insulated dielectric layer surface, a conductive precoating layer was first deposited, at the expense of electrical conductivity. Using the precoating layer as the anode, a polypyrrole layer was then deposited electrochemically in preparation for the fabrication of a solid electrolytic capacitor in which the composite conducting polymer layer was used as a solid electrolyte. Soluble polyaniline could be used as a conductive precoating layer as well as polypyrrole formed by chemical oxidizing polymerization. The capacitor using the composite solid electrolyte presented excellent impedance frequency and temperature characteristics; moreover, the solid electrolyte showed 'self-healing' and non-polar behaviour.

  19. Ionic Transport Across Interfaces of Solid Glass and Polymer Electrolytes

    SciTech Connect

    Tenhaeff, Wyatt E; Yu, Xiang; Hong, Kunlun; Perry, Kelly A; Dudney, Nancy J

    2011-01-01

    A study of lithium cation transport across solid-solid electrolyte interfaces to identify critical resistances in nanostructured solid electrolytes is reported. Bilayers of glass and polymer thin film electrolytes were fabricated and characterized for this study. The glass electrolyte was lithium phosphorous oxynitride (Lipon), and two polymer electrolytes were studied: poly(methyl methacrylate-co-poly(ethylene glycol) methyl ether methacrylate) and poly(styrene-co-poly(ethylene glycol) methyl ether methacrylate). Both copolymers contained LiClO{sub 4} salt. In bilayers where polymer electrolyte layers are fabricated on top of Lipon, the interfacial resistance dominates transport. At 25 C, the interfacial resistance is at least three times greater than the sum of the Lipon and polymer electrolyte resistances. By reversing the structure and fabricating Lipon on top of the polymer electrolytes, the interfacial resistance is eliminated. Experiments to elucidate the origin of the interfacial resistance in the polymer-on-Lipon bilayers reveal that the solvent mixtures used to fabricate the polymer layers do not degrade the Lipon layer. The importance of the polymer electrolytes' mechanical properties is also discussed.

  20. Fluid and electrolyte therapy in ruminants.

    PubMed

    Constable, Peter

    2003-11-01

    Five important questions always must be asked and answered regarding fluid and electrolyte therapy in ruminants: (1) Is therapy needed? (2) What type of therapy? (3) What route of administration? (4) How much should be administered? and (5) How fast should the solution be administered? Food animal veterinarians routinely should carry the following commercially available crystalloid solutions and have the knowledge of how to use the products appropriately: Ringer's solution, 1.3% NaHCO3, acetated Ringer's solution, HS (7.2% NaCl), 8% NaHCO3, 23% calcium gluconate, calcium-magnesium solutions, and 50% dextrose. Ruminants with a blood pH less than 7.20 should be treated intravenously with 1.3% or 8.0% NaHCO3, and those animals with a blood pH greater than 7.45 should be treated intravenously with Ringer's solution. Oral electrolyte solutions or intravenous acetated Ringer's solution should be administered to ruminants with a blood pH greater than 7.20 but less than 7.45, and acetated Ringer's solution is preferred to lactated Ringer's solution. HS solution should be administered whenever rapid resuscitation is required. Oral administration of electrolyte solutions is underused in neonatal and adult ruminants. The optimal solution for oral administration to neonatal ruminants has a sodium concentration between 90 and 130 mmol/L; a potassium concentration between 10 and 20 mmol/L; a chloride concentration between 40 and 80 mmol/L; 40 to 80 mmol/L of metabolizable (nonbicarbonate) base, such as acetate or propionate; and glucose as an energy source. The optimal formulation for adult ruminants is unknown, but such a solution should contain sodium, potassium, calcium, magnesium, phosphate, and propionate to facilitate sodium absorption and to provide an additional source of energy to the animal. Acidemia is treated best by intravenous or oral administration of NaHCO3. Alkalemia is treated best by intravenous administration of Ringer's solution and oral administration of

  1. Investigation of a novel ternary electrolyte based on dimethyl sulfite and lithium difluoromono(oxalato)borate for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Chen, Renjie; Zhu, Lu; Wu, Feng; Li, Li; Zhang, Rong; Chen, Shi

    2014-01-01

    Lithium difluoromono(oxalato)borate (LiODFB) has been used as a novel lithium salt for battery in recent studies. In this study, a series of novel electrolytes has been prepared by adding 30 vol% dimethyl sulfite (DMS) or dimethyl carbonate (DMC) as co-solvent into an ethylene carbonate (EC)/ethyl methyl carbonate (EMC) + LiX mixture, in which the LiX could be LiClO4, LiODFB, LiBOB, LiTFSI, or LiCF3SO3. These ternary electrolytes have been investigated for use in lithium ion batteries. FT-IR spectroscopy analysis shows that characteristic functional groups (-CO3, -SO3) undergo red-shift or blue-shift with the addition of different lithium salts. The LiODFB-EC/EMC/DMS electrolyte exhibits high ionic conductivity, which is mainly because of the low melting point of DMS, and LiODFB possessing high solubility. The Li/MCMB cells containing this novel electrolyte exhibit high capacities, good cycling performance, and excellent rate performance. These performances are probably because both LiODFB and DMS can assist in the formation of SEI films by reductive decomposition. Additionally, the discharge capacity of Li/LiCoO2 half cell containing LiODFB-EC/EMC/DMS electrolyte is 130.9 mAh g-1 after 50 cycles, and it is very comparable with the standard-commercial electrolyte. The results show that this study produces a promising electrolyte candidate for lithium ion batteries.

  2. Application of the thin electrolyte layer technique to corrosion testing of dental materials

    NASA Astrophysics Data System (ADS)

    Ledvina, Martin

    activity of pores and seemed to produce an inhibitive action against localized corrosion. The same trends were observed in human saliva. To clarify the mechanisms of protein-surface interaction, electrochemical impedance spectroscopy (EIS) was employed with the same alloy-electrolyte combinations. Based on the results, it was hypothesized that proteins are adsorbed to the anodic areas where pits may be forming or casting porosity exists. The electrostatic interaction and affinity of proteins for metallic ions plays a significant role. The absorbed macromolecules physically block transport of reactants to and from the interface and slow down the corrosion reaction appreciably. Overall, this investigation contributed to the further understanding of the electrochemistry of the oral environment, particularly the contribution of proteinaceous species.

  3. Interface Engineering of Garnet Solid Electrolytes

    NASA Astrophysics Data System (ADS)

    Cheng, Lei

    Solid lithium ion conductors represent a promising class of materials for next generation high energy density batteries, with the potential for enabling use of high capacity Li metal anodes and providing opportunities for novel lithium-free cathode materials. However, highly resistive interfaces stymie their practical use. This urgent scientific challenge requires mechanistic understanding of ion transport at interfaces, as well as development of novel processes to achieve low interfacial resistances. The goal of this PhD dissertation was to generate fundamental understandings of garnet-structured Al substituted Li7La3Zr2O 12 (LLZO) electrolyte surfaces and interfaces with lithium metal electrodes. Specifically in this research, the topmost surface microstructure, local chemical environment, and surface chemistry were carefully studied. The ceramic processing of garnet is discussed and ways to control the sintering behavior and microstructures were explored and successfully demonstrated. Factors contributing to high interfacial resistance were systematically studied. The source of the high interfacial impedance has been traced to the presence of Li2CO 3 on pellet surfaces resulting from air exposure after processing. In addition, it was discovered that surface grain boundaries are surprisingly fast ion transport pathways and surface microstructure is critically important to lithium ion transport at interfaces. Complex homo- and heterostructured LLZO solid electrolytes with controllable surface and bulk microstructures were successfully fabricated, which allowed the comparison and separation of the contribution from the surface and the bulk. Engineered pellet surfaces allowed us to achieve the lowest interfacial resistance ever reported for this composition, resulting in significantly improved cycling behavior. Lastly, it was found that LLZO surfaces can be effectively stabilized under air exposure conditions, preventing Li2CO3 formation and maintaining low

  4. Electrolytic decontamination of the 3013 inner can

    SciTech Connect

    Wedman, D.E.; Nelson, T.O.; Rivera, Y.; Weisbrod, K.; Martinez, H.E.; Limback, S.

    1998-12-31

    Disposition of plutonium recovered from nuclear weapons or production residues must be stored in a manner that ensures safety. The criteria that has been established to assure the safety of stored materials for a minimum of 50 years is DOE-STD-3013. This standard specifies both the requirements for containment and furthermore specifies that the inner container be decontaminated to a level of {le}20 dpm/100 cm{sup 2} swipable and {le}500 dpm/100 cm{sup 2} direct alpha such that a failure of the outer containment barrier will have a lower probability of resulting in a spread of contamination. The package consists of an optional convenience (food pack) can, a welded type 304L stainless steel inner (primary) can, and a welded type 304L stainless steel outer (secondary) can. Following the welding process, the can is checked for leaks and then sent down the line for decontamination. Once decontaminated, the sealed primary can may be removed from the glove box line. Welding of the secondary container takes place outside the glove box line. The highly automated decontamination process that has been developed to support the packaging of Special Nuclear Materials is based on an electrolytic process similar to the wide spread industrial technique of electropolishing. The can is placed within a specially designed stainless steel fixture built within a partition of a glove box. The passage of current through this electrolytic cell results in a uniform anodic dissolution of the surface metal layers of the can. This process results in a rapid decontamination of the can. The electrolyte is fully recyclable, and the separation of the chromium from the actinides results in a compact, non RCRA secondary waste product.

  5. Cantera and Cantera Electrolyte Thermodynamics Objects

    2015-10-19

    Cantera is a suite of object-oriented software tools for problems involving chemical kinetics, thermodynamics, and/or transport processes. It is a multi-organizational effort to create and formulate high quality 0D and 1D constitutive modeling tools for reactive transport codes.Institutions involved with the effort include Sandia, MIT, Colorado School of Mines, U. Texas, NASA, and Oak Ridge National Labs. Specific to Sandia’s contributions, the Cantera Electrolyte Thermo Objects (CETO) packages is comprised of add-on routines for Canteramore » that handle electrolyte thermochemistry and reactions within the overall Cantera package. Cantera is a C++ Cal Tech code that handles gas phase species transport, reaction, and thermodynamics. With this addition, Cantera can be extended to handle problems involving liquid phase reactions and transport in electrolyte systems, and phase equilibrium problemsinvolving concentrated electrolytes and gas/solid phases. A full treatment of molten salt thermodynamics and transport has also been implemented in CETO. The routines themselves consist of .cpp and .h files containing C++ objects that are derived from parent Cantera objects representing thermodynamic functions. They are linked unto the main Cantera libraries when requested by the user. As an addendum to the main thermodynamics objects, several utility applications are provided. The first is multiphase Gibbs free energy minimizer based on the vcs algorithm, called vcs_cantera. This code allows for the calculation of thermodynamic equilibrium in multiple phases at constant temperature and pressure. Note, a similar code capability exists already in Cantera. This version follows the same algorithm, but gas a different code-base starting point, and is used as a research tool for algorithm development. The second program, cttables, prints out tables of thermodynamic and kinetic information for thermodynamic and kinetic objects within Cantera. This program serves as a “Get the

  6. Nephrology/hypertension/fluid and electrolyte disorders.

    PubMed

    Slick, G L

    1993-01-01

    The following annotated bibliography has been developed for the purpose of providing to primary care physicians a handy source of review articles and major studies in the field of nephrology, hypertension, and fluid and electrolyte disorders. Almost all of the articles are review articles of clinical topics that would be of interest to the practicing physician. JAOA will be publishing additional annotated bibliographies in various fields of internal medicine over the next several months. The second in this series will appear in a forthcoming issue of THE JOURNAL.

  7. Polarization of anthracite electrodes in electrolyte solutions

    SciTech Connect

    A.N. Lopanov; E.V. Blaido; O.V. Smirnova

    2007-10-15

    The regularities of the polarization of anthractie electrodes for the liberation of hydrogen from electrolyte (potassium chloride and hydrogen chloride) solutions were found, and electrode processes occurring at the surface of coals in the Fe{sup 2+}/Fe{sup 3+} redox system were studied. It was found that the deviations of standard electrode potentials from the equilibrium values of redox systems depend on the exchange current densities of electrochemical processes occurring at the surface of coal matter. Low transfer coefficients (0.04-0.051) for the discharge reaction of hydrogen ions on anthracites indicate that the reaction occurs under conditions close to those of an activationless process.

  8. Electrolytic production of oxygen from lunar resources

    NASA Technical Reports Server (NTRS)

    Keller, Rudolf

    1991-01-01

    Some of the most promising approaches to extract oxygen from lunar resources involve electrochemical oxygen generation. In a concept called magma electrolysis, suitable oxides (silicates) which are molten at 1300 to 1500 C are then electrolyzed. Residual melt can be discarded after partial electrolysis. Alternatively, lunar soil may be dissolved in a molten salt and electrolyzed. In this approach, temperatures are lower and melt conductances higher, but electrolyte constituents need to be preserved. In a different approach ilmenite is reduced by hydrogen and the resulting water is electrolyzed.

  9. The Radioimmunoassay of Fluid and Electrolyte Hormones

    NASA Technical Reports Server (NTRS)

    Keil, Lanny C.

    1985-01-01

    The subject of the paper will be the assay of fluid/electrolyte hormones. ADH (antidiuretic hormone also referred to as vasopressin) reduces fluid loss by increasing water reabsorption by the kidney. The stimuli for its release from the pituitary are loss of blood, dehydration, or increased salt intake. Angiotensin II is the next hormone of interest. It is "generated" from a blood protein by the release of renin from the kidney. One of its functions is to stimulate the secretion of aldosterone from the adrenal gland. Release of renin is also stimulated by volume and sodium loss.

  10. Electrolyte additive for improved battery performance

    DOEpatents

    Bellows, Richard J.; Kantner, Edward

    1989-04-04

    In one embodiment of the present invention, there is provided an electrochemical cell having a metal bromine couple. The cell includes an electrode structure on which to deposit the metal of the couple and a counterelectrode at which to generate bromine. A microporous membrane separates the electrode and counterelectrode. Importantly, the aqueous electrolyte comprises an aqueous metal bromide solution containing a water soluble bromine complexing agent capable of forming a water immiscible complex with bromine and an additive capable of decreasing the wettability of the microporous separators employed in such cells by such water immiscible bromine complexes.

  11. Electrocatalysis issues in polymer electrolyte fuel cells

    NASA Astrophysics Data System (ADS)

    Wilson, M. S.; Derouin, C. R.; Valerio, J. A.; Gottesfeld, S.

    Various electrocatalysis issues of importance to low platinum loading polymer electrolyte fuel cells (PEFCs) are discussed. Thin film catalyst layer assemblies are used to investigate the effects of CO and CO2 on the anode as well as efforts to restore performance by oxygen bleeding into the anode feedstream. These electrodes behave differently than ionomer-impregnated E-TEK electrodes because of the extra, exposed Pt in the latter case. The tolerance of Pt-Ru alloy thin film anodes to CO and CO2 are also evaluated. Thin film electrodes are also used to study Pt particle growth in aged electrodes as well as particle size effects on specific activity.

  12. Cantera and Cantera Electrolyte Thermodynamics Objects

    SciTech Connect

    John Hewson, Harry Moffat

    2015-10-19

    Cantera is a suite of object-oriented software tools for problems involving chemical kinetics, thermodynamics, and/or transport processes. It is a multi-organizational effort to create and formulate high quality 0D and 1D constitutive modeling tools for reactive transport codes.Institutions involved with the effort include Sandia, MIT, Colorado School of Mines, U. Texas, NASA, and Oak Ridge National Labs. Specific to Sandia’s contributions, the Cantera Electrolyte Thermo Objects (CETO) packages is comprised of add-on routines for Cantera that handle electrolyte thermochemistry and reactions within the overall Cantera package. Cantera is a C++ Cal Tech code that handles gas phase species transport, reaction, and thermodynamics. With this addition, Cantera can be extended to handle problems involving liquid phase reactions and transport in electrolyte systems, and phase equilibrium problemsinvolving concentrated electrolytes and gas/solid phases. A full treatment of molten salt thermodynamics and transport has also been implemented in CETO. The routines themselves consist of .cpp and .h files containing C++ objects that are derived from parent Cantera objects representing thermodynamic functions. They are linked unto the main Cantera libraries when requested by the user. As an addendum to the main thermodynamics objects, several utility applications are provided. The first is multiphase Gibbs free energy minimizer based on the vcs algorithm, called vcs_cantera. This code allows for the calculation of thermodynamic equilibrium in multiple phases at constant temperature and pressure. Note, a similar code capability exists already in Cantera. This version follows the same algorithm, but gas a different code-base starting point, and is used as a research tool for algorithm development. The second program, cttables, prints out tables of thermodynamic and kinetic information for thermodynamic and kinetic objects within Cantera. This program serves as a “Get the numbers

  13. Effect of zwitterion on the lithium solid electrolyte interphase in ionic liquid electrolytes

    NASA Astrophysics Data System (ADS)

    Byrne, N.; Howlett, P. C.; MacFarlane, D. R.; Smith, M. E.; Howes, A.; Hollenkamp, A. F.; Bastow, T.; Hale, P.; Forsyth, M.

    An understanding of the solid electrolyte interphase (SEI) that forms on the lithium-metal surface is essential to the further development of rechargeable lithium-metal batteries. Currently, the formation of dendrites during cycling, which can lead to catastrophic failure of the cell, has mostly halted research on these power sources. The discovery of ionic liquids as electrolytes has rekindled the possibility of safe, rechargeable, lithium-metal batteries. The current limitation of ionic liquid electrolytes, however, is that when compared with conventional non-aqueous electrolytes the device rate capability is limited. Recently, we have shown that the addition of a zwitterion such as N-methyl- N-(butyl sulfonate) pyrrolidinium resulted in enhancement of the achievable current densities by 100%. It was also found that the resistance of the SEI layer in the presence of a zwitterion is 50% lower. In this study, a detailed chemical and electrochemical analysis of the SEI that forms in both the presence and absence of a zwitterion has been conducted. Clear differences in the chemical nature and also the thickness of the SEI are observed and these may account for the enhancement of operating current densities.

  14. Influence of aluminum salt addition on in situ sintering of electrolyte matrices for molten carbonate fuel cells

    NASA Astrophysics Data System (ADS)

    Lee, Insung; Kim, Wonsun; Moon, Youngjoon; Lim, Heechun; Lee, Dokyol

    Three aluminum salts are investigated as a sintering aid for the in situ sintering of electrolyte matrices for molten carbonate fuel cells (MCFCs). Only aluminum acetylacetonate shows a potential. At or above 420°C, aluminum acetylacetonate changes to Al 2O 3 and reacts with Li 2CO 3 in the electrolyte to produce γ-LiAlO 2. This reaction product forms necks between matrix particles. Necks grow with increasing sintering time and correspondingly, the mechanical strength of the electrolyte matrix shows an abrupt increase, starting at a sintering time of about 100 h until it levels off at about 250 h. The porosity of the matrices fabricated with aluminum acetylacetonate is in the range acceptable for use in MCFCs.

  15. The role of electrolyte pH on phase evolution and magnetic properties of CoFeW codeposited films

    NASA Astrophysics Data System (ADS)

    Ghaferi, Z.; Sharafi, S.; Bahrololoom, M. E.

    2016-07-01

    In this research, nanocrystalline Co-Fe-W alloy coatings were electrodeposited from a citrate-borate bath. The influence of electrolyte pH on the morphology, microstructure and magnetic properties of these films was also studied. By increasing pH value, the amount of iron content increased from 30 to 55 wt.% which indicates anomalous fashion at higher pH electrolytes. X-ray diffraction patterns showed that the structure of these films depend on electrolyte pH effectively. However, two-phase structure coatings showed smaller average grain size compared with one- phase solid solutions. Vibrating sample magnetometer measurements indicated that the coercivity of the coatings was in the range of 21-76 Oe. However, the highest pH value produced coating with superior magnetic behaviour. Microhardness of the coatings reached its maximum value at about 260HV which is referred to the highest tungsten content.

  16. In situ Poly(methyl methacrylate)/Graphene Composite Gel Electrolytes for Highly Stable Dye-Sensitized Solar Cells.

    PubMed

    Kang, Yu-il; Moon, Jun Hyuk

    2015-11-01

    Dye-sensitized solar cells (DSCs) with long-term stability are produced using polymer-gel electrolytes (PGEs). In this study, we introduce the formation of PGEs using in situ gelation with poly(methyl methacrylate) (PMMA) particles and graphene fillers that are pre-deposited on the counter electrodes. We obtain a high concentration PMMA-based PGEs (i.e., over 10 wt%). A DSC composed of a PMMA/graphene composite PGEs exhibits an 8.49% photon-to-electric conversion efficiency, which is comparable to conventional liquid electrolyte DSCs. This finding is attributed to increased ion diffusivity and conductivity of the PMMA-based PGEs resulting from the incorporation of graphene nanofillers. The PMMA-based PGE DSCs exhibit highly stable long-term efficiencies, maintaining up to 90% of their initial efficiency during thermal soaking, whereas the efficiencies of liquid electrolyte cells decrease significantly, by up to 60%. PMID:26471468

  17. Effects of a coal-fired power plant on the rock lichen Rhizoplaca melanophthalma: chlorophyll degradation and electrolyte leakage

    USGS Publications Warehouse

    Belnap, Jayne; Harper, Kimball T.

    1990-01-01

    Chlorophyll degradation and electrolyte leakage were measured for the umbilicate desert lichen Rhizoplaca melanophthalma (Ram.) Leuck. & Poelt in the vicinity of a coal-fired power plant near Page, Arizona. Patterns of lichen damage indicated by chlorophyll degradation were similar to those indicated by electrolyte leakage. Regression analyses of chlorophyll degradation as well as electrolyte leakage on distance from the power plant were significant (p < 0.001), suggesting that lichen damage decreased with increasing distance from the power plant. Mean values for both variables at the two sites closest to the power plant (7 and 12 km) differed significantly from values for the two sites farthest from the plant (21 and 42 km; p < 0.001). Mean values within each group (7 and 12 km; 21 and 42 km) do not differ significantly for either parameter. It is suggested that effluents from the power plant combine with local weather factors to produce the observed levels of damage.

  18. In situ Poly(methyl methacrylate)/Graphene Composite Gel Electrolytes for Highly Stable Dye-Sensitized Solar Cells.

    PubMed

    Kang, Yu-il; Moon, Jun Hyuk

    2015-11-01

    Dye-sensitized solar cells (DSCs) with long-term stability are produced using polymer-gel electrolytes (PGEs). In this study, we introduce the formation of PGEs using in situ gelation with poly(methyl methacrylate) (PMMA) particles and graphene fillers that are pre-deposited on the counter electrodes. We obtain a high concentration PMMA-based PGEs (i.e., over 10 wt%). A DSC composed of a PMMA/graphene composite PGEs exhibits an 8.49% photon-to-electric conversion efficiency, which is comparable to conventional liquid electrolyte DSCs. This finding is attributed to increased ion diffusivity and conductivity of the PMMA-based PGEs resulting from the incorporation of graphene nanofillers. The PMMA-based PGE DSCs exhibit highly stable long-term efficiencies, maintaining up to 90% of their initial efficiency during thermal soaking, whereas the efficiencies of liquid electrolyte cells decrease significantly, by up to 60%.

  19. Synthesis of Mesoporous Carbons from Rice Husk for Supercapacitors with High Energy Density in Ionic Liquid Electrolytes.

    PubMed

    He, Xiaojun; Zhang, Hebao; Xie, Kang; Xia, Youyi; Zhao, Zhigang; Wang, Xiaoting

    2016-03-01

    High-performance mesoporous carbons (MCs) for supercapacitors were made from rice husk by one-step microwave-assisted ZnCl2 activation. The microstructures of MCs as-made were characterized by field emission scanning electron microscopy and transmission electron microscopy. The pore structure parameters of MCs were obtained by N2 adsorption technique. The electrochemical properties of MC electrodes were studied by constant current charge-discharge, cyclic voltammetry and electrochemical impedance spectroscopy in different electrolytes. The results showed that the specific surface area of MC4 made at the ZnCl2/rice husk mass of 4:1 reached 1737 m2 g(-1). The specific capacitance and energy density of the electrodes fabricated from the mixture of MC4 and microporous carbon increased with the mass percentage of MC4, reaching 157 F g(-1) and 84 Wh kg(-1) at 0.05 A g(-1), and showed good cycle stability in 1-butyl-3-methylimidazolium hexafluorophosphate electrolyte. Compared to the often-used aqueous and organic electrolytes, MC4 capacitor exhibited extremely high energy density in ionic liquid electrolyte, remaining at 28 Wh kg(-1) at 1684 W kg(-1). This work paves a new way to produce cost-effective MCs from biomass for supercapacitors with extremely high energy density in ionic liquid electrolytes.

  20. Sulfone-carbonate ternary electrolyte with further increased capacity retention and burn resistance for high voltage lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Xue, Leigang; Lee, Seung-Yul; Zhao, Zuofeng; Angell, C. Austen

    2015-11-01

    Safety and high energy density are the two focus issues for current lithium ion batteries. For safety, it has been demonstrated that sulfone electrolytes are much less flammable than the prevailing all-carbonate type, and they are also promising for high voltage batteries due to the high oxidization resistance. However, the high melting points and viscosities greatly restricted their application. Based on our previous work on use of fluidity-enhancing cosolvents to make binary sulfone-carbonate electrolytes, we report here a three-component system that is more conductive and should be even less flammable while additionally having better low temperature stability. The conductivity-viscosity relations have been determined for this electrolyte and are comparable to those of the "standard" carbonate electrolyte. The additional component also produces much improved capacity retention for the LiNi0.5Mn1.5O4 cathode. As with carbonate electrolytes, increase of temperature to 55 °C leads to rapid capacity decrease during cycling, but the capacity loss is due to the salt, not the solvent. The high discharge capacity observed at 25 °C when LiBF4 replaces LiPF6, is fully retained at 55 °C.

  1. Synthesis of Mesoporous Carbons from Rice Husk for Supercapacitors with High Energy Density in Ionic Liquid Electrolytes.

    PubMed

    He, Xiaojun; Zhang, Hebao; Xie, Kang; Xia, Youyi; Zhao, Zhigang; Wang, Xiaoting

    2016-03-01

    High-performance mesoporous carbons (MCs) for supercapacitors were made from rice husk by one-step microwave-assisted ZnCl2 activation. The microstructures of MCs as-made were characterized by field emission scanning electron microscopy and transmission electron microscopy. The pore structure parameters of MCs were obtained by N2 adsorption technique. The electrochemical properties of MC electrodes were studied by constant current charge-discharge, cyclic voltammetry and electrochemical impedance spectroscopy in different electrolytes. The results showed that the specific surface area of MC4 made at the ZnCl2/rice husk mass of 4:1 reached 1737 m2 g(-1). The specific capacitance and energy density of the electrodes fabricated from the mixture of MC4 and microporous carbon increased with the mass percentage of MC4, reaching 157 F g(-1) and 84 Wh kg(-1) at 0.05 A g(-1), and showed good cycle stability in 1-butyl-3-methylimidazolium hexafluorophosphate electrolyte. Compared to the often-used aqueous and organic electrolytes, MC4 capacitor exhibited extremely high energy density in ionic liquid electrolyte, remaining at 28 Wh kg(-1) at 1684 W kg(-1). This work paves a new way to produce cost-effective MCs from biomass for supercapacitors with extremely high energy density in ionic liquid electrolytes. PMID:27455718

  2. Effect of current mode on PEO treatment of magnesium in Ca- and P-containing electrolyte and resulting coatings

    NASA Astrophysics Data System (ADS)

    Gao, Yonghao; Yerokhin, Aleksey; Matthews, Allan

    2014-10-01

    Plasma electrolytic oxidation (PEO) coatings were produced on commercially pure magnesium in a biologically friendly electrolyte composed of 2 g L-1 Ca(OH)2 and 12 g L-1 Na3PO4·12H2O using pulsed unipolar and bipolar current regimes with negative biasing varying from 0 to 20 mA cm-2. Analysis of voltage transients was performed to characterise the PEO processes. The coating morphology and phase composition were studied by scanning electron microscopy and X-ray diffraction technique, respectively. In vitro corrosion performance of the coatings was evaluated in a simulated body fluid at 37 ± 1 °C, using electrochemical techniques including open circuit potential monitoring, electrochemical impedance spectroscopy and potentiodynamic polarisation scans. The influence of the negative biasing on the PEO process and resulting coating characteristics is discussed. Unlike generally recognised beneficial effects of the negative biasing in PEO treatments of some other metal-electrolyte systems, it was found that detrimental effects are induced to the coatings on cp-Mg produced in the studied electrolyte when the negative current amplitude increases, which may be attributed to hydrogen liberation at the coating/substrate interface during the negative biasing cycles. As a result, a deterioration of vitro corrosion performance was observed for the pulsed bipolar PEO coatings compared to those produced using the pulsed unipolar regime which provides better quality coatings.

  3. Transparent conducting oxide induced by liquid electrolyte gating

    PubMed Central

    ViolBarbosa, Carlos; Karel, Julie; Kiss, Janos; Gordan, Ovidiu-dorin; Altendorf, Simone G.; Utsumi, Yuki; Samant, Mahesh G.; Wu, Yu-Han; Tsuei, Ku-Ding; Felser, Claudia; Parkin, Stuart S. P.

    2016-01-01

    Optically transparent conducting materials are essential in modern technology. These materials are used as electrodes in displays, photovoltaic cells, and touchscreens; they are also used in energy-conserving windows to reflect the infrared spectrum. The most ubiquitous transparent conducting material is tin-doped indium oxide (ITO), a wide-gap oxide whose conductivity is ascribed to n-type chemical doping. Recently, it has been shown that ionic liquid gating can induce a reversible, nonvolatile metallic phase in initially insulating films of WO3. Here, we use hard X-ray photoelectron spectroscopy and spectroscopic ellipsometry to show that the metallic phase produced by the electrolyte gating does not result from a significant change in the bandgap but rather originates from new in-gap states. These states produce strong absorption below ∼1 eV, outside the visible spectrum, consistent with the formation of a narrow electronic conduction band. Thus WO3 is metallic but remains colorless, unlike other methods to realize tunable electrical conductivity in this material. Core-level photoemission spectra show that the gating reversibly modifies the atomic coordination of W and O atoms without a substantial change of the stoichiometry; we propose a simple model relating these structural changes to the modifications in the electronic structure. Thus we show that ionic liquid gating can tune the conductivity over orders of magnitude while maintaining transparency in the visible range, suggesting the use of ionic liquid gating for many applications. PMID:27647884

  4. Chemical Passivation of Li(exp +)-Conducting Solid Electrolytes

    NASA Technical Reports Server (NTRS)

    West, William; Whitacre, Jay; Lim, James

    2008-01-01

    Plates of a solid electrolyte that exhibits high conductivity for positive lithium ions can now be passivated to prevent them from reacting with metallic lithium. Such passivation could enable the construction and operation of high-performance, long-life lithium-based rechargeable electrochemical cells containing metallic lithium anodes. The advantage of this approach, in comparison with a possible alternative approach utilizing lithium-ion graphitic anodes, is that metallic lithium anodes could afford significantly greater energy-storage densities. A major impediment to the development of such cells has been the fact that the available solid electrolytes having the requisite high Li(exp +)-ion conductivity are too highly chemically reactive with metallic lithium to be useful, while those solid electrolytes that do not react excessively with metallic lithium have conductivities too low to be useful. The present passivation method exploits the best features of both extremes of the solid-electrolyte spectrum. The basic idea is to coat a higher-conductivity, higher-reactivity solid electrolyte with a lower-conductivity, lower-reactivity solid electrolyte. One can then safely deposit metallic lithium in contact with the lower-reactivity solid electrolyte without incurring the undesired chemical reactions. The thickness of the lower-reactivity electrolyte must be great enough to afford the desired passivation but not so great as to contribute excessively to the electrical resistance of the cell. The feasibility of this method was demonstrated in experiments on plates of a commercial high-performance solid Li(exp +)- conducting electrolyte. Lithium phosphorous oxynitride (LiPON) was the solid electrolyte used for passivation. LiPON-coated solid-electrolyte plates were found to support electrochemical plating and stripping of Li metal. The electrical resistance contributed by the LiPON layers were found to be small relative to overall cell impedances.

  5. Diminution of supercooling of electrolytes by carbon particles

    SciTech Connect

    Ding, S.P.; Xu, K.; Zhang, S.S.; Jow, T.R.; Amine, K.; Henriksen, G.L.

    1999-11-01

    A liquid solution composed of a pure or mixed solvent and a dissolved salt is the most common form of electrolyte used in electrochemical devices for energy storage and conversion, such as batteries and capacitors. For such an electrolyte, one of the most important properties is its crystallization temperature, which limits the low-temperature operation of a device containing such an electrolyte. If thermodynamic equilibria were strictly followed, crystallization of an electrolyte would start as soon as it is cooled to its liquidus temperature. But such is seldom the case, as an electrolyte by itself often supercools well below this temperature. This supercooling can delay or even eliminate the crystallization of an electrolyte, thus substantially extending its apparent liquid range. The authors studied the supercooling behavior of a number of solutions of LiPF{sub 6} in ethylene carbonate-ethyl methyl carbonate in 1:1 weight ratio with and without the presence of one of these carbons: activated carbon, carbon black, and mesocarbon microbeads. The results of differential scanning calorimetry (DSC) show that the supercooling of less concentrated solutions is significantly diminished by the presence of a carbon, the degree and the nature of which depends on the concentration of the electrolyte and the type of carbon present. The results of conductivity measurements also indicate precipitation in some of the electrolytes at low temperatures, which correlates well with the DSC results. The authors therefore conclude that the temperature range in which an electrolyte supercools without a nucleating material is unreliable for the operation of an electrochemical device containing such an electrolyte. Instead, the liquidus temperature of an electrolyte should be used as the lower limit of operation if the possibility of its crystallization is to be excluded.

  6. Anodic polymerization of vinyl ethylene carbonate in Li-Ion battery electrolyte

    SciTech Connect

    Chen, Guoying; Zhuang, Guorong V.; Richardson, Thomas J.; Gao, Liu; Ross Jr., Philip N.

    2005-02-28

    A study of the anodic oxidation of vinyl ethylene carbonate (VEC) was conducted with post-mortem analysis of reaction products by ATR-FTIR and gel permeation chromatography (GPC). The half-wave potential (E1/2) for oxidation of VEC is ca. 3.6 V producing a resistive film on the electrode surface. GPC analysis of the film on a gold electrode produced by anodization of a commercial Li-ion battery electrolyte containing 2 percent VEC at 4.1 V showed the presence of a high molecular weight polymer. IR analysis indicated polycarbonate with alkyl carbonate rings linked by aliphatic methylene and methyl branches.

  7. Organometallic electrochemistry based on electrolytes containing weakly-coordinating fluoroarylborate anions.

    PubMed

    Geiger, William E; Barrière, Frédéric

    2010-07-20

    Electrochemistry is a powerful tool for the study of oxidative electron-transfer reactions (anodic processes). Since the 1960s, the electrolytes of choice for nonaqueous electrochemistry were relatively small (heptaatomic or smaller) inorganic anions, such as perchlorate, tetrafluoroborate, or hexafluorophosphate. Owing to the similar size-to-charge ratios of these "traditional" anions, structural alterations of the electrolyte anion are not particularly valuable in effecting changes in the corresponding redox reactions. Systematic variations of supporting electrolytes were largely restricted to cathodic processes, in which interactions of anions produced in the reactions are altered by changes in electrolyte cations. A typical ladder involves going from a weakly ion-pairing tetraalkylammonium cation, [N(C(n)H(2n+1))(4)](+), with n > or = 4, to more strongly ion-pairing counterparts with n < 4, and culminating in very strongly ion-pairing alkali metal ions. A new generation of supporting electrolyte salts that incorporate a weakly coordinating anion (WCA) expands anodic applications by providing a dramatically different medium in which to generate positively charged electrolysis products. A chain of electrolyte anions is now available for the control of anodic reactions, beginning with weakly ion-pairing WCAs, progressing through the traditional anions, and culminating in halide ions. Although the electrochemical properties of a number of different WCAs have been reported, the most systematic work involves fluoro- or trifluoromethyl-substituted tetraphenylborate anions (fluoroarylborate anions). In this Account, we focus on tetrakis(perfluorophenyl)borate, [B(C(6)F(5))(4)](-), which has a significantly more positive anodic window than tetrakis[(3,5-bis(trifluoromethyl)phenyl)]borate, [BArF(24)](-), making it suitable in a larger range of anodic oxidations. These WCAs also have a characteristic of specific importance to organometallic redox processes. Many electron

  8. Performance of capacitors using organic electrolytes

    SciTech Connect

    Morimoto, T.; Tsushima, M.; Che, Y.

    2000-07-01

    Electric double-layer capacitors (EDLC) based on charge storage at the interface between a high surface area activated carbon electrode and an electrolyte solution are characterized by their long cycle life and high power density in comparison with batteries. However, energy density of electric double-layer capacitors obtained at present is at most 1Wh/kg at a power density of 600W/kg and smaller compared with that of batteries, which limits the applications of the capacitor. Therefore, new capacitors which show larger energy density than that of electric-double layer capacitors are proposed. The new capacitors are hybrid capacitors consisting of activated carbon cathode, Li-doped graphite anode and an organic electrolyte. Maximum voltage applicable to the cell becomes over 4.0V which is larger than that of the electric double-layer capacitor. As a result, discharged energy density of the cell becomes 4Wh/kg at a power density of 600W/kg.

  9. Common electrolyte imbalances associated with malignancy.

    PubMed

    Hawthorne, J L; Schneider, S M; Workman, M L

    1992-08-01

    More than one million Americans will be diagnosed with cancer during 1992, and 50% will be cured of their disease. Of those individuals not cured of the malignancy, survival time after diagnosis has increased tremendously compared to 1980. Because of advances in therapy and the increase in long-term survival, the presence of cancer patients in critical care units should no longer represent either a medical contradiction or an ethical dilemma when the condition requiring critical care is potentially reversible. Many of these individuals may become patients in critical care settings as a result of specific electrolyte imbalances caused by the malignant disease or treatment of malignancy. Although the imbalances often are temporary, they can be life-threatening without intervention. The most common temporary electrolyte imbalances associated with malignant conditions are hypercalcemia, hyperkalemia, and tumor lysis syndrome. Critical care nurses can contribute skill and knowledge in ameliorating these conditions so that the person with cancer can have better quality and longer survival time.

  10. ELECTROLYTIC MEMBRANE DIALYSIS FOR TREATING WASTEWATER STREAMS

    SciTech Connect

    Ronald C. Timpe

    2000-04-01

    This project will determine whether electrolytic dialysis has promise in the separation of charged particles in an aqueous solution. The ability to selectively move ions from one aqueous solution to another through a semipermeable membrane will be studied as a function of emf, amperage, and particle electrical charge. The ions selected for the study are Cl{sup -} and SO{sub 4}{sup 2-}. These ions are of particular interest because of their electrical conduction properties in aqueous solution resulting with their association with the corrosive action of metals. The studies will be performed with commercial membranes on solutions prepared in the laboratory from reagent salts. pH adjustments will be made with dilute reagent acid and base. Specific objectives of the project include testing a selected membrane currently available for electrolytic dialysis, membrane resistance to extreme pH conditions, the effectiveness of separating a mixture of two ions selected on the basis of size, the efficiency of the membranes in separating chloride (Cl{sup 1-}) from sulfate (SO{sub 4}{sup 2-}), and separation efficiency as a function of electromotive force (emf).

  11. Bending response of polymer electrolyte actuator

    NASA Astrophysics Data System (ADS)

    Onishi, Kazuo; Sewa, Shingo; Asaka, Kinji; Fujiwara, Naoko; Oguro, Keisuke

    2000-06-01

    To induce bending motion in a perfluorinated polymer electrolyte by electric stimuli in water or saline solution, plating with metal is required. To fabricate electrodes, a perfluorocarboxylic acid membrane was soaked in Au(III) di- chloro phenanthroline complex solution, and then any adsorbed Au(III) cation complex was reduced in aqueous sodium sulfite. Optimizing the motion response depends on control of the chemical plating procedure. By sequential adsorption/reduction cycling, a suitable pair of gold electrodes with a fractal-like structure have been grown. We illustrate the advantage of optimizing the interfacial area between electrode and membrane to enhance deformation response. To achieve this, gold deposits in the film are accumulated by sequential adsorption/reduction plating cycles. Actuator displacement increased with the number of plating gold deposition cycles up to roughly 6 times, but showed no clear improvement beyond. It is believed that with excessive plating, the interfacial area begins to decrease and/or the hardness of the electrode increases, thus countering any improvement in electrical conductance. Displacement rates were proportional to current. This high interfacial area between the electrodes and polymer electrolyte leads to larger deformation. The measured deformation progressively improves with cycling. Its motional response and versatility are illustrated by some examples.

  12. Annealing Would Improve beta" - Alumina Solid Electrolyte

    NASA Technical Reports Server (NTRS)

    Williams, Roger; Homer, Margie; Ryan, Margaret; Cortez, Roger; Shields, Virgil; Kisor, Adam

    2003-01-01

    A pre-operational annealing process is under investigation as a potential means of preventing a sudden reduction of ionic conductivity in a Beta"-alumina solid electrolyte (BASE) during use. On the basis of tests, the sudden reduction of ionic conductivity, followed by a slow recovery, has been found to occur during testing of the solid electrolyte and electrode components of an alkali metal thermal-to-electric converter (AMTEC) cell. At this time, high-temperature tests of limited duration have indicated the superiority of the treated BASE, but reproducible tests over thousands of hours are necessary to confirm that microcracking has been eliminated. The ionic conductivity of the treated BASE is also measured to be higher than untreated BASE at 1,073 K in low-pressure sodium vapor. Microcracking resulting in loss of conductivity was not observed with treated BASE in one high-temperature experiment, but this result must be duplicated over very long testing times to be sure of the effect. Shorter annealing times (10 to 20 hours) were found to result in significantly less loss of mass; it may be necessary for the packed powder mixture to evolve some Na2O before the Na2O can leave the ceramic.

  13. Endurance testing with Li/Na electrolyte

    SciTech Connect

    Ong, E.T.; Remick, R.J.; Sishtla, C.I.

    1996-12-31

    The Institute of Gas Technology (IGT), under subcontract to M-C Power Corporation under DOE funding, has been operating bench-scale fuel cells to investigate the performance and endurance issues of the Li/Na electrolyte because it offers higher ionic conductivity, higher exchange current densities, lower vapor pressures, and lower cathode dissolution rates than the Li/K electrolyte. These cells have continued to show higher performance and lower decay rates than the Li/K cells since the publication of our two previous papers in 1994. In this paper, test results of two long-term 100-cm{sup 2} bench scale cells are discussed. One cell operated continuously at 160 mA/cm{sup 2} for 17,000 hours with reference gases (60H{sub 2}/20CO{sub 2}/20H{sub 2}O fuel at 75% utilization and 30CO{sub 2}/70 air oxidant humidified at room temperature at 50% utilization). The other cell operated at 160 mA/cm{sup 2} for 6900 hours at 3 atm with system gases (64H{sub 2}/16CO{sub 2}/20H{sub 2}O at 75% utilization and an M-C Power system-defined oxidant at 40% utilization). Both cells have shown the highest performance and longest endurance among IGT cells operated to date.

  14. Electrolytic coloration below 100°C and spectral properties of potassium alum crystals.

    PubMed

    Gu, Hongen; Li, Yutong

    2015-03-15

    Potassium alum crystals are colored electrolytically below 100°C and under various voltages using a pointed cathode and a flat anode. SO3(-), SO2(-), O3(-), O2(-), O(-) hole-trapped centers and O(0), O(2-), H(+) radicals are produced in colored potassium alum crystals. No obvious characteristic absorption band in ultraviolet and visible wavelength regions is observed in absorption spectrum of uncolored potassium alum crystal. Characteristic absorption bands of SO3(-), SO2(-) and O3(-) hole-trapped centers are observed in the absorption spectra of the colored potassium alum crystals. The hole-trapped centers and radicals come from electric- and thermal-induced decomposition of SO4(2-) radicals and crystalline water molecules. Current-time curve for electrolytic coloration of potassium alum crystal is given. Electron exchanges from electrons and small charged radicals to electrodes induce complete current.

  15. Electrolytic coloration below 100 °C and spectral properties of potassium alum crystals

    NASA Astrophysics Data System (ADS)

    Gu, Hongen; Li, Yutong

    2015-03-01

    Potassium alum crystals are colored electrolytically below 100 °C and under various voltages using a pointed cathode and a flat anode. SO3-, SO2-, O3-, O2-, O- hole-trapped centers and O0, O2-, H+ radicals are produced in colored potassium alum crystals. No obvious characteristic absorption band in ultraviolet and visible wavelength regions is observed in absorption spectrum of uncolored potassium alum crystal. Characteristic absorption bands of SO3-, SO2- and O3- hole-trapped centers are observed in the absorption spectra of the colored potassium alum crystals. The hole-trapped centers and radicals come from electric- and thermal-induced decomposition of SO42- radicals and crystalline water molecules. Current-time curve for electrolytic coloration of potassium alum crystal is given. Electron exchanges from electrons and small charged radicals to electrodes induce complete current.

  16. Electrode assembly for use in a solid polymer electrolyte fuel cell

    DOEpatents

    Raistrick, Ian D.

    1989-01-01

    A gas reaction fuel cell may be provided with a solid polymer electrolyte membrane. Porous gas diffusion electrodes are formed of carbon particles supporting a catalyst which is effective to enhance the gas reactions. The carbon particles define interstitial spaces exposing the catalyst on a large surface area of the carbon particles. A proton conducting material, such as a perfluorocarbon copolymer or ruthenium dioxide contacts the surface areas of the carbon particles adjacent the interstitial spaces. The proton conducting material enables protons produced by the gas reactions adjacent the supported catalyst to have a conductive path with the electrolyte membrane. The carbon particles provide a conductive path for electrons. A suitable electrode may be formed by dispersing a solution containing a proton conducting material over the surface of the electrode in a manner effective to coat carbon surfaces adjacent the interstitial spaces without impeding gas flow into the interstitial spaces.

  17. A computational study of electrolyte adsorption in a simple model for intercalated clays

    NASA Astrophysics Data System (ADS)

    Lomba, E.; Weis, J.-J.

    2010-03-01

    A pillared interlayered clay is represented by a two-dimensional quenched charged disordered medium, in which the pillar configuration is produced by the quench of a two-dimensional electrolyte and the subsequent removal of the anions (that act as a template). The cation charge is counterbalanced by a neutralizing background that is an ideal representation of the layer's negative charge in the experimental system. In this paper we investigate the adsorption of electrolyte particles in this charged disordered medium resorting both to the use of the replica Ornstein-Zernike equation in the hypernetted chain approximation and grand canonical Monte Carlo simulations. The theoretical approach qualitatively reproduces the simulated behavior of the adsorbed fluids. Theoretical estimates of the material porosities obtained for various types of pillar distributions are in good agreement with the simulation. We investigate the influence of the matrix on correlation functions and adsorption isotherms.

  18. Highly conductive electrolyte composites containing glass and ceramic, and method of manufacture

    DOEpatents

    Hash, Mark C.; Bloom, Ira D.

    1992-01-01

    An electrolyte composite is manufactured by pressurizing a mixture of sodium ion conductive glass and an ionically conductive compound at between 12,000 and 24,000 pounds per square inch to produce a pellet. The resulting pellet is then sintered at relatively lower temperatures (800.degree. C.-1200.degree. C.), for example 1000.degree. C., than are typically required (1400.degree. C.) when fabricating single constituent ceramic electrolytes. The resultant composite is 100 percent conductive at 250.degree. C. with conductivity values of 2.5 to 4.times.10.sup.-2 (ohm-cm).sup.-1. The matrix exhibits chemical stability against sodium for 100 hours at 250.degree. to 300.degree. C.

  19. A comparison of three oral electrolyte solutions in the treatment of diarrheic calves.

    PubMed

    Naylor, J M; Petrie, L; Rodriguez, M I; Skilnick, P

    1990-11-01

    Thirty-six diarrheic calves infected with rota- and coronaviruses were randomly allocated to one of three oral electrolyte treatments: Ion-Aid (Syntex Agribusiness), Life-Guard (Norden Inc), or Revibe (Langford Inc). The calves were also allowed voluntary access to milk which was offered at the rate of 5% of body weight per feeding in two feedings daily. There were significant differences in recovery rate among calves treated with the different electrolytes. Only 33% of Ion-Aid-treated calves recovered; Revibe- and Life-Guard-treated calves had high recovery rates of 92% and 83%, respectively. The much higher recovery rates with Life-Guard and Revibe were attributed to the presence of an alkalizing agent in these preparations. Life-Guard uses bicarbonate to counteract acidosis and there was some evidence that this may have interfered with milk digestion. Revibe uses acetate; this was effectively metabolized within the calves' tissues and produced alkalization without interference with milk digestion.

  20. Quantification Method for Electrolytic Sensors in Long-Term Monitoring of Ambient Air Quality

    PubMed Central

    Masson, Nicholas; Piedrahita, Ricardo; Hannigan, Michael

    2015-01-01

    Traditional air quality monitoring relies on point measurements from a small number of high-end devices. The recent growth in low-cost air sensing technology stands to revolutionize the way in which air quality data are collected and utilized. While several technologies have emerged in the field of low-cost monitoring, all suffer from similar challenges in data quality. One technology that shows particular promise is that of electrolytic (also known as amperometric) sensors. These sensors produce an electric current in response to target pollutants. This work addresses the development of practical models for understanding and quantifying the signal response of electrolytic sensors. Such models compensate for confounding effects on the sensor response, such as ambient temperature and humidity, and address other issues that affect the usability of low-cost sensors, such as sensor drift and inter-sensor variability. PMID:26516860

  1. Covering anodized aluminum with electropolymerized polypyrrole via manganese oxide layer and application to solid electrolytic capacitor

    NASA Astrophysics Data System (ADS)

    Kudoh, Yasuo; Kojima, Toshikuni; Fukuyama, Masao; Tsuchiya, Sohji; Yoshimura, Susumu

    A new technology for covering an etched and anodized aluminum (Al) foil with polypyrrole (PPy) was developed. PPy was electropolymerized from an external electrode via an extremely thin semiconducting manganese oxide layer prepared on the etched and anodized Al foil in advance. Pyrolytic and reduced manganese oxide could be used with little difference in the performance of the PPy layer growth. To obtain a high coverage ratio, the optimal starting materials were manganese nitrate for the pyrolysis process and sodium permanganate for the reduction process. On the basis of the technology, two kinds of Al solid electrolytic capacitors, in which the PPy layers are used as electrolytes, were produced and characterized. These capacitors showed almost equal ideal impedance-frequency characteristics, excellent temperature characteristics and environmental stability, and independence of the manganese oxide synthesis route.

  2. Characterization of ι-carrageenan and its derivative based green polymer electrolytes

    SciTech Connect

    Jumaah, Fatihah Najirah; Mobaraka, Nadhratun Naiim; Ahmad, Azizan; Ramli, Nazaruddin

    2013-11-27

    The new types of green polymer electrolytes based on ι-carrageenan derivative have been prepared. ι-carrageenan act as precursor was reacted with monochloroacetic acid to produce carboxymethyl ι-carrageenan. The powders were characterized by Attenuated Total Reflection Fourier Transform infrared (ATR-FTIR) spectroscopy and {sup 1}H nuclear magnetic resonance (NMR) to confirm the substitution of targeted functional group in ι-carrageenan. The green polymer electrolyte based on ι-carrageenan and carboxymethyl ι-carrageenan was prepared by solution-casting technique. The films were characterized by electrochemical impedance spectroscopy to determine the ionic conductivity. The ionic conductivity ι-carrageenan film were higher than carboxymethyl ι-carrageenan which 4.87 ×10{sup −6} S cm{sup −1} and 2.19 ×10{sup −8} S cm{sup −1}, respectively.

  3. Effect of surface nanostructuring of aluminum alloy on post plasma electrolytic oxidation

    NASA Astrophysics Data System (ADS)

    Masiha, H. R.; Bagheri, H. R.; Gheytani, M.; Aliofkhazraei, M.; Sabour Rouhaghdam, A.; Shahrabi, T.

    2014-10-01

    AA1230 aluminum alloy samples were coated by plasma electrolytic oxidation (PEO). The samples with and without surface mechanical attrition treatment (SMAT) were coated in phosphate- and silicate-based electrolytes and in the presence of Si3N4 nanoparticles. Besides, morphology and properties of the produced coatings were examined. To determine the corrosion resistance of the coatings, potentiodynamic polarization technique was used. All coated samples were subjected to wear test in order to compare coating wear properties of the SMATed and unSMATed samples. Then the effects of SMAT preprocessing and its duration on the properties of the coatings prepared by PEO were investigated. The results indicated that the mean coefficient of friction of the coated samples decreased by near 83% with respect to the uncoated (raw) samples. Furthermore, the SMATed samples showed thicker coatings as compared to unSMATed samples due to an increase in their matrix reactivity.

  4. Growth of thin, c-axis oriented Sr-doped LaP3O9 electrolyte membranes in condensed phosphoric acid solutions

    NASA Astrophysics Data System (ADS)

    Hatada, Naoyuki; Takahashi, Kota; Adachi, Yoshinobu; Uda, Tetsuya

    2016-08-01

    Proton-conducting Sr-doped LaP3O9 has potential application as electrolytes in intermediate temperature fuel cells, but reduction of the electrical resistance of the electrolyte membranes is necessary for practical applications. In this study, we focused on reducing the resistance by reducing the electrolyte thickness, while maintaining a preferable microstructure for proton conduction (c-axis orientation and absence of the small-crystal layer). Thin, c-axis oriented Sr-doped LaP3O9 membranes were successfully obtained in condensed phosphoric acid solutions by a novel "two-step precipitation method". In this method, Sr-doped LaP3O9 powder was artificially deposited on the surface of the carbon paper supports as seeds, and then columnar crystals were grown "downward" in the solutions. We expect that this method will be utilized to produce LaP3O9 electrolyte membranes with lower electrical resistance.

  5. 40 CFR 424.60 - Applicability; description of the electrolytic manganese products subcategory.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... electrolytic manganese products subcategory. 424.60 Section 424.60 Protection of Environment ENVIRONMENTAL... CATEGORY Electrolytic Manganese Products Subcategory § 424.60 Applicability; description of the electrolytic manganese products subcategory. The provisions of this subpart are applicable to...

  6. 40 CFR 424.60 - Applicability; description of the electrolytic manganese products subcategory.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... electrolytic manganese products subcategory. 424.60 Section 424.60 Protection of Environment ENVIRONMENTAL... CATEGORY Electrolytic Manganese Products Subcategory § 424.60 Applicability; description of the electrolytic manganese products subcategory. The provisions of this subpart are applicable to...

  7. 40 CFR 424.60 - Applicability; description of the electrolytic manganese products subcategory.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... electrolytic manganese products subcategory. 424.60 Section 424.60 Protection of Environment ENVIRONMENTAL... CATEGORY Electrolytic Manganese Products Subcategory § 424.60 Applicability; description of the electrolytic manganese products subcategory. The provisions of this subpart are applicable to...

  8. 40 CFR 424.60 - Applicability; description of the electrolytic manganese products subcategory.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... electrolytic manganese products subcategory. 424.60 Section 424.60 Protection of Environment ENVIRONMENTAL... CATEGORY Electrolytic Manganese Products Subcategory § 424.60 Applicability; description of the electrolytic manganese products subcategory. The provisions of this subpart are applicable to...

  9. 40 CFR 424.60 - Applicability; description of the electrolytic manganese products subcategory.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... electrolytic manganese products subcategory. 424.60 Section 424.60 Protection of Environment ENVIRONMENTAL... CATEGORY Electrolytic Manganese Products Subcategory § 424.60 Applicability; description of the electrolytic manganese products subcategory. The provisions of this subpart are applicable to...

  10. Fuel cells with solid polymer electrolyte and their application on vehicles

    SciTech Connect

    Fateev, V.

    1996-04-01

    In Russia, solid polymer electrolyte MF-4-SK has been developed for fuel cells. This electrolyte is based on perfluorinated polymer with functional sulfogroups. Investigations on electrolyte properties and electrocatalysts have been carried out.

  11. Highly concentrated water-in-oil emulsions: Influence of electrolyte on their properties and stability

    SciTech Connect

    Aronson, M.P.; Petko, M.F. )

    1993-08-01

    Concentrated water-in-oil emulsions of over 95% internal phase by volume were prepared using a variety of low HLB emulsifiers. These emulsions coarsened with time to produce a fraction of large droplets that grow at the expense of smaller droplets. This resulted in a decrease in yield stress and eventually to visible phase separation of water. There was a significant effect of emulsifier type, and the optimum HLB appears to be [approximately]5 for mineral oil. None of the emulsions prepared with distilled water as the internal phase could withstand a single freeze/thaw cycle. In contrast to the gradual coarsening process at room temperature, freeze/thaw instability was sudden and involved an inversion process that took place in the frozen state. The properties of these concentrated emulsions changed dramatically when electrolyte was introduced into the aqueous phase at concentrations as low as 0.02 M. The rate of coarsening decreased, and coalescence of water droplets during the freeze/thaw process was inhibited. The emulsions retained their yield stress over prolonged storage and a lower droplet size was often produced under the same conditions of emulsification. These effects seemed to be general and were observed with a variety of emulsifiers and electrolytes. The electrolytes appeared to enhance the stability of these water-in-oil emulsions by increasing the resistance of the water droplets to coalescence. It is proposed that this was achieved by a higher adsorption density of emulsifier at room temperature storage, and in the frozen state by the fractionation of a concentrated electrolyte solution that wetted the ice crystals and prevented their fusion. Analysis of emulsion rheology and processing suggested that this enhanced coalescence stability was adequate to account for the changes in yield stress and droplet sizes observed.

  12. Performance of electric double layer capacitors with polymer gel electrolytes

    SciTech Connect

    Ishikawa, Masashi; Kishino, Takahiro; Katada, Naoji; Morita, Masayuki

    2000-07-01

    Polymer gel electrolytes consisting of poly(vinylidene fluoride) (PVdF), tetraethylammonium tetrafluoroborate (TEABF{sub 4}), and propylene carbonate (PC) as a plasticizer have been investigated for electric double layer capacitors. The PVdF gel electrolytes showed high ionic conductivity (ca. 6 mS/cm at 298 K). To assemble model capacitors with the PVdF gel electrolytes and activated carbon fiber cloth electrodes, a pair of the fixed electrodes was soaked in a precursor solution containing PC, PVdF, and TEABF{sub 4}, followed by evaporation of the PC solvent in a vacuum oven. The resulting gel electrolytes were in good contact with the electrodes. The model capacitors with the PVdF gel electrolytes showed a large value of capacitance and high coulombic efficiency in operation voltage ranges of 1--2 and 1--3 V. It is worth noting that the capacitors with the PVdF electrolytes showed long voltage retention in a self-discharge test. These good characteristics of the gel capacitors were comparable to those of typical double layer capacitors with a liquid organic electrolyte containing PC and TEABF{sub 4}; rather, the voltage retentivity of the PVdF gel capacitors was much superior to that of the capacitors with the organic electrolyte.

  13. Solid electrolyte-electrode system for an electrochemical cell

    DOEpatents

    Tuller, Harry L.; Kramer, Steve A.; Spears, Marlene A.

    1995-01-01

    An electrochemical device including a solid electrolyte and solid electrode composed of materials having different chemical compositions and characterized by different electrical properties but having the same crystalline phase is provided. A method for fabricating an electrochemical device having a solid electrode and solid electrolyte characterized by the same crystalline phase is also provided.

  14. Metallography of Aluminum and Its Alloys : Use of Electrolytic Polishing

    NASA Technical Reports Server (NTRS)

    Jacquet, Pierre A

    1955-01-01

    Recent methods are described for electropolishing aluminum and aluminum alloys. Numerous references are included of electrolytic micrographic investigations carried out during the period 1948 to 1952. A detailed description of a commercial electrolytic polishing unit, suitable for micrographic examination of aluminum and its alloys, is included.

  15. Electrolyte Loss Tendencies of Primary Silver-Zinc Cells

    NASA Technical Reports Server (NTRS)

    Thaller, Lawrence H.; Juvinall, Gordon L.

    1997-01-01

    Since silver zinc cells are not hermetically sealed, care must be taken to prevent the loss of electrolyte which can result in shorting paths within the battery box. Prelaunch battery processing is important in being able to minimize any problems with expelled electrolyte.

  16. 64 FR 23675 - Electrolytic Manganese Dioxide From Greece and Japan

    Federal Register 2010, 2011, 2012, 2013, 2014

    1999-05-03

    ... orders on imports of electrolytic manganese dioxide from Greece and Japan (54 FR 15243). The Commission..., including the text of subpart F of part 207, are published at 63 FR 30599, June 5, 1998, and may be... COMMISSION Electrolytic Manganese Dioxide From Greece and Japan AGENCY: United States International...

  17. Solid electrolyte-electrode system for an electrochemical cell

    DOEpatents

    Tuller, H.L.; Kramer, S.A.; Spears, M.A.

    1995-04-04

    An electrochemical device including a solid electrolyte and solid electrode composed of materials having different chemical compositions and characterized by different electrical properties but having the same crystalline phase is provided. A method for fabricating an electrochemical device having a solid electrode and solid electrolyte characterized by the same crystalline phase is also provided. 17 figures.

  18. Electrochemical Stability of Model Polymer Electrolyte/Electrode Interfaces

    NASA Astrophysics Data System (ADS)

    Hallinan, Daniel; Yang, Guang

    2015-03-01

    Polymer electrolytes are promising materials for high energy density rechargeable batteries. However, typical polymer electrolytes are not electrochemically stable at the charging voltage of advanced positive electrode materials. Although not yet reported in literature, decomposition is expected to adversely affect the performance and lifetime of polymer-electrolyte-based batteries. In an attempt to better understand polymer electrolyte oxidation and design stable polymer electrolyte/positive electrode interfaces, we are studying electron transfer across model interfaces comprising gold nanoparticles and organic protecting ligands assembled into monolayer films. Gold nanoparticles provide large interfacial surface area yielding a measurable electrochemical signal. They are inert and hence non-reactive with most polymer electrolytes and lithium salts. The surface can be easily modified with ligands of different chemistry and molecular weight. In our study, poly(ethylene oxide) (PEO) will serve as the polymer electrolyte and lithium bis(trifluoromethanesulfonyl) imide salt (LiTFSI) will be the lithium salt. The effect of ligand type and molecular weight on both optical and electrical properties of the gold nanoparticle film will be presented. Finally, the electrochemical stability of the electrode/electrolyte interface and its dependence on interfacial properties will be presented.

  19. Lithium-ion transport in inorganic solid state electrolyte

    NASA Astrophysics Data System (ADS)

    Jian, Gao; Yu-Sheng, Zhao; Si-Qi, Shi; Hong, Li

    2016-01-01

    An overview of ion transport in lithium-ion inorganic solid state electrolytes is presented, aimed at exploring and designing better electrolyte materials. Ionic conductivity is one of the most important indices of the performance of inorganic solid state electrolytes. The general definition of solid state electrolytes is presented in terms of their role in a working cell (to convey ions while isolate electrons), and the history of solid electrolyte development is briefly summarized. Ways of using the available theoretical models and experimental methods to characterize lithium-ion transport in solid state electrolytes are systematically introduced. Then the various factors that affect ionic conductivity are itemized, including mainly structural disorder, composite materials and interface effects between a solid electrolyte and an electrode. Finally, strategies for future material systems, for synthesis and characterization methods, and for theory and calculation are proposed, aiming to help accelerate the design and development of new solid electrolytes. Project supported by the National Natural Science Foundation of China (Grant No. 51372228), the Shanghai Pujiang Program, China (Grant No. 14PJ1403900), and the Shanghai Institute of Materials Genome from the Shanghai Municipal Science and Technology Commission, China (Grant No. 14DZ2261200).

  20. Solid polymer electrolyte composite membrane comprising laser micromachined porous support

    DOEpatents

    Liu, Han; LaConti, Anthony B.; Mittelsteadt, Cortney K.; McCallum, Thomas J.

    2011-01-11

    A solid polymer electrolyte composite membrane and method of manufacturing the same. According to one embodiment, the composite membrane comprises a rigid, non-electrically-conducting support, the support preferably being a sheet of polyimide having a thickness of about 7.5 to 15 microns. The support has a plurality of cylindrical pores extending perpendicularly between opposing top and bottom surfaces of the support. The pores, which preferably have a diameter of about 5 microns, are made by laser micromachining and preferably are arranged in a defined pattern, for example, with fewer pores located in areas of high membrane stress and more pores located in areas of low membrane stress. The pores are filled with a first solid polymer electrolyte, such as a perfluorosulfonic acid (PFSA) polymer. A second solid polymer electrolyte, which may be the same as or different than the first solid polymer electrolyte, may be deposited over the top and/or bottom of the first solid polymer electrolyte.