Science.gov

Sample records for lithium salt nature

  1. Molten salt lithium cells

    DOEpatents

    Raistrick, Ian D.; Poris, Jaime; Huggins, Robert A.

    1983-01-01

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

  2. Molten salt lithium cells

    DOEpatents

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

    1980-07-18

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

  3. Molten salt lithium cells

    DOEpatents

    Raistrick, Ian D.; Poris, Jaime; Huggins, Robert A.

    1982-02-09

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

  4. 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.

  5. 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.

  6. Glyme-lithium salt phase behavior.

    PubMed

    Henderson, Wesley A

    2006-07-01

    Phase diagrams are reported for glyme mixtures with simple lithium salts. The glymes studied include monoglyme (DME), diglyme, triglyme, and tetraglyme. The lithium salts include LiBETI, LiAsF6, LiI, LiClO4, LiBF4, LiCF3SO3, LiBr, LiNO3, and LiCF3CO2. The phase diagrams clearly illustrate how solvate formation and thermophysical properties are dictated by the ionic association strength of the salt (i.e., the properties of the anions) and chain length of the solvating molecules. This information provides critical predictive capabilities for solvate formation and ionic interactions common in organometallic reagents and battery electrolytes. PMID:16805630

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

    SciTech Connect

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

    2010-01-01

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

  8. Antiproliferative Potential of Officinal Forms and Nanoparticles of Lithium Salts.

    PubMed

    Lykov, A P; Poveshchenko, O V; Bondarenko, N A; Bogatova, N P; Makarova, O P; Konenkov, V I

    2016-04-01

    We studied the effect of officinal forms and nanoparticles of lithium carbonate and lithium citrate on proliferative activity of hepatoma-29 cells. Lithium carbonate nanoparticles suppressed proliferation of hepatoma-29 cells in lower concentrations than officinal form of this salt. The antiproliferative effect of lithium salts i activation of apoptosis and arrest of hepatoma-29 cells in the G2/M phase of the cell cycle. PMID:27165073

  9. 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.

  10. A Molten Salt Lithium-Oxygen Battery.

    PubMed

    Giordani, Vincent; Tozier, Dylan; Tan, Hongjin; Burke, Colin M; Gallant, Betar M; Uddin, Jasim; Greer, Julia R; McCloskey, Bryan D; Chase, Gregory V; Addison, Dan

    2016-03-01

    Despite the promise of extremely high theoretical capacity (2Li + O2 ↔ Li2O2, 1675 mAh per gram of oxygen), many challenges currently impede development of Li/O2 battery technology. Finding suitable electrode and electrolyte materials remains the most elusive challenge to date. A radical new approach is to replace volatile, unstable and air-intolerant organic electrolytes common to prior research in the field with alkali metal nitrate molten salt electrolytes and operate the battery above the liquidus temperature (>80 °C). Here we demonstrate an intermediate temperature Li/O2 battery using a lithium anode, a molten nitrate-based electrolyte (e.g., LiNO3-KNO3 eutectic) and a porous carbon O2 cathode with high energy efficiency (∼95%) and improved rate capability because the discharge product, lithium peroxide, is stable and moderately soluble in the molten salt electrolyte. The results, supported by essential state-of-the-art electrochemical and analytical techniques such as in situ pressure and gas analyses, scanning electron microscopy, rotating disk electrode voltammetry, demonstrate that Li2O2 electrochemically forms and decomposes upon cycling with discharge/charge overpotentials as low as 50 mV. We show that the cycle life of such batteries is limited only by carbon reactivity and by the uncontrolled precipitation of Li2O2, which eventually becomes electrically disconnected from the O2 electrode. PMID:26871485

  11. A new lithium salt with dihydroxybenzene and lithium tetrafluoroborate for lithium battery electrolytes

    NASA Astrophysics Data System (ADS)

    Xue, Zhao-Ming; Sun, Bin-Bin; Zhou, Wei; Chen, Chun-Hua

    2011-10-01

    A new unsymmetrical lithium salt containing F-, C6H4O22- [dianion of 1,2-benzenediol], lithium difluoro(1,2-benzene-diolato(2-)-o,o‧)borate (LDFBDB) is synthesized and characterized. Its thermal decomposition in nitrogen begins at 170 °C. The cyclic voltammetry study shows that the LDFBDB solution in propylene carbonate (PC) is stable up to 3.7 V versus Li+/Li. It is soluble in common organic solvents. The ionic dissociation properties of LDFBDB are examined by conductivity measurements in PC, PC+ ethyl methyl carbonate (EMC), PC + dimethyl ether (DME), PC + ethylene carbonate (EC) + EMC solutions. The conductivity values of the 0.564 mol dm-3 LDFBDB electrolyte in PC + DME solution is 3.90 mS cm-1. All these properties of the new lithium salt including the thermal characteristics, electrochemical stabilities, solubilities, ionic dissociation properties are studied and compared with those of its derivatives, lithium difluoro(3-fluoro-1,2-benzene-diolato(2-)-o,o‧)borate (FLDFBDB), lithium [3-fluoro-1,2-benzenediolato(2-)-o,o‧ oxalato]borate (FLBDOB), and lithium bis(oxalate)borate (LBOB).

  12. Application of lithium in molten-salt reduction processes.

    SciTech Connect

    Gourishankar, K. V.

    1998-11-11

    Metallothermic reductions have been extensively studied in the field of extractive metallurgy. At Argonne National Laboratory (ANL), we have developed a molten-salt based reduction process using lithium. This process was originally developed to reduce actinide oxides present in spent nuclear fuel. Preliminary thermodynamic considerations indicate that this process has the potential to be adapted for the extraction of other metals. The reduction is carried out at 650 C in a molten-salt (LiCl) medium. Lithium oxide (Li{sub 2}O), produced during the reduction of the actinide oxides, dissolves in the molten salt. At the end of the reduction step, the lithium is regenerated from the salt by an electrowinning process. The lithium and the salt from the electrowinning are then reused for reduction of the next batch of oxide fuel. The process cycle has been successfully demonstrated on an engineering scale in a specially designed pyroprocessing facility. This paper discusses the applicability of lithium in molten-salt reduction processes with specific reference to our process. Results are presented from our work on actinide oxides to highlight the role of lithium and its effect on process variables in these molten-salt based reduction processes.

  13. New MALDI matrices based on lithium salts for the analysis of hydrocarbons and wax esters.

    PubMed

    Horká, Petra; Vrkoslav, Vladimír; Hanus, Robert; Pecková, Karolina; Cvačka, Josef

    2014-07-01

    Lithium salts of organic aromatic acids (lithium benzoate, lithium salicylate, lithium vanillate, lithium 2,5-dimethoxybenzoate, lithium 2,5-dihydroxyterephthalate, lithium α-cyano-4-hydroxycinnamate and lithium sinapate) were synthesized and tested as potential matrices for the matrix-assisted laser desorption/ionization (MALDI)-mass spectrometry analysis of hydrocarbons and wax esters. The analytes were desorbed using nitrogen laser (337.1 nm) and ionized via the attachment of a lithium cation, yielding [M + Li](+) adducts. The sample preparation and the experimental conditions were optimized for each matrix using stearyl behenate and n-triacontane standards. The performance of the new matrices in terms of signal intensity and reproducibility, the mass range occupied by matrix ions and the laser power threshold were studied and compared with a previously recommended lithium 2,5-dihydroxybenzoate matrix (LiDHB) (Cvačka and Svatoš, Rapid Commun. Mass Spectrom. 2003, 17, 2203). Several of the new matrices performed better than LiDHB. Lithium vanillate offered a 2-3 times and 7-9 times higher signal for wax esters and hydrocarbons, respectively. Also, the signal reproducibility improved substantially, making this matrix a suitable candidate for imaging applications. In addition, the diffuse reflectance spectra and solubility of the synthesized compounds were investigated and discussed with respect to the compound's ability to serve as MALDI matrices. The applicability of selected matrices was tested on natural samples of wax esters and hydrocarbons. PMID:25044848

  14. Electronic structure calculations on lithium battery electrolyte salts.

    PubMed

    Johansson, Patrik

    2007-03-28

    New lithium salts for non-aqueous liquid, gel and polymeric electrolytes are crucial due to the limiting role of the electrolyte in modern lithium batteries. The solvation of any lithium salt to form an electrolyte solution ultimately depends on the strength of the cation-solvent vs. the cation-anion interaction. Here, the latter is probed via HF, B3LYP and G3 theory gas-phase calculations for the dissociation reaction: LiX <--> Li(+) + X(-). Furthermore, a continuum solvation method (C-PCM) has been applied to mimic solvent effects. Anion volumes were also calculated to facilitate a discussion on ion conductivities and cation transport numbers. Judging from the present results, synthesis efforts should target heterocyclic anions with a size of ca. 150 A(3) molecule(-1) to render new highly dissociative lithium salts that result in electrolytes with high cation transport numbers. PMID:17356757

  15. 40 CFR 721.9538 - Lithium salt of sulfophenyl azo phenyl azo disulfostilbene (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Lithium salt of sulfophenyl azo phenyl... Significant New Uses for Specific Chemical Substances § 721.9538 Lithium salt of sulfophenyl azo phenyl azo... substance identified generically as lithium salt of sulfophenyl azo phenyl azo disulfostilbene (PMN...

  16. 40 CFR 721.9538 - Lithium salt of sulfophenyl azo phenyl azo disulfostilbene (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Lithium salt of sulfophenyl azo phenyl... Significant New Uses for Specific Chemical Substances § 721.9538 Lithium salt of sulfophenyl azo phenyl azo... substance identified generically as lithium salt of sulfophenyl azo phenyl azo disulfostilbene (PMN...

  17. 40 CFR 721.9538 - Lithium salt of sulfophenyl azo phenyl azo disulfostilbene (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Lithium salt of sulfophenyl azo phenyl... Significant New Uses for Specific Chemical Substances § 721.9538 Lithium salt of sulfophenyl azo phenyl azo... substance identified generically as lithium salt of sulfophenyl azo phenyl azo disulfostilbene (PMN...

  18. 40 CFR 721.9538 - Lithium salt of sulfophenyl azo phenyl azo disulfostilbene (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Lithium salt of sulfophenyl azo phenyl... Significant New Uses for Specific Chemical Substances § 721.9538 Lithium salt of sulfophenyl azo phenyl azo... substance identified generically as lithium salt of sulfophenyl azo phenyl azo disulfostilbene (PMN...

  19. 40 CFR 721.9538 - Lithium salt of sulfophenyl azo phenyl azo disulfostilbene (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Lithium salt of sulfophenyl azo phenyl... Significant New Uses for Specific Chemical Substances § 721.9538 Lithium salt of sulfophenyl azo phenyl azo... substance identified generically as lithium salt of sulfophenyl azo phenyl azo disulfostilbene (PMN...

  20. Role of Constituent Hard Polymer in Enhancing Lithium Transference Number of Lithium Salt-Polymer Complexes

    NASA Astrophysics Data System (ADS)

    Jo, Gyuha; Park, Moon Jeong

    2015-03-01

    Lithium polymer batteries have been projected as promising energy storage systems, owing to their unique advantages such as long cycle life, high specific capacity, and high cell potential. While the polymer electrolytes such as poly(ethylene oxide) (PEO) employed in lithium polymer batteries have high ionic conductivity and low volatility, the PEO-lithium salt complexes indicated immense shortcomings of concentration polarization, ascribed to the motion of free anions within PEO. This has limited charge/discharge rate of lithium batteries. In this study, we present a new methodology for improving the ionic conductivity and lithium transference number of PEO, by block copolymerization with a hard polymer, namely poly(dithiooxamide) (PDTOA). Compared to a simple PEO/PDTOA blend, lithium-salt doped PEO-b-PDTOA block copolymers exhibited significantly improved ionic conductivity values. Further, lithium transference numbers as high as 0.66 were observed, which are much higher than the corresponding values for conventional PEO-salt electrolytes (~ 0 . 25).

  1. Study of novel lithium salt-based, plasticized polymer electrolytes

    NASA Astrophysics Data System (ADS)

    Silva, Maria Manuela; Barros, Sandra Cerqueira; Smith, Michael J.; MacCallum, James R.

    The results of a preliminary investigation of a series of polymer electrolytes based on a novel polymer host, poly(trimethylene carbonate) (p(TMC)), with lithium triflate or lithium perchlorate and various plasticizing additives, are described in this presentation. Electrolytes with lithium salt compositions of about n=10 (where n represents the molar ratio of (OCOCH 2CH 2CH 2O) units per lithium ion) and additive compositions between 5 and 15 wt.% (with respect to p(TMC)), were prepared by co-dissolution of salt and polymer in anhydrous solvent with a controlled amount of additive. The homogeneous solutions obtained were evaporated within a preparative glovebox and under a dry argon atmosphere to form thin films of electrolyte. The solvent-free electrolyte films produced were characterized by measurements of total ionic conductivity, differential scanning calorimetry and thermogravimetry. In general the triflate-based electrolytes were found to show moderate ionic conductivity and good thermal stability while perchlorate-based electrolytes showed higher levels of conductivity but lower thermal stability. Electrolytes based on this host polymer, with both lithium salts, were obtained as very flexible, transparent, completely amorphous films.

  2. Effect of organo and inorganic lithium salt on human blood plasma glutathione- A comparative study.

    PubMed

    Ullah, Hashmat; Khan, Muhammad Farid; Jan, Syed Umer; Hashmat, Farwa

    2016-03-01

    Investigation of toxicological effect of various metals is the field of interest for toxicological scientists since four to five decades and especially the toxicological effect of those drugs containing metals and there use is common because there is no other choice except to use these metal containing drugs. Inorganic as well as organic salts of lithium are commonly used in prophylaxis and treatments of many psychiatric disorders. The aim of the present study was to see the difference between the effect of organic and inorganic salt of lithium commonly used in psychiatric disorders on the GSH of human blood plasma. It is the scientific fact that ionic dissociation of organic and inorganic salts of any metal is always quite different hence to prove this fact, the effect of lithium citrate (organic salt of lithium) and lithium carbonate (inorganic salt of lithium) was investigated on human blood plasma GSH to find the difference between the effect of two. Ellman's method was used for the quantification of glutathione contents in plasma. It was found that lithium citrate decrease plasma GSH contents less than lithium carbonate indicating that organic salts of lithium are safe than inorganic salts of lithium when are used in psychiatric disorders. Further to analyze the effect of organic and inorganic salt of lithium on blood plasma GSH with the increase in incubation time was also evaluated and was found that both concentration and time dependent effect of organic salt of lithium shows that this salt has decreased plasma GSH contents of human blood less than inorganic salt of lithium either by promoting oxidation of GSH into GSSG or by lithium glutathione complex formation. These results suggest the physicians that the use of organic lithium salts is much safer than inorganic salts of lithium in terms of depletion of blood plasma GSH contents. PMID:27087067

  3. Kinetic investigation of the solvation of lithium salts in siloxanes.

    SciTech Connect

    Chen, Z.; Wang, H. H.; Vissers, D. R.; Zhang, L.; West, R.; Lyons, L. J.; Amine, K.; Chemical Sciences and Engineering Division; Univ. of Wisconsin; Grinnell Coll.

    2008-02-14

    The solvation of lithium salts in siloxanes was investigated with the aim to understand the key barriers that limit the ionic conductivity of siloxane-based electrolytes. The conductivity and kinetic data were measured for electrolytes with different salts, different salt concentrations, and solvents. The results show that both the conductivity and the kinetics of ionic transportation were greatly impacted by the specific interactions between ions and the solvent molecules. The high content of ion pairs in the electrolytes can be one of the main reasons for the low ionic conductivity observed in the siloxane-based electrolytes.

  4. A Stable Fluorinated and Alkylated Lithium Malonatoborate Salt for Lithium Ion Battery Application

    SciTech Connect

    Dai, Sheng; Sun, Xiao-Guang

    2015-01-01

    A new fluorinated and alkylated lithium malonatoborate salt, lithium bis(2-methyl-2-fluoromalonato)borate (LiBMFMB), has been synthesized for lithium ion battery application. A 0.8 M LiBMFMB solution is obtained in a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) (1:2 by wt.). The new LiBMFMB based electrolyte exhibits good cycling stability and rate capability in LiNi0.5Mn1.5O4 and graphite based half-cells.

  5. A Stable Fluorinated and Alkylated Lithium Malonatoborate Salt for Lithium Ion Battery Application

    DOE PAGESBeta

    Wan, Shun; Jiang, Xueguang; Guo, Bingkun; Dai, Sheng; Goodenough, John B.; Sun, Xiao-Guang

    2015-04-27

    A new fluorinated and alkylated lithium malonatoborate salt, lithium bis(2-methyl-2-fluoromalonato)borate (LiBMFMB), has been synthesized for lithium ion battery application. A 0.8 M LiBMFMB solution is obtained in a mixture of ethylene carbonate (EC) and ethyl methyl carbonate (EMC) (1:2 by wt.). The new LiBMFMB based electrolyte exhibits good cycling stability and rate capability in LiNi0.5Mn1.5O4 and graphite based half-cells.

  6. Stable lithium electrodeposition in salt-reinforced electrolytes

    NASA Astrophysics Data System (ADS)

    Lu, Yingying; Tu, Zhengyuan; Shu, Jonathan; Archer, Lynden A.

    2015-04-01

    Development of high-energy lithium-based batteries that are safe remains a challenge due to the non-uniform lithium electrodeposition during repeated charge and discharge cycles. We report on the effectiveness of lithium bromide (LiBr) salt additives in a common liquid electrolyte (i.e. propylene carbonate (PC)) on the stability of lithium electrodeposition. From galvanostatic cycling measurements, we find that the presence of LiBr in PC provides more than 20-fold enhancement in cell lifetime over the control LiTFSI/PC electrolyte. Batteries containing 30 mol% LiBr additive in the electrolytes are able to cycle stably for at least 1.8 months with no observations of cell failure. From galvanostatic polarization measurements, an electrolyte containing 30 mol% LiBr shows a maximum improvement in lifetime. The formation of uneven lithium electrodeposits is significantly suppressed by the Br-containing SEI layers, evidenced by impedance spectra, post-mortem SEM and XPS analyses. The study also concludes that good solubility of halogenated salts is not necessary for achieving the observed improvements in cell lifetime.

  7. Lithium salts for advanced lithium batteries: Li-metal, Li-O2, and Li-S

    SciTech Connect

    Younesi, Reza; Veith, Gabriel M.; Johansson, Patrik; Edstrom, Kristina; Vegge, Tejs

    2015-06-01

    Presently lithium hexafluorophosphate (LiPF6) is the dominant Li-salt used in commercial rechargeable lithium-ion batteries (LIBs) based on a graphite anode and a 3-4 V cathode material. While LiPF6 is not the ideal Li-salt for every important electrolyte property, it has a uniquely suitable combination of properties (temperature range, passivation, conductivity, etc.) rendering it the overall best Li-salt for LIBs. However, this may not necessarily be true for other types of Li-based batteries. Indeed, next generation batteries, for example lithium-metal (Li-metal), lithium-oxygen (Li-O2), and lithium sulphur (Li-S), require a re-evaluation of Li-salts due to the different electrochemical and chemical reactions and conditions within such cells. Furthermore, this review explores the critical role Li-salts play in ensuring in these batteries viability.

  8. Lithium salts for advanced lithium batteries: Li-metal, Li-O2, and Li-S

    DOE PAGESBeta

    Younesi, Reza; Veith, Gabriel M.; Johansson, Patrik; Edstrom, Kristina; Vegge, Tejs

    2015-06-01

    Presently lithium hexafluorophosphate (LiPF6) is the dominant Li-salt used in commercial rechargeable lithium-ion batteries (LIBs) based on a graphite anode and a 3-4 V cathode material. While LiPF6 is not the ideal Li-salt for every important electrolyte property, it has a uniquely suitable combination of properties (temperature range, passivation, conductivity, etc.) rendering it the overall best Li-salt for LIBs. However, this may not necessarily be true for other types of Li-based batteries. Indeed, next generation batteries, for example lithium-metal (Li-metal), lithium-oxygen (Li-O2), and lithium sulphur (Li-S), require a re-evaluation of Li-salts due to the different electrochemical and chemical reactions andmore » conditions within such cells. Furthermore, this review explores the critical role Li-salts play in ensuring in these batteries viability.« less

  9. Salting the landscapes in Transbaikalia: natural and technogenic factors

    NASA Astrophysics Data System (ADS)

    Peryazeva, E. G.; Plyusnin, A. M.; Chinavlev, A. M.

    2010-05-01

    Salting the soils, surface and subsurface waters is widespread in Transbaikalia. Hearths of salting occur within intermountain depressions of the Mesozoic and Cenozoic age both in the steppe arid and forest humid landscapes. Total water mineralization reaches 80 g/dm3 in lakes and 4-5 g/dm3 in subsurface waters. The waters belong to hydrocarbonate sodium and sulfate sodium types by chemical composition. The soda type of waters is widely spread through the whole area. Sulfate waters are found in several hearths of salting. Deposition of salts takes place in some lakes. Mirabilite and soda depositions are most commonly observed in muds of salt lakes. Deposition of salts occurs both as a result of evaporative concentrating and during freezing out the solvent. In the winter period, efflorescences of salts, where decawater soda is main mineral, are observed on ice surface. Solonchaks are spread in areas of shallow ground waters (1-2m). Soil salting is most intense in the lower parts of depressions, where surface of ground waters is at depth 0.5-1.0m. In soil cover of solonchaks, salt horizon is of various thicknesses, and it has various morphological forms of occurrence, i.e. as thick deposits of salts on soil surface and salting the surficial horizons. The soil has low alkaline reaction of medium and is characterized by high content of exchangeable bases with significant content of exchangeable sodium in the absorbing complex. Total amount of salts varies from 0.7 to 1.3%. Their maximal quantity (3.1%) is confined to the surficial layer. Sulfate-sodium type of salting is noted in the solonchak upper horizons and sulfate-magnesium-calcium one in the lower ones (Ubugunov et al, 2009). Formation of salting hearths is associated with natural and technogenic conditions. The Mesozoic depressions of Transbaikalia are characterized by intense volcanism. Covers of alkaline and moderately alkaline basalts that are enriched in potassium, sodium, carbon dioxide, fluorine, chlorine

  10. Aggregation of 12-Hydroxystearic Acid and Its Lithium Salt in Hexane: Molecular Dynamics Simulations.

    PubMed

    Gordon, Ryan; Stober, Spencer T; Abrams, Cameron F

    2016-07-28

    12-Hydroxystearic acid (12HSA) is a well-known organogelator, and its metal salts and derivatives find roles in many important applications. The structures of aggregates of 12-hydroxysteric acid and its salts depend sensitively on cation type, but a fundamental understanding of this phenomenon is lacking. In this study, molecular dynamics simulations were conducted on the microsecond long time scales for (1) 12HSA and (2) its lithium salt, each at 12.5 wt % in explicit hexane solvent. Self-assembly was accelerated by using a modified potential to prohibit alkane chain dihedral gauche states (all-trans-12HSA) and then verified by continuation using standard force-field parameters. In three independent simulation, acceleration using "gauche-less" potentials resulted in self-assembled pseudocrystalline aggregates through formation of polarized five- and six-membered rings between inter-12-hydroxyl groups and head-to-head carboxylic acid dimerization. When subjected to the unmodified dihedral potential, two of the three structures remained stable after 1 μs of MD. Stable structures exhibited a "ring-of-rings" motif, composed of two six-membered acetic acid-dimerized ring bundles with six satellite rings, while the unstable structure did not. In strong contrast, the lithium salt produced a network of fibrils that spanned the volume of the sample. When lithium ions were substituted for carboxylic acid protons in the stable acid structures, they remained intact but lost their chiral nature. Both the acid and lithium structures displayed scattering peaks that agreed with experiment. Taken together, our results suggest that this ring-of-rings structure could be a primary feature of the self-assembly of 12HSA in organic solvents. PMID:27387154

  11. Characterization of Lithium Polysulfide Salts in Homopolymers and Block Copolymers

    NASA Astrophysics Data System (ADS)

    Wang, Dunyang; Wujcik, Kevin; Balsara, Nitash

    Ion-conducting polymers are important for solid-state batteries due to the promise of better safety and the potential to produce higher energy density batteries. Nanostructured block copolymer electrolytes can provide high ionic conductivity and mechanical strength through microphase separation. One of the potential use of block copolymer electrolytes is in lithium-sulfur batteries, a system that has high theoretical energy density wherein the reduction of sulfur leads to the formation of lithium polysulfide intermediates. In this study we investigate the effect of block copolymer morphology on the speciation and transport properties of the polysulfides. The morphology and conductivities of polystyrene-b-poly(ethylene oxide) (SEO) containing lithium polysulfides were studies using small-angle X-ray scattering and ac impedance spectroscopy. UV-vis spectroscopy is being used to determine nature of the polysulfide species in poly(ethylene oxide) and SEO. Department of Energy, Soft Matter Electron Microscopy Program and Battery Materials Research Program.

  12. Enhanced charging capability of lithium metal batteries based on lithium bis(trifluoromethanesulfonyl)imide-lithium bis(oxalato)borate dual-salt electrolytes

    NASA Astrophysics Data System (ADS)

    Xiang, Hongfa; Shi, Pengcheng; Bhattacharya, Priyanka; Chen, Xilin; Mei, Donghai; Bowden, Mark E.; Zheng, Jianming; Zhang, Ji-Guang; Xu, Wu

    2016-06-01

    Rechargeable lithium (Li) metal batteries with conventional LiPF6-carbonate electrolytes have been reported to fail quickly at charging current densities of about 1.0 mA cm-2 and above. In this work, we demonstrate the rapid charging capability of Li||LiNi0.8Co0.15Al0.05O2 (NCA) cells can be enabled by a dual-salt electrolyte of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and lithium bis(oxalato)borate (LiBOB) in a carbonate solvent mixture. The cells using the LiTFSI-LiBOB dual-salt electrolyte significantly outperform those using the LiPF6 electrolyte at high charging current densities. At the charging current density of 1.50 mA cm-2, the Li||NCA cells with the dual-salt electrolyte can still deliver a discharge capacity of 131 mAh g-1 and a capacity retention of 80% after 100 cycles. The Li||NCA cells with the LiPF6 electrolyte start to show fast capacity fading after the 30th cycle and only exhibit a low capacity of 25 mAh g-1 and a low retention of 15% after 100 cycles. The reasons for the good chargeability and cycling stability of the cells using the LiTFSI-LiBOB dual-salt electrolyte can be attributed to the good film-formation ability of the electrolyte on the Li metal anode and the highly conductive nature of the sulfur-rich interphase layer.

  13. Correlating Microstructural Lithium Metal Growth with Electrolyte Salt Depletion in Lithium Batteries Using ⁷Li MRI.

    PubMed

    Chang, Hee Jung; Ilott, Andrew J; Trease, Nicole M; Mohammadi, Mohaddese; Jerschow, Alexej; Grey, Clare P

    2015-12-01

    Lithium dendrite growth in lithium ion and lithium rechargeable batteries is associated with severe safety concerns. To overcome these problems, a fundamental understanding of the growth mechanism of dendrites under working conditions is needed. In this work, in situ (7)Li magnetic resonance (MRI) is performed on both the electrolyte and lithium metal electrodes in symmetric lithium cells, allowing the behavior of the electrolyte concentration gradient to be studied and correlated with the type and rate of microstructure growth on the Li metal electrode. For this purpose, chemical shift (CS) imaging of the metal electrodes is a particularly sensitive diagnostic method, enabling a clear distinction to be made between different types of microstructural growth occurring at the electrode surface and the eventual dendrite growth between the electrodes. The CS imaging shows that mossy types of microstructure grow close to the surface of the anode from the beginning of charge in every cell studied, while dendritic growth is triggered much later. Simple metrics have been developed to interpret the MRI data sets and to compare results from a series of cells charged at different current densities. The results show that at high charge rates, there is a strong correlation between the onset time of dendrite growth and the local depletion of the electrolyte at the surface of the electrode observed both experimentally and predicted theoretical (via the Sand's time model). A separate mechanism of dendrite growth is observed at low currents, which is not governed by salt depletion in the bulk liquid electrolyte. The MRI approach presented here allows the rate and nature of a process that occurs in the solid electrode to be correlated with the concentrations of components in the electrolyte. PMID:26524078

  14. Ionic liquid-based electrolyte with binary lithium salts for high performance lithium-sulfur batteries

    NASA Astrophysics Data System (ADS)

    Wu, Feng; Zhu, Qizhen; Chen, Renjie; Chen, Nan; Chen, Yan; Ye, Yusheng; Qian, Ji; Li, Li

    2015-11-01

    Rechargeable Li-S batteries have suffered several technical obstacles, such as rapid capacity fading and low coulombic efficiency. To overcome these problems, we design new electrolytes containing N-methoxyethyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)-imide (Pyr1,2O1TFSI) and tri(ethylene glycol)dimethyl ether (TEGDME) in mass ratio of 7:3. Moreover, Lithium difluoro(oxalate)borate (LiODFB) is introduced for the modification. Although the addition of LiODFB as additive lead to extremely high viscosity of electrolyte and inferior performance of the cells, the electrolyte containing lithium bis(trifluoromethanesulfonyl)imide (LiTFSI, 0.84 nm) and LiODFB (0.60 nm) mixture with a total molar concentration of 0.4 mol kg-1 as binary lithium salt shows excellent electrochemical performance. The Pyr1,2O1TFSI/TEGDME electrolyte with LiTFSI/LiODFB binary lithium salts in mole ratio of 6:4 is obtained after optimizing ratio. The Li-S cells containing this electrolyte system show excellent capacity and cycle performance, whose initial discharge capacity is 1264.4 mAh g-1, and retains 911.4 mAh g-1 after 50 cycles with the coulombic efficiency more than 95%. It can be attributed the solid-electrolyte interphase (SEI)-forming ability of LiODFB which protect Li anode from suffering lithium dendrites and prevent the shuttle phenomenon. The novel electrolytes provide good cycling stability and high coulombic efficiency for the Li-S batteries, which is suggested as a promising electrolyte for Li-S batteries.

  15. Structural Interactions within Lithium Salt Solvates. Acyclic Carbonates and Esters

    SciTech Connect

    Afroz, Taliman; Seo, D. M.; Han, Sang D.; Boyle, Paul D.; Henderson, Wesley A.

    2015-03-06

    Solvate crystal structures serve as useful models for the molecular-level interactions within the diverse solvates present in liquid electrolytes. Although acyclic carbonate solvents are widely used for Li-ion battery electrolytes, only three solvate crystal structures with lithium salts are known for these and related solvents. The present work, therefore, reports six lithium salt solvate structures with dimethyl and diethyl carbonate: (DMC)2:LiPF6, (DMC)1:LiCF3SO3, (DMC)1/4:LiBF4, (DEC)2:LiClO4, (DEC)1:LiClO4 and (DEC)1:LiCF3SO3 and four with the structurally related methyl and ethyl acetate: (MA)2:LiClO4, (MA)1:LiBF4, (EA)1:LiClO4 and (EA)1:LiBF4.

  16. LBDOB, a new lithium salt with benzenediolato and oxalato complexes of boron for lithium battery electrolytes

    NASA Astrophysics Data System (ADS)

    Xue, Zhao-Ming; Zhao, Jun-Fei; Ding, Jia; Chen, Chun-Hua

    A new unsymmetrical lithium salt containing C 6H 4O 2 2-[dianion of 1,2-benzenediol] and C 2O 4 2-[dianion of oxalic acid], lithium [1,2-benzenediolato(2-)-O,O‧ oxalato]borate (LBDOB), is synthesized and characterized. The thermal characteristics of it, lithium bis[1,2-benzenediolato(2-)-O,O‧]borate (LBBB) and lithium bis(oxalate)borate (LiBOB) are examined by thermogravimetric (TG) analysis. The thermal decomposition in Ar begins at 250, 256, and 302 °C for LBBB, LBDOB, and LBOB, respectively. The order of the stability toward oxidation of these organoborates is LBOB > LBDOB > LBBB, which is in the same order of the thermal stability. The cyclic voltammetry study shows that the LBDOB solution in PC is stable up to 3.7 V vs. Li +/Li. They are soluble in common organic solvents. Ionic dissociation properties of LBDOB and its derivatives are examined by conductivity measurements in PC, PC + DME, EC + DME, PC + THF, EC + THF (molar ratio 1:1) solutions. The conductivity values of the 0.10 mold m -3 LBDOB electrolyte in PC, PC + DME, EC + DME, PC + THF, EC + THF solutions are higher than those of LBBB, but lower than those of LBOB electrolytes.

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

    SciTech Connect

    Yang, Li; Zhang, Hanjun; Driscoll, Peter; Lucht, Brett; Kerr, John

    2011-09-30

    A new class of lithium salts of malonatoborate anions has been synthesized. These six-membered-ring salts provided slightly lower ionic conductivity than that of LiBOB and LiBF4. Nevertheless, compared with LiBOB and LiPF6, the lowered ring strains in the malonatoborate structures and reduced numbers of fluorine atoms in the molecules was found to enhance the thermal and water stabilities and compatibilities of these salts with ether solvents. Small amount LiDMMDFB when used as an additive, was found to stabilize LiPF6 in carbonate electrolytes at 80°C for one month. Employing LiMDFB as the electrolyte in Li/Li cells and full cells, large interfacial impedances were observed on lithium metal and the cathode. Moreover, the large impedances are at least partially attributed to the acidic hydrogen atoms in the malonate structure. This issue can be addressed by replacing the acidic atoms with methyl groups.

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

    SciTech Connect

    Ding, Fei; Xu, Wu; Chen, Xilin; Zhang, Jian; Engelhard, Mark H.; Zhang, Yaohui; Johnson, Bradley R.; Crum, Jarrod V.; Blake, Thomas A.; Liu, Xingjiang; Zhang, Jiguang

    2013-09-04

    The application of lithium (Li) metal anode in rechargeable batteries is hindered by Li dendrite growth during Li deposition and low Li Coulombic efficiency (CE), where the nonaqueous electrolyte plays a critical role. In this work, the effects of different carbonate solvents and Li salts on Li deposition morphology and CE were systematically investigated. Typically cyclic carbonates are found to favor the formation of uniform Li film and improve Li CE than linear carbonates do. Several specific cyclic carbonates that are conventionally used as solid electrolyte interface formation additives in Li ion batteries can also improve the CE of Li anode. Furthermore, among the nine electrolyte salts studied, LiAsF6 and LiBOB lead to the highest CE for Li anode. LiBOB also leads to much smoother Li morphology than other salts do. Considering the better safety of LiBOB as compared to LiAsF6, LiBOB is a promising Li salt for rechargeable Li metal batteries with high CE. By combining the best electrolyte solvent/salt that can lead to high Li CE and novel electrolyte additives that can prevent dendrite formation, it is possible to find an electrolyte that not only prevents Li dendrite formation but also lead to high CE during Li deposition/stripping processes.

  19. Lithium in the brines of Fish Lake Valley and Columbus Salt Marsh, Nevada

    USGS Publications Warehouse

    Smith, C.L.; Meier, Allen L.; Downey, H.D.

    1977-01-01

    Analyses of waters-from springs in Nevada have led to the identification of an area containing anomalous amounts of lithium northwest of the Clayton Valley-area. Fish Lake Valley and Columbus Salt Marsh contain waters having, relatively high lithium and potassium concentrations. At least a part of these waters is probably derived from the leaching of Tertiary rocks containing saline minerals. The high-lithium waters at Columbus Salt Marsh could be derived not only by the leaching of rocks with a high soluble lithium ands, potassium content but also by subsurface outflow from Fish Lake Valley.

  20. Lithium clearance in man: effects of dietary salt intake, acute changes in extracellular fluid volume, amiloride and frusemide.

    PubMed

    Atherton, J C; Green, R; Hughes, S; McFall, V; Sharples, J A; Solomon, L R; Wilson, L

    1987-12-01

    1. The effects of amiloride and frusemide on lithium clearance were studied during changes in dietary sodium chloride intake and during infusion of 0.9% NaCl in normal human volunteers. 2. Lithium and fractional lithium clearances were less on the low than on the high salt diet. Values for the medium salt diet were intermediate. Acute extracellular fluid volume expansion with 0.9% NaCl infusion and extracellular fluid volume contraction 3-4 h after intravenous frusemide caused lithium and fractional lithium clearances to increase and decrease respectively. 3. Amiloride caused small changes in lithium and fractional lithium clearances on a low salt diet, but was without effect when salt intake was medium or high. 4. Increases in lithium clearance occurred immediately after frusemide irrespective of dietary salt intake and in subjects infused with 0.9% NaCl. Only in salt-depleted subjects did frusemide cause a substantial increase in fractional lithium clearance. Changes induced under other circumstances were small. 5. It is concluded that the lithium clearance method for assessment of proximal tubule salt and water reabsorption can be used with some degree of confidence in certain circumstances (medium and high salt intake as well as in acute volume expansion) but may not be reliable when dietary salt intake is low. PMID:3690979

  1. Electrochemical studies on lithium intercalatin materials in molten salts

    SciTech Connect

    Gauthier, M.; Vassort, G.; Belanger, A.; Adams, W.A.

    1982-05-01

    Using an electrochemical device for investigating powdered reagents, we studied various intercalation compounds in the LiCl-KCl electrolyte at about 430/degree/C and found TiS/sub 2/, TiSe/sub 2/, NbSe/sub 2/, and TaS/sub 2/ sufficiently stable to be studied under test conditions. The electrochemical techniques used include cyclic voltammetry and the study of discharge-voltage curves, simultaneously with coulometry. The tests showed that these compounds, all with lamellar structures, nonstoichiometrically intercalate one lithium ion per mol of the host structure and that intercalation is rapid as well as reversible, with the reactions taking place close to equilibrium conditions at utilizations of almost 100%. In addition, a cycling test on stoichiometric TiS/sub 2/ show that the performance of the electrode remains unaltered after more than 300 discharge-charge cycles. However, although the intercalation compounds investigated here have remarkable electrochemical properties, they do not represent attractive substitutes for the FeS electrode now used in molten-salt batteries. 20 refs.

  2. Concentrated dual-salt electrolytes for improving the cycling stability of lithium metal anodes

    NASA Astrophysics Data System (ADS)

    Pin, Liu; Qiang, Ma; Zheng, Fang; Jie, Ma; Yong-Sheng, Hu; Zhi-Bin, Zhou; Hong, Li; Xue-Jie, Huang; Li-Quan, Chen

    2016-07-01

    Lithium (Li) metal is an ideal anode material for rechargeable Li batteries, due to its high theoretical specific capacity (3860 mAh/g), low density (0.534 g/cm3), and low negative electrochemical potential (‑3.040 V vs. standard hydrogen electrode). In this work, the concentrated electrolytes with dual salts, composed of Li[N(SO2F)2] (LiFSI) and Li[N(SO2CF3)2] (LiTFSI) were studied. In this dual-salt system, the capacity retention can even be maintained at 95.7% after 100 cycles in Li|LiFePO4 cells. A Li|Li cell can be cycled at 0.5 mA/cm2 for more than 600 h, and a Li|Cu cell can be cycled at 0.5 mA/cm2 for more than 200 cycles with a high average Coulombi efficiency of 99%. These results show that the concentrated dual-salt electrolytes exhibit superior electrochemical performance and would be a promising candidate for application in rechargeable Li batteries. Project supported by the National Nature Science Foundation of China (Grant Nos. 51222210, 51472268, 51421002, and 11234013) and the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA09010300).

  3. Studies on the Properties of Plasticizer and Lithium Salt on PMMA-based Solid Polymer Electrolytes

    SciTech Connect

    Chew, K. W.; Tan, C. G.; Osman, Z.

    2010-03-11

    The effects of plasticizer and lithium salt on PMMA-based solid polymer electrolyte have been investigated. In current project, three system samples consisted of pure poly(methyl methacrylate (PMMA) system, plasticized poly(methyl methacrylate)(PMMA-EC) system and the LiCF{sub 3}SO{sub 3} salted-poly(methyl methacrylate) containing a fixed amount of plasticizer ([PMMA-EC]-LiCF{sub 3}SO{sub 3}) system have been prepared using solution casting technique. The conductivities of the films from each system are characterized by impedance spectroscopy and infrared spectrum. With the addition of plasticizer, results show improvement on the ionic conductivity value where the value of 6.25x10{sup -10} Scm{sup -1} is obtained. This may be due to the nature of plasticizer that softens the polymer and hence enhanced the ionic transportation across the polymer. The room temperature conductivity for the highest conducting sample in the ([PMMA-EC]-LiCF{sub 3}SO{sub 3}) system is 1.36x10{sup -5} Scm{sup -1}. Fourier Transform Infrared Spectroscopy (FTIR) indicates complexation between the polymer and the plasticizer and the polymer, the plasticizer and the salts, and the result of XRD further supports the observation.

  4. Lithium and cesium acidities of some terminal acethylenes and aggregation of their salts in tetrahydrofuran

    SciTech Connect

    Gareyev, R.; Streitwieser, A.

    1995-12-01

    Ion-pair acidity equilibria have been determined for 4-ethynylbiphenyl (1), 1-ethynyladamantane (2) and 3,3,3-triphenylpropyne (3) with lithium and cesium as counterions in tetrahydrofuran. The pK values increase, 1 < 3 < 2, with lithium as the counterion. With the cesium gegenion the pK of compound 2 is also higher than that of 3. The cesium salt of 1 is insoluble in tetrahydrofuran. Comparison of lithium and cesium acidities shows a difference of 6 pK units for both 2 and 3, the lithium pK being lower. In some cases, the measured equilibrium acidities depend on the concentration of the acetylene salt, which indicates aggregation of ion pairs into higher ionic clusters. The average aggregation numbers were determined from the equilibrium studies.

  5. A new lithium salt with 3-fluoro-1,2-benzenediolato and oxalato complexes of boron for lithium battery electrolytes

    NASA Astrophysics Data System (ADS)

    Xue, Zhao-Ming; Ji, Chun-Qin; Zhou, Wei; Chen, Chun-Hua

    A new unsymmetrical lithium salt, lithium [3-fluoro-1,2-benzenediolato(2-)-o,o‧ oxalato]borate (FLBDOB), is synthesized and characterized. The thermal characteristics of FLBDOB and its counterparts lithium bis[3-fluoro-1,2-benzenediolato(2-)-o,o]borate (FLBBB) and lithium bis[oxalate]borate (LBOB) are examined and compared by thermogravimetric analysis (TG). The thermal decomposition of these salts in air is found to begin at 302, 262 and 256 °C for LBOB, FLBDOB and FLBBB, respectively. The order of the stability toward oxidation of these organoborates is LBOB > FLBDOB > FLBBB, which is in the same order of the thermal stability. The cyclic voltammetry study shows that the FLBDOB solution in PC is stable up to 4.0 V versus Li +/Li. It is soluble in common organic solvents such as propylene carbonate (PC), ethylene carbonate (EC), 1,2-dimethoxyethane (DME), and tetrahydrofuran (THF). Ionic dissociation properties of FLBDOB and the counterparts in PC, PC + THF, PC + DME, EC + DME, EC + THF (molar ratio 1:1) solutions are also examined by conductivity measurements. The conductivity values of the 0.10 mol dm -3 FLBDOB electrolyte in PC, PC + THF, PC + DME, EC + DME, EC + THF solutions are higher than those of FLBBB, but lower than those of LBOB electrolytes.

  6. Dual effectiveness of lithium salt in controlling both delayed ettringite formation and ASR in concretes

    SciTech Connect

    Ekolu, S.O. . E-mail: stephen.ekolu@wits.ac.za; Thomas, M.D.A.; Hooton, R.D.

    2007-06-15

    The influence of lithium nitrate on expansions due to delayed ettringite formation (DEF) and alkali-silica reaction (ASR) has been investigated. Effects of the lithium salt were examined in heat-cured mortars and concretes containing one or both damage mechanisms. The mortars and concretes made using reactive and/or non-reactive aggregates were subjected to heat treatment consisting of a hydration delay period of 4 h at 23 deg. C followed by steam-curing at 95 deg. C and then stored in limewater. Results showed that the lithium salt admixture was able to reduce the occurrence of deleterious expansion due to delayed ettringite formation in addition to controlling alkali-silica reaction in cementitious systems containing one or both mechanisms. In concretes made using non-reactive limestone aggregates, incorporation of lithium nitrate in a proportion of 0.74 M ratio of Li to (Na + K) was found to control delayed ettringite formation during the one-year period of this study. By analyzing the leaching properties of lithium and other alkalis from mortars during storage, it was found that a substantial amount of lithium was retained in the cementitious system in a slightly soluble form, and is expected to be responsible for reducing DEF.

  7. Modified natural graphite as anode material for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Wu, Y. P.; Jiang, C.; Wan, C.; Holze, R.

    A concentrated nitric acid solution was used as an oxidant to modify the electrochemical performance of natural graphite as anode material for lithium ion batteries. Results of X-ray photoelectron spectroscopy, electron paramagnetic resonance, thermogravimmetry, differential thermal analysis, high resolution electron microscopy, and measurement of the reversible capacity suggest that the surface structure of natural graphite was changed, a fresh dense layer of oxides was formed. Some structural imperfections were removed, and the stability of the graphite structure increased. These changes impede decomposition of electrolyte solvent molecules, co-intercalation of solvated lithium ions and movement of graphene planes along the a-axis direction. Concomitantly, more micropores were introduced, and thus, lithium intercalation and deintercalation were favored and more sites were provided for lithium storage. Consequently, the reversible capacity and the cycling behavior of the modified natural graphite were much improved by the oxidation. Obviously, the liquid-solid oxidation is advantageous in controlling the uniformity of the products.

  8. Deep eutectic solvents based on N-methylacetamide and a lithium salt as suitable electrolytes for lithium-ion batteries.

    PubMed

    Boisset, Aurélien; Menne, Sebastian; Jacquemin, Johan; Balducci, Andrea; Anouti, Mérièm

    2013-12-14

    In this work, we present a study on the physical and electrochemical properties of three new Deep Eutectic Solvents (DESs) based on N-methylacetamide (MAc) and a lithium salt (LiX, with X = bis[(trifluoromethyl)sulfonyl]imide, TFSI; hexafluorophosphate, PF6; or nitrate, NO3). Based on DSC measurements, it appears that these systems are liquid at room temperature for a lithium salt mole fraction ranging from 0.10 to 0.35. The temperature dependences of the ionic conductivity and the viscosity of these DESs are correctly described by using the Vogel-Tammann-Fulcher (VTF) type fitting equation, due to the strong interactions between Li(+), X(-) and MAc in solution. Furthermore, these electrolytes possess quite large electrochemical stability windows up to 4.7-5 V on Pt, and demonstrate also a passivating behavior toward the aluminum collector at room temperature. Based on these interesting electrochemical properties, these selected DESs can be classified as potential and promising electrolytes for lithium-ion batteries (LIBs). For this purpose, a test cell was then constructed and tested at 25 °C, 60 °C and 80 °C by using each selected DES as an electrolyte and LiFePO4 (LFP) material as a cathode. The results show a good compatibility between each DES and LFP electrode material. A capacity of up to 160 mA h g(-1) with a good efficiency (99%) is observed in the DES based on the LiNO3 salt at 60 °C despite the presence of residual water in the electrolyte. Finally preliminary tests using a LFP/DES/LTO (lithium titanate) full cell at room temperature clearly show that LiTFSI-based DES can be successfully introduced into LIBs. Considering the beneficial properties, especially, the cost of these electrolytes, such introduction could represent an important contribution for the realization of safer and environmentally friendly LIBs. PMID:24153449

  9. Electrolytic Deposition and Diffusion of Lithium onto Magnesium-9 Wt Pct Yttrium Bulk Alloy in Low-Temperature Molten Salt of Lithium Chloride and Potassium Chloride

    NASA Astrophysics Data System (ADS)

    Dong, Hanwu; Wu, Yaoming; Wang, Lidong; Wang, Limin

    2009-10-01

    The electrolytic deposition and diffusion of lithium onto bulk magnesium-9 wt pct yttrium alloy cathode in molten salt of 47 wt pct lithium chloride and 53 wt pct potassium chloride at 693 K were investigated. Results show that magnesium-yttrium-lithium ternary alloys are formed on the surface of the cathodes, and a penetration depth of 642 μm is acquired after 2 hours of electrolysis at the cathodic current density of 0.06 A·cm-2. The diffusion of lithium results in a great amount of precipitates in the lithium containing layer. These precipitates are the compound of Mg41Y5, which arrange along the grain boundaries and hinder the diffusion of lithium, and solid solution of yttrium in magnesium. The grain boundaries and the twins of the magnesium-9 wt pct yttrium substrate also have negative effects on the diffusion of lithium.

  10. Natural gas storage in bedded salt formations

    SciTech Connect

    Macha, G.

    1996-09-01

    In 1990 Western Resources Inc. (WRI) identified the need for additional natural gas storage capacity for its intrastate natural gas system operated in the state of Kansas. Western Resources primary need was identified as peak day deliverability with annual storage balancing a secondary objective. Consequently, an underground bedded salt storage facility, Yaggy Storage Field, was developed and placed in operation in November 1993. The current working capacity of the new field is 2.1 BCF. Seventy individual caverns are in service on the 300 acre site. The caverns vary in size from 310,000 CF to 2,600,000 CF. Additional capacity can be added on the existing acreage by increasing the size of some of the smaller existing caverns by further solution mining and by development of an additional 30 potential well sites on the property.

  11. Influence of Lithium Salts on the Discharge Chemistry of Li-Air Cells.

    PubMed

    Veith, Gabriel M; Nanda, Jagjit; Delmau, Laetitia H; Dudney, Nancy J

    2012-05-17

    In this work, we show that the use of a high boiling point ether solvent (tetraglyme) promotes the formation of Li2O2 in a lithium-air cell. However, another major constituent in the discharge product of a Li-air cell contains halides from the lithium salts and C-O from the tetraglyme used as the solvent. This information is critical to the development of Li-air electrolytes, which are stable and promote the formation of the desired Li2O2 products. PMID:26286765

  12. Influence of lithium salts on the discharge chemistry of Li-air cells

    SciTech Connect

    Veith, Gabriel M; Nanda, Jagjit; Delmau, Laetitia Helene; Dudney, Nancy J

    2012-01-01

    In this work we show that the use of a high boiling point ether solvent (tetraglyme) promotes the formation of Li2O2 in a lithium-air cell. In addition, another major constituent in the discharge product of a Li-air cell contains halides, from the lithium salt, and the tetraglyme used as the solvent. This information is critical to the development of Li-air electrolytes which are stable and promote the formation of the desired Li2O2 products.

  13. Anion Coordination Interactions in Solvates with the Lithium Salts LiDCTA and LiTDI

    SciTech Connect

    McOwen, Dennis W.; Delp, Samuel A.; Paillard, Elie; Herriot, Cristelle; Han, Sang D.; Boyle, Paul D.; Sommer, Roger D.; Henderson, Wesley A.

    2014-04-17

    Lithium 4,5-dicyano-1,2,3-triazolate (LiDCTA) and lithium 2-trifluoromethyl-4,5-dicyanoimidazole (LiTDI) are two salts proposed for lithium battery electrolyte applications, but little is known about the manner in which the DCTA- and TDI- anions coordinate Li+ cations. To explore this in-depth, crystal structures are reported here for two solvates with LiDCTA: (G2)1:LiDCTA and (G1)1:LiDCTA with diglyme and monoglyme, respectively, and seven solvates with LiTDI: (G1)2:LiTDI, (G2)2:LiTDI, (G3)1:LiTDI, (THF)1:LiTDI, (EC)1:LiTDI, (PC)1:LiTDI and (DMC)1/2:LiTDI with monoglyme, diglyme, triglyme, tetrahydrofuran, ethylene carbonate, propylene carbonate and dimethyl carbonate, respectively. These latter solvate structures are compared with the previously reported acetonitrile (AN)2:LiTDI structure. The solvates indicate that the LiTDI salt is much less associated than the LiDCTA salt and that the ions in LiTDI, when aggregated in solvates, have a very similar TDI-...Li+ cation mode of coordination through both the anion ring and cyano nitrogen atoms. Such coordination facilitates the formation of polymeric ion aggregates, instead of dimers. Insight into such ion speciation is instrumental for understanding the electrolyte properties of aprotic solvent mixtures with these salts.

  14. Quantitative analysis of the hydration of lithium salts in water using multivariate curve resolution of near-infrared spectra.

    PubMed

    Barba, M Isabel; Larrechi, M Soledad; Coronas, Alberto

    2016-05-01

    The hydration process of lithium iodide, lithium bromide, lithium chloride and lithium nitrate in water was analyzed quantitatively by applying multivariate curve resolution alternating least squares (MCR-ALS) to their near infrared spectra recorded between 850 nm and 1100 nm. The experiments were carried out using solutions with a salt mass fraction between 0% and 72% for lithium bromide, between 0% and 67% for lithium nitrate and between 0% and 62% for lithium chloride and lithium iodide at 323.15 K, 333.15 K, 343.15 K and 353.15 K, respectively. Three factors were determined for lithium bromide and lithium iodide and two factors for the lithium chloride and lithium nitrate by singular value decomposition (SVD) of their spectral data matrices. These factors are associated with various chemical environments in which there are aqueous clusters containing the ions of the salts and non-coordinated water molecules. Spectra and concentration profiles of non-coordinated water and cluster aqueous were retrieved by MCR-ALS. The amount of water involved in the process of hydration of the various salts was quantified. The results show that the water absorption capacity increases in the following order LiI < LiBr < LiNO3 < LiCl. The salt concentration at which there is no free water in the medium was calculated at each one of the temperatures considered. The values ranged between 62.6 and 65.1% for LiBr, 45.5-48.3% for LiCl, 60.4-61.2% for LiI and 60.3-63.7% for LiNO3. These values are an initial approach to determining the concentration as from which crystal formation is favored. PMID:27086095

  15. Discharge characteristics of lithium/molten nitrate thermal battery cells using silver salts as solid cathode materials

    NASA Astrophysics Data System (ADS)

    McManis, G. E.; Miles, M. H.; Fletcher, A. N.

    1985-12-01

    Thermal battery cells using molten nitrate electrolytes and liquid lithium anodes have been evaluated using several silver salts with low solubility in molten nitrates as solid cathode materials. These cathode materials do not readily diffuse into the anolyte and, thus, do not have parasitic reactions with the lithium anode. Furthermore, the solid cathode materials have voltammetric characteristics as favorable as many soluble silver salt cathodes. This paper presents the effects of temperature, current density, and cathode material on cell discharge characteristics.

  16. Liquid Fluoride Salt Experimentation Using a Small Natural Circulation Cell

    SciTech Connect

    Yoder Jr, Graydon L; Heatherly, Dennis Wayne; Williams, David F; Elkassabgi, Yousri M.; Caja, Joseph; Caja, Mario; Jordan, John; Salinas, Roberto

    2014-04-01

    A small molten fluoride salt experiment has been constructed and tested to develop experimental techniques for application in liquid fluoride salt systems. There were five major objectives in developing this test apparatus: Allow visual observation of the salt during testing (how can lighting be introduced, how can pictures be taken, what can be seen) Determine if IR photography can be used to examine components submerged in the salt Determine if the experimental configuration provides salt velocity sufficient for collection of corrosion data for future experimentation Determine if a laser Doppler velocimeter can be used to quantify salt velocities. Acquire natural circulation heat transfer data in fluoride salt at temperatures up to 700oC All of these objectives were successfully achieved during testing with the exception of the fourth: acquiring velocity data using the laser Doppler velocimeter. This paper describes the experiment and experimental techniques used, and presents data taken during natural circulation testing.

  17. Lithium recovery from salt lake brine by H2TiO3.

    PubMed

    Chitrakar, Ramesh; Makita, Yoji; Ooi, Kenta; Sonoda, Akinari

    2014-06-21

    The details of the ion exchange properties of layered H2TiO3, derived from the layered Li2TiO3 precursor upon treatment with HCl solution, with lithium ions in the salt lake brine (collected from Salar de Uyuni, Bolivia) are reported. The lithium adsorption rate is slow, requiring 1 d to attain equilibrium at room temperature. The adsorption of lithium ions by H2TiO3 follows the Langmuir model with an adsorptive capacity of 32.6 mg g(-1) (4.7 mmol g(-1)) at pH 6.5 from the brine containing NaHCO3 (NaHCO3 added to control the pH). The total amount of sodium, potassium, magnesium and calcium adsorbed from the brine was <0.30 mmol g(-1). The H2TiO3 was found capable of efficiently adsorbing lithium ions from the brine containing competitive cations such as sodium, potassium, magnesium and calcium in extremely large excess. The results indicate that the selectivity order Li(+) ≫ Na(+), K(+), Mg(2+), Ca(2+) originates from a size effect. The H2TiO3 can be regenerated and reused for lithium exchange in the brine with an exchange capacity very similar to the original H2TiO3. PMID:24801244

  18. A new look at an old drug: neuroprotective effects and therapeutic potentials of lithium salts

    PubMed Central

    Dell’Osso, Liliana; Del Grande, Claudia; Gesi, Camilla; Carmassi, Claudia; Musetti, Laura

    2016-01-01

    Increasing evidence highlights bipolar disorder as being associated with impaired neurogenesis, cellular plasticity, and resiliency, as well as with cell atrophy or loss in specific brain regions. This has led most recent research to focus on the possible neuroprotective effects of medications, and particularly interesting findings have emerged for lithium. A growing body of evidence from preclinical in vitro and in vivo studies has in fact documented its neuroprotective effects from different insults acting on cellular signaling pathways, both preventing apoptosis and increasing neurotrophins and cell-survival molecules. Furthermore, positive effects of lithium on neurogenesis, brain remodeling, angiogenesis, mesenchymal stem cells functioning, and inflammation have been revealed, with a key role played through the inhibition of the glycogen synthase kinase-3, a serine/threonine kinase implicated in the pathogenesis of many neuropsychiatric disorders. These recent evidences suggest the potential utility of lithium in the treatment of neurodegenerative diseases, neurodevelopmental disorders, and hypoxic–ischemic/traumatic brain injury, with positive results at even lower lithium doses than those traditionally considered to be antimanic. The aim of this review is to briefly summarize the potential benefits of lithium salts on neuroprotection and neuroregeneration, emphasizing preclinical and clinical evidence suggesting new therapeutic potentials of this drug beyond its mood stabilizing properties. PMID:27468233

  19. A new look at an old drug: neuroprotective effects and therapeutic potentials of lithium salts.

    PubMed

    Dell'Osso, Liliana; Del Grande, Claudia; Gesi, Camilla; Carmassi, Claudia; Musetti, Laura

    2016-01-01

    Increasing evidence highlights bipolar disorder as being associated with impaired neurogenesis, cellular plasticity, and resiliency, as well as with cell atrophy or loss in specific brain regions. This has led most recent research to focus on the possible neuroprotective effects of medications, and particularly interesting findings have emerged for lithium. A growing body of evidence from preclinical in vitro and in vivo studies has in fact documented its neuroprotective effects from different insults acting on cellular signaling pathways, both preventing apoptosis and increasing neurotrophins and cell-survival molecules. Furthermore, positive effects of lithium on neurogenesis, brain remodeling, angiogenesis, mesenchymal stem cells functioning, and inflammation have been revealed, with a key role played through the inhibition of the glycogen synthase kinase-3, a serine/threonine kinase implicated in the pathogenesis of many neuropsychiatric disorders. These recent evidences suggest the potential utility of lithium in the treatment of neurodegenerative diseases, neurodevelopmental disorders, and hypoxic-ischemic/traumatic brain injury, with positive results at even lower lithium doses than those traditionally considered to be antimanic. The aim of this review is to briefly summarize the potential benefits of lithium salts on neuroprotection and neuroregeneration, emphasizing preclinical and clinical evidence suggesting new therapeutic potentials of this drug beyond its mood stabilizing properties. PMID:27468233

  20. Solvation of lithium salts in protic ionic liquids: a molecular dynamics study.

    PubMed

    Méndez-Morales, Trinidad; Carrete, Jesús; Cabeza, Óscar; Russina, Olga; Triolo, Alessandro; Gallego, Luis J; Varela, Luis M

    2014-01-23

    The structure of solutions of lithium nitrate in a protic ionic liquid with a common anion, ethylammonium nitrate, at room temperature is investigated by means of molecular dynamics simulations. Several structural properties, such as density, radial distribution functions, hydrogen bonds, spatial distribution functions, and coordination numbers, are analyzed in order to get a picture of the solvation of lithium cations in this hydrogen-bonded, amphiphilically nanostructured environment. The results reveal that the ionic liquid mainly retains its structure upon salt addition, the interaction between the ammonium group of the cation and the nitrate anion being only slightly perturbed by the addition of the salt. Lithium cations are solvated by embedding them in the polar nanodomains of the solution formed by the anions, where they coordinate with the latter in a solid-like fashion reminiscent of a pseudolattice structure. Furthermore, it is shown that the average coordination number of [Li](+) with the anions is 4, nitrate coordinating [Li](+) in both monodentate and bidentate ways, and that in the second coordination layer both ethylammonium cations and other lithiums are also found. Additionally, the rattling motion of lithium ions inside the cages formed by their neighboring anions, indicative of the so-called caging effect, is confirmed by the analysis of the [Li](+) velocity autocorrelation functions. The overall picture indicates that the solvation of [Li](+) cations in this amphiphilically nanostructured environment takes place by means of a sort of inhomogeneous nanostructural solvation, which we could refer to as nanostructured solvation, and which could be a universal solvation mechanism in ionic liquids. PMID:24405468

  1. Structural Interactions within Lithium Salt Solvates: Cyclic Carbonates and Esters

    SciTech Connect

    Seo, D. M.; Afroz, Taliman; Allen, Joshua L.; Boyle, Paul D.; Trulove, Paul C.; De Long, Hugh C.; Henderson, Wesley A.

    2014-11-13

    Only limited information is available regarding the manner in which cyclic carbonate and ester solvents coordinate Li+ cations in electrolyte solutions for lithium batteries. One approach to gleaning significant insight into these interactions is to examine crystalline solvate structures. To this end, eight new solvate structures are reported with ethylene carbonate, γ-butyrolactone and γ-valerolactone: (EC)3:LiClO4, (EC)2:LiClO4, (EC)2:LiBF4, (GBL)4:LiPF6, (GBL)1:LiClO4, (GVL)1:LiClO4, (GBL)1:LiBF4 and (GBL)1:LiCF3SO3. The crystal structure of (EC)1:LiCF3SO3 is also re-reported for comparison. These structures enable the factors which govern the manner in which the ions are coordinated and the ion/solvent packing—in the solid-state—to be scrutinized in detail.

  2. Ionic conductivity of dual-phase polymer electrolytes comprised of NBR/SBR latex films swollen with lithium salt solutions

    SciTech Connect

    Matsumoto, Morihiko; Ichino, Toshihiro; Rutt, J.S.; Nishi, Shiro . NTT Interdisciplinary Research Lab.)

    1994-08-01

    Dual-phase polymer electrolytes (DPE) with high ionic conductivity and good mechanical strength were prepared by swelling poly(acrylonitrile-co-butadiene) rubber (NBR) and poly(styrene-co-butadiene) rubber (SBR) mixed latex films with lithium salt solutions (e.g., 1M LiClO[sub 4]/[gamma]-butyrolactone). The latex films retain particle morphology in the solid state. The NBR phase (formed from fused NBR latex particles) is polar and is impregnated selectively with polar lithium salt solutions, yielding ion-conductive channels, whereas the SBR phase (formed from fused SBR latex particles) is nonpolar and is not impregnated, providing a mechanically supportive matrix. The ionic conductivity of the DPE increased dramatically with increasing content of lithium salt solution, and higher amounts of solution were imbibed with increasing content of NBR relative to SBR. Several factors which affect the ionic conductivity of this system were examined, and the highest ionic conductivity (>10[sup [minus]3] S/cm) was obtained when either an NBR/SBR 70/30 (w/w) or a 50/50 (w/w) latex film was saturated with 1M LiClO[sub 4]/[gamma]-BL solution or 1M LiClO[sub 4]/[gamma]-BL/DME solution. Ion-conductive behavior changed critically with increasing lithium salt solution uptake. At low levels of lithium salt solution uptake, evidence suggested that ionic conductivity of the absorbed lithium salt solution was strongly influenced by the presence of the NBR in the ion-conductive channel, but at higher levels, the effects of the NBR were reduced and free'' lithium salt solution was present.

  3. Enhanced cycling performance of a Li metal anode in a dimethylsulfoxide-based electrolyte using highly concentrated lithium salt for a lithium-oxygen battery

    NASA Astrophysics Data System (ADS)

    Togasaki, Norihiro; Momma, Toshiyuki; Osaka, Tetsuya

    2016-03-01

    Stable charge-discharge cycling behavior for a lithium metal anode in a dimethylsulfoxide (DMSO)-based electrolyte is strongly desired of lithium-oxygen batteries, because the Li anode is rapidly exhausted as a result of side reactions during cycling in the DMSO solution. Herein, we report a novel electrolyte design for enhancing the cycling performance of Li anodes by using a highly concentrated DMSO-based electrolyte with a specific Li salt. Lithium nitrate (LiNO3), which forms an inorganic compound (Li2O) instead of a soluble product (Li2S) on a lithium surface, exhibits a >20% higher coulombic efficiency than lithium bis(trifluoromethanesulfonyl)imide, lithium bis(fluorosulfonyl)imide, and lithium perchlorate, regardless of the loading current density. Moreover, the stable cycling of Li anodes in DMSO-based electrolytes depends critically on the salt concentration. The highly concentrated electrolyte 4.0 M LiNO3/DMSO displays enhanced and stable cycling performance comparable to that of carbonate-based electrolytes, which had not previously been achieved. We suppose this enhancement is due to the absence of free DMSO solvent in the electrolyte and the promotion of the desolvation of Li ions on the solid electrolyte interphase surface, both being consequences of the unique structure of the electrolyte.

  4. Excess lithium salt functions more than compensating for lithium loss when synthesizing Li6.5La3Ta0.5Zr1.5O12 in alumina crucible

    NASA Astrophysics Data System (ADS)

    Liu, Kai; Ma, Jiang-Tao; Wang, Chang-An

    2014-08-01

    Garnet type electrolyte "Li6.5La3Ta0.5Zr1.5O12" (LLZTO) was prepared by conventional solid-state reaction in alumina crucibles and excess lithium salt (from 0% to 50 mol%) was added into the starting materials to investigate the effects of excess lithium salt on the property of LLZTO. SEM, XRD and AC impedance were used to determine the microstructure, phase formation and Li-ion conductivity. Cubic garnet with a minor second phase LiAlO2 in the grain boundary was obtained for the pellets with excess lithium salt. As the amount of excess lithium salt increased, more Al element diffused from alumina crucibles to LLZTO pellets and reacted with excess lithium salt to form liquid Li2O-Al2O3 phase in the grain boundary, which accelerated the pellets' densification and reduced lithium loss at a high temperature. Ionic conductivity of LLZTO pellets increased with the amount of excess lithium salt added and leveled off at ∼4 × 10-4 S cm-1 when lithium salt exceeded 30 mol%. The performance of Li-air batteries with hybrid electrolytes, using homemade LLZTO thin pellets as solid electrolytes, was investigated. The LLZTO thin pellet with more excess lithium salt in starting material had a higher density and resulted in better cell performance.

  5. Lithium recovery by means of electrochemical ion pumping: a comparison between salt capturing and selective exchange.

    PubMed

    Trocoli, Rafael; Bidhendi, Ghoncheh Kasiri; La Mantia, Fabio

    2016-03-23

    Currently, lithium carbonate is mainly produced through evaporation of lithium-rich brines, which are located in South American countries such as Bolivia, Chile, and Argentina. The most commonly used process, the lime-soda evaporation, requires a long time and several purification steps, which produces a considerable amount of chemical waste. Recently, several alternative electrochemical methods, based on LiFePO4 as a selective lithium capturing electrode and differing for the reaction at the counter electrode, have been proposed. In this work a comparison between the salt capturing method, based on silver / silver chloride reaction, and the selective exchange method, based on ion intercalation reaction in a Prussian Blue derivative, is performed in terms of energy consumption. In particular, the energy consumption is divided in thermodynamic and kinetic contribution, and the theoretical calculations are compared with the experimental results. The experimental results show a good agreement with the theoretical calculation. The selective exchange method shows superior performances to the salt exchange in terms of purity and efficiency, however the energy consumption is higher. PMID:26910577

  6. Thermophysical properties and corrosion characterization of low cost lithium containing nitrate salts produced in northern Chile for thermal energy storage

    NASA Astrophysics Data System (ADS)

    Fernández, Ángel G.; Gomez, Judith C.; Galleguillos, Hector; Fuentealba, Edward

    2016-05-01

    In recent years, lithium containing salts have been studied for thermal energy storage (TES) systems applications, because of their optimal thermophysical properties. In solar power plants, lithium is seen as a way to improve the properties of molten salts used today. Lithium nitrate is a good candidate for sensible heat storage, due to its ability to increase the salt mixture's working temperature range. In the present research, thermophysical properties characterization of lithium nitrate containing salts, produced in Chile, have been carried out. Corrosion evaluations of carbon and low chromium steels were performed at 390°C for 1000 hours. Thermophysical properties of the salt mixtures, such as thermal stability and heat capacity, were measured before and after corrosion tests. Chemical composition of the salts was also determined and an estimation of Chilean production costs is reported. Results showed that purity, thermal stability and heat capacity of the salts were reduced, caused by partial thermal decomposition and incorporation of corrosion products from the steel.

  7. Solvation structure around the Li(+) ion in succinonitrile-lithium salt plastic crystalline electrolytes.

    PubMed

    Shen, Yuneng; Deng, Gang-Hua; Ge, Chuanqi; Tian, Yuhuan; Wu, Guorong; Yang, Xueming; Zheng, Junrong; Yuan, Kaijun

    2016-06-01

    Herein, we discuss the study of solvation dynamics of lithium-succinonitrile (SN) plastic crystalline electrolytes by ultrafast vibrational spectroscopy. The infrared absorption spectra indicated that the CN stretch of the Li(+) bound and unbound succinonitrile molecules in a same solution have distinct vibrational frequencies (2276 cm(-1)vs. 2253 cm(-1)). The frequency difference allowed us to measure the rotation decay times of solvent molecules bound and unbound to Li(+) ion. The Li(+) coordination number of the Li(+)-SN complex was found to be 2 in the plastic crystal phase (22 °C) and 2.5-3 in the liquid phase (80 °C), which is independent of the concentration (from 0.05 mol kg(-1) to 2 mol kg(-1)). The solvation structures along with DFT calculations of the Li(+)-SN complex have been discussed. In addition, the dissociation percentage of lithium salt was also determined. In 0.5 mol kg(-1) LiBF4-SN solutions at 80 °C, 60% ± 10% of the salt dissociates into Li(+), which is bound by 2 or 3 solvent molecules. In the 0.5 mol kg(-1) LiClO4-SN solutions at 80 °C, the salt dissociation ratio can be up to 90% ± 10%. PMID:27189266

  8. Disordered lithium niobate rock-salt materials prepared by hydrothermal synthesis.

    PubMed

    Modeshia, Deena R; Walton, Richard I; Mitchell, Martin R; Ashbrook, Sharon E

    2010-07-14

    An investigation of the one-step hydrothermal crystallisation of lithium niobates reveals that reaction between Nb(2)O(5) and aqueous LiOH at 240 degrees C yields materials with a disordered rock-salt structure where the metals are statistically distributed over the cation sites. This contrasts with the well-studied reaction between Nb(2)O(5) and NaOH or KOH that produces ANbO(3) (A = Na, K) perovskites. Powder neutron diffraction shows that materials prepared at short reaction times and lower LiOH concentration (2.5 M) are lithium deficient and have a slight excess of niobium, but that at longer periods of reaction in 5 M LiOH, close to the ideal, stoichiometric Li(0.75)Nb(0.25)O composition is produced. Upon annealing this phase cleanly transforms into the known ordered rock-salt material Li(3)NbO(4), a process we have followed using thermodiffractometry, which indicates that transformation begins at approximately 700 degrees C. Solid-state (93)Nb and (7)Li NMR of the disordered and ordered rock-salt phases shows that both contain single metal sites but there is clear evidence for local disorder in the disordered samples. For the ordered material, NMR parameters derived from experiment are also compared to those calculated using density functional theory and are shown to be in good agreement. PMID:20442945

  9. Solid lithium electrolyte via addition of lithium salts to metal-organic frameworks

    DOEpatents

    Wiers, Brian M.; Balsara, Nitash P.; Long, Jeffrey R.

    2016-03-29

    Various embodiments of the invention disclose that the uptake of LiO.sup.iPr in Mg.sub.2(dobdc) (dobdc.sup.4-=1,4-dioxido-2,5-benzenedicarboxylate) followed by soaking in a typical electrolyte solution leads to a new solid lithium electrolyte Mg.sub.2(dobdc).0.35LiO.sup.iPr.0.25LiBF.sub.4.EC.DEC. Two-point ac impedance data show a pressed pellet of this material to have a conductivity of 3.1.times.10.sup.-4 S/cm at 300 K. In addition, the results from variable-temperature measurements reveal an activation energy of approximately 0.15 eV, while single-particle data suggest that intraparticle transport dominates conduction.

  10. The corrosion protection of AA2024-T3 aluminium alloy by leaching of lithium-containing salts from organic coatings.

    PubMed

    Visser, Peter; Liu, Yanwen; Zhou, Xiaorong; Hashimoto, Teruo; Thompson, George E; Lyon, Stuart B; van der Ven, Leendert G J; Mol, Arjan J M C; Terryn, Herman A

    2015-01-01

    Lithium carbonate and lithium oxalate were incorporated as leachable corrosion inhibitors in model organic coatings for the protection of AA2024-T3. The coated samples were artificially damaged with a scribe. It was found that the lithium-salts are able to leach from the organic coating and form a protective layer in the scribe on AA2024-T3 under neutral salt spray conditions. The present paper shows the first observation and analysis of these corrosion protective layers, generated from lithium-salt loaded organic coatings. The scribed areas were examined by scanning and transmission electron microscopy before and after neutral salt spray exposure (ASTM-B117). The protective layers typically consist of three different layered regions, including a relatively dense layer near the alloy substrate, a porous middle layer and a flake-shaped outer layer, with lithium uniformly distributed throughout all three layers. Scanning electron microscopy and white light interferometry surface roughness measurements demonstrate that the formation of the layer occurs rapidly and, therefore provides an effective inhibition mechanism. Based on the observation of this work, a mechanism is proposed for the formation of these protective layers. PMID:25927079

  11. Carbon Cathodes in Rechargeable Lithium-Oxygen Batteries Based on Double-Lithium-Salt Electrolytes.

    PubMed

    Yoo, Eunjoo; Zhou, Haoshen

    2016-06-01

    The use of carbon materials as air electrodes in lithium-oxygen (Li-O2 ) batteries is known to be advantageous owing to their good conductivity and because they offer sites suitable for the reversible electrode reactions. However, the exact influence of carbon materials on the electrochemical performance of Li-O2 batteries is not clear. In this study the electrochemical performance of four different types of carbon materials (multiwalled carbon nanotubes (MWCNTs), CMK-3, graphene nanosheets (GNSs), and Ketjen Black (KB)) as air electrodes is examined. We find that a Li-O2 cell based on an electrode of multiwalled carbon nanotubes (MWCNTs) demonstrates good rate performance and cycle stability, when using LiNO3 -LiTFSI/DMSO as electrolyte. Li-O2 cells based on such MWCNT electrodes, with a cut-off capacity of 1000 mAh g(-1) at 500 mA g(-1) , can undergo around 90 cycles without obvious losses of capacity. Even when the discharge depth is increased to 2000 mA h g(-1) , stable cycling is maintained for 45 cycles at a charge potential below 4.0 V. PMID:27120298

  12. Nanostructure of mixtures of protic ionic liquids and lithium salts: effect of alkyl chain length.

    PubMed

    Méndez-Morales, Trinidad; Carrete, Jesús; Rodríguez, Julio R; Cabeza, Óscar; Gallego, Luis J; Russina, Olga; Varela, Luis M

    2015-02-21

    The bulk structure of mixtures of two protic ionic liquids, propylammonium nitrate and butylammonium nitrate, with a salt with a common anion, is analyzed at room temperature by means of small angle X-ray scattering and classical molecular dynamics simulations. The study of several structural properties, such as density, radial distribution functions, spatial distribution functions, hydrogen bonds, coordination numbers and velocity autocorrelation functions, demonstrates that increasing the alkyl chain length of the alkylammonium cation results in more segregated, better defined polar and apolar domains, the latter having a larger size. This increase, ascribed to the erosion of the H-bond network in the ionic liquid polar regions as salt is added, is confirmed by means of small angle X-ray scattering measurements, which show a clear linear increase of the characteristic spatial sizes of the studied protic ionic liquids with salt concentration, similar to that previously reported for ethylammonium nitrate (J. Phys. Chem. B, 2014, 118, 761-770). In addition, larger ionic liquid cations lead to a lower degree of hydrogen bonding and to more sparsely packed three-dimensional structures, which are more easily perturbed by the addition of lithium salts. PMID:25609558

  13. Effects of lithium salt concentration on graphited carbon microbead anodes in the piperidinium-based hybrid electrolytes

    SciTech Connect

    Gao, Kun; Li, Shu-Dan

    2015-01-15

    Graphical abstract: “Lithium aggregates” usually cause a significant decrease in Li{sup +} mobility and transfer efficiency. Therefore, as important as the problem of SEI, the content of lithium salt and the interaction between Li{sup +} and ILs’ anions should be taken into consideration in the optimization of ILs-based electrolytes for Li-ion batteries. - Highlights: • “Lithium aggregates” in piperidinium-based electrolytes are evidenced by IR and NMR. • High LiPF{sub 6} content could decrease Li{sup +} mobility due to “ionic aggregates”. • Lithium salt concentration is an important factor affecting graphite performances. - Abstract: The variations in LiPF{sub 6} concentration lead to the very different electrochemical performances of carbon microbeads anodes in the piperidinium-based hybrid electrolytes. The “two peaks” behaviors of lithium plating observed in cyclic voltammetry tests, and some detailed changes in infrared spectra and nuclear magnetic resonance indicates that the formation of “ionic aggregates” related to lithium ions”. Therefore, the excessive lithium salts in the piperidinium-based hybrid electrolytes, usually cause a significant decrease in Li{sup +} mobility and transfer efficiency. The main behaviors are that, when LiPF{sub 6} concentrations increased from 0.2 to 1.2 mol kg{sup −1}, the apparent migration energies (E{sub a}) increase largely from 8.83 to 21.16 kJ mol{sup −1}, while the lithium transference numbers (t{sub Li{sup +}}) drop markedly from 0.538 to 0.292.

  14. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2011-01-01

    In 2010, lithium consumption in the United States was estimated to have been about 1 kt (1,100 st) of contained lithium, a 23-percent decrease from 2009. The United States was estimated to be the fourth largest consumer of lithium. It remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. Only one company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic resources. In 2010, world lithium consumption was estimated to have been about 21 kt (22,000 st) of lithium contained in minerals and compounds, a 12-percent increase from 2009.

  15. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2010-01-01

    In 2009, lithium consumption in the United States was estimated to have been about 1.2 kt (1,300 st) of contained lithium, a 40-percent decrease from 2008. The United States was estimated to be the fourth largest consumer of lithium, and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. Only one company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic resources. In 2009, world lithium consumption was estimated to have been about 18.7 kt (20,600 st) of lithium contained in minerals and compounds.

  16. Analysis of cell performance and thermal regeneration of a lithium-tin cell having an immobilized fused-salt electrolyte

    NASA Technical Reports Server (NTRS)

    Cairns, E. J.; Shimotake, H.

    1969-01-01

    Cell performance and thermal regeneration of a thermally regenerative cell uses lithium and tin and a fused-salt electrolyte. The emf of the Li-Sn cell, as a function of cathode-alloy composition, is shown to resemble that of the Na-Bi cell.

  17. Lithium salt with a super-delocalized perfluorinated sulfonimide anion as conducting salt for lithium-ion cells: Physicochemical and electrochemical properties

    NASA Astrophysics Data System (ADS)

    Zhang, Heng; Han, Hongbo; Cheng, Xiaorong; Zheng, Liping; Cheng, Pengfei; Feng, Wenfang; Nie, Jin; Armand, Michel; Huang, Xuejie; Zhou, Zhibin

    2015-11-01

    Lithium salt with a super-delocalized imide anion, namely (trifluoromethane(S-trifluoromethanesulfonylimino)sulfonyl) (trifluoromethanesulfonyl)imide ([CF3SO(=NSO2CF3)2]-), [sTFSI]-), has been prepared and studied as conducting salt for Li-ion cells. The fundamental physicochemical and electrochemical properties of neat Li[sTFSI] and its carbonate-based liquid electrolyte have been characterized with various chemical and electrochemical tools. Li[sTFSI] shows a low melting point at 118 °C, and is thermally stable up to 300 °C without decomposition on the spectra of differential scanning calorimetry-thermogravimetry-mass spectrometry (DSC-TG-MS). The electrolyte of 1.0 M (mol dm-3) Li[sTFSI] in ethylene carbonate (EC)/ethyl-methyl-carbonate (EMC) (3:7, v/v) containing 0.3% water does not show any hydrolytic decomposition on the spectra of 1H and 19F NMR, after storage at 85 °C for 10 days. The conductivities of 1.0 M Li[sTFSI]-EC/EMC (3:7, v/v) are slightly lower than those of Li[(CF3SO2)2N] (LiTFSI), but higher than those of Li[(C2F5SO2)2N] (LiBETI). The electrochemical behavior of Al foil in the Li[sTFSI]-based electrolyte has been investigated by using cyclic voltammetry and chronoamperometry, and scanning electron microscope (SEM). It is illustrated that Al metal does not corrode in the high potential region (3-5 V vs. Li/Li+) in the Li[sTFSI]-based electrolyte. On Pt electrode, the Li[sTFSI]-based electrolyte is highly resistant to oxidation (ca. 5 V vs. Li/Li+), and is also resistant to reduction to allow Li deposition and stripping. The applicability of Li[sTFSI] as conducting salt for Li-ion cells has been tested using graphite/LiCoO2 cells. It shows that the cell with Li[sTFSI] displays better cycling performance than that with LiPF6.

  18. Association constants in solutions of lithium salts in butyrolactone and a mixture of propylene carbonate with 1,2-dimethoxyethane (1 : 1), according to conductometric data

    NASA Astrophysics Data System (ADS)

    Chernozhuk, T. V.; Sherstyuk, Yu. S.; Novikov, D. O.; Kalugin, O. N.

    2016-02-01

    A conductometric study is performed with solutions of lithium bis(oxalato)borate (LiBOB) in γ-butyrolactone (γ-BL) at 278.15-388.15 K and lithium bis(trifluoromethylsulfonyl)imide (LiTFSI), LiBOB, and lithium tetrafluoroborate (LiBF4) in mixtures of propylene carbonate and 1,2-dimethoxyethane (PC + 1,2-DME) (1 : 1) at 278.15-348.15 K. Limiting molar electrical conductivities (LMECs) and association constants ( K a) in the studied solutions of electrolytes are determined using the Lee-Wheaton equation. The effect temperature, the nature of the solvent, and the properties of the anion have on the conductivity and interparticle interactions in solutions of lithium salts in γ-BL and PC + 1,2-DME (1 : 1) is established. It was concluded that the studied solutions are characterized by low values of their association constants. It was found that the BOB;- anion destroys the structure of the solvent.The thickness of the dynamic solvation shell of ions (Δ R) remains constant for both solvents over the studied range of temperatures, and Δ R is significantly greater for Li+ than for other ions.

  19. Lithium

    USGS Publications Warehouse

    Jaskula, B.W.

    2012-01-01

    In 2011, world lithium consumption was estimated to have been about 25 kt (25,000 st) of lithium contained in minerals and compounds, a 10-percent increase from 2010. U.S. consumption was estimated to have been about 2 kt (2,200 st) of contained lithium, a 100-percent increase from 2010. The United States was estimated to be the fourth-ranked consumer of lithium and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. One company, Chemetall Foote Corp. (a subsidiary of Chemetall GmbH of Germany), produced lithium compounds from domestic brine resources near Silver Peak, NV.

  20. Lithium

    USGS Publications Warehouse

    Ober, J.A.

    2006-01-01

    In 2005, lithium consumption in the United States was at 2.5 kt of contained lithium, nearly 32% more than the estimate for 2004. World consumption was 14.1 kt of lithium contained in minerals and compounds in 2003. Exports from the US increased slightly compared with 2004. Due to strong demand for lithium compounds in 2005, both lithium carbonate plants in Chile were operating at or near capacity.

  1. Toward the design of high voltage magnesium-lithium hybrid batteries using dual-salt electrolytes.

    PubMed

    Cheng, Yingwen; Choi, Daiwon; Han, Kee Sung; Mueller, Karl T; Zhang, Ji-Guang; Sprenkle, Vincent L; Liu, Jun; Li, Guosheng

    2016-04-01

    We report a design of high voltage magnesium-lithium (Mg-Li) hybrid batteries through rational control of the electrolyte chemistry, electrode materials and cell architecture. Prototype devices with a structure of Mg-Li/LiFePO4 (LFP) and Mg-Li/LiMn2O4 (LMO) have been investigated. A Mg-Li/LFP cell using a dual-salt electrolyte 0.2 M [Mg2Cl2(DME)4][AlCl4]2 and 1.0 M LiTFSI exhibits voltages higher than 2.5 V (vs. Mg) and a high specific energy density of 246 W h kg(-1) under conditions that are amenable for practical applications. The successful demonstrations reported here could be a significant step forward for practical hybrid batteries. PMID:26959513

  2. Lithium salts of [1,12-dialkyl-CB11Me10]- anions.

    PubMed

    Valášek, Michal; Štursa, Jan; Pohl, Radek; Michl, Josef

    2010-11-15

    We report the syntheses of several [1-R-CB(11)-Me(11)](-) and [1-R-12-R'-CB(11)-Me(10)](-) anions (R, R' = alkyl) and the solubilities of their lithium salts in cyclohexane. These solutions are of interest as Lewis acid catalysts. The new anions are not directly accessible by methylation with methyl triflate because of intervening triflyloxy substitution on one or more boron vertices. The difficulty has been circumvented in two ways. Either (i) an iodo substituent is first introduced into position 12, permitting a clean decamethylation, and then replaced with a methyl by reaction with trimethylaluminum or (ii) the offending triflyloxy substituents are replaced with methyls by reaction with trimethylaluminum. PMID:20932023

  3. Lithium salt of end-substituted nanotube: Structure and large nonlinear optical property

    NASA Astrophysics Data System (ADS)

    Ma, Fang; Zhou, Zhong-Jun; Li, Zhi-Ru; Wu, Di; Li, Ying; Li, Ze-Sheng

    2010-03-01

    Lithium salt of substituted nanotube is suggested as a new kind of nonlinear optical (NLO) material. It is found that the combination of the lithiation effect and the donor substitution effect can greatly enhance the static first hyperpolarizability ( β0). Specially, the unusual donor - acceptor(nanotube) - donor system Li-NT(6,0)-(NH 2) 2 has considerable β0 to be 6.8 × 10 5 au, due to its small transition energy and large transition moment. Further, the relationships between β0 and the number of Li atoms m and the substituents R for Li m-NT(6,0)-( R) 2 ( m = 1, 6 and R = -CN, -NH 2) systems are explored.

  4. New boron based salts for lithium-ion batteries using conjugated ligands.

    PubMed

    Jankowski, P; Wieczorek, W; Johansson, P

    2016-06-28

    A new anion design concept, based on combining a boron atom as the central atom and conjugated systems as ligands, is presented as a route for finding alternative Li-salts for lithium-ion batteries. The properties of a wide range of novel anions designed in this way have been evaluated by DFT calculations focusing on three different fundamental success factors/measures: the strength of the cation-anion interaction, ultimately determining both the solubility and the ionic conductivity, the oxidation limit, determining their possible use vs. high voltage cathodes, and the reduction stability, revealing a possible role of the anion in the SEI-formation at the anode. For a few anions superior properties vs. today's existing or suggested anions are predicted, especially the very low cation-anion interaction strengths are promising features. The design route itself is shown to be versatile in determining the correlation between different choices of ligands and the resulting overall properties - where the most striking feature is the decreased lithium cation interaction energy upon using the (1Z,3Z)-buta-1,3-diene-1,2,3,4-tetracarbonitrile ligands. This also opens avenues for the further design of novel anions beyond those with a boron central atom. PMID:27253752

  5. Mixed-salt Effects on the Ionic Conductivity of Lithium-doped PEO-containing Block Copolymers

    SciTech Connect

    W Young; J Albert; A Schantz; T Epps

    2011-12-31

    We demonstrate a simple, yet effective, mixed-salt method to increase the room temperature ionic conductivity of lithium-doped block copolymer electrolyte membranes by suppressing the crystalline phases in the conducting block. We examined a mixed-salt system of LiClO{sub 4} and LiN(SO{sub 2}CF{sub 3}){sub 2} (LiTFSI) doped into a lamellae-forming poly(styrene-b-ethylene oxide) (PS-PEO) diblock copolymer. The domain spacings, morphologies, thermal behavior, and crystalline phases of salt-doped PS-PEO samples were characterized, and the ionic conductivities of block copolymer electrolytes were obtained through ac impedance measurements. Comparing the ionic conductivity profiles of salt-doped PS-PEO samples at different mixed-salt ratios and total salt concentrations, we found that the ionic conductivity at room temperature can be improved by more than an order of magnitude when coinhibition of crystallite growth is promoted by the concerted behavior of the PEO:LiClO{sub 4} and PEO:LiTFSI phases. Additionally, we examined the influence of mixed-salt ratio and total salt concentration on copolymer energetics, and we found that the slope of the effective interaction parameter (x{sub eff}) vs salt concentration in our lamellae-forming PS-PEO system was lower than that reported for a cylinder-forming PS-PEO system due to the balance between chain stretching and salt segregation in the PEO domains.

  6. Mixed-Salt Effects on the Ionic Conductivity of Lithium-Doped PEO-Containing Block Copolymers

    SciTech Connect

    Young, Wen-Shiue; Albert, Julie N.L.; Schantz, A. Benjamin; Epps, III, Thomas H.

    2012-10-10

    We demonstrate a simple, yet effective, mixed-salt method to increase the room temperature ionic conductivity of lithium-doped block copolymer electrolyte membranes by suppressing the crystalline phases in the conducting block. We examined a mixed-salt system of LiClO{sub 4} and LiN(SO{sub 2}CF{sub 3}){sub 2} (LiTFSI) doped into a lamellae-forming poly(styrene-b-ethylene oxide) (PS-PEO) diblock copolymer. The domain spacings, morphologies, thermal behavior, and crystalline phases of salt-doped PS-PEO samples were characterized, and the ionic conductivities of block copolymer electrolytes were obtained through ac impedance measurements. Comparing the ionic conductivity profiles of salt-doped PS-PEO samples at different mixed-salt ratios and total salt concentrations, we found that the ionic conductivity at room temperature can be improved by more than an order of magnitude when coinhibition of crystallite growth is promoted by the concerted behavior of the PEO:LiClO{sub 4} and PEO:LiTFSI phases. Additionally, we examined the influence of mixed-salt ratio and total salt concentration on copolymer energetics, and we found that the slope of the effective interaction parameter ({chi}{sub eff}) vs salt concentration in our lamellae-forming PS-PEO system was lower than that reported for a cylinder-forming PS-PEO system due to the balance between chain stretching and salt segregation in the PEO domains.

  7. CAVERN ROOF STABILITY FOR NATURAL GAS STORAGE IN BEDDED SALT

    SciTech Connect

    DeVries, Kerry L; Mellegard, Kirby D; Callahan, Gary D; Goodman, William M

    2005-06-01

    This report documents research performed to develop a new stress-based criterion for predicting the onset of damage in salt formations surrounding natural gas storage caverns. Laboratory tests were conducted to investigate the effects of shear stress, mean stress, pore pressure, temperature, and Lode angle on the strength and creep characteristics of salt. The laboratory test data were used in the development of the new criterion. The laboratory results indicate that the strength of salt strongly depends on the mean stress and Lode angle. The strength of the salt does not appear to be sensitive to temperature. Pore pressure effects were not readily apparent until a significant level of damage was induced and the permeability was increased to allow penetration of the liquid permeant. Utilizing the new criterion, numerical simulations were used to estimate the minimum allowable gas pressure for hypothetical storage caverns located in a bedded salt formation. The simulations performed illustrate the influence that cavern roof span, depth, roof salt thickness, shale thickness, and shale stiffness have on the allowable operating pressure range. Interestingly, comparison of predictions using the new criterion with that of a commonly used criterion indicate that lower minimum gas pressures may be allowed for caverns at shallow depths. However, as cavern depth is increased, less conservative estimates for minimum gas pressure were determined by the new criterion.

  8. Particle formation above natural and simulated salt lakes

    NASA Astrophysics Data System (ADS)

    Kamilli, Katharina; Ofner, Johannes; Sattler, Tobias; Krause, Torsten; Zetzsch, Cornelius; Held, Andreas

    2013-04-01

    Western Australia was originally covered by natural eucalyptus forests, but land-use has changed considerably after large scale deforestation from 1950 to 1970. Thus, the ground-water level rose and brought dissolved salts and minerals to the surface. Nowadays, Western Australia is known for a great plenty of salt lakes with pH levels reaching from 2.5 to 7.1. The land is mainly used for wheat farming and livestock and becomes drier due to the lack of rain periods. One possible reason could be the formation of ultrafine particles from salt lakes, which increases the number of cloud condensation nuclei and thus potentially suppresses precipitation. Several field campaigns have been conducted between 2006 and 2011 with car-based and airborne measurements, where new particle formation has been observed and has been related to the Western Australian salt lakes (Junkermann et al., 2009). To identify particle formation directly above the salt lakes, a 1.5 m³ Teflon chamber was set up above several lakes in 2012. Inside the chamber, photochemistry may take place whereas mixing through wind or advection of already existing particles is prevented. Salt lakes with a low pH level lead to strongly increased aerosol formation. As salt lakes have been identified as a source for reactive halogen species (RHS; Buxmann et al., 2012) and RHS seem to interact with precursors of secondary organic aerosol (SOA), they could be producers of halogen induced secondary organic aerosol (XOA) (Ofner et al., 2012). As reference experiments, laboratory based aerosol smog-chamber runs were performed to examine XOA formation under atmospheric conditions using simulated sunlight and the chemical composition of a chosen salt lake. After adding α-pinene to the simulated salt lake, a strong nucleation event began in the absence of ozone comparable to the observed events in Western Australia. First results from the laboratory based aerosol smog-chamber experiments indicate a halogen-induced aerosol

  9. PC based electrolytes with LiDFOB as an alternative salt for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Knight, Brandon M.

    Lithium-ion batteries (LIBs) have been greatly sought after as a source of renewable energy storage. LIBs have a wide range of applications including but not limited portable electronic devices, electric vehicles, and power tools. As a direct result of their commercial viability an insatiable hunger for knowledge, advancement within the field of LIBs has been omnipresent for the last two decades. However, there are set backs evident within the LIB field; most notably the limitations of standard electrolyte formulations and LiPF6 lithium salt. The standard primary carbonate of ethylene carbonate (EC) has a very limited operating range due to its innate physical properties, and the LiPF6 salt is known to readily decompose to form HF which can further degrade LIB longevity. The goal of our research is to explore the use of a new primary salt LiDFOB in conjunction with a propylene carbonate based electrolyte to establish a more flexible electrolyte formulation by constructing coin cells and cycling them under various conditions to give a clear understanding of each formulation inherent performance capabilities. Our studies show that 1.2M LiDFOB in 3:7 PC/EMC + 1.5% VC is capable of performing comparably to the standard 1.2M LiPF6 in 3:7 EC/EMC at 25°C and the PC electrolyte also illustrates performance superior to the standard at 55°C. The degradation of lithium manganese spinel electrodes, including LiNi 0.5Mn1.5O4, is an area of great concern within the field of lithium ion batteries (LIBs). Manganese containing cathode materials frequently have problems associated with Mn dissolution which significantly reduces the cycle life of LIB. Thus the stability of the cathode material is paramount to the performance of Mn spinel cathode materials in LIBs. In an effort to gain a better understanding of the stability of LiNi0.5 Mn1.5O4 in common LiPF6/carbonate electrolytes, samples were stored at elevated temperature in the presence of electrolyte. Then after storage both

  10. Chemistry of carbon nanomaterials: Uses of lithium nanotube salts in organic syntheses and functionalization of graphite

    NASA Astrophysics Data System (ADS)

    Chattopadhyay, Jayanta

    The effective utilization of carbon nanomaterials, such as single-walled carbon nanotubes (SWNTs) and graphite, has been hindered due to difficulties (poor solubility, poly-dispersity) in processing. Therefore, a high degree of sidewall functionalization, either covalent or non-covalent, is often required to overcome these difficulties as the functionalized nanomaterials exhibit better solubility (either in organic solvents or in water), dispersity, manipulation, and processibility. This thesis presents a series of convenient and efficient organic synthetic routes to functionalize carbon nanomaterials. Carbon nanotube salts, prepared by treating SWNTs with lithium in liquid ammonia, react readily with aryl halides to yield aryl-functionalized SWNTs. These arylated SWNTs are soluble in methanol and water upon treatment with oleum. Similarly, SWNTs can be covalently functionalized by different heteroatoms (nitrogen, oxygen, and sulfur). Using the reductive alkylation approach, a synthetic scheme is designed to prepare long chain carboxylic acid functionalized SWNTs [SWNTs-(RCOOH)] that can react with (1) amine-terminated polyethylene glycol (PEG) chains to yield water-soluble biocompatible PEGylated SWNTs that are likely to be useful in a variety of biomedical applications; (2) polyethyleneimine (PEI) to prepare a SWNTs-PEI based adsorbent material that shows a four-fold improvement in the adsorption capacity of carbon dioxide over commonly used materials, making it useful for regenerable carbon dioxide removal in spaceflight; (3) chemically modified SWNTs-(RCOOH) to permit covalent bonding to the nylon matrix, thus allowing the formation of nylon 6,10 and nylon 6,10/SWNTs-(RCOOH) nanocomposites. Furthermore, we find that the lithium salts of carbon nanotubes serve as a source of electrons to induce polymerization of simple alkenes and alkynes onto the surface of carbon nanotubes. In the presence of sulfide/disulfide bonds, SWNT salts can initiate the single electron

  11. Lithium

    USGS Publications Warehouse

    Ober, J.

    1998-01-01

    The lithium industry can be divided into two sectors: ore concentrate producers and chemical producers. Ore concentrate producers mine lithium minerals. They beneficiate the ores to produce material for use in ceramics and glass manufacturing.

  12. Determination of lithium isotopes at natural abundance levels by atomic absorption spectrometry

    USGS Publications Warehouse

    Meier, A.L.

    1982-01-01

    The relationships of the absorption of 6Li and 7Li hollow cathode lamp emissions are used to determine lithium isotopic composition in the natural abundance range of geologic materials. Absorption was found to have a nonlinear dependence upon total lithium concentration and isotopic composition. A method using nonlinear equations to describe the relationship of the absorption of 6Li and 7Li lamp radiation is proposed as a means of calculating isotopic composition that is independent of total lithium concentration.

  13. Parametric study of natural circulation flow in molten salt fuel in molten salt reactor

    SciTech Connect

    Pauzi, Anas Muhamad; Cioncolini, Andrea; Iacovides, Hector

    2015-04-29

    The Molten Salt Reactor (MSR) is one of the most promising system proposed by Generation IV Forum (GIF) for future nuclear reactor systems. Advantages of the MSR are significantly larger compared to other reactor system, and is mainly achieved from its liquid nature of fuel and coolant. Further improvement to this system, which is a natural circulating molten fuel salt inside its tube in the reactor core is proposed, to achieve advantages of reducing and simplifying the MSR design proposed by GIF. Thermal hydraulic analysis on the proposed system was completed using a commercial computation fluid dynamics (CFD) software called FLUENT by ANSYS Inc. An understanding on theory behind this unique natural circulation flow inside the tube caused by fission heat generated in molten fuel salt and tube cooling was briefly introduced. Currently, no commercial CFD software could perfectly simulate natural circulation flow, hence, modeling this flow problem in FLUENT is introduced and analyzed to obtain best simulation results. Results obtained demonstrate the existence of periodical transient nature of flow problem, hence improvements in tube design is proposed based on the analysis on temperature and velocity profile. Results show that the proposed system could operate at up to 750MW core power, given that turbulence are enhanced throughout flow region, and precise molten fuel salt physical properties could be defined. At the request of the authors and the Proceedings Editor the name of the co-author Andrea Cioncolini was corrected from Andrea Coincolini. The same name correction was made in the Acknowledgement section on page 030004-10 and in reference number 4. The updated article was published on 11 May 2015.

  14. Parametric study of natural circulation flow in molten salt fuel in molten salt reactor

    NASA Astrophysics Data System (ADS)

    Pauzi, Anas Muhamad; Cioncolini, Andrea; Iacovides, Hector

    2015-04-01

    The Molten Salt Reactor (MSR) is one of the most promising system proposed by Generation IV Forum (GIF) for future nuclear reactor systems. Advantages of the MSR are significantly larger compared to other reactor system, and is mainly achieved from its liquid nature of fuel and coolant. Further improvement to this system, which is a natural circulating molten fuel salt inside its tube in the reactor core is proposed, to achieve advantages of reducing and simplifying the MSR design proposed by GIF. Thermal hydraulic analysis on the proposed system was completed using a commercial computation fluid dynamics (CFD) software called FLUENT by ANSYS Inc. An understanding on theory behind this unique natural circulation flow inside the tube caused by fission heat generated in molten fuel salt and tube cooling was briefly introduced. Currently, no commercial CFD software could perfectly simulate natural circulation flow, hence, modeling this flow problem in FLUENT is introduced and analyzed to obtain best simulation results. Results obtained demonstrate the existence of periodical transient nature of flow problem, hence improvements in tube design is proposed based on the analysis on temperature and velocity profile. Results show that the proposed system could operate at up to 750MW core power, given that turbulence are enhanced throughout flow region, and precise molten fuel salt physical properties could be defined. At the request of the authors and the Proceedings Editor the name of the co-author Andrea Cioncolini was corrected from Andrea Coincolini. The same name correction was made in the Acknowledgement section on page 030004-10 and in reference number 4. The updated article was published on 11 May 2015.

  15. Effect of lithium salts addition on the ionic liquid based extraction of essential oil from Farfarae Flos.

    PubMed

    Li, Zhen-Yu; Zhang, Sha-Sha; Jie-Xing; Qin, Xue-Mei

    2015-01-01

    In this study, an ionic liquids (ILs) based extraction approach has been successfully applied to the extraction of essential oil from Farfarae Flos, and the effect of lithium chloride was also investigated. The results indicated that the oil yields can be increased by the ILs, and the extraction time can be reduced significantly (from 4h to 2h), compared with the conventional water distillation. The addition of lithium chloride showed different effect according to the structures of ILs, and the oil yields may be related with the structure of cation, while the chemical compositions of essential oil may be related with the anion. The reduction of extraction time and remarkable higher efficiency (5.41-62.17% improved) by combination of lithium salt and proper ILs supports the suitability of the proposed approach. PMID:25459951

  16. Structural and aggregate analyses of (Li salt + glyme) mixtures: the complex nature of solvate ionic liquids.

    PubMed

    Shimizu, Karina; Freitas, Adilson A; Atkin, Rob; Warr, Gregory G; FitzGerald, Paul A; Doi, Hiroyuki; Saito, Soshi; Ueno, Kazuhide; Umebayashi, Yasuhiro; Watanabe, Masayoshi; Canongia Lopes, José N

    2015-09-14

    The structure and interactions of different (Li salt + glyme) mixtures, namely equimolar mixtures of lithium bis(trifluoromethylsulfonyl)imide, nitrate or trifluoroacetate salts combined with either triglyme or tetraglyme molecules, are probed using Molecular Dynamics simulations. structure factor functions, calculated from the MD trajectories, confirmed the presence of different amounts of lithium-glyme solvates in the aforementioned systems. The MD results are corroborated by S(q) functions derived from diffraction and scattering data (HEXRD and SAXS/WAXS). The competition between the glyme molecules and the salt anions for the coordination to the lithium cations is quantified by comprehensive aggregate analyses. Lithium-glyme solvates are dominant in the lithium bis(trifluoromethylsulfonyl)imide systems and much less so in systems based on the other two salts. The aggregation studies also emphasize the existence of complex coordination patterns between the different species (cations, anions, glyme molecules) present in the studied fluid media. The analysis of such complex behavior is extended to the conformational landscape of the anions and glyme molecules and to the dynamics (solvate diffusion) of the bis(trifluoromethylsulfonyl)imide plus triglyme system. PMID:26245295

  17. Lithium difluoro(oxalate)borate and LiBF4 blend salts electrolyte for LiNi0.5Mn1.5O4 cathode material

    NASA Astrophysics Data System (ADS)

    Zhou, Hongming; Xiao, Kaiwen; Li, Jian

    2016-01-01

    The electrochemical behaviors of lithium difluoro(oxalate)borate (LiODFB) and LiBF4 blend salts in ethylene carbonate + dimethyl carbonate + ethyl(methyl) carbonate (EC + DMC + EMC, 1:1:1, by wt.) have been investigated for LiNi0.5Mn1.5O4 cathode in lithium-ion batteries. The electric conductivity tests are utilized to examine the relationship among solution conductivity, the electrolyte composition and temperature. Through cyclic voltammetry, charge-discharge test and AC impedance measurements, we compare the capacity and cycling efficiency of LNMO cathode in different electrolyte systems at different temperatures and discharge current rates. Scanning electron microscopy (SEM) analysis and X-ray photoelectron spectroscopy (XPS) are served to analyze the surface nature of LNMO cathode after cycles at elevated temperature. These results demonstrate that LNMO cathode can exert excellent electrochemical performance with the increase of LiODFB concentration at room temperature and elevated temperature and it is found that just slight LiBF4, mixed with LiODFB as blend salts, can strikingly improve the cyclability at -20 °C, especially in high-rate cycling. Grouped together, the optimum LiODFB/LiBF4 molar ratio is around 4:1, which can present an excellent affinity to LNMO cathode in a wide electrochemical window.

  18. An approach of ionic liquids/lithium salts based microwave irradiation pretreatment followed by ultrasound-microwave synergistic extraction for two coumarins preparation from Cortex fraxini.

    PubMed

    Liu, Zaizhi; Gu, Huiyan; Yang, Lei

    2015-10-23

    Ionic liquids/lithium salts solvent system was successfully introduced into the separation technique for the preparation of two coumarins (aesculin and aesculetin) from Cortex fraxini. Ionic liquids/lithium salts based microwave irradiation pretreatment followed by ultrasound-microwave synergy extraction (ILSMP-UMSE) procedure was developed and optimized for the sufficient extraction of these two analytes. Several variables which can potentially influence the extraction yields, including pretreatment time and temperature, [C4mim]Br concentration, LiAc content, ultrasound-microwave synergy extraction (UMSE) time, liquid-solid ratio, and UMSE power were optimized by Plackett-Burman design. Among seven variables, UMSE time, liquid-solid ratio, and UMSE power were the statistically significant variables and these three factors were further optimized by Box-Behnken design to predict optimal extraction conditions and find out operability ranges with maximum extraction yields. Under optimum operating conditions, ILSMP-UMSE showed higher extraction yields of two target compounds than those obtained by reference extraction solvents. Method validation studies also evidenced that ILSMP-UMSE is credible for the preparation of two coumarins from Cortex fraxini. This study is indicative of the proposed procedure that has huge application prospects for the preparation of natural products from plant materials. PMID:26411478

  19. Preparation and electrochemical performance of polyphosphazene based salt-in-polymer electrolyte membranes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Jankowsky, S.; Hiller, M. M.; Wiemhöfer, H.-D.

    2014-05-01

    This work presents a detailed study of the electrochemical performance of polyphosphazene based electrolyte membranes consisting of a linear polymer with -(Ndbnd PR2)- units, grafted with ethylene oxide side chains of the type R = -(OCH2CH2)3OCH3 and containing LiTFSI and LiBOB as dissolved lithium salts. The average molecular weight was 105 g mol-1. Mechanical stability was achieved by UV induced in-situ cross-linking of the thin polymer electrolyte films. Favorable properties of this type of polymer electrolytes are the good thermal and electrochemical stability of the electrolyte membranes, the broad electrochemical stability window ranging between 0 V and 4.7 V versus the Li/Li+ reference and a very good interface stability at lithium metal electrodes where a stable SEI was formed during initial contact. Total ionic conductivities up to 10-4 S cm-1 were measured at 30 °C. The transference numbers of lithium ions at 50 °C ranged between 0.06 and 0.07 and hence are lower by a factor of about three as compared to other typical polymer electrolytes. Nevertheless, the partial lithium ion conductivity estimated from the product of total conductivity and lithium ion transference number is as high or slightly higher compared to PEO based polymer electrolytes.

  20. Analysis of secondary cells with lithium anodes and immobilized fused-salt electrolytes

    NASA Technical Reports Server (NTRS)

    Cairns, E. J.; Rogers, G. L.; Shimotake, H.

    1969-01-01

    Secondary cells with liquid lithium anodes, liquid bismuth or tellurium cathodes, and fused lithium halide electrolytes immobilized as rigid pastes operate between 380 and 485 degrees. Applications include power sources in space, military vehicle propulsion and special commercial vehicle propulsion.

  1. Novel benzimidazole salts for lithium ion battery electrolytes: effects of substituents.

    PubMed

    Sriana, T; Leggesse, E G; Jiang, J C

    2015-07-01

    In this paper, we report on our effort to design a novel lithium salt derived from bis(trifluoroborane)benzimidazolide by using density functional theory (DFT) calculations. The effects of different substituents are investigated with respect to ion pair dissociation energies and intrinsic anion oxidation potential of the molecules. Based on our calculations, we have found that ion pair dissociation energies and intrinsic anion oxidation potentials of the anions are mainly affected by the position and the type of substituents introduced into the parent structure. Compared to -CH3, substitution at the C2 position of the parent bis(trifluoroborane)benzimidazole (BTB(-)) by -CF3 results in an increase in anion oxidation stability. However, we observed a negligible change in the intrinsic anion oxidation potential as the length of the fluoroalkyl group increased to -C2F5. The most promising anions are generated by considering double-substitution at C2 and C5 positions. Among the possible anions, bis(trifluoroborane)-5-nitro-2-(trifluoromethyl) benzimidazolide (BTNTB(-)), with the calculated intrinsic anion oxidation potential of 5.50 V vs. Li(+)/Li, can be considered as a potential candidate for high voltage Li-ion batteries. PMID:26051990

  2. Crystal structure of a lithium salt of a glucosyl derivative of lithocholic acid.

    PubMed

    Gubitosi, Marta; Meijide, Francisco; D'Annibale, Andrea; Vázquez Tato, José; Jover, Aida; Galantini, Luciano; Travaglini, Leana; di Gregorio, Maria Chiara; Pavel, Nicolae V

    2016-09-01

    The crystal structure of a Li(+) salt of a glucosyl derivative of lithocholic acid (lithium 3α-(α-d-glucopyranosyl)-5β-cholan-24-oate) has been solved. The crystal belongs to the orthorhombic system, P212121 spatial group, and includes acetone and water in the structure with a 1:1:2 stoichiometry. Monolayers, having a hydrophobic interior and hydrophilic edges, are recognized in the crystal structure. Li(+) is coordinated to three hydroxyl groups of three different glucose residues, with two of them belonging to the same monolayer. A fourth molecule, located in this monolayer, is involved in the coordination of the cation through the carboxylate ion by an electrostatic interaction, thus completing a distorted tetrahedron. All Li(+)-oxygen distances values are very close to the sum of the ionic radius of Li(+) and van der Waals radius of oxygen. Each steroid molecule is linked to other five steroid molecules through hydrogen bonds. Water and acetone are also involved in the hydrogen bond network. A hierarchical organization can be recognized in the crystal, the helical assembly along 21 screw axes being left-handed. PMID:27394960

  3. Ionic conduction properties of PVDF-HFP type gel polymer electrolytes with lithium imide salts

    SciTech Connect

    Saito, Yuria; Kataoka, Hiroshi; Capiglia, C.; Yamamoto, Hitoshi

    2000-03-09

    Conduction properties of gel polymer electrolytes composed of lithium imide salts, LiN(CF{sub 3}SO{sub 2}){sub 2}, LiN(C{sub 2}F{sub 5}SO{sub 2}){sub 2}, and PVDF-HFP copolymer were investigated using the pulsed-field gradient NMR and complex impedance techniques. The diffusion coefficients of the gel decreased with an increase in the polymer fraction in the gel. Carrier concentration exhibited 3 orders of magnitude variation in the fraction change in polymer from 80% to 20%. These results suggest that the polymer interacts with the electrolyte to affect the carrier concentration and mobility of the gel electrolytes. The interactive effect of polymer would be detected in the measurements of spin-lattice relaxation time (T{sub 1}). The deviation of the symmetric curve of the temperature dependence of T{sub 1} could be divided into two components, one was consistent with the component of solution and independent of the polymer fraction and the other depended on the polymer fraction in the gel.

  4. Lithium

    MedlinePlus

    ... bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). Lithium ... Lithium is also sometimes used to treat depression, schizophrenia (a mental ... emotions), disorders of impulse control (inability to resist the urge ...

  5. Electrical Conductivity Study of Polymer Electrolyte Magnetic Nanocomposite Based Poly(Vinyl) Alcohol (PVA) Doping Lithium and Nickel Salt

    NASA Astrophysics Data System (ADS)

    Aji, Mahardika Prasetya; Rahmawati, Silvia, Bijaksana, Satria; Khairurrijal, Abdullah, Mikrajuddin

    2010-10-01

    Composite polymer electrolyte magnetic systems composed of poly(vinyl) alcohol (PVA) as the host polymer, lithium and nickel salt as dopant were studied. The effect upon addition of lithium ions in polimer PVA had been enhanced conductivity with the increase of lithium concentration. The conductivity values were 1.19x10-6, 1.25x10-5, 4.89x-5, 1.88x10-4, and 1.33x10-3 Sṡcm-1 for pure PVA and 1%, 3%, 5% and 7% LiOH complexed PVA, respectively. Meanwhile, the addition nickel salt into polymer electrolyte PVA-LiOH does not significantly change of conductivity value, on order 10-3 Sṡcm-1. The ionic transport is dominantly regarded by Li+ ions present in polymer electrolyte magnetic because the atomic mass Li+ is smaller than Ni2+. The absence of external magnetic field in polimer electrolyte magnetic causes the existence Ni2+ ions not significantly affected of conductivity.

  6. Determination of the electrochemical performance and stability of the lithium-salt, lithium 4,5-dicyano-2-(trifluoromethyl) imidazolide, with various anodes in Li-ion cells

    NASA Astrophysics Data System (ADS)

    Paillet, Sabrina; Schmidt, Gregory; Ladouceur, Sébastien; Fréchette, Joël; Barray, Francis; Clément, Daniel; Hovington, Pierre; Guerfi, Abdelbast; Vijh, Ashok; Cayrefourcq, Ian; Zaghib, Karim

    2015-12-01

    The electrochemical performance and stability of lithium 4,5-dicyano-2-(trifluoromethyl) imidazolide (LiTDI), which is a promising lithium salt for electrolytes in lithium-ion batteries, are discussed. The power capability of LiTDI in EC/DEC (3/7 v/v) in half cells was evaluated with standard anodes used in the lithium-ion battery industry: graphite and Li4Ti5O12 (LTO). The effects of two additives, vinylene carbonate (VC) and fluoro-ethylene carbonate (FEC), were investigated (2% weight in EC/DEC) and compared with a reference electrolyte, 1 M LiPF6 (EC/DEC + 2%VC). LiTDI forms a thin SEI with FEC that is uniformly deposited on graphite, which allows high power capability with 93.9% of the specific capacity at 10C (92.3% for 1 M LiPF6 + 2%VC). Excellent results were also obtained for LiTDI with LTO, 91.1% of the specific capacity was recovered at 10C vs. 91.5% for LiPF6. The stability of LiTDI was evaluated in pouch-cells: LFP/LTO (1C-rate) and NMC/LTO (C/4-rate). The results show that the performance of LiTDI is comparable to that of LiPF6, 85.4% of the capacity was recovered after 900 cycles (87.6% for LiPF6) for LFP/LTO, and 85.8% of capacity was obtained after 450 cycles (86.3% for LiPF6) for NMC/LTO.

  7. Synthesis of rock-salt type lithium borohydride and its peculiar Li+ ion conduction properties

    NASA Astrophysics Data System (ADS)

    Miyazaki, R.; Maekawa, H.; Takamura, H.

    2014-05-01

    The high energy density and excellent cycle performance of lithium ion batteries makes them superior to all other secondary batteries and explains why they are widely used in portable devices. However, because organic liquid electrolytes have a higher operating voltage than aqueous solution, they are used in lithium ion batteries. This comes with the risk of fire due to their flammability. Solid electrolytes are being investigated to find an alternative to organic liquid. However, the nature of the solid-solid point contact at the interface between the electrolyte and electrode or between the electrolyte grains is such that high power density has proven difficult to attain. We develop a new method for the fabrication of a solid electrolyte using LiBH4, known for its super Li+ ion conduction without any grain boundary contribution. The modifications to the conduction pathway achieved by stabilizing the high pressure form of this material provided a new structure with some LiBH4, more suitable to the high rate condition. We synthesized the H.P. form of LiBH4 under ambient pressure by doping LiBH4 with the KI lattice by sintering. The formation of a KI - LiBH4 solid solution was confirmed both macroscopically and microscopically. The obtained sample was shown to be a pure Li+ conductor despite its small Li+ content. This conduction mechanism, where the light doping cation played a major role in ion conduction, was termed the "Parasitic Conduction Mechanism." This mechanism made it possible to synthesize a new ion conductor and is expected to have enormous potential in the search for new battery materials.

  8. Mechanism of dissolution of a lithium salt in an electrolytic solvent in a lithium ion secondary battery: a direct ab initio molecular dynamics (AIMD) study.

    PubMed

    Tachikawa, Hiroto

    2014-06-01

    The mechanism of dissolution of the Li(+) ion in an electrolytic solvent is investigated by the direct ab initio molecular dynamics (AIMD) method. Lithium fluoroborate (Li(+)BF4(-)) and ethylene carbonate (EC) are examined as the origin of the Li(+) ion and the solvent molecule, respectively. This salt is widely utilized as the electrolyte in the lithium ion secondary battery. The binding of EC to the Li(+) moiety of the Li(+)BF4(-) salt is exothermic, and the binding energies at the CAM-B3LYP/6-311++G(d,p) level for n=1, 2, 3, and 4, where n is the number of EC molecules binding to the Li(+) ion, (EC)n(Li(+)BF4(-)), are calculated to be 91.5, 89.8, 87.2, and 84.0 kcal mol(-1) (per EC molecule), respectively. The intermolecular distances between Li(+) and the F atom of BF4(-) are elongated: 1.773 Å (n=0), 1.820 Å (n=1), 1.974 Å (n=2), 1.942 Å (n=3), and 4.156 Å (n=4). The atomic bond populations between Li(+) and the F atom for n=0, 1, 2, 3, and 4 are 0.202, 0.186, 0.150, 0.038, and 0.0, respectively. These results indicate that the interaction of Li(+) with BF4(-) becomes weaker as the number of EC molecules is increased. The direct AIMD calculation for n=4 shows that EC reacts spontaneously with (EC)3(Li(+)BF4(-)) and the Li(+) ion is stripped from the salt. The following substitution reaction takes place: EC+(EC)3(Li(+)BF4(-))→(EC)4Li(+)-(BF4(-)). The reaction mechanism is discussed on the basis of the theoretical results. PMID:24616076

  9. Investigation of the Decomposition Mechanism of Lithium Bis(oxalate)borate (LiBOB) Salt in the Electrolyte of an Aprotic Li–O2 Battery

    SciTech Connect

    Lau, Kah Chun; Lu, Jun; Low, John; Peng, Du; Wu, Huiming; Albishri, Hassan M.; Al-Hady, D. Abd; Curtiss, Larry A.; Amine, Khalil

    2014-03-13

    The stability of the lithium bis(oxalate) borate (LiBOB) salt against lithium peroxide (Li2O2) formation in an aprotic Li–O2 (Li–air) battery is investigated. From theoretical and experimental findings, we find that the chemical decomposition of LiBOB in electrolytes leads to the formation lithium oxalate during the discharge of a Li–O2 cell. According to density functional theory (DFT) calculations, the formation of lithium oxalate as the reaction product is exothermic and therefore is thermodynamically feasible. This reaction seems to be independent of solvents used in the Li–O2 cell, and therefore LiBOB is probably not suitable to be used as the salt in Li–O2 cell electrolytes.

  10. Synthesis of Ultrathin Si Nanosheets from Natural Clays for Lithium-Ion Battery Anodes.

    PubMed

    Ryu, Jaegeon; Hong, Dongki; Choi, Sinho; Park, Soojin

    2016-02-23

    Two-dimensional Si nanosheets have been studied as a promising candidate for lithium-ion battery anode materials. However, Si nanosheets reported so far showed poor cycling performances and required further improvements. In this work, we utilize inexpensive natural clays for preparing high quality Si nanosheets via a one-step simultaneous molten salt-induced exfoliation and chemical reduction process. This approach produces high purity mesoporous Si nanosheets in high yield. As a control experiment, two-step process (pre-exfoliated silicate sheets and subsequent chemical reduction) cannot sustain their original two-dimensional structure. In contrast, one-step method results in a production of 5 nm-thick highly porous Si nanosheets. Carbon-coated Si nanosheet anodes exhibit a high reversible capacity of 865 mAh g(-1) at 1.0 A g(-1) with an outstanding capacity retention of 92.3% after 500 cycles. It also delivers high rate capability, corresponding to a capacity of 60% at 20 A g(-1) compared to that of 2.0 A g(-1). Furthermore, the Si nanosheet electrodes show volume expansion of only 42% after 200 cycles. PMID:26789405

  11. Electrochemical performance of lithium-sulfur batteries based on a sulfur cathode obtained by H2S gas treatment of a lithium salt

    NASA Astrophysics Data System (ADS)

    Dressel, Carina B.; Jha, Himendra; Eberle, Anna-Marietta; Gasteiger, Hubert A.; Fässler, Thomas F.

    2016-03-01

    A new technique to produce Li2S/C composites and Li2S cathodes as well as their application in high-capacity Li-S batteries is demonstrated. The simple but effective method converts an easy-to-handle lithium salt-containing composite or electrode to Li2S using H2S. The main advantage is that the conversion to Li2S can be performed towards the final stage of the electrode preparation process, which significantly reduces the need of controlled atmosphere otherwise required for Li2S handling. LiOH is used to demonstrate the technique, and such fabricated Li2S electrode is successfully used in a Li-S battery (half-cell) where it shows discharge capacities of up to 770 mAh g-1(Li2S) and retained >410 mAh g-1(Li2S) after 100 cycles at C/5.

  12. Rock-salt structure lithium deuteride formation in liquid lithium with high-concentrations of deuterium: a first-principles molecular dynamics study

    NASA Astrophysics Data System (ADS)

    Chen, Mohan; Abrams, T.; Jaworski, M. A.; Carter, Emily A.

    2016-01-01

    Because of lithium’s possible use as a first wall material in a fusion reactor, a fundamental understanding of the interactions between liquid lithium (Li) and deuterium (D) is important. We predict structural and dynamical properties of liquid Li samples with high concentrations of D, as derived from first-principles molecular dynamics simulations. Liquid Li samples with four concentrations of inserted D atoms (LiDβ , β =0.25 , 0.50, 0.75, and 1.00) are studied at temperatures ranging from 470 to 1143 K. Densities, diffusivities, pair distribution functions, bond angle distribution functions, geometries, and charge transfer between Li and D atoms are calculated and analyzed. The analysis suggests liquid-solid phase transitions can occur at some concentrations and temperatures, forming rock-salt LiD within liquid Li. We also observe formation of some D2 molecules at high D concentrations.

  13. 76 FR 28074 - Notice of Inventory Completion: Utah Museum of Natural History, Salt Lake City, UT

    Federal Register 2010, 2011, 2012, 2013, 2014

    2011-05-13

    ... National Park Service Notice of Inventory Completion: Utah Museum of Natural History, Salt Lake City, UT... inventory of human remains in the possession and control of the Utah Museum of Natural History, Salt Lake... remains was made by the Utah Museum of Natural History professional staff and a report sent...

  14. 75 FR 57288 - Notice of Inventory Completion: Utah Museum of Natural History, Salt Lake City, UT

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-09-20

    ... National Park Service Notice of Inventory Completion: Utah Museum of Natural History, Salt Lake City, UT... of Natural History, Salt Lake City, UT. The human remains and associated funerary objects were... Utah Museum of Natural History professional staff and a report sent to representatives of...

  15. Physicochemical and electrochemical properties of N-methyl-N-methoxymethylpyrrolidinium bis(fluorosulfonyl)amide and its lithium salt composites

    NASA Astrophysics Data System (ADS)

    Horiuchi, Shunsuke; Yoshizawa-Fujita, Masahiro; Takeoka, Yuko; Rikukawa, Masahiro

    2016-09-01

    The ionic liquid (IL) N-Methyl-N-methoxymethylpyrrolidinium bis(fluorosulfonyl)amide ([Pyr1,1O1][FSA]) was synthesized, and its physicochemical and electrochemical properties were investigated with respect to its application as an electrolyte in lithium-ion secondary batteries operating over a wide temperature range. [Pyr1,1O1][FSA]/Li salt (0.34 mol kg-1) composites were prepared by adding lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) into the IL. [Pyr1,1O1][FSA] and [Pyr1,1O1][FSA]/LiTFSA exhibited melting temperatures (Tm) below -30 °C. [Pyr1,1O1][FSA] exhibited a higher ionic conductivity value as compared with that of the corresponding IL with only alkyl substituents. The electrochemical window for both [Pyr1,1O1][FSA] and [Pyr1,1O1][FSA]/LiTFSA was 5.1 V. Stable lithium deposition and dissolution occurred on a Ni electrode at 25 °C.

  16. Lithium

    MedlinePlus

    ... mania (frenzied, abnormally excited mood) in people with bipolar disorder (manic-depressive disorder; a disease that causes episodes of depression, episodes of mania, and other abnormal moods). Lithium is in a ... antimanic agents. It works by decreasing abnormal activity in the brain.

  17. 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.

  18. STORAGE OF CHILLED NATURAL GAS IN BEDDED SALT STORAGE CAVERNS

    SciTech Connect

    JOel D. Dieland; Kirby D. Mellegard

    2001-11-01

    This report provides the results of a two-phase study that examines the economic and technical feasibility of converting a conventional natural gas storage facility in bedded salt into a refrigerated natural gas storage facility for the purpose of increasing the working gas capacity of the facility. The conceptual design used to evaluate this conversion is based on the design that was developed for the planned Avoca facility in Steuben County, New York. By decreasing the cavern storage temperature from 43 C to -29 C (110 F to -20 F), the working gas capacity of the facility can be increased by about 70 percent (from 1.2 x 10{sup 8} Nm{sup 3} or 4.4 billion cubic feet (Bcf) to 2.0 x 10{sup 8} Nm{sup 3} or 7.5 Bcf) while maintaining the original design minimum and maximum cavern pressures. In Phase I of the study, laboratory tests were conducted to determine the thermal conductivity of salt at low temperatures. Finite element heat transfer calculations were then made to determine the refrigeration loads required to maintain the caverns at a temperature of -29 C (-20 F). This was followed by a preliminary equipment design and a cost analysis for the converted facility. The capital cost of additional equipment and its installation required for refrigerated storage is estimated to be about $13,310,000 or $160 per thousand Nm{sup 3} ($4.29 per thousand cubic feet (Mcf)) of additional working gas capacity. The additional operating costs include maintenance refrigeration costs to maintain the cavern at -29 C (-20 F) and processing costs to condition the gas during injection and withdrawal. The maintenance refrigeration cost, based on the current energy cost of about $13.65 per megawatt-hour (MW-hr) ($4 per million British thermal units (MMBtu)), is expected to be about $316,000 after the first year and to decrease as the rock surrounding the cavern is cooled. After 10 years, the cost of maintenance refrigeration based on the $13.65 per MW-hr ($4 per MMBtu) energy cost is

  19. Conductivity and stability towards lithium metal of lithium triflate (LiSO 3CF 3) and lithium bistrifluorosulfonylimide (Li(SO 2CF 3)N) in amines and their mixtures with ammonia

    NASA Astrophysics Data System (ADS)

    Fahys, Bernard; Akturk, Necmettin; Herlem, Michel

    The solvates based on combinations of lithium salts with ammonia (called liquid ammoniates) form highly conductive and low cost electrolytes. The generalizing of this fact is possible with amines. Like ammoniates, their solvates possess properties which can widely vary with the composition, the nature of the amine and the anion. Mixtures of NH 3, amine(s) and lithium salt(s) were also investigated. These properties include the glass-transition temperature, the conductivity, the vapour pressure and the corrosion rate of lithium. The conductivity can be as high as 1 × 10 -2 Ω -1 cm -1 at 60 °C. The lithium stability depends on the anion and on the nature of the amines: with n-propylamine and isopropylamine charged with lithium triflate (only 1.5 M) lithium metal is very stable even at +70 °C during several months.

  20. Solvation of the fluorine containing anions and their lithium salts in propylene carbonate and dimethoxyethane.

    PubMed

    Chaban, Vitaly

    2015-07-01

    Electrolyte solutions based on the propylene carbonate (PC)-dimethoxyethane (DME) mixtures are of significant importance and urgency due to emergence of lithium-ion batteries. Solvation and coordination of the lithium cation in these systems have been recently attended in detail. However, analogous information concerning anions (tetrafluoroborate, hexafluorophosphate) is still missed. This work reports PM7-MD simulations (electronic-structure level of description) to include finite-temperature effects on the anion solvation regularities in the PC-DME mixture. The reported result evidences that the anions appear weakly solvated. This observation is linked to the absence of suitable coordination sites in the solvent molecules. In the concentrated electrolyte solutions, both BF4(-) and PF6(-) prefer to exist as neutral ion pairs (LiBF4, LiPF6). PMID:26067106

  1. Growth of lithium triborate single crystals from molten salt solution under various temperature gradients

    NASA Astrophysics Data System (ADS)

    Guretskii, S. A.; Ges, A. P.; Zhigunov, D. I.; Ignatenko, A. A.; Kalanda, N. A.; Kurnevich, L. A.; Luginets, A. M.; Milovanov, A. S.; Molchan, P. V.

    1995-12-01

    Single crystals of lithium triborate LiB 3O 5 (LBO) have been grown by the top-seeded solution growth method with B 2O 3 as a solvent using different temperature gradients in the zone of crystallization. Optical and nonlinear optical properties of LBO single crystals have been investigated. The influence of post-growth thermal treatment in oxygen atmosphere on the optical properties has been studied.

  2. The Salts of Mars: A Rich and Ubiquitous Natural Resource

    NASA Astrophysics Data System (ADS)

    Kargel, Jeff S.

    1998-01-01

    The Viking and Pathfinder Mars landers have shown that martian soil is highly enriched in Cl, S, P, and perhaps Br. which, in all likelihood, occur as salts (chlorides, sulfates, phosphates, and perhaps bromides). Carbonates also may be present Many martian salt minerals are believed to be hydrated. These water-soluble constituents of the soil will offer the first colonists a rich source of many industrial commodities needed to sustain and grow the colony. Being hydrous, martian salts hold a tremendous potential to supply water in regions of Mars where otherwise preferable ice may be absent or difficult to access A caliche-like form of concrete or adobe may be manufactured by the drying of briny mud. Sulfates and phosphates may be used as additives for the manufacture of soil prepared and balanced for agriculture. Sulfates and chlorides offer a raw material for the manufacture of sulfuric and hydrochloric acids. Electrolytic processes applied to magnesium sulfate solution may yield metallic Mg. In short, martian salts will offer colonists abroad industrial base of chemical substances potentially useful in development of indigenous construction, chemical, and agricultural industries. Best of all, such salty dust deposits are among the most widespread and chemically uniform (i.e., dependable) raw materials on Mars. A simple method of preprocessing martian soil to extract and isolate the major salt consituents and to obtain water will be presented, as will a more thorough presentation of possible industrial uses of these materials in a Mars base.

  3. Polymer electrolytes with multiple conductive channels prepared from NBR/SBR latex films impregnated with lithium salt and plasticizer

    SciTech Connect

    Matsumoto, Morihiko; Rutt, J.S.; Nishi, Shiro

    1995-09-01

    Polymer electrolytes, composed of a polar polymer acting as a host matrix for lithium-salt solutions, have high ionic conductivity and have been studied for application in advanced electronic devices such as the rechargeable lithium battery. Polymer electrolytes with high ionic conductivity (> 10{sup {minus}3} S/cm) and good tensile strength were prepared by swelling poly(acrylonitrile-co-butadiene) (NBR)/poly(styrene-co-butadiene) (SBR)/LiClO{sub 4} latex films with {gamma}-butyrolactone ({gamma}-BL) or LiClO{sub 4}/{gamma}-BL plasticizer. Before swelling, the LiClO{sub 4} phase is formed at the particle interface. After politicization, two ion-conductive channels are present: the LiClO{sub 4} phase is present at the interface of the latex particles, and the NBR phase is formed from NBR latex particles. These regions are polar and impregnated selectively with polar {gamma}-BL solvent or LiClO{sub 4}/{gamma}-BL solution, building primary and secondary ion-conductive channels, respectively. The SBR phase (formed from SBR latex particles) is nonpolar and not impregnated, providing a mechanically supportive matrix. High ionic conductivity on the order of 10{sup {minus}3} S/cm is achieved when NBR/SBR(50/50)/LiClO{sub 4} latex film was saturated on 0.2 to 0.4M LiClO{sub 4}/{gamma}-BL solutions. Various microscopic and macroscopic analyses suggest that two types of ion-conductive channels exist in the polymer electrolyte film.

  4. Particle formation above natural and simulated salt lakes

    NASA Astrophysics Data System (ADS)

    Kamilli, Katharina A.; Ofner, Johannes; Sattler, Tobias; Krause, Torsten; Held, Andreas

    2014-05-01

    Originally, Western Australia was covered with Eucalyptus trees. Large scale deforestation for agricultural purposes led to rising ground water levels and brought dissolved salts and minerals to the surface. Nowadays, Western Australia is known for a great plenty of salt lakes with pH levels reaching from 2.5 to 7.1. The land is mainly used for wheat farming and livestock and becomes drier due to the lack of rain periods. One possible reason could be the formation of ultrafine particles from salt lakes, which increases the number of cloud condensation nuclei, and thus potentially suppresses precipitation. Several field campaigns have been conducted between 2006 and 2011 with car-based and airborne measurements, where new particle formation has been observed and has been related to the Western Australian salt lakes (Junkermann et al., 2009). To identify particle formation directly above the salt lakes, a 2.35 m³ PTFE chamber was set up above several lakes in 2012 and 2013. Inside the chamber, photochemistry may take place whereas mixing through wind or advection of already existing particles is prevented. Salt lakes with a low pH level led to strongly increased aerosol formation. Also, the dependence on meteorological conditions has been examined. To obtain chemical information of the newly formed particles, during the chamber experiments also aerosol filter samples have been taken. The analysis of the anions by ion chromatography in 2012 showed an 8 to 17 times higher concentration of Cl- than SO42-, which led to the assumption that particle formation may have been influenced by halogens. As reference experiments, laboratory based aerosol smog-chamber runs were performed to examine halogen induced aerosol formation under atmospheric conditions using simulated sunlight and the simplified chemical composition of a salt lake. The mixture included FeSO4, NaCl and Na2SO4. After adding α-pinene to the simulated salt lake, a strong nucleation event began comparable to

  5. 78 FR 2434 - Notice of Inventory Completion: Natural History Museum of Utah, Salt Lake City, UT

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... National Park Service Notice of Inventory Completion: Natural History Museum of Utah, Salt Lake City, UT AGENCY: National Park Service, Interior. ACTION: Notice. SUMMARY: The Natural History Museum of Utah has... may contact the Natural History Museum of Utah. Repatriation of the human remains and...

  6. 78 FR 2430 - Notice of Inventory Completion: Natural History Museum of Utah, Salt Lake City, UT

    Federal Register 2010, 2011, 2012, 2013, 2014

    2013-01-11

    ... National Park Service Notice of Inventory Completion: Natural History Museum of Utah, Salt Lake City, UT AGENCY: National Park Service, Interior. ACTION: Notice. SUMMARY: The Natural History Museum of Utah has... may contact the Natural History Museum of Utah. Repatriation of the human remains and...

  7. Materials corrosion in molten lithium fluoride-sodium fluoride-potassium fluoride eutectic salt

    NASA Astrophysics Data System (ADS)

    Olson, Luke Christopher

    Static corrosion studies were undertaken to determine the compatibility of several candidate high temperature materials for a heat transfer loop in a molten alkali fluoride eutectic salt, LiF-NaF-KF: 46.5-11.5-42 mol % (commonly referred to as FLiNaK), as well as a molten chloride near eutectic salt, KCl-MgCl2: 68-32 mol %. Several high temperature alloys: Hastelloy-N, Hastelloy-X, Haynes-230, Inconel-617, and Incoloy-800H, Nb-1Zr, a nearly pure Ni alloy Ni-201, and a C/SiSiC ceramic were exposed to molten FLiNaK at 850°C for 500 h in sealed graphite crucibles under an argon cover gas. Corrosion occurred predominantly from dealloying of Cr from the Cr bearing alloys, an effect that was particularly pronounced at the grain boundaries. Corrosion was noted to occur from selective attack of the Si phase in the C/SiSiC ceramic. Alloy weight-loss/area due to molten fluoride salt exposure correlated with the initial Cr-content of the alloys, and was consistent with the Cr-content measured in the salts after corrosion tests. The alloys' weight-loss/area was also found to correlate to the concentration of carbon present in the nominally 20% Cr containing alloys, due to the formation of chromium carbide phases at the grain boundaries. The corrosion mechanisms for the chloride based salt were found to be similar to those observed in FLiNaK, but the chemical attack was found to be less aggressive. Sulfamate Ni electroplating and Mo plasma spraying of Fe-Ni-Cr alloy coupons was investigated to mitigate Cr dissolution. A chemical vapor deposited pyrolytic carbon and SiC coating was also investigated to protect the C/SiSiC composites. Results indicate that Ni-plating has the potential to provide protection against alloy corrosion in molten fluoride salts. Furthermore, the presence of a chromium-oxide interlayer at the interface of the Ni-plating and alloy substrate can further improve the efficacy of the Ni-plating. The pyrolytic carbon and SiC coating on the C/SiSiC composites

  8. Graphitized needle cokes and natural graphites for lithium intercalation

    SciTech Connect

    Tran, T.D.; Spellman, L.M.; Pekala, R.W.; Goldberger, W.M.; Kinoshita, K.

    1996-05-10

    This paper examined effects of heat treatment and milling (before or after heat treatment) on the (electrochemical) intercalating ability of needle petroleum coke; natural graphite particles are included for comparison. 1 tab, 4 figs, 7 refs.

  9. Lithium salt of tetrahydroxybenzoquinone: toward the development of a sustainable Li-ion battery.

    PubMed

    Chen, Haiyan; Armand, Michel; Courty, Matthieu; Jiang, Meng; Grey, Clare P; Dolhem, Franck; Tarascon, Jean-Marie; Poizot, Philippe

    2009-07-01

    The use of lithiated redox organic molecules containing electrochemically active C=O functionalities, such as lithiated oxocarbon salts, is proposed. These represent alternative electrode materials to those used in current Li-ion battery technology that can be synthesized from renewable starting materials. The key material is the tetralithium salt of tetrahydroxybenzoquinone (Li(4)C(6)O(6)), which can be both reduced to Li(2)C(6)O(6) and oxidized to Li(6)C(6)O(6). In addition to being directly synthesized from tetrahydroxybenzoquinone by neutralization at room temperature, we demonstrate that this salt can readily be formed by the thermal disproportionation of Li(2)C(6)O(6) (dilithium rhodizonate phase) under an inert atmosphere. The Li(4)C(6)O(6) compound shows good electrochemical performance vs Li with a sustained reversibility of approximately 200 mAh g(-1) at an average potential of 1.8 V, allowing a Li-ion battery that cycles between Li(2)C(6)O(6) and Li(6)C(6)O(6) to be constructed. PMID:19476355

  10. Rock-salt-type lithium metal sulphides as novel positive-electrode materials

    PubMed Central

    Sakuda, Atsushi; Takeuchi, Tomonari; Okamura, Kazuhiro; Kobayashi, Hironori; Sakaebe, Hikari; Tatsumi, Kuniaki; Ogumi, Zempachi

    2014-01-01

    One way of increasing the energy density of lithium-ion batteries is to use electrode materials that exhibit high capacities owing to multielectron processes. Here, we report two novel materials, Li2TiS3 and Li3NbS4, which were mechanochemically synthesised at room temperature. When used as positive-electrode materials, Li2TiS3 and Li3NbS4 charged and discharged with high capacities of 425 mA h g−1 and 386 mA h g−1, respectively. These capacities correspond to those resulting from 2.5- and 3.5-electron processes. The average discharge voltage was approximately 2.2 V. It should be possible to prepare a number of high-capacity materials on the basis of the concept used to prepare Li2TiS3 and Li3NbS4. PMID:24811191

  11. Advanced Surface and Microstructural Characterization of Natural Graphite Anodes for Lithium Ion Batteries

    SciTech Connect

    Gallego, Nidia C; Contescu, Cristian I; Meyer III, Harry M; Howe, Jane Y; Meisner, Roberta Ann; Payzant, E Andrew; Lance, Michael J; Yoon, Steve; Denlinger, Matthew; Wood III, David L

    2014-01-01

    Natural graphite powders were subjected to a series of thermal treatments in order to improve the anode irreversible capacity loss (ICL) and capacity retention during long-term cycling of lithium ion batteries. A baseline thermal treatment in inert Ar or N2 atmosphere was compared to cases with a proprietary additive to the furnace gas environment. This additive substantially altered the surface chemistry of the natural graphite powders and resulted in significantly improved long-term cycling performance of the lithium ion batteries over the commercial natural graphite baseline. Different heat-treatment temperatures were investigated ranging from 950-2900 C with the intent of achieving the desired long-term cycling performance with as low of a maximum temperature and thermal budget as possible. A detailed summary of the characterization data is also presented, which includes X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Raman spectroscopy, and temperature-programed desorption mass spectroscopy (TPD-MS). This characterization data was correlated to the observed capacity fade improvements over the course of long-term cycling at high charge-discharge rates in full lithium-ion coin cells. It is believed that the long-term performance improvements are a result of forming a more stable solid electrolyte interface (SEI) layer on the anode graphite surfaces, which is directly related to the surface chemistry modifications imparted by the proprietary gas environment during thermal treatment.

  12. Salinity tolerance in soybean is modulated by natural variation in GmSALT3.

    PubMed

    Guan, Rongxia; Qu, Yue; Guo, Yong; Yu, Lili; Liu, Ying; Jiang, Jinghan; Chen, Jiangang; Ren, Yulong; Liu, Guangyu; Tian, Lei; Jin, Longguo; Liu, Zhangxiong; Hong, Huilong; Chang, Ruzhen; Gilliham, Matthew; Qiu, Lijuan

    2014-12-01

    The identification of genes that improve the salt tolerance of crops is essential for the effective utilization of saline soils for agriculture. Here, we use fine mapping in a soybean (Glycine max (L.) Merr.) population derived from the commercial cultivars Tiefeng 8 and 85-140 to identify GmSALT3 (salt tolerance-associated gene on chromosome 3), a dominant gene associated with limiting the accumulation of sodium ions (Na+) in shoots and a substantial enhancement in salt tolerance in soybean. GmSALT3 encodes a protein from the cation/H+ exchanger family that we localized to the endoplasmic reticulum and which is preferentially expressed in the salt-tolerant parent Tiefeng 8 within root cells associated with phloem and xylem. We identified in the salt-sensitive parent, 85-140, a 3.78-kb copia retrotransposon insertion in exon 3 of Gmsalt3 that truncates the transcript. By sequencing 31 soybean landraces and 22 wild soybean (Glycine soja) a total of nine haplotypes including two salt-tolerant haplotypes and seven salt-sensitive haplotypes were identified. By analysing the distribution of haplotypes among 172 Chinese soybean landraces and 57 wild soybean we found that haplotype 1 (H1, found in Tiefeng 8) was strongly associated with salt tolerance and is likely to be the ancestral allele. Alleles H2-H6, H8 and H9, which do not confer salinity tolerance, were acquired more recently. H1, unlike other alleles, has a wide geographical range including saline areas, which indicates it is maintained when required but its potent stress tolerance can be lost during natural selection and domestication. GmSALT3 is a gene associated with salt tolerance with great potential for soybean improvement. PMID:25292417

  13. Dynamics and relaxation of charge carriers in poly(methylmethacrylate)-lithium salt based polymer electrolytes plasticized with ethylene carbonate

    NASA Astrophysics Data System (ADS)

    Pal, P.; Ghosh, A.

    2016-07-01

    In this paper, we have studied the dynamics and relaxation of charge carriers in poly(methylmethacrylate)-lithium salt based polymer electrolytes plasticized with ethylene carbonate. Structural and thermal properties have been examined using X-ray diffraction and differential scanning calorimetry, respectively. We have analyzed the complex conductivity spectra by using power law model coupled with the contribution of electrode polarization at low frequencies and high temperatures. The temperature dependence of the ionic conductivity and crossover frequency exhibits Vogel-Tammann-Fulcher type behavior indicating a strong coupling between the ionic and the polymer chain segmental motions. The scaling of the ac conductivity indicates that relaxation dynamics of charge carriers follows a common mechanism for all temperatures and ethylene carbonate concentrations. The analysis of the ac conductivity also shows the existence of a nearly constant loss in these polymer electrolytes at low temperatures and high frequencies. The fraction of free anions and ion pairs in polymer electrolyte have been obtained from the analysis of Fourier transform infrared spectra. It is observed that these quantities influence the behavior of the composition dependence of the ionic conductivity.

  14. Novel polymer electrolytes based on thermoplastic polyurethane and ionic liquid/lithium bis(trifluoromethanesulfonyl)imide/propylene carbonate salt system

    NASA Astrophysics Data System (ADS)

    Lavall, R. L.; Ferrari, S.; Tomasi, C.; Marzantowicz, M.; Quartarone, E.; Magistris, A.; Mustarelli, P.; Lazzaroni, S.; Fagnoni, M.

    Polymer electrolytes were prepared from thermoplastic polyurethane with addition of mixture of ionic liquid N-ethyl(methylether)-N-methylpyrrolidinium trifluoromethanesulfonimmide (PYRA 12O1TFSI), lithium bis(trifluoromethanesulfoneimide) salt and propylene carbonate. The electrolytes characterization was performed by thermogravimetric analysis, differential scanning calorimetry and scanning electron microscopy. The electrical properties were investigated in detail by impedance spectroscopy with the aid of equivalent circuit fitting of the impedance spectra. A model describing temperature evolution of ionic conductivity and the properties of electrolyte/blocking electrode interface was developed. The electrochemical stability of the electrolytes was studied by linear voltammetry. Our results indicate that the studied electrolytes have good self-standing characteristics, and also a sufficient level of thermal stability and a fairly good electrochemical window. The ionic conductivity increases with increasing amount of mixture, and the character of temperature dependence of conductivity indicates decoupling of ion transport from polymer matrix. For studied system, the highest value of ionic conductivity measured at room temperature was 10 -4 S cm -1.

  15. Intergranular fracture of lithium fluoride-22 percent calcium fluoride hypereutectic salt at 800 K

    NASA Technical Reports Server (NTRS)

    Raj, Subramanium V.; Whittenberger, J. Daniel

    1990-01-01

    Substantial strain-hardening was noted during the initial stages of deformation in constant-velocity compression tests conducted on as-cast samples of the LiF-22 mol pct CaF2 hypereutectic salt at 800 K. The deformed specimens exhibited extensive grain-boundary cracking and cavitation, suggesting that such cracking, in conjunction with interfacial sliding, is important for cavity nucleation at grain boundaries and at the LiF-CaF2 interfaces. Cavity growth and interlinkage occur through the preferential failure of the weaker LiF phase.

  16. Ion pairing in aqueous lithium salt solutions with monovalent and divalent counter-anions.

    PubMed

    Pluhařová, Eva; Mason, Philip E; Jungwirth, Pavel

    2013-11-21

    Molecular dynamics simulations of concentrated aqueous solutions of LiCl and Li2SO4 were conducted in order to provide molecular insight into recent neutron scattering data. The structures predicted from the molecular dynamics simulations using standard nonpolarizable force fields provided a very poor fit to the experiment; therefore, refinement was needed. The electronic polarizability of the medium was effectively accounted for by implementing the electronic continuum correction, which practically means rescaling the ionic charges. Consistent with previous studies, we found that this approach in each case provided a significantly improved fit to the experimental data, which was further enhanced by slightly adjusting the radius of the lithium ion. The polarization effect was particularly pronounced in the Li2SO4 solution where the ions in the nonpolarizable simulations tended to cluster unphysically. With the above alterations, the employed force field displayed an excellent fit to the neutron scattering data and provided a useful interpretative framework for the experimental measurements. At the same time, the present study underlines the importance of solvent polarization effects in hydration of ions with high charge density. PMID:23581250

  17. Risk assessment of converting salt caverns to natural gas storage. Final report, November 1994-July 1995

    SciTech Connect

    Harrison, M.R.; Ellis, P.F.

    1995-10-01

    The objective of this paper was an assessment of the risks of release of large quantities of natural gas from salt caverns converted from other uses to the storage of compressed natural gas (CNG). A total of 22 potential root causes for large releases of natural gas from converted salt converns were identified and ranked in terms of relative risk. While this project assessed the relative risks of major gas releases, the absolute risk was determined by implication to be extremely low, as indicated by the historical record.

  18. Synthesis of rock-salt type lithium borohydride and its peculiar Li{sup +} ion conduction properties

    SciTech Connect

    Miyazaki, R.; Maekawa, H.; Takamura, H.

    2014-05-01

    The high energy density and excellent cycle performance of lithium ion batteries makes them superior to all other secondary batteries and explains why they are widely used in portable devices. However, because organic liquid electrolytes have a higher operating voltage than aqueous solution, they are used in lithium ion batteries. This comes with the risk of fire due to their flammability. Solid electrolytes are being investigated to find an alternative to organic liquid. However, the nature of the solid-solid point contact at the interface between the electrolyte and electrode or between the electrolyte grains is such that high power density has proven difficult to attain. We develop a new method for the fabrication of a solid electrolyte using LiBH{sub 4,} known for its super Li{sup +} ion conduction without any grain boundary contribution. The modifications to the conduction pathway achieved by stabilizing the high pressure form of this material provided a new structure with some LiBH{sub 4}, more suitable to the high rate condition. We synthesized the H.P. form of LiBH{sub 4} under ambient pressure by doping LiBH{sub 4} with the KI lattice by sintering. The formation of a KI - LiBH{sub 4} solid solution was confirmed both macroscopically and microscopically. The obtained sample was shown to be a pure Li{sup +} conductor despite its small Li{sup +} content. This conduction mechanism, where the light doping cation played a major role in ion conduction, was termed the “Parasitic Conduction Mechanism.” This mechanism made it possible to synthesize a new ion conductor and is expected to have enormous potential in the search for new battery materials.

  19. Corrosion behavior of Ni-based structural materials for electrolytic reduction in lithium molten salt

    NASA Astrophysics Data System (ADS)

    Cho, Soo Haeng; Park, Sung Bin; Lee, Jong Hyeon; Hur, Jin Mok; Lee, Han Soo

    2011-05-01

    In this study, the corrosion behavior of new Ni-based structural materials was studied for electrolytic reduction after exposure to LiCl-Li 2O molten salt at 650 °C for 24-216 h under an oxidizing atmosphere. The new alloys with Ni, Cr, Al, Si, and Nb as the major components were melted at 1700 °C under an inert atmosphere. The melt was poured into a preheated metallic mold to prepare an as-cast alloy. The corrosion products and fine structures of the corroded specimens were characterized by scanning electron microscope (SEM), Energy Dispersive X-ray Spectroscope (EDS), and X-ray diffraction (XRD). The corrosion products of as cast and heat treated low Si/high Ti alloys were Cr 2O 3, NiCr 2O 4, Ni, NiO, and (Al,Nb,Ti)O 2; those of as cast and heat treated high Si/low Ti alloys were Cr 2O 3, NiCr 2O 4, Ni, and NiO. The corrosion layers of as cast and heat treated low Si/high Ti alloys were continuous and dense. However, those of as cast and heat treated high Si/low Ti alloys were discontinuous and cracked. Heat treated low Si/high Ti alloy showed the highest corrosion resistance among the examined alloys. The superior corrosion resistance of the heat treated low Si/high Ti alloy was attributed to the addition of an appropriate amount of Si, and the metallurgical evaluations were performed systematically.

  20. Carbon catalysis of reactions in the lithium SOCl2 and SO2 systems

    NASA Technical Reports Server (NTRS)

    Kilroy, W. P.

    1981-01-01

    Certain hazards associated with lithium batteries have delayed widespread acceptance of these power sources. The reactivity of ground lithium carbon mixtures was examined. The effect of carbon types on this reactivity was determined. The basic reaction involved mixtures of lithium and carbon with battery electrolyte. The various parameters that influenced this reactivity included: the nature and freshness of the carbon; the freshness, the purity, and the conductive salt of the electrolyte; and the effect of Teflon or moisture.

  1. Seven-coordinate iron complex as a ditopic receptor for lithium salts: study of host-guest interactions and substitution behavior.

    PubMed

    Sarauli, David; Popova, Vesselina; Zahl, Achim; Puchta, Ralph; Ivanović-Burmazović, Ivana

    2007-09-17

    Interactions between the seven-coordinate tweezerlike [Fe(dapsox)(H2O)2]ClO4 complex (H2dapsox = 2,6-diacetylpyridine-bis(semioxamazide)) with different lithium salts (LiOTf, LiClO4, LiBF4, and LiPF6) in CH3CN have been investigated by electrochemical, spectrophotometric, 7Li and 19F NMR, kinetic, and DFT methods. It has been demonstrated that this complex acts as ditopic receptor, showing spectral and electrochemical ion-pair-sensing capability for different lithium salts. In general, the apparent binding constants for lithium salts increase in the order LiOTf < LiClO4 < LiBF4. From the electrochemical measurements, the apparent lithium salt binding constants for the Fe(III) and Fe(II) forms of the complex have been obtained, suggesting a stronger host-guest interaction with the reduced form of the complex. In the presence of LiPF6, the solution chemistry is more complex because of the hydrolysis of PF6-. The kinetics of the complexation of [Fe(dapsox)(CH3CN)2]+ by thiocyanate at -15 degrees C in acetonitrile in the presence of 0.2 M NBu4OTf shows two steps with the following rate constants and activation parameters: k(1) = 411 +/- 14 M(-1) s(-1); DeltaH(1) not equal = 9 +/- 2 kJ mol(-1); DeltaS1 not equal = -159 +/- 6 J K(-1) mol(-1); k(2) = 52 +/- 1 M(-1) s(-1); DeltaH(2) not equal = 4 +/- 1 kJ mol(-1); DeltaS(2) not equal = -195 +/- 3 J K(-1) mol(-1). The very negative DeltaS not equal values are consistent with an associative (A) mechanism. Under the same conditions but with 0.2 M LiOTf, k1Li and k2Li are 1605 +/- 51 and 106 +/- 2 M(-1) s(-1), respectively. The increased rate constants for the {[Fe(dapsox)(CH3CN)2] x LiOTf}+ adduct are in agreement with an associative mechanism. Kinetic and spectrophotometric titration measurements show stronger interaction between the lithium salt and the anion-substituted forms, [Fe(dapsox)(CH3CN)(NCS)] and [Fe(dapsox)(NCS)2]-, of the complex. These experiments demonstrate that in nonaqueous media lithium salts cannot be

  2. Resistivity and induced polarization monitoring of salt transport under natural hydraulic gradients

    SciTech Connect

    Slater, L.D.; Sandberg, S.K.

    2000-04-01

    The authors demonstrate the use of resistivity/induced polarization (IP) monitoring of salt transport under natural hydraulic loads. Electrical monitoring of saline tracer transport during forced injection has been demonstrated previously. Detection of tracer transport under natural hydraulic loading is difficult because neither the hydraulic load nor the tracer resistivity can be controlled. In one study, the authors identify the electrical response to salt transport in a dynamic beach environment. Resistivity/IP imagine resolved the structure of the saltwater-freshwater interface and evidence for tide-induced groundwater transport. Resistivity increases in the near surface and at depth, upbeach of the high-tide mark, accompanied by tidal transgression. They attribute this to desaturation and decreasing salinity in the near surface and to decreasing salinity at depth, despite tidal transgression. Monitoring of groundwater levels indicates a phase lag between the tide level and groundwater level, supporting the electrical data. IP was insensitive to groundwater salinity variation. In a second study, the authors identify the electrical response to recharge-induced salt transport from a road-sale storage facility. Conductivity and IP models for monitoring lines, located on the basis of an EM31 survey, resolved the subsurface salt distribution, IP modeling resolved the sediment-bedrock interface. Modeling of monthly conductivity differences revealed conductivity increases and decreases at the locations of salt contamination, which correlate with the recharge pattern. They attribute near-surface conductivity increases after heavy rainfall to increasing saturation and ion dissolution. Corresponding conductivity decreases at depth are attributed to flushing of the bedrock with freshwater. Essentially, the opposite response was observed during a quiet monitoring period following heavy recharge. Near-surface IP changes are consistent with this interpretation. Salt

  3. Second hyperpolarizability of the calcium-doped lithium salt of pyridazine Li-H3C4N2 ⋯ Ca

    NASA Astrophysics Data System (ADS)

    Marques, Suélio; Castro, Marcos A.; Leão, Salviano A.; Fonseca, Tertius L.

    2016-08-01

    In this work we report results of coupled cluster calculations for the second hyperpolarizability of the calcium-doped lithium salt of pyridazine (Li-H3C4N2 ⋯ Ca) molecule. In the static limit an unusual value of 4.34 ×106 au was obtained at the CCSD level of calculation. Results obtained for the dc-Kerr effect through SCF, CCS and CCSD methods show that γ (- ω; ω, 0, 0) is strongly dependent of the electron correlation treatment. Dynamic results obtained at the CCSD level are also reported for the IDRI, dc-SHG and THG nonlinear optical processes.

  4. Preparation of nanocrystalline silicon from SiCl4 at 200 °C in molten salt for high-performance anodes for lithium ion batteries.

    PubMed

    Lin, Ning; Han, Ying; Wang, Liangbiao; Zhou, Jianbin; Zhou, Jie; Zhu, Yongchun; Qian, Yitai

    2015-03-16

    Crystalline Si nanoparticles are prepared by reduction of SiCl4 with metallic magnesium in the molten salt of AlCl3 at 200 °C in an autoclave. AlCl3 not only acts as molten salt, but also participates in the reaction. The related experiments confirm that metallic Mg reduces AlCl3 to create nascent Al which could immediately reduce SiCl4 to Si, and the by-product MgCl2 would combine with AlCl3 forming complex of MgAl2Cl8. As anode for rechargeable lithium ion batteries, the as-prepared Si delivers the reversible capacity of 3083 mAh g(-1) at 1.2 A g(-1) after 50 cycles, and 1180 mAh g(-1) at 3 A g(-1) over 500 cycles. PMID:25631549

  5. ASSESSMENT OF LITHIUM USING THE IEHR EVALUATIVE PROCESS FOR ASSESSING HUMAN DEVELOPMENTAL AND REPRODUCTIVE TOXICITY OF AGENTS

    EPA Science Inventory

    This document presents an evaluation of the reproductive and developmental effects of lithium and reviews toxicologic information on several specific lithium salts: ithium carbonate, lithium chloride, lithium citrate, and lithium hypochlorite. ithium (Li), an alkali metal, is a n...

  6. Surface passivation of natural graphite electrode for lithium ion battery by chlorine gas.

    PubMed

    Suzuki, Satoshi; Mazej, Zoran; Zemva, Boris; Ohzawa, Yoshimi; Nakajima, Tsuyoshi

    2013-01-01

    Surface lattice defects would act as active sites for electrochemical reduction of propylene carbonate (PC) as a solvent for lithium ion battery. Effect of surface chlorination of natural graphite powder has been investigated to improve charge/discharge characteristics of natural graphite electrode in PC-containing electrolyte solution. Chlorination of natural graphite increases not only surface chlorine but also surface oxygen, both of which would contribute to the decrease in surface lattice defects. It has been found that surface-chlorinated natural graphite samples with surface chlorine concentrations of 0.5-2.3 at% effectively suppress the electrochemical decomposition of PC, highly reducing irreversible capacities, i.e. increasing first coulombic efficiencies by 20-30% in 1 mol L-1 LiClO4-EC/DEC/PC (1:1:1 vol.). In 1 mol L-1 LiPF6-EC/EMC/PC (1:1:1 vol.), the effect of surface chlorination is observed at a higher current density. This would be attributed to decrease in surface lattice defects of natural graphite powder by the formation of covalent C-Cl and C=O bonds. PMID:24169705

  7. Novel binary deep eutectic electrolytes for rechargeable Li-ion batteries based on mixtures of alkyl sulfonamides and lithium perfluoroalkylsulfonimide salts

    NASA Astrophysics Data System (ADS)

    Geiculescu, O. E.; DesMarteau, D. D.; Creager, S. E.; Haik, O.; Hirshberg, D.; Shilina, Y.; Zinigrad, E.; Levi, M. D.; Aurbach, D.; Halalay, I. C.

    2016-03-01

    Ionic liquids (IL's) were proposed for use in Li-ion batteries (LIBs), in order to mitigate some of the well-known drawbacks of LiPF6/mixed organic carbonates solutions. However, their large cations seriously decrease lithium transference numbers and block lithium insertion sites at electrode-electrolyte interfaces, leading to poor LIB rate performance. Deep eutectic electrolytes (DEEs) (which share some of the advantages of ILs but possess only one cation, Li+), were then proposed, in order to overcome the difficulties associated with ILs. We report herein on the preparation, thermal properties (melting, crystallization, and glass transition temperatures), transport properties (specific conductivity and viscosity) and thermal stability of binary DEEs based on mixtures of lithium bis(trifluoromethane)sulfonimide or lithium bis(fluoro)sulfonimide salts with an alkyl sulfonamide solvent. Promise for LIB applications is demonstrated by chronoamperometry on Al current collectors, and cycling behavior of negative and positive electrodes. Residual current densities of 12 and 45 nA cm-2 were observed at 5 V vs. Li/Li+ on aluminum, 1.5 and 16 nA cm-2 at 4.5 V vs. Li/Li+, respectively for LiFSI and LiTFSI based DEEs. Capacities of 220, 130, and 175 mAh· g-1 were observed at low (C/13 or C/10) rates, respectively for petroleum coke, LiMn1/3Ni1/3Co1/3O2 (a.k.a. NMC 111) and LiAl0.05Co0.15Ni0.8O2 (a.k.a. NCA).

  8. A Facile Molten-Salt Route for Large-Scale Synthesis of NiFe2O4 Nanoplates with Enhanced Lithium Storage Capability.

    PubMed

    Huang, Gang; Du, Xinchuan; Zhang, Feifei; Yin, Dongming; Wang, Limin

    2015-09-28

    Binary metal oxides have been deemed as a promising class of electrode materials for high-performance lithium ion batteries owing to their higher conductivity and electrochemical activity than corresponding monometal oxides. Here, NiFe2O4 nanoplates consisting of nanosized building blocks have been successfully fabricated by a facile, large-scale NaCl and KCl molten-salt route, and the changes in the morphology of NiFe2O4 as a function of the molten-salt amount have been systemically investigated. The results indicate that the molten-salt amount mainly influences the diameter and thickness of the NiFe2O4 nanoplates as well as the morphology of the nanosized building blocks. Cyclic voltammetry (CV) and galvanostatic charge-discharge measurements have been conducted to evaluate the lithium storage properties of the NiFe2O4 nanoplates prepared with a Ni(NO3)2/Fe(NO3)3/KCl/NaCl molar ratio of 1:2:20:60. A high reversible capacity of 888 mAh g(-1) is delivered over 100 cycles at a current density of 100 mA g(-1). Even at a current density of 5000 mA g(-1) , the discharge capacity could still reach 173 mAh g(-1). Such excellent electrochemical performances of the NiFe2O4 nanoplates are contributed to the short Li(+) diffusion distance of the nanosized building blocks and the synergetic effect of the Ni(2+) and Fe(3+) ions. PMID:26251115

  9. Nature of chalcogen hor ellipsis chalcogen contact interactions in organic donor-molecule salts

    SciTech Connect

    Novoa, J.J.; Whangbo, Myung-Hwan . Dept. of Chemistry); Williams, J.M. )

    1990-01-01

    The nature of chalcogen{hor ellipsis}chalcogen contact interactions in organic donor-molecule salts was examined by performing ab initio SCF-MO/MP2 calculations on H{sub 2}X{hor ellipsis}XH{sub 2}(X = O, S, SE, Te) and MM2 calculations on donor dimers (TXF){sub 2} (X = S, SE, Te) and (BEDX-TTF){sub 2} (X = O, S). 14 refs., 4 figs., 4 tabs.

  10. Fry spacing of deformed and undeformed modeled and natural salt domes

    SciTech Connect

    Roennlund, P.; Koyi, H.

    1988-05-01

    Fry's center-point spacing strain analysis is applied to experiments of gravity-driven overturn of horizontal fluid layers on scales of centimeters or decimeters, and to natural salt diapirs on scales of kilometers to tens of kilometers. Laboratory experiments in which about 100 diapirs formed from initially plane horizontal layers resulted in laterally isotropic spacing and yielded an open circle on a Fry plot with a radius equal to the wavelength (W). Lateral deformation and initial departures from horizontal layers with uniform properties may influence W. Sample experiments of diapirism with and without lateral deformation are compared to natural equivalents. The spacing of post-Late Triassic diapirs in the Zechstein salt of Germany and of post-Jurassic diapirs in the Hormuz salt of Arabia yields circles on Fry plots which indicate that these gravity structures developed without additional lateral forces. Fry plots of the spacing of salt diapirs in the Zagros Mountains define a strain ellipse with the long axis (=W in Arabia) parallel and the short axis perpendicular to post-Miocene regional fold axes. The ratio of the Zagros strain ellipse is about 1.7, which suggests a northeast-southwest shortening of 41%, rather than 10%-21% as estimated from folding alone. This mismatch may be a result of unquantified shortening due to thrusts and/or layer-parallel shortening. Center-point spacing of post-Late Triassic domes of Zechstein salt in the central North Sea also gives an ellipse. Here, the long axis coincides with the direction of Middle Jurassic to Cretaceous extension. The axial ratio of the North Sea strain ellipse is about 2.8, compared to estimates of about 1.5-2.0 by Sclater and Christie, and 1.8 by Wood and Barton.

  11. EXAMINE AND EVALUATE A PROCESS TO USE SALT CAVERNS TO RECEIVE SHIP BORNE LIQUEFIED NATURAL GAS

    SciTech Connect

    Michael M. McCall; William M. Bishop; D. Braxton Scherz

    2003-04-24

    The goal of the U.S. Department of Energy cooperative research project is to define, describe, and validate, a process to utilize salt caverns to receive and store the cargoes of LNG ships. The project defines the process as receiving LNG from a ship, pumping the LNG up to cavern injection pressures, warming it to cavern compatible temperatures, injecting the warmed vapor directly into salt caverns for storage, and distribution to the pipeline network. The performance of work under this agreement is based on U.S. Patent 5,511,905, and other U.S. and Foreign pending patent applications. The cost sharing participants in the research are The National Energy Technology Laboratory (U.S. Department of Energy), BP America Production Company, Bluewater Offshore Production Systems (U.S.A.), Inc., and HNG Storage, L.P. Initial results indicate that a salt cavern based receiving terminal could be built at about half the capital cost, less than half the operating costs and would have significantly higher delivery capacity, shorter construction time, and be much more secure than a conventional liquid tank based terminal. There is a significant body of knowledge and practice concerning natural gas storage in salt caverns, and there is a considerable body of knowledge and practice in handling LNG, but there has never been any attempt to develop a process whereby the two technologies can be combined. Salt cavern storage is infinitely more secure than surface storage tanks, far less susceptible to accidents or terrorist acts, and much more acceptable to the community. The project team developed conceptual designs of two salt cavern based LNG terminals, one with caverns located in Calcasieu Parish Louisiana, and the second in Vermilion block 179 about 50 miles offshore Louisiana. These conceptual designs were compared to conventional tank based LNG terminals and demonstrate superior security, economy and capacity. The potential for the development of LNG receiving terminals

  12. Spindletop salt-cavern points way for future natural-gas storage

    SciTech Connect

    Shotts, S.A.; Neal, J.R.; Solis, R.J. ); Oldham, C. )

    1994-09-12

    Spindletop underground natural-gas storage complex began operating in 1993, providing 1.7 bcf of working-gas capacity in its first cavern. The cavern and related facilities exemplify the importance and advantages of natural-gas storage in leached salt caverns. Development of a second cavern, along with continued leaching of the initial cavern, target 5 bcf of available working-gas capacity in both caverns by the end of this year. The facilities that currently make up the Spindletop complex include two salt dome gas-storage wells and a 24,000-hp compression and dehydration facility owned by Sabine Gas; two salt dome gas-storage wells and a 15,900-hp compression and dehydration facility owned by Centana; a 7,000-hp leaching plant; and three jointly owned brine-disposal wells. The paper discusses the development of the storage facility, design goals, leaching plant and wells, piping and compressors, dehydration and heaters, control systems, safety and monitoring, construction, first years operation, and customer base.

  13. From the Disordered State to the Frank-Kasper Sigma Phase: Readily Tuning the Phase Behavior of Block Polymers via Lithium Salt Addition

    NASA Astrophysics Data System (ADS)

    Irwin, Matthew; Hickey, Robert; Bates, Frank; Lodge, Timothy

    Sphere-forming block copolymers have long been known to assemble onto a body-centered cubic (BCC) lattice, but recent work has demonstrated that with the correct thermal treatments, more exotic morphologies such as dodecagonal quasicrystals or the Frank-Kasper sigma phase can be observed. In this presentation, we show that a similar variety of morphologies can be obtained by simply adding small amounts of lithium bis(trifluoromethane)sulfonimide (LiTFSI), which preferentially partitions into one of the domains. Using small-angle X-ray scattering, we have found that block copolymers, which are disordered when neat, can form spheres with liquid-like packing, BCC crystals, the Frank-Kasper sigma phase, or hexagonally close packed crystals upon increasing the salt loading. This work demonstrates a unique, alternative route to highly segregated sphere-forming block copolymers and examines the universality of the formation of these complex morphologies.

  14. Marine fungal diversity: a comparison of natural and created salt marshes of the north-central Gulf of Mexico.

    PubMed

    Walker, Allison K; Campbell, Jinx

    2010-01-01

    Marine fungal communities of created salt marshes of differing ages were compared with those of two reference natural salt marshes. Marine fungi occurring on the lower 30 cm of salt marsh plants Spartina alterniflora and Juncus roemerianus were inventoried with morphological and molecular methods (ITS T-RFLP analysis) to determine fungal species richness, relative frequency of occurrence and ascomata density. The resulting profiles revealed similar fungal communities in natural salt marshes and created salt marshes 3 y old and older with a 1.5 y old created marsh showing less fungal colonization. A 26 y old created salt marsh consistently exhibited the highest fungal species richness. Ascomata density of the dominant fungal species on each host was significantly higher in natural marshes than in created marshes at all three sampling dates. This study indicates marine fungal saprotroph communities are present in these manmade coastal salt marshes as early as 1 y after marsh creation. The lower regions of both plant hosts were dominated by a small number of marine ascomycete species consistent with those species previously reported from salt marshes of the East Coast of USA. PMID:20524584

  15. Comparison of wetland structural characteristics between created and natural salt marshes in southwest Louisiana, USA

    USGS Publications Warehouse

    Edwards, K.R.; Proffitt, C.E.

    2003-01-01

    The use of dredge material is a well-known technique for creating or restoring salt marshes that is expected to become more common along the Gulf of Mexico coast in the future. However, the effectiveness of this restoration method is still questioned. Wetland structural characteristics were compared between four created and three natural salt marshes in southwest Louisiana, USA. The created marshes, formed by the pumping of dredge material into formerly open water areas, represent a chronosequence, ranging in age from 3 to 19 years. Vegetation and soil structural factors were compared to determine whether the created marshes become more similar over time to the natural salt marshes. Vegetation surveys were conducted in 1997, 2000, and 2002 using the line-intercept technique. Site elevations were measured in 2000. Organic matter (OM) was measured in 1996 and 2002, while bulk density and soil particle-size distribution were determined in 2002 only. The natural marshes were dominated by Spartina alterniflora, as were the oldest created marshes; these marshes had the lowest mean site elevations ( 35 cm NGVD) and became dominated by high marsh (S. patens, Distichlis spicata) and shrub (Baccharis halimifolia, Iva frutescens) species. The higher elevation marsh seems to be following a different plant successional trajectory than the other marshes, indicating a relationship between marsh elevation and species composition. The soils in both the created and natural marshes contain high levels of clays (30-65 %), with sand comprising < 1 % of the soil distribution. OM was significantly greater and bulk density significantly lower in two of the natural marshes when compared to the created marshes. The oldest created marsh had significantly greater OM than the younger created marshes, but it may still take several decades before equivalency is reached with the natural marshes. Vegetation structural characteristics in the created marshes take only a few years to become similar

  16. Process for recovering tritium from molten lithium metal

    DOEpatents

    Maroni, Victor A.

    1976-01-01

    Lithium tritide (LiT) is extracted from molten lithium metal that has been exposed to neutron irradiation for breeding tritium within a thermonuclear or fission reactor. The extraction is performed by intimately contacting the molten lithium metal with a molten lithium salt, for instance, lithium chloride - potassium chloride eutectic to distribute LiT between the salt and metal phases. The extracted tritium is recovered in gaseous form from the molten salt phase by a subsequent electrolytic or oxidation step.

  17. An Aliphatic Solvent-Soluble Lithium Salt of the Perhalogenated Weakly Coordinating Anion [Al(OC(CCl3)(CF3)2)4](-).

    PubMed

    Zheng, Xin; Zhang, Zaichao; Tan, Gengwen; Wang, Xinping

    2016-02-01

    The facile synthesis of a new highly aliphatic solvent-soluble Li(+) salt of the perhalogenated weakly coordinating anion [Al(OC(CCl3)(CF3)2)4](-) and its application in stabilizing the Ph3C(+) cation were investigated. The lithium salt Li[Al(OC(CCl3)(CF3)2)4] (4) was prepared by the treatment of 4 mol equiv of HOC(CCl3)(CF3)2 with purified LiAlH4 in n-hexane from -20 °C to room temperature. Compound 4 is highly soluble in both polar and nonpolar solvents, and it bears both CCl3 and CF3 groups, resulting in a lower symmetry around the Al center compared to that of Li[Al(OC(CF3)3)4] (1). Treatment of 4 with Ph3CCl afforded the ionic compound [Ph3C][Al(OC(CCl3)(CF3)2)4] (5) bearing the Ph3C(+) cation with concomitant elimination of LiCl, suggesting the potential application of [Al(OC(CCl3)(CF3)2)4](-) in stabilizing reactive cationic species. Compounds 4 and 5 were fully characterized by spectroscopic and structural methods. PMID:26784742

  18. Radiation defects and energy storage in natural polycrystalline rock salt. Results of an in-situ test in the Permian rock salt of the Asse

    SciTech Connect

    Gies, H.; Rothfuchs, T.; Celma, A.G.; Haas, J.B.M. de; Pederson, L.

    1994-12-31

    Radiation damage development and the corresponding energy storage in pure undeformed single crystals have frequently been studied in laboratory experiments, however little is known of irradiation experiments on natural rock salt (polycrystalline, deformed and impure) under geological conditions. The relevance of these parameters to the defect formation was revealed by a joint United States/Federal Republic of Germany in-situ test in the Asse Mine. Natural rock salt was heated and irradiated using Co-60 sources. Calculations of the amount of halite expected to be decomposed by radiolysis during the experiment were performed using the 1985 version of the Jain-Lidiard model. Qualitative agreement between theory and analyses was found for all the performed analyses. Quantitative and qualitative deviations of the natural samples behaviour from that of single undeformed crystals were observed and attributed to the influence of sulfatic admixtures, polycrystallinity and strain on radiation damage development and anneal. Special chemical methods, such as iodometric titration and uv-visible spectroscopy were applied in order to measure the hypochlorite ion, which forms in irradiated salt. Composite samples located closet to the Co-60 source averaged 0,4 micromoles neutral chlorine atoms per gram salt, a factor of two more than from other positions. Uv-vis analyses revealed more than a factor of ten greater neutral chlorine concentrations in coloured halite. Similarly, optical absorption measurements indicated a factor of ten difference in sodium metal colloid concentrations.

  19. Lithium orotate, carbonate and chloride: pharmacokinetics, polyuria in rats.

    PubMed Central

    Smith, D F

    1976-01-01

    1 The pharmacokinetics of the lithium ion administered as lithium orotate were studied in rats. Parallel studies were carried out with lithium carbonate and lithium chloride. 2 No differences in the uptake, distribution and excretion of the lithium ion were observed between lithium orotate, lithium carbonate and lithium chloride after single intraperitoneal, subcutaneous or intragastric injections (0.5-1.0 mEq lithium/kg) or after administration of the lithium salts for 20 days in the food. 3 The findings oppose the notion that the pharmacokinetics of the lithium ion given as lithium orotate differ from lithium chloride or lithium carbonate. 4 Polyuria and polydipsia developed more slowly in rats given lithium orotate than in those given lithium carbonate or lithium chloride, perhaps due to an effect of the orotate anion. PMID:1260219

  20. On the nature of lithium-rich giant stars. Constraints from beryllium abundances

    NASA Astrophysics Data System (ADS)

    Melo, C. H. F.; de Laverny, P.; Santos, N. C.; Israelian, G.; Randich, S.; Do Nascimento, J. D., Jr.; de Medeiros, J. R.

    2005-08-01

    We have derived beryllium abundances for 7 Li-rich giant (A(Li) > 1.5) stars and 10 other Li-normal giants with the aim of investigating the origin of the lithium in the Li-rich giants. In particular, we test the predictions of the engulfment scenario proposed by Siess & Livio (1999, MNRAS, 308, 1133), where the engulfment of a brown dwarf or one or more giant planets would lead to simultaneous enrichment of 7Li and 9Be. We show that regardless of their nature, none of the stars studied in this paper were found to have detectable beryllium. Using simple dilution arguments we show that engulfment of an external object as the sole source of Li enrichment is ruled out by the Li and Be abundance data. The present results favor the idea that Li has been produced in the interior of the stars by a Cameron-Fowler process and brought up to the surface by an extra mixing mechanism.

  1. Synthesis of Ti-based electrodes using Ti-salt flocculated sludge and their application in lithium-ion batteries

    SciTech Connect

    Kang, Jungwon; Rai, Alok Kumar; Kim, Sungjin; Choi, Eunseok; Yoo, Insun; Kim, Jongho; Kim, Jaekook

    2012-10-15

    We report a simple strategy to synthesize the nanostructured TiO{sub 2} samples by a solid state reaction using Ti-salt flocculated sludge. The structure and morphology of the Ti-salt flocculated sludge, nanostructured TiO{sub 2} samples and pure commercial Aldrich TiO{sub 2} powder were characterized by powder X-ray diffraction and field emission scanning electron microscopy (FE-SEM). The electrochemical performances were evaluated in coin type cells. Nanostructured TiO{sub 2} samples, obtained by Ti-salt flocculated sludge shows a higher capacity and better cycling performances than pure commercial Aldrich TiO{sub 2} powder at the cutoff of 1.0–2.5 V especially at high current rate. The enhanced cycling performance can be attributed to the facts that their high crystallinity and uniform nano-sized distribution.

  2. Salt Lakes of Western Australia - Emissions of natural volatile organic compounds

    NASA Astrophysics Data System (ADS)

    Sattler, Tobias; Krause, Torsten; Schöler, Heinfried; Kamilli, Katharina; Held, Andreas; Zetzsch, Cornelius; Ofner, Johannes; Junkermann, Wolfgang; Atlas, Elliot

    2013-04-01

    Western Australia is a semi-/arid region that is heavily influenced by global climate change and agricultural land use. The area is known for its many saline lakes with a wide range of hydrogeochemical parameters. This area has been repeatedly investigated since 2006 and consists of ephemeral saline and saline groundwater sourced lakes with a pH reaching from 2.5 to 7.1. The semi-/arid region was originally covered by natural eucalyptus forests, but land-use has changed considerably after large scale deforestation from 1950 to 1970. Today the region is mostly used for growing wheat and live stock. The deforestation led to a rising groundwater table, bringing dissolved salts and minerals to the surface. In the last decades, a concurrent alteration of rain periods has been observed. A reason could be the regional formation of ultra-fine particles that were measured with car-based and airborne instruments around the salt lakes in several campaigns between 2006 and 2011. These ultra-fine particles emitted from the lakes and acting as cloud condensation nuclei can modify cloud microphysics and thus suppress rain events [1]. New data from a campaign in 2012 accentuates the importance of these hyper saline environments for the local climate. Ground-based particle measurements around the salt lakes in 2012 were accompanied by novel chamber experiments directly on the lakes. The 1.5 m³ cubic chamber was constructed from transparent PTFE foil permitting photochemistry within while preventing dilution of the air due to lateral wind transport. This experimental setup allows linking the measured data directly to the chemistry of and above the salt lakes. Another advantage of the PTFE chamber is the enrichment of volatile organic compounds (VOC) that are emitted from salt lakes as possible precursors for the ultra-fine particles. Chamber air was sampled using stainless steel canisters. Sediment, crust and water samples were taken for investigation of potential VOC emissions in

  3. Potassium Retention under Salt Stress Is Associated with Natural Variation in Salinity Tolerance among Arabidopsis Accessions

    PubMed Central

    Sun, Yanling; Kong, Xiangpei; Li, Cuiling; Liu, Yongxiu; Ding, Zhaojun

    2015-01-01

    Plants are exposed to various environmental stresses during their life cycle such as salt, drought and cold. Natural variation mediated plant growth adaptation has been employed as an effective approach in response to the diverse environmental cues such as salt stress. However, the molecular mechanism underlying this process is not well understood. In the present study, a collection of 82 Arabidopsis thaliana accessions (ecotypes) was screened with a view to identify variation for salinity tolerance. Seven accessions showed a higher level of tolerance than Col-0. The young seedlings of the tolerant accessions demonstrated a higher K+ content and a lower Na+/K+ ratio when exposed to salinity stress, but its Na+ content was the same as that of Col-0. The K+ transporter genes AtHAK5, AtCHX17 and AtKUP1 were up-regulated significantly in almost all the tolerant accessions, even in the absence of salinity stress. There was little genetic variation or positive transcriptional variation between the selections and Col-0 with respect to Na+-related transporter genes, as AtSOS genes, AtNHX1 and AtHKT1;1. In addition, under salinity stress, these selections accumulated higher compatible solutes and lower reactive oxygen species than did Col-0. Taken together, our results showed that natural variation in salinity tolerance of Arabidopsis seems to have been achieved by the strong capacity of K+ retention. PMID:25993093

  4. 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.

  5. 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.

  6. The Stereoselective Reductions of Ketones to the Most Thermodynamically Stable Alcohols Using Lithium and Hydrated Salts of Common Transition Metals.

    PubMed

    Kennedy, Nicole; Cohen, Theodore

    2015-08-21

    A simple method is presented for the highly stereoselective reductions of ketones to the most thermodynamically stable alcohols. In this procedure, the ketone is treated with lithium dispersion and either FeCl2·4H2O or CuCl2·2H2O in THF at room temperature. This protocol is applied to a large number and variety of ketones and is both more convenient and efficient than those commonly reported for the diastereoselective reduction of five- and six-membered cyclic ketones. PMID:26226182

  7. Non-aqueous electrolytes for lithium batteries

    SciTech Connect

    Bakos, V.W.; Steklenski, D.J.

    1989-02-14

    An electrochemical cell is described comprising a lithium anode, a cathode and an electrolyte having a conductivity, and reciprocal ohms per cm, of at least 3.5 in, comprising a lithium salt, propylene carbonate and 1,2-dimethoxypropane.

  8. Performance evaluation of two protective treatments on salt-laden limestones and marble after natural and artificial weathering.

    PubMed

    Salvadori, Barbara; Pinna, Daniela; Porcinai, Simone

    2014-02-01

    Salt crystallization is a major damage factor in stone weathering, and the application of inappropriate protective products may amplify its effects. This research focuses on the evaluation of two protective products' performance (organic polydimethylsiloxane and inorganic ammonium oxalate (NH4)2(COO)2·H2O) in the case of a salt load from behind. Experimental laboratory simulations based on salt crystallization cycles and natural weathering in an urban area were carried out. The effects were monitored over time, applying different methods: weight loss evaluation, colorimetric and water absorption by capillarity measurements, stereomicroscope observations, FTIR and SEM-EDS analyses. The results showed minor impact exerted on the short term on stones, particularly those treated with the water repellent, by atmospheric agents compared to salt crystallization. Lithotypes with low salt load (Gioia marble) underwent minor changes than the heavily salt-laden limestones (Lecce and Ançã stones), which were dramatically damaged when treated with polysiloxane. The results suggest that the ammonium oxalate treatment should be preferred to polysiloxane in the presence of soluble salts, even after desalination procedures which might not completely remove them. In addition, the neo-formed calcium oxalate seemed to effectively protect the stone, improving its resistance against salt crystallization without occluding the pores and limiting the superficial erosion caused by atmospheric agents. PMID:23996736

  9. Ionic liquids-lithium salts pretreatment followed by ultrasound-assisted extraction of vitexin-4″-O-glucoside, vitexin-2″-O-rhamnoside and vitexin from Phyllostachys edulis leaves.

    PubMed

    Hou, Kexin; Chen, Fengli; Zu, Yuangang; Yang, Lei

    2016-01-29

    An efficient method for the extraction of vitexin, vitexin-4″-O-glucoside, and vitexin-2″-O-rhamnoside from Phyllostachys edulis leaves comprises heat treatment using an ionic liquid-lithium salt mixture (using 1-butyl-3-methylimidazolium bromide as the solvent and lithium chloride as the additive), followed by ultrasound-assisted extraction. To obtain higher extraction yields, the effects of the relevant experimental parameters (including heat treatment temperature and time, relative amounts of 1-butyl-3-methylimidazolium bromide and lithium chloride, power and time of the ultrasound irradiation, and the liquid-solid ratio) are evaluated and response surface methodology is used to optimize the significant factors. The morphologies of the treated and untreated P. edulis leaves are studied by scanning electron microscopy. The improved extraction method proposed provides high extraction yield, good repeatability and precision, and has wide potential applications in the analysis of plant samples. PMID:26763300

  10. Culturable halophilic archaea at the initial and crystallization stages of salt production in a natural solar saltern of Goa, India

    PubMed Central

    2012-01-01

    Background Goa is a coastal state in India and salt making is being practiced for many years. This investigation aimed in determining the culturable haloarchaeal diversity during two different phases of salt production in a natural solar saltern of Ribandar, Goa. Water and sediment samples were collected from the saltern during pre-salt harvesting phase and salt harvesting phase. Salinity and pH of the sampling site was determined. Isolates were obtained by plating of the samples on complex and synthetic haloarchaeal media. Morphology of the isolates was determined using Gram staining and electron microscopy. Response of cells to distilled water was studied spectrophotometrically at 600nm. Molecular identification of the isolates was performed by sequencing the 16S rRNA. Results Salinity of salt pans varied from 3-4% (non-salt production phase) to 30% (salt production phase) and pH varied from 7.0-8.0. Seven haloarchaeal strains were isolated from water and sediment samples during non-salt production phase and seventeen haloarchaeal strains were isolated during the salt production phase. All the strains stained uniformly Gram negative. The orange-red acetone extract of the pigments showed similar spectrophotometric profile with absorption maxima at 393, 474, 501 and 535 nm. All isolates obtained from the salt dilute phase were grouped within the genus Halococcus. This was validated using both total lipid profiling and 16S rRNA data sequencing. The isolates obtained from pre-salt harvesting phase were resistant to lysis. 16S rRNA data showed that organisms belonging to Halorubrum, Haloarcula, Haloferax and Halococcus genera were obtained during the salt concentrated phase. The isolates obtained from salt harvesting phase showed varied lysis on suspension in distilled water and /or 3.5% NaCl. Conclusion Salterns in Goa are transiently operated during post monsoon season from January to May. During the pre-salt harvesting phase, all the isolates obtained belonged to

  11. Aquatic macroinvertebrate communities of natural and ditched potholes in a San Francisco Bay salt marsh

    NASA Astrophysics Data System (ADS)

    Barnby, Mark A.; Collins, Joshua N.; Resh, Vincent H.

    1985-03-01

    Differences in macroinvertebrate community structure and composition were examined from April 1980 to March 1981 in three potholes that had been ditched for mosquito control and three natural (i.e. unditched) potholes, which are located in a San Francisco Bay, California, U.S.A. salt marsh. Measurements of incipient tidal flooding into potholes (i.e. pothole inundation threshold) indicated that these sites comprise a gradient of tidal influences. Exponential decreases in the frequency and duration of tidal inundation corresponded to linear increases in inundation threshold. Since ditched study sites had low thresholds they tended to be more uniformly and regularly influenced by tides, were less saline, had less variable temperature regimens, and supported less filamentous algae than natural potholes. Habitat conditions were generally more similar among ditched than unditched potholes, but environmental conditions were most severe at natural sites near the upper limit of the inundation threshold gradient, where some potholes desiccate during the dry season each year. Differences in macroinvertebrate communities corresponded to differences in habitat conditions. Species richness and diversity (Simpson's Index) were generally highest near the middle of the inundation threshold gradient, which is a pattern predicted by the Intermediate Disturbance Hypothesis. Analysis of faunal composition using discriminant functions indicated more similarity among potholes located at the lowest positions of the inundation gradient than among potholes with intermediate thresholds. Since ditching lowers the inundation thresholds of potholes, it reduces species richness and diversity, while increasing faunal similarity. As a result, extensive ditching to control salt marsh mosquitoes can reduce the overall complexity of lentic macroinvertebrate communities.

  12. Dispersion of Louisiana crude oil in salt water environment by Corexit 9500A in the presence of natural coastal materials

    NASA Astrophysics Data System (ADS)

    Tansel, Berrin; Lee, Mengshan; Berbakov, Jillian; Tansel, Derya Z.; Koklonis, Urpiana

    2014-04-01

    Effectiveness of Corexit 9500A for dispersing Louisiana crude oil was evaluated in salt water solutions containing natural materials in relation to salinity and dispersant-to-oil ratio (DOR). Experimental results showed that both salinity and DOR had significant effects on dispersion of Louisiana crude oil in the presence of different natural materials. The natural materials added to the salt water solutions included sea sand (South Beach, Miami, Florida), red mangrove leaves (Rhizophora mangle), seaweed (Sargassum natans), and sea grass (Halodule wrightii). Dispersant effectiveness (amount of oil dispersed into the water) was reduced significantly with increasing salinity with the minimum effectiveness observed in the salinity range between 30 and 50 ppt in all aqueous samples containing natural materials. When significant amounts of floating oil were present, the partially submerged natural materials enhanced the transfer of oil into the water column, which improved the dispersion effectiveness. However, dispersant effectiveness was significantly reduced when the amount of floating oil was relatively small and could not be released back to the water column. Surface tension may not be an adequate parameter for monitoring the effectiveness of dispersants in salt water environment. When distilled water was used (i.e., zero salinity), surface tension was significantly reduced with increasing dispersant concentration. However, there was no clear trend in the surface tension of the salt water solutions (17-51 ppt) containing crude oil and natural materials with increasing dispersant concentration.

  13. Natural macromolecule based carboxymethyl cellulose as a gel polymer electrolyte with adjustable porosity for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Zhu, Y. S.; Xiao, S. Y.; Li, M. X.; Chang, Z.; Wang, F. X.; Gao, J.; Wu, Y. P.

    2015-08-01

    A porous membrane of carboxymethyl cellulose (CMC) from natural macromolecule as a host of a gel polymer electrolyte for lithium ion batteries is reported. It is prepared, for the first time, by a simple non-solvent evaporation method and its porous structure is fine-adjusted by varying the composition ratio of the solvent and non-solvent mixture. The electrolyte uptake of the porous membrane based on CMC is 75.9%. The ionic conductivity of the as-prepared gel membrane saturated with 1 mol L-1 LiPF6 electrolyte at room temperature can be up to 0.48 mS cm-1. Moreover, the lithium ion transference in the gel membrane at room temperature is as high as 0.46, much higher than 0.27 for the commercial separator Celgard 2730. When evaluated by using LiFePO4 cathode, the prepared gel membrane exhibits very good electrochemical performance including higher reversible capacity, better rate capability and good cycling behaviour. The obtained results suggest that this porous polymer membrane shows great attraction to the lithium ion batteries requiring high safety, low cost and environmental friendliness.

  14. Lithium in Medicine: Mechanisms of Action.

    PubMed

    Mota de Freitas, Duarte; Leverson, Brian D; Goossens, Jesse L

    2016-01-01

    In this chapter, we review the mechanism of action of lithium salts from a chemical perspective. A description on how lithium salts are used to treat mental illnesses, in particular bipolar disorder, and other disease states is provided. Emphasis is not placed on the genetics and the psychopharmacology of the ailments for which lithium salts have proven to be beneficial. Rather we highlight the application of chemical methodologies for the characterization of the cellular targets of lithium salts and their distribution in tissues. PMID:26860311

  15. 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.

  16. Electrochemical and impedance investigation of the effect of lithium malonate on the performance of natural graphite electrodes in lithium-ion batteries

    SciTech Connect

    Sun, Xiao-Guang; Dai, Sheng

    2010-01-01

    Lithium malonate (LM) was coated on the surface of a natural graphite (NG) electrode, which was then tested as the negative electrode in the electrolytes of 0.9 M LiPF6/EC-PC-DMC (1/1/3, by weight) and 1.0 M LiBF4/EC-PC-DMC (1/1/3, by weight) under a current density of 0.075 mA cm-2. LM was also used as an additive to the electrolyte of 1.0 M LiPF6/EC-DMC-DEC (1/1/1, by volume) and tested on a bare graphite electrode. It was found that both the surface coating and the additive approach were effective in improving first charge discharge capacity and coulomb efficiency. Electrochemical impedance spectra showed that the decreased interfacial impedance was coupled with improved coulomb efficiency of the cells using coated graphite electrodes. Cyclic voltammograms (CVs) on fresh bare and coated natural graphite electrodes confirmed that all the improvement in the half-cell performance was due to the suppression of the solvent decomposition through the surface modification with LM. The CV data also showed that the carbonate electrolyte with LM as the additive was not stable against oxidation, which resulted in lower capacity of the full cell with commercial graphite and LiCoO2 electrodes.

  17. Characterization of halophiles in natural MgSO 4 salts and laboratory enrichment samples: Astrobiological implications for Mars

    NASA Astrophysics Data System (ADS)

    Foster, Ian S.; King, Penelope L.; Hyde, Brendt C.; Southam, Gordon

    2010-03-01

    The presence of sulfate salts and limited subsurface water (ice) on Mars suggests that any liquid water on Mars today will occur as (magnesium) sulfate-rich brines in regions containing sources of magnesium and sulfur. The Basque Lakes of British Columbia, Canada, represent a hypersaline terrestrial analogue site, which possesses chemical and physical properties similar to those observed on Mars. The Basque Lakes also contain diverse halophilic organisms representing all three Kingdoms of life, growing in surface and near-subsurface environments. Of interest from an astrobiological perspective, crushed magnesium sulfate samples that were analyzed using a modified Lowry protein assay contained biomass in every crystal inspected, with biomass values from 0.078 to 4.21 mg biomass/g salt; average=0.74±0.7 mg biomass/g salt. Bacteria and Archaea cells were easily observed even in low-biomass samples using light microscopy, and bacteria trapped within magnesium sulfate crystals were observed using confocal microscopy. Regions within the salt also contained bacterial pigments, e.g., carotenoids, which were separate from the cells, indicating that cell lysis might have occurred during entrapment within the salt matrix. These biosignatures, cells, and any 'soluble' organic constituents were primarily found trapped within fluid inclusions or fluid-filled void spaces between intergrown crystals. Diffuse reflectance infrared Fourier transform spectroscopy (reflectance IR) analysis of enrichment cultures, containing cyanobacteria, Archaea, or dissimilatory sulfate-reducing bacteria, highlighted molecular biosignature features between 550-1650 and 2400-3000 cm -1. Spectra from natural salts demonstrated that we can detect biomass within salt crystals using the most sensitive biosignatures, which are the 1530-1570 cm -1, C-N, N-H, -COOH absorptions and the 1030-1050 cm -1 C-OH, C-N, PO 43- bond features. The lowest detection limit for a biosignature absorption feature using

  18. Effects of solvents and salt on the thermal stability of lithiated graphite used in lithium ion battery.

    PubMed

    Wang, Qingsong; Sun, Jinhua; Chen, Chunhua

    2009-08-15

    The thermal stability of lithiated graphite in the presence of solvents, electrolytes and LiPF(6) salt was studied using C80 micro-calorimeter. The presence of cyclic carbonates or linear carbonates increases the activity of Li(x)C(6)-solvent coexisting system, especially for the Li(x)C(6)-linear carbonates one. LiPF(6) was detected that it increases the activity greatly of its coexisting system with lithiated graphite. The coexisting system of Li(x)C(6) with the electrolyte of LiPF(6)/ethylene carbonate+diethyl carbonate shows less thermal stability, which is attributed to the activity between diethyl carbonate and Li(x)C(6). This also agrees with the experiment result of Li(x)C(6)-diethyl carbonate coexisting system. PMID:19261386

  19. Favorable combination of positive and negative electrode materials with glyme-Li salt complex electrolytes in lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Orita, A.; Kamijima, K.; Yoshida, M.; Dokko, K.; Watanabe, M.

    Tetraglyme (G4)-lithium bis(trifluoromethanesulfonyl)amide (TFSA) complexes with different G4 ratio were investigated. An increase in the amount of G4 led to the decrease in the viscosity, and increase in the ionic conductivity of the complex, and G4-LiTFSA showed higher thermal stabilities than the conventional organic electrolyte, when the molar ratio of G4 was more than 40 mol%. The increase in the G4 amount improved the rate capabilities of Li/LiCoO 2 cells in the range where the molar ratio of G4 was between 40 mol% and 60 mol%. The stable Li ion intercalation-deintercalation was not observed in the Li/graphite cell of [Li(G4)][TFSA] (G4: 50 mol%) without additives. However, the additives for forming solid electrolyte interface (SEI) film, such as vinylene carbonate, vinylethylene carbonate, and 1,3-propane sultone, led to the charge-discharge performance comparable to that of the conventional organic electrolyte. The adoption of Li 4Ti 5O 12 and LiFePO 4 led to excellent reversibilities of the Li half cells using [Li(G4)][TFSA], probably because of the favorable operation voltage. In the case of the LiFePO 4/Li 4Ti 5O 12 cell, the cell with [Li(G4)][TFSA] showed the better rate capability than that with the conventional organic electrolyte, when the rate was less than 1 CmA, and it is concluded that [Li(G4)][TFSA] can be the candidate as the alternative of organic electrolytes when the most appropriate electrode-active materials are used.

  20. Surface natures of conductive carbon materials and their contributions to charge/discharge performance of cathodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Lin, H. B.; Huang, W. Z.; Rong, H. B.; Hu, J. N.; Mai, S. W.; Xing, L. D.; Xu, M. Q.; Li, X. P.; Li, W. S.

    2015-08-01

    The surface natures of five carbon materials, acetylene black, Super P, ECP600JD, KS-6 and CNTs, are compared in terms of morphology, specific surface area and activity towards electrolyte decomposition and anion insertion, and their contributions as conductive additives to cathode performance of lithium ion batteries are understood. With the characterizations from scanning electron microscopy, Brunauer-Emmett-Teller analysis and cyclic voltammetry, it's demonstrated that: (1) the morphology is granular for acetylene black, Super P and ECP600JD, flake-like for KS-6 and wire-like for CNTs; (2) ECP600JD exhibits the largest specific surface area but KS-6 has the smallest one; (3) the activity is the same for all the samples towards the electrolyte decomposition but different from each other towards anion insertion. Charge/discharge tests of LiMn2O4 and LiNi0.5Mn1.5O4 cathodes indicate that the surface natures of carbon materials play an important role in charge/discharge performance of cathodes for lithium ion batteries. ECP600JD with smallest particle size provides the largest site for electrolyte decomposition leading to the lowest coulombic efficiency, while KS-6 with a layered structure exhibits the highest activity towards anion insertion leading to the lowest charge and discharge capacity of cathode materials. These negative effects become more significant when high voltage cathode materials are used.

  1. Qualitative evaluation of the adesive interface between lithium disilicate, luting composite and natural tooth.

    PubMed

    Mobilio, Nicola; Fasiol, Alberto; Catapano, Santo

    2016-01-01

    Aim of this work was to qualitatively evaluate the interface between tooth, luting composite and lithium disilicate surface using a scanning electron microscope (SEM). An extracted restoration-free human molar was stored in physiological solution until it was embedded in an autopolimerysing acrylic resin. A standard preparation for overlay was completed and after preparation an anatomic overlay was waxed on the tooth and then hot pressed using lithium disilicate ceramic. After cementation the sample was dissected and the section was analysed using an Automatic Micromet (Remet s.a.s) and the section was analyzed using a scanning electron microscope (SEM). SEM evaluation of the tooth showed the three layers seamlessly; by increasing the enlargement the interface did not change. PMID:27486504

  2. Qualitative evaluation of the adesive interface between lithium disilicate, luting composite and natural tooth

    PubMed Central

    Mobilio, Nicola; Fasiol, Alberto; Catapano, Santo

    2016-01-01

    Summary Aim of this work was to qualitatively evaluate the interface between tooth, luting composite and lithium disilicate surface using a scanning electron microscope (SEM). An extracted restoration-free human molar was stored in physiological solution until it was embedded in an autopolimerysing acrylic resin. A standard preparation for overlay was completed and after preparation an anatomic overlay was waxed on the tooth and then hot pressed using lithium disilicate ceramic. After cementation the sample was dissected and the section was analysed using an Automatic Micromet (Remet s.a.s) and the section was analyzed using a scanning electron microscope (SEM). SEM evaluation of the tooth showed the three layers seamlessly; by increasing the enlargement the interface did not change. PMID:27486504

  3. Palmitoleic acid calcium salt: a lubricant and bactericidal powder from natural lipids.

    PubMed

    Yamamoto, Yoshiaki; Kawamura, Yuki; Yamazaki, Yuki; Kijima, Tatsuro; Morikawa, Toshiya; Nonomura, Yoshimune

    2015-01-01

    Palmitoleic acid is a promising bactericidal agent for cleansing products with alternative bactericidal abilities. In this study, we focus on the physical and biological activity of palmitoleic acid calcium salt (C16:1 fatty acid Ca salt) because it forms via an ion-exchange reaction between palmitoleic acid and Ca ions in tap water, and remains on the skin surface during the cleansing process. Here, we prepared C16:1 fatty acid Ca salt to investigate its crystal structure and physical and bactericidal properties. The Ca salt was a plate-shaped lamellar crystalline powder with a particle diameter of several micrometers to several tens of micrometers; it exhibited significant lubricity and alternative bactericidal activity against Staphylococcus aureus (S. aureus) and Propionibacterium acnes (P. acnes). We also examined other fatty acid Ca salts prepared from lauric acid (C12:0 fatty acid), palmitic acid (C16:0 fatty acid), and oleic acid (C18:1 fatty acid). The bactericidal activities and lubricity of the fatty acid Ca salts changed with the alkyl chain length and the degree of unsaturation. The C16:1 fatty acid Ca salt exhibited the strongest selective bactericidal ability among the four investigated fatty acid Ca salts. These findings suggest that C16:1 fatty acid and its Ca salt have potential applications in cleansing and cosmetic products. PMID:25757432

  4. In vivo and in vitro biotransformation of the lithium salt of gamma-linolenic acid by three human carcinomas.

    PubMed Central

    de Antueno, R.; Elliot, M.; Ells, G.; Quiroga, P.; Jenkins, K.; Horrobin, D.

    1997-01-01

    Lipid metabolism has been considered recently as a novel target for cancer therapy. In this field, lithium gamma-linolenate (LiGLA) is a promising experimental compound for use in the treatment of human tumours. In vivo and in vitro studies allowed us to assess the metabolism of radiolabelled LiGLA by tumour tissue and different organs of the host. In vitro studies demonstrated that human pancreatic (AsPC-1), prostatic (PC-3) and mammary carcinoma (ZR-75-1) cells were capable of elongating GLA from LiGLA to dihomo-gamma-linolenic acid (DGLA) and further desaturating it to arachidonic acid (AA). AsPC-1 cells showed the lowest delta5-desaturase activity on DGLA. In the in vivo studies, nude mice bearing the human carcinomas were given Li[1-(14)C]GLA (2.5 mg kg(-1)) by intravenous injection for 30 min. Mice were either sacrificed after infusion or left for up to 96 h recovery before sacrifice. In general, the organs showed a maximum uptake of radioactivity 30 min after the infusion started (t = 0). Thereafter, in major organs the percentage of injected radioactivity per g of tissue declined below 1% 96 h after infusion. In kidney, brain, testes/ovaries and all three tumour tissues, labelling remained constant throughout the experiment. The ratio of radioactivity in liver to tumour tissues ranged between 16- and 24-fold at t = 0 and between 3.1- and 3.7-fold at 96 h. All tissues showed a progressive increase in the proportion of radioactivity associated with AA with a concomitant decrease in radiolabelled GLA as the time after infusion increased. DGLA declined rapidly in liver and plasma, but at a much slower rate in brain and malignant tissue. Seventy-two hours after the infusion, GLA was only detected in plasma and tumour tissue. The sum of GLA + DGLA varied among tumour tissues, but it remained 2-4 times higher than in liver and plasma. In brain, DGLA is the major contributor to the sum of these fatty acids. Data showed that cytotoxic GLA and DGLA, the latter

  5. Experimental study of natural convection melting of ice in salt solutions

    SciTech Connect

    Fang, L.J.; Cheung, F.B.; Linehan, J.H.; Pedersen, D.R.

    1984-01-01

    The solid-liquid interface morphology and the micro-physical process near the moving phase boundary during natural convection melting of a horizontal layer of ice by an overlying pool of salt solution were studied experimentally. A cathetometer which amplifies the interface region was used to measure the ice melting rate. Also measured were the temperature transients of the liquid pool. Within the temperature and the density ratio ranges explored, the ice melting rate was found to be very sensitive to the ratio of pool-to-ice melt density but independent of pool-to-ice temperature difference. By varying the density ratio, three different flow regimes and morphologies of the solid-liquid interface were observed, with melt streamers emanating from the crests of the wavy interface into the pool in all three cases. The measured wavelengths (spacing) between the streamers for four different pairs of materials were correlated with the density ratio and found to agree favorably with the predictions of Taylor instability theory.

  6. Preservation of artifacts in salt mines as a natural analog for the storage of transuranic wastes at the WIPP repository

    SciTech Connect

    Martell, M.A.; Hansen, F.; Weiner, R.

    1998-10-01

    Use of nature`s laboratory for scientific analysis of complex systems is a largely untapped resource for understanding long-term disposal of hazardous materials. The Waste Isolation Pilot Plant (WIPP) in the US is a facility designed and approved for storage of transuranic waste in a salt medium. Isolation from the biosphere must be ensured for 10,000 years. Natural analogs provide a means to interpret the evolution of the underground disposal setting. Investigations of ancient sites where manmade materials have experienced mechanical and chemical processes over millennia provide scientific information unattainable by conventional laboratory methods. This paper presents examples of these pertinent natural analogs, provides examples of features relating to the WIPP application, and identifies potential avenues of future investigations. This paper cites examples of analogical information pertaining to the Hallstatt salt mine in Austria and Wieliczka salt mine in Poland. This paper intends to develop an appreciation for the applicability of natural analogs to the science and engineering of a long-term disposal facility in geomedia.

  7. Characteristics of natural salt licks located in the Colombian Amazon foothills.

    PubMed

    Molina, Eduardo; León, Tomás Enrique; Armenteras, Dolors

    2014-02-01

    Salt licks are key places for the ecological dynamics of wildlife communities around the world and are locations where animals develop geophagical behaviours. Geophagy is a method for animals to supplement their diets or facilitate their digestive processes and is related to the health of individuals and populations. This study characterises a series of salt licks located in the Colombian Amazon foothills and describes their structural, mineralogical and physicochemical properties, as well as the fauna that visit these locations. The results are analysed in reference to the geological characteristics of the study area and in relation to the role of the salt lick in the nutritional ecology of the Amazonian fauna. Located in the study area are two types of salt licks that are significantly different in composition. These salt licks are located in an area where young geological materials have been exposed. The characteristics of the salt licks supports the hypothesis that they are used to solve nutritional problems that result from herbivorous diets. The clear importance of salt licks in the ecology of several Amazonian animal species emphasises the need to prioritise conservation areas by maximising the complementarities of salt lick sites. PMID:23595632

  8. A natural carbonized leaf as polysulfide diffusion inhibitor for high-performance lithium-sulfur battery cells.

    PubMed

    Chung, Sheng-Heng; Manthiram, Arumugam

    2014-06-01

    Attracted by the unique tissue and functions of leaves, a natural carbonized leaf (CL) is presented as a polysulfide diffusion inhibitor in lithium-sulfur (Li-S) batteries. The CL that is covered on the pure sulfur cathode effectively suppresses the polysulfide shuttling mechanism and enables the use of pure sulfur as the cathode. A low charge resistance and a high discharge capacity of 1320 mA h g(-1) arise from the improved cell conductivity due to the innately integral conductive carbon network of the CL. The unique microstructure of CL leads to a high discharge/charge efficiency of >98 %, low capacity fade of 0.18 % per cycle, and good long-term cyclability over 150 cycles. The structural gradient and the micro/mesoporous adsorption sites of CL effectively intercept/trap the migrating polysulfides and facilitate their reutilization. The green CL polysulfide diffusion inhibitor thus offers a viable approach for developing high-performance lithium-sulfur batteries. PMID:24700745

  9. Effects of natural and anthropogenic change on habitat use and movement of endangered salt marsh harvest mice.

    PubMed

    Smith, Katherine R; Barthman-Thompson, Laureen; Gould, William R; Mabry, Karen E

    2014-01-01

    The northern salt marsh harvest mouse (Reithrodontomys raviventris halicoetes) is an endangered species endemic to the San Francisco Bay Estuary. Using a conservation behavior perspective, we examined how salt marsh harvest mice cope with both natural (daily tidal fluctuations) and anthropogenic (modification of tidal regime) changes in natural tidal wetlands and human-created diked wetlands, and investigated the role of behavioral flexibility in utilizing a human-created environment in the Suisun Marsh. We used radio telemetry to determine refuge use at high tide, space use, and movement rates to investigate possible differences in movement behavior in tidal versus diked wetlands. We found that the vast majority of the time salt marsh harvest mice remain in vegetation above the water during high tides. We also found no difference in space used by mice during high tide as compared to before or after high tide in either tidal or diked wetlands. We found no detectable difference in diurnal or nocturnal movement rates in tidal wetlands. However, we did find that diurnal movement rates for mice in diked wetlands were lower than nocturnal movement rates, especially during the new moon. This change in movement behavior in a relatively novel human-created habitat indicates that behavioral flexibility may facilitate the use of human-created environments by salt marsh harvest mice. PMID:25310800

  10. Effects of Natural and Anthropogenic Change on Habitat Use and Movement of Endangered Salt Marsh Harvest Mice

    PubMed Central

    Smith, Katherine R.; Barthman-Thompson, Laureen; Gould, William R.; Mabry, Karen E.

    2014-01-01

    The northern salt marsh harvest mouse (Reithrodontomys raviventris halicoetes) is an endangered species endemic to the San Francisco Bay Estuary. Using a conservation behavior perspective, we examined how salt marsh harvest mice cope with both natural (daily tidal fluctuations) and anthropogenic (modification of tidal regime) changes in natural tidal wetlands and human-created diked wetlands, and investigated the role of behavioral flexibility in utilizing a human-created environment in the Suisun Marsh. We used radio telemetry to determine refuge use at high tide, space use, and movement rates to investigate possible differences in movement behavior in tidal versus diked wetlands. We found that the vast majority of the time salt marsh harvest mice remain in vegetation above the water during high tides. We also found no difference in space used by mice during high tide as compared to before or after high tide in either tidal or diked wetlands. We found no detectable difference in diurnal or nocturnal movement rates in tidal wetlands. However, we did find that diurnal movement rates for mice in diked wetlands were lower than nocturnal movement rates, especially during the new moon. This change in movement behavior in a relatively novel human-created habitat indicates that behavioral flexibility may facilitate the use of human-created environments by salt marsh harvest mice. PMID:25310800

  11. Charge-discharge characteristics of natural graphite electrode in N, N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)amide containing lithium ion for lithium-ion secondary batteries

    NASA Astrophysics Data System (ADS)

    Towada, Jun; Karouji, Tomohiro; Sato, Hiroki; Kadoma, Yoshihiro; Shimada, Kazuaki; Ui, Koichi

    2015-02-01

    We investigated the electrochemical characteristics of a natural graphite electrode in room-temperature ionic liquids not containing additives. N, N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)amide (DEME-TFSA) containing lithium bis(trifluoromethylsulfonyl)amide (Li-TFSA) as the electrolyte and a natural graphite electrode as the negative electrode material were employed. The charge-discharge tests showed that the discharge capacity and the charge-discharge efficiency of the natural graphite electrode at the 1st cycle were 318 mAh g-1 and 75.6%, respectively. The cycle performance showed that the discharge capacity and the charge-discharge efficiency were stably maintained at ca. 320 mAh g-1 and 100%, respectively, until the initial 10th cycle. The ex-situ X-ray diffraction measurements showed that lithium-graphite intercalation compounds, such as LiC12 and LiC6, were formed after the 1st charge. The structural change in the natural graphite electrode was reversible because graphite recovered to its original structure after the 1st discharge. These results clarified that the graphite electrode could operate as a negative electrode for lithium-ion secondary batteries in DEME-TFSA containing Li-TFSA without organic solvents.

  12. 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.

  13. 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.

  14. 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.

  15. Rechargeable lithium battery technology - A survey

    NASA Technical Reports Server (NTRS)

    Halpert, Gerald; Surampudi, Subbarao

    1990-01-01

    The technology of the rechargeable lithium battery is discussed with special attention given to the types of rechargeable lithium cells and to their expected performance and advantages. Consideration is also given to the organic-electrolyte and polymeric-electrolyte cells and to molten salt lithium cells, as well as to technical issues, such as the cycle life, charge control, rate capability, cell size, and safety. The role of the rechargeable lithium cell in future NASA applications is discussed.

  16. Evidence of sealing and brine distribution at grain boundaries in natural fine-grained Halite (Qum Kuh salt fountain, Central Iran): implications for rheology of salt extrusions

    NASA Astrophysics Data System (ADS)

    Desbois, Guillaume; Urai, Janos L.; de Bresser, J. H. P.

    2010-05-01

    When grain boundary movement is stopped, surface energy related forces reassert themselves driving the system to its equilibrium conditions ([2], [6], [7], [8]). This could result in growth of islands and shrinking of channels and hence in healing the boundary by internal redistribution of fluid and solid in the contact region. Such islands are proposed to grow preferentially close to the contact rim and promote the healing of the grain-grain contact, which in turn prevents transport in or out the boundary region and thus traps the fluids in isolated inclusions. This contribution is focused on observation of grain boundary microstructures in natural mylonitic rocksalt collected from the distal part of Kum-Quh salt fountain (central Iran) in order to give unprecedented insight of grain boundary microstructures using argon-beam cross-sectioning to prepare high quality polished surfaces suitable for high-resolution SEM imaging. The possibility to use our SEM under cryogenic conditions allows also imaging the in-situ distribution of fluids. Results show that brine at grain boundaries occurs as thick layers (> µm in scale) corresponding to cross-sectioned wetted triple junction tubes, as filling at triple junction and as array of isolated fluids inclusions at grain-grain contacts. Close observations at islands contacts suggest the presence of a very thin fluid film (<100 nm). The most remarkable is evidence for sealing of pore space appearing as subhedral crystals filling the void space and decoupled from surrounding crystals by a thin brine layer. In parallel to this microstructural study, we deformed the same samples in order to simulate the simple shear flow at very low mean stress as in the salt fountain. First results suggest a complicated rheology. Samples loaded at σ < 0.7 MPa show no measurable deformation in a month, indicating strain rates less than 10-12 s-1 though, in fully activated pressure-solution (PS) creep, strain rates of several orders of magnitude

  17. Nature and Origin of Volcanogenic Salts Deposits around the Crater of Erebus volcano, Antarctica

    NASA Astrophysics Data System (ADS)

    Kammerer, M. M.; Kyle, P. R.; Dunbar, N. W.

    2010-12-01

    Volcanogenic salt deposits (VSD) are widespread around the summit crater of the active 3794-meter high Erebus volcano in Antarctica. The distribution, composition and formation of the salts provide insight into degassing of the phonolite lava lake and the interaction of the gas plume with the snow and rocks around the summit crater. The greatest accumulations of VSD are located within 1 km of the active crater and are found under rocks and in crevices in the lava flows as white to yellow incrustations, massive deposits, efflorescences, and needles. The VSD are most abundant downwind of the crater where individual VSD accumulations of 20g or more are common. The VSD are not associated with fumaroles or fumarolic ice towers but form under the ambient -20 to -60 oC temperatures. The formation of the salts under such extreme temperatures conditions may have application to salt formation at other active planetary volcanoes. Previous XRD analyses of Erebus VSD have positively identified halite, gypsum, alunite, thenardite, sylvite, mirabilite, and calcite, with numerous tentatively identified phases. SEM observations of VSD indicate that the salts are well crystallized on a very fine scale, with crystal size ranging between 1 to 20 microns. One of the most common crystal morphologies consists of well-formed columnar crystals, although blocky, platy and acicular crystals are also observed. Qualitative electron microprobe chemical scans indicate that a wide range of elements are present in the various VSD phases, including Al, Cl, F, Fe, K, Mg, Mn, Na, P, S, and Ti, with multiple salt phases present in each sample. Different crystal morphologies of salt are chemically distinct; the columnar crystals appear to be largely composed of Al, Cl, F, and Fe, platier crystals appear to be composed largely of Na and S, and flat, rectangular crystals are composed of Na and Cl. The Erebus plume, snow, and ice samples around the summit region contain large quantities of Cl, F, and S

  18. Lithium batteries with laminar anodes

    SciTech Connect

    Bruder, A.H.

    1986-11-04

    This patent describes a laminar electrical cell, comprising an anode, a cathode, and an electrolyte permeable separator between the anode and the cathode. The anode consists essentially of a layer of lithium having at least one surface of unreacted lithium metal in direct contact with and adhered to a layer of conductive plastic with no intermediate adhesive promoting adjuncts. The cathode comprises a slurry of MnO/sub 2/ and carbon particles in a solution of a lithium salt in an organic solvent, the solution permeating the separator and being in contact with the lithium.

  19. Lithium Dinitramide as an Additive in Lithium Power Cells

    NASA Technical Reports Server (NTRS)

    Gorkovenko, Alexander A.

    2007-01-01

    Lithium dinitramide, LiN(NO2)2 has shown promise as an additive to nonaqueous electrolytes in rechargeable and non-rechargeable lithium-ion-based electrochemical power cells. Such non-aqueous electrolytes consist of lithium salts dissolved in mixtures of organic ethers, esters, carbonates, or acetals. The benefits of adding lithium dinitramide (which is also a lithium salt) include lower irreversible loss of capacity on the first charge/discharge cycle, higher cycle life, lower self-discharge, greater flexibility in selection of electrolyte solvents, and greater charge capacity. The need for a suitable electrolyte additive arises as follows: The metallic lithium in the anode of a lithium-ion-based power cell is so highly reactive that in addition to the desired main electrochemical reaction, it engages in side reactions that cause formation of resistive films and dendrites, which degrade performance as quantified in terms of charge capacity, cycle life, shelf life, first-cycle irreversible capacity loss, specific power, and specific energy. The incidence of side reactions can be reduced through the formation of a solid-electrolyte interface (SEI) a thin film that prevents direct contact between the lithium anode material and the electrolyte. Ideally, an SEI should chemically protect the anode and the electrolyte from each other while exhibiting high conductivity for lithium ions and little or no conductivity for electrons. A suitable additive can act as an SEI promoter. Heretofore, most SEI promotion was thought to derive from organic molecules in electrolyte solutions. In contrast, lithium dinitramide is inorganic. Dinitramide compounds are known as oxidizers in rocket-fuel chemistry and until now, were not known as SEI promoters in battery chemistry. Although the exact reason for the improvement afforded by the addition of lithium dinitramide is not clear, it has been hypothesized that lithium dinitramide competes with other electrolyte constituents to react with

  20. Porous carbon particles derived from natural peanut shells as lithium ion battery anode and its electrochemical properties

    NASA Astrophysics Data System (ADS)

    Cao, Xiaoyu; Chen, Shuangqiang; Wang, Guoxiu

    2014-07-01

    Abandoned peanut shells, a common farm waste, have caused tremendous environmental pollution and huge waste deposits through burned and buried disposal approaches. In targeting to enhance the potential value of peanut shells and discover a new alternative candidate for lithium ion batteries, we adopted an easy to scale-up and highly repeated method to treat fresh and dry peanut shells via acid-treatment and pyrolysis, making porous structures on carbonized peanut shells. The pyrolysis process transformed the peanut shells to porous carbon (PC) materials in a quartz tube furnace at a series of temperatures from 500°C to 700°C in N2 under the condition of 40°C gradient temperatures with a heating rate of 2°C min-1. Scanning electron microscopy (SEM) images show that the irregular porous structures and hundreds of micropores are distributed on the PC materials. The cyclic voltammogram (CV) test and particle size analysis are employed to investigate their characteristics of voltammetry and particle size distribution. PC material obtained at 620°C (PC-620) exhibited good particle distribution, porous structure and less agglomerated particles. When applied as anode materials in lithium ion batteries, the PC-620 electrode displayed the high reversible capacity of 608 mAh g-1. Moreover, the cycling performance of PC-620 was the most stable, with a high Coulombic efficiency of 98.9% at the 20th cycle, demonstrating a reversible capacity of 418 mAh g-1, which is higher than the theoretical capacity of graphite. Most importantly, the PC materials harvested from the wastes of natural resources are turned into valuable electrode materials for the high demand energy storage devices, which can significantly reduce severe environmental pollution and alleviate an energy shortage. [Figure not available: see fulltext.

  1. Impact of solid second phases on deformation mechanisms of naturally deformed salt rocks (Kuh-e-Namak, Dashti, Iran) and rheological stratification of the Hormuz Salt Formation

    NASA Astrophysics Data System (ADS)

    Závada, P.; Desbois, G.; Urai, J. L.; Schulmann, K.; Rahmati, M.; Lexa, O.; Wollenberg, U.

    2015-05-01

    Viscosity contrasts displayed in flow structures of a mountain namakier (Kuh-e-Namak - Dashti), between 'weak' second phase bearing rock salt and 'strong' pure rock salt types are studied for deformation mechanisms using detailed quantitative microstructural study. While the solid inclusions rich ("dirty") rock salts contain disaggregated siltstone and dolomite interlayers, "clean" salts reveal microscopic hematite and remnants of abundant fluid inclusions in non-recrystallized cores of porphyroclasts. Although the flow in both, the recrystallized "dirty" and "clean" salt types is accommodated by combined mechanisms of pressure-solution creep (PS), grain boundary sliding (GBS), transgranular microcracking and dislocation creep accommodated grain boundary migration (GBM), their viscosity contrasts observed in the field outcrops are explained by: 1) enhanced ductility of "dirty" salts due to increased diffusion rates along the solid inclusion-halite contacts than along halite-halite contacts, and 2) slow rates of intergranular diffusion due to dissolved iron and inhibited dislocation creep due to hematite inclusions for "clean" salt types Rheological contrasts inferred by microstructural analysis between both salt rock classes apply in general for the "dirty" salt forming Lower Hormuz and the "clean" salt forming the Upper Hormuz of the Hormuz Formation and imply strain rate gradients or decoupling along horizons of mobilized salt types of different composition and microstructure.

  2. FT-Raman spectroscopy study of solvent-in-salt electrolytes

    NASA Astrophysics Data System (ADS)

    Liumin, Suo; Fang, Zheng; Yong-Sheng, Hu; Liquan, Chen

    2016-01-01

    Cation-anion interaction with different ratios of salt to solvent is investigated by FT-Raman spectroscopy. The fitting result of the C-N-C bending vibration manifests that the cation-anion coordination structure changes tremendously with the variation of salt concentration. It is well known that lithium-ion transport in ultrahigh salt concentration electrolyte is dramatically different from that in dilute electrolyte, due to high viscosity and strong cation-anion interaction. In ultrahigh salt concentrated “solvent-in-salt” electrolyte (SIS-7#), we found, on one hand, that the cation and anion in the solution mainly formed cation-anion pairs with a high Li+ coordination number (≥ 1), including intimate ion pairs (20.1%) and aggregated ion pairs (79.9%), which not only cause low total ionic conductivity but also cause a high lithium transference number (0.73). A possible lithium transport mechanism is proposed: in solvent-in-salt electrolytes, lithium ions’ direct movement presumably depends on Li-ion exchange between aggregated ion pairs and solvent molecules, which repeats a dissolving and re-complexing process between different oxygen groups of solvent molecules. Project supported by the National Basic Research Program of China (Grant No. 2014CB932300), the National Natural Science Foundation of China (Grant Nos. 51222210, 51472268, and 11234013), and the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA09010300).

  3. Design of Complex Systems to Achieve Passive Safety: Natural Circulation Cooling of Liquid Salt Pebble Bed Reactors

    NASA Astrophysics Data System (ADS)

    Scarlat, Raluca Olga

    This dissertation treats system design, modeling of transient system response, and characterization of individual phenomena and demonstrates a framework for integration of these three activities early in the design process of a complex engineered system. A system analysis framework for prioritization of experiments, modeling, and development of detailed design is proposed. Two fundamental topics in thermal-hydraulics are discussed, which illustrate the integration of modeling and experimentation with nuclear reactor design and safety analysis: thermal-hydraulic modeling of heat generating pebble bed cores, and scaled experiments for natural circulation heat removal with Boussinesq liquids. The case studies used in this dissertation are derived from the design and safety analysis of a pebble bed fluoride salt cooled high temperature nuclear reactor (PB-FHR), currently under development in the United States at the university and national laboratories level. In the context of the phenomena identification and ranking table (PIRT) methodology, new tools and approaches are proposed and demonstrated here, which are specifically relevant to technology in the early stages of development, and to analysis of passive safety features. A system decomposition approach is proposed. Definition of system functional requirements complements identification and compilation of the current knowledge base for the behavior of the system. Two new graphical tools are developed for ranking of phenomena importance: a phenomena ranking map, and a phenomena identification and ranking matrix (PIRM). The functional requirements established through this methodology were used for the design and optimization of the reactor core, and for the transient analysis and design of the passive natural circulation driven decay heat removal system for the PB-FHR. A numerical modeling approach for heat-generating porous media, with multi-dimensional fluid flow is presented. The application of this modeling

  4. The electrorheological behavior of suspensions based on molten-salt synthesized lithium titanate nanoparticles and their core-shell titanate/urea analogues.

    PubMed

    Plachy, T; Mrlik, M; Kozakova, Z; Suly, P; Sedlacik, M; Pavlinek, V; Kuritka, I

    2015-02-18

    This paper concerns the preparation of novel electrorheological (ER) materials using microwave-assisted synthesis as well as utilizing a suitable shell-providing system with enhanced ER performance. Lithium titanate nanoparticles were successfully synthesized, and their composition was confirmed via X-ray diffraction. Rheological properties were investigated in the absence as well as in the presence of an external electric field. Dielectric properties clarified the response of the particles to the application of an electric field. The urea-coated lithium titanate nanoparticle-based suspension exhibits higher ER performance in comparison to suspensions based on bare particles. PMID:25633327

  5. Solid Polymer Electrolytes Based on Functionalized Tannic Acids from Natural Resources for All-Solid-State Lithium-Ion Batteries.

    PubMed

    Shim, Jimin; Bae, Ki Yoon; Kim, Hee Joong; Lee, Jin Hong; Kim, Dong-Gyun; Yoon, Woo Young; Lee, Jong-Chan

    2015-12-21

    Solid polymer electrolytes (SPEs) for all-solid-state lithium-ion batteries are prepared by simple one-pot polymerization induced by ultraviolet (UV) light using poly(ethylene glycol) methyl ether methacrylate (PEGMA) as an ion-conducting monomeric unit and tannic acid (TA)-based crosslinking agent and plasticizer. The crosslinking agent and plasticizer based on natural resources are obtained from the reaction of TA with glycidyl methacrylate and glycidyl poly(ethylene glycol), respectively. Dimensionally stable free-standing SPE having a large ionic conductivity of 5.6×10(-4)  Scm(-1) at room temperature can be obtained by the polymerization of PEGMA into P(PEGMA) with a very small amount (0.1 wt %) of the crosslinking agent and 2.0 wt % of the plasticizer. The ionic conductivity value of SPE with a crosslinked structure is one order of magnitude larger than that of linear P(PEGMA) in the waxy state. PMID:26609912

  6. EVALUATING MONITORED NATURAL ATTENUATION FOR RADIONUCLIDE & ORGANIC CONTAMINATION IN GROUNDWATER (SALT LAKE CITY, UT)

    EPA Science Inventory

    Monitored Natural Attenuation (MNA) for radionuclides and inorganic contaminants is dependent on naturally occurring processes in the subsurface that act without human intervention to reduce the mass, toxicity, mobility, volume or concentration of contaminants. EPA is developing ...

  7. Validity and slopes of the linear equation of state for natural brines in salt lake systems

    NASA Astrophysics Data System (ADS)

    Kohfahl, C.; Post, V. E. A.; Hamann, E.; Prommer, H.; Simmons, C. T.

    2015-04-01

    Many density-dependent groundwater flow simulations rely on a linear equation of state that relates the fluid density to the total dissolved solute content (TDS). This approach ignores non-linear volume of mixing effects, as well as the impact of any chemical reactions. These effects can be considered by using geochemical codes that implement algorithms that calculate the density of a fluid based on the concentration of individual solute species. While in principle such algorithms could be used in-lieu of a linear equation of state in a groundwater model, the computational overhead is such that the use of a more simplified equation of state is preferred. This requires that the assumption of linearity as well as the appropriate value of the linear slope have to be determined. Here, published density measurements of 7 chemically-distinct salt lake brines are compared with densities calculated by PHREEQC-3, confirming the applicability of PHREEQC's algorithm to salt lake brines, as well as to seawater brines and artificial brines from laboratory experiments. Further, calculations with PHREEQC-3 are used to assess the impact of mineral precipitation reactions during evaporative concentration. Results show that the density-TDS relationship is essentially linear over a wide concentration range, and that slopes range between 0.64 and 0.75, with the upper end of the range applying to Na-CO3-Cl brines and the lower end to Na-Cl brines. Mineral precipitation of highly-soluble evaporate minerals such as halite and trona limit TDS, and may lead to considerable errors in coupled flow simulations based on a linear equation of state at high concentrations. Misrepresentation of the slope may lead to an error of up to 20% in the calculated length of the brine nose bordering a salt lake, or of the Rayleigh number, which indicates if a density stratification is stable or not.

  8. Salton Sea Geothermal Field, California, as a near-field natural analog of a radioactive waste repository in salt

    SciTech Connect

    Elders, W.A.; Cohen, L.H.

    1983-11-01

    Since high concentrations of radionuclides and high temperatures are not normally encountered in salt domes or beds, finding an exact geologic analog of expected near-field conditions in a mined nuclear waste repository in salt will be difficult. The Salton Sea Geothermal Field, however, provides an opportunity to investigate the migration and retardation of naturally occurring U, Th, Ra, Cs, Sr and other elements in hot brines which have been moving through clay-rich sedimentary rocks for up to 100,000 years. The more than thirty deep wells drilled in this field to produce steam for electrical generation penetrate sedimentary rocks containing concentrated brines where temperatures reach 365/sup 0/C at only 2 km depth. The brines are primarily Na, K, Ca chlorides with up to 25% of total dissolved solids; they also contain high concentrations of metals such as Fe, Mn, Li, Zn, and Pb. This report describes the geology, geophysics and geochemistry of this system as a prelude to a study of the mobility of naturally occurring radionuclides and radionuclide analogs within it. The aim of this study is to provide data to assist in validating quantitative models of repository behavior and to use in designing and evaluating waste packages and engineered barriers. 128 references, 33 figures, 13 tables.

  9. Thermoluminescence (TL) Analysis and Fading Studies of Naturally Occurring Salt Irradiated by 500 mGy Gamma Rays

    SciTech Connect

    Tiwari, Ramesh Chandra; Pau, Kham Suan

    2011-10-20

    The aim of the present study was to investigate the potential of the naturally occurring salt for the dosimetry purposes, using TL. The fine powder samples (20 mg) were irradiated by {gamma}- rays from 500 mGy to 2500 mGy by using Theratron-780C Cobalt-60 source, however, this paper discusses about 500 mGy only. The TL glow curve peak parameters were studied by using Chen's peak shape equation. TL glow curves were compared with fitted curves using glow curve deconvolution (GCD) method by using Kitis expression. The kinetic parameter values (E, b and s) so calculated, are in good agreement with those available in literature. The calculated energy values were also verified by using various heating rate (VHR) method. {chi}{sup 2} test and figure of merit (FOM) calculation was done to accept the goodness of fit between the curves. Fading studies of the sample showed a good fitting between the curves. The analysis suggests that natural salt should be considered for dosimetry purposes.

  10. Sulfide variation in the pore and surface waters of artificial salt-marsh ditches and a natural tidal creek

    SciTech Connect

    Rey, J.R.; Shaffer, J.; Kain, T.; Stahl, R.; Crossman, R. )

    1992-09-01

    Pore and surface water sulfide variation near artificial ditches and a natural creek are examined in salt marshes bordering the Indian River Lagoon in east-central Florida. Pore water sulfide concentrations ranged from 0 [mu]g-at l[sup [minus]1] to 1,640 [mu]g-at l[sup [minus]1]. On average, the natural creek had the lowest sulfide concentrations (mean < 1.0 [mu]g-at l[sup [minus]1]) and the perimeter ditch of a managed salt marsh impoundment the highest (436.5 [mu]g-at l[sup [minus]1]). There was a trend of increasing sulfide concentration in the summer, and sharp peaks in late fall-early winter which correspond with peak litter input into the sediments. Significant differences in sulfide concentration between sites are attributed to differences in water flow and in organic matter content. Delaying the seasonal opening of culverts (which connect impounded marshes with the lagoon) until lagoon water levels rise in fall may prevent massive fish kills that have been associated with high sulfide levels in the impoundment perimeter ditches. 35 refs., 7 figs., 5 tabs.

  11. Effect of the nature of the salt precursor of an oxide-hydroxide sorbent on the sorption of oxalate ions

    NASA Astrophysics Data System (ADS)

    Pechenyuk, S. I.; Kuz'mich, L. F.; Semushina, Yu. P.

    2012-09-01

    Generalizations are made on the effect of the nature of a precursor (the original salt of a metal) on the sorption activity of hydrogels of oxidehydroxides (OHes) towards oxalate ions using the example of an OH obtained by the alkaline hydrolysis of chloride, perchlorate, and sulfate of Fe(III); chloride, sulfate, and nitrate of Al; and nitrate of Zr(IV). It is established that the sorption of C2O{4/2-} on the studied OHes is described by the Langmuir equation. We find that the sorption activity depends on the nature of the precursor: Al2(SO4)3 > Al(NO3)3 > AlCl3 > ZrO(NO3)2 > Fe2(SO4)3 > FeCl3 > Fe(ClO4)3.

  12. A rapid method for the determination of lithium transference numbers

    SciTech Connect

    Zawodzinski, T.A. Jr.; Dai, H.; Sanderson, S.; Davey, J.; Uribe, F.

    1997-05-01

    Lithium ion-conducting polymer electrolytes are of increasing interest for use in lithium-polymer batteries. Lithium transference numbers, the net fraction of current carried by lithium in a cell, are key figures of merit for potential lithium battery electrolytes. The authors describe the Electrophoretic NMR (ENMR) method for the determination of lithium ion transference numbers (T{sub Li}). The work presented is a proof-of-concept of the application of the ENMR method to lithium ion transference measurements for several different lithium salts in gelled electrolytes. The NMR method allows accurate determination of T{sub Li} values, as indicated by the similarity of T{sub Li} in the gelled electrolytes to those in aqueous electrolyte solutions at low salt concentration. Based on calculated tradeoffs of various experimental parameters, they also discuss some conclusions concerning the range of applicability of the method to other electrolytes with lower lithium mobility.

  13. Alignment nature of ZnO nanowires grown on polished and nanoscale etched lithium niobate surface through self-seeding thermal evaporation method

    SciTech Connect

    Mohanan, Ajay Achath; Parthiban, R.; Ramakrishnan, N.

    2015-08-15

    Highlights: • ZnO nanowires were grown directly on LiNbO{sub 3} surface for the first time by thermal evaporation. • Self-alignment of the nanowires due to step bunching of LiNbO{sub 3} surface is observed. • Increased roughness in surface defects promoted well-aligned growth of nanowires. • Well-aligned growth was then replicated in 50 nm deep trenches on the surface. • Study opens novel pathway for patterned growth of ZnO nanowires on LiNbO{sub 3} surface. - Abstract: High aspect ratio catalyst-free ZnO nanowires were directly synthesized on lithium niobate substrate for the first time through thermal evaporation method without the use of a buffer layer or the conventional pre-deposited ZnO seed layer. As-grown ZnO nanowires exhibited a crisscross aligned growth pattern due to step bunching of the polished lithium niobate surface during the nanowire growth process. On the contrary, scratches on the surface and edges of the substrate produced well-aligned ZnO nanowires in these defect regions due to high surface roughness. Thus, the crisscross aligned nature of high aspect ratio nanowire growth on the lithium niobate surface can be changed to well-aligned growth through controlled etching of the surface, which is further verified through reactive-ion etching of lithium niobate. The investigations and discussion in the present work will provide novel pathway for self-seeded patterned growth of well-aligned ZnO nanowires on lithium niobate based micro devices.

  14. Salt lakes of Western Australia - Natural abiotic formation of volatile organic compounds

    NASA Astrophysics Data System (ADS)

    Krause, T.; Studenroth, S.; Mulder, I.; Tubbesing, C.; Kotte, K.; Ofner, J.; Junkermann, W.; Schöler, H. F.

    2012-04-01

    Western Australia is a semi-/arid region that is heavily influenced by global climate change and agricultural land use. The area is known for its many ephemeral saline and hypersaline lakes with a wide range of hydrogeochemical parameters that have gradually changed over the last fifty years. Historically, the region was covered by eucalyptus trees and shrubs, but was cleared mainly within 10 years after WWII to make room for wheat and live stock. After the clearance of the deep rooted native plants the groundwater started to rise, bringing increased amounts of dissolved salts and minerals to the surface and discharging them into streams and lakes. Thus most of Western Australia is influenced by secondary salinisation (soil salting) [1]. Another problem is that the discharged minerals affect the pH of ground and surface water, which ranges from acidic to slightly basic. During the 2011 campaign surface water was measured with a pH between 2.5 and 7.1. Another phenomenon in Western Australia is the decrease of rainfall over the last decades assumed to be linked to the secondary salinisation. The rising saline and mineral rich groundwater increases the biotical and abiotical activity of the salt lakes. Halogenated and non-halogenated volatile organic compounds emitted from those lakes undergo fast oxidation and chemical reactions to form small particles modifying cloud microphysics and thus suppressing rain events [2]. Our objective is to gain a better understanding of this extreme environment with its hypersaline acidic lakes with regard to the potential abiotic formation of volatile organic compounds and its impact on the local climate. In spring 2011 fifty-three sediment samples from ten salt lakes in the Lake King region where taken, freeze-dried and ground. In order to simulate the abiotic formation of volatile organic compounds the soil samples were resuspended with water in gas-tight headspace vials. The headspace was measured using a purge and trap GC

  15. Nuclear magnetic resonance studies on the rotational and translational motions of ionic liquids composed of 1-ethyl-3-methylimidazolium cation and bis(trifluoromethanesulfonyl)amide and bis(fluorosulfonyl)amide anions and their binary systems including lithium salts

    NASA Astrophysics Data System (ADS)

    Hayamizu, Kikuko; Tsuzuki, Seiji; Seki, Shiro; Umebayashi, Yasuhiro

    2011-08-01

    Room temperature ionic liquids (ILs) are stable liquids composed of anions and cations. 1-ethyl-3-methyl-imidazolium (EMIm, EMI) is a popular and important cation that produces thermally stable ILs with various anions. In this study two amide-type anions, bis(trifluoro-methanesulfonyl)amide [N(SO2CF3)2, TFSA, TFSI, NTf2, or Tf2N] and bis(fluorosulfonyl)amide [(N(SO2F)2, FSA, or FSI] were investigated by multinuclear NMR spectroscopy. In addition to EMIm-TFSA and EMIm-FSA, lithium-salt-doped binary systems were prepared (EMIm-TFSA-Li and EMIm-FSA-Li). The spin-lattice relaxation times (T1) were measured by 1H, 19F, and 7Li NMR spectroscopy and the correlation times of 1H NMR, τc(EMIm) (8 × 10-10 to 3 × 10-11 s) for the librational molecular motion of EMIm and those of 7Li NMR, τc(Li) (5 × 10-9 to 2 × 10-10 s) for a lithium jump were evaluated in the temperature range between 253 and 353 K. We found that the bulk viscosity (η) versus τc(EMIm) and cation diffusion coefficient DEMIm versus the rate 1/τc(EMIm) have good relationships. Similarly, linear relations were obtained for the η versus τc(Li) and the lithium diffusion coefficient DLi versus the rate 1/τc(Li). The mean one-jump distances of Li were calculated from τc(Li) and DLi. The experimental values for the diffusion coefficients, ionic conductivity, viscosity, and density in our previous paper were analyzed by the Stokes-Einstein, Nernst-Einstein, and Stokes-Einstein-Debye equations for the neat and binary ILs to clarify the physicochemical properties and mobility of individual ions. The deviations from the classical equations are discussed.

  16. The application of high resolution X-ray computed tomography on naturally deformed rock salt: Multi-scale investigations of the structural inventory

    NASA Astrophysics Data System (ADS)

    Thiemeyer, Nicolas; Habersetzer, Jörg; Peinl, Mark; Zulauf, Gernold; Hammer, Jörg

    2015-08-01

    X-ray computed tomography (CT) represents a useful technique providing new perspectives and insights for the structural investigation of naturally-deformed rock salt. Several samples of Permian rock salt from Gorleben, Asse and Teutschenthal (Germany) were investigated by exploiting the non-destructive nature of μCT and nCT techniques particularly for salt rocks. CT imaging enabled the visualization and quantification of anhydrite impurities, pore space and fluid phases located along grain-boundaries or trapped as intracrystalline inclusions. Disseminated grains and aggregates of anhydrite in rock salt of the Gorleben salt dome have been visualized and quantified by μCT for the first time in order to portray their spatial occurrence. The visualization of anhydrite aggregates and pore space shows no correlation between their spatial distributions. This independence excludes the anhydrite to be responsible for elevated porosity (0.87 ± 0.07 vol.-%). High-resolution nCT scans (≤1 μm voxel size) of single intracrystalline and grain-boundary fluid inclusions from Gorleben and Asse rock salt allowed the visualization and quantification of their various phase components. A major achievement is the detailed description of the morphology and shape of the fluid inclusions and of their phase components, which has not been conducted in rock salt research by high-resolution X-ray CT imaging before.

  17. Design of Complex Systems to Achieve Passive Safety: Natural Circulation Cooling of Liquid Salt Pebble Bed Reactors

    NASA Astrophysics Data System (ADS)

    Scarlat, Raluca Olga

    This dissertation treats system design, modeling of transient system response, and characterization of individual phenomena and demonstrates a framework for integration of these three activities early in the design process of a complex engineered system. A system analysis framework for prioritization of experiments, modeling, and development of detailed design is proposed. Two fundamental topics in thermal-hydraulics are discussed, which illustrate the integration of modeling and experimentation with nuclear reactor design and safety analysis: thermal-hydraulic modeling of heat generating pebble bed cores, and scaled experiments for natural circulation heat removal with Boussinesq liquids. The case studies used in this dissertation are derived from the design and safety analysis of a pebble bed fluoride salt cooled high temperature nuclear reactor (PB-FHR), currently under development in the United States at the university and national laboratories level. In the context of the phenomena identification and ranking table (PIRT) methodology, new tools and approaches are proposed and demonstrated here, which are specifically relevant to technology in the early stages of development, and to analysis of passive safety features. A system decomposition approach is proposed. Definition of system functional requirements complements identification and compilation of the current knowledge base for the behavior of the system. Two new graphical tools are developed for ranking of phenomena importance: a phenomena ranking map, and a phenomena identification and ranking matrix (PIRM). The functional requirements established through this methodology were used for the design and optimization of the reactor core, and for the transient analysis and design of the passive natural circulation driven decay heat removal system for the PB-FHR. A numerical modeling approach for heat-generating porous media, with multi-dimensional fluid flow is presented. The application of this modeling

  18. 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.

  19. Air breathing lithium power cells

    DOEpatents

    Farmer, Joseph C.

    2014-07-15

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

  20. RECOVERY AND SEPARATION OF LITHIUM VALUES FROM SALVAGE SOLUTIONS

    DOEpatents

    Hansford, D.L.; Raabe, E.W.

    1963-08-20

    Lithium values can be recovered from an aqueous basic solution by reacting the values with a phosphate salt soluble in the solution, forming an aqueous slurry of the resultant aqueous insoluble lithium phosphate, contacting the slurry with an organic cation exchange resin in the acid form until the slurry has been clarified, and thereafter recovering lithium values from the resin. (AEC)

  1. Electrophysical behavior of ion-conductive organic-inorganic polymer system based on aliphatic epoxy resin and salt of lithium perchlorate

    NASA Astrophysics Data System (ADS)

    Matkovska, Liubov; Iurzhenko, Maksym; Mamunya, Yevgen; Matkovska, Olga; Demchenko, Valeriy; Lebedev, Eugene; Boiteux, Gisele; Serghei, Anatoli

    2014-12-01

    In the present work, ion-conductive hybrid organic-inorganic polymers based on epoxy oligomer of diglycide aliphatic ester of polyethylene glycol (DEG) and lithium perchlorate (LiClO4) were synthesized. The effect of LiClO4 content on the electrophysical properties of epoxy polymers has been studied by differential scanning calorimetry (DSC) and broadband dielectric spectroscopy (BDS). The effect of LiClO4 content on the structure has been studied by wide-angle X-ray scattering (WAXS). It was found that LiClO4 impacts on the structure of the synthesized hybrid epoxy polymers, probably, by formation of coordinative complexes {ether oxygen-lithium cations-ether oxygen} as evidenced from a significant increase in their glass transition temperatures with increasing LiClO4 concentration and WAXS studies. The presence of ether oxygen in DEG macromolecules provides a transfer mechanism of the lithium cations with the ether oxygen similar to polyethylene oxide (PEO). Thus, the obtained hybrid polymers have high values of ionic conductivity σ' (approximately 10-3 S/cm) and permittivity ɛ' (6 × 105) at elevated temperatures (200°C). On the other hand, DEG has higher heat resistance compared to PEO that makes these systems perspective as solid polymer electrolytes able to operate at high temperature.

  2. Lithium Treatment for Psychiatric Disorders

    PubMed Central

    Maletzky, Barry M.; Shore, James H.

    1978-01-01

    Although used around the world since 1949, lithium has come into extensive use in psychiatry in the United States only within the past decade. Before initiating treatment with this drug, physicians must be familiar with the diagnostic scheme of the major affective disorders, the indications and contraindications to lithium's use, and its principles of treatment, including evaluation before lithium therapy, criteria for monitoring blood levels and signs of impending toxicity. Despite earlier reports about the toxicity of lithium when it was promoted as a salt substitute, lithium is a safe drug. Its use not only has revolutionized the treatment of the major affective disorders, but has opened up new and broad avenues of research into the regulation of man's emotions. PMID:664651

  3. Liquid surface skimmer apparatus for molten lithium and method

    DOEpatents

    Robinson, Samuel C.; Pollard, Roy E.; Thompson, William F.; Stark, Marshall W.; Currin, Jr., Robert T.

    1995-01-01

    This invention relates to an apparatus for separating two fluids having different specific gravities. The invention also relates to a method for using the separating apparatus of the present invention. This invention particularly relates to the skimming of molten lithium metal from the surface of a fused salt electrolyte in the electrolytic production of lithium metal from a mixed fused salt.

  4. Electrochemical performance of cobalt vanadium oxide/natural graphite as anode for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Ni, Shibing; Ma, Jianjun; Zhang, Jicheng; Yang, Xuelin; Zhang, Lulu

    2015-05-01

    CoV2O6/natural graphite electrode with sodium alginate binder is prepared, which shows excellent electrochemical performance as anode for Li-ion batteries. It exhibits initial discharge and charge capacity of 902 and 638 mAh g-1 at a specific current of 110 mA g-1. After 100 cycles, the discharge and charge capacity maintain of 669 and 665 mAh g-1, respectively. The charge/discharge mechanism of CoV2O6 is also studied, suggesting a structure variation in discharging, which involves the initial formation of LiV2O5 and Co3V2O8, the subsequent transition from Co3V2O8 to LixV2O5 and CoO, and the later reduction of CoO into Co. The structure variation of Co3V2O8 accompanies by an amorphization process, which maintains in the subsequent discharging and charging process.

  5. Natural abundance 17O nuclear magnetic resonance and computational modeling studies of lithium based liquid electrolytes

    NASA Astrophysics Data System (ADS)

    Deng, Xuchu; Hu, Mary Y.; Wei, Xiaoliang; Wang, Wei; Chen, Zhong; Liu, Jun; Hu, Jian Zhi

    2015-07-01

    Natural abundance 17O NMR measurements were conducted on electrolyte solutions consisting of Li[CF3SO2NSO2CF3] (LiTFSI) dissolved in the solvents of ethylene carbonate (EC), propylene carbonate (PC), ethyl methyl carbonate (EMC), and their mixtures at various concentrations. It was observed that 17O chemical shifts of solvent molecules change with the concentration of LiTFSI. The chemical shift displacements of carbonyl oxygen are evidently greater than those of ethereal oxygen, strongly indicating that Li+ ion is coordinated with carbonyl oxygen rather than ethereal oxygen. To understand the detailed molecular interaction, computational modeling of 17O chemical shifts was carried out on proposed solvation structures. By comparing the predicted chemical shifts with the experimental values, it is found that a Li+ ion is coordinated with four double bond oxygen atoms from EC, PC, EMC and TFSI- anion. In the case of excessive amount of solvents of EC, PC and EMC the Li+ coordinated solvent molecules are undergoing quick exchange with bulk solvent molecules, resulting in average 17O chemical shifts. Several kinds of solvation structures are identified, where the proportion of each structure in the liquid electrolytes investigated depends on the concentration of LiTFSI.

  6. Natural Abundance 17O Nuclear Magnetic Resonance and Computational Modeling Studies of Lithium Based Liquid Electrolytes

    SciTech Connect

    Deng, Xuchu; Hu, Mary Y.; Wei, Xiaoliang; Wang, Wei; Chen, Zhong; Liu, Jun; Hu, Jian Z.

    2015-07-01

    Natural abundance 17O NMR measurements were conducted on electrolyte solutions consisting of Li[CF3SO2NSO2CF3] (LiTFSI) dissolved in the solvents of ethylene carbonate (EC), propylene carbonate (PC), ethyl methyl carbonate (EMC), and their mixtures at various concentrations. It was observed that 17O chemical shifts of solvent molecules change with the concentration of LiTFSI. The chemical shift displacements of carbonyl oxygen are evidently greater than those of ethereal oxygen, strongly indicating that Li+ ion is coordinated with carbonyl oxygen rather than ethereal oxygen. To understand the detailed molecular interaction, computational modeling of 17O chemical shifts was carried out on proposed solvation structures. By comparing the predicted chemical shifts with the experimental values, it is found that a Li+ ion is coordinated with four double bond oxygen atoms from EC, PC, EMC and TFSI- anion. In the case of excessive amount of solvents of EC, PC and EMC the Li+ coordinated solvent molecules are undergoing quick exchange with bulk solvent molecules, resulting in average 17O chemical shifts. Several kinds of solvation structures are identified, where the proportion of each structure in the liquid electrolytes investigated depends on the concentration of LiTFSI.

  7. Lithium isotopes in large rivers reveal the cannibalistic nature of modern continental weathering and erosion

    NASA Astrophysics Data System (ADS)

    Dellinger, Mathieu; Gaillardet, Jérôme; Bouchez, Julien; Calmels, Damien; Galy, Valier; Hilton, Robert G.; Louvat, Pascale; France-Lanord, Christian

    2014-09-01

    The erosion of major mountain ranges is thought to be largely cannibalistic, recycling sediments that were deposited in the ocean or on the continents prior to mountain uplift. Despite this recognition, it has not yet been possible to quantify the amount of recycled material that is presently transported by rivers to the ocean. Here, we have analyzed the Li content and isotope composition (δLi7) of suspended sediments sampled along river depth profiles and bed sands in three of the largest Earth's river systems (Amazon, Mackenzie and Ganga-Brahmaputra rivers). The δLi7 values of river-sediments transported by these rivers range from +5.3 to -3.6‰ and decrease with sediment grain size. We interpret these variations as reflecting a mixture of unweathered rock fragments (preferentially transported at depth in the coarse fraction) and present-day weathering products (preferentially transported at the surface in the finest fraction). Only the finest surface sediments contain the complementary reservoir of Li solubilized by water-rock interactions within the watersheds. Li isotopes also show that river bed sands can be interpreted as a mixture between unweathered fragments of igneous and sedimentary rocks. A mass budget approach, based on Li isotopes, Li/Al and Na/Al ratios, solved by an inverse method allows us to estimate that, for the large rivers analyzed here, the part of solid weathering products formed by present-day weathering reactions and transported to the ocean do not exceed 35%. Li isotopes also show that the sediments transported by the Amazon, Mackenzie and Ganga-Brahmaputra river systems are mostly sourced from sedimentary rocks (>60%) rather than igneous rocks. This study shows that Li isotopes in the river particulate load are a good proxy for quantifying both the erosional rock sources and the fingerprint of present-day weathering processes. Overall, Li isotopes in river sediments confirm the cannibalistic nature of erosion and weathering.

  8. Natural sources of salinity in the Brazos River, Texas with particular reference to the Croton and salt Croton Creek basins

    USGS Publications Warehouse

    Baker, R.C.; Hughes, Leon S.; Yost, I.D.

    1964-01-01

    The salt water may be disposed of by impounding it in reservoirs for evaporation or by injecting it underground through oil wells, oil tests, or wells drilled for saltwater disposal. Sediments in which the salt water possibly could be injected underlie the. Dove Creek Salt Flats at depths of less than 7,000 feet.

  9. LITHIUM PROPHYLAXIS IN AFFECTIVE DISORDER

    PubMed Central

    Rao, A. Venkoba; Hariharasubramanian, N.; Devi, S. Parvathi; Sugumar, A.; Srinivasan, V.

    1982-01-01

    SUMMARY Out of 108 patients on the rolls in the Lithium clinic, Madurai Medical College and Govt. Rajaji Hospital, Madurai, India, 47 patients suffering from affective disorders receiving lithium continuously for more than three years were analysed with a view to study the recurrences. Thirteen suffered no relapses while on lithium while nineteen experienced them while on lithium. Four were free from recurrences after lithium was withdrawn- Seven defaulted but suffered recurrences while in four the drug was withdrawn and in both the groups remission was achieved with re-administration of lithium. The study reveals that lithium besides averting the recurrences can reduce the frequency, number, duration, intensity of episodes and improve the amenability to drugs. Among the symptoms, suicidal ideas and behaviour and insight were found to be influenced favourably by lithium. Among the factors that help favourable response to lithium were a positive family history of affective disorder, in the first degree relatives and lesser frequency and number of episodes in the pre-lithium period. A reappraisal of the natural history of the illness is called for in the light of lithium prophylaxis of manic depressive psychosis. PMID:21965880

  10. Lithium to the Rescue.

    PubMed

    Jope, Richard S; Nemeroff, Charles B

    2016-01-01

    Lithium, an element that Mother Nature has put in some drinking water sources, has been used for its curative powers for centuries. Today, it's given in capsule form as a mood stabilizer for bipolar disorder and depression. New research, however, reveals its role as a neuroprotector, and suggests that a better understanding of the role enzymes modulated by lithium play could lead to new treatments for Alzheimer's disease, Parkinson's disease, multiple sclerosis, and other neurodegenerative disorders. PMID:27408673

  11. Defining cooking salt intakes for patient counselling and policy making.

    PubMed

    Sánchez-Castillo, C P; James, W P

    1995-12-01

    The role of salt (NaCl) in the development of high blood pressure has been a matter of debate, however, the Intersalt Study showed that sodium (Na) intake in various areas of the World is related to the slope of blood pressure with age. Accurate amounts of the total salt intake or that coming from a particular source are needed, both, for physicians who need to consider the salt intake of their patients and for public health workers who are in charge of the implementation of public health programs where salt is used as a carrier of other nutrients. An analysis of the literature suggests that exaggerated values for total salt intakes have often been obtained from indirect estimates; discretionary salt use, i.e. home-cooking salt has invariably been overestimated. A method is described for measuring the contribution of cooking salt to total salt intake since it is a confusing area where inappropriate methods have been used to assess its contribution. The method described is based on the use of small amounts of lithium carbonate fused with NaCl. Validation experiments were undertaken to determine the naturally occurring lithium (Li) in a number of foods including fresh, frozen and tinned vegetables, and the use of Li tagged salt for cooking vegetables and for direct use in cooked foods. We also assessed whether Li was taken up proportionally with Na into foods during cooking. In general vegetables contained variable but only small amounts of Li except aubergine and spinach, and Li was taken up proportionally with Na in a variety of vegetables. Results showed that 36, 35 and 21% of the salt added during cooking was recovered in carrots, runner beans and potatoes respectively, the rest being discarded in the cooking water. This suggest that about a third of salt added during the cooking of vegetables will be ingested by the household. Attempts to rely simply on the total use of household salt supplies will clearly exaggerate, markedly, the true intake of individuals

  12. Synthesis of tetraaza bromide macrocyclic and studies of its effect on poly(methyl methacrylate) grafted natural rubber (MG49) - lithium tertrafluoroborate (LiBF{sub 4}) films

    SciTech Connect

    Mariam, Siti Nor; Yamin, Bohari M.; Ahmad, Azizan

    2013-11-27

    Good Poly(Methyl Methacrylate) Grafted natural Rubber (MG49) films with homogeneous and smooth surface were obtained in the presence of Lithium Tertrafluoroborate (LiBF{sub 4}) and 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-7,14-dienium bromide, (Me{sub 6}N{sub 4}H{sub 4})Br{sub 2} as dopants. The conductivity was found to be 3.63×10{sup −6} S/cm an increase by seven fold compare to the undoped MG49.

  13. Synthesis of tetraaza bromide macrocyclic and studies of its effect on poly(methyl methacrylate) grafted natural rubber (MG49) - lithium tertrafluoroborate (LiBF4) films

    NASA Astrophysics Data System (ADS)

    Mariam, Siti Nor; Yamin, Bohari M.; Ahmad, Azizan

    2013-11-01

    Good Poly(Methyl Methacrylate) Grafted natural Rubber (MG49) films with homogeneous and smooth surface were obtained in the presence of Lithium Tertrafluoroborate (LiBF4) and 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-7,14-dienium bromide, (Me6N4H4)Br2 as dopants. The conductivity was found to be 3.63×10-6 S/cm an increase by seven fold compare to the undoped MG49.

  14. 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).

  15. 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.

  16. Recovery of lithium and cobalt from waste lithium ion batteries of mobile phone

    SciTech Connect

    Jha, Manis Kumar Kumari, Anjan; Jha, Amrita Kumari; Kumar, Vinay; Hait, Jhumki; Pandey, Banshi Dhar

    2013-09-15

    Graphical abstract: Recovery of valuable metals from scrap batteries of mobile phone. - Highlights: • Recovery of Co and Li from spent LIBs was performed by hydrometallurgical route. • Under the optimum condition, 99.1% of lithium and 70.0% of cobalt were leached. • The mechanism of the dissolution of lithium and cobalt was studied. • Activation energy for lithium and cobalt were found to be 32.4 kJ/mol and 59.81 kJ/mol, respectively. • After metal recovery, residue was washed before disposal to the environment. - Abstract: In view of the stringent environmental regulations, availability of limited natural resources and ever increasing need of alternative energy critical elements, an environmental eco-friendly leaching process is reported for the recovery of lithium and cobalt from the cathode active materials of spent lithium-ion batteries of mobile phones. The experiments were carried out to optimize the process parameters for the recovery of lithium and cobalt by varying the concentration of leachant, pulp density, reductant volume and temperature. Leaching with 2 M sulfuric acid with the addition of 5% H{sub 2}O{sub 2} (v/v) at a pulp density of 100 g/L and 75 °C resulted in the recovery of 99.1% lithium and 70.0% cobalt in 60 min. H{sub 2}O{sub 2} in sulfuric acid solution acts as an effective reducing agent, which enhance the percentage leaching of metals. Leaching kinetics of lithium in sulfuric acid fitted well to the chemical controlled reaction model i.e. 1 − (1 − X){sup 1/3} = k{sub c}t. Leaching kinetics of cobalt fitted well to the model ‘ash diffusion control dense constant sizes spherical particles’ i.e. 1 − 3(1 − X){sup 2/3} + 2(1 − X) = k{sub c}t. Metals could subsequently be separated selectively from the leach liquor by solvent extraction process to produce their salts by crystallization process from the purified solution.

  17. Studies on the translational and rotational motions of ionic liquids composed of N-methyl-N-propyl-pyrrolidinium (P13) cation and bis(trifluoromethanesulfonyl)amide and bis(fluorosulfonyl)amide anions and their binary systems including lithium salts

    NASA Astrophysics Data System (ADS)

    Hayamizu, Kikuko; Tsuzuki, Seiji; Seki, Shiro; Fujii, Kenta; Suenaga, Masahiko; Umebayashi, Yasuhiro

    2010-11-01

    Room-temperature ionic liquids (RTIL, IL) are stable liquids composed of anions and cations. N-methyl-N-propyl-pyrrolidinium (P13, Py13, PYR13, or mppy) is an important cation and produces stable ILs with various anions. In this study two amide-type anions, bis(trifluoromethanesulfonyl)amide [N(SO2CF3)2, TFSA, TFSI, NTf2, or Tf2N] and bis(fluorosulfonyl)amide [N(SO2F)2, FSA, or FSI], were investigated. In addition to P13-TFSA and P13-FSA, lithium salt doped samples were prepared (P13-TFSA-Li and P13-FSA-Li). The individual ion diffusion coefficients (D) and spin-lattice relaxation times (T1) were measured by H1, F19, and L7i NMR. At the same time, the ionic conductivity (σ), viscosity (η), and density (ρ) were measured over a wide temperature range. The van der Waals volumes of P13, TFSA, FSA, Li(TFSA)2, and Li(FSA)3 were estimated by molecular orbital calculations. The experimental values obtained in this study were analyzed by the classical Stokes-Einstein, Nernst-Einstein (NE), and Stokes-Einstein-Debye equations and Walden plots were also made for the neat and binary ILs to clarify physical and mobile properties of individual ions. From the temperature-dependent velocity correlation coefficients for neat P13-TFSA and P13-FSA, the NE parameter 1-ξ was evaluated. The ionicity (electrochemical molar conductivity divided by the NE conductivity from NMR) and the 1-ξ had exactly the same values. The rotational and translational motions of P13 and jump of a lithium ion are also discussed.

  18. Natural variation in rosette size under salt stress conditions corresponds to developmental differences between Arabidopsis accessions and allelic variation in the LRR-KISS gene.

    PubMed

    Julkowska, Magdalena M; Klei, Karlijn; Fokkens, Like; Haring, Michel A; Schranz, M Eric; Testerink, Christa

    2016-04-01

    Natural variation among Arabidopsis accessions is an important genetic resource to identify mechanisms underlying plant development and stress tolerance. To evaluate the natural variation in salinity stress tolerance, two large-scale experiments were performed on two populations consisting of 160 Arabidopsis accessions each. Multiple traits, including projected rosette area, and fresh and dry weight were collected as an estimate for salinity tolerance. Our results reveal a correlation between rosette size under salt stress conditions and developmental differences between the accessions grown in control conditions, suggesting that in general larger plants were more salt tolerant. This correlation was less pronounced when plants were grown under severe salt stress conditions. Subsequent genome wide association study (GWAS) revealed associations with novel candidate genes for salinity tolerance such as LRR-KISS (At4g08850),flowering locus KH-domain containing protein and a DUF1639-containing protein Accessions with high LRR-KISS expression developed larger rosettes under salt stress conditions. Further characterization of allelic variation in candidate genes identified in this study will provide more insight into mechanisms of salt stress tolerance due to enhanced shoot growth. PMID:26873976

  19. Natural variation in rosette size under salt stress conditions corresponds to developmental differences between Arabidopsis accessions and allelic variation in the LRR-KISS gene

    PubMed Central

    Julkowska, Magdalena M.; Klei, Karlijn; Fokkens, Like; Haring, Michel A.; Schranz, M. Eric; Testerink, Christa

    2016-01-01

    Natural variation among Arabidopsis accessions is an important genetic resource to identify mechanisms underlying plant development and stress tolerance. To evaluate the natural variation in salinity stress tolerance, two large-scale experiments were performed on two populations consisting of 160 Arabidopsis accessions each. Multiple traits, including projected rosette area, and fresh and dry weight were collected as an estimate for salinity tolerance. Our results reveal a correlation between rosette size under salt stress conditions and developmental differences between the accessions grown in control conditions, suggesting that in general larger plants were more salt tolerant. This correlation was less pronounced when plants were grown under severe salt stress conditions. Subsequent genome wide association study (GWAS) revealed associations with novel candidate genes for salinity tolerance such as LRR-KISS (At4g08850), flowering locus KH-domain containing protein and a DUF1639-containing protein. Accessions with high LRR-KISS expression developed larger rosettes under salt stress conditions. Further characterization of allelic variation in candidate genes identified in this study will provide more insight into mechanisms of salt stress tolerance due to enhanced shoot growth. PMID:26873976

  20. Ternary compound electrode for lithium cells

    DOEpatents

    Raistrick, Ian D.; Godshall, Ned A.; Huggins, Robert A.

    1982-01-01

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

  1. Ternary compound electrode for lithium cells

    DOEpatents

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

    1980-07-30

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

  2. Synthesis of nano-sized silicon from natural halloysite clay and its high performance as anode for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Zhou, Xiangyang; Wu, Lili; Yang, Juan; Tang, Jingjing; Xi, Lihua; Wang, Biao

    2016-08-01

    Recently, nanostructured Si has been intensively studied as a promising anode candidate for lithium ion batteries due to its ultrahigh capacity. However, the downsizing of Si to nanoscale dimension is often impeded by complicated and expensive methods. In this work, natural halloysite clay was utilized for the production of Si nanoparticles through selective acid etching and modified magnesiothermic reduction processes. The physical and chemical changes of these samples during the various processes have been analyzed. The as-prepared Hsbnd Si from halloysite clay is composed of many interconnected Si nanoparticles with an average diameter of 20-50 nm. Owing to the small size and porous nature, the Hsbnd Si nanoparticles exhibit a satisfactory performance as an anode for lithium ion batteries. Without further modification, a stable capacity over 2200 mAh g-1 at a rate of 0.2 C after 100 cycles and a reversible capacity above 800 mAh g-1 at a rate of 1 C after 1000 cycles can be obtained. As a result, this synthetic route is cost-effective and can be scaled up for mass production of Si nanoparticles, which may facilitate valuable utilization of halloysite clay and further commercial application of Si-based anode materials.

  3. 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.

  4. Tungsten carbide production from ore concentrates by molten salt-natural gas sparging treatment

    SciTech Connect

    Carnahan, T.G.; Kazonich, G.; Raddatz, A.E.

    1988-01-01

    The U.S. Bureau of Mines conducted a bench-scale study to delineate the important parameters in a three-step process to produce commercial-quality tungsten carbide (WC) directly from tungsten minerals. In the process, tungsten concentrates of wolframite or wolframite and scheelite are decomposed at 1,050{sup 0}C in a molten mixture of NcCl and Na{sub 2}SiO{sub 3} that forms two immiscible phases. Tungsten, as sodium tungstate, reports to the halide phase and is separated from the gangue constituents, which report to the silicate phase. After decanting to separate the two phases, natural gas is sparged into the molten halide phase a 1,070{sup 0}C. Submicrometer crystals of WC are initially produced. These crystals grow into thin triangular-shaped plates up to 100 {mu}m on a side or into popcorn-shaped conglomerates. Sparged WC was examined for its suitability for use in sintered carbide products. In physical evaluations, sparged WC ground to an average particle size of 1.52 {mu}m and compacted with 10 pct Co binder into standard 6-by 22-mm test bars had a density of 14.35 and a Rockwell A hardness of 89.6. This compared favorably with 14.39 and 89.7 respectively, for test bars made from a standard commercial 1.52-{mu}m WC powder. Test bars made from Bureau of Mines WC had no C'' porosity or eta phase.

  5. Endogenous siRNAs derived from a pair of natural cis-antisense transcripts regulate salt tolerance in Arabidopsis.

    PubMed

    Borsani, Omar; Zhu, Jianhua; Verslues, Paul E; Sunkar, Ramanjulu; Zhu, Jian-Kang

    2005-12-29

    In higher eukaryotes, miRNAs and siRNAs guide translational inhibition, mRNA cleavage, or chromatin regulation. We found that the antisense overlapping gene pair of Delta(1)-pyrroline-5-carboxylate dehydrogenase (P5CDH), a stress-related gene, and SRO5, a gene of unknown function, generates two types of siRNAs. When both transcripts are present, a 24-nt siRNA is formed by a biogenesis pathway dependent on DCL2, RDR6, SGS3, and NRPD1A. Initial cleavage of the P5CDH transcript guided by the 24-nt siRNA establishes a phase for the subsequent generation of 21-nt siRNAs by DCL1 and further cleavage of P5CDH transcripts. The expression of SRO5 is induced by salt, and this induction is required to initiate siRNA formation. Our data suggest that the P5CDH and SRO5 proteins are also functionally related, and that the P5CDH-SRO5 gene pair defines a mode of siRNA function and biogenesis that may be applied to other natural cis-antisense gene pairs in eukaryotic genomes. PMID:16377568

  6. Synthesis, characterization, thermolysis and performance evaluation studies on alkali metal salts of TABA and NTO.

    PubMed

    Kulkarni, P B; Purandare, G N; Nair, J K; Talawar, M B; Mukundan, T; Asthana, S N

    2005-03-17

    The lithium (Li) and potassium (K) salts of 3-nitro-1,2,4-triazol-5-one (NTO) and 2,4,6-trinitroanilino benzoic acid (TABA) were prepared and characterized during this work. The synthesis was carried out by addition of a solution of lithium/potassium hydroxide to the aqueous solution of NTO and TABA, respectively. The products were characterized by elemental analysis, metal content determination and Fourier Transform Infrared (FTIR) Spectrum. Differential scanning calorimetry (DSC) profile indicated that Li and K salts of NTO and TABA undergo exothermic decomposition in the temperature range of 257-360 degrees C suggesting their energetic nature. The thermo gravimetric (TG) weight loss pattern revealed loss of water for Li/K salts of NTO and TABA in the temperature range of 115-155 degrees C. Sensitivity results revealed that the compounds are insensitive to impact and friction (impact sensitivity--height of 50% explosion>170 cm and friction insensitivity up to 36 kg) stimuli despite even the parent molecule of NTO salts (NTO) being HEM in the hazard category of 1.1. The FTIR spectra of the gaseous products evolved during TGA of NTO and TABA salts indicated the release of NO2. The formation of products such as LiNCO and KNCO was also observed in case of NTO salts, whereas that of CO2 and NH containing products was indicated in case of TABA salts during this study. In order to assess the performance as energetic ballistic modifiers (EBMs), NTO and TABA salts were incorporated in the ammonium perchlorate-hydroxyl terminated polybutadiene (AP-HTPB) composite propellants. The potassium salts enhanced the burning rate of the propellant. The best catalytic effect was obtained with K-TABA salt, which increased the burning rate to the extent of approximately 81% as well as brought down the n-value to 0.15 (pressure 2-9 MPa). PMID:15752848

  7. Three-dimensional characterization of electrodeposited lithium microstructures using synchrotron X-ray phase contrast imaging.

    PubMed

    Eastwood, David S; Bayley, Paul M; Chang, Hee Jung; Taiwo, Oluwadamilola O; Vila-Comamala, Joan; Brett, Daniel J L; Rau, Christoph; Withers, Philip J; Shearing, Paul R; Grey, Clare P; Lee, Peter D

    2015-01-01

    The electrodeposition of metallic lithium is a major cause of failure in lithium batteries. The 3D microstructure of electrodeposited lithium 'moss' in liquid electrolytes has been characterised at sub-micron resolution for the first time. Using synchrotron X-ray phase contrast imaging we distinguish mossy metallic lithium microstructures from high surface area lithium salt formations by their contrasting X-ray attenuation. PMID:24898258

  8. Lithium-aluminum-iron electrode composition

    DOEpatents

    Kaun, Thomas D.

    1979-01-01

    A negative electrode composition is presented for use in a secondary electrochemical cell. The cell also includes an electrolyte with lithium ions such as a molten salt of alkali metal halides or alkaline earth metal halides that can be used in high-temperature cells. The cell's positive electrode contains a a chalcogen or a metal chalcogenide as the active electrode material. The negative electrode composition includes up to 50 atom percent lithium as the active electrode constituent in an alloy of aluminum-iron. Various binary and ternary intermetallic phases of lithium, aluminum and iron are formed. The lithium within the intermetallic phase of Al.sub.5 Fe.sub.2 exhibits increased activity over that of lithium within a lithium-aluminum alloy to provide an increased cell potential of up to about 0.25 volt.

  9. Surface characterization of the carbon cathode and the lithium anode of Li-O₂ batteries using LiClO₄ or LiBOB salts.

    PubMed

    Younesi, Reza; Hahlin, Maria; Edström, Kristina

    2013-02-01

    The surface compositions of a MnO₂ catalyst containing carbon cathode and a Li anode in a Li-O₂ battery were investigated using synchrotron-based photoelectron spectroscopy (PES). Electrolytes comprising LiClO₄ or LiBOB salts in PC or EC:DEC (1:1) solvents were used for this study. Decomposition products from LiClO₄ or LiBOB were observed on the cathode surface when using PC. However, no degradation of LiClO₄ was detected when using EC/DEC. We have demonstrated that both PC and EC/DEC solvents decompose during the cell cycling to form carbonate and ether containing compounds on the surface of the carbon cathode. However, EC/DEC decomposed to a lesser degree compared to PC. PES revealed that a surface layer with a thickness of at least 1-2 nm remained on the MnO₂ catalyst at the end of the charged state. It was shown that the detachment of Kynar binder influences the surface composition of both the carbon cathode and the Li anode of Li-O₂ cells. The PES results indicated that in the charged state the SEI on the Li anode is composed of PEO, carboxylates, carbonates, and LiClO₄ salt. PMID:23336349

  10. Novel pseudo-delocalized anions for lithium battery electrolytes.

    PubMed

    Jónsson, Erlendur; Armand, Michel; Johansson, Patrik

    2012-05-01

    A novel anion concept of pseudo-delocalized anions, anions with distinct positive and negative charge regions, has been studied by a computer aided synthesis using DFT calculations. With the aim to find safer and better performing lithium salts for lithium battery electrolytes two factors have been evaluated: the cation-anion interaction strength via the dissociation reaction LiAn ⇌ Li(+) + An(-) and the anion oxidative stability via a vertical ionisation from anion to radical. Based on our computational results some of these anions have shown promise to perform well as lithium salts for modern lithium batteries and should be interesting synthetic targets for future research. PMID:22441354

  11. Hydrogen, lithium, and lithium hydride production

    SciTech Connect

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

    2014-03-25

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

  12. Ionic liquid based lithium battery electrolytes: charge carriers and interactions derived by density functional theory calculations.

    PubMed

    Angenendt, Knut; Johansson, Patrik

    2011-06-23

    The solvation of lithium salts in ionic liquids (ILs) leads to the creation of a lithium ion carrying species quite different from those found in traditional nonaqueous lithium battery electrolytes. The most striking differences are that these species are composed only of ions and in general negatively charged. In many IL-based electrolytes, the dominant species are triplets, and the charge, stability, and size of the triplets have a large impact on the total ion conductivity, the lithium ion mobility, and also the lithium ion delivery at the electrode. As an inherent advantage, the triplets can be altered by selecting lithium salts and ionic liquids with different anions. Thus, within certain limits, the lithium ion carrying species can even be tailored toward distinct important properties for battery application. Here, we show by DFT calculations that the resulting charge carrying species from combinations of ionic liquids and lithium salts and also some resulting electrolyte properties can be predicted. PMID:21591707

  13. Lithium peroxide crystal clusters as a natural growth feature of discharge products in Li-O2 cells.

    PubMed

    Zakharchenko, Tatiana K; Kozmenkova, Anna Ya; Itkis, Daniil M; Goodilin, Eugene A

    2013-01-01

    The often observed and still unexplained phenomenon of the growth of lithium peroxide crystal clusters during the discharge of Li-O2 cells is likely to happen because of self-assembling Li2O2 platelets that nucleate homogeneously right after the intermediate formation of superoxide ions by a single-electron oxygen reduction reaction (ORR). This feature limits the rechargeability of Li-O2 cells, but at the same time it can be beneficial for both capacity improvement and gain in recharge rate if a proper liquid phase mediator can be found. PMID:24367744

  14. Charge carrier dynamics and relaxation in (polyethylene oxide-lithium-salt)-based polymer electrolyte containing 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide as ionic liquid.

    PubMed

    Karmakar, A; Ghosh, A

    2011-11-01

    In this paper we report the dynamics of charge carriers and relaxation in polymer electrolytes based on polyethylene oxide (PEO), lithium bis(trifluoromethylsulfonyl)imide (LiTFSI) and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (BMPTFSI) ionic liquid prepared by solution cast technique. It has been observed that the incorporation of BMPTFSI into PEO-LiTFSI electrolyte is an effective way for increasing the amorphous phase to a large extent. It has also been observed that both the glass transition and melting temperatures decrease with the increase of BMPTFSI concentration. The ionic conductivity of these polymer electrolytes increases with the increase of BMPTFSI concentration. The highest ionic conductivity obtained at 25 °C is ~3×10(-4) S cm(-1) for the electrolyte containing 60 wt % BMPTFSI and ethylene oxide (EO)/Li ratio of 20. The temperature dependence of the dc conductivity and the hopping frequency show Vogel-Tamman-Fulcher type behavior indicating a strong coupling between the ionic and the polymer chain segmental motions. The frequency dependence of the ac conductivity exhibits a power law with an exponent n which decreases with the increase of temperature. The scaling of the ac conductivity indicates that relaxation dynamics of charge carriers follows a common mechanism for all temperatures and BMPTFSI concentrations. We have also presented the electric modulus data which have been analyzed in the framework of a Havriliak-Negami equation and the shape parameters obtained by the analysis show slight temperature dependence, but change sharply with BMPTFSI concentration. The stretched exponent β obtained from Kohlrausch-Williams-Watts fit to the modulus data is much lower than unity signifying that the relaxation is highly nonexponential. The decay function obtained from analysis of experimental modulus data is highly asymmetric with time. PMID:22181434

  15. Novel hierarchically porous carbon materials obtained from natural biopolymer as host matrixes for lithium-sulfur battery applications.

    PubMed

    Zhang, Bin; Xiao, Min; Wang, Shuanjin; Han, Dongmei; Song, Shuqin; Chen, Guohua; Meng, Yuezhong

    2014-08-13

    Novel hierarchically porous carbon materials with very high surface areas, large pore volumes and high electron conductivities were prepared from silk cocoon by carbonization with KOH activation. The prepared novel porous carbon-encapsulated sulfur composites were fabricated by a simple melting process and used as cathodes for lithium sulfur batteries. Because of the large surface area and hierarchically porous structure of the carbon material, soluble polysulfide intermediates can be trapped within the cathode and the volume expansion can be alleviated effectively. Moreover, the electron transport properties of the carbon materials can provide an electron conductive network and promote the utilization rate of sulfur in cathode. The prepared carbon-sulfur composite exhibited a high specific capacity and excellent cycle stability. The results show a high initial discharge capacity of 1443 mAh g(-1) and retain 804 mAh g(-1) after 80 discharge/charge cycles at a rate of 0.5 C. A Coulombic efficiency retained up to 92% after 80 cycles. The prepared hierarchically porous carbon materials were proven to be an effective host matrix for sulfur encapsulation to improve the sulfur utilization rate and restrain the dissolution of polysulfides into lithium-sulfur battery electrolytes. PMID:25025228

  16. Lithium metal reduction of plutonium oxide to produce plutonium metal

    DOEpatents

    Coops, Melvin S.

    1992-01-01

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

  17. Chemical and morphological characteristics of lithium electrode surfaces

    NASA Technical Reports Server (NTRS)

    Yen, S. P. S.; Shen, D.; Vasquez, R. P.; Grunthaner, F. J.; Somoano, R. B.

    1981-01-01

    Lithium electrode surfaces were analyzed for chemical and morphological characteristics, using electron spectroscopy chemical analysis (ESCA) and scanning electron microscopy (SEM). Samples included lithium metal and lithium electrodes which were cycled in a 1.5 M lithium arsenic hexafluoride/two-methyl tetrahydrofuran electrolyte. Results show that the surface of the as-received lithium metal was already covered by a film composed of LiO2 and an Li2O/CO2 adduct with a thickness of approximately 100-200 A. No evidence of Ni3 was found. Upon exposure of the lithium electrode to a 1.5 M LiAsF6/2-Me-THF electrochemical environment, a second film was observed to form on the surface, consisting primarily of As, Si, and F, possibly in the form of lithium arsenic oxyfluorides or lithium fluorosilicates. It is suggested that the film formation may be attributed to salt degradation.

  18. Retrospective salt tectonics

    SciTech Connect

    Jackson, M.P.A.

    1996-12-31

    The conceptual breakthroughs in understanding salt tectonics can be recognized by reviewing the history of salt tectonics, which divides naturally into three parts: the pioneering era, the fluid era, and the brittle era. The pioneering era (1856-1933) featured the search for a general hypothesis of salt diapirism, initially dominated by bizarre, erroneous notions of igneous activity, residual islands, in situ crystallization, osmotic pressures, and expansive crystallization. Gradually data from oil exploration constrained speculation. The effects of buoyancy versus orogeny were debated, contact relations were characterized, salt glaciers were discovered, and the concepts of downbuilding and differential loading were proposed as diapiric mechanisms. The fluid era (1933-{approximately}1989) was dominated by the view that salt tectonics resulted from Rayleigh-Taylor instabilities in which a dense fluid overburden having negligible yield strength sinks into a less dense fluid salt layer, displacing it upward. Density contrasts, viscosity contrasts, and dominant wavelengths were emphasized, whereas strength and faulting of the overburden were ignored. During this era, palinspastic reconstructions were attempted; salt upwelling below thin overburdens was recognized; internal structures of mined diapirs were discovered; peripheral sinks, turtle structures, and diapir families were comprehended; flow laws for dry salt were formulated; and contractional belts on divergent margins and allochthonous salt sheets were recognized. The 1970s revealed the basic driving force of salt allochthons, intrasalt minibasins, finite strains in diapirs, the possibility of thermal convection in salt, direct measurement of salt glacial flow stimulated by rainfall, and the internal structure of convecting evaporites and salt glaciers. The 1980`s revealed salt rollers, subtle traps, flow laws for damp salt, salt canopies, and mushroom diapirs.

  19. Lithium nephrotoxicity.

    PubMed

    Azab, Abed N; Shnaider, Alla; Osher, Yamima; Wang, Dana; Bersudsky, Yuly; Belmaker, R H

    2015-12-01

    Reports of toxic effects on the kidney of lithium treatment emerged very soon after lithium therapy was introduced. Lithium-induced nephrogenic diabetes insipidus is usually self-limiting or not clinically dangerous. Some reports of irreversible chronic kidney disease and renal failure were difficult to attribute to lithium treatment since chronic kidney disease and renal failure exist in the population at large. In recent years, large-scale epidemiological studies have convincingly shown that lithium treatment elevates the risk of chronic kidney disease and renal failure. Most patients do not experience renal side effects. The most common side effect of polyuria only weakly predicts increasing creatinine or reduced kidney function. Among those patients who do experience decrease in creatinine clearance, some may require continuation of lithium treatment even as their creatinine increases. Other patients may be able to switch to a different mood stabilizer medication, but kidney function may continue to deteriorate even after lithium cessation. Most, but not all, evidence today recommends using a lower lithium plasma level target for long-term maintenance and thereby reducing risks of severe nephrotoxicity. PMID:26043842

  20. Expanding Mg-Zn hybrid chemistry: inorganic salt effects in addition reactions of organozinc reagents to trifluoroacetophenone and the implications for a synergistic lithium-magnesium-zinc activation.

    PubMed

    Armstrong, David R; Clegg, William; García-Álvarez, Pablo; Kennedy, Alan R; McCall, Matthew D; Russo, Luca; Hevia, Eva

    2011-07-18

    Numerous organic transformations rely on organozinc compounds made through salt-metathesis (exchange) reactions from organolithium or Grignard reagents with a suitable zinc precursor. By combining X-ray crystallography, NMR spectroscopy and DFT calculations, this study sheds new light on the constitution of the organometallic species involved in this important synthetic tool. Investigations into the metathesis reactions of equimolar amounts of Grignard reagents (RMgX) and ZnCl(2) in THF led to the isolation of novel magnesium-zinc hybrids, [{(thf)(2)Mg(μ-Cl)(3)ZnR}(2)] (R=Et, tBu, nBu or o-OMe-C(6)H(4)), which exhibit an unprecedented structural motif in mixed magnesium-zinc chemistry. Furthermore, theoretical modelling of the reaction of EtMgCl with ZnCl(2) reveals that formation of the mixed-metal compound is thermodynamically preferred to that of the expected homometallic products, RZnCl and MgCl(2). This study also assesses the alkylating ability of hybrid 3 towards the sensitive ketone trifluoroacetophenone, revealing a dramatic increase in the chemoselectivity of the reaction when LiCl is introduced as an additive. This observation, combined with recent related breakthroughs in synthesis, points towards the existence of a trilateral Li/Mg/Zn synergistic effect. PMID:21656589

  1. Lithium Ion Polymer Electrolyte Based on Pva-Pan

    NASA Astrophysics Data System (ADS)

    Genova, F. Kingslin Mary; Selvasekarapandian, S.; Rajeswari, N.; Devi, S. Siva; Karthikeyan, S.; Raja, C. Sanjeevi

    2013-07-01

    The polymer blend electrolytes based on polyvinylalcohol(PVA) and polyacrylonitrile (PAN) doped with lithium per chlorate (LiClO4) have been prepared by solution casting technique using DMF as solvent. The complex formation between blend polymer and the salt has been confirmed by Fourier transform infrared spectroscopy. The amorphous nature of the blend polymer electrolyte has been confirmed by X-ray diffraction analysis. The ionic conductivity of the prepared blend polymer electrolyte has been found by ac impedence spectroscopic analysis. The highest ionic conductivity has been found to be 5.0 X10-4 S cm -1 at room temperature for 92.5 PVA: 7.5PAN: 20 molecular wt. % of LiClO4. The effect of salt concentration on the conductivity of the blend polymer electrolyte has been discussed.

  2. Permeability of natural rock salt from the Waste Isolation Pilot Plant (WIPP) during damage evolution and healing

    SciTech Connect

    Pfeifle, T.W.

    1998-06-01

    The US Department of Energy has developed the Waste Isolation Pilot Plant (WIPP) in the bedded salt of southeastern New Mexico to demonstrate the safe disposal of radioactive transuranic wastes. Four vertical shafts provide access to the underground workings located at a depth of about 660 meters. These shafts connect the underground facility to the surface and potentially provide communication between lithologic units, so they will be sealed to limit both the release of hazardous waste from and fluid flow into the repository. The seal design must consider the potential for fluid flow through a disturbed rock zone (DRZ) that develops in the salt near the shafts. The DRZ, which forms initially during excavation and then evolves with time, is expected to have higher permeability than the native salt. The closure of the shaft openings (i.e., through salt creep) will compress the seals, thereby inducing a compressive back-stress on the DRZ. This back-stress is expected to arrest the evolution of the DRZ, and with time will promote healing of damage. This paper presents laboratory data from tertiary creep and hydrostatic compression tests designed to characterize damage evolution and healing in WIPP salt. Healing is quantified in terms of permanent reduction in permeability, and the data are used to estimate healing times based on considerations of first-order kinetics.

  3. Lithium ion battery with improved safety

    DOEpatents

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

    2006-04-11

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

  4. Review of lithium-ion technology

    SciTech Connect

    Levy, S.C.; Cieslak, W.R.

    1993-12-31

    The first practical use of graphite intercalation compounds (GIC) as battery anodes was reported in a 1981 patent by Basu in which a molten salt cell was described having a negative electrode that consisted of lithium intercalated in graphite. A second patent by Basu, issued in 1983, described an ambient temperature rechargeable system which also utilized lithium intercalated in graphite as the anode. Work in this area progressed at a low level, however, until interest was sparked in 1990 when Sony Corporation announced a new ``lithium-ion`` rechargeable cell containing a lithium ion intercalating carbon anode. These cells have the advantages of metallic lithium systems; i.e., high energy density, high voltage, and light weight, without the disadvantages of dendrite formation on charge and the safety considerations associated with metallic lithium. Materials other than carbon have been studied as intercalation anodes. Examples are Fe{sub 2}O{sub 3}, WO{sub 2} and TiS{sub 2}. Although these alternate anode materials are of interest academically and for specialty applications, they do not hold much promise for widespread general use due to their increased weight and lower cell voltage. Studies of cathode materials for lithium-ion systems have centered on the transition metal chalcogenides. A number of these materials are capable of reversibly intercalating lithium ions at a useful potential versus lithium. Both organic liquids and polymers are candidate electrolytes for this technology.

  5. Resource Assessment of the In-Place and Potentially Recoverable Deep Natural Gas Resource of the Onshore Interior Salt Basins, North Central and Northeastern Gulf of Mexico

    SciTech Connect

    Ernest A. Mancini; Donald A. Goddard

    2004-10-28

    The objectives of the study are: to perform resource assessment of the in-place deep (>15,000 ft) natural gas resource of the onshore interior salt basins of the North Central and Northeastern Gulf of Mexico areas through petroleum system identification, characterization and modeling and to use the petroleum system based resource assessment to estimate the volume of the in-place deep gas resource that is potentially recoverable and to identify those areas in the interior salt basins with high potential to recover commercial quantities of the deep gas resource. The principal research effort for Year 1 of the project is data compilation and petroleum system identification. The research focus for the first nine (9) months of Year 1 is on data compilation and for the remainder of the year the emphasis is on petroleum system identification.

  6. Method for forming thin composite solid electrolyte film for lithium batteries

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, Ganesan (Inventor); Attia, Alan I. (Inventor)

    1994-01-01

    A composite solid electrolyte film is formed by dissolving a lithium salt such as lithium iodide in a mixture of a first solvent which is a co-solvent for the lithium salt and a binder polymer such as polyethylene oxide and a second solvent which is a solvent for the binder polymer and has poor solubility for the lithium salt. Reinforcing filler such as alumina particles are then added to form a suspension followed by the slow addition of binder polymer. The binder polymer does not agglomerate the alumina particles. The suspension is cast into a uniform film.

  7. Method for forming thin composite solid electrolyte film for lithium batteries

    NASA Technical Reports Server (NTRS)

    Nagasubramanian, Ganesan (Inventor); Attia, Alan I. (Inventor)

    1997-01-01

    A composite solid electrolyte film is formed by dissolving a lithium salt such as lithium iodide in a mixture of a first solvent which is a cosolvent for the lithium salt and a binder polymer such as polyethylene oxide and a second solvent which is a solvent for the binder polymer and has poor solubility for the lithium salt. Reinforcing filler such as alumina particles are then added to form a suspension followed by the slow addition of binder polymer. The binder polymer does not agglomerate the alumina particles. The suspension is cast into a uniform film.

  8. Lithium batteries with organic slurry cathodes

    SciTech Connect

    Bruder, A.H.

    1986-04-01

    This patent describes a laminar electrical cell. This cell consists of a sheet of conductive plastic, a separator, a cathode consisting essentially of a slurry of dewatered MnO/sub 2/ and carbon particles in a solution of a lithium salt in a substantially anhydrous organic solvent between and in contact with the conductive plastic sheet and the separator with the solution permeating the separator. The slurry is free of any binder material, and a thin sheet of lithium is in contact with the separator. The separator being interposed between the cathode and the lithium sheet.

  9. 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.

  10. 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.

  11. [Lithium carbonate-induced hyperparathyroidism in a patient after removal of a parathyroid adenoma].

    PubMed

    Krysiak, Robert; Okopień, Bogusław

    2015-01-01

    Lithium compounds are widely used and effective drugs in the treatment of mood disorders. However, despite their efficacy, the use of lithium salts is limited by their narrow therapeutic window. Treatment with lithium salts may be associated with the risk of development of numerous adverse effects. Endocrine complications include: thyroid dysfunction, nephrogenic diabetes insipidus and hyperparathyroidism. Because symptoms of lithium-induced hyperparathyroidism may resemble those of the underlying disorder, hyperparathyroidism sometimes remains undetected. The pathogenic mechanism for parathyroid dysfunction in lithium-treated patients is still unclear. We report a patient who had undergone removal of a parathyroid adenoma and later developed lithium-induced hyperparathyroidism. Cessation of lithium treatment normalised parathyroid function. The described case suggests that patients with pre-existing parathyroid disorders may be particularly susceptible to the development of lithium-induced hyperparathyroidism. PMID:26094339

  12. Seed dispersal and seedling emergence in a created and a natural salt marsh on the Gulf of Mexico coast in Southwest Louisiana, U.S.A

    USGS Publications Warehouse

    Elsey-Quirk, T.; Middleton, B.A.; Proffitt, C.E.

    2009-01-01

    Early regeneration dynamics related to seed dispersal and seedling emergence can contribute to differences in species composition among a created and a natural salt marsh. The objectives of this study were to determine (1) whether aquatic and aerial seed dispersal differed in low and high elevations within a created marsh and a natural marsh and (2) whether seedling emergence was influenced by marsh, the presence of openings in the vegetation, and seed availability along the northern Gulf of Mexico coast. Aerial seed traps captured a greater quantity of seeds than aquatic traps. Several factors influenced aquatic and aerial seed dispersal in a created and a natural salt marsh, including distance from the marsh edge, cover of existing vegetation, and water depth. The natural marsh had a high seed density of Spartina alterniflora and Distichlis spicata, the low-elevation created marsh had a high seed density of S. alterniflora, and the high-elevation created marsh had a high seed density of Aster subulatus and Iva frutescens. The presence of adult plants and water depth above the marsh surface influenced seed density. In the natural marsh, openings in vegetation increased seedling emergence for all species, whereas in the low-elevation created marsh, S. alterniflora had higher seedling density under a canopy of vegetation. According to the early regeneration dynamics, the future vegetation in areas of the low-elevation created marsh may become similar to that in the natural marsh. In the high-elevation created marsh, vegetation may be upland fringe habitat dominated by high-elevation marsh shrubs and annual herbaceous species. ?? 2009 Society for Ecological Restoration International.

  13. Cooking without salt

    MedlinePlus

    ... flavor and nutrition. Plant-based foods -- carrots, spinach, apples, and peaches -- are naturally salt-free. Sun-dried ... types of pepper, including black, white, green, and red. Experiment with vinegars (white and red wine, rice ...

  14. Molten salt battery having inorganic paper separator

    DOEpatents

    Walker, Jr., Robert D.

    1977-01-01

    A high temperature secondary battery comprises an anode containing lithium, a cathode containing a chalcogen or chalcogenide, a molten salt electrolyte containing lithium ions, and a separator comprising a porous sheet comprising a homogenous mixture of 2-20 wt.% chrysotile asbestos fibers and the remainder inorganic material non-reactive with the battery components. The non-reactive material is present as fibers, powder, or a fiber-powder mixture.

  15. Technical report on galvanic cells with fused-salt electrolytes

    NASA Technical Reports Server (NTRS)

    Cairns, E. J.; Crouthamel, C. E.; Fischer, A. K.; Foster, M. S.; Hesson, J. C.; Johnson, C. E.; Shimotake, H.; Tevebaugh, A. D.

    1969-01-01

    Technical report is presented on sodium and lithium cells using fused salt electrolytes. It includes a discussion of the thermally regenerative galvanic cell and the secondary bimetallic cell for storage of electricity.

  16. Molten salt electrolyte battery cell with overcharge tolerance

    DOEpatents

    Kaun, Thomas D.; Nelson, Paul A.

    1989-01-01

    A molten salt electrolyte battery having an increased overcharge tolerance employs a negative electrode with two lithium alloy phases of different electrochemical potential, one of which allows self-discharge rates which permits battery cell equalization.

  17. Electrolyte Suitable for Use in a Lithium Ion Cell or Battery

    NASA Technical Reports Server (NTRS)

    McDonald, Robert C. (Inventor)

    2014-01-01

    Electrolyte suitable for use in a lithium ion cell or battery. According to one embodiment, the electrolyte includes a fluorinated lithium ion salt and a solvent system that solvates lithium ions and that yields a high dielectric constant, a low viscosity and a high flashpoint. In one embodiment, the solvent system includes a mixture of an aprotic lithium ion solvating solvent and an aprotic fluorinated solvent.

  18. Electroactive compositions with poly(arylene oxide) and stabilized lithium metal particles

    SciTech Connect

    Zhang, Zhengcheng; Yuan, Shengwen; Amine, Khalil

    2015-05-12

    An electroactive composition includes an anodic material; a poly(arylene oxide); and stabilized lithium metal particles; where the stabilized lithium metal particles have a size less than about 200 .mu.m in diameter, are coated with a lithium salt, are present in an amount of about 0.1 wt % to about 5 wt %, and are dispersed throughout the composition. Lithium secondary batteries including the electroactive composition along with methods of making the electroactive composition are also discussed.

  19. Fluid distribution in grain boundaries of natural fine-grained rock salt deformed at low shear stress: implications for rheology and transport properties

    NASA Astrophysics Data System (ADS)

    Desbois, G.; Urai, J. L.; De Bresser, J. H. P.

    2012-04-01

    We used a combination of broad ion beam (BIB) cross-sectioning and high resolution (cryogenic) SEM to image polished surfaces and corresponding pairs of fractured grain boundaries in an investigation of grain boundary (GB) microstructures and fluid distribution in naturally deformed halite from a salt glacier (Kum Quh, central Iran). At the scale of observations, four types of fluid or gas filled grain boundaries can be distinguished: (1) straight boundaries with thick (up to 10 µm) GB tubes (2) straight boundaries with narrow (about 50 nm) GB tubes (3) wavy (tens of µm wavelength) GB with isolated inclusions of a few µm, and (4) wavy (µm wavelength) GB with small (µm) isolated inclusions. Grain boundary fluid inclusions can have three types of morphologies: the inclusion of Type 1 is intruded completely in one grain, inclusion of Type 2 has its major part included in one grain with a minor part in the second grain and the inclusion of Type 3 is located in both grains. Solid second phases in GB are mainly euhedral anhydrite crystals. The mobility of the brine is shown after cutting the inclusions by BIB in vacuum and fine-grained halite forms efflorescence and precipitates on internal walls of inclusions. At cryogenic temperature, in-situ brine is seen as continuous film in GB of type (1) and (2), and in isolated inclusions in GB of type (3) and (4). The structure of halite-halite contact between isolated fluid inclusions in GB of type (3) and (4) is below the resolution of SEM. GB of type (3) and (4) are interpreted to have formed by healing of mobile fluid films. First results of deformation experiments on the same samples under shear stress corresponding to conditions of natural salt glacier, show very low strain rates (7.43x10-10 s-1 and 1x10-9 s-1), up to one order of magnitude below of expected strain rates by solution precipitation creep. Both microstructures and deformation experiments suggest interfacial energy-driven GB healing, in agreement with the

  20. RESOURCE ASSESSMENT OF THE IN-PLACE AND POTENTIALLY RECOVERABLE DEEP NATURAL GAS RESOURCE OF THE ONSHORE INTERIOR SALT BASINS, NORTH CENTRAL AND NORTHEASTERN GULF OF MEXICO

    SciTech Connect

    Ernest A. Mancini

    2004-04-16

    The University of Alabama and Louisiana State University have undertaken a cooperative 3-year, advanced subsurface methodology resource assessment project, involving petroleum system identification, characterization and modeling, to facilitate exploration for a potential major source of natural gas that is deeply buried (below 15,000 feet) in the onshore interior salt basins of the North Central and Northeastern Gulf of Mexico areas. The project is designed to assist in the formulation of advanced exploration strategies for funding and maximizing the recovery from deep natural gas domestic resources at reduced costs and risks and with minimum impact. The results of the project should serve to enhance exploration efforts by domestic companies in their search for new petroleum resources, especially those deeply buried (below 15,000 feet) natural gas resources, and should support the domestic industry's endeavor to provide an increase in reliable and affordable supplies of fossil fuels. The principal research effort for Year 1 of the project is data compilation and petroleum system identification. The research focus for the first nine (9) months of Year 1 is on data compilation and for the remainder of the year the emphasis is on petroleum system identification. The objectives of the study are: to perform resource assessment of the in-place deep (>15,000 ft) natural gas resource of the onshore interior salt basins of the North Central and Northeastern Gulf of Mexico areas through petroleum system identification, characterization and modeling and to use the petroleum system based resource assessment to estimate the volume of the in-place deep gas resource that is potentially recoverable and to identify those areas in the interior salt basins with high potential to recover commercial quantities of the deep gas resource. The project objectives will be achieved through a 3-year effort. First, emphasis is on petroleum system identification and characterization in the North

  1. Low temperature electrolytes for lithium/silver vanadium oxide cells

    NASA Technical Reports Server (NTRS)

    Tuhovak, Denise R.; Takeuchi, Esther S.

    1991-01-01

    Combinations of methyl formate (MF) and propylene carbonate (PC) using salt concentrations of 0.6 to 2.4 M, with lithium hexafluoroarsenate and lithium tetrafluoroborate in a five to one molar ratio, were investigated as electrolytes in lithium/silver vanadium oxide batteries. The composition of the electrolyte affected cell performance at low temperature, self-discharge and abuse resistance as characterized by short circuit and crush testing. The electrolyte that provided the best combination of good low temperature performance, low cell self-discharge and abuse resistance was 0.6 M salt in 10:90 PC/MF.

  2. Δ17O Isotopic Investigation of Nitrate Salts Found in Co-Occurrence with Naturally Formed Perchlorate in the Mojave Desert, California, USA and the Atacama Desert, Chile

    NASA Astrophysics Data System (ADS)

    Lybrand, R. A.; Parker, D.; Rech, J.; Prellwitz, J.; Michalski, G.

    2009-12-01

    Perchlorate is both a naturally occurring and manmade contaminant that has been identified in soil, groundwater and surface water. Perchlorate directly affects human health by interfering with iodide uptake in the thyroid gland, which may in turn lower the production of key hormones that are needed for proper growth and development. Until recently, the Atacama Desert, Chile was thought to be the only location where perchlorate salts formed naturally. Recent work has documented the occurrence of these salts in several semi-arid regions of the United States. This study identified putatively natural sources of perchlorate in the Mojave Desert of California. Soil samples were collected from six field sites varying in geologic age. The co-occurrence of perchlorate and nitrate in caliches from the Atacama Desert and soils from the Mojave Desert was also investigated. Although the former are richer in NO3-, near-ore-grade (~5%) deposits occur in the vicinity of Death Valley National Park. Weak but significant correlations exist between ClO4- and NO3- at both locations, but the perchlorate levels are much higher (up to 800 mg/kg) in the Chilean samples than in California (<25 mg/kg). Oxygen isotopes in the nitrate were examined to identify variation within the Mojave Desert field sites, and to compare with those in samples collected from the Atacama Desert. The Mojave Desert Δ17O values ranged from 7-13‰ and those from the Atacama were between 17-21‰. This isotopic analysis revealed a dominantly atmospheric origin for the Atacama nitrate salts, and a mixture between biological nitrate and atmospherically-derived nitrate for the Mojave samples. When corrected for the percentage of atmospheric nitrate measured in the Atacama samples, the Mojave samples still contain much lower perchlorate concentrations than would be expected if the occurrence of perchlorate correlated strictly with atmospherically derived nitrate. These results indicate that the variation in the

  3. Structural chemistry of new lithium bis(oxalato)borate solvates.

    PubMed

    Zavalij, Peter Y; Yang, Shoufeng; Whittingham, M Stanley

    2004-12-01

    Recently lithium bis(oxalato)borate, LiB(C2O4)2, has been proposed as an alternative lithium salt for the electrolyte in rechargeable batteries that do not contain explosive perchlorate, reactive fluoride or toxic arsenic. This lithium salt crystallizes in the form of solvates from such solvents as water, acetonitrile, acetone, dimethoxyethane, 1,3-dioxolane and ethylene carbonate. Their crystal structures were determined in order to explore the crystal chemistry of this lithium salt. It was found that most of the solvents consist of a lithium bis(oxalato)borate dimer in which the ligand acts as both a chelating and a bridging agent. Lithium has octahedral coordination that typically includes one or, less commonly, two solvent molecules. An exception to this rule is the ethylene carbonate solvate where the lithium is tetrahedrally surrounded exclusively by the solvent and bis(oxalato)borate plays the role of counter-ion only. The ethylene carbonate solvates were also studied for LiPF6 and LiAsF6 salts and they have similar structures to the bis(oxalato)borate tetrahedral complexes. PMID:15534382

  4. Lithium Ion Electrolytes and Lithium Ion Cells With Good Low Temperature Performance

    NASA Technical Reports Server (NTRS)

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

    2014-01-01

    There is provided in one embodiment of the invention an electrolyte for use in a lithium ion electrochemical cell. The electrolyte comprises a mixture of an ethylene carbonate (EC), an ethyl methyl carbonate (EMC), an ester cosolvent, and a lithium salt. The ester cosolvent comprises methyl propionate (MP), ethyl propionate (EP), methyl butyrate (MB), ethyl butyrate (EB), propyl butyrate (PB), or butyl butyrate (BB). The electrochemical cell operates in a temperature range of from about -60 C to about 60 C. In another embodiment there is provided a lithium ion electrochemical cell using the electrolyte of the invention.

  5. Lithium brines: A global perspective: Chapter 14

    USGS Publications Warehouse

    Munk, LeeAnn; Hynek, Scott; Bradley, Dwight C.; Boutt, David; Labay, Keith A.; Jochens, Hillary

    2016-01-01

    Lithium is a critical and technologically important element that has widespread use, particularly in batteries for hybrid cars and portable electronic devices. Global demand for lithium has been on the rise since the mid-1900s and is projected to continue to increase. Lithium is found in three main deposit types: (1) pegmatites, (2) continental brines, and (3) hydrothermally altered clays. Continental brines provide approximately three-fourths of the world’s Li production due to their relatively low production cost. The Li-rich brine systems addressed here share six common characteristics that provide clues to deposit genesis while also serving as exploration guidelines. These are as follows: (1) arid climate; (2) closed basin containing a salar (salt crust), a salt lake, or both; (3) associated igneous and/or geothermal activity; (4) tectonically driven subsidence; (5) suitable lithium sources; and (6) sufficient time to concentrate brine. Two detailed case studies of Li-rich brines are presented; one on the longest produced lithium brine at Clayton Valley, Nevada, and the other on the world’s largest producing lithium brine at the Salar de Atacama, Chile.

  6. Benzimidazole-derived anion for lithium-conducting electrolytes

    NASA Astrophysics Data System (ADS)

    Niedzicki, Leszek; Oledzki, Piotr; Bitner, Anna; Bukowska, Maria; Szczecinski, Przemyslaw

    2016-02-01

    In this work we announce new lithium salt of 5,6-dicyano-2-(trifluoromethyl)benzimidazolide (LiTDBI) designed for application in lithium conductive electrolytes. It was synthesized and completely characterized by NMR techniques. Studies show salt's thermal stability up to 270 °C and electrochemical stability in liquid solvents up to +4.7 V vs. metallic lithium anode. Basic characterization of electrolytes made with this salt show conductivity over 1 mS cm-1 and unusually high transference number at high concentrations (0.74 in EC:DMC 1:2 ratio mixture) along with low onset of conductivity peak. As a final proof of concept, cycling in half-cell was performed and electrolyte based on LiTDBI showed perfect capacity retention. Such properties show remarkable progress in creating efficient lithium-conducting electrolytes with use of weakly-coordinating anions.

  7. A case with reversible neurotoxicity after 2 years of dementia secondary to maintenance lithium treatment.

    PubMed

    Soriano-Barceló, Juan; Alonso, María Tajes; Traba, María Begoña Portela; Vilar, Alberte Araúxo; Kahn, David A

    2015-03-01

    Chronic neurotoxicity caused by lithium salts can be reversible or irreversible and may appear after years of treatment, even at serum levels considered within the usual therapeutic range. The authors present the case of a patient with bipolar disorder who developed dementia at the age of 54 after being treated with lithium carbonate at therapeutic levels for 4 years. Nevertheless, lithium treatment was continued. At age 56, the patient presented with an acute encephalopathy caused by toxic lithium levels, which resolved only after lithium carbonate was discontinued. Full recovery from the dementia, which had started 2 years earlier, occurred only after cessation of lithium. The authors conclude that when patients treated with lithium develop subacute cognitive impairment, the possibility of lithium toxicity should be considered, even if the serum levels are considered within the therapeutic range. A long duration of neurotoxicity associated with lithium treatment does not necessarily indicate an irreversible prognosis. PMID:25782766

  8. LMWOA (low molecular weight organic acid) exudation by salt marsh plants: Natural variation and response to Cu contamination

    NASA Astrophysics Data System (ADS)

    Mucha, Ana P.; Almeida, C. Marisa R.; Bordalo, Adriano A.; Vasconcelos, M. Teresa S. D.

    2010-06-01

    This work aimed to evaluate, in vitro, the capability of roots of two salt marsh plants to release low molecular weight organic acids (LMWOAs) and to ascertain whether Cu contamination would stimulate or not organic acids exudation. The sea rush Juncus maritimus and the sea-club rush Scirpus maritimus, both from the lower Douro river estuary (NW Portugal), were used. Plants were collected seasonally, four times a year in 2004, during low tide. After sampling, plant roots were washed for removal of adherent particles and immersed for 2 h in a solution that matched salinity (3) and pH (7.5) of the pore water from the same location to obtain plant exudates. In one of the seasons, similar experiments were carried out but spiking the solution with different amounts of Cu in order to embrace the range between 0 and 1600 nM. In the final solutions as well as in sediment pore water LMWOAs were determined by high performance liquid chromatography. Plants were able to release, in a short period of time, relatively high amounts of LMWOAs (oxalate, citrate, malate, malonate, and succinate). In the sediment pore water oxalate, succinate and acetate were also detected. Therefore, plant roots probably contributed to the presence of some of these organic compounds in pore water. Exudation differed between the plant species and also showed some seasonally variation, particularly for S. maritimus. The release of oxalate by J. maritimus increased with Cu increase in the media. However, exudation of the other LMWOAs did not seem to be stimulated by Cu contamination in the media. This fact is compatible with the existence of alternative internal mechanisms for Cu detoxification, as denoted by the fact that in media contaminated with Cu both plant species accumulated relatively high amounts (29-83%) of the initially dissolved Cu. This study expands our knowledge on the contribution of globally dominant salt marsh plants to the release of LMWOAs into the environment.

  9. [Fluoride in children saliva with its natural low intake in cases of fluoridated salt or water consumption].

    PubMed

    Popruzhenko, T V; Terekhova, T N

    2008-01-01

    Fluoride content dynamics in whole saliva in 3 groups of 5-6 year old children before and after meal. All children lived in the region with lov F-0,2 ppm in water, used fluoridated toothpaste and went to kindergartens. Children from group A (n=10) did not have other sources of F, group B children (n=10) drink one glass a day of F-water (1 ppm), participants from group C (n=11) eat F-salt 250+/-100 ppm. The F in saliva samples gathered prior to and following meal was determined. Before the meal children saliva in group A contains 0,058 ppm F, in group B - 0,078 ppm F, in group C - 0,074 ppm F. Saliva of group A children shows the increase of F after the meal (0,067 ppm), F decreases lower the starting point after the 5th minute (0,056 ppm) and restores to normal by minute 40. Group B showed the decrease of F right after the meal, lasting to minute 20 (0,060 ppm), than a small increase followed (0,063 ppm), and finally the restoration to normal by minute 50. In group C immediate raise of F (0,085 ppm) was noticed, by minute 10 - some decline (0,076 ppm), from minute 20 F rises to level 0,090 ppm, after that it is decreasing slowly, but by minute 60 remains higher tan the starting point (0, 076 ppm). Thus, F-salt use allows to raise a basic level of F, and also to positively change F dynamics in oral fluid during the risk period (after the meal intake). PMID:19156108

  10. Single-Ion Block Copoly(ionic liquid)s as Electrolytes for All-Solid State Lithium Batteries.

    PubMed

    Porcarelli, Luca; Shaplov, Alexander S; Salsamendi, Maitane; Nair, Jijeesh R; Vygodskii, Yakov S; Mecerreyes, David; Gerbaldi, Claudio

    2016-04-27

    Polymer electrolytes have been proposed as replacement for conventional liquid electrolytes in lithium-ion batteries (LIBs) due to their intrinsic enhanced safety. Nevertheless, the power delivery of these materials is limited by the concentration gradient of the lithium salt. Single-ion conducting polyelectrolytes represent the ideal solution since their nature prevents polarization phenomena. Herein, the preparation of a new family of single-ion conducting block copolymer polyelectrolytes via reversible addition-fragmentation chain transfer polymerization technique is reported. These copolymers comprise poly(lithium 1-[3-(methacryloyloxy)propylsulfonyl]-1-(trifluoromethylsulfonyl)imide) and poly(ethylene glycol) methyl ether methacrylate blocks. The obtained polyelectrolytes show low Tg values in the range of -61 to 0.6 °C, comparatively high ionic conductivity (up to 2.3 × 10(-6) and 1.2 × 10(-5) S cm(-1) at 25 and 55 °C, respectively), wide electrochemical stability (up to 4.5 V versus Li(+)/Li), and a lithium-ion transference number close to unity (0.83). Owing to the combination of all mentioned properties, the prepared polymer materials were used as solid polyelectrolytes and as binders in the elaboration of lithium-metal battery prototypes with high charge/discharge efficiency and excellent specific capacity (up to 130 mAh g(-1)) at C/15 rate. PMID:27043201

  11. Effect of electrode density on cycle performance and irreversible capacity loss for natural graphite anode in lithium ion batteries

    SciTech Connect

    Shim, Joongpyo; Striebel, Kathryn A.

    2002-12-02

    The effect of electrode thickness and density for unpressed and pressed natural graphite electrodes were studied using electrochemical characterization. Pressing the graphite electrode decreases the reversible capacity and the irreversible capacity loss during formation. As electrode density increased, the capacity retention at high rate increased until 0.9g/cm{sup 3}, and then decreased. The cycle performances of the pressed graphite electrodes were more stable than the unpressed one. Pressing graphite electrode affected on its electrochemical characterization such as irreversible capacity loss, high rate cycling and cycle performance.

  12. Transparent plastic scintillators for neutron detection based on lithium salicylate

    NASA Astrophysics Data System (ADS)

    Mabe, Andrew N.; Glenn, Andrew M.; Carman, M. Leslie; Zaitseva, Natalia P.; Payne, Stephen A.

    2016-01-01

    Transparent plastic scintillators with pulse shape discrimination containing 6Li salicylate have been synthesized by bulk polymerization with a maximum 6Li loading of 0.40 wt%. Photoluminescence and scintillation responses to gamma-rays and neutrons are reported herein. Plastics containing 6Li salicylate exhibit higher light yields and permit a higher loading of 6Li as compared to previously reported plastics based on lithium 3-phenylsalicylate. However, pulse shape discrimination performance is reduced in lithium salicylate plastics due to the requirement of adding more nonaromatic monomers to the polymer matrix as compared to those based on lithium 3-phenylsalicylate. Reduction in light yield and pulse shape discrimination performance in lithium-loaded plastics as compared to pulse shape discrimination plastics without lithium is interpreted in terms of energy transfer interference by the aromatic lithium salts.

  13. Integrated Salt Studies

    NASA Astrophysics Data System (ADS)

    Urai, Janos L.; Kukla, Peter A.

    2015-04-01

    The growing importance of salt in the energy, subsurface storage, and chemical and food industries also increases the challenges with prediction of geometries, kinematics, stress and transport in salt. This requires an approach, which integrates a broader range of knowledge than is traditionally available in the different scientific and engineering disciplines. We aim to provide a starting point for a more integrated understanding of salt, by presenting an overview of the state of the art in a wide range of salt-related topics, from (i) the formation and metamorphism of evaporites, (ii) rheology and transport properties, (iii) salt tectonics and basin evolution, (iv) internal structure of evaporites, (v) fluid flow through salt, to (vi) salt engineering. With selected case studies we show how integration of these domains of knowledge can bring better predictions of (i) sediment architecture and reservoir distribution, (ii) internal structure of salt for optimized drilling and better cavern design, (iii) reliable long-term predictions of deformations and fluid flow in subsurface storage. A fully integrated workflow is based on geomechanical models, which include all laboratory and natural observations and links macro- and micro-scale studies. We present emerging concepts for (i) the initiation dynamics of halokinesis, (ii) the rheology and deformation of the evaporites by brittle and ductile processes, (iii) the coupling of processes in evaporites and the under- and overburden, and (iv) the impact of the layered evaporite rheology on the structural evolution.

  14. Lithium in 2012

    USGS Publications Warehouse

    Jaskula, B.W.

    2013-01-01

    In 2012, estimated world lithium consumption was about 28 kt (31,000 st) of lithium contained in minerals and compounds, an 8 percent increase from that of 2011. Estimated U.S. consumption was about 2 kt (2,200 st) of contained lithium, the same as that of 2011. The United States was thought to rank fourth in consumption of lithium and remained the leading importer of lithium carbonate and the leading producer of value-added lithium materials. One company, Rockwood Lithium Inc., produced lithium compounds from domestic brine resources near Silver Peak, NV.

  15. A new application of high-efficient silver salts-based photocatalyst under natural indoor weak light for wastewater cleaning.

    PubMed

    Hua, Xia; Teng, Fei; Zhao, Yunxuan; Xu, Juan; Xu, Chuangye; Yang, Yang; Zhang, Qiqi; Paul, Shashi; Zhang, Yi; Chen, Mindong; Zhao, Xudong

    2015-09-15

    As a high-quantum-efficiency photocatalyst, the serious photo-corrosion of silver phosphate (Ag3PO4), limits the practical applications in water purification and challenges us. Herein, Ag3PO4 is found to have a high stability under natural indoor weak light irradiation, suggesting that we can employ it by adopting a new application strategy. In our studies, rhodamine B (RhB, cationic dye), methyl orange (MO, anionic dye) and RhB-MO mixture aqueous solutions are used as the probing reaction for the degradation of organic wastewater. It is found that RhB, MO and RhB-MO can be completely degraded after 28 h under natural indoor weak light irradiation, indicating that multi-component organic contaminants can be efficiently degraded by Ag3PO4 under natural indoor weak light irradiation. The density of natural indoor weak light is measured to be 72cd, which is merely one-thousandth of 300 W xenon lamp (68.2 × 10(3)cd). Most importantly, Ag3PO4 shows a high stability under natural indoor weak light irradiation, demonstrated by the formation of fairly rare Ag. Furthermore, we also investigate the influence of inorganic ions on organic dyes degradation. It shows that the Cl(-) and Cr(6+) ions with high concentrations in wastewater have significantly decreased the degradation rate. From the viewpoint of energy saving and stability, this study shows us that we can utilize the Ag-containing photocatalysts under natural indoor weak light, which could be extended to indoor air cleaning process. PMID:26107659

  16. Arctic Sea Salt Aerosol from Blowing Snow and Sea Ice Surfaces - a Missing Natural Source in Winter

    NASA Astrophysics Data System (ADS)

    Frey, M. M.; Norris, S. J.; Brooks, I. M.; Nishimura, K.; Jones, A. E.

    2015-12-01

    Atmospheric particles in the polar regions consist mostly of sea salt aerosol (SSA). SSA plays an important role in regional climate change through influencing the surface energy balance either directly or indirectly via cloud formation. SSA irradiated by sunlight also releases very reactive halogen radicals, which control concentrations of ozone, a pollutant and greenhouse gas. However, models under-predict SSA concentrations in the Arctic during winter pointing to a missing source. It has been recently suggested that salty blowing snow above sea ice, which is evaporating, to be that source as it may produce more SSA than equivalent areas of open ocean. Participation in the 'Norwegian Young Sea Ice Cruise (N-ICE 2015)' on board the research vessel `Lance' allowed to test this hypothesis in the Arctic sea ice zone during winter. Measurements were carried out from the ship frozen into the pack ice North of 80º N during February to March 2015. Observations at ground level (0.1-2 m) and from the ship's crows nest (30 m) included number concentrations and size spectra of SSA (diameter range 0.3-10 μm) as well as snow particles (diameter range 50-500 μm). During and after blowing snow events significant SSA production was observed. In the aerosol and snow phase sulfate is fractionated with respect to sea water, which confirms sea ice surfaces and salty snow, and not the open ocean, to be the dominant source of airborne SSA. Aerosol shows depletion in bromide with respect to sea water, especially after sunrise, indicating photochemically driven release of bromine. We discuss the SSA source strength from blowing snow in light of environmental conditions (wind speed, atmospheric turbulence, temperature and snow salinity) and recommend improved model parameterisations to estimate regional aerosol production. N-ICE 2015 results are then compared to a similar study carried out previously in the Weddell Sea during the Antarctic winter.

  17. Effects of electrolyte salts on the performance of Li-O2 batteries

    SciTech Connect

    Nasybulin, Eduard N.; Xu, Wu; Engelhard, Mark H.; Nie, Zimin; Burton, Sarah D.; Cosimbescu, Lelia; Gross, Mark E.; Zhang, Jiguang

    2013-02-05

    It is well known that the stability of nonaqueous electrolyte is critical for the rechargeable Li-O2 batteries. Although stability of many solvents used in the electrolytes has been investigated, considerably less attention has been paid to the stability of electrolyte salt which is the second major component. Herein, we report the systematic investigation of the stability of seven common lithium salts in tetraglyme used as electrolytes for Li-O2 batteries. The discharge products of Li-O2 reaction were analyzed by X-ray diffraction, X-ray photoelectron spectroscopy and nuclear magnetic resonance spectroscopy. The performance of Li-O2 batteries was strongly affected by the salt used in the electrolyte. Lithium tetrafluoroborate (LiBF4) and lithium bis(oxalato)borate (LiBOB) decompose and form LiF and lithium borates, respectively during the discharge of Li-O2 batteries. Several other salts, including lithium bis(trifluoromethane)sulfonamide (LiTFSI), lithium trifluoromethanesulfonate (LiTf), lithium hexafluorophosphate (LiPF6), lithium perchlorate (LiClO4) , and lithium bromide (LiBr) led to the discharge products which mainly consisted of Li2O2 and only minor signs of decomposition of LiTFSI, LiTf, LPF6 and LiClO4 were detected. LiBr showed the best stability during the discharge process. As for the cycling performance, LiTf and LiTFSI were the best among the studied salts. In addition to the instability of lithium salts, decomposition of tetraglyme solvent was a more significant factor contributing to the limited cycling stability. Thus a more stable nonaqueous electrolyte including organic solvent and lithium salt still need to be further developed to reach a fully reversible Li-O2 battery.

  18. Low-Cost Al2O3 Coating Layer As a Preformed SEI on Natural Graphite Powder To Improve Coulombic Efficiency and High-Rate Cycling Stability of Lithium-Ion Batteries.

    PubMed

    Feng, Tianyu; Xu, Youlong; Zhang, Zhengwei; Du, Xianfeng; Sun, Xiaofei; Xiong, Lilong; Rodriguez, Raul; Holze, Rudolf

    2016-03-01

    Coulombic efficiency especially in the first cycle, cycling stability, and high-rate performance are crucial factors for commercial Li-ion batteries (LIBs). To improve them, in this work, Al2O3-coated natural graphite powder was obtained through a low-cost and facile sol-gel method. Based on a comparison of various coated amounts, 0.5 mol % Al(NO3)3 (vs mole of graphite) could bring about a smooth Al2O3 coating layer with proper thickness, which could act as a preformed solid electrolyte interface (SEI) to reduce the regeneration of SEI and lithium-ions consumption during subsequent cycling. Furthermore, we examined the advantages of Al2O3 coating by relating energy levels in LIBs using density functional theory calculations. Owing to its proper bandgap and lithium-ion conduction ability, the coating layer performs the same function as a SEI does, preventing an electron from getting to the outer electrode surface and allowing lithium-ion transport. Therefore, as a preformed SEI, the Al2O3 coating layer reduces extra cathode consumption observed in commercial LIBs. PMID:26913475

  19. Comparative Study of Ether-Based Electrolytes for Application in Lithium-Sulfur Battery.

    PubMed

    Carbone, Lorenzo; Gobet, Mallory; Peng, Jing; Devany, Matthew; Scrosati, Bruno; Greenbaum, Steve; Hassoun, Jusef

    2015-07-01

    Herein, we report the characteristics of electrolytes using various ether-solvents with molecular composition CH3O[CH2CH2O]nCH3, differing by chain length, and LiCF3SO3 as the lithium salt. The electrolytes, considered as suitable media for lithium-sulfur batteries, are characterized in terms of thermal properties (TGA, DSC), lithium ion conductivity, lithium interface stability, cyclic voltammetry, self-diffusion properties of the various components, and lithium transference number measured by NMR. Furthermore, the electrolytes are characterized in lithium cells using a sulfur-carbon composite cathode by galvanostatic charge-discharge tests. The results clearly evidence the influence of the solvent chain length on the species mobility within the electrolytes that directly affects the behavior in lithium sulfur cell. The results may effectively contribute to the progress of an efficient, high-energy lithium-sulfur battery. PMID:26057152

  20. Lithium in drinking water and suicide mortality: interplay with lithium prescriptions

    PubMed Central

    Helbich, Marco; Leitner, Michael; Kapusta, Nestor D.

    2015-01-01

    Background Little is known about the effects of lithium intake through drinking water on suicide. This intake originates either from natural rock and soil elution and/or accumulation of lithium-based pharmaceuticals in ground water. Aims To examine the interplay between natural lithium in drinking water, prescribed lithium-based pharmaceuticals and suicide in Austria. Method Spatial Bayesian regressions for males, females and pooled suicide mortality rates were estimated. Results Although the expected inverse association between lithium levels in drinking water and suicide mortality was confirmed for males and for total suicide rates, the relationship for females was not significant. The models do not indicate that lithium from prescriptions, assumed to accumulate in drinking water, is related to suicide risk patterns either as an individual effect or as a moderator of lithium levels in drinking water. Gender-specific differences in risk factors and local risk hot spots are confirmed. Conclusions The findings do not support the hypotheses that lithium prescriptions have measureable protective effects on suicide or that they interact with lithium in drinking water. PMID:25953888

  1. Resource Assessment of the In-Place and Potentially Recoverable Deep Natural Gas Resource of the Onshore Interior Salt Basins, North Central and Northeastern Gulf of Mexico

    SciTech Connect

    Ernest A. Mancini

    2006-09-30

    The objectives of the study were: (1) to perform resource assessment of the thermogenic gas resources in deeply buried (>15,000 ft) natural gas reservoirs of the onshore interior salt basins of the north central and northeastern Gulf of Mexico areas through petroleum system identification, characterization and modeling; and (2) to use the petroleum system based resource assessment to estimate the volume of the deep thermogenic gas resource that is available for potential recovery and to identify those areas in the interior salt basins with high potential for this thermogenic gas resource. Petroleum source rock analysis and petroleum system characterization and modeling, including thermal maturation and hydrocarbon expulsion modeling, have shown that the Upper Jurassic Smackover Formation served as the regional petroleum source rock in the North Louisiana Salt Basin, Mississippi Interior Salt Basin, Manila Subbasin and Conecuh Subbasin. Thus, the estimates of the total hydrocarbons, oil, and gas generated and expelled are based on the assumption that the Smackover Formation is the main petroleum source rock in these basins and subbasins. The estimate of the total hydrocarbons generated for the North Louisiana Salt Basin in this study using a petroleum system approach compares favorably with the total volume of hydrocarbons generated published by Zimmermann (1999). In this study, the estimate is 2,870 billion barrels of total hydrocarbons generated using the method of Schmoker (1994), and the estimate is 2,640 billion barrels of total hydrocarbons generated using the Platte River software application. The estimate of Zimmermann (1999) is 2,000 to 2,500 billion barrels of total hydrocarbons generated. The estimate of gas generated for this basin is 6,400 TCF using the Platte River software application, and 12,800 TCF using the method of Schmoker (1994). Barnaby (2006) estimated that the total gas volume generated for this basin ranges from 4,000 to 8,000 TCF. Seventy

  2. [Use of metal salts for radioprotection of plants during radioactive pollution of the territory].

    PubMed

    Gudkov, I N; Kitsno, V E; Grisiuk, S N; Tkachenko, G M; Ivanova, E A; Saenko, K V; Gural'chuk, Zh Z

    1999-01-01

    The applying salts of some metals to radionuclide contaminated soddy-podzolic soil in the zone of Chernobyl nuclear power station or the spraying of plants by its solutions are showing the radioprotective effect (salts of iron, zinc, cobalt and manganese) and decreasing the uptake of 90Sr and 137Cs through roots (salts of zinc, manganese, boron, lithium, cobalt and copper). PMID:10366969

  3. Partitioning of Pb, Cd, and Cu in natural and disturbed salt marshes of eastern San Francisco Bay

    SciTech Connect

    Alai, M.; Fegan, N. . Dept. of Geological Sciences)

    1993-04-01

    Sediment from different marsh systems along eastern San Francisco Bay was analyzed to determine how metals are partitioned in different environments influenced by human activity. Human influences in the marshes may have altered the geochemical processes controlling the metal partitioning. The three marsh systems analyzed include a natural marsh (San Francisco Wildlife Refuge), a natural marsh influenced by landfill leachate (Triangle Marsh), and a disturbed marsh constructed of artificial fill (Hayward Landing). The trace metal concentrations were compared in: easily exchangeable, weakly acid soluble, reducible, and oxidizable fractions representing the sediment phases of: clays, carbonates, Mn or Fe oxyhydroxides, and sulfides or organic material, respectively. The sediment fractions were analyzed for Pb, Cd, and Cu. In all three marshes, the pattern of metal partitioning with depth is similar; however, there are some inconsistencies. The Pb, Cd, and Cu in the reducible fraction typically decrease with depth while the metals in the oxidizable fraction generally increase or remain approximately constant with depth. This data suggests that the partitioning of metals in all three environments is initially controlled by sorption of metals onto Mn or Fe oxyhydroxides at the surface and shifts to organic or sulfides as the sediments is buried and the environment becomes more reducing.

  4. Process for manufacturing a lithium alloy electrochemical cell

    DOEpatents

    Bennett, William R.

    1992-10-13

    A process for manufacturing a lithium alloy, metal sulfide cell tape casts slurried alloy powders in an organic solvent containing a dissolved thermoplastic organic binder onto casting surfaces. The organic solvent is then evaporated to produce a flexible tape removable adhering to the casting surface. The tape is densified to increase its green strength and then peeled from the casting surface. The tape is laminated with a separator containing a lithium salt electrolyte and a metal sulfide electrode to form a green cell. The binder is evaporated from the green cell at a temperature lower than the melting temperature of the lithium salt electrolyte. Lithium alloy, metal sulfide and separator powders may be tape cast.

  5. Strong tendency of homeotropic alignment and anisotropic lithium ion conductivity of sulfonate functionalized zwitterionic imidazolium ionic liquid crystals.

    PubMed

    Rondla, Rohini; Lin, Joseph C Y; Yang, C T; Lin, Ivan J B

    2013-09-17

    Here, we report the first attempt to investigate the liquid crystal (LC) behavior of SO3(-) functionalized imidazolium zwitterionic (SO3(-)ImZI) salts, which display homeotropic alignment on a glass slide without the aid of any aligning approach. Doping lithium salt to ImZI salts lowers the melting temperatures and raises the clearing temperatures substantially to form room temperature ImZILCs. Excellent anisotropic lithium ion conductivity is achieved; which is strengthened by their tendency for homeotropic alignment. PMID:24010889

  6. Lithium-associated hyperthyroidism.

    PubMed

    Siyam, Fadi F; Deshmukh, Sanaa; Garcia-Touza, Mariana

    2013-08-01

    Goiters and hypothyroidism are well-known patient complications of the use of lithium for treatment of bipolar disease. However, the occurrence of lithium-induced hyperthyroidism is a more rare event. Many times, the condition can be confused with a flare of mania. Monitoring through serial biochemical measurement of thyroid function is critical in patients taking lithium. Hyperthyroidism induced by lithium is a condition that generally can be controlled medically without the patient having to discontinue lithium therapy, although in some circumstances, discontinuation of lithium therapy may be indicated. We report on a patient case of lithium-associated hyperthyroidism that resolved after discontinuation of the medication. PMID:23948626

  7. Large natural pH, CO2 and O2 fluctuations in a temperate tidal salt marsh on diel, seasonal, and interannual time scales

    USGS Publications Warehouse

    Baumann, Hannes; Wallace, Ryan; Tagliaferri, Tristen N.; Gobler, Christopher J.

    2014-01-01

    Coastal marine organisms experience dynamic pH and dissolved oxygen (DO) conditions in their natural habitats, which may impact their susceptibility to long-term anthropogenic changes. Robust characterizations of all temporal scales of natural pH and DO fluctuations in different marine habitats are needed; however, appropriate time series of pH and DO are still scarce. We used multiyear (2008–2012), high-frequency (6 min) monitoring data to quantify diel, seasonal, and interannual scales of pH and DO variability in a productive, temperate tidal salt marsh (Flax Pond, Long Island, US). pHNBS and DO showed strong and similar seasonal patterns, with average (minimum) conditions declining from 8.2 (8.1) and 12.5 (11.4) mg l−1 at the end of winter to 7.6 (7.2) and 6.3 (2.8) mg l−1 in late summer, respectively. Concomitantly, average diel fluctuations increased from 0.22 and 2.2 mg l−1 (February) to 0.74 and 6.5 mg l−1 (August), respectively. Diel patterns were modulated by tides and time of day, eliciting the most extreme minima when low tides aligned with the end of the night. Simultaneous in situ pCO2 measurements showed striking fluctuations between ∼330 and ∼1,200 (early May), ∼2,200 (mid June), and ∼4,000 μatm (end of July) within single tidal cycles. These patterns also indicate that the marsh’s strong net heterotrophy influences its adjacent estuary by ‘outwelling’ acidified and hypoxic water during ebb tides. Our analyses emphasize the coupled and fluctuating nature of pH and DO conditions in productive coastal and estuarine environments, which have yet to be adequately represented by experiments.

  8. Lithium and magnesium isotopes fractionation by zone melting

    NASA Astrophysics Data System (ADS)

    Akimov, D. V.; Egorov, N. B.; Dyachenko, A. N.; Pustovalova, M. P.; Podoinikov, I. R.

    2016-06-01

    The process of changing isotopic composition of the lithium and magnesium salts was studied by using the process of zone melting. It was founded in the paper that the process of separation of the lithium isotopes is more effective than for magnesium isotopes when the conditions of process were the same. The coefficients of isotopes separation were calculated and have the next value: α = 1.006 for 26Mg isotope and α = 1.0022 for 6Li isotope.

  9. SEPARATION OF METAL SALTS BY ADSORPTION

    DOEpatents

    Gruen, D.M.

    1959-01-20

    It has been found that certain metal salts, particularly the halides of iron, cobalt, nickel, and the actinide metals, arc readily absorbed on aluminum oxide, while certain other salts, particularly rare earth metal halides, are not so absorbed. Use is made of this discovery to separate uranium from the rare earths. The metal salts are first dissolved in a molten mixture of alkali metal nitrates, e.g., the eutectic mixture of lithium nitrate and potassium nitrate, and then the molten salt solution is contacted with alumina, either by slurrying or by passing the salt solution through an absorption tower. The process is particularly valuable for the separation of actinides from lanthanum-group rare earths.

  10. High rate and stable cycling of lithium metal anode

    PubMed Central

    Qian, Jiangfeng; Henderson, Wesley A.; Xu, Wu; Bhattacharya, Priyanka; Engelhard, Mark; Borodin, Oleg; Zhang, Ji-Guang

    2015-01-01

    Lithium metal is an ideal battery anode. However, dendrite growth and limited Coulombic efficiency during cycling have prevented its practical application in rechargeable batteries. Herein, we report that the use of highly concentrated electrolytes composed of ether solvents and the lithium bis(fluorosulfonyl)imide salt enables the high-rate cycling of a lithium metal anode at high Coulombic efficiency (up to 99.1%) without dendrite growth. With 4 M lithium bis(fluorosulfonyl)imide in 1,2-dimethoxyethane as the electrolyte, a lithium|lithium cell can be cycled at 10 mA cm−2 for more than 6,000 cycles, and a copper|lithium cell can be cycled at 4 mA cm−2 for more than 1,000 cycles with an average Coulombic efficiency of 98.4%. These excellent performances can be attributed to the increased solvent coordination and increased availability of lithium ion concentration in the electrolyte. Further development of this electrolyte may enable practical applications for lithium metal anode in rechargeable batteries. PMID:25698340

  11. Phosphoryl-rich flame-retardant ions (FRIONs): towards safer lithium-ion batteries.

    PubMed

    Rectenwald, Michael F; Gaffen, Joshua R; Rheingold, Arnold L; Morgan, Alexander B; Protasiewicz, John D

    2014-04-14

    The functionalized catecholate, tetraethyl (2,3-dihydroxy-1,4-phenylene)bis(phosphonate) (H2 -DPC), has been used to prepare a series of lithium salts Li[B(DPC)(oxalato)], Li[B(DPC)2], Li[B(DPC)F2], and Li[P(DPC)3]. The phosphoryl-rich character of these anions was designed to impart flame-retardant properties for their use as potential flame-retardant ions (FRIONs), additives, or replacements for other lithium salts for safer lithium-ion batteries. The new materials were fully characterized, and the single-crystal structures of Li[B(DPC)(oxalato)] and Li[P(DPC)3] have been determined. Thermogravimetric analysis of the four lithium salts show that they are thermally stable up to around 200 °C. Pyrolysis combustion flow calorimetry reveals that these salts produce high char yields upon combustion. PMID:24615890

  12. Salt stress or salt shock: which genes are we studying?

    PubMed

    Shavrukov, Yuri

    2013-01-01

    Depending on the method of NaCl application, whether gradual or in a single step, plants may experience either salt stress or salt shock, respectively. The first phase of salt stress is osmotic stress. However, in the event of salt shock, plants suffer osmotic shock, leading to cell plasmolysis and leakage of osmolytes, phenomena that do not occur with osmotic stress. Patterns of gene expression are different in response to salt stress and salt shock. Salt stress initiates relatively smooth changes in gene expression in response to osmotic stress and a more pronounced change in expression of significant numbers of genes related to the ionic phase of salt stress. There is a considerable time delay between changes in expression of genes related to the osmotic and ionic phases of salt stress. In contrast, osmotic shock results in strong, rapid changes in the expression of genes with osmotic function, and fewer changes in ionic-responsive genes that occur earlier. There are very few studies in which the effects of salt stress and salt shock are described in parallel experiments. However, the patterns of changes in gene expression observed in these studies are consistently as described above, despite the use of diverse plant species. It is concluded that gene expression profiles are very different depending the method of salt application. Imposition of salt stress by gradual exposure to NaCl rather than salt shock with a single application of a high concentration of NaCl is recommended for genetic and molecular studies, because this more closely reflects natural incidences of salinity. PMID:23186621

  13. An Attempt to Asses Suitability of Middle-Poland Salt Domes for Natural Gas Storage / Ocena Przydatności Środkowopolskich Wysadów Solnych Do Magazynowania Gazu Ziemnego

    NASA Astrophysics Data System (ADS)

    Ślizowski, Jarosław; Urbańczyk, Kazimierz

    2012-11-01

    The aim of the paper is to assess geological conditions in Middle-Poland salt domes and their suitability for natural gas storage. The starting point to the assessment were statistical distributions of caverns depth and volume in Mogilno CUGS. The distributions were generalized to other domes using the part of anticline forms in the salt mirror surface. The expected average cavern volumes, depths with their standard deviations are evaluated. Storing capacity of the caverns and the risk of a borehole unsuitable for cavern location are also given.

  14. A diverse group of halophilic bacteria exist in Lunsu, a natural salt water body of Himachal Pradesh, India.

    PubMed

    Gupta, Sonika; Sharma, Parul; Dev, Kamal; Srivastava, Malay; Sourirajan, Anuradha

    2015-01-01

    Five halophilic bacterial isolates namely SS1, SS2, SS3, SS5 and SS8 were isolated from soil sediments of Lunsu, a salty water body. All the bacterial isolates showed growth in LB medium containing up to 8.7% NaCl, pH 7-8 and at temperature range of 30-37°C. The bacterial isolates SS1 and SS3 require at least 3.8% NaCl for their growth, indicating their strict halophilic nature. Interestingly, bacterial isolates SS2, SS5 and SS8 but not SS1 and SS3 exhibited growth in medium supplemented with KCl. Accordingly, Na(+) and K(+) ions were detected at 1.39 and 0.0035%, respectively in Lunsu water. All the bacterial isolates were analyzed by random amplification of polymorphic DNA (RAPD) using four different random primers and produced PCR fragments ranging from 0.1 to 5 kb in size. Phylogenetic tree based on RAPD finger prints showed that SS1 and SS3 formed one group, while SS2 and SS5 formed the second group, whereas SS8 was out group. Sequence analysis of 16S rDNA identified SS1 and SS3 as Halobacillus trueperi, SS2 as Shewanella algae, SS5 as Halomonas venusta, and SS8 as Marinomonas sp. were deposited in GenBank with accession numbers of KM260166, KF751761, KF751760, KF751762 and KF751763, respectively. This is the first report on the presence of diverse halophilic bacteria in the foot hills of Himalayas. PMID:26090321

  15. Dynamics of salt playa polygons

    NASA Astrophysics Data System (ADS)

    Goehring, L.; Fourrière, A.

    2014-12-01

    In natural salt playa or in evaporation pools for the salt extraction industry, one can sometimes see surprising regular structures formed by ridges of salt. These ridges connect together to form a self-organized network of polygons one to two meters in diameter, which we call salt polygons. Here we propose a mechanism based on porous media convection of salty water in soil to explain the formation and the scaling of the salt polygons. Surface evaporation causes a steady upward flow of salty water, which can cause precipitation near the surface. A vertical salt gradient then builds up in the porous soil, with heavy salt-saturated water lying over the less salty source water. This can drive convection when a threshold is reached, given by a critical Rayleigh number of about 7. We suggest that the salt polygons are the surface expression of the porous medium convection, with salt crystallizing along the positions of the convective downwellings. To study this instability directly, we developed a 2D analogue experiment using a Hele-Shaw cell filled with a porous medium saturated with a salt solution and heated from above. We perform a linear stability analysis of this system, and find that it is unstable to convection, with a most unstable wavelength that is set by a balance between salt diffusion and water evaporation. The Rayleigh number in our experiment is controlled by the particle size of our model soil, and the evaporation rate. We obtain results that scale with the observation of natural salt polygons. Using dye, we observe the convective movement of salty water and find downwelling convective plumes underneath the spots where surface salt ridges form, as shown in the attached figure.

  16. Performance and properties of arsenic passivated lithium-titanium disulfide cells

    NASA Technical Reports Server (NTRS)

    Yen, S. P. S.; Shen, D.; Fitzgerald, D.; Vasquez, R. P.; Somoano, R. B.

    1986-01-01

    In order to inhibit chemical degradation associated with the lithium-electrolyte interaction in ambient temperature lithium cells, an attempt was made to synthetically passivate the anode via ion implantation of arsenic. Solvent reduction is reduced although salt reaction with lithium is still present. The performance of the Li-TiS2 cell differs from those with standard electrodes, but further work is necessary to clarify the efficacy of this mode of passivation.

  17. A review of clinical trials of lithium in medicine.

    PubMed

    Yung, C Y

    1984-01-01

    Since the approval of lithium use in treatment of acute mania, there have been numerous clinical trials of lithium in medical and psychiatric disorders. This paper gives a brief review of the literature on lithium trials in approximately fourteen medical conditions. These are: hyperthyroidism, metabolizing thyroid cancer, syndrome of inappropriate secretion of antidiuretic hormone, premenstrual tension syndrome, anorexia nervosa, Felty's syndrome, chemotherapy-induced neutropenia, aplastic anemia, seborrheic dermatitis, eczematoid dermatitis, cyclic vomiting, diabetes mellitus and asthma. Most of the case reports cited showed the efficacy of the side effects from lithium salt in the management of the symptoms and signs of these disorders, however, well-designed and controlled studies give negative results. The positive results are reported in the group of disorders having an underlying subdromal affective syndrome such as premenstrual tension syndrome and anorexia nervosa. Other encouraging reports include the effect of lithium to induce leucocytosis in Felty's syndrome and chemotherapy-induced neutropenia. PMID:6395135

  18. All Solid State Rechargeable Lithium Batteries using Block Copolymers

    NASA Astrophysics Data System (ADS)

    Hallinan, Daniel; Balsara, Nitash

    2011-03-01

    The growing need for alternative energy and increased demand for mobile technology require higher density energy storage. Existing battery technologies, such as lithium ion, are limited by theoretical energy density as well as safety issues. Other battery chemistries are promising options for dramatically increasing energy density. Safety can be improved by replacing the flammable, reactive liquids used in existing lithium-ion battery electrolytes with polymer electrolytes. Block copolymers are uniquely suited for this task because ionic conductivity and mechanical strength, both important properties in battery formulation, can be independently controlled. In this study, lithium batteries were assembled using lithium metal as negative electrode, polystyrene-b-poly(ethylene oxide) copolymer with lithium salt as electrolyte, and a positive electrode. The positive electrode consisted of polymer electrolyte for ion conduction, carbon for electron conduction, and an active material. Batteries were charged and discharged over many cycles. The battery cycling results were compared to a conventional battery chemistry.

  19. 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.

  20. Improving Lithium Therapeutics by Crystal Engineering of Novel Ionic Cocrystals

    PubMed Central

    2013-01-01

    Current United States Food and Drug Administration (FDA)-approved lithium salts are plagued with a narrow therapeutic window. Recent attempts to find alternative drugs have identified new chemical entities, but lithium’s polypharmacological mechanisms for treating neuropsychiatric disorders are highly debated and are not yet matched. Thus, re-engineering current lithium solid forms in order to optimize performance represents a low cost and low risk approach to the desired therapeutic outcome. In this contribution, we employed a crystal engineering strategy to synthesize the first ionic cocrystals (ICCs) of lithium salts with organic anions. We are unaware of any previous studies that have assessed the biological efficacy of any ICCs, and encouragingly we found that the new speciation did not negatively affect established bioactivities of lithium. We also observed that lithium ICCs exhibit modulated pharmacokinetics compared to lithium carbonate. Indeed, the studies detailed herein represent an important advancement in a crystal engineering approach to a new generation of lithium therapeutics. PMID:24191685

  1. Lithium-aluminum-magnesium electrode composition

    DOEpatents

    Melendres, Carlos A.; Siegel, Stanley

    1978-01-01

    A negative electrode composition is presented for use in a secondary, high-temperature electrochemical cell. The cell also includes a molten salt electrolyte of alkali metal halides or alkaline earth metal halides and a positive electrode including a chalcogen or a metal chalcogenide as the active electrode material. The negative electrode composition includes up to 50 atom percent lithium as the active electrode constituent and a magnesium-aluminum alloy as a structural matrix. Various binary and ternary intermetallic phases of lithium, magnesium, and aluminum are formed but the electrode composition in both its charged and discharged state remains substantially free of the alpha lithium-aluminum phase and exhibits good structural integrity.

  2. Boric Ester-Type Molten Salt via Dehydrocoupling Reaction

    PubMed Central

    Matsumi, Noriyoshi; Toyota, Yoshiyuki; Joshi, Prerna; Puneet, Puhup; Vedarajan, Raman; Takekawa, Toshihiro

    2014-01-01

    Novel boric ester-type molten salt was prepared using 1-(2-hydroxyethyl)-3-methylimidazolium chloride as a key starting material. After an ion exchange reaction of 1-(2-hydroxyethyl)-3-methylimidazolium chloride with lithium (bis-(trifluoromethanesulfonyl) imide) (LiNTf2), the resulting 1-(2-hydroxyethyl)-3-methylimidazolium NTf2 was reacted with 9-borabicyclo[3.3.1]nonane (9-BBN) to give the desired boric ester-type molten salt in a moderate yield. The structure of the boric ester-type molten salt was supported by 1H-, 13C-, 11B- and 19F-NMR spectra. In the presence of two different kinds of lithium salts, the matrices showed an ionic conductivity in the range of 1.1 × 10−4–1.6 × 10−5 S cm−1 at 51 °C. This was higher than other organoboron molten salts ever reported. PMID:25405738

  3. Resource Assessment of the In-Place and Potentially Recoverable Deep Natural Gas Resource of the Onshore Interior Salt Basins, North Central and Northeastern Gulf of Mexico

    SciTech Connect

    Ernest A. Mancini; Donald A. Goddard

    2005-04-15

    The principal research effort for the first six months of Year 2 of the project has been petroleum system characterization. Understanding the burial and thermal maturation histories of the strata in the onshore interior salt basins of the North Central and Northeastern Gulf of Mexico areas is important in petroleum system characterization. The underburden and overburden rocks in these basins and subbasins are a product of their rift-related geohistory. Petroleum source rock analysis and thermal maturation and hydrocarbon expulsion modeling indicate that an effective regional petroleum source rock in the onshore interior salt basins, the North Louisiana Salt Basin, Mississippi Interior Salt Basin, Manila Subbasin and Conecuh Subbasin, was the Upper Jurassic Smackover lime mudstone. The Upper Cretaceous Tuscaloosa shale was an effective local petroleum source rock in the Mississippi Interior Salt Basin and a possible local source bed in the North Louisiana Salt Basin. Hydrocarbon generation and expulsion was initiated in the Early Cretaceous and continued into the Tertiary in the North Louisiana Salt Basin and the Mississippi Interior Salt Basin. Hydrocarbon generation and expulsion was initiated in the Late Cretaceous and continued into the Tertiary in the Manila Subbasin and Conecuh Subbasin. Reservoir rocks include Jurassic, Cretaceous and Tertiary siliciclastic and carbonate strata. Seal rocks include Jurassic, Cretaceous and Tertiary anhydrite and shale beds. Petroleum traps include structural and combination traps.

  4. Hartmannibacter diazotrophicus gen. nov., sp. nov., a phosphate-solubilizing and nitrogen-fixing alphaproteobacterium isolated from the rhizosphere of a natural salt-meadow plant.

    PubMed

    Suarez, Christian; Ratering, Stefan; Geissler-Plaum, Rita; Schnell, Sylvia

    2014-09-01

    A phosphate-mobilizing, Gram-negative bacterium was isolated from rhizospheric soil of Plantago winteri from a natural salt meadow as part of an investigation of rhizospheric bacteria from salt-resistant plant species and evaluation of their plant-growth-promoting abilities. Cells were rods, motile, strictly aerobic, oxidase-positive and catalase-negative. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain E19(T) was distinct from other taxa within the class Alphaproteobacteria. Strain E19(T) showed less than 93.5 % 16S rRNA gene sequence similarity with members of the genera Rhizobium (≤93.5 %), Labrenzia (≤93.1 %), Stappia (≤93.1 %), Aureimonas (≤93.1 %) and Mesorhizobium (≤93.0 %) and was most closely related to Rhizobium rhizoryzae (93.5 % 16S rRNA gene sequence similarity to the type strain). The sole respiratory quinone was Q-10, and the polar lipids comprised phosphatidylglycerol, phosphatidylcholine, phosphatidylethanolamine, an aminolipid and an unidentified phospholipid. Major fatty acids were C18 : 1ω7c (71.4 %), summed feature 2 (C14 : 0 3-OH and/or iso-C16 : 1; 8.3 %), C20 : 0 (7.9 %) and C16 : 0 (6.1 %). The DNA G+C content of strain E19(T) was 59.9±0.7 mol%. The capacity for nitrogen fixation was confirmed by the presence of the nifH gene and the acetylene reduction assay. On the basis of the results of our polyphasic taxonomic study, the new isolate represents a novel genus and species, for which the name Hartmannibacter diazotrophicus gen. nov., sp. nov. is proposed. The type strain of Hartmannibacter diazotrophicus is E19(T) ( = LMG 27460(T) = KACC 17263(T)). PMID:24961682

  5. Immobilization of IFR salt wastes in mortar

    SciTech Connect

    Fischer, D.F.; Johnson, T.R.

    1988-01-01

    Portland cement-base mortars are being considered for immobilizing chloride salt wastes produced by the fuel cycles of Integral Fast Reactors (IFR). The IFR is a sodium-cooled fast reactor with metal alloy fuels. It has a close-coupled fuel cycle in which fission products are separated from the actinides in an electrochemical cell operating at 500/degree/C. This cell has a liquid cadmium anode in which the fuels are dissolved and a liquid salt electrolyte. The salt will be a mixture of either lithium, potassium, and sodium chlorides or lithium, calcium, barium, and sodium chlorides. One method being considered for immobilizing the treated nontransuranic salt waste is to disperse the salt in a portland cement-base mortar that will be sealed in corrosion-resistant containers. For this application, the grout must be sufficiently fluid that it can be pumped into canister-molds where it will solidify into a strong, leach-resistant material. The set times must be longer than a few hours to allow sufficient time for processing, and the mortar must reach a reasonable compressive strength (/approximately/7 MPa) within three days to permit handling. Because fission product heating will be high, about 0.6 W/kg for a mortar containing 10% waste salt, the effects of elevated temperatures during curing and storage on mortar properties must be considered.

  6. Conductive polymeric compositions for lithium batteries

    DOEpatents

    Angell, Charles A.; Xu, Wu

    2009-03-17

    Novel chain polymers comprising weakly basic anionic moieties chemically bound into a polyether backbone at controllable anionic separations are presented. Preferred polymers comprise orthoborate anions capped with dibasic acid residues, preferably oxalato or malonato acid residues. The conductivity of these polymers is found to be high relative to that of most conventional salt-in-polymer electrolytes. The conductivity at high temperatures and wide electrochemical window make these materials especially suitable as electrolytes for rechargeable lithium batteries.

  7. Electrochemical analysis of lithium polymer batteries

    NASA Astrophysics Data System (ADS)

    Han, Yong-Bong

    Lithium batteries consist of lithium anode, polymer electrolyte separator, and the porous, composite cathode. Lithium batteries have been very attractive to the battery industries because lithium metal has an extremely high energy density. The use of lithium metal can cause dendrite formation by uneven electro-deposition during charge. The lithium battery can explode in a liquid electrolyte when it is shorted by the dendrite. It has been reported that the mechanical properties of a polymer electrolyte can retard the dendrite initiation. We have attempted to study the dendrite initiation quantitatively by developing a mathematical model that evaluates the behavior of the interface and by performing dendrite-initiation experiments with the use of cross-linked polymer electrolytes to vary the mechanical properties of the electrolyte. Cross-linking the polymer backbone may decrease the transport properties of the polymer electrolyte. The transport properties are diffusion coefficient, ionic conductivity, and transference number of the electrolyte. When poor transport properties of the polymer electrolyte cause salt depletion at the cathode at low salt concentrations, side reactions and dendrite initiation can be accelerated. In order to study how cross-linking the polymer backbone affects the transport properties, the transport properties are measured experimentally by LBNL method which is based on concentrated solution theory. Porous electrodes are commonly used as the cathode in lithium battery systems. Because the electrochemical reaction occurs at the active particles in the porous, composite cathode during charge and discharge, the kinetics of the electrochemical reaction at the active particles in the cathode affects the battery performance. AC impedance has been broadly used to study the kinetics of the electrochemical reaction in the cathode. However, the AC impedance spectra have been analyzed by regarding the porous cathode as a planar electrode by most

  8. Resource Assessment of the In-Place and Potentially Recoverable Deep Natural Gas Resource of the Onshore Interior Salt Basins, North Central and Northeastern Gulf of Mexico

    SciTech Connect

    Ernest A. Mancini; Paul Aharon; Donald A. Goddard; Roger Barnaby

    2005-10-28

    The principal research effort for Year 2 of the project has been petroleum system characterization and modeling. Understanding the burial, thermal maturation, and hydrocarbon expulsion histories of the strata in the onshore interior salt basins of the North Central and Northeastern Gulf of Mexico areas is important in hydrocarbon resource assessment. The underburden and overburden rocks in these basins and subbasins are a product of their rift-related geohistory. Petroleum source rock analysis and initial thermal maturation and hydrocarbon expulsion modeling indicated that an effective regional petroleum source rock in the onshore interior salt basins and subbasins, the North Louisiana Salt Basin, Mississippi Interior Salt Basin, Manila Subbasin and Conecuh Subbasin, was Upper Jurassic Smackover lime mudstone. The initial modeling also indicated that hydrocarbon generation and expulsion were initiated in the Early Cretaceous and continued into the Tertiary in the North Louisiana Salt Basin and the Mississippi Interior Salt Basin and that hydrocarbon generation and expulsion were initiated in the Late Cretaceous and continued into the Tertiary in the Manila Subbasin and Conecuh Subbasin. Refined thermal maturation and hydrocarbon expulsion modeling and additional petroleum source rock analysis have confirmed that the major source rock in the onshore interior salt basins and subbasins is Upper Jurassic Smackover lime mudstone. Hydrocarbon generation and expulsion were initiated in the Early to Late Cretaceous and continued into the Tertiary.

  9. Novel solid polymer electrolytes based on poly(trimethylene carbonate) and lithium hexafluoroantimonate

    NASA Astrophysics Data System (ADS)

    Manuela Silva, Maria; Barbosa, Paula; Evans, Alan; Smith, Michael John

    2006-11-01

    The results of the characterization of a polymer electrolyte system based on the poly(trimethylene carbonate) host matrix, with lithium hexafluoroantimonate as guest salt, are described in this study. Electrolytes with lithium salt compositions with values of n between 5 and 100 (where n represents the total number of monomeric cation-coordinating units sbnd (O dbnd COCH 2CH 2CH 2O) sbnd per lithium ion) were prepared by co-dissolution and deposition from acetonitrile. The solvent-casting technique was used to prepare flexible, transparent and self-supporting films of electrolytes which were characterized by measurements of conductivity, cyclic voltammetry, differential scanning calorimetry and thermogravimetry.

  10. Equilibrium distribution of lanthanum, neodymium, and thorium between lithium chloride melt and liquid bismuth

    NASA Astrophysics Data System (ADS)

    Zagnit'ko, A. V.; Ignat'ev, V. V.

    2013-04-01

    The distribution of lanthanum, neodymium, and thorium between a lithium chloride melt and liquid bismuth with additions of lithium as a reducing agent are investigated at 650°C. Equilibrium values of their distribution constants are measured. It is shown that in contrast to neodymium and lanthanum, thorium cannot be extracted from bismuth into lithium chloride. This allows us to propose an efficient scheme for separating lanthanides and thorium in a system for the extraction of fuel salts in molten-salt nuclear reactors.

  11. Remote Estimation of Salt Marsh Biophysical Parameters in the Georgia Coast: Model Cal/Val using NASA Sensors to Improve Monitoring and Restoration Efforts by the Georgia Department of Natural Resources

    NASA Astrophysics Data System (ADS)

    White, J. A.; Padgett-Vasquez, S.; Ghosh, S.; Baruch, A.; Chen, N.; Mote, J.; Mishra, D. R.

    2013-12-01

    Salt marshes are highly productive ecosystems that provide habitat and nutrition to wildlife, offer protection from flooding and storm surges, and help filter polluted run-off from upland areas. This study demonstrates the ability to identify ';hotspots' of early stages of marsh degradation which can only be delineated by evaluating marsh biophysical characteristics including distribution of chlorophyll content (Chl), leaf area index (LAI) (a ratio of green foliage area vs. ground area), and green vegetation fraction (VF) (percent green canopy cover). These biophysical characteristics are primary indicators of photosynthetic capacity, nitrogen content, and physiological status of vegetation. Through use of NASA's Moderate Resolution Imaging Spectroradiometer (MODIS) sensor, we retrieve the above described biophysical characteristics in Georgia salt marshes. This work is significant because it allows for the first time the use of NASA satellite data to study the biophysical characteristics of salt marshes along Georgia's coast. Our results show an efficient and non-destructive biophysical mapping protocol for emergent wetlands to be used in restoration decision-making by the Georgia Department of Natural Resources. Our primary objectives are (1) to calibrate and validate a range of MODIS-based vegetation indices (VIs) and develop prototype weekly and monthly composites of the salt marsh biophysical characteristics for the coast of Georgia from 2000 through 2013, for the growing season (March-November) and (2) to perform a time-series analysis, with map products developed from MODIS imagery, to study the overall trend of salt marsh productivity during the last decade. These VIs (NDVI, WDRVI, EVI2, SAVI, and VARI) have been widely used and tested for monitoring terrestrial vegetation, but not for salt marsh ecosystems.

  12. Veins in Paleo-reservoir as a Natural Indication of Coupled Changes in Pore Pressure and Stress, Salt Wash Graben of SE Utah, USA

    NASA Astrophysics Data System (ADS)

    Gwon, S.; Edwards, P.; Kim, Y. S.

    2015-12-01

    Hydrofracturing associated with elevated fluid pressure coupled with changes in stress has been crucial in enhancing the production and recovery of hydrocarbons. Furthermore, it is also an important issue to access the efficiency and stability of long-term CO2 geologic storage reservoirs. Veins are mineral-filled extension fractures developed along the plane of σ1-σ2 and perpendicular to σ3, and the fluid pressure must exceed σ3applied to the plane when the vein opens. Therefore, vein is a well-known natural analogue for fluid migration in a paleo-reservoir. In the Salt Wash Graben of SE Utah, CO2-charged vein systems hosted in the bleached Entrada Formation are well developed and examined to understand the conditions of fluid pressure and stress during the injections of CO2-charged fluid. Based on color and relative cross-cutting relationship in the field, veins are subdivided into two sets; sub-vertical black mineral-rich veins and orthogonal calcite veins that have previously been described as 'grid-lock fractures'. The vein distribution and fluid leakage along through-going fractures in mechanic units allow us to determine the stress regime and driving stress condition through 3D-Mohr circle reconstruction. The results of this statistical analysis for the veins show that the orthogonal veins indicate a 'stress transition' with maximum principal stress direction changing from vertical to NNW-SSE sub-horizontal which coincides with the current regional stress regime. The possible causes of the stress transition can be considered. The process of repeated sealing, reactivation and localization of veins within the bleached zone is a natural indication of a coupled change in pore pressure and stress in the reservoir. Thus, an understanding of the effect of stress changes due to the volumetric injection of CO2 in the subsurface as well as a knowledge of how pre-existing fractures affect fluid flow with respect to elevated pore pressures in layered rocks are

  13. Trichloroacetic acid in the vegetation of polluted and remote areas of both hemispheres—Part II: salt lakes as novel sources of natural chlorohydrocarbons

    NASA Astrophysics Data System (ADS)

    Weissflog, Ludwig; Elansky, Nikolai; Putz, Erich; Krueger, Gert; Lange, Christian A.; Lisitzina, Lida; Pfennigsdorff, Andrea

    One of the issues provided for by the 1993 existing substances regulation (793/93/EEC) is the assessment of the environmental risk emanating from waste materials. One such material is the highly volatile substance perchloroethene (PER; TECE). PER is produced in large quantities all over the world by the chemical industry. There are many industrial processes in which PER escapes into the environment, especially the atmosphere. It has since been proven that after entering plants via the air/leaf pathway, airborne PER can be metabolised into the phytotoxic substance trichloroacetic acid. However our own studies detected relatively high levels of TCA in environmental compartments in regions far away from industry which cannot be explained by the anthropogenic input of airborne substances into the relevant ecosystems. This indicates that natural PER emittents also exist and must be identified, in order to find out more about the global spread of PER. This paper reports on the findings of related fieldwork in the Kalmykian Steppe. This area of steppe in southern Russia spans an area extending west-to-east from the Black Sea and the Caspian Sea and north-to-south between the Greater Caucasus and Volgograd. The main aim of the experiments in the Kalmykian Steppe was to study water from lakes, rivers and springs with differing levels of salinity. The concentrations of the chlorinated hydrocarbons (VCHCs) chloroform (CHCl 3), tetrachloromethane (CCl 4), 1,1,1-trichloroethane (1,1,1-C 2H 3Cl 3), trichloroethene (TRI; C 2HCl 3), tetrachloroethene (PER; C 2Cl 4) and TCA in these waters were measured, along with the levels of cations and anions and the pH-value of the waters. The measurements indicate that in particular water from salt lakes located in semiarid/arid areas of the study region must be considered as new types of natural emittents of PER and other chlorinated hydrocarbons as well as trichloroacetic acid. Furthermore, attention is drawn to ecological impacts

  14. Review of lithium effects on brain and blood.

    PubMed

    Young, Wise

    2009-01-01

    Clinicians have long used lithium to treat manic depression. They have also observed that lithium causes granulocytosis and lymphopenia while it enhances immunological activities of monocytes and lymphocytes. In fact, clinicians have long used lithium to treat granulocytopenia resulting from radiation and chemotherapy, to boost immunoglobulins after vaccination, and to enhance natural killer activity. Recent studies revealed a mechanism that ties together these disparate effects of lithium. Lithium acts through multiple pathways to inhibit glycogen synthetase kinase-3beta (GSK3 beta). This enzyme phosphorylates and inhibits nuclear factors that turn on cell growth and protection programs, including the nuclear factor of activated T cells (NFAT) and WNT/beta-catenin. In animals, lithium upregulates neurotrophins, including brain-derived neurotrophic factor (BDNF), nerve growth factor, neurotrophin-3 (NT3), as well as receptors to these growth factors in brain. Lithium also stimulates proliferation of stem cells, including bone marrow and neural stem cells in the subventricular zone, striatum, and forebrain. The stimulation of endogenous neural stem cells may explain why lithium increases brain cell density and volume in patients with bipolar disorders. Lithium also increases brain concentrations of the neuronal markers n-acetyl-aspartate and myoinositol. Lithium also remarkably protects neurons against glutamate, seizures, and apoptosis due to a wide variety of neurotoxins. The effective dose range for lithium is 0.6-1.0 mM in serum and >1.5 mM may be toxic. Serum lithium levels of 1.5-2.0 mM may have mild and reversible toxic effects on kidney, liver, heart, and glands. Serum levels of >2 mM may be associated with neurological symptoms, including cerebellar dysfunction. Prolonged lithium intoxication >2 mM can cause permanent brain damage. Lithium has low mutagenic and carcinogenic risk. Lithium is still the most effective therapy for depression. It "cures" a third

  15. Crystallization of lithium borate glasses

    NASA Technical Reports Server (NTRS)

    Goktas, A. A.; Neilson, G. F.; Weinberg, M. C.

    1992-01-01

    The glass-forming ability and crystallization behavior of lithium borate compositions, in the diborate-to-metaborate-range, were studied. In particular, the nature and sequence of formation of crystalline phases and the tendency toward devitrification were investigated as functions of temperature, thermal history and batch composition. It was found that the sequence of crystalline phase formation was sensitive to all of the three latter factors, and it was observed that under certain conditions metastable defect structures of the metaborate can appear.

  16. Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries

    NASA Astrophysics Data System (ADS)

    Kim, Myeong-Seong; Kim, Hyun-Kyung; Lee, Suk-Woo; Kim, Dong-Hyun; Ruan, Dianbo; Chung, Kyung Yoon; Lee, Sang Hyun; Roh, Kwang Chul; Kim, Kwang-Bum

    2016-05-01

    Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.25PO4/reduced graphene oxide microspheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precursor salt and graphene oxide and a subsequent heat treatment. During this process, it was found that the type of metal salt used has significant effects on the morphology, phase purity, and electrochemical properties of the synthesized samples. Furthermore, the amount of the chelating agent used also affects the phase purity and electrochemical properties of the samples. The composite exhibited a high tap density (1.1 g cm‑3) as well as a gravimetric capacity of 161 mA h g‑1 and volumetric capacity of 281 mA h cm‑3 at 0.05 C-rate. It also exhibited excellent rate capability, delivering a discharge capacity of 90 mA h g‑1 at 60 C-rate. Furthermore, the microspheres exhibited high energy efficiency and good cyclability, showing a capacity retention rate of 93% after 1000 cycles at 10 C-rate.

  17. Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries

    PubMed Central

    Kim, Myeong-Seong; Kim, Hyun-Kyung; Lee, Suk-Woo; Kim, Dong-Hyun; Ruan, Dianbo; Chung, Kyung Yoon; Lee, Sang Hyun; Roh, Kwang Chul; Kim, Kwang-Bum

    2016-01-01

    Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.25PO4/reduced graphene oxide microspheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precursor salt and graphene oxide and a subsequent heat treatment. During this process, it was found that the type of metal salt used has significant effects on the morphology, phase purity, and electrochemical properties of the synthesized samples. Furthermore, the amount of the chelating agent used also affects the phase purity and electrochemical properties of the samples. The composite exhibited a high tap density (1.1 g cm−3) as well as a gravimetric capacity of 161 mA h g−1 and volumetric capacity of 281 mA h cm−3 at 0.05 C-rate. It also exhibited excellent rate capability, delivering a discharge capacity of 90 mA h g−1 at 60 C-rate. Furthermore, the microspheres exhibited high energy efficiency and good cyclability, showing a capacity retention rate of 93% after 1000 cycles at 10 C-rate. PMID:27220812

  18. Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries.

    PubMed

    Kim, Myeong-Seong; Kim, Hyun-Kyung; Lee, Suk-Woo; Kim, Dong-Hyun; Ruan, Dianbo; Chung, Kyung Yoon; Lee, Sang Hyun; Roh, Kwang Chul; Kim, Kwang-Bum

    2016-01-01

    Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.25PO4/reduced graphene oxide microspheres synthesized by one-step salt-assisted spray drying using a mixed solution containing a precursor salt and graphene oxide and a subsequent heat treatment. During this process, it was found that the type of metal salt used has significant effects on the morphology, phase purity, and electrochemical properties of the synthesized samples. Furthermore, the amount of the chelating agent used also affects the phase purity and electrochemical properties of the samples. The composite exhibited a high tap density (1.1 g cm(-3)) as well as a gravimetric capacity of 161 mA h g(-1) and volumetric capacity of 281 mA h cm(-3) at 0.05 C-rate. It also exhibited excellent rate capability, delivering a discharge capacity of 90 mA h g(-1) at 60 C-rate. Furthermore, the microspheres exhibited high energy efficiency and good cyclability, showing a capacity retention rate of 93% after 1000 cycles at 10 C-rate. PMID:27220812

  19. Aluminum-lithium alloys in helicopters

    SciTech Connect

    Smith, A.F.

    1997-10-01

    Aluminium-lithium alloys are widely applied on the EH101 helicopter, designed and built jointly by GKN Westland Helicopters of England and Agusta S.p.A. of Italy. With the exception of the powder metallurgy alloy AA 5091, all the current commercially available aluminum-lithium alloys are produced by direct-chill casting, and require a precipitation-aging heat treatment to achieve the required properties. In aluminum-lithium alloys containing greater than 1.3% (by weight) of lithium, the intermetallic phase {delta}{prime}-Al{sub 3}Li precipitates upon natural or artificial aging, but the associated strengthening effect is insufficient to meet the medium or high strength levels usually required (the damage tolerant temper in AA 8090 is an exception).

  20. Lithium use in batteries

    USGS Publications Warehouse

    Goonan, Thomas G.

    2012-01-01

    Lithium has a number of uses but one of the most valuable is as a component of high energy-density rechargeable lithium-ion batteries. Because of concerns over carbon dioxide footprint and increasing hydrocarbon fuel cost (reduced supply), lithium may become even more important in large batteries for powering all-electric and hybrid vehicles. It would take 1.4 to 3.0 kilograms of lithium equivalent (7.5 to 16.0 kilograms of lithium carbonate) to support a 40-mile trip in an electric vehicle before requiring recharge. This could create a large demand for lithium. Estimates of future lithium demand vary, based on numerous variables. Some of those variables include the potential for recycling, widespread public acceptance of electric vehicles, or the possibility of incentives for converting to lithium-ion-powered engines. Increased electric usage could cause electricity prices to increase. Because of reduced demand, hydrocarbon fuel prices would likely decrease, making hydrocarbon fuel more desirable. In 2009, 13 percent of worldwide lithium reserves, expressed in terms of contained lithium, were reported to be within hard rock mineral deposits, and 87 percent, within brine deposits. Most of the lithium recovered from brine came from Chile, with smaller amounts from China, Argentina, and the United States. Chile also has lithium mineral reserves, as does Australia. Another source of lithium is from recycled batteries. When lithium-ion batteries begin to power vehicles, it is expected that battery recycling rates will increase because vehicle battery recycling systems can be used to produce new lithium-ion batteries.

  1. Stable lithium electrodeposition in liquid and nanoporous solid electrolytes.

    PubMed

    Lu, Yingying; Tu, Zhengyuan; Archer, Lynden A

    2014-10-01

    Rechargeable lithium, sodium and aluminium metal-based batteries are among the most versatile platforms for high-energy, cost-effective electrochemical energy storage. Non-uniform metal deposition and dendrite formation on the negative electrode during repeated cycles of charge and discharge are major hurdles to commercialization of energy-storage devices based on each of these chemistries. A long-held view is that unstable electrodeposition is a consequence of inherent characteristics of these metals and their inability to form uniform electrodeposits on surfaces with inevitable defects. We report on electrodeposition of lithium in simple liquid electrolytes and in nanoporous solids infused with liquid electrolytes. We find that simple liquid electrolytes reinforced with halogenated salt blends exhibit stable long-term cycling at room temperature, often with no signs of deposition instabilities over hundreds of cycles of charge and discharge and thousands of operating hours. We rationalize these observations with the help of surface energy data for the electrolyte/lithium interface and impedance analysis of the interface during different stages of cell operation. Our findings provide support for an important recent theoretical prediction that the surface mobility of lithium is significantly enhanced in the presence of lithium halide salts. Our results also show that a high electrolyte modulus is unnecessary for stable electrodeposition of lithium. PMID:25108613

  2. Phosphate salts

    MedlinePlus

    ... taken by mouth or used as enemas. Indigestion. Aluminum phosphate and calcium phosphate are FDA-permitted ingredients ... Phosphate salts containing sodium, potassium, aluminum, or calcium are LIKELY SAFE for most people when taken by mouth short-term, when sodium phosphate is inserted into the ...

  3. Halocyclization of Unsaturated Guanidines Mediated by Koser's Reagent and Lithium Halides.

    PubMed

    Daniel, Marion; Blanchard, Florent; Nocquet-Thibault, Sophie; Cariou, Kevin; Dodd, Robert H

    2015-11-01

    The synthesis of halogenated cyclic guanidines through iodine(III)-mediated umpolung of halide salts is described. Cyclic guanidines of various sizes can be obtained with generally excellent regioselectivities through either a chloro- or a bromocyclization, using Koser's reagent and the corresponding lithium salt. PMID:26492553

  4. Coating protects magnesium-lithium alloys against corrosion

    NASA Technical Reports Server (NTRS)

    1967-01-01

    Coating protects newly developed magnesium-lithium alloys against corrosion. The procedure includes heating the ingots in a salt bath and rolling them to the desired sheet thickness. The black coating, which is tough though thin and ductile, is derived mainly from chromium.

  5. Hot filament technique for measuring the thermal conductivity of molten lithium fluoride

    NASA Technical Reports Server (NTRS)

    Jaworske, Donald A.; Perry, William D.

    1990-01-01

    Molten salts, such as lithium fluoride, are attractive candidates for thermal energy storage in solar dynamic space power systems because of their high latent heat of fusion. However, these same salts have poor thermal conductivities which inhibit the transfer of heat into the solid phase and out of the liquid phase. One concept for improving the thermal conductivity of the thermal energy storage system is to add a conductive filler material to the molten salt. High thermal conductivity pitch-based graphite fibers are being considered for this application. Although there is some information available on the thermal conductivity of lithium fluoride solid, there is very little information on lithium fluoride liquid, and no information on molten salt graphite fiber composites. This paper describes a hot filament technique for determining the thermal conductivity of molten salts. The hot filament technique was used to find the thermal conductivity of molten lithium fluoride at 930 C, and the thermal conductivity values ranged from 1.2 to 1.6 W/mK. These values are comparable to the slightly larger value of 5.0 W/mK for lithium fluoride solid. In addition, two molten salt graphite fiber composites were characterized with the hot filament technique and these results are also presented.

  6. 21 CFR 172.626 - Salts of carrageenan.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Salts of carrageenan. 172.626 Section 172.626 Food... Gums, Chewing Gum Bases and Related Substances § 172.626 Salts of carrageenan. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  7. 21 CFR 172.660 - Salts of furcelleran.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Salts of furcelleran. 172.660 Section 172.660 Food... Gums, Chewing Gum Bases and Related Substances § 172.660 Salts of furcelleran. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  8. 21 CFR 172.660 - Salts of furcelleran.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Salts of furcelleran. 172.660 Section 172.660 Food... Gums, Chewing Gum Bases and Related Substances § 172.660 Salts of furcelleran. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  9. 21 CFR 172.626 - Salts of carrageenan.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Salts of carrageenan. 172.626 Section 172.626 Food... Gums, Chewing Gum Bases and Related Substances § 172.626 Salts of carrageenan. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  10. 21 CFR 172.626 - Salts of carrageenan.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Salts of carrageenan. 172.626 Section 172.626 Food... Gums, Chewing Gum Bases and Related Substances § 172.626 Salts of carrageenan. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  11. 21 CFR 172.626 - Salts of carrageenan.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Salts of carrageenan. 172.626 Section 172.626 Food... Gums, Chewing Gum Bases and Related Substances § 172.626 Salts of carrageenan. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  12. 21 CFR 172.660 - Salts of furcelleran.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Salts of furcelleran. 172.660 Section 172.660 Food... Gums, Chewing Gum Bases and Related Substances § 172.660 Salts of furcelleran. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  13. 21 CFR 172.660 - Salts of furcelleran.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Salts of furcelleran. 172.660 Section 172.660 Food... Gums, Chewing Gum Bases and Related Substances § 172.660 Salts of furcelleran. The food additive salts... the concentration of one of the naturally occurring salts (ammonium, calcium, potassium, or sodium)...

  14. Influence of Phosphatidylcholine and Calcium on Self-Association and Bile Salt Mixed Micellar Binding of the Natural Bile Pigment, Bilirubin Ditaurate.

    PubMed

    Neubrand, Michael W; Carey, Martin C; Laue, Thomas M

    2015-11-17

    Recently [Neubrand, M. W., et al. (2015) Biochemistry 54, 1542-1557], we determined a concentration-dependent monomer-dimer-tetramer equilibrium in aqueous bilirubin ditaurate (BDT) solutions and explored the nature of high-affinity binding of BDT monomers with monomers and micelles of the common taurine-conjugated bile salts (BS). We now investigate, employing complementary physicochemical methods, including fluorescence emission spectrophotometry and quasi-elastic light scattering spectroscopy, the influence of phosphatidylcholine (PC), the predominant phospholipid of bile and calcium, the major divalent biliary cation, on these self-interactions and heterointeractions. We have used short-chain, lyso and long-chain PC species as models and contrasted our results with those of parallel studies employing unconjugated bilirubin (UCB) as the fully charged dianion. Both bile pigments interacted with the zwitterionic headgroup of short-chain lecithins, forming water-soluble (BDT) and insoluble ion-pair complexes (UCB), respectively. Upon micelle formation, BDT monomers apparently remained at the headgroup mantle of short-chain PCs, but the ion pairs with UCB became internalized within the micelle's hydrophobic core. BDT interacted with the headgroups of unilamellar egg yolk (EY) PC vesicles; however, with the simultaneous addition of CaCl2, a reversible aggregation took place, but not vesicle fusion. With mixed EYPC/BS micelles, BDT became bound to the hydrophilic surface (as with simple BS micelles), and in turn, both BDT and BS bound calcium, but not other divalent cations. The calcium complexation of BDT and BS was enhanced strongly with increases in micellar EYPC, suggesting calcium-mediated cross-bridging of hydrophilic headgroups at the micelle's surface. Therefore, the physicochemical binding of BDT to BS in an artificial bile medium is influenced not only by BS species and concentration but also by long-chain PCs and calcium ions that exert a specific rather

  15. Natural protein engineering: a uniquely salt-tolerant, but not halophilic, alpha-type carbonic anhydrase from algae proliferating in low- to hyper-saline environments.

    PubMed

    Bageshwar, Umesh K; Premkumar, Lakshmanane; Gokhman, Irena; Savchenko, Tatyana; Sussman, Joel L; Zamir, Ada

    2004-02-01

    Dunaliella salina is a unicellular green alga thriving in environments ranging from fresh water to hyper-saline lakes, such as the Dead Sea. An unusual, internally duplicated, 60 kDa alpha-type carbonic anhydrase (dCA I), located on the surface of this alga, is expected to function over a broad range of salinities. It would therefore differ from other carbonic anhydrases that already lose activity at low salinities and also from halophilic proteins that require high salinities for conformational stability. Enzymatic analyses indeed indicated that dCA I retained activity at salt concentrations ranging from low salt to at least 1.5 M NaCl or KCl for CO(2) hydration, 2.0 M NaCl for esterase activity and 0.5 M for bicarbonate dehydration. Although measurements at higher salinities were constrained by the interference of salt in the respective assayed reactions, activity was noticeable even at 4.0 M NaCl. Comparisons of the internally duplicated dCA I to single-domain derivatives indicated that inter-domain interactions played a decisive role in the stability, activity, salt tolerance and pH responses of dCA I. Hence dCA I is a uniquely salt- tolerant protein, retaining an active conformation over a large range of salinities and, as a Zn metalloenzyme, largely immune to the specific inhibitory effects of anions. Its unique features make dCA I a useful model to understand the physico-chemical basis of halotolerance and protein-salt interactions in general. PMID:15047915

  16. Lithium: a key to the genetics of bipolar disorder

    PubMed Central

    2009-01-01

    Since the 1950s, lithium salts have been the main line of treatment for bipolar disorder (BD), both as a prophylactic and as an episodic treatment agent. Like many psychiatric conditions, BD is genetically and phenotypically heterogeneous, but evidence suggests that individuals who respond well to lithium treatment have more homogeneous clinical and molecular profiles. Response to lithium seems to cluster in families and can be used as a predictor for recurrence of BD symptoms. While molecular studies have provided important information about possible genes involved in BD predisposition or in lithium response, neither the mechanism of action of this drug nor the genetic profile of bipolar disorder is, as yet, completely understood. PMID:19691823

  17. Direct Lit Electrolysis In A Metallic Lithium Fusion Blanket

    SciTech Connect

    Colon-Mercado, H.; Babineau, D.; Elvington, M.; Garcia-Diaz, B.; Teprovich, J.; Vaquer, A.

    2015-10-13

    A process that simplifies the extraction of tritium from molten lithium based breeding blankets was developed.  The process is based on the direct electrolysis of lithium tritide using a ceramic Li ion conductor that replaces the molten salt extraction step. Extraction of tritium in the form of lithium tritide in the blankets/targets of fission/fusion reactors is critical in order to maintained low concentrations.  This is needed to decrease the potential tritium permeation to the surroundings and large releases from unforeseen accident scenarios. Because of the high affinity of tritium for the blanket, extraction is complicated at the required low levels. This work identified, developed and tested the use of ceramic lithium ion conductors capable of recovering the hydrogen and deuterium thru an electrolysis step at high temperatures. 

  18. The synergetic effect of lithium polysulfide and lithium nitrate to prevent lithium dendrite growth.

    PubMed

    Li, Weiyang; Yao, Hongbin; Yan, Kai; Zheng, Guangyuan; Liang, Zheng; Chiang, Yet-Ming; Cui, Yi

    2015-01-01

    Lithium metal has shown great promise as an anode material for high-energy storage systems, owing to its high theoretical specific capacity and low negative electrochemical potential. Unfortunately, uncontrolled dendritic and mossy lithium growth, as well as electrolyte decomposition inherent in lithium metal-based batteries, cause safety issues and low Coulombic efficiency. Here we demonstrate that the growth of lithium dendrites can be suppressed by exploiting the reaction between lithium and lithium polysulfide, which has long been considered as a critical flaw in lithium-sulfur batteries. We show that a stable and uniform solid electrolyte interphase layer is formed due to a synergetic effect of both lithium polysulfide and lithium nitrate as additives in ether-based electrolyte, preventing dendrite growth and minimizing electrolyte decomposition. Our findings allow for re-evaluation of the reactions regarding lithium polysulfide, lithium nitrate and lithium metal, and provide insights into solving the problems associated with lithium metal anodes. PMID:26081242

  19. The synergetic effect of lithium polysulfide and lithium nitrate to prevent lithium dendrite growth

    NASA Astrophysics Data System (ADS)

    Li, Weiyang; Yao, Hongbin; Yan, Kai; Zheng, Guangyuan; Liang, Zheng; Chiang, Yet-Ming; Cui, Yi

    2015-06-01

    Lithium metal has shown great promise as an anode material for high-energy storage systems, owing to its high theoretical specific capacity and low negative electrochemical potential. Unfortunately, uncontrolled dendritic and mossy lithium growth, as well as electrolyte decomposition inherent in lithium metal-based batteries, cause safety issues and low Coulombic efficiency. Here we demonstrate that the growth of lithium dendrites can be suppressed by exploiting the reaction between lithium and lithium polysulfide, which has long been considered as a critical flaw in lithium-sulfur batteries. We show that a stable and uniform solid electrolyte interphase layer is formed due to a synergetic effect of both lithium polysulfide and lithium nitrate as additives in ether-based electrolyte, preventing dendrite growth and minimizing electrolyte decomposition. Our findings allow for re-evaluation of the reactions regarding lithium polysulfide, lithium nitrate and lithium metal, and provide insights into solving the problems associated with lithium metal anodes.

  20. Resource Assessment of the In-Place and Potentially Recoverable Deep Natural Gas Resource of the Onshore Interior Salt Basins, North Central and Northeastern Gulf of Mexico

    SciTech Connect

    Ernest A. Mancini; Paul Aharon; Donald A. Goddard; Roger Barnaby

    2006-04-26

    The principal research effort for the first half of Year 3 of the project has been resource assessment. Emphasis has been on estimating the total volume of hydrocarbons generated and the potential amount of this resource that is classified as deep (>15,000 ft) gas in the North Louisiana Salt Basin, the Mississippi Interior Salt Basin, the Manila Subbasin and the Conecuh Subbasin. The amount of this resource that has been expelled, migrated and entrapped is also the focus of the first half of Year 3 of this study.

  1. Lithium Resources for the 21st Century

    NASA Astrophysics Data System (ADS)

    Kesler, S.; Gruber, P.; Medina, P.; Keolian, G.; Everson, M. P.; Wallington, T.

    2011-12-01

    (Great Salt Lake, Searles Lake), geothermal systems (Salton Sea) and oil fields contain lithium, but in low concentrations that add relatively little to estimated global resources. Igneous deposits, which constitute 26% of estimated global resources, consist largely of pegmatites, including past and present producers at Kings Mountain-Bessemer City (USA), Greenbushes (Australia) and Bikita (Zimbabwe), as well as numerous active prospects, especially in Canada and China. Amenability of these deposits to economic extraction is controlled by mineralogy and zoning of lithium, which vary considerably from deposit to deposit. An additional 8% of global lithium resources is estimated to be present in unusual deposits including largely hectorite clays in volcaniclastic rocks at Kings Valley (USA) and jadarite in lacustrine evaporite deposits (Serbia), which present new challenges to both mining and processing. If this highly varied population of deposits can be converted to reserves, lithium supplies for the 21st century EV market are relatively secure.

  2. Selective Reduction of Active Metal Chlorides from Molten LiCl-KCl using Lithium Drawdown

    SciTech Connect

    Michael F. Simpson; Daniel LaBrier; Michael Lineberry; Tae-Sic Yoo

    2012-10-01

    In support of optimizing electrorefining technology for treating spent nuclear fuel, lithium drawdown has been investigated for separating actinides from molten salt electrolyte. Drawdown reaction selectivity is a major issue that needs to be investigated, since the goal is to remove actinides while leaving the fission products in the salt. A series of lithium drawdown tests with surrogate fission product chlorides was run to obtain selectivity data with non-radioactive salts, develop a predictive model, and draw conclusions about the viability of using this process with actinide-loadd salt. Results of tests with CsCl, LaCl3, CeCl3, and NdCl3 are reported here. An equilibrium model has been formulated and fit to the experimental data. Excellent fits to the data were achieved. Based on analysis and results obtained to date, it is concluded that clean separation between minor actinides and lanthanides will be difficult to achieve using lithium drawdown.

  3. A lithium-rich composite metal oxide used as a SALDI-MS matrix for the determination of small biomolecules.

    PubMed

    Li, Ze; Zhang, Yi-Wei; Xin, Yue-Long; Bai, Yu; Zhou, Heng-Hui; Liu, Hu-Wei

    2014-12-18

    A lithium-rich composite metal oxide was evaluated as a novel matrix for matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-MS). The low background interference and lithium-rich feature made it a highly efficient matrix for the analysis of small molecules with high reproducibility, sensitivity and strong salt tolerance. PMID:25349979

  4. Method of recycling lithium borate to lithium borohydride through diborane

    DOEpatents

    Filby, Evan E.

    1976-01-01

    This invention provides a method for the recycling of lithium borate to lithium borohydride which can be reacted with water to generate hydrogen for utilization as a fuel. The lithium borate by-product of the hydrogen generation reaction is reacted with hydrogen chloride and water to produce boric acid and lithium chloride. The boric acid and lithium chloride are converted to lithium borohydride through a diborane intermediate to complete the recycle scheme.

  5. Lithium dendrite growth through solid polymer electrolyte membranes

    NASA Astrophysics Data System (ADS)

    Harry, Katherine; Schauser, Nicole; Balsara, Nitash

    2015-03-01

    Replacing the graphite-based anode in current batteries with a lithium foil will result in a qualitative increase in the energy density of lithium batteries. The primary reason for not adopting lithium-foil anodes is the formation of dendrites during cell charging. In this study, stop-motion X-ray microtomography experiments were used to directly monitor the growth of lithium dendrites during electrochemical cycling of symmetric lithium-lithium cells with a block copolymer electrolyte. In an attempt to understand the relationship between viscoelastic properties of the electrolyte on dendrite formation, a series of complementary experiments including cell cycling, tomography, ac impedance, and rheology, were conducted above and below the glass transition temperature of the non-conducting poly(styrene) block; the conducting phase is a mixture of rubbery poly(ethylene oxide) and a lithium salt. The tomography experiments enable quantification of the evolution of strain in the block copolymer electrolyte. Our work provides fundamental insight into the dynamics of electrochemical deposition of metallic films in contact with high modulus polymer electrolytes. Rational approaches for slowing down and, perhaps, eliminating dendrite growth are proposed.

  6. Materials issues in lithium ion rechargeable battery technology

    SciTech Connect

    Doughty, D.H.

    1995-07-01

    Lithium ion rechargeable batteries are predicted to replace Ni/Cd as the workhorse consumer battery. The pace of development of this battery system is determined in large part by the availability of materials and the understanding of interfacial reactions between materials. Lithium ion technology is based on the use of two lithium intercalating electrodes. Carbon is the most commonly used anode material, while the cathode materials of choice have been layered lithium metal chalcogenides (LiMX{sub 2}) and lithium spinel-type compounds. Electrolytes may be either organic liquids or polymers. Although the first practical use of graphite intercalation compounds as battery anodes was reported in 1981 for molten salt cells and in 1983 for ambient temperature systems, it was not until Sony Energytech announced a new lithium ion intercalating carbon anode in 1990, that interest peaked. The reason for this heightened interest is that these electrochemical cells have the high energy density, high voltage and light weight of metallic lithium, but without the disadvantages of dendrite formation on charge, improving their safety and cycle life.

  7. Lithium Redistribution in Lithium-Metal Batteries

    SciTech Connect

    Ferrese, A; Albertus, P; Christensen, J; Newman, J

    2012-01-01

    A model of a lithium-metal battery with a CoO2 positive electrode has been modeled in order to predict the movement of lithium in the negative electrode along the negative electrode/separator interface during cell cycling. A finite-element approach was used to incorporate an intercalation positive electrode using superposition, electrode tabbing, transport using concentrated solution theory, as well as the net movement of the lithium electrode during cycling. From this model, it has been found that movement of lithium along the negative electrode/separator interface does occur during cycling and is affected by three factors: the cell geometry, the slope of the open-circuit-potential function of the positive electrode, and concentration gradients in both the solid and liquid phases in the cell. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.027210jes] All rights reserved.

  8. Electrohydrodynamic ion emission from molten lithium nitrate

    SciTech Connect

    Panitz, J.A.; Pregenzer, A.L.; Gerber, R.A.

    1989-01-01

    Positive ions have been generated at the surface of molten lithium nitrate by applying a high electrostatic field to a thin layer of the molten salt on the apex of a field emitter tip. The ion emission process is characteristic of electrohydrodynamic ion formation, usually observed when a high electric field is applied to the surface of a liquid metal or alloy. With molten lithium nitrate, a single emission site appears at threshold. The divergence of the ion beam is several degrees. At higher field strengths multiple emission sites are observed. An ion species at m/e = 76 amu dominates the mass spectrum at all field strengths. This species is identified as a cluster ion (LiNO/sub 3/ )Li/sup +/ . At low source temperatures, (LiNO/sub 3/ )/sub 2/ Li/sup +/ is also observed. Despite the low ionization potential of lithium (5.4 eV), Li/sup +/ accounts for <8% of the total ion current generated by the source under all operating conditions. Multiply charged lithium is not detected in the mass spectra, suggesting the electric field at the Taylor cone apex is not sufficient to field-ionize singly charged species by a postionization process.

  9. Ionic liquids for rechargeable lithium batteries

    SciTech Connect

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

    2005-09-29

    We have investigated possible anticipated advantages of ionic-liquid electrolytes for use in lithium-ion batteries. Thermal stabilities and phase behavior were studied by thermal gravimetric analysis and differential scanning calorimetry. The ionic liquids studied include various imidazoliumTFSI systems, pyrrolidiniumTFSI, BMIMPF{sub 6}, BMIMBF{sub 4}, and BMIMTf. Thermal stabilities were measured for neat ionic liquids and for BMIMBF{sub 4}-LiBF{sub 4}, BMIMTf-LiTf, BMIMTFSI-LiTFSI mixtures. Conductivities have been measured for various ionic-liquid lithium-salt systems. We show the development of interfacial impedance in a Li|BMIMBF{sub 4} + LiBF{sub 4}|Li cell and we report results from cycling experiments for a Li|BMIMBF{sub 4} + 1 mol/kg LIBF{sub 4}|C cell. The interfacial resistance increases with time and the ionic liquid reacts with the lithium electrode. As expected, imidazolium-based ionic liquids react with lithium electrodes. We seek new ionic liquids that have better chemical stabilities.

  10. Determination of lithium in rocks: Fluorometric method

    USGS Publications Warehouse

    White, C.E.; Fletcher, M.H.; Parks, J.

    1951-01-01

    The gravimetric method in general use for the determination of lithium is tedious, and the final weighed product often contains other alkali metals. A fluorometric method was developed to shorten the time required for the analysis and to assure that the final determination is for lithium alone. This procedure is based on the complex formed between lithium and 8-hydroxyquinoline. The fluorescence is developed in a slightly alkaline solution of 95% alcohol and measurement is made on a photoelectric fluorometer. Separation from the ore is carried out by the wet method or by the distillation procedure. Sodium and potassium are removed by alcohol and ether, but complete separation is not necessary. Comparison of analyzed samples shows excellent agreement with spectrographic and gravimetric methods. The fluorometric method is more rapid than the gravimetric and produces more conclusive results. Another useful application is in the preparation of standard lithium solutions from reagent quality salts when a known standard is available. In this case no separations are necessary.

  11. Perchlorate (ClO4) and Perchlorate Salts

    Integrated Risk Information System (IRIS)

    Perchlorate ( ClO4 - ) and Perchlorate Salts CASRN 7790 - 98 - 9 Ammonium perchlorate CASRN 7791 - 03 - 9 Lithium perchlorate CASRN 7778 - 74 - 7 Potassium perchlorate CASRN 7601 - 89 - 0 Sodium perchlorate This U.S . EPA IRIS Summary is based on the U.S . Government - sponsored technical review of

  12. Lithium and symptomatic hyperparathyroidism.

    PubMed Central

    Ananth, J; Dubin, S E

    1983-01-01

    Hyperparathyroidism with or without adenoma has occasionally been reported in association with lithium treatment, and in symptomatic patients depression, psychosis and an exacerbation of existing psychopathology may occur. Three lithium-treated patients with hyperparathyroidism are reported, in whom discontinuation of lithium in one and removal of parathyroid adenomata in two led to both a reduction in plasma calcium levels and an improvement in their psychopathology. PMID:6423822

  13. Lithium purification technique

    DOEpatents

    Keough, R.F.; Meadows, G.E.

    1984-01-10

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

  14. Lithium purification technique

    DOEpatents

    Keough, Robert F.; Meadows, George E.

    1985-01-01

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

  15. The Lithium Isotopic Signature of Hawaiian Basalts

    NASA Astrophysics Data System (ADS)

    Harrison, L.; Weis, D.; Hanano, D. W.

    2013-12-01

    shield stage volcanoes or amongst individual volcanoes; 2) differences in degree of mantle melt and spatial structure of the mantle heterogeneity melting in the case of pre-shield, shield, and post-shield differences. In Hawaiian basalts, lithium isotopes help distinguish between 'enriched' Loa source components: Ko';olau Makapu';u shield stage lavas may have between 4-10% of a carbonate input and Hualalai post-shield and shield lavas may reflect incorporation of subduction eroded lower continental crust. Comparison of this dataset with worldwide OIB published lithium isotopic data indicates that the lithium isotopic system behaves systematically on a mantle-wide scale. Hawai'i is generally characterized as EM-I like, with Hualalai post-shield lavas exhibiting both the lightest lithium isotopic signature and the most extreme EM-I characteristics. Lithium isotopes thus provide an additional insight into the nature of EM-I type mantle. [1] Weis, D. et al. (2011) Nature Geoscience 4, doi:10.1038/NGEO1328. [2] Nobre Silva, I.G. et al. (2013) Geochem. Geophy. Geosys. 14(3), doi: doi:10.1002/ggge.20047. [3] Chan, L.H., and Frey, F.A. (2003) Geochem. Geophy. Geosys. 4(3), doi: 10.1029/2002GC000365.

  16. Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes

    PubMed Central

    Reddy, Arava Leela Mohana; Nagarajan, Subbiah; Chumyim, Porramate; Gowda, Sanketh R.; Pradhan, Padmanava; Jadhav, Swapnil R.; Dubey, Madan; John, George; Ajayan, Pulickel M.

    2012-01-01

    Current lithium batteries operate on inorganic insertion compounds to power a diverse range of applications, but recently there is a surging demand to develop environmentally friendly green electrode materials. To develop sustainable and eco-friendly lithium ion batteries, we report reversible lithium ion storage properties of a naturally occurring and abundant organic compound purpurin, which is non-toxic and derived from the plant madder. The carbonyl/hydroxyl groups present in purpurin molecules act as redox centers and reacts electrochemically with Li-ions during the charge/discharge process. The mechanism of lithiation of purpurin is fully elucidated using NMR, UV and FTIR spectral studies. The formation of the most favored six membered binding core of lithium ion with carbonyl groups of purpurin and hydroxyl groups at C-1 and C-4 positions respectively facilitated lithiation process, whereas hydroxyl group at C-2 position remains unaltered. PMID:23233879

  17. Effects of Long-Term Acid-Mine Drainage Contamination on Diversity and Activity of Sulfate-Reducing Bacteria in a Natural Salt Marsh.

    NASA Astrophysics Data System (ADS)

    Moreau, J. W.; Banfield, J. F.

    2003-12-01

    Constructed wetlands have been studied as sites or analogs for in situ bioremediation of metal contaminants from acid mine drainage (AMD) or industrial sources (e.g. Webb et al. 1998). Wetlands bioremediation necessarily invokes the ubiquity and robustness of sulfate-reducing bacteria (SRB) to sequester dissolved metals into various poorly soluble metal-sulfides (e.g. PbS, CdS). However, few studies of natural wetlands under long-term ecological forcing by AMD or other contaminant sources are available for context. We are investigating the microbial diversity, mineralogy and geochemistry of a highly contaminated salt marsh along the East Central San Francisco Bay. For nearly a half-century, areas within this marsh have received acidic and/or metal-rich groundwaters from near-surface pyrite tailings (transported there from Iron Mountain Mine, near Redding, CA) and local industrial sources (e.g. paint and explosives manufacturers). Sediment cores (30-40 cm long) were taken from six contaminated sites in the marsh with pH range of ˜2 to ˜8. Previous analyses (URS Corp. 2001) reported As, Cd, Cu, Se, Zn, and Pb present in sediments at extremely high concentrations (100s of ppm), yet our ICP-AES analyses of pore waters showed only As present at concentrations of 10-50 ppb. We infer, from high-resolution transmission electron microscope (HRTEM) studies of biogenic (SRB biofilm) ZnS (Moreau et al. 2003, in review) and marsh sediments, that contaminant metals have been sequestered into aggregates of nanocrystalline metal-sulfides. Continuous-flow isotope ratio mass spectrometer (CF-IRMS) analyses of pore-water sulfate and sedimentary sulfides allow resolution of contributions to dissolved sulfate and sulfide from tailings oxidation and dissimilatory sulfate reduction. Sulfate analyses from subsections of three cores (pH 2-3, 6-7, 7-8, respectively) all yield δ 34S values consistent with bacterial sulfate reduction. We note that all three cores also contain very fine

  18. Phosphate-stabilized Lithium intercalation compounds

    SciTech Connect

    Richardson, Thomas J.

    2002-07-22

    Four manganese and iron phosphates with alluaudite or fillowite structures have been prepared by solid state reactions: Na2FeMn2(PO4)3, LiNaFeMn2(PO4)3, NaFe3(PO4)3, and Na2Mn3(PO4)3. LixNa2-xFeMn2(PO4)3 with x close to 2 was prepared from Na2FeMn2(PO4)3 by molten salt ion exchange. These materials are similar in stoichiometry to the phospho-olivines LiFe(Mn)PO4, but have a more complex structure that can accommodate mixed transition metal oxidation states. They are of interest as candidates for lithium battery cathodes because of their somewhat higher electronic conductivity, high intercalant ion mobility, and ease of preparation. Their performance as intercalation electrodes in non-aqueous lithium cells was, however, poor.

  19. The nature of the salt error in the Sn(II)-reduced molybdenum blue reaction for determination of dissolved reactive phosphorus in saline waters.

    PubMed

    Nagul, Edward A; McKelvie, Ian D; Kolev, Spas D

    2015-10-01

    Sn(II) is a well-known reductant used in the formation of phosphomolybdenum blue for the determination of dissolved reactive phosphorus (DRP) in waters because it provides rapid and quantitative reduction. However, in saline waters, this method suffers from a salt error which causes a significant decrease in sensitivity. This phenomenon has never been adequately explained in the literature. The Murphy and Riley method, which uses Sb(III) and ascorbic acid for the reduction step, is preferred for DRP determination in saline waters because it is unaffected by salinity, but it exhibits a sensitivity approximately 30% lower than that when Sn(II) is used as the reductant without Cl(-) interference. This study investigates the processes causing the salt error and possible ways of minimizing it, so that the benefits of Sn(II) reduction on the molybdenum blue reaction rate and sensitivity may be exploited in the determination of low levels of DRP in marine and estuarine waters. It has been established that the salt error is caused by the formation of Sn(IV) chloro-complexes which compete with the formation of Sn(IV)-substituted phosphomolybdenum blue, forcing the reaction to proceed via the much slower, less favourable process of direct reduction that occurs in methods using organic reductants such as ascorbic acid. PMID:26481995

  20. Thermodynamics of salt-doped polymers

    NASA Astrophysics Data System (ADS)

    Wang, Zhen-Gang

    2013-03-01

    There is much current interest in salt-doped polymers as materials for energy applications. For example, a promising system for rechargeable battery applications consists of diblock copolymers of an ion-dissolving block, such as polyethylene oxide (PEO) and a nonconducting block such as polystyrene. Experimentally, it has been shown that the addition of lithium salts significantly alters the order-order and order-disorder transition (ODT) temperatures. In particular, the ODT temperature can increase substantially upon adding even a small amount of lithium salt, and the domain spacing in the ordered phases also increases significantly. Both changes are found to depend on the anion type. In this talk, I describe a simple theory for explaining these phenomena. A key effect is the solvation energy of the anions by the polymers, which we approximate using the Born solvation model. The difference in the Born energy between different polymers provides a driving force towards phase separation. By studying the shift in the mean-field spinodal of the disordered phase, we can identify an effective χ parameter, with a systematic dependence on the anion radius, in agreement with available experimental data. Furthermore, by studying the behavior of the domain spacing with salt concentration, we clarify the relationship between different definitions of the effective χ parameter. We propose that the effective χ parameter determined from the structure factor of the disordered phase is a more robust measure of the change in miscibility between the two blocks. Finally, we demonstrate that salt doping induces a strongly first-order transition from the disordered phase to the lamellar phase, with different salt concentrations in the two phases.

  1. Composite Electrolytes for Lithium Batteries: Ionic Liquids in APTES Crosslinked Polymers

    NASA Technical Reports Server (NTRS)

    Tigelaar, Dean M.; Meador, Mary Ann B.; Bennett, William R.

    2007-01-01

    Solvent free polymer electrolytes were made consisting of Li(+) and pyrrolidinium salts of trifluoromethanesulfonimide added to a series of hyperbranched poly(ethylene oxide)s (PEO). The polymers were connected by triazine linkages and crosslinked by a sol-gel process to provide mechanical strength. The connecting PEO groups were varied to help understand the effects of polymer structure on electrolyte conductivity in the presence of ionic liquids. Polymers were also made that contain poly(dimethylsiloxane) groups, which provide increased flexibility without interacting with lithium ions. When large amounts of ionic liquid are added, there is little dependence of conductivity on the polymer structure. However, when smaller amounts of ionic liquid are added, the inherent conductivity of the polymer becomes a factor. These electrolytes are more conductive than those made with high molecular weight PEO imbibed with ionic liquids at ambient temperatures, due to the amorphous nature of the polymer.

  2. Thermal Characterization of Molten Salt Systems

    SciTech Connect

    Toni Y. Gutknecht; Guy L. Fredrickson

    2011-09-01

    The phase stability of molten salts in an electrorefiner (ER) may be adversely affected by the buildup of sodium, fission products, and transuranics in the electrolyte. Potential situations that need to be avoided are the following: (1) salt freezing due to an unexpected change in the liquidus temperature, (2) phase separation or non-homogeneity of the molten salt due to the precipitation of solids or formation of immiscible liquids, and (3) any mechanism that can result in the separation and concentration of fissile elements from the molten salt. Any of these situations would result in an off-normal condition outside the established safety basis for electrorefiner (ER) operations. The stability (and homogeneity) of the phases can potentially be monitored through the thermal characterization of the salts, which can be a function of impurity concentration. This report describes the experimental results of typical salts compositions, which consist of chlorides of potassium, lithium, strontium, samarium, praseodymium, lanthanum, barium, cerium, cesium, neodymium, sodium and gadolinium chlorides as a surrogate for both uranium and plutonium, used for the processing of used nuclear fuels.

  3. Synthesis of nanocrystalline transition metal and oxides for lithium storage

    NASA Astrophysics Data System (ADS)

    Wang, G. X.; Chen, Y.; Yang, L.; Yao, Jane; Needham, Scott; Liu, H. K.; Ahn, J. H.

    Nanosize silver and tin dioxide powders were synthesised by a novel reverse micelle technique. The reverse micelles were formed from a microemulsion of organic solvents, water based salts and surfactants. The spherical nanosize Ag powders were formed via in situ reduction. The tin hydroxide precipitates were formed in reverse micelles and converted to tin dioxide nanopowders after heat treatment. The Ag and SnO 2 powders have a particle size in the range of 20-50 nm. The as-prepared nanosize Ag and SnO 2 nanopowders were used in lithium-ion cells for lithium storage.

  4. High Performance Batteries Based on Hybrid Magnesium and Lithium Chemistry

    SciTech Connect

    Cheng, Yingwen; Shao, Yuyan; Zhang, Jiguang; Sprenkle, Vincent L.; Liu, Jun; Li, Guosheng

    2014-01-01

    Magnesium and lithium (Mg/Li) hybrid batteries that combine Mg and Li electrochemistry, consisting of a Mg anode, a lithium-intercalation cathode and a dual-salt electrolyte with both Mg2+ and Li+ ions, were constructed and examined in this work. Our results show that hybrid (Mg/Li) batteries were able to combine the advantages of Li-ion and Mg batteries, and delivered outstanding rate performance (83% for capacities at 15C and 0.1C) and superior cyclic stability (~5% fade after 3000 cycles).

  5. Laminar Multicell Lithium Batteries

    SciTech Connect

    Bruder, A. H.

    1984-01-31

    Laminar batteries of series connected cells comprising lithium anodes and an electrolyte containing a passivating solvent reactive with lithium in which the cells are electrically connected in series by intercell barriers comprising outer layers of electrochemically inert electronically conducting material in contact with the electrochemically active anode and cathode of adjacent cells and a layer of metal foil between the electrochemically inert layers.

  6. Cathode material for lithium batteries

    DOEpatents

    Park, Sang-Ho; Amine, Khalil

    2015-01-13

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

  7. Cathode material for lithium batteries

    DOEpatents

    Park, Sang-Ho; Amine, Khalil

    2013-07-23

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

  8. Lithium and autophagy.

    PubMed

    Motoi, Yumiko; Shimada, Kohei; Ishiguro, Koichi; Hattori, Nobutaka

    2014-06-18

    Lithium, a drug used to treat bipolar disorders, has a variety of neuroprotective mechanisms, including autophagy regulation, in various neuropsychiatric conditions. In neurodegenerative diseases, lithium enhances degradation of aggregate-prone proteins, including mutated huntingtin, phosphorylated tau, and α-synuclein, and causes damaged mitochondria to degrade, while in a mouse model of cerebral ischemia and Alzheimer's disease autophagy downregulation by lithium is observed. The signaling pathway of lithium as an autophagy enhancer might be associated with the mammalian target of rapamycin (mTOR)-independent pathway, which is involved in myo-inositol-1,4,5-trisphosphate (IP3) in Huntington's disease and Parkinson's disease. However, the mTOR-dependent pathway might be involved in inhibiting glycogen synthase kinase-3β (GSK3β) in other diseases. Lithium's autophagy-enhancing property may contribute to the therapeutic benefit of patients with neuropsychiatric disorders. PMID:24738557

  9. Long life lithium batteries with stabilized electrodes

    DOEpatents

    Amine, Khalil; Liu, Jun; Vissers, Donald R.; Lu, Wenquan

    2009-03-24

    The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In some embodiments the additives include a substituted or unsubstituted cyclic or spirocyclic hydrocarbon containing at least one oxygen atom and at least one alkenyl or alkynyl group. When used in electrochemical devices with, e.g., lithium manganese oxide spinel electrodes or olivine or carbon-coated olivine electrodes, the new electrolytes provide batteries with improved calendar and cycle life.

  10. Lithium-Ion Electrolytes Containing Flame Retardant Additives for Increased Safety Characteristics

    NASA Technical Reports Server (NTRS)

    Smart, Marshall C. (Inventor); Smith, Kiah A. (Inventor); Bugga, Ratnakumar V. (Inventor); Prakash, Surya G. (Inventor); Krause, Frederick Charles (Inventor)

    2014-01-01

    The invention discloses various embodiments of Li-ion electrolytes containing flame retardant additives that have delivered good performance over a wide temperature range, good cycle life characteristics, and improved safety characteristics, namely, reduced flammability. In one embodiment of the invention there is provided an electrolyte for use in a lithium-ion electrochemical cell, the electrolyte comprising a mixture of an ethylene carbonate (EC), an ethyl methyl carbonate (EMC), a fluorinated co-solvent, a flame retardant additive, and a lithium salt. In another embodiment of the invention there is provided an electrolyte for use in a lithium-ion electrochemical cell, the electrolyte comprising a mixture of an ethylene carbonate (EC), an ethyl methyl carbonate (EMC), a flame retardant additive, a solid electrolyte interface (SEI) film forming agent, and a lithium salt.

  11. Evaluation of the Impacts of Marine Salts and Asian Dust on the Forested Yakushima Island Ecosystem, a World Natural Heritage Site in Japan.

    PubMed

    Nakano, Takanori; Yokoo, Yoriko; Okumura, Masao; Jean, Seo-Ryong; Satake, Kenichi

    2012-11-01

    To elucidate the influence of airborne materials on the ecosystem of Japan's Yakushima Island, we determined the elemental compositions and Sr and Nd isotope ratios in streamwater, soils, vegetation, and rocks. Streamwater had high Na and Cl contents, low Ca and HCO(3) contents, and Na/Cl and Mg/Cl ratios close to those of seawater, but it had low pH (5.4 to 7.1), a higher Ca/Cl ratio than seawater, and distinct (87)Sr/(86)Sr ratios that depended on the bedrock type. The proportions of rain-derived cations in streamwater, estimated by assuming that Cl was derived from sea salt aerosols, averaged 81 % for Na, 83 % for Mg, 36 % for K, 32 % for Ca, and 33 % for Sr. The Sr value was comparable to the 28 % estimated by comparing Sr isotope ratios between rain and granite bedrock. The soils are depleted in Ca, Na, P, and Sr compared with the parent materials. At Yotsuse in the northwestern side, plants and the soil pool have (87)Sr/(86)Sr ratios similar to that of rainwater with a high sea salt component. In contrast, the Sr and Nd isotope ratios of soil minerals in the A and B horizons approach those of silicate minerals in northern China's loess soils. The soil Ca and P depletion results largely from chemical weathering of plagioclase and of small amounts of apatite and calcite in granitic rocks. This suggests that Yakushima's ecosystem is affected by large amounts of acidic precipitation with a high sea salt component, which leaches Ca and its proxy (Sr) from bedrock into streams, and by Asian dust-derived apatite, which is an important source of P in base cation-depleted soils. PMID:23136452

  12. Reduction of the spent nuclear fuel of a VVER-1000 reactor by lithium in a lithium chloride melt

    NASA Astrophysics Data System (ADS)

    Bychkov, A. V.; Ishunin, V. S.; Kormilitsyn, M. V.

    2010-08-01

    Researchers at FGUP GNTs RF NIIAR performed a series of experiments on the lithium reduction of the spent nuclear fuel (SNF) of a VVER-1000 reactor to a metal in a lithium chloride melt. The depletion of the nuclear fuel taken before experiments is about 30000 (MW day)/t, and the cooling time is 5 years. The experiments are performed on 5.8-kg samples of a prepared SNF powder. Data are obtained on a decrease in the heat release, the specific activity of the processed powder, and the distribution of actinides and the main fission products between a salt phase and a reduced SNF powder.

  13. Lithium: a versatile tool for understanding renal physiology

    PubMed Central

    Ecelbarger, Carolyn M.

    2013-01-01

    By virtue of its unique interactions with kidney cells, lithium became an important research tool in renal physiology and pathophysiology. Investigators have uncovered the intricate relationships of lithium with the vasopressin and aldosterone systems, and the membrane channels or transporters regulated by them. While doing so, their work has also led to 1) questioning the role of adenylyl cyclase activity and prostaglandins in lithium-induced suppression of aquaporin-2 gene transcription; 2) unraveling the role of purinergic signaling in lithium-induced polyuria; and 3) highlighting the importance of the epithelial sodium channel (ENaC) in lithium-induced nephrogenic diabetes insipidus (NDI). Lithium-induced remodeling of the collecting duct has the potential to shed new light on collecting duct remodeling in disease conditions, such as diabetes insipidus. The finding that lithium inhibits glycogen synthase kinase-3β (GSK3β) has opened an avenue for studies on the role of GSK3β in urinary concentration, and GSK isoforms in renal development. Finally, proteomic and metabolomic profiling of the kidney and urine in rats treated with lithium is providing insights into how the kidney adapts its metabolism in conditions such as acquired NDI and the multifactorial nature of lithium-induced NDI. This review provides state-of-the-art knowledge of lithium as a versatile tool for understanding the molecular physiology of the kidney, and a comprehensive view of how this tool is challenging some of our long-standing concepts in renal physiology, often with paradigm shifts, and presenting paradoxical situations in renal pathophysiology. In addition, this review points to future directions in research where lithium can lead the renal community. PMID:23408166

  14. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

    Thackeray, Michael M.; Kim, Jeom-Soo; Johnson, Christopher S.

    2008-01-01

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

  15. Conductivity through Polymer Electrolytes and Its Implications in Lithium-Ion Batteries: Real-World Application of Periodic Trends

    ERIC Educational Resources Information Center

    Compton, Owen C.; Egan, Martin; Kanakaraj, Rupa; Higgins, Thomas B.; Nguyen, SonBinh T.

    2012-01-01

    Periodic conductivity trends are placed in the scope of lithium-ion batteries, where increases in the ionic radii of salt components affect the conductivity of a poly(ethyleneoxide)-based polymer electrolyte. Numerous electrolytes containing varying concentrations and types of metal salts are prepared and evaluated in either one or two laboratory…

  16. Effect of the size-selective silver clusters on lithium peroxide morphology in lithium-oxygen batteries

    NASA Astrophysics Data System (ADS)

    Lu, Jun; Cheng, Lei; Lau, Kah Chun; Tyo, Eric; Luo, Xiangyi; Wen, Jianguo; Miller, Dean; Assary, Rajeev S.; Wang, Hsien-Hau; Redfern, Paul; Wu, Huiming; Park, Jin-Bum; Sun, Yang-Kook; Vajda, Stefan; Amine, Khalil; Curtiss, Larry A.

    2014-09-01

    Lithium-oxygen batteries have the potential needed for long-range electric vehicles, but the charge and discharge chemistries are complex and not well understood. The active sites on cathode surfaces and their role in electrochemical reactions in aprotic lithium-oxygen cells are difficult to ascertain because the exact nature of the sites is unknown. Here we report the deposition of subnanometre silver clusters of exact size and number of atoms on passivated carbon to study the discharge process in lithium-oxygen cells. The results reveal dramatically different morphologies of the electrochemically grown lithium peroxide dependent on the size of the clusters. This dependence is found to be due to the influence of the cluster size on the formation mechanism, which also affects the charge process. The results of this study suggest that precise control of subnanometre surface structure on cathodes can be used as a means to improve the performance of lithium-oxygen cells.

  17. Hybrid Lithium-Sulfur Batteries with a Solid Electrolyte Membrane and Lithium Polysulfide Catholyte.

    PubMed

    Yu, Xingwen; Bi, Zhonghe; Zhao, Feng; Manthiram, Arumugam

    2015-08-01

    Lithium-sulfur (Li-S) batteries are receiving great attention as the most promising next-generation power source with significantly high charge-storage capacity. However, the implementation of Li-S batteries is hampered by a critical challenge because of the soluble nature of the intermediate polysulfide species in the liquid electrolyte. The use of traditional porous separators unavoidably allows the migration of the dissolved polysulfide species from the cathode to the lithium-metal anode and results in continuous loss of capacity. In this study, a LiSICON (lithium super ionic conductor) solid membrane is used as a cation-selective electrolyte for lithium-polysulfide (Li-PS) batteries to suppress the polysulfide diffusion. Ionic conductivity issue at the lithium metal/solid electrolyte interface is successfully addressed by insertion of a "soft", liquid-electrolyte integrated polypropylene interlayer. The solid LiSICON lithium-ion conductor maintains stable ionic conductivity during the electrochemical cycling of the cells. The Li-PS battery system with a hybrid solid/liquid electrolyte exhibits significantly enhanced cyclability relative to the cells with the traditional liquid-electrolyte integrated porous separator. PMID:26161547

  18. Rotation, inflation, and lithium in the Pleiades

    NASA Astrophysics Data System (ADS)

    Somers, Garrett; Pinsonneault, Marc H.

    2015-06-01

    The rapidly rotating cool dwarfs of the Pleiades are rich in lithium relative to their slowly rotating counterparts. Motivated by observations of inflated radii in young, active stars, and by calculations showing that radius inflation inhibits pre-main-sequence (pre-MS) Li destruction, we test whether this pattern could arise from a connection between stellar rotation rate and radius inflation on the pre-MS. We demonstrate that pre-MS radius inflation can efficiently suppress lithium destruction by rotationally induced mixing in evolutionary models, and that the net effect of inflation and rotational mixing is a pattern where rotation correlates with lithium abundance for M* < M⊙, and anticorrelates with lithium abundance for M* > M⊙, similar to the empirical trend in the Pleiades. Next, we adopt different prescriptions for the dependence of inflation on rotation, and compare their predictions to the Pleiades lithium/rotation pattern. We find that if a connection between rotation and radius inflation exists, then the important qualitative features of this pattern naturally and generically emerge in our models. This is the first consistent physical model to date that explains the Li-rotation correlation in the Pleiades. We discuss plausible mechanisms for inducing this correlation and suggest an observational test using granulation.

  19. Size effects in lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Hu-Rong, Yao; Ya-Xia, Yin; Yu-Gao, Guo

    2016-01-01

    Size-related properties of novel lithium battery materials, arising from kinetics, thermodynamics, and newly discovered lithium storage mechanisms, are reviewed. Complementary experimental and computational investigations of the use of the size effects to modify electrodes and electrolytes for lithium ion batteries are enumerated and discussed together. Size differences in the materials in lithium ion batteries lead to a variety of exciting phenomena. Smaller-particle materials with highly connective interfaces and reduced diffusion paths exhibit higher rate performance than the corresponding bulk materials. The thermodynamics is also changed by the higher surface energy of smaller particles, affecting, for example, secondary surface reactions, lattice parameter, voltage, and the phase transformation mechanism. Newly discovered lithium storage mechanisms that result in superior storage capacity are also briefly highlighted. Project supported by the National Natural Science Foundation of China (Grant Nos. 51225204 and 21303222), the Shandong Taishan Scholarship, China, the Ministry of Science and Technology, China (Grant No. 2012CB932900), and the Strategic Priority Research Program of the Chinese Academy of Sciences (Grant No. XDA09010000).

  20. Is violence in part a lithium deficiency state?

    PubMed

    Goldstein, Mark R; Mascitelli, Luca

    2016-04-01

    Violence, particularly firearm violence, leading to suicide and homicide is a significant problem worldwide. A majority of suicidal and homicidal violence involves males; homicidal violence is prevalent among young men and suicide is the leading cause of violence worldwide. Lithium, in pharmacological doses, has been used successfully for decades in treating bipolar disorders, and has been shown to decrease violent crime in this situation. Interestingly, lithium, in trace amounts, as occurs in some drinking water, has been inversely related to aggression, and suicidal and homicidal violence. Lithium is naturally found in vegetables, grains and drinking water, and dietary intake varies from nearly zero to 3mg daily. Elemental lithium, in trace doses, has been shown to improve mood in weeks. Moreover, lithium, in trace amounts, has no toxicity. In order to ensure adequate dietary intakes of elemental lithium daily for the purpose of decreasing aggression and violence, we propose considering the fortification of cereal grain products with lithium and also the addition of lithium to vitamin preparations for adults. Importantly, randomized trials in various populations are needed to test this hypothesis. PMID:26968907

  1. Silver manganese oxide electrodes for lithium batteries

    DOEpatents

    Thackeray, Michael M.; Vaughey, John T.; Dees, Dennis W.

    2006-05-09

    This invention relates to electrodes for non-aqueous lithium cells and batteries with silver manganese oxide positive electrodes, denoted AgxMnOy, in which x and y are such that the manganese ions in the charged or partially charged electrodes cells have an average oxidation state greater than 3.5. The silver manganese oxide electrodes optionally contain silver powder and/or silver foil to assist in current collection at the electrodes and to improve the power capability of the cells or batteries. The invention relates also to a method for preparing AgxMnOy electrodes by decomposition of a permanganate salt, such as AgMnO4, or by the decomposition of KMnO4 or LiMnO4 in the presence of a silver salt.

  2. Community solar salt production in Goa, India

    PubMed Central

    2012-01-01

    Traditional salt farming in Goa, India has been practised for the past 1,500 years by a few communities. Goa’s riverine estuaries, easy access to sea water and favourable climatic conditions makes salt production attractive during summer. Salt produced through this natural evaporation process also played an important role in the economy of Goa even during the Portuguese rule as salt was the chief export commodity. In the past there were 36 villages involved in salt production, which is now reduced to 9. Low income, lack of skilled labour, competition from industrially produced salt, losses incurred on the yearly damage of embankments are the major reasons responsible for the reduction in the number of salt pans. Salt pans (Mithagar or Mithache agor) form a part of the reclaimed waterlogged khazan lands, which are also utilised for aquaculture, pisciculture and agriculture. Salt pans in Goa experience three phases namely, the ceased phase during monsoon period of June to October, preparatory phase from December to January, and salt harvesting phase, from February to June. After the monsoons, the salt pans are prepared manually for salt production. During high tide, an influx of sea water occurs, which enters the reservoir pans through sluice gates. The sea water after 1–2 days on attaining a salinity of approximately 5ºBé, is released into the evaporator pans and kept till it attains a salinity of 23 - 25ºBé. The brine is then released to crystallizer pans, where the salt crystallises out 25 - 27ºBé and is then harvested. Salt pans form a unique ecosystem where succession of different organisms with varying environmental conditions occurs. Organisms ranging from bacteria, archaea to fungi, algae, etc., are known to colonise salt pans and may influence the quality of salt produced. The aim of this review is to describe salt farming in Goa’s history, importance of salt production as a community activity, traditional method of salt production and the

  3. Community solar salt production in Goa, India.

    PubMed

    Mani, Kabilan; Salgaonkar, Bhakti B; Das, Deepthi; Bragança, Judith M

    2012-01-01

    Traditional salt farming in Goa, India has been practised for the past 1,500 years by a few communities. Goa's riverine estuaries, easy access to sea water and favourable climatic conditions makes salt production attractive during summer. Salt produced through this natural evaporation process also played an important role in the economy of Goa even during the Portuguese rule as salt was the chief export commodity. In the past there were 36 villages involved in salt production, which is now reduced to 9. Low income, lack of skilled labour, competition from industrially produced salt, losses incurred on the yearly damage of embankments are the major reasons responsible for the reduction in the number of salt pans.Salt pans (Mithagar or Mithache agor) form a part of the reclaimed waterlogged khazan lands, which are also utilised for aquaculture, pisciculture and agriculture. Salt pans in Goa experience three phases namely, the ceased phase during monsoon period of June to October, preparatory phase from December to January, and salt harvesting phase, from February to June. After the monsoons, the salt pans are prepared manually for salt production. During high tide, an influx of sea water occurs, which enters the reservoir pans through sluice gates. The sea water after 1-2 days on attaining a salinity of approximately 5ºBé, is released into the evaporator pans and kept till it attains a salinity of 23 - 25ºBé. The brine is then released to crystallizer pans, where the salt crystallises out 25 - 27ºBé and is then harvested.Salt pans form a unique ecosystem where succession of different organisms with varying environmental conditions occurs. Organisms ranging from bacteria, archaea to fungi, algae, etc., are known to colonise salt pans and may influence the quality of salt produced.The aim of this review is to describe salt farming in Goa's history, importance of salt production as a community activity, traditional method of salt production and the biota

  4. Electrolyte Solvation and Ionic Association. V. Acetonitrile-Lithium Bis(fluorosulfonyl)imide (LiFSI) Mixtures

    SciTech Connect

    Han, Sang D.; Borodin, Oleg; Seo, D. M.; Zhou, Zhi B.; Henderson, Wesley A.

    2014-09-30

    Electrolytes with the salt lithium bis(fluorosulfonyl)imide (LiFSI) have been evaluated relative to comparable electrolytes with other lithium salts. Acetonitrile (AN) has been used as a model electrolyte solvent. The information obtained from the thermal phase behavior, solvation/ionic association interactions, quantum chemical (QC) calculations and molecular dynamics (MD) simulations (with an APPLE&P many-body polarizable force field for the LiFSI salt) of the (AN)n-LiFSI mixtures provides detailed insight into the coordination interactions of the FSI- anions and the wide variability noted in the electrolyte transport property (i.e., viscosity and ionic conductivity).

  5. Rheological contrasts in salt and their effects on flow in salt

    NASA Astrophysics Data System (ADS)

    Urai, Janos L.; Kukla, Peter A.

    2014-05-01

    The majority of numerical and analogue models of salt tectonics assume homogeneous rheological models, and consequently produce simple internal structures. This is in contrast to observations in salt mines and 3D seismic, showing complex folding at a wide range of scales, in combination with boudinage and fracturing, which point to large rheological contrasts in salt bodies. The rheology of rock salt during slow deformation can be both Newtonian and Power law. Dislocation creep and dissolution-precipitation processes, such as solution-precipitation creep and dynamic recrystallisation, both play a significant role and grain boundary healing in deforming salt may result in cyclic softening and hardening behaviour. The switch between these processes can cause major changes in rock salt rheology, at time scales both relevant to geologic evolution and subsurface operations. In the dislocation creep field, a compilation of laboratory data show that different rock salts can creep at four orders of magnitude different strain rates under otherwise the same conditions. Potassium - Magnesium salts are in turn much weaker, and Anhydrite much stronger than rock salt. Anhydrite - carbonate inclusions embedded in deforming salt bodies respond to the movements of the salt in a variety of ways including boudinage and folding. New methods of microstructure analysis integrated with paleorheology indicators observed in natural laboratories allows an integration of these data and the development of a unified model for salt creep for both underground cavities and natural deformation, including the effect of high fluid pressures in salt which lead to a dramatic increases in permeability. For example, modeling of anhydrite stringer sinking is an important way to obtain the long term rheology of the halite, indicating that the rheology of Zechstein salt during the Tertiary was dominated by dislocation creep. These form the basis of a new generation of mechanical models to predict the

  6. Lithium-Ion Electrolytes with Improved Safety Tolerance to High Voltage Systems

    NASA Technical Reports Server (NTRS)

    Smart, Marshall C. (Inventor); Bugga, Ratnakumar V. (Inventor); Prakash, Surya G. (Inventor); Krause, Frederick C. (Inventor)

    2015-01-01

    The invention discloses various embodiments of electrolytes for use in lithium-ion batteries, the electrolytes having improved safety and the ability to operate with high capacity anodes and high voltage cathodes. In one embodiment there is provided an electrolyte for use in a lithium-ion battery comprising an anode and a high voltage cathode. The electrolyte has a mixture of a cyclic carbonate of ethylene carbonate (EC) or mono-fluoroethylene carbonate (FEC) co-solvent, ethyl methyl carbonate (EMC), a flame retardant additive, a lithium salt, and an electrolyte additive that improves compatibility and performance of the lithium-ion battery with a high voltage cathode. The lithium-ion battery is charged to a voltage in a range of from about 2.0 V (Volts) to about 5.0 V (Volts).

  7. A stable graphite negative electrode for the lithium-sulfur battery.

    PubMed

    Jeschull, Fabian; Brandell, Daniel; Edström, Kristina; Lacey, Matthew J

    2015-12-14

    Efficient, reversible lithium intercalation into graphite in ether-based electrolytes is enabled through a protective electrode binder, polyacrylic acid sodium salt (PAA-Na). In turn, this enables the creation of a stable "lithium-ion-sulfur" cell, using a lithiated graphite negative electrode with a sulfur positive electrode, using the common DME:DOL solvent system suited to the electrochemistry of the lithium-sulfur battery. Graphite-sulfur lithium-ion cells show average coulombic efficiencies of ∼99.5%, compared with <95% for lithium-sulfur cells, and significantly better capacity retention, taking into account cell balancing considerations. The high efficiency derives from the considerably better interfacial stability of the graphite electrode, which suppresses the polysulfide redox shuttle and self-discharge. PMID:26451894

  8. Multiphase Flow and Cavern Abandonment in Salt

    SciTech Connect

    Ehgartner, Brian; Tidwell, Vince

    2001-02-13

    This report will explore the hypothesis that an underground cavity in gassy salt will eventually be gas filled as is observed on a small scale in some naturally occurring salt inclusions. First, a summary is presented on what is known about gas occurrences, flow mechanisms, and cavern behavior after abandonment. Then, background information is synthesized into theory on how gas can fill a cavern and simultaneously displace cavern fluids into the surrounding salt. Lastly, two-phase (gas and brine) flow visualization experiments are presented that demonstrate some of the associated flow mechanisms and support the theory and hypothesis that a cavity in salt can become gas filled after plugging and abandonment

  9. Helping crops stand up to salt

    SciTech Connect

    Raeburn, P.

    1985-05-01

    A new approach to the problem of increasing soil salinity is to raise salt-tolerant plants. The search for such plants involves finding new applications for naturally occurring salt-resistant plants (halophytes), using conventional breeding techniques to identify and strengthen crop varieties known to have better-than-average salt tolerance, and applying recombinant DNA methods to introduce salt resistance into existing plants. One promising plant is salicornia, which produces oil high in polyunsaturates at a greater yield than soybeans. Two varieties of atriplex yield as much animal feed as alfalfa and can be harvested several times a year. Seed companies are supporting the research.

  10. Molten salt safety study. Final report

    SciTech Connect

    Not Available

    1980-01-01

    The considerations concerning safety in using molten salt (40% potassium nitrate, 60% sodium nitrate) in a solar central receiver plant are addressed. The considerations are of a general nature and do not cover any details of equipment or plant operation. The study includes salt chemical reaction, experiments with molten salt, dry storage and handling constraints, and includes data from the National Fire Protection Association. The contents of this report were evaluated by two utility companies and they concluded that no major safety problems exist in using a molten salt solar system.

  11. Lithium cell test results

    NASA Technical Reports Server (NTRS)

    Bragg, B. J.

    1977-01-01

    Three lithium SO2 cells, two lithium CF cells, and a vinyl chloride cell, all with crimped seals, and all strictly experimental, were independently discharged on resistors. Three temperatures were used and several different storage temperatures. Discharge rate generally on the nominal discharges were 0.1 amp, 0.5 amp, and 1 amp. Tests results show that the crimp seals are inadequate, especially for the SO2 cells. Normal discharges present no hazards. All cells discharge to zero. The problem of lithium cell explosions, such as occurred during off-limits testing, is discussed.

  12. Lithium Dendrite Formation

    SciTech Connect

    2015-03-06

    Scientists at the Department of Energy’s Oak Ridge National Laboratory have captured the first real-time nanoscale images of lithium dendrite structures known to degrade lithium-ion batteries. The ORNL team’s electron microscopy could help researchers address long-standing issues related to battery performance and safety. Video shows annular dark-field scanning transmission electron microscopy imaging (ADF STEM) of lithium dendrite nucleation and growth from a glassy carbon working electrode and within a 1.2M LiPF6 EC:DM battery electrolyte.

  13. Toxic Effects of Lithium Chloride during Early Neonatal Period of Rat Development.

    PubMed

    Menshanov, P N; Bannova, A V; Dygalo, N N

    2016-02-01

    Lithium chloride (85, 255, or 255+127 μg/kg) or dexamethasone (0.2 or 2 mg/kg) were subcutaneously injected to 3-day-old rat pups, whose excretory system did not yet attain functional maturity. Both agents retarded the growth of rat pups and delayed the appearance of negative geotaxis. LD50 and therapeutic index of lithium chloride were 255 μg/kg and TI≤3, respectively. Thus, lithium salts even in low doses can be highly toxic for the developing organism. PMID:26906201

  14. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

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

    2010-06-08

    An uncycled preconditioned electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula xLi.sub.2-yH.sub.yO.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 in which 0lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. The xLi.sub.2-yH.sub.y.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 material is prepared by preconditioning a precursor lithium metal oxide (i.e., xLi.sub.2M'O.sub.3.(1-x)LiMO.sub.2) with a proton-containing medium with a pH<7.0 containing an inorganic acid. Methods of preparing the electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

  15. Diffusive Fractionation of Lithium Isotopes in Olivine

    NASA Astrophysics Data System (ADS)

    Homolova, V.; Richter, F. M.; Watson, E. B.; Chaussidon, M.

    2014-12-01

    Systematic lithium isotope variations along concentration gradients found in olivine and pyroxene grains from terrestrial, lunar and martian rocks have been attributed to diffusive isotopic fractionation [Beck et al., 2006; Tang et al., 2007]. In some cases, these isotopic excursions are so large that a single grain may display isotopic variability that spans almost the entire range of documented terrestrial values [Jeffcoate et al., 2007]. In this study, we present the results of experiments to examine diffusive isotopic fractionation of lithium in olivine. The experiments comprised crystallographically oriented slabs of San Carlos olivine juxtaposed with either spodumene powder or a lithium rich pyroxene crystal. Experiments were conducted at 1 GPa and 0.1MPa over a temperature range of 1000 to 1125⁰C. Oxygen fugacity in the 0.1MPa experiments was controlled using the wustite-magnetite and nickel-nickel oxide solid buffer assemblages. Lithium concentrations generally decrease smoothly away from the edges of the grains; however, experiments involving diffusion parallel to the a-axis consistently show peculiar wavy or segmented concentration profiles. Lithium diffusivity parallel to the c-axis is on the order of 1E-14m2/s at 1100⁰C. The diffusivity parallel to the c-axis is more than an order of magnitude faster than diffusion parallel to the b-axis and correlates positively with oxygen fugacity. The lithium isotopic composition, δ7Li = 1000‰ * ((δ7Lisample- δ7Ligrain center)/ δ7Ligrain center), shows a decrease away from the edge of the grain to a minimum value (up to 70‰ lighter) and then an abrupt increase back to the initial isotopic composition of the olivine grain. This isotopic profile is similar to those found in natural grains and an experimental study on diffusive fractionation of lithium isotopes in pyroxene [Richter et al., 2014]. Results from the present study are modeled using the approach of Dohmen et al. [2010], which assumes lithium

  16. Geospatial examination of lithium in drinking water and suicide mortality

    PubMed Central

    2012-01-01

    Background Lithium as a substance occurring naturally in food and drinking water may exert positive effects on mental health. In therapeutic doses, which are more than 100 times higher than natural daily intakes, lithium has been proven to be a mood-stabilizer and suicide preventive. This study examined whether natural lithium content in drinking water is regionally associated with lower suicide rates. Methods Previous statistical approaches were challenged by global and local spatial regression models taking spatial autocorrelation as well as non-stationarity into account. A Geographically Weighted Regression model was applied with significant independent variables as indicated by a spatial autoregressive model. Results The association between lithium levels in drinking water and suicide mortality can be confirmed by the global spatial regression model. In addition, the local spatial regression model showed that the association was mainly driven by the eastern parts of Austria. Conclusions According to old anecdotic reports the results of this study support the hypothesis of positive effects of natural lithium intake on mental health. Both, the new methodological approach and the results relevant for health may open new avenues in the collaboration between Geographic Information Science, medicine, and even criminology, such as exploring the spatial association between violent or impulsive crime and lithium content in drinking water. PMID:22695110

  17. Stabilizing lithium metal using ionic liquids for long-lived batteries.

    PubMed

    Basile, A; Bhatt, A I; O'Mullane, A P

    2016-01-01

    Suppressing dendrite formation at lithium metal anodes during cycling is critical for the implementation of future lithium metal-based battery technology. Here we report that it can be achieved via the facile process of immersing the electrodes in ionic liquid electrolytes for a period of time before battery assembly. This creates a durable and lithium ion-permeable solid-electrolyte interphase that allows safe charge-discharge cycling of commercially applicable Li|electrolyte|LiFePO4 batteries for 1,000 cycles with Coulombic efficiencies >99.5%. The tailored solid-electrolyte interphase is prepared using a variety of electrolytes based on the N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide room temperature ionic liquid containing lithium salts. The formation is both time- and lithium salt-dependant, showing dynamic morphology changes, which when optimized prevent dendrite formation and consumption of electrolyte during cycling. This work illustrates that a simple, effective and industrially applicable lithium metal pretreatment process results in a commercially viable cycle life for a lithium metal battery. PMID:27292652

  18. Studies of ionic liquids in lithium-ion battery test systems

    SciTech Connect

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

    2006-06-01

    In this work, thermal and electrochemical properties of neat and mixed ionic liquid - lithium salt systems have been studied. The presence of a lithium salt causes both thermal and phase-behavior changes. Differential scanning calorimeter DSC and thermal gravimetric analysis TGA were used for thermal analysis for several imidazolium bis(trifluoromethylsulfonyl)imide, trifluoromethansulfonate, BF{sub 4}, and PF{sub 6} systems. Conductivities and diffusion coefficient have been measured for some selected systems. Chemical reactions in electrode - ionic liquid electrolyte interfaces were studied by interfacial impedance measurements. Lithium-lithium and lithium-carbon cells were studied at open circuit and a charged system. The ionic liquids studied include various imidazolium systems that are already known to be electrochemically unstable in the presence of lithium metal. In this work the development of interfacial resistance is shown in a Li|BMIMBF{sub 4} + LiBF{sub 4}|Li cell as well as results from some cycling experiments. As the ionic liquid reacts with the lithium electrode the interfacial resistance increases. The results show the magnitude of reactivity due to reduction of the ionic liquid electrolyte that eventually has a detrimental effect on battery performance.

  19. Stabilizing lithium metal using ionic liquids for long-lived batteries

    PubMed Central

    Basile, A.; Bhatt, A. I.; O'Mullane, A. P.

    2016-01-01

    Suppressing dendrite formation at lithium metal anodes during cycling is critical for the implementation of future lithium metal-based battery technology. Here we report that it can be achieved via the facile process of immersing the electrodes in ionic liquid electrolytes for a period of time before battery assembly. This creates a durable and lithium ion-permeable solid–electrolyte interphase that allows safe charge–discharge cycling of commercially applicable Li|electrolyte|LiFePO4 batteries for 1,000 cycles with Coulombic efficiencies >99.5%. The tailored solid–electrolyte interphase is prepared using a variety of electrolytes based on the N-propyl-N-methylpyrrolidinium bis(fluorosulfonyl)imide room temperature ionic liquid containing lithium salts. The formation is both time- and lithium salt-dependant, showing dynamic morphology changes, which when optimized prevent dendrite formation and consumption of electrolyte during cycling. This work illustrates that a simple, effective and industrially applicable lithium metal pretreatment process results in a commercially viable cycle life for a lithium metal battery. PMID:27292652

  20. Nonflammable perfluoropolyether-based electrolytes for lithium batteries

    PubMed Central

    Wong, Dominica H. C.; Thelen, Jacob L.; Fu, Yanbao; Devaux, Didier; Pandya, Ashish A.; Battaglia, Vincent S.; Balsara, Nitash P.; DeSimone, Joseph M.

    2014-01-01

    The flammability of conventional alkyl carbonate electrolytes hinders the integration of large-scale lithium-ion batteries in transportation and grid storage applications. In this study, we have prepared a unique nonflammable electrolyte composed of low molecular weight perfluoropolyethers and bis(trifluoromethane)sulfonimide lithium salt. These electrolytes exhibit thermal stability beyond 200 °C and a remarkably high transference number of at least 0.91 (more than double that of conventional electrolytes). Li/LiNi1/3Co1/3Mn1/3O2 cells made with this electrolyte show good performance in galvanostatic cycling, confirming their potential as rechargeable lithium batteries with enhanced safety and longevity. PMID:24516123

  1. Transient existence of crystalline lithium disulfide Li2S2 in a lithium-sulfur battery

    NASA Astrophysics Data System (ADS)

    Paolella, Andrea; Zhu, Wen; Marceau, Hugues; Kim, Chi-su; Feng, Zimin; Liu, Dongqiang; Gagnon, Catherine; Trottier, Julie; Abdelbast, Guerfi; Hovington, Pierre; Vijh, Ashok; Demopoulos, George P.; Armand, Michel; Zaghib, Karim

    2016-09-01

    Crystalline lithium disulfide (Li2S2) is identified, for the first time, as a transient species in the lithium-sulfur cell, by using an operando X-ray diffraction (XRD) technique. The observed XRD pattern precisely matches with the predicted pattern based on the density function theory. The formation of Li2S2 crystals is repetitively found in the highly concentrated (7 M Li+) electrolyte at high voltage region (>2 V) near the end of the first charge cycle and before the end of the second discharge cycle. These conditions indicate that crystalline Li2S2 exists in the non-equilibrium regime. The formation of crystalline Li2S2 under only the specified conditions suggests that it is not formed as an intermediate discharge product, contrary to what is generally believed, but as a transient species by the disproportionation reaction from higher order polysulfides which is facilitated by the "solvent-in-salt" conditions.

  2. Current status of environmental, health, and safety issues of lithium polymer electric vehicle batteries

    SciTech Connect

    Corbus, D; Hammel, C J

    1995-02-01

    Lithium solid polymer electrolyte (SPE) batteries are being investigated by researchers worldwide as a possible energy source for future electric vehicles (EVs). One of the main reasons for interest in lithium SPE battery systems is the potential safety features they offer as compared to lithium battery systems using inorganic and organic liquid electrolytes. However, the development of lithium SPE batteries is still in its infancy, and the technology is not envisioned to be ready for commercialization for several years. Because the research and development (R&D) of lithium SPE battery technology is of a highly competitive nature, with many companies both in the United States and abroad pursuing R&D efforts, much of the information concerning specific developments of lithium SPE battery technology is proprietary. This report is based on information available only through the open literature (i.e., information available through library searches). Furthermore, whereas R&D activities for lithium SPE cells have focused on a number of different chemistries, for both electrodes and electrolytes, this report examines the general environmental, health, and safety (EH&S) issues common to many lithium SPE chemistries. However, EH&S issues for specific lithium SPE cell chemistries are discussed when sufficient information exists. Although lithium batteries that do not have a SPE are also being considered for EV applications, this report focuses only on those lithium battery technologies that utilize the SPE technology. The lithium SPE battery technologies considered in this report may contain metallic lithium or nonmetallic lithium compounds (e.g., lithium intercalated carbons) in the negative electrode.

  3. Current status of environmental, health, and safety issues of lithium polymer electric vehicle batteries

    NASA Astrophysics Data System (ADS)

    Corbus, D.; Hammel, C. J.

    1995-02-01

    Lithium solid polymer electrolyte (SPE) batteries are being investigated by researchers worldwide as a possible energy source for future electric vehicles (EV's). One of the main reasons for interest in lithium SPE battery systems is the potential safety features they offer as compared to lithium battery systems using inorganic and organic liquid electrolytes. However, the development of lithium SPE batteries is still in its infancy, and the technology is not envisioned to be ready for commercialization for several years. Because the research and development (R&D) of lithium SPE battery technology is of a highly competitive nature, with many companies both in the United States and abroad pursuing R&D efforts, much of the information concerning specific developments of lithium SPE battery technology is proprietary. This report is based on information available only through the open literature (i.e., information available through library searches). Furthermore, whereas R&D activities for lithium SPE cells have focused on a number of different chemistries, for both electrodes and electrolytes, this report examines the general environmental, health, and safety (EH&S) issues common to many lithium SPE chemistries. However, EH&S issues for specific lithium SPE cell chemistries are discussed when sufficient information exists. Although lithium batteries that do not have a SPE are also being considered for EV applications, this report focuses only on those lithium battery technologies that utilize the SPE technology. The lithium SPE battery technologies considered in this report may contain metallic lithium or nonmetallic lithium compounds (e.g., lithium intercalated carbons) in the negative electrode.

  4. Lithium drifted germanium system

    NASA Technical Reports Server (NTRS)

    Fjarlie, E. J.

    1969-01-01

    General characteristics of the lithium-drifted germanium photodiode-Dewar-preamplifier system and particular operating instructions for the device are given. Information is included on solving operational problems.

  5. APPARATUS FOR THE PRODUCTION OF LITHIUM METAL

    DOEpatents

    Baker, P.S.; Duncan, F.R.; Greene, H.B.

    1961-08-22

    Methods and apparatus for the production of high-purity lithium from lithium halides are described. The apparatus is provided for continuously contacting a molten lithium halide with molten barium, thereby forming lithium metal and a barium halide, establishing separate layers of these reaction products and unreacted barium and lithium halide, and continuously withdrawing lithium and barium halide from the reaction zone. (AEC)

  6. Scoping studies: behavior and control of lithium and lithium aerosols

    SciTech Connect

    Jeppson, D W

    1982-01-01

    The HEDL scoping studies examining the behavior of lithium and lithium aerosols have been conducted to determine and examine potential safety and environmental issues for postulated accident conditions associated with the use of lithium as a fusion reactor blanket and/or coolant. Liquid lithium reactions with air, nitrogen, carbon dioxide and concretes have been characterized. The effectiveness of various powder extinguishing agents and methods of application were determined for lithium-air reactions. The effectiveness of various lithium aerosol collection methods were determined and the volatilization and transport of radioactive metals potentially associated with lithium-air reactions were evaluated. Liquid lithium atmosphere reactions can be safely controlled under postulated accident conditions, but special handling practices must be provided. Lithium-concrete reactions should be avoided because of the potential production of high temperatures, corrosive environment and hydrogen. Carbon microspheres are effective in extinguishing well established lithium-air reactions for the lithium quantities tested (up to 10 kg). Large mass loading of lithium aerosols can be efficiently collected with conventional air cleaning systems. Potentially radioactive species (cobalt, iron and manganese) will be volatilized in a lithium-air reaction in contact with neutron activated stainless steel.

  7. A green and efficient technology for the degradation of cellulosic materials: structure changes and enhanced enzymatic hydrolysis of natural cellulose pretreated by synergistic interaction of mechanical activation and metal salt.

    PubMed

    Zhang, Yanjuan; Li, Qian; Su, Jianmei; Lin, Ye; Huang, Zuqiang; Lu, Yinghua; Sun, Guosong; Yang, Mei; Huang, Aimin; Hu, Huayu; Zhu, Yuanqin

    2015-02-01

    A new technology for the pretreatment of natural cellulose was developed, which combined mechanical activation (MA) and metal salt treatments in a stirring ball mill. Different valent metal nitrates were used to investigate the changes in degree of polymerization (DP) and crystallinity index (CrI) of cellulose after MA+metal salt (MAMS) pretreatment, and Al(NO3)3 showed better pretreatment effect than NaNO3 and Zn(NO3)2. The destruction of morphological structure of cellulose was mainly resulted from intense ball milling, and the comparative studies on the changes of DP and crystal structure of MA and MA+Al(NO3)3 pretreated cellulose samples showed a synergistic interaction of MA and Al(NO3)3 treatments with more effective changes of structural characteristics of MA+Al(NO3)3 pretreated cellulose and substantial increase of reducing sugar yield in enzymatic hydrolysis of cellulose. In addition, the results indicated that the presence of Al(NO3)3 had significant enhancement for the enzymatic hydrolysis of cellulose. PMID:25490099

  8. Lithium battery management system

    DOEpatents

    Dougherty, Thomas J.

    2012-05-08

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

  9. Solid-state lithium battery

    SciTech Connect

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

    2014-11-04

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

  10. Comparative study on lithium borates as corrosion inhibitors of aluminum current collector in lithium bis(fluorosulfonyl)imide electrolytes

    NASA Astrophysics Data System (ADS)

    Park, Kisung; Yu, Sunghun; Lee, Chulhaeng; Lee, Hochun

    2015-11-01

    Lithium bis(fluorosulfonyl)imide (LiFSI) is a promising salt that can possibly overcome the limitations of lithium hexafluorophosphate (LiPF6) in current Li-ion batteries (LIBs). Aluminum (Al) corrosion issue, however, is a major bottleneck for the wide use of LiFSI. This study investigates lithium borate salts as Al corrosion inhibitors in LiFSI electrolytes. Through a systematic comparison among lithium tetrafluoroborate (LiBF4), lithium bis(oxalato)borate (LiBOB), and lithium difluoro(oxalato)borate (LiDFOB), and LiPF6, the inhibition ability of the additives is revealed to be in the following order: LiDFOB > LiBF4 ≈ LiPF6 > LiBOB. In particular, the inhibition effect of LiDFOB is outstanding; the anodic behavior of Al in 0.8 M LiFSI + 0.2 M LiDFOB ethylene carbonate (EC)-based electrolyte is comparable to that of corrosion-free 1 M LiPF6 solution. The superior inhibition ability of LiDFOB is attributed to the formation of a passive layer composed of Al-F, Al2O3, and B-O species, as evidenced by X-ray photoelectron spectroscopy (XPS) measurements. A LiCoO2/graphite cell with 0.8 M LiFSI + 0.2 M LiDFOB electrolyte exhibits a rate capability comparable to a cell with 1 M LiPF6 solution, whereas a cell with 0.8 M LiFSI solution without LiDFOB suffers from poor power performance resulting from severe Al corrosion.

  11. A Car-Parrinello and path integral molecular dynamics study of the intramolecular lithium bond in the lithium 2-pyridyl-N-oxide acetate

    NASA Astrophysics Data System (ADS)

    Durlak, Piotr; Latajka, Zdzisław; Berski, Sławomir

    2009-07-01

    Lithium bonding in lithium 2-pyridyl-N-oxide acetate has been investigated using classic Car-Parrinello molecular dynamics (CPMD) and the path integral approach [path integrals molecular dynamics (PIMD)]. The simulations have been performed in 300 K. Structures, energies, and lithium trajectories have been determined. The CPMD results show that the lithium atom is generally equidistant between heavy atoms in the (O⋯Li⋯O) bridge. Applying quantum effects through the PIMD leads to similar conclusion. The theoretical lithium 2-pyridyl-N-oxide acetate infrared spectrum has also been determined using the CPMD calculations. This shows very good agreement with available experimental results and reproduces well the broad low-frequency band observed experimentally. In order to gain deeper understanding of the nature of the lithium bonding topological analysis of the electron localization function has been applied.

  12. Hydrogen Outgassing from Lithium Hydride

    SciTech Connect

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

    2006-04-20

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

  13. Energy Storage Materials from Nature through Nanotechnology: A Sustainable Route from Reed Plants to a Silicon Anode for Lithium-Ion Batteries.

    PubMed

    Liu, Jun; Kopold, Peter; van Aken, Peter A; Maier, Joachim; Yu, Yan

    2015-08-10

    Silicon is an attractive anode material in energy storage devices, as it has a ten times higher theoretical capacity than its state-of-art carbonaceous counterpart. However, the common process to synthesize silicon nanostructured electrodes is complex, costly, and energy-intensive. Three-dimensional (3D) porous silicon-based anode materials have been fabricated from natural reed leaves by calcination and magnesiothermic reduction. This sustainable and highly abundant silica source allows for facile production of 3D porous silicon with very good electrochemical performance. The obtained silicon anode retains the 3D hierarchical architecture of the reed leaf. Impurity leaching and gas release during the fabrication process leads to an interconnected porosity and the reductive treatment to an inside carbon coating. Such anodes show a remarkable Li-ion storage performance: even after 4000 cycles and at a rate of 10 C, a specific capacity of 420 mA h g(-1) is achieved. PMID:26119499

  14. Characterization of natural wax esters by MALDI-TOF mass spectrometry.

    PubMed

    Vrkoslav, Vladimír; Míková, Radka; Cvacka, Josef

    2009-01-01

    The applicability of matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF MS) to the analysis of wax esters (WEs) was investigated. A series of metal salts of 2,5-dihydroxybenzoic acid (DHB) was synthesized and tested as possible matrices. Alkali metal (Li, Na, K, Rb, Cs) and transition metal (Cu, Ag) salts were studied. The matrix properties were evaluated, including solubility in organic solvents, threshold laser power that should be applied for successful desorption/ionization of WEs, the nature of the matrix ions and the mass range occupied by them, and the complexity of the isotope clusters for individual metals. Lithium salt of dihydroxybenzoic acid (LiDHB) performed the best and matrices with purified lithium isotopes ((6)LiDHB or (7)LiDHB) were recommended for WEs. Three sample preparation procedures were compared: (1) mixing the sample and matrix in a glass vial and deposition of the mixture on a MALDI plate (Mix), (2) deposition of sample followed by deposition of matrix (Sa/Ma), and (3) deposition of matrix followed by deposition of sample (Ma/Sa). Morphology of the samples was studied by scanning electron microscopy. The best sample preparation technique was Ma/Sa with the optimum sample to matrix molar ratio 1 : 100. Detection limit was in the low picomolar range. The relative response of WEs decreased with their molecular weight, and minor differences between signals of saturated and monounsaturated WEs were observed. MALDI spectra of WEs showed molecular adducts with lithium [M + Li](+). Fragments observed in postsource decay (PSD) spectra were related to the acidic part of WEs [RCOOH + Li](+) and they were used for structure assignment. MALDI with LiDHB was used for several samples of natural origin, including insect and plant WEs. A good agreement with GC/MS data was achieved. Moreover, MALDI allowed higher WEs to be analyzed, up to 64 carbon atoms in Ginkgo biloba leaves extract. PMID:18821728

  15. Comparison of shallow-water and marsh-surface habitats associated with pipeline canals and natural channels in Louisiana salt marshes

    SciTech Connect

    Rozas, L.P.

    1992-11-01

    The primary objective of the study was to assess the effects of pipeline canals on the habitat function of inside-levee marshes. The degree to which inside-levee marshes function as nursery habitat for nekton residing in canals was examined by comparing densities of nekton on marshes adjacent to pipeline canals (inside-levee marshes) and natural tidal creeks. In addition, shallow subtidal habitats in the two environments (canals and natural channels) were compared by sampling nekton along the marsh edge at low tide and measuring predator encounter rates in both habitats.

  16. Environmental aspects of produced-water salt releases in onshore and coastal petroleum-producing areas of the conterminous U.S. - a bibliography

    USGS Publications Warehouse

    Otton, James K.

    2006-01-01

    Environmental effects associated with the production of oil and gas have been reported since the first oil wells were drilled in the Appalachian Basin in Pennsylvania and Kentucky in the early to mid-1800s. The most significant of these effects are the degradation of soils, ground water, surface water, and ecosystems they support by releases of suspended and dissolved hydrocarbons and co-produced saline water. Produced water salts are less likely than hydrocarbons to be adsorbed by mineral phases in the soil and sediment and are not subject to degradation by biologic processes. Sodium is a major dissolved constituent in most produced waters and it causes substantial degradation of soils through altering of clays and soil textures and subsequent erosion. Produced water salts seem to have the most wide-ranging effects on soils, water quality, and ecosystems. Trace elements, including boron, lithium, bromine, fluorine, and radium, also occur in elevated concentrations in some produced waters. Many trace elements are phytotoxic and are adsorbed and may remain in soils after the saline water has been flushed away. Radium-bearing scale and sludge found in oilfield equipment and discarded on soils pose additional hazards to human health and ecosystems. This bibliography includes studies from across the oil- and natural-gas-producing areas of the conterminous United States that were published in the last 80 yrs. The studies describe the effects of produced water salts on soils, water quality, and ecosystems. Also included are reports that describe (1) the inorganic chemistry of produced waters included in studies of formation waters for various purposes, (2) other sources of salt affecting water quality that may be mistaken for produced water effects, (3) geochemical and geophysical techniques that allow discrimination of salt sources, (4) remediation technologies designed to repair damage caused to soils and ground water by produced water salts, and (5) contamination by

  17. Lithium: for harnessing renewable energy

    USGS Publications Warehouse

    Bradley, Dwight; Jaskula, Brian

    2014-01-01

    Lithium, which has the chemical symbol Li and an atomic number of 3, is the first metal in the periodic table. Lithium has many uses, the most prominent being in batteries for cell phones, laptops, and electric and hybrid vehicles. Worldwide sources of lithium are broken down by ore-deposit type as follows: closed-basin brines, 58%; pegmatites and related granites, 26%; lithium-enriched clays, 7%; oilfield brines, 3%; geothermal brines, 3%; and lithium-enriched zeolites, 3% (2013 statistics). There are over 39 million tons of lithium resources worldwide. Of this resource, the USGS estimates there to be approximately 13 million tons of current economically recoverable lithium reserves. To help predict where future lithium supplies might be located, USGS scientists study how and where identified resources are concentrated in the Earth’s crust, and they use that knowledge to assess the likelihood that undiscovered resources also exist.

  18. Rechargeable ambient temperature lithium cells

    NASA Technical Reports Server (NTRS)

    Holleck, G. L.

    1980-01-01

    The cycling performance of a secondary lithium cell with a 2-methyl THF lithium hectofluorarsenate electrolyte is discussed. Stripping efficiency, dendritization, passivation on standing, and discharge efficiency are considered.

  19. [Lithium gluconate 8% in the treatment of seborrheic dermatitis].

    PubMed

    Dréno, B; Blouin, E; Moyse, D

    2007-04-01

    Seborrheic dermatitis is a chronic from of inflammatory dermatitis characterized by erythema and desquamation with predominant localization on the face (nasolabial folds, eyebrows, hair-line and ears). It appears to be caused by proliferation of Malassezia yeasts. Lithium gluconate 8% gel (Lithioderm 8% gel) is the only drug containing topical lithium salt commercially available in France for the treatment of seborrheic dermatitis. The mechanism of action of topical lithium is not well known; it may act through anti-inflammatory and antifungal action. Efficacy and safety were assessed in 2 clinical studies, one versus placebo and the other versus ketoconazole 2% foaming gel using the same principal criterion defined as the rate of patients showing complete remission after 2 months of treatment (complete disappearance of both erythema and desquamation). Lithium gluconate 8% was significantly more effective than placebo and than ketoconazole 2% foaming gel and was well tolerated. Adverse events observed were cutaneous (burning sensation, erythema and pruritus), for the most part of mild severity. No cutaneous side effects contributed to those reported with the use of systemic lithium in psychiatric disorders were noted. Pharmacokinetic studies have shown that systemic absorption after topical application is low. Lithioderm 8% gel is applied twice daily over a recommended period of 2 months. It constitutes a new alternative in the treatment of facial seborrheic dermatitis, regardless of severity. PMID:17483754

  20. Treatment of oxide spent fuel using the lithium reduction process

    SciTech Connect

    Karell, E.J.; Pierce, R.D.; Mulcahey, T.P.

    1996-05-01

    The wide variety in the composition of DOE spent nuclear fuel complicates its long-term disposition because of the potential requirement to individually qualify each type of fuel for repository disposal. Argonne National Laboratory (ANL) has developed the electrometallurgical treatment technique to convert all of these spent fuel types into a single set of disposal forms, simplifying the qualification process. While metallic fuels can be directly processed using the electrometallurgical treatment technique, oxide fuels must first be reduced to the metallic form. The lithium reduction process accomplishes this pretreatment. In the lithium process the oxide components of the fuel are reduced using lithium at 650 C in the presence of molten LiCl, yielding the corresponding metals and Li{sub 2}O. The reduced metal components are then separated from the LiCl salt phase and become the feed material for electrometallurgical treatment. A demonstration test of the lithium reduction process was successfully conducted using a 10-kg batch of simulated oxide spent fuel and engineering-scale equipment specifically constructed for that purpose. This paper describes the lithium process, the equipment used in the demonstration test, and the results of the demonstration test.

  1. Natural abundance 17O, 6Li NMR and molecular modeling studies of the solvation structures of lithium bis(fluorosulfonyl)imide/1,2-dimethoxyethane liquid electrolytes

    NASA Astrophysics Data System (ADS)

    Wan, Chuan; Hu, Mary Y.; Borodin, Oleg; Qian, Jiangfeng; Qin, Zhaohai; Zhang, Ji-Guang; Hu, Jian Zhi

    2016-03-01

    Natural abundance 17O and 6Li NMR experiments, quantum chemistry and molecular dynamics studies were employed to investigate the solvation structures of Li+ at various concentrations of LiFSI in DME electrolytes. It was found that the chemical shifts of both 17O and 6Li changed with the concentration of LiFSI, indicating the changes of solvation structures with concentration. For the quantum chemistry calculations, the coordinated cluster LiFSI(DME)2 forms at first, and its relative ratio increases with increasing LiFSI concentration to 1 M. Then the solvation structure LiFSI(DME) become the dominant component. As a result, the coordination of forming contact ion pairs between Li+ and FSI- ion increases, but the association between Li+ and DME molecule decreases. Furthermore, at LiFSI concentration of 4 M the solvation structures associated with Li+(FSI-)2(DME), Li+2(FSI-)(DME)4 and (LiFSI)2(DME)3 become the dominant components. For the molecular dynamics simulation, with increasing concentration, the association between DME and Li+ decreases, and the coordinated number of FSI- increases, which is in perfect accord with the DFT results.

  2. Effect of acid scavengers on electrochemical performance of lithium-sulfur batteries: Functional additives for utilization of LiPF6

    NASA Astrophysics Data System (ADS)

    Yim, Taeeun; Kang, Kyoung Seok; Yu, Ji-Sang; Kim, Ki Jae; Park, Min-Sik; Woo, Sang-Gil; Jeong, Goojin; Jo, Yong Nam; Im, Keun Yung; Kim, Jae-Hun; Kim, Young-Jun

    2014-08-01

    We investigated a novel approach for utilizing LiPF6 as the lithium salt for Li-S batteries and verifying its chemical reactivity with the main solvent. It is found that the main obstacle for the adoption of LiPF6 is the undesired acid-catalyzed, cascade-type polymerization reaction between cyclic ether components in the solvent and LiPF6. Therefore, several kinds of acid scavengers are proposed to enhance the chemical stability between the main solvent and LiPF6. Simple storage tests indicate that polymerization occurred as acid residue is removed from the electrolyte. Consequently, the cell with a modified electrolyte shows excellent discharge capacity and moderate retention based on its improved chemical stability. These results indicate that assuring the chemical stability is the most important factor to utilizing LiPF6 as the main lithium salt for a Li-S cell. Additionally, it is believed that an understanding of the nature of chemical reactivity will be beneficial to constructing more efficient electrolyte systems owing to enhanced electrochemical performance of many kinds of energy storage systems including Li-S, Li-air, and metal-air batteries.

  3. Interior cavern conditions and salt fall potential

    SciTech Connect

    Munson, D.E.; Molecke, M.A.; Myers, R.E.

    1998-03-01

    A relatively large number of salt caverns are used for fluid hydrocarbon storage, including an extensive set of facilities in the Gulf Coast salt domes for the Strategic Petroleum Reserve (SPR) Program. Attention is focused on the SPR caverns because of available histories that detail events involving loss and damage of the hanging string casing. The total number of events is limited, making the database statistically sparse. The occurrence of the events is not evenly distributed, with some facilities, and some caverns, more susceptible than others. While not all of these events could be attributed to impacts from salt falls, many did show the evidence of such impacts. As a result, a study has been completed to analyze the potential for salt falls in the SPR storage caverns. In this process, it was also possible to deduce some of the cavern interior conditions. Storage caverns are very large systems in which many factors could possibly play a part in casing damage. In this study, all of the potentially important factors such as salt dome geology, operational details, and material characteristics were considered, with all being logically evaluated and most being determined as secondary in nature. As a result of the study, it appears that a principal factor in determining a propensity for casing damage from salt falls is the creep and fracture characteristics of salt in individual caverns. In addition the fracture depends strongly upon the concentration of impurity particles in the salt. Although direct observation of cavern conditions is not possible, the average impurity concentration and the accumulation of salt fall material can be determined. When this is done, there is a reasonable correlation between the propensity for a cavern to show casing damage events and accumulation of salt fall material. The accumulation volumes of salt fall material can be extremely large, indicating that only a few of the salt falls are large enough to cause impact damage.

  4. Salt: a sacred substance.

    PubMed

    De Santo, N G; Bisaccia, C; De Santo, R M; De Santo, L S; Petrelli, L; Gallo, L; Cirillo, M; Capasso, G

    1997-11-01

    Salt is the last relic of the ocean where life was born. Its presence has influenced the whole gamut of history and its name is linked to hundred of geographical locations. Its importance for nutrition is supported by the discovery of Aeneolithic salt cellars. Salt cellars and pyramids of salt have been included in paintings and other works of art. In Japan where salt was and still is obtained from the sea, a salt culture has developed that can be traced in the rituals of everyday life, including meal preparation, sports, and Shinto ceremonies. PMID:9350697

  5. Salt tectonics on Venus

    SciTech Connect

    Wood, C.A.; Amsbury, D.

    1986-05-01

    The discovery of a surprisingly high deuterium/hydrogen ratio on Venus immediately led to the speculation that Venus may have once had a volume of surface water comparable to that of the terrestrial oceans. The authors propose that the evaporation of this putative ocean may have yielded residual salt deposits that formed various terrain features depicted in Venera 15 and 16 radar images. By analogy with models for the total evaporation of the terrestrial oceans, evaporite deposits on Venus should be at least tens to hundreds of meters thick. From photogeologic evidence and in-situ chemical analyses, it appears that the salt plains were later buried by lava flows. On Earth, salt diapirism leads to the formation of salt domes, anticlines, and elongated salt intrusions - features having dimensions of roughly 1 to 100 km. Due to the rapid erosion of salt by water, surface evaporite landforms are only common in dry regions such as the Zagros Mountains of Iran, where salt plugs and glaciers exist. Venus is far drier than Iran; extruded salt should be preserved, although the high surface temperature (470/sup 0/C) would probably stimulate rapid salt flow. Venus possesses a variety of circular landforms, tens to hundreds of kilometers wide, which could be either megasalt domes or salt intrusions colonizing impact craters. Additionally, arcurate bands seen in the Maxwell area of Venus could be salt intrusions formed in a region of tectonic stress. These large structures may not be salt features; nonetheless, salt features should exist on Venus.

  6. Reversibility of anodic lithium in rechargeable lithium-oxygen batteries.

    PubMed

    Shui, Jiang-Lan; Okasinski, John S; Kenesei, Peter; Dobbs, Howard A; Zhao, Dan; Almer, Jonathan D; Liu, Di-Jia

    2013-01-01

    Non-aqueous lithium-air batteries represent the next-generation energy storage devices with very high theoretical capacity. The benefit of lithium-air batteries is based on the assumption that the anodic lithium is completely reversible during the discharge-charge process. Here we report our investigation on the reversibility of the anodic lithium inside of an operating lithium-air battery using spatially and temporally resolved synchrotron X-ray diffraction and three-dimensional micro-tomography technique. A combined electrochemical process is found, consisting of a partial recovery of lithium metal during the charging cycle and a constant accumulation of lithium hydroxide under both charging and discharging conditions. A lithium hydroxide layer forms on the anode separating the lithium metal from the separator. However, numerous microscopic 'tunnels' are also found within the hydroxide layer that provide a pathway to connect the metallic lithium with the electrolyte, enabling sustained ion-transport and battery operation until the total consumption of lithium. PMID:23929396

  7. A theoretical study of pericyclic rearrangements catalyzed by lithium.

    PubMed

    Montero-Campillo, M Merced; Cabaleiro-Lago, Enrique M; Rodríguez-Otero, Jesús

    2008-06-12

    The role of lithium cation in the isomerization from diademane to triquinacene and in the Claisen reaction from phenyl allyl ether to 6-allyl-2,4-cyclohexadienone was analyzed. The nature of the interaction of the lithium ion with the reacting molecules in the transition state was studied using supermolecule and perturbational methods. The aromaticity of the transition state in presence of lithium was compared with that for the same reaction in absence of catalyst, employing tools such as nucleus-independent chemical shift and anisotropy of the induced current density. Our results support that the catalytic effect is caused principally by a more favorable electrostatic interaction of lithium cation with the transition states of both reactions. PMID:18491853

  8. Li(+) solvation in glyme-Li salt solvate ionic liquids.

    PubMed

    Ueno, Kazuhide; Tatara, Ryoichi; Tsuzuki, Seiji; Saito, Soshi; Doi, Hiroyuki; Yoshida, Kazuki; Mandai, Toshihiko; Matsugami, Masaru; Umebayashi, Yasuhiro; Dokko, Kaoru; Watanabe, Masayoshi

    2015-03-28

    Certain molten complexes of Li salts and solvents can be regarded as ionic liquids. In this study, the local structure of Li(+) ions in equimolar mixtures ([Li(glyme)]X) of glymes (G3: triglyme and G4: tetraglyme) and Li salts (LiX: lithium bis(trifluoromethanesulfonyl)amide (Li[TFSA]), lithium bis(pentafluoroethanesulfonyl)amide (Li[BETI]), lithium trifluoromethanesulfonate (Li[OTf]), LiBF4, LiClO4, LiNO3, and lithium trifluoroacetate (Li[TFA])) was investigated to discriminate between solvate ionic liquids and concentrated solutions. Raman spectra and ab initio molecular orbital calculations have shown that the glyme molecules adopt a crown-ether like conformation to form a monomeric [Li(glyme)](+) in the molten state. Further, Raman spectroscopic analysis allowed us to estimate the fraction of the free glyme in [Li(glyme)]X. The amount of free glyme was estimated to be a few percent in [Li(glyme)]X with perfluorosulfonylamide type anions, and thereby could be regarded as solvate ionic liquids. Other equimolar mixtures of [Li(glyme)]X were found to contain a considerable amount of free glyme, and they were categorized as traditional concentrated solutions. The activity of Li(+) in the glyme-Li salt mixtures was also evaluated by measuring the electrode potential of Li/Li(+) as a function of concentration, by using concentration cells against a reference electrode. At a higher concentration of Li salt, the amount of free glyme diminishes and affects the electrode reaction, leading to a drastic increase in the electrode potential. Unlike conventional electrolytes (dilute and concentrated solutions), the significantly high electrode potential found in the solvate ILs indicates that the solvation of Li(+) by the glyme forms stable and discrete solvate ions ([Li(glyme)](+)) in the molten state. This anomalous Li(+) solvation may have a great impact on the electrode reactions in Li batteries. PMID:25733406

  9. A review of lithium deposition in lithium-ion and lithium metal secondary batteries

    NASA Astrophysics Data System (ADS)

    Li, Zhe; Huang, Jun; Yann Liaw, Bor; Metzler, Viktor; Zhang, Jianbo

    2014-05-01

    Major aspects related to lithium deposition in lithium-ion and lithium metal secondary batteries are reviewed. For lithium-ion batteries with carbonaceous anode, lithium deposition may occur under harsh charging conditions such as overcharging or charging at low temperatures. The major technical solutions include: (1) applying electrochemical models to predict the critical conditions for deposition initiation; (2) preventions by improved battery design and material modification; (3) applying adequate charging protocols to inhibit lithium deposition. For lithium metal secondary batteries, the lithium deposition is the inherent reaction during charging. The major technical solutions include: (1) the use of mechanistic models to elucidate and control dendrite initiation and growth; (2) engineering surface morphology of the lithium deposition to avoid dendrite formation via adjusting the composition and concentration of the electrolyte; (3) controlling battery working conditions. From a survey of the literature, the areas that require further study are proposed; e.g., refining the lithium deposition criteria, developing an effective AC self pre-heating method for low-temperature charging of lithium-ion batteries, and clarifying the role the solid electrolyte interphase (SEI) plays in determining the deposition morphology; to facilitate a refined control of the lithium deposition.

  10. Effect of composition on the density of multi-component molten nitrate salts.

    SciTech Connect

    Bradshaw, Robert W.

    2009-12-01

    The density of molten nitrate salts was measured to determine the effects of the constituents on the density of multi-component mixtures. The molten salts consisted of various proportions of the nitrates of potassium, sodium, lithium and calcium. Density measurements ere performed using an Archimedean method and the results were compared to data reported in the literature for the individual constituent salts or simple combinations, such as the binary Solar Salt mixture of NaNO3 and KNO3. The addition of calcium nitrate generally ncreased density, relative to potassium nitrate or sodium nitrate, while lithium nitrate decreased density. The temperature dependence of density is described by a linear equation regardless of composition. The molar volume, and thereby, density of multi-component mixtures an be calculated as a function of temperature using a linear additivity rule based on the properties of the individual constituents.

  11. Use of Ionic Liquids in Rod-Coil Block Copolyimides for Improved Lithium Ion Conduction

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann B.; Tigelaar, Dean M.; Chapin, Kara; Bennett, William R.

    2007-01-01

    Solvent-free, solid polymer electrolytes (SPE) have the potential to improve safety, increase design flexibility and enhance performance of rechargeable lithium batteries. Solution based electrolytes are flammable and typically incompatible with lithium metal anodes, limiting energy density. We have previously demonstrated use of polyimide rod coil block copolymers doped with lithium salts as electrolytes for lithium polymer batteries. The polyimide rod blocks provide dimensional stability while the polyethylene oxide (PEO) coil portions conduct ions. Phase separation of the rods and coils in these highly branched polymers provide channels with an order of magnitude improvement in lithium conduction over polyethylene oxide itself at room temperature. In addition, the polymers have been demonstrated in coin cells to be compatible with lithium metal. For practical use at room temperature and below, however, at least an order of magnitude improvement in ion conduction is still required. The addition of nonvolatile, room temperature ionic liquids has been shown to improve the ionic conductivity of high molecular weight PEO. Herein we describe use of these molten salts to improve ionic conductivity in the rod-coil block copolymers.

  12. [Is there an increased risk for renal tumors during long-term treatment with lithium?].

    PubMed

    Conell, J; Lewitzka, U; Ritter, P; Severus, E; Pilhatsch, M; Pfennig, A; Berghöfer, M; Bauer, M

    2015-09-01

    Lithium salts are the recommended first-line treatment (gold standard) in national and international treatment guidelines for acute and maintenance treatment of affective disorders, such as bipolar disorders. Lithium has also been shown to have a unique protective effect against suicide in patients suffering from affective disorders. Despite the well-known acute and long-term adverse effects lithium therapy can be safely administered if patients are properly educated and carefully monitored. A recent study from France now shows that patients with severely impaired renal function who had been treated with lithium salts for more than 10 years could have an increased risk for kidney tumors (benign and malignant). This resulted in an adjustment concerning information within the package leaflet by European authorities. The authors of this article reflect the currently available data in order to better understand and handle this new finding and to warn about uncritical reactions including withdrawal of lithium in successfully treated patients. This article provides clinical recommendations to provide further insight relating to the risk of kidney cancer in long-term lithium therapy. PMID:26341836

  13. What Are Bath Salts?

    MedlinePlus

    ... Are bath salts becoming more popular? Marsha Lopez Hi, Lauren. Nope! Actually quite the opposite! This family ... and how dangerous for your body? Michelle Rankin Hi ParkerPanella - Bath salts are drugs known as synthetic ...

  14. Low-salt diet

    MedlinePlus

    ... seasonings. Pepper, garlic, herbs, and lemon are good choices. Avoid packaged spice blends. They often contain salt. Use garlic and onion powder, not garlic and onion salt. Do not eat foods with monosodium glutamate (MSG). When you go out ...

  15. 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.

  16. Utah: Salt Lake Region

    Atmospheric Science Data Center

    2014-05-15

    article title:  Winter and Summer Views of the Salt Lake Region     View Larger Image Magnificent views of the region surrounding Salt Lake City, Utah are captured in these winter and summer images from the ...

  17. Lithium overdosage and related tests.

    PubMed

    Pigatto, Paolo D; Dell'Osso, Bernardo; Guzzi, Gianpaolo

    2016-12-01

    Lithium acts biochemically through the inositol depletion in brain cortex. At low doses, however, it is partly effective and/or ineffective, whereas in high concentrations is toxic. We would like to make one point about this review. In fact, in our view, the patient should be given a support to correct hypernatremia and even sodium levels should be tested serially-along with serum lithium concentrations-because high sodium levels reduce the rate of elimination of lithium. Lithium is mainly a neurotoxicant. Lithium-related central nervous system toxicity as well as the cardiovascular and thyroid changes are most likely due to the cations (Na2 (+) and K(+)) competition. PMID:26753697

  18. Phytotoxicity of salt and plant salt uptake: Modeling ecohydrological feedback mechanisms

    NASA Astrophysics Data System (ADS)

    Bauer-Gottwein, Peter; Rasmussen, Nikolaj F.; Feificova, Dagmar; Trapp, Stefan

    2008-04-01

    A new model of phytotoxicity of salt and plant salt uptake is presented and is coupled to an existing three-dimensional groundwater simulation model. The implementation of phytotoxicity and salt uptake relationships is based on experimental findings from willow trees grown in hydroponic solution. The data confirm an s-shaped phytotoxicity relationship as found in previous studies. Uptake data were explained assuming steady state salt concentration in plant roots, passive salt transport into the roots, and active enzymatic removal of salt from plant roots. On the one hand, transpiration strongly depends on groundwater salinity (phytotoxicity); on the other hand, transpiration significantly changes the groundwater salinity (uptake). This feedback loop generates interesting dynamic phenomena in hydrological systems that are dominated by transpiration and are influenced by significant salinity gradients. Generic simulations are performed for the Okavango island system and are shown to reproduce essential phenomena observed in nature.

  19. Conductivity and self-diffusivity measurements on molten lithium electrolytes for battery applications

    NASA Astrophysics Data System (ADS)

    Videa, Marcelo Vargas

    Several lithium salt systems, classified in this work as solvent-free and solvent containing, have been investigated with the purpose of determining their qualities as potential electrolytes for applications in lithium batteries. With this objective, their thermal. properties, of which the glassforming ability was considered of fundamental importance, and their experimental conductivities and lithium self-diffusivities were determined to build a body of information that could be considered complete insofar as the evaluation of the material was concerned. Mixtures of lithium salts with fluorine-based anions, including LiCF 3SO3, LiBF4 and LiN(SO2CF3) 2 (or LiIm), were studied as part of a search for chemically and electrochemically stable glassforming lithium salts. Although the observation of the glassforming ability of some binary and ternary systems was considered a partial success, the high glass transition temperatures recorded and their inability to avoid crystallization discouraged the author from any attempt of using these materials as practical electrolytes. Attention was then placed on a family of tetrahaloaluminate lithium salts among which LiAlCl4, although non-glassforming when pure, can be easely vitrified upon the addition of small amounts of a second component or plasticizing agent. By extrapolation to zero content of plasticizing agent it was found that Tg for this salt is -35°C, the lowest value recorded for an ionic system. Although the LiAlCl4-based systems obtained by introducing LiIm, LiIm-AlCl3 or LiAl(SO3Cl)4 as second components produce room temperature, non-crystallizing liquids, they unfortunately fail in providing conductivities with values acceptable for the applications intended. In the case of the system LiAlC14-LiAl(SO3Cl) 4, lithium self-diffusivity measurements are compared via the Nernst-Einstein relation to the conductivity values in order to obtain insight on lithium-ion transport properties. Solvent-containing electrolytes

  20. Molten salt technology

    SciTech Connect

    Lovering, D.G.

    1982-01-01

    In this volume, the historical background, scope, problems, economics, and future applications of molten salt technologies are discussed. Topics presented include molten salts in primary production of aluminum, general principles and handling and safety of the alkali metals, first-row transition metals, group VIII metals and B-group elements, solution electrochemistry, transport phenomena, corrosion in different molten salts, cells with molten salt electrolytes and reactants, fuel cell design, hydrocracking and liquefaction, heat storage in phase change materials, and nuclear technologies.

  1. Salt weathering on Mars

    NASA Technical Reports Server (NTRS)

    Malin, M. C.

    1974-01-01

    Mariner 9 photographs of Mars indicate that significant erosion has occurred on that planet. Although several possible erosion mechanisms have been proposed, most terrestrial weathering mechanisms cannot function in the present Martian environment. Salt weathering, believed to be active in the Antarctic dry valleys, is especially suited to Mars, given the presence of salts and small amounts of water. Volcanic salts are probably available, and the association of salts and water is likely from both thermodynamic and geologic considerations.

  2. Lithium Ion Batteries

    NASA Technical Reports Server (NTRS)

    1997-01-01

    Lithium ion batteries, which use a new battery chemistry, are being developed under cooperative agreements between Lockheed Martin, Ultralife Battery, and the NASA Lewis Research Center. The unit cells are made in flat (prismatic) shapes that can be connected in series and parallel to achieve desired voltages and capacities. These batteries will soon be marketed to commercial original-equipment manufacturers and thereafter will be available for military and space use. Current NiCd batteries offer about 35 W-hr/kg compared with 110 W-hr/kg for current lithium ion batteries. Our ultimate target for these batteries is 200 W-hr/kg.

  3. Thermoluminescence of ultra-high dilutions of lithium chloride and sodium chloride

    NASA Astrophysics Data System (ADS)

    Rey, Louis

    2003-05-01

    Ultra-high dilutions of lithium chloride and sodium chloride (10 -30 g cm -3) have been irradiated by X- and γ-rays at 77 K, then progressively rewarmed to room temperature. During that phase, their thermoluminescence has been studied and it was found that, despite their dilution beyond the Avogadro number, the emitted light was specific of the original salts dissolved initially.

  4. Two-Dimensional Wavelike Spinel Lithium Titanate for Fast Lithium Storage

    PubMed Central

    Liu, Jiehua; Wei, Xiangfeng; Liu, Xue-Wei

    2015-01-01

    Safe fast-charging lithium-ion batteries (LIBs) have huge potential market size on demand according to their shortened charging time for high-power devices. Zero-strain spinel Li4Ti5O12 is one of ideal candidates for safe high-power batteries owing to its good cycling performance, low cost and safety. However, the inherent insulating characteristic of LTO seriously limits its high-rate capability. In this work, we successfully synthesize novel wavelike spinel LTO nanosheets using a facile ‘co-hydrolysis’ method, which is superior to molten-salt approach and traditional solvothermal method in some respects. The unique 2D structures have single-crystal framework with shortened path for Li ion transport. As a result, the N-doped 2D wavelike LTO with 0.6 wt.% of ‘carbon joint’ not only exhibits exciting capacity of ~180 and ~150 mA h g−1 for fast lithium storage at high discharge/charge rates of 1.7 and 8.5 A g−1 (10C and 50C) respectively, but also shows excellent low-temperature performance at −20°C. In addition, the cost may be further decreased due to recycled functional reagents. This novel nanostructured 2D LTO anode material makes it possible to develop safe fast-charging high-power lithium ion batteries. PMID:25985465

  5. Measurement of Solubility of Metallic Lithium Dissolved in Molten LiCl-Li2O

    NASA Astrophysics Data System (ADS)

    Burak, Adam J.; Simpson, Michael F.

    2016-07-01

    The solubility of lithium metal in molten LiCl-Li2O mixtures has been measured at various concentrations of Li2O ranging from 0 wt.% to 2.7 wt.% at a temperature of approximately 670-680°C. After contacting molten lithium with molten LiCl-Li2O for several hours to achieve equilibrium saturation, samples were taken by freezing the salt onto a room-temperature steel rod and dissolving in water for analysis. Both volume of hydrogen gas generated and volume of titrated HCl were measured to investigate two different approaches to calculating the lithium concentration. There appeared to be no effect of Li2O concentration on the Li solubility in the salt. But the results vary between different methods of deducing the amount of dissolved Li. The H2 collection method is recommended, but care must be taken to ensure all of the H2 has been included.

  6. Observations of the freeze/thaw performance of lithium fluoride by motion picture photography

    NASA Technical Reports Server (NTRS)

    Jaworske, D. A.; Perry, W. D.

    1991-01-01

    To gain direct observation of the molten salt phase change, a novel containerless technique was developed where the high surface tension of lithium fluoride was used to suspend a bead of the molten salt inside a specially designed wire cage. By varying the current passing through the wire, the cage also served as a variable heat source. In this way, the freeze/thaw performance of the lithium fluoride could be photographed by motion picture photography without the influence of container walls. The motion picture photography of the lithium fluoride sample revealed several zones during the phase change, a solid zone and a liquid zone, as expected, and a slush zone that was predicted by thermal analysis modeling.

  7. 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.

  8. 21 CFR 100.155 - Salt and iodized salt.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 2 2011-04-01 2011-04-01 false Salt and iodized salt. 100.155 Section 100.155... FOR HUMAN CONSUMPTION GENERAL Specific Administrative Rulings and Decisions § 100.155 Salt and iodized salt. (a) For the purposes of this section, the term iodized salt or iodized table salt is...

  9. 21 CFR 100.155 - Salt and iodized salt.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 2 2014-04-01 2014-04-01 false Salt and iodized salt. 100.155 Section 100.155... FOR HUMAN CONSUMPTION GENERAL Specific Administrative Rulings and Decisions § 100.155 Salt and iodized salt. (a) For the purposes of this section, the term iodized salt or iodized table salt is...

  10. 21 CFR 100.155 - Salt and iodized salt.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 2 2010-04-01 2010-04-01 false Salt and iodized salt. 100.155 Section 100.155... FOR HUMAN CONSUMPTION GENERAL Specific Administrative Rulings and Decisions § 100.155 Salt and iodized salt. (a) For the purposes of this section, the term iodized salt or iodized table salt is...

  11. 21 CFR 100.155 - Salt and iodized salt.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 2 2012-04-01 2012-04-01 false Salt and iodized salt. 100.155 Section 100.155... FOR HUMAN CONSUMPTION GENERAL Specific Administrative Rulings and Decisions § 100.155 Salt and iodized salt. (a) For the purposes of this section, the term iodized salt or iodized table salt is...

  12. 21 CFR 100.155 - Salt and iodized salt.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 2 2013-04-01 2013-04-01 false Salt and iodized salt. 100.155 Section 100.155... FOR HUMAN CONSUMPTION GENERAL Specific Administrative Rulings and Decisions § 100.155 Salt and iodized salt. (a) For the purposes of this section, the term iodized salt or iodized table salt is...

  13. Fracture and Healing of Rock Salt Related to Salt Caverns

    SciTech Connect

    Chan, K.S.; Fossum, A.F.; Munson, D.E.

    1999-03-01

    In recent years, serious investigations of potential extension of the useful life of older caverns or of the use of abandoned caverns for waste disposal have been of interest to the technical community. All of the potential applications depend upon understanding the reamer in which older caverns and sealing systems can fail. Such an understanding will require a more detailed knowledge of the fracture of salt than has been necessary to date. Fortunately, the knowledge of the fracture and healing of salt has made significant advances in the last decade, and is in a position to yield meaningful insights to older cavern behavior. In particular, micromechanical mechanisms of fracture and the concept of a fracture mechanism map have been essential guides, as has the utilization of continuum damage mechanics. The Multimechanism Deformation Coupled Fracture (MDCF) model, which is summarized extensively in this work was developed specifically to treat both the creep and fracture of salt, and was later extended to incorporate the fracture healing process known to occur in rock salt. Fracture in salt is based on the formation and evolution of microfractures, which may take the form of wing tip cracks, either in the body or the boundary of the grain. This type of crack deforms under shear to produce a strain, and furthermore, the opening of the wing cracks produce volume strain or dilatancy. In the presence of a confining pressure, microcrack formation may be suppressed, as is often the case for triaxial compression tests or natural underground stress situations. However, if the confining pressure is insufficient to suppress fracture, then the fractures will evolve with time to give the characteristic tertiary creep response. Two first order kinetics processes, closure of cracks and healing of cracks, control the healing process. Significantly, volume strain produced by microfractures may lead to changes in the permeability of the salt, which can become a major concern in

  14. 77 FR 28259 - Mailings of Lithium Batteries

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-05-14

    ... for mailpieces containing lithium metal or lithium-ion cells or batteries and applies regardless of...'' instead of ``lithium content'' for secondary lithium-ion batteries when describing maximum quantity limits...-ion (Rechargeable) Cells and Batteries Small consumer-type lithium-ion cells and batteries like...

  15. 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.

  16. LiGa(OTf)(sub 4) as an Electrolyte Salt for Li-Ion Cells

    NASA Technical Reports Server (NTRS)

    Reddy, V. Prakash; Prakash, G. K. Syria; Hu, Jinbo; Yan, Ping; Smart, Marshall; Bugga, ratnakumar; Chin, Keith; Surampudi, Subarao

    2008-01-01

    Lithium tetrakis(trifluoromethane sulfo - nato)gallate [abbreviated "LiGa(OTf)4" (wherein "OTf" signifies trifluoro - methanesulfonate)] has been found to be promising as an electrolyte salt for incorporation into both liquid and polymer electrolytes in both rechargeable and non-rechargeable lithium-ion electrochemical cells. This and other ingredients have been investigated in continuing research oriented toward im proving the performances of rechargeable lithium-ion electrochemical cells, especially at low temperatures. This research at earlier stages, and the underlying physical and chemical principles, were reported in numerous previous NASA Tech Briefs articles. As described in more detail in those articles, lithiumion cells most commonly contain nonaqueous electrolyte solutions consisting of lithium hexafluorophosphate (LiPF6) dissolved in mixtures of cyclic and linear alkyl carbonates, including ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), diethyl carbonate (DEC), and ethyl methyl carbonate (EMC). Although such LiPF6-based electrolyte solutions are generally highly ionically conductive and electrochemically stable, as needed for good cell performance, there is interest in identifying alternate lithium electrolyte salts that, relative to LiPF6, are more resilient at high temperature and are less expensive. Experiments have been performed on LiGa(OTf)4 as well as on several other candidate lithium salts in pursuit of this interest. As part of these experiments, LiGa(OTf)4 was synthesized by the reaction of Ga(OTf)3 with an equimolar portion of LiOTf in a solvent consisting of anhydrous acetonitrile. Evaporation of the solvent yielded LiGa(OTf)4 as a colorless crystalline solid. The LiGa(OTf)4 and the other salts were incorporated into solutions with PC and DMC. The resulting electrolyte solutions exhibited reasonably high ionic conductivities over a relatively wide temperature range down to 40 C (see figure). In cyclic

  17. Electrochemistry of LiCl-Li2O-H2O Molten Salt Systems

    SciTech Connect

    Natalie J. Gese; Batric Pesic

    2013-03-01

    Uranium can be recovered from uranium oxide (UO2) spent fuel through the combination of the oxide reduction and electrorefining processes. During oxide reduction, the spent fuel is introduced to molten LiCl-Li2O salt at 650 degrees C and the UO2 is reduced to uranium metal via two routes: (1) electrochemically, and (2) chemically by lithium metal (Li0) that is produced electrochemically. However, the hygroscopic nature of both LiCl and Li2O leads to the formation of LiOH, contributing hydroxyl anions (OH-), the reduction of which interferes with the Li0 generation required for the chemical reduction of UO2. In order for the oxide reduction process to be an effective method for the treatment of uranium oxide fuel, the role of moisture in the LiCl-Li2O system must be understood. The behavior of moisture in the LiCl-Li2O molten salt system was studied using cyclic voltammetry, chronopotentiometry and chronoamperometry, while reduction to hydrogen was confirmed with gas chromatography.

  18. Thin lithium cobalt dioxide rechargeable cells using polyacrylonitrile-based polymer electrolytes. Technical report

    SciTech Connect

    Slane, S.

    1994-07-01

    Rechargeable Li/LiCoO2 cells with polymer electrolytes have achieved 100 mAh/g capacity and over 75 charge/discharge cycles with an average discharge potential of 3.7 volts. Solid-state polymer lithium electrolytes based on poly(acrylonitrile) (PAN) have achieved room temperature conductivities of 0,001 siemens per cm, equal to that of some liquid organic electrolytes. Polymer films of ethylene carbonate, propylene carbonate, PAN, and lithium salts have yielded conductivities as high as 4x10-4 siemens per cm at 25 deg C. These high conductivities made the use of polymer electrolytes a viable possibility in advanced lithium batteries. Reported here are the film preparation techniques, conductivities from -70 to 70 deg C, and discharge curves of Li/LiCoO2 cells. Rechargeable battery, Lithium, Polymer electrolyte, Ionic conductivity.

  19. Electrochemical properties of a lithium-impregnated metal foam anode for thermal batteries

    NASA Astrophysics Data System (ADS)

    Choi, Yu-Song; Yu, Hye-Ryeon; Cheong, Hae-Won

    2015-02-01

    Lithium-impregnated metal foam anodes (LIMFAs) are fabricated and investigated. The LIMFAs are prepared by the impregnation of lithium into molten-salt-coated nickel metal foam. A single cell with the LIMFA exhibits a specific capacity of 3009 As g-1. For comparison, a single cell with a LiSi alloy anode is also discharged, demonstrating a specific capacity of 1050 As g-1. These significant improvements can be attributed to the large amount of lithium impregnated into the metal foam as well as the molten lithium holding capability of the foam. Due to their excellent electrochemical properties, LIMFAs are suitable for use in thermal batteries.

  20. [Nursing care of a patient with bipolar disorder and lithium-induced nephrogenic diabetes insipidus].

    PubMed

    García de la Orden, Lucía; García Carretero, Rafael

    2015-01-01

    Bipolar disorder is one of the most common, severe and persistent mental disorders. The evaluation of all data and variables related to bipolar disorder is a difficult task, because there is no clear agreement on what should be included in this category. One of the traditional treatments for this disease is the lithium metal that is administered in the form of lithium salt. Lithium has a narrow therapeutic window and there is a significant risk of complications arising from its use, mainly neurological and renal. In the case presented, the preparation of a care plan is described for a patient diagnosed with bipolar disorder who suffered a complication with lithium treatment. To do this, it was decided to use a standardized care plan and later completed it with diagnostic, objectives and interventions to the specific needs of the patient, aimed at achieving optimal levels of independence. PMID:25600576

  1. Effect of Branching on Rod-coil Polyimides as Membrane Materials for Lithium Polymer Batteries

    NASA Technical Reports Server (NTRS)

    Meador, Mary Ann B.; Cubon, Valerie A.; Scheiman, Daniel A.; Bennett, William R.

    2003-01-01

    This paper describes a series of rod-coil block co-polymers that produce easy to fabricate, dimensionally stable films with good ionic conductivity down to room temperature for use as electrolytes for lithium polymer batteries. The polymers consist of short, rigid rod polyimide segments, alternating with flexible, polyalkylene oxide coil segments. The highly incompatible rods and coils should phase separate, especially in the presence of lithium ions. The coil phase would allow for conduction of lithium ions, while the rigid rod phase would provide a high degree of dimensional stability. An optimization study was carried out to study the effect of four variables (degree of branching, formulated molecular weight, polymerization solvent and lithium salt concentration) on ionic conductivity, glass transition temperature and dimensional stability in this system.

  2. Bioavailability of lithium from lithium citrate syrup versus conventional lithium carbonate tablets.

    PubMed

    Guelen, P J; Janssen, T J; De Witte, T C; Vree, T B; Benson, K

    1992-10-01

    The bioavailability of lithium citrate syrup was compared with that of regular lithium carbonate tablets in 18 healthy male human volunteers. Blood samples were collected up to 48 h after dosing. Lithium serum concentrations were determined by means of AAS. The absorption rate following oral administration of the syrup was greater (tmax 0.8 h) than following administration of regular tablets (tmax 1.4 h). Maximum lithium serum concentrations, however, were only about 10 per cent higher after syrup dosing and serum concentrations resulting from syrup and tablets were almost superimposable from 2 h after dosing. The terminal half-life of lithium was found to be 22 h after syrup as well as after tablet dosing. No side-effects were observed during the study. The bioavailability of lithium from syrup relative to tablets was found to be bioequivalent with respect to the maximum lithium serum concentration and the extent of drug absorption (AUC). PMID:1489941

  3. Lithium disulfide battery

    DOEpatents

    Kaun, Thomas D.

    1988-01-01

    A negative electrode limited secondary electrochemical cell having dense FeS.sub.2 positive electrode operating exclusively on the upper plateau, a Li alloy negative electrode and a suitable lithium-containing electrolyte. The electrolyte preferably is 25 mole percent LiCl, 38 mole percent LiBr and 37 mole percent KBr. The cell may be operated isothermally.

  4. Lithium and Pregnancy

    MedlinePlus

    ... role in the rate of miscarriage, which include maternal age, gestational age, and history of previous miscarriage that ... Studies on children up to seven years of age who were exposed to lithium during pregnancy did not find significant physical, mental, or behavioral ...

  5. Lithium thionyl chloride battery

    SciTech Connect

    Saathoff, D.J.; Venkatasetty, H.V.

    1982-10-19

    The discharge rate and internal conductivity of electrochemical cell including a lithium anode, and a cathode and an electrolyte including LiAlCl4 and SOC2 is improved by the addition of an amount of a mixture containing AlCl3 and butyl pyridinium chloride.

  6. Lithium battery discharge tests

    NASA Technical Reports Server (NTRS)

    Johnson, C. J.

    1980-01-01

    The long term discharge of a variety of lithium cells was characterized and the susceptibility of the cells to chemical variation during the slow discharge was tested. A shunt resistor was set across the terminals to monitor the voltage as a function of time. Failures were identified by premature voltage drops.

  7. Mixed solvent electrolytes for ambient temperature secondary lithium cells

    NASA Technical Reports Server (NTRS)

    Shen, David H. (Inventor); Surampudi, Subbarao (Inventor); Deligiannis, Fotios (Inventor); Halpert, Gerald (Inventor)

    1991-01-01

    The present invention comprises an improved electrolyte for secondary lithium-based cells as well as batteries fabricated using this electrolyte. The electrolyte is a lithium containing salt dissolved in a non-aqueous solvent, which is made from a mixture of ethylene carbonate, ethylene propylene diene terpolymer, 2-methylfuran, and 2-methyltetrahydrofuran. This improved, mixed solvent electrolyte is more conductive than prior electrolytes and much less corrosive to lithium anodes. Batteries constructed with this improved electrolyte utilize lithium or lithium alloy anodes and cathodes made of metal chalcogenides or oxides, such as TiS.sub.2, NbSe.sub.3, V.sub.6 O.sub.13, V.sub.2 O.sub.5, MoS.sub.2, MoS.sub.3, CoO.sub.2, or CrO.sub.2, dissolved in a supporting polymer matrix, like EPDM. The preferred non-aqueous solvent mixture comprises approximately 5 to 30 volume percent ethylene carbonate, approximately 0.01 to 0.1 weight percent ethylene propylene diene terpolymer, and approximately 0.2 to 2 percent 2-methylfuran, with the balance being 2-methyltetrahydrofuran. The most preferred solvent comprises approximately 10 to 20 volume percent ethylene carbonate, about 0.05 weight percent ethylene propylene diene terpolymer, and about 1.0 percent 2-methylfuran, with the balance being 2-methyltetrahydrofuran. The concentration of lithium arsenic hexafluoride can range from about 1.0 to 1.8 M; a concentration 1.5 M is most preferred. Secondary batteries made with the improved electrolyte of this invention have lower internal impedance, longer cycle life, higher energy density, low self-discharge, and longer shelf life.

  8. Lithium recovery from brine using a λ-MnO2/activated carbon hybrid supercapacitor system.

    PubMed

    Kim, Seoni; Lee, Jaehan; Kang, Jin Soo; Jo, Kyusik; Kim, Seonghwan; Sung, Yung-Eun; Yoon, Jeyong

    2015-04-01

    Lithium is one of the most important elements in various fields including energy storage, medicine manufacturing and the glass industry, and demands for lithium are constantly increasing these days. The lime soda evaporation process using brine lake water is the major extraction method for lithium, but this process is not only inefficient and time-consuming but also causes a few environmental problems. Electrochemical recovery processes of lithium ions have been proposed recently, but the better idea for the silver negative electrodes used in these systems is required to reduce its cost or increase long term stability. Here, we report an electrochemical lithium recovery method based on a λ-MnO2/activated carbon hybrid supercapacitor system. In this system, lithium ions and counter anions are effectively captured at each electrode with low energy consumption in a salt solution containing various cationic species or simulated Salar de Atacama brine lake water in Chile. Furthermore, we designed this system as a flow process for practical applications. By experimental analyses, we confirmed that this system has high selectivity and long-term stability, with its performance being retained even after repetitive captures and releases of lithium ions. PMID:25681679

  9. Cold neutron depth profiling of lithium-ion battery materials

    NASA Astrophysics Data System (ADS)

    Lamaze, G. P.; Chen-Mayer, H. H.; Becker, D. A.; Vereda, F.; Goldner, R. B.; Haas, T.; Zerigian, P.

    We report the characterization of two thin-film battery materials using neutron techniques. Neutron depth profiling (NDP) has been employed to determine the distribution of lithium and nitrogen simultaneously in lithium phosphorous oxynitride (LiPON) deposited by ion beam assisted deposition (IBAD). The depth profiles are based on the measurement of the energy of the charged particle products from the 6Li(n,α) 3H and 14N(n,p) 14C reactions for lithium and nitrogen, respectively. Lithium at the level of 10 22 atoms/cm 3 and N of 10 21 atoms/cm 3, distributed in the film thickness on the order of 1 μm, have been determined. This information provides insights into nitrogen incorporation and lithium concentration in the films under various fabrication conditions. NDP of lithium has also been performed on IBAD LiCoO 2 films, in conjunction with instrumental neutron activation analysis (INAA) to determine the cobalt concentration. The Li/Co ratio thus obtained serves as an ex situ control for the thin-film evaporation process. The non-destructive nature of the neutron techniques is especially suitable for repeated analysis of these materials and for actual working devices.

  10. Lithium-oxygen batteries-Limiting factors that affect performance

    NASA Astrophysics Data System (ADS)

    Padbury, Richard; Zhang, Xiangwu

    2011-05-01

    Lithium-oxygen batteries have recently received attention due to their extremely high theoretical energy densities, which far exceed that of any other existing energy storage technology. The significantly larger theoretical energy density of the lithium-oxygen batteries is due to the use of a pure lithium metal anode and the fact that the cathode oxidant, oxygen, is stored externally since it can be readily obtained from the surrounding air. Before the lithium-oxygen batteries can be realized as high performance, commercially viable products, there are still many challenges to overcome, from designing their cathode structure, to optimizing their electrolyte compositions and elucidating the complex chemical reactions that occur during charge and discharge. The scientific obstacles that are related to the performance of the lithium-oxygen batteries open up an exciting opportunity for researchers from many different backgrounds to utilize their unique knowledge and skills to bridge the knowledge gaps that exist in current research projects. This article is a summary of the most significant limiting factors that affect the performance of the lithium-oxygen batteries from the perspective of the authors. The article indicates the relationships that form between various limiting factors and highlights the complex yet captivating nature of the research within this field.

  11. Lithium ferrite nanoparticles for ferrofluid applications

    NASA Astrophysics Data System (ADS)

    Sankaranarayanan, V. K.; Prakash, Om; Pant, R. P.; Islam, Mohammad

    2002-11-01

    Nanoparticles of Lithium ferrite in the particle size range of 10 nm have been prepared by a citrate precursor method at a relatively low temperature of 200°C. The particles show characteristic infra red (IR) spectrum of lithium ferrite and broadened X-ray diffraction (XRD) patterns typical of the nanoparticle nature. The sample decomposed at 200°C has the β-LiFe 5O 8 type (a disordered type of spinel) structure which on annealing at 350°C transforms to the α-LiFe 5O 8 type (an ordered type spinel) structure as shown by both IR spectra and XRD studies. Magnetization curves indicate a particle size distribution consisting of both ferromagnetic particles and a superparamagnetic fraction. With 4 ΠMs values of 2000 G these particles could be useful for applications in certain low magnetization ferrofluids.

  12. Interfacial transport in lithium-ion conductors

    NASA Astrophysics Data System (ADS)

    Shaofei, Wang; Liquan, Chen

    2016-01-01

    Physical models of ion diffusion at different interfaces are reviewed. The use of impedance spectroscopy (IS), nuclear magnetic resonance (NMR), and secondary ion mass spectrometry (SIMS) techniques are also discussed. The diffusion of ions is fundamental to the operation of lithium-ion batteries, taking place not only within the grains but also across different interfaces. Interfacial ion transport usually contributes to the majority of the resistance in lithium-ion batteries. A greater understanding of the interfacial diffusion of ions is crucial to improving battery performance. Project supported by the Beijing S&T Project, China (Grant No. Z13111000340000), the National Natural Science Foundation of China (Grant Nos. 51325206 and 11234013) and the National Basic Research Program of China (Grant No. 2012CB932900).

  13. Environmental fatigue in aluminum-lithium alloys

    NASA Technical Reports Server (NTRS)

    Piascik, Robert S.

    1992-01-01

    Aluminum-lithium alloys exhibit similar environmental fatigue crack growth characteristics compared to conventional 2000 series alloys and are more resistant to environmental fatigue compared to 7000 series alloys. The superior fatigue crack growth behavior of Al-Li alloys 2090, 2091, 8090, and 8091 is due to crack closure caused by tortuous crack path morphology and crack surface corrosion products. At high R and reduced closure, chemical environment effects are pronounced resulting in accelerated near threshold da/dN. The beneficial effects of crack closure are minimized for small cracks resulting in rapid growth rates. Limited data suggest that the 'chemically small crack' effect, observed in other alloy system, is not pronounced in Al-Li alloys. Modeling of environmental fatigue in Al-Li-Cu alloys related accelerated fatigue crack growth in moist air and salt water to hydrogen embrittlement.

  14. High cycle life secondary lithium battery

    NASA Technical Reports Server (NTRS)

    Yen, Shiao-Ping S. (Inventor); Carter, Boyd J. (Inventor); Shen, David H. (Inventor); Somoano, Robert B. (Inventor)

    1985-01-01

    A secondary battery (10) of high energy density and long cycle is achieved by coating the separator (18) with a film (21) of cationic polymer such as polyvinyl-imidazoline. The binder of the positive electrode (14) such as an ethylene-propylene elastomer binder (26) containing particles (28) of TiS.sub.2 chalcogenide can also be modified to contain sulfone functional groups by incorporating liquid or solid sulfone materials such as 0.1 to 5 percent by weight of sulfolane into the binder. The negative lithium electrode (14), separator (18) and positive electrode (16) are preferably spirally wound and disposed within a sealed casing (17) containing terminals (32, 34). The modified separator and positive electrode are more wettable by the electrolytes in which a salt is dissolved in a polar solvent such as sulfolane.

  15. Examination of Liquid Fluoride Salt Heat Transfer

    SciTech Connect

    Yoder Jr, Graydon L

    2014-01-01

    equipment designs. All of the data discussed above were taken under forced convective conditions (both laminar and turbulent). Some recent data taken at ORNL under free convection conditions are also presented and results discussed. This data was taken using a simple crucible experiment with an instrumented nickel heater inserted in the salt to induce natural circulation within the crucible. The data was taken over a temperature range of 550oC to 650oC in FLiNaK salt. This data covers both laminar and turbulent natural convection conditions, and is compared to existing forms of natural circulation correlations.

  16. Development of encapsulated lithium hydride sink-side thermal energy storage for pulsed space power systems

    SciTech Connect

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

    1988-01-01

    Value analysis indicates that inclusion of thermal energy storage (TES) as an element in a pulsed space power supply will reduce the mass of the heat rejection system. A candidate design for the TES component utilizes lithium hydride (LiH) encapsulated in 304L stainless steel or molybdenum in a packed-bed configuration with a lithium or sodium-potassium (NaK) heat transport fluid. Critical concerns with this concept are the need to (1) accommodate shell stresses induced by volumetric expansion of the melting salt or surface gripping by the freezing salt and (2) minimize hydrogen loss through the shell due to LiH dissociation at high temperatures. Experimental observation of significant cracking of the LiH during cooling mitigates the first of these issues by providing a leakage path into the interior void as melting occurs at the salt-containment interface, thus allowing use of thin shells.

  17. SALT Science Conference 2015

    NASA Astrophysics Data System (ADS)

    Buckley, David; Schroeder, Anja

    The Southern African Large Telescope (SALT) has seen great changes in the last years following the beginning of full time science operations in 2011. The three first generation instruments, namely the SALTICAM imager, the Robert Stobie Spectrograph (RSS) and its multiple modes and finally in 2014, the new High Resolution Spectrograph (HRS), have commissioned it. The SALT community now eagerly anticipate the installation and commissioning of the near-infrared arm of RSS, likely to commence in 2016. The the third "Science with SALT" conference was held at the Stellenbosch Institute of Advanced Study from 1-5 June 2015. The goals of this conference were to: -Present and discuss recent results from SALT observations; -Anticipate scientific programs that will be carried out with new SALT instrumentation such as RSS-NIR; -Provide a scientific environment in which to foster inter-institutional and inter-facility collaborations between scientists at the different SALT partners; -Provide an opportunity for students and postdocs to become more engaged in SALT science and operations; -Encourage the scientific strategic planning that will be necessary to insure an important role for SALT in an era of large astronomical facilities in the southern hemisphere such as MeerKAT, the SKA, LSST, and ALMA; -Consider options for future instrumentation and technical development of SALT; and, -Present, discuss, and engage in the SALT Collateral Benefits program led by SAAO. Conference proceedings editors: David Buckley and Anja Schroeder

  18. Electrochemical properties of quaternary ammonium salts for electrochemical capacitors

    SciTech Connect

    Ue, Makoto; Takeda, Masayuki; Takehara, Masahiro; Mori, Shoichiro

    1997-08-01

    The limiting reduction and oxidation potentials and electrolytic conductivities of new quaternary ammonium salts were examined for electrochemical capacitor applications, whose anions have already been tested as lithium salts for lithium battery applications. The anodic stability was in the following order BR{sub 4}{sup {minus}} < ClO{sub 4}{sup {minus}} {le} CF{sub 3}SO{sub 3}{sup {minus}} < (CF{sub 3}SO{sub 2}){sub 2}N{sup {minus}} {le} C{sub 4}F{sub 9}SO{sub 3}{sup {minus}} < BF{sub 4}{sup {minus}} < PF{sub 6}{sup {minus}} {le} AsF{sub 6}{sup {minus}} < SbF{sub 6}{sup {minus}}. The electrolytic conductivities of Me{sub 4{minus}n}Et{sub n}N(CF{sub 3}SO{sub 2}){sub 2}N (n = 0--4) were examined in comparison with Me{sub 4{minus}n}Et{sub n}NBF{sub 4} counterparts. These imide salts showed good solubility, relatively high conductivity, and anodic stability in propylene carbonate. Et{sub 4}N(CF{sub 3}SO{sub 2}){sub 2}N was found to be a good supporting salt for low permittivity organic solvents, and it afforded a highly conductive electrolyte system based on the ethylene carbonate-dimethyl carbonate mixed solvent, which is useful for electrochemical capacitor applications.

  19. Synthesis and Characterization of Lithium Bis(fluoromalonato)borate (LiBFMB) for Lithium Ion Battery Applications

    SciTech Connect

    Liao, Chen; Han, Kee Sung; Baggetto, Loic; Hillesheim, Daniel A; Custelcean, Radu; Lee, Dr. Eun-Sung; Guo, Bingkun; Bi, Zhonghe; Jiang, Deen; Veith, Gabriel M; Hagaman, Edward {Ed} W; Brown, Gilbert M; Bridges, Craig A; Paranthaman, Mariappan Parans; Manthiram, Arumugam; Dai, Sheng; Sun, Xiao-Guang

    2014-01-01

    A new orthochelated salt, lithium bis(monofluoromalonato)borate (LiBFMB), has been synthesized and purified for the first time for application in lithium ion batteries. The presence of fluorine in the borate anion of LiBFMB increases its oxidation potential and also facilitates ion dissociation, as reflected by the ratio of ionic conductivity measured by electrochemical impedance spectroscopy ( exp) and that by ion diffusivity coefficients obtained using pulsed field gradient nuclear magnetic resonance (PFG-NMR) technique ( NMR). Half-cell tests using 5.0 V lithium nickel manganese oxide (LiNi0.5Mn1.5O4) as a cathode and EC/DMC/DEC as a solvent reveals that the impedance of the LiBFMB cell is much larger than those of LiPF6 and LiBOB based cells, which results in lower capacity and poor cycling performance of the former. XPS spectra of the cycled cathode electrode suggest that because of the stability of the LiBFMB salt, the solid electrolyte interphase (SEI) formed on the cathode surface is significantly different from those of LiPF6 and LiBOB based electrolytes, resulting in more solvent decomposition and thicker SEI layer. Initial results also indicate that using high dielectric constant solvent PC alters the surface chemistry, reduces the interfacial impedance, and enhances the performance of LiBFMB based 5.0V cell.

  20. The history of lithium therapy

    PubMed Central

    Shorter, Edward

    2013-01-01

    The use of lithium in psychiatry goes back to the mid-19th century. Early work, however, was soon forgotten, and John Cade is credited with reintroducing lithium to psychiatry for mania in 1949. Mogens Schou undertook a randomly controlled trial for mania in 1954, and in the course of that study became curious about lithium as a prophylactic for depressive illness. In 1970, the United States became the 50th country to admit lithium to the marketplace. Meanwhile, interest in lithium for the prophylaxis of depression was growing apace and today the agent is widely prescribed for that indication, even though it has not been accepted by the Food and Drug Administration. Lithium was almost derailed by a small group of opponents from the Maudsley Hospital and its status today is threatened by the “mood stabilizers.” PMID:19538681