Relevant bibliographies by topics / Lithium chlorides

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Lithium chlorides'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Lithium chlorides"

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Novoselova, Alena, Vladimir Shishkin, and Vladimir Khokhlov. "Redox Potentials of Samarium and Europium in Molten Lithium Chloride." Zeitschrift für Naturforschung A 56, no. 11 (November 1, 2001): 754–56. http://dx.doi.org/10.1515/zna-2001-1110.

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Abstract The samarium (III)/(II) and europium (III)/(II) redox potentials in molten lithium chloride were measured using the direct potentiometric method in the temperature range from 923 to 1094 K. Glassy carbon was used as the indifferent working electrode, and the standard chlorine electrode as a reference. The total concentration of rare-earth chlorides dissolved in molten lithium chloride did not exceed 4.5 mol%.
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Hahn, F. Ekkehardt, and Stefan Rupprecht. "Synthese und Kristallstruktur von [LiCl · 2THF]2 / Synthesis and Crystal Structure of [LiCl · 2THF]2." Zeitschrift für Naturforschung B 46, no. 2 (February 1, 1991): 143–46. http://dx.doi.org/10.1515/znb-1991-0203.

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The reaction of lithiated catechol ligands with W (0)Cl4 produces LiCl as a side product. The lithium chloride from this reaction crystallizes as (THF)2Li(μ-Cl)-,Li(THF)2. The X -ray analysis shows lithium in the center of a distorted tetrahedron made up from two THF molecules and two bridging chlorides with d(Li-Cl) = 2.342(3) and 2.308(3)Å.
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Dippel, Kerstin, Nayla K. Keweloh, Peter G. Jones, Uwe Klingebiel, and Dieter Schmidt. "Synthese und Kristallstruktur eines Lithium(trimethylacetoxy-di-tert-butylsilanolats) / Synthesis and Crystal Structure of a Lithium(trimethylacetoxy-di-tert-butylsilanolate)." Zeitschrift für Naturforschung B 42, no. 10 (October 1, 1987): 1253–55. http://dx.doi.org/10.1515/znb-1987-1008.

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Abstract In an acid medium di-tert-butylsilanediol reacts with acyl chlorides to give the di-tert-butylchlorosilanol (2) and the carboxylic acid. A lithium salt of a silanol-carboxylic acid ester (5) is formed in the reaction of the lithiated diol with 2,2-dimethylpropionyl chloride. 5 reacts with phenylacetyl chloride to give the first mixed dicarboxyl-silane. The crystal structure determination of 5 shows a Li-O-cubane with C = 0 ···Li chelate bonds.
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Rocha e Silva, M., I. T. Velasco, R. I. Nogueira da Silva, M. A. Oliveira, G. A. Negraes, and M. A. Oliveira. "Hyperosmotic sodium salts reverse severe hemorrhagic shock: other solutes do not." American Journal of Physiology-Heart and Circulatory Physiology 253, no. 4 (October 1, 1987): H751—H762. http://dx.doi.org/10.1152/ajpheart.1987.253.4.h751.

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Severe hemorrhage in pentobarbital-anesthetized dogs (25 mg/kg) is reversed by intravenous NaCl (4 ml/kg, 2,400 mosmol/l, 98% long-term survival). This paper compares survival rates and hemodynamic and metabolic effects of hypertonic NaCl with sodium salts (acetate, bicarbonate, and nitrate), chlorides [lithium and tris(hydroxymethyl)aminomethane (Tris)], and nonelectrolytes (glucose, mannitol, and urea) after severe hemorrhage (44.5 +/- 2.3 ml/kg blood loss). Sodium salts had higher survival rates (chloride, 100%; acetate, 72%; bicarbonate, 61%; nitrate, 55%) with normal stable arterial pressure after chloride and nitrate; near normal cardiac output after sodium chloride; normal acid-base equilibrium after all sodium salts; and normal mean circulatory filling pressure after chloride, acetate, and bicarbonate. Chlorides and nonelectrolytes produced low survival rates (glucose and lithium, 5%; mannitol, 11%; Tris, 22%; urea, 33%) with low cardiac output, low mean circulatory filling pressure, and severe metabolic acidosis. Plasma sodium, plasma bicarbonate, mean circulatory filling pressure, cardiac output, and arterial pressure correlated significantly with survival; other parameters, including plasma volume expansion or plasma osmolarity, did not. It is proposed that high plasma sodium is essential for survival.
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Knochel, Paul, Andreas Steib, Sarah Fernandez, Olesya Kuzmina, Martin Corpet, and Corinne Gosmini. "Chromium(II)-Catalyzed Amination of N-Heterocyclic Chlorides with Magnesium Amides." Synlett 26, no. 08 (February 26, 2015): 1049–54. http://dx.doi.org/10.1055/s-0034-1380178.

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We report a ligand-free chromium(II)-catalyzed amination reaction of various N-heterocyclic chlorides. CrCl2 regioselectively catalyzes the reaction of chloropyridines and dichloropyridines, dichloroquinolines, dichloroisoquinolines and dichloroquinoxalines with a range of aliphatic, allylic, benzylic and saturated (hetero)cyclic magnesium amides in the presence of lithium chloride as additive. The reactions were performed at 50 °C in THF and led to the desired aminated products in 56–96% yield.
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Masset, Patrick J., Armand Gabriel, and Jean-Claude Poignet. "Reprocessing of LiH in Molten Chlorides." Zeitschrift für Naturforschung A 63, no. 5-6 (June 1, 2008): 377–84. http://dx.doi.org/10.1515/zna-2008-5-619.

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LiH was used as inactive material to stimulate the reprocessing of lithium tritiate in molten chlorides. The electrochemical properties (diffusion coefficients, apparent standard potentials) were measured by means of transient electrochemical techniques (cyclic voltammetry and chronopotentiometry). At 425 ºC the diffusion coefficient and the apparent standard potential were 2.5 · 10−5 cm2 s−1 and −1.8 V vs. Ag/AgCl, respectively. For the process design the LiH solubility was measured by means of DTA to optimize the LiH concentration in the molten phase. In addition electrolysis tests were carried out at 460 ºC with current densities up to 1 A cm−2 over 24 h. These results show that LiH may be reprocessed in molten chlorides consisting in the production of hydrogen gas at the anode and molten metallic lithium at the cathode.
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Liu, Shuanshuan, Weichen Huang, Decai Wang, Ping Wei, and Qilong Shen. "Cobalt-catalyzed cross-coupling of lithium (hetero)aryl zincates with heteroaryl chlorides and bromides." Organic Chemistry Frontiers 6, no. 15 (2019): 2630–34. http://dx.doi.org/10.1039/c9qo00551j.

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A mild, efficient and practical Co-catalyzed cross coupling reaction of a variety of activated heteroaryl chlorides and bromides with lithium aryl zincates that were in situ generated from lithium aryl boronates with ZnBr2 was described.
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Obafemi, Craig A., and Choi Chuck Lee. "Lithium aluminium hydride reduction of some triarylvinyl bromides and acetates catalyzed by some transition metal chlorides." Canadian Journal of Chemistry 68, no. 11 (November 1, 1990): 1998–2000. http://dx.doi.org/10.1139/v90-306.

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A number of triarylvinyl halides and acetates were reduced with lithium aluminium hydride using various transition metal chlorides as catalysts. The vinylic halides were reduced to the corresponding alkenes while the vinylic acetates were reduced to mixtures of triarylketones and alcohols. The reduction of labeled vinylic halides did not result in any scrambling of the label from C-2 to C-1. The reactions took place under mild conditions and relatively fast reaction times. Keywords: triarylvinyl chlorides, triarylvinyl acetates, lithium aluminium hydride reduction, 1,2,2-triarylethanol, 1,1,2-tri-p-tolyl[1-13C]ethane.
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Reckeweg, Olaf, Björn Blaschkowski, and Thomas Schleid. "Li5OCl3and Li3OCl: Two Remarkably Different Lithium Oxide Chlorides." Zeitschrift für anorganische und allgemeine Chemie 638, no. 12-13 (August 20, 2012): 2081–86. http://dx.doi.org/10.1002/zaac.201200143.

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Lutz, Heinz Dieter, Klaus Wussow, and Peter Kuske. "Ionic Conductivity, Structural, IR and Raman Spectroscopic Data of Olivine, Sr2PbO4, and Na2CuF4 Type Lithium and Sodium Chlorides Li2ZnCl4 and Na2MCl4 (M = Mg, Ti, Cr, Mn, Co, Zn, Cd)." Zeitschrift für Naturforschung B 42, no. 11 (November 1, 1987): 1379–86. http://dx.doi.org/10.1515/znb-1987-1103.

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The ionic conductivities (complex impedance measurements) of the olivine type Li2ZnCl4, Na2ZnCl4 and Na2CoCl4, the Sr2PbO4 type Na2MgCl4, Na2MnCl4, and Na2CdCl4, and the novel Na2CrCl4 with monoclinically distorted Sr2PbO4 structure (Na2CuF4 type) are presented. The specific conductivities of Li2ZnCl4 and the Na2MCl4 are about three orders of magnitude lower than those of the fast ionic conducting lithium chloride spinels Li[LiM ]Cl4 (M = Mg, Mn. Fe. Cd. etc.) indicating that in the latter compounds the tetrahedrally coordinated lithium ions exhibit higher mobility than those on octahedral sites. The X-ray data including those of Sr2PbO4 type Na2TiCl4 and both the IR and Raman spectra (together with a group theoretical treatment) are also given. The spectra obtained confirm the different structure types of the ternary chlorides.
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Dissertations / Theses on the topic "Lithium chlorides"

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FERNANDES, DAMARIS. "Estudo tecnologico do reprocessamento eletroquimico de combustiveis de uranio em meio de cloretos fundidos." reponame:Repositório Institucional do IPEN, 2002. http://repositorio.ipen.br:8080/xmlui/handle/123456789/11020.

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Instituto de Pesquisas Energeticas e Nucleares - IPEN/CNEN-SP
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Aojula, Kuldip Singh. "Electrodeposition of lithium from dimethylsulphoxide/lithium chloride medium." Thesis, University of Southampton, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305484.

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Green, Susan. "The optimisation of lithium sulphuryl chloride cells." Thesis, Loughborough University, 1988. https://dspace.lboro.ac.uk/2134/27797.

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Kruesi, William H. "The electrowinning of lithium from chloride-carbonate melts." Thesis, University of Cambridge, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.386113.

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Bradley, Jonathan. "Optimisation of anode characteristics of calcium thionyl chloride cells." Thesis, Loughborough University, 1991. https://dspace.lboro.ac.uk/2134/10399.

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In the field of high performance primary battery systems lithium anoded cells have been shown to have an excellent performance and extremely good shelf life. The major drawback with the lithium technology is one of safety, whereby abuse conditions (such as charging of the cell) lead to an unstable system with the very real possibility of a cell explosion. For a commercially available cell consideration of safety issues would preclude the marketing of a high performance lithium cell for general use, rather, it will be reserved for specialist e.g. Military use where the personnel having contact with the power source can be trained in its safe operation. The work described in this thesis is concerned with the development of a high performance battery system utilising calcium as the anode material. Calcium has received attention as an anode material for a high performance battery system because it removes many of the safety problems associated with lithium. The major disadvantages of calcium have been addressed namely the shelf life and discharge performance. The electrochemical techniques of cyclic voltammetry and a.c. impedance have been used in conjunction with physical methods such as scanning electron microscopy to define the mode of operation of these cells.
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周士明 and Shi-ming Chau. "Investigation of the electrochemical, spectroscopic and physical properties of the low melting 1-methyl-3-ethylimidazolium chloride /alcl3 / licl system for lithium battery application." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1992. http://hub.hku.hk/bib/B31232991.

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Chau, Shi-ming. "Investigation of the electrochemical, spectroscopic and physical properties of the low melting 1-methyl-3-ethylimidazolium chloride / alcl3 / licl system for lithium battery application /." [Hong Kong : University of Hong Kong], 1992. http://sunzi.lib.hku.hk/hkuto/record.jsp?B13880949.

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Cui, Qingzhou. "CURRENT OSCILLATIONS DURING COPPER ELECTRODISSOLUTION IN LITHIUM ION BATTERY AND ACIDIC CHLORIDE ELECTROLYTES." Ohio University / OhioLINK, 2006. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1162242616.

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Saunders, Tim G. "The performance evaluation of lithium thionyl chloride batteries for long-life meter applications." Thesis, Loughborough University, 1998. https://dspace.lboro.ac.uk/2134/13855.

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A research project has been carried out to provide BG plc with service life predictions of lithium primary batteries capable of supplying a continuous pulsed power supply to two new electronic domestic gas meters over a desired design life of 11.5 years, in UK weather conditions. The paper study includes investigations of the range of suitable lithium technologies and test methods, and detailed reviews of the discharge processes, polarisation and self-discharge failure modes of the lithium thionyl chloride system. A new multi-channel load test rig and a high resolution measurement system, and software analysis tools were designed and constructed, and some 440 accelerated discharge tests were carried out at different stress levels on 4 cell types. The results provide a unique database of the voltage/temperature/load trends through discharge, and generate a ranking order of performance. Basic statistical analyses have been carried out to quantify the variability of performance trends. A hitherto unreported behaviour pattern is characterised. Qualitative models are postulated to account for deviations from normal behaviour exhibited by two cell types. The analysis suggests that catholyte additives could predispose a system to early failure (due to modification of the crystal structure of the reaction products), and that manufacturing tolerances define the degree of failure. Mathematical models of self-discharge rate for both low and medium rate discharge were developed from laboratory measurements. Meter load profiles were also measured, which together with the self-discharge model enabled prediction of operational energy utilisation rates. A sample of 50 batteries was extracted from customers homes, after operating in the field for periods of up to 2 years, and the battery capacity loss rates were measured by the residual capacity method. A comparison of predicted and actual capacity utilisation rates yielded a discrepancy of approximately 1.28. Analysis implied that the source of the discrepancy could be adduced to an under estimate of the impact of self-discharge, but that a factor of up to six times the predicted value was required. Evidence was provided to show that self-discharge rate under operational stresses could be significantly higher than that under the steady-state laboratory measurement conditions, but that that the amplitude and time constant associated with a selfdischarge peak was unknown and not predictable. Mean service lives of 14 and 10 years for the respective battery types in the two types of meter are predicted, the worst case (probability of 0.13% of the population) being failure within approximately 5.9 years.
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Brown, L. D. "The combined electrochemical and microstructural characterisation of the electrochemical reduction of uranium dioxide to uranium metal in molten lithium chloride-potassium chloride eutectic." Thesis, University College London (University of London), 2015. http://discovery.ucl.ac.uk/1469912/.

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The electrochemical reduction of uranium (IV) oxide to metallic uranium has been studied in lithium chloride-potassium chloride eutectic at 450°C using electrochemical and advanced material characterisation techniques. Electrochemical characterisation identified a single reduction peak occurring at -2.57V with respect to the Ag|Ag+ reference electrode. Sweep voltammetry has identified that the electroreduction of uranium dioxide to metallic uranium occurs via a single, 4-electron transfer, process. The electrochemical reduction has also been observed to be dependent on the activity of O2- ions: An increase in the bulk activity of the oxygen anion impeded the electroreduction process. This phenomena was thermodynamically predicted using Littlewood diagrams produced for the system. In addition, in situ energy dispersive X-ray diffraction investigations were carried out on the I12 JEEP beamline at the Diamond Light Source which resulted in the direct observation of the formation of uranium metal when a uranium dioxide electrode was exposed to electroreduction potentials. No intermediate phases were observed which supports the electrochemical characterisation of this process occurring in a single step. Moreover, microstructural characterisation has been performed on micro-bucket electrodes and metallic cavity electrodes. A coral-like structure was identified after reduction of uranium dioxide and has been attributed to the volume change associated with the reduction. Microstructural reconstructions were performed on four separate sub-volumes in the direction of propagation of the electroreduction process. The porosity was seen to decrease significantly from 16% to 4%. The pore connectivity was also observed to decrease from 93% to 18%. This drastic change in porosity and pore connectivity is reflected in the pore tortuosity which is seen to increase to infinity. This microstructural evaluation is concluded to impede the diffusion of O2- ions out of the electrode resulting in an increased probability of impediment of the electrochemical reduction process.
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Books on the topic "Lithium chlorides"

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White, Ralph E. Optimization of the lithium/thionyl chloride battery: A final report. College Station, Tex: Dept. of Chemical Engineering, Texas A&M University, 1987.

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White, Ralph E. Optimization of the lithium/thionyl chloride battery: A final report for NASA GRANT NAG 9-177, for the period January 1, 1988 to December 31, 1988. [Washington, D.C: National Aeronautics and Space Administration, 1989.

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Garrett, Donald E. Handbook of lithium and natural calcium chloride. Amsterdam: Elsevier Academic Press, 2004.

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Murray, David P. Environmental enrichment: Its effects on lithium chloride-pilocarpine induced seizure activity. Sudbury, Ont: Laurentian University, Department of Psychology, 1986.

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Handbook of Lithium and Natural Calcium Chloride. Elsevier, 2004. http://dx.doi.org/10.1016/b978-0-12-276152-2.x5035-x.

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G, Halpert, Stein Irving, and Jet Propulsion Laboratory (U.S.), eds. Safety considerations of lithium-thionyl chloride cells. Pasadena, Calif: National Aeronautics and Space Administration, Jet Propulsion Laboratory, California Institute of Technology, 1986.

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A mathematical model of a lithium thionyl chloride primary cell. [Washington, DC: National Aeronautics and Space Administration, 1987.

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Saunders, Tim G. The performance evaluation of lithium thionyl chloride batteries for long-life meter applications. 1998.

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Ekolu, Stephen Okurut. Role of heat curing in concrete durability: Effects of lithium salts and chloride ingress on delayed ettringite formation. 2004.

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Book chapters on the topic "Lithium chlorides"

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Masset, P. J. "Lithium Hydride Solubility in Molten Chlorides." In Molten Salts Chemistry and Technology, 213–18. Chichester, UK: John Wiley & Sons, Ltd, 2014. http://dx.doi.org/10.1002/9781118448847.ch3h.

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Levy, Samuel C., and Per Bro. "Lithium/Thionyl Chloride Batteries." In Battery Hazards and Accident Prevention, 211–32. Boston, MA: Springer US, 1994. http://dx.doi.org/10.1007/978-1-4899-1459-0_10.

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Striegel, André M., and Judy D. Timpa. "Size Exclusion Chromatography of Polysaccharides in Dimethylacetamide—Lithium Chloride." In ACS Symposium Series, 366–78. Washington, DC: American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0635.ch020.

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Winkelmann, J. "Diffusion of oxygen (1); water (2); lithium chloride (3)." In Gases in Gases, Liquids and their Mixtures, 2315. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-49718-9_1800.

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Cohen-Adad, R. "Lithium Chloride." In Alkali Metal and Ammonium Chlorides in Water and Heavy Water (Binary Systems), 1–63. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-08-023918-7.50007-7.

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Jancsó, G., and J. W. Lorimer. "Lithium Chloride." In Alkali Metal and Ammonium Chlorides in Water and Heavy Water (Binary Systems), 499–502. Elsevier, 1991. http://dx.doi.org/10.1016/b978-0-08-023918-7.50014-4.

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Rossi, L. "Reaction of Alkylcarbamoyl Chlorides with Lithium Butaneselenolate." In Four Carbon-Heteroatom Bonds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-018-00785.

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Niecke, E., A. Ruban, and M. Raab. "Condensation Reactions of Tris(trimethylsilyl)phosphine or Its Lithium Salt with Acyl Chlorides." In Heteroatom Analogues of Aldehydes and Ketones, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-027-00804.

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Saito, S. "Lithium Aluminum Hydride with Various Metal Chloride Salts for the ­Catalytic Reduction of Alkynes, Alkenes, and Aryl and Alkyl Chlorides." In Compounds of Groups 13 and 2 (Al, Ga, In, Tl, Be...Ba), 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-007-00030.

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Garrett, Donald E. "Lithium." In Handbook of Lithium and Natural Calcium Chloride, 1–235. Elsevier, 2004. http://dx.doi.org/10.1016/b978-012276152-2/50037-2.

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Conference papers on the topic "Lithium chlorides"

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Agafonova, N. A., E. V. Shchegolkov, Ya V. Burgart, V. I. Saloutin, and M. V. Ulitko. "Synthesis of biological active compounds based on trifluoromethylcontaining 4-nitrosopyrazoles." In VIII Information school of a young scientist. Central Scientific Library of the Urals Branch of the Russian Academy of Sciences, 2020. http://dx.doi.org/10.32460/ishmu-2020-8-0009.

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e-pot nitrosation of 1,3-diketones or their lithium salts followed by treatment of hydrazines. Reduction of the nitroso-derivatives made it possible to obtain the 4-amino-3-trifluoromethylpyrazoles chlorides. Cytotoxic activity of the compounds wase evaluated in vitro
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Kharina, E. A., R. Yu Kaychenkova, A. S. Dedyukhin, A. V. Shchetinskiy, and L. F. Yamshchikov. "Potentiometric study of lanthanum containing melts based on the eutectic mixture of lithium, potassium and cesium chlorides." In PHYSICS, TECHNOLOGIES AND INNOVATION (PTI-2018): Proceedings of the V International Young Researchers’ Conference. Author(s), 2018. http://dx.doi.org/10.1063/1.5055110.

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Strepetov, K. E., A. A. Osipenko, and V. A. Volkovich. "Electronic absorption spectra of palladium(II) ions in molten eutectic mixture of lithium, potassium and cesium chlorides." In THE 2ND INTERNATIONAL CONFERENCE ON PHYSICAL INSTRUMENTATION AND ADVANCED MATERIALS 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0032407.

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Amamoto, Ippei, Naoki Mitamura, Tatsuya Tsuzuki, Yasushi Takasaki, Atsushi Shibayama, Tetsuji Yano, Masami Nakada, and Yoshihiro Okamoto. "Removal of Fission Products in the Spent Electrolyte Using Iron Phosphate Glass as a Sorbent." In ASME 2010 13th International Conference on Environmental Remediation and Radioactive Waste Management. ASMEDC, 2010. http://dx.doi.org/10.1115/icem2010-40272.

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This study is carried out to make the pyroprocessing hold a competitive advantage from the viewpoint of environmental load reduction and economical improvement. As one of the measures to reduce the volume of the high-level radioactive waste (HLW), the phosphate conversion method is applied for removal of fission products (FP) from the melt, referring to the spent electrolyte in this paper. Among the removing target chlorides in the spent electrolyte i.e., alkali metals, alkaline earth metals and rare earth elements, only the rare earth elements and lithium form the precipitates as insoluble phosphates by reaction with Li3PO4. The sand filtration method was applied to separate FP precipitates from the spent electrolyte. The iron phosphate glass (IPG) powder, which is a compatible material for the immobilization of FP, was used as a filter medium. After filtration experiment, it was proven that insoluble FP could almost be completely removed from the spent electrolyte. Subsequently, we attempted to separate the dissolved FP from the spent electrolyte. The IPG was being used once again but this time as a sorbent instead. This is possible because the IPG has some unique characteristics, e.g., changing the valence of iron, which is one of its network modifiers due to its manufacturing temperature. Therefore, it would be likely to sorb some FP when the chemical condition of IPG is unstable. We produced three kinds of IPG under different manufacturing temperature and confirmed that those glasses could sorb FP as anticipated. According to the experimental result, its sorption efficiency of metal cations was attained at around 20–40%.
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"Development of a 250 Ah lithium thionyl chloride battery." In Intersociety Energy Conversion Engineering Conference. Reston, Virigina: American Institute of Aeronautics and Astronautics, 1994. http://dx.doi.org/10.2514/6.1994-4111.

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Reuter, Sebastian, Nina Dehzad, Michael Stassen, Helen Martin, Roland Buhl, Leonid Eshkind, and Christian Taube. "Lithium Chloride Affects The Development Of Allergic Airway Disease." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2856.

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Nelson, E. J., M. L. Fulcher, and F. W. Dampier. "Low Temperature Performance of the Rechargeable Lithium-Copper Chloride Battery." In SAE Aerospace Power Systems Conference. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1997. http://dx.doi.org/10.4271/971229.

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Ehrenreich, Dan. "The Lithium Thionyl Chloride Battery-A New Source for Automotive Applications." In SAE International Congress and Exposition. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 1986. http://dx.doi.org/10.4271/860571.

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SCHNEIDER, IRWIN, and CHARLES L. MARQUARDT. "Broadly tunable oscillator-amplifier system using lithium ( F 2 + ) A centers in potassium chloride." In Conference on Lasers and Electro-Optics. Washington, D.C.: OSA, 1985. http://dx.doi.org/10.1364/cleo.1985.the2.

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Der Pal, Michel Van, and Jakobert Veldhuis. "Thermodynamic Properties of Lithium Chloride Ammonia Complexes Under Heat Pump Type II Working Conditions." In Innovative Materials for Processes in Energy Systems 2010. Singapore: Research Publishing Services, 2010. http://dx.doi.org/10.3850/978-981-08-7614-2_impres032.

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Reports on the topic "Lithium chlorides"

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Dampier, F. W. Lithium-Thionyl Chloride Cell System Safety Hazard Analysis. Fort Belvoir, VA: Defense Technical Information Center, March 1985. http://dx.doi.org/10.21236/ada157089.

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Eisenmann, E. T. Lithium: Thionyl chloride battery state-of-the-art assessment. Office of Scientific and Technical Information (OSTI), March 1996. http://dx.doi.org/10.2172/221912.

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Hoier, S. N., and E. T. Eisenmann. The faradaic efficiency of the lithium-thionyl chloride battery. Office of Scientific and Technical Information (OSTI), April 1996. http://dx.doi.org/10.2172/219339.

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Cooper, George, Ashley Stowe, Jeff Preston, Brendon Wiggins, Keivan Stassun, and Arnold Burger. The Characterization and Optimization of Lithium Hafnium Chloride Crystal Scintillators for Neutron Detection. Office of Scientific and Technical Information (OSTI), September 2017. http://dx.doi.org/10.2172/1410677.

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Cieslak, W., F. Delnick, and C. Crafts. Compatibility study of 316L stainless steel bellows for XMC3690 reserve lithium/thionyl-chloride battery. Office of Scientific and Technical Information (OSTI), February 1986. http://dx.doi.org/10.2172/6130076.

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Higgins, Michaela. Loss of PTEN as a Predictive Biomarker of Response to Lithium Chloride, A Potential Targeted Treatment for Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, June 2012. http://dx.doi.org/10.21236/ada564012.

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Higgins, Michaela. Loss of PTEN as a Predictive Biomarker of REsponse to Lithium Chloride, a Potential Targeted Treatment for Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, September 2011. http://dx.doi.org/10.21236/ada547534.

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