Relevant bibliographies by topics / Lithium compounds. Lithium

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

Academic literature on the topic 'Lithium compounds. Lithium'

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

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Journal articles on the topic "Lithium compounds. Lithium"

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Tang, Yao, Zhao Lin Zhan, Xiao Hua Yu, Miao Ma, and Xiao Yu Li. "Development and Application of Manganese Cobalt Lithium Compounds in the Field of Lithium Batteries." Advanced Materials Research 1088 (February 2015): 275–78. http://dx.doi.org/10.4028/www.scientific.net/amr.1088.275.

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Manganese lithium cobalt compounds have been used in the preparation of lithium battery cathode material because of its excellent electrochemical characteristics and gradually in recent years. This paper introduces the different methods of preparing the compounds, analyzes the structural characteristics of the manganese cobalt lithium compounds and the differences in the electrochemical properties, the end of the article has carried on the forecast to the future development direction of the compound.
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Julien, C. M. "Lithium intercalated compounds." Materials Science and Engineering: R: Reports 40, no. 2 (2003): 47–102. http://dx.doi.org/10.1016/s0927-796x(02)00104-3.

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Liu, Jingwei, Daixi Xie, Wei Shi, and Peng Cheng. "Coordination compounds in lithium storage and lithium-ion transport." Chemical Society Reviews 49, no. 6 (2020): 1624–42. http://dx.doi.org/10.1039/c9cs00881k.

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Ehrenberg, H., B. Hasse, K. Schwarz, and M. Epple. "Structure determination of lithium chloroacetate, lithium bromoacetate and lithium iodoacetate by powder diffraction." Acta Crystallographica Section B Structural Science 55, no. 4 (1999): 517–24. http://dx.doi.org/10.1107/s0108768199003614.

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Most halogenoacetates of alkali salts readily undergo a thermally induced polymerization reaction to poly-(hydroxyacetic acid) in the solid state. The lithium salts represent a remarkable exception. The crystal structures of lithium chloroacetate, lithium bromoacetate and lithium iodoacetate were determined ab initio from synchrotron powder diffraction data. The three compounds are isostructural and differ considerably from the structures of sodium chloroacetate and silver chloroacetate, two compounds that undergo polymerization. Most likely, the strong polarizing effect of the small lithium cation is responsible for the unfavorable crystal structure in which each lithium cation is coordinated to four O atoms from four different halogenoacetate molecules. Lithium chloroacetate: a = 9.3882 (9), b = 4.8452 (4), c = 9.0119 (7) Å, β = 94.330 (5)°; lithium bromoacetate: a = 9.7165 (11), b = 4.8610 (6), c = 9.0228 (11) Å, β = 93.946 (5)°; lithium iodoacetate: a = 10.1812 (10), b = 4.8922 (8), c = 9.0468 (10) Å, β = 93.251 (5)°, all crystallizing in space group P21/c with Z = 4.
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Conard, Jacques, and Pierre Lauginie. "Lithium NMR in Lithium-Carbon Solid State Compounds." TANSO 2000, no. 191 (2000): 62–70. http://dx.doi.org/10.7209/tanso.2000.62.

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Krat, S. A., A. S. Popkov, Yu M. Gasparyan, et al. "Wetting properties of liquid lithium on lithium compounds." Fusion Engineering and Design 117 (April 2017): 199–203. http://dx.doi.org/10.1016/j.fusengdes.2016.06.038.

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Tsuji, Junichi, Hirohide Nakamatsu, Takeshi Mukoyama, Kazuo Kojima, Shigero Ikeda, and Kazuo Taniguchi. "Lithium K-edge XANES spectra for lithium compounds." X-Ray Spectrometry 31, no. 4 (2002): 319–26. http://dx.doi.org/10.1002/xrs.577.

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Capece, A. M., M. I. Patino, Y. Raitses, and B. E. Koel. "Secondary electron emission from lithium and lithium compounds." Applied Physics Letters 109, no. 1 (2016): 011605. http://dx.doi.org/10.1063/1.4955461.

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Georgiev, M. K., D. V. Elenkov, and V. T. Tomov. "Stopping times of lithium ions in lithium compounds." Atomic Energy 78, no. 5 (1995): 338–40. http://dx.doi.org/10.1007/bf02419261.

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Taguchi, N., M. Kitta, H. Sakaebe, M. Kohyama, and T. Akita. "Lithium analysis using reflection EELS for lithium compounds." Journal of Electron Spectroscopy and Related Phenomena 203 (August 2015): 40–44. http://dx.doi.org/10.1016/j.elspec.2015.05.014.

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Dissertations / Theses on the topic "Lithium compounds. Lithium"

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Khosravi, Javad. "Production of lithium peroxide and lithium oxide in an alcohol medium." Thesis, McGill University, 2007. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=103204.

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Experiments to measure (i) the reactivity of lithium peroxide and lithium oxide in ambient air as a function of relative humidity and reactant particle size, (ii) the solubility of lithium hydroxide and lithium hydroxide monohydrate in three alcohols, namely methanol, ethanol and 1 and 2-propanol, as a function of time and temperature, (iii) the efficiency of the production of lithium peroxide in alcohol medium as a function of the concentration of LiOH.H 2O in methanol, the concentration of hydrogen peroxide, the kind of alcohol, the kind of feed material, and temperature and the time of mixing, (iv) the analysis of the precipitates, (v) the temperature of the precipitate decomposition in isothermal and non-isothermal conditions in ambient and neutral conditions as function of time, (vi) the activation energy of the precipitate decomposition, (vii) the temperature of the lithium peroxide decomposition in isothermal and non-isothermal conditions as function of time and (viii) the activation energy of lithium peroxide decomposition were performed.<br>The purpose of the study was to gather the data necessary to evaluate the production of lithium peroxide, Li2O2, and subsequently lithium oxide, Li2O, to be used as a feed for a silicothermic reduction process for the production of metallic lithium. The proposed basis for the production of Li2O2 was the conversion of lithium hydroxide or lithium hydroxide monohydrate by hydrogen peroxide in an alcohol medium. Alcohols were chosen because they are members of a class of non-aqueous solvents that can selectively dissolve the anticipated contaminants while precipitating the desired products.<br>It was found that the addition of hydrogen peroxide to alcohol solutions containing lithium hydroxide monohydrate resulted in the formation of lithium peroxide as lithium hydroperoxidate trihydrate with eight adduct molecules of methanol, i.e., Li2O2•H2O 2•3H2O•8CH3OH and involved the peroxide group transfer. The optimum conditions for the production of lithium peroxide were found to be (i) the least water concentration in the system (ii) the use of the temperature lower than ambient temperature and (iii) fast separation of the precipitate and raffinate to prevent dissociation of the precipitate or dissolving into the raffinate.<br>The high solubility of LiOH.H2O and at the same time the low solubility of Li2CO3 and of Li2O2 in methanol resulted in selection of methanol as the best alcohol of those studied for the proposed method of Li2O2 production. It also yielded high purity lithium peroxide. The production of Li2O 2 using H2O2 (35 %wt) required an excess of hydrogen peroxide equal to 2.6 times the stoichiometric amount.<br>The thermal decomposition of the lithium hydroperoxidate trihydrate precipitate started with the rejection of the adduct methanol molecules, followed by co-evolution of H2O and H2O2 from the resulting Li 2O2•H2O2•H2O. The activation energy of the decomposition reaction of the precipitate was measured as 141 kJ/mol. At temperatures greater than 200°C, lithium peroxide was found to be very reactive with atmospheric air. However, in an argon atmosphere, it rapidly decomposed losing the majority of the oxygen atoms, followed by the gradual slow diffusion of oxygen gas absorbed on the lithium oxide.
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Hodgson, Susan Marie. "Structural studies of lithium compounds." Thesis, University of Newcastle Upon Tyne, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.244863.

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Imanishi, Nobuyuki. "STUDY ON LITHIUM INSERTION COMPOUNDS AS ELECTRODE MATERIALS FOR LITHIUM SECONDARY BATTERY." Kyoto University, 1993. http://hdl.handle.net/2433/168867.

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本文データは平成22年度国立国会図書館の学位論文(博士)のデジタル化実施により作成された画像ファイルを基にpdf変換したものである<br>Kyoto University (京都大学)<br>0048<br>新制・論文博士<br>博士(工学)<br>乙第8064号<br>論工博第2663号<br>新制||工||898(附属図書館)<br>UT51-93-B336<br>(主査)教授 竹原 善一郎, 教授 曽我 直弘, 教授 小久見 善八<br>学位規則第4条第2項該当
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Selvaraj, Peter Rajan. "Exploratory study of ionophoric spiroethers and spiroketals." Columbus, Ohio : Ohio State University, 2006. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=osu1158620953.

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Ma, Miaomiao. "Layered LiMn0.4Ni0.4Co0.2O2 as cathode for lithium batteries." Diss., Online access via UMI:, 2005.

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Thesis (Ph. D.)--State University of New York at Binghamton, Materials Science, 2005.<br>Numerals in chemical formula in title are "subscript" in t.p. of printed version. Includes bibliographical references.
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Hamilton, A. L. "Applications of lithium compounds in organic synthesis." Thesis, Swansea University, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.637209.

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The lithiation and subsequent condensation with an electrophile is a useful reaction in many 'total' syntheses. This study was undertaken to investigate the lithiation reactions of several organic molecules. In Chapters 2 and 3, the lithiation of a range of <I>N-</I>pivaloyl-<I>o</I>-toluidines was studied, with the resultant formation of indoles (Chapter 2) and reaction with carbon monoxide to form a carbonylated product (Chapter 3). The lithiation reaction was then applied to 2,5-dimethyl-1,4-phenylene-di-<I>N</I>-pivaloylamine as an attempt to effect quadruple lithiation. However, only double lithiation was observed. In Chapter 4, the attempted lithiation of trifluoroacetylanilines, was studied to see whether it is possible to effect lithiation on the aromatic ring to yield a dianion. Both alkyl and aryllithium reagents were observed to act as nucleophiles towards the substrates, resulting in displacement of the trifluoromethyl group. In Chapters 5, 6 and 7, lithiation of pyridones was investigated. Lithiation and electrophile trapping were found to readily occur for 3-methyl- (Chapter 6) and 6-methyl-2-pyridone (Chapter 5). However, the research on 4-methyl-2-pyridone (Chapter 6) showed that <I>n</I>-butyllithium caused either (i) lithiation at the 4-position in the ring or (ii) acted as a nucleophile, with the addition of a butyl group at the 6-position in the ring. The reaction of <I>n</I>-butyllithium and 3-cyano-6-methyl-2-pyridone was studied (Chapter 7). <I>n</I>-Butyllithium was found to act as a nucleophile towards 3-cyano-6-methyl-2-pyridone, resulting in the addition of a butyl group.
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Chen, Jiajun. "The hydrothermal synthesis and characterization of olivine compounds for electrochemical applications." Diss., Online access via UMI:, 2007.

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Agåker, Marcus. "Double Excitations in Helium Atoms and Lithium Compounds." Doctoral thesis, Uppsala University, Atomic and molecular physics, 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6889.

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<p>This thesis addresses the investigation of doubly excited <i>2l´nl</i> states in helium atoms and double core excitations in solid lithium compounds.</p><p>Measurements on <i>He</i> are made in field free environments and under the influence of electric and magnetic fields, using synchrotron based inelastic photon scattering. Cross sections for scattering to singly excited final states are directly determined and compared to theoretical results and are found to be in excellent agreement. Radiative and spin-orbit effects are quantified and are shown to play an important role in the overall characterization of highly excited <i>He </i>states below the <i>N =2</i> threshold. A dramatic electric field dependence is also observed in the flourecence yield already for relatively weak fields. This signal increase, induced by electric as well as magnetic fields, is interpreted in terms of mixing with states of higher fluorescence branching ratios.</p><p>Double core excitations at the lithium site in solid lithium compounds are investigated using resonant inelastic x-ray scattering (RIXS). The lithium halides <i>LiF, LiCl, LiBr</i> and <i>LiI </i>are studied as well as the molecular compounds <i>Li</i><i>2</i><i>O, Li</i><i>2</i><i>CO</i><i>3</i> and <i>LiBF</i><i>4</i>. States with one, as well as both, of the excited electrons localized at the site of the bare lithium nucleus are identified, and transitions which involve additional band excitations are observed. A strong influence of the chemical surrounding is found, and it is discussed in terms of the ionic character of the chemical bond.</p>
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Agåker, Marcus. "Double excitations in helium atoms and lithium compounds /." Uppsala : Acta Universitatis Upsaliensis : Universitetsbiblioteket [distributör], 2006. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-6889.

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Rudisch, Christian. "Nuclear Magnetic Resonance on Selected Lithium Based Compounds." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2014. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-130485.

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This thesis presents the NMR measurements on the single crystals LiMnPO4 and Li0.9FeAs. Therefore, the thesis is divided into two separated sections. The first part reports on the competitive next generation cathode material LiMnPO4 with a stable reversible capacity up to 145 mAh/g and a rather flat discharge voltage curve at 4.1 V. For the basic understanding of the material the magnetic properties have been investigated by a Li and P NMR study in the paramagnetic and antiferromagnetic phase. LiMnPO4 shows a strong anisotropy of the dipolar hyperfine coupling due to the strong local magnetic moments at the Mn site. The corresponding dipole tensor of the Li- and P-nuclei is fully determined by orientation and temperature dependent NMR experiments and compared to the calculated values from crystal structure data. Deviations of the experimentally determined values from the theoretical ones are discussed in terms of Mn disorder which could have an impact on the mobility of the Li ions. The disorder is corroborated by diffuse x-ray diffraction experiments which indicate a shift of the heavy elements in the lattice, namely the Mn atoms. Furthermore, the spin arrangement in the relative strong field of 7.0494 T in the antiferromagnetic state is understood by the NMR measurements. In order to obtain parameters of the Li ion diffusion in LiMnPO4 measurements of the spin lattice relaxation rate were performed. Due to the strong dipolar coupling between the Li-nuclei and the magnetic moments at the Mn site it is difficult to extract parameters which can characterize the diffusive behavior of the Li ions. The second section reports on the AC/DC susceptibility and NMR/NQR studies on Li deficit samples labeled as Li0.9FeAs. LiFeAs belongs to the family of the superconducting Pnictides which are discovered in 2008 by H. Hosono et al. In recent studies the stoichiometric compound reveals triplet superconductivity below Tc ∼ 18 K which demands ferromagnetic coupling of the electrons in the Cooper pairs. In Li0.9FeAs the Li deficit acts like hole doping which suppresses the superconductivity. Then ferromagnetism can arise which is very interesting because of the vicinity to the triplet superconductivity. With the microscopic methods NMR/NQR on the Li and As nuclei, it was investigated where the ferromagnetism can be located in Li0.9FeAs. Recent susceptibility, ESR and µSR studies reveal an internal field due to the ferromagnetism. In contrast, the internal field could not be used to perform zero field NMR measurements. Possible reasons for this discrepancy are discussed. In addition, the automatic insitu AC susceptibility technique by using the NMR radio frequency circuit has been tested by a reference compound Co2TiGa which shows itinerant ferromagnetism. Similar curves are observed for Li0.9FeAs which indicate the existence of itinerant magnetic moments in Li0.9FeAs. Furthermore, in order to determine the size of the dipolar contribution from the magnetic moments of the Fe the dipolar hyperfine coupling tensor was calculated from the crystal structure data. The comparison of the experimental and calculated hyperfine coupling elements reveals transferred hyperfine fields in LiFeAs.
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Books on the topic "Lithium compounds. Lithium"

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Luisi, Renzo, and Vito Capriati, eds. Lithium Compounds in Organic Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2014. http://dx.doi.org/10.1002/9783527667512.

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Cheruvally, Gouri. Lithium iron phosphate: A promising cathode-active material for lithium secondary batteries. Trans Tech Publications Ltd., 2008.

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Li li zi dian chi yong lin suan tie li zheng ji cai liao: LiFePO4 Cathode Material Used for Li-ion Battery. Ke xue chu ban she, 2013.

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Greiner, Simon. Novel Decavanadate Compounds for Lithium-Ion Batteries. Springer Fachmedien Wiesbaden, 2020. http://dx.doi.org/10.1007/978-3-658-28985-0.

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International, Symposium on Fabrication and Properties of Lithium Ceramics (1987 Pittsburgh Pa ). Fabrication and properties of lithium ceramics. American Ceramic Society, 1989.

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Luliński, Sergiusz. Otrzymywanie wybranych fluorowco- i cyjanopochodnych arylolitowych i ich zastosowanie w syntezie: Generation of selected halogen- and cyano-substituted aryllithiums and their application in synthesis. Oficyna Wydawnicza Politechniki Warszawskiej, 2010.

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Collins, W. K. Hexagonal phase transformation in the engineered scavenger compound lithium titanate. U.S. Dept. of the Interior, Bureau of Mines, 1993.

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Anne-Marie, Sapse, and Schleyer, Paul von R., 1930-, eds. Lithium chemistry: A theoretical and experimental overview. Wiley, 1995.

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Lithium chemistry: A theoretical and experimental overview. Wiley, 1995.

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Lithium Chemistry: A Theoretical and Experimental Overview. Wiley-Interscience, 1995.

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Book chapters on the topic "Lithium compounds. Lithium"

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Julien, Christian, Alain Mauger, Ashok Vijh, and Karim Zaghib. "Disordered Compounds." In Lithium Batteries. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-19108-9_9.

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Julien, Christian, Alain Mauger, Ashok Vijh, and Karim Zaghib. "Fluoro-polyanionic Compounds." In Lithium Batteries. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-19108-9_8.

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Julien, Christian, Alain Mauger, Ashok Vijh, and Karim Zaghib. "Polyanionic Compounds as Cathode Materials." In Lithium Batteries. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-19108-9_7.

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Macintyre, J. E., F. M. Daniel, D. J. Cardin, et al. "Li Lithium." In Dictionary of Organometallic Compounds. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4757-4966-3_30.

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MacIntyre, Jane E. "Li Lithium." In Dictionary of Organometallic Compounds. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-6848-7_30.

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Macintyre, J. E. "Li Lithium." In Dictionary of Organometallic Compounds. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4615-6847-6_27.

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Barpanda, P., and J. M. Tarascon. "Fluorine-Based Polyanionic Compounds for High-Voltage Electrode Materials." In Lithium Batteries. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118615515.ch7.

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Murphy, D. W., S. M. Zahurak, C. J. Chen, and M. Greenblatt. "Lithium Insertion Compounds." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132555.ch59.

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Murphy, D. W., S. M. Zahurak, C. J. Chen, and M. Greenblatt. "Lithium Insertion Compounds." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132616.ch36.

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Nagy, Zoltán. "Li—Lithium." In Electrochemical Synthesis of Inorganic Compounds. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4899-0545-1_36.

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Conference papers on the topic "Lithium compounds. Lithium"

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ESAKA, Takao. "SYNTHESIS AND ELECTROCHEMICAL PROPERTY OF LITHIUM STORAGE INTERMETALLIC COMPOUNDS." In Proceedings of the 8th Asian Conference. WORLD SCIENTIFIC, 2002. http://dx.doi.org/10.1142/9789812776259_0007.

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Billaud, D., F. X. Henry, and P. Willmann. "New methods for the synthesis of lithium-polyacetylene intercalation compounds." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835607.

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Meng, Ying, and Minghao Zhang. "Quantifying the Unusual Anion Redox Activity in Lithium Intercalation Compounds." In American Physical Society Meeting, Los Angeles, CA (USA), March 5-9, 2018. US DOE, 2018. http://dx.doi.org/10.2172/1770700.

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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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Andrade, Osvaldo, Irfan Prasetia, and Kazuyuki Torii. "The Diffusivity of Lithium Compounds Through Cement Pastes and Its Effects on ASR Mitigation." In Research, Development and Practice in Structural Engineering and Construction. Research Publishing Services, 2012. http://dx.doi.org/10.3850/978-981-08-7920-4_m-18-0163.

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Chakoumakos, Bryan C. "DATA MINING CRYSTAL STRUCTURES OF LITHIUM MINERALS AND COMPOUNDS TO REVEAL CRYSTAL CHEMICAL SYSTEMATICS." In GSA Annual Meeting in Phoenix, Arizona, USA - 2019. Geological Society of America, 2019. http://dx.doi.org/10.1130/abs/2019am-336506.

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Billaud, D., F. X. Henry, S. Lemont, and P. Willmann. "Compared electrochemical behaviour of lithium-graphite intercalation compounds in liquid and solid electrolyte based cells." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.835867.

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Alcántara, Ricardo, Uche G. Nwokeke, Francisco Nacimiento, Pedro Lavela, and José L. Tirado. "Recent advances in nanocrystalline intermetallic tin compounds for the negative electrode of lithium ion batteries." In SPIE Defense, Security, and Sensing, edited by Nibir K. Dhar, Priyalal S. Wijewarnasuriya, and Achyut K. Dutta. SPIE, 2011. http://dx.doi.org/10.1117/12.882863.

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Pal, Himangshu, Mainak Seal, Anirudha Deogaonkar, Rajat Mahapatra, and Somenath Chatterjee. "Finding the suitability of reduced graphene oxide and lithium based compounds for flexible battery application." In PROCEEDINGS OF ADVANCED MATERIAL, ENGINEERING & TECHNOLOGY. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0024621.

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Lestariningsih, Titik, Etty Marty Wigayati, Qolby Sabrina, Bambang Prihandoko, and Slamet Priyono. "The effect of Li2CO3 substitution on synthesis of LiBOB compounds as salt of electrolyte battery lithium ion." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON MATERIALS AND METALLURGICAL ENGINEERING AND TECHNOLOGY (ICOMMET 2017) : Advancing Innovation in Materials Science, Technology and Applications for Sustainable Future. Author(s), 2018. http://dx.doi.org/10.1063/1.5030250.

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Reports on the topic "Lithium compounds. Lithium"

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Apblett, Christopher A., and Jaclyn Coyle. Lithium Oxysilicate Compounds Final Report. Office of Scientific and Technical Information (OSTI), 2017. http://dx.doi.org/10.2172/1390680.

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Cox, S. O. Criteria for the safe storage of lithium metal and lithium compounds at the Y-12 Plant. Office of Scientific and Technical Information (OSTI), 1995. http://dx.doi.org/10.2172/162490.

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Apblett, Christopher A. Lithium Thiophosphate Compounds as Stable High Rate Li-Ion Separators. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1171577.

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LR Greenwood. Radiation Damage Calculations for the FUBR and BEATRIX Irradiations of Lithium Compounds in EBR-II and FFTF. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/7826.

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Greenwood, Lawrence R. Radiation Damage Calculations for the FUBR and BEATRIX Irradiations of Lithium Compounds in EBR-II and FFTF. Office of Scientific and Technical Information (OSTI), 1999. http://dx.doi.org/10.2172/15001054.

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