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Journal articles on the topic 'Lithium compounds. Lithium'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

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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2

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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3

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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4

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 c

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5

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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6

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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7

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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8

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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9

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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10

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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11

Radwan, Fae`q A. A. "Anisotropy of Lithium Compounds." Journal of Applied Sciences 1, no. 4 (2001): 512–13. http://dx.doi.org/10.3923/jas.2001.512.513.

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12

Mischenko, A. V., Yu V. Moronov, P. P. Samojlov, and V. E. Fedorov. "Lithium intercalation cluster compounds." Journal of Inclusion Phenomena 5, no. 2 (1987): 263–64. http://dx.doi.org/10.1007/bf00655661.

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13

Deng, Hongyang, Xuanchun Wei, Shaoyan Liu, Shan Li, and Xinhua Cai. "Influence of Different Lithium Compounds on Hydration and Mechanical Properties of Calcium Sulfoaluminate Cement." Materials 13, no. 16 (2020): 3465. http://dx.doi.org/10.3390/ma13163465.

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This work investigated the influence of three different lithium compounds, lithium carbonate (Li2CO3), lithium sulfate (Li2SO4) and lithium chloride (LiCl), on the hydration and mechanical properties of calcium sulfoaluminate (CSA) cement mixtures. Five concentrations of Li+, 0, 0.05, 0.11, 0.16 and 0.22 mmol/g of cement, were chosen, and then the proportions (by mass) of three lithium compounds were determined. Compressive strengths at 8 h, 24 h and 28 days were tested. Meanwhile, an early hydration heat test, thermogravimetric (TG) analysis, X-ray diffraction (XRD) and scanning electron micr

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14

Lin, Zhan, Zengcai Liu, Wujun Fu, Nancy J. Dudney, and Chengdu Liang. "Lithium Polysulfidophosphates: A Family of Lithium-Conducting Sulfur-Rich Compounds for Lithium-Sulfur Batteries." Angewandte Chemie International Edition 52, no. 29 (2013): 7460–63. http://dx.doi.org/10.1002/anie.201300680.

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15

Lin, Zhan, Zengcai Liu, Wujun Fu, Nancy J. Dudney, and Chengdu Liang. "Lithium Polysulfidophosphates: A Family of Lithium-Conducting Sulfur-Rich Compounds for Lithium-Sulfur Batteries." Angewandte Chemie 125, no. 29 (2013): 7608–11. http://dx.doi.org/10.1002/ange.201300680.

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16

Dessemond, Colin, Francis Lajoie-Leroux, Gervais Soucy, Nicolas Laroche, and Jean-François Magnan. "Spodumene: The Lithium Market, Resources and Processes." Minerals 9, no. 6 (2019): 334. http://dx.doi.org/10.3390/min9060334.

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This literature review gives an overview of the lithium industry, including the lithium market, global resources, and processes of lithium compounds production. It focuses on the production of lithium compounds from spodumene minerals. Spodumene is one of the most critical minerals nowadays, due to its high lithium content and high rate of extraction. Lithium is one of the most sought-after metals, due to the ever-growing demand for lithium-ion batteries (LiBs). The data on lithium extraction from minerals is scattered through years of patents, journal articles, and proceedings; hence, requiri

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17

Uxa, Daniel, Erwin Hüger, Lars Dörrer, and Harald Schmidt. "Lithium-Silicon Compounds as Electrode Material for Lithium-Ion Batteries." Journal of The Electrochemical Society 167, no. 13 (2020): 130522. http://dx.doi.org/10.1149/1945-7111/abb9cc.

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18

Yanase, Satoshi, Wakana Hayama, and Takao Oi. "Lithium Isotope Effect Accompanying Electrochemical Intercalation of Lithium into Graphite." Zeitschrift für Naturforschung A 58, no. 5-6 (2003): 306–12. http://dx.doi.org/10.1515/zna-2003-5-610.

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Lithium has been electrochemically intercalated from a 1:2 (v/v) mixed solution of ethylene carbonate (EC) and methylethyl carbonate (MEC) containing 1 M LiClO4 into graphite, and the lithium isotope fractionation accompanying the intercalation was observed. The lighter isotope was preferentially fractionated into graphite. The single-stage lithium isotope separation factor ranged from 1.007 to 1.025 at 25 °C and depended little on the mole ratio of lithium to carbon of the lithium-graphite intercalation compounds (Li-GIC) formed. The separation factor inceased with the relative content of lit

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19

O'Shaughnessy, Cedrick, Grant S. Henderson, Benjamin J. A. Moulton, Lucia Zuin, and Daniel R. Neuville. "A LiK-edge XANES study of salts and minerals." Journal of Synchrotron Radiation 25, no. 2 (2018): 543–51. http://dx.doi.org/10.1107/s1600577518000954.

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The first comprehensive LiK-edge XANES study of a varied suite of Li-bearing minerals is presented. Drastic changes in the bonding environment for lithium are demonstrated and this can be monitored using the position and intensity of the main LiK-absorption edge. The complex silicates confirm the assignment of the absorption edge to be a convolution of triply degeneratep-like states as previously proposed for simple lithium compounds. The LiK-edge position depends on the electronegativity of the element to which it is bound. The intensity of the first peak varies depending on the existence of

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20

Fan, Min, Xin Chang, Yu-Jie Guo, et al. "Increased residual lithium compounds guided design for green recycling of spent lithium-ion cathodes." Energy & Environmental Science 14, no. 3 (2021): 1461–68. http://dx.doi.org/10.1039/d0ee03914d.

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21

Gutiérrez-Flórez, M. T., A. Kuhn, and F. Garcı́a-Alvarado. "Lithium intercalation in KxTi8O16 compounds." International Journal of Inorganic Materials 1, no. 1 (1999): 117–21. http://dx.doi.org/10.1016/s1463-0176(99)00018-6.

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22

Zamoshchina, T., V. Isupov, and A. Matveyenko. "The new prolonged lithium compounds." European Neuropsychopharmacology 10 (September 2000): 269. http://dx.doi.org/10.1016/s0924-977x(00)80256-4.

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23

Lumley, J. S. "ASR suppression by lithium compounds." Cement and Concrete Research 27, no. 2 (1997): 235–44. http://dx.doi.org/10.1016/s0008-8846(97)00003-3.

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24

Richardson, Thomas J. "Phosphate-stabilized lithium intercalation compounds." Journal of Power Sources 119-121 (June 2003): 262–65. http://dx.doi.org/10.1016/s0378-7753(03)00244-1.

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25

Gorelik, V. S., Dongxue Bi, Y. P. Voinov, et al. "Raman spectra of lithium compounds." Journal of Physics: Conference Series 918 (November 2017): 012035. http://dx.doi.org/10.1088/1742-6596/918/1/012035.

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26

Gonopolsky, A. M., D. A. Makarenkov, V. I. Nazarov, M. I. Klyushenkova, and A. P. Popov. "Recycling Lithium-containing Compounds from Spent Current Sources." Ecology and Industry of Russia 23, no. 5 (2019): 10–15. http://dx.doi.org/10.18412/1816-0395-2019-5-10-15.

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The work is devoted to the development of an assessment of existing methods of utilization of lithium chemical current sources. Modern types of lithium-ion current sources are analyzed. It is shown that the cathode and electrolyte materials are most valuable for the process of separating commercial lithium. A modern technological disposal scheme is proposed, where mechanical activation processes are used using ball mills and baromembrane technologies (ultrafiltration and reverse osmosis). The results of experimental studies on the pilot plant.

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27

Ducros, J. B., S. Bach, J. P. Pereira-Ramos, and P. Willmann. "Layered lithium cobalt nitrides: A new class of lithium intercalation compounds." Journal of Power Sources 175, no. 1 (2008): 517–25. http://dx.doi.org/10.1016/j.jpowsour.2007.09.052.

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28

Kotani, Shunsuke, Kenji Kukita, Kana Tanaka, Tomonori Ichibakase, and Makoto Nakajima. "Lithium Binaphtholate-Catalyzed Asymmetric Addition of Lithium Acetylides to Carbonyl Compounds." Journal of Organic Chemistry 79, no. 11 (2014): 4817–25. http://dx.doi.org/10.1021/jo5005394.

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29

Hashikawa, Satoru, Satoshi Yanase, and Takao Oi. "Lithium Isotope Effect Accompanying Chemical Insertion of Lithium into Graphite." Zeitschrift für Naturforschung A 57, no. 11 (2002): 857–62. http://dx.doi.org/10.1515/zna-2002-1104.

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Lithiumwas chemically intercalated from 1-methoxybutane solution of lithiumand naphthalene into graphite and vice versa, and lithium isotope fractionation accompanying those intercalation and deintercalation processes was observed. 6Li was always preferentially fractionated into the graphite phase. The single-stage lithium isotope separation factor upon intercalation was about 1.023 at 25 ºC, nearly independent of the structure of the lithium-graphite intercalation compounds formed. A much smaller separation factor was observed for the deintercalation process, suggesting the existence of lithi

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30

Sorokin, Vladimir I., Valery A. Ozeryanskii, Gennady S. Borodkin, Anatoly V. Chernyshev, Max Muir, and Jon Baker. "Preparation of Dialkylamino-Substituted Benzenes and Naphthalenes by Nucleophilic Replacement of Fluorine in the Corresponding Perfluoroaromatic Compounds." Zeitschrift für Naturforschung B 61, no. 5 (2006): 615–25. http://dx.doi.org/10.1515/znb-2006-0519.

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The reactions between hexafluorobenzene (HFB) and octafluoronaphthalene (OFN) with secondary aliphatic amines (pyrrolidine, dimethylamine and piperidine) and lithium amides (pyrrolidide, dimethylamide and piperidide) have been investigated both experimentally and (in part) theoretically. With amines HFB, depending on the selected conditions, gives either di-substituted products or a complex mixture of di-, tri- and tetrasubstituted compounds. Under similar conditions OFN produces almost exclusively the 2,3,6,7-tetrasubstituted compound. Interaction of HFB with the more nucleophilic lithium ami

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31

Zhecheva, E., R. Stoyanova, R. Alcántara, P. Lavela, and J. L. Tirado. "Cation order/disorder in lithium transition-metal oxides as insertion electrodes for lithium-ion batteries." Pure and Applied Chemistry 74, no. 10 (2002): 1885–94. http://dx.doi.org/10.1351/pac200274101885.

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Results on the local cation ordering in layered lithium-nickel/cobalt oxides and metal-substituted lithium-manganese spinels are presented. It is shown that electron spin resonance of Ni3+ and Mn4+ and magnetic susceptibility measurements are powerful tools to monitor the short-range cation ordering in these compounds, which is not accessible by diffraction techniques. Thus, owing to the different strength of the 90° and 180° Ni3+–O–Ni3+/2+ exchange interactions, the distribution of Ni3+/Ni2+ between the lithium and nickel layers in Li1–xNi1+xO2 with 0 &lt; x &lt; 0.4 can be determined

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32

Sato, Kunihiko, Shun Saito, Satoshi Yanase, and Takao Oi. "Estimation of Reduced Partition Function Ratios of Lithium-Graphite Intercalation Compounds by Density Functional Theory." Zeitschrift für Naturforschung A 69, no. 3-4 (2014): 122–28. http://dx.doi.org/10.5560/zna.2013-0085.

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The reduced partition function ratio (RPFR) of lithium in lithium-graphite intercalation compounds (Li-GICs) was evaluated at the UB3LYP=6-311G(d) level of theory. The partition functions were written in the usual rigid-rotor harmonic oscillator approximation.With a C24H12 coronene molecule as the model of graphene, lithium-coronene sandwich, and club sandwich compounds were considered as models of Li-GICs. The estimated value of the 6Li-to-7Li RPFR was 1.0402 at 25 °C, which yielded 1.034 as the value of the equilibrium constant, K, of the lithium isotope exchange reaction between a lithium i

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33

Zaidi, S. Z. J., S. Hassan, M. Raza, C. Harito, B. Yuliarto, and F. C. Walsh. "Conceptualized Simulation for Templating Carbon Based Nano Structures for Li-ion Batteries: A DFT Investigation." Journal of New Materials for Electrochemical Systems 24, no. 2 (2021): 66–72. http://dx.doi.org/10.14447/jnmes.v24i2.a02.

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CNT (10, 0) is carbon nanotube; Graphene is a 2-dimensional carbon allotrope being light weight and Chitosan is a linear polysaccharide. In this work, detailed analysis of the above three stated compounds as anode for lithium-ion batteries is stated. The density function theory (DFT) computations were used to carry out the investigation of the above stated compound as anode materials for the lithium-ion batteries. The analysis shows that Graphene and Chitosan are highly favorable to be used as anodes materials for the lithium-ion batteries. The results show that the Vcell of Graphene and Chito

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34

Havlíček, David, Zdeněk Mička, Václav Barbořák, and Petr Šmejkal. "Cesium and Cesium-Lithium Selenates." Collection of Czechoslovak Chemical Communications 65, no. 2 (2000): 167–78. http://dx.doi.org/10.1135/cccc20000167.

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The Cs2SeO4-H2SeO4-H2O and Cs2SeO4-Li2SeO4-H2O systems were studied at 30 °C as a basis for determining the conditions for formation of the compound Cs4LiH3(SeO4)4, which has been observed to undergo a ferroelectric phase transition. The results of a solubility study were used to construct a pseudo-ternary cross-section for CsLiSeO4-CsHSeO4-H2O in the quaternary system Cs2SeO4-Li2SeO4-H2SeO4-H2O, which demonstrated that, in the region of crystallization of the compound of interest, a substance with the composition Cs4LiH3(SeO4)4 is actually formed. Attention was further paid to the following n

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35

Yang, Y., L. Buzi, A. O. Nelson, R. Kaita, and B. E. Koel. "Post exposure time dependence of deuterium retention in lithium and lithium compounds." Nuclear Materials and Energy 19 (May 2019): 161–65. http://dx.doi.org/10.1016/j.nme.2019.01.031.

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36

Aspinall, Garreth M., May C. Copsey, John C. Jeffery, Angela P. Breakspear (neé Leedham), Christopher A. Russell, and John M. Slattery. "Lithium–nitrogen and lithium–boron–nitrogencage compounds formed using the phenylhydrazido backbone." Dalton Trans., no. 9 (2006): 1234–38. http://dx.doi.org/10.1039/b510103d.

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37

Chun, Jinyoung, Hyojin Kim, Changshin Jo, Eunho Lim, Jinwoo Lee, and Youngsik Kim. "Reversibility of Lithium-Ion-Air Batteries Using Lithium Intercalation Compounds as Anodes." ChemPlusChem 80, no. 2 (2014): 349–53. http://dx.doi.org/10.1002/cplu.201402035.

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38

Funabiki, Atsushi, Minoru Inaba, Takeshi Abe, and Zempachi Ogumi. "Stage Transformation of Lithium‐Graphite Intercalation Compounds Caused by Electrochemical Lithium Intercalation." Journal of The Electrochemical Society 146, no. 7 (1999): 2443–48. http://dx.doi.org/10.1149/1.1391953.

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39

Boyle, Timothy J., Todd M. Alam, Kelly P. Peters, and Mark A. Rodriguez. "Structural Diversity of Lithium Neopentoxide Compounds." Inorganic Chemistry 40, no. 24 (2001): 6281–86. http://dx.doi.org/10.1021/ic0106569.

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40

Rabii, S., and D. Guérard. "Stability of superdense lithium graphite compounds." Journal of Physics and Chemistry of Solids 69, no. 5-6 (2008): 1165–67. http://dx.doi.org/10.1016/j.jpcs.2007.10.023.

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41

Julien, C. M., A. Ait-Salah, A. Mauger, and F. Gendron. "Magnetic properties of lithium intercalation compounds." Ionics 12, no. 1 (2006): 21–32. http://dx.doi.org/10.1007/s11581-006-0007-5.

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42

Jug, Karl, Eckhard Fasold, and Andres M. Köster. "Charge and valence in lithium compounds." Chemical Physics Letters 188, no. 3-4 (1992): 294–98. http://dx.doi.org/10.1016/0009-2614(92)90025-i.

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43

Raston, CL, WT Robinson, BW Skelton, CR Whitaker, and AH White. "Lewis-Base Adducts of Main Group 1 Metal-Compounds. XIII. Synthesis and Structures of Some Pyridine Base Lithium Bromide and Iodide Adducts." Australian Journal of Chemistry 43, no. 7 (1990): 1163. http://dx.doi.org/10.1071/ch9901163.

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The syntheses and single-crystal X-ray structure determinations of adducts of the lithium(I) halides with the following stoichiometries are reported: 1 : 3 lithium(I) bromide, iodide/ pyridine, monomers; 1 : 2 lithium(I) bromide/ quinoline and lithium(I) iodide/ quinaldine , both as [L2LiX2LiL2] dimers ; and 1 : 1� lithium(I) iodide/2,4,6-trimethylpyridine, 'step' tetramer.

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44

Carper, H. J., A. Ertas, and O. Cuvalci. "Rating Thread Compounds for Galling Resistance." Journal of Tribology 117, no. 4 (1995): 639–45. http://dx.doi.org/10.1115/1.2831529.

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Results are presented from an experimental study which demonstrates the feasibility of using an existing galling tester and test method as a screening device for evaluating thread compound additives for galling protection. The galling tester employs tubular pin and box specimen pairs fabricated from steel tubing used in the oil field. For the test thread compounds, four different additive packages were used, all with the same grease base of lithium stearate. For reference purposes, the lithium stearate grease base without any additives was tested as one of the thread compounds. The data obtain

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45

Zhang, Hui Zong, Dong Liang Shen, Dao Lin Gao, Shi Qiang Wang, Ya Fei Guo, and Tian Long Deng. "Lithium Recovery Techniques from Solid and Liquid Mineral Resources." Advanced Materials Research 549 (July 2012): 528–31. http://dx.doi.org/10.4028/www.scientific.net/amr.549.528.

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Lithium and its compounds are important materials in industry. In this paper, lithium recovery methods both from solid ores and brines were summarized, and the key problems existed were also pointed out. More details for lithium recovery from brines by solvent extraction, ion-exchange, precipitation and calcination leaching methods were discussed, and the new trend for lithium recovery in the future was also carried out.

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46

Nazarenko, O. A., V. I. Demidov, O. A. Gromova, E. L. Aleksakhina, and I. Yu Torshin. "Comparative study of the neuroprotective activity of lithium compounds and their effect on the course of experimental alloxan diabetes mellitus in rats." Pharmacokinetics and Pharmacodynamics, no. 3 (June 22, 2021): 40–47. http://dx.doi.org/10.37489/2587-7836-2020-3-40-47.

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A comparative study of the effects of an inorganic lithium salt (lithium carbonate) and an organic lithium salt (lithium ascorbate) on a model of alloxan diabetes mellitus was conducted. The use of lithium ascorbate for a month in experimental alloxan diabetes mellitus facilitates its course – the survival rate of animals increases, the level of glycemia decreases (especially when administered at a dose of 10 mg/kg). Morphometric analysis showed that lithium ascorbate in alloxan diabetes has a neuroprotective effect, which is manifested in a decrease in toxic damage to neurocytes with an incre

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47

Schirmer, Thomas, Michael Wahl, Wolfgang Bock, and Michael Kopnarski. "Determination of the Li Distribution in Synthetic Recycling Slag with SIMS." Metals 11, no. 5 (2021): 825. http://dx.doi.org/10.3390/met11050825.

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The recovery of technically important elements like lithium from slag of pyrometallurgical recycling of lithium traction batteries will be very important in future due to the expected increasing demand of this element with the upcoming world-wide implementation of electro mobility. Therefore, the investigation of possibilities to recover lithium from pyrometallurgical slag from the recycling of lithium traction batteries is mandatory. In this context, the EnAM (engineered artificial mineral) approach is very promising. Solidified melt of synthetic recycling slag with the compounds Li2O-MgO-Al2

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48

OKUMURA, Toyoki, Tomokazu FUKUTSUKA, Yoshiharu UCHIMOTO, Morihiro SAITO, and Jun KUWANO. "Lithium-Ion Conductivity in Lithium Lanthanum Titanates as Different Local Distortion Model Compounds." Electrochemistry 78, no. 5 (2010): 457–59. http://dx.doi.org/10.5796/electrochemistry.78.457.

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49

Jackman, Lloyd M., L. M. Scarmoutzos, and C. W. DeBrosse. "Lithium quadrupole coupling constants and the structures of organic lithium compounds in solution." Journal of the American Chemical Society 109, no. 18 (1987): 5355–61. http://dx.doi.org/10.1021/ja00252a009.

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50

Kotani, Shunsuke, Kenji Kukita, Kana Tanaka, Tomonori Ichibakase, and Makoto Nakajima. "ChemInform Abstract: Lithium Binaphtholate-Catalyzed Asymmetric Addition of Lithium Acetylides to Carbonyl Compounds." ChemInform 45, no. 47 (2014): no. http://dx.doi.org/10.1002/chin.201447027.

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