Rozprawy doktorskie na temat „Lithium”
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Nguyen, Hanh D. "Structural Elucidation of tert-Butyllithium/Lithium Alkoxide and Lithium Hydride/Lithium Alkoxide Mixed Aggregates". Thesis, University of North Texas, 1997. https://digital.library.unt.edu/ark:/67531/metadc278525/.
Pełny tekst źródłaAojula, 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.
Pełny tekst źródłaHarrison, Hollie. "The electrodialysis of lithium sulphate to lithium hydroxide". Thesis, Harrison, Hollie (2018) The electrodialysis of lithium sulphate to lithium hydroxide. Honours thesis, Murdoch University, 2018. https://researchrepository.murdoch.edu.au/id/eprint/40456/.
Pełny tekst źródłaChinyama, Luzendu Gabriel. "Recovery of Lithium from Spent Lithium Ion Batteries". Thesis, Luleå tekniska universitet, Institutionen för samhällsbyggnad och naturresurser, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-59866.
Pełny tekst źródłaBjörkman, Carl Johan. "Detection of lithium plating in lithium-ion batteries". Thesis, KTH, Kemiteknik, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-266369.
Pełny tekst źródłaMed en ökande efterfråga på hållbara transportlösningar så finns det ett behov av elektrifierade fordon. Ett sätt att lagra energi ombord ett elektrifierat fordon är att använda et litium-jon-batteri. Denna batteriteknologi har många fördelar: t.ex. är dessa batterier återladdningsbara, och de kan leverera höga uteffekter samtidigt som de kan ha ett stort energiinnehåll. för att säkerställa en säker drift av litium-jon-batterier måste batteriets styrsystem vara designat med hänsyn till den elektrokemiska dynamiken inuti batteriet. Dock åldras batteriet med tiden, vilket innebär att denna dynamik ändras med tiden, vilket innebär att styrningen av batteriet måste anpassa sig till denna föråldring. Det är möjligt att förutspå åldring av batterier, men vissa åldringsmekanismer kan ske slumpartat, t.ex. via slumpmässiga förändringar i tillverkningsprocessen av batteriet, eller variationer i användningen av batteriet. Genom att därmed bevaka dessa åldringsmekanismer in situ så kan styrsystemets algoritm anpassa sig utmed batteriåldringen, trots dessa slumpartade effekter. En åldringmekanism hos litium-jon-batterier är s.k. litiumplätering. Denna mekanism innebär att litium-joner elektrokemiskt pläteras i form av metalliskt litium på ytan av litium-jon-batteriets negativa elektrod. Mekanismen kan också inducera andra åldringsmekanismer, t.ex. gasutveckling eller elektrolytreduktion. Detta projekt har undersökt en metod för att detektera litiumplätering in situ efter att plätering har skett, genom att både analysera öppencellspänningens (OCV) förändring med tiden direkt efter uppladdning samt analysera de svällande krafterna som uppstår under uppladdning av batteriet. Resultaten visar på en korrelation mellan en hög sannolikhet för litiumplätering och observationen av en topp i svällningskraft och en platå i OCV-kurvan. resultaten visar också en möjlig korrelation mellan påbörjandet av litium-plätering och påbörjandet av toppen i svällningskraft. Vidare visar även resultaten ett troligt samband mellan signalernas magnitud och mängden pläterat litium. Slutligen visar resultaten också ett möjligt samband mellan irreversibelt pläterat litium och ett svällningstryck som ackumuleras med varje uppladdningscykel. Dock krävs det en validering med mer avancerade analysmetoder för att säkerställa användningsbarheten av dessa två signaler, vilket ej var möjligt inom detta projekt.
Harvey, Norman Stewart. "Lithium treatment". Thesis, University of Sheffield, 1990. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.321423.
Pełny tekst źródłaMyalo, Zolani. "Graphenised Lithium Iron Phosphate and Lithium Manganese Silicate Hybrid Cathode Systems for Lithium-Ion Batteries". University of the Western Cape, 2017. http://hdl.handle.net/11394/6036.
Pełny tekst źródłaThis research was based on the development and characterization of graphenised lithium iron phosphate-lithium manganese silicate (LiFePO4-Li2MnSiO4) hybrid cathode materials for use in Li-ion batteries. Although previous studies have mainly focused on the use of a single cathode material, recent works have shown that a combination of two or more cathode materials provides better performances compared to a single cathode material. The LiFePO4- Li2MnSiO4 hybrid cathode material is composed of LiFePO4 and Li2MnSiO4. The Li2MnSiO4 contributes its high working voltage ranging from 4.1 to 4.4 V and a specific capacity of 330 mA h g-1, which is twice that of the LiFePO4 which, in turn, offers its long cycle life, high rate capacity as well as good electrochemical and thermal stability. The two cathode materials complement each other's properties however they suffer from low electronic conductivities which were suppressed by coating the hybrid material with graphene nanosheets. The synthetic route entailed a separate preparation of the individual pristine cathode materials, using a sol-gel protocol. Then, the graphenised LiFePO4-Li2MnSiO4 and LiFePO4-Li2MnSiO4 hybrid cathodes were obtained in two ways: the hand milling (HM) method where the pristine cathodes were separately prepared and then mixed with graphene using a pestle and mortar, and the in situ sol-gel (SG) approach where the Li2MnSiO4 and graphene were added into the LiFePO4 sol, stirred and calcined together.
2021-04-30
Popovic, Jelena. "Novel lithium iron phosphate materials for lithium-ion batteries". Phd thesis, Universität Potsdam, 2011. http://opus.kobv.de/ubp/volltexte/2011/5459/.
Pełny tekst źródłaKonventionelle Energiequellen sind weder nachwachsend und daher nachhaltig nutzbar, noch weiterhin langfristig verfügbar. Sie benötigen Millionen von Jahren um gebildet zu werden und verursachen in ihrer Nutzung negative Umwelteinflüsse wie starke Treibhausgasemissionen. Im 21sten Jahrhundert ist es unser Ziel nachhaltige und umweltfreundliche, sowie möglichst preisgünstige Energiequellen zu erschließen und nutzen. Neuartige Technologien assoziiert mit transportablen Energiespeichersystemen spielen dabei in unserer mobilen Welt eine große Rolle. Li-Ionen Batterien sind in der Lage wiederholt Energie aus entsprechenden Prozessen nutzbar zu machen, indem sie reversibel chemische in elektrische Energie umwandeln. Die Leistung von Li-Ionen Batterien hängen sehr stark von den verwendeten Funktionsmaterialien ab. Aktuell verwendete Elektrodenmaterialien haben hohe Produktionskosten, verfügen über limitierte Energiespeichekapazitäten und sind teilweise gefährlich in der Nutzung für größere Bauteile. Dies beschränkt die Anwendungsmöglichkeiten der Technologie insbesondere im Gebiet der hybriden Fahrzeugantriebe. Die vorliegende Dissertation beschreibt bedeutende Fortschritte in der Entwicklung von LiFePO4 als Kathodenmaterial für Li-Ionen Batterien. Mithilfe einfacher Syntheseprozeduren konnten eine vollkommen neue Morphologie (mesokristallines LiFePo4) sowie ein nanostrukturiertes Material mit exzellenten elektrochemischen Eigenschaften hergestellt werden. Die neu entwickelten Verfahren zur Synthese von LiFePo4 sind einschrittig und bei signifikant niedrigeren Temperaturen im Vergleich zu konventionellen Methoden. Die Verwendung von preisgünstigen und umweltfreundlichen Ausgangsstoffen stellt einen grünen Herstellungsweg für die large scale Synthese dar. Mittels des neuen Synthesekonzepts konnte meso- und nanostrukturiertes LiFe PO4 generiert werden. Die Methode ist allerdings auch auf andere phospho-olivin Materialien (LiCoPO4, LiMnPO4) anwendbar. Batterietests der besten Materialien (nanostrukturiertes LiFePO4 mit Kohlenstoffnanobeschichtung) ergeben eine mögliche Energiespeicherung von 94%.
Cvitaš, Marko Tomislav. "Interactions and collisions of cold molecules : lithium + lithium dimer". Thesis, Durham University, 2004. http://etheses.dur.ac.uk/3667/.
Pełny tekst źródłaRoß, Sebastian [Verfasser]. "Lithium conductivity characteristics of amorphous lithium silicate and lithium alumosilicate materials and their compaction / Sebastian Roß". Hannover : Technische Informationsbibliothek und Universitätsbibliothek Hannover (TIB), 2015. http://d-nb.info/1068347899/34.
Pełny tekst źródłaPark, Bongjin. "Single electron transfer in reactions involving alkyl halides with lithium alkylamide, lithium alkyl and lithium metal". Diss., Georgia Institute of Technology, 1988. http://hdl.handle.net/1853/27052.
Pełny tekst źródłaTaubert, Franziska. "Thermodynamische Untersuchungen in den Systemen Lithium-Silicium und Lithium-Zinn". Doctoral thesis, Technische Universitaet Bergakademie Freiberg Universitaetsbibliothek "Georgius Agricola", 2017. http://nbn-resolving.de/urn:nbn:de:bsz:105-qucosa-229567.
Pełny tekst źródłaAlmohareb, Muneerah. "Novel Lithium Ionic Conducting Perovskite Materials for Lithium-Air Batteries". Thesis, Université d'Ottawa / University of Ottawa, 2017. http://hdl.handle.net/10393/36515.
Pełny tekst źródłaBest, Adam Samuel 1976. "Lithium-ion conducting electrolytes for use in lithium battery applications". Monash University, School of Physics and Materials Engineering, 2001. http://arrow.monash.edu.au/hdl/1959.1/9240.
Pełny tekst źródłaLi, Juchuan. "UNDERSTANDING DEGRADATION AND LITHIUM DIFFUSION IN LITHIUM ION BATTERY ELECTRODES". UKnowledge, 2012. http://uknowledge.uky.edu/cme_etds/12.
Pełny tekst źródłaHein, Smon [Verfasser]. "Modeling of lithium plating in lithium-ion-batteries / Smon Hein". Ulm : Universität Ulm, 2018. http://d-nb.info/1162539917/34.
Pełny tekst źródłaLin, Jian. "Novel Lithium Salt and Polymer Electrolytes for Polymer Lithium Batteries". Case Western Reserve University School of Graduate Studies / OhioLINK, 2008. http://rave.ohiolink.edu/etdc/view?acc_num=case1215572988.
Pełny tekst źródłaDamen, Libero <1980>. "Advanced lithium and lithium-ion rechargeable batteries for automotive applications". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/3427/1/Damen_Libero_Tesi.pdf.
Pełny tekst źródłaDamen, Libero <1980>. "Advanced lithium and lithium-ion rechargeable batteries for automotive applications". Doctoral thesis, Alma Mater Studiorum - Università di Bologna, 2011. http://amsdottorato.unibo.it/3427/.
Pełny tekst źródłaKruchinin, Dennis. "Lithium amide mechanisms". Thesis, University of Oxford, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.437356.
Pełny tekst źródłaKhosravi, 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.
Pełny tekst źródłaThe 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.
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.
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.
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.
Petzl, Mathias [Verfasser]. "Zerstörungsfreie Charakterisierung von Lithium-Plating in Lithium-Ionen-Batterien / Mathias Petzl". Ulm : Universität Ulm. Fakultät für Naturwissenschaften, 2015. http://d-nb.info/1076828515/34.
Pełny tekst źródłaTaylor, David Wayne. "The Lithium concentration dependence of creep in binary Aluminum-Lithium alloys". Thesis, Monterey, California. Naval Postgraduate School, 1989. http://hdl.handle.net/10945/26044.
Pełny tekst źródłaJang, Young-Il 1968. "Stability of lithium aluminum manganese oxide cathodes for rechargeable lithium batteries". Thesis, Massachusetts Institute of Technology, 1999. http://hdl.handle.net/1721.1/9162.
Pełny tekst źródłaIncludes bibliographical references.
Lithium manganese oxides have attracted wide attention as low-cost, nontoxic intercalation cathode materials for rechargeable lithium batteries. In this work, the stability of these compounds during synthesis and in use has been studied in several respects. (1) Phase stability of LiMnO2 polymorphs has been determined under the high temperature synthesis conditions. Effects of temperature, oxygen partial pressure, and dopant (Al) content on the phase stability have been discussed based on a possible stability mechanism. (2) The mechanism of improved cycling stability of electrochemically transformed spinel compared to conventional spinel has been identified. Atomic rearrangement from the ordered rocksalt to spinel type cation ordering results in an antiphase nanodomain structure, which becomes a ferroelastic domain structure during the cubic ---> tetragonal Jahn-Teller transformation, and thereby accommodates the transformation strains. (3) Al-doped spinels exhibit much improved capacity stability at elevated temperatures compared to undoped spinels. This effect has been discussed with respect to proposed mechanisms of Mn dissolution and capacity loss. (4) Magnetic properties are critically influenced by phase stability, cation ordering, and Mn valence in lithium manganese oxides. In the paramagnetic temperature regime, it has been observed that antiferromagnetic interactions between the Mn ions are strongest in the orthorhombic phase among LiMnO2 polymorphs having the average Mn valence of 3+, while decreasing Mn valence strengthens the antiferromagnetic interactions in LixMn2O4 spinel. At temperatures below the paramagnetic temperature regime, spin-glass behavior is observed in both LixMn2O4 and monoclinic LiMnO2 compounds, which is attributed to geometrical frustration due to structure ( cation ordering) and magnetic disorder due to a disordered distribution of Mn valence. As spin-glass behavior is commonly observed in both well-crystallized, conventional spinel and highly disordered, transformed spinel, magnetic characterization cannot easily be used to distinguish the two different spinels.
by Young Il-Jang.
Ph.D.
Kwabi, David G. (David Gator). "Electrochemical studies of lithium-oxygen reactions for lithium-air battery applications". Thesis, Massachusetts Institute of Technology, 2013. http://hdl.handle.net/1721.1/81607.
Pełny tekst źródłaCataloged from PDF version of thesis.
Includes bibliographical references (p. 61-63).
Fundamentally understanding reaction mechanisms during Li-O₂ cell operation is critical for implementing Li-air batteries with high reversibility and long cycle life. In this thesis, the rotating ring disk electrode (RRDE) technique has been used to probe the influence of different electrolyte solvents on the stability of the superoxide radical produced on planar glassy carbon and Au electrodes. It was found that the fraction of oxygen reduction reaction current attributable to superoxide generation exhibits a solvent-invariant potential dependence on carbon, with a higher fraction of superoxide produced at lower discharge overpotentials. This trend is in support of a proposed growth model for different Li-O₂ morphologies, where Li-O₂ growth is governed primarily by disproportionation of superoxide at low overpotentials and direct electron transfer at high overpotentials. On Au, superoxide stability exhibits a strong solvent dependence, which can be explained in terms of the effect of the electrolyte solvent basicity on the stability of the Li+-O₂- ion pair. This study highlights the potential use of RRDE as a tool to gain insights into Li-O₂ reaction and growth mechanisms and the contribution of soluble intermediate species to parasitic reactions in practical Li-air batteries.
by David G. Kwabi.
S.M.
Valdivia, Christopher E. "Light-induced ferroelectric domain engineering in lithium niobate & lithium tantalate". Thesis, University of Southampton, 2007. https://eprints.soton.ac.uk/65500/.
Pełny tekst źródłaWellington, Iain. "Direct UV writing of structures in lithium niobate and lithium tantalate". Thesis, University of Southampton, 2007. https://eprints.soton.ac.uk/50699/.
Pełny tekst źródłaBrinkhaus, Linda [Verfasser], i Dirk [Akademischer Betreuer] Guldi. "Degradation Phenomena of Lithium-rich Lithium-Nickel-Cobalt- Manganese-Oxide in Lithium-Ion-Batteries / Linda Brinkhaus. Gutachter: Dirk Guldi". Erlangen : Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), 2015. http://d-nb.info/1075837618/34.
Pełny tekst źródłaPaul, Marcus. "Synthesis and characterisation of transition metal-doped lithium niobate and lithium tantalate". Thesis, University of Aberdeen, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.319341.
Pełny tekst źródłaNordh, Tim. "Lithium titanate as anode material in lithium-ion batteries : -A surface study". Licentiate thesis, Uppsala universitet, Strukturkemi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-267567.
Pełny tekst źródłaImanishi, Nobuyuki. "STUDY ON LITHIUM INSERTION COMPOUNDS AS ELECTRODE MATERIALS FOR LITHIUM SECONDARY BATTERY". Kyoto University, 1993. http://hdl.handle.net/2433/168867.
Pełny tekst źródłaKyoto University (京都大学)
0048
新制・論文博士
博士(工学)
乙第8064号
論工博第2663号
新制||工||898(附属図書館)
UT51-93-B336
(主査)教授 竹原 善一郎, 教授 曽我 直弘, 教授 小久見 善八
学位規則第4条第2項該当
Madsen, Alex. "Lithium iron sulphide as a positive electrode material for rechargeable lithium batteries". Thesis, University of Southampton, 2013. https://eprints.soton.ac.uk/355748/.
Pełny tekst źródłaRossouw, Margaretha Hendrina. "Synthesis and characterization of lithium-manganese-oxide electrodes for lithium battery applications". Master's thesis, University of Cape Town, 1994. http://hdl.handle.net/11427/18339.
Pełny tekst źródłaRida, Hania. "Nouvelles données sur les systèmes graphite-lithium-europium et graphite-lithium-calcium". Thesis, Nancy 1, 2011. http://www.theses.fr/2011NAN10019/document.
Pełny tekst źródłaThe molten alloy solid-liquid method containing lithium has recently enabled the synthesis of several bulk graphite intercalation compounds (GICs) in graphite-lithium-alkaline earth metal systems. As part of this thesis, this synthesis method was extended to graphite-lithium-lanthanide systems, with an additional difficulty which is the lack of knowledge of lithium-lanthanide binary phase diagrams whose data are crucial for determining the temperature range and chemical composition of alloys that may lead to GICs.The immersion of pyrographite platelets in some europium-lithium alloys wisely chosen led to a binary EuC6 compound as well as a graphite-lithium-europium first stage ternary compound.Kinetics study of EuC6 compound was followed by ex situ X-ray diffraction in order to understand the different reaction steps and identify intermediate phases leading to the thermodynamically stable final compound. This mechanism revealed a reaction process more "cooperative" than that leading to CaC6 binary compound and was described by a succession of steps that contribute to the bulk insertion of europium.The elementary composition of the ternary compound was determined by ions beam analysis allowing the simultaneous quantification of the three elements lithium, carbon and europium. The refinement of these analyses led to the chemical formula Li0,25Eu1,95C6 for the ternary compound. EuC6 has also been studied by nuclear microprobe analysis, and especially the C/Eu atomic ratio equal to 6 has been confirmed.Structural studies have been undertaken for binary and ternary compounds. On one hand, it was possible to fully resolve the three-dimensional structure of the binary EuC6, which crystallizes in a hexagonal unit cell with P63/mmc space group. On the other hand, the c axis stacking sequence of the poly-layered intercalated sheet of the ternary compound was modeled by combining structural data with information from the ions beam analysis. The graphite intercalation compounds are low-dimensional solids that are ideal for the study of structure-properties relations. Thus in graphite-lithium-calcium system, superconducting character has been studied for CaC6 and Li3Ca2C6 compounds by muons spin spectroscopy ([mu]SR). For the graphite-lithium-europium system, previous magnetic measurements have been continued and supplemented by [mu]SR analysis (for Li0,25Eu1,95C6 and EuC6) and by low temperature 151Eu Mössbauer spectroscopy (for Li0,25Eu1,95C6)
Hsiao, Kuang-Che. "Synthesis, characterisation and properties of lithium pyrophosphate materials for lithium battery applications". Thesis, University of Sheffield, 2014. http://etheses.whiterose.ac.uk/6693/.
Pełny tekst źródłaBramham, Janice. "Lithium-7 NMR investigations of the biological behaviour of the lithium ion". Thesis, University of St Andrews, 1993. http://hdl.handle.net/10023/14768.
Pełny tekst źródłaMast, Ernest. "Lithium production from spodumene". Thesis, McGill University, 1989. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=55633.
Pełny tekst źródłaMuller, Catherine R. "Lithium amides in synthesis". Thesis, University of Oxford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.413176.
Pełny tekst źródłaBroughton, Duncan Andrew. "Hydrolysis of lithium hydride". Thesis, University of Reading, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394063.
Pełny tekst źródłaFlack, Keith W. "Defects in lithium oxide". Thesis, University of Kent, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238119.
Pełny tekst źródłaThomas, Geraint Mark Howard. "Lithium and phosphoinositide metabolism". Thesis, University of Wolverhampton, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.238120.
Pełny tekst źródłaBarry, Ian Eric. "Microstructuring of lithium niobate". Thesis, University of Southampton, 2000. https://eprints.soton.ac.uk/15498/.
Pełny tekst źródłaSenyshyn, A., M. Monchak, O. Dolotko i H. Ehrenberg. "Lithium Diffusion and Diffraction". Diffusion fundamentals 21 (2014) 4, S.1, 2014. https://ul.qucosa.de/id/qucosa%3A32392.
Pełny tekst źródłaMargheim, Steven J. "Lithium in the Pleiades". [Bloomington, Ind.] : Indiana University, 2007. http://gateway.proquest.com/openurl?url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:dissertation&res_dat=xri:pqdiss&rft_dat=xri:pqdiss:3252776.
Pełny tekst źródłaTitle from PDF t.p. (viewed Nov. 19, 2008). Source: Dissertation Abstracts International, Volume: 68-02, Section: B, page: 1022. Adviser: Constantine Deliyannis.
Wise, David. "Processing hard rock lithium". Thesis, Wise, David (2018) Processing hard rock lithium. Honours thesis, Murdoch University, 2018. https://researchrepository.murdoch.edu.au/id/eprint/41925/.
Pełny tekst źródłaQueval, Pierre. "Phosphures borane de lithium". Caen, 2011. http://www.theses.fr/2011CAEN2053.
Pełny tekst źródłaLithium phosphido-boranes are anionic species prepared by deprotonation of secondary phosphane-boranes using an organolithium base. Multinuclear NMR analysis of these poorly studied compounds evidenced lithium-hydrides interactions and absence of lithium-phosphorus one. According to their structure, these compounds develop a dual reactivity behaving as both P-nucleophile and reducing agent using carbonyl compounds as substrates. The issue of the reaction depends on the kinetic or thermodynamic control imposed to the reaction medium: P-addition or reduction, respectively. Linear polyphosphinoboranes have also been formed during the reduction process. In a second part, P-enantioenriched phosphane-boranes have been synthesized starting form sterically hindered phosphane-boranes using enantiopure amines derived from 3-aminopyrrolidine as chiral agents. This approach, involving a thermodynamic dynamic resolution process, leads for the first time to tertiary P-stereogenic phosphane-boranes, having the (S)-configuration
Ecker, Madeleine [Verfasser]. "Lithium Plating in Lithium-Ion Batteries : An Experimental and Simulation Approach / Madeleine Ecker". Aachen : Shaker, 2016. http://d-nb.info/1106838440/34.
Pełny tekst źródłaTsukamoto, Hisashi. "Synthesis and electrochemical studies of lithium transition metal oxides for lithium-ion batteries". Thesis, University of Aberdeen, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327428.
Pełny tekst źródłaNguyen, Trang Thi Thu. "Hydrogen release and absorption in mixed anion lithium amide/lithium ternary nitride systems". Thesis, University of Birmingham, 2016. http://etheses.bham.ac.uk//id/eprint/6671/.
Pełny tekst źródłaDU, PASQUIER AURELIEN. "Synthese et evaluation d'electrolytes polymeres pour generateurs secondaires au lithium et ion lithium". Paris 6, 1996. http://www.theses.fr/1996PA066318.
Pełny tekst źródła