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Artykuły w czasopismach na temat "Li+ and F- ions"

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Jiang, Hongfu, Haiyan Song, Zuoxing Zhou, Xingqin Liu, and Guangyao Meng. "The roles of Li+ and F− ions in Li–F-codoped TiO2 system." Journal of Physics and Chemistry of Solids 68, no. 10 (2007): 1830–35. http://dx.doi.org/10.1016/j.jpcs.2007.01.027.

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Hao, Tingting, Xu Wang, Yuchun Zhai, and Yunlong Chang. "Y(III) Ion Migration in AlF3–(Li,Na)F–Y2O3 Molten Salt." Applied Sciences 12, no. 4 (2022): 2200. http://dx.doi.org/10.3390/app12042200.

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In this study, three slots containing an anode chamber, a cathode chamber, and a middle pole chamber were designed by applying the Hittorf method, and a two-way coupling model of the flow field and electric field was established using the COMSOL system. The electric field distribution in the constructed model was simulated, and the model reliability, boundary conditions, and related parameters were verified. A three-chamber tank was utilized to investigate the migration numbers change rule and migration mechanism of Y(III) ions in the AlF3–(Li,Na)F system. The migration number of Y(III) ions i
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Norikawa, Yutaro, and Toshiyuki Nohira. "Electrodeposition of Ti in molten AF–ACl–A3TiF6 (A = Li, Na, K)." ECS Transactions 114, no. 6 (2024): 23–31. http://dx.doi.org/10.1149/11406.0023ecst.

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Electrochemical behaviors of Ti(III) ions and electrodeposition of Ti were investigated in molten AF–ACl–A3TiF6 (A = Li, Na, K) at 973 K. Redox currents corresponding to Ti(III)/Ti(0) and Ti(IV)/Ti(III) reactions were observed by cyclic voltammetry. The redox potentials of the reactions with reference to Cl2/Cl− and F2/F− were most positive for the Li system, followed by the Na system, and most negative for the K system. The differences in the potential can be explained by the interactions of alkali cations and F- ions; smaller cations interact more strongly with F−, resulting in a weaker inte
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Liu, Lili, and Shimou Chen. "Theoretical Study on Cyclopeptides as the Nanocarriers for Li+, Na+, K+and F−, Cl−, Br−." Journal of Nanomaterials 2015 (2015): 1–7. http://dx.doi.org/10.1155/2015/276191.

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The interaction process between a series of cyclopeptide compounds cyclo(Gly)n (n=4,6,8)and monovalent ions (Li+, Na+, K+, F−, Cl−, and Br−) was studied using theoretical calculation. The mechanism of combination between the cyclo(Gly)nand ions was discussed through binding energy, Mulliken electron population, and hydrogen bond. It was found that for the same cyclopeptide the binding energy has the order of cyclo(Gly)n–Li+> cyclo(Gly)n–Na+> cyclo(Gly)n–K+and cyclo(Gly)n–F−> cyclo(Gly)n–Br−> cyclo(Gly)n–Cl−. The binding energy manifests the stable complex of cyclo(Gly)nand ions can
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DalleDonne, Isabella, Aldo Milzani, Umberto Fascio, Antonia Ratti, and Roberto Colombo. "Lithium preserves F-actin from the disarrangement induced by either DNase I or cytochalasin D." Biochemistry and Cell Biology 71, no. 9-10 (1993): 440–46. http://dx.doi.org/10.1139/o93-065.

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Light scattering at 546 nm, which is mainly related to the presence of rodlike particles longer than 50 nm, showed that Li+ accelerates the formation of actin filaments. Intermolecular cross-linking with N,N′-1,4-phenylene-bismaleimide proved that the observed enhancement in the light-scattering intensity is caused by the increase in the concentration of actin oligomers, which gradually elongate to form longer filaments. DNase-I-related F-actin disassembly was reduced in the presence of lithium ions, as demonstrated by fluorimetric and viscometric experiments. Li+–F-actin showed an apparently
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Wang, Yuhu, Akiyoshi Osaka, Yoshinari Miura, and Katsuaki Takahashi. "Effect of halide ions on Li+ ionic conductivity in oxyhalo-borate glasses." Journal of Materials Research 2, no. 5 (1987): 606–9. http://dx.doi.org/10.1557/jmr.1987.0606.

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The electrical conductivity has been measured for the glasses in the system B2O3–Li2O–Li2X2(X = F, Cl, Br), where Li2O is replaced by Li2X2 with Li content kept constant. The conductivity decreases for F glasses and increases for Cl and Br glasses with increasing halide ion content, which is caused by the increase in the activation energy for F glasses and the decrease for Cl and Br glasses. The analysis of the activation energy in terms of the Anderson-Stuart model indicates that, with the increase in LiX, Δ Eb, (the electrostatic energy) increases for F glass, whereas ΔEs (the strain energy)
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Journal, Baghdad Science. "Energy Calculation for Excited Lithium Atom in Position Space." Baghdad Science Journal 12, no. 4 (2015): 808–13. http://dx.doi.org/10.21123/bsj.12.4.808-813.

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The energy expectation values for Li and Li-like ions ( , and ) have been calculated and examined within the ground state and the excited state in position space. The partitioning technique of Hartree-Fock (H-F) has been used for existing wave functions.
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AL-Bayati, Khalil H., and Khalid Omar Al-Baiti. "Energy Calculation for Excited Lithium Atom in Position Space." Baghdad Science Journal 12, no. 4 (2015): 808–13. http://dx.doi.org/10.21123/bsj.2015.12.4.808-813.

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The energy expectation values for Li and Li-like ions ( , and ) have been calculated and examined within the ground state and the excited state in position space. The partitioning technique of Hartree-Fock (H-F) has been used for existing wave functions.
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Galashev, Alexander. "Computational Study of the Physical Properties of a High Temperature Molten Salt Mixture of FLiNaK and CeF3." Applied Sciences 13, no. 2 (2023): 1085. http://dx.doi.org/10.3390/app13021085.

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In this work, we study the diffusion characteristics and structure of the molten salt FLiNaK with dissolved CeF3 in the operating temperature range of the molten-salt reactor. The temperature dependence of the self-diffusion coefficients of the ions that make up the salt mixture is represented with good accuracy as a linear dependence, except for the case of self-diffusion of Ce ions. As a rule, Li and F ions are more mobile than Na and K ions and significantly more so than slow Ce ions. The coordination numbers and their increase upon dissolution of CeF3 in FLiNaK were determined based on the
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PATTANAYAK, SUBRAT KUMAR, and SNEHASIS CHOWDHURI. "SIZE DEPENDENCE OF SOLVATION STRUCTURE AND DYNAMICS OF IONS IN LIQUID N-METHYLACETAMIDE: A MOLECULAR DYNAMICS SIMULATION STUDY." Journal of Theoretical and Computational Chemistry 11, no. 02 (2012): 361–77. http://dx.doi.org/10.1142/s0219633612500241.

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The solvation structure and dynamics of alkali metal (Li+, Na+, K+, Rb+, Cs+) and halide (F-, Cl-, Br-, I-) ions in liquid N -methylacetamide (NMA) are calculated at two different temperatures T = 313 K and 453 K, by using classical molecular dynamics simulations. We have also considered [Formula: see text] and some larger cations such as I +, Me 4 N +, and Et4N+ in this study to investigate the size dependence solvation structure and dynamics of ions in liquid NMA. With the increase of ion size, the self-diffusion coefficients of cations are found to increase and the maximum is observed at Me
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Rozprawy doktorskie na temat "Li+ and F- ions"

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Yeung, Vincent Hon Kuen. "Latest RF Li-ions battery charger and its applications." access abstract and table of contents access full-text, 2004. http://libweb.cityu.edu.hk/cgi-bin/ezdb/dissert.pl?msc-ap-b21175299a.pdf.

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Thesis (M.Sc.)--City University of Hong Kong, 2004.<br>At head of title: City University of Hong Kong, Department of Physics and Materials Science, Master of Science in materials engineering & nanotechnology dissertation. Title from title screen (viewed on Sept. 4, 2006) Includes bibliographical references.
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Kerns, John William. "Quadrupole moment effects in Li elastic scattering /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487263399024843.

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Epp, Viktor, Özgül Gün, Hans-Jörg Deiseroth, and Martin Wilkening. "Extreme mobility: low-temperature NMR probes highly diffusive Li+ ions in argyrodite-type Li 6 PSe 5 Cl and Li 6 PS 5 Br." Diffusion fundamentals 20 (2013) 85, S. 1-2, 2013. https://ul.qucosa.de/id/qucosa%3A13672.

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Pattee, Dorothée. "Les Acides dialkyldithiophosphoriques propriétés, extraction des ions 4 f et 5 f /." Grenoble 2 : ANRT, 1986. http://catalogue.bnf.fr/ark:/12148/cb376002556.

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Wang, Ying. "Enhanced Li-ion intercalation properties of vanadium oxides /." Thesis, Connect to this title online; UW restricted, 2006. http://hdl.handle.net/1773/10561.

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Li, Chunmei. "Study of rechargeable aprotic Li-O2 batteries." Amiens, 2014. http://www.theses.fr/2014AMIE0111.

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Est-il possible d'augmenter la densité d'énergie des batteries au lithium pour apporter l'autonomie souhaitée pour les applications véhicules électriques, voire réseaux? Une note d'espoir peut effectivement provenir des systèmes métaux-air et plus spécialement du Lithium-air qui suscite aujourd'hui l'engouement des fabricants d'automobiles. Sur la base de calculs théoriques, la technologie Li-air pourrait fournir des densités d'énergie de 3500 Wh kg(-1), soit environ 15 fois plus que celles des accumulateurs à ions lithium. Cependant, pour rendre de tels systèmes opérationnels, de nombreux ver
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Kone, Joël-Louis. "Modélisation et suivi du vieillissement d’accumulateurs Li-ions par couplage avec modèle Dual-tank." Thesis, Université Grenoble Alpes, 2021. http://www.theses.fr/2021GRALI003.

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Les modèles de batterie utilisés dans les études systèmes sont généralement basés sur des modèles électriques à un seul réservoir (« one tank »), auxquels sont couplés des modèles de vieillissement semi-empiriques prédisant l’évolution de la capacité de ce réservoir.Dans ces modèles, l’état de santé d’une cellule est donc représenté par une seule valeur, ce qui est trop limitant. Par ailleurs, ces approches permettent difficilement d’appréhender les phénomènes de ruptures de pentes observés expérimentalement.Dans cette thèse, des modèles de vieillissement empiriques ou inspirés de la physique
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Saint, Juliette. "Matériaux d'électrode négative pour accumulateurs à ions lithium : étude des systèmes binaires Li-Ga et Li-B et des composites silicium-carbone." Amiens, 2005. http://www.theses.fr/2005AMIE0530.

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La mise au point d’un matériau d’électrode négative pour accumulateurs au lithium pouvant supplanter le graphite, en vue de nouvelles applications comme le véhicule électrique, génère un nombre croissant d’études de par le monde. Parmi les prétendants, les alliages à base de lithium (LixMy) sont les plus prometteurs et de nombreuses voies sont à explorer. Les alliages LixSiy présentent la plus forte capacité électrochimique (4200 mAh/g; plus de dix fois celle du graphite) mais leur très mauvaise réversibilité empêche leur utilisation. Pour pallier ce problème, différentes approches ont été dév
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Chable, Johann. "Électrolytes solides fluorés pour batteries tout solide à ions F-." Thesis, Bordeaux, 2015. http://www.theses.fr/2015BORD0276/document.

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Ce travail porte sur la synthèse, la mise en forme et la caractérisation desolutions solides de type tysonite RE1-xMxF3-x (RE = La, Sm, Ce et M = Ba, Ca, Sr). Dans unpremier temps, une démarche d’étude rigoureuse est mise en place pour la solution solide ditede référence, La1-xBaxF3-x. Les synthèses menées à l’état solide aboutissent à une maîtrise dela composition chimique et à l'établissement de lois de variations des paramètres structuraux.Une meilleure compréhension de l’influence de la structure sur la mobilité des ions F- estégalement acquise. L’influence du frittage dans l’obtention de
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Giesecke, Marianne. "Characterizing ions in solution by NMR methods." Doctoral thesis, KTH, Tillämpad fysikalisk kemi, 2014. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-149552.

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NMR experiments performed under the effect of electric fields, either continuous or pulsed, can provide quantitative parameters related to ion association and ion transport in solution.  Electrophoretic NMR (eNMR) is based on a diffusion pulse-sequence with electric fields applied in the form of pulses. Magnetic field gradients enable the measurement of the electrophoretic mobility of charged species, a parameter that can be related to ionic association. The effective charge of the tetramethylammonium cation ion in water, dimethylsulphoxide (DMSO), acetonitrile, methanol and ethanol was estima
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Książki na temat "Li+ and F- ions"

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Dar-El, E. Hagbarat ha-piryon be-m. u-f.: Sikum sadna li-menahale m. u-f. ha-Ṭekhniyon, Mosad Shemuʼel Neʼeman, 1992.

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Barnett, C. F. Collision of H, H2, He and Li atoms and ions with atoms and molecules. Controlled Fusion Atomic Data Center, Oak Ridge National Laboratory, 1990.

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Kuriata, Jerzy. Rozszczepienie zeropolowe jonów ⁸S₇/₂(4f⁷) w polu krystalicznym niskiej symetrii i ich oddziaływania nadsubtelne z ligandami ¹⁹F. Wydawn. Uczelniane Politechniki Szczecińskiej, 1990.

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1933-, Seginer Ido, Israel. Miśrad ha-energyah ṿeha-tashtit. Agaf meḥḳar u-fituaḥ. та Minhal ha-meḥḳar ha-ḥaḳlaʼi, ред. M. u-f. energyah ba-ḥaḳlaʼut: Duaḥ li-shenat 1992. Faḳulṭah le-handasah ḥaḳlaʼit, Ṭekhniyon, 1993.

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1933-, Seginer Ido, Israel. Miśrad ha-energyah ṿeha-tashtit. Agaf meḥḳar u-fituaḥ. та Minhal ha-meḥḳar ha-ḥaḳlaʼi, ред. M. u-f. energyah ba-ḥaḳlaʼut: Duaḥ li-shenat 1993. Faḳulṭah le-handasah ḥaḳlaʼit, Ṭekhniyon, 1994.

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ping, Guo ji. Jing ji f an li yu kao shi yao dian. Shang hai ren min chu ban she, 1989.

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Dr, Segal Y., Israel. Miśrad ha-energyah ṿeha-tashtit. Agaf meḥḳar u-fituaḥ. та Minhal ha-meḥḳar ha-ḥaḳlaʼi (Israel), ред. M. u-f. energyah ba-ḥaḳlaʼut: Duaḥ li-shenat 1989-90. Miśrad ha-energyah ṿeha-tashtit, 1990.

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G, Felsenshtein, Israel. Miśrad ha-energyah ṿeha-tashtit. Agaf meḥḳar u-fituaḥ. та Minhal ha-meḥḳar ha-ḥaḳlaʼi, ред. M. u-f. energyah ba-ḥaḳlaʼut: Duaḥ li-shenat 1990-91. ha-Makhon le-handasah ḥaḳlaʼit, 1991.

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Drucker, Peter F. Guan li de shi jian: The practice of management / Peter F. Drucker. Ji xie gong ye chu ban she, 2006.

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Conference on d and f Electrons Systems (3rd 1990 Zakopane, Poland). Proceedings of the 3rd Conference on d and f Electrons Systems, Zakopane, 4-8 October 1990. Nakł. Uniwersytetu Jagiellońskiego, 1990.

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Części książek na temat "Li+ and F- ions"

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Holze, Rudolf. "Transport numbers of ions in Li based ionic liquids." In Electrochemistry. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-642-02723-9_1725.

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Kalaiselvam, S., Kanthan Bharathi A. Lakshmi, Jacquline B. Mercy, Kumar U. Harish, and M. Bhuvanesh. "Bioleaching of Lithium Ions from Li-Ion Battery Waste." In Advanced Bioseparation of Industrial Wastes. CRC Press, 2024. https://doi.org/10.1201/9781003415541-4.

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Tanis, J. A., and N. Stolterfoht. "Ionization and Excitation of Atomic Li by Fast Ions." In The Physics of Multiply and Highly Charged Ions. Springer Netherlands, 2003. http://dx.doi.org/10.1007/978-94-017-0544-8_11.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Li-7 (Lithium)." In Supplement to I/25 A-F. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48875-1_10.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Li-8 (Lithium)." In Supplement to I/25 A-F. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48875-1_11.

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Sukhoruchkin, S. I., and Z. N. Soroko. "Excited Nuclear States for Li-11 (Lithium)." In Supplement to I/25 A-F. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-48875-1_12.

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Reeder, P. L., R. A. Warner, W. K. Hensley, D. J. Vieira, and J. M. Wouters. "Delayed-Neutron Emission Probabilities of Li-F Nuclides." In Exotic Nuclear Spectroscopy. Springer US, 1990. http://dx.doi.org/10.1007/978-1-4615-3684-0_35.

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Feng, Chuan Qi, Keli Zhang, and Jutang Sun. "Synthesis and Electrochemical Properties of Nonstoichiometric Spinel Phase (Li1.02Mn1.90Y0.02O4-yF0.08) for Lithium Ion Battery." In Materials Science Forum. Trans Tech Publications Ltd., 2005. http://dx.doi.org/10.4028/0-87849-960-1.1809.

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Boehly, T., D. McCoy, M. Russotto, J. Wang, and B. Yaakobi. "Observation of Gain on XUV Transitions in Ne-Like and Li-Like Ions." In Laser Interaction and Related Plasma Phenomena. Springer US, 1991. http://dx.doi.org/10.1007/978-1-4615-3804-2_12.

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Edelstein, Norman. "Electronic Structure and Optical Spectroscopy of fn Ions and Compounds." In Fundamental and Technological Aspects of Organo-f-Element Chemistry. Springer Netherlands, 1985. http://dx.doi.org/10.1007/978-94-009-5406-9_7.

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Streszczenia konferencji na temat "Li+ and F- ions"

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Duffy, Michael, and Tony Samaritano. "The LIFT! Project - Modular, Electric Vertical Lift System." In Vertical Flight Society 71st Annual Forum & Technology Display. The Vertical Flight Society, 2015. http://dx.doi.org/10.4050/f-0071-2015-10502.

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The LIFT! Project explored scaling of all-electric multi-rotor propulsion and methods of cooperation between multiple VTOL aircraft. Multi-rotor aircraft have become pervasive throughout the hobby industry, toy industry and research institutions due - in part - to very powerful, inexpensive inertial measurement devices and increased energy density of Li-Ion batteries driven by the mobile phone industry. This research demonstrates the viability of large multi-rotor systems up to two magnitudes of gross weight larger than a typical COTS hobby multi-rotor vehicle. Furthermore, this research demon
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Carranza, Ricardo M., Martín A. Rodríguez, and Raúl B. Rebak. "Inhibition of Chloride Induced Crevice Corrosion in Alloy 22 by Fluoride Ions." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06626.

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Abstract Alloy 22 (N06022) is highly resistant to localized corrosion. Alloy 22 may be susceptible to crevice corrosion in pure chloride (Cl-) solutions under aggressive environmental conditions. The effect of the fluoride (F-) over the crevice corrosion induced by chloride ions is still not well established. The objective of the present work was to explore the crevice corrosion resistance of this alloy to different mixtures of fluorides and chlorides. Cyclic potentiodynamic polarization (CPP) tests were conducted in deaerated aqueous solutions of pure halide ions and also in different mixture
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Ghanbari, Elmira, Alireza Saatchi, Danyil Kovalov, Bruno Kursten, and Digby D. Macdonald. "The Influence of Halide Ions on the Passivity Breakdown of Carbon Steel Based on the Point Defect Model." In CORROSION 2018. NACE International, 2018. https://doi.org/10.5006/c2018-11025.

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Abstract An important factor in determining the breakdown of the barrier layer of the passive film on carbon steel in halide-containing solutions is the anion size. In this study, the influence of the size of aggressive anions on the passivity breakdown of UNS K02700 grade carbon steel exposed to saturated Ca(OH)2 solutions with the addition of different halides was investigated by using the potentiodynamic polarization (PDP) experiments. The PDP results were interpreted by using a mechanistic description based on the Point Defect Model (PDM). The experimental results revealed a linear depende
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Economy, G., and F. W. Pement. "Temperature Effects on Alloy 600 PWSCC from 310 to 330 C (590 to 626 F)." In CORROSION 1989. NACE International, 1989. https://doi.org/10.5006/c1989-89493.

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Abstract The initiation time for primary water stress corrosion cracking (PWSCC) of mill annealed Alloy 600 tubing was studied in simulated pressurized water reactor (PWR) coolant environments at steam generator hot-leg inlet temperatures of 310, 320, and 330 C (590, 608, and 626 F). The coolant chemistry, common to all three temperature conditions, consisted of 2.0 ppm Li (as LiOH), 1200 ppm B (as H3BO3), and 50 cc H2 (STP)/kg H2O. A second test at 310 C (590 F) used 32 cc H2 (STP)/kg H2O to match the hydrogen fugacity of 50 cc H2 (STP)/kg H2O at 330 C (626 F). A comparative test in 400 C (75
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Crolet, Jean-Louis, and Tong E. Pou. "Identification of a Critical Pitting Potential for film-Forming Inhibitors, Using Classical and New Electrochemical Techniques." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95039.

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Abstract In facilities operating in a sour environment, oxygen ingress converts the H2S to thiosulfate ions, whose oxidizing effect can induce pitting attack in the presence of certain corrosion inhibitors. The present paper shows that this process involves a slight increase in the corrosion potential, associated with the existence of a critical pitting potential. The critical potential has been identified either with the aid of "pseudo-polarization" curves, corresponding to the locus of the free corrosion point, Ucorr(t) = f(log icorr(t)), in the presence of thiosulfate but without applied po
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Grubb, John F. "Comparison of Laboratory Pitting and Crevice Corrosion Tests of Stainless Steels and Estimates of Expected Performance." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01251.

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Abstract Stainless steels resist corrosion through formation of an oxygen-rich passive film. Halide ions damage this film and promote localized attack. Chloride ions are the most prevalent halide ions in our environment and are involved in many stainless steel corrosion failures. Failures typically are manifested as pitting or crevice corrosion. Several laboratory tests are used to measure resistance to these modes of attack. Among the commonly-used tests are the ASTM(1) G1501 Electrochemical Critical Pitting Temperature (CPT) test, the ASTM G482 Practices A, C, and E CPT tests, the ASTM G48 P
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Chiang, K. T., D. S. Dunn, and G. A. Cragnolino. "The Combined Effect of Bicarbonate and Chloride Ions on the Stress Corrosion Cracking Susceptibility of Alloy 22." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06506.

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Abstract The potential engineering barriers for the permanent disposal of high-level waste at the Yucca Mountain site include an Alloy 22 outer container. One of the anticipated degradation modes for the container is stress corrosion cracking of Alloy 22. Slow strain rate tests were performed to evaluate the combined effect of bicarbonate and chloride ions on the stress corrosion cracking susceptibility of mill-annealed Alloy 22. Tests were conducted in which the solution chemistry, electrochemical potentials, and solution temperatures were varied. Stress corrosion cracking was observed in sim
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Shao, Linato, Auhuan Xie, Jiandong Cai, Yunzheng Zhu, and Shiqiang Zhu. "The Battery Cooling Design and Simulation Study in Multirotor eVTOL Aircraft." In Vertical Flight Society 79th Annual Forum & Technology Display. The Vertical Flight Society, 2023. http://dx.doi.org/10.4050/f-0079-2023-18051.

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High-specific energy Li-ion batteries are widely used in eVTOL aircraft and usually rapidly heat up during flight. Therefore, proper and efficient cooling strategies should be adopted during eVTOL design in order to prevent overheating. This paper collected and compared the battery cooling strategies adopted by different eVTOL aircraft manufacturers based on published patents. The choice of battery cooling strategies could be influenced by aircraft configurations. The ZJCopter eVTOL aircraft developed by Zhejiang Lab adopted the PCM cooling method as a fast-cooling and lightweight battery cool
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Wada, M., H. Tsuda, and M. Sasao. "Compact Li− ion source for plasma diagnostics." In Production and neutralization of negative ions and beams. AIP, 1992. http://dx.doi.org/10.1063/1.44763.

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Chatterjee, A., and A. Ghosh. "Dynamics of Li+ ions in Li2O-TeO2-P2O5 glasses." In DAE SOLID STATE PHYSICS SYMPOSIUM 2017. Author(s), 2018. http://dx.doi.org/10.1063/1.5028828.

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Raporty organizacyjne na temat "Li+ and F- ions"

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Grice, M. E., and Peter Politzer. Computational Investigation of the Stabilities of Some N, O, F Ions. Defense Technical Information Center, 1995. http://dx.doi.org/10.21236/ada292305.

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Alnesafi, Lateef. Lithium-ion Batteries; The Intercalation of Lithium Ions and the Plating Phenomenon in Li-ion Batteries. Iowa State University, 2024. https://doi.org/10.31274/cc-20250502-3.

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Zhang, Hong, D. Sampson, and C. Fontes. Relativistic distorted wave collision strengths and oscillator strengths for the 85 Li-like ions with 8 le Z le 92. Office of Scientific and Technical Information (OSTI), 1989. http://dx.doi.org/10.2172/5474113.

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Fernando, P. U. Ashvin Iresh, Gilbert Kosgei, Matthew Glasscott, Garrett George, Erik Alberts, and Lee Moores. Boronic acid functionalized ferrocene derivatives towards fluoride sensing. Engineer Research and Development Center (U.S.), 2022. http://dx.doi.org/10.21079/11681/44762.

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In this technical report (TR), a robust, readily synthesized molecule with a ferrocene core appended with one or two boronic acid moieties was designed, synthesized, and used toward F- (free fluoride) detection. Through Lewis acid-base interactions, the boronic acid derivatives are capable of binding with F- in an aqueous solution via ligand exchange reaction and is specific to fluoride ion. Fluoride binding to ferrocene causes significant changes in fluorescence or electrochemical responses that can be monitored with field-portable instrumentation at concentrations below the WHO recommended l
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Scavuzzo, Sebastian, Jonathan Cedeño, and Jaroslava Miksovska. In Silico Calculation of Interhelical Angles in NCS1. Florida International University, 2025. https://doi.org/10.25148/fiuurj.3.1.16.

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Proteins are important macromolecules responsible for a variety of processes in living organisms. One of the most important features of proteins is their ability to respond to environmental stimuli, such as changes in intracellular metal concentration by binding metal ions, which in turns triggers structural changes within the protein that can modify its function or allow the protein to participate in a signaling pathway. One such signaling protein is the so-called neuronal calcium sensor 1 protein or NCS1, which binds Ca2+ along with other abiogenic metals such as Li+, and the metal binding r
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