Academic literature on the topic 'Room temperature sodium battery'

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Journal articles on the topic "Room temperature sodium battery"

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Liu, Wen, Hong Li, Jing-Ying Xie, and Zheng-Wen Fu. "Rechargeable Room-Temperature CFx-Sodium Battery." ACS Applied Materials & Interfaces 6, no. 4 (2014): 2209–12. http://dx.doi.org/10.1021/am4051348.

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Park, Cheol-Wan, Jou-Hyeon Ahn, Ho-Suk Ryu, Ki-Won Kim, and Hyo-Jun Ahn. "Room-Temperature Solid-State Sodium∕Sulfur Battery." Electrochemical and Solid-State Letters 9, no. 3 (2006): A123. http://dx.doi.org/10.1149/1.2164607.

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Hartmann, Pascal, Conrad L. Bender, Miloš Vračar, et al. "A rechargeable room-temperature sodium superoxide (NaO2) battery." Nature Materials 12, no. 3 (2012): 228–32. http://dx.doi.org/10.1038/nmat3486.

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Xin, Sen, Ya-Xia Yin, Yu-Guo Guo, and Li-Jun Wan. "A High-Energy Room-Temperature Sodium-Sulfur Battery." Advanced Materials 26, no. 8 (2013): 1261–65. http://dx.doi.org/10.1002/adma.201304126.

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McCormick, Colin. "Energy Focus: Rechargeable room-temperature sodium-air battery involves sodium superoxide." MRS Bulletin 38, no. 2 (2013): 119. http://dx.doi.org/10.1557/mrs.2013.30.

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Kim, T. B., J. W. Choi, H. S. Ryu, et al. "Electrochemical properties of sodium/pyrite battery at room temperature." Journal of Power Sources 174, no. 2 (2007): 1275–78. http://dx.doi.org/10.1016/j.jpowsour.2007.06.093.

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Feng, Jinkui, Zhen Zhang, Lifei Li, Jian Yang, Shenglin Xiong, and Yitai Qian. "Ether-based nonflammable electrolyte for room temperature sodium battery." Journal of Power Sources 284 (June 2015): 222–26. http://dx.doi.org/10.1016/j.jpowsour.2015.03.038.

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Brutti, S., M. A. Navarra, G. Maresca, et al. "Ionic liquid electrolytes for room temperature sodium battery systems." Electrochimica Acta 306 (May 2019): 317–26. http://dx.doi.org/10.1016/j.electacta.2019.03.139.

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Wang, Yanjie, Yingjie Zhang, Hongyu Cheng, et al. "Research Progress toward Room Temperature Sodium Sulfur Batteries: A Review." Molecules 26, no. 6 (2021): 1535. http://dx.doi.org/10.3390/molecules26061535.

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Lithium metal batteries have achieved large-scale application, but still have limitations such as poor safety performance and high cost, and limited lithium resources limit the production of lithium batteries. The construction of these devices is also hampered by limited lithium supplies. Therefore, it is particularly important to find alternative metals for lithium replacement. Sodium has the properties of rich in content, low cost and ability to provide high voltage, which makes it an ideal substitute for lithium. Sulfur-based materials have attributes of high energy density, high theoretica
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Kim, Icpyo, Chang Hyeon Kim, Sun hwa Choi, et al. "A singular flexible cathode for room temperature sodium/sulfur battery." Journal of Power Sources 307 (March 2016): 31–37. http://dx.doi.org/10.1016/j.jpowsour.2015.12.035.

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Dissertations / Theses on the topic "Room temperature sodium battery"

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Martine, Milena. "Na-Sb-Sn-based negative electrode materials for room temperature sodium cells for stationary applications." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-226494.

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The implementation of energy storage systems in the current electrical grid will increase the grid's reliability and e ciency. Room temperature sodium batteries are seen as potential technology, especially to assist renewable energy generation sources. Currently, suggested negative electrode materials, however, are still not satisfactory for practical use in terms of fabrication costs, gravimetric /volumetric energy densities, cyclability, and irreversible capacity losses occur at the rst cycle. The literature describes various strategies that enhance the specific capacity and/or the cyclabili
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Gray, Gary E. "Stability of sodium electrodeposited from a series of room temperature chloroaluminate molten salts." Diss., Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/11107.

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YANG, HUAN. "Functional Electrolytes for Advanced Electrochemical Performance in Sodium and Potassium Secondary Batteries." Kyoto University, 2020. http://hdl.handle.net/2433/259756.

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Li, Si. "HIGHLY CONDUCTIVE SOLID POLYMER ELECTROLYTE CONTAINING LiBOB AT ROOM TEMPERATURE FOR ALL SOLID STATE BATTERY." University of Akron / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=akron1490481514905008.

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Martinsson, Patrik. "State of Charge Estimation in a High Temperature Sodium Nickel Chloride Battery Using Kalman Filter." Thesis, Linköping University, Department of Electrical Engineering, 2008. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-11173.

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<p>In today’s heavy industry there are applications demanding high power supply in certain periods of a working cycle. A typical case might be startup of heavy machinery or just keeping a certain point in a distribution network at a certain energy level. To deal with this different techniques might be used, one way is to introduce a battery as an energy reserve in the system. One battery studied at ABB for this purpose is the so called High Temperature Sodium Nickel Chloride battery and a model of this battery has been developed at ABB. When operating a battery of the mentioned type in an appli
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Lodge, Andrew. "The electrochemical reduction of oxygen in room temperature ionic liquids for use in a lithium-air battery." Thesis, University of Southampton, 2015. https://eprints.soton.ac.uk/380892/.

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Experiments were undertaken to investigate the electrochemical reduction of oxygen (O2) in various room temperature ionic liquids (RTILs) with the aim of using a RTIL as an electrolyte in a lithium-air battery cell. Cyclic voltammetry (CV) in oxygenated RTILs was undertaken at Au and Pt microdisc electrodes. It was confirmed that the reduction of O2 in pyrrolidinium based RTILs occurs in two one-electron reduction steps, from O2 to superoxide (O2•−) and from O2•− to peroxide (O22−). It was found that the reduction of O2 was fully reversible in pyrrolidinium based ionic liquids. It was found th
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Yang, Run. "A Superionic Conductive Solid Polymer Electrolyte Based Solid Sodium Metal Batteries with Stable Cycling Performance at Room Temperature." University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1619741453185762.

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SHUBHAM, KAUSHIK. "A Study on Phosphides-based Negative Electrode Materials for Sodium Secondary Batteries Using Ionic Liquid Electrolytes." Kyoto University, 2020. http://hdl.handle.net/2433/259063.

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Fischer, Pauline Josephine [Verfasser], Fritz E. [Akademischer Betreuer] Kühn, Fritz E. [Gutachter] Kühn, and Tom [Gutachter] Nilges. "Room Temperature Ionic Liquids as Electrolytes for Sodium Ion Batteries / Pauline Josephine Fischer ; Gutachter: Fritz E. Kühn, Tom Nilges ; Betreuer: Fritz E. Kühn." München : Universitätsbibliothek der TU München, 2019. http://d-nb.info/1189815613/34.

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Pye, Stephen L. "The electrochemical behavior of iron, copper, and nickel electrodes in sodium chloride buffered, neutral room temperature aluminum chloride : 1-methyl-3-ethylimidazolium chloride molten salt." Thesis, Georgia Institute of Technology, 1996. http://hdl.handle.net/1853/11126.

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Books on the topic "Room temperature sodium battery"

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Pitt, Matthew. Investigation of channelopathies. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198754596.003.0008.

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The chapter begins with a general description of the clinical findings in conditions where hyperexcitability occurs. These are divided into the dystrophic conditions, such as myotonia dystrophy, and the non-dystrophic conditions, which include myotonia congenita, paramyotonia congenita, and potassium-aggravated myotonia. Conditions where hypoexcitability occurs such as periodic paralysis are next discussed. The associated disorders of sodium, calcium, chloride, and potassium channels are described. Next, the protocols for the neurophysiological tests that are used in myotonia, and the short ex
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Book chapters on the topic "Room temperature sodium battery"

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Wagner, D., A. Rost, J. Schilm, M. Fritsch, M. Kusnezoff, and A. Michaelis. "Glass Ceramic Separators for Room Temperature Operating Sodium Batteries." In Ceramic Materials for Energy Applications V. John Wiley & Sons, Inc., 2015. http://dx.doi.org/10.1002/9781119211709.ch6.

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Choudhury, Snehashis. "A Highly Reversible Room-Temperature Lithium Metal Battery Based on Cross-Linked Hairy Nanoparticles." In Springer Theses. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-030-28943-0_3.

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Cheng, Reynold, and Sunil Prabhakar. "Sensors, Uncertainty Models, and Probabilistic Queries." In Encyclopedia of Database Technologies and Applications. IGI Global, 2005. http://dx.doi.org/10.4018/978-1-59140-560-3.ch101.

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Sensors are often used to monitor the status of an environment continuously. The sensor readings are reported to the application for making decisions and answering user queries. For example, a fire alarm system in a building employs temperature sensors to detect any abrupt change in temperature. An aircraft is equipped with sensors to track wind speed, and radars are used to report the aircraft’s location to a military application. These applications usually include a database or server to which the sensor readings are sent. Limited network bandwidth and battery power imply that it is often not practical for the server to record the exact status of an entity it monitors at every time instant. In particular, if the value of an entity (e.g., temperature, location) monitored is constantly evolving, the recorded data value may differ from the actual value. Querying the database can then produce incorrect results. Consider a simple example where a user asks the database: “Which room has a temperature between 10oF and 20oF?” If we represent temperature values of rooms A and B stored in the database by A0 and B0 respectively, we can see from Figure 1(a) that the answer to the user query is “Room B”. In reality, the temperature values of both rooms may have changed to newer values, A1 and B1, as shown in Figure 1(b), where the true query answer should be “Room A”. Unfortunately, because of transmission delay, these newest pieces of information are not propagated in time to the system to supply fresh data to the query, and consequently the query is unable to yield a correct answer.
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"Technology of Heat and Moisture Regeneration for Ventilation Systems." In Technology Development for Adsorptive Heat Energy Converters. IGI Global, 2021. http://dx.doi.org/10.4018/978-1-7998-4432-7.ch006.

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The chapter is focused on technology of heat and moisture regeneration for ventilation systems. In the first sub-division recent progress in adsorptive technologies for air dehumidification, heating and conditioning is analyzed. In the next sub-divisions results of original researches of authors on adsorptive heat and moisture regeneration are given. The design of adsorptive heat-moisture regenerator for ventilation systems is shown. Its operation and the results of field tests are described. The technology of regeneration of low-potential heat and moisture by composite sorbent ‘silica gel – sodium sulphate' is suggested. Experimental plots of temperature, absolute and relative humidity at the inlet and the outlet of the apparatus and between cassettes with the composite are given. Correlation of flows switch-over time, airflow rate and temperature drop is stated. The relationships temperature efficiency factor vs. dimensionless temperature drop and moisture efficiency factor vs. absolute humidity dimensionless drop are derived with fair accuracy for engineering calculation. Ability of purposeful modification of the above-mentioned characteristics within broad ranges by changing the half-cycle time, the size of the granules of the adsorbent and its amount is revealed. The mathematical model and algorithm for determining the basic parameters of adsorptive regenerator operating processes are developed. The proposed algorithm involves calculating the volume of air passed through the layer of adsorptive heat-storage material, the concentration of water in the airflow at the outlet of the regenerator, the adsorption, the heat of adsorption, the final temperature of the cold air, the air temperature after mixing the cold air from the street and the warm air in the room at the warm end of the regenerator during inflow, calculation of the final concentration of water in the flow at the cold end of the regenerator, the volume of air passing through the layer of heat-accumulating material, adsorption and heat of adsorption, the final temperature of the air at the cold end of the regenerator, the air temperature after mixing of the cold air from the street and the warm air from the room at the cold end of regenerator during outflow, determining the temperature efficiency coefficient, summarized adsorption and maximal adsorption time. The correlation of air temperatures near the warm and cold end of the regenerator, as well as the temperature efficiency factors calculated according to the proposed algorithm and obtained by experimental way is confirmed. The mathematical modeling of the processes of operation of adsorption regenerators based on composites ‘silica gel – sodium sulphate' and ‘sodium acetate' in the conditions of the typical ventilation system of residential premises is carried out. The dependences of the temperature efficiency factor vs. the time of switching air flows and the velocity of air flow, as well as the temperatures of external and internal air under stationary conditions are shown. An optimal composition of composite adsorbents is stated to be 20% of silica gel and 80% of salt, that is, sodium sulphate or sodium acetate. Due to higher value of maximal adsorption composite ‘silica gel – Na2SO4' is shown to be required in half as much as compared with ‘silica gel – CH3COONa'. The results of the research can be used in the development of energy-efficient ventilation systems and devices for residential and warehouse premises.
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Li, Jie Jack, Chris Limberakis, and Derek A. Pflum. "Reductions." In Modern Organic Synthesis in the Laboratory. Oxford University Press, 2008. http://dx.doi.org/10.1093/oso/9780195187984.003.0010.

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The Barton deoxygenation (or Barton–McCombie deoxygenation) is a two-step reaction sequence for the reduction of an alcohol to an alkane. The alcohol is first converted to a methyl xanthate or thioimidazoyl carbamate. Then, the xanthate or thioimidazoyl carbamate is reduced with a tin hydride reagent under radical conditions to afford the alkane. Trialkylsilanes have also been used as the hydride source. Reviews: (a) McCombie, S. W. In Comprehensive Organic Synthesis; Trost, B. M.; Fleming, I., Eds.; Pergamon Press: Oxford, U. K., 1991; Vol. 8, Chapter 4.2: Reduction of Saturated Alcohols and Amines to Alkanes, pp. 818–824. (b) Crich, D.; Quintero, L. Chem. Rev. 1989, 89, 1413–1432. To a solution of the â-hydroxy-N-methyl-O-methylamide (0.272 g, 1.55 mol) in tetrahydrofuran (THF) (30 mL) were added carbon disulfide (6.75 mL, 112 mmol) and iodomethane (6.70 mL, 108 mmol) at 0 °C. The mixture was stirred at this temperature for 0.25 h, and then sodium hydride (60% suspension in mineral, 136.3 mg, 3.4 mmol) was added. After 20 min at 0 °C, the reaction was quenched by slow addition to 60 g of crushed ice. (Caution: hydrogen gas evolution!). The mixture was raised to room temperature and separated, and the aqueous layer was extracted with CH2Cl2 (4 × 15 mL). The combined organic extracts were dried (Na2SO4&lt;/aub&gt;), concentrated in vacuo, and purified (SiO2, 5% EtOAc in hexanes) to afford 0.354 g (86%) of the xanthate. To a solution of the xanthate (2.95 g, 11.1 mmol) in toluene (100 mL) was added tributyltin hydride (15.2 mL, 56.6 mmol) and 2,2´-azobisisobutyronitrile (AIBN, 0.109 g, 0.664 mmol). The reaction mixture was then heated to reflux for 1 h. The mixture was cooled, concentrated in vacuo, and purified (SiO2, 100% hexanes to remove tin byproducts, followed by 10% EtOAc in hexanes to elute product) to afford 1.69 g (96%) of the N-methyl-O-methylamide.
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Lambert, Tristan H. "Functional Group Interconversion." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0004.

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Chaozhong Li of the Shanghai Institute of Organic Chemistry reported (J. Am. Chem. Soc. 2012, 134, 10401) the silver nitrate catalyzed decarboxylative fluorination of carboxylic acids, which shows interesting chemoselectivity in substrates such as 1. A related decarboxylative chlorination was also reported by Li (J. Am. Chem. Soc. 2012, 134, 4258). Masahito Ochiai at the University of Tokushima has developed (Chem. Commun. 2012, 48, 982) an iodobenzene-catalyzed Hofmann rearrangement (e.g., 3 to 4) that proceeds via hypervalent iodine intermediates. The dehydrating agent T3P (propylphosphonic anhydride), an increasingly popular reagent for acylation chemistry, has been used (Tetrahedron Lett. 2012, 53, 1406) by Vommina Sureshbabu at Bangalore University to convert amino or peptide acids such as 5 to the corresponding thioacids with sodium sulfide. Jianqing Li and co-workers at Bristol-Myers Squibb have shown (Org. Lett. 2012, 14, 214) that trimethylaluminum, which has long been known to effect the direct amidation of esters, can also achieve the direct coupling of acids and amines, such as in the preparation of amide 8. The propensity of severely hindered 2,2,6,6-tetramethylpiperidine (TMP) amides such as 9 to undergo solvolysis at room temperature has been shown (Angew. Chem. Int. Ed. 2012, 51, 548) by Guy Lloyd-Jones and Kevin Booker-Milburn at the University of Bristol. The reaction proceeds by way of the ketene and is enabled by sterically induced destabilization of the usual conformation that allows conjugation of the nitrogen lone pair with the carbonyl. Matthias Beller at Universität Rostock has found (Angew. Chem. Int. Ed. 2012, 51, 3905) that primary amides may be transamidated via copper(II) catalysis. The conditions are mild enough that an epimerization-prone amide such as 11 undergoes no observable racemization during conversion to amide 13. A photochemical transamidation has been achieved (Chem. Sci. 2012, 3, 405) by Christian Bochet at the University of Fribourg that utilizes 385-nm light to activate a dinitroindoline amide in the presence of amines such as 15, which produces the amide 16. Notably, photochemical cleavage of the Ddz protecting group occurs at a shorter wavelength of 300 nm.
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Taber, Douglass F. "Substituted Benzenes: The Subba Reddy Synthesis of 7-Desmethoxyfusarentin." In Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0064.

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Andrey P. A ntonchick of the Max-Planck-Institut Dortmund devised (Org. Lett. 2012, 14, 5518) a protocol for the direct amination of an arene 1 to give the amide 3. Douglass A. Klumpp of Northern University showed (Tetrahedron Lett. 2012, 53, 4779) that under strong acid conditions, an arene 4 could be carboxylated to give the amide 6. Eiji Tayama of Niigata University coupled (Tetrahedron Lett. 2012, 53, 5159) an arene 7 with the α-diazo ester 8 to give 9. Guy C. Lloyd-Jones and Christopher A. Russell of the University of Bristol activated (Science 2012, 337, 1644) the aryl silane 11 to give an intermediate that coupled with the arene 10 to give 12. Ram A. Vishwakarma and Sandip P. Bharate of the Indian Institute of Integrative Medicine effected (Tetrahedron Lett. 2012, 53, 5958) ipso nitration of an areneboronic acid 13 to give 14. Stephen L. Buchwald of MIT coupled (J. Am. Chem. Soc. 2012, 134, 11132) sodium isocyanate with the aryl chloride 15 (aryl triflates also worked well) to give the isocyanate 16, which could be coupled with phenol to give the carbamate or carried onto the unsymmetrical urea. Zhengwu Shen of the Shanghai University of Traditional Chinese Medicine used (Org. Lett. 2012, 14, 3644) ethyl cyanoacetate 18 as the donor for the conversion of the aryl bromide 17 to the nitrile 19. Kuo Chu Hwang of the National Tsig Hua University showed (Adv. Synth. Catal. 2012, 354, 3421) that under the stimulation of blue LED light the Castro-Stephens coupling of 20 with 21 proceeded efficiently at room temperature. Lutz Ackermann of the Georg-August-Universität Göttingen employed (Org. Lett. 2012, 14, 4210) a Ru catalyst to oxidize the amide 23 to the phenol 24. Both Professor Ackermann (Org. Lett. 2012, 14, 6206) and Guangbin Dong of the University of Texas (Angew. Chem. Int. Ed. 2012, 51, 13075) described related work on the ortho hydroxylation of aryl ketones. George A. Kraus of Iowa State University rearranged (Tetrahedron Lett. 2012, 53, 7072) the aryl benzyl ether 25 to the phenol 26. The synthetic utility of the triazene 27 was demonstrated (Angew. Chem. Int. Ed. 2012, 51, 7242) by Yong Huang of the Shenzen Graduate School of Peking University.
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Conference papers on the topic "Room temperature sodium battery"

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Xie, J., and T. L. Riechel. "Room temperature molten salt batteries." In Fourteenth Annual Battery Conference on Applications and Advances. Proceedings of the Conference (Cat. No.99TH8371). IEEE, 1999. http://dx.doi.org/10.1109/bcaa.1999.795980.

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Myers, H. F., C. H. Champness, and I. Shih. "Room temperature transport measurements on Bridgman-grown CuInSe 2 with added sodium." In Photonics North 2010, edited by Henry P. Schriemer and Rafael N. Kleiman. SPIE, 2010. http://dx.doi.org/10.1117/12.869576.

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Frutschy, Kris, Troy Chatwin, Leng Mao, Chris R. Smith, and Roger Bull. "Sodium Nickel Chloride Battery Design and Testing." In ASME 2012 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/imece2012-86379.

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The main subsystems in a GE Durathon™ sodium nickel chloride battery are cells, Battery Management System (BMS), and packaging (see Figure 1). This cell chemistry requires an internal operating temperature of about 300°C, which provides unique challenges for battery thermal insulation and cooling. Electrical insulation between the cells and enclosures is another challenge, because traditional polymer-based insulations cannot operate at this elevated temperature range. Similarly, mechanical support structures must be high-temperature capable and also provide adequate protection to the cells and
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Peng, Kang-wei, Zhi-gang Zhang, Ming Guo, Chao Wang, and Shu-bin Sun. "Experimental Study on Sodium Column Fire of Sodium-Cooled Fast Reactor." In 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-16089.

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In the operation of sodium-cooled fast reactor, accident caused by the leakage and combustion of liquid sodium is common, and it is a pivotal and difficult problem in research, construction and operation of sodium-cooled fast reactor internationally. In actual operation of sodium-cooled fast reactor, liquid sodium in sodium fire accident is difficult to form fog but mainly in columnar flow form due to low operation pressure and thermal insulation material wrapping the pipe, so experimental research about columnar fire is of much more practical significance. This paper focuses on combustion pro
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Das, Susanta K., Salma Rahman, Jianfang Chai, et al. "Experimental Performance Evaluation of a Rechargeable Lithium-Air Battery Operating at Room Temperature." In ASME 2014 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/imece2014-39004.

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The effects of electrolyte, catalyst, and the process of preparation of the air-cathode on the performance of Li-air batteries were investigated. An ether based electrolyte was the best choice for Ketjen Black carbon based air cathodes and delivered high specific capacity (1050 mAh/gC) under dry air with cobalt oxide as catalyst. The introduction of an ultrasonication step in the air-cathode fabrication process improved the air-cathode microstructure. BET analyses revealed that the cathode has a higher surface area and mesopore volume when ultrasonication was used compared to those for the cat
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Xiao, Yong, Zhihao Zhang, Ming Yang, Haifeng Yang, Mingyu Li, and Yong Cao. "Study of the Fast Sintering of Silver Nanoparticle Ink Induced by Sodium chloride solution at Room Temperature." In 2018 19th International Conference on Electronic Packaging Technology (ICEPT). IEEE, 2018. http://dx.doi.org/10.1109/icept.2018.8480763.

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Garcia-Plaza, M., D. Serrano-Jimenez, J. Eloy-Garcia Carrasco, and J. Alonso-Martinez. "State of charge, hysteresis and room temperature effects on the Ni-Cd battery modeling." In 2015 IEEE International Conference on Industrial Technology (ICIT). IEEE, 2015. http://dx.doi.org/10.1109/icit.2015.7125259.

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Du, Haiou, Chen Liu, Rongdong Wang, and Wenjun Hu. "Experimental Study on the Sodium Spray Fire." In 2013 21st International Conference on Nuclear Engineering. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/icone21-16237.

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Sodium fire is a design basis accident of sodium-cooled fast reactor. Sodium spray fire experiments were conducted in enclosed cell in this study to understand the sodium spray fire status and how to have an influence on the plant under realistic sodium spray. The process of spray fire experiment was described in the paper. Pressure transducers and thermocouples can be mounted on the room to record pressures and temperatures, respectively. Control and data acquisition system were designed to record most of data for the various instruments. Three experimental results showed realistic sodium spr
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Pei, X., J. Liu, and X. Lu. "Measurement of reactive species density in the battery-operated, handheld room temperature atmospheric plasma jet for biomedical applications." In 2013 IEEE 40th International Conference on Plasma Sciences (ICOPS). IEEE, 2013. http://dx.doi.org/10.1109/plasma.2013.6633328.

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Hecq, JD, M. Closset, S. Onorati, et al. "PP-013 Long term stability of 5-fluorouracil at standardised rounded doses in sodium chloride infusion polyolefin bags, stored at room temperature." In 22nd EAHP Congress 22–24 March 2017 Cannes, France. British Medical Journal Publishing Group, 2017. http://dx.doi.org/10.1136/ejhpharm-2017-000640.460.

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Reports on the topic "Room temperature sodium battery"

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Tao, Greg, and Neill Weber. A High Temperature (400 to 650oC) Secondary Storage Battery Based on Liquid Sodium and Potassium Anodes. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/908547.

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