Primary chemical current source
专利摘要:
An electrolytic cell comprising a negative electrode having as the active material a light metal and a positive electrode as the main active material a poly-dicarbon monofluoride represented by the formula (C2F)n has been found to exhibit a high discharge voltage as compared with the conventional electrolytic cell of the type using as the active material of the positive electrode a polycarbon monofluoride represented by the formula (CF)n and also been found to be excellent in flatness of discharge voltage and shelf-life. The electrolytic cell of the present invention can be produced at low cost due to high yield of (C2F)n in production, and is useful as the energy source of such devices as watch, clock, desk type computer, small type radio, etc. 公开号:SU867333A3 申请号:SU792805307 申请日:1979-08-20 公开日:1981-09-23 发明作者:Ватанабе Нобуатсу;Моригаки Кенити 申请人:Эплайд Сайенс Рисерч Институт; IPC主号:
专利说明:
one This invention relates to chemical current sources and relates to a positive electrode based on carbon fluoride. Current sources are known, which contain a negative light metal electrode, an electrolyte and a positive carbon fluoride-based electrode containing a formula (CFx), where O X 0.25 1 and 0.9 X 1.3 2, However, the degradation temperature of such: polycarbon-fluoride compounds is close to the temperature of their synthesis, and the electrical characteristics, especially the discharge voltage, are not high enough. The purpose of the invention is to increase the electrical characteristics. For this, in the proposed current source, polyficarbon monofluoride is taken as carbon fluoride with the general formula 50100 mol.% in the positive electrode. Although the polycarbon monofluoride compound theoretical content fluorine is less than in a conventional polycarbon-single-fluoride compound, but when used as an active substance in a current source, it gives a high electromotive force and good current-voltage characteristics, for example, in terms of uniformity of discharge voltage, high energy density and no leakage. ten The specific gravity of the compound () n is about 2.8, while the specific gravity (CF) is about 2/7. Polydicarbon-single-fluoride compound (CrjF) receive 15 by the reaction of microparticles of carbon material having a Franklin index of approximately from O to 0.6 with fluorine at a temperature of 3OO-ZOO C up to those Tjop, until it reaches 20 complete fluorination of carbonaceous material consisting of microparticles. The product yield is 100%. Decomposition of this product does not occur at all. FIG. 1-7 are given characteristics 25 proposed current source. Example. Powder of polydicarbon-single-fluoride compound (C (F) obtained by the reaction of natural graphite with fluorine, at a temperature of 375 C, 30 under a pressure of fluorine of 760 mm Hg). For 120 hours, mixed with an electrically conductive agent, such as powdered coal, acetylene black, or a similar material, and a binder, such as a porous polyethylene or fluoropolymer, such as polytetrafluoroethylene, or expanded graphite, to prepare a mixture of the active substance. for a positive electrode. This can be easily molded to form a positive electrode. Carbon black, or acetylene black, as an electrically conductive agent, can be used in an amount of 3-20 wt.%, Preferably 3-15 wt.%. The binder may be used in an amount of 1-10% by weight. The higher the content (CrH) l in the mixture of active material, the better the electrochemical characteristics of the positive electrode Since polydicarbon monofluoride compound (C, P) y is more electrically conductive than polydicarbon monofluoride compound (CF) vi, the amount of electrically conductive agent included in this mixture may be less in the case of use ( use case (CF). A positive electrode is obtained simply by forming a mixture, preferably around a metal collector. The negative electrode is a light alkali metal or alkaline earth metal. The electrolyte used in the proposed current source is generally non-aqueous. The positive electrode from the compound (C, P) "gave a small overvoltage, compared with the positive electrode from the compound (CP)". The discharge voltage is 3 V from 2.8 V for the electrode {CF) ".
权利要求:
Claims (1) [1] Invention Formula A primary chemical source of current containing a negative light metal electrode, an electrolyte, and a positive carbon fluoride-based electrode, characterized in that, in order to improve electrical characteristics, polycarbonic fluorocarbon is taken using the general formula (), where n is an integer crystal structure with interplanar spacing between the layers of 9.0 Au peak in the X-ray powder diffraction pattern at 10, which is positive electrode 50-100 mol.%. Sources of information taken into account in the examination 1. US Patent 3700502, cl. 136-6, 0 1974. . US patent 3985577,4292194,1976. 10 0 .8 I about tj 0.6 tir MOS b, 5v water atmosphere ny L. ff {tffffOO teine rotoffo, C Vely X 600 FIG. one go {CzF) n. Rich. 9.0 80 AT J 7. (7 6.0 3fO ifOS ( Yu; 3ff mz 50 Fui.Z LCF ndictt S.O 600 500 Temperature, C Fy-W ® (CrPp 0: (CF) n I 1550 Percentage of yes SO 15 FiL five S nomsHttiiHUi, fvs Li .f
类似技术:
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同族专利:
公开号 | 公开日 IT7925224D0|1979-08-21| IN152156B|1983-11-05| CH628775B| FR2434492A1|1980-03-21| FR2434492B1|1984-03-30| GB2028570A|1980-03-05| DE2933497A1|1980-03-13| IT1162573B|1987-04-01| DE2933497C3|1982-02-04| US4247608A|1981-01-27| CA1121449A|1982-04-06| JPS5528246A|1980-02-28| CH628775A|1982-03-31| DE2933497B2|1981-02-19| JPS6142378B2|1986-09-20| GB2028570B|1982-09-29| NL7906307A|1980-02-25|
引用文献:
公开号 | 申请日 | 公开日 | 申请人 | 专利标题 IT500094A|1968-04-12| JPS4825566B1|1968-04-17|1973-07-30| JPS4825565A|1971-08-03|1973-04-03| US3956018A|1974-12-30|1976-05-11|Union Carbide Corporation|Primary electric current-producing dry cell using a n cathode and an aqueous alkaline electrolyte| US4166888A|1978-10-30|1979-09-04|Exxon Research & Engineering Co.|Cell having an alkali metal anode, a fluorinated carbon cathode and an electrolyte which includes an alkali metal halide salt and a solvent system containing a substituted amide solvent and a cyclic carbonate cosolvent|JPS56125498A|1980-03-06|1981-10-01|Gosei Kagaku Kenkyusho:Kk|Lubricant for hot forging| US4327166A|1980-09-29|1982-04-27|Union Carbide Corporation|Nonaqueous cell having a MNO2 /poly-carbon fluoride cathode| JPS6335068B2|1980-11-14|1988-07-13|Matsushita Electric Ind Co Ltd| JPS5816468A|1981-07-22|1983-01-31|Central Glass Co Ltd|Cell active substance| JPS6220127B2|1981-09-10|1987-05-06|Oyo Kagaku Kenkyusho| JPH0258738B2|1981-11-17|1990-12-10|Matsushita Electric Ind Co Ltd| US4578327A|1983-04-05|1986-03-25|Asahikasei Kabushiki Kaisha|Electric cells using fluorinated graphite as active material of positive electrode| FR2546153B1|1983-05-19|1990-05-04|Lorraine Carbone|GRAPHITE INSERTING COMPOUNDS WITH IMPROVED PERFORMANCE AND ELECTROCHEMICAL APPLICATIONS THEREOF| EP0126701B1|1983-05-19|1987-10-14|Le Carbone-Lorraine S.A.|Graphite intercalation compounds with improved performance, and electrochemical application of these compounds| EP0128560B1|1983-06-09|1989-09-06|Daikin Kogyo Co., Ltd.|Active materials for batteries| US4524119A|1983-07-25|1985-06-18|Allied Corporation|Electrophotographic carriers incorporating fluorinated carbon and process of using same| JPH0677458B2|1984-11-12|1994-09-28|信淳 渡辺|Battery active material| US4548881A|1985-02-08|1985-10-22|Allied Corporation|High energy density battery with cathode composition| US4618548A|1985-03-18|1986-10-21|Combustion Engineering, Inc.|Electrolyte additive| US4770797A|1986-03-31|1988-09-13|Allied-Signal Inc.|Carbon fluoride chloride lubricant| US4681823A|1986-05-19|1987-07-21|Allied Corporation|Lithium/fluorinated carbon battery with no voltage delay| US5484675A|1994-09-19|1996-01-16|Xerox Corporation|Toner compositions with halosilanated pigments| US6180311B1|1994-09-19|2001-01-30|Xerox Corporation|Carrier particles with halosilanated pigments| US5849399A|1996-04-19|1998-12-15|Xerox Corporation|Bias transfer members with fluorinated carbon filled fluoroelastomer outer layer| JP4423699B2|1999-05-27|2010-03-03|ソニー株式会社|Semiconductor laser device and manufacturing method thereof| US6406741B1|2000-11-28|2002-06-18|Xerox Corporation|Method of making a polyimide layer containing fluorinated carbon material| US6677076B2|2002-01-15|2004-01-13|Quallion Llc|Electric storage battery construction and method of manufacture| AU2003251798A1|2003-01-15|2005-10-07|Quallion Llc|Battery| US6670071B2|2002-01-15|2003-12-30|Quallion Llc|Electric storage battery construction and method of manufacture| WO2005089422A2|2004-03-17|2005-09-29|California Institute Of Technology|Methods for purifying carbon materials| US8080329B1|2004-03-25|2011-12-20|Quallion Llc|Uniformly wound battery| US20100221603A1|2006-03-03|2010-09-02|Rachid Yazami|Lithium ion fluoride battery| US8377586B2|2005-10-05|2013-02-19|California Institute Of Technology|Fluoride ion electrochemical cell| US8658309B2|2006-08-11|2014-02-25|California Institute Of Technology|Dissociating agents, formulations and methods providing enhanced solubility of fluorides| US20070218364A1|2005-10-05|2007-09-20|Whitacre Jay F|Low temperature electrochemical cell| US7563542B2|2005-10-05|2009-07-21|California Institute Of Technology|Subfluorinated graphite fluorides as electrode materials| US8232007B2|2005-10-05|2012-07-31|California Institute Of Technology|Electrochemistry of carbon subfluorides| US7794880B2|2005-11-16|2010-09-14|California Institute Of Technology|Fluorination of multi-layered carbon nanomaterials| US20090111021A1|2007-03-14|2009-04-30|Rachid Yazami|High discharge rate batteries| CN101678310A|2007-05-09|2010-03-24|加州理工学院|lithium fluoropolymer and fluoro-organic batteries| US9029019B2|2007-08-17|2015-05-12|Nanotek Instruments, Inc.|Carbon anode compositions for lithium ion batteries| US7993780B2|2007-10-05|2011-08-09|Nanotek Instruments, Inc.|Process for producing carbon anode compositions for lithium ion batteries| WO2009153051A1|2008-06-20|2009-12-23|MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V.|Use of a superfine expanded graphite and preparation thereof| CN102203984A|2008-11-04|2011-09-28|加州理工学院|Hybrid electrochemical generator with a soluble anode| WO2012174710A1|2011-06-21|2012-12-27|Dow Global Technologies Llc|Isocyanate-based polymer foam with improved thermal insulation properties| US9328859B2|2011-07-26|2016-05-03|Dow Global Technologies Llc|Isocyanate-based polymer foam composite with improved thermal insulation properties| CN103022493A|2012-12-14|2013-04-03|天津大学|Fluoridized graphite/polythiophene composite material and preparation method thereof| GB2532035B|2014-11-06|2018-01-10|Schlumberger Holdings|Lithium carbon fluoride primary battery| CN104538580B|2014-12-18|2017-01-11|复旦大学|Primary thermal battery based on fluorine carbon electrode and preparation method of one-order thermal battery|
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申请号 | 申请日 | 专利标题 JP53100911A|JPS6142378B2|1978-08-21|1978-08-21| 相关专利
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