CN102800899B - A kind of preparation method of electrolyte of nickel hydrogen battery - Google Patents

A kind of preparation method of electrolyte of nickel hydrogen battery Download PDF

Info

Publication number
CN102800899B
CN102800899B CN201210315866.2A CN201210315866A CN102800899B CN 102800899 B CN102800899 B CN 102800899B CN 201210315866 A CN201210315866 A CN 201210315866A CN 102800899 B CN102800899 B CN 102800899B
Authority
CN
China
Prior art keywords
electrolyte
battery
preparation
electrolysis additive
alkaline solution
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201210315866.2A
Other languages
Chinese (zh)
Other versions
CN102800899A (en
Inventor
姜波
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Qinzhou Industry Research Institute
Original Assignee
SHANGHAI JINZHONG INFORMATION TECHNOLOGY Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by SHANGHAI JINZHONG INFORMATION TECHNOLOGY Co Ltd filed Critical SHANGHAI JINZHONG INFORMATION TECHNOLOGY Co Ltd
Priority to CN201210315866.2A priority Critical patent/CN102800899B/en
Publication of CN102800899A publication Critical patent/CN102800899A/en
Application granted granted Critical
Publication of CN102800899B publication Critical patent/CN102800899B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/10Energy storage using batteries
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P70/00Climate change mitigation technologies in the production process for final industrial or consumer products
    • Y02P70/50Manufacturing or production processes characterised by the final manufactured product

Landscapes

  • Battery Electrode And Active Subsutance (AREA)
  • Secondary Cells (AREA)

Abstract

The invention discloses the preparation method of the electrolyte of Ni-MH battery, the component proportion of its alkaline solution is: is 23: 12: 0.5 1: 0.3 0.6 potassium hydroxide, NaOH, lithium hydroxide by mass ratio and can make Mn2+Reach saturated MnSO4The mixture of three, under conditions of 40 50 DEG C and stirring, is dissolved by aqueous solvent, is made into the solution that molality is 8 10mol/L;Its electrolysis additive is: lithium nitrate, sodium formate, ethylene glycol, nickel nitrate.Trying out through battery producer, compared with other Ni-MH battery electrolyte on market, uses the discharge capability of the ni-mh of the electrolyte of the present invention to be greatly improved, and service life is effectively extended.

Description

A kind of preparation method of electrolyte of nickel hydrogen battery
Technical field
The present invention relates to the preparation method of a kind of battery electrolyte, particularly relate to a kind of Ni-MH battery electrolyte and prepare Method.
Background technology
Ni-MH battery can be used for military affairs, Aero-Space, navigation, oil, coal, geological prospecting and operation, ice Go up and the mountain-climbing field such as sports items, antarctic investigation.At present, Ni-MH battery manufactured by existing industry, used Electrolyte is mainly the mixing electrolysis of potassium hydroxide aqueous solution or potassium hydroxide, NaOH and lithium hydroxide Liquid.Research is thought: electrolyte is very big on battery performance impact, and this is owing to bath composition and concentration are led with it Electrically and electrode reaction is closely related, the electric conductivity of electrolyte and the invertibity of electrode reaction directly affect electricity Tank discharge capacity and mean voltage.Therefore, the electrolyte of Ni-MH battery for the discharge capability of Ni-MH battery and makes With the life-span etc., there is vital effect.
Content of the invention
It is an object of the invention to provide the preparation method of the electrolyte of a kind of Ni-MH battery, use the method to prepare The Ni-MH battery of electrolyte has that discharge capability is strong, the advantage of length in service life.
To achieve these goals, the preparation method of the electrolyte of the Ni-MH battery that the present invention provides includes walking as follows Rapid:
Step 1, prepares alkaline solution:
Mass ratio is 2-3: 1-2: 0.5-1: 0.3-0.6 potassium hydroxide, NaOH, lithium hydroxide and Mn can be made2+Reach saturated MnSO4Mixture, 40-50 DEG C and stirring under conditions of, use aqueous solvent Dissolve, be made into Mn2+Molar concentration is the solution of 8-10mol/L;
Step 2, preparation electrolysis additive:
Electrolysis additive is by following mass ratio:
Alkaline solution and electrolysis additive are mixed by step 3, prepare Ni-MH battery electrolyte:
Under conditions of 40-50 DEG C and stirring, by the electrolysis additive of 1-1.5% that mass ratio is alkaline solution Join in the aqueous slkali that the first step is prepared, dissolve, continue stirring 5-10 minute, i.e. prepare Ni-MH battery Electrolyte.
Wherein, described aqueous solvent is redistilled water or deionized water.
Wherein, described carboxylic acid sodium is sodium formate or sodium acetate.
Wherein, described polyalcohol is dihydroxylic alcohols and/or trihydroxylic alcohol.
Wherein, described dihydroxylic alcohols is ethylene glycol and/or propane diols.
Wherein, described trihydroxylic alcohol is glycerine.
Using Ni-MH battery electrolyte prepared by the manufacture method of the present invention, trying out through battery producer, with market On other electrolyte compare, discharge capability is greatly improved, and service life is effectively extended.
Detailed description of the invention
Embodiment one
Prepare alkaline solution
It is 2: 1: 0.5:0.3 potassium hydroxide, NaOH, lithium hydroxide by mass ratio and Mn can be made2+Reach To saturated MnSO4The mixture of three, is dissolved in redistilled water and deionized water in glass container, It is then placed in heating stirring container, at a temperature of 40 DEG C, with the speed of 1000 revs/min, stir 5 minutes, It is made into Mn2+Molar concentration is the solution of 8mol/L.
Prepare electrolysis additive
Electrolysis additive is by following mass ratio:
Four kinds of materials of above-mentioned mass parts are sufficiently mixed.
Alkaline solution and electrolysis additive are mixed, prepares Ni-MH battery electrolyte
By mixed electrolysis additive, add in the alkaline solution to above-mentioned heating stirring container, its matter Amount ratio is the 1% of alkaline solution, dissolves, and continues in stirring 5 points under the mixing speed of 40 DEG C and 1000 turns Clock, i.e. prepares Ni-MH battery electrolyte.
Embodiment two
Prepare alkaline solution
It is 3: 2: 1:0.6 potassium hydroxide, NaOH, lithium hydroxide by mass ratio and Mn can be made2+Reach To saturated MnSO4The mixture of three, is dissolved in redistilled water and deionized water in glass container, It is then placed in heating stirring container, at a temperature of 50 DEG C, with the speed of 1500 revs/min, stir 10 minutes, It is made into2+Molar concentration is the solution of 10mol/L.
Prepare electrolysis additive
Electrolysis additive is by following proportion by weight:
Four kinds of materials of above-mentioned mass parts are sufficiently mixed.
Alkaline solution and electrolysis additive are mixed, prepares Ni-MH battery electrolyte
By mixed electrolysis additive, add in the alkaline solution to above-mentioned heating stirring container, its matter Amount ratio is the 1.5% of alkaline solution, dissolves, and continues in stirring 10 under the mixing speed of 50 DEG C and 1500 turns Minute, i.e. prepare Ni-MH battery electrolyte.
Electrolyte that embodiment 1 and 2 prepares and general electrolytic liquid (comparative example) are for the property of Ni-MH battery Can detect as follows:
General electrolytic liquid Embodiment 1 Embodiment 2
Normal temperature charge/discharge capacity 1500mAh 1600mAh 1650mAh
Service life 2-3 3-4 3-4
Being described in detail the specific embodiment of the present invention above, but it being intended only as example, the present invention is simultaneously It is not restricted to particular embodiments described above.To those skilled in the art, any the present invention is carried out Equivalent modifications and replacement also all among scope of the invention.Therefore, without departing from the spirit of the present invention and model Enclose lower made impartial conversion and modification, all should cover within the scope of the invention.

Claims (3)

1. the preparation method of the electrolyte of a Ni-MH battery, it is characterised in that comprise the steps:
Step 1, prepares alkaline solution:
It is 3: 2: 1:0.6 potassium hydroxide, NaOH, lithium hydroxide by mass ratio and Mn can be made2+Reach To saturated MnSO4Mixture, 50 DEG C and stirring under conditions of, with aqueous solvent dissolve, be made into Mn2+ Molar concentration is the solution of 10mol/L;
Step 2, preparation electrolysis additive:
Electrolysis additive is by following mass ratio:
Alkaline solution and electrolysis additive are mixed by step 3, prepare Ni-MH battery electrolyte:
Under conditions of 40-50 DEG C and stirring, by the electrolysis additive of 1-1.5% that mass ratio is alkaline solution Join in the aqueous slkali that the first step is prepared, dissolve, continue stirring 5-10 minute, i.e. prepare Ni-MH battery Electrolyte.
2. a preparation method for Ni-MH battery electrolyte as claimed in claim 1, wherein, described aqueous solvent is Redistilled water or deionized water.
3. a preparation method for Ni-MH battery electrolyte as claimed in claim 1, wherein, described carboxylic acid sodium is Sodium formate or sodium acetate.
CN201210315866.2A 2012-08-30 2012-08-30 A kind of preparation method of electrolyte of nickel hydrogen battery Expired - Fee Related CN102800899B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201210315866.2A CN102800899B (en) 2012-08-30 2012-08-30 A kind of preparation method of electrolyte of nickel hydrogen battery

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201210315866.2A CN102800899B (en) 2012-08-30 2012-08-30 A kind of preparation method of electrolyte of nickel hydrogen battery

Publications (2)

Publication Number Publication Date
CN102800899A CN102800899A (en) 2012-11-28
CN102800899B true CN102800899B (en) 2016-11-09

Family

ID=47199929

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201210315866.2A Expired - Fee Related CN102800899B (en) 2012-08-30 2012-08-30 A kind of preparation method of electrolyte of nickel hydrogen battery

Country Status (1)

Country Link
CN (1) CN102800899B (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101369672A (en) * 2008-10-07 2009-02-18 湖南科力远新能源股份有限公司 Special electrolytic solution for alkaline nickel-hydrogen battery
CN101871060A (en) * 2010-06-21 2010-10-27 桂林电子科技大学 Nickel-hydrogen battery negative electrode hydrogen storage material capable of being used at low temperature and matched electrolytic solution thereof
CN101924253A (en) * 2009-06-15 2010-12-22 浙江师范大学 Electrolyte additive of novel nickel-metal hydride secondary battery

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101369672A (en) * 2008-10-07 2009-02-18 湖南科力远新能源股份有限公司 Special electrolytic solution for alkaline nickel-hydrogen battery
CN101924253A (en) * 2009-06-15 2010-12-22 浙江师范大学 Electrolyte additive of novel nickel-metal hydride secondary battery
CN101871060A (en) * 2010-06-21 2010-10-27 桂林电子科技大学 Nickel-hydrogen battery negative electrode hydrogen storage material capable of being used at low temperature and matched electrolytic solution thereof

Also Published As

Publication number Publication date
CN102800899A (en) 2012-11-28

Similar Documents

Publication Publication Date Title
Zhang et al. Issues and rational design of aqueous electrolyte for Zn‐ion batteries
CN103985906B (en) A kind of lithium-ion battery electrolytes taking into account high temperature performance
CN105428719B (en) Wide temperature lithium-ion battery electrolytes of high voltage and preparation method and application
CN103384004B (en) Storage battery cathode formula and preparation technology thereof
CN109796006B (en) Application of ionic liquid in preparation of nitrogen-doped carbon quantum dots, and preparation method and application of nitrogen-doped carbon quantum dots
CN106876778B (en) A kind of lithium ion secondary battery
CN106328938A (en) Low-temperature lithium iron phosphate battery and preparation method
CN108390096A (en) A kind of application of tetrafluoroborate, composite electrolyte and composite positive pole comprising tetrafluoroborate
CN103928707A (en) High voltage lithium ion battery functional electrolyte and preparation method and application
CN110867612B (en) Low-temperature charging and discharging electrolyte for lithium ion battery
CN101840784A (en) Electrolyte for super capacitor and super capacitor
CN106785037B (en) A kind of lithium-ion battery electrolytes for ternary material battery
CN102417500A (en) Fluorine-containing carbonic ester solvent, its preparation method and electrolyte for lithium ion batteries
CN101420053A (en) Guanidinium type ionic liquid electrolyzing solution for lithium secondary cell
CN102800899B (en) A kind of preparation method of electrolyte of nickel hydrogen battery
CN106340664B (en) Full electrolyte of vanadium redox battery and preparation method thereof
CN103107364B (en) A kind of electrolyte of low temp lithium ion battery and lithium ion battery
CN107359367A (en) A kind of high voltage withstanding flame-retardant lithium ion battery electrolyte and preparation method thereof
US9923242B2 (en) Lithium bromide battery
CN113793984B (en) Electrolyte for double-ion battery and preparation method thereof
CN108832201A (en) A kind of electrolysis additive, electrolyte and the lithium ion battery using it
CN108511812A (en) A kind of mixing water system lithium cell electrolyte solution and preparation method
CN107256983A (en) Wide-temperature high-efficiency flame-retardant electrolyte for lithium ion battery and preparation method thereof
CN201210498Y (en) Air cell connection structure
CN102328949A (en) Preparation method for copper oxide nanoribbon with high hydrogen storage capacity

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CB03 Change of inventor or designer information

Inventor after: Lu Hongxian

Inventor before: Jiang Bo

CB03 Change of inventor or designer information
TR01 Transfer of patent right

Effective date of registration: 20171218

Address after: 535000 the Guangxi Zhuang Autonomous Region, Qinzhou, Qinnan District Building Street, No. 9

Patentee after: Qinzhou Industry Research Institute

Address before: 201203 Shanghai Guo Shou Jing Road, Zhangjiang High Tech Park of Pudong New Area No. 351 Building No. 2 room 662-16

Patentee before: Shanghai Jinzhong Information Technology Co., Ltd.

TR01 Transfer of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20161109

Termination date: 20180830

CF01 Termination of patent right due to non-payment of annual fee