Process for synthesizing lithium difluoro(oxalate)borate from lithium bis(oxalate)borate

The technology of lithium difluorooxalate borate and lithium bisoxalate borate is applied in the field of synthesis technology of electrolyte lithium salt, can solve the problems of difficult separation of by-products, low reaction yield and high requirements for reaction equipment, and achieves great implementation value and social economy. Benefit, mild preparation conditions, less three wastes

Active Publication Date: 2017-10-03
SHANGHAI ROLECHEM CO LTD
View PDF8 Cites 10 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] The typical preparation method of lithium difluorooxalate borate mainly contains LiBF in European Patent EP1195834A2 by Tsujioka.S et al. 4 、CH(CF 3 ) 2 OLi, H 2 C 2 o 4 , the reaction medium is a polar aprotic solvent such as carbonate or acetonitrile for synthesis, unreacted LiBF 4 Up to more than 15%; Tsujioka.S and others in the European patent EP1308449A2 with H 2 C 2 o 4 、LiBF 4 and AlCl 3 or SiCl 4 Synthesis of lithium difluorooxalate borate in dimethyl carbonate; HerzigT, ShchreinerC, GerhardD, et al. J Fluorine Chem, 2007, 128: 612-618 using H 2 C 2 o 4 and LiBF 4 AlCl in carbonate or acetonitrile 3 or SiCl 4 Synthesis under the action of additives, the above methods all have the characteristics of high requirements for reaction equipment, a large amount of hydrochloric acid gas and silicon tetrafluoride gas are emitted during the reaction, and it is easy to produce by-products that are not easy to separate or difficult to filter insolubles in the reaction mixture.
To overcome the above shortcomings, ZhangSS.Electrochem.Commun, 2006, 8: 1423-1428; Uno AKIRA, Uchiyama Hatsuo, Kawaswa Yoshio.JP59-50018, 1984 used BF 3 (CH 2 CH 3 ) 2 with Li 2 C 2 o 4 Synthesis of lithium difluorooxalate borate products in DMC, the process is simple, the cost is low, but at the same time there is a by-product LiBF 4 Formed and difficult to separate, resulting in low reaction yield
In recent years, Chinese published patents such as "CN101643481A", "CN102260282A", "CN1031113396A", "CN105399761A" and other published patents are similar to the above-mentioned patents. The purity of the LiODFB samples obtained is relatively low, and the generated by-product LiBF4 is difficult to separate. Purified before it can be used as an electrolyte for lithium-ion batteries

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Process for synthesizing lithium difluoro(oxalate)borate from lithium bis(oxalate)borate

Examples

Experimental program
Comparison scheme
Effect test

Embodiment approach

[0032] As an embodiment of the present invention, the compound containing fluorine, boron, and lithium is lithium tetrafluoroborate, fluoroboric acid, boron trifluoride dimethyl carbonate complex, lithium fluoride, boron trifluoride, trifluoride Boron trifluoride acetonitrile, boron trifluoride ether, boron trifluoride dimethyl carbonate, boron trifluoride ethyl acetate, boron trifluoride tetrahydrofuran, boron trifluoride methyl ether complex, boron trioxide, borax , boric acid, lithium carbonate, lithium oxalate, lithium chloride, lithium hydrogen oxalate, lithium hydroxide, lithium sulfate, lithium dihydrogen phosphate, lithium fluoride, lithium oxide, lithium bromide, lithium amide, lithium diisopropylamide one or a combination.

[0033] As a preferred form of the present invention, the compound containing fluorine, boron, and lithium is lithium tetrafluoroborate, fluoroboric acid, lithium fluoride, boron trifluoride, boron trifluoride acetonitrile, boron trifluoride ether...

Embodiment approach 1

[0040] Embodiment 1: This embodiment provides a synthesis process for preparing lithium difluorooxalate borate with lithium bisoxalate borate. The synthesis process includes the following steps:

[0041] 1), mixing lithium bisoxalate borate with compounds containing fluorine, boron, and lithium in proportion to obtain a mixture;

[0042] 2) Add the mixture in step 1) to the solvent, and react at 0-150° C. with a reaction pressure of 101kpa-150kpa to obtain the product, which is crystallized and vacuum-dried to obtain lithium difluorooxalate borate.

Embodiment approach 2

[0043] Embodiment 2: The synthesis process as described in Embodiment 1, the compound containing fluorine, boron, and lithium is lithium tetrafluoroborate, fluoroboric acid, boron trifluoride dimethyl carbonate complex, lithium fluoride, three Boron fluoride, boron trifluoride acetonitrile, boron trifluoride ether, boron trifluoride dimethyl carbonate, boron trifluoride ethyl acetate, boron trifluoride tetrahydrofuran, boron trifluoride methyl ether complex, three Diboron oxide, borax, boric acid, lithium carbonate, lithium oxalate, lithium chloride, lithium hydrogen oxalate, lithium hydroxide, lithium sulfate, lithium dihydrogen phosphate, lithium fluoride, lithium oxide, lithium bromide, lithium amide, diisopropyl Any one or combination of lithium amides.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses a process for synthesizing lithium difluoro(oxalate)borate from lithium bis(oxalate)borate. The process comprises the following steps: mixing lithium bis(oxalate)borate with a compound containing fluorine, boron and lithium; carrying out a reaction in a solvent system at a temperature of 0 to 150 DEG C and a reaction pressure of 101 kpa and 150 kpa to produce a product; and carrying out a reaction at a certain temperature and then carrying out crystallization and vacuum drying so as to obtain battery-grade lithium difluoro(oxalate)borate. The process provided by the invention is novel in process and mild in conditions and can prepare high-purity battery-grade lithium difluoro(oxalate)borate.

Description

technical field [0001] The invention relates to a synthesis process of an electrolyte lithium salt used in the lithium ion battery industry, in particular to a synthesis process of lithium difluorooxalate borate. technical background [0002] Electrolyte salt is an important part of lithium-ion batteries, and its research and development is very important to the performance and development of lithium-ion secondary batteries. At present, the electrolyte of commonly used lithium-ion batteries is mainly lithium hexafluorophosphate (LiPF 6 ), lithium bisoxalate borate (LiBOB), lithium tetrafluoroborate (LiBF 4 )Wait. [0003] LiPF 6 The thermal stability of carbon dioxide is poor, easy to deliquescence, and must be used with ethylene carbonate (EC) to form a stable solid electrolyte interface (SEI) film on the surface of the carbon negative electrode; while the melting point of EC is 37 ° C, which will affect the low temperature performance. influences. LiBF 4 The charge t...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Applications(China)
IPC IPC(8): C07F5/02
CPCC07F5/022
Inventor 杨焜
Owner SHANGHAI ROLECHEM CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products