Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Synthesis method for bis(fluorosulfonyl)imide salt

A technology of bisfluorosulfonimide salt and bischlorosulfonimide salt, which is applied in the field of halogen exchange fluorination synthesis, can solve the problems of difficult separation and purification operation, inability to remove, cumbersome and the like, and achieves simple process operation and high product quality. The effect of high yield and high product purity

Active Publication Date: 2015-06-03
JIANGSU GUOTAI SUPER POWER NEW MATERIALS
View PDF4 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0010]J.K.Ruff et al. used AsF3 fluorinating agent in the process of fluorinating bischlorosulfonimide, which used highly toxic As element, not Suitable for industrial production (J.K.Ruff et al, Inorg.Synth. 1968, 11, 138); the antimony trichloride contained in the fluorinating agent compound fluorinating agent used by B.Krumm et al. has a very strong sublimation property , can not go out in the late stage of the reaction (B.Krumm et al, Inorg.Chem.1998, 37, 6295); although Zhou Zhibin and others use potassium carbonate to neutralize antimony trichloride, it will lead to difluorosulfonimide after neutralization The salt cannot be separated (Zhou Zhibin et al., application number: CN 102786451 A)
A.Hammami et al. used excess potassium fluoride (KF) and dichlorosulfonimide to react in an organic solvent to directly prepare the potassium salt of H[FSI]; this preparation route not only generates highly toxic gas HF, but also reacts excessively Since the potassium salt of the product KF and the product H[FSI] is insoluble in the organic solvent, the reaction system will coagulate into blocks, and the separation and purification operations are difficult and cumbersome, etc. (A.Hammami et al, US 2007043231, 2007)

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0022] Embodiment 1: Potassium difluorosulfonimide ([KN(SO 2 F)] 2 , referred to as KFSI) preparation.

[0023] Under nitrogen protection, 504g (2mol) of potassium dichlorosulfonimide (KCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.

[0024] Under the condition of stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 7 batches, and adjacent batches are added to the above-mentioned 2000ml three-necked flask at intervals of 45 minutes. The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.

[0025] After the reaction, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 300 g, and cooled to 5° C. to crystallize. Then filter, wash, and dry to obtain 218.6 g (0.998 mol) of potassium...

Embodiment 2

[0026] Embodiment 2: Sodium bisfluorosulfonimide ([NaN(SO 2 F)] 2 , referred to as NaFSI).

[0027]Under nitrogen protection, 472g (2mol) of sodium bischlorosulfonimide (NaCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.

[0028] Under stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 9 batches, and adjacent batches are added in the above-mentioned 2000ml three-necked flask at intervals of 40 minutes. The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.

[0029] After the reaction was completed, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 360 g, and cooled to 5° C. for crystallization. Then filter, wash, and dry to obtain 268g (1.32mol) of sodium bisfluorosulfonimid...

Embodiment 3

[0030] Embodiment 3: Lithium difluorosulfonimide ([LiN(SO 2 F)] 2 , referred to as LiFSI).

[0031] Under nitrogen protection, 440g (2mol) of lithium bischlorosulfonimide (LiCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.

[0032] Under the condition of stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 10 batches, and adjacent batches are added in the above-mentioned 2000ml three-necked flask at intervals of 50 minutes, The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.

[0033] After the reaction was completed, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 360 g, and cooled to 5° C. for crystallization. Then filtered, washed, and dried to obtain 195 g (1.04 mol) o...

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 synthesis method for a bis(fluorosulfonyl)imide salt, wherein the method comprises the following steps: (one) under the protection of nitrogen, dissolving a bis(chlorosulfonyl)imide salt in a nonprotic organic solvent to obtain a bis(chlorosulfonyl)imide salt organic solution; (two) under a stirring condition, adding an excess compound fluridizer into the organic solution, then heating to a temperature being 8 DEG C-20 DEG C higher than an organic solvent boiling point temperature, and making the bis(chlorosulfonyl)imide salt to undergo an effective fluorination reaction in the organic solvent, wherein the compound fluridizer is selected from at least two substances of antimony trifluoride, potassium fluoride, zinc fluoride and aluminum fluoride; (three) after the reaction is finished, filtering the reaction liquid, and concentrating the filtrate to obtain a concentrated solution; and (four) crystallizing the concentrated solution, filtering, drying, and thus obtaining the high-purity bis(fluorosulfonyl)imide salt. The synthesis method has the advantages of simple operation, high product productive rate, no toxic reagent to pollute the environment, and high purity of the product, and is suitable for large-scale production in industry.

Description

technical field [0001] The invention belongs to halogen exchange fluorination synthesis and relates to a preparation method of alkali metal salt of bisfluorosulfonimide. Background technique [0002] Fluorine is the most electronegative element known so far. The introduction of fluorine atoms into molecules can cause drastic changes in its physical and chemical properties, resulting in many strange properties in terms of optical, electrical and magnetic properties. At present, fluorine-containing compounds have shown great research value and economic value in the research and application of energy storage electronic materials and biological materials. Some fluorine-containing compounds have ultra-high electrical conductivity, which makes them have important applications in electrochemical energy storage materials and devices such as secondary lithium-ion batteries and supercapacitors. For example, lithium bistrifluoromethylsulfonylimide (LiTFSI), lithium tetrafluoroborate (...

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): C01B21/096
Inventor 邹凯赵世勇闻立新施苏萍徐晓强何永刚陶荣辉赵金保张鹏
Owner JIANGSU GUOTAI SUPER POWER NEW MATERIALS
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
Eureka Blog
Learn More
PatSnap group products