Method for producing phosphoryl imide salt, method for producing nonaqueous electrolyte solution containing said salt, and method for producing nonaqueous secondary battery

Patent metadata

Field	Value
Publication number	US-10851124-B2
Application number	US-201816603866-A
Country	US
Kind code	B2
Filing date	Apr 9, 2018
Priority date	Apr 10, 2017
Publication date	Dec 1, 2020
Grant date	Dec 1, 2020

Abstract

To provide a method for producing a phosphoryl imide salt represented by the following general formula (1) at a satisfactory yield by cation exchange. The method comprises the step of performing cation exchange by bringing a phosphoryl imide salt represented by the following general formula (2) into contact with a cation exchange resin having M 1 n+ or a metal salt represented by the general formula (4) in an organic solvent having a water content of 0.3% by mass or less.

First claim

The invention claimed is:

1. A method for producing a phosphoryl imide salt represented by the following general formula (1), comprising the step of performing cation exchange by bringing a phosphoryl imide salt represented by the following general formula (2) into contact with a cation exchange resin having M 1 n+ or a metal salt represented by the general formula (4) in an organic solvent having a water content of 0.3% by mass or less:

wherein M 1 n+ is an alkali metal cation, an alkaline earth metal cation, a quaternary ammonium cation or a quaternary phosphonium cation,
M 2 n+ is any one of an alkali metal cation, an alkaline earth metal cation, a quaternary ammonium cation, a tertiary ammonium cation (a protonated form of a tertiary organic amine base), or a mixture thereof,
a cation M 1 n+ of the product is different from a cation M 2 n+ of the raw material,
N is a nitrogen atom, P is a phosphorus atom, and X is a sulfur atom or a phosphorus atom,
n is 1 or 2,
when X is a sulfur atom, m is 2 and R 4 is absent,
when X is a phosphorus atom, m is 1,
B is a chloride ion, a sulfate ion, a sulfonate ion or a carbonate ion, and
R 1 , R 2 , R 3 and R 4 are each independently selected from a fluorine atom, an alkyl group, an alkoxy group, an alkenyl group, an alkenyloxy group, an alkynyloxy group and an aryloxy group.

2. The method for producing a phosphoryl imide salt according to claim 1 , wherein the water content of the organic solvent is 0.05% by mass or less.

3. The method for producing a phosphoryl imide salt according to claim 1 , wherein M 1 n+ is a lithium ion, a sodium ion, a potassium ion, a magnesium ion, a calcium ion, a tetraalkylammonium cation, a tetraalkylphosphonium cation, an imidazolium cation, a pyrazolium cation, a pyridinium cation or a pyrimidinium cation.

4. The method for producing a phosphoryl imide salt according to claim 1 , wherein M 1 n+ is a lithium ion and the water content of the organic solvent is 0.0001 to 0.03% by mass.

5. The method for producing a phosphoryl imide salt according to claim 1 , wherein M 1 n+ is a sodium ion and the water content of the organic solvent is 0.001 to 0.05% by mass.

6. The method for producing a phosphoryl imide salt according to claim 1 , wherein M 2 n+ is a proton adduct of an aliphatic tertiary amine.

7. The method for producing a phosphoryl imide salt according to claim 6 , wherein the proton adduct of the aliphatic tertiary amine is a proton adduct of triethylamine, a proton adduct of tri-n-butylamine or a doubly protonated adduct of tetramethylethylenediamine.

8. The method for producing a phosphoryl imide salt according to claim 1 , wherein B is a chloride ion, a sulfate ion or a carbonate ion.

9. The method for producing a phosphoryl imide salt according to claim 1 , wherein R 1 and R 2 are each independently a methoxy group or a fluorine atom,
R 3 is a trifluoromethyl group, a methyl group, a vinyl group, a methoxy group, a propargyloxy group, a 1,1,1,3,3,3-hexafluoroisopropoxy group, a trifluoroethoxy group or a fluorine atom, and
R 4 is a fluorine atom.

10. The method for producing a phosphoryl imide salt according to claim 1 , wherein the cation exchange resin is a cation exchange resin having a sulfonate group.

11. The method for producing a phosphoryl imide salt according to claim 1 , wherein the organic solvent is at least one selected from the group consisting of carbonate esters, chain esters, ethers and ketones.

12. The method for producing a phosphoryl imide salt according to claim 11 , wherein the carbonate esters are selected from the group consisting of dimethyl carbonate, ethyl methyl carbonate and diethyl carbonate,
the chain esters are selected from the group consisting of methyl acetate, ethyl acetate, methyl propionate and ethyl propionate,
the ethers are selected from the group consisting of tetrahydrofuran, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, triethylene glycol dimethyl ether, tetraethylene glycol dimethyl ether and 1,2-dimethoxyethane, and
the ketones are selected from the group consisting of acetone and ethyl methyl ketone.

13. A method for producing a nonaqueous electrolyte solution, which comprises the steps of:
(1) performing cation exchange by bringing a phosphoryl imide salt represented by the following general formula (2) into contact with a cation exchange resin having M 1 n+ or a metal salt represented by the general formula (4) in an organic solvent having a water content of 0.3% by mass or less, so as to produce a phosphoryl imide salt represented by the following general formula (1):

wherein M 1 n+ is an alkali metal cation, an alkaline earth metal cation, a quaternary ammonium cation or a quaternary phosphonium cation,
M 2 n+ any one of an alkali metal cation, an alkaline earth metal cation, a quaternary ammonium cation, a tertiary ammonium cation (a protonated form of a tertiary organic amine base), or a mixture thereof,
a cation M 1 n+ of the product is different from a cation M 2 n+ of the raw material,
N is a nitrogen atom, P is a phosphorus atom, and X is a sulfur atom or a phosphorus atom,
n is 1 or 2,
when X is a sulfur atom, m is 2 and R 4 is absent,
when X is a phosphorus atom, m is 1,
B is a chloride ion a sulfate ion a sulfonate ion or a carbonate ion, and
R 1 , R 2 , R 3 and R 4 are each independently selected from a fluorine atom, an alkyl group, an alkoxy group, an alkenyl group, an alkenyloxy group, an alkynyloxy group and an aryloxy group; and

(2) dissolving at least the resultant phosphoryl imide salt and a solute in a nonaqueous solvent.

14. The method for producing a nonaqueous electrolyte solution according to claim 13 , wherein the solute is at least one selected from the group consisting of LiPF 6 , LiBF 4 , LiPF 2 (C 2 O 4 ) 2 , LiPF 4 (C 2 O 4 ), LiP(C 2 O 4 ) 3 , LiBF 2 (C 2 O 4 ), LiB(C 2 O 4 ) 2 , LiPO 2 F 2 , LiN(F 2 PO) 2 , LiN(FSO 2 ) 2 , LiN(CF 3 SO 2 ) 2 , LiN(CF 3 SO 2 )(FSO 2 ), LiSO 3 F, NaPF 6 , NaBF 4 , NaPF 2 (C 2 O 4 ) 2 , NaPF 4 (C 2 O 4 ), NaP(C 2 O 4 ) 3 , NaBF 2 (C 2 O 4 ), NaB(C 2 O 4 ) 2 , NaPO 2 F 2 , NaN(F 2 PO) 2 , NaN(FSO 2 ) 2 , NaSO 3 F, NaN(CF 3 SO 2 ) 2 and NaN(CF 3 SO 2 )(FSO 2 ).

15. The method for producing a nonaqueous electrolyte solution according to claim 13 , wherein an amount of the phosphoryl imide salt to be added is in a range of 0.005 to 12.0% by mass based on the total amount of the nonaqueous solvent, the solute and the phosphoryl imide salt.

16. The method for producing a nonaqueous electrolyte solution according to claim 13 , further adding at least one additive selected from the group consisting of a fluorine-containing cyclic carbonate ester, an unsaturated bond-containing cyclic carbonate ester, a fluorine-containing chain carbonate ester, an ester, a cyclic sulfate ester, a cyclic sulfonate ester, an oxalatoborate, an oxalatophosphate, a difluorophosphate, a fluorosulfonate, a bissulfonyl imide salt, a bisphosphoryl imide salt, an aromatic compound, a nitrile compound and an alkylsilane.

17. The method for producing a nonaqueous electrolyte solution according to claim 13 , wherein the nonaqueous solvent is at least one selected

Assignees

• Central Glass Co Ltd

Inventors

• Takahashi Mikihiro
• Morinaka Takayoshi
• Shinmen Masutaka
• Terada Ryosuke

Classifications

• Y02T10/70

  Energy storage systems for electromobility, e.g. batteries · CPC title

• H01M2300/0028

  characterised by the solvent · CPC title

• H01M2300/0025

  Organic electrolyte · CPC title

• C07F9/26 Primary

  containing P-halide groups · CPC title

• C07F9/2483

  containing the structure P(=X)n-N-S (X = O, S, Se; n = 0, 1) · CPC title