Abstract: An electrolyte composition includes: a sulfonylimide compound represented by the following general formula (1) as an electrolyte salt; and an amidosulfuric acid component. LiN(X1SO2)(X2SO2)??(1) (where X1 and X2 are identical to or different from each other, and each represent a fluorine atom, an alkyl group with a carbon number of 1 to 6, or a fluoroalkyl group with a carbon number of 1 to 6).

Abstract: In the present invention, a bis (fluorosulfonyl) imide metal salt is an alkali metal salt of bis (fluorosulfonyl) imide or an alkaline earth metal salt of bis (fluorosulfonyl) imide. The bis (fluorosulfonyl) imide metal salt has an average particle diameter of not less than 0.1 mm, or has an average moisture absorption rate of not more than 2.5 mass ppm/cm2·min when sealed in a PE bag having a thickness of 80 ?m and left for 30 minutes at 23° C. and 65% humidity.

Abstract: Provided is a method the enables easy production of bis(fluorosulfonyl)imide suitable for a non-aqueous electrolytic solution for a lithium ion secondary battery, etc. The method for producing a bis(fluorosulfonyl)imide alkali metal salt according to the present invention comprises reacting bis(fluorosulfonyl)imide with an alkali metal compound in a reaction solution containing an organic solvent, wherein the organic solvent includes at least one organic solvent (A) selected from the group consisting of carbonate solvents, cyclic ether solvents, linear ether solvents having two or more oxygen atoms in the molecule, cyclic ester solvents, sulfolane solvents, N,N-dimethyl formamide, dimethyl sulfoxide, and N-methyl oxazolidinone.

Abstract: Provided is a method the enables easy production of bis(fluorosulfonyl)imide suitable for a non-aqueous electrolytic solution for a lithium ion secondary battery, etc. The method for producing a bis(fluorosulfonyl)imide alkali metal salt according to the present invention comprises reacting bis(fluorosulfonyl)imide with an alkali metal compound in a reaction solution containing an organic solvent, wherein the organic solvent includes at least one organic solvent (A) selected from the group consisting of carbonate solvents, cyclic ether solvents, linear ether solvents having two or more oxygen atoms in the molecule, cyclic ester solvents, sulfolane solvents, N,N-dimethyl formamide, dimethyl sulfoxide, and N-methyl oxazolidinone.

Abstract: Provided is a method with which it is possible to conveniently produce bis(fluorosulfonyl)imide suitable as a nonaqueous electrolyte of a lithium ion secondary cell. The method for producing a bis(fluorosulfonyl)imide alkali metal salt of the invention is a production method for producing a bis(fluorosulfonyl)imide alkali metal salt by reacting bis(fluorosulfonyl)imide and an alkali metal halide in a reaction solution including an organic solvent, the method including a purification step for filtering out the bis(fluorosulfonyl)imide alkali metal from the solution after the reaction.

Abstract: A compound represented by the following formula (1): wherein R1, R2 and R3 each independently represent fluorine, an alkyl group having 1 to 6 carbon atoms or a fluoroalkyl group having 1 to 6 carbon atoms; and M+ represents an alkali metal ion.

Abstract: The present invention provides a method for producing a bis (fluorosulfonyl) imide alkali metal salt by a reaction of a mixture containing bis (fluorosulfonyl) imide and an alkali metal compound is provided. According to this method for producing a bis (fluorosulfonyl) imide alkali metal salt, a total of weight ratios of the bis (fluorosulfonyl) imide, the alkali metal compound and the bis (fluorosulfonyl) imide alkali metal salt to an entire reacted mixture is not less than 0.8, after the reaction.

Abstract: In the present invention, a bis (fluorosulfonyl) imide metal salt is an alkali metal salt of bis (fluorosulfonyl) imide or an alkaline earth metal salt of bis (fluorosulfonyl) imide. The bis (fluorosulfonyl) imide metal salt has an average particle diameter of not less than 0.1 mm, or has an average moisture absorption rate of not more than 2.5 mass ppm/cm2·min when sealed in a PE bag having a thickness of 80 ?m and left for 30 minutes at 23° C. and 65% humidity.