IP Library Granted Patent US 7,867,294
Granted Patent B2
US 7,867,294 · App. 12/760,102 · Granted Jan 11, 2011

Triazine compounds for removing acids and water from nonaqueous electrolytes for electrochemical cells

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Quick Facts
Patent No.
US 7,867,294
App. No.
12/760,102
Granted
Jan 11, 2011
Kind
B2
Abstract

A process is provided to produce non-aqueous electrolytic solution for use in batteries having low acid content and low water content. The invention involves removing acids and water from non-aqueous electrolytic solutions typically found in lithium or lithium-ion batteries by using nitrogen-containing compounds such as triazines. After treatment by a triazine such as melamine, the concentrations of acids and water in the electrolytic solutions are substantially decreased. The present invention provides a process to prepare extremely pure electrolytic solutions having low (<20 ppm) concentrations of both water and acids.

Claims (44)

1. A method of making a secondary battery comprising:

providing an electrolytic solution comprising

i. a non-aqueous electrolytic solvent and

ii. a lithium containing salt;

contacting the electrolytic solution with a triazine compound selected from the group consisting of

2,6-bis-(2,4-dimethylphenyl)-4-(2-hydroxy-4-octyloxyphenyl)-s-triazine;

2,6-bis(2,4-dimethylphenyl)-4-(2,4-dihydroxyphenyl)-s-triazine;

2,4-bis(2,4-dihydroxyphenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2-hydroxy(2-hydroxyethoxy)phenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2-hydroxy-4-(2-hydroxyethoxy)phenyl)-phenyl-s-triazine;

2,4-bis(2-hydroxy-4-(2-hydroxyethoxy)-phenyl)-6-(2,4-dimethylphenyl)-s-triazine;

2,4-bis(2-hydroxy(2-hydroxyethoxy)phenyl)-6-(4-bromophenyl)-s-triazine;

2,4-bis(2-hydroxy-4-(2-acetoryethoxy)phenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2,4-dihydroxyphenyl)-6-(2,4-dimethylphenyl)-1-s-triazine;

2,4,6-trimethoxy-1,3,5-triazine;

2,4,6-triphenyoxy-1,3,5-triazine;

2,4,6-triethoxy-1,3,5-triazine;

2,4,6-tripropoxy-1,3,5-triazine;

2,4,6-tributoxy-1,3,5-triazine, and combinations thereof;

removing substantially all of the triazine compound from the electrolytic solution;

laminating and winding a cathode, a first porous separator, an anode, and a second porous separator;

placing the wound laminated electrodes and separators in a battery case;

infusing the electrolytic solution into the battery case; and,

sealing the battery case containing the electrodes, electrolytic solution and separators.

2. The method of claim 1 wherein the non-aqueous electrolytic solvent is selected from the group consisting of ethylene carbonate, propylene carbonate, butylene carbonate, dimethyl carbonate, diethyl carbonate, dipropyl carbonate, dibutyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, ethyl propyl carbonate, tetrahydrofuran, 2-methyl tetrahydrofuran, 1,3-dioxolane, 1,4-dioxane, 1,2-dimethoxyethane, 1,2-diethoxyethane, 1,2-dibutoxyethane, acetonitrile, dimethylformamide, methyl formate, ethyl formate, propyl formate, butyl formate, methyl acetate, ethyl acetate, propyl acetate, butyl acetate, methyl propionate, ethyl propionate, propyl propionate, butyl propionate, methyl butyrate, ethyl butyrate, propyl butyrate, butyl butyrate, γ-butyrolactone, 2-methyl-γ-butyrolactone, 3-methyl-γ-butyrolactone, 4-methyl-γ-butyrolactone, β-propiolactone, δ-valerolactone, trimethyl phosphate, triethyl phosphate, tris(2-chloroethyl) phosphate, tris(2,2,2-trifluoroethyl) phosphate, tripropyl phosphate, triisopropyl phosphate, tributyl phosphate, trihexyl phosphate, triphenyl phosphate, tritolyl phosphate, and combinations thereof.

3. The method of claim 1 wherein the lithium containing salt is selected from the group consisting of LiPF 6 , LiBF 4 , LiSbF 6 , LiAsF 6 , LiTaF 6 , LiAlCl 4 , Li 2 B 10 Cl 10 , LiBOB, LiBMB, LiBDFMB, LiMOB, LiDFMOB, LiTOP, LiTDFMP, LiClO 4 , LiCF 3 SO 3 ; LiN(SO 2 C m F 2m+1 )(SO 2 C n F 2n+1 ), and LiC(SO 2 C k F 2k+1 )(SO 2 C m F 2m+1 )(SO 2 C n F 2n+1 ), wherein k=1-10, m=1-10, and n=1-10, respectively; LiN(SO 2 C p F 2p SO 2 ), and LiC(SO 2 C p F 2p SO 2 )(SO 2 C q F 2q+1 ) wherein p=1-10 and q=1-10; and LiPF x (R F ) 6−x and LiBF y (R F ) 4−y , wherein R F represents perfluorinated C 1 -C 20 alkyl groups or perfluorinated aromatic groups, x=0-5, and y=0-3.

4. The method of claim 1 wherein the cathode comprises: a lithium mixed metal oxide selected from the group consisting of LiMnO 2 , LiMn 2 O 4 , LiCoO 2 , Li 2 Cr 2 O 7 , Li 2 CrO 4 , LiNiO 2 , LiFeO 2 , LiNi z Co 1−z O 2 (0<z<1), LiFePO 4 , Li 3 VPO 4 , LiMn 0.5 Ni 0.5 O 2 , LiMn 1/3 Co 1/3 Ni 1/3 O 2 , LiNi r Co s Me t O 2 wherein Me may be one or more of Al, Mg, Ti, B, Ga, or Si and 0<r,s,t<1, and LiMc 0.5 Mn 1.5 O 4 wherein Mc is a divalent metal, and mixtures thereof.

5. The method of claim 1 wherein the anode comprises a material selected from the group consisting of crystalline carbon, lithium metal, LiMnO 2 , Li 4 Ti 5 O 12 , LiAl, LiZn, Li 3 Bi, Li 3 Cd, Li 3 Sb, Li 4 Si, Li 4.4 Pb, Li 4.4 Sn, LiC 6 , Li 3 FeN 2 , Li 2.6 Co 0.4 N, Li 2.6 Cu 0.4 N, and combinations thereof.

6. A method of preparing a non-aqueous electrolytic solution for a lithium battery wherein the method comprises: contacting a non aqueous electrolyte with a triazine compound to produce an electrolytic solution comprising less than about 20 ppm water and less than about 50 ppm acids, wherein the triazine compound is selected from the group consisting of

2,6-bis-(2,4-dimethylphenyl)-4-(2-hydroxy-4-octyloxyphenyl)-s-triazine;

2,6-bis(2,4-dimethylphenyl)-4-(2,4-dihydroxyphenyl)-s-triazine;

2,4-bis(2,4-dihydroxyphenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2-hydroxy(2-hydroxyethoxy)phenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2-hydroxy-4-(2-hydroxyethoxy)phenyl)-phenyl-s-triazine;

2,4-bis(2-hydroxy-4-(2-hydroxyethoxy)-phenyl)-6-(2,4-dimethylphenyl)-s-triazine;

2,4-bis(2-hydroxy(2-hydroxyethoxy)phenyl)-6-(4-bromophenyl)-s-triazine;

2,4-bis(2-hydroxy-4-(2-acetoryethoxy)phenyl)-6-(4-chlorophenyl)-s-triazine;

2,4-bis(2,4-dihydroxyphenyl)-6-(2,4-dimethylphenyl)-1-s-triazine;

2,4,6-trimethoxy-1,3,5-triazine;

2,4,6-triphenyoxy-1,3,5-triazine;

2,4,6-triethoxy-1,3,5-triazine;

2,4,6-tripropoxy-1,3,5-triazine;

2,4,6-tributoxy-1,3,5-triazine, and combinations thereof.

7. The method of claim 6 wherein the method produces an electrolytic solution comprising less than about 10 ppm water and less than about 20 ppm acids.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 27, 2017
From: BASF CORPORATION
To: SHENZHEN CAPCHEM TECHNOLOGY CO., LTD.
Reel/Frame 043964/0545 →
CHANGE OF NAME Recorded Oct 12, 2016
From: NOVOLYTE TECHNOLOGIES INC.
To: NOVOLYTE LEGACY TECHNOLOGIES LLC.
Reel/Frame 040324/0215 →
MERGER Recorded Oct 12, 2016
From: NOVOLYTE LEGACY TECHNOLOGIES LLC.
To: BASF CORPORATION
Reel/Frame 040336/0890 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2012
From: SQUARE 1 BANK
To: SQUARE 1 BANK; NOVOLYTE TECHNOLOGIES, INC
Reel/Frame 028195/0781 →
RELEASE OF SECURITY INTEREST Recorded May 11, 2012
From: SQUARE 1 BANK
To: NOVOLYTE TECHNOLOGIES, INC
Reel/Frame 028195/0871 →