IP Library Granted Patent US 7,629,300
Granted Patent B2
US 7,629,300 · App. 12/333,938 · Granted Dec 8, 2009

Detergent / anti-oxidant additives for lubricants

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Quick Facts
Patent No.
US 7,629,300
App. No.
12/333,938
Granted
Dec 8, 2009
Kind
B2
Abstract

A composition is disclosed that comprises the reaction product of an acidic organic compound, a boron compound, and a basic organic compound. The composition is useful as a detergent additive for lubricants and hydrocarbon fuels.

Claims (61)

1. A composition comprising:

A) a lubricant, and

B) at least one reaction product of an acidic organic compound, a boron compound, and a basic organic compound, wherein the reaction product is a metal free detergent and wherein the acidic organic compound is selected from the group consisting of:

(A) alkyl substituted salicylic acids,

(B) di-substituted salicylic acids,

(C) oil soluble hydroxy carboxylic acids,

(D) salicylic acid calixarenes,

(E) sulfur-containing calixarenes,

(F) acids of the formula:

wherein R 1 is hydrocarbon or halogen, R 2 is hydrocarbon, and Ar is substituted or unsubstituted aryl,

(G) acids of the formula:

wherein X and X′ are independently selected from the group consisting of hydrogen, hydrocarbyl, and halogen, R is polymethylene or branched or unbranched alkylene, x is 0 or 1, and R 1 is hydrogen or hydrocarbyl,

(H) acids of the formula:

wherein

R 1 and R 2 are independently selected from the group consisting of hydrogen, hydrocarbyl groups, tertiary alkyl groups, and tertiary aralkyl groups, provided that both R 1 and R 2 are not hydrogen,

R 3 and R 4 are independently selected from the group consisting of hydrogen, hydrocarbyl groups, aralkyl groups, and cycloalkyl groups, and

x is from 0 to 24, inclusive; and

(I) salts of the foregoing acids; and

wherein the basic organic compound is selected from the group consisting of N-hydroxyalkyl-N′-alkyl-imidazolines, N-hydroxyalkyl-piperazines, N-hydroxyalkyl-N′-alkyl piperazines, N-hydroxyalkyl-N′-cycloalkyl-piperazines, N-hydroxyalkyl-N′-alkyl hexahydropyrimidines, N-hydroxyalkyl-N′-cycloalkyl hexahydropyrimidines, N-hydroxyalkyl-N′-alkyl hexahydropyridazines, N-hydroxyalkyl-N′-cycloalkyl hexahydropyridazines, N-hydroxyalkyl-piperidines, N-hydroxyalkyl-N′-alkyl-imidazolidines, N-hydroxyalkyl-N′-cycloalkyl-imidazolidines, N-hydroxyalkyl-pyrrolidine, N-hydroxyalkyl-pyrazolidine, N-hydroxyalkyl-hydrogenated 1,2,3,-triazole, N-hydroxyalkyl-hydrogenated 1,2,4,-triazole, N-hydroxyalkyl-hydrogenated indole, N-hydroxyalkyl-hydrogenated carbazole, N-hydroxyalkyl-hydrogenated quinoline, N-hydroxyalkyl-hydrogenated acridine, N-hydroxyalkyl-hydrogenated phenazine, N-oxyalkyl-N′-hydrocarbyl-saturated cyclic diazines, and N-hydroxyalkyl-N′-hydrocarbyl-saturated cyclic diazines.

2. The composition of claim 1 , wherein the boron compound is selected from the group consisting of boric acid, trialkyl borates, alkyl boric acids, dialkyl boric acids, boric oxide, boric acid complex, cycloalkyl boric acids, aryl boric acids, dicycloalkyl boric acids, diaryl boric acids, and substitution products of the foregoing with alkoxy groups, alkyl groups, alkyl groups, and combinations thereof.

3. The composition of claim 1 , wherein the basic organic compound is an organic nitrogen base compound comprising an N-hydroxyalkyl-N′-alkyl-imidazoline.

4. The composition of claim 1 , wherein the reaction product is:

wherein R 1 and R 2 are independently selected hydrocarbyl groups, a is an integer of 1 or 2, provided that, where a is 2, the R 1 groups are independently selected.

5. The composition of claim 4 , wherein the R 1 and R 2 groups are independently selected hydrocarbyl groups of from 1 to 50 carbon atoms.

6. The composition of claim 1 wherein the lubricant is a lubricating oil.

7. A method for reducing the formation of deposits in an internal combustion engine which comprises operating the engine with a lubricating oil containing the reaction product of an acidic organic compound, a boron compound, and a basic organic compound, wherein the reaction product is in an amount effective to reduce the friction, wherein the acidic organic compound is selected from the group consisting of

(A) alkyl substituted salicylic acids,

(B) di-substituted salicylic acids,

(C) oil soluble hydroxy carboxylic acids,

(D) salicylic acid calixarenes,

(E) sulfur-containing calixarenes,

(F) acids of the formula:

wherein R 1 is hydrocarbon or halogen, R 2 is hydrocarbon, and Ar is substituted or unsubstituted aryl,

(G) acids of the formula:

wherein X and X′ are independently selected from the group consisting of hydrogen, hydrocarbyl, and halogen, R is polymethylene or branched or unbranched alkylene, x is 0 or 1, and R 1 is hydrogen or hydrocarbyl,

H acids of the formula:

wherein

R 1 and R 2 are independently selected from the group consisting of hydrogen, hydrocarbyl groups, tertiary alkyl groups, and tertiary aralkyl groups, provided that both R 1 and R 2 are not hydrogen,

R 3 and R 4 are independently selected from the group consisting of hydrogen, hydrocarbyl groups, aralkyl groups, and cycloalkyl groups, and

x is from 0 to 24, inclusive; and

(I) salts of the foregoing acids; and

wherein the basic organic compound is selected from the group consisting of N-hydroxyalkyl-N′-alkyl-imidazolines, N-hydroxyalkyl-piperazines, N-hydroxyalkyl-N′-alkyl piperazines, N-hydroxyalkyl-N′-cycloalkyl-piperazines, N-hydroxyalkyl-N′-alkyl hexahydropyrimidines, N-hydroxyalkyl-N′-cycloalkyl hexahydropyrimidines, N-hydroxyalkyl-N′-alkyl hexahydropyridazines, N-hydroxyalkyl-N′-cycloalkyl hexahydropyridazines, N-hydroxyalkyl-piperidines, N-hydroxyalkyl-N′-alkyl-imidazolidines, N-hydroxyalkyl-N′-cycloalkyl imidazolidines, N-hydroxyalkyl-pyrrolidine, N-hydroxyalkyl-pyrazolidine, N-hydroxyalkyl-hydrogenated 1,2,3,-triazole, N-hydroxyalkyl-hydrogenated 1,2,4,-triazole, N-hydroxyalkyl-hydrogenated indole, N-hydroxyalkyl-hydrogenated carbazole, N-hydroxyalkyl-hydrogenated quinoline, N-hydroxyalkyl-hydrogenated acridine, N-hydroxyalkyl-hydrogenated phenazine, N-oxyalkyl-N′-hydrocarbyl-saturated cyclic diazines, N-hydroxyalkyl-N′-hydrocarbyl-saturated cyclic diazines.

8. The method of claim 7 , wherein the acidic organic compound is selected from the group consisting of:

(A) alkyl substituted salicylic acids, and

(B) di-substituted salicylic acids.

9. The method of claim 7 , wherein the boron compound is selected from the group consisting of boric acid, trialkyl borates, alkyl boric acids, dialkyl boric acids, boric oxide, boric acid complex, cycloalkyl boric acids, aryl boric acids, dicycloalkyl boric acids, diaryl boric acids, and substitution products of the foregoing with alkoxy groups, alkyl groups, alkyl groups, and combinations thereof.

10. The method of claim 7 , wherein the basic organic compound is an organic nitrogen base compound comprising an N-hydroxyalkyl-N′-alkyl-imidazoline.

11. The method of claim 7 , wherein the reaction product:

wherein R 1 and R 2 are independently selected hydrocarbyl groups, a is an integer of 1 or 2, provided that, where a is 2, the R 1 groups are independently selected.

12. The method of claim 11 wherein the R 1 and R 2 groups are independently selected hydrocarbyl groups of from 1 to 50 carbon atoms.

13. The composition of claim 1 , wherein the reaction product is in the range of from about 0.01 to about 15 wt % based on the total weight of the composition.

14. The composition of claim 1 , wherein the reaction product is a metal-free detergent and anti-oxidant.

15. A composition comprising:

A) a lubricant, and

B) at least one reaction product of (i) an acidic organic compound selected from the group consisting of alkyl substituted salicylic acids and di-substituted salicylic acids, (ii) a boron compound, and (iii) a N-hydroxy alkyl moiety, and the reaction product is:

wherein R 1 and R 2 are independently selected hydrocarbyl groups, a is an integer of 1 or 2, provided that, where a is 2, the R 1 groups are independently selected.

16. The composition of claim 15 , wherein the boron compound is selected from the group consisting of boric acid, trialkyl borates, alkyl boric acids, dialkyl boric acids, boric oxide, boric acid complex, cycloalkyl boric acids, aryl boric acids, dicycloalkyl boric acids, diaryl boric acids, and substitution products of the foregoing with alkoxy groups, alkyl groups, alkyl groups, and combinations thereof.

17. The composition of claim 15 , wherein the basic organic compound is N-hydroxyalkyl-N′-alkyl-imidazoline.

18. The composition of claim 15 , wherein the reaction product is in the range of from about 0.01 to about 15 wt % based on the total weight of the composition.

19. The composition of claim 15 , wherein the reaction product is a metal-free detergent.

20. The composition of claim 15 , wherein the reaction product is a metal-free detergent and anti-oxidant.

Assignments (12)
MERGER AND CHANGE OF NAME Recorded Jun 15, 2017
From: CHEMTURA CANADA CO./CIE; LANXESS CANADA CO./CIE
To: LANXESS CANADA CO./CIE
Reel/Frame 042826/0839 →
RELEASE OF AMENDED AND RESTATED SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 12, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
Reel/Frame 042452/0759 →
RELEASE OF THIRD LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 12, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
Reel/Frame 042452/0894 →
RELEASE OF FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042447/0508 →
RELEASE OF SECOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded May 11, 2017
From: BANK OF AMERICA, N.A.
To: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
Reel/Frame 042449/0001 →
CHANGE OF NAME Recorded May 9, 2017
From: CROMPTON CO./CIE
To: CHEMTURA CANADA CO./CIE
Reel/Frame 042490/0967 →
AMENDED AND RESTATED SECOND LIEN INTELLECTUAL PROPERY SECURITY AGREEMENT Recorded Jul 18, 2014
From: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 033360/0225 →
THIRD LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Jul 18, 2014
From: CHEMTURA CORPORATION; CROMPTON COLORS INCORPORATED; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION
To: BANK OF AMERICA, N.A.
Reel/Frame 033360/0325 →
FIRST LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT. Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N.A.
Reel/Frame 026028/0622 →
INTELLECTUAL PROPERTY SECURITY RELEASE AGREEMENT Recorded Mar 21, 2011
From: CITIBANK, N.A.
To: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; ASCK, INC; BIOLAB COMPANY STORE, LLC; AQUA CLEAR INDUSTRIES, LLC; ASEPSIS, INC.; BIOLAB TEXTILES ADDITIVES, LLC; BIOLAB, INC.; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GT SEED TREATMENT, INC.; ISCI, INC; GREAT LAKES CHEMICAL GLOBAL, INC.; HOMECARE LABS, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; NAUGATUCK TREATMENT COMPANY; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); MONOCHEM, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC; WRL OF INDIANA, INC.; BIOLAB FRANCHISE COMPANY, LLC
Reel/Frame 026039/0142 →
SECDOND LIEN INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Mar 21, 2011
From: CHEMTURA CORPORATION; BIOLAB FRANCHISE COMPANY, LLC; BIO-LAB, INC.; CROMPTON COLORS INCORORATED; CROMPTON HOLDING CORPORATION; CLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; HAOMECARE LABS, INC.; LAUREL INDUSTRIES HOLDINGS, INC.; RECREATIONAL WATER PRODUCTS, INC.; WEBER CITY ROAD LLC
To: BANK OF AMERICA, N. A.
Reel/Frame 027881/0347 →
AMENDED AND RESTATED INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Feb 22, 2010
From: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; AQUA CLEAR INDUSTRIES, LLC; ASCK, INC.; ASEPSIS, INC.; BIOLAB COMPANY STORE, LLC; BIOLAB FRANCHISE COMPANY, LLC; BIOLAB TEXTILE ADDITIVES, LLC; BIO-LAB, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON COLORS INCORPORATED; CROMPTON HOLDING CORPORATION; CROMPTON MONOCHEM, INC.; GLCC LAUREL, LLC; GREAT LAKES CHEMICAL CORPORATION; GREAT LAKES CHEMICAL GLOBAL, INC.; GT SEED TREATMENT, INC.; HOMECARE LABS, INC.; ISCI, INC.; KEM MANUFACTURING CORPORATION; LAUREL INDUSTRIES HOLDINGS, INC.; MONOCHEM, INC.; NAUGATUCK TREATMENT COMPANY; RECREATIONAL WATER PRODUCTS, INC.; UNIROYAL CHEMICAL COMPANY LIMITED (DELAWARE); WEBER CITY ROAD LLC; WRL OF INDIANA, INC.
To: CITIBANK, N.A.
Reel/Frame 023998/0001 →