IP Library Granted Patent US 7,621,971
Granted Patent B2
US 7,621,971 · App. 12/334,065 · Granted Nov 24, 2009

Detergent/anti-oxidant additives for fuels

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Quick Facts
Patent No.
US 7,621,971
App. No.
12/334,065
Granted
Nov 24, 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 (32)

1. A composition comprising:

A) a hydrocarbon fuel, and

B) at least one reaction product of an acidic organic compound, a boron compound, and a basic organic compound selected from the group consisting of: 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, 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.

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 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.

4. The composition of claim 3 , wherein the R 1 and R 2 groups are independently selected hydrocarbyl groups of from 1 to 50 carbon atoms.

5. 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.

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

7. A composition comprising:

A) a hydrocarbon fuel, 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) an organic nitrogen base compound comprising an N-hydroxy alkyl moiety, selected from the group consisting of: 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 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.

8. The composition 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.

9. The composition of claim 7 , 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.

10. The composition of claim 7 , wherein the reaction product is a metal-free detergent.

11. The composition of claim 7 , wherein the reaction product is a metal-free detergent and anti-oxidant.

Assignments (8)
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 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 →
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 →
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 →