IP Library Granted Patent US 7,521,401
Granted Patent B2
US 7,521,401 · App. 11/273,797 · Granted Apr 21, 2009

Dithiocarbamyl β-hydroxy fatty acid esters as additives for lubricants and fuels

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Quick Facts
Patent No.
US 7,521,401
App. No.
11/273,797
Granted
Apr 21, 2009
Kind
B2
Abstract

Fuels, especially hydrocarbon fuels, and lubricants, especially lubricating oils, contain dithiocarbamyl β-hydroxy fatty acid esters, a class of anti-corrosion, anti-wear, anti-fatigue, and extreme pressure additives that are derived from epoxidized fatty acid esters. The additives exhibit synergistic anti-wear activity in combination with phosphorus containing additives.

Claims (52)

1. A composition comprising at least one dithiocarbamyl β-hydroxy fatty acid ester having formula I or II:

wherein m=1 to about 20, R 1 is a hydrocarbyl group possessing from 1 to about 50 carbon atoms with or without substituents selected from alkyl, cycloalkyl, alkenyl, aryl and alkoxy groups, and with or without heteroatoms selected from oxygen, nitrogen, and sulfur, R 2 is a hydrocarbyl group possessing from 1 to about 20 carbon atoms with or without olefin, dialkyldithiocarbamyl, OH, ether, oxirane, SH, or thiirane functionalities, R 3 and R 4 can be the same or different and are independently hydrocarbyl groups possessing from 1 to about 12 carbon atoms.

2. The composition of claim 1 wherein m is from 1 to about 12, R 1 possesses from 1 to about 18 carbon atoms, and R 2 possesses from 1 to about 12 carbon atoms.

3. The composition of claim 1 wherein R 1 is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl, docosyl, tricosyl, tetracosyl, pentacosyl, triacontyl, isopropyl, isobutyl, isopentyl, isohexyl, isoheptyl, isooctyl, 2-ethyl hexyl, sec-butyl, 1-methylbutyl, 1-ethylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, phenyl, tolyl, xylyl, benzyl, methoxyphenyl, methoxylmethyl, methoxyethyl, ethoxymethyl, ethoxyethyl and isomers thereof.

4. The composition of claim 1 wherein R 3 and R 4 are alkyl groups fused together to form a ring with or without N, O, or S, and with or without alkyl, alkenyl, aryl, or alkoxy substituents.

5. The composition of claim 1 wherein the dithiocarbamyl β-hydroxy fatty acid ester having formula I or II is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized fatty acid ester.

6. The composition of claim 1 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized oleic acid ester, or an epoxidized linoleic acid ester, or a mixture thereof.

7. The composition of claim 1 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a tallate ester.

8. The composition of claim 1 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a 2-ethylhexyl tallate ester.

9. The composition of claim 1 wherein the dithiocarbamyl β-hydroxy fatty acid ester has one of the following structures (A) or (B), or isomers thereof:

wherein:

R 1 is butyl, pentyl, hexyl, heptyl, 2-ethyl hexyl, or octyl, and R 3 and R 4 are independently butyl, pentyl, hexyl, heptyl, octyl, or 2-ethyl hexyl.

10. A composition comprising:

a) an oil of lubricant viscosity; and

b) at least one dithiocarbamyl β-hydroxy fatty acid ester having formula I or II:

wherein m=1 to about 20, R 1 is a hydrocarbyl group possessing from 1 to about 50 carbon atoms with or without substituents selected from alkyl, cycloalkyl, alkenyl, aryl and alkoxy groups, and with or without heteroatoms selected from oxygen, nitrogen, and sulfur, R 2 is a hydrocarbyl group possessing from 1 to about 20 carbon atoms with or without olefin, dialkyldithiocarbamyl, OH, ether, oxirane, SH, or thiirane functionalities, R 3 and R 4 can be the same or different and are independently hydrocarbyl groups possessing from 1 to about 12 carbon atoms.

11. The composition of claim 10 wherein m is from 1 to about 12, R 1 possesses from 1 to about 18 carbon atoms, and R 2 possesses from 1 to about 12 carbon atoms.

12. The composition of claim 10 wherein R 1 is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl, docosyl, tricosyl, tetracosyl, pentacosyl, triacontyl, isopropyl, isobutyl, isopentyl, isohexyl, isoheptyl, isooctyl, 2-ethyl hexyl, sec-butyl, 1-methylbutyl, 1-ethylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, phenyl, tolyl, xylyl, benzyl, methoxyphenyl, methoxylmethyl, methoxyethyl, ethoxymethyl, ethoxyethyl and isomers thereof.

13. The composition of claim 10 wherein R 3 and R 4 are alkyl groups fused together to form a ring with or without N, O, or S, and with or without alkyl, alkenyl, aryl, or alkoxy substituents.

14. The composition of claim 10 wherein the dithiocarbamyl β-hydroxy fatty acid ester having formula I or II is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized fatty acid ester.

15. The composition of claim 10 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized oleic acid ester, or an epozidized linoleic acid ester, or a mixture thereof.

16. The composition of claim 10 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a tallate ester.

17. The composition of claim 10 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a 2-ethylhexyl tallate ester.

18. The composition of claim 10 wherein the dithiocarbamyl β-hydroxy fatty acid ester has one of the following structures (A) or (B), or isomers thereof:

wherein:

R 1 is butyl, pentyl, hexyl, heptyl, 2-ethyl hexyl, or octyl, and R 3 and R 4 are independently butyl, pentyl, hexyl, heptyl, octyl, or 2-ethyl hexyl.

19. The composition according to claim 10 , further containing a zinc dihydrocarbyldithiophosphate.

20. The composition of claim 10 further containing one or more additives selected from the group consisting of:

at least one dispersant selected from the group consisting of polyisobutylene succinimides, polyisobutylene succinate esters and Mannich Base ashless dispersants,

at least one detergent selected from the group consisting of metallic and ashless alkyl phenates, metallic and ashless sulfurized alkyl phenates, metallic and ashless alkyl sulfonates, metallic and ashless alkyl salicylates, and metallic and ashless saligenin derivatives,

at least one antioxidant selected from the group consisting of alkylated diphenylamines, N-alkylated phenylenediamines, phenyl-α-naphthylamine, alkylated phenyl-α-naphthylamine, dimethyl quinolines, trimethyldihydroquinolines and oligomeric compositions derived therefrom, hindered phenolics, alkylated hydroquinones, hydroxylated thiodiphenyl ethers, alkylidenebisphenols, thiopropionates, metallic dithiocarbamates, 1,3,4-dimercaptothiadiazole and derivatives and oil soluble copper compounds,

at least one anti-wear additive selected from the group consisting of organo borates, organo-phosphites, organo-phosphates, organic sulfur-containing compounds, sulfurized olefins, sulfurized fatty acid derivatives (esters), chlorinated paraffins, zinc dialkyldithiophosphates, zinc diaryldithiophosphates, dialkyldithiophosphate esters, diaryl dithiophosphate esters and phosphosulfurized hydrocarbons,

at least one friction modifier selected from the group consisting of fatty acid esters and amides, organo molybdenum compounds, molybdenum dialkyldithiocarbamates, molybdenum dialkyl dithiophosphates, molybdenum disulfide, tri-molybdenum cluster dialkyldithiocarbamates and non-sulfur molybdenum compounds,

at least one polysiloxane anti-foamant,

at least one rust inhibitor selected from the group consisting of polyoxyalkylene polyol and benzotriazole derivatives,

at least one viscosity index improver selected from the group consisting of olefin copolymers and dispersant olefin copolymers and

at least one polymethacrylate pour point depressant.

21. The composition of claim 10 wherein the oil of lubricant viscosity is a natural or synthetic lubricating oil base stock fraction having a kinematic viscosity at 100° C. of about 2 to about 200 cSt.

22. A composition comprising:

a) a hydrocarbon fuel; and

b) at least one dithiocarbamyl β-hydroxy fatty acid ester having formula I or II:

wherein m=1 to about 20, R 1 is a hydrocarbyl group possessing from 1 to about 50 carbon atoms with or without substituents selected from alkyl, cycloalkyl, alkenyl, aryl and alkoxy groups, and with or without heteroatoms selected from oxygen, nitrogen, and sulfur, R 2 is a hydrocarbyl group possessing from 1 to about 20 carbon atoms with or without olefin, dialkyldithiocarbamyl, OH, ether, oxirane, SH, or thiirane functionalities, R 3 and R 4 can be the same or different and are independently hydrocarbyl groups possessing from 1 to about 12 carbon atoms.

23. The composition of claim 22 wherein m is from 1 to about 12, R 1 possesses from 1 to about 18 carbon atoms, and R 2 possesses from 1 to about 12 carbon atoms.

24. The composition of claim 22 wherein R 1 is selected from the group consisting of methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, hexadecyl, heptadecyl, octadecyl, nonadecyl, eicosyl, heneicosyl, docosyl, tricosyl, tetracosyl, pentacosyl, triacontyl, isopropyl, isobutyl, isopentyl, isoheptyl, isooctyl, sec-butyl, 1-methylbutyl, 1-ethylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclooctyl, phenyl, tolyl, xylyl, benzyl, methoxyphenyl, methoxylmethyl, methoxyethyl, ethoxymethyl, ethoxyethyl and isomers thereof.

25. The composition of claim 22 wherein R 3 and R 4 are alkyl groups fused together to form a ring with or without N, O, or S, and with or without alkyl, alkenyl, aryl, or alkoxy substituents.

26. The composition of claim 22 wherein the dithiocarbamyl β-hydroxy fatty acid ester having formula I or II is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized fatty acid ester.

27. The composition of claim 22 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with an epoxidized oleic acid ester, or an epozidized linoleic acid ester, or a mixture thereof.

28. The composition of claim 22 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a tallate ester.

29. The composition of claim 22 wherein the dithiocarbamyl β-hydroxy fatty acid ester of formula (I) and (II) is prepared by the reaction of an alkali metal dithiocarbamate or an ammonium dithiocarbamate with a 2-ethylhexyl tallate ester.

30. The composition of claim 22 wherein the dithiocarbamyl β-hydroxy fatty acid ester has one of the following structures, or isomers thereof:

wherein:

R 1 is butyl, pentyl, hexyl, heptyl, 2-ethyl hexyl, or octyl, and R 3 and R 4 are independently butyl, pentyl, hexyl, heptyl, octyl, or 2-ethyl hexyl.

Assignments (10)
MERGER AND CHANGE OF NAME Recorded Sep 7, 2018
From: CHEMTURA CORPORATION; LANXESS SOLUTIONS US INC.
To: LANXESS SOLUTIONS US INC.
Reel/Frame 046811/0266 →
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 →
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 →
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 →