IP Library Granted Patent US 7,608,568
Granted Patent B2
US 7,608,568 · App. 11/706,116 · Granted Oct 27, 2009

Tetraaromatic diamine compounds as antioxidants

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Quick Facts
Patent No.
US 7,608,568
App. No.
11/706,116
Granted
Oct 27, 2009
Kind
B2
Abstract

Tetraaromatic diamine compounds having the general formula: are provided wherein a is 0-3; b, c and d independently are integers from 0-5, R 1 and R 2 together with the carbon atoms to which they are bonded are joined together to form a substituted or unsubstituted C 3 to about C 30 ring, saturated, partially unsaturated or fully unsaturated, optionally substituted with one or more heteroatoms, a is 0-3; b, c and d independently are integers from 0-5, R 3 , R 4 , R 5 and R 6 are independently hydrogen, a straight or branched C 1 -C 30 alkyl or alkylene group optionally substituted with one or more substituents, a substituted or unsubstituted C 3 -C 12 cycloalkyl, a substituted or unsubstituted C 5 -C 25 aryl, a substituted or unsubstituted C 6 -C 25 arylalkyl, a straight or branched C 1 -C 30 alkoxy group optionally substituted with one or more substituents or two R 4 substituents and/or two R 5 substituents and/or two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith can be joined together to form a substituted or unsubstituted C 3 to about C 30 ring, saturated, partially unsaturated or fully unsaturated, optionally substituted with one or more heteroatoms. Lubricating oil compositions containing the tetraaromatic diamine compound additives are also provided.

Claims (32)

1. A tetraaromatic diamine compound having the general formula:

wherein a is 0-3;

b, c and d independently are integers from 0-5,

R 1 and R 2 together with the carbon atoms to which they are bonded are joined together to form a saturated or partially saturated C 3 to about C 30 ring,

R 3 , R 4 , R 5 and R 6 are independently hydrogen, a straight or branched C 1 -C 30 alkyl or alkylene group optionally substituted with one or more substituents, a substituted or unsubstituted C 3 -C 12 cycloalkyl, a substituted or unsubstituted C 5 -C 25 aryl, a substituted or unsubstituted C 6 -C 25 arylalkyl, a straight or branched C 1 -C 30 alkoxy group optionally substituted with one or more substituents.

2. The tetraaromatic diamine compound of claim 1 , wherein R 1 and R 2 are joined together to form a saturated 5-, 6-, or 7-membered ring.

3. The tetraaromatic diamine compound of claim 1 , wherein R 1 and R 2 are joined together to form a partially unsaturated 5-, 6-, or 7-membered ring.

4. The tetraaromatic diamine compound of claim 1 , wherein two R 4 substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated or partially unsaturated C 3 to about C 30 ring.

5. The tetraaromatic diamine compound of claim 1 , wherein two substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated 5-, 6-, or 7-membered ring.

6. The tetraaromatic diamine compound of claim 1 , wherein two R 4 substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a partially unsaturated 5-, 6-, or 7-membered ring.

7. The tetraaromatic diamine compound of claim 1 , wherein R 1 and R 2 are joined together to form a saturated or partially unsaturated 5-, 6-, or 7-membered ring and two R 4 substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a substituted or unsubstituted and saturated or partially unsaturated 5-, 6-, or 7-membered ring.

8. A lubricating oil composition comprising

(a) at least one oil of lubricating viscosity and

(b) an antioxidant improving effective amount of at least one tetraaromatic diamine compound having the general formula:

wherein a is 0-3;

b, c and d independently are integers from 0-5,

R 1 and R 2 together with the carbon atoms to which they are bonded are joined together to form a saturated or partially saturated C 3 to about C 30 ring

R 3 , R 4 , R 5 and R 6 are independently hydrogen, a straight or branched C 1 -C 30 alkyl or alkylene group optionally substituted with one or more substituents, a substituted or unsubstituted C 3 -C 12 cycloalkyl, a substituted or unsubstituted C 5 -C 25 aryl, a substituted or unsubstituted C 6 -C 25 arylalkyl, a straight or branched C 1 -C 30 alkoxy group optionally substituted with one or more substituents.

9. The lubricating oil composition of claim 8 , wherein in the tetraaromatic diamine compound R 1 and R 2 are joined together to form a saturated 5-, 6-, or 7-membered ring.

10. The lubricating oil composition of claim 8 , wherein in the tetraaromatic diamine compound R 1 and R 2 are joined together to form a partially unsaturated 5-, 6-, or 7-membered ring.

11. The lubricating oil composition of claim 1 , wherein two R 4 substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated or partially unsaturated C 3 to about C 30 ring.

12. The lubricating oil composition of claim 8 , wherein in the tetraaromatic diamine compound R 1 and R 2 are joined together to form a saturated or partially unsaturated 5-, 6-, or 7-membered ring and two R 4 substituents and two R 5 substituents and two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated or partially unsaturated 5-, 6-, or 7-membered ring.

13. The lubricating oil composition of claim 8 , wherein the at least one oil of lubricating viscosity is selected from the group consisting of engine oils, transmission fluids, hydraulic fluids, gear oils, marine cylinder oils, compressor oils, refrigeration lubricants and mixtures thereof.

14. The lubricating oil composition of claim 8 , further comprising at least one lubricating oil additive selected from the group consisting of antioxidants, anti-wear agents, detergents, rust inhibitors, dehazing agents, demulsifying agents, metal deactivating agents, friction modifiers, pour point depressants, antifoaming agents, co-solvents, package compatibilisers, corrosion-inhibitors, ashless dispersants, dyes, extreme pressure agents and mixtures thereof.

15. The lubricating oil composition of claim 8 , further comprising at least one lubricating oil additive selected from the group consisting of an alkylated diphenylamine, alkylated hindered phenolic, alkylated substituted or unsubstituted phenylenediamine, alkylated oil soluble copper compound, alkylated sulfur containing compound known to impart oxidation stability and mixtures thereof.

16. The lubricating oil composition of claim 15 , wherein the alkylated sulfur containing compound known to impart oxidation stability is selected from the group consisting of phenothiazines, sulfurized olefins, thiocarbamates, sulfur bearing hindered phenolics, zinc dialkyldithiophosphates and mixtures thereof.

17. The lubricating oil composition of claim 8 , having a phosphorous content of less than about 0.1 weight percent.

18. An additive package comprising about 1 to about 75 weight of at least one tetraaromatic diamine compound of claim 1 .

19. A stabilizer-containing composition comprising (a) an organic material subject to oxidative, thermal, and/or light-induced degradation and in need of stabilization to prevent or inhibit such degradation; and (b) a stabilization effective amount of at least one tetraaromatic diamine compound of claim 1 .

20. A method for stabilizing an organic material subject to oxidative, thermal, and/or light-induced degradation and in need of stabilization to prevent or inhibit such degradation, the method comprising adding to the organic material a stabilizing amount of at least one tetraaromatic diamine compound of claim 1 .

21. The tetraaromatic diamine compound of claim 1 , wherein two R 4 substituents and/or two R 5 substituents and/or two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated or partially saturated C 3 to about C 30 ring.

22. The lubricating oil composition of claim 8 , wherein two R 4 substituents and/or two R 5 substituents and/or two R 6 substituents on adjacent carbon atoms of the aromatic ring associated therewith are joined together to form a saturated or partially saturated C 3 to about C 30 ring.

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 →