IP Library Granted Patent US 7,956,205
Granted Patent B2
US 7,956,205 · App. 11/634,745 · Granted Jun 7, 2011

Peroxide reduction in functionalized vegetable oils

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Quick Facts
Patent No.
US 7,956,205
App. No.
11/634,745
Granted
Jun 7, 2011
Kind
B2
Abstract

Disclosed is a method for the reduction of residual peroxides in vegetable oils, preferably epoxidized vegetable oils using a phosphorous compound preferably alkyl/aryl substituted phosphite compounds or hypophosphorous acid and its derivatives.

Claims (20)

1. A method for producing a reduced peroxide content epoxidized vegetable oil product, consisting of:

providing a first composition consisting of epoxidized vegetable oil having an initial amount of peroxide; and

adding to the first composition a peroxide-reducing effective amount of hypophosphorous acid or a hydrocarbyl phosphite to form a mixture to yield a reduced peroxide content epoxidized vegetable oil product having a reduced amount of peroxide;

wherein the reduced amount is at least 25% less than the initial amount;

wherein said hydrocarbyl phosphite is represented by the general formula (I):

wherein R 1 , R 2 , and R 3 are independently selected from hydrogen, aryl hydrocarbon groups, and alkyl hydrocarbon group.

2. The method of claim 1 wherein the hydrocarbyl phosphite is added to the first composition in an amount of 0.001 to 10 weight percent by weight of the first composition.

3. The method of claim 1 wherein the hydrocarbyl phosphite is added to the first composition in an amount of 0.001 to about 1 weight percent by weight of the first composition.

4. The method according to claim 1 wherein the alkyl hydrocarbon group is a C1 to C20 branched or straight chain alkyl.

5. The method according to claim 1 wherein the aryl group is a phenyl or naphthyl group optionally substituted by C1 to C20 branched or straight chain alkyl or aryl groups.

6. The method according to claim 1 wherein R1, R2, and R3 are the same hydrocarbyl group.

7. The method according to claim 1 wherein R1 is hydrogen and R2 and R3 are independently alkyl or aryl.

8. The method according to claim 1 wherein R1, R2, and R3 are all alkyl.

9. The method according to claim 1 wherein R1, R2, and R3 are all aryl.

10. The method according to claim 1 wherein R1 is alkyl and R2 and R3 are aryl.

11. The method according to claim 1 wherein at least one of R1, R2, and R3 is a substituted aryl moiety in which a hydrogen has been replaced by an alkoxy radical, a thioalkyl radical, a halogen or other substituent which will not react with oxygen to produce undesirable hydroperoxide compounds.

12. The method according to claim 1 wherein said epoxidized vegetable oil is selected from the group consisting of soybean oil, sunflower seed oil, corn oil, coconut oil, hydrogenated soybean oil, groundnut oil, olive oil, hydrogenated cottonseed oil, rapeseed oil, palm olein, palm oil, hydrogenated rapeseed oil, and linseed oil.

13. The method according to claim 1 wherein said epoxidized vegetable oil is selected from the group consisting of soybean oil, linseed oil and rapeseed oil.

14. The method according to claim 1 wherein the epoxidized vegetable oil is selected from the group consisting of epoxidized soybean oil, epoxidized octyl tallate ester, and epoxidized linseed oil.

15. The method according to claim 1 wherein said hydrocarbyl phosphite is selected from the group consisting of triisodecyl phosphite, diphenyl 2-ethylhexyl phosphite, tris (nonyl phenyl) phosphite, tris (butyl phenyl) phosphite, trimethyl phosphite, triethyl phosphite, tris (2-ethylhexyl) phosphite, triisopropyl phosphite, triisoctyl phosphite, diisoctyl phosphite, distearyl phosphite, triisodecyl phosphite, triisoetyl phosphite, trilauryl phosphite, triphenyl phosphite, tristearyl phosphite, diphenyl phosphite, diphenyl isodecyl phosphite, diphenyl isooctyl phosphite, phenyl isodecyl phosphite, dilauryl phosphite, di-tridecyl phosphite, ethylhexyl diphenyl phosphite, diisoctyl octylphenyl phosphite, trioctyl phosphite, tridecyl phosphite, tridodecyl phosphite, tritridecyl phosphite, tripentadecyl phosphite, trioleyl phosphite, tricresyl phosphite, tris(2,4-tert-butylphenyl) phosphite, tricyclohexyl phosphite, phenyl dioctyl phosphite, phenyl didecyl phosphite, phenyl didodecyl phosphite, phenyl ditridecyl phosphite, phenyl ditetradecyl phosphite, phenyl dipentadecyl phosphite, octyl diphenyl phosphite, decyl diphenyl phosphite, undecyl diphenyl phosphite, dodecyl diphenyl phosphite, tridecyl diphenyl phosphite, tetradeyl diphenyl phosphite, pentadecyl diphenyl phosphite, oleyl diphenyl phosphite, stearyl diphenyl phosphite and dodecyl bis(2,4-di-tert-butylphenyl) phosphite.

Assignments (5)
AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Aug 28, 2015
From: GALATA CHEMICALS HOLDING COMPANY, LLC; GALATA CHEMICALS, LLC
To: WELLS FARGO BANK, NATIONAL ASSOCIATION, AS AGENT
Reel/Frame 036503/0794 →
RELEASE OF SECURITY INTEREST Recorded Aug 17, 2015
From: GARRISON LOAN AGENCY SERVICES, LLC, AS COLLATERAL AGENT
To: GALATA CHEMICALS LLC
Reel/Frame 036335/0503 →
SECURITY INTEREST Recorded Apr 4, 2014
From: GALATA CHEMICALS, LLC
To: GARRISON LOAN AGENCY SERVICES LLC, AS COLLATERAL AGENT
Reel/Frame 032601/0253 →
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 →