IP Library Patent Application 12036877
Patent Application
App. No. 12/036,877

HIGH PERFORMANCE POLYURETHANE ELASTOMERS FROM MDI PREPOLYMERS WITH REDUCED CONTENT OF FREE MDI MONOMER

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Patent No.
US None
App. No.
12/036,877
Abstract

The invention is directed to polyurethane prepolymers having a reduced amount of unreacted monomeric diisocyanate, particularly diphenylmethane diisocyanate (MDI), prepared by distilling the prepolymer reaction product in the presence of at least one inert solvent whose boiling point is slightly below that of the monomeric diisocyanate; and to high performance cast polyurethane elastomers from the thus obtained prepolymers using diamine and/or diol chain extenders.

Claims (46)

1 . A polyurethane elastomer comprising the reaction product of:

A) a prepolymer comprising the reaction product of a polyol and diphenyl methane diisocyanate wherein unreacted diphenyl methane diisocyanate has been partially removed; and

B) methylenedianiline or its complex with sodium chloride.

2 . The polyurethane elastomer of claim 1 , wherein the polyol is selected from the group consisting of a polyester of adipic acid; a polyether of ethylene oxide, propylene oxide, or tetrahydrofuran; a polycaprolactone; a polycarbonate; a hydrocarbon polyol; ethylene glycol, isomers of propylene glycol, isomers of butane diol, hexanediol, trimethylolpropane, pentaerythritol, poly(tetramethylene ether) glycol, diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, and mixtures thereof.

3 . The polyurethane elastomer of claim 1 , wherein the polyol comprises a first polyol and a second polyol.

4 . The polyurethane elastomer of claim 3 , wherein the first polyol has a molecular weight in the range of from about 62 to about 400.

5 . The polyurethane elastomer of claim 3 , wherein the second polyol has a molecular weight in the range of from about 400 to about 5000.

6 . The polyurethane elastomer of claim 3 , wherein the molar ratio of the first polyol to the second polyol is in the range of from about 0.25 to about 2.5:1.

7 . The polyurethane elastomer of claim 1 , wherein the prepolymer contains less than 2% by weight of the unreacted diphenyl methane diisocyanate.

8 . The polyurethane elastomer of claim 1 , wherein the prepolymer contains less than 0.3% by weight of the unreacted diphenyl methane diisocyanate.

9 . The polyurethane elastomer of claim 1 , wherein the prepolymer contains less than 0.1% by weight of the unreacted diphenyl methane diisocyanate.

10 . The polyurethane elastomer of claim 1 , wherein the prepolymer contains less than 0.05% by weight of the unreacted diphenyl methane diisocyanate.

11 . The polyurethane elastomer of claim 1 , wherein the prepolymer contains at least about 80% of the theoretical NCO content for a pure ABA structure.

12 . The polyurethane elastomer of claim 1 , wherein the equivalent ratio of the prepolymer to the methylenedianiline is in the range of from about 0.7:1 to about 1.2:1.

13 . The polyurethane elastomer of claim 1 , wherein the unreacted diphenylmethane diisocyanate monomer is removed from the prepolymer by a process comprising distilling a solution comprising the prepolymer, the unreacted diphenylmethane diisocyanate and a solvent, the solvent consisting of an inert solvent having a boiling point about 1° C. to about 100° C. below the boiling point of the diphenylmethane diisocyanate monomer at a pressure of 10 torr, wherein the weight ratio of the inert solvent to the unreacted diphenylmethane diisocyanate monomer ranges from about 90:10 to about 10:90, and the inert solvent comprises about 5% to about 85% by weight of the total weight of the combination of the prepolymer plus solvents.

14 . The polyurethane elastomer of claim 1 , wherein the unreacted diphenylmethane diisocyanate monomer is removed from the prepolymer in a vacuum distillation operation.

15 . The polyurethane elastomer of claim 14 , wherein the vacuum distillation operation comprises at least three agitated film vacuum distillation stages in series, each at an evaporative temperature of up to about 150° C.

16 . The polyurethane elastomer of claim 1 , wherein the polyurethane elastomer has a tear split strength of at least 75 pli or more.

17 . The polyurethane elastomer of claim 1 , wherein the polyurethane elastomer has a Bashore rebound value of at least 50 or more.

18 . A tire, wheel or roll comprising the polyurethane elastomer of claim 1 .

19 . A tire, wheel or roll comprising the reaction product of:

A) a prepolymer comprising the reaction product of a polyol and diphenyl methane diisocyanate wherein unreacted diphenyl methane diisocyanate has been partially removed; and

B) an amine or diol chain extender.

20 . The tire, wheel or roll of claim 19 , further comprising a core and a cover, wherein the cover comprises the reaction product.

21 . The tire, wheel or roll of claim 19 , wherein the diol chain extender is selected from the group consisting of 1,4-butanediol; 1,3-propanediol; ethylene glycol; 1,6-hexanediol; hydroquinone-bis-hydroxyethyl ether; resorcinol di(beta-hydroxyethyl)ether; resorcinol di(beta-hydroxypropyl)ether; 1,4-cyclohexane dimethanol; an aliphatic triol; an aliphatic tetrol; and mixture thereof.

22 . The tire, wheel or roll of claim 19 , wherein the amine chain extender is selected from the group consisting of 4,4′-methylene-bis(2-chloroaniline); 4,4′-methylene-bis(3-chloro-2,6-diethylaniline); diethyl toluene diamine; t-butyl toluene diamine; dimethylthio-toluene diamine; trimethylene glycol di-p-amino-benzoate; methylenedianiline; methylenedianiline-sodium chloride complex; and mixtures thereof.

23 . The tire, wheel or roll of claim 19 , wherein the amine chain extender is methylenedianiline or its complex with sodium chloride.

24 . The tire, wheel or roll of claim 19 , wherein the polyol is selected from the group consisting of a polyester of adipic acid; a polyether of ethylene oxide, propylene oxide, or tetrahydrofuran; a polycaprolactone; a polycarbonate; a hydrocarbon polyol; ethylene glycol, isomers of propylene glycol, isomers of butane diol, hexanediol, trimethylolpropane, pentaerythritol, poly(tetramethylene ether) glycol, diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, and mixtures thereof.

25 . The tire, wheel or roll of claim 19 , wherein the prepolymer contains less than 2% by weight of the unreacted diphenyl methane diisocyanate.

26 . A process for producing a polyurethane elastomer comprising:

reacting a polyol and diphenyl methane diisocyanate to form a prepolymer;

distilling the prepolymer to at least partially remove excess diphenyl methane diisocyanate in the prepolymer; and

curing the prepolymer with methylenedianiline or its complex with sodium chloride.

27 . The process of claim 26 , further comprising mixing the diphenyl methane diisocyanate with a solvent, the solvent consisting of an inert solvent having a boiling point about 1° C. to about 100° C. below the boiling point of the diphenylmethane diisocyanate monomer at a pressure of 10 torr, wherein the weight ratio of the inert solvent to the unreacted diphenylmethane diisocyanate monomer ranges from about 90:10 to about 10:90, and the inert solvent comprises about 5% to about 85% by weight of the total weight of the combination of the prepolymer plus solvents.

28 . The process of claim 26 , wherein the prepolymer is distilled in at least three agitated film vacuum distillation stages in series, each at an evaporative temperature of up to about 150° C.

29 . The process of claim 26 , wherein the polyol is selected from the group consisting of a polyester of adipic acid; a polyether of ethylene oxide, propylene oxide, or tetrahydrofuran; a polycaprolactone; a polycarbonate; a hydrocarbon polyol; ethylene glycol, isomers of propylene glycol, isomers of butane diol, hexanediol, trimethylolpropane, pentaerythritol, poly(tetramethylene ether) glycol, diethylene glycol, triethylene glycol, dipropylene glycol, tripropylene glycol, and mixtures thereof.

30 . The process of claim 26 , wherein the polyol comprises a first polyol and a second polyol.

31 . The process of claim 30 , wherein the first polyol has a molecular weight in the range of from about 62 to about 400.

32 . The process of claim 30 , wherein the second polyol has a molecular weight in the range of from about 400 to about 5000.

33 . The process of claim 30 , wherein the molar ratio of the first polyol to the second polyol is in the range of from about 0.25 to about 2.5:1.

34 . The process of claim 26 , wherein the prepolymer contains less than 2% by weight of the unreacted diphenyl methane diisocyanate.

35 . The process of claim 26 , wherein the prepolymer contains less than 0.3% by weight of the unreacted diphenyl methane diisocyanate.

36 . The process of claim 26 , wherein the prepolymer contains less than 0.1% by weight of the unreacted diphenyl methane diisocyanate.

37 . The process of claim 26 , wherein the prepolymer contains less than 0.05% by weight of the unreacted diphenyl methane diisocyanate.

38 . The process of claim 26 , wherein the prepolymer contains at least about 80% of the theoretical NCO content for a pure ABA structure.

39 . The process of claim 26 , wherein the equivalent ratio of the prepolymer to the chain extender is in the range of from about 0.7:1 to about 1.2:1.

Assignments (9)
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 →
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 →
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 →
CHANGE OF NAME Recorded May 17, 2010
From: CROMPTON CORPORATION
To: CHEMTURA CORPORATION
Reel/Frame 024396/0850 →
CHANGE OF NAME Recorded May 17, 2010
From: CK WITCO CORPORATION
To: CROMPTON CORPORATION
Reel/Frame 024396/0891 →
CHANGE OF NAME Recorded May 17, 2010
From: WITCO CORPORATION
To: CK WITCO CORPORATION
Reel/Frame 024398/0108 →
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 →