IP Library Granted Patent US 6,943,202
Granted Patent B2
US 6,943,202 · App. 10/629,273 · Granted Sep 13, 2005

Radiation-curable polyurethane

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Quick Facts
Patent No.
US 6,943,202
App. No.
10/629,273
Granted
Sep 13, 2005
Kind
B2
Abstract

A radiation-curable polyurethane is obtained from the reaction of a low free diisocyanate polyurethane prepolymer and an acrylic monomer.

Claims (54)

1. A radiation-curable polyurethane produced by the process which comprises:

(a) reacting at least one diisocyanate monomer with a combination of a high molecular weight polyol and a low molecular weight polyol to provide a polyurethane prepolymer containing unreacted diisocyanate monomer, wherein each polyol is selected from the group consisting of polyether, polyester, polycarbonate, polycaprolactone and hydrocarbon polyols having a number average molecular weight of from about 60 to about 12,000;

b) removing unreacted diisocyanate monomer from the polyurethane prepolymer to provide polyurethane prepolymer of reduced unreacted diisocyanate monomer content; and,

c) reacting the polyurethane prepolymer of reduced unreacted diisocyanate monomer content with an acrylic monomer to provide radiation-curable polyurethane.

2. The radiation-curable polyurethane of claim 1 wherein the diisocyanate monomer is at least one diisocyanate monomer selected from the group consisting of 2,4 and 2,6 toluene diisocyanate, 4,4′-diphenyl methane diisocyanate, p-phenylene diisocyanate, tolidene diisocyanate, hexamethylene diisocyanate, tetramethylxylene diisocyanate, isophorone diisocyanate and dicyclohexylmethane diisocyanate.

3. The radiation-curable polyurethane of claim 1 wherein the polyether polyol is represented by the general formula HO(RO) n H, wherein R is an alkylene radical and n is an integer large enough that the polyether polyol has a number average molecular weight of at least about 250.

4. The radiation-curable polyurethane of claim 3 wherein the polyether polyol is a polytetramethylene ether glycol.

5. The radiation-curable polyurethane of claim 1 wherein the low molecular weight polyol is an aliphatic polyol selected from the group consisting of ethylene glycol, diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, neopentyl glycol, 1,3-butanediol, 1,4-butanediol, and the like.

6. The radiation-curable polyurethane of claim 1 wherein the low molecular weight polyol is less than about 20% of the combination of high molecular weight polyol and low molecular weight polyol.

7. The radiation-curable polyurethane of claim 6 wherein the low molecular weight polyol is up to about 15% of the combination of high molecular weight polyol and low molecular weight polyol.

8. A radiation-curable polyurethane produced by the process which comprises:

(a) reacting at least one diisocyanate monomer with at least one polyol to provide a polyurethane prepolymer containing unreacted diisocyanate monomer, wherein the polyol is selected from the group consisting of polyether, polyester, polycarbonate, polycaprolactone and hydrocarbon polyols having a number average molecular weight of from about 100 to about 12,000, and wherein the polyester polyol is a mixture of a polyester of butanediol, hexanediol and adipic acid;

(b) removing unreacted diisocyanate monomer from the polyurethane prepolymer to provide polyurethane prepolymer of reduced unreacted diisocyanate monomer content; and,

(c) reacting the polyurethane prepolymer of reduced unreacted diisocyanate monomer content with an acrylic monomer to provide radiation-curable polyurethane.

9. The radiation-curable polyurethane of claim 1 wherein the polyurethane prepolymer is of the general structure ABA wherein A denotes diisocyanate and B denotes a polyol.

10. The radiation-curable polyurethane of claim 1 wherein the removal of unreacted diisocyanate monomer from the polyurethane prepolymer is accomplished through a process of distillation.

11. The radiation-curable polyurethane of claim 10 wherein the process of distillation is accomplished through an agitated film distillation system.

12. The radiation-curable polyurethane of claim 11 wherein the agitated film distillation system comprises continuous units with internal condensers that can be combined in series.

13. The radiation-curable polyurethane of claim 10 wherein the process of distillation utilizes a wiped film vacuum distillation process.

14. The radiation-curable polyurethane of claim 1 wherein the removal of unreacted diisocyanate monomer from the polyurethane prepolymer reduces the content of unreacted diisocyanate monomer polyurethane prepolymer to less than about 2% by weight.

15. The radiation-curable polyurethane of claim 14 wherein the removal of unreacted diisocyanate monomer from the polyurethane prepolymer reduces the content of unreacted diisocyanate monomer polyurethane prepolymer to less than about 0.5% by weight.

16. A radiation-curable polyurethane produced by the process which comprises:

(a) reacting at least one diisocyanate monomer with at least one polyol to provide a polyurethane prepolymer containing unreacted diisocyanate monomer;

(b) removing unreacted diisocyanate monomer from the polyurethane prepolymer to provide polyurethane prepolymer of reduced unreacted diisocyanate monomer content, wherein the removal of unreacted diisocyanate monomer from the polyurethane prepolymer reduces the content of unreacted diisocyanate monomer polyurethane prepolymer to less than about 0.1% by weight; and,

(c) reacting the polyurethane prepolymer of reduced unreacted diisocyanate monomer content with an acrylic monomer to provide radiation-curable polyurethane.

17. The radiation-curable polyurethane of claim 1 wherein the acrylic monomer possesses at least one reactive functionality.

18. The radiation-curable polyurethane of claim 17 wherein the acrylic monomer possessing at least one reactive functionality is selected from the group consisting of vinyl carboxylic acid, acrylic acid, methacrylic acid, aminoalkyl acrylates, aminoalkyl methacrylates, hydroxyalkyl acrylates, hydroxyalkyl methacrylates and mixtures thereof.

19. The radiation-curable polyurethane of claim 18 wherein the hydroxyalkyl acrylate is selected from the group consisting of hydroxyethyl acrylate, hydroxyethyl methacrylate, hydroxypropyl acrylate, hydroxypropyl methacrylate, hydroxybutylacrylate and mixtures thereof.

20. The radiation-curable composition of claim 1 wherein the polyurethane prepolymer of reduced unreacted diisocyanate monomer content is end-capped with an acrylate.

21. The radiation-curable polyurethane of claim 1 wherein the reaction of at least one diisocyanate monomer with the combination of polyols provides for a molar excess of diisocyanate monomer over polyol.

22. The radiation-curable polyurethane of claim 21 wherein the molar excess of diisocyanate monomer over polyol is from about 2:1 to about 30:1 molar ratio.

23. The radiation-curable polyurethane of claim 22 wherein the molar excess of diisocyanate monomer over polyol is from about 3:1 to about 18:1 molar ratio.

24. The radiation-curable polyurethane of claim 23 wherein the reaction of at least one diisocyanate monomer with the combination of polyols has a solvent added thereto.

25. A radiation-curable polyurethane produced by the process which comprises:

(a) reacting at least one diisocyanate monomer with at least one polyol to provide a polyurethane prepolymer containing unreacted diisocyanate monomer, wherein the reaction of at least one diisocyanate monomer with at least one polyol provides for a molar excess of diisocyanate monomer over polyol from about 3:1 to about 20:1 molar ratio, and wherein the reaction of at least one diisocyanate monomer with at least one polyol has a solvent added thereto, wherein the solvent is selected from the group consisting of dimethyl adipate and dimethyl phthalate;

(b) removing unreacted diisocyanate monomer from the polyurethane prepolymer to provide polyurethane prepolymer of reduced unreacted diisocyanate monomer content; and,

(c) reacting the polyurethane prepolymer of reduced unreacted diisocyanate monomer content with an acrylic monomer to provide radiation-curable polyurethane.

26. The radiation-curable polyurethane of claim 1 formed from a prepolymer of step (b) having a NCO content of at least about 70% of the theoretical NCO content.

27. The radiation-curable polyurethane of claim 1 formed from a prepolymer of step (b) having a NCO content of at least about 80% of the theoretical NCO content.

28. The radiation-curable polyurethane of claim 18 wherein the hydroxyalkyl acrylate has a ratio of available hydroxyl functionality to the available NCO content of the polyurethane prepolymer of reduced unreacted diisocyanate monomer content of from about 0.9:1 to about 1.2:1.

29. The radiation-curable polyurethane of claim 28 wherein the hydroxyalkyl acrylate has a ratio of available hydroxyl functionality to the available NCO content of the polyurethane prepolymer of reduced unreacted diisocyanate monomer content of from about 1.05:1 to about 1.10:1.

30. The radiation-curable polyurethane of claim 1 wherein step (c) can have added thereto one or more inhibitors of free radical reactions in an amount of from about 50 ppm to about 1% by weight.

31. The radiation-curable polyurethane of claim 30 wherein the inhibitor of free radical reactions is 4-methoxyphenol.

32. The radiation-curable polyurethane of claim 1 wherein step (c) can have added thereto one or more catalysts in an amount of up to about 3% by weight.

33. The radiation-curable polyurethane of claim 1 wherein at the temperature of about 50° C. the viscosity is from about 500 to about 28,000 cps.

34. A radiation-curable polyurethane comprising:

a) a polyurethane prepolymer terminated with a diisocyanate monomer selected from the group consisting of 2,4- and 2,6-toluene diisocyanate, 4,4′-diphenyl methane diisocyanate, p-phenylene diisocyanate, tolidene diisocyanate, hexamethylene diisocyanate, tetramethylxylene diisocyanate, isophorone diisocyanate, and dicyclohexylmethane diisocyanate, said polyurethane prepolymer being the reaction product of one or more of the said diisocyanate monomers and at least one polyol selected from the group consisting of polyether, polyester, polycarbonate, polycaprolactone and hydrocarbon polyols having a number average molecular weight of from about 250 to about 10,000 from which unreacted diisocyanate monomer has been removed; said polyurethane prepolymer comprising no more than about 2 wt % free diisocyanate monomer and having at least about 80% of theoretical NCO content for pure ABA structure and;

b) an acrylic monomer possessing at least one reactive functionality selected from the group consisting of vinyl carboxylic acids, acrylic acid, methacrylic acid, aminoalkyl acrylates, aminoalkyl methacrylates, hydroxyalkyl acrylates, hydroxyalkyl methacrylates and mixtures thereof, said radiation-curable polyurethane containing a ratio of available hydroxy functionality of the hydroxyalkyl acrylate to NCO content of the prepolymer of reduced unreacted diisocyanate monomer content of from about 0.9:1 to about 1.2:1.

35. A substrate coated with a radiation-curable polyurethane produced by the process of claim 1 .

36. A substrate coated with a radiation-curable polyurethane produced by the process of claim 8 .

37. A substrate coated with a radiation-curable polyurethane produced by the process of claim 16 .

38. A substrate coated with a radiation-curable polyurethane produced by the process of claim 25 .

39. The radiation-curable polyurethane of claim 1 wherein the high molecular weight polyol has a number average molecular weight of from about 250 to about 12,000 and the low molecular weight polyol has a number average molecular weight of from 60 to about 250.

40. The radiation-curable polyurethane of claim 1 wherein the high molecular weight polyol has a number average molecular weight of from about 400 to about 6,000.

Assignments (11)
CHANGE OF NAME Recorded Sep 25, 2018
From: CROMPTON CORPORATION
To: CHEMTURA CORPORATION
Reel/Frame 047141/0152 →
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 →
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 →
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 →
SECURITY AGREEMENT Recorded May 12, 2009
From: CHEMTURA CORPORATION; A & M CLEANING PRODUCTS, LLC; AQUA CLEAR INDUSTRIES, LLC; ASCK, INC.; ASEPSIS, INC.; BIOLAB TEXTILE ADDITIVES, LLC; BIO-LAB, INC.; CNK CHEMICAL REALTY CORPORATION; CROMPTON HOLDING CORPORATION; CROMPTON COLORS INCORPORATED; CROMPTON MONOCHEM, INC.; 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.; BIOLAB COMPANY STORE, LLC; BIOLAB FRANCHISE COMPANY, LLC; GLCC LAUREL, LLC
To: CITIBANK, N.A.
Reel/Frame 022668/0658 →
RELEASE OF LIEN IN PATENTS Recorded Jul 13, 2005
From: DEUTSCHE BANK AG, NEW YORK BRANCH
To: CROMPTON CORPORATION
Reel/Frame 016513/0745 →
SECURITY AGREEMENT Recorded Nov 10, 2004
From: CROMPTON CORPORATION
To: DEUTSCHE BANK AG NEW YORK BRANCH
Reel/Frame 015370/0467 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 17, 2003
From: ZHU, ZHENYA; KHUDYAKOV, IGOR V.; ROSENBERG, RONALD O.
To: CROMPTON CORPORATION
Reel/Frame 014696/0538 →