US4184031A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Control of cure rate of polyurethane resins
Assignee: ATK Launch Systems LLC
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Filing: 1977-10-11
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Granted: 1980-01-15
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Expires: 1997-10-11
Abstract
Abstract Curing catalysts comprising organo metallic compounds, and carboxylic acids or compounds convertible thereto, processes for their use and compositions containing them are disclosed. The compositions enable the control of the curing rate profile of hydroxy terminated polybutadiene based urethane propellant binders, and the cure rate profile of polyurethane resin systems generally.
Inventors
- 👤 William H. Graham
- 👤 Inella G. Shepard
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-26 03:33
CPC Classifications
C; C06; C06B; C06B45/00; C06B45/04; C06B45/06; C06B45/10; C08; C08G; C08G18/00; C08G18/06; C08G18/08; C08G18/089; C08G18/16; C08G18/161; C08G18/28; C08G18/67; C08G18/69
Claims Analysis
Total Claims: 10
Claim 1
Independent Claim
88 words
A curable composition comprising a hydroxy terminated polybutadiene, a polyisocyanate and an effective amount of a cure catalyst therefor, said catalyst comprising a metallo organic compound of the formula MR m where M is an m-valent metal selected from bismuth, lead, tin, arsenic, zinc, copper, cadmium or potassium and R is phenyl, tolyl, benzyl, naphthyl, alkyl of 1 to 20 carbon atoms or cycloalkyl of 5 to 20 carbon atoms and a carboxylic acid or a compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen.
Claim 2
Dependent Claim
88 words
A curable composition comprising a hydroxy terminated polybutadiene, a polyisocyanate and an effective amount of a cure catalyst therefor, said catalyst comprising a metallo organic compound of the formula MR m where M is an m-valent metal selected from bismuth, lead, tin, arsenic, zinc, copper, cadmium or potassium and R is phenyl, tolyl, benzyl, naphthyl, alkyl of 1 to 20 carbon atoms or cycloalkyl of 5 to 20 carbon atoms and a carboxylic acid or a compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen.
Claim 3
Dependent Claim
64 words
A curable composition which comprises a liquid polyurethane prepolymer, a polyurethane prepolymer curing agent and an effective amount of a cure catalyst therefor, said catalyst comprising a metallo organic compound of the formula MR m wherein M, R and m are as defined in claim 1, and a carboxylic acid or a compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen.
Claim 4
Dependent Claim
81 words
A process for the control of the pot life and the curing rate of a polyurethane casting or molding resin which comprises admixing with a curable liquid polyurethane prepolymer and a polyurethane prepolymer curing agent and an effective amount of a catalyst, said catalyst comprising a metallo organic compound of the formula MR m wherein M, R and m are as defined in claim 1 and a carboxylic acid or a compound convertible to a carboxylic acid by Zerewitinoff active hydrogen.
Claim 5
Dependent Claim
62 words
An article of manufacture comprising the reaction products of a liquid polyurethane prepolymer, a polyurethane prepolymer curing agent and a cure catalyst therefor, said cure catalyst comprising a metallo organic compound of the formula MR m wherein M, R and m are as defined in claim 1 and a carboxylic acid or a compound convertible thereto by reaction with Zerewitinoff active hydrogen.
Claim 6
Dependent Claim
162 words
A curable composition as defined in claim 2 wherein the liquid polyurethane prepolymer is selected from: polyester polyols, alkane diols of from 2 to 20 carbon atoms, alkene diols, cycloalkylene diols, carbocyclic aromatic diols, heterocyclic containing diols, polyalkylene ether polyols, polyalkylene thioether polyols, polyalkylene ether-thioether polyols, polyalkylenearylene ether polyols, polyalkylenearylene thioether polyols, polyalkylenearylene ether-thioether polyols, polyesteramide polyols, polyamino alcohols, ethylene disulfide, liquid polysulfide polymers, or polysulfide polymers having glycol end caps; and the polyurethane prepolymer curing agent is selected from polyisocyanates; or the liquid polyurethane prepolymer is selected from isocyanate terminated moieties derived from: polyester polyols, alkane diols of from 2 to 20 carbon atoms, alkene diols, cycloalkylene diols, carbocyclic aromatic diols, heterocyclic containing diols, polyalkylene ether polyols, polyalkylene thioether polyols, polyalkylene ether-thioether polyols, polyalkylenearylene ether polyols, polyalkylenearylene thioether polyols, polyesteramide polyols, polyamino alcohols, ethylene disulfide, liquid polysulfide polymers, or polysulfide polymers having glycol end caps; and the polyurethane prepolymer curing agent is selected from: polyhydroxyl compounds, polythiols, polyamines, or hydroxy amines.
Claim 7
Dependent Claim
29 words
A curable composition as defined in claim 5 wherein the liquid polyurethane prepolymer is selected from: polyester polyols, polyether polyols; or polyester polyols and polyether polyols terminated with isocyanates.
Claim 8
Dependent Claim
27 words
A curable composition as defined in claim 2 wherein the compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen is a carboxylic acid anhydride.
Claim 9
Dependent Claim
27 words
A curable composition as defined in claim 5 wherein the compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen is a carboxylic acid anhydride.
Claim 10
Dependent Claim
27 words
A curable composition as defined in claim 6 wherein the compound convertible to a carboxylic acid by reaction with Zerewitinoff active hydrogen is a carboxylic acid anhydride.
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USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1983-01-14 | 1983-07-16 | 1984-01-15 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1987-01-14 | 1987-07-16 | 1988-01-15 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1991-01-14 | 1991-07-16 | 1992-01-15 | $7700.00 | Window Closed / Lapsed |