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US4334052A Expired / Lapsed US ⏱️ 0.0 years remaining

Rigid, non-cellular polyurethane modified with reaction product of an isocyanate and an alcohol

Assignee: BASF Corp
•
Filing: 1981-03-13
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Granted: 1982-06-08
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Expires: 2001-03-13
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Abstract

Abstract Rigid, solid, non-cellular, urethane polymer compositions can be prepared which are the reaction product of at least one polyhydric alcohol with at least one organic polyisocyanate in the presence of a low molecular weight urethane modifier adduct which is the reaction product prepared, for instance, by reacting (1) at least one polyisocyanate and at least one monohydric alcohol or (2) at least one monofunctional isocyanate with at least one monohydric or polyhydric alcohol. Said adduct can also consist of mixtures of (1) and (2). Such polymers when prepared in the presence of any catalyst for urethane formation which is a liquid or solid at ambient temperature, set quickly to solid, rigid polymers having a density of at least one gram per cubic centimeter. They can be demolded after combining the materials, without the addition of heat from an external source, within a period of less than one minute to about 15 minutes. By proper selection of the urethane modifier adduct, flame-retardant polymers can be prepared.

Inventors

  • 👤 John T. Patton, Jr.
  • 👤 Herwart C. Vogt
  • 👤 Manher Parekh

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-27 15:11
CPC Classifications
C; C08; C08K; C08K5/00; C08K5/16; C08K5/205; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/80; C08G18/8003; C08G18/8061; C08G18/8064; C08G18/8083; C08G18/8087; C08L; C08L75/00; C08L75/04; C08L75/08

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 97 words
In the process for the preparation of a noncellular, solid urethane polymer composition prepared by the reaction of a polyoxyalkylene polyether polyol with an organic polyisocyanate in the absence of a trimization catalyst, the improvement comprising the addition of from about 2 percent by weight to 75 percent by weight based upon the total weight of the polyether polyol and the organic polyisocyanate, an isocyanate-free, hydroxyl group-free reaction product of an organic isocyanate with a monohydric or polyhydric compound containing from 1 to 4 hydroxyl groups and from 2 to 18 carbon atoms prior to said reaction.
Claim 2
Dependent Claim 97 words
In the process for the preparation of a noncellular, solid urethane polymer composition prepared by the reaction of a polyoxyalkylene polyether polyol with an organic polyisocyanate in the absence of a trimization catalyst, the improvement comprising the addition of from about 2 percent by weight to 75 percent by weight based upon the total weight of the polyether polyol and the organic polyisocyanate, an isocyanate-free, hydroxyl group-free reaction product of an organic isocyanate with a monohydric or polyhydric compound containing from 1 to 4 hydroxyl groups and from 2 to 18 carbon atoms prior to said reaction.
Claim 3
Dependent Claim 23 words
The process of claim 1 wherein said organic isocyanate is selected from the group consisting of phenyl isocyanate, toluene diisocyanate and diphenylmethane diisocyanate.
Claim 4
Dependent Claim 29 words
The process of claim 1 wherein said monohydric or polyhydric compound is selected from the group consisting of butanol, 2-ethylhexanol, glycerine, cyclohexanol, dipropylene glycol, butylene glycol, trimethylolpropane and pentaerythritol.
Claim 5
Dependent Claim 34 words
The process of claim 1 wherein said monohydric or polyhydric compound is selected from the group consisting of 2,4,4,4-tetrachloro-1-butanol, 2,3-dichloropropanol, 2,3,-dibromopropanol, 2-chloroethanol, 1,1,1,3,3,3-hexachloro-2-propanol, pentachlorophenol, 2-methylol-1,4,5,6,7,7-hexachlorobicyclo-2.2.1)-5-heptene, tetrabromobisphenol A, dibromobisphenol A, 2,3,-dibromobutanediol-1,4, dibromoneopentyl glycol, and 1,1,1-trichloro-2-propanol.

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-06-07 1985-12-07 1986-06-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-06-07 1989-12-07 1990-06-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-06-07 1993-12-07 1994-06-08 $7700.00 Window Closed / Lapsed

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