Patent US4191818A successfully refreshed from Google Patents.
← Back to Patent Explorer
US4191818A Expired / Lapsed US ⏱️ 0.0 years remaining

Process for preparing heat-resistant polyurethane elastomers having no secondary softening range

Assignee: BASF Corp
•
Filing: 1978-07-10
•
Granted: 1980-03-04
•
Expires: 1998-07-10
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract Polyurethane elastomers of improved heat stability are made by a process in which a polyisocyanate is reacted with a polyol of high molecular weight with an OH:NCO ratio of 1:0.66 to 1:0.85, and the resulting adduct is later reacted with an excess of symmetrical diisocyanate and a diol as chain extender.

Inventors

  • 👤 Karl H. Illers
  • 👤 Herbert Stutz

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-23 13:50
CPC Classifications
C; C08; C08G; C08G18/00; C08G18/06; C08G18/70; C08G18/72; C08G18/74; C08G18/76; C08G18/7657; C08G18/7664; C08G18/7671; C08G18/08; C08G18/10; C08G18/721; C08G2250/00

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 164 words
A process for the production of a castable heat-resistant polyurethane elastomer from primarily linear and substantially difunctional high-molecular-weight polyhydroxyl compound, polyisocyanate, and chain extender, characterized in that the high-molecular-weight polyhydroxyl compound is first reacted with such a quantity of polyisocyanate that the ratio of OH:NCO groups amounts to 1:0.66 to 1:0.85 to obtain an adduct of polyhydroxyl compound and an organic diisocyanate, which adduct is substantially anhydrous, and contains terminal hydroxyl groups, the adduct with terminal hydroxyl groups is then reacted with a diol as a chain extender and an excess of a symmetrical aromatic diisocyanate and with the provisos that the ratio of the number of isocyanate groups to the total number of all hydrogen atoms capable of reacting with the isocyanate groups amounts to approximately 1.0 to 1.2:1, and said chain extender forms a crystalline or crystallizable urethane with said aromatic diisocyanate, thereby obtaining a castable material exhibiting a start of softening at an advanced temperature of about 180° C. or greater.
Claim 2
Dependent Claim 164 words
A process for the production of a castable heat-resistant polyurethane elastomer from primarily linear and substantially difunctional high-molecular-weight polyhydroxyl compound, polyisocyanate, and chain extender, characterized in that the high-molecular-weight polyhydroxyl compound is first reacted with such a quantity of polyisocyanate that the ratio of OH:NCO groups amounts to 1:0.66 to 1:0.85 to obtain an adduct of polyhydroxyl compound and an organic diisocyanate, which adduct is substantially anhydrous, and contains terminal hydroxyl groups, the adduct with terminal hydroxyl groups is then reacted with a diol as a chain extender and an excess of a symmetrical aromatic diisocyanate and with the provisos that the ratio of the number of isocyanate groups to the total number of all hydrogen atoms capable of reacting with the isocyanate groups amounts to approximately 1.0 to 1.2:1, and said chain extender forms a crystalline or crystallizable urethane with said aromatic diisocyanate, thereby obtaining a castable material exhibiting a start of softening at an advanced temperature of about 180° C. or greater.
Claim 3
Dependent Claim 29 words
A process according to claim 1 characterized by the fact that the symmetrical aromatic diisocyanate used as one selected from the group consisting of 4,4'-phenylenediisocyanate, 4,4'-diisocyanatodiphenylmethane, and 1,5-naphthalene diisocyanate.
Claim 4
Dependent Claim 28 words
A process according to claim 1 characterized by the fact that the chain extender used is one selected from the group consisting of ethylene glycol, 1,4-butanediol and 1,6-hexanediol.
Claim 5
Dependent Claim 24 words
A process according to claim 1 characterized by the fact that the poly- and diisocyanate consists of 4,4'-diisocyanatodiphenylmethane, and the chain extender is 1,4-butanediol.

References Cited (Backward Citations)

US2723935A Cited
US2871226A Cited
US2981719A Cited
US3192186A Cited
US3730927A Cited
US3905925A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-03-04 1983-09-03 1984-03-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-03-04 1987-09-03 1988-03-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-03-04 1991-09-03 1992-03-04 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag