US2003065046A1PendingUtilityA1
Process for rigid polyurethane foams
Est. expiryApr 2, 2018(expired)· nominal 20-yr term from priority
Inventors:Alan J. Hamilton
Y10T428/239C08G 2330/50C08J 2205/10Y10T428/233Y10T428/249987C08G 18/3848Y10T428/231Y10T428/249984C08J 2375/04C08J 9/0028C08G 18/10C08J 2205/05C08G 18/38C08G 2110/0025
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Claims
Abstract
Process for the preparation of open celled rigid polyurethane or urethane-modified polyisocyanurate foams by reaction of a polyfunctional isocyanate-reactive composition with a polyisocyanate composition comprising a prepolymer of NCO-value 21-30% based on a high molecular weight oxyethylene-containing polyol.
Claims
exact text as granted — not AI-modified1 . Process for the preparation of an open-celled (semi-)rigid polyurethane or urethane-modified polyisocyanurate foam by reaction of a polyisocyanate composition with a polyfunctional isocyanate-reactive composition under foam-forming conditions, characterised in that the polyisocyanate composition has a free NCO-value of 21 to 30% by weight and comprises the reaction product of a stoichiometric excess of an organic polyisocyanate and an isocyanate-reactive material comprising a polyether polyol having a number average molecular weight between 1000 and 10000 and an average nominal hydroxyl functionality of from 2 to 6 and containing from 10 to 50% by weight of oxyethylene units.
2 . Process according to claim 1 wherein the free NCO-value of the polyisocyanate composition is between 23 and 29 wt %.
3 . Process according to claim 2 wherein the free NCO-value of the polyisocyanate composition is between 24 and 26 wt %.
4 . Process according to any one of the preceding claims wherein the polyether polyol has a number average molecular weight between 1000 and 6000.
5 . Process according to any one of the preceding claims wherein the polyether polyol has an average nominal hydroxyl functionality of from 2 to 4.
6 . Process according to any one of the preceding claims wherein the polyether polyol has an oxyethylene content of between 15 and 35% by weight.
7 . Process according to any one of the preceding claims wherein the polyether polyol is a poly(oxyethylene-oxypropylene) polyol.
8 . Process according to any one of the preceding claims wherein at least 50% of the oxyethylene groups are present at the end of the polyether polyol.
9 . Process according to any one of the preceding claims wherein the isocyanate-reactive material in the reaction product is used in an amount from 2 to 25% by weight based on the reaction product.
10 . Process according to any one of the preceding claims wherein the organic polyisocyanate is polymethylene polyphenylene polyisocyanate.
11 . Process according to any one of the preceding claims carried out in the presence of an isocyanate-reactive cyclic compound corresponding to the formula :
wherein Y is O or NR 1 wherein each R 1 independently is a lower alkyl radical of C 1 -C 6 or a lower alkyl radical substituted with an isocyanate-reactive group; each R independently is hydrogen, a lower alkyl radical of C 1 -C 6 or (CH 2 ) m —X wherein X is an isocyanate-reactive group which is OH or NH 2 and m is 0, 1 or 2;
and n is 1 or 2; with the proviso that at least one of R 1 or R is or comprises an isocyanate-reactive group.
12 . Process according to claim 11 wherein the isocyanate-reactive cyclic compound corresponds to the formula (II) or (III):
13 . (Semi-)rigid open-celled polyurethane or urethane-modified polyisocyanurate foam obtainable by a process as defined in any one of claims 1 to 12 .
14 . Evacuated insulation panel comprising a filler material and vessel formed of a gastight film enveloping said filler, characterised in that said filler material comprises a (semi-)rigid open-celled polyurethane or urethane-modified polyisocyanurate foam as defined in claim 13 .
15 . Polyisocyanate composition having a free NCO-value of 21 to 30% by weight comprising the reaction product of a stoichiometric excess of an organic polyisocyanate and an isocyanate-reactive material comprising a polyether polyol having a number average molecular weight between 1000 and 10000 and an average nominal hydroxyl functionality of from 2 to 6 and containing from 10 to 50% by weight of oxyethylene units.Join the waitlist — get patent alerts
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