US 4,038,239 AGranted

Moisture curable polyurethane systems

AssigneeConTech Inc.

InventorsRobert N. Coyner, Peter Skujins

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Abstract

The disclosed process for making a high % solids, one-part, curable, essentially flowable or pumpable, high equivalent weight polyurethane (i.e., polyol-polyisocyanate adduct) prepolymer composition involves de-watering the polyol component of the reaction mixture with an alkaline earth metal oxide, preferably calcium oxide; adding the minimum acceptable level of catalyst for the NCO/polyol reaction; exothermically reacting a partially hindered aliphatic polyisocyanate such as isophorone diisocyanate (IPDI) and a partially hindered aromatic polyisocyanate such as 2,4-tolylene diisocyanate seriatim, so that at least about one-fourth of the IPDI reacts before the 2,4-TDI is added; and then adding more catalyst for the curing (e.g. moisture cure) reaction. Careful control over the amounts and selection of raw materials, proper selection of sequences of addition of these amounts and materials, careful de-watering of the reaction mixture, and proper adjustment or selection of isocyanate functionality minimizes random and undesired reactions and side reactions (e.g. chain extension) during prepolymer formation and insures good elastomeric properties in the ultimately cured product. As a result, this well-controlled prepolymer composition can be made efficiently with simple mixing equipment. One of the preferred coating or sealant uses for the prepolymer product is cured elastomeric coatings for the building industry, e.g. as a primary seal in roofing.

Claims10

Dependent claims

A process for making a one-part, moisture-reactive composition comprising a moisture-reactive isocyanate-terminated polyether-urethane prepolymer, said process comprising the steps of:

a. providing an isocyanate-reactive composition comprising:
an alkaline earth metal oxide, wherein the metal has an atomic weight ranging from 40 to 138, a catalyst for isocyanate/active hydrogen reations, and a liquid polyol composition having an average equivalent weight greater than 1000 and an average functionality greater than 2, said polyol containing at least one polyoxyalkylene chain;
the amounts of alkaline earth metal oxide being greater than the stoichiometric amount for reacting with all the water in said isocyanate-reactive composition;
b. exothermically reacting an aliphatic polyisocyanate, at least one of the free isocyanate radicals of said aliphatic polyisocyanate being substantially kinetically more reactive with respect to active hydrogen than any other said free isocyanate radicals;
c. after at least 25% of said free isocyanate radicals of said aliphatic polyisocyanate have reacted with said isocyanate-reactive composition, exothermically reacting said isocyanate-reactive composition with an aromatic polyisocyanate, at least one of the free isocyanate radicals of said aromatic polyisocyanate being substantially kinetically more reactive with respect to active hydrogen than any other said free isocyanate radicals of said aromatic polyisocyanate, the amounts of polyisocyanate being controlled such that the ratio of aromatic NCO equivalents to aliphatic NCO equivalents reacted with said isocyanate-reactive composition is at least about 1:1 but less than 7:1 and the NCO/OH ratio for the entire moisture curable composition is greater than about 1.8:1 but no more than about 3:1;
whereby a moisture-reactive isocyanate-terminated polyurethane prepolymer composition having an average NCO functionality greater than 1.8 but less than 3.0 is obtained as a result of steps (b) and (c), said isocyanate-terminated prepolymer composition, upon the addition of a curing catalyst for the isocyanate/water reaction, being curable under normal ambient conditions to a solid elastomer, which, in the form of a sheet-like article, has a tensile strength at break greater than 25 psi and an elongation at break greater than 200%;
d. applying said moisture-reactive isocyanate-terminated polyurethane prepolymer composition to a substrate and curing said composition.

4 more elements

A process for making a moisture-curable polyurethane coating composition having a viscosity less than 800,000 centipoise at 25.degree. C. and containing an organo-tin/tertiary amine moisture cure catalyst, said process comprising the steps of:

a. blending, at normal ambient temperatures, the components comprising:
(1) a liquid polyoxyalkylene polyol component having an average functionality of at least 2.5 but no greater than about 3.0 and an equivalent weight greater than 1000 but less than 3300;
(2) a minor amount, by weight, of a particulate solid component containing at least some pigment;
(3) an amount of particulate calcium oxide in excess of the amount needed to scavenge all the water in said polyol component and said filler component and to provide an alkaline environment for the resulting blend of components;
(4) 0.1-5% by weight of a petroleum distillate which is inert to isocyanate radicals and active-hydrogen-bearing radicals and has a boiling point greater than 30.degree. C. and a measurable vapor pressure at 0.degree. C. under normal atmospheric pressure;
and (5) no more than about 80% by weight of the total of the organo-tin component of said organo-tin/tertiary amine catalyst;
b. mixing the resulting blend until the water/calcium oxide reaction is completed and all water in the blend has been scavenged;
c. providing a polyurethane reaction mixture by adding, without the addition of heat, 2/7 to 5/6 NCO equivalents of isophorone diisocyanate per equivalent of polyol active hydrogen and permitting an essentially adiabatic exotherm to develop until the temperature of the resulting mixture indicates that at least 25% of the isocyanate radicals of the isophorone diisocyanate have been converted to urethane linkages;
d. adding, without any further addition of heat, sufficient tolylene diisocyanate to bring said reaction mixture including both reacted and unreacted isophorone diisocyanate, to an NCO/OH ratio of about 2:1 to about 2.5:1, and permitting an additional essentially adiabatic exotherm to develop until substantially all of the free hydroxyl in said reaction mixture has been converted to urethane linkages;
said tolylene diisocyanate consisting essentially of the 2,4-isomer thereof;
e. adding to said reaction mixture:
said tertiary amine catalyst component of said organo-tin/tertiary amine moisture-cure catalyst, an amount of monofunctional alcohol sufficient to adjust the isocyanate functionality of the adduct resulting from said reaction mixture to less than 3.0 but greater than about 2.7, and the balance of said organo-tin catalyst component of said organo-tin/tertiary amine moisture catalyst;
f. packaging the resulting product in substantially hermetically sealed containers;
g. coating said resulting product onto a roof for a building at normal ambient temperatures to a thickness of 1-200 mils, and
h. curing the coating with atmospheric moisture at normal ambient conditions to an essentially non-cellular elastomeric layer having a tensile strength at break of 50 - 300 psi and an elongation at break of 500 - 2000%.

12 more elements

Dependencies are inferred from the claim text.