US4192937A — Process for the preparation of isocyanate polyadd…

Claim 1

Independent Claim 96 words

A process for the preparation of substantially linear isocyanate polyaddition products containing hydroxyl groups derived from oxazolidine groups in sidechains by the reaction of reactive systems which contain free isocyanate groups and oxazolidine groups with water, characterized in that (a) substantially linear prepolymers which have both isocyanate end groups and oxazolidine end groups or (b) a mixture containing substantially linear isocyanate prepolymers and bis-oxazolidines are chain lengthened by mixing with water, using a quantity of water calculated to provide at least about 1 mol of water per mol of oxazolidine groups present in the reaction mixture.

Claim 2

Dependent Claim 96 words

A process for the preparation of substantially linear isocyanate polyaddition products containing hydroxyl groups derived from oxazolidine groups in sidechains by the reaction of reactive systems which contain free isocyanate groups and oxazolidine groups with water, characterized in that (a) substantially linear prepolymers which have both isocyanate end groups and oxazolidine end groups or (b) a mixture containing substantially linear isocyanate prepolymers and bis-oxazolidines are chain lengthened by mixing with water, using a quantity of water calculated to provide at least about 1 mol of water per mol of oxazolidine groups present in the reaction mixture.

Claim 3

Dependent Claim 46 words

A process according to claim 1, characterized in that the prepolymers used are hydrophilically modified and/or contain an external emulsifier and water is used in a large excess in the chain-lengthening reaction so that the polyaddition products are directly obtained as an aqueous dispersion or solution.

Claim 4

Dependent Claim 20 words

Isocyanate polyaddition products containing hydroxyl groups derived from oxazolidine groups in side-chains obtainable according to the process of claim 1.

Claim 5

Dependent Claim 214 words

A process for the production of substantially linear isocyanate polyaddition products containing pendant hydroxyl groups derived from oxazolidine groups comprising reacting A. a reactive system selected from the group consisting of i. a mixture comprising a. bis-oxazolidines and b. a substantially linear, isocyanate prepolymer having (1) an average isocyanate functionality of from about 1.8 to 2.2, (2) an average molecular weight of from about 500 to 10,000, and (3) dispersing centers selected from the group consisting of chemically incorporated cationic or anionic groups present in said isocyanate prepolymer in from about 0 to 100 milliequivalents per 100 g of isocyanate prepolymer, chemically incorporated ethylene oxide units present in said isocyanate present in from about 0 to 30% by weight, based on the weight of the isocyanate prepolymer, and external emulsifiers present in about 0 to 30% by weight, based on the weight of the isocyanate prepolymer, and ii. the substantially linear, isocyanate prepolymer of (ib) above which in addition contains oxazolidine groups, said reactive system containing from about 0.6 to 1.1 mols of oxazolidine groups per mol of isocyanate groups, with B. water, wherein the water is present in the process in a sufficient amount to provide at least about 1 mol of water per mol of oxazolidine groups present in the reactive system.

Claim 6

Dependent Claim 214 words

A process for the production of substantially linear isocyanate polyaddition products containing pendant hydroxyl groups derived from oxazolidine groups comprising reacting A. a reactive system selected from the group consisting of i. a mixture comprising a. bis-oxazolidines and b. a substantially linear, isocyanate prepolymer having (1) an average isocyanate functionality of from about 1.8 to 2.2, (2) an average molecular weight of from about 500 to 10,000, and (3) dispersing centers selected from the group consisting of chemically incorporated cationic or anionic groups present in said isocyanate prepolymer in from about 0 to 100 milliequivalents per 100 g of isocyanate prepolymer, chemically incorporated ethylene oxide units present in said isocyanate present in from about 0 to 30% by weight, based on the weight of the isocyanate prepolymer, and external emulsifiers present in about 0 to 30% by weight, based on the weight of the isocyanate prepolymer, and ii. the substantially linear, isocyanate prepolymer of (ib) above which in addition contains oxazolidine groups, said reactive system containing from about 0.6 to 1.1 mols of oxazolidine groups per mol of isocyanate groups, with B. water, wherein the water is present in the process in a sufficient amount to provide at least about 1 mol of water per mol of oxazolidine groups present in the reactive system.

Claim 7

Dependent Claim 111 words

The process of claim 4 wherein isocyanate prepolymer (ib) has (1) an average isocyanate functionality of from about 1.8 to 2.2, (2) an average molecular weight of from about 500 to 10,000, and (3) dispersing centers selected from the group consisting of chemically incorporated cationic or anionic groups present in said isocyanate prepolymer in from about 0.1 to 100 milliequivalents per 100 g. of isocyanate prepolymer, chemically incorporated ethylene oxide units present in said isocyanate present in from about 0.5 to 30% by weight, based on the weight of the isocyanate prepolymer, and external emulsifiers present in about 1 to 30% by weight, based on the weight of the isocyanate prepolymer.

Claim 8

Dependent Claim 30 words

The process of claim 5 wherein the substantially linear hydrophilic isocyanate prepolymers are prepared using a ratio of isocyanate groups to isocyanate-reactive hydrogen atoms of from about 1.05:1 to 10:1.

Claim 9

Dependent Claim 15 words

The process of claim 5 wherein the substantially linear, hydrophilic isocyanate prepolymers are prepared solvent-free.

Claim 10

Dependent Claim 161 words

The process of claim 4 wherein the oxazolidine groups of the isocyanate prepolymers and bis-oxazolidines are represented by the structural formula ##STR15## wherein R 1 and R 2 , which may be the same or different, represent hydrogen, aliphatic hydrocarbon groups having from 1 to 4 carbon atoms, cycloaliphatic hydrocarbon groups having from 5 to 7 carbon atoms or aromatic hydrocarbon groups having from 6 to 10 carbon atoms, or R 1 and R 2 together with the ring carbon atom may form a 5-membered or 6-membered cycloaliphatic hydrocarbon ring, X represents a group represented by the following formula: ##STR16## in which R 3 and R 4 which may be the same or different, represent hydrogen or C 1 -C 4 alkyl groups, and m represents 2 or 3, Y represents a group represented by the following formula: ##STR17## in which R 3 and R 4 have the meanings indicated above and n represents an integer of from 2 to 6.

Claim 11

Dependent Claim 31 words

The process of claim 4 wherein the water is present in the process in at least about 2 mols of water per mol of oxazolidine groups present in the reactive system.

Claim 12

Dependent Claim 20 words

Isocyanate polyaddition products containing pendant hydroxyl groups derived from oxazolidine groups produced by the processes of claims 4 or 5.

Annuity Stage	Window Opens	Payment Deadline	Surcharge Period Until	Estimated Fee	Status
3.5 Years (Year 4)	1983-03-11	1983-09-10	1984-03-11	$2000.00	Window Closed / Lapsed
7.5 Years (Year 8)	1987-03-11	1987-09-10	1988-03-11	$3760.00	Window Closed / Lapsed
11.5 Years (Year 12)	1991-03-11	1991-09-10	1992-03-11	$7700.00	Window Closed / Lapsed

Process for the preparation of isocyanate polyaddition products which have hydroxyl groups in side chains

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