Polysiloxane-modified polyisocyanates, processes for preparing the same, and polyurethanes containing the same
Processes for preparing siloxane-modified polyisocyanates, the processes comprising: providing a polyisocyanate reactant; and reacting the polyisocyanate reactant with a hydroxyl-containing siloxane having a number-average molecular weight of 200 to 3000 g/mol and an average OH functionality of greater than or equal to 1.8, and corresponding to the general formula (I): wherein X represents an aliphatic, unbranched or branched C 1 to C 20 radical optionally containing ether groups; R represents a hydroxyl-functional radical; R 1 represents a hydrogen or an optionally heteroatom-containing C 1 to C 20 hydrocarbon radical; and n is 1 to 40; siloxane-modified polyisocyanates prepared thereby, and uses therefor.
1. A process for producing a siloxane-modified polyisocyanate, the process comprising:
providing a polyisocyanate reactant; and
reacting the polyisocyanate reactant with a hydroxyl-containing siloxane and optionally, a blocking agent, to form a siloxane-modified polyisocyanate, wherein the hydroxyl-containing siloxane has a number-average molecular weight of 200 to 3000 g/mol and an average OH functionality of greater than or equal to 2, and corresponding to the general formula (I):
wherein each X independently represents an aliphatic, unbranched or branched C 1 to C 10 radical optionally containing one or more ether groups selected from the group consisting of —[—[O—CH 2 —CHZ] n′ —O—]— wherein each Z independently represents an H or a methyl group and n′ is 1 to 12, and —[—CH2-O—(CH2) r -]- wherein r is 1 to 4;
wherein each R independently represents a hydroxyl-functional radical selected from the group consisting of: (i) hydroxyfunctional carbon acid ester moieties of the formula (a)
wherein x is 3 to 5; and (ii) hydroxyalkyl-functional amino group of Formula (b)
wherein R 2 represents a substituent selected from the group consisting of H, methyl, ethyl, n-propyl, iso-propyl, cyclohexyl radicals, 2-hydroxyethyl, 2-hydroxypropyl, and 3-hydroxypropyl, and wherein R 3 represents a substituent selected from the group consisting of 2-hydroxyethyl, 2-hydroxypropyl and 3-hydroxypropyl; each R 1 independently represents a hydrogen or an optionally heteroatom-containing C 1 to C 10 hydrocarbon radical; and n is 1 to 40.
2. The process according to claim 1 , wherein the polyisocyanate reactant is reacted with the hydroxyl-containing siloxane and a blocking agent.
3. The process according to claim 1 , wherein the polyisocyanate reactant comprises one or more functional groups selected from the group consisting of uretdione, isocyanurate, allophanate, biuret, iminooxadiazinedione, oxadiazinetrione and combinations thereof.
4. The process according to claim 1 , wherein the polyisocyanate reactant comprises one or more compounds prepared from one or more diisocyanates selected from the group consisting of isophorone diisocyanate, diisocyanatodiphenylmethane, diisocyanatotoluene, diisocyanatohexane, and mixtures thereof.
5. The process according to claim 1 , wherein R 1 represents a phenyl or a methyl group.
6. The process according to claim 1 , wherein the polyisocyanate reactant has an amount of free NCO groups, the hydroxyl-containing siloxane of the formula (I) has an amount of NCO-reactive OH groups, and a ratio of the free NCO groups to the NCO-reactive OH groups is 1:0.001 to 1:0.4.
7. The process according to claim 2 , wherein free NCO groups in the polyisocyanate reactant are blocked with the blocking agent.
8. The process according to claim 1 , wherein reacting the polyisocyanate reactant with the hydroxyl-containing siloxane is carried out in the absence of compounds having two or more hydroxyl groups, other than the hydroxyl-containing siloxane.