Reaction injection molding of stimuli-responsive thermosets
Disclosed are methods of using reaction injection molding to mold stimuli-responsive thermosets such as urethane linked poly(caprolactone) networks from polyols and polyisocyanates, as well as polymers prepared by such methods.
1. A method of making a stimuli-responsive thermoset, comprising:
combining at a pressure of from about 1100 psi to about 2000 psi a reaction mixture consisting essentially of a multifunctional isocyanate with a linear composite diol comprising a linear semi-crystalline polymer segment having a low polydispersity and one or more non-crystalline segments and an optional catalyst; and
injecting the reaction mixture into a mold where the multifunctional isocyanate crosslinks the linear composite diol, thereby forming a stimuli-responsive thermoset.
2. The method of claim 1 , wherein the multifunctional isocyanate and linear composite diol are recirculated before being combined.
3. The method of claim 1 , wherein mold is heated to about 30° C. or more.
4. The method of claim 1 , wherein the pressure is from about 1450 psi to about 1600 psi.
5. The method of claim 1 , wherein the amounts of multifunctional isocyanate and linear composite diol are such that hydroxyl groups and isocyanate groups are at a molar ratio of 0.8:1 to 1:0.8.
6. The method of claim 1 , wherein a portion of the linear composite diol is first combined with the multifunctional isocyanate followed by addition of the remainder of the linear or branched composite diol.
7. The method of claim 1 , wherein the linear semi-crystalline polymer segment is a linear polycaprolactone.
8. The method of claim 1 , wherein the non-crystalline segment comprises C 2 -C 10 alkyl.
9. The method of claim 1 , wherein the multifunctional polyisocyanate has from 2 to 6 isocyanate groups.
10. The method of claim 1 , wherein the multifunctional polyisocyanate is 1,3,5-tris(6-isocyanatohexyl)-1,3,5-triazinane-2,4,6-trione.
11. The method of claim 1 , wherein the reaction mixture further comprises a tin catalyst.
12. The method of claim 1 , wherein the multifunctional polyisocyanate is 1,3,5-tris(6-isocyanatohexyl)-1,3,5-triazinane-2,4,6-trione and the linear composite diol has linear polycaprolactone semi-crystalline segments and butyl non-crystalline segments and terminal hydroxyl groups.
13. The method of claim 1 , wherein the linear composite diol has a number average molecular weight of 500 g/mol or greater.
14. The method of claim 1 , wherein the reaction mixture comprises a prepolymer that is crystalline at room temperature.