Copolyester polyols, prepolymers, and polyurethane elastomers formed therefrom and processes for making same
View Patent ↗Polyurethane elastomers formed from prepolymers derived from copolyester polyols. The copolyester polyols have segments derived from one or more polyesters and caprolactone or polycaprolactone. The polyurethane elastomers have good hardness stability at temperatures ranging from 0° C. to 30° C. and preferably have good hydrolytic stability.
1. A process for making a polyurethane elastomer, comprising:
transesterifying
one or more polyesters selected from the group consisting of poly(ethylene adipate) glycol, poly(diethylene adipate) glycol, poly(ethylene/diethylene adipate) glycol, poly(ethylene/propylene adipate) glycol, poly(butylene adipate) glycol, poly(ethylene/butylene adipate) glycol, poly(butylene/hexamethylene adipate) glycol, poly(hexamethylene adipate) glycol, poly(neopentyl adipate) glycol, poly(hexamethylene/neopentyl adipate) glycol, poly(ethylene succinate) glycol, poly(diethylene succinate) glycol, poly(ethylene/diethylene succinate) glycol, poly(ethylene/propylene succinate) glycol, poly(butylene succinate) glycol, poly(ethylene/butylene succinate) glycol, poly(butylene/hexamethylene succinate) glycol, poly(hexamethylene succinate) glycol, poly(neopentyl succinate) glycol, poly(hexamethylene/neopentyl succinate) glycol, poly(hexamethylene decanedioate) glycol, poly(butylene/hexamethylene decanedioate) glycol, poly(hexamethylene dodecanedioate) glycol, poly(butylene/hexamethylene dodecanedioate) glycol, poly(hexamethylene adipate/dodecanedioate) glycol, poly(butylene/hexamethylene adipate/dodecanedioate) glycol, poly(hexamethylene azelate) glycol, poly(butylene/hexamethylene azelate) glycol, poly(hexamethylene adipate/azelate) glycol, poly(butylene/hexamethylene adipate/azelate) glycol, and mixtures thereof, with
a polycaprolactone to form a copolyester polyol wherein the polycaprolactone has a weight average molecular weight of from 400 to 10,000 amu and the weight ratio of the one or more polyesters to the polycaprolactone is from 1:5 to 5:1;
reacting the copolyester polyol with diphenylmethane diisocyanate or 2,4-toluene diisocyanate to form a prepolymer; and
curing the prepolymer with a diamine chain extender or a polyol chain extender selected from the group consisting of polybutadiene polyol, resorcinol di(beta-hydroxyethyl) ether , resorcinol di(beta-hydroxypropyl) ether, hydroquinone-bis-hydroxyethyl ether, 1,4-cyclohexane dimethanol, trimethylol propane, triisopropanolamine, triethanolamine; adducts of propylene oxide having molecular weights in the range of from 190 to 500 and adducts of ethylene oxide having molecular weights in the range of from 190 to 500, to form the polyurethane elastomer.
2. A process for making a polyurethane elastomer, comprising:
reacting (a) a dicarboxylic acid, or a dialkyl ester of a dicarboxylic acid selected from the group consisting of adipic acid, succinic acid, dimethyl succinate, decanedioic acid, dodecanedioic acid, azelaic acid, and mixtures thereof with (b) a glycol, and (c) a polycaprolactone in a reaction mixture to form a copolyester polyol wherein the polycaprolactone is present in an amount of 5 wt. % to 60 wt. %, based on the total weight of the reaction mixture;
reacting the copolyester polyol with diphenylmethane diisocyanate or 2,4-toluene diisocyanate to form a prepolymer; and
curing the prepolymer with a diamine chain extender or a polyol chain extender selected from the group consisting of polybutadiene polyol, resorcinol di(beta-hydroxyethyl) ether, resorcinol di(beta-hydroxypropyl) ether, hydroquinone-bis-hydroxyethyl ether, 1,4-cyclohexane dimethanol, trimethylol propane, triisopropanolamine, triethanolamine; adducts of propylene oxide having molecular weights in the range of from 190 to 500 and adducts of ethylene oxide having molecular weights in the range of from 190 to 500, to form the polyurethane elastomer.
3. The process of claim 2 , wherein the glycol is selected from the group consisting of ethylene glycol, propylene glycol, 1,3-propanediol, diethylene glycol, dipropylene glycol, 1,4-butanediol, 1,6-hexanediol, neopentyl glycol, 1,9-nonanediol, 1,10-decanediol, or 1,12-dodecaendiol; and mixtures thereof.
4. The process according to claim 1 wherein the diamine chain extender is selected from the group consising of 4,4′-methylene-bis(2-chloroaniline); 4,4′-methylene-bis(3-chloro-2,6-diethylaniline; diethyl toluene diamine; tertiary butyl toluene diamine; dimethylthio-toluene diamine; trimethylene glycol di-p-amino-benzoate; methylene bis orthochloroaniline, methylene bis diethylaniline; methylenedianiline; and
methylenedianiline-salt complexes.
5. The process according to claim 1 wherein the polyol chain extender is selected from the group consisting of polybutadiene polyol, resorcinol di(beta-hydroxyethyl) ether, trimethylol propane, triisopropanolamine, triethanolamine; and trimethylol propane ethylene oxide adducts.
6. The process according to claim 2 wherein the diamine chain extender is selected from the group consising of 4,4′-methylene-bis(2-chloroaniline); 4,4′-methylene-bis(3-chloro-2,6-diethylaniline; diethyl toluene diamine; tertiary butyl toluene diamine; dimethylthio-toluene diamine; trimethylene glycol di-p-amino-benzoate; methylene bis orthochloroaniline, methylene bis diethylaniline; methylenedianiline; and
methylenedianiline-salt complexes.
7. The process according to claim 2 wherein the polyol chain extender is selected from the group consisting of polybutadiene polyol, resorcinol di(beta-hydroxyethyl) ether , trimethylol propane, triisopropanolamine, triethanolamine;and trimethylol propane ethylene oxide adducts.