Hard, optically clear polyurethane articles

• US 4,101,529 A
• Filed: 02/04/1976
• Issued: 07/18/1978
• Est. Priority Date: 02/04/1976
• Status: Expired due to Term

• Current Assignee: PPG Industries Incorporated (Nouryon BV)
• Original Assignee: PPG Industries Incorporated (Nouryon BV)
• Inventors: Ammons, Vernon G.
• Primary Examiner(s): Rzucidlo, Eugene C.
• Application Number:
  US05/655,184
• Time in Patent Office: 895 Days
• Field of Search: 260/2.5 AP, 260/2.5 AM, 260/2.5 AT, 260/77.5 AM, 260/77.5 AT
• US Class Current: 528/67
• CPC Class Codes: C08G 18/3206 aliphatic
• CPC Class Codes: C08G 18/44 Polycarbonates
• CPC Class Codes: C08G 18/6644 having at least three hydroxy groups
• CPC Class Codes: C08G 18/758 containing two or more cycloaliphatic rings

Abstract

Polyurethane compositions characterized by being heat curable to yield hard, impact-resistant articles having a high heat distortion temperature are disclosed. The cured polyurethane articles are transparent and also hydrolytic and UV light stable as well as being abrasion resistant. The polyurethane is prepared from a cycloaliphatic polyisocyanate, low molecular weight active hydrogen-containing material and optionally a polycarbonate diol. The weight percentage of the urethane moieties and the crosslinked density are carefully controlled so as to provide the proper balance of physical properties, particularly between hardness, flexibility and heat distortion temperature. The polyurethane articles are particularly useful in glazing applications such as aircraft glazing.

Claims

1. A polyurethane composition substantially free of ether linkages characterized by being heat curable to yield hard, impact-resistant articles having a Shore D hardness at room temperature of at least 75, said articles having a heat distortion temperature as determined according to ASTM D-648 of at least 190°

F. (88°

C.) and showing no visual change when exposed to ultraviolet light in accordance with ASTM G-25-70, Method A, comprising the reaction product of;

(A) a cycloaliphatic polyisocyanate,

(B) a low molecular weight active hydrogen-containing material containing only two active hydrogens per molecule,

(C) a low molecular weight active hydrogen-containing material having at least three active hydrogens per molecule, and optionally,

(D) a polymeric polycarbonate diol;

the equivalent ratio of (B)/(C) being within the range of 0.5 to 10/1, said reaction product having a calculated weight percentage of urethane linkages of at least 20 percent, a calculated molecular weight between branch points of 600-4,000 and the percentage by weight of cycloaliphatic structural units being within the range of 45 to 50.

2. The composition of claim 1 which when cured has a Shore D hardness at room temperature of at least 75;

a Gardner impact for a 1/8 inch thick specimen of at least 40 inch/pounds.

3. The composition of claim 1 which when cured has a tensile strength as determined according to ASTM D-638 of at least 12,000 pounds per square inch.

4. The composition of claim 3 which when cured retains at least 70 percent of its tensile strength after a 1000 hour exposure to a Weather-O-Meter according to ASTM D-1499-64.

5. The composition of claim 1 which when cured has less than an 18 percent increase in haze when subjected to 100 cycles on a Taber abrader using a CS-10F abrasion wheel at 500 grams of weight.

6. The composition of claim 1 in which the equivalent ratio of (B) plus (D) to (C) is within the range of 0.8 to 4.0/1.

7. The composition of claim 1 in which the cycloaliphatic polyisocyanate is a diisocyanate containing cyclohexyl moiety.

8. The composition of claim 7 in which the diisocyanate is 4,4'"'"'-methylene-bis-(cyclohexyl isocyanate).

9. The composition of claim 8 in which the 4,4'"'"'-methylene-bis-(cyclohexyl isocyanate) is in a stereo:

isomer ratio of 55 percent trans and 45 percent cis.

10. The composition of claim 1 in which (B) is a hydroxyterminated alkylene diol containing from 2 to 10 carbon atoms.

11. The composition of claim 10 in which the alkylene diol is selected from the class consisting of ethylene glycol, 1,4-butanediol and 1,6-hexanediol.

12. The composition of claim 1 in which (C) is an aliphatic triol.

13. The composition of claim 12 in which the aliphatic triol is selected from the class consisting of trimethylolpropane and trimethylolethane.

14. The composition of claim 1 in which the polycarbonate diol has a molecular weight of 700-2000.

15. The composition of claim 14 in which the polycarbonate diol is a poly(alkylenecarbonate) diol in which the alkylene groups contain from 5 to 10 carbon atoms.

16. The composition of claim 15 in which the alkylene moiety of the poly(alkylenecarbonate) diol is a cycloalkylene moiety.

17. The composition of claim 16 in which the cycloalkylene moiety is cyclohexyl.

18. The composition of claim 15 in which the alkylene moiety of the poly(alkylenecarbonate) diol is a mixed moiety selected from linear alkylene and cycloalkylene moieties.

19. The composition of claim 18 in which the cycloalkylene moiety is cyclohexyl dimethyl moiety.

20. The composition of claim 18 in which the mixed alkylene moieties are hexyl and cyclohexyl dimethyl moieties.

21. A polyurethane composition substantially free of ether linkages characterized by being heat curable to yield hard, impact-resistant articles having a Shore D hardness at room temperature of at least 75, said articles having a heat distortion temperature according to ASTM D-648 of at least 190°

F. (88°

C.) and showing no visual change when exposed to ultraviolet light in accordance with ASTM G-25-70, comprising the reaction product of;

(A) 4,4'"'"'-methylene-bis(cyclohexyl isocyanate),

(B) a low molecular weight active hydrogen-containing material selected from the class consisting of ethylene glycol, 1,4-butanediol and 1,6-hexanediol and mixtures thereof,

(C) trimethylolpropane;

the equivalent ratio of (A) to (B) and (C) being about 1 to 1, the equivalent ratio of (B) to (C) being within the range of 0.5 to 10/1;

said reaction product having a calculated weight percentage of urethane linkages of at least 20 percent, a calculated molecular weight between branch points of 600-4000 and the percentage by weight of the cycloaliphatic structural units being within the range of 45 to 50.