US2021317036A1PendingUtilityA1

Thermoplastic cycloaliphatic polyamide matrix resins for next-generation energy absorbing applications

Assignee: U S ARMY RES LABORATORY ATTN RDRL LOC IPriority: Aug 10, 2015Filed: Jun 24, 2021Published: Oct 14, 2021
Est. expiryAug 10, 2035(~9 yrs left)· nominal 20-yr term from priority
C03C 25/50C03C 25/328B32B 2260/046C08J 2377/06B32B 27/12F41H 5/0485B32B 2262/106D06M 15/59B32B 2262/0269B32B 2262/14B32B 2571/02C08J 2375/04B32B 2262/101B32B 5/08D06M 17/00C08J 5/043B32B 2260/021B32B 2262/0253D06M 15/564B32B 2307/702B32B 2307/732C08J 5/042B32B 27/34C03C 25/1095
60
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

Provided are materials that include one or more cycloaliphatic polyamides integrated into or coated onto one or more structural fibers such as polyethylene fibers, aramid-fibers, glass fibers or carbon fibers. The resulting materials may be incorporated into composite articles suitable for use as protective equipment or structural layers.

Claims

exact text as granted — not AI-modified
I claim: 
     
         1 . An energy dissipating composite material comprising:
 a cycloaliphatic polyamide; and   a structural fiber, said cycloaliphatic polyamide impregnated into or coated onto said structural fiber.   
     
     
         2 . The material of  claim 1  wherein said cycloaliphatic polyamide matrix resin is amorphous. 
     
     
         3 . The material of  claim 1  wherein said thermoplastic cycloaliphatic polyamide matrix resin comprises a structure as a result of a stoichiometric reaction between a diamine and a diacid. 
     
     
         4 . The material of  claim 3  wherein said diamine is selected from the group consisting of: hexamethylenediamine; 1,4-phenyl-diamine (para-phenylenediamine); 1,3-phenyl-diamine (m-phenylenediamine); 1,4-diaminocyclohexane; 1,3-diaminocyclohexane; m-xylylenediamine; 4,4′-methylenebis(cyclohexylamine); 2,2,4-trimethyl hexamethylene diamine;
 2,4,4-trimethyl hexamethylene diamine; and any mixture thereof. 
 
     
     
         5 . The material of  claim 3  wherein said diacid is selected from the group consisting of: terephthalic acid; isophthalic acid; succinic acid; glutaric acid; adipic acid; sebacic acid; dodecanedioic acid; azelaic acid; trimethyl adipic acid; 1,4-cyclohexanedicarboxylic acid; 1,3-cyclohexanedicarboxylic acid; and any mixture thereof. 
     
     
         6 . The material of  claim 3  wherein said diacid and diamine each have a functionality of 2. 
     
     
         7 . The material of  claim 1  wherein said cycloaliphatic polyamide comprises a cyclohexyl moiety. 
     
     
         8 . The material of  claim 1  wherein said structural fiber comprises polyethylene fiber, aramid fiber, carbon fibers, glass fibers, or combinations thereof. 
     
     
         9 . The material of  claim 8  wherein said wherein said fibers are provided in the form of an open woven fiber fabric. 
     
     
         10 . An energy dissipating composite material comprising:
 a first layer comprising a poly(urethane urea) impregnated into a first structural fiber; and   a second layer on said first layer, said second layer comprising a thermoplastic cycloaliphatic polyamide.   
     
     
         11 . The composite material of  claim 10  wherein said poly(urethane urea) and said thermoplastic cycloaliphatic polyamide are predominantly amorphous. 
     
     
         12 . The composite material of  claim 10  wherein said composite material excludes resin absent intermolecular hydrogen bonding. 
     
     
         13 . The composite material of  claim 10  excluding polycarbonate. 
     
     
         14 . The composite material of  claim 10  wherein said thermoplastic cycloaliphatic polyamide comprises a structure as a result of a stoichiometric reaction between a diamine and a diacid. 
     
     
         15 . The material of  claim 14  wherein said diamine is selected from the group consisting of: hexamethylenediamine; 1,4-phenyl-diamine (para-phenylenediamine); 1,3-phenyl-diamine (m-phenylenediamine); 1,4-diaminocyclohexane; 1,3-diaminocyclohexane; m-xylylenediamine; 4,4′-methylenebis(cyclohexylamine); 2,2,4-trimethyl hexamethylene diamine; 2,4,4-trimethyl hexamethylene diamine; and any mixture thereof. 
     
     
         16 . The material of  claim 14  wherein said diacid is selected from the group consisting of: terephthalic acid; isophthalic acid; succinic acid; glutaric acid; adipic acid; sebacic acid; dodecanedioic acid; azelaic acid; trimethyl adipic acid; 1,4-cyclohexanedicarboxylic acid; 1,3-cyclohexanedicarboxylic acid; and any mixture thereof. 
     
     
         17 . The material of  claim 10  wherein said poly(urethane urea) is formed of 4,4′-dicyclohexylmethane diisocyanate, diethyltoluenediamine, and poly(tetramethylene oxide). 
     
     
         18 . The material of  claim 10  formed into a helmet, armor, a face shield, or a transparent window element. 
     
     
         19 . The material of  claim 18  wherein said first layer is positioned outside of said second layer. 
     
     
         20 . The material of  claim 10 , wherein said cycloaliphatic polyamide is characterized by compressive flow stress values at strain rates of 2,200 per second that are higher in comparison with compressive flow stress values at strain rates of 0.01 per second.

Join the waitlist — get patent alerts

Track US2021317036A1 — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.