PL75714B2 - - Google Patents

Info

Publication number

PL75714B2

PL75714B2 PL15632672A PL15632672A PL75714B2 PL 75714 B2 PL75714 B2 PL 75714B2 PL 15632672 A PL15632672 A PL 15632672A PL 15632672 A PL15632672 A PL 15632672A PL 75714 B2 PL75714 B2 PL 75714B2

Authority

PL

Poland

Prior art keywords

carbon fibers

matrix

resin

synthetic plastics

composition

Prior art date

1972-06-28

Links

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• 229920000049 Carbon (fiber) Polymers 0.000 claims description 15
• 239000004917 carbon fiber Substances 0.000 claims description 15
• 229920005989 resin Polymers 0.000 claims description 15
• 239000011347 resin Substances 0.000 claims description 15
• 238000000034 method Methods 0.000 claims description 14
• 239000011159 matrix material Substances 0.000 claims description 12
• 239000000203 mixture Substances 0.000 claims description 12
• 230000008569 process Effects 0.000 claims description 6
• JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 5
• 239000003822 epoxy resin Substances 0.000 claims description 5
• 229920000647 polyepoxide Polymers 0.000 claims description 5
• 239000011248 coating agent Substances 0.000 claims description 2
• 238000000576 coating method Methods 0.000 claims description 2
• LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 2
• 229920000642 polymer Polymers 0.000 claims description 2
• 239000004033 plastic Substances 0.000 claims 6
• 229920003023 plastic Polymers 0.000 claims 6
• 229920002994 synthetic fiber Polymers 0.000 claims 1
• KUBDPQJOLOUJRM-UHFFFAOYSA-N 2-(chloromethyl)oxirane;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol Chemical compound ClCC1CO1.C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 KUBDPQJOLOUJRM-UHFFFAOYSA-N 0.000 description 6
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
• 239000000835 fiber Substances 0.000 description 6
• 238000010438 heat treatment Methods 0.000 description 5
• RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 4
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
• WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 4
• JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
• 238000005452 bending Methods 0.000 description 3
• XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 2
• 229910015900 BF3 Inorganic materials 0.000 description 2
• BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
• 239000004593 Epoxy Substances 0.000 description 2
• QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
• 239000003795 chemical substances by application Substances 0.000 description 2
• 238000009833 condensation Methods 0.000 description 2
• 230000005494 condensation Effects 0.000 description 2
• GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical class C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
• WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
• 235000014655 lactic acid Nutrition 0.000 description 2
• 239000004310 lactic acid Substances 0.000 description 2
• 239000007788 liquid Substances 0.000 description 2
• 230000009467 reduction Effects 0.000 description 2
• 150000003839 salts Chemical class 0.000 description 2
• 239000007787 solid Substances 0.000 description 2
• 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
• DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
• 101000682328 Bacillus subtilis (strain 168) 50S ribosomal protein L18 Proteins 0.000 description 1
• MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
• 150000004982 aromatic amines Chemical class 0.000 description 1
• 230000015572 biosynthetic process Effects 0.000 description 1
• BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
• 230000015556 catabolic process Effects 0.000 description 1
• 150000001875 compounds Chemical class 0.000 description 1
• -1 cyano compound Chemical class 0.000 description 1
• 238000006731 degradation reaction Methods 0.000 description 1
• MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 1
• 230000006872 improvement Effects 0.000 description 1
• 239000011229 interlayer Substances 0.000 description 1
• 239000010410 layer Substances 0.000 description 1
• 239000002075 main ingredient Substances 0.000 description 1
• 239000000463 material Substances 0.000 description 1
• VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
• 239000004014 plasticizer Substances 0.000 description 1
• 229920003225 polyurethane elastomer Polymers 0.000 description 1
• 238000002360 preparation method Methods 0.000 description 1
• 229920006395 saturated elastomer Polymers 0.000 description 1
• 239000002904 solvent Substances 0.000 description 1
• 239000000758 substrate Substances 0.000 description 1
• 230000007704 transition Effects 0.000 description 1