TW200514B - - Google Patents
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- Publication number
- TW200514B TW200514B TW080106300A TW80106300A TW200514B TW 200514 B TW200514 B TW 200514B TW 080106300 A TW080106300 A TW 080106300A TW 80106300 A TW80106300 A TW 80106300A TW 200514 B TW200514 B TW 200514B
- Authority
- TW
- Taiwan
- Prior art keywords
- atoms
- polyacetal
- resin
- patent application
- nylon
- Prior art date
Links
- 229920005989 resin Polymers 0.000 claims description 84
- 239000011347 resin Substances 0.000 claims description 84
- 229920006324 polyoxymethylene Polymers 0.000 claims description 78
- 229930182556 Polyacetal Natural products 0.000 claims description 70
- 229920006122 polyamide resin Polymers 0.000 claims description 30
- 239000000945 filler Substances 0.000 claims description 28
- 239000011342 resin composition Substances 0.000 claims description 28
- 125000004429 atom Chemical group 0.000 claims description 26
- -1 binary Chemical class 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000002270 dispersing agent Substances 0.000 claims description 22
- 229920001577 copolymer Polymers 0.000 claims description 21
- 238000011049 filling Methods 0.000 claims description 21
- 239000002245 particle Substances 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 238000002844 melting Methods 0.000 claims description 16
- 230000008018 melting Effects 0.000 claims description 16
- 229920000299 Nylon 12 Polymers 0.000 claims description 12
- 125000003118 aryl group Chemical group 0.000 claims description 12
- 239000011521 glass Substances 0.000 claims description 12
- 239000003365 glass fiber Substances 0.000 claims description 12
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 239000000835 fiber Substances 0.000 claims description 10
- 229920002292 Nylon 6 Polymers 0.000 claims description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 239000007789 gas Substances 0.000 claims description 8
- 239000000454 talc Substances 0.000 claims description 8
- 229910052623 talc Inorganic materials 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 6
- 239000000378 calcium silicate Substances 0.000 claims description 6
- 229910052918 calcium silicate Inorganic materials 0.000 claims description 6
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 claims description 6
- 229920002647 polyamide Polymers 0.000 claims description 6
- 239000004677 Nylon Substances 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229920001778 nylon Polymers 0.000 claims description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims description 3
- 150000001412 amines Chemical class 0.000 claims description 3
- 239000011324 bead Substances 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims description 3
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims description 3
- NJLLQSBAHIKGKF-UHFFFAOYSA-N dipotassium dioxido(oxo)titanium Chemical compound [K+].[K+].[O-][Ti]([O-])=O NJLLQSBAHIKGKF-UHFFFAOYSA-N 0.000 claims description 3
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims description 3
- 239000011159 matrix material Substances 0.000 claims description 3
- 150000003672 ureas Chemical class 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 229920000571 Nylon 11 Polymers 0.000 claims description 2
- KXBFLNPZHXDQLV-UHFFFAOYSA-N [cyclohexyl(diisocyanato)methyl]cyclohexane Chemical compound C1CCCCC1C(N=C=O)(N=C=O)C1CCCCC1 KXBFLNPZHXDQLV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004927 clay Substances 0.000 claims description 2
- 238000005516 engineering process Methods 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 150000007974 melamines Chemical class 0.000 claims description 2
- 229920000962 poly(amidoamine) Polymers 0.000 claims description 2
- 239000000377 silicon dioxide Substances 0.000 claims description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims 2
- 150000001298 alcohols Chemical class 0.000 claims 2
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims 2
- USKJMUFHXCJSGV-UHFFFAOYSA-N N=C=O.N=C=O.N=C=O Chemical compound N=C=O.N=C=O.N=C=O USKJMUFHXCJSGV-UHFFFAOYSA-N 0.000 claims 1
- 125000004849 alkoxymethyl group Chemical group 0.000 claims 1
- 125000005907 alkyl ester group Chemical group 0.000 claims 1
- 150000003862 amino acid derivatives Chemical class 0.000 claims 1
- 150000008064 anhydrides Chemical group 0.000 claims 1
- 239000006229 carbon black Substances 0.000 claims 1
- 238000007334 copolymerization reaction Methods 0.000 claims 1
- RAABOESOVLLHRU-UHFFFAOYSA-N diazene Chemical class N=N RAABOESOVLLHRU-UHFFFAOYSA-N 0.000 claims 1
- 125000005442 diisocyanate group Chemical group 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 239000002657 fibrous material Substances 0.000 claims 1
- 125000000524 functional group Chemical group 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- 229940037201 oris Drugs 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 33
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 15
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 13
- 238000005299 abrasion Methods 0.000 description 10
- 238000004898 kneading Methods 0.000 description 10
- 229930040373 Paraformaldehyde Natural products 0.000 description 8
- 239000011152 fibreglass Substances 0.000 description 8
- 229920001519 homopolymer Polymers 0.000 description 7
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 235000019256 formaldehyde Nutrition 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- 229920002959 polymer blend Polymers 0.000 description 5
- 229920005992 thermoplastic resin Polymers 0.000 description 5
- 229920000877 Melamine resin Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 229920002302 Nylon 6,6 Polymers 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 150000001336 alkenes Chemical group 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 235000013877 carbamide Nutrition 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229910052704 radon Inorganic materials 0.000 description 3
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- UYVWNPAMKCDKRB-UHFFFAOYSA-N 1,2,4,5-tetraoxane Chemical compound C1OOCOO1 UYVWNPAMKCDKRB-UHFFFAOYSA-N 0.000 description 2
- FQERLIOIVXPZKH-UHFFFAOYSA-N 1,2,4-trioxane Chemical compound C1COOCO1 FQERLIOIVXPZKH-UHFFFAOYSA-N 0.000 description 2
- BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 229920000305 Nylon 6,10 Polymers 0.000 description 2
- 229920001744 Polyaldehyde Polymers 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- XKKFHYIHXAEDLW-UHFFFAOYSA-N methoxymethylcarbamic acid Chemical compound COCNC(O)=O XKKFHYIHXAEDLW-UHFFFAOYSA-N 0.000 description 2
- 238000001000 micrograph Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000003014 reinforcing effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000012756 surface treatment agent Substances 0.000 description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
- 238000004627 transmission electron microscopy Methods 0.000 description 2
- VTLOQWKTMLAQKF-UHFFFAOYSA-N 1-methoxy-1,3,3-trimethylurea Chemical compound CON(C)C(=O)N(C)C VTLOQWKTMLAQKF-UHFFFAOYSA-N 0.000 description 1
- QHSJQEMESPRTBF-UHFFFAOYSA-N 2-(dimethoxymethyl)guanidine Chemical compound COC(OC)N=C(N)N QHSJQEMESPRTBF-UHFFFAOYSA-N 0.000 description 1
- BOLVKBXIEFIFQF-UHFFFAOYSA-N 2-(methoxymethyl)guanidine Chemical compound COCN=C(N)N BOLVKBXIEFIFQF-UHFFFAOYSA-N 0.000 description 1
- SYURNNNQIFDVCA-UHFFFAOYSA-N 2-propyloxirane Chemical group CCCC1CO1 SYURNNNQIFDVCA-UHFFFAOYSA-N 0.000 description 1
- 241000255789 Bombyx mori Species 0.000 description 1
- YVZDOAURMSVEEQ-UHFFFAOYSA-N CNNC1=NC(=NC(=N1)N)N Chemical compound CNNC1=NC(=NC(=N1)N)N YVZDOAURMSVEEQ-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 229920002614 Polyether block amide Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 206010041349 Somnolence Diseases 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000006230 acetylene black Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- NLEPDOASNNDPBD-UHFFFAOYSA-N bis(methoxymethyl)carbamic acid Chemical compound COCN(C(O)=O)COC NLEPDOASNNDPBD-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical compound Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- ASQQEOXYFGEFKQ-UHFFFAOYSA-N dioxirane Chemical group C1OO1 ASQQEOXYFGEFKQ-UHFFFAOYSA-N 0.000 description 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- RZMZBHSKPLVQCP-UHFFFAOYSA-N ethyl 2-amino-2-oxoacetate Chemical compound CCOC(=O)C(N)=O RZMZBHSKPLVQCP-UHFFFAOYSA-N 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000002309 gasification Methods 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- UUVWYPNAQBNQJQ-UHFFFAOYSA-N hexamethylmelamine Chemical compound CN(C)C1=NC(N(C)C)=NC(N(C)C)=N1 UUVWYPNAQBNQJQ-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- HJYNGRZUBXMFGB-UHFFFAOYSA-N methoxymethylurea Chemical compound COCNC(N)=O HJYNGRZUBXMFGB-UHFFFAOYSA-N 0.000 description 1
- VFKBNRYIYZIRMD-UHFFFAOYSA-N methyl n-(methoxymethyl)carbamate Chemical compound COCNC(=O)OC VFKBNRYIYZIRMD-UHFFFAOYSA-N 0.000 description 1
- NWXPCXZSHMVPFK-UHFFFAOYSA-N methyl n-acetylcarbamate Chemical compound COC(=O)NC(C)=O NWXPCXZSHMVPFK-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- SHHGHQXPESZCQA-UHFFFAOYSA-N oxiran-2-ylmethylsilicon Chemical compound [Si]CC1CO1 SHHGHQXPESZCQA-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 125000005704 oxymethylene group Chemical group [H]C([H])([*:2])O[*:1] 0.000 description 1
- 125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SYUHGPGVQRZVTB-UHFFFAOYSA-N radon atom Chemical compound [Rn] SYUHGPGVQRZVTB-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000003017 thermal stabilizer Substances 0.000 description 1
- 239000013638 trimer Substances 0.000 description 1
- 229940124543 ultraviolet light absorber Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/4009—Two or more macromolecular compounds not provided for in one single group of groups C08G18/42 - C08G18/64
- C08G18/4054—Mixtures of compounds of group C08G18/60 with other macromolecular compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/205—Compounds containing groups, e.g. carbamates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/29—Compounds containing one or more carbon-to-nitrogen double bonds
- C08K5/31—Guanidine; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
- C08L59/02—Polyacetals containing polyoxymethylene sequences only
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L61/00—Compositions of condensation polymers of aldehydes or ketones; Compositions of derivatives of such polymers
- C08L61/20—Condensation polymers of aldehydes or ketones with only compounds containing hydrogen attached to nitrogen
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21714990 | 1990-08-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW200514B true TW200514B (en, 2012) | 1993-02-21 |
Family
ID=16699628
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW080106300A TW200514B (en, 2012) | 1990-08-20 | 1991-08-09 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US5354798A (en, 2012) |
| EP (1) | EP0475127B1 (en, 2012) |
| JP (1) | JP3109753B2 (en, 2012) |
| KR (1) | KR950006140B1 (en, 2012) |
| BE (1) | BE1004773B3 (en, 2012) |
| DE (1) | DE69117840T2 (en, 2012) |
| FR (1) | FR2665904B1 (en, 2012) |
| GB (1) | GB2247684B (en, 2012) |
| TW (1) | TW200514B (en, 2012) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5298537A (en) * | 1992-04-09 | 1994-03-29 | E. I. Du Pont De Nemours And Company | Polyoxymethylene compositions containing at least one encapsulated nucleant |
| US5446086A (en) * | 1992-06-30 | 1995-08-29 | Polyplastics Co., Ltd. | Polyoxymethylene composition |
| AU669567B2 (en) * | 1992-10-30 | 1996-06-13 | Basf Corporation | Water dispersible ionic and nonionic polyamide modified polyurethane resins for use in coating compositions |
| JP3285480B2 (ja) * | 1995-09-29 | 2002-05-27 | ポリプラスチックス株式会社 | ポリアセタール樹脂組成物 |
| US5902517A (en) * | 1996-10-28 | 1999-05-11 | Cabot Corporation | Conductive polyacetal composition |
| WO2003054084A1 (fr) * | 2001-12-21 | 2003-07-03 | Mitsubishi Gas Chemical Company, Inc. | Composition de resine thermoplastique |
| DE10297570B4 (de) * | 2001-12-25 | 2008-02-21 | Asahi Kasei Chemicals Corporation | Verwendung einer Harzzusammensetzung mit Polyoxymethylenharz als Rampe |
| US6974849B2 (en) * | 2003-03-03 | 2005-12-13 | Ticona Llc | Polyacetals with improved resistance to bleach |
| JP5325792B2 (ja) * | 2006-11-22 | 2013-10-23 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 静電気拡散性ポリアセタール組成物 |
| CN105121495A (zh) | 2013-02-15 | 2015-12-02 | 英派尔科技开发有限公司 | 酚类环氧化合物 |
| US9868683B2 (en) | 2013-06-13 | 2018-01-16 | Empire Technology Development Llc | Multi-functional phenolic resins |
| CN105814014B (zh) | 2013-12-02 | 2018-06-12 | 英派尔科技开发有限公司 | 新型双子表面活性剂和它们的用途 |
| CN105980351B (zh) * | 2013-12-02 | 2018-11-02 | 英派尔科技开发有限公司 | 双子型表面活性剂和它们的制备方法以及用途 |
| US9896637B2 (en) * | 2015-04-08 | 2018-02-20 | Jtekt Corporation | Sliding member, method of manufacturing sliding member, and gear |
| JP2017061638A (ja) * | 2015-09-25 | 2017-03-30 | 富士ゼロックス株式会社 | 樹脂組成物、樹脂成形体、及び樹脂組成物の製造方法 |
| WO2017064778A1 (ja) * | 2015-10-14 | 2017-04-20 | Ykk株式会社 | ポリアセタール樹脂組成物、ファスニング部材及びスライドファスナー |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE626284A (en, 2012) * | 1962-04-28 | |||
| US3549734A (en) * | 1967-06-27 | 1970-12-22 | Takeshi Yasuda | Method of forming microfibers |
| GB1455314A (en) * | 1973-01-30 | 1976-11-10 | Asahi Chemical Ind | Resin composition |
| JPS5915948B2 (ja) * | 1974-12-16 | 1984-04-12 | 旭化成株式会社 | ポリアミド組成物 |
| JPS5381562A (en) * | 1976-12-24 | 1978-07-19 | Toyobo Co Ltd | Flame-retardant polyamide composition |
| JPS59105047A (ja) * | 1982-12-07 | 1984-06-18 | Mitsubishi Gas Chem Co Inc | アセタ−ル樹脂組成物 |
| DE3248330A1 (de) * | 1982-12-28 | 1984-06-28 | Bayer Ag, 5090 Leverkusen | Brandwidrig ausgeruestete polyamidformmassen |
| CA1235246A (en) * | 1984-10-25 | 1988-04-12 | Kavilipalayam M. Natarajan | Oxymethylene polymer molding compositions having enhanced resistance to speck formation |
| JPS63112650A (ja) * | 1986-10-23 | 1988-05-17 | ヘキスト・セラニーズ・コーポレーション | 安定化オキシメチレンポリマー組成物 |
| CN1011040B (zh) * | 1986-11-18 | 1991-01-02 | 赫希斯特人造丝公司 | 颜色稳定度得到改善的聚缩醛稳定剂组合物 |
| US4873282A (en) * | 1987-05-15 | 1989-10-10 | Mitsubishi Petrochemical Co., Ltd. | Polyacetal resin composition |
| GB2210048B (en) * | 1987-09-22 | 1992-04-15 | Asahi Chemical Ind | Polyacetal composition |
| MY104161A (en) * | 1988-08-12 | 1994-02-28 | Toshiba Kk | Material for use in manufacturing movable mechanical elements. |
| DE3834547A1 (de) * | 1988-10-11 | 1990-04-19 | Basf Ag | Polyoxymethylen-formmassen mit verbesserter thermischer stabilitaet, verfahren zu deren herstellung und deren verwendung |
| AU5842290A (en) * | 1989-06-15 | 1991-01-08 | E.I. Du Pont De Nemours And Company | Stabilized polyacetal compositions |
| KR0146285B1 (ko) * | 1989-08-09 | 1998-08-17 | 마에다 가쓰노스께 | 폴리옥시메틸렌 다원공중합체 및 그의 성형품 |
| JPH06334377A (ja) * | 1993-05-19 | 1994-12-02 | Toshiba Chem Corp | 電子機器筐体 |
-
1991
- 1991-08-09 TW TW080106300A patent/TW200514B/zh active
- 1991-08-13 FR FR9110275A patent/FR2665904B1/fr not_active Expired - Fee Related
- 1991-08-15 JP JP03228520A patent/JP3109753B2/ja not_active Expired - Fee Related
- 1991-08-16 US US07/746,341 patent/US5354798A/en not_active Expired - Fee Related
- 1991-08-19 GB GB9117870A patent/GB2247684B/en not_active Expired - Fee Related
- 1991-08-19 DE DE69117840T patent/DE69117840T2/de not_active Expired - Fee Related
- 1991-08-19 EP EP91113855A patent/EP0475127B1/en not_active Expired - Lifetime
- 1991-08-19 BE BE9100752A patent/BE1004773B3/fr not_active IP Right Cessation
- 1991-08-20 KR KR1019910014355A patent/KR950006140B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| KR950006140B1 (ko) | 1995-06-09 |
| JPH05239313A (ja) | 1993-09-17 |
| JP3109753B2 (ja) | 2000-11-20 |
| FR2665904A1 (fr) | 1992-02-21 |
| KR920004498A (ko) | 1992-03-27 |
| DE69117840T2 (de) | 1996-11-07 |
| GB2247684A (en) | 1992-03-11 |
| EP0475127B1 (en) | 1996-03-13 |
| BE1004773B3 (fr) | 1994-11-03 |
| FR2665904B1 (fr) | 1993-12-31 |
| GB2247684B (en) | 1993-10-06 |
| BE1004773A0 (fr) | 1993-01-26 |
| EP0475127A1 (en) | 1992-03-18 |
| DE69117840D1 (de) | 1996-04-18 |
| US5354798A (en) | 1994-10-11 |
| GB9117870D0 (en) | 1991-10-09 |
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