JP6626444B2 - 射出成形用の耐熱性強化熱可塑性組成物 - Google Patents
射出成形用の耐熱性強化熱可塑性組成物 Download PDFInfo
- Publication number
- JP6626444B2 JP6626444B2 JP2016538995A JP2016538995A JP6626444B2 JP 6626444 B2 JP6626444 B2 JP 6626444B2 JP 2016538995 A JP2016538995 A JP 2016538995A JP 2016538995 A JP2016538995 A JP 2016538995A JP 6626444 B2 JP6626444 B2 JP 6626444B2
- Authority
- JP
- Japan
- Prior art keywords
- injection molded
- molded part
- thermoplastic composition
- part according
- polyarylene sulfide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims description 220
- 229920001169 thermoplastic Polymers 0.000 title claims description 123
- 239000004416 thermosoftening plastic Substances 0.000 title claims description 123
- 238000001746 injection moulding Methods 0.000 title claims description 7
- 229920000412 polyarylene Polymers 0.000 claims description 118
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims description 107
- 238000002347 injection Methods 0.000 claims description 90
- 239000007924 injection Substances 0.000 claims description 90
- 239000004609 Impact Modifier Substances 0.000 claims description 84
- -1 polydimethylsiloxane Polymers 0.000 claims description 84
- 229920000642 polymer Polymers 0.000 claims description 69
- 238000012360 testing method Methods 0.000 claims description 43
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims description 33
- 239000000945 filler Substances 0.000 claims description 33
- 238000000034 method Methods 0.000 claims description 33
- 239000000835 fiber Substances 0.000 claims description 25
- 239000003431 cross linking reagent Substances 0.000 claims description 24
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 24
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 23
- 125000000524 functional group Chemical group 0.000 claims description 19
- 239000007822 coupling agent Substances 0.000 claims description 16
- 229920002725 thermoplastic elastomer Polymers 0.000 claims description 16
- 239000004593 Epoxy Substances 0.000 claims description 15
- 239000000155 melt Substances 0.000 claims description 14
- 238000000465 moulding Methods 0.000 claims description 14
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 13
- 230000032683 aging Effects 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 12
- 239000000654 additive Substances 0.000 claims description 11
- 230000014759 maintenance of location Effects 0.000 claims description 11
- 229920001897 terpolymer Polymers 0.000 claims description 11
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims description 10
- 229910021485 fumed silica Inorganic materials 0.000 claims description 9
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 8
- 239000004734 Polyphenylene sulfide Substances 0.000 claims description 8
- 229920000570 polyether Polymers 0.000 claims description 8
- 229920000069 polyphenylene sulfide Polymers 0.000 claims description 8
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical group [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 5
- 229920002647 polyamide Polymers 0.000 claims description 5
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical group OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 4
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 4
- WVDRSXGPQWNUBN-UHFFFAOYSA-N 4-(4-carboxyphenoxy)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1OC1=CC=C(C(O)=O)C=C1 WVDRSXGPQWNUBN-UHFFFAOYSA-N 0.000 claims description 2
- NEQFBGHQPUXOFH-UHFFFAOYSA-N 4-(4-carboxyphenyl)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1 NEQFBGHQPUXOFH-UHFFFAOYSA-N 0.000 claims description 2
- 238000007599 discharging Methods 0.000 claims description 2
- DFFZOPXDTCDZDP-UHFFFAOYSA-N naphthalene-1,5-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1C(O)=O DFFZOPXDTCDZDP-UHFFFAOYSA-N 0.000 claims description 2
- ZQVKTHRQIXSMGY-UHFFFAOYSA-N 4-Ethylbenzoic acid Chemical compound CCC1=CC=C(C(O)=O)C=C1 ZQVKTHRQIXSMGY-UHFFFAOYSA-N 0.000 claims 1
- ABMFBCRYHDZLRD-UHFFFAOYSA-N naphthalene-1,4-dicarboxylic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=C(C(O)=O)C2=C1 ABMFBCRYHDZLRD-UHFFFAOYSA-N 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 32
- 150000001875 compounds Chemical class 0.000 description 25
- 125000004432 carbon atom Chemical group C* 0.000 description 24
- 239000004971 Cross linker Substances 0.000 description 23
- 229920001577 copolymer Polymers 0.000 description 21
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 21
- 238000006116 polymerization reaction Methods 0.000 description 18
- 239000000049 pigment Substances 0.000 description 15
- 230000008569 process Effects 0.000 description 15
- 239000000463 material Substances 0.000 description 14
- 238000010128 melt processing Methods 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- 238000007306 functionalization reaction Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 10
- 238000002156 mixing Methods 0.000 description 9
- 229910052977 alkali metal sulfide Inorganic materials 0.000 description 8
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 7
- 229910052736 halogen Inorganic materials 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 150000003568 thioethers Chemical class 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 6
- 238000012668 chain scission Methods 0.000 description 6
- 239000003086 colorant Substances 0.000 description 6
- 150000002367 halogens Chemical group 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 239000004738 Fortron® Substances 0.000 description 5
- 239000006087 Silane Coupling Agent Substances 0.000 description 5
- 239000012963 UV stabilizer Substances 0.000 description 5
- 229910052783 alkali metal Inorganic materials 0.000 description 5
- 150000001491 aromatic compounds Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 239000000986 disperse dye Substances 0.000 description 5
- 125000003700 epoxy group Chemical group 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 5
- 230000000704 physical effect Effects 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 230000035882 stress Effects 0.000 description 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 5
- WYTZZXDRDKSJID-UHFFFAOYSA-N (3-aminopropyl)triethoxysilane Chemical compound CCO[Si](OCC)(OCC)CCCN WYTZZXDRDKSJID-UHFFFAOYSA-N 0.000 description 4
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- SJECZPVISLOESU-UHFFFAOYSA-N 3-trimethoxysilylpropan-1-amine Chemical compound CO[Si](OC)(OC)CCCN SJECZPVISLOESU-UHFFFAOYSA-N 0.000 description 4
- 241000218642 Abies Species 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 125000003545 alkoxy group Chemical group 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- KDKYADYSIPSCCQ-UHFFFAOYSA-N but-1-yne Chemical compound CCC#C KDKYADYSIPSCCQ-UHFFFAOYSA-N 0.000 description 4
- 150000003857 carboxamides Chemical class 0.000 description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 239000003365 glass fiber Substances 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- 239000008188 pellet Substances 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 229920005604 random copolymer Polymers 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 125000003396 thiol group Chemical group [H]S* 0.000 description 4
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 4
- 238000004073 vulcanization Methods 0.000 description 4
- PBKONEOXTCPAFI-UHFFFAOYSA-N 1,2,4-trichlorobenzene Chemical compound ClC1=CC=C(Cl)C(Cl)=C1 PBKONEOXTCPAFI-UHFFFAOYSA-N 0.000 description 3
- ZPQOPVIELGIULI-UHFFFAOYSA-N 1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1 ZPQOPVIELGIULI-UHFFFAOYSA-N 0.000 description 3
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 125000000732 arylene group Chemical group 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 230000015556 catabolic process Effects 0.000 description 3
- 238000006731 degradation reaction Methods 0.000 description 3
- 150000004985 diamines Chemical class 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000806 elastomer Substances 0.000 description 3
- 239000012765 fibrous filler Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 239000011256 inorganic filler Substances 0.000 description 3
- 229910003475 inorganic filler Inorganic materials 0.000 description 3
- 239000000314 lubricant Substances 0.000 description 3
- 238000012423 maintenance Methods 0.000 description 3
- 125000005395 methacrylic acid group Chemical group 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 2
- CRSBERNSMYQZNG-UHFFFAOYSA-N 1-dodecene Chemical compound CCCCCCCCCCC=C CRSBERNSMYQZNG-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 2
- FZZMTSNZRBFGGU-UHFFFAOYSA-N 2-chloro-7-fluoroquinazolin-4-amine Chemical compound FC1=CC=C2C(N)=NC(Cl)=NC2=C1 FZZMTSNZRBFGGU-UHFFFAOYSA-N 0.000 description 2
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 2
- HXLAEGYMDGUSBD-UHFFFAOYSA-N 3-[diethoxy(methyl)silyl]propan-1-amine Chemical compound CCO[Si](C)(OCC)CCCN HXLAEGYMDGUSBD-UHFFFAOYSA-N 0.000 description 2
- ZYAASQNKCWTPKI-UHFFFAOYSA-N 3-[dimethoxy(methyl)silyl]propan-1-amine Chemical compound CO[Si](C)(OC)CCCN ZYAASQNKCWTPKI-UHFFFAOYSA-N 0.000 description 2
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical class C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 2
- GPAPPPVRLPGFEQ-UHFFFAOYSA-N 4,4'-dichlorodiphenyl sulfone Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC=C(Cl)C=C1 GPAPPPVRLPGFEQ-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- PMDCZENCAXMSOU-UHFFFAOYSA-N N-ethylacetamide Chemical compound CCNC(C)=O PMDCZENCAXMSOU-UHFFFAOYSA-N 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920004482 WACKER® Polymers 0.000 description 2
- PXAJQJMDEXJWFB-UHFFFAOYSA-N acetone oxime Chemical compound CC(C)=NO PXAJQJMDEXJWFB-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001345 alkine derivatives Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 2
- 125000002344 aminooxy group Chemical group [H]N([H])O[*] 0.000 description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 150000004984 aromatic diamines Chemical class 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 229940067597 azelate Drugs 0.000 description 2
- 239000000987 azo dye Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 125000002228 disulfide group Chemical group 0.000 description 2
- 150000002019 disulfides Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229940012017 ethylenediamine Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- NYMPGSQKHIOWIO-UHFFFAOYSA-N hydroxy(diphenyl)silicon Chemical class C=1C=CC=CC=1[Si](O)C1=CC=CC=C1 NYMPGSQKHIOWIO-UHFFFAOYSA-N 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 2
- 125000005647 linker group Chemical group 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- PHQOGHDTIVQXHL-UHFFFAOYSA-N n'-(3-trimethoxysilylpropyl)ethane-1,2-diamine Chemical compound CO[Si](OC)(OC)CCCNCCN PHQOGHDTIVQXHL-UHFFFAOYSA-N 0.000 description 2
- QHJABUZHRJTCAR-UHFFFAOYSA-N n'-methylpropane-1,3-diamine Chemical compound CNCCCN QHJABUZHRJTCAR-UHFFFAOYSA-N 0.000 description 2
- KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- KJFMBFZCATUALV-UHFFFAOYSA-N phenolphthalein Chemical compound C1=CC(O)=CC=C1C1(C=2C=CC(O)=CC=2)C2=CC=CC=C2C(=O)O1 KJFMBFZCATUALV-UHFFFAOYSA-N 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000515 polycarbonate Polymers 0.000 description 2
- 239000004417 polycarbonate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920001195 polyisoprene Polymers 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 229920002635 polyurethane Polymers 0.000 description 2
- 239000004814 polyurethane Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 229920005573 silicon-containing polymer Polymers 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000012321 sodium triacetoxyborohydride Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000010561 standard procedure Methods 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- CNHDIAIOKMXOLK-UHFFFAOYSA-N toluquinol Chemical compound CC1=CC(O)=CC=C1O CNHDIAIOKMXOLK-UHFFFAOYSA-N 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 description 1
- NAQWICRLNQSPPW-UHFFFAOYSA-N 1,2,3,4-tetrachloronaphthalene Chemical compound C1=CC=CC2=C(Cl)C(Cl)=C(Cl)C(Cl)=C21 NAQWICRLNQSPPW-UHFFFAOYSA-N 0.000 description 1
- YPFCYPZKFQPCOC-UHFFFAOYSA-N 1,2,3,5-tetrabromobenzene Chemical compound BrC1=CC(Br)=C(Br)C(Br)=C1 YPFCYPZKFQPCOC-UHFFFAOYSA-N 0.000 description 1
- RELMFMZEBKVZJC-UHFFFAOYSA-N 1,2,3-trichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Cl RELMFMZEBKVZJC-UHFFFAOYSA-N 0.000 description 1
- DMFMMVMUXPAZKT-UHFFFAOYSA-N 1,2,4-tribromo-6-methylnaphthalene Chemical compound BrC1=C(Br)C=C(Br)C2=CC(C)=CC=C21 DMFMMVMUXPAZKT-UHFFFAOYSA-N 0.000 description 1
- KSXFNGRHPAHIQJ-UHFFFAOYSA-N 1,2,4-triiodobenzene Chemical compound IC1=CC=C(I)C(I)=C1 KSXFNGRHPAHIQJ-UHFFFAOYSA-N 0.000 description 1
- VMNISWKTOHUZQN-UHFFFAOYSA-N 1,3,5-trichloro-2,4,6-trimethylbenzene Chemical compound CC1=C(Cl)C(C)=C(Cl)C(C)=C1Cl VMNISWKTOHUZQN-UHFFFAOYSA-N 0.000 description 1
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 1
- MWQBXOFZQBEAQV-UHFFFAOYSA-N 1,3-diamino-1,3-dinitrourea Chemical compound [N+](=O)([O-])N(N)C(=O)N([N+](=O)[O-])N MWQBXOFZQBEAQV-UHFFFAOYSA-N 0.000 description 1
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 1
- SWJPEBQEEAHIGZ-UHFFFAOYSA-N 1,4-dibromobenzene Chemical compound BrC1=CC=C(Br)C=C1 SWJPEBQEEAHIGZ-UHFFFAOYSA-N 0.000 description 1
- QKMNFFSBZRGHDJ-UHFFFAOYSA-N 1,4-dichloro-2-methoxybenzene Chemical compound COC1=CC(Cl)=CC=C1Cl QKMNFFSBZRGHDJ-UHFFFAOYSA-N 0.000 description 1
- KFAKZJUYBOYVKA-UHFFFAOYSA-N 1,4-dichloro-2-methylbenzene Chemical compound CC1=CC(Cl)=CC=C1Cl KFAKZJUYBOYVKA-UHFFFAOYSA-N 0.000 description 1
- DXAQJSDEJGVDQP-UHFFFAOYSA-N 1,7-diaminoheptan-4-yl trimethyl silicate Chemical compound CO[Si](OC)(OC)OC(CCCN)CCCN DXAQJSDEJGVDQP-UHFFFAOYSA-N 0.000 description 1
- ZFPGARUNNKGOBB-UHFFFAOYSA-N 1-Ethyl-2-pyrrolidinone Chemical compound CCN1CCCC1=O ZFPGARUNNKGOBB-UHFFFAOYSA-N 0.000 description 1
- DZHFFMWJXJBBRG-UHFFFAOYSA-N 1-bromo-3,5-dichlorobenzene Chemical compound ClC1=CC(Cl)=CC(Br)=C1 DZHFFMWJXJBBRG-UHFFFAOYSA-N 0.000 description 1
- URUJZHZLCCIILC-UHFFFAOYSA-N 1-chloro-4-(4-chlorophenoxy)benzene Chemical compound C1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1 URUJZHZLCCIILC-UHFFFAOYSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- QORAVNMWUNPXAO-UHFFFAOYSA-N 2,2',4,4'-tetrachlorobiphenyl Chemical group ClC1=CC(Cl)=CC=C1C1=CC=C(Cl)C=C1Cl QORAVNMWUNPXAO-UHFFFAOYSA-N 0.000 description 1
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- ZWMYTAHVFFRQTD-UHFFFAOYSA-N 2,4-dibromo-3-(2,6-dibromo-3,5-dimethylphenyl)-1,5-dimethylbenzene Chemical group CC1=CC(C)=C(Br)C(C=2C(=C(C)C=C(C)C=2Br)Br)=C1Br ZWMYTAHVFFRQTD-UHFFFAOYSA-N 0.000 description 1
- BXHXGRWITCQYFW-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yldisulfanyl)-1,3-benzoxazole Chemical compound C1=CC=C2OC(SSC=3OC4=CC=CC=C4N=3)=NC2=C1 BXHXGRWITCQYFW-UHFFFAOYSA-N 0.000 description 1
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- PMOATLADBGHBMF-UHFFFAOYSA-N 2-(2,5-diiodophenyl)-1,4-diiodobenzene Chemical group IC1=CC=C(I)C(C=2C(=CC=C(I)C=2)I)=C1 PMOATLADBGHBMF-UHFFFAOYSA-N 0.000 description 1
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
- DLLMHEDYJQACRM-UHFFFAOYSA-N 2-(carboxymethyldisulfanyl)acetic acid Chemical compound OC(=O)CSSCC(O)=O DLLMHEDYJQACRM-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- YYYOQURZQWIILK-UHFFFAOYSA-N 2-[(2-aminophenyl)disulfanyl]aniline Chemical compound NC1=CC=CC=C1SSC1=CC=CC=C1N YYYOQURZQWIILK-UHFFFAOYSA-N 0.000 description 1
- VNAWKNVDKFZFSU-UHFFFAOYSA-N 2-ethyl-2-methylpropane-1,3-diol Chemical compound CCC(C)(CO)CO VNAWKNVDKFZFSU-UHFFFAOYSA-N 0.000 description 1
- AAAWJUMVTPNRDT-UHFFFAOYSA-N 2-methylpentane-1,5-diol Chemical compound OCC(C)CCCO AAAWJUMVTPNRDT-UHFFFAOYSA-N 0.000 description 1
- BHWUCEATHBXPOV-UHFFFAOYSA-N 2-triethoxysilylethanamine Chemical compound CCO[Si](CCN)(OCC)OCC BHWUCEATHBXPOV-UHFFFAOYSA-N 0.000 description 1
- QHQNYHZHLAAHRW-UHFFFAOYSA-N 2-trimethoxysilylethanamine Chemical compound CO[Si](OC)(OC)CCN QHQNYHZHLAAHRW-UHFFFAOYSA-N 0.000 description 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
- PKXHXOTZMFCXSH-UHFFFAOYSA-N 3,3-dimethylbut-1-ene Chemical compound CC(C)(C)C=C PKXHXOTZMFCXSH-UHFFFAOYSA-N 0.000 description 1
- CXKCZFDUOYMOOP-UHFFFAOYSA-N 3,5-dichlorobenzoic acid Chemical compound OC(=O)C1=CC(Cl)=CC(Cl)=C1 CXKCZFDUOYMOOP-UHFFFAOYSA-N 0.000 description 1
- YCLSOMLVSHPPFV-UHFFFAOYSA-N 3-(2-carboxyethyldisulfanyl)propanoic acid Chemical compound OC(=O)CCSSCCC(O)=O YCLSOMLVSHPPFV-UHFFFAOYSA-N 0.000 description 1
- NMSZFQAFWHFSPE-UHFFFAOYSA-N 3-(oxiran-2-ylmethoxycarbonyl)but-3-enoic acid Chemical compound OC(=O)CC(=C)C(=O)OCC1CO1 NMSZFQAFWHFSPE-UHFFFAOYSA-N 0.000 description 1
- YURPISYZTZHYBW-UHFFFAOYSA-N 3-(pyridin-3-yldisulfanyl)pyridine Chemical compound C=1C=CN=CC=1SSC1=CC=CN=C1 YURPISYZTZHYBW-UHFFFAOYSA-N 0.000 description 1
- YHQXBTXEYZIYOV-UHFFFAOYSA-N 3-methylbut-1-ene Chemical compound CC(C)C=C YHQXBTXEYZIYOV-UHFFFAOYSA-N 0.000 description 1
- DCQBZYNUSLHVJC-UHFFFAOYSA-N 3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCS DCQBZYNUSLHVJC-UHFFFAOYSA-N 0.000 description 1
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 1
- YTBRNEUEFCNVHC-UHFFFAOYSA-N 4,4'-dichlorobiphenyl Chemical group C1=CC(Cl)=CC=C1C1=CC=C(Cl)C=C1 YTBRNEUEFCNVHC-UHFFFAOYSA-N 0.000 description 1
- MERLDGDYUMSLAY-UHFFFAOYSA-N 4-[(4-aminophenyl)disulfanyl]aniline Chemical compound C1=CC(N)=CC=C1SSC1=CC=C(N)C=C1 MERLDGDYUMSLAY-UHFFFAOYSA-N 0.000 description 1
- HCUNREWMFYCWAQ-UHFFFAOYSA-N 4-[2-(4-carboxyphenyl)ethyl]benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1CCC1=CC=C(C(O)=O)C=C1 HCUNREWMFYCWAQ-UHFFFAOYSA-N 0.000 description 1
- ODPYDILFQYARBK-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-1,3,5-triene Chemical group C1=CC=C2SC2=C1 ODPYDILFQYARBK-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 229920002748 Basalt fiber Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical group OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- DOJDCOIUSNKGCO-UHFFFAOYSA-N CC1(C([ClH]C2=NC(=NC(=N2)Cl)Cl)(C)C)CO1 Chemical compound CC1(C([ClH]C2=NC(=NC(=N2)Cl)Cl)(C)C)CO1 DOJDCOIUSNKGCO-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000005046 Chlorosilane Substances 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- FANBESOFXBDQSH-UHFFFAOYSA-N Ethyladipic acid Chemical compound CCC(C(O)=O)CCCC(O)=O FANBESOFXBDQSH-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- OPBCASKIMIECAF-UHFFFAOYSA-N N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)NC1=CC=CC=C1 Chemical compound N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)NC1=CC=CC=C1 OPBCASKIMIECAF-UHFFFAOYSA-N 0.000 description 1
- DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- KYPYTERUKNKOLP-UHFFFAOYSA-N Tetrachlorobisphenol A Chemical compound C=1C(Cl)=C(O)C(Cl)=CC=1C(C)(C)C1=CC(Cl)=C(O)C(Cl)=C1 KYPYTERUKNKOLP-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- OCWCVKQSJSKTHM-UHFFFAOYSA-N [bis(3-aminopropyl)-ethoxysilyl] triethyl silicate Chemical compound NCCC[Si](OCC)(CCCN)O[Si](OCC)(OCC)OCC OCWCVKQSJSKTHM-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 239000003929 acidic solution Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001348 alkyl chlorides Chemical group 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000001118 alkylidene group Chemical group 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 239000001000 anthraquinone dye Substances 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 206010003549 asthenia Diseases 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 1
- IHWUGQBRUYYZNM-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene-3,4-dicarboxylic acid Chemical compound C1CC2(C(O)=O)C(C(=O)O)=CC1C2 IHWUGQBRUYYZNM-UHFFFAOYSA-N 0.000 description 1
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 description 1
- 238000000071 blow moulding Methods 0.000 description 1
- 239000001045 blue dye Substances 0.000 description 1
- 238000006664 bond formation reaction Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000006309 butyl amino group Chemical group 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 150000001718 carbodiimides Chemical class 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 150000001244 carboxylic acid anhydrides Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- AJPXTSMULZANCB-UHFFFAOYSA-N chlorohydroquinone Chemical compound OC1=CC=C(O)C(Cl)=C1 AJPXTSMULZANCB-UHFFFAOYSA-N 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 150000004292 cyclic ethers Chemical class 0.000 description 1
- FOTKYAAJKYLFFN-UHFFFAOYSA-N decane-1,10-diol Chemical compound OCCCCCCCCCCO FOTKYAAJKYLFFN-UHFFFAOYSA-N 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- AFZSMODLJJCVPP-UHFFFAOYSA-N dibenzothiazol-2-yl disulfide Chemical compound C1=CC=C2SC(SSC=3SC4=CC=CC=C4N=3)=NC2=C1 AFZSMODLJJCVPP-UHFFFAOYSA-N 0.000 description 1
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- QTNDMWXOEPGHBT-UHFFFAOYSA-N dicesium;sulfide Chemical compound [S-2].[Cs+].[Cs+] QTNDMWXOEPGHBT-UHFFFAOYSA-N 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 229940069096 dodecene Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- FWDBOZPQNFPOLF-UHFFFAOYSA-N ethenyl(triethoxy)silane Chemical compound CCO[Si](OCC)(OCC)C=C FWDBOZPQNFPOLF-UHFFFAOYSA-N 0.000 description 1
- NKSJNEHGWDZZQF-UHFFFAOYSA-N ethenyl(trimethoxy)silane Chemical compound CO[Si](OC)(OC)C=C NKSJNEHGWDZZQF-UHFFFAOYSA-N 0.000 description 1
- WOXXJEVNDJOOLV-UHFFFAOYSA-N ethenyl-tris(2-methoxyethoxy)silane Chemical compound COCCO[Si](OCCOC)(OCCOC)C=C WOXXJEVNDJOOLV-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- JPZROSNLRWHSQQ-UHFFFAOYSA-N furan-2,5-dione;prop-2-enoic acid Chemical compound OC(=O)C=C.O=C1OC(=O)C=C1 JPZROSNLRWHSQQ-UHFFFAOYSA-N 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- NWVVVBRKAWDGAB-UHFFFAOYSA-N hydroquinone methyl ether Natural products COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 150000002500 ions Chemical group 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- GLNWILHOFOBOFD-UHFFFAOYSA-N lithium sulfide Chemical compound [Li+].[Li+].[S-2] GLNWILHOFOBOFD-UHFFFAOYSA-N 0.000 description 1
- 230000007774 longterm Effects 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
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000012768 molten material Substances 0.000 description 1
- BVFWLVGGBZGWPF-UHFFFAOYSA-N n,n-dimethylacetamide;1-methylazepan-2-one Chemical compound CN(C)C(C)=O.CN1CCCCCC1=O BVFWLVGGBZGWPF-UHFFFAOYSA-N 0.000 description 1
- KBJFYLLAMSZSOG-UHFFFAOYSA-N n-(3-trimethoxysilylpropyl)aniline Chemical compound CO[Si](OC)(OC)CCCNC1=CC=CC=C1 KBJFYLLAMSZSOG-UHFFFAOYSA-N 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- OTYIADUBGFZFSV-UHFFFAOYSA-N n-[4-(acetylsulfamoyl)phenyl]-2-[[2-[[4-(acetylsulfamoyl)phenyl]carbamoyl]phenyl]disulfanyl]benzamide Chemical compound C1=CC(S(=O)(=O)NC(=O)C)=CC=C1NC(=O)C1=CC=CC=C1SSC1=CC=CC=C1C(=O)NC1=CC=C(S(=O)(=O)NC(C)=O)C=C1 OTYIADUBGFZFSV-UHFFFAOYSA-N 0.000 description 1
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 description 1
- DVYVMJLSUSGYMH-UHFFFAOYSA-N n-methyl-3-trimethoxysilylpropan-1-amine Chemical compound CNCCC[Si](OC)(OC)OC DVYVMJLSUSGYMH-UHFFFAOYSA-N 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 150000001282 organosilanes Chemical class 0.000 description 1
- RPQRDASANLAFCM-UHFFFAOYSA-N oxiran-2-ylmethyl prop-2-enoate Chemical compound C=CC(=O)OCC1CO1 RPQRDASANLAFCM-UHFFFAOYSA-N 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 239000011236 particulate material Substances 0.000 description 1
- 238000005453 pelletization Methods 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- QQBPIHBUCMDKFG-UHFFFAOYSA-N phenazopyridine hydrochloride Chemical group Cl.NC1=NC(N)=CC=C1N=NC1=CC=CC=C1 QQBPIHBUCMDKFG-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 150000008301 phosphite esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
- 239000006187 pill Substances 0.000 description 1
- IWELDVXSEVIIGI-UHFFFAOYSA-N piperazin-2-one Chemical class O=C1CNCCN1 IWELDVXSEVIIGI-UHFFFAOYSA-N 0.000 description 1
- 150000003053 piperidines Chemical class 0.000 description 1
- 125000003386 piperidinyl group Chemical class 0.000 description 1
- 125000005936 piperidyl group Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 238000009428 plumbing Methods 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 229920005594 polymer fiber Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- DPLVEEXVKBWGHE-UHFFFAOYSA-N potassium sulfide Chemical compound [S-2].[K+].[K+] DPLVEEXVKBWGHE-UHFFFAOYSA-N 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000012066 reaction slurry Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- AHKSSQDILPRNLA-UHFFFAOYSA-N rubidium(1+);sulfide Chemical compound [S-2].[Rb+].[Rb+] AHKSSQDILPRNLA-UHFFFAOYSA-N 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 238000004513 sizing Methods 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229920002397 thermoplastic olefin Polymers 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- JXUKBNICSRJFAP-UHFFFAOYSA-N triethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CCO[Si](OCC)(OCC)CCCOCC1CO1 JXUKBNICSRJFAP-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 125000005591 trimellitate group Chemical group 0.000 description 1
- DQZNLOXENNXVAD-UHFFFAOYSA-N trimethoxy-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane Chemical compound C1C(CC[Si](OC)(OC)OC)CCC2OC21 DQZNLOXENNXVAD-UHFFFAOYSA-N 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- YUYCVXFAYWRXLS-UHFFFAOYSA-N trimethoxysilane Chemical compound CO[SiH](OC)OC YUYCVXFAYWRXLS-UHFFFAOYSA-N 0.000 description 1
- FJOMYOIAMDJAAY-UHFFFAOYSA-N undecane-1,1,1-tricarboxylic acid Chemical compound CCCCCCCCCCC(C(O)=O)(C(O)=O)C(O)=O FJOMYOIAMDJAAY-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000012463 white pigment Substances 0.000 description 1
- 239000010456 wollastonite Substances 0.000 description 1
- 229910052882 wollastonite Inorganic materials 0.000 description 1
- 239000001043 yellow dye Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- 150000007934 α,β-unsaturated carboxylic acids Chemical class 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/0005—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor using fibre reinforcements
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C45/00—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor
- B29C45/0001—Injection moulding, i.e. forcing the required volume of moulding material through a nozzle into a closed mould; Apparatus therefor characterised by the choice of material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D63/00—Flexible elongated elements, e.g. straps, for bundling or supporting articles
- B65D63/10—Non-metallic straps, tapes, or bands; Filamentary elements, e.g. strings, threads or wires; Joints between ends thereof
- B65D63/1018—Joints produced by application of integral securing members, e.g. buckles, wedges, tongue and slot, locking head and teeth or the like
- B65D63/1027—Joints produced by application of integral securing members, e.g. buckles, wedges, tongue and slot, locking head and teeth or the like the integral securing member being formed as a female and male locking member, e.g. locking head and locking teeth, or the like
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/285—Feeding the extrusion material to the extruder
- B29C48/297—Feeding the extrusion material to the extruder at several locations, e.g. using several hoppers or using a separate additive feeding
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/395—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders
- B29C48/40—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders
- B29C48/402—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die using screws surrounded by a cooperating barrel, e.g. single screw extruders using two or more parallel screws or at least two parallel non-intermeshing screws, e.g. twin screw extruders the screws having intermeshing parts
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C48/00—Extrusion moulding, i.e. expressing the moulding material through a die or nozzle which imparts the desired form; Apparatus therefor
- B29C48/25—Component parts, details or accessories; Auxiliary operations
- B29C48/36—Means for plasticising or homogenising the moulding material or forcing it through the nozzle or die
- B29C48/50—Details of extruders
- B29C48/76—Venting, drying means; Degassing means
- B29C48/765—Venting, drying means; Degassing means in the extruder apparatus
- B29C48/766—Venting, drying means; Degassing means in the extruder apparatus in screw extruders
- B29C48/767—Venting, drying means; Degassing means in the extruder apparatus in screw extruders through a degassing opening of a barrel
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2021/00—Use of unspecified rubbers as moulding material
- B29K2021/003—Thermoplastic elastomers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2081/00—Use of polymers having sulfur, with or without nitrogen, oxygen or carbon only, in the main chain, as moulding material
- B29K2081/04—Polysulfides, e.g. PPS, i.e. polyphenylene sulfide or derivatives thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0005—Condition, form or state of moulded material or of the material to be shaped containing compounding ingredients
- B29K2105/0032—Pigments, colouring agents or opacifiyng agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0088—Blends of polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/0094—Condition, form or state of moulded material or of the material to be shaped having particular viscosity
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/06—Condition, form or state of moulded material or of the material to be shaped containing reinforcements, fillers or inserts
- B29K2105/16—Fillers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2105/00—Condition, form or state of moulded material or of the material to be shaped
- B29K2105/24—Condition, form or state of moulded material or of the material to be shaped crosslinked or vulcanised
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0016—Non-flammable or resistant to heat
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0012—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds having particular thermal properties
- B29K2995/0017—Heat stable
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0082—Flexural strength; Flexion stiffness
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2995/00—Properties of moulding materials, reinforcements, fillers, preformed parts or moulds
- B29K2995/0037—Other properties
- B29K2995/0089—Impact strength or toughness
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2005/00—Elements of slide fasteners
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2007/00—Flat articles, e.g. films or sheets
- B29L2007/007—Narrow strips, e.g. ribbons, tapes, bands
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/727—Fastening elements
- B29L2031/7276—Straps or the like
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29L—INDEXING SCHEME ASSOCIATED WITH SUBCLASS B29C, RELATING TO PARTICULAR ARTICLES
- B29L2031/00—Other particular articles
- B29L2031/727—Fastening elements
- B29L2031/7282—Snap fasteners, clips, press-buttons
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T24/00—Buckles, buttons, clasps, etc.
- Y10T24/14—Bale and package ties, hose clamps
- Y10T24/1498—Plastic band
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T24/00—Buckles, buttons, clasps, etc.
- Y10T24/44—Clasp, clip, support-clamp, or required component thereof
Landscapes
- Mechanical Engineering (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Chemical & Material Sciences (AREA)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Installation Of Indoor Wiring (AREA)
- Clamps And Clips (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Health & Medical Sciences (AREA)
- Organic Insulating Materials (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
Description
[0001]本出願は、本明細書中、その全体が参照として含まれる2013年8月27日出願の米国特許仮出願シリアル番号第61/870,356号の出願の利益を主張する。
[0135]引張特性:引張弾性率、降伏応力、降伏歪み、破断点強さ、降伏点伸び、破断点伸びなどを含む引張特性は、ISO試験No.527(技術的にASTM D638と同等)に従って試験する。弾性率、歪み及び強さの測定は、長さ80mm、厚さ10mm、及び幅4mmをもつ同一試験ストリップサンプルで行う。試験温度は23℃であり、試験速度は5または50mm/分である。
[0137]ポリフェニレンスルフィド(Fortron(登録商標)0214、Ticonaより市販)を超高分子量ポリジメチルシロキサンとフュームドシリカ(Genioplast(登録商標)ペレットS、Wacker Chemie AGより市販)との混合物をタンブル混合して、一つのサンプルではアミノシランカップリング剤とも混合した。この混合物を310℃でWLE-25mmを通して溶融押出し、ペレット化した。配合物と機械的特性の試験結果を以下の表に示す。
[0139]組成物を成形するのに使用した材料は以下のものを含んでいた:
ポリアリーレンスルフィド:PPS1−Fortron(登録商標)0203 ポリフェニレンスルフィド、Ticona Engineering Polymers of Florence製、Kentucky。
本発明の具体的態様は以下のとおりである。
[1]
約100ミリメートル以下の厚さをもつ射出成形部品であって、前記射出成形部品は、ポリアリーレンスルフィドと架橋耐衝撃性改良剤とを含む熱可塑性組成物から成形され、前記射出成形部品は、温度23℃でISO試験No.179-1に従って測定して約3kJ/m 2 以上のノッチ付きシャルピー衝撃強さを示し、前記射出成形部品は、165℃で1000時間の加熱老化後で約60%以上の強度保持率を示す、前記射出成形部品。
[2]
前記射出成形部品がファスナーである、[1]に記載の射出成形部品。
[3]
前記ファスナーがケーブルタイ、クリップ、バンド、ハーネス、テープ、クランプまたはケーブルタイ・サドルである、[2]に記載の射出成形部品。
[4]
前記射出成形部品が、−30℃の温度でISO試験No.179-1に従って測定して、約8kJ/m 2 以上のノッチ付きシャルピー衝撃強さを示す、[1]に記載の射出成形部品。
[5]
前記射出成形部品が、0.2ミリメートルの厚さでV-0難燃性規格を満たす、[1]に記載の射出成形部品。
[6]
前記射出成形部品が、ISO試験No.178に従って測定して、約2500MPa以下の曲げ弾性率を示す、[1]に記載の射出成形部品。
[7]
前記ポリアリーレンスルフィドがポリフェニレンスルフィドである、[1]に記載の射出成形部品。
[8]
前記耐衝撃性改良剤がオレフィン性ターポリマーである、[1]に記載の射出成形部品。
[9]
[1]に記載の射出成形部品であって、架橋耐衝撃性改良剤が耐衝撃性改良剤のエポキシ官能基と架橋剤との反応生成物、または耐衝撃性改良剤の無水マレイン酸官能基と架橋剤との反応生成物を含む、前記射出成形部品。
[10]
前記架橋剤がテレフタル酸である、[9]に記載の射出成形部品。
[11]
前記熱可塑性組成物がさらにシロキサンポリマーを含む、[1]に記載の射出成形部品。
[12]
前記シロキサンポリマーが、ポリジメチルシロキサンである、[11]に記載の射出成形部品。
[13]
前記ポリジメチルシロキサンが、超高分子量ポリジメチルシロキサンである、[12]に記載の射出成形部品。
[14]
前記熱可塑性組成物がさらに、フュームドシリカを含む、[11]に記載の射出成形部品。
[15]
前記熱可塑性組成物がさらに、カップリング剤を含む、[11]に記載の射出成形部品。
[16]
前記カップリング剤が、アミノシランカップリング剤である、[15]に記載の射出成形部品。
[17]
前記熱可塑性組成物がさらに熱可塑性エラストマーを含む、[1]に記載の射出成形部品。
[18]
前記熱可塑性エラストマーが、(A-B) n {式中、Aはハードセグメントであり、Bはソフトセグメントである}より表される繰り返し構造をもつ、[17]に記載の射出成形部品。
[19]
前記熱可塑性エラストマーが、ポリアミドとポリエーテルの交互ブロックを含む、[18]に記載の射出成形部品。
[20]
前記熱可塑性組成物がさらに一種以上の添加剤を含む、[1]に記載の射出成形部品。
[21]
前記一種以上の添加剤が一種以上の充填剤を含む、[20]に記載の射出成形部品。
[22]
前記一種以上の充填剤が、繊維充填剤を含む、[21]に記載の射出成形部品。
[23]
[1]に記載の射出成形部品の成形方法であって、
温度310℃及び剪断速度1200秒 -1 においてキャピラリーレオメーターで測定して約3キロポアズ以下の溶融粘度をもつ熱可塑性組成物をモールドキャビティに射出する工程;及び
モールドキャビティから成形部品を排出する工程、
を含む前記方法。
Claims (23)
- 約100ミリメートル以下の厚さをもつ射出成形部品であって、前記射出成形部品は、ポリアリーレンスルフィドと架橋耐衝撃性改良剤とを含む熱可塑性組成物から成形され、前記架橋耐衝撃性改良剤が耐衝撃性改良剤の官能基と多官能性カルボン酸架橋剤との反応生成物を含み、前記射出成形部品は、温度23℃でISO試験No.179-1に従って測定して約3kJ/m2以上のノッチ付きシャルピー衝撃強さを示し、前記射出成形部品は、165℃で1000時間の加熱老化後で約60%以上の強度保持率を示し、前記射出成形部品がファスナーである、前記射出成形部品。
- 約100ミリメートル以下の厚さをもつ射出成形部品であって、前記射出成形部品は、ポリアリーレンスルフィドと架橋耐衝撃性改良剤とを含む熱可塑性組成物から成形され、前記架橋耐衝撃性改良剤が耐衝撃性改良剤の官能基と多官能性カルボン酸架橋剤との反応生成物を含み、前記多官能性カルボン酸架橋剤が、イソフタル酸、テレフタル酸、フタル酸、1,2-ジ(p-カルボキシフェニル)エタン、4,4'-ジカルボキシジフェニルエーテル、4,4'-二安息香酸、1,4-ナフタレンジカルボン酸、1,5-ナフタレンジカルボン酸、及びデカヒドロナフタレンジカルボン酸からなる群から選択され、前記射出成形部品は、温度23℃でISO試験No.179-1に従って測定して約3kJ/m 2 以上のノッチ付きシャルピー衝撃強さを示し、前記射出成形部品は、165℃で1000時間の加熱老化後で約60%以上の強度保持率を示す、前記射出成形部品。
- 前記ファスナーがケーブルタイ、クリップ、バンド、ハーネス、テープ、クランプまたはケーブルタイ・サドルである、請求項1に記載の射出成形部品。
- 前記射出成形部品が、−30℃の温度でISO試験No.179-1に従って測定して、約8kJ/m2以上のノッチ付きシャルピー衝撃強さを示す、請求項1又は2に記載の射出成形部品。
- 前記射出成形部品が、0.2ミリメートルの厚さでV-0難燃性規格を満たす、請求項1又は2に記載の射出成形部品。
- 前記射出成形部品が、ISO試験No.178に従って測定して、約2500MPa以下の曲げ弾性率を示す、請求項1又は2に記載の射出成形部品。
- 前記ポリアリーレンスルフィドがポリフェニレンスルフィドである、請求項1又は2に記載の射出成形部品。
- 前記耐衝撃性改良剤がオレフィン性ターポリマーである、請求項1又は2に記載の射出成形部品。
- 請求項1又は2に記載の射出成形部品であって、前記耐衝撃性改良剤の前記官能基がエポキシ官能基または無水マレイン酸官能基である、前記射出成形部品。
- 前記多官能性カルボン酸架橋剤がテレフタル酸である、請求項9に記載の射出成形部品。
- 前記熱可塑性組成物がさらにシロキサンポリマーを含む、請求項1又は2に記載の射出成形部品。
- 前記シロキサンポリマーが、ポリジメチルシロキサンである、請求項11に記載の射出成形部品。
- 前記ポリジメチルシロキサンが、超高分子量ポリジメチルシロキサンである、請求項12に記載の射出成形部品。
- 前記熱可塑性組成物がさらに、フュームドシリカを含む、請求項11に記載の射出成形部品。
- 前記熱可塑性組成物がさらに、カップリング剤を含む、請求項11に記載の射出成形部品。
- 前記カップリング剤が、アミノシランカップリング剤である、請求項15に記載の射出成形部品。
- 前記熱可塑性組成物がさらに熱可塑性エラストマーを含む、請求項1又は2に記載の射出成形部品。
- 前記熱可塑性エラストマーが、(A-B)n{式中、Aはハードセグメントであり、Bはソフトセグメントである}より表される繰り返し構造をもつ、請求項17に記載の射出成形部品。
- 前記熱可塑性エラストマーが、ポリアミドとポリエーテルの交互ブロックを含む、請求項18に記載の射出成形部品。
- 前記熱可塑性組成物がさらに一種以上の添加剤を含む、請求項1又は2に記載の射出成形部品。
- 前記一種以上の添加剤が一種以上の充填剤を含む、請求項20に記載の射出成形部品。
- 前記一種以上の充填剤が、繊維充填剤を含む、請求項21に記載の射出成形部品。
- 請求項1又は2に記載の射出成形部品の成形方法であって、
温度310℃及び剪断速度1200秒-1においてキャピラリーレオメーターで測定して約3キロポアズ以下の溶融粘度をもつ熱可塑性組成物をモールドキャビティに射出する工程;及び
モールドキャビティから成形部品を排出する工程、
を含む前記方法。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201361870356P | 2013-08-27 | 2013-08-27 | |
US61/870,356 | 2013-08-27 | ||
PCT/US2014/052462 WO2015031233A1 (en) | 2013-08-27 | 2014-08-25 | Heat resistant toughened thermoplastic composition for injection molding |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2017500404A JP2017500404A (ja) | 2017-01-05 |
JP6626444B2 true JP6626444B2 (ja) | 2019-12-25 |
Family
ID=52583642
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2016538995A Active JP6626444B2 (ja) | 2013-08-27 | 2014-08-25 | 射出成形用の耐熱性強化熱可塑性組成物 |
Country Status (3)
Country | Link |
---|---|
US (2) | US9718225B2 (ja) |
JP (1) | JP6626444B2 (ja) |
WO (1) | WO2015031233A1 (ja) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9494262B2 (en) | 2012-04-13 | 2016-11-15 | Ticona Llc | Automotive fuel lines including a polyarylene sulfide |
US9494260B2 (en) | 2012-04-13 | 2016-11-15 | Ticona Llc | Dynamically vulcanized polyarylene sulfide composition |
US9493646B2 (en) | 2012-04-13 | 2016-11-15 | Ticona Llc | Blow molded thermoplastic composition |
SE538496C2 (en) * | 2014-07-11 | 2016-08-09 | Resorbable Devices Ab | Cable tie based medical device |
US10926928B2 (en) | 2015-04-17 | 2021-02-23 | Abb Schweiz Ag | High strength cable tie |
WO2018190782A1 (en) * | 2015-04-17 | 2018-10-18 | Abb Technology Ag | High strength cable tie |
WO2017100395A1 (en) | 2015-12-11 | 2017-06-15 | Ticona Llc | Crosslinkable polyarylene sulfide composition |
CN108368339A (zh) * | 2015-12-11 | 2018-08-03 | 提克纳有限责任公司 | 聚芳硫醚组合物 |
US11383491B2 (en) | 2016-03-24 | 2022-07-12 | Ticona Llc | Composite structure |
WO2017214106A1 (en) * | 2016-06-09 | 2017-12-14 | Abb Schweiz Ag | Fiber guides for injection molding of fiber-reinfored cable ties |
RU2660874C2 (ru) * | 2016-08-10 | 2018-07-10 | Общество с ограниченной ответственностью "Конструкторское бюро электроаппаратуры" (ООО "КБЭА") | Полимерная композиция |
RU2635136C1 (ru) * | 2016-08-30 | 2017-11-09 | Общество с ограниченной ответственностью "Терморан" (ООО "Терморан") | Стеклонаполненная композиция на основе полифениленсульфида |
CA2994583C (en) | 2017-02-16 | 2022-07-05 | Abb Schweiz Ag | Reinforced cable tie strap and method of manufacture |
DE102018110191A1 (de) * | 2018-04-27 | 2019-10-31 | Deutsches Zentrum für Luft- und Raumfahrt e.V. | Kabelbinder umfassend faserartige Struktur |
JP7096454B1 (ja) * | 2020-12-25 | 2022-07-05 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物、成形品、及び光フェルール |
CN112724675A (zh) * | 2020-12-29 | 2021-04-30 | 富海(东营)新材料科技有限公司 | 一种聚苯硫醚复合材料及其制备方法 |
FR3139164B1 (fr) | 2022-08-26 | 2024-08-23 | Nexans | Colliers de serrage résistants au feu |
KR102615592B1 (ko) * | 2023-01-16 | 2023-12-20 | 주식회사 파이프랜드 | 강성과 탄성이 향상된 폴리에틸렌 합성수지관의 제조 방법 |
Family Cites Families (118)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3184439A (en) * | 1961-09-27 | 1965-05-18 | Hercules Powder Co Ltd | Polyesters of epoxidized aliphatic acids and crosslinked products |
US3354129A (en) | 1963-11-27 | 1967-11-21 | Phillips Petroleum Co | Production of polymers from aromatic compounds |
US3845010A (en) | 1971-12-17 | 1974-10-29 | Ford Motor Co | Thermoset molding powders employing glycidyl methacrylate functional polymer and dibasic acid crosslinking agent and moldings thereof |
US3919177A (en) | 1973-11-19 | 1975-11-11 | Phillips Petroleum Co | P-phenylene sulfide polymers |
DE2539132C2 (de) | 1975-09-03 | 1987-04-09 | Bayer Ag, 5090 Leverkusen | Verwendung hydrierter Dien-Copolymere als temperaturbeständige Materialien auf dem Dichtungssektor |
US4337329A (en) | 1979-12-06 | 1982-06-29 | Nippon Zeon Co., Ltd. | Process for hydrogenation of conjugated diene polymers |
JPS5682803A (en) | 1979-12-08 | 1981-07-06 | Nippon Zeon Co Ltd | Preparation of hydrogenated conjugated polymer |
JPS5817103A (ja) | 1981-07-24 | 1983-02-01 | Nippon Zeon Co Ltd | 共役ジエン系重合体の水素化方法 |
US4368321A (en) | 1981-09-01 | 1983-01-11 | Phillips Petroleum Company | Elevated, declining pressure dehydration of poly(arylene sulfide) prepolymerization mixture |
US4371671A (en) | 1981-09-01 | 1983-02-01 | Phillips Petroleum Company | Controlled, elevated pressure dehydration of poly(arylene sulfide) prepolymerization mixture |
CA1203047A (en) | 1982-12-08 | 1986-04-08 | Hormoz Azizian | Polymer hydrogenation process |
CA1220300A (en) | 1982-12-08 | 1987-04-07 | Polysar Limited | Polymer hydrogenation process |
DE3329974A1 (de) | 1983-08-19 | 1985-02-28 | Bayer Ag, 5090 Leverkusen | Herstellung von hydrierten nitrilkautschuken |
JPH0635544B2 (ja) * | 1985-03-11 | 1994-05-11 | 大日本インキ化学工業株式会社 | ポリアリ−レンスルフイド樹脂組成物 |
DE3671458D1 (de) | 1985-12-27 | 1990-06-28 | Toray Industries | Polyphenylensulfidharzzusammensetzung und verfahren zu ihrer herstellung. |
JPH0717750B2 (ja) | 1986-04-28 | 1995-03-01 | 呉羽化学工業株式会社 | ポリアリ−レンスルフイドの製造方法 |
US4810590A (en) | 1987-02-19 | 1989-03-07 | Phillips Petroleum Company | Poly(arylene sulfide) encapsulation process and article |
JPH0822930B2 (ja) | 1987-05-15 | 1996-03-06 | 呉羽化学工業株式会社 | 二軸延伸ポリアリーレンスルフィド系樹脂組成物フィルムおよびその製造法 |
FR2617176A1 (fr) | 1987-06-25 | 1988-12-30 | Charbonnages Ste Chimique | Compositions de polymeres thermoplastiques |
US5625002A (en) | 1988-06-02 | 1997-04-29 | Toray Industries, Inc. | Polyphenylene sulfide composition and shaped articles made therefrom |
JPH01306467A (ja) * | 1988-06-02 | 1989-12-11 | Toray Ind Inc | ポリフェニレンスルフィド組成物 |
JPH0759667B2 (ja) * | 1988-07-19 | 1995-06-28 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物並びにその成形品 |
US5047465A (en) | 1989-07-07 | 1991-09-10 | Hoechst Celanese Corporation | Impact modified polyphenylene sulfide |
US5270305A (en) | 1989-09-08 | 1993-12-14 | Glaxo Group Limited | Medicaments |
DE69026461T2 (de) | 1989-10-26 | 1996-11-28 | Idemitsu Petrochemical Co | Polyarylensulfid-Mischungen |
DE3937754A1 (de) | 1989-11-14 | 1991-05-16 | Bayer Ag | Mischungen aus polyarylensulfiden, nitrogruppenhaltigen vernetzern und glasfasern |
JP2943187B2 (ja) * | 1989-11-30 | 1999-08-30 | ダイキン工業株式会社 | ポリフェニレンスルフィド樹脂組成物及びその製法 |
DE3941564A1 (de) | 1989-12-16 | 1991-06-20 | Bayer Ag | Elastomermodifizierte polyarylensulfid-formmassen |
JPH0649789B2 (ja) | 1990-01-23 | 1994-06-29 | 工業技術院長 | 熱可塑性樹脂成形体の表面活性化方法 |
JP2736279B2 (ja) | 1990-04-25 | 1998-04-02 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物 |
WO1991018055A1 (en) | 1990-05-15 | 1991-11-28 | General Electric Company | Blends from carboxy-functionalized polyphenylene resins and ethylene-glycidyl methacrylate copolymers |
US5087666A (en) | 1990-07-10 | 1992-02-11 | Phillips Petroleum Company | Modified poly(arylene sulfide) composition with improved impact strength and reduced shrinkage |
JPH04170466A (ja) * | 1990-11-02 | 1992-06-18 | Asahi Chem Ind Co Ltd | Pps樹脂を含む樹脂組成物 |
JP2942635B2 (ja) | 1990-12-07 | 1999-08-30 | 出光石油化学株式会社 | ポリアリーレンスルフィド樹脂組成物 |
US6699946B1 (en) | 1991-12-13 | 2004-03-02 | Solvay (Societe Anonyme) | Polyphenylene sulphide-based compositions with improved impact strength and process for preparing them |
US5652287A (en) | 1992-06-15 | 1997-07-29 | Hoechst Celanese Corporation | Ductile poly(arylene sulfide) resin compositions |
JPH0665376A (ja) | 1992-08-19 | 1994-03-08 | Dainippon Ink & Chem Inc | ポリアリーレンスルフィド樹脂の架橋方法 |
CA2105211A1 (en) * | 1992-09-15 | 1994-03-16 | Lachhman H. Wadhwa | Reinforced poly(arylene sulfide) resins having reduced flash |
JP3245253B2 (ja) | 1992-09-17 | 2002-01-07 | 呉羽化学工業株式会社 | ポリアリーレンスルフィド樹脂組成物 |
JPH08506128A (ja) | 1993-01-08 | 1996-07-02 | カワサキ ケミカル ホールディング シーオー.アイエヌシー. | 強靭化ポリフェニレンスルフィド組成物およびそれを製造する方法 |
BE1007649A3 (fr) | 1993-10-21 | 1995-09-05 | Solvay | Compositions a base de polysulfure de phenylene de resistance au choc amelioree et procede pour les preparer. |
US5397839A (en) | 1993-12-13 | 1995-03-14 | Advanced Elastomer Systems, L.P. | Polyester-hydrogenated diene rubber compositions |
US5578679A (en) | 1993-12-28 | 1996-11-26 | Kureha Kagaku Kogyo Kabushiki Kaisha | Flame-resisting resin composition |
WO1995021217A1 (fr) | 1994-02-01 | 1995-08-10 | Asahi Kasei Kogyo Kabushiki Kaisha | Nouvelle composition de resine |
US5589544A (en) | 1994-07-06 | 1996-12-31 | Advanced Elastomer Systems, L.P. | Soft thermoplastic elastomers having improved resistance to oil swell and compression set |
DE4439766C1 (de) | 1994-11-07 | 1996-04-04 | Hoechst Ag | Formteile aus Polyacetal mit direkt angeformten Funktionselementen |
JPH0940865A (ja) | 1995-05-23 | 1997-02-10 | Kureha Chem Ind Co Ltd | ポリアリ−レンスルフィド樹脂組成物 |
JPH09124931A (ja) | 1995-06-07 | 1997-05-13 | General Electric Co <Ge> | ポリ(フェニレンエーテル)、ポリ(アリーレンスルフィド)及びオルトエステル化合物からなる組成物 |
JPH0959514A (ja) | 1995-08-28 | 1997-03-04 | Dainippon Ink & Chem Inc | 非強化ポリフェニレンスルフィド樹脂組成物およびその製造方法 |
US5817723A (en) | 1995-09-07 | 1998-10-06 | E. I. Du Pont De Nemours And Company | Toughened thermoplastic polymer compositions |
JP3618018B2 (ja) | 1995-09-22 | 2005-02-09 | 呉羽化学工業株式会社 | ポリフェニレンスルフィド樹脂組成物 |
US5840830A (en) | 1996-02-21 | 1998-11-24 | Kureha Kagaku Kogyo K.K. | Process for producing poly(arylene sulfide) |
US6020431A (en) | 1996-07-26 | 2000-02-01 | Advanced Elastomer Systems, L.P. | Dynamic vulcanizates of engineering thermoplastic and acrylate rubber blends with dissimilar cure sites using a common curative |
JP3889122B2 (ja) | 1997-08-06 | 2007-03-07 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物 |
US6001934A (en) | 1997-09-03 | 1999-12-14 | Tonen Chemical Co. | Process for the preparation of a functional group-containing polyarylene sulfide resin |
JPH11124476A (ja) | 1997-10-24 | 1999-05-11 | Dainippon Ink & Chem Inc | 熱可塑性樹脂組成物 |
US6015858A (en) | 1998-09-08 | 2000-01-18 | Dow Corning Corporation | Thermoplastic silicone elastomers based on fluorocarbon resin |
JP4295848B2 (ja) * | 1998-12-24 | 2009-07-15 | 出光興産株式会社 | 電子部品封止用ポリアリーレンスルフィド樹脂組成物 |
US6608136B1 (en) | 1999-07-26 | 2003-08-19 | E. I. Du Pont De Nemours And Company | Polyphenylene sulfide alloy composition |
JP4062828B2 (ja) | 1999-08-20 | 2008-03-19 | 日本ゼオン株式会社 | 架橋性ゴム組成物および架橋物 |
DE19942743A1 (de) | 1999-09-07 | 2001-03-08 | Bayer Ag | Kautschukmischungen für Walzenbeläge |
US6281286B1 (en) | 1999-09-09 | 2001-08-28 | Dow Corning Corporation | Toughened thermoplastic resins |
JP2001115020A (ja) | 1999-10-22 | 2001-04-24 | Dainippon Ink & Chem Inc | 水廻り部品用樹脂組成物 |
US6362287B1 (en) | 2000-03-27 | 2002-03-26 | Dow Corning Corportion | Thermoplastic silicone elastomers formed from nylon resins |
JP2001279097A (ja) | 2000-03-31 | 2001-10-10 | Dainippon Ink & Chem Inc | ポリアリーレンスルフィド組成物 |
DE10025257A1 (de) | 2000-05-22 | 2001-12-06 | Ticona Gmbh | Verbund-Formteile enthaltend Polyarylensulfid und Siliconkautschuk |
US6362288B1 (en) | 2000-07-26 | 2002-03-26 | Dow Corning Corporation | Thermoplastic silicone elastomers from compatibilized polyamide resins |
US6417293B1 (en) | 2000-12-04 | 2002-07-09 | Dow Corning Corporation | Thermoplastic silicone elastomers formed from polyester resins |
JP2002226604A (ja) | 2001-01-31 | 2002-08-14 | Toyoda Gosei Co Ltd | 樹脂成形体 |
JP3811012B2 (ja) | 2001-01-31 | 2006-08-16 | 豊田合成株式会社 | 燃料系部品 |
JP4049580B2 (ja) | 2001-01-31 | 2008-02-20 | 豊田合成株式会社 | 高圧ガス容器用ライナー及び高圧ガス容器 |
KR100788855B1 (ko) | 2001-03-27 | 2007-12-27 | 다이니혼 잉키 가가쿠 고교 가부시키가이샤 | 산화 가교된 폴리아릴렌설파이드의 제조 방법 |
US6569958B1 (en) | 2001-10-19 | 2003-05-27 | Dow Corning Corporation | Thermoplastic silicone elastomers from compatibilized polyester resins |
US6569955B1 (en) | 2001-10-19 | 2003-05-27 | Dow Corning Corporation | Thermoplastic silicone elastomers from compatibilized polyamide resins |
DE10209420A1 (de) | 2002-03-05 | 2003-09-18 | Ticona Gmbh | Langfaserverstärkte thermoplastische Kunststoffstrukturen |
WO2003085681A1 (en) * | 2002-04-01 | 2003-10-16 | World Properties, Inc. | Electrically conductive polymeric foams and elastomers and methods of manufacture thereof |
US6743868B2 (en) | 2002-07-18 | 2004-06-01 | Dow Corning Corporation | Polyamide based thermoplastic silicone elastomers |
JP2004300270A (ja) | 2003-03-31 | 2004-10-28 | Dainippon Ink & Chem Inc | 流体配管用部材 |
JP4235893B2 (ja) | 2003-03-31 | 2009-03-11 | Dic株式会社 | 燃料系部品 |
JP4307908B2 (ja) | 2003-06-05 | 2009-08-05 | ポリプラスチックス株式会社 | ポリアリーレンサルファイド樹脂組成物および塗装成形品 |
JP3938169B2 (ja) | 2003-09-30 | 2007-06-27 | 東海ゴム工業株式会社 | 自動車用燃料系ホース |
US6888719B1 (en) | 2003-10-16 | 2005-05-03 | Micron Technology, Inc. | Methods and apparatuses for transferring heat from microelectronic device modules |
JP4600015B2 (ja) | 2003-12-02 | 2010-12-15 | 東レ株式会社 | 樹脂組成物およびその製造方法 |
JP4552434B2 (ja) | 2003-12-19 | 2010-09-29 | Dic株式会社 | 多層成形体 |
US7041741B2 (en) | 2004-01-08 | 2006-05-09 | Teknor Apex Company | Toughened polymer compositions |
JP2005299629A (ja) | 2004-03-18 | 2005-10-27 | Tokai Rubber Ind Ltd | 自動車用燃料系ホースおよびその製法 |
US7803856B2 (en) * | 2004-05-04 | 2010-09-28 | Sabic Innovative Plastics Ip B.V. | Halogen-free flame retardant polyamide composition with improved electrical and flammability properties |
JP4600016B2 (ja) | 2004-08-27 | 2010-12-15 | 東レ株式会社 | 熱可塑性樹脂組成物およびその製造方法 |
JP5132031B2 (ja) * | 2004-08-30 | 2013-01-30 | Dic株式会社 | ポリアリーレンスルフィド樹脂組成物より成る流体配管部材 |
PL1814704T3 (pl) * | 2004-10-22 | 2009-12-31 | Dow Global Technologies Inc | Wyroby kompozytowe z tworzyw sztucznych i sposób ich wytwarzania |
US20060229417A1 (en) | 2005-04-07 | 2006-10-12 | Frederic Ferrate | Polyphenylene sulfide- silicone vulcanizates |
US7718736B2 (en) * | 2005-06-30 | 2010-05-18 | Freudenberg-Nok General Partnership | Base resistant FKM-TPV elastomers |
JP2007169550A (ja) | 2005-12-26 | 2007-07-05 | Dainippon Ink & Chem Inc | 樹脂成型体用組成物及び燃料電池用セパレータ |
WO2007102827A1 (en) | 2006-03-09 | 2007-09-13 | Ticona Llc | Flexible, hydrocarbon-resistant polyarylenesulfide compounds and articles |
CN102585494B (zh) | 2006-03-23 | 2014-09-03 | 东丽株式会社 | 热塑性树脂组合物、其制造方法以及成形品 |
WO2008048266A1 (en) | 2006-10-20 | 2008-04-24 | Ticona Llc | Polyether ether ketone/ polyphenylene sulfide blend |
JP5051428B2 (ja) | 2006-10-31 | 2012-10-17 | Dic株式会社 | 多層成形体 |
JP5092833B2 (ja) | 2007-03-23 | 2012-12-05 | 東レ株式会社 | ポリフェニレンスルフィド樹脂組成物を成形してなる車載燃料ポンプモジュール用部品 |
JP5029881B2 (ja) | 2007-03-29 | 2012-09-19 | Dic株式会社 | ポリアリーレンスルフィド樹脂組成物 |
JP5206492B2 (ja) * | 2008-03-28 | 2013-06-12 | 東レ株式会社 | ポリフェニレンスルフィド樹脂組成物の製造方法およびポリフェニレンスルフィド樹脂組成物 |
RU2011124512A (ru) | 2008-11-21 | 2012-12-27 | Дик Корпорейшн | Композиция полиариленсульфидной смолы и элемент трубопровода для текучей среды |
JP5454877B2 (ja) | 2009-07-17 | 2014-03-26 | Dic株式会社 | 多層成形体及びそれを用いた燃料用部品 |
KR101759185B1 (ko) | 2010-05-26 | 2017-07-31 | 디아이씨 가부시끼가이샤 | 블로우 중공 성형품용 수지 조성물, 블로우 중공 성형품 및 제조 방법 |
JP5872191B2 (ja) * | 2010-06-11 | 2016-03-01 | ティコナ・エルエルシー | ブロー成形品およびその製造方法 |
US20120037397A1 (en) | 2010-08-10 | 2012-02-16 | General Cable Technologies Corporation | Polymer compositions and their use as cable coverings |
MY177797A (en) * | 2010-10-29 | 2020-09-23 | Toray Industries | Method for producing polyarylene sulfide, and polyarylene sulfide |
JP2014517104A (ja) * | 2011-05-12 | 2014-07-17 | ハンツマン・アドバンスド・マテリアルズ・アメリカズ・エルエルシー | 高い熱安定性とじん性を示すエポキシ樹脂 |
JP5905877B2 (ja) * | 2011-05-20 | 2016-04-20 | 旭化成ケミカルズ株式会社 | 難燃樹脂フィルム及びそれを用いた太陽電池バックシート |
KR20140063838A (ko) | 2011-09-20 | 2014-05-27 | 티코나 엘엘씨 | 전자 장치용의 오버몰딩된 복합 구조체 |
WO2013066663A2 (en) | 2011-10-31 | 2013-05-10 | Ticona Llc | Thermoplastic composition for use in forming a laser direct structured substrate |
JP6062924B2 (ja) * | 2012-03-30 | 2017-01-18 | 株式会社クレハ | 粒状ポリアリーレンスルフィド及びその製造方法 |
US9758674B2 (en) * | 2012-04-13 | 2017-09-12 | Ticona Llc | Polyarylene sulfide for oil and gas flowlines |
US9765219B2 (en) * | 2012-04-13 | 2017-09-19 | Ticona Llc | Polyarylene sulfide components for heavy duty trucks |
US9494262B2 (en) * | 2012-04-13 | 2016-11-15 | Ticona Llc | Automotive fuel lines including a polyarylene sulfide |
US9494260B2 (en) * | 2012-04-13 | 2016-11-15 | Ticona Llc | Dynamically vulcanized polyarylene sulfide composition |
US9493646B2 (en) * | 2012-04-13 | 2016-11-15 | Ticona Llc | Blow molded thermoplastic composition |
US9061807B2 (en) * | 2012-05-08 | 2015-06-23 | Thomas & Betts International, Inc. | Cable tie head |
US20150111794A1 (en) * | 2013-10-21 | 2015-04-23 | Ticona Gmbh | Two Component Polyoxymethylene Based Systems |
-
2014
- 2014-08-25 JP JP2016538995A patent/JP6626444B2/ja active Active
- 2014-08-25 US US14/467,374 patent/US9718225B2/en active Active
- 2014-08-25 WO PCT/US2014/052462 patent/WO2015031233A1/en active Application Filing
-
2017
- 2017-07-31 US US15/664,307 patent/US20180015648A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US20180015648A1 (en) | 2018-01-18 |
US20150064437A1 (en) | 2015-03-05 |
US9718225B2 (en) | 2017-08-01 |
JP2017500404A (ja) | 2017-01-05 |
WO2015031233A1 (en) | 2015-03-05 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6626444B2 (ja) | 射出成形用の耐熱性強化熱可塑性組成物 | |
JP6836490B2 (ja) | ブロー成形された熱可塑性組成物 | |
KR102695731B1 (ko) | 가교결합성 폴리아릴렌 설파이드 조성물 | |
JP7033624B2 (ja) | シランカップリング剤及びシリコーンエラストマーを含むポリアリーレンスルフィド組成物 | |
US10359129B2 (en) | Automotive fuel lines including a polyarylene sulfide | |
US20200216667A1 (en) | Polyarylene Sulfide Composition | |
JP6672218B2 (ja) | 自動車用途用のポリアリーレンスルフィド部品 | |
JP6714510B2 (ja) | 炭化水素取り込みの低い熱可塑性組成物 | |
WO2013155425A2 (en) | Polyarylene sulfide composition including a functionalized siloxane polymer and a non-aromatic impact modifier | |
WO2015122941A1 (en) | Toughened polyarylene sulfide composition | |
KR20240042088A (ko) | 연료 전지 시스템에 사용하기 위한 유체 부재 | |
US20160168382A1 (en) | Stabilized Flexible Thermoplastic Composition and Products Formed Therefrom | |
JP5103763B2 (ja) | 樹脂組成物およびそれからなる成形品 | |
JP2008214383A (ja) | ポリアリ−レンスルフィド樹脂組成物 | |
CN118139743A (zh) | 用于燃料电池系统的流体构件 | |
JP2017031310A (ja) | ポリ(エーテルイミド−シロキサン)共重合体樹脂組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20170731 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20180713 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20180720 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20181019 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20181205 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20190515 |
|
A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20190806 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20191010 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20191031 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20191129 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 6626444 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313113 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |