CN109071946A - 具有优异的耐化学性的聚芳硫醚树脂组合物 - Google Patents
具有优异的耐化学性的聚芳硫醚树脂组合物 Download PDFInfo
- Publication number
- CN109071946A CN109071946A CN201780029329.2A CN201780029329A CN109071946A CN 109071946 A CN109071946 A CN 109071946A CN 201780029329 A CN201780029329 A CN 201780029329A CN 109071946 A CN109071946 A CN 109071946A
- Authority
- CN
- China
- Prior art keywords
- resin combination
- iodine
- glass fibre
- hydrotalcite
- silane
- 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.)
- Granted
Links
- 239000000126 substance Substances 0.000 title claims abstract description 22
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 title claims description 5
- 229920000412 polyarylene Polymers 0.000 title claims description 4
- 239000011342 resin composition Substances 0.000 title description 5
- 229920005989 resin Polymers 0.000 claims abstract description 63
- 239000011347 resin Substances 0.000 claims abstract description 63
- -1 poly arylidene thio-ester Chemical class 0.000 claims abstract description 56
- 239000003365 glass fiber Substances 0.000 claims abstract description 25
- 229910001701 hydrotalcite Inorganic materials 0.000 claims abstract description 23
- 229960001545 hydrotalcite Drugs 0.000 claims abstract description 23
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims abstract description 22
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 15
- 239000011734 sodium Substances 0.000 claims abstract description 15
- 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 claims abstract description 14
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 14
- 229910052740 iodine Inorganic materials 0.000 claims description 43
- 239000011630 iodine Substances 0.000 claims description 41
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 24
- 229910000077 silane Inorganic materials 0.000 claims description 20
- 238000000465 moulding Methods 0.000 claims description 18
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 16
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 239000000155 melt Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000007788 liquid Substances 0.000 claims description 3
- 239000002216 antistatic agent Substances 0.000 claims description 2
- 239000011152 fibreglass Substances 0.000 claims description 2
- 239000000314 lubricant Substances 0.000 claims description 2
- 239000002667 nucleating agent Substances 0.000 claims description 2
- 239000000049 pigment Substances 0.000 claims description 2
- 239000012748 slip agent Substances 0.000 claims description 2
- 239000005388 borosilicate glass Substances 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 abstract description 2
- 239000004734 Polyphenylene sulfide Substances 0.000 description 35
- 229920000069 polyphenylene sulfide Polymers 0.000 description 35
- 238000006116 polymerization reaction Methods 0.000 description 27
- 238000000034 method Methods 0.000 description 18
- 238000006243 chemical reaction Methods 0.000 description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 239000005864 Sulphur Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 8
- 239000000835 fiber Substances 0.000 description 8
- 238000002156 mixing Methods 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 239000000376 reactant Substances 0.000 description 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 6
- 238000005452 bending Methods 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 6
- 150000003839 salts Chemical group 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- IOJUPLGTWVMSFF-UHFFFAOYSA-N cyclobenzothiazole Natural products C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- UUEWCQRISZBELL-UHFFFAOYSA-N 3-trimethoxysilylpropane-1-thiol Chemical compound CO[Si](OC)(OC)CCCS UUEWCQRISZBELL-UHFFFAOYSA-N 0.000 description 4
- GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 239000000395 magnesium oxide Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- TXDNPSYEJHXKMK-UHFFFAOYSA-N sulfanylsilane Chemical compound S[SiH3] TXDNPSYEJHXKMK-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 150000004756 silanes Chemical class 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- BBOLNFYSRZVALD-UHFFFAOYSA-N 1,2-diiodobenzene Chemical compound IC1=CC=CC=C1I BBOLNFYSRZVALD-UHFFFAOYSA-N 0.000 description 2
- SCCCFNJTCDSLCY-UHFFFAOYSA-N 1-iodo-4-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(I)C=C1 SCCCFNJTCDSLCY-UHFFFAOYSA-N 0.000 description 2
- DCQBZYNUSLHVJC-UHFFFAOYSA-N 3-triethoxysilylpropane-1-thiol Chemical compound CCO[Si](OCC)(OCC)CCCS DCQBZYNUSLHVJC-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- 235000021355 Stearic acid Nutrition 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- MCEBKLYUUDGVMD-UHFFFAOYSA-N [SiH3]S(=O)=O Chemical compound [SiH3]S(=O)=O MCEBKLYUUDGVMD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000002528 anti-freeze Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- OCKPCBLVNKHBMX-UHFFFAOYSA-N butylbenzene Chemical compound CCCCC1=CC=CC=C1 OCKPCBLVNKHBMX-UHFFFAOYSA-N 0.000 description 2
- 238000011088 calibration curve Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229940125904 compound 1 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- 229910052593 corundum Inorganic materials 0.000 description 2
- 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 2
- 238000000113 differential scanning calorimetry Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000009955 starching Methods 0.000 description 2
- 239000008117 stearic acid Substances 0.000 description 2
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 2
- 229960002447 thiram Drugs 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 229910001845 yogo sapphire Inorganic materials 0.000 description 2
- QQFIQWBUKYSUHM-UHFFFAOYSA-N (2,3-diiodophenyl)-phenylmethanone Chemical compound IC1=CC=CC(C(=O)C=2C=CC=CC=2)=C1I QQFIQWBUKYSUHM-UHFFFAOYSA-N 0.000 description 1
- QFLWZFQWSBQYPS-AWRAUJHKSA-N (3S)-3-[[(2S)-2-[[(2S)-2-[5-[(3aS,6aR)-2-oxo-1,3,3a,4,6,6a-hexahydrothieno[3,4-d]imidazol-4-yl]pentanoylamino]-3-methylbutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-[1-bis(4-chlorophenoxy)phosphorylbutylamino]-4-oxobutanoic acid Chemical compound CCCC(NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)CCCCC1SC[C@@H]2NC(=O)N[C@H]12)C(C)C)P(=O)(Oc1ccc(Cl)cc1)Oc1ccc(Cl)cc1 QFLWZFQWSBQYPS-AWRAUJHKSA-N 0.000 description 1
- UYHYZAYIQAVJCN-UHFFFAOYSA-N 1,2-diiodonaphthalene Chemical compound C1=CC=CC2=C(I)C(I)=CC=C21 UYHYZAYIQAVJCN-UHFFFAOYSA-N 0.000 description 1
- YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- JTPNRXUCIXHOKM-UHFFFAOYSA-N 1-chloronaphthalene Chemical compound C1=CC=C2C(Cl)=CC=CC2=C1 JTPNRXUCIXHOKM-UHFFFAOYSA-N 0.000 description 1
- VREPHMROZZKOOL-UHFFFAOYSA-N 12-trimethoxysilyldodecane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCCCCCCCCCS VREPHMROZZKOOL-UHFFFAOYSA-N 0.000 description 1
- UAXHQOHEACNJSR-UHFFFAOYSA-N 18-trimethoxysilyloctadecane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCCCCCCCCCCCCCCCS UAXHQOHEACNJSR-UHFFFAOYSA-N 0.000 description 1
- 229940069744 2,2'-dithiobisbenzothiazole Drugs 0.000 description 1
- VALABLHQPAMOBO-UHFFFAOYSA-N 2,4-diiodo-1-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(I)C=C1I VALABLHQPAMOBO-UHFFFAOYSA-N 0.000 description 1
- JEVDBSPYZIVTGM-UHFFFAOYSA-N 2,6-diiodonaphthalene Chemical compound C1=C(I)C=CC2=CC(I)=CC=C21 JEVDBSPYZIVTGM-UHFFFAOYSA-N 0.000 description 1
- KFEVWIIWNXMTGM-UHFFFAOYSA-N 2-(2,2-dimethoxyethoxysilyl)ethanethiol Chemical compound SCC[SiH2]OCC(OC)OC KFEVWIIWNXMTGM-UHFFFAOYSA-N 0.000 description 1
- FTJVOUKRKPQVRL-UHFFFAOYSA-N 2-ethylhexoxysilane Chemical compound CCCCC(CC)CO[SiH3] FTJVOUKRKPQVRL-UHFFFAOYSA-N 0.000 description 1
- KQDJTBPASNJQFQ-UHFFFAOYSA-N 2-iodophenol Chemical compound OC1=CC=CC=C1I KQDJTBPASNJQFQ-UHFFFAOYSA-N 0.000 description 1
- LOSLJXKHQKRRFN-UHFFFAOYSA-N 2-trimethoxysilylethanethiol Chemical compound CO[Si](OC)(OC)CCS LOSLJXKHQKRRFN-UHFFFAOYSA-N 0.000 description 1
- UZEBPNPRXOYGRA-UHFFFAOYSA-N 2-tripropoxysilylethanethiol Chemical compound CCCO[Si](CCS)(OCCC)OCCC UZEBPNPRXOYGRA-UHFFFAOYSA-N 0.000 description 1
- DQMRXALBJIVORP-UHFFFAOYSA-N 3-[methoxy(dimethyl)silyl]propane-1-thiol Chemical compound CO[Si](C)(C)CCCS DQMRXALBJIVORP-UHFFFAOYSA-N 0.000 description 1
- BUZICZZQJDLXJN-UHFFFAOYSA-N 3-azaniumyl-4-hydroxybutanoate Chemical compound OCC(N)CC(O)=O BUZICZZQJDLXJN-UHFFFAOYSA-N 0.000 description 1
- QSUKAUDXXCSABB-UHFFFAOYSA-N 3-trimethoxysilylcyclohexane-1-thiol Chemical compound CO[Si](OC)(OC)C1CCCC(S)C1 QSUKAUDXXCSABB-UHFFFAOYSA-N 0.000 description 1
- DECHJJJXDGPZHY-UHFFFAOYSA-N 3-tripropoxysilylpropane-1-thiol Chemical compound CCCO[Si](CCCS)(OCCC)OCCC DECHJJJXDGPZHY-UHFFFAOYSA-N 0.000 description 1
- GSOFTRZWLZLBLR-UHFFFAOYSA-N 4-(1h-pyrrol-2-yl)morpholine Chemical class C1COCCN1C1=CC=CN1 GSOFTRZWLZLBLR-UHFFFAOYSA-N 0.000 description 1
- LMAFAQBMCIYHQS-UHFFFAOYSA-N 4-trimethoxysilylbutane-1-thiol Chemical compound CO[Si](OC)(OC)CCCCS LMAFAQBMCIYHQS-UHFFFAOYSA-N 0.000 description 1
- JRYUZCLLNMIMQM-UHFFFAOYSA-N 4-tripropoxysilylbutane-1-thiol Chemical compound CCCO[Si](OCCC)(OCCC)CCCCS JRYUZCLLNMIMQM-UHFFFAOYSA-N 0.000 description 1
- 229930185605 Bisphenol Natural products 0.000 description 1
- VXMAETDNBRYZJO-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)C1=CC=CC=C1.[I] Chemical compound C(C1=CC=CC=C1)(=O)C1=CC=CC=C1.[I] VXMAETDNBRYZJO-UHFFFAOYSA-N 0.000 description 1
- WGINUBKWLUSQGI-UHFFFAOYSA-N C1(=CC=CC=C1)C1=CC=CC=C1.[I] Chemical group C1(=CC=CC=C1)C1=CC=CC=C1.[I] WGINUBKWLUSQGI-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XAQHXGSHRMHVMU-UHFFFAOYSA-N [S].[S] Chemical compound [S].[S] XAQHXGSHRMHVMU-UHFFFAOYSA-N 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- JIFPTBLGXRKRAO-UHFFFAOYSA-K aluminum;magnesium;hydroxide;sulfate Chemical compound [OH-].[Mg+2].[Al+3].[O-]S([O-])(=O)=O JIFPTBLGXRKRAO-UHFFFAOYSA-K 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- XWQLYVIMMBLXPY-UHFFFAOYSA-N butan-2-yloxysilane Chemical compound CCC(C)O[SiH3] XWQLYVIMMBLXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- BWDDKSQGVQKNAM-UHFFFAOYSA-L calcium octadecanoate octadecanoic acid Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC(O)=O.CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O BWDDKSQGVQKNAM-UHFFFAOYSA-L 0.000 description 1
- 235000012241 calcium silicate Nutrition 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- JYYOBHFYCIDXHH-UHFFFAOYSA-N carbonic acid;hydrate Chemical compound O.OC(O)=O JYYOBHFYCIDXHH-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000004035 construction material Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- UBHZUDXTHNMNLD-UHFFFAOYSA-N dimethylsilane Chemical compound C[SiH2]C UBHZUDXTHNMNLD-UHFFFAOYSA-N 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000012760 heat stabilizer Substances 0.000 description 1
- 229960002163 hydrogen peroxide Drugs 0.000 description 1
- 238000002354 inductively-coupled plasma atomic emission spectroscopy Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229940006461 iodide ion Drugs 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 238000005342 ion exchange Methods 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229960004018 magaldrate Drugs 0.000 description 1
- UIUXUFNYAYAMOE-UHFFFAOYSA-N methylsilane Chemical compound [SiH3]C UIUXUFNYAYAMOE-UHFFFAOYSA-N 0.000 description 1
- CMAUJSNXENPPOF-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)-n-cyclohexylcyclohexanamine Chemical compound C1CCCCC1N(C1CCCCC1)SC1=NC2=CC=CC=C2S1 CMAUJSNXENPPOF-UHFFFAOYSA-N 0.000 description 1
- DEQZTKGFXNUBJL-UHFFFAOYSA-N n-(1,3-benzothiazol-2-ylsulfanyl)cyclohexanamine Chemical compound C1CCCCC1NSC1=NC2=CC=CC=C2S1 DEQZTKGFXNUBJL-UHFFFAOYSA-N 0.000 description 1
- RRHNGIRRWDWWQQ-UHFFFAOYSA-N n-iodoaniline Chemical compound INC1=CC=CC=C1 RRHNGIRRWDWWQQ-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- HCIWORWMHIXTLB-UHFFFAOYSA-N octylsulfanylsilane Chemical compound C(CCCCCCC)S[SiH3] HCIWORWMHIXTLB-UHFFFAOYSA-N 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 1
- 229920006389 polyphenyl polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 238000012805 post-processing Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- HCOKJWUULRTBRS-UHFFFAOYSA-N propan-2-yloxysilane Chemical compound CC(C)O[SiH3] HCOKJWUULRTBRS-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- YWWOEPOBDHZQEJ-UHFFFAOYSA-N s-(4-cyclohexyl-1,3-benzothiazol-2-yl)thiohydroxylamine Chemical compound C1=CC=C2SC(SN)=NC2=C1C1CCCCC1 YWWOEPOBDHZQEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- FCEHBMOGCRZNNI-UHFFFAOYSA-N thianaphthalene Natural products C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 1
- RKQOSDAEEGPRER-UHFFFAOYSA-L zinc diethyldithiocarbamate Chemical compound [Zn+2].CCN(CC)C([S-])=S.CCN(CC)C([S-])=S RKQOSDAEEGPRER-UHFFFAOYSA-L 0.000 description 1
- MBBWTVUFIXOUBE-UHFFFAOYSA-L zinc;dicarbamodithioate Chemical compound [Zn+2].NC([S-])=S.NC([S-])=S MBBWTVUFIXOUBE-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/0209—Polyarylenethioethers derived from monomers containing one aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G75/00—Macromolecular compounds obtained by reactions forming a linkage containing sulfur with or without nitrogen, oxygen, or carbon in the main chain of the macromolecule
- C08G75/02—Polythioethers
- C08G75/0204—Polyarylenethioethers
- C08G75/025—Preparatory processes
- C08G75/0263—Preparatory processes using elemental sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K13/00—Use of mixtures of ingredients not covered by one single of the preceding main groups, each of these compounds being essential
- C08K13/02—Organic and inorganic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/34—Silicon-containing compounds
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/40—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/548—Silicon-containing compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/02—Fibres or whiskers
- C08K7/04—Fibres or whiskers inorganic
- C08K7/14—Glass
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/12—Adsorbed ingredients, e.g. ingredients on carriers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L81/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing sulfur with or without nitrogen, oxygen or carbon only; Compositions of polysulfones; Compositions of derivatives of such polymers
- C08L81/02—Polythioethers; Polythioether-ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/50—Physical properties
- C08G2261/63—Viscosity
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/24—Acids; Salts thereof
- C08K3/26—Carbonates; Bicarbonates
- C08K2003/267—Magnesium carbonate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/003—Additives being defined by their diameter
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/004—Additives being defined by their length
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/005—Additives being defined by their particle size in general
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
项目 | 性质 |
PPS 1 | MV:2150泊,Tm:280℃,Mn:17420 |
PPS 2 | MV:715泊,Tm:281℃,Mn:13290 |
PPS 3 | MV:3650泊,Tm:281℃,Mn:19010 |
PPS 4 | Celanese 0205P4,MV:700泊,Tm:280℃ |
PPS 5 | Solvay P-6,MI(380g/10min,@316℃,5kg),Tm:281℃ |
PPS 6 | R4-220(Solvay) |
玻璃纤维1 | Jushi-584,平均直径11μm,平均长度4.5mm,氨基硅烷上浆 |
玻璃纤维2 | FT-562(Owens Corning),直径10μm,长度3.0mm,环氧硅烷上浆 |
巯基硅烷化合物1 | Momentive公司,Silquest A-189,3-巯基丙基三甲氧基硅烷 |
巯基硅烷化合物2 | 干燥硅烷(A-189/硅酸钙=7/3重量比) |
环氧硅烷化合物 | Momentive A-187,环氧硅烷化合物 |
水滑石 | 平均长度0.5μm,MgO/Al<sub>2</sub>O<sub>3</sub>重量比:4.5,kyowa化学公司,DHT-4A |
金属基硬脂酸 | 硬脂酸钙,Tm:150℃ |
项目(重量含量%) | 实施例1 | 实施例2 | 实施例3 | 实施例4 | 实施例5 | 实施例6 |
PPS 1 | 59.2 | - | - | 59.2 | 59.0 | 59.0 |
PPS 2 | - | 59.2 | - | - | - | - |
PPS 3 | - | - | 59.2 | - | - | - |
玻璃纤维1 | 40 | 40 | 40 | 40 | 40 | - |
玻璃纤维2 | - | - | - | - | - | 40 |
巯基硅烷化合物1 | 0.3 | 0.3 | 0.3 | - | 0.5 | 0.5 |
巯基硅烷化合物2 | - | - | - | 0.3 | - | - |
水滑石 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 |
Claims (13)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2016-0061468 | 2016-05-19 | ||
KR1020160061468A KR102503262B1 (ko) | 2016-05-19 | 2016-05-19 | 내화학성이 우수한 폴리아릴렌 설파이드 수지 조성물 |
PCT/KR2017/003544 WO2017200203A1 (ko) | 2016-05-19 | 2017-03-31 | 내화학성이 우수한 폴리아릴렌 설파이드 수지 조성물 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN109071946A true CN109071946A (zh) | 2018-12-21 |
CN109071946B CN109071946B (zh) | 2022-03-04 |
Family
ID=60325954
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201780029329.2A Active CN109071946B (zh) | 2016-05-19 | 2017-03-31 | 具有优异的耐化学性的聚芳硫醚树脂组合物 |
Country Status (7)
Country | Link |
---|---|
US (1) | US20190144609A1 (zh) |
EP (1) | EP3460004A4 (zh) |
JP (1) | JP7155014B2 (zh) |
KR (1) | KR102503262B1 (zh) |
CN (1) | CN109071946B (zh) |
TW (1) | TWI757281B (zh) |
WO (1) | WO2017200203A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111574832A (zh) * | 2019-02-18 | 2020-08-25 | 现代摩比斯株式会社 | 聚芳硫醚树脂组合物及汽车前照灯组件 |
CN115151605A (zh) * | 2020-03-26 | 2022-10-04 | 帝斯曼知识产权资产管理有限公司 | 注射成型零件 |
CN115678278A (zh) * | 2022-10-28 | 2023-02-03 | 金发科技股份有限公司 | 一种pps复合材料及其制备方法和应用 |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102492258B1 (ko) * | 2016-04-26 | 2023-01-26 | 에이치디씨폴리올 주식회사 | 내가수분해성이 우수한 폴리아릴렌 설파이드 수지 조성물 |
KR102625849B1 (ko) * | 2017-12-28 | 2024-01-16 | 에이치디씨폴리올 주식회사 | 기계적 특성 및 부식 특성이 우수한 폴리아릴렌 설파이드 수지 조성물 |
JP2019156987A (ja) * | 2018-03-14 | 2019-09-19 | 帝人株式会社 | 樹脂組成物 |
JP7260317B2 (ja) * | 2019-02-05 | 2023-04-18 | 帝人株式会社 | 樹脂組成物 |
WO2022080129A1 (ja) * | 2020-10-16 | 2022-04-21 | ポリプラスチックス株式会社 | 水を含む流体と接触し得る車両用冷却系部品 |
US20230383428A1 (en) * | 2022-05-09 | 2023-11-30 | Ticona Llc | Fluidic Member for Use in an Electrolyzer System |
Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0106319A2 (en) * | 1982-10-15 | 1984-04-25 | Phillips Petroleum Company | Poly(arylene sulfide) containing talc |
US4448918A (en) * | 1982-10-15 | 1984-05-15 | Phillips Petroleum Company | Poly(arylene sulfide) composition containing titanium dioxide and 3-mercaptopropyltrimethoxysilane |
US4482665A (en) * | 1982-09-14 | 1984-11-13 | Phillips Petroleum Company | Encapsulation of electronic components with calcium silicate-containing poly(arylene sulfide) compositions |
US4529769A (en) * | 1983-12-06 | 1985-07-16 | Phillips Petroleum Company | Poly(arylene sulfide) composition, molding method and article of manufacture |
JPS6317549A (ja) * | 1986-07-10 | 1988-01-25 | Toray Ind Inc | 樹脂封止電子部品 |
CN1048397A (zh) * | 1989-06-27 | 1991-01-09 | 汎塑料株式会社 | 聚亚芳基硫醚树脂组合物 |
EP0485644A1 (en) * | 1989-11-13 | 1992-05-20 | Phillips Petroleum Company | Poly(arylene sulfide) compositions with strengthened weldline |
KR19980027827A (ko) * | 1996-10-18 | 1998-07-15 | 김준웅 | 폴리아릴렌 설파이드 수지 조성물 |
JP2000080274A (ja) * | 1998-09-04 | 2000-03-21 | Matsushita Electric Works Ltd | 電子部品封止用樹脂組成物およびその製造方法、ならびにこの電子部品封止用樹脂組成物を用いた封止電子部品 |
CN1709975A (zh) * | 2005-07-18 | 2005-12-21 | 四川大学 | 聚苯硫醚电子封装材料及其制备方法 |
CN1902275A (zh) * | 2003-12-19 | 2007-01-24 | 罗狄亚工程塑料有限责任公司 | 基于热塑性基质的阻燃组合物 |
CN101084273A (zh) * | 2004-12-21 | 2007-12-05 | 旭化成化学株式会社 | 聚苯硫醚树脂组合物 |
CN101595165A (zh) * | 2006-08-24 | 2009-12-02 | Sk化学株式会社 | 聚(亚芳基硫醚)的制备方法 |
CN101709148A (zh) * | 2008-08-13 | 2010-05-19 | 北美泰密克汽车公司 | 对碳氢化合物流体具有抗性的胺固化的硅酮组合物及其应用 |
CN103052683A (zh) * | 2010-07-30 | 2013-04-17 | 沙伯基础创新塑料知识产权有限公司 | 抗水性聚醚酰亚胺共混物、及其制造方法和由其形成的制品 |
CN103387746A (zh) * | 2012-05-09 | 2013-11-13 | 合肥杰事杰新材料股份有限公司 | 一种纤维增强聚苯硫醚/聚酰胺合金材料及其制备方法 |
CN103443205A (zh) * | 2011-03-31 | 2013-12-11 | 东丽株式会社 | 聚苯硫醚树脂组合物及由该组合物形成的成型体 |
CN103987769A (zh) * | 2011-09-20 | 2014-08-13 | 提克纳有限责任公司 | 低氯填充的熔融加工的聚芳硫醚组合物 |
CN104861163A (zh) * | 2008-12-31 | 2015-08-26 | Sk化学株式会社 | 制备自由碘含量降低的聚芳撑硫醚的方法 |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2583941A (en) | 1946-11-13 | 1952-01-29 | Jr Thurlow M Gordon | Device for detecting variations in fluid pressure |
US2513188A (en) | 1948-09-10 | 1950-06-27 | Macallum Alexander Douglas | Mixed phenylene sulfide resins |
JP2513188B2 (ja) | 1986-08-30 | 1996-07-03 | 日本電気株式会社 | 加工順序制御式外形加工機 |
WO1988001977A1 (en) * | 1986-09-09 | 1988-03-24 | Calp Kogyo Kabushiki Kaisha | Roll unit and combined rolls |
JP2583941B2 (ja) | 1988-02-12 | 1997-02-19 | 株式会社テック | 表面処理装置 |
CA2014561A1 (en) * | 1989-06-05 | 1990-12-05 | Roy F. Wright | Glass-filled poly(arylene sulfide) compositions and methods |
KR910006413A (ko) * | 1989-09-13 | 1991-04-29 | 원본미기재 | 폴리(아릴렌 술파이드)를 함유한 성형 조성물 |
JPH05239354A (ja) * | 1991-12-06 | 1993-09-17 | Phillips Petroleum Co | ポリ(アリーレンスルフィド)組成物 |
JPH06256569A (ja) * | 1993-03-02 | 1994-09-13 | Idemitsu Petrochem Co Ltd | ガラス繊維強化熱可塑性樹脂組成物 |
JPH1121451A (ja) * | 1997-04-21 | 1999-01-26 | Toray Ind Inc | エンジン冷却水系部品用ポリアミド樹脂組成物および成形体 |
KR101681682B1 (ko) * | 2015-07-31 | 2016-12-01 | 에스케이케미칼 주식회사 | 유리 요오드 저감 폴리아릴렌 설파이드의 제조 방법 |
KR102492258B1 (ko) | 2016-04-26 | 2023-01-26 | 에이치디씨폴리올 주식회사 | 내가수분해성이 우수한 폴리아릴렌 설파이드 수지 조성물 |
-
2016
- 2016-05-19 KR KR1020160061468A patent/KR102503262B1/ko active IP Right Grant
-
2017
- 2017-03-31 JP JP2018560620A patent/JP7155014B2/ja active Active
- 2017-03-31 EP EP17799561.0A patent/EP3460004A4/en not_active Withdrawn
- 2017-03-31 US US16/099,575 patent/US20190144609A1/en not_active Abandoned
- 2017-03-31 CN CN201780029329.2A patent/CN109071946B/zh active Active
- 2017-03-31 WO PCT/KR2017/003544 patent/WO2017200203A1/ko unknown
- 2017-04-13 TW TW106112374A patent/TWI757281B/zh active
Patent Citations (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4482665A (en) * | 1982-09-14 | 1984-11-13 | Phillips Petroleum Company | Encapsulation of electronic components with calcium silicate-containing poly(arylene sulfide) compositions |
EP0106319A2 (en) * | 1982-10-15 | 1984-04-25 | Phillips Petroleum Company | Poly(arylene sulfide) containing talc |
US4448918A (en) * | 1982-10-15 | 1984-05-15 | Phillips Petroleum Company | Poly(arylene sulfide) composition containing titanium dioxide and 3-mercaptopropyltrimethoxysilane |
US4529769A (en) * | 1983-12-06 | 1985-07-16 | Phillips Petroleum Company | Poly(arylene sulfide) composition, molding method and article of manufacture |
JPS6317549A (ja) * | 1986-07-10 | 1988-01-25 | Toray Ind Inc | 樹脂封止電子部品 |
CN1048397A (zh) * | 1989-06-27 | 1991-01-09 | 汎塑料株式会社 | 聚亚芳基硫醚树脂组合物 |
EP0485644A1 (en) * | 1989-11-13 | 1992-05-20 | Phillips Petroleum Company | Poly(arylene sulfide) compositions with strengthened weldline |
KR19980027827A (ko) * | 1996-10-18 | 1998-07-15 | 김준웅 | 폴리아릴렌 설파이드 수지 조성물 |
JP2000080274A (ja) * | 1998-09-04 | 2000-03-21 | Matsushita Electric Works Ltd | 電子部品封止用樹脂組成物およびその製造方法、ならびにこの電子部品封止用樹脂組成物を用いた封止電子部品 |
CN1902275A (zh) * | 2003-12-19 | 2007-01-24 | 罗狄亚工程塑料有限责任公司 | 基于热塑性基质的阻燃组合物 |
CN101084273A (zh) * | 2004-12-21 | 2007-12-05 | 旭化成化学株式会社 | 聚苯硫醚树脂组合物 |
CN1709975A (zh) * | 2005-07-18 | 2005-12-21 | 四川大学 | 聚苯硫醚电子封装材料及其制备方法 |
CN101595165A (zh) * | 2006-08-24 | 2009-12-02 | Sk化学株式会社 | 聚(亚芳基硫醚)的制备方法 |
CN101709148A (zh) * | 2008-08-13 | 2010-05-19 | 北美泰密克汽车公司 | 对碳氢化合物流体具有抗性的胺固化的硅酮组合物及其应用 |
CN104861163A (zh) * | 2008-12-31 | 2015-08-26 | Sk化学株式会社 | 制备自由碘含量降低的聚芳撑硫醚的方法 |
CN103052683A (zh) * | 2010-07-30 | 2013-04-17 | 沙伯基础创新塑料知识产权有限公司 | 抗水性聚醚酰亚胺共混物、及其制造方法和由其形成的制品 |
CN103443205A (zh) * | 2011-03-31 | 2013-12-11 | 东丽株式会社 | 聚苯硫醚树脂组合物及由该组合物形成的成型体 |
CN103987769A (zh) * | 2011-09-20 | 2014-08-13 | 提克纳有限责任公司 | 低氯填充的熔融加工的聚芳硫醚组合物 |
CN103387746A (zh) * | 2012-05-09 | 2013-11-13 | 合肥杰事杰新材料股份有限公司 | 一种纤维增强聚苯硫醚/聚酰胺合金材料及其制备方法 |
Non-Patent Citations (1)
Title |
---|
何建新等: "《新型纤维材料学》", 31 July 2014, 东华大学出版社 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111574832A (zh) * | 2019-02-18 | 2020-08-25 | 现代摩比斯株式会社 | 聚芳硫醚树脂组合物及汽车前照灯组件 |
CN111574832B (zh) * | 2019-02-18 | 2023-04-07 | 现代摩比斯株式会社 | 聚芳硫醚树脂组合物及汽车前照灯组件 |
CN115151605A (zh) * | 2020-03-26 | 2022-10-04 | 帝斯曼知识产权资产管理有限公司 | 注射成型零件 |
CN115678278A (zh) * | 2022-10-28 | 2023-02-03 | 金发科技股份有限公司 | 一种pps复合材料及其制备方法和应用 |
CN115678278B (zh) * | 2022-10-28 | 2024-02-13 | 金发科技股份有限公司 | 一种pps复合材料及其制备方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
TWI757281B (zh) | 2022-03-11 |
EP3460004A1 (en) | 2019-03-27 |
JP7155014B2 (ja) | 2022-10-18 |
JP2019516840A (ja) | 2019-06-20 |
WO2017200203A1 (ko) | 2017-11-23 |
US20190144609A1 (en) | 2019-05-16 |
CN109071946B (zh) | 2022-03-04 |
TW201809145A (zh) | 2018-03-16 |
EP3460004A4 (en) | 2020-02-19 |
KR20170130802A (ko) | 2017-11-29 |
KR102503262B1 (ko) | 2023-02-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN109071946A (zh) | 具有优异的耐化学性的聚芳硫醚树脂组合物 | |
CN108884318B (zh) | 具有优异的耐水解性的聚亚芳基硫醚树脂组合物 | |
EP2883900A1 (en) | Polyarylene sulfide resin and method for preparing same | |
WO2011093685A2 (ko) | 요오드 저감 폴리아릴렌 설파이드의 제조 방법 | |
KR102502509B1 (ko) | 유동성이 우수한 폴리아릴렌 설파이드 수지 조성물 | |
US20210002428A1 (en) | Polyarylene sulfide resin and preparation method thereof | |
CN111712545B (zh) | 具有优异的机械特性和腐蚀特性的聚芳硫醚树脂组合物 | |
TWI740858B (zh) | 聚芳硫醚樹脂組合物及成形物件 | |
KR102463662B1 (ko) | 연성 및 치수 안정성이 우수한 폴리아릴렌 설파이드 수지 조성물 | |
CN107207856A (zh) | 具有优异的金属粘接性的聚芳硫醚组合物 | |
KR20170128880A (ko) | 내부식성 및 열충격성이 우수한 폴리아릴렌 설파이드 수지 조성물 | |
CN108603030B (zh) | 对金属具有优异粘附性的聚芳硫醚组合物 | |
JP2015105303A (ja) | ポリアリーレンスルフィドの製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20191227 Address after: 310 Banqiao Road, pantang District, Chengnan, Gyeonggi do, South Korea Applicant after: SK Chemicals Co., Ltd. Address before: 119, 616fan street, Churong Road, Shinan District, Weishan, South Korea Applicant before: British Car Corporation |
|
TA01 | Transfer of patent application right | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
TR01 | Transfer of patent right |
Effective date of registration: 20220406 Address after: 591-1 Xinhang Road, Ulsan South District, Korea Patentee after: HDC polymerization Co.,Ltd. Address before: Gyeonggi Do City South Korea Panchiao road Bundang 310 Patentee before: SK CHEMICALS Co.,Ltd. |
|
TR01 | Transfer of patent right |