TW482805B - Curable perfluoroelastomer composition - Google Patents
Curable perfluoroelastomer composition Download PDFInfo
- Publication number
- TW482805B TW482805B TW088113901A TW88113901A TW482805B TW 482805 B TW482805 B TW 482805B TW 088113901 A TW088113901 A TW 088113901A TW 88113901 A TW88113901 A TW 88113901A TW 482805 B TW482805 B TW 482805B
- Authority
- TW
- Taiwan
- Prior art keywords
- perfluoroelastomer
- ammonia
- patent application
- item
- scope
- Prior art date
Links
- 229920006169 Perfluoroelastomer Polymers 0.000 title claims abstract description 60
- 239000000203 mixture Substances 0.000 title claims abstract description 53
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims abstract description 77
- 229910021529 ammonia Inorganic materials 0.000 claims abstract description 37
- 239000000178 monomer Substances 0.000 claims abstract description 27
- 229920001971 elastomer Polymers 0.000 claims abstract description 8
- 239000000806 elastomer Substances 0.000 claims abstract description 5
- -1 perfluoro Chemical group 0.000 claims description 23
- 150000002825 nitriles Chemical class 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 17
- 150000002170 ethers Chemical class 0.000 claims description 13
- 229920002554 vinyl polymer Polymers 0.000 claims description 7
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 5
- 230000005070 ripening Effects 0.000 claims description 5
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 4
- 238000001179 sorption measurement Methods 0.000 claims description 4
- LOUICXNAWQPGSU-UHFFFAOYSA-N 2,2,3,3-tetrafluorooxirane Chemical compound FC1(F)OC1(F)F LOUICXNAWQPGSU-UHFFFAOYSA-N 0.000 claims description 3
- CRHIAMBJMSSNNM-UHFFFAOYSA-N tetraphenylstannane Chemical group C1=CC=CC=C1[Sn](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 CRHIAMBJMSSNNM-UHFFFAOYSA-N 0.000 claims description 3
- VRVRGVPWCUEOGV-UHFFFAOYSA-N 2-aminothiophenol Chemical compound NC1=CC=CC=C1S VRVRGVPWCUEOGV-UHFFFAOYSA-N 0.000 claims description 2
- KYHOPNYZFIFAOH-UHFFFAOYSA-N 3,4-diamino-2-(2-hydroxyphenyl)phenol Chemical group NC1=CC=C(O)C(C=2C(=CC=CC=2)O)=C1N KYHOPNYZFIFAOH-UHFFFAOYSA-N 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 125000005192 alkyl ethylene group Chemical group 0.000 claims description 2
- 239000003125 aqueous solvent Substances 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 150000007857 hydrazones Chemical class 0.000 claims description 2
- NITMACBPVVUGOJ-UHFFFAOYSA-N 2,2,2-trifluoroethanimidamide Chemical compound NC(=N)C(F)(F)F NITMACBPVVUGOJ-UHFFFAOYSA-N 0.000 claims 1
- KSSJBGNOJJETTC-UHFFFAOYSA-N COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC Chemical compound COC1=C(C=CC=C1)N(C1=CC=2C3(C4=CC(=CC=C4C=2C=C1)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC(=CC=C1C=1C=CC(=CC=13)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)N(C1=CC=C(C=C1)OC)C1=C(C=CC=C1)OC)C1=CC=C(C=C1)OC KSSJBGNOJJETTC-UHFFFAOYSA-N 0.000 claims 1
- 206010011878 Deafness Diseases 0.000 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- 231100000895 deafness Toxicity 0.000 claims 1
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
- 208000016354 hearing loss disease Diseases 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 abstract description 16
- 125000002560 nitrile group Chemical group 0.000 abstract description 4
- 229920000642 polymer Polymers 0.000 description 22
- 239000006229 carbon black Substances 0.000 description 11
- 235000019241 carbon black Nutrition 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000004810 polytetrafluoroethylene Substances 0.000 description 10
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 9
- 239000000945 filler Substances 0.000 description 7
- 230000035800 maturation Effects 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 6
- 239000000654 additive Substances 0.000 description 6
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 229920002313 fluoropolymer Polymers 0.000 description 6
- 238000002329 infrared spectrum Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000004575 stone Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 5
- 239000004811 fluoropolymer Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 230000002079 cooperative effect Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000003863 ammonium salts Chemical class 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 230000006835 compression Effects 0.000 description 3
- 238000007906 compression Methods 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 125000004093 cyano group Chemical group *C#N 0.000 description 3
- FOKCKXCUQFKNLD-UHFFFAOYSA-N pent-1-enyl hypofluorite Chemical compound C(CC)C=COF FOKCKXCUQFKNLD-UHFFFAOYSA-N 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 238000007789 sealing Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- BBMCTIGTTCKYKF-UHFFFAOYSA-N 1-heptanol Chemical compound CCCCCCCO BBMCTIGTTCKYKF-UHFFFAOYSA-N 0.000 description 2
- 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 2
- HSTOKWSFWGCZMH-UHFFFAOYSA-N 3,3'-diaminobenzidine Chemical group C1=C(N)C(N)=CC=C1C1=CC=C(N)C(N)=C1 HSTOKWSFWGCZMH-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 101100273965 Solanum lycopersicum HCR9-0 gene Proteins 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 238000009434 installation Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 2
- 229920005548 perfluoropolymer Polymers 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000010557 suspension polymerization reaction Methods 0.000 description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 1
- RRZIJNVZMJUGTK-UHFFFAOYSA-N 1,1,2-trifluoro-2-(1,2,2-trifluoroethenoxy)ethene Chemical group FC(F)=C(F)OC(F)=C(F)F RRZIJNVZMJUGTK-UHFFFAOYSA-N 0.000 description 1
- BTJWLDDXZYWBNY-UHFFFAOYSA-N 2,2,3,3,4,4,5,5,6,6,6-undecafluorohexanimidamide Chemical compound NC(=N)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F BTJWLDDXZYWBNY-UHFFFAOYSA-N 0.000 description 1
- HDGLPTVARHLGMV-UHFFFAOYSA-N 2-amino-4-(1,1,1,3,3,3-hexafluoropropan-2-yl)phenol Chemical compound NC1=CC(C(C(F)(F)F)C(F)(F)F)=CC=C1O HDGLPTVARHLGMV-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- ZOYBGDLDYYDOJZ-UHFFFAOYSA-N FOC=CC1=CC=CC2=C1CC1=CC=CC=C21 Chemical compound FOC=CC1=CC=CC2=C1CC1=CC=CC=C21 ZOYBGDLDYYDOJZ-UHFFFAOYSA-N 0.000 description 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
- STGGUFIDDWNMRA-UHFFFAOYSA-N N'-chloro-2,2,2-trifluoroethanimidamide Chemical compound N\C(=N/Cl)C(F)(F)F STGGUFIDDWNMRA-UHFFFAOYSA-N 0.000 description 1
- 239000006057 Non-nutritive feed additive Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241000872198 Serjania polyphylla Species 0.000 description 1
- SXEHKFHPFVVDIR-UHFFFAOYSA-N [4-(4-hydrazinylphenyl)phenyl]hydrazine Chemical compound C1=CC(NN)=CC=C1C1=CC=C(NN)C=C1 SXEHKFHPFVVDIR-UHFFFAOYSA-N 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- YOALFLHFSFEMLP-UHFFFAOYSA-N azane;2,2,3,3,4,4,5,5,6,6,7,7,8,8,8-pentadecafluorooctanoic acid Chemical compound [NH4+].[O-]C(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F YOALFLHFSFEMLP-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Chemical group 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical group 0.000 description 1
- 206010061592 cardiac fibrillation Diseases 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000010382 chemical cross-linking Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004939 coking Methods 0.000 description 1
- 238000010961 commercial manufacture process Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000010556 emulsion polymerization method Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 230000002600 fibrillogenic effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000002220 fluorenes Chemical class 0.000 description 1
- 238000003682 fluorination reaction Methods 0.000 description 1
- 239000006232 furnace black Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 230000010198 maturation time Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 150000002902 organometallic compounds Chemical class 0.000 description 1
- 239000010702 perfluoropolyether Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- FUTGSLRCERHDMB-UHFFFAOYSA-N propan-2-yl hypofluorite Chemical compound CC(C)OF FUTGSLRCERHDMB-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229920013730 reactive polymer Polymers 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 238000010074 rubber mixing Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- AGGKEGLBGGJEBZ-UHFFFAOYSA-N tetramethylenedisulfotetramine Chemical compound C1N(S2(=O)=O)CN3S(=O)(=O)N1CN2C3 AGGKEGLBGGJEBZ-UHFFFAOYSA-N 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 150000003606 tin compounds Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000004073 vulcanization Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
Landscapes
- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9591598P | 1998-08-10 | 1998-08-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| TW482805B true TW482805B (en) | 2002-04-11 |
Family
ID=22254183
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW088113901A TW482805B (en) | 1998-08-10 | 1999-08-18 | Curable perfluoroelastomer composition |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6221970B1 (enExample) |
| EP (1) | EP1114094B1 (enExample) |
| JP (1) | JP4362258B2 (enExample) |
| KR (1) | KR100589103B1 (enExample) |
| DE (1) | DE69918698T2 (enExample) |
| TW (1) | TW482805B (enExample) |
| WO (1) | WO2000009569A2 (enExample) |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6559238B1 (en) * | 1998-06-29 | 2003-05-06 | E. I. Du Pont De Nemours And Company | Thermally cross-linked fluoropolymer |
| JP3514155B2 (ja) * | 1999-02-19 | 2004-03-31 | 富士写真光機株式会社 | 内視鏡装置 |
| JP4547735B2 (ja) * | 1999-07-14 | 2010-09-22 | ダイキン工業株式会社 | 含フッ素重合体の硬化方法 |
| JP5122056B2 (ja) * | 2000-09-18 | 2013-01-16 | スリーエム イノベイティブ プロパティズ カンパニー | 金属アミン錯体含有フルオロポリマー組成物 |
| CA2421708A1 (en) * | 2000-09-18 | 2002-03-28 | 3M Innovative Properties Company | Imidate-containing fluoropolymer compositions |
| DE60126336T2 (de) * | 2000-12-14 | 2007-11-08 | Dupont Dow Elastomers L.L.C., Wilmington | Verfahren zur herstellung von hochreinen durchscheinenden perfluorelastomer-gegenständen |
| US6890995B2 (en) | 2001-01-31 | 2005-05-10 | 3M Innovative Properties Company | Fluoropolymer compositions |
| US6844388B2 (en) | 2001-04-12 | 2005-01-18 | 3M Innovative Properties Company | Fluoropolymer compositions containing a nitrogen cure site monomer |
| US6803425B2 (en) | 2001-04-12 | 2004-10-12 | 3M Innovative Properties Company | Fluoropolymers having pendant imidate structures |
| US6794457B2 (en) | 2001-04-30 | 2004-09-21 | 3M Innovative Properties Company | Fluoropolymer curing system containing a nitrogen cure site monomer |
| US6956085B2 (en) | 2003-02-14 | 2005-10-18 | 3M Innovative Properties Company | Fluoroelastomer compositions |
| EP1699829A1 (en) | 2003-12-30 | 2006-09-13 | 3M Innovative Properties Company | Fluoropolymer coagulation method and composition |
| US7402630B2 (en) | 2004-12-16 | 2008-07-22 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| JP5029359B2 (ja) * | 2005-05-02 | 2012-09-19 | ダイキン工業株式会社 | 架橋性ポリテトラフルオロエチレン組成物、ポリテトラフルオロエチレン架橋体粉末、ポリテトラフルオロエチレン成形体、樹脂ブレンド組成物、および樹脂ブレンド成形体 |
| JP4998267B2 (ja) | 2005-07-26 | 2012-08-15 | ダイキン工業株式会社 | 硬化性組成物、それからなる成形品および成形品の製造方法 |
| US8069833B2 (en) | 2006-10-20 | 2011-12-06 | Bando Kiko Co., Ltd. | Reciprocating engine |
| JP2009001748A (ja) * | 2007-06-25 | 2009-01-08 | Daikin Ind Ltd | 半導体等製造用物品 |
| US9650479B2 (en) | 2007-10-04 | 2017-05-16 | W. L. Gore & Associates, Inc. | Dense articles formed from tetrafluoroethylene core shell copolymers and methods of making the same |
| US9040646B2 (en) | 2007-10-04 | 2015-05-26 | W. L. Gore & Associates, Inc. | Expandable TFE copolymers, methods of making, and porous, expanded articles thereof |
| US8637144B2 (en) * | 2007-10-04 | 2014-01-28 | W. L. Gore & Associates, Inc. | Expandable TFE copolymers, method of making, and porous, expended articles thereof |
| JP5452508B2 (ja) * | 2008-02-29 | 2014-03-26 | スリーエム イノベイティブ プロパティズ カンパニー | 低カルボニル末端基率を有するペルフルオロエラストマー |
| JP5549668B2 (ja) * | 2008-06-30 | 2014-07-16 | ダイキン工業株式会社 | 硬化性組成物およびそれからなる成形品 |
| WO2010151610A2 (en) | 2009-06-25 | 2010-12-29 | 3M Innovative Properties Company | Curing compositions for fluoropolymers |
| JP5549419B2 (ja) * | 2009-07-15 | 2014-07-16 | ダイキン工業株式会社 | 硬化性パーフルオロエラストマー組成物の製造方法、硬化性パーフルオロエラストマー組成物およびそれからなる成形品 |
| CN102725503B (zh) | 2010-02-01 | 2015-08-26 | 坂东机工株式会社 | 往复式发动机 |
| US8772997B2 (en) | 2010-09-13 | 2014-07-08 | Baker Hughes Incorporated | Electrical submersible pump system having high temperature slot, end bell and phase-to-phase insulation |
| US9644054B2 (en) | 2014-12-19 | 2017-05-09 | W. L. Gore & Associates, Inc. | Dense articles formed from tetrafluoroethylene core shell copolymers and methods of making the same |
| US20230027292A1 (en) * | 2019-12-13 | 2023-01-26 | Chromis Fiberoptics, Inc. | Amorphous fluorinated copolymers and methods of making and using the same |
| US12160183B2 (en) | 2020-01-03 | 2024-12-03 | C-Motive Technologies, Inc. | Method of producing an electrostatic motor |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3332907A (en) | 1963-06-17 | 1967-07-25 | Du Pont | Oxy aromatic polyamides and process for preparation |
| US3956000A (en) | 1972-07-21 | 1976-05-11 | Hoechst Aktiengesellschaft | Fluorocarbon waxes and process for producing them |
| US4281092A (en) | 1978-11-30 | 1981-07-28 | E. I. Du Pont De Nemours And Company | Vulcanizable fluorinated copolymers |
| US4242498A (en) | 1979-04-09 | 1980-12-30 | Frosch Robert A | Process for the preparation of fluorine containing crosslinked elastomeric polytriazine and product so produced |
| US4394489A (en) | 1982-02-25 | 1983-07-19 | E. I. Du Pont De Nemours & Co. | Fluoroelastomer curatives |
| US4879362A (en) | 1987-12-31 | 1989-11-07 | E. I. Dupont De Nemours And Company | Modified polytetrafluoroethylene resins |
| US5693748A (en) * | 1989-02-01 | 1997-12-02 | Asahi Kasei Kogyo Kabushiki Kaisha | High molecular weight polyimidoylamidine and a polytriazine derived therefrom |
| EP0708797B1 (en) | 1993-07-16 | 1998-02-04 | E.I. Du Pont De Nemours And Company | High purity fluoroelastomer compositions |
| US5554680A (en) | 1994-02-16 | 1996-09-10 | E. I. Du Pont De Nemours And Company | Heat-resistant perfluoroelastomer composition |
| JPH08143535A (ja) | 1994-11-17 | 1996-06-04 | Nippon Mektron Ltd | ビスアミノチオフェノール化合物、その製造法およびそれよりなる含フッ素エラストマー用硬化剤 |
| JP3223776B2 (ja) * | 1995-03-31 | 2001-10-29 | 日本メクトロン株式会社 | 含フッ素エラストマー組成物 |
| US5677389A (en) | 1996-11-25 | 1997-10-14 | E. I. Du Pont De Nemours | Perfluoroelastomer composition having enhanced curing performance |
| US5877264A (en) | 1996-11-25 | 1999-03-02 | E. I. Du Pont De Nemours And Company | Fast-curing perfluoroelastomer composition |
| WO1998023655A1 (en) | 1996-11-25 | 1998-06-04 | E.I. Du Pont De Nemours And Company | Perfluoroelastomer composition having improved processability |
-
1999
- 1999-08-06 WO PCT/US1999/017868 patent/WO2000009569A2/en not_active Ceased
- 1999-08-06 JP JP2001576397A patent/JP4362258B2/ja not_active Expired - Fee Related
- 1999-08-06 DE DE69918698T patent/DE69918698T2/de not_active Expired - Lifetime
- 1999-08-06 EP EP99940932A patent/EP1114094B1/en not_active Expired - Lifetime
- 1999-08-06 KR KR1020007009680A patent/KR100589103B1/ko not_active Expired - Fee Related
- 1999-08-06 US US09/369,801 patent/US6221970B1/en not_active Expired - Lifetime
- 1999-08-18 TW TW088113901A patent/TW482805B/zh not_active IP Right Cessation
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|---|---|
| US6221970B1 (en) | 2001-04-24 |
| JP2003531222A (ja) | 2003-10-21 |
| KR20010041511A (ko) | 2001-05-25 |
| WO2000009569A3 (en) | 2000-06-29 |
| KR100589103B1 (ko) | 2006-06-14 |
| EP1114094A2 (en) | 2001-07-11 |
| JP4362258B2 (ja) | 2009-11-11 |
| WO2000009569A2 (en) | 2000-02-24 |
| EP1114094B1 (en) | 2004-07-14 |
| DE69918698T2 (de) | 2005-08-04 |
| DE69918698D1 (de) | 2004-08-19 |
| WO2000009569A8 (en) | 2001-02-08 |
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