JP5837619B2 - ジルコニウム酸化物ナノ粒子を含む非晶質ペルフルオロポリマー - Google Patents
ジルコニウム酸化物ナノ粒子を含む非晶質ペルフルオロポリマー Download PDFInfo
- Publication number
- JP5837619B2 JP5837619B2 JP2013552557A JP2013552557A JP5837619B2 JP 5837619 B2 JP5837619 B2 JP 5837619B2 JP 2013552557 A JP2013552557 A JP 2013552557A JP 2013552557 A JP2013552557 A JP 2013552557A JP 5837619 B2 JP5837619 B2 JP 5837619B2
- Authority
- JP
- Japan
- Prior art keywords
- zirconium oxide
- oxide nanoparticles
- nanoparticles
- minutes
- inch
- 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.)
- Expired - Fee Related
Links
- 239000002105 nanoparticle Substances 0.000 title claims description 48
- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 title claims description 27
- 229910001928 zirconium oxide Inorganic materials 0.000 title claims description 27
- 229920005548 perfluoropolymer Polymers 0.000 title claims description 14
- 239000000203 mixture Substances 0.000 claims description 33
- 229920002313 fluoropolymer Polymers 0.000 claims description 17
- 239000004811 fluoropolymer Substances 0.000 claims description 17
- 230000002378 acidificating effect Effects 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 55
- 239000007787 solid Substances 0.000 description 29
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 23
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 22
- 238000000034 method Methods 0.000 description 22
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 description 16
- 229910052740 iodine Inorganic materials 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 230000000052 comparative effect Effects 0.000 description 12
- 239000000377 silicon dioxide Substances 0.000 description 11
- 239000011787 zinc oxide Substances 0.000 description 11
- 229920001971 elastomer Polymers 0.000 description 10
- 239000004816 latex Substances 0.000 description 10
- 229920000126 latex Polymers 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 229920006169 Perfluoroelastomer Polymers 0.000 description 9
- 229910052794 bromium Inorganic materials 0.000 description 9
- 239000002131 composite material Substances 0.000 description 9
- 239000008367 deionised water Substances 0.000 description 9
- 229910021641 deionized water Inorganic materials 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- KOMNUTZXSVSERR-UHFFFAOYSA-N 1,3,5-tris(prop-2-enyl)-1,3,5-triazinane-2,4,6-trione Chemical compound C=CCN1C(=O)N(CC=C)C(=O)N(CC=C)C1=O KOMNUTZXSVSERR-UHFFFAOYSA-N 0.000 description 7
- 239000004971 Cross linker Substances 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 7
- 150000001451 organic peroxides Chemical class 0.000 description 7
- 230000004580 weight loss Effects 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000001914 filtration Methods 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- 239000004065 semiconductor Substances 0.000 description 6
- 229920001973 fluoroelastomer Polymers 0.000 description 5
- 150000002894 organic compounds Chemical class 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000000691 measurement method Methods 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- 229910019142 PO4 Inorganic materials 0.000 description 3
- -1 carbide Chemical class 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000011630 iodine Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 238000001020 plasma etching Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-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
- 101150065749 Churc1 gene Proteins 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 102100038239 Protein Churchill Human genes 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 150000001409 amidines Chemical class 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 238000004364 calculation method Methods 0.000 description 2
- JJWKPURADFRFRB-UHFFFAOYSA-N carbonyl sulfide Chemical compound O=C=S JJWKPURADFRFRB-UHFFFAOYSA-N 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 238000009616 inductively coupled plasma Methods 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 229910021645 metal ion Inorganic materials 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 150000003016 phosphoric acids Chemical class 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000011164 primary particle Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 239000013585 weight reducing agent Substances 0.000 description 2
- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- LDQKDAUATAVUHZ-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2,3,3-hexafluoro-3-methoxypropane Chemical compound COC(F)(F)C(F)(F)C(F)(F)OC=C LDQKDAUATAVUHZ-UHFFFAOYSA-N 0.000 description 1
- LYIPDZSLYLDLCU-UHFFFAOYSA-N 2,2,3,3-tetrafluoro-3-[1,1,1,2,3,3-hexafluoro-3-(1,2,2-trifluoroethenoxy)propan-2-yl]oxypropanenitrile Chemical compound FC(F)=C(F)OC(F)(F)C(F)(C(F)(F)F)OC(F)(F)C(F)(F)C#N LYIPDZSLYLDLCU-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
- 229920001774 Perfluoroether Polymers 0.000 description 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
- 239000012963 UV stabilizer Substances 0.000 description 1
- 238000005411 Van der Waals force Methods 0.000 description 1
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 description 1
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical class OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 1
- 229910001413 alkali metal ion Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- HFEHLDPGIKPNKL-UHFFFAOYSA-N allyl iodide Chemical compound ICC=C HFEHLDPGIKPNKL-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 125000000438 amidrazone group Chemical group 0.000 description 1
- 150000001412 amines Chemical group 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000001636 atomic emission spectroscopy Methods 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- UUEDINPOVKWVAZ-UHFFFAOYSA-N bis(2-ethylhexyl) 3,4,5,6-tetrabromobenzene-1,2-dicarboxylate Chemical compound CCCCC(CC)COC(=O)C1=C(Br)C(Br)=C(Br)C(Br)=C1C(=O)OCC(CC)CCCC UUEDINPOVKWVAZ-UHFFFAOYSA-N 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910002090 carbon oxide Inorganic materials 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- SFZULDYEOVSIKM-UHFFFAOYSA-N chembl321317 Chemical compound C1=CC(C(=N)NO)=CC=C1C1=CC=C(C=2C=CC(=CC=2)C(=N)NO)O1 SFZULDYEOVSIKM-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 238000001246 colloidal dispersion Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000002296 dynamic light scattering Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- CEIPQQODRKXDSB-UHFFFAOYSA-N ethyl 3-(6-hydroxynaphthalen-2-yl)-1H-indazole-5-carboximidate dihydrochloride Chemical compound Cl.Cl.C1=C(O)C=CC2=CC(C3=NNC4=CC=C(C=C43)C(=N)OCC)=CC=C21 CEIPQQODRKXDSB-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- GHXZPUGJZVBLGC-UHFFFAOYSA-N iodoethene Chemical compound IC=C GHXZPUGJZVBLGC-UHFFFAOYSA-N 0.000 description 1
- MGFYSGNNHQQTJW-UHFFFAOYSA-N iodonium Chemical compound [IH2+] MGFYSGNNHQQTJW-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000002114 nanocomposite Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000003129 oil well Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical group FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000011417 postcuring Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/12—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
-
- 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F14/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F14/18—Monomers containing fluorine
-
- 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
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
-
- 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
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/184—Monomers containing fluorine with fluorinated vinyl ethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161439421P | 2011-02-04 | 2011-02-04 | |
| US61/439,421 | 2011-02-04 | ||
| PCT/US2012/022663 WO2012106172A2 (en) | 2011-02-04 | 2012-01-26 | Amorphous perfluoropolymers comprising zirconium oxide nanoparticles |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014504674A JP2014504674A (ja) | 2014-02-24 |
| JP2014504674A5 JP2014504674A5 (cg-RX-API-DMAC7.html) | 2015-03-05 |
| JP5837619B2 true JP5837619B2 (ja) | 2015-12-24 |
Family
ID=46603240
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013552557A Expired - Fee Related JP5837619B2 (ja) | 2011-02-04 | 2012-01-26 | ジルコニウム酸化物ナノ粒子を含む非晶質ペルフルオロポリマー |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9309370B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2670802B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5837619B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR101862899B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN103443195B (cg-RX-API-DMAC7.html) |
| TW (1) | TWI530518B (cg-RX-API-DMAC7.html) |
| WO (1) | WO2012106172A2 (cg-RX-API-DMAC7.html) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101862899B1 (ko) * | 2011-02-04 | 2018-05-30 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 산화지르코늄 나노입자를 포함하는 비결정성 퍼플루오로중합체 |
| US10498435B2 (en) * | 2017-02-14 | 2019-12-03 | Qualcomm Incorporated | Narrowband time-division duplex frame structure for narrowband communications |
| EP3807344B1 (en) | 2018-06-12 | 2023-12-27 | 3M Innovative Properties Company | Fluoropolymer coating compositions comprising aminosilane curing agents, coated substrates and related methods |
| WO2019239320A1 (en) | 2018-06-12 | 2019-12-19 | 3M Innovative Properties Company | Fluoropolymer compositions comprising fluorinated additives, coated substrates and methods |
| TW202033573A (zh) * | 2018-12-17 | 2020-09-16 | 美商3M新設資產公司 | 包括可固化氟聚合物及固化劑之組成物及製造及使用其之方法 |
| WO2020261089A1 (en) * | 2019-06-28 | 2020-12-30 | 3M Innovative Properties Company | Functionalized triazine compounds, compositions comprising such compounds and cured fluoropolymer articles |
| CN114269844A (zh) * | 2019-08-27 | 2022-04-01 | 3M创新有限公司 | 包含金属氟化物颗粒的可固化含氟聚合物组合物及其制品 |
| EP4055109A1 (en) * | 2019-11-04 | 2022-09-14 | 3M Innovative Properties Company | Fluoropolymer compositions comprising a curing agent with ethylenically unsaturated and electron donor groups, and substrates coated therewith |
| WO2021088198A1 (en) * | 2019-11-04 | 2021-05-14 | 3M Innovative Properties Company | Electronic telecommunications articles comprising crosslinked fluoropolymers and methods |
| EP4563645A1 (en) * | 2022-07-25 | 2025-06-04 | Daikin Industries, Ltd. | Crosslinkable composition and molded article |
| KR102700169B1 (ko) | 2022-09-08 | 2024-08-27 | 강원대학교산학협력단 | 락토바실러스 람노서스에 의해 합성되며 테트라사이클린 클로라이드로 로드된 산화지르코늄 나노입자 및 그 제조방법 |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5037579A (en) | 1990-02-12 | 1991-08-06 | Nalco Chemical Company | Hydrothermal process for producing zirconia sol |
| WO1997001599A1 (en) | 1995-06-28 | 1997-01-16 | E.I. Du Pont De Nemours And Company | Fluoropolymer nanocomposites |
| DE19544912A1 (de) | 1995-12-01 | 1997-06-05 | Gore W L & Ass Gmbh | PTFE-Körper aus mikroporösem Polytetrafluorethylen mit Füllstoff und Verfahren zu dessen Herstellung |
| AU5484499A (en) * | 1998-08-18 | 2000-03-14 | Ppg Industries Ohio, Inc. | Process for producing durable antireflective surfaces and antireflective articles |
| JP2000119468A (ja) | 1998-10-16 | 2000-04-25 | Nippon Valqua Ind Ltd | 含フッ素エラストマー組成物、その架橋体、並びにその用途 |
| US6376590B2 (en) | 1999-10-28 | 2002-04-23 | 3M Innovative Properties Company | Zirconia sol, process of making and composite material |
| WO2001032782A1 (en) | 1999-11-04 | 2001-05-10 | Daikin Industries, Ltd. | Molded elastomer for semiconductor production apparatus and crosslinkable fluoroelastomer composition |
| JP2002037666A (ja) | 2000-07-24 | 2002-02-06 | Toshiba Ceramics Co Ltd | 耐プラズマ性部材およびその製造方法 |
| US7351471B2 (en) | 2000-12-06 | 2008-04-01 | 3M Innovative Properties Company | Fluoropolymer coating compositions with multifunctional fluoroalkyl crosslinkers for anti-reflective polymer films |
| JP3979845B2 (ja) | 2001-12-28 | 2007-09-19 | 日本バルカー工業株式会社 | 表面改質フッ素ゴムの製造方法、得られた表面改質フッ素ゴムおよびその用途 |
| ITMI20021202A1 (it) * | 2002-06-04 | 2003-12-04 | Ausimont Spa | Composizioni di fluoropolimeri e particelle inorganiche nanometriche |
| US20050107544A1 (en) | 2003-11-13 | 2005-05-19 | Shuhong Wang | Plasma resistant curable fluoroelastomer composition |
| CN100471877C (zh) | 2003-12-30 | 2009-03-25 | 3M创新有限公司 | 含氟聚合物的凝聚方法及组合物 |
| US7323514B2 (en) * | 2004-12-30 | 2008-01-29 | 3M Innovative Properties Company | Low refractive index fluoropolymer coating compositions for use in antireflective polymer films |
| US7495049B2 (en) | 2005-02-04 | 2009-02-24 | Du Pont - Mitsoi Fluorochemicals Co, Ltd. | Melt processible fluoropolymer composition containing nano particles |
| JP4628814B2 (ja) | 2005-02-15 | 2011-02-09 | 日本バルカー工業株式会社 | 半導体製造装置用シール材 |
| WO2006128128A2 (en) | 2005-05-27 | 2006-11-30 | University Of Florida Research Foundation, Inc. | Inert wear resistant ptfe-based solid lubricant nanocomposite |
| ATE501212T1 (de) | 2005-09-26 | 2011-03-15 | Asahi Glass Co Ltd | Perfluoroelastomerzusammensetzung und formteil aus einem perfluorkautschuk |
| JP5044999B2 (ja) | 2005-09-26 | 2012-10-10 | 旭硝子株式会社 | パーフルオロエラストマー組成物およびパーフルオロゴム成形品 |
| EP1937762B1 (en) * | 2005-09-30 | 2011-06-29 | DuPont-Mitsui Fluorochemicals Company, Ltd. | A polymer composition with uniformly distributed nano-sized inorganic particles |
| WO2007120122A1 (en) | 2006-01-31 | 2007-10-25 | Dupont-Mitsui Fluorochemicals Co Ltd. | Melt processible fluoropolymer composition containing nano particles |
| JP4992897B2 (ja) | 2006-06-22 | 2012-08-08 | ダイキン工業株式会社 | シール材、該シール材を有するプラズマ処理装置用部品および該シール材の製造方法 |
| JP2008115336A (ja) | 2006-11-07 | 2008-05-22 | Du Pont Mitsui Fluorochem Co Ltd | 接着性フッ素樹脂複合体組成物 |
| US20100297433A1 (en) | 2007-12-19 | 2010-11-25 | E. I. Du Pont De Nemours And Company | Bilayer anti-reflective films containing nonoparticles |
| EP2620413B1 (en) | 2007-12-28 | 2020-07-01 | 3M Innovative Properties Company | Continuous hydrothermal reactor system comprising a fluorinated polymer tubular reactor |
| EP2239284A4 (en) * | 2008-01-28 | 2011-02-16 | Asahi Glass Co Ltd | HARDENED COMPOSITION, FLUOR CONTAINING HARDENED PRODUCT, OPTICAL MATERIAL USING THIS HARDENED PRODUCT, AND LIGHT EMITTING DEVICE |
| WO2010011368A1 (en) | 2008-07-22 | 2010-01-28 | E. I. Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing inorganic nanoparticles |
| WO2010147867A1 (en) | 2009-06-15 | 2010-12-23 | Arkema Inc. | Organic/inorganic composite blend membrane compositions of polyelectrolye blends with nanoparticles |
| CN102958987A (zh) | 2010-06-24 | 2013-03-06 | 3M创新有限公司 | 不含有机乳化剂的可聚合组合物以及其聚合物和制造方法 |
| WO2012067937A2 (en) | 2010-11-18 | 2012-05-24 | 3M Innovative Properties Company | Method of coagulating an amorphous fluoropolymer using modified inorganic nanoparticles |
| EP2640781B1 (en) * | 2010-11-18 | 2016-12-28 | 3M Innovative Properties Company | Method of coagulating an amorphous fluoropolymer latex |
| KR101862899B1 (ko) * | 2011-02-04 | 2018-05-30 | 쓰리엠 이노베이티브 프로퍼티즈 컴파니 | 산화지르코늄 나노입자를 포함하는 비결정성 퍼플루오로중합체 |
-
2012
- 2012-01-26 KR KR1020137022981A patent/KR101862899B1/ko not_active Expired - Fee Related
- 2012-01-26 CN CN201280015155.1A patent/CN103443195B/zh not_active Expired - Fee Related
- 2012-01-26 EP EP12741594.1A patent/EP2670802B1/en not_active Not-in-force
- 2012-01-26 WO PCT/US2012/022663 patent/WO2012106172A2/en not_active Ceased
- 2012-01-26 US US13/983,321 patent/US9309370B2/en active Active
- 2012-01-26 JP JP2013552557A patent/JP5837619B2/ja not_active Expired - Fee Related
- 2012-02-03 TW TW101103571A patent/TWI530518B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP2670802A2 (en) | 2013-12-11 |
| TW201237079A (en) | 2012-09-16 |
| KR101862899B1 (ko) | 2018-05-30 |
| US9309370B2 (en) | 2016-04-12 |
| WO2012106172A2 (en) | 2012-08-09 |
| CN103443195B (zh) | 2017-10-10 |
| KR20140008365A (ko) | 2014-01-21 |
| TWI530518B (zh) | 2016-04-21 |
| EP2670802B1 (en) | 2018-04-25 |
| US20140011933A1 (en) | 2014-01-09 |
| CN103443195A (zh) | 2013-12-11 |
| WO2012106172A3 (en) | 2013-01-17 |
| EP2670802A4 (en) | 2015-02-11 |
| JP2014504674A (ja) | 2014-02-24 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5837619B2 (ja) | ジルコニウム酸化物ナノ粒子を含む非晶質ペルフルオロポリマー | |
| EP3074430B1 (en) | Employing polyalkylene oxides for nucleation in aqueous polymerization of fluoromonomer | |
| US8623963B2 (en) | High purity perfluoroelastomer composites and a process to produce the same | |
| US10557031B2 (en) | Composition including amorphous fluoropolymer and fluoroplastic particles and methods of making the same | |
| JP4051929B2 (ja) | 架橋用フッ素系エラストマー組成物 | |
| JPWO2000029479A1 (ja) | 含フッ素エラストマーおよびその架橋用組成物 | |
| US20210292451A1 (en) | Fluoropolymer-containing composition and molded article | |
| US8969469B2 (en) | Method of coagulating an amorphous fluoropolymer latex | |
| JP4748125B2 (ja) | フッ素ゴム架橋用組成物 | |
| WO2020204082A1 (ja) | 含フッ素弾性共重合体組成物、フッ素ゴム及びこれらの製造方法 | |
| JP5863060B2 (ja) | フルオロエラストマ組成物 | |
| EP2585532A2 (en) | Process for preparing curable perfluoroelastomer compositions | |
| WO2025018379A1 (ja) | 含フッ素エラストマーの製造方法、水性分散液、固体組成物 | |
| JP5070805B2 (ja) | クリーンフィラーを配合した架橋性フッ素系エラストマー組成物 | |
| US12091537B2 (en) | Composition and molded article containing fluorine-containing polymer | |
| WO2025263537A1 (ja) | パーフルオロエラストマー、組成物、架橋ゴム物品、パーフルオロエラストマーの製造方法 | |
| JP2025110424A (ja) | フッ素含有ポリマーの分解方法 | |
| WO2025143165A1 (ja) | パーフルオロエラストマー、架橋ゴム物品 | |
| JP2025036050A (ja) | フッ素含有ポリマーの分解方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20150114 |
|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20150114 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20150417 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20150512 |
|
| 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: 20151006 |
|
| A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20151105 |
|
| R150 | Certificate of patent or registration of utility model |
Ref document number: 5837619 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 |
|
| R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
| LAPS | Cancellation because of no payment of annual fees |