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 (enExample) | 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 (enExample) |
| EP (1) | EP2670802B1 (enExample) |
| JP (1) | JP5837619B2 (enExample) |
| KR (1) | KR101862899B1 (enExample) |
| CN (1) | CN103443195B (enExample) |
| TW (1) | TWI530518B (enExample) |
| WO (1) | WO2012106172A2 (enExample) |
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 |
| US10958337B2 (en) * | 2017-02-14 | 2021-03-23 | Qualcomm Incorporated | Narrowband time-division duplex frame structure for narrowband communications |
| WO2019241186A1 (en) | 2018-06-12 | 2019-12-19 | 3M Innovative Properties Company | Fluoropolymer coating compositions comprising amine 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 |
| TWI918597B (zh) * | 2018-12-17 | 2026-03-21 | 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 |
| WO2021038424A1 (en) * | 2019-08-27 | 2021-03-04 | 3M Innovative Properties Company | Curable fluoropolymer compositions comprising metal fluoride particles and articles therefrom |
| CN114630874B (zh) | 2019-11-04 | 2023-12-05 | 3M创新有限公司 | 包含具有烯键式不饱和基团和电子供体基团的固化剂的含氟聚合物组合物及用其涂覆的基底 |
| WO2021088198A1 (en) * | 2019-11-04 | 2021-05-14 | 3M Innovative Properties Company | Electronic telecommunications articles comprising crosslinked fluoropolymers and methods |
| CN119604576A (zh) * | 2022-07-25 | 2025-03-11 | 大金工业株式会社 | 交联性组合物和成型品 |
| 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 |
| EP0837901A1 (en) | 1995-06-28 | 1998-04-29 | 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 |
| WO2000010934A1 (en) * | 1998-08-18 | 2000-03-02 | 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 |
| US6803402B2 (en) | 1999-11-04 | 2004-10-12 | Daikin Industries, Ltd. | Elastomer molded article and crosslinkable fluorine-containing elastomer composition for semi-conductor production apparatuses |
| 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 |
| US7790658B2 (en) * | 2005-05-27 | 2010-09-07 | University of Florida Research Foundaction, Inc. | Inert wear resistant PTFE-based solid lubricant nanocomposite |
| 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 |
| ATE501212T1 (de) | 2005-09-26 | 2011-03-15 | Asahi Glass Co Ltd | Perfluoroelastomerzusammensetzung und formteil aus einem perfluorkautschuk |
| WO2007041227A2 (en) | 2005-09-30 | 2007-04-12 | 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 |
| US20100239867A1 (en) | 2006-06-22 | 2010-09-23 | Daikin Industries, Ltd. | Sealing material, parts for plasma treating equipment having said sealing material, and process for preparing said sealing material |
| 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 |
| WO2009085926A2 (en) | 2007-12-28 | 2009-07-09 | 3M Innovative Properties Company | Method of making zirconia-containing nanoparticles |
| CN101925622A (zh) * | 2008-01-28 | 2010-12-22 | 旭硝子株式会社 | 固化性组合物、含氟固化物、使用其的光学材料及发光元件 |
| CN102099871A (zh) | 2008-07-22 | 2011-06-15 | E.I.内穆尔杜邦公司 | 包含无机纳米颗粒的导电聚合物的含水分散体 |
| US8889316B2 (en) * | 2009-06-15 | 2014-11-18 | Arkema Inc. | Organic/inorganic composite blend membrane compositions of polyelectrolye blends with nanoparticles |
| WO2011162971A2 (en) | 2010-06-24 | 2011-12-29 | 3M Innovative Properties Company | Polymerizable compositions free of organic emulsifier and polymers and methods of making thereof |
| CN103221479B (zh) * | 2010-11-18 | 2016-06-22 | 3M创新有限公司 | 凝聚无定形含氟聚合物胶乳的方法 |
| WO2012067937A2 (en) | 2010-11-18 | 2012-05-24 | 3M Innovative Properties Company | Method of coagulating an amorphous fluoropolymer using modified inorganic nanoparticles |
| 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 US US13/983,321 patent/US9309370B2/en active Active
- 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 CN CN201280015155.1A patent/CN103443195B/zh not_active Expired - Fee Related
- 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 |
|---|---|
| CN103443195B (zh) | 2017-10-10 |
| WO2012106172A2 (en) | 2012-08-09 |
| US9309370B2 (en) | 2016-04-12 |
| JP2014504674A (ja) | 2014-02-24 |
| WO2012106172A3 (en) | 2013-01-17 |
| EP2670802A2 (en) | 2013-12-11 |
| KR20140008365A (ko) | 2014-01-21 |
| CN103443195A (zh) | 2013-12-11 |
| TW201237079A (en) | 2012-09-16 |
| EP2670802A4 (en) | 2015-02-11 |
| EP2670802B1 (en) | 2018-04-25 |
| TWI530518B (zh) | 2016-04-21 |
| US20140011933A1 (en) | 2014-01-09 |
| KR101862899B1 (ko) | 2018-05-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| TWI530518B (zh) | 包含氧化鋯奈米粒子之非晶形全氟聚合物 | |
| EP3074430B1 (en) | Employing polyalkylene oxides for nucleation in aqueous polymerization of fluoromonomer | |
| US10557031B2 (en) | Composition including amorphous fluoropolymer and fluoroplastic particles and methods of making the same | |
| US20060270780A1 (en) | High purity perfluoroelastomer composites and a processes to produce the same | |
| JP7848945B2 (ja) | 水性分散液の製造方法、第２含フッ素重合体の製造方法、水性分散液、固体組成物 | |
| 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 | |
| WO2025121351A1 (ja) | 含フッ素エラストマーの製造方法、組成物、固体組成物、及び架橋ゴム物品 | |
| 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 | |
| EP2640781B1 (en) | Method of coagulating an amorphous fluoropolymer latex | |
| 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 | |
| JP2007246928A (ja) | フッ素ゴム架橋用組成物 | |
| US12091537B2 (en) | Composition and molded article containing fluorine-containing polymer | |
| JP5863060B2 (ja) | フルオロエラストマ組成物 | |
| JP7845517B2 (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 | |
| WO2011163575A2 (en) | Process for preparing curable perfluoroelastomer compositions | |
| JP2007084832A (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 | |
| JP2025110424A (ja) | フッ素含有ポリマーの分解方法 | |
| JP2025036050A (ja) | フッ素含有ポリマーの分解方法 | |
| WO2020027046A1 (ja) | 含フッ素ポリマーを含有する組成物および成形品 | |
| HK1108708B (en) | High purity perfluoroelastomer composites and a process to produce the same |
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 |