DE60020911T2 - Perfluorpolyätherschmiermittel, enthaltend Sulfonylfluorgruppen - Google Patents
Perfluorpolyätherschmiermittel, enthaltend Sulfonylfluorgruppen Download PDFInfo
- Publication number
- DE60020911T2 DE60020911T2 DE60020911T DE60020911T DE60020911T2 DE 60020911 T2 DE60020911 T2 DE 60020911T2 DE 60020911 T DE60020911 T DE 60020911T DE 60020911 T DE60020911 T DE 60020911T DE 60020911 T2 DE60020911 T2 DE 60020911T2
- Authority
- DE
- Germany
- Prior art keywords
- cof
- range
- perfluoropolyether
- ocf
- temperature
- 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 - Lifetime
Links
- 239000010702 perfluoropolyether Substances 0.000 title claims description 46
- 239000000314 lubricant Substances 0.000 title claims description 29
- 125000001153 fluoro group Chemical group F* 0.000 title description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 title 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 27
- 229910052760 oxygen Inorganic materials 0.000 claims description 27
- 239000001301 oxygen Substances 0.000 claims description 27
- 239000000178 monomer Substances 0.000 claims description 25
- VQUGQIYAVYQSAB-UHFFFAOYSA-N 1,1,2,2-tetrafluoro-2-(1,2,2-trifluoroethenoxy)ethanesulfonyl fluoride Chemical compound FC(F)=C(F)OC(F)(F)C(F)(F)S(F)(=O)=O VQUGQIYAVYQSAB-UHFFFAOYSA-N 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 22
- 239000007788 liquid Substances 0.000 claims description 19
- 230000005855 radiation Effects 0.000 claims description 19
- 239000002904 solvent Substances 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 10
- 229910052731 fluorine Inorganic materials 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- 238000006116 polymerization reaction Methods 0.000 claims description 9
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 7
- 239000012429 reaction media Substances 0.000 claims description 7
- 229920001774 Perfluoroether Polymers 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 5
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 4
- LGPPATCNSOSOQH-UHFFFAOYSA-N 1,1,2,3,4,4-hexafluorobuta-1,3-diene Chemical compound FC(F)=C(F)C(F)=C(F)F LGPPATCNSOSOQH-UHFFFAOYSA-N 0.000 claims description 3
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 3
- -1 hydrogen fluoride ethers Chemical class 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 229910052708 sodium Inorganic materials 0.000 claims description 3
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical group FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 claims description 3
- 238000005903 acid hydrolysis reaction Methods 0.000 claims description 2
- 238000005904 alkaline hydrolysis reaction Methods 0.000 claims description 2
- 150000001993 dienes Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 238000003682 fluorination reaction Methods 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims 1
- 239000000047 product Substances 0.000 description 55
- 229920000642 polymer Polymers 0.000 description 44
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 22
- 238000006243 chemical reaction Methods 0.000 description 19
- 238000001816 cooling Methods 0.000 description 15
- 150000003457 sulfones Chemical group 0.000 description 14
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- 239000010453 quartz Substances 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- 238000004448 titration Methods 0.000 description 10
- 239000004721 Polyphenylene oxide Substances 0.000 description 9
- 239000011521 glass Substances 0.000 description 9
- 229920000570 polyether Polymers 0.000 description 9
- 239000007789 gas Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 7
- 238000002411 thermogravimetry Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 6
- 125000000524 functional group Chemical group 0.000 description 6
- 239000003999 initiator Substances 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 5
- 238000004821 distillation Methods 0.000 description 5
- 238000001704 evaporation Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 230000009477 glass transition Effects 0.000 description 5
- 230000001590 oxidative effect Effects 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 230000001105 regulatory effect Effects 0.000 description 5
- 239000012265 solid product Substances 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 230000008859 change Effects 0.000 description 4
- 238000000113 differential scanning calorimetry Methods 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000003776 cleavage reaction Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000005342 ion exchange Methods 0.000 description 3
- 239000000395 magnesium oxide Substances 0.000 description 3
- 150000002924 oxiranes Chemical class 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- 230000007017 scission Effects 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- PGFXOWRDDHCDTE-UHFFFAOYSA-N hexafluoropropylene oxide Chemical compound FC(F)(F)C1(F)OC1(F)F PGFXOWRDDHCDTE-UHFFFAOYSA-N 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 239000006193 liquid solution Substances 0.000 description 2
- 239000012454 non-polar solvent Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000007539 photo-oxidation reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- 150000003456 sulfonamides Chemical class 0.000 description 2
- 238000001308 synthesis method Methods 0.000 description 2
- 238000004293 19F NMR spectroscopy Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000012668 chain scission Methods 0.000 description 1
- 150000005827 chlorofluoro hydrocarbons Chemical class 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000011147 inorganic material Substances 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical group 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000003930 superacid Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/002—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds
- C08G65/005—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens
- C08G65/007—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from unsaturated compounds containing halogens containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/38—Lubricating compositions characterised by the base-material being a macromolecular compound containing halogen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/02—Macromolecular compounds obtained by reactions of monomers involving only carbon-to-carbon unsaturated bonds
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Polyethers (AREA)
- Lubricants (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ITMI991756 | 1999-08-04 | ||
| IT1999MI001756A IT1313597B1 (it) | 1999-08-04 | 1999-08-04 | Lubrificanti perfluoropolieterei contenenti gruppi solfonilfluoruro |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60020911D1 DE60020911D1 (de) | 2005-07-28 |
| DE60020911T2 true DE60020911T2 (de) | 2006-04-27 |
Family
ID=11383503
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60020911T Expired - Lifetime DE60020911T2 (de) | 1999-08-04 | 2000-07-27 | Perfluorpolyätherschmiermittel, enthaltend Sulfonylfluorgruppen |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US6403539B1 (enExample) |
| EP (1) | EP1074584B1 (enExample) |
| JP (1) | JP4837164B2 (enExample) |
| DE (1) | DE60020911T2 (enExample) |
| IT (1) | IT1313597B1 (enExample) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2001114750A (ja) * | 1999-10-19 | 2001-04-24 | Daikin Ind Ltd | パーフルオロビニルエーテルスルホン酸誘導体の製造法 |
| ITMI20010008A1 (it) * | 2001-01-03 | 2002-07-03 | Ausimont Spa | Additivi per fluoropolieterei per applicazioni elettromagnetiche |
| ITMI20011340A1 (it) | 2001-06-26 | 2002-12-26 | Ausimont Spa | Pfpe aventi almeno un terminale alchiletereo e relativo processo dipreparazione |
| US7425601B2 (en) * | 2002-12-20 | 2008-09-16 | Exxonmobil Chemical Patents Inc. | Polymers with new sequence distributions |
| JP5193424B2 (ja) * | 2002-12-20 | 2013-05-08 | エクソンモービル・ケミカル・パテンツ・インク | 長鎖分子を実質的に含まないポリマー |
| WO2004058828A1 (en) * | 2002-12-20 | 2004-07-15 | Exxonmobil Chemical Patents Inc. | Polymerization processes |
| US7723447B2 (en) * | 2002-12-20 | 2010-05-25 | Exxonmobil Chemical Patents Inc. | Polymerization processes |
| AU2004276302B2 (en) * | 2003-09-23 | 2011-02-03 | California Institute Of Technology | Photocurable perfluoropolyethers for use as novel materials in microfluidic devices |
| US8481468B2 (en) * | 2005-09-12 | 2013-07-09 | HGST Netherlands B.V. | Lubricant with non-terminal functional groups |
| WO2010063745A1 (en) * | 2008-12-05 | 2010-06-10 | Solvay Solexis S.P.A. | Polyfunctional (per)fluoropolyethers |
| WO2017131059A1 (ja) * | 2016-01-27 | 2017-08-03 | 株式会社ニッペコ | 異物除去潤滑組成物、異物除去潤滑組成物の塗布部材、及び、異物除去潤滑組成物の使用方法 |
| WO2017144413A1 (en) * | 2016-02-23 | 2017-08-31 | Solvay Specialty Polymers Italy S.P.A. | Method for the manufacture of fluorinated polymers and polymers obtainable therefrom |
| JP2019123759A (ja) * | 2016-05-19 | 2019-07-25 | ダイキン工業株式会社 | フッ素含有共重合体 |
| EP3677570B1 (en) * | 2017-09-01 | 2023-11-08 | AGC Inc. | Fluorosulfonyl group-containing compound, fluorosulfonyl group-containing monomer, and production methods for same |
| JP7345454B2 (ja) | 2017-09-08 | 2023-09-15 | ソルベイ スペシャルティ ポリマーズ イタリー エス．ピー．エー． | フルオロポリマーを製造する方法 |
| WO2019084498A2 (en) | 2017-10-27 | 2019-05-02 | The Board Of Trustees Of The Leland Stanford Junior University | ELECTROCALLY CONDUCTIVE HYDROGELS WITH LITHOGRAPHIC PATTERNS, PHOTOCURABLE COMPOSITIONS, AND ELASTOMERS FORMED FROM SUCH COMPOSITIONS |
| JPWO2022059682A1 (enExample) * | 2020-09-16 | 2022-03-24 | ||
| JP2024547081A (ja) | 2021-12-21 | 2024-12-26 | ソルベイ スペシャルティ ポリマーズ イタリー エス．ピー．エー． | ペンダント官能基を含むパーフルオロポリエーテルポリマー |
| EP4594370A1 (en) | 2022-09-28 | 2025-08-06 | Solvay Specialty Polymers Italy S.p.A. | Perfluoropolyether polymers |
| WO2024068677A1 (en) | 2022-09-28 | 2024-04-04 | Solvay Specialty Polymers Italy S.P.A. | Perfluoropolyether polymers |
| WO2024068676A1 (en) | 2022-09-28 | 2024-04-04 | Solvay Specialty Polymers Italy S.P.A. | Perfluoropolyether polymers |
| WO2024149802A1 (en) * | 2023-01-12 | 2024-07-18 | Solvay Specialty Polymers Italy S.P.A. | Perfluoropolyether polymers |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3282875A (en) * | 1964-07-22 | 1966-11-01 | Du Pont | Fluorocarbon vinyl ether polymers |
| US4610829A (en) * | 1968-08-21 | 1986-09-09 | Produits Chimiques Ugine Kuhlmann | Polyfluorinated sulphonic acids and their derivatives |
| US4360645A (en) * | 1981-04-03 | 1982-11-23 | E. I. Du Pont De Nemours And Company | Perfluoroglycidyl ethers |
| US4384128A (en) * | 1981-04-03 | 1983-05-17 | E. I. Du Pont De Nemours And Company | Perfluoroglycidyl ethers |
| IT1213071B (it) | 1986-05-07 | 1989-12-07 | Ausimont Spa | Perfluoropolieteri esenti da ossigeno perossidico e contenenti gruppi perfluoroepossidici disposti lungo la catena perfluoropolieterea. |
| US4940525A (en) * | 1987-05-08 | 1990-07-10 | The Dow Chemical Company | Low equivalent weight sulfonic fluoropolymers |
| IT1229845B (it) | 1989-04-20 | 1991-09-13 | Ausimont Srl | Procedimento per la preparazione di perfluoropolieteri perossidici. |
| IT1237887B (it) * | 1989-12-12 | 1993-06-18 | Ausimont Spa | Lubrificanti perfluoropolieterei aventi proprieta' antiusura |
| US5142842A (en) | 1989-12-13 | 1992-09-01 | W. R. Grace & Co.-Conn. | Method for making a film/foil panel |
| IT1246357B (it) * | 1990-07-12 | 1994-11-17 | Ausimont Spa | Processo per la preparazione di composti perfluoroalcossisolfonici |
| US6019909A (en) * | 1993-01-22 | 2000-02-01 | Daikin Industries, Ltd. | Fluorinated hydrocarbon compound and process for its preparation, and refrigerator oil and magnetic recording medium lubricant |
| IT1264977B1 (it) | 1993-11-17 | 1996-10-17 | Ausimont Spa | Processo per preparare perfluoropolietri |
| US5872157A (en) * | 1996-01-30 | 1999-02-16 | The University Of North Carolina At Chapel Hill | Method for olefin oxidation |
| EP0831110B9 (en) * | 1996-09-18 | 2005-09-07 | E.I. Du Pont De Nemours And Company | Perfluoroalkylene oxide copolymer composition containing functional groups |
| DE19644942A1 (de) | 1996-10-29 | 1998-04-30 | Kba Planeta Ag | Stapellogistik |
| US6184187B1 (en) * | 1998-04-07 | 2001-02-06 | E. I. Dupont De Nemours And Company | Phosphorus compounds and their use as corrosion inhibitors for perfluoropolyethers |
-
1999
- 1999-08-04 IT IT1999MI001756A patent/IT1313597B1/it active
-
2000
- 2000-07-27 EP EP00116064A patent/EP1074584B1/en not_active Expired - Lifetime
- 2000-07-27 DE DE60020911T patent/DE60020911T2/de not_active Expired - Lifetime
- 2000-08-02 US US09/631,880 patent/US6403539B1/en not_active Expired - Lifetime
- 2000-08-04 JP JP2000237581A patent/JP4837164B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP1074584A3 (en) | 2001-11-21 |
| JP2001049276A (ja) | 2001-02-20 |
| EP1074584B1 (en) | 2005-06-22 |
| ITMI991756A0 (it) | 1999-08-04 |
| IT1313597B1 (it) | 2002-09-09 |
| JP4837164B2 (ja) | 2011-12-14 |
| EP1074584A2 (en) | 2001-02-07 |
| US6403539B1 (en) | 2002-06-11 |
| DE60020911D1 (de) | 2005-07-28 |
| ITMI991756A1 (it) | 2001-02-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE60020911T2 (de) | Perfluorpolyätherschmiermittel, enthaltend Sulfonylfluorgruppen | |
| DE3750786T2 (de) | Perfluorpolyether frei von peroxidischem Sauerstoff und Perfluorepoxygruppen entlang der Perfluorpolyetherkette enthaltend. | |
| DE69500674T2 (de) | Fluorierte Polymere und Copolymere die cyclische Strukturen enthalten | |
| DE69402473T2 (de) | Perfluorodioxole, ihre Herstellung und deren Homopolymere und Copolymere | |
| DE60133497T2 (de) | Perfluorpolyether und verfahren zur ihrer herstellung | |
| DE69424124T2 (de) | Verfahren zur Herstellung von Perfluorpolyethers | |
| DE60125012T2 (de) | Perfluoropolyether Additive für elektrochemische Anwendungen | |
| DE60213723T2 (de) | Perfluoropolyether (PFPEs) mit minderstens einer Alkylrtherendgruppe und Verfahren zur Herstellung derselben | |
| DE69126339T2 (de) | Perfluorether und Verfahren zu ihrer Herstellung | |
| DE68921891T2 (de) | Flüssigphase-fluorieren. | |
| DD259629A5 (de) | Verfahren zur polymerisation und copolymerisation fluorierter monomerer | |
| DD298941A5 (de) | Verfahren zur herstellung von peroxidischen perfluorpolyethern | |
| DE60010936T2 (de) | Sulfonierte perfluorvinylfunktionalisierte monomere | |
| DE602004010980T2 (de) | Perfluoropolyether | |
| JP2594798B2 (ja) | 元素状ふっ素を用いたふっ素化によるペルフルオルエーテルの製造方法 | |
| DE69702550T2 (de) | Verfahren zur Herstellung von peroxiperfluoropolyxyalkylene | |
| DE69403692T2 (de) | Radikalisches (co)Polymerisationsverfahren von fluorhaltigen olefinischen Monomeren | |
| DE69017281T2 (de) | Verfahren zur Herstellung von perhalogenierten Ethern aus perhalogenierten Olefinen und so erhaltene perhalogenierte Ether. | |
| JP2001049276A5 (enExample) | ||
| DE60023948T2 (de) | Fluoro-olefinpolymerisation | |
| DE69918229T2 (de) | Hydrofluoroalkylvinylether sowie deren Herstellungsverfahren | |
| DE60036962T2 (de) | Verfahren zur polymerisation von fluorenthaltenden monomeren in wässriger emulsion | |
| DE60028021T2 (de) | Fluoriertes polymer von allylether | |
| DE69202764T2 (de) | Perfluorierte cyclische polyether, verwendbar als schmiermittel und wärmeübertragungsflüssigkeiten. | |
| EP0223238B1 (en) | Process for preparing perfluoropolyethers of regulated molecular weight having neutral and functional end groups |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition |