CS276635B6 - Perfluoroethers containing halogen different from fluorine with terminal acid group and process for preparing thereof - Google Patents
Perfluoroethers containing halogen different from fluorine with terminal acid group and process for preparing thereof Download PDFInfo
- Publication number
- CS276635B6 CS276635B6 CS892693A CS269389A CS276635B6 CS 276635 B6 CS276635 B6 CS 276635B6 CS 892693 A CS892693 A CS 892693A CS 269389 A CS269389 A CS 269389A CS 276635 B6 CS276635 B6 CS 276635B6
- Authority
- CS
- Czechoslovakia
- Prior art keywords
- formula
- fluorine
- group
- groups
- chlorine
- Prior art date
Links
- 229910052731 fluorine Inorganic materials 0.000 title claims abstract description 21
- 239000011737 fluorine Substances 0.000 title claims abstract description 19
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 title abstract description 13
- 239000002253 acid Substances 0.000 title abstract description 10
- UJMWVICAENGCRF-UHFFFAOYSA-N oxygen difluoride Chemical class FOF UJMWVICAENGCRF-UHFFFAOYSA-N 0.000 title description 4
- 229920001774 Perfluoroether Polymers 0.000 title description 3
- 229910052736 halogen Inorganic materials 0.000 title description 3
- 150000002367 halogens Chemical class 0.000 title description 3
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000007539 photo-oxidation reaction Methods 0.000 claims abstract description 20
- 239000010702 perfluoropolyether Substances 0.000 claims abstract description 12
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims abstract description 11
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 10
- 125000005843 halogen group Chemical group 0.000 claims abstract description 9
- 125000002081 peroxide group Chemical group 0.000 claims abstract description 8
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims abstract description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 4
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical compound FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 20
- 229910052801 chlorine Inorganic materials 0.000 claims description 19
- 239000000460 chlorine Chemical group 0.000 claims description 17
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 12
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 239000001301 oxygen Substances 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 11
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 230000002378 acidificating effect Effects 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 230000005855 radiation Effects 0.000 claims description 7
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 6
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 3
- 239000002574 poison Substances 0.000 claims 1
- 231100000614 poison Toxicity 0.000 claims 1
- 150000001265 acyl fluorides Chemical class 0.000 abstract description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract description 2
- 238000000354 decomposition reaction Methods 0.000 abstract description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 7
- 125000001309 chloro group Chemical group Cl* 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 6
- 230000008020 evaporation Effects 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000004721 Polyphenylene oxide Substances 0.000 description 5
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 5
- 229920000570 polyether Polymers 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 239000010453 quartz Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000008246 gaseous mixture Substances 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 230000007935 neutral effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- AYCANDRGVPTASA-UHFFFAOYSA-N 1-bromo-1,2,2-trifluoroethene Chemical group FC(F)=C(F)Br AYCANDRGVPTASA-UHFFFAOYSA-N 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- -1 alkali metal salt Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- 125000005702 oxyalkylene group Chemical group 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- UPVJEODAZWTJKZ-OWOJBTEDSA-N (e)-1,2-dichloro-1,2-difluoroethene Chemical group F\C(Cl)=C(\F)Cl UPVJEODAZWTJKZ-OWOJBTEDSA-N 0.000 description 1
- PGJHURKAWUJHLJ-UHFFFAOYSA-N 1,1,2,3-tetrafluoroprop-1-ene Chemical compound FCC(F)=C(F)F PGJHURKAWUJHLJ-UHFFFAOYSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- LDTMPQQAWUMPKS-UHFFFAOYSA-N 1-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=CCl LDTMPQQAWUMPKS-UHFFFAOYSA-N 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- 238000001632 acidimetric titration Methods 0.000 description 1
- 125000000777 acyl halide group Chemical group 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
- 239000000292 calcium oxide Substances 0.000 description 1
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000012986 chain transfer agent Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical compound F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 238000004141 dimensional analysis Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- BPQPBEVHMFRECG-UHFFFAOYSA-N fluoro formate Chemical compound FOC=O BPQPBEVHMFRECG-UHFFFAOYSA-N 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 239000001307 helium Substances 0.000 description 1
- 229910052734 helium Inorganic materials 0.000 description 1
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000002798 spectrophotometry method Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000012916 structural analysis Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- 230000004580 weight loss Effects 0.000 description 1
- 238000010626 work up procedure Methods 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
-
- 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
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/321—Polymers modified by chemical after-treatment with inorganic compounds
- C08G65/324—Polymers modified by chemical after-treatment with inorganic compounds containing oxygen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/125—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups
- C07C59/135—Saturated compounds having only one carboxyl group and containing ether groups, groups, groups, or groups containing halogen
-
- 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
- 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
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
-
- 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
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/3311—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group
- C08G65/3312—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group acyclic
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyethers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT20406/88A IT1217452B (it) | 1988-05-02 | 1988-05-02 | Perfluoropolieteri contenenti un alogeno diverso da fluoro e aventi un gruppo terminale a funzione acida |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CS269389A3 CS269389A3 (en) | 1992-02-19 |
| CS276635B6 true CS276635B6 (en) | 1992-07-15 |
Family
ID=11166452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CS892693A CS276635B6 (en) | 1988-05-02 | 1989-05-02 | Perfluoroethers containing halogen different from fluorine with terminal acid group and process for preparing thereof |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5143589A (xx) |
| EP (1) | EP0340740B1 (xx) |
| JP (2) | JP3073497B2 (xx) |
| KR (1) | KR0134375B1 (xx) |
| AU (1) | AU615054B2 (xx) |
| CA (1) | CA1339425C (xx) |
| CS (1) | CS276635B6 (xx) |
| DE (1) | DE68924800T2 (xx) |
| ES (1) | ES2079362T3 (xx) |
| IL (1) | IL90157A (xx) |
| IT (1) | IT1217452B (xx) |
| RU (1) | RU1838337C (xx) |
| UA (1) | UA12836A (xx) |
| ZA (1) | ZA893231B (xx) |
Families Citing this family (46)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1231758B (it) * | 1989-04-20 | 1991-12-21 | Ausimont Srl | Fluoropolieteri funzionalizzati |
| IT1217453B (it) * | 1988-05-02 | 1990-03-22 | Ausimont Spa | Procedimento per la produzione di perfluoropolieteri a peso molecolare controllato,aventi gruppi terminali perfluoroalchilici o perfluorocloroalchilici |
| IT1217838B (it) * | 1988-06-17 | 1990-03-30 | Ausimont Spa | Microemulsioni per tipo acqua in olio elettricamente conduttrici,a base di composti perfluorurati usate come catolita in processi elettrochimici |
| IT1217839B (it) * | 1988-06-17 | 1990-03-30 | Ausimont Spa | Microemulsioni del tipo olio in acqua elettricamente conduttrici,a base di composti perfluorurati,usate come catolita in processi elettrochimici |
| US5211861A (en) * | 1988-09-19 | 1993-05-18 | Ausimont S.R.L. | Liquid aqueous compositions comprising perfluoropolyethereal compounds suitable as lubricants in the plastic processing of metals |
| IT1229845B (it) * | 1989-04-20 | 1991-09-13 | Ausimont Srl | Procedimento per la preparazione di perfluoropolieteri perossidici. |
| IT1256304B (it) * | 1992-11-10 | 1995-11-30 | Ausimont Spa | Derivati fosfazenici e loro impiego come stabilizzanti per oli e grassi a base di perfluoropolieteri |
| IT1256721B (it) * | 1992-12-16 | 1995-12-15 | Ausimont Spa | Processo per impartire oleo- ed idro-repellenza alla superficie di materiali ceramici porosi |
| IT1264977B1 (it) * | 1993-11-17 | 1996-10-17 | Ausimont Spa | Processo per preparare perfluoropolietri |
| IT1269886B (it) * | 1994-06-14 | 1997-04-15 | Ausimont Spa | Processo per il trattamento superficiale di materiali cellulosici, metallici,vetrosi,oppure cementi,marmi,graniti e simili |
| IT1270703B (it) * | 1994-11-17 | 1997-05-07 | Ausimont Spa | Microemulsioni di fluoropoliossialchileni in miscela con idrocarburi, e loro uso in processi di (co)polimerizzazione di monomeri fluorurati |
| IT1275972B1 (it) * | 1995-03-24 | 1997-10-24 | Ausimont Spa | Dispersioni di politetrafluoroetilene in un solvente organico ed agenti disperdenti ivi impiegati |
| IT1276072B1 (it) * | 1995-10-31 | 1997-10-24 | Ausimont Spa | Processo di (co)polimerizzazione di monomeri fluorurati per ottenere polimeri contenenti idrogeno |
| US5872157A (en) * | 1996-01-30 | 1999-02-16 | The University Of North Carolina At Chapel Hill | Method for olefin oxidation |
| US6211415B1 (en) | 1996-11-22 | 2001-04-03 | Daikin Industries, Ltd. | Process for thermal decomposition of hexafluoropropylene oxide oligomers |
| AU4458797A (en) | 1997-09-15 | 1999-04-05 | Sofitech N.V. | Electrically conductive non-aqueous wellbore fluids |
| US6405809B2 (en) | 1998-01-08 | 2002-06-18 | M-I Llc | Conductive medium for openhold logging and logging while drilling |
| ITMI20010554A1 (it) | 2001-03-16 | 2002-09-16 | Ausimont Spa | Additivi per resine idrogenate |
| ITMI20011306A1 (it) | 2001-06-21 | 2002-12-21 | Ausimont Spa | Poliuretani vulcanizzabili |
| ITMI20011424A1 (it) | 2001-07-05 | 2003-01-05 | Ausimont Spa | Dispersioni di polimeri fluorurati |
| ITMI20020029A1 (it) | 2002-01-10 | 2003-07-10 | Ausimont Spa | Composizioni idro- oleo repellenti |
| ITMI20020056A1 (it) | 2002-01-15 | 2003-07-15 | Ausimont Spa | Composizioni acquose di fosfati di perfluoropolieteri e loro uso per conferire oleorepellenza alla carta |
| ITMI20020057A1 (it) | 2002-01-15 | 2003-07-15 | Ausimont Spa | Composizioni acquose di fosfati di perfluoropolieteri e loro uso per conferire oleorepellenza alla carta |
| ITMI20020198A1 (it) * | 2002-02-05 | 2003-08-05 | Ausimont Spa | (per)aloeteri |
| ITMI20021228A1 (it) | 2002-06-06 | 2003-12-09 | Ausimont Spa | Composizioni di poliuretani reticolabili |
| ITMI20021277A1 (it) | 2002-06-11 | 2003-12-11 | Ausimont Spa | Perfluoropolieteri comprendenti unita' ripetitive ottenute dall'ossidazione di perfluorodiossoli |
| ITMI20040106A1 (it) | 2004-01-27 | 2004-04-27 | Solvay Solexis Spa | Poliuretani |
| ITMI20040133A1 (it) | 2004-01-29 | 2004-04-29 | Solvay Solexis Spa | Processo per preparare fluoroalogenoeteri |
| ITMI20040345A1 (it) * | 2004-02-26 | 2004-05-26 | Solvay Solexis Spa | Perfluororpolieteri perossidici |
| ITMI20040346A1 (it) * | 2004-02-26 | 2004-05-26 | Solvay Solexis Spa | Perfluoropolieteri perossidici |
| ITMI20042238A1 (it) | 2004-11-19 | 2005-02-19 | Solvay Solexis Spa | Composti per fluoropolirterei |
| ITMI20050817A1 (it) | 2005-05-05 | 2006-11-06 | Solvay Solexis Spa | Processo di dealogenazione |
| ITMI20060681A1 (it) * | 2006-04-06 | 2007-10-07 | Solvay Solexis Spa | Processo per preparare perfluoropolieteri mono-carbossilici ad elevata purezza |
| CN100479643C (zh) * | 2007-04-10 | 2009-04-22 | 西北农林科技大学 | 西藏嵩草种子萌发处理方法 |
| CN103073410A (zh) * | 2012-12-30 | 2013-05-01 | 江苏梅兰化工有限公司 | 一种氟醚羧酸表面活性剂的制备方法 |
| CN105170018B (zh) * | 2015-09-30 | 2016-08-17 | 成都晨光博达橡塑有限公司 | 一种不含全氟辛酸的含氟表面活性剂及其制备方法和工艺系统 |
| CN105344288A (zh) * | 2015-09-30 | 2016-02-24 | 成都晨光博达橡塑有限公司 | 一种不含全氟辛酸的含氟表面活性剂的连续化生产工艺 |
| CN105344289B (zh) * | 2015-09-30 | 2016-07-13 | 成都晨光博达橡塑有限公司 | 不含全氟辛酸及其盐的含氟表面活性剂 |
| CN105170017B (zh) * | 2015-09-30 | 2016-08-17 | 成都晨光博达橡塑有限公司 | 一种不含全氟辛酸的含氟表面活性剂 |
| CN105148794A (zh) * | 2015-09-30 | 2015-12-16 | 成都晨光博达橡塑有限公司 | 一种制备不含全氟辛酸的含氟表面活性剂的生产工艺 |
| EP3638704B1 (en) | 2017-06-14 | 2021-11-10 | Solvay Specialty Polymers Italy S.p.A. | Ferroelectric fluoropolymer |
| KR102277461B1 (ko) | 2019-08-29 | 2021-07-14 | 한서대학교 산학협력단 | 양식장용 산소공급장치 |
| KR102336611B1 (ko) * | 2020-02-12 | 2021-12-07 | 권태우 | 용존산소 생성 장치 및 이를 이용한 멀티 수질 정화기 |
| CN114015033B (zh) * | 2021-09-30 | 2024-06-18 | 四川弘氟新材料有限公司 | 一种含氟聚醚羧酸型表面活性剂及其制备方法 |
| CN114031762A (zh) * | 2021-09-30 | 2022-02-11 | 四川弘氟新材料有限公司 | 全氟聚醚表面活性剂的制备工艺及全氟聚醚表面活性剂 |
| CN114395117B (zh) * | 2021-12-31 | 2023-10-20 | 西安近代化学研究所 | 一种双端全氟聚醚及其制备方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1745169B2 (de) * | 1967-02-09 | 1977-04-21 | Montecatini Edison S.P.A., Mailand (Italien) | Fluorierte lineare polyaether und verfahren zu ihrer herstellung |
| US4451646A (en) * | 1967-02-09 | 1984-05-29 | Montedison, S.P.A. | High molecular weight polymeric perfluorinated copolyethers and process for their preparation from tetrafluoroethylene |
| US4647413A (en) * | 1983-12-27 | 1987-03-03 | Minnesota Mining And Manufacturing Company | Perfluoropolyether oligomers and polymers |
| IT1207492B (it) * | 1985-02-22 | 1989-05-25 | Montefluos Spa | Impiego di derivati dei perfluoropo lieteri per la protezione dei materiali lapidei dagli agenti atmosferici |
| KR900007874B1 (ko) * | 1985-02-26 | 1990-10-22 | 몬테디손 에스. 페. 아. | 브롬화된 말단기 및 조절된 분자량을 갖는 이작용성 및 단작용성 과플루오로폴리에테르의 제조방법 |
| US4820588A (en) * | 1986-08-29 | 1989-04-11 | Minnesota Mining And Manufacturing Company | Shaped articles of polyfluoropolyethers having pendant perfluoroalkoxy groups |
| DE3767132D1 (de) * | 1986-10-24 | 1991-02-07 | Atochem | Polyfluorierte verbindungen und verfahren zu deren herstellung. |
| JPS63137922A (ja) * | 1986-11-28 | 1988-06-09 | Nippon Mektron Ltd | 新規パーフルオロポリエーテルの製造法 |
| US4952735A (en) * | 1986-11-28 | 1990-08-28 | Nipon Mektron Ltd | Novel perfluoropolyether and process for producing the same |
-
1988
- 1988-05-02 IT IT20406/88A patent/IT1217452B/it active
-
1989
- 1989-04-28 RU SU894614118A patent/RU1838337C/ru active
- 1989-04-28 CA CA000598194A patent/CA1339425C/en not_active Expired - Fee Related
- 1989-04-28 UA UA4614118A patent/UA12836A/uk unknown
- 1989-05-02 ES ES89107958T patent/ES2079362T3/es not_active Expired - Lifetime
- 1989-05-02 CS CS892693A patent/CS276635B6/cs unknown
- 1989-05-02 JP JP01113551A patent/JP3073497B2/ja not_active Expired - Lifetime
- 1989-05-02 ZA ZA893231A patent/ZA893231B/xx unknown
- 1989-05-02 DE DE68924800T patent/DE68924800T2/de not_active Expired - Lifetime
- 1989-05-02 EP EP89107958A patent/EP0340740B1/en not_active Expired - Lifetime
- 1989-05-02 AU AU33962/89A patent/AU615054B2/en not_active Ceased
- 1989-05-02 IL IL9015789A patent/IL90157A/en not_active IP Right Cessation
- 1989-05-02 KR KR1019890005937A patent/KR0134375B1/ko not_active IP Right Cessation
-
1991
- 1991-01-29 US US07/648,328 patent/US5143589A/en not_active Expired - Lifetime
-
2000
- 2000-01-27 JP JP2000019327A patent/JP3133304B2/ja not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| IL90157A (en) | 1994-06-24 |
| AU615054B2 (en) | 1991-09-19 |
| EP0340740A2 (en) | 1989-11-08 |
| DE68924800D1 (de) | 1995-12-21 |
| KR890017282A (ko) | 1989-12-15 |
| ES2079362T3 (es) | 1996-01-16 |
| EP0340740A3 (en) | 1991-05-15 |
| IL90157A0 (en) | 1989-12-15 |
| JP2000178224A (ja) | 2000-06-27 |
| KR0134375B1 (ko) | 1998-04-20 |
| US5143589A (en) | 1992-09-01 |
| EP0340740B1 (en) | 1995-11-15 |
| RU1838337C (ru) | 1993-08-30 |
| DE68924800T2 (de) | 1996-04-25 |
| UA12836A (uk) | 1997-02-28 |
| IT1217452B (it) | 1990-03-22 |
| CS269389A3 (en) | 1992-02-19 |
| JP3133304B2 (ja) | 2001-02-05 |
| JP3073497B2 (ja) | 2000-08-07 |
| CA1339425C (en) | 1997-09-02 |
| AU3396289A (en) | 1989-11-02 |
| JPH0222245A (ja) | 1990-01-25 |
| IT8820406A0 (it) | 1988-05-02 |
| ZA893231B (en) | 1990-01-31 |
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