WO1999041313A1 - Mixtures of thermoplastic fluoropolymers - Google Patents
Mixtures of thermoplastic fluoropolymers Download PDFInfo
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- WO1999041313A1 WO1999041313A1 PCT/EP1999/000795 EP9900795W WO9941313A1 WO 1999041313 A1 WO1999041313 A1 WO 1999041313A1 EP 9900795 W EP9900795 W EP 9900795W WO 9941313 A1 WO9941313 A1 WO 9941313A1
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/44—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins
- H01B3/443—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from vinylhalogenides or other halogenoethylenic compounds
- H01B3/445—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes vinyl resins; acrylic resins from vinylhalogenides or other halogenoethylenic compounds from vinylfluorides or other fluoroethylenic compounds
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- 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
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- 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
- C08L27/18—Homopolymers or copolymers or tetrafluoroethene
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B3/00—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
- H01B3/18—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
- H01B3/30—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes
- H01B3/42—Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances plastics; resins; waxes polyesters; polyethers; polyacetals
- H01B3/427—Polyethers
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- 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
- C08J2300/00—Characterised by the use of unspecified polymers
- C08J2300/22—Thermoplastic resins
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2207/00—Properties characterising the ingredient of the composition
- C08L2207/32—Properties characterising the ingredient of the composition containing low molecular weight liquid component
- C08L2207/324—Liquid component is low molecular weight polymer
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/04—Macromolecular compounds according to groups C08L7/00 - C08L49/00, or C08L55/00 - C08L57/00; Derivatives thereof
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
Definitions
- This invention relates to thermoplastic polymers having tetrafluoroethylene units and perfluoro alkyl vinyl ether units, mixtures of such polymers that contain low molecular weight and high molecular weight components, and to processes and articles that employ such polymers.
- Copolymers of tetrafluoroethylene (TFEs below) and perfluoro alkyl vinyl ethers having from 1 to 4 carbon atoms in the alkyl moiety (PANEs below), in particular perfluoro n-propyl vinyl ether (PPNEs below) have been known for a long time. Such copolymers are commercially available under the designation
- PFA poly(ethylene glycol)
- these partially crystalline copolymers have excellent technical performance, for example exceptional chemical stability, combined with high service temperatures. They can be processed from the melt as thermoplastics, for example by compression molding, extruding or injection molding. Preferred applications are, inter alia, extruded pipes, tubes and cable sheathing. Processing from the melt takes place at temperatures of from 350 up to 450°C. Under these conditions, both thermal and mechanical degradation occur.
- the thermal degradation takes place predominantly via the thermally unstable end groups formed in the polymerization, i.e. from the end of the chain.
- the mechanism of this degradation is described in more detail in "Modern Fluoropolymers", Jolin Wiley & Sons, 1997, K. Hintzer and G. L ⁇ hr, Melt Processable Tetrafluoroethylene-Perfluoropropylvinyl Ether Copolymers (PFA), page 223.
- the degradation can be substantially suppressed by converting the thermally unstable end groups into stable CF 3 end groups by postfluorination, as described, for example in US-A-4 743 658 and DE-C-19 01 872.
- CoiTosive gases arise during the thermal degradation, and these considerably impair the quality of the final product by metal contamination or bubble formation, and can corrode tooling and processing machinery.
- a PFA has now been found which has good melt processability and which contains at least one high-molecular- weight PFA with an MFI ⁇ 15, preferably from 0.01 to 15, and at least one low-molecular-weight PFA with MFI > 30.
- the mixtures of the invention are particularly useful in applications where chemical resistance and .high temperature resistance are important.
- the invention therefore relates to mixtures of thermoplastic fluoropolymers essentially comprising units of TFE and subordinate amounts of units of one or more PANEs having from 1 to 4 carbon atoms in the alkyl moiety and a total concentration of from 0.5 to 10 mol%, the mixture comprising A) at least one low molecular weight component with an MFI A > 30 and B) at least one high molecular weight component with an MFI B ⁇ 15.
- These components are selected in such a way that the ratio of the MFI A of component A) to the MFI B of component B) is in the range from 80 to 2500, preferably in the range of from
- Essentially comprising units of TFE and of a PANE means that small amounts, up to about 5 mol%, of other fluoromonomers not containing hydrogen, such as hexafluoropropene or chlorotrifluoroethylene, are not to be excluded.
- the composition of the copolymer of the two components may differ within the limits mentioned above.
- the mixing ratio of high- and low-molecular- weight components may vary within wide limits and can be determined for the desired application by means of simple preliminary experiments.
- the ratio is generally from 10:90 to 90: 10, preferably in the range from 25:75 to 75:25 parts by weight and in particular from
- the invention also relates to a novel low-molecular- weight PFA with an MFI > 30, preferably > 120 with preference from 120 to 1000, in particular from 120 to 700, especially from 200 to 600.
- Another aspect of the invention relates to mixtures of the novel low-molecular-weight PFA(s) mentioned with the high-molecular-weight PFA(s) mentioned above, the MFI ratio mentioned above corresponding approximately to a molecular weight ratio of the high-molecular- weight to the low-molecular- weight component(s) > 3.5, preferably from 3.5 to 10, in particular from 3.5 to 7.
- the MFI gives the amount of a melt in grams per 10 min which is extruded from a holding cylinder through a die by the action of a piston loaded with weights.
- the dimensions of the die, the piston, the holding cylinder and the weights are standardized (DIN 53735, ASTM D-1238). All of the MFIs mentioned here have been measured with a die of diameter 2.1 mm and length 8 mm using a superimposed weight of 5 kg and a temperature of 372°C. The values 0.01 and 1000 are practically the limiting values of this measurement method.
- the present invention further provides a process for making a shaped article from the mixtures of the invention. This process involves providing the mixture, extruding, compression molding, or injection molding the mixture, and preferably, cooling the mixture to provide a self-supporting shaped article.
- the present invention provides shaped articles comprising the mixture.
- articles include molded or extruded goods such as films, pellets, wire and cable insulation, tubes and pipes, containers, vessel liners, and the like.
- novel mixtures may be prepared in a conventional manner, i.e. for example by mixing the pulverulent products, mixing dispersions of the components, or by conducting the polymerization in an appropriate manner ("step polymerization") with controlled use of initiator and chain transfer agent, such as short-chain alkanes and haloalkanes, and also hydrogen.
- step polymerization i.e. for example by mixing the pulverulent products, mixing dispersions of the components, or by conducting the polymerization in an appropriate manner (“step polymerization") with controlled use of initiator and chain transfer agent, such as short-chain alkanes and haloalkanes, and also hydrogen.
- An advantageous procedure here is as follows: at the start of the polymerization, for a low desired MFI, relatively little initiator and relatively little chain transfer agent are metered in.
- polymerization conditions are changed at the desired juncture in the polymerization, depending on the type of composition by weight to be achieved, for example after 50% of the TFE addition, by metering in further initiator and chain transfer agent, so that the polymer produced as the polymerization continues has the desired high MFI.
- the desired high MFI may also be created by increasing the temperature during the polymerization. The advantage of this preparation process is that a "perfect" mixture of the two components is created in situ.
- the novel mixtures are distinguished by considerably increased extrusion speed without melt fracture.
- MFI determination before and after processing this is not at the cost of significantly increased degradation.
- novel mixtures have a noticeably increased zero-shear viscosity and a lower complex viscosity at higher shear rates, compared with a commercially available polymer component with identical MFI.
- the PFA with MFI > 30 differs from the hitherto conventional grades of
- PFA in its low molecular weight It therefore has a relatively large number of labile end groups, which limit the thermal stability of the material.
- elemental fluorine GB-A-1 210 794, EP-A-0 150 953 and US-A-4 743 658) .
- This same process may be used to post fluorinate the mixtures of the invention.
- the success of the postfluorination is checked by IR-spectroscopic determination of the residual carboxyl and/or carbonyl fluoride end groups, as described in US-A-4 743 658.
- complete fluorination of the end groups is not necessary.
- Reduction of the thermally unstable end groups (COOH + COF) to from 10 to 15 end groups/10 6 carbon atoms is sufficient to achieve the desired improvements in properties. This significantly shortens the reaction time and therefore makes the postfluorination more cost-effective.
- the novel PFA mixture postfluorinated in this way shows no discoloration, even at 450°C.
- a further advantage of the increased high-temperature resistance is that when production failures occur, the novel PFA mixture remains for a longer residence time at high temperatures without degradation and thus there is no discoloration or bubble formation at elevated temperature and no corrosion of the processing machinery or of the substrates which come into contact with the polymer mixture.
- the preferred process for preparing the novel mixtures consists in blending the two components as dispersions, agglomerating these, drying and melt granulation followed by water-treatment (DE-A-195 47 909) of the granules obtained from the melt and, if desired, postfluorination of the same.
- the novel mixtures are advantageously suitable for producing thin-walled articles by extrusion or extrusion blow molding and injection molding.
- the higher processing speeds wliich are possible here do not have to be obtained at the cost of impairment of properties; on the contrary, the products obtained surprisingly have increased stiffness (increased modulus of elasticity) and yield stress, i.e. the novel mixtures can resist .higher mechanical stresses in particular applications, since an increased yield stress means an enlargement of the elastic range of these materials. This makes it possible to create moldings with longer service lives, and this in turn permits the use of tubes with thinner walls.
- the polymerization may be carried out by .known processes of aqueous free-radical emulsion polymerization (US-A-3 635 926, US-A-4 262 101), or in a non-aqueous phase (US-A-3 642 742).
- aqueous free-radical emulsion polymerization US-A-3 635 926, US-A-4 262 101
- a non-aqueous phase US-A-3 642 742
- the perfluoro propyl vinyl ether content is determined by IR spectroscopy
- EP-B-362 868 has already disclosed mixtures of fluoropolymers, including investigation of high-molecular- weight and low-molecular-weight PFA grades.
- the low-molecular-weight component here is defined by a melt viscosity at 380°C of from 5000 to 280,000 Poise, corresponding to an MFI at 372°C of from 80 to 1.6. It is expressly mentioned here that a melt viscosity of less than
- the resultant amount of 31.5 kg of polymer dispersion with a solids content of 22.8% is discharged from the bottom of the reactor. .
- the dispersion has been transferred into a 180 1 stirring vessel, its volume is increased to 100 1 with demineralized water and it is mixed with 200 ml of concentrated hydrochloric acid and stirred until the solid has separated from the aqueous phase.
- the flocculant powder precipitated after stirring is granulated with 6.9 1 of a petroleum fraction, the petroleum fraction is driven off using steam, and the granules are then washed six times by vigorous and thorough stirring with 100 1 of demineralized water on each occasion.
- the moist powder is dried for 12 hours at 260°C in a drying cabinet under nitrogen. This gives 7.1 kg of a low molecular weight bipolymer according to the invention which has a PPVE content of 3.9% and an MFI of 40.
- a PFA mixture according to the invention having an MFI of 2.3 is prepared from a 50/50 mixture composed of a dispersion of the material from Example 1 and a dispersion of a PFA having an .MFI of 0.5.
- the ratio of MFI A to MFI B is 80.
- Example 1 but 6.7 g of methylene chloride and 1.8 g of .APS are pumped in, giving a bipolymer which has 3.9% of PPVE and an MFI of 0.5.
- Example 1 The dispersion mixture is worked up as in Example 1. This gives a bipolymer which has a PPVE content of 3.9% and an MFI of 2.3. After melt granulation, the MFI rises to 2.4.
- Example 2 The PFA mixture of Example 2 is compared with a commercially available PFA having an MFI of 2 in the extrusion of a tube having an external diameter of 28.3 mm and an internal diameter of 27.7 mm. Extruder data
- the mixture of Example 2 allows a throughput of 20 kg/h, without adverse effects on the quality of the tube.
- the MFI change shows that the commercially available product, even at a low throughput of 8 kg/h, is degraded to about the same extent as the novel material from Example 2 at a throughput of 20 kg/h.
- the yield stress of the novel material is increased. This means that the final article has a higher dimensional stability and/or stiffness.
- the tubes extruded with the mixture of Example 2 prepared according to the invention also show, compared with the commercially available PFA2 material, increased cold bursting strength.
- the test took place on a bursting strength test apparatus (in-house construction), in which a firmly secured plastic pipe was filled with water and placed under pressure using a pneumatic pump.
- the pressure test is regarded as having been passed if the pipe survives without damage after pressure has been maintained for 6 min at a test pressure dependent on the dimensions of the pipe. After this test has been carried out, the test pressure is raised by 2 bar/min until the pipe bursts, in order to determine the residual bursting strength.
- Example 4 The PFA mixture of Example 2 is processed to give a pressed sheet, and long-term failure is determined on specimens of this pressed sheet.
- the PFA2 defined in Example 3 served as comparison. Whereas the mean value of the times to failure for PFA2 is 194 h, after 793 h only two of three specimens of the mixture of Example 2 had failed.
- the tests were long-term tensile creep tests based on the specification of the Deutscher Nerband ftir Schweisstechnik [German Association for Welding Technology], DNS 2203, Part 4, on notched specimens.
- the specimens were compression-molded plates of 5 mm thickness. The force applied was 4 ⁇ /mm 2 .
- the medium used is demineralized water containing 2%> of non-ionic surfactant (ARKOPAL® ⁇ 100).
- the tests are carried out at a temperature of 80°C. In each case, the measurements are carried out on three identical test specimens. This test method, and therefore also the results, permit coirelation with DIN 8075 measurements of the effects of long-term internal hydrostatic pressure on pipes.
- Example 1 The procedure of Example 1 is followed, but 200 g of methylene chloride and 20 g of APS are pumped in, resulting in a low molecular weight bipolymer according to the invention having a PPNE content of 4% and an MFI of 500.
- a PFA mixture according to the invention having an MFI of 9.8 is prepared as agglomerate from a 50/50 mixture composed of a dispersion of the material from Example 5 and a dispersion of a PFA with an MFI of 1.6.
- the ratio of MFI A to MFI B is 312.5.
- the dispersion mixture is worked up as in Example 1. This gives a bipolymer which has a PPVE content of 4.1 mol % and an MFI of 9.8.
- Example 6 The PFA mixture of Example 6 (MFI 9.8) is compared with commercially available products in pellet form having an MFI of 10 (for example PFA10) in the injection molding of specimens. For this the materials are firstly converted into melt pellets, the MFI changing as shown in the table.
- Modulus of elasticity and yield stress are measured on dumbbell specimens (DIN 53455, Test specimen No. 3) by the DIN 53457 measurement method.
- the novel material shows lower degradation, higher modulus of elasticity and higher yield stress, without change in mechanical properties, such as TS and EB.
- the improved flowability of the novel mixture is also apparent in the injection molding of spirals.
- the degradation occurring in this procedure can be assessed from the MFI ratio.
- the injection conditions are as follows:
- the PFA mixture of Example 6 shows markedly better flowability with the same degradation and a lower tendency to delaminate when lower temperatures and higher injection rates are used.
- the PFA mixture of Example 6 is converted into melt pellets which show an MFI of 11. 1.5 kg of this mixture is melted in the melt container in a convection heating cabinet at 370°C for 5 h, and injection molded within a period of 4 min into a mold, likewise heated to 370°C and having complicated injection geometry.
- the shape to be encapsulated is that of a magnetic coupling. After cooling for 30 min with water, the molded specimen has no defects, in particular neither gas inclusions nor any discoloration.
- the MFI of the molding is 11.3.
- a standard PFA with MFI 10 or 15 showed delaminations in the molding, making the component unusable.
- Example 7 It is apparent during this that the postfluorinated PFA mixture of Example 9 can withstand higher thermal stresses.
- Example 1 The procedure (I e the preparation of the polymerization reactor, the polymerization conditions, and the work-up) of Example 1 is followed However, for preparing a novel mixture by step polymerization, at the start of the polymerization 7 g of methylene chloride and 2 g of APS are added Following 50% of the amount of TFE to be run in, 35 g of methylene chloride and 10 g of APS are metered in This gives a bipolymer having a PPNE content of 3 9% and an MFI of 2 1
- the first part of the polymerization gives a PFA having an MFI of 0 3
- the MFI created in the second step is calculated from the MFI of 2 1 of the end product via the following equation
- the MFI is therefore 75
- the ratio of MFI A to MFI B is 250
- Example 11 The procedure (i.e., the preparation of the polymerization reactor, the polymerization conditions, and the work-up) of Example 1 is followed. However, for preparing a novel mixture by step polymerization, at the start of the polymerization 3 g of methylene chloride and 2 g of APS are added. Following the addition of 30% of the amount of TFE to be run in, 100 g of methylene chloride and 10 g of APS are metered in. This gives a bipolymer having a PPVE content of
- the swell index is defined by the following formula: [DE/DD - 1]100, where DE is the diameter of the extrudate and DD the diameter of the die.
- the first part of the polymerization gives a PFA having an MFI of 0J.
- An MFI of 130 created in the second stage is calculated from the MFI of 2.6 of the end product, using the equation given in Example 10.
- the ratio of MFI A to MFI B is 1300.
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- Extrusion Moulding Of Plastics Or The Like (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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Abstract
Description
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020007008841A KR20010040930A (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
EP99932501A EP1053284B1 (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
DE69909247T DE69909247T2 (en) | 1998-02-13 | 1999-02-06 | MIXTURES OF THERMOPLASTIC FLUOROPOLYMERS |
AU44811/99A AU4481199A (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
JP2000531502A JP4252210B2 (en) | 1998-02-13 | 1999-02-06 | Mixture of thermoplastic fluoropolymers |
CA002320130A CA2320130A1 (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
PL99342370A PL342370A1 (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19805832.2 | 1998-02-13 | ||
DE19805832A DE19805832A1 (en) | 1998-02-13 | 1998-02-13 | Blends of thermoplastic fluoropolymers |
Publications (1)
Publication Number | Publication Date |
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WO1999041313A1 true WO1999041313A1 (en) | 1999-08-19 |
Family
ID=7857556
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/EP1999/000795 WO1999041313A1 (en) | 1998-02-13 | 1999-02-06 | Mixtures of thermoplastic fluoropolymers |
Country Status (11)
Country | Link |
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US (2) | US6696526B1 (en) |
EP (1) | EP1053284B1 (en) |
JP (1) | JP4252210B2 (en) |
KR (1) | KR20010040930A (en) |
AU (1) | AU4481199A (en) |
CA (1) | CA2320130A1 (en) |
DE (2) | DE19805832A1 (en) |
PL (1) | PL342370A1 (en) |
RU (1) | RU2214428C2 (en) |
WO (1) | WO1999041313A1 (en) |
ZA (1) | ZA991139B (en) |
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WO2000069967A1 (en) * | 1999-05-13 | 2000-11-23 | Dyneon Llc | Polymer processing additive containing a multimodalfluoropolymer and a melt processable thermoplastic polymer composition employing the same |
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WO2002004560A1 (en) * | 2000-07-11 | 2002-01-17 | 3M Innovative Properties Company | Fep with increased flexural fatigue strength and a low level of die deposits |
US6531559B1 (en) | 1998-08-06 | 2003-03-11 | Eidgenössische Technische Hochschule Zürich | Melt-processible poly (tetrafluoroethylene) |
US6583226B1 (en) | 2001-06-28 | 2003-06-24 | 3M Innovative Properties Company | FEP with increased flexural fatigue strength and a low level of die deposits |
US6653379B2 (en) | 2001-07-12 | 2003-11-25 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US6737165B1 (en) | 1998-08-06 | 2004-05-18 | Omlidon Technologies Llc | Melt-processible poly(tetrafluoroethylene) |
US7060772B2 (en) | 2001-09-20 | 2006-06-13 | 3M Innovative Properties Company | Fluoropolymers from tetrafluoroethylene and perfluoro(alkoxyalkyl vinyl) ether |
US7276287B2 (en) | 2003-12-17 | 2007-10-02 | Eidgenössische Technische Hochschule Zürich | Melt-processible poly(tetrafluoroethylene) |
WO2019236289A1 (en) | 2018-06-07 | 2019-12-12 | Chemours-Mitsui Fluoroproducts Co., Ltd. | Melt processible fluororesin composition and injection molded article formed from same |
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US6642310B2 (en) | 2001-02-16 | 2003-11-04 | Dupont Dow Elastomers L.L.C. | Process aid for melt processable polymers |
US20050161858A1 (en) * | 2004-01-28 | 2005-07-28 | Cyril Chevillard | Method to improve melt processing of styrenic resins at high shear rates |
CN100455611C (en) * | 2004-04-13 | 2009-01-28 | 大金工业株式会社 | Chlorotrifluoroethylene copolymer |
WO2005108051A1 (en) | 2004-04-13 | 2005-11-17 | Daikin Industries, Ltd. | Fluid transfer member |
JP4533115B2 (en) * | 2004-12-03 | 2010-09-01 | 三井・デュポンフロロケミカル株式会社 | Fluororesin molding method and fluororesin molding |
JP4530972B2 (en) * | 2005-11-08 | 2010-08-25 | 三井・デュポンフロロケミカル株式会社 | Tetrafluoroethylene copolymer composition for injection molding |
WO2007096347A1 (en) * | 2006-02-23 | 2007-08-30 | Solvay Solexis S.P.A. | Lan cables |
EP1849828A1 (en) * | 2006-04-25 | 2007-10-31 | Solvay Solexis S.p.A. | Thermoplastic fluoropolymer composition |
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US20090152776A1 (en) | 2007-12-12 | 2009-06-18 | E. I. Du Pont De Nemours And Company | Core/Shell Polymer and Fluoropolymer Blending Blown Film Process |
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- 1999-02-06 DE DE69909247T patent/DE69909247T2/en not_active Expired - Lifetime
- 1999-02-06 KR KR1020007008841A patent/KR20010040930A/en not_active Application Discontinuation
- 1999-02-06 EP EP99932501A patent/EP1053284B1/en not_active Expired - Lifetime
- 1999-02-06 WO PCT/EP1999/000795 patent/WO1999041313A1/en not_active Application Discontinuation
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EP1063245A4 (en) * | 1998-03-10 | 2002-02-27 | Daikin Ind Ltd | Perfluorochemical molding material and blow-molded container |
EP1063245A1 (en) * | 1998-03-10 | 2000-12-27 | Daikin Industries, Ltd. | Perfluorochemical molding material and blow-molded container |
US7872081B2 (en) | 1998-08-06 | 2011-01-18 | Omlidon Technologies Llc | Melt-processible poly(tetrafluoroethylene) |
US7160623B2 (en) | 1998-08-06 | 2007-01-09 | Eidgenossische Technische Hochschule Zurich | Melt-processible poly(tetrafluoroethylene) |
US6531559B1 (en) | 1998-08-06 | 2003-03-11 | Eidgenössische Technische Hochschule Zürich | Melt-processible poly (tetrafluoroethylene) |
US6548612B2 (en) | 1998-08-06 | 2003-04-15 | Eidgenossische Technische Hochschule Zürich | Melt-processible poly(tetrafluoroethylene) |
US6737165B1 (en) | 1998-08-06 | 2004-05-18 | Omlidon Technologies Llc | Melt-processible poly(tetrafluoroethylene) |
US6277919B1 (en) | 1999-05-13 | 2001-08-21 | Dyneon Llc | Polymer processing additive containing a multimodal fluoropolymer and melt processable thermoplastic polymer composition employing the same |
EP1591484A1 (en) * | 1999-05-13 | 2005-11-02 | Dyneon LLC | Polymer processing additive containing a multimodalfluoropolymer and a melt processable thermoplastic polymer composition employing the same |
WO2000069967A1 (en) * | 1999-05-13 | 2000-11-23 | Dyneon Llc | Polymer processing additive containing a multimodalfluoropolymer and a melt processable thermoplastic polymer composition employing the same |
WO2002004560A1 (en) * | 2000-07-11 | 2002-01-17 | 3M Innovative Properties Company | Fep with increased flexural fatigue strength and a low level of die deposits |
EP2821435A1 (en) * | 2000-07-11 | 2015-01-07 | 3M Innovative Properties Company | FEP with increased flexural fatigue strength and a low level of die deposits |
US6583226B1 (en) | 2001-06-28 | 2003-06-24 | 3M Innovative Properties Company | FEP with increased flexural fatigue strength and a low level of die deposits |
US6984697B2 (en) * | 2001-07-12 | 2006-01-10 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US6653379B2 (en) | 2001-07-12 | 2003-11-25 | 3M Innovative Properties Company | Fluoropolymers resistant to stress cracking |
US7060772B2 (en) | 2001-09-20 | 2006-06-13 | 3M Innovative Properties Company | Fluoropolymers from tetrafluoroethylene and perfluoro(alkoxyalkyl vinyl) ether |
US7276287B2 (en) | 2003-12-17 | 2007-10-02 | Eidgenössische Technische Hochschule Zürich | Melt-processible poly(tetrafluoroethylene) |
WO2019236289A1 (en) | 2018-06-07 | 2019-12-12 | Chemours-Mitsui Fluoroproducts Co., Ltd. | Melt processible fluororesin composition and injection molded article formed from same |
US11236226B2 (en) | 2018-06-07 | 2022-02-01 | The Chemours Company Fc, Llc | Melt processible fluororesin composition and injection molded article formed from same |
US11623984B2 (en) | 2018-06-07 | 2023-04-11 | Chemours-Mitsui Fluoroproducts Co., Ltd | Melt processible fluororesin composition and injection molded article formed from same |
Also Published As
Publication number | Publication date |
---|---|
DE69909247D1 (en) | 2003-08-07 |
DE19805832A1 (en) | 1999-08-19 |
JP4252210B2 (en) | 2009-04-08 |
US20020010277A1 (en) | 2002-01-24 |
EP1053284B1 (en) | 2003-07-02 |
KR20010040930A (en) | 2001-05-15 |
US6713141B2 (en) | 2004-03-30 |
DE69909247T2 (en) | 2004-04-15 |
RU2214428C2 (en) | 2003-10-20 |
US6696526B1 (en) | 2004-02-24 |
PL342370A1 (en) | 2001-06-04 |
EP1053284A1 (en) | 2000-11-22 |
JP2002503744A (en) | 2002-02-05 |
ZA991139B (en) | 1999-08-13 |
AU4481199A (en) | 1999-08-30 |
CA2320130A1 (en) | 1999-08-19 |
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