WO1997023570A1 - Composition comprenant un fluoroelastomere et un polyamide thermoplastique et film obtenu - Google Patents
Composition comprenant un fluoroelastomere et un polyamide thermoplastique et film obtenu Download PDFInfo
- Publication number
- WO1997023570A1 WO1997023570A1 PCT/FR1996/002050 FR9602050W WO9723570A1 WO 1997023570 A1 WO1997023570 A1 WO 1997023570A1 FR 9602050 W FR9602050 W FR 9602050W WO 9723570 A1 WO9723570 A1 WO 9723570A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- blocks
- polyamide
- fluoroelastomer
- extruder
- film
- Prior art date
Links
Classifications
-
- 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
- C08J5/18—Manufacture of films or sheets
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
-
- 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
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L77/00—Compositions of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Compositions of derivatives of such polymers
-
- 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
- C08J2327/00—Characterised by the use 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; Derivatives of such polymers
- C08J2327/02—Characterised by the use 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; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use 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; 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
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2377/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
-
- 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
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31725—Of polyamide
Definitions
- the subject of the present invention is a composition comprising a fluoroelastomer and a thermoplastic polyamide. Intended to improve the processing of plastics.
- Another subject of the invention relates to a composition based on hydrocarbon polymers comprising a fluoroelastomer and a thermoplastic polyamide.
- the present invention further relates to a homogeneous thermoplastic film having improved optical and mechanical properties and comprising modifying agents such as a fluoroelastomer and a thermoplastic polyamide. It is generally accepted that during the extrusion of a plastic material, flow irregularities appear at the outlet of the die when a critical shear rate is exceeded. Below, the extrudates are smooth so that * above the critical rate is observed for surface defects.
- melt fracture defects come in several forms.
- the films obtained by extrusion blow-molding lose their transparency and their gloss.
- homogeneity defects with smooth areas in a rough surface appear. These defects significantly reduce the optical and mechanical properties of the film. The same phenomena can be observed on extruded rods. When the surface of the rods loses their shine and becomes dull and rough, it is often compared to an "orange peel".
- composition which improves the transformation of plastics, during their processing by extrusion, without however having the drawbacks set out above.
- This composition comprising a fluoroelastomer and a thermoplastic polyamide, forms the subject of the present invention
- the present invention not only makes it possible to move the “melt fractures” towards high shear rates but also to obtain homogeneous films with a reduced duration of setting in operation of the extruder.
- the present invention therefore provides a composition of modifying agents for improving the transformation of plastics, characterized in that it comprises
- Polymers with polyamide blocks and polyether blocks result from the copolycondensation of polyamide blocks with reactive ends with polyether blocks with reactive ends, such as, inter alia •
- polyamide sequences with dicarboxylic chain ends originate, for example, from the condensation of alpha-omega aminocarboxylic acids of lactams or of dicarboxylic acids and diamines in the presence of a chain-limiting dicarboxylic acid.
- the polyamide blocks are advantageously made of polyamide- 12_or in polyamide- 6
- the number-average molar mass Mn of the polyamide blocks is between 300 and 15,000 and preferably between 600 and 5,000
- the mass Mn of the polyether blocks is between 100 and 6,000 and preferably between 200 and 3,000
- Polymers with polyamide blocks and polyether blocks can also comprise randomly distributed units. These polymers can be prepared by the simultaneous reaction of the polyether and of the precursors of the polyamide blocks.
- polyetherdiol, a lactam (or an alpha-omega amino acid) and a chain-limiting diacid can be reacted in the presence of a little water.
- a polymer is obtained which essentially has polyether blocks, polyamide blocks of very variable length, but also the different reactants which reacted randomly which are distributed statistically along the polymer chain
- polymers containing polyamide blocks and polyether blocks whether they originate from the copolycondensation of polyamide and polyether blocks prepared beforehand or from a reaction in one step, exhibit, for example, shore D hardnesses which may be between 20 and 75 and advantageously between 30 and 70 and an intrinsic viscosity between 0.8 and 2.5 measured in metacresol at 250 ° C for an initial concentration of 0.8 g / 100 ml
- polyether blocks are derived from polyethylene glycol, polyoxypropylene glycol or polyoxytetramethylene glycol, they are either used as such and copolycondensed with polyamide blocks having carboxylic ends, or they are aminated to be transformed into polyether diamines and condensed with polyamide blocks to carboxylic ends They can also be mixed with polyamide precursors and a chain limiter to make polymers with polyamide blocks and polyether blocks having randomly distributed units Polymers with polyamide and polyether blocks are described in US Patents 4,331,786, US 4,115,475, US 4,195,015, US 4,839,441, US 4,864,014, US 4,230,838 and US 4,332,920.
- polyether blocks are in the polymer chain with polyamide blocks and polyether blocks in the form of diols or diamines, they are called for simplification PEG blocks or PPG blocks or even PTMG blocks. It would not be departing from the scope of the invention if the polyether blocks contained different units such as units derived from ethylene glycol, propylene glycol or even tetramethylene glycol.
- the polymer with polyamide blocks and polyether blocks is such that the polyamide which is in the form of blocks and that which is optionally distributed statistically in the chain, represents 50% by weight or more of the polymer with polyamide blocks and polyether blocks.
- the amount of polyamide and the amount of polyether are in the ratio (polyamide / polyether) 2/3 to 3/1 and preferably close to 1/1.
- films of the invention are antistatic.
- plastic material polymers comprising olefin units such as for example ethylene, propylene, butene-1 units, etc.
- olefin units such as for example ethylene, propylene, butene-1 units, etc.
- the film according to the invention can be obtained for a period of warm-up of the extruder of less than 2 hours, preferably for a period of less than or equal to one hour.
- the KAUFMAN extruder transforms the final compositions by extrusion blow molding of sheath.
- the characteristics of the extruder and of its die are given in table 1.
- the different zones of the extruder screw are presented in table 2.
- the temperature profile of the different zones recorded in table 3, is constant for all attempts.
- the mass of the projectile is varied so as to obtain both broken test pieces and intact test pieces in the same group of 10 test pieces and with at least 3 different rupture rates between 0% and
- ⁇ W is the increase in mass used successively from one test to another (in grams)
- S is the sum of the percentages of ruptures for each mass of projectile (this sum includes the percentages corresponding to all the masses of projectile used from the mass corresponding to no rupture up to the mass W
- the antistatic properties of the film are evaluated by a method based on the ability of a surface to run off static charges. This method consists first of all in charging the film surface for a few seconds via a high voltage After cutting from the high-voltage source, note the half-discharge time, which is the time necessary to go from the maximum potential V max reached to half this value V max / 2 An antistatic material will more easily discharge the charges and therefore the half-discharge time will be shorter b) Conduct of the tests (i) Stabilization of the extruder with LDPE LL0209AA,
- a film width 500 mm
- a film thickness 50 ⁇ m
- a final composition is used containing only the plastic material (PEbdl LL0209AA) to be transformed.
- This final composition is transformed into a rod using the HAAKE RHEOLEX extruder.
- the parameters and samples were taken one hour after starting the extrusion at a screw rotation speed of 20 revolutions / min and at a die temperature equal to 215 ° C.
- a film is obtained by the extrusion blow molding of sheath using the KAUFMAN extruder.
- the appearance of the rods and film thus obtained is shown in Table 4.
- IRGANOX B 900 (antioxidant agent) 0.1% in the plastic material (PEbdl LL0209 AA) to be transformed.
- the final composition thus obtained contains:
- Example 3 A final composition is prepared in the same way as in Example 2 except that I add 2% of MMF15C from SCHULMANN containing about 15% of natural silica.
- a final composition is prepared in an identical manner to Example 3 except that 2% of MMF15C is replaced by 4% of MM CMPF 59080 of SYNTHECOLOR containing 2% of anti-slip agent ERUCAMIDE
- the final composition contains
- Example 2 The final composition of Example 2 is taken up again and its behavior as a function of time is studied during the extrusion blow molding process on the KAUFMAN extruder. The parameters noted and the appearance of the film obtained are shown in Table 5.
- Examples 6 to 8 were carried out on the KAUFMAN extruder.
- MM 29790 PG antioxidant (SANTONOX)
- a final composition is prepared from a masterbatch containing LDPE LL0209 AA (granules) 97.7% KYNAR 2821 2.0%
- PE polyethylene
- Example 7 The procedure is identical to Example 6 except that the masterbatch used additionally contains 4% of PEBAX M. The final composition contains
- PE polyethylene
- Example 7 The procedure is identical to that in Example 7 except that the masterbatch contains 8% of PEBAX M instead of 4%.
- the final composition contains PEbdl LL0209 AA 97.794%
- PE polyethylene
- the optical and mechanical properties of the film obtained, as a function of the operating time of the extruder, are shown in Tables 6 and 7 respectively.
- the PE polyethylene comes from the masterbatches MM F 15C and MM
- Tables 8 and 9 show that the film obtained by extrusion blow molding of a final composition comprising a fluoroelastomer and a thermoplastic polyamide is more homogeneous than a film obtained by transformation of a final composition comprising a fluoroelastomer alone.
- the antistatic character of the film obtained from the compositions of Examples 6 and 8 was evaluated according to the method described above.
- the half-discharge time of the film from Example 6 is 169 seconds
- a composition of LDPE comprising 400 ppm of KYNAR and 1600 ppm of PEBAX results in a film whose half-time charge reduced to 18 seconds
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)
- Extrusion Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/894,622 US5986005A (en) | 1995-12-22 | 1996-12-20 | Composition including a fluoroelastomer and a thermoplastic polyamide and resulting film |
KR1019970705800A KR100312055B1 (ko) | 1995-12-22 | 1996-12-20 | 플루오로엘라스토머및열가소성폴리아미드를함유하는조성물,및생성된필름 |
JP9523368A JPH11501083A (ja) | 1995-12-22 | 1996-12-20 | フルオロエラストマーおよび熱可塑性ポリアミドを含む組成物と、得られたフィルム |
AU11985/97A AU1198597A (en) | 1995-12-22 | 1996-12-20 | Composition including a fluoroelastomer and a thermoplastic polyamide, and resulting film |
EP96943166A EP0811038A1 (fr) | 1995-12-22 | 1996-12-20 | Composition comprenant un fluoroelastomere et un polyamide thermoplastique et film obtenu |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9515352 | 1995-12-22 | ||
FR95/15352 | 1995-12-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1997023570A1 true WO1997023570A1 (fr) | 1997-07-03 |
Family
ID=9485853
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR1996/002050 WO1997023570A1 (fr) | 1995-12-22 | 1996-12-20 | Composition comprenant un fluoroelastomere et un polyamide thermoplastique et film obtenu |
Country Status (8)
Country | Link |
---|---|
US (1) | US5986005A (fr) |
EP (1) | EP0811038A1 (fr) |
JP (1) | JPH11501083A (fr) |
KR (1) | KR100312055B1 (fr) |
CN (1) | CN1102616C (fr) |
AU (1) | AU1198597A (fr) |
CA (1) | CA2211806A1 (fr) |
WO (1) | WO1997023570A1 (fr) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7353756B2 (en) | 2002-04-10 | 2008-04-08 | Accutec Usa | Lead free reduced ricochet limited penetration projectile |
CA3220464A1 (fr) | 2021-08-12 | 2023-02-16 | Nova Chemicals Corporation | Auxiliaires de traitement de polymere a base de copolymeres sequences |
WO2023238032A1 (fr) | 2022-06-10 | 2023-12-14 | Nova Chemicals (International) S.A. | Auxiliaires de traitement de polymères exempts de fluor |
WO2023241955A1 (fr) | 2022-06-15 | 2023-12-21 | Nova Chemicals (International) S.A. | Auxiliaires de traitement des polymères à base de copolymères séquencés |
WO2024079553A1 (fr) | 2022-10-11 | 2024-04-18 | Nova Chemicals (International) S.A. | Sel métallique en tant qu'auxiliaire de traitement de polymère |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2168332A1 (fr) * | 1972-01-18 | 1973-08-31 | Solvay | |
EP0432911A1 (fr) * | 1989-11-16 | 1991-06-19 | Minnesota Mining And Manufacturing Company | Composition de polymères |
US5304422A (en) * | 1990-09-19 | 1994-04-19 | Bando Chemical Industries, Ltd. | Low friction polyamide, polyethylene, P.T.F.E. resin |
EP0626424A1 (fr) * | 1992-12-10 | 1994-11-30 | Daikin Industries, Limited | Composition de resine thermoplastique |
WO1995001396A1 (fr) * | 1993-06-30 | 1995-01-12 | Peach State Labs, Inc. | Fibres resistantes aux salissures |
WO1995011940A1 (fr) * | 1993-10-29 | 1995-05-04 | Daikin Industries, Ltd. | Composition de resine thermoplastique et stratifie a base de cette composition |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3334157A (en) * | 1963-12-03 | 1967-08-01 | Union Carbide Canada Ltd | Polyethylene blends containing trace amounts of polytetrafluoroethylene |
FR2273021B1 (fr) * | 1974-05-31 | 1977-03-11 | Ato Chimie | |
FR2318185A1 (fr) * | 1975-07-17 | 1977-02-11 | Ato Chimie | Procede de preparation de copolyesteramides comme produits a mouler |
US4195015A (en) * | 1976-07-30 | 1980-03-25 | Ato Chimie | Heat and aging stable copolyetheresteramides and method of manufacturing same |
US4230836A (en) * | 1979-04-26 | 1980-10-28 | Mobil Oil Corporation | Chemically cross-linked poly(p-methylstyrene) |
FR2466478B2 (fr) * | 1979-10-02 | 1986-03-14 | Ato Chimie | Procede de preparation de copolyetheresteramides aliphatiques elastomeres |
FR2611727B1 (fr) * | 1987-02-26 | 1989-06-16 | Atochem | Polyesteramides et polyetheresteramides - leur procede de fabrication |
FR2611726B1 (fr) * | 1987-02-26 | 1989-06-16 | Atochem | Polyesteramides et polyetherthioether-ester-amides - leur procede de fabrication |
US4855360A (en) * | 1988-04-15 | 1989-08-08 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
US4983677A (en) * | 1988-04-15 | 1991-01-08 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
US5015693A (en) * | 1988-04-15 | 1991-05-14 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
US4863983A (en) * | 1988-04-15 | 1989-09-05 | Minnesota Mining And Manufacturing Company | Extrudable thermoplastic hydrocarbon polymer composition |
WO1991005007A1 (fr) * | 1989-10-06 | 1991-04-18 | E.I. Du Pont De Nemours And Company | Procede d'extrusion pour polymeres difficiles a mouler par fusion |
-
1996
- 1996-12-20 US US08/894,622 patent/US5986005A/en not_active Expired - Fee Related
- 1996-12-20 CN CN96193411A patent/CN1102616C/zh not_active Expired - Fee Related
- 1996-12-20 WO PCT/FR1996/002050 patent/WO1997023570A1/fr not_active Application Discontinuation
- 1996-12-20 JP JP9523368A patent/JPH11501083A/ja active Pending
- 1996-12-20 AU AU11985/97A patent/AU1198597A/en not_active Abandoned
- 1996-12-20 EP EP96943166A patent/EP0811038A1/fr not_active Withdrawn
- 1996-12-20 KR KR1019970705800A patent/KR100312055B1/ko not_active IP Right Cessation
- 1996-12-20 CA CA002211806A patent/CA2211806A1/fr not_active Abandoned
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2168332A1 (fr) * | 1972-01-18 | 1973-08-31 | Solvay | |
EP0432911A1 (fr) * | 1989-11-16 | 1991-06-19 | Minnesota Mining And Manufacturing Company | Composition de polymères |
US5304422A (en) * | 1990-09-19 | 1994-04-19 | Bando Chemical Industries, Ltd. | Low friction polyamide, polyethylene, P.T.F.E. resin |
EP0626424A1 (fr) * | 1992-12-10 | 1994-11-30 | Daikin Industries, Limited | Composition de resine thermoplastique |
WO1995001396A1 (fr) * | 1993-06-30 | 1995-01-12 | Peach State Labs, Inc. | Fibres resistantes aux salissures |
WO1995011940A1 (fr) * | 1993-10-29 | 1995-05-04 | Daikin Industries, Ltd. | Composition de resine thermoplastique et stratifie a base de cette composition |
EP0726293A1 (fr) * | 1993-10-29 | 1996-08-14 | Daikin Industries, Limited | Composition de resine thermoplastique et stratifie a base de cette composition |
Also Published As
Publication number | Publication date |
---|---|
CN1182449A (zh) | 1998-05-20 |
KR100312055B1 (ko) | 2002-05-09 |
KR19980702401A (ko) | 1998-07-15 |
CA2211806A1 (fr) | 1997-07-03 |
US5986005A (en) | 1999-11-16 |
AU1198597A (en) | 1997-07-17 |
EP0811038A1 (fr) | 1997-12-10 |
CN1102616C (zh) | 2003-03-05 |
JPH11501083A (ja) | 1999-01-26 |
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