GB2262101A - Insulating material - Google Patents

Insulating material Download PDF

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Publication number
GB2262101A
GB2262101A GB9220872A GB9220872A GB2262101A GB 2262101 A GB2262101 A GB 2262101A GB 9220872 A GB9220872 A GB 9220872A GB 9220872 A GB9220872 A GB 9220872A GB 2262101 A GB2262101 A GB 2262101A
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Prior art keywords
porous
ptfe
tape
wire
copolymer
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GB9220872A
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GB2262101B (en
GB9220872D0 (en
Inventor
Jnr William Patrick Mortimer
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WL Gore and Associates UK Ltd
WL Gore and Associates Inc
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WL Gore and Associates UK Ltd
WL Gore and Associates Inc
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Priority claimed from GB909009407A external-priority patent/GB9009407D0/en
Application filed by WL Gore and Associates UK Ltd, WL Gore and Associates Inc filed Critical WL Gore and Associates UK Ltd
Priority claimed from GB9219772A external-priority patent/GB2261668B/en
Publication of GB9220872D0 publication Critical patent/GB9220872D0/en
Publication of GB2262101A publication Critical patent/GB2262101A/en
Application granted granted Critical
Publication of GB2262101B publication Critical patent/GB2262101B/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/17Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/29Protection against damage caused by extremes of temperature or by flame
    • H01B7/292Protection against damage caused by extremes of temperature or by flame using material resistant to heat
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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
    • C08L27/02Compositions 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
    • C08L27/12Compositions 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
    • C08L27/18Homopolymers or copolymers or tetrafluoroethene
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B3/00Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties
    • H01B3/18Insulators or insulating bodies characterised by the insulating materials; Selection of materials for their insulating or dielectric properties mainly consisting of organic substances
    • H01B3/30Insulators 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
    • H01B3/44Insulators 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
    • H01B3/443Insulators 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
    • H01B3/445Insulators 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/02Disposition of insulation
    • H01B7/0241Disposition of insulation comprising one or more helical wrapped layers of insulation
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/17Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/28Protection against damage caused by moisture, corrosion, chemical attack or weather
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01BCABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
    • H01B7/00Insulated conductors or cables characterised by their form
    • H01B7/17Protection against damage caused by external factors, e.g. sheaths or armouring
    • H01B7/29Protection against damage caused by extremes of temperature or by flame
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions 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 an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/10Homopolymers or copolymers of unsaturated ethers
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A30/00Adapting or protecting infrastructure or their operation
    • Y02A30/14Extreme weather resilient electric power supply systems, e.g. strengthening power lines or underground power cables

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Organic Insulating Materials (AREA)

Abstract

An electrical insulating tape comprises (a) 5-90 weight percent of a thermoplastic copolymer of tetrafluroethylene and perfluoro (propyl vinyl ether); and (b) 90-5 weight percent of polytetrafluroethylene (PTFE). The copolymer may be entrapped in the pores of the PTFE. The tape may be prepared from pellets comprising the said polymeric components and then stretched.

Description

ELECTRICAL INSULATING MATERIAL TECHNICAL FIELD The present invention relates to an electrical insulating composite material, particularly though not exclusively for insulating wire. The invention also includes a method of forming the insulating material, and insulated conductors.
DESCRIPTION OF PRIOR ART The use of polytetrafluoroethylene (PTFE) or copolymers formed from tetrafluoroethylene (TFE) and perfluoro (propyl vinyl ether) (PPVE) is well known for the insulation of wire. These polymers have good heat resistance, high resistance to solvent attack and good dielectric properties. These attributes are desirable where high reliability is required, for example in aerospace applications.
Other desirable attributes for such applications include mechanical properties such as resistance to abrasion and resistance to cut-through of insulation by sharp edges. However, the properties of the aforesaid materials are poor in these respects.
Attempts have been made in the past to improve the mechanical properties of TFE base polymers by including additives such as glass spheres, silica flake, etc.
However, the improvements achieved with such compositions are generally limited and often at the expense of other desirable features, for example leading to degradation of electrical properties or mechanical properties such as flexibility.
Attempts have also been made in the past to improve the mechanical properties of the fluoropolymers by mixing with other polymers having better mechanical properties, such as polyphenylene sulphide, polyphenylene oxide, etc. However, these other polymers are in general incompatible with fluoropolymers so that there is difficulty in producing intimate blends.
It is an object of the present invention to mitigate these problems.
SUMMARY OF THE INVENTION The present invention provides an electrical insulating composite material which comprises an intimate admixture of: (a) 5-90 weight percent of a thermoplastic copolymer of tetrafluoroethylene and perfluoro (propyl vinyl ether); and (b) 90-5 weight percent of polytetrafluoroethylene (PTFE) selected from the class consisting t coagulated dispersion type PTFE and porous expanded PTFE.
The composite material itself may be non-porous or may be expanded to produce porous material.
The TFE/PPVE copolymer is preferably used in particulate form and preferably has a particle size in the range 1 to 180 microns, especially 20 to 100 microns. The particles may have a wide range of particle sizes and preferably include particles having sizes right across the ranges. However, particles of narrow size range may also be used. The TFE/PPVE copolymer particles preferably have a substantially regular shape, such as oblong or spherical.
The polytetrafluoroethylene component is of the coagulated dispersion type. As is well known, polytetrafluoroethylene (PTFE) can be produced in three quite distinct forms having different properties viz; granular PTFE, coagulated dispersion PTFE, and liquid PTFE dispersions. Coagulated dispersion PTFE is also referred to as fine powder PTFE. In the present invention, the PTFE resin can be used in powder form; or alternatively, the PTFE resin can be coagulated from an aqueous dispersion in the presence of perfluoroalkoxy TFE/PVE copolymer powder or dispersion. The coagulation of PTFE in the presence of a dispersion of the copolymer results in a co-coagulation of PTFE and copolymer. The flocculated mixture may then be decanted and dried.
The electrically insulating material may be used for producing a covering for wire, or other electrically conductive substrate to which bonding is not normally required.
DESCRIPTION OF PREFERRED EMBODIMENTS One particular aspect of the present invention provides a non-porous electrical insulating material for an electrical conductor comprising an intimate admixture of 5 to 40 weight percent of a thermoplastic copolymer of tetrafluoroethylene and perfluoro (propyl vinyl ether); and 60 to 95 weight percent of coagulated dispersion type polytetrafluoroethylene.
Advantageous, the composite material comprises 5 to 40 wt% of copolymer (and 60 to 95 wtt PTFE); more particularly 8 to 20 wt% of copolymer (and 80 to 92 wt% of PTFE).
The non-porous material typically has a density of 2.0 to 2.2 g/cc.
There is also provided a method of insulating an electrical conductor comprising; paste extruding an electrically insulating material formed from an intimate mixture of 5 to 40 weight percent of a particulate thermoplastic copolymer of tetrafluoroethylene and perfluoro (propyl vinyl ether); and 60 to 95 weight percent of coagulated dispersion type polytetrafluoroethylene; applying said material to an electrically conductive substrate; and sintering the material before or after application to the substrate.
The paste extrusion step may be carried out using conventional PTFE extrusion techniques (for example in admixture with a liquid carrier, such as a hydrocarbon). The extruded composition is generally of thin section so as to allow efficient removal of the liquid carrier and formation of a solid material, usually in the form of a sheet, tape or filament. If necessary, the solid material may be mechanically worked, such as by calendering, to modify its shape or thickness prior to application to the substrate.
In the case of wire, usually the solid material in the form of a tape is wrapped around the wire in overlapping turns. The overlapping areas of the material may then be fused together, for example at temperatures of 350 to 4500C (for 0.5 to 20 minutes).
The time will be in correspondence with the temperature employed. Temperatures as low as 320"C may be used at long sintering times. Lower temperatures tend to minimise degradation of the material. The time and temperature conditions also depend on the construction of the insulated conductor, such as thickness of the insulation and number of cores in the wire.
It has been found that wire electrical insulation made from wrapped and sintered tape produced from the composition has an unexpectedly better cut-through resistance and abrasion resistance than equivalent wire insulation made from fine powder PTFE alone.
A second particular aspect of the invention provides a porous material which is a composite of: a) 5-90 weight percent of a thermoplastic copolymer of tetrafluoroethylene and perfluoro(propyl vinyl ether), and complementarily, intermingled therewith, b) 90-5 weight percent of a porous expanded structure of polytetrafluoroethylene.
In one embodiment, the thermoplastic copolymer will constitute about 5-50 weight percent of the composite.
In this embodiment, the composite is useful as insulation on wire or cable, especially as electrical insulation.
In another embodiment, the thermoplastic copolymer will constitute about 50-95 weight percent of the composite. In this embodiment, the composite is useful as a reinforced thermoplastic copolymer film.
This aspect of the invention also provides a process for preparing the composites which comprises mixing the thermoplastic copolymer with a dispersion of the coagulated fine powder polytetrafluoroethylene resin or with a dispersion of the fine powder and coagulating the solids to obtain a resin blend, preparing pellets of the resin blend, forming a tape of the pellets and stretching the tape until a desired degree of porosity is attained in the resulting composite.
In a preferred embodiment a flocculated mixture of the TFE/PPVE copolymer and PTFE, in particulate form, is lubricated for paste extrusion with an ordinary lubricant known for use in paste extrusion, and is pelletized. The pellets are preferably aged at 40-60 C and are then paste extruded into a desired shape, usually a film. The extruded shape is then stretched, preferably in a series of at least two stretch steps while heating at between 35-360 C until a desired degree of porosity is attained. The porosity occurs through the formation of a network of interconnected nodes and fibrils in the structure of the stretched PTFE film, as more fully described in U.S. Patent 3,953,566. The density of the porous material will usually be less than 2.0 g/cc.
At the stretch temperatures employed, the TFE/PPVE copolymer melts and, depending on the amount present, may become entrapped in the pores or nodes formed, may coat the nodes or fibrils, or may be present on the outer surface of the membrane formed. Most likely a combination of each embodiment occurs, depending on whether the copolymer and the PTFE remain as distinct moieties.
The porous composite is useful as an insulation covering for wire and cable, particularly in electrical applications. In tape form, the composite can simply be wrapped around the wire or cable in overlapping turns.
It is believed that the presence of the TFE/PPVE copolymer aids in adhering the layers of tape wrap to one another. The porous composite can be sintered either before or after wrapping if desired to improve cohesiveness and strength of the tape per se. Once the porous composite is prepared, it can be compressed, if desired, to increase the density of the composite. Such compression does not significantly affect the increased matrix strength that is associated with expanded porous PTFE. Compression improves properties such as dielectric strength and cut-through resistance.
It has been found that wire and cable insulation made from the non-porous or porous composites of this invention have unexpectedly better cut-through resistance, strength and abrasion resistance than insulation made from the TFE/PPVE copolymer alone or from non-expanded PTFE.
A third particular aspect of the present invention provides an insulated electrical conductor, which comprises a wire having wrapped around it two adjacent layers of the composite material, one layer being formed of non-porous composite material and the second layer being formed of porous composite material.
Generally, the layers are applied in the form of tapes wrapped (preferably counter-wrapped) around the wire in overlapping turns. The layers may also be applied longitudinally with a longitudinal overlapping seam. Preferably, sintering takes place after the two tapes have been applied; so that the layers become fused into an integral structure. Sintering may be brought about under the conditions previously described.
It has been found that generally speaking the non-porous non-expanded material has good electrical (particularly dielectric) properties; whilst the porous expanded material (whether compressed after expansion or not) has good mechanical properties (particularly cut-through resistance). Surprisingly these properties are retained in the two-layer insulated electrical conductor notwithstanding sintering, so that an insulating layer having both good mechanical and electrical properties is obtained.
Either the porous or the non-porous layer may be adjacent the wire. Placing the non-porous layer adjacent the wire facilitates stripping of the wire when a connection is to be made. Placing the non-porous layer uppermost allows better overprinting (e.g. for colour coding).
If required more than two layers of material may be used, for example non-porous/porous/non-porous which provides good stripping and printing characteristics.
Also, one or more porous or non-porous layers of the material of the present invention may be wrapped together with one or more layers of conventional expanded or non-expanded PTFE tape prior to sintering.
In particular, the combination of layers of non-porous composite material with conventional expanded PTFE; and the combination of layers porous composite material with non-expanded PTFE may be used.
EXAMPLES Embodiments of the present invention will now be described by way of example only. Figure 1 shows a wire construction.
Example 1 (non-porous tape) 181g (9wt %) of the TFE/PPVE copolymer powder of wide particle size distribution which had been screened to a particle size in the range 1-150 microns was added to 1.81kg (9lwt t) of Hostaflon (Registered Trade Mark) 2023 PTFE resin powder and tumbled in a Pascall tumble mixer at 40 revs/min for 60 minutes.
620 ml of Shellsol (Registered Trade Mark) TD liquid hydrocarbon was then added to this powder mixture and tumbled for a further 30 minutes to form a paste.
The paste was then left overnight before being compressed at 200 psi into a 4 inch diameter pellet.
The pellet was left for 24 hours at a temperature of 35 to 39"C before extrusion on a standard PTFE ram extruder at room temperature.
The extrudate of thickness 0.035 inch (890 microns) was then calendered down to 0.004 inch (101 microns) in three stages, using rollers heated to approximately 50 C.
The 0.004" tape was slit and wrapped on to 22 AWG (American Wire Gauge) 19 strand silver plated electrical wire conductor, to an insulation wall thickness of 0.008" (200 microns) and sintered in air at 400"C for 0.5 minute.
A similar wire sample was made using only the PTFE resin for comparison.
Both wire samples were tested for dynamic cut-through resistance and scrape abrasion resistance according to the test method given in BS G 230 (British Standard, Group 230). The results are given in Table 1 and demonstrate the improvement in the mechanical performance of the PTFE wire insulation when blended with TFE/PPVE copolymer over and above that of the base PTFE resin.
Table 1 DYNAMIC CUT THROUGH SCRAPE ABRASION (4 Newtons Load) in Newtons (N) SAMPLE (Room TemDerature) (Room Temperature) A 63 2,000 cycles B (comparison) 28 200 cycles Sample A: 22 AWG, 19 strand, silver plated copper conductor with 0.008" wall of PTFE and TFE/PPVE blended insulation material.
(according to Example 1).
Sample B: 22 AWG, 19 strand, silver plated copper conductor with 0.008" wall of PTFE insulation.
Example 2 (non-porous tape) 1.2Kg of TFE/PPVE copolymer powder of particle size was dispersed in 3.75Kg of Shellsol (Trademark) TD liquid hydrocarbon.
This was achieved by grinding the suspension in a colloid mill down to approximately 0.002" (50 microns + 12 microns). The resultant slurry was added to 13.61Kg of Hostaflon (Trade mark) 2023 PTFE resin and tumbled for 7 minutes.
The powder/lubricant mixture was then compressed into a 4 inch pellet. Tape of thickness 0.003" (75 microns) was made from the resultant pellet by a similar method to that described in Example 1.
Example 3 (expanded tape) 302g. (16.7 wt.%) of a tetrafluoroethylene/perfluoro(propyl vinyl ether) copolymer powder (PFA powder) was added to 1.5 liters of methanol and diluted with 20.1 liters of deionized water to form a dispersion. This was mixed for 30 seconds in a baffled 5 gallow container.
Next, 6500g. of aqueous dispersion containing 1600g. (12.8 wt.%) of dispersion-produced polytetrafluoroethylene was mixed with the PFA powder dispersion. Then, 6.4g. polyethylene imine was added to coagulate the solids from the mixture. After about 20 seconds of stirring, the phases separated. The clear liquid was decanted and the remaining solids dried at 1600C for 24 hours.
The solids, in particulate form, were lubricated with mineral spirits (19% by weight) and pelletized under vacuum. The pellets were aged at 49"C for about 24 hours, and were then extruded into tape. The tape was calendared to a thickness of 16.5 mil. and then dried to remove lubricant.
The dried tape was stretched in three steps. In the first stretch step, the tape was expanded longitudinally 93% (1.93 to 1) at 270"C at an output rate of 105 feet per minute. In the second step, the tape was expanded longitudinally at a rate of 20:1 at 290"C at an output rate of 3.8 feet per minute. In the third step, the tape was expanded longitudinally at a ratio of 2:1 at 325"C at an output of 75 feet per minute.
The resulting porous tape was then subjected to heat at 3300C for about 6 seconds.
It was then compressed to almost full density. The bulk density was 2.0 gm/cc.
Example 4 (expanded tape) The procedure of Example 3 was followed, except that in the first stretch step the stretch was at 1.9 to 1 instead of 1.93 to 1, and in the second stretch step the temperature was 300"C, and, in the third stretch step, the temperature was 360"C.
The tape was not compressed. The resulting density was 0.7 gm/cc.
Example 5 (mechanical properties) Expanded tapes produced by the method given in Example 3 that had been compressed to almost full density to a thickness of 0.0007" (18 microns) were slit and wrapped onto 20 AWG, 19 strand silver plated electrical wire conductor, to an insulation wall finished thickness of 0.003" (75 microns) post-sinter.
The insulated wire was then heat treated in air at 350"C for 15 minutes, to fuse the insulation material.
The resultant wire was tested for dynanmic cut-through resistance according to the test method given in BS G 230.
BS G 230 (British Standard Group 230) is a test specification for general requirements for aircraft electrical cables. Test results are given in Table 2.
Table 2.
Dynamic Cut-Through in Sample Newtons (N) at Room Temnerature 20 AWG, 19 strand, 91 silver plated copper 92 conductor, with 0.003" 65 wall of fused insulation 89 tape. Average = 84 Example 6 (mechanical properties) The expanded tape made by the method given in Example 3 was slit and a 0.15mm thick layer (0.lmm post-sinter) was wrapped (layer A) on to 20 AWG (American Wire Gauge) 19 strand nickel plated copper conductor (C).
Tape made by the method given in Example 2 was slit and then a 0.20mm thick layer (0.15mm post-sinter) was counter-wrapped (layer B) on the above insulated wire (See Figure 1). Counter-wrapping means that the tapes were wound as spirals of opposite hand.
The resultant composite wire was then sintered in air at 400oC for 1.5 minutes. The insulation had a final post-sinter thickness of 0.25mm. Similar insulated wires were made with only the tape manufactured as in Example 3 or Example 4.
For the purposes of comparison, separate samples of conductor were insulated with standard PTFE or with TFE/PPVE jackets (Samples 1 and 2 respectively).
The overall diameter of all samples was maintained at 1.5mm, resulting in similar wall thicknesses to allow the samples to be compared with one another.
The mechanical properties, with respect to scrape abrasion and cut through resistance of the insulated wire samples, were measured according to the test method given in BS G 230. The results are given in Table 3 and show the overall improvement in the mechanical properties of the composite insulation materials when compared with the individual homogeneous insulation materials.
Table 3 DYNAMIC CUT THROUGH SCRAPE ABRASION in Newtons (N) 8 Newtons 4 Newtons Load Load Sample ~ Room Temperature (Room TemPerature) 1 (comparison) 35 12 310 2 (comparison) 45 46 610 3 56 54 1,900 4 115 66 260 5 81 120 10,000 Sample 1 20AWG, 19 strand, nickel plated copper conductor with 0.25mm wall of PTFE insulation.
Sample 2 20AWG, 19 strand, nickel plated copper conductor with 0.25mm wall of TFE/PPVE insulation.
Sample 3 20AWG, 19 strand, nickel plated copper conductor with 0.25mm wall of PTFE and TFE/PPVE blended insulation material (according to Example 2).
Sample 4 20AWG, 19 strand, nickel plated copper conductor with 0.25mm wall of (expanded and densified) PTFE and TFE/PPVE blended insulation material (according to Example 3).
Samnle 5 2OAWG, 19 strand, nickel plated copper conductor with 0.25mm wall of composite insulation consisting of O.lmm of PTFE and TFE/PPVE blended material (according to Example 3) and 0.15mm PTFE and TFE/PPVE blended material (according to Example 2) fused together.
Example 7 (electrical performance) When Samples 4 and 5, manufactured by the method given in Example 5 are subject to the High Voltage Immersion Test given in BS G 230, Test Method 16a, the following test results are obtained: Sample 4 : 3.5 KV Sample 5 : 5 KV From these test results it is apparent that Sample 5, containing the dual counter-wrapped tapes manufactured by the methods given in Examples 2 and 3, has improved electrical properties with respect to voltage withstand characteristics over and above that of Sample 4.
Thus, for overall mechanical and electrical performance the dual, counter-wrapped construction is the preferred construction.
Example 8 (expanded/non-porous dual wrap) Expanded tape made by the method given in Example 3 was slit and a 50 microns thick (post-sinter thickness) layer (A) was wrapped onto 20AWG (American Wire Gauge) 19 strand nickel plated copper conductor (C)..
Tape made by the method given in Example 2 was slit and a 150 microns thick (post-sinter thickness) layer (B) was then counter-wrapped on the above insulated wire.
The resultant composite wire was then fused by heat treatment in air at 350"C for 20 minutes.
Figures of 113 - 151 cycles to failure (8 Newton load), and 110 - 130 Newtons were obtained when tested respectively, at room temperature, for scrape abrasion and dynamic cut-through resistance, according to Test Methods 30 and 26 given in BS G 230.
Example 9 (non-porous/expanded dual wrap) Tape made by the method given in Example 2 was slit and a 150 microns thick (post-sinter thickness) layer (A) was wrapped onto 20AWG (American Wire Gauge) 19 strand nickel plated copper conductor (C).
Expanded tape made by the method given in Example 3 was slit and a 50 microns thick (post-s inter thickness) layer (8) was counter-wrapped on the above insulated wire.
The resultant composite wire was then fused by heat-treatment in air for 1.5 minutes at 400"C followed by 20 minutes at 350 C.
When tested to Test Methods 16a, 26 and 30 in BS G 230, the results in Table 4 were obtained.
Table 4 Test Test Method Result High Voltage BS G 230 5 KV Immersion Test Test 16a Dynamic Cut-Through BS G 230 139 N Test 26 (Room Temperature) Scrape Abrasion BS G 230 95 Cycles Test 30 (8N Load, Room Temperature)

Claims (9)

  1. CLAIMS 1. A composite sheet material of a porous membrane of expanded polytetrafluoroethylene (PTFE) and a thermoplastic copolymer of tetrafluoroethylene and perfluoro(propylvinylether) wherein at least a portion of the thermoplastic copolymer is entrapped within the pores of the porous polytetrafluoroethylene.
  2. 2. A material according to claim 1 which comprises 5 to 95 wt.% of copolymer.
  3. 3. A material according to claim 1 which comprises 50 to 95 wt.% of copolymer.
  4. 4. A material according to any preceding claim which has a density less than 2.0 g/cc.
  5. 5. A material according to any preceding claim in which the porous structure has been compressed to increase its density.
  6. 6. An insulated electrical conductor which comprises a wire (C) having an electrically insulating layer (A) formed of a film or tape of a material according to claim 1 around the wire.
  7. 7. A conductor according to claim 6 which has been sintered.
  8. 8. A process for preparing a composite material which comprises mixing 5-90 wt.% of a thermoplastic copolymer of tetrafluoroethylene and perfluoro(propylvinylether) with a dispersion of coagulated polytetrafluoroethylene resin comprising 90-5 wt.% of polytetrafluoroethylene, coagulating the solids to form a resin blend, preparing pellets from the resin blend, forming a tape from the pellets, and stretching the tape until a desired degree of porosity is attained in the resulting porous composite.
  9. 9. A process according to claim 8 which further comprises compressing the porous composite material.
GB9220872A 1990-04-27 1991-04-26 Electrical insulating material Expired - Fee Related GB2262101B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US51530290A 1990-04-27 1990-04-27
GB909009407A GB9009407D0 (en) 1990-04-27 1990-04-27 Electrical insulating material
GB9219772A GB2261668B (en) 1990-04-27 1992-09-18 Electrical insulating material

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GB9220872D0 GB9220872D0 (en) 1992-11-18
GB2262101A true GB2262101A (en) 1993-06-09
GB2262101B GB2262101B (en) 1995-01-11

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996007529A1 (en) * 1994-09-02 1996-03-14 W. L. Gore & Associates, Inc. Porous polytetrafluoroethylene compositions
EP0779334A1 (en) * 1995-12-13 1997-06-18 Eilentropp Kg Polymer compositions and their use as high temperature resistant seals and connectors
WO1998012255A1 (en) * 1996-09-19 1998-03-26 W.L. Gore & Associates Gmbh Co-continuous blend of a fluoropolymer and a thermoplastic and method
EP2147023B1 (en) * 2007-05-21 2012-09-05 E. I. du Pont de Nemours and Company Process for coagulating fluoroelastomers
US10194528B2 (en) * 2011-05-06 2019-01-29 Guangdong Shengyi Sci. Tech Co., Ltd. Composite material, high-frequency circuit baseboard made therefrom and production method thereof
US11535017B2 (en) 2017-04-04 2022-12-27 W. L. Gore & Associates Gmbh Dielectric composite with reinforced elastomer and integrate electrode

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US4379858A (en) * 1981-08-28 1983-04-12 Hirosuke Suzuki Foamed plastics
US4454249A (en) * 1981-08-28 1984-06-12 Junkosha Co., Ltd. Reinforced plastics with porous resin fragments
EP0416806A1 (en) * 1989-09-01 1991-03-13 Junkosha Co. Ltd. A porous polytetrafluoroethylene resin material

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US4379858A (en) * 1981-08-28 1983-04-12 Hirosuke Suzuki Foamed plastics
US4454249A (en) * 1981-08-28 1984-06-12 Junkosha Co., Ltd. Reinforced plastics with porous resin fragments
EP0416806A1 (en) * 1989-09-01 1991-03-13 Junkosha Co. Ltd. A porous polytetrafluoroethylene resin material

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1996007529A1 (en) * 1994-09-02 1996-03-14 W. L. Gore & Associates, Inc. Porous polytetrafluoroethylene compositions
US5708044A (en) * 1994-09-02 1998-01-13 W. L. Gore & Associates, Inc. Polyetrafluoroethylene compositions
EP0779334A1 (en) * 1995-12-13 1997-06-18 Eilentropp Kg Polymer compositions and their use as high temperature resistant seals and connectors
WO1998012255A1 (en) * 1996-09-19 1998-03-26 W.L. Gore & Associates Gmbh Co-continuous blend of a fluoropolymer and a thermoplastic and method
US6127486A (en) * 1996-09-19 2000-10-03 W. L. Gore & Associates, Gmbh Co-continuous blend of a fluoropolymer and a thermoplastic and method
EP2147023B1 (en) * 2007-05-21 2012-09-05 E. I. du Pont de Nemours and Company Process for coagulating fluoroelastomers
US10194528B2 (en) * 2011-05-06 2019-01-29 Guangdong Shengyi Sci. Tech Co., Ltd. Composite material, high-frequency circuit baseboard made therefrom and production method thereof
US11535017B2 (en) 2017-04-04 2022-12-27 W. L. Gore & Associates Gmbh Dielectric composite with reinforced elastomer and integrate electrode

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GB2262101B (en) 1995-01-11
GB9220872D0 (en) 1992-11-18

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