WO1994019400A1 - Improved composition of expanded polytetrafluoroethylene and similar polymers and method for producing same - Google Patents
Improved composition of expanded polytetrafluoroethylene and similar polymers and method for producing same Download PDFInfo
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- WO1994019400A1 WO1994019400A1 PCT/US1993/003853 US9303853W WO9419400A1 WO 1994019400 A1 WO1994019400 A1 WO 1994019400A1 US 9303853 W US9303853 W US 9303853W WO 9419400 A1 WO9419400 A1 WO 9419400A1
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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
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/32—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof from compositions containing microballoons, e.g. syntactic foams
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
- C08K9/10—Encapsulated ingredients
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B11/00—Communication cables or conductors
- H01B11/18—Coaxial cables; Analogous cables having more than one inner conductor within a common outer conductor
- H01B11/1834—Construction of the insulation between the conductors
- H01B11/1839—Construction of the insulation between the conductors of cellular structure
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B7/00—Insulated conductors or cables characterised by their form
- H01B7/02—Disposition of insulation
- H01B7/0233—Cables with a predominant gas dielectric
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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
- 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
- C08J2327/18—Homopolymers or copolymers of tetrafluoroethylene
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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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/903—Sewing threads
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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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/905—Bicomponent material
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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
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S57/00—Textiles: spinning, twisting, and twining
- Y10S57/907—Foamed and/or fibrillated
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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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
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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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2927—Rod, strand, filament or fiber including structurally defined particulate matter
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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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2929—Bicomponent, conjugate, composite or collateral fibers or filaments [i.e., coextruded sheath-core or side-by-side type]
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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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2935—Discontinuous or tubular or cellular core
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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
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/294—Coated or with bond, impregnation or core including metal or compound thereof [excluding glass, ceramic and asbestos]
Definitions
- the present invention relates to expanded polytetrafluoro ⁇ ethylene (PTFE) and similar polymer compositions and methods for producing them. More particularly, the present invention relates to improved processes for expanding such compositions at least in part through non-mechanical means and compositions produced through such processes.
- PTFE polytetrafluoro ⁇ ethylene
- Patent 4,273,806 issued June 16, 1981, to Stechler (employing naturally occurring microspheres of silica and alumina in a polymer such as polyolefin or polyester); United States Patent 5,115,103 issued May 19, 1992, to Ya anishi et al . (employing silica or polymer microspheres in an ultraviolet (u.v.) radiation curable polymer such as fluoroacrylate, silicone, or silicone acrylate); and United States Patent 5,128,175 issued July 7, 1992, to Yamanishi et al .
- a primary purpose of the present invention to produce a PTFE or similar polymer product which is capable of expanding in three dimensions yet retains advantages of mechanically expanded PTFE products, such as increased strength, increased porosity, and low dielectric constant.
- the present Invention provides improved compositions of expanded polytetrafluoroethylene (PTFE) and similar long-chain polymers and a method for producing such compositions.
- PTFE polytetrafluoroethylene
- the present invention comprises a mixture of polymer, such as PTFE dispersion, and expandable thermoplastic microspheres.
- polymer such as PTFE dispersion
- expandable thermoplastic microspheres By expanding the microspheres in the mixture through exposure to heat or other energy source, 1t has been determined that a three dimensional scaffold or lattice network is formed of coherent expanded polymeric nodes and fibrils and expanded microspheres.
- This scaffold has many of the same desirable properties of mechanically expanded PTFE, including improved tensile strength, liquid repellency with moisture vapor permeability, filtration selectivity, and low dielectric constant.
- compositions of the present invention have numerous beneficial properties which have eluded previous fine powder PTFE products.
- the interaction of the PTFE and the microspheres causes the PTFE to expand in three dimensions- -providing length, width and depth to a cohesive expanded product.
- this provides for PTFE products are: unsintered dimensional stability, resilience and resistance to deformation, thermal insulation, buoyancy, padding, moisture retention, moldabiHty, and selective expandability.
- wire produced from the composition of the present invention have proven to have extremely low dielectric constants and high velocities of propagation.
- the present invention provides a myriad of improved manufacturing advantages.
- Improved processes of the present invention are: simplified polymer expansion procedures; simplified expanded PTFE application procedures; the ability to create seamless PTFE wire Insulation and other products; simplified and improved seam sealing procedures; and the ability to mold and create uniquely shaped articles from fine powder PTFE.
- Figure 1 is a graph showing the typical sizes and ranges of expansion of one form of expandable thermoplastic micropheres employed with the present invention
- Figure 2 1s a scanning electron microscopic (SEM) image of a composition of the present invention, enlarged 150X;
- Figure 3 is an SEM image of a composition of the present invention, enlarged 150X;
- Figure 4 is an SEM image of a composition of the present invention, enlarged 1280X;
- Figure 5 is a cross-sectional SEM image of a conductive substrate (wire) coated with the composition of the present invention and contained within a sheath, enlarged 30X;
- Figure 6A is a cross-sectional view of one embodiment of a thread formed in accordance with the present invention.
- Figure 6B is a cross-sectional view of another embodiment of a thread formed in accordance with the present invention
- Figure 7A is a cross-sectional view of yet another embodiment of a thread formed in accordance with the present invention.
- Figure 7B is a cross-sectional view of still another embodiment of a thread formed in accordance with the present invention.
- Figure 8 is a three-quarter isometric view of a gasket made in accordance with the present invention.
- the present invention provides improved methods for producing expanded polytetrafluoroethylene (PTFE) and similar polymer products and improved compositions of such polymer products for use in a variety of applications.
- PTFE polytetrafluoroethylene
- a tetraf1uoroethylene polymer material can be created with a micro-structure characterized by nodes interconnected with fibrils. Once sintered to establish expanded dimensional stability, this material is highly porous, has high strength, and has very good electric insulative properties. Among the numerous useful forms of this material is as films/membranes, tubes, rods, and continuous filaments.
- PTFE may be expanded by employing expandable microspheres blended Into a PTFE composition.
- Such microspheres comprise a plastic coating surrounding an expandable liquid or gaseous volatile fluid.
- thermoplastic microspheres are adapted to expand dramatically when exposed to heat. These microspheres are monocellular particles comprising a body of resinous material encapsulating a volatile fluid. When heated, the resinous material of thermoplastic microspheres softens and the volatile material expands--causing the entire microsphere to increase substantially in size. On cooling, the resinous material in the shell of the microspheres ceases flowing and tends to retain its enlarged dimension; the volatile fluid inside the microsphere tends to condense, causing a reduced pressure in the microsphere.
- thermoplastic microspheres are now commercially available from Nobel Industries Sweden, Sundsvall, Sweden, under the trademark EXPANCEL 0 . These microspheres may be obtained in a variety of sizes and forms, with expansion temperatures generally ranging from 80 to 130 ⁇ C.
- a typical EXPANCEL microsphere has an initial average diameter of 9 to 17 microns and an average expanded diameter of 40 to 60 microns. According to Nobel Industries, the microspheres have an unexpanded true density of 1250-1300 kg/m 3 and an expanded density below 20 kg/m 3 .
- expandable microsphere herein is Intended to encompass any hollow resilient container filled with volatile fluid which is adapted to expand.
- presently available microspheres are essentially ball- shaped particles adapted to expand when exposed to an energy source, it should be understood that such microspheres are quite resilient in their expanded form and can be compressed and released (e.g. through extrusion) to achieve the expansion required for the present invention. Additionally, it may be possible to form such products in a variety of other shapes, such as tubes, ellipsoids, cubes, particles, etc. As such, the term “expandable microsphere” in the context of the present invention is intended to include all applicable forms and uses of these products now known or later developed.
- EXPANCEL type 091 DU is employed.
- This product comprises an off-white dry powder with a particle size between 5 and 50 microns.
- the shell of the microsphere comprises acrylonitrile or ethacrylonitrile.
- the volatile liquid comprises isopentane. It has been found that by mixing a dry preparation of EXPANCEL microspheres with a dispersion of PTFE or similar polymer and then heating the resulting composition, the polymer will undergo expansion in three-dimensions to achieve a porous network of polymeric nodes and fibrils.
- a mixture of PTFE, in the form of paste, dispersion or powder, and microspheres, in the form of dry powder or solution, are mixed in proportions of 1 to 90% by weight icropheres, with 5 to 85% by weight of microspheres being preferred. It should be appreciated that a wide range of products may be created even with a percentage of microspheres of merely 0.1 to 5% by weight; similarly, for some uses, filled products may be created with a percentage of microspheres and/or other fillers between 90 to 99 or more percent by weight. Mixture may occur by any suitable means, Including dry blending of powders, wet blending, co-coagulation of aqueous dispersions and slurry filler, high shear mixing, etc.
- the resulting composition is heated to a temperature of 80 to 170°C for a period of 0.5 to 10 minutes to activate the microspheres.
- the composition may be re-heated to a temperature of 40 to 200°C and mechanically expanded through any conventional means, such as those disclosed in United States Patent 3,963,566.
- any conventional means such as those disclosed in United States Patent 3,963,566.
- the present invention is believed to lend Itself to incorporation with many existing mechanical expansion techniques, whether before, during and/or after microsphere expansion.
- compositions made in accordance with the present invention have tremendous applications in the electrical industries for uses such as high VP cable, sheathing, circuit board insulation, etc.
- compositions of the present invention have proven to have a variety of surprising properties previously unattainable with expanded PTFE compositions.
- the interaction of the PTFE and the microspheres causes the PTFE to expand in three dimensions—providing length, width and depth to the expanded product.
- this provides for PTFE products are: thermal insulation, buoyancy, padding, moisture retention, moldability, extremely low densities, and selective expandability.
- the present invention provides a wide selection of improved manufacturing techniques.
- compositions of the present invention Two of the more startling improved properties discovered to date of the new expanded PTFE compositions of the present invention are their substantial non-amorphously locked ("unsintered") dimensional stability and their exceptional elasticity/resilience to deformation. Each of these properties was unexpected and each provides many new utilities for expanded PTFE products. It is quite remarkable that the PTFE products made in accordance with the present invention are dimensionally stable in their unsintered form. As is known, existing expanded PTFE products must be sintered after expansion in order to have the products retain their expanded dimensions. Unexpectedly, the compositions of the present invention form a coherent mass which tends to retain its expanded dimensions with no further treatment. Equally surprising is that this coherent mass can be formed even without pre-treatment of the PTFE polymer (i.e. allowing new applications for expanded PTFE without the need to extrude or otherwise treat the PTFE polymer before expansion).
- Another equally remarkable property of the present invention is its ability to "puff" into a resilient cushion-like coherent mass with substantial proportions of open air spaces therein.
- the mass can expand in all dimensions and, very surprisingly, remains highly self-cohesive despite the dramatic increase in its dimensions and typical air space contents from 10 to 50 to 80% or more.
- the resulting product becomes even less dense.
- the "puffed" mass of the present invention has proven to be remarkably elastic and resilient to deformation. For instance, a typical expanded mass will withstand compression of 50% or more with nearly 100% rebound to original shape.
- FIGS. 2 and 3 show SEM images of compositions of the present invention enlarged 150 times.
- the composition comprises many expanded microspheres 10 interconnected by polymeric fibrils 12 (I.e. thread-like elements) and nodes 14 (i.e. particles from which fibrils emerge).
- This "scaffold” or “lattice” structure of fibrils and nodes incorporating microspheres defines substantial areas of open air spaces within the composition. It is believed to be both the voids within the microspheres 10 and these air spaces which create many of the unique properties of the present invention.
- microspheres 10 can be seen attached to and embedded within fibrils 12 and nodes 14.
- the polymer actually becomes attached to the microspheres, apparently with some fibrils 16 extending directly from the microspheres 10 and some nodes 18 attached directly to the surface of the microspheres 10.
- composition of the present invention is in creating molded articles. Unlike previous co positions made with fine powder PTFE, the present invention will readily expand to fill molds or other forms. Shown in Figure 5 is a cross-sectional view of a conductor 20 housed within a sheath material 22, such as PTFE or acrylic. By partially filling the sheath 22 (or, as is explained below, by coating the conductor 20) with the polymer/microsphere composition 24 of the present invention, the composition can be expanded to fill in the sheath thoroughly and provide an even coating around the conductor 20. An alternative coating may be created by heating the conductor itself to institute composition expansion.
- a sheath material 22 such as PTFE or acrylic.
- This unique property of the present invention can be readily applied to create coherent expanded PTFE products in virtually any imaginable shape, including inducing expansion to occur in only predetermined directions. At least three different mechanisms may be employed in this regard—selective heating, external constriction, and/or internal constriction.
- compositions made in accordance with the present invention may be selectively heated to activate expansion in only certain directions or in certain areas.
- heat may be focused through any known means to activate the microspheres only in the desired locations (e.g. use of focused heat through conduction or convection, directed electrical current, or a laser).
- molding methods may be applied in concert to provide unique application-specific properties.
- many different characteristics can be imparted, such as continuous PTFE products with variable densities or shapes, ribbed PTFE products, etc.
- Another important application for the present invention is as a thread material.
- One common problem in virtually all instances where a sewn seam is created e.g. in fabric or medical (i.e. suture) uses
- the needle creates an opening larger than the thread.
- leakage e.g. in waterproof fabrics or in a medical procedure
- the seam must then be sealed or wrapped through one or more various time-consuming procedures.
- seams By forming threads using the present invention, the need for seam-sealing may be significantly reduced or eliminated. At least two possible options are available for seam-sealing using the composition of the present invention. First, by forming a thread from a composition of polymer and unexpanded microspheres (e.g.. through extrusion), seams can be created and sewn using conventional methods. Once the thread is in place, the seams can then be treated to cause the polymer/microspheres to expand, swelling the thread and sealing the openings caused by the needle.
- Figures 6A and 6B illustrate two options for a thread 24a, 24b which is "puffed” once sewn in place.
- the thread 24a comprises a composition 26 of polymer/unexpanded microspheres and a conductive filler, such as carbon black.
- the thread 24b comprises a conductive core 28 (e.g. a wire or conductive fiber) surrounded by a composition 30 of polymer/unexpanded microspheres.
- microsphere activation energy e.g. heat through conduction, convention, or electrical resistance
- the advantage of providing an expandable thread 24a, 24b with some form of conductive element in the thread itself is that the thread can be expanded with minimal impact on the material or tissue surrounding the thread.
- the thread may also be constructed from a polymer/microsphere composition with no core or fillers; in this event, the thread is expanded merely through the application of activation energy directly to the outside of the thread (e.g. by generally heating the seam or subjecting the seam to a localized energy source, like a laser).
- Figures 7A and 7B illustrate two examples of threads 30a, 30b which are "pre-puffed" before being sewn in place.
- the thread 30a of Figure 7A comprises a core 32 of pre-expanded polymer/ microspheres housed within a sheath 34.
- the sheath 34 should provide sufficient resilience to allow deformation and rebound of the polymer/microsphere core and a smooth surface for ease, in sewing. Suitable material includes PTFE, acrylic, etc.
- Figure 6B shows an example of a thread 30b with the reverse construction having a strong core 36 (e.g. KEVLAR, PTFE, etc.) and a sheath 38 of pre-expanded polymer/microsphere composition.
- a strong core 36 e.g. KEVLAR, PTFE, etc.
- a gasket 40 can be readily formed from a polymer/microsphere composition of the present Invention and employed in any conventional manner. Depending upon application, it may be possible to create a superior seal with such a product by activating the microspheres after the gasket 40 is in place, such as between fittings 42, 44. To control expansion in this context, the polymer/microsphere composite can be wrapped in a film (e.g. a plastic tube or a tape of PTFE). Another surprising property of the present invention is that the composition will attach itself to a variety of substrates with limited "flaking off" after expansion.
- an effective insulative layer can be formed around the conductor.
- This process is a vastly more expedient method of providing a PTFE insulation on a conductor than any present available.
- This same procedure can be applied to produce numerous other expanded PTFE products.
- a dip or coating process can be applied over a thin substrate (e.g. a film of latex or expanded PTFE) to produce seamless PTFE gloves, socks, footwear, dry- suits/wetsults, etc. This process not only eliminates the labor intensive task of forming and sealing seams, but also may allow for greater dexterity and improved performance.
- certain products such as gloves or boots, can be created by expanding the PTFE/microsphere composition while being worn by a user to create a customized fit.
- a wide number of unique molded items can be created, Including ones with variable polymer densities. For instance, by placing the polymer/microsphere composition in a mold having selective constricted areas, once the coherent polymer/microsphere mass is expanded, 1t will comprise greater and lesser thicknesses, with generally greater polymer density in those areas of lesser thickness.
- Another useful application for the present invention is in its use as a filter element. Not only can the composition of the present invention be formed to provide selective chemical permeability, but it also has other attributes not previously attainable with PTFE filter material. For example, it has been determined that, once saturated under forced liquid pressure, an expanded PTFE/microsphere material of the present invention has the ability to retain moisture for long periods of time. As such, filter elements now requiring pre-wetting or other pre-installation treatment can be supplied in a ready-to-use form, significantly reducing labor and costs associated with filter replacement procedures.
- a 5% EXPANCEL / 95% PTFE by weight sample was made by the following method: A slurry of 7.8 g of EXPANCEL - 091 DU obtained from Nobel Industries, 1519 Johnson Ferry Road, Marietta, GA 30062, and 551.2 g of de-Ionized water was prepared in a 2 liter baffled stainless steel container. While the slurry was agitating at 800 RPM, 148.2 g of PTFE in the form of a 20.0 % dispersion was rapidly poured Into the vessel. The PTFE dispersion was an aqueous dispersion obtained from ICI Americas, Inc.
- the coagulum was dried at 110°C in a convection oven.
- the dried cake was chilled below 0°C. It was hand ground through a 0.635 cm mesh stainless steel screen.
- a 35 g sample of screened powder was lubricated with mineral spirits at a ratio of 0.375 cc solvent per gram of powder. The mixture was chilled, passed through a 0.635 cm mesh screen again, tumbled, then allowed to sit at 18°C for 16 hours and was re-tumbled.
- a 2.54 cm diameter pellet was formed in a cylinder at 200 psi.
- the pellet was then extruded through a 0.254 cm diameter die at a ram rate of 50.8 cm/min.
- the extruded beading was then dried at 105°C in a convection oven for 1 hour.
- a 19.04 cm long piece of the dried extrudate measuring 0.297 cm in diameter, weighing 1.924 gms, and a calculated density of 1.457 g/cc was then placed in a convection oven at 165°C for 3 minutes to "puff" the microspheres (i.e. heat activating and subsequent growing of the spheres).
- the sample was measured to be 28.1 cm long, having a diameter of 0.569 cm, a weight of 1.918 g, and a calculated density of 0.268 g/cc.
- a 15.0 cm long section was cut from the sample produced in Example 1.
- a 5.0 cm long section was marked off in the center of this piece using an indelible marker.
- the sample was placed in a convection oven at 165°C for 3 minutes. The sample was then grabbed by hand outside of the marks using high temperature gloves. Upon removal from the oven, the sample was Immediately and rapidly stretched by separating hands. The time of stretch was estimated to be approximately 0.25 seconds.
- the sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 49.0 cm long, 0.399 cm in diameter, weight of 0.343 g., with a calculated density of 0.056 g/cc.
- a 15.0 cm long section was cut from the sample produced in Example 2.
- a 5.0 cm long section was marked off in the center of this piece using an indelible marker.
- the sample was placed in a convection oven at 165°C for 3 minutes. The sample was then grabbed by hand outside of the marks using high temperature gloves. Upon removal from the oven, the sample was immediately and rapidly stretched by separating hands. The time of stretch was estimated to be approximately 0.25 seconds.
- the sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 21.5 cm long, 0683 cm in diameter, weight of 0.239 g, and a calculated density of 0.030 g/cc.
- Example 2a Using the same procedure and sample size as Example 2a the following sample was produced.
- the sample measured to be 42.0 cm long, 0.612 cm in diameter, weight of 0.240 g, and a calculated density of 0.019 g/cc.
- a 15.0 cm long section of dried extrudate was cut from Example 2 measuring 0.297 in diameter.
- a 5.0 cm long section was marked off in the center of this piece using an indelible marker.
- the sample was placed in a convection oven at 115°C for 7 minutes. The sample was then grabbed by hand outside of the marks using high temperature gloves. Upon removal from the oven, the sample was immediately and rapidly stretched by separating hands. The time of stretch was estimated to be approximately 0.25 seconds.
- the sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 64.1 cm long, 0.287 cm in diameter, weight of 0.474 g, with a calculated density of 0.114 g/cc.
- This sample was then placed unrestrained in a convection oven at 165°C for 3 minutes. Upon removal from the oven, the sample had a length of 30 cm, a diameter of 0.533 cm, a weight of 0.471 g and a calculated density of 0.070 g/cc.
- a 19.04 cm long piece of dried extrudate measuring 0.297 cm in diameter weighing 1.690 g and a calculated density of 1.280 g/cc was then placed in a convection oven at 165°C for 3 minutes. Upon removal from the oven the sample was measured to be 40.2 cm long, having a diameter of 0.955 cm, and a weight of 1.666 g, and a calculated density of 0.058 g/cc.
- a 15.0 cm long section was cut from the 0.955 cm diameter sample produced in Example 3.
- a 5.0 cm long section was marked off in the center of this piece using an indelible marker.
- the sample was placed in a convection oven at 165°C for 3 minutes. The sample was then grabbed by hand outside of the marks using high temperature gloves. Upon removal from the oven, the sample was immediately and rapidly stretched by separating hands. The time of stretch was estimated to be approximately 0.25 seconds.
- the sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 27.0 cm long, 0.648 cm in diameter, weight of 0.203 g, and a calculated density of 0.023 g/cc.
- a sample of the dried extrudate measuring 0.297 cm in diameter from Example 3 was then tested for breakstrength on a Instron Model 1130. Gauge length (distance between clamps) was two inches. Samples were pulled apart at 10 inches/min with maximum tensile force being recorded. The sample was measured to have a breakstrength of 0.77 lbs.
- Example 3 A sample of the 0.955 cm diameter from Example 3 was then tested for breakstrength on a Instron Model 1130. Gauge length (distance between clamps) was two inches. Samples were pulled apart at 10 inches/min with maximum tensile force being recorded. The sample was measured to have a breakstrength of 1.78 lbs.
- a slurry of 78 g of EXPANCEL - 091 DU and 867 g of de-ionized water was prepared in a 2 liter baffled stainless steel container. While the slurry was agitating at 800 RPM, 78 g of PTFE in the form of a 20.0 % dispersion was rapidly poured into the vessel. The PTFE dispersion was an aqueous dispersion obtained from ICI Americas, Inc. After 30 seconds, 3.0 g of a 0.4% solution of a cationic modified polyacryli ide was added to initiate the co- coagulation. After a total of 1 minute, the mixer was stopped. The coagulum settled to the bottom of the vessel and the effluent was slightly cloudy.
- the coagulum was dried at 110°C in a convection oven.
- the dried cake was chilled below 0°C. It was hand ground through a 0.635 cm mesh stainless steel screen.
- a 35 g sample of screened powder was lubricated with mineral spirits at a ratio of 0.309 cc solvent per gram of powder. The mixture was chilled, passed through a 0.635 cm mesh screen again, tumbled, then allowed to sit at 18°C for 16 hours and was re-tumbled.
- a 2.54 cm diameter pellet was formed in a cylinder at 200 psi. The pellet was then extruded through a 0.254 cm diameter die at a ram rate of 50.8 cm / min.
- a 30.0 length of the extrudate was then placed in a convection oven at 165°C for 6 minutes. Upon removal from the oven the sample was measured to be 58.0 cm long, having a diameter of 1.524 cm, a weight of 2.352 g, and a calculated density of 0.022 g/cc.
- a 15.0 cm long section was cut from the 1.524 cm diameter sample produced in Example 4.
- a 5.0 cm long section was marked off in the center of this piece using an indelible marker.
- the sample was placed in a convection oven at 165°C for 3 minutes. The sample was then grabbed by hand outside of the marks. The sample was stretched inside the oven by separating hands. The time of stretch was estimated to be approximately 5.0 seconds. The sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 13.1 cm long, 1.283 cm in diameter, weight of 0.200 g, and a calculated density of 0.012 g/cc.
- EXPANCEL/25% PTFE by weight was made by using the same method as Example 4 except the following component amounts were used: Slurry of 117 g of EXPANCEL - 091 DU and 950 g of de-ionized water
- a 30.0 cm length of the sample was then placed in a convection oven at 165°C for 6 minutes. Upon removal from the oven the sample was measured to be 51.0 cm long, having a diameter of 1.702 cm, weight of 1.834 g, and a calculated density of 0.016 g/cc.
- a slurry of 2610 g of EXPANCEL - 091 DU and 45.2 Kg of de- ionized water was prepared in a 30 gallon stainless steel container. While the slurry was agitating, 7.83 Kg of PTFE in the form of a 20.0 % dispersion was rapidly poured into the vessel.
- the PTFE dispersion was an aqueous dispersion obtained from ICI Americas, Inc. After 20 seconds, 147 g of a 0.4% solution of a cationic modified polyacrylimide was added to Initiate the co- coagulation. After a total of 1 minute 44 seconds, the mixer was stopped. The coagulum settled to the bottom of the vessel and the effluent was clear.
- the coagulum was dried at about 110°C in a convection oven.
- the dried cake was chilled below 0°C. It was hand ground through a 0.635 cm mesh stainless steel screen.
- a sample of screened powder was lubricated with mineral spirits at a ratio of 0.265 cc solvent per gram of powder. The mixture was chilled, passed through a 0.635 cm mesh screen again, tumbled, then allowed to sit at 18°C for 16 hours and was re-tumbled.
- the powder was then extruded through a 10.1 cm diameter barrel and a 0.203 x 15.2 cm die at a ram rate of 100 cm/min.
- a piece of the dried extrudate made in accordance with Example 6 was then placed in a convection oven at 165°C for 5 minutes. Upon removal from the oven the sample was measured to be 33.3 cm long, 19.4 cm wide, 1.4 cm thick, a weight of 69.72 g, and a calculated density of 0.077 g/cc.
- Example 6 Another sample was produced in the same manner as Example 6. A 10 cm long section was marked off in the center of this piece using an indelible marker. The sample was placed in a convection oven at 165°C for 3 minutes. The sample was then grabbed by hand outside of the marks using high temperature gloves. Upon removal from the oven, the sample was immediately and rapidly stretched by separating hands. The time of stretch was estimated to be approximately 0.25 seconds. The sample was then cut at the marks and measurements were taken on the center section. The sample measured to be 34.7 cm long, 14.3 cm wide, 1.21 cm thick, a weight of 19.64 g, and a calculated density of 0.033 g/cc.
- Example 6 Another sample was produced in the same manner as Example 6. This material was measured to have a thickness of 0.208 cm and a width of 14.8 cm. The material was then additionally processed by calendering between two metal rolls using the following gap sizes and output speeds in nine successive steps:
- the calendered material had a thickness of 0.0077 cm and a width of 13.2 cm. The material was then placed in a convection oven at 165°C for 5 minutes. A length of material was cut from the sample and measured to be 44.5 cm long, 39.4 cm wide, 0.036 cm thick, a weight of 5.30 g, and a calculated density of 0.084 g/cc.
- AIR SPACE VOLUME should be interpreted as the volume of air contained within the sample which is not inside the microspheres.
- AIR SPACE VOLUME is calculated using the equations below and is based on the following definitions and assumptions:
- PTFE VOLUME 1 s the calculated volume of PTFE within sample.
- MICROSPHERE VOLUME is the calculated volume of the microsphere shell, including contents, within sample.
- BULK VOLUME is the di ensionally measured volume of the sample.
- Puffed microspheres for this example were assumed to have an average density of 0.03 g/cc.
- the density of PTFE was assumed to be 2.20 g/cc.
- a water resistance test on samples of Examples 6a, 6b and 6c was conducted.
- Two 8 inch square waterproof bags were prepared by cutting an approximate 3.0 inch square window into one side of each of the bags.
- a 5 inch square sample cut from each of the Examples 6a-6c was placed inside the bags.
- the window perimeters were sealed to the samples using duct tape thereby exposing only a 2.5 inch square portion of the sample to the outside.
- An absorbent paper towel was place behind each of the samples, opposite of the cut window, then the bags were sealed.
- the bags were placed flat on the floor inside a simulated rain room with the windows facing upward towards the rain. The rain impinged upon the samples for 30 minutes at a rate of 3 inches of water per hour.
- the samples were examined immediately after the rain test for water penetration by visually checking for wetness of the paper towels. In all the examples, the paper towels were completely dry.
- MVTR moisture vapor transmission rate test
- This test apparatus consists of a reservoir filled with distilled water maintained at 23°C. The reservoir is covered by a porous expanded polytetrafluoroethylene (ePTFE) membrane having a high moisture vapor transmission rate (MVTR). Cups having a mouth diameter of 3.5 inches are prepared by partially filling the cup with potassium acetate and then covering the mouth of the cup with the same high MVTR ePTFE membrane.
- ePTFE expanded polytetrafluoroethylene
- a thermal conductivity test was conducted on the above sample 6a.
- a sample measuring 12 inches was tested according to ASTM C518 procedures using the Holometrics Rapid K Thermal Conductivity Instrument Model RK 80.
- a constant 20°C water bath was supplied by Neslab.
- ⁇ T for testing was 30°C with the upper face at 60°C and the lower face at 30°C
- Thermal conductivity ( ⁇ ) for sample 6a was calculated to be 0.268 BTU-INCH/(HR-FT 2 -F).
- a slurry was mixed consisting of 15.14 g of PTFE in the form of a 60.0 % dispersion and 14.91 g of EXPANCEL - 091 DU and 5.14 g of distilled water. This yields a solids content of 50% PTFE to 50% EXPANCEL.
- the PTFE dispersion used was part number TE 30, an aqueous dispersion obtained from E. I. Dupont.
- a plain weave 50 denier ePTFE fabric of approximately 112 x 112 picks per inch was dipped in the above slurry and the excess slurry wiped off. The fabric was allowed to air dry for approximately 1 hour in ambient conditions.
- the fabric was then placed between two heated platens at 165°C with a fixed gap of approximately 2 mm for 1 minute. The platens were then opened and the sample was removed. The sample was found to be a flexible, stable, membrane-like material with good adhesion of the coating to the fabric.
- a water penetration test was conducted on this fabric by cupping the fabric within a 3 inch diameter beaker and pouring 10 ml of water into the cupped portion of the fabric. After one minute there was no visible leakage of the water through the fabric.
- a slurry was mixed consisting of 15.14 g of PTFE in the form of a 60.0 % dispersion and 14.91 g of EXPANCEL - 091 DU and 10.19 g of distilled water. This yields a solids content of 50% PTFE to 50% EXPANCEL.
- the PTFE dispersion used was part number TE 30, an aqueous dispersion obtained from E. I. Dupont.
- a slurry was mixed consisting of 15.14 g of PTFE in the form of a 60.0 % dispersion and 14.91 g of EXPANCEL - 091 DU and 10.19 g of distilled water. This yields a solids content of 50% PTFE to 50% EXPANCEL.
- the PTFE dispersion used was part number TE 30, an aqueous dispersion obtained from E. I. Dupont.
- the slurry was then painted onto a 3/8 inch diameter copper tube using a conventional paint brush and allow to air dry at ambient conditions for 1 hour. The tube was then placed in a convection oven at 165°C for 3 minutes to expand the EXPANCEL micro-balloons. The tube was then removed and inspected. Good adhesion properties between the coating and the tube were observed.
- a slurry was mixed consisting of 20.94 g of PTFE in the form of a 60.0 % dispersion and 27.88 g of EXPANCEL - 091 DU and 3.5 g of distilled water. This yields a solids content of 43% PTFE to 57% EXPANCEL.
- the PTFE dispersion used was part number TE 30, an aqueous dispersion obtained from E. I. Dupont.
- a 24 gauge silver plated copper wire was "dipped" coated with the above slurry by inserting the wire through a small hole in the bottom of the mix container and drawing the wire upwards through the bath. The wire was then hung vertically to dry for approximately 30 minutes at ambient conditions.
- the 3.5 ft section of dried coated wire was inserted inside an expanded PTFE tube (e.g. tubing produced according to Gore U.S. Patent 3,953,566) of the same length having an inside diameter
- the assembly was then placed in a convection oven for 3 minutes at 165°C in order to puff the wire coating so that it fills the annular space between the wire and the PTFE tubing. The sample was removed and allowed to cool. The density of the puffed coating was calculated to be 0.096 g/cc using the known weight and volume of the puffed coating.
- V.P. velocity of propagation
- a Techtronics Model CSA 803 was used in TDR mode (time domain reflectometry) to measure velocity of propagation.
- a slurry was mixed consisting of 7.36 g of PTFE in the form of a 60.0 % dispersion and 13.67 gms of EXPANCEL - 091 DU and 4.5 g of distilled water. This yields a solids content of 35% PTFE to 65% EXPANCEL.
- the PTFE dispersion used was part number TE 30, an aqueous dispersion obtained from E. I. Dupont.
- a 33 gauge silver plated copper wire was dipped coated with the above slurry by inserting the wire through a small hole in the bottom of the mix container and drawing the wire upwards through the bath. The wire was then hung vertically to dry for approximately 30 minutes at ambient conditions.
- the 3.5 ft section of dried coated wire was inserted inside a 43 mil I.D. copper tube of the same length.
- the assembly was then placed in a convection oven for 4 minutes at 165°C in order to puff the wire coating so that it fills the annular space between the wire and the copper tubing.
- the sample was removed and allowed to cool.
- a Techtronics Model CSA 803 was used in TDR mode (time domain reflectometry) to measure velocity of propagation.
- a cable length of 3.240 ft was measured to have a signal delay of 1.037 ns/ft, which converts to a signal speed of 2.939 x 10 8 meters/sec. This
- Solutions of UHMW-PE were prepared in a jacketed reaction vessel capable of maintaining solutions temperatures in excess of 130°C.
- the vessel was purged with flowing nitrogen.
- the vessel was also fitted with a thermocouple for determining the solution temperature, and a stirring paddle.
- the vessel was initially heated to approximately 79°C, at which time 200 g of reagent grade mixed xylenes were added, and equilibrated at temperature.
- a piece of the resulting product from the above procedure was measured to be 4.70 cm long, 1.10 cm wide, and 0.358 cm thick, a weight of 0.570 g, and a calculated density of 0.308 g/cc. This piece was placed in a convection oven at 165°C for 5 minutes and removed. The sample had a puffed appearance. A piece was cut from the puffed sample and was measured to be 8.92 cm long, 2.04 cm wide, and 0.767 cm thick, a weight of 0.534 g, and a calculated density of 0.038 g/cc.
- the following example demonstrates ability to mold and/or selectively puff regions of a sample.
- a 1/2-20 inch threaded sleeve was placed between two heat platens set at 200°C and allowed to reach temperature.
- a length was cut from the dried extruded beading of Example 4, part of which was inserted into the metal sleeve.
- the sleeve removed from the sample, and the following observations were made.
- the region of the sample that had been placed within the sleeve had a puffed outside diameter (O.D.) of 1/2 inch which matched the inside diameter (I.D.) of the sleeve including the threaded profile.
- the region which was not inserted within the metal sleeve had a smooth profile and an O.D. of approximately 1/8 inch.
- a slurry of 13.8 g of EXPANCEL - 091 DU, 23.07 g of Carbon Black, and 987 g of de-ionized water was prepared in a 2 liter baffled stainless steel container. While the slurry was agitating at 500 RPM for 3 minutes, 55.38 g of PTFE in the form of 20.0% dispersion was rapidly poured Into the vessel now mixing at 800 RPM. The carbon black used was Ketjen Black type 300J obtained from Akzo Chemical, Inc. After a total of 1 minute 3 seconds, the mixer was stopped. The coagulum settled to the bottom of the vessel and the effluent was clear.
- the coagulum was dried at 103°C in convention oven.
- the dried cake was chilled below 0°C. It was hand ground through a 0.635 cm mesh screen again, tumbled, then allowed to sit at 18°C for 16 hours and was re-tumbled.
- a 2.54 cm diameter pellet was formed in a cylinder at 200 psi.
- the cylinder was heated to 100°C and the pellet was then extruded through a 0.254 cm diameter die at a ram rate of 50.8 cm/min.
- a 20 cm long piece of extrudate having a diameter of 0.302 cm was then placed in a convection oven at 165°C for 3 minutes. Upon removal from the oven the sample was measured to be 21.2 cm long, having a diameter of 0.922 cm, and a weight of 0.989 gms with a calculated density of 0.070 g/cc.
- the sample was tested for electrical resistivity using Mil G 83528A standard modified to a 4 point probe instead of a 2 point probe. During testing, the sample was compressed approximately 50%. The surface measurement was 110 ohms yielding a volume resistivity of 191 ohm-cm. An alternative testing method was also used by attaching alligator clips to the sample at a 4 inch spacing. This test yielded a result of 241 ohm-cm. A z-axis test was measured between two plates and also compressed 50%. This test yielded a result of 5.7 ohm-cm.
- compositions of the present invention can be formed with various fillers to provide specific utility.
- suitable fillers include: carbon black, ceramics, chemically activated materials (e.g. silica gel, activated carbon), thermoplastics, metals, metal oxides, elastomers particulates (including particles, rods, or flakes), etc.
- a coagulum was prepare as in Example 6.
- the coagulum was dried at 110°C in a convection oven.
- the dried cake was chilled below 0°C. It was hand ground through a 0.635 cm mesh stainless steel screen.
- the screened powder was lubricated with mineral spirits at a ratio of 0.265 c solvent per gram of powder.
- the mixture was chilled, passed through a 0.635 mesh screen again, tumbled, then allowed to sit at 18°C for 16 hours and was re- tumbled.
- a 10 cm diameter pellet was formed in a cylinder at 200 psi and then extruded through a .203 x 15.2 cm die at a ram rate of 100 cm/min.
- the extruded tape was allowed to air dry in ambient conditions overnight.
- a piece of the dried extrudate was cut and measured to be 15.2 cm long, 14.0 cm wide, and 0.0206 cm thick.
- the piece was placed in a convection oven at 165°C for 6 minutes to puff the material.
- the piece measured to be 39.8 cm long, 27.8 cm wide, and 0.940 cm thick, thus showing growth in the length (x), width (y), and thickness (z) dimensions.
- the ratio of growth in the x direction was 2.6, in the y direction was 2.8, and in the z direction was 4.6.
- Comparative tensile properties of the before and after puffed materials were performed using ASTM D882 test method for the x and y dimensions, and ASTM D952 for the z dimension. All of the samples tested were of the same cut x and y dimensions, however, since the samples grew significantly in all dimensions when puffed, it was necessary to normalize the data to account for this growth in order to simulate the total strength gained by the entire sample.
- the puffed tensile value For the x-direction tensile measurements, the puffed tensile value must be multiplied by the ratio of y-direction growth in order to normalize the data ("normalizing ratio"). Conversely, for the y-direction tensile measurements the puffed tensile value must be multiplied by the ratio of x-direction growth in order to normalize the data. For the z-direction tensile measurements, the puffed tensile value must be multiplied by the product of the ratios of both the x and y direction growth in order to normalize the data. The following table shows the raw and normalized data for the tensile tests.
Abstract
Description
Claims
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EP93910768A EP0686169A1 (en) | 1993-02-26 | 1993-04-26 | Improved composition of expanded polytetrafluoroethylene and similar polymers and method for producing same |
AU41151/93A AU675220B2 (en) | 1993-02-26 | 1993-04-26 | Improved composition of expanded polytetrafluoroethylene and similar polymers and method for producing same |
JP6518929A JPH08507316A (en) | 1993-02-26 | 1993-04-26 | Improved composites of expanded polytetrafluoroethylene and similar polymers and methods of making the same |
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US08/023,642 US5429869A (en) | 1993-02-26 | 1993-02-26 | Composition of expanded polytetrafluoroethylene and similar polymers and method for producing same |
US08/023,642 | 1993-02-26 |
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EP (1) | EP0686169A1 (en) |
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Also Published As
Publication number | Publication date |
---|---|
AU4115193A (en) | 1994-09-14 |
EP0686169A1 (en) | 1995-12-13 |
JPH08507316A (en) | 1996-08-06 |
CA2155328A1 (en) | 1994-09-01 |
US5429869A (en) | 1995-07-04 |
AU675220B2 (en) | 1997-01-30 |
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