EP3408316A1

EP3408316A1 - Porous articles formed from polyparaxylylene and processes for forming the same

Info

Publication number: EP3408316A1
Application number: EP17706599.2A
Authority: EP
Inventors: Guy A. SBRIGLIA; Peter J. Walsh
Original assignee: WL Gore and Associates Inc
Current assignee: WL Gore and Associates Inc
Priority date: 2016-01-27
Filing date: 2017-01-23
Publication date: 2018-12-05
Also published as: CN108699263B; CN112239556B; AU2017212317A1; CA3005270A1; CN112239556A; KR20180104705A; WO2017132077A1; CN108699263A; JP2018538403A; CA3005270C; AU2017212317B2; JP6767487B2; KR102134982B1

Abstract

Polyparaxylylene (PPX) polymer films that can be expanded into porous articles that have a node and fibril microstructure are provided. The fibrils contain PPX polymer chains oriented with the fibril axis. The PPX polymer may contain one or more comonomer. PPX polymer articles may be formed by applying PPX to one or both sides of a substrate, such as by vapor deposition. The nominal thickness of the PPX polymer film(s) is less than about 50 microns. The PPX polymer film(s) may be removed from the substrate to form a free-standing PPX polymer film(s), which may then be stretched into a porous article.

Description

POROUS ARTICLES FORMED FROM POLYPARAXYLYLENE

AND PROCESSES FOR FORMING THE SAME

FIELD

[0001] The present invention relates generaiiy to polyparaxylylene, and more specifically to porous articles containing polyparaxylylene polymers where the articles have a node and fibril structure. A process for the formation of porous articles from polyparaxylylene polymers is also provided.

BACKGROUND

{0002] Polyparaxylylene (PPX) and its derivatives are well known in the art. Artides made from PPX possess physical properties such as resistance to chemical attack, resistance to gamma radiation, thermo-oxidative stability at elevated temperatures, biocompatibility, high dielectric strength, high mechanical strength, and excellent barrier properties. Because of the favorable attributes associated with it, PPX has been utilized as a monolithic coating or film in a variet of applications including thin film dielectrics, electrical insulation, chemical resistance, and barrier coatings.

[0003] Unfortunately, PPX polymers cannot be made into useful forms by conventional processing routes such as compression molding, extrusion, solvent casting, gel spinning, or sintering because there is no melt state or solution state. However, porous PPX articles have been made through the addition of porogens, by coating a porous scaffold composed of another polymer, and fay thermal exposure that causes degradation of the PPX polymer introducing localized holes. These approaches to creating porous microstructures limit the possible microstructures and/or degrade the physical properties of the porous PPX material.

(0004] Thus, there exists a need in the art for a process for making a PPX article and a PPX article that is porous and maintains the excellent physical properties of PPX. SUMMARY

(0005] One embodiment relates to a process for forming a porous

polyparaxyiylene article that includes (1) depositing a poiyparaxyiylene (PPX) polymer film on a first side and a second side of a substrate to form a PPX composite structure and (2) expanding the PPX composite structure to form a first porous PPX polymer article on the first side of the substrate and a second porous PPX polymer article on the second side of the substrate. Each of the porous PPX polymer articles have a node and fibril structure. In one embodiment, the process further includes removing at least one of the porous PPX polymer articles from the substrate. The PPX polymer films have a thickness less than about 50 microns. The PPX composite structure may be expanded at a temperature from about 80°C to about 450°C, or from 220°C to about 450°C. Polymer chains in the fibrils are oriented along a fibril axis. In at least one embodiment, PPX is deposited onto the first and second sides of the substrate by vapor deposition. The substrate is a substrate that is capable of substantia! deformation.

[00061 A second embodiment relates to a porous polyparaxyiylene (PPX) polymer article that includes (1) a substrate having a first side and a second side, (2) a first expanded PPX polymer film on the first side of the substrate, and (3) a second expanded PPX polymer film on the second side of the substrate, The porous PPX polyme article includes nodes and fibrils. The fibriis include polymer chains oriented along a fibril axis. In addition, the substrate may be an expanded

polytetrafSuoroethylene (ePTFE) membrane, a polytetrafluoroethylene (PTFE) tape, a PTFE membrane, an expanded po!ytetrafluorethylene (ePTFE) tape, poiyimide, polyamide-imide, silicon, glass, or zinc,

(0GG7J A third embodiment relates to a process for forming a porous polyparaxyiylene article that includes (1) forming a polyparaxyiylene (PPX) compostte article and (2) expanding the PPX composite article to form a porous PPX polymer article having a node and fibril structure. The composite article is formed by (1) depositing a first PPX polymer film on a first side of a substrate and (2) forming a second PPX polymer film on the second side of the substrate. The PPX polymer films have a thickness less than about 50 microns, in some embodiments, the first PPX polymer film has a microstructure that is different from the microstructure of th second PPX polymer film. In other embodiments, the microstructures of the first and second PPX polymer films are the same or substantially the same. BRIEF DESCRIPTION OF THE DRAWINGS

[0008] The accompanying drawings are included to provide a further understanding of the disclosure and are incorporated in and constitute a part of this specification, illustrate embodiments, and together with the description serve to explain the principles of the disclosure.

[0009] FIG. 1 is a scanning electron micrograph (SE ) of the surface of the non-expanded, non-porous polyparaxylylene-AF4 film of the Comparative Example taken at 5,000x magnification;

[Όθθΐβ] FiG. 2 is a scanning electron micrograph (SEM) of the cross-section of the non-expanded:, non-porous poiyparaxylylene-AF4 film of the Comparative Example taken at 5,000x magnification;

[00011] FIG. 3 is a scanning electron micrograph (SEM) of the surface of the expanded porous polyparaxylylene-AF4 membrane of Example 1 taken at 50,000x magnification where the machine direction (MD) is horizontal in accordance with one embodiment of the invention;

[6001.2] FIG. 4 is a scanning electron micrograph (SEM) of the cross-section of the expanded porous po!yparaxyiylene-AF4 sheet of Example 1 taken at 1 ,000x magnification in accordance with one embodiment of the invention;

[00013] FIG . 5 is a wide angle x-ray diffraction (WAXD) pattern of the non- expanded, non-porous polyparaxylylene~AF4 film of the Comparative Example;

[00014] FIG. 6 is wide angle x-ray diffraction (WAXD) pattern of the biaxially expanded porous polyparaxyiylene-AF4 membrane of Example 1 with the machine direction oriented in the vertical direction according to at feast one embodiment of the invention;

[00015] FIG. 7A is a scanning electron micrograph (SEM) of the surface of the expanded porous polyparaxy!yJene~AF4 article of Example 3 taken at 20,000x magnification in accordance with an embodiment of the invention;

[00016] FIG. 7B is a scanning electron micrograph (SEM) of the surface of the expanded porous expanded porous poiyparaxy!ylene-AF4 article of Example 3 taken at 5000x magnification according to at least one embodiment of the invention;

[10017] FIG. 8 is a scanning electron micrograph (SEM) of the surface of the expanded pofyparaxylylene-AF4 article of Example 6 taken at 20,000x magnification in accordance with an embodiment of the invention; [000183 F'G- 9 ^is a scanning electron micrograph (SEM) of the surface of the expanded pQiyparaxyly!ene-AF4 article of Example 9 taken at 45,000x magnification according to at least one embodiment of the invention;

[00019] FIG. 10 is a scanning electron micrograph (SEM) of the surface of the PPX-N membrane of Example 11 drawn to an extension ratio of 2,2 at an

engineering strain rate of 50 percent per second taken at 20,Q0Gx magnification in accordance with an embodiment of the invention;

[0ΟΘ2Θ] FIG. 11 is a scanning electron micrograph (SEM) of the PPX-N fine powder of Example 12 taken at 4,000x magnification according to at least one embodiment of the invention;

[00021] F!G. 12 is a differentia! scanning thermogram (DSC) of the non- expanded, non-porous PPX-AF4 membrane of the Comparative Example; and

[§0022] FIG. 13 is a differential scanning thermogram (DSC) of the expanded, porous PPX-AF4 membrane of Example 1 according to an embodiment of the invention;

[00023] FIG. 14 is a scanning electron micrograph (SEM) of the surface of the co-expanded PTFE/PPX-AF4 membrane of Example 14 taken at 40,000x

magnification according to at least one embodiment of the invention;

[00024] FIG , 15 is a scanning electron micrograph (SEM) of the cross-section of the co-expanded PTFE/PPX-AF4 membrane of Example 1 taken at 3000x magnification in accordance with one embodiment of the invention;

[00025] FIG. 16 is a scanning electron micrograph (SEM) of the cross-section of the expanded PTFE/PPX-AF4 composite article of Example 16 taken at 500x magnification in accordance with one embodiment of the invention; and

[00026] FIG. 17 is a scanning electron micrograph (SEM) of the cross-section of the expanded PTFE/PPX-AF4 composite article of Example 16 taken at 500x magnification according to an embodiment.

GLOSSARY

[9Θ027] As used herein, the term "PPX" refers to polyparaxylylene.

[00028) As used herein, the term "PPX polymer" is meant to include ail forms of PPX, including PPX-N, PPX-AF4, PPX-VT4, and combinations thereof.

[00029] The term "PPX polymer film" as used herein is meant to denote unexpended PPX polymer, either free-standing or on a substrate, (60030] The term "PPX polymer membrane" as used herein is meant to denote a PPX polymer film that has been expanded in one or more directions,

[60031] The term "PPX composite structure" as used herein is meant to describe a PPX polymer film that has been formed on one or both sides of a substrate,

[60032] As used herein, a porous PPX polymer article, is meant to denote an expanded PPX polymer film (e.g. , PPX polymer membrane), either free-standing or as a co-expanded PPX poiymer film/substrate or a co-expanded PPX polymer filrn/substrate/PPX. polymer film.

[00633] As used herein, the term "lubricant" is meant to describe a processing aid that includes, and in some embodiments, consists of, an incompressible fluid that is not a solvent for the polymer at processing conditions, The fluid-polymer surface interactions are such that it is possible to create a homogenous mixture.

100034] As used herein, the term "extension ratio" is meant to define strain as the final length divided by the original length.

[00035] As used herein, the term "node" is meant to describe the connection point of at least two fibrils.

100036] As used herein, the term "thin" is meant to describe a thickness of less than about 50 microns.

[00037] As used herein, the term "fibril axis" is meant to describe direction parallel to the long dimension of the fibril.

[60038] As used herein, the term "substantial deformation" is meant to describe a substrate that is capable of elongating in one or more direction without breaking.

DETAILED DESCRIPTION

[00039] Persons skilled in the art will readily appreciate that various aspects of the present disclosure can be realized by any number of methods and apparatus configured to perform the intended functions. It should also be noted that the accompanying drawing figures referred to herein are not necessarily drawn to scale, but may be exaggerated to illustrate various aspects of the present disclosure, and in that regard, the drawing figures should not be construed as limiting.

[0ΘΘ40] The present invention relates to poiyparaxyly!ene (PPX) poiymers that can be expanded into porous articles that have a node and fibril mtcrostructure. in at least one embodiment, the fibrils contain PPX polymer chains oriented with the fibril axis, Optionally, the PPX polymer may contain one or more comonomer. As used herein, the term "PPX polymer" is meant to include all forms of PPX, including PPX- N, PPX-AF4, PPX-VT4, and combinations thereof.

100041]: In forming a porous PPX polymer article, PPX may be applied to one or both sides of a substrate, such as by any conventional vapor deposition method. The substrate is not particularly limiting so iong as the substrate is dimensionaily stable and the PPX polymer film formed thereon can be removed from the substrate, if desired. Non-limiting examples of suitable substrates include a

polytetrafiuoroethytene (PTFE) tape or membrane, an expanded

polytetraftuorethylene (ePTFE) tape or membrane, poiyimide, polyamide-imide, silicon, glass, zinc, or any substrate that can withstand expansion temperatures above about 220°C. In exemplar embodiments, the substrate is capable of substantial deformation in one or more directions, such as a PTFE film or

membrane.

[00042] The PPX polymer film, either free-standing or formed on a substrate, may have a nominal thickness less than about 50 microns, in exemplary

embodiments, the PPX polymer film has a thickness from about 0.1 microns to about 50 microns, from about 0.1 microns to about 40 microns, from about 0.1 microns to about 30 microns, from about 0, 1 microns to about 20 microns, from about 0.1 microns to about 10 microns, from about 0, 1 microns to about 5 microns, from about 0, 1 microns to about 2 microns, or from about 0.1 microns to about 1 micron.

[00043] The ability to apply a thin PPX polymer film on one side of a substrate, for example a PTFE substrate, enables the formation of a composite structure containing two different polymer layers with two different microsiructures. Applying a PPX polymer ftlm to both sides of a substrate, such as a PTFE substrate, enables the formation of a composite structure containing three polymer layers (e.g. , a PPX polymer film on either side of the substrate) and potentially three different

microstructures. It is to be appreciated that the PPX polymer film on one side of the substrate may or may not have the same microstructure as the PPX polymer film on the opposing side of the substrate. If the PPX polymer films have different microstructures, the composite structure contains three different microstructures, If the PPX polymer films have the same microstructure (or substantiall the same microstructure such that the microstructures cannot be distinguished from each other), the composite structure contains two different microstructures. The difference between the first mi.cFOstructu.re, the second micro-structure, and the third microstructure can be measured by, for example, a difference in pore size (porosity), a difference in node and/or fibril geometry or size, and/or a difference in density, ft is to be appreciated thai the composite structure may include additional PPX polymer fllm(s) and/or substrate(s) and may therefore have more than three microstructures within the composite structure,

[60044] The PPX polymer film{s) may be removed from the substrate to form a free-standing PPX polymer fifm(s). The free-standing PPX polymer film may be stretched or expanded in one or more directions to form a porous PPX membrane. Alternatively, a PPX composite structure (e.g. , th PPX polymer fiim(s) on a substrate) may be co-expanded in one or more directions to form a porous PPX poiymer article (e.g. , co-expanded PTFE/PPX membrane or co-expanded PPX polymer film /PTFE/PPX polymer film). It is to be appreciated that even though the substrate and the PPX polymer fi!ni(s) are expanded together, the expanded PPX polymer may be removed from the expanded substrate to form a free standing expanded PPX poiymer membrane{s). The expanded PPX polymer membrane may be referred to herein as a porous PPX polymer article, it is to be noted that the expanded composite structure (e.g., the expanded PPX polymer film/expanded substrate or expanded PPX polymer film/expanded substrate/expanded PPX polymer film) may remain as a singie unit in some embodiments, in other embodiments, a PPX polymer film is deposited on one or both sides of a substrate and co-expanded into a PPX composite structure, after which one or both of the expanded PPX poiymer films Is removed.

]00045j lⁿ aⁿ alternate embodiment, a PPX polymer film(s) may be deposited onto a partially expanded substrate, such as a partiaiiy expanded PTFE tape o membrane. The PPX polymer fllm(s) and the partially expanded substrate may then be co-expanded. The expanded PPX poiymer film(s) may be removed from the expanded substrate to become a free-standing PPX expanded poiymer membrane or porous PPX article.

[00046] The PPX polymer film (with or without an expandable substrate) may be cut into suitable sizes for expansion. Expansion of the free-standing PPX polymer film(s) occur at a temperature from about 80°C to about 220°C or from about 22Q°C to about 290°C or from about 290°C to about 450°C. Expansion of a composite structure of a PPX poiymer fs!m/PTFE substrate or PPX polymer fflm/PTFE substrate/PPX polymer film may occur at temperatures from about 80°C to about 220X, from about 220°C to about 340X, or from about 290X to about 340°C (i.e., below the melt temperature of the PTFE substrate). It is to be noted that the maximum temperature for expanding any composite structure described herein is the temperature at which the substrate degrades or melts. Expansion may be conducted at engineering strain rates (ESR) up to 10,000%/second, or from 1% to 10,000%/ second or from 10% to 5000%/second to form an expanded, porous PPX article.

f00047j The expanded PPX membrane has a microstructure of nodes interconnected by fibrils, optionally with regions of unexpanded PPX, such as may be seen in FIGS.3, 4, 7, 8, 9 and 10. FIGS. 4 and 78, fo example, show expanded regions 40 and unexpanded regions 50 in the expanded PPX membranes. The microporous structure and the geometry of the interconnected fibrils can be controlled by the deposition conditions, the rate of expansion, temperature of expansion, and ultimate expansion ratio in each direction.

[00048] Looking at FIG. 5, a wide angle x-ray diffraction (WAXD) pattern consistent with highly crystalline, randomly oriented lamella of the unexpanded or as-deposited PPX sample is depicted. In contrast, the WAXD pattern of an expanded PPX article oriented with the larger expansion in the vertical direction is depicted in FIG. 8, which shows a new diffraction peak at reference numeral 30. This WAXD pattern shows an emergence of two additional equatorial reflections (at 3 o'clock and 9 o^'clock) in a d-spacing of about 0.45 nm and two distinct meridonal reflections (at 12 o'clock and 6 o'clock) in a d-spacing of about 0.32 nm. These reflections are associated with oriented polymer chains in the fibrils in the expanded PPX article. In other words, the polymer chains in the fibrils are oriented along the fibril axis. As would be understood by one of ordinary skill in the art, with a more balanced biaxial expansion, the expanded PPX article would display a WAXD pattern illustrating an additional signal at the 0.45 nm d-spacing, which may show up as additional diffraction spots or a concentric ring.

[00049] Additionally, the expanded PPX articles are porous, and may have a percent porosity of at least about .5%, at least about 10%, at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, ai least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, or up to (and: including) 90%. In exemplary embodiments, the expanded PPX articles may have a percent porosity from about 5% to about 75%, from about 10% to about 50%, or from about 10% to about 25%.

[00050] In an alternate embodiment, a porous PPX article may be formed from a crystalline PPX polymer in the form of a powder. In at least one embodiment, PPX polymer and a lubricant are mixed so as to uniformly or substantially uniformly distribute the lubricant in the mixture. It is to be appreciated that the term lubricant", as used herein, is meant to describe a processing aid that is an incompressible fluid that is not a solvent for the polymer at the process conditions, The fluid-polymer surface Interactions are such that it is possible to create a homogenous mixture, it is also to be noted that that choice of lubricant is not particularly limiting and the selection of lubricant is largely a matter of safety and convenience. Non-limiting examples of lubricants for use herein include light mineral oil, aliphatic

hydrocarbons, aromatic hydrocarbons, haiogenafed hydrocarbons, and the like, and may be selected according to fiammabiiity, evaporation rate, and economic considerations.

[90051] It is to be appreciated that various times and mixing methods may be used to distribute the PPX polymer in the mixture. For example, for PPX-AF4, the lubricated PPX polymer is heated to a temperature about 80°C to about 22Q°C or from about 220°C to about 290°C or from about 29G°C to about 450"C. For those PPX variants that are subject to thermal decomposition and oxidation, such as PPX- N and PPX-VT4, the lubricated PPX polymer is heated to at a temperature from about 220°C and below the temperature at which the polymer would decompose during processing, and in exemplar embodiments, from about 220°C to about 250°C {in an inert atmosphere). Along with the heating of the PPX polymer, sufficient pressure and shear is applied so as to form inter-particle connections and create a solid form. Non-limiting examples of methods of applying pressure and shear include ram extrusion (ø,<?., typically called paste extrusion or paste

processing when lubricant is present) and calendering.

[09052] In one exemplary embodiment, the lubricated PPX polymer is calendered or ram extruded to produce a cohesive sheet that may be used as a preform. As used herein, the term "cohesive" is meant to describe a sheet that is sufficiently strong for further processing. For PPX-AF4, the calendering or ram extrusion occurs at a temperature about 80°C to about 220X or from about 220°C to about 290°C or from about 290^eC to about 450°C, For PPX-N and PPX-VT4, the calendering or ram extrusion occurs from about 220°^'C and below the temperature at which the polymer would decompose during processing, and in exemplary embodiments, from about 220°C to about 250°C (in an inert atmosphere), In at least one other embodiment, the lubricated PPX polymer may be ram extruded to produce a cohesive sheet, tube, or cylinde preform, in either calendering or ram extruding, the PPX polymer preform may be subsequently expanded as described above to form a porous PPX polymer article.

TEST METHODS

[00053]; It should be understood that although certain methods and equipment are described below, other methods or equipment determined suitable by one of ordinary skill in the art may be alternatively utilized,

SBM Sample Preparation Method

[00054] SElvl images were collected using an Hitachi SU8000 FE Ultra High Resolution Scanning Electron Microscope with Dual SE detectors. Cross-sectioned samples were prepared using a Cooled straight-razor blade method. Surface and cross-sectioned samples were mounted onto a 25 mm diameter mefai stub with a 25 mm carbon double sided adhesive. The mounted samples were sputter coated with platinum.

W de Angle X-ray Diffraction (WAXD)

[Θ0055| Diffraction patterns from as-deposited and expanded films were collected using a Molecular Metrology instrument configured for 2-D WAXD observations. The X-Ray source was a Rigaku icro^'Max Sealed Micro Source CuKa element with a wavelength of 0.1542 nm running at 45 kV/66 mA. To collect two- dimensional diffraction information at wide angles a 20 cm x 20 cm Fujifiim BAS SR2040 imaging plate was placed in the instrument vacuum chamber perpendicular to the X-Ray beam line at a camera length of 146 mm. Camera length was calibrated by collecting a WAXD pattern from a tricosane standard and calculating the camera length from the 110 reflection at q of 15.197 nm^" or d =0.4134 nm. Films approximately 10 pm thick were placed on a motorized stage and aligned perpendicular to the beam line. The vacuum chamber was then sealed and evacuated to 500 mTorr below atmospheric pressure and the beam shutter opened. Diffraction patterns were collected at ambient temperature for a period of 1-6 hours depending on the thickness and scattering intensity of the film sample. The diffraction data were collected from the Fujifi!m BAS SR204Q image plates using a General Electric Typhoon FLA7000 image piate reader. Diffraction pattern images were saved as grayscale TIFF files and subsequently analyzed using POLAR analysts software.

Powder X-ray Diffraction

[00056] Diffraction patterns from calendered PPX powder were collected using a Bruker Discovery D-8 instrument. The X-Ray source was CuKa element with a wavelength of 0.1542 nm running at 40 kV/60 mA. The instrument was configured in a Srentano-Bragg geometry. Diffraction intensity was measured using a OD scintillation counter rotating at 0.0.2 degree 2-theta increments for a one second duration. The range of 2-theta was 10 degrees to 45 degrees. The instrument was calibrated using a polycrystaine silicon and an automated interna! calibration algorithm. A PPX polymer was placed on the Bruker Discovery D-8 stage and aligned with the beam line.

Gurley Flow

[00057] The Gurle air flow test measures the time in seconds for 100 cm³ of air to flow through a 6.45 cm² aperture at 12.4 cm of water pressure. If the sample size was smaller than 6.45 cm² an aperture of 0.645 cm² was used and the time observed divided by a factor of 10 to normalize observations made with both apertures. The samples were measured in a Gurley Densometer Model 4110 Automatic Densometer equipped with a Gurley Model 4320 automated digital timer. The reported results are the average of multiple (3-5) measurements.

DSC Measurements

[00058] DSC data were coilected using a TA Instruments Q2000 DSC between 0°C and 425°C using a heating and a cooling rate of 10 °G/min. The expanded porous membrane samples and the solid film samples were prepared by punching out .4 mm disks. The 4 mm disk was placed flat n the pan and the ltd was crimped to sandwich the disk between the pan and lid. EXAMPLES

Comparative Example

[00059] A film of PPX-AF4 having a nominal thickness of 10 pm was deposited onto a blended, extruded, and dried PTFE tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive,

Indianapolis, IN 46278).

[00060 j The coated article was then cut to dimensions of 200 mm x 200 mm and placed i the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 35Q°C for 300 seconds. The heat treated article was aiowed to cool to room temperature under restraint of the pantograph biaxial expander grips. After cooling, the article was removed from the expander grips, the PPX-AF4 film was removed from the melted PTFE carrier tape to yield a free-standing, non-expanded, non- porous film of PPX-AF4.

[00061] A scanning electron micrograph (SE ) of the surface and cross- section of the non-expanded, non-porous PPX-AF4 film are shown in FIGS, 1 and 2, respectively. A wide angle x-ray diffraction (WAXD) pattern of the PPX-AF4 film is shown in FIG. 5. A differential scanning thermogram (DSC) of the PPX-AF4 film is shown in FIG. 12, As shown in FIG, 12, the non-expanded, non-porous PPX-AF4 film, on cooling, exhibits a single exothermic peak at approximately 3S0°C. A Gurley number of the non-expanded, non-porous PPX AF4 film was determined to be greater than 3600 seconds and is reported in Table 1.

Example 1

[00062] A film of PPX-AF4 having a nominal thickness of 10 pm was deposited onto a blended, extruded, and dried PTFE tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a

commercially available vapor depositio process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, I 46278).

[00063] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 350°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 100 percent/second to an extension ratio in the tape machine direction of 1:1 and 4:1 in the tape transverse direction. The expanded article was allowed to coo! to room temperature under restraint of the pantograph biaxial expander grips. After cooling, the article was removed from the expander grips and a film of porous PPX-AF4 was removed from the melted PTFE tape to yield a free-standing porous membrane of PPX-AF4.

[006643 Scanning electron micrographs (SEI Is) of the surface and the cross* section of the expanded porous PPX-AF4 membrane are shown in FIGS. 3 and 4, respectively. A wide angle x-ray diffraction (WAXD) pattern of the expanded porous PPX-AF4 membrane is shown in FIG. 6. A differential scanning: thermogram (DSC) of the expanded , porous PPX-AF4 membrane is shown in FIG. 13. As shown in FIG. 13, the free-standing expanded, porous PPX-AF4 membrane, on cooling, exhibits two exothermic peaks, namely a first peak at 378.8°C and the second peak at 401 ,36°C. The second peak Is associated with the fibrils of the porous

membrane. A Gurley number of the expanded PPX-AF4 membrane was determined to be 127.5 seconds and is reported in Table 1.

Example 2

[00065] A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto a blended, extruded, and dried poiytetrafiuoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953.566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[000661 T e coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 7 percenf second to an extension ratio in the extrudate machine direction of 4: 1 and 4: 1 in the extrudafe transverse direction. The expanded PPX-AF4 article was removed from the oven, and aliowed to cool to room temperature under restraint of the biaxial batch expander grips.. After cooling the expanded PPX-AF4 article {i.e., co-expanded PTFE PPX-AF4 membrane) was removed from the grips. A.Guriey number of the expanded PPX-AF4 article was determined to be 68.38 and is reported in Table 1.

Example 3

100667] A film of PPX-AF4 having a nominal thickness of S pm was deposited onto a blended, extruded, and dried poiytetrafluoroethyiene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,568 to Gore by a commercially available vapor deposition process (Specialt Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278). The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ES ) of 70

percent second to an extension ratio in the extrudate machine direction of 4:1 and 4:1 in the extrudate transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to cool to room temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article (i.e. , co-expanded PTFE/PPX-AF4 membrane) was removed from the grips.

j 0068] A scanning electron micrograph (SE ) of the surface of the expanded PPX-AF4 membrane taken at 20,000x magnification is shown in FIG. 7A, A representative node is depicted by reference numeral 10 and a representative fibril is depicted by reference numeral 20. F!G. 7B is an SEM of the surface of the expanded PPX-AF4 membrane taken at SOOOx magnification depicting therein an expanded region 40 and an unexpanded region 50. A Gurley number of the expanded PPX-AF4 article was determined to be 89.1 seconds and is reported in Table 1.

Exam le 4

[06069] A film of PPX-AF4 having a nominal thickness of 5 um was deposited onto a b!ended, extruded, and dried poiytetrafluoroethyiene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No, 3,953,566 to Gore by a commercially available vapor deposition process {Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00070] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 700 percent/second to an extension ratio in the extrudate machine direction of 4:1 and 4:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and owed to cool to room temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article {i.e., co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. A Gurley number of the expanded PPX-AF4 article was determined to be 111.7 seconds and is reported in Table 1.

Example 5

[00071] A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto a blended, extruded, and dried po!ytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00072] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds, The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 7 percent second to an extension ratio in the extrudate machine direction of 6:1 and 6:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to coo! to room temperature under restraint of the pantograph biaxial expander grips. After cooling, the expanded PPX-AF4 article (i.e. , co-expanded PTFE/PPX-AF4 membrane) was removed from the expander grips. A Gurley number of the expanded PPX-AF4 article was determined to be 60.92 seconds and is reported in Table 1. Example 8

[00973] A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto blended, extruded, and dried polytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process {Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00074] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 70 percent/second to an extension ratio in the tape machine direction of 6:1 and 6:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to cool to room

temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article (i.e., co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. A Gurley number of the expanded PPX-AF4 article was determined to be 54.36 seconds and is reported in Table 1.

Example 7

[00075] A film of PPX-AF4 having a nominal thickness of 5pm was deposited onto a blended, extruded, and dried polytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process {Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00076] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 300°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 700 percent/second to an extension ratio in the extrudate tape machine direction of 6:1 and 6:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to cool to room temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article {i.e., co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. A Guriey number of the expanded PPX-AF4 article was determined to be 85,06 and is reported in Table 1.

Example 8

[ 0Θ77] A film of PPX-AF4 having a nominal thickness of 5 μηι was deposited onto blended, extruded, and dried poiytetrafluoroethyiene (PTFE) tape made generally in accordance wit the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00078} The coated article was then cut to dimensions of 200 mm x 200 mm and placed i the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 250°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 7 percent/second to an extension ratio in the tape machine direction of 4:1 and 4:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to cool to room

temperature under restraint of the biaxiai batch expander grips. After cooling, the expanded PPX-AF4 article (/.&, co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. A Guriey number of the expanded PPX-AF4 article was determined to be 109.0 seconds and is reported in Table 1.

Example 9

[00079] A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto a blended, extruded, and dried poiytetrafluoroethyiene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[09080] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 250°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 70 percent second to an extension ratio in the tape machine direction of 6: 1 and 6:1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to coo! to room

temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article {i.e. , co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. FIG. 9 is a scanning electron micrograph (SEM) of the surface of the expanded PPX-AF4 article of taken at 45,00Qx magnification showing a fibriilated region. A Gurley number of the expanded PPX-AF4 article was determined to be 03.26 seconds and is reported in Table 1.

Example 10

|00081 | A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto a blended, extruded, and dried pofytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN, 46278).

{00082] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 250°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 700 percent/second to an extension ratio in the tape machine direction of 6:1 and 6: 1 in the tape transverse direction. The expanded PPX-AF4 article was removed from the oven and allowed to cool to room

temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PPX-AF4 article (i.e., co-expanded PTFE/PPX-AF4 membrane) was removed from the grips. A Gurley number of the expanded PPX-AF4 article was determined to be 1 19.3 seconds and is reported in Table 1.

Table 1

Example 11

[00083] A film of PPX-N having a nominal thickness of 10 pro was deposited onto a blended, extruded, and dried polytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process {.Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278).

[00084] The coated article was then cut into a 35 rnm x 13 mm rectangle with the samples long dimension aligned with the ExampSe 1 tape machine direction (MD) direction. The rectangular sample was drawn to an extension ratio of 2.2 at an engineering strain rate (ESR) of 50 percent per second in a RSA 3 Dynamic

Mechanical Analyzer (DMA), the gauge length was 10 mm, TA Instruments,

Newcastle, DE using the standard TA film grips. The atmosphere in the DMA oven was a continuous purge of nitrogen gas. Oven temperature was set to 290°C and the film sample was heat soaked for 300 seconds. A scanning electron micrograph (SEM) of the surface of the PPX-N membrane taken at 20,000x magnification is shown in FIG. 10,

Example 12

|6 085] Approximately 1000 grams of anhydrous p-xylene was charged into 2 liter round bottom flask with a magnetic stirrer at room temperature. Approximately 16 grams of potassium t-butoxide was added to the reaction flask. The flask was heated to 90°C. When all of the potassium t-butoxide was dissolved, 15 grams of alpha-ch!oro p-xylene was added the flask. The mixture immediately turned yellow. The reaction mixture was then heated to reflux at approximately 135°C. After 30 minutes, 5.7 grams of the alpha chloro p-xylene dissolved in approximately 87 grams of p-xyiene was added dropwise to the reaction mixture over 40 minutes. The reaction mixture was allowed to stir for approximately 16 hours. The solution was a cloudy suspension. The solution was cooled and then vacuum filtered to remove the xylene. The resulting product was dispersed into 2 liters of a 50/50 IP A/water mixture and filtered again. This was done two times. The product was allowed to dr overnight. The dried product was then mixed into an IPA/water mixture, boiled, and filtered 2 more times. The product was allowed to dry in a hood overnight. Final drying was done at 120°C for 4 hours in a vacuum oven. The final product was a PPX-N powder. FIG. 11 is a scanning electron micrograph (SEM) of the PPX-N powder taken at 4,G00x magnification.

Exam pie 13

100086] The PPX-N powder of Example 12 was lubricated with mineral oil and calendered at 150°C to form a thin PPX-N sheet about 0,5 mm thick.

Example 14

[09687] A film of PPX-AF4 having a nominal thickness of 10 pm was deposited onto a blended, extruded, and dried polytetrafiuoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,568 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278). [00088] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated article was heat soaked at a constant temperature of 300^CC for 300 seconds. The coated article was then simultaneously stretched at an engineering strain rate (ESR) of 100 percent/second to an extension ratio of 2:1 in both the extrudate machine and transverse directions. The expanded PPX-AF4 article was removed from the oven, and allowed to cool to room temperature under restraint of the biaxial batch expander grips. After cooling, the co-expanded

PTFE/PPX-AF4 membrane was removed from the grips. A scanning electron micrograph (SEM) of a surface of the above co-expanded PTFE/PPX-AF4 membrane taken at 40,000x magnification is shown in FIG.. 14. FIG. 15 shows a scanning electron micrograph (SEW) of the cross-section of the above co-expanded PTFE/PPX-AF4 membrane taken at 3000x magnification. FIG. 15 illustrates a first tight microstructure (60) and a second open mierostructure (70) of the above composite structure. Gurley number of the expanded PPX-AF4 article was determined to be 407.7 seconds.

Example 15

[00089] A film of PPX-AF4 having a nominal thickness of 5 pm was deposited onto the external surfaces of a blended, extruded, and dried poiytetrafluoroethylene (PTFE) tape made generally in accordance with the teachings of U.S. Patent No. 3,953,566 to Gore by a commercially available vapor deposition process (Specialty Coating Systems, 7645 Woodland Drive, Indianapolis, IN 46278,

[00090] The coated article was then cut to dimensions of 200 mm x 200 mm and placed in the grips of a pantograph type biaxial batch expander equipped with a convection oven. The coated tape was heat soaked at a constant temperature of 335°C for 300 seconds. The coated tape was then simultaneously stretched at an engineering strain rate (ESR) of 10 percent second to an extension ratio in the extrudate machine direction of 2: 1 and 2: 1 in the extrudate transverse direction. The article was then heat soaked at a constant temperature of Z Q°C for 30 seconds. The expanded PTFE/PPX-AF4 composite article was formed of a first layer of expanded PPX-AF4, a layer of expanded PTFE, and a second layer of expanded PPX-AF4. The expanded PTFE/PPX-AF4 composite article was removed from the oven and allowed to cool to room temperature under restraint of the biaxial batch expander grips. After cooling, the expanded PTFE/PPX-AF4 composite article (i.e., co-expanded PTFE/PPX-AF4 film) was removed from the grips.

[00091] FIG, 16 shows a scanning electron micrograph (SEW) of the cross- section of the co-expanded PTFE/PPX-AF4 composite article taken at 5Q0x magnification. FIG, 16 illustrates the first tight microstructure (80) (first expanded PPX-AF4 film), the open microstructure (90) (ePTFE membrane), and the second tight microstructure (100) (second expanded PPX-AF4 film) of the expanded composite article on a carbon tape SEM mount (110). The Gurley number of the expanded PPX-AF4 polymer article was determined to be 137.5 seconds,

Example 18

[00092] A layer of PPX-AF4 was removed from one side of the co-expanded PPX-AF4 article of Example 15 to form an expanded PTFE/PPX-AF4 composite article formed of a layer of expanded PPX-AF4 and a layer of expanded PTFE (having a tight/open microstructure).

[00093} FIG, 17 shows a scanning electron micrograph (SEM) of the cross- section of the co-expanded PTFE/PPX-AF4 composite article taken at 500x magnification, FIG. 17 illustrates the tight microstructure of the expanded PPX-AF4 film (120) and the open microstructure of the ePTFE (130). The Gurley number of the porous PTFE/PPX-AF4 composite article was determined to be 79.0 seconds.

[90094] The invention of this application has been described above both generieally and with regard to specific embodiments, it will be apparent to those skilled in the art that various modifications and variations can be made in the embodiments without departing from the scope of the disclosure, Thus, it is intended that the embodiments cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.

Claims

WHAT IS CLAIMED IS:

1. A process for forming a porous po!yparaxyiylene articie comprising:

depositing a polyparaxyiy!ene (PPX) film on a first side and a second side of a substrate to form a PPX composite structure; and

expanding said PPX composite structure to form a first porous PPX polymer articie on said first side and a second porous PPX polymer articie on said second side, each said porous PPX polymer articie having a node and fibrii structure.

2. The process of claim 1 , further comprising removing at least one of said first porous PPX polymer articie and said second porous PPX polymer article from said substrate.

3. The process of claim 1 , wherein said PPX film has a thickness less than about 50 microns.

4. The process of claim 1 , wherein said expanding of said PPX composite structure occurs at a temperature from about 80°C to about 450°C.

5. The process of claim 1 , wherein said expanding of said PPX composite structure occurs at a temperature from: about 220^QC to about 450°C.

6. The process of claim 1 , wherein said fibrils comprise polymer chains and said polymer chains are oriented along a fibril axis.

7. The process of claim 1 , wherein said depositing comprises vapor depositing said poiyparaxyfylene onto said first side and said second side of said substrate.

8 The process of claim 1 , wherein said substrate comprises a deformable substrate.

9. The process of claim 8, wherein said substrate is a member selected from the group consisting of a polytetraf!uoroethy!ene (PTFE) tape and a PTFE membrane.

10. The process of claim 9, wherein said expanding of said PPX composite structure occurs at temperatures from about 80°C to about 45G°G.

11. The process of claim 10, wherein said expanding of said PPX composite structure occurs at temperatures from about 220°C. to about 450°C.

12. A porous poiyparaxylylene (PPX) polymer article comprising;

a substrate having a first side and a second side;

a first expanded PPX polymer film: on said first side of said substrate; and a second expanded PPX polymer film on said second side of said substrate, wherein said porous PPX polymer article comprises nodes and fibrils,

13. The PPX polymer article of claim 12, wherein said first and second expanded PPX polymer films have a thickness less than about 50 microns.

14. The PPX polymer article of claim 12, wherein said substrate comprises a deformab!e substrate.

15. The PPX polymer article of claim 12, wherein substrate comprises a member seiected from the group consisting of an expanded polytetrafluoroethylene (ePTFE) membrane, a polytetrafiuoroethylene (PTFE) tape, a PTFE membrane, an expanded pofytetrafiuorethyiene (ePTFE) tape, polyimide, polyamide-imide, silicon, glass and zinc.

16. The PPX polymer article of claim 12, wherein said fibrils comprise polymer chains and said polymer chains are oriented along a fibril axis.

17. The PPX polymer article of claim 12, wherein said PPX polymer film contains one or more comonomer.

18. A process for forming a porous poiyparaxylylene article comprising:

forming a poiyparaxylylene (PPX) composite article by: depositing a first poiyparaxyiyiene (PPX) film on a first side of a substrate; and

depositing a second PPX film on a second side of said substrate; and expanding said PPX composite article to form a porous PPX polymer article having a node and fibril structure.

1.9. The process of claim 18, wherein said first and second PPX films have a thickness less than about 50 microns,

20. The process of claim 18, wherein said first PPX film has a first microstructure and said second PPX film has a second microstructure and said first microstructure is different from said second microstructure,

21. The process of claim 18, wherein said first PPX film has a first microstructure and said second PPX fiim; has a second microstructure and said first microstructure is substantially the same as said second microstructure,