WO2006127946A2 - Multi-functional coatings on microporous substrates - Google Patents

Multi-functional coatings on microporous substrates Download PDF

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Publication number
WO2006127946A2
WO2006127946A2 PCT/US2006/020322 US2006020322W WO2006127946A2 WO 2006127946 A2 WO2006127946 A2 WO 2006127946A2 US 2006020322 W US2006020322 W US 2006020322W WO 2006127946 A2 WO2006127946 A2 WO 2006127946A2
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WO
WIPO (PCT)
Prior art keywords
composite
functional additive
microporous
coating
functional
Prior art date
Application number
PCT/US2006/020322
Other languages
French (fr)
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WO2006127946A3 (en
Inventor
Donald Freese
Manish K. Nandi
Original Assignee
Gore Enterprise Holdings, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gore Enterprise Holdings, Inc. filed Critical Gore Enterprise Holdings, Inc.
Priority to PL06760389T priority Critical patent/PL1885476T3/en
Priority to CA2609519A priority patent/CA2609519C/en
Priority to EP06760389.4A priority patent/EP1885476B1/en
Priority to KR1020077029969A priority patent/KR101393173B1/en
Priority to JP2008513728A priority patent/JP5307536B2/en
Publication of WO2006127946A2 publication Critical patent/WO2006127946A2/en
Publication of WO2006127946A3 publication Critical patent/WO2006127946A3/en
Priority to NO20076525A priority patent/NO341096B1/en
Priority to HK08102372.6A priority patent/HK1108852A1/en

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Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D67/00—Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
    • B01D67/0081—After-treatment of organic or inorganic membranes
    • B01D67/0088—Physical treatment with compounds, e.g. swelling, coating or impregnation
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/02—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D69/00—Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor
    • B01D69/14—Dynamic membranes
    • B01D69/141—Heterogeneous membranes, e.g. containing dispersed material; Mixed matrix membranes
    • B01D69/1411—Heterogeneous membranes, e.g. containing dispersed material; Mixed matrix membranes containing dispersed material in a continuous matrix
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D71/00—Semi-permeable membranes for separation processes or apparatus characterised by the material; Manufacturing processes specially adapted therefor
    • B01D71/06—Organic material
    • B01D71/30—Polyalkenyl halides
    • B01D71/32—Polyalkenyl halides containing fluorine atoms
    • B01D71/36—Polytetrafluoroethene

Definitions

  • the present invention relates to microporous substrates having a multifunctional coating thereon.
  • Coated microporous substrates are used in many applications to take advantage of the properties of the microporous substrate while also taking advantage of the functionality of the coating material for a variety of applications.
  • Substrates of particular interest are polytetrafluoroethylene (“PTFE”) and microporous polytetrafluoroethylene. Due to the inherent hydrophobicity of PTFE, membranes of these materials are of particular interest when in the form of repellant products such as rainwear. Expanded microporous, liquid waterproof polytetrafluoroethylene materials, such as those available from W. L. Gore and Associates, Inc., sold under the trademark GORE-TEX®, as well as expanded PTFE products available from other suppliers, are especially well suited for this purpose. The expanded PTFE materials are liquid waterproof, but allow water vapor, such as perspiration, to pass through. Polyurethanes and other polymers have been used for this purpose also.
  • U.S. Patent No. 4,194,041 describes the use of an additional coating on microporous polymers which is based on a thin, air-impermeable coating composed of a polyetherpolyurethane or polyperfluorosulfonic acid that transports water vapor molecules by diffusion.
  • the thin coating completely fills at least a portion of the pores in the microporous structure.
  • the thin coating is employed to reduce transmission of surface active agents and contaminating substances through the polymers. Owing to the chemical structure of the polymer, this monolithic coating on the microporous structure exhibits a high transport of water molecules, (high permeability to water vapor) through the polymeric material.
  • Suitable coatings for microporous low surface energy materials are described in the art, many of which rely on solvents to wet the desired substrate.
  • EP 0581168 Mitsubishi describes the use of perfluoroalkyl methacrylates and perfluoroalkylethyl acrylates to coat porous polyethylene and polypropylene membranes where the coated substances are held in physical contact with the surface of the polyolefin porous membrane.
  • the fluorinated monomer or fluorinated monomer and a crosslinking monomer together with a polymerization initiator are dissolved in a suitable solvent to produce a solution.
  • this solution typically may comprise about 15% wt. monomer and 85% wt. acetone.
  • This solvent solution is coated onto the porous substrate. After coating, the solvent is vaporized off.
  • U.S. Patent No. 6,228,477 teaches a means to coat a low surface energy, microporous PTFE substrate with an otherwise non-wetting, aqueous fluoropolymer dispersion through the use of significant percentages of isopropanol ("IPA").
  • IPA isopropanol
  • U.S. Patent No. 5,460,872 to Wu et. al. teaches the use of fluorinated surfactants to lower the surface energy and contact angle with microporous PTFE as a means to produce a uniformly coated microporous PTFE substrate.
  • Perfluoropolyethers in conjunction with ePTFE for use as water-repellent finish are mentioned in WO 92/21715.
  • U. S. Patent No. 6,676,993 teaches a process that uses a mixture of isopropanol and water to wet microporous ePTFE substrates and when specific fluoroacrylates are dispersed in this solvent-laden solution, it can be used to coating to the ePTFE surfaces it wets.
  • microporous substrate coating technologies have focused on depositing a single homogenous material on the microstructure of the microporous substrate.
  • Solvent wetting systems and aqueous wetting systems have not been compatible with a range of additives or multiple additives.
  • these wetting systems have been compatible with isolated, unique oleophobic monomer, polymers or emulsions.
  • a need has existed for added flexibility in coating technology to provide two or more functionalities in a single conformal coating on a low surface energy microporous substrate without occluding the micropores of the substrate.
  • the present invention overcomes the limitation of the prior art by providing a single conformal coating on a microporous substrate, such as a low surface energy microporous substrate, which provides multiple functionalities to the underlying microporous material, while still maintaining porosity within at least a portion of the microporous substrate.
  • Fig. 1 is a schematic sectional view of a coated microporous polymer layer.
  • Fig. 2 is a schematic angled cross-sectional view of a coated fibril of a coated, expanded polytetrafluoroethylene membrane.
  • Fig. 3 is a schematic full cross-sectional view of a coated fibril of a coated, expanded polytetrafluoroethylene membrane.
  • a microporous coated substrate is produced wherein the coating contains two or more functionalities.
  • the multifunctional coating includes at least two additives and each additive provides at least one functionality.
  • the first additive may form a film around, encompass or otherwise bind the second additive to the microporous structure.
  • the first additive provides some functionality to the composite, such as hydrophobicity, hydrophilicity, etc., and the second additive provides some further functionality to the composite.
  • the multi-functional coating combines a first functional additive such as but not limited to surface energy modifying (e.g., lowering, etc.) polymeric binders with additional functional additives wherein the resulting multi-functional coating exists on the pore surfaces of the microporous substrate.
  • the term "functional additive" is intended to refer to any additional material which renders further functionality to the coated microporous substrate than what otherwise exists in the absence of the functional additive, such as by changing the chemical, physical or mechanical properties of the microporous substrate.
  • One class of polymeric binders of this invention are fluoropolymer binders since they can be used to alter the surface energy or wetting characteristics of the otherwise inherently hydrophobic expanded PTFE substrate.
  • additional functional additives can be included in the polymeric binder mix so that the resultant coated microporous substrate exhibits both a surface energy change due to the fluoropolymer binder but also a second functional change due to the additional functional additive.
  • binders While surface energy altering polymeric binders are of particular interest in this invention, other embodiments encompass incorporating a non-polymeric binder.
  • the multi-functionality results from the incorporation of more than one functional additive onto the surfaces of the microporous substrate, where at least one of the functional additives also acts as a binder.
  • binder refers to a material which adheres or otherwise attaches to at least a portion of the underlying microporous structure and assists in retention of the second functional component.
  • the multi-functional coatings of this invention can be applied to the microporous substrate by any means which produces the desired coating uniformity on the surfaces of the microstructure and preferably does not occlude the pores of the microporous substrate.
  • One aspect of this invention dissolves the functional polymeric binder in an organic solvent into which the additional functional additives, such as particles are added.
  • the organic solvent selected must be capable of wetting the microporous substrate surface.
  • This multi-functional-additive, solvent mix is then coated onto the microporous substrate and the solvent vaporized.
  • the functional polymeric binder and the functional additive particles contained therein are deposited onto substrate surface in order to create a desired effect.
  • Examples of functions that can be provided in such a multi-functional coating include, but are not limited to, color change in the case of a pigment, or hydrophilicity change in the case of pH sensitive materials, and infrared reflectivity changes in the case of infrared absorbing materials. Carbon particles are of particular interest in applications where a change in an electromagnetic spectral response or electric or thermal conductivity of the substrate is desired.
  • a critical aspect of this invention is that the resultant microporous substrate must exhibit multiple functionalities such as that of the surface energy altering polymeric binder and a change in spectral, electromagnetic, or thermal response.
  • the coating mix must be able to wet the substrate to which it is applied.
  • the coating mix typically should have a surface tension around 30 dynes/cm or less.
  • a multi-functional coating can be produced using an aqueous wetting system.
  • a polymeric binder and a second functional additive are stabilized in an aqueous wetting system which is then coated onto the desired microporous substrate.
  • An aqueous wetting system containing a water insoluble alcohol (e.g., C 5 -C 10 linear backbone) emulsified by a surfactant is one suitable system.
  • the surfactant or surfactants can be selected to be compatible with the additives and any surfactants that may be used to stabilize the additives.
  • the water is vaporized and the multi-functional coating is produced on the surfaces of the microporous substrate.
  • Suitable functional additives include materials which have suitable stability to be delivered and which are either soluble in the wetting system (either the water or wetting agent) or dispersible in the wetting system.
  • the substrate is a polymer layer that is not naturally oleophobic, it can be rendered oleophobic by incorporating within the aqueous delivery system a functional additive which is an oleophobic material.
  • suitable microporous materials can include fluoropolymers, e.g.
  • polytetrafluoroethylene or polyvinylidene fluorides polyolefins, e.g. polyethylene or polypropylene; polyamides; polyesters; polysulfone, poly(ethersulfone) and combinations thereof, polycarbonate, polyurethanes.
  • the present invention should be designed to preserve the open microporous structure, as filling the micropores may destroy or severely lessen the water-vapor transmitting property of the microporous substrate.
  • the walls defining the voids in the microporous polymer preferably have only a very thin coating in such an embodiment.
  • oleophobic functional additive compositions suitable for this invention include oleophobic fluorocarbon compounds.
  • the fluorocarbon can be one that contains perfluoroalkyl groups CF 3 ⁇ (CF 2 ) n — , where n is >0.
  • the following compounds or classes of oleophobic materials, while not exhaustive, can be used:
  • Apolar perfluoropolyethers having CF 3 side groups such as Fomblin Y- Ausimont; Krytox-DuPont;
  • Polar water-insoluble PFPE such as, for example, Galden MF with phosphate, silane, or amide, end groups;
  • Emulsions based on perfluoroalkyl-substituted poly(meth)acrylates and copolymers products of Asahi Glass, Hoechst, DuPont and others.
  • the concentration of the functional material provided by this invention can vary greatly depending on the desired outcome.
  • an oleophobic fluoropolymer such as but not limited to, polymers having ⁇ (CF 2 ) n -CF 3 pendant groups
  • functional materials of this type can impart very low surface energy values to the polymer and thus impart good oil and water resistance properties.
  • Representative oleophobic polymers can be made from organic monomers having pendant perfluoroalkyl groups. These include fluoroalkyl acrylates and fluoroalkyl methacrylates having terminal perfluoroalkyl groups of the formula:
  • n is a cardinal number of 1-21
  • m is a cardinal number of 1-10
  • R is H or CH 3
  • fluoroalkyl aryl urethanes fluoroalkyl allyl urethanes, fluoroalkyl urethane acrylates; fluoroalkyl acrylamides; fluoroalkyl sulfonamide acrylates and the like.
  • concentrations from about 1 % wt. up to about 30% wt. solids of oleophobic material based on total coating mix weight may be effective.
  • the concentration of the oleophobic functional material preferably is between about 3% wt.
  • the present invention can be used to deliver particulate functional materials to surfaces, provided that the particulate can be dispersed in the wetting system. In some instances, it may be advantageous to disperse the particulates in a dispersing agent which can subsequently be dispersed in the wetting system. In applications involving particulates, such as carbon, concentrations ranging from about 0.1% wt. up to about 5% wt. based on total mix weight are often appropriate to impart the desired functional effect of this additional functional additive.
  • the optional functional material of the present invention may also be materials that are either soluble in the inventive aqueous wetting system or dispersible in the inventive aqueous wetting system.
  • the list of soluble materials that can be used in conjunction with the present invention include but are not limited to polyacrylic acid, polyacrylamide, melamine, polyvinyl alcohol, salts, and dyes.
  • the list of dispersible materials that can be used in conjunction with the present invention include but are not limited to fluoroacrylates, polystyrene, pigments, carbon black, and aluminum oxide.
  • One requirement for these dispersible materials is that the particle size be sufficiently small so that then can physically enter the pores of the microporous substrate to which they are being applied. When the microporous substrate is inherently hydrophobic, such a coating can change the surface characteristic from hydrophobic to hydrophilic.
  • a wide range of functionalities can be incorporated into the low surface energy microporous substrate.
  • Some examples include but are not limited to functional additives that can be provided to change water absorption, hydrophobicity, oleophobicity, light shielding, color change, flame resistance and fire retardancy, antimicrobial, antistatic, elasticity, infrared and near infrared absorption, UV absorption, catalysts, photo catalysts, biocompatibility, and controlled release of therapeutic agents.
  • One primary aspect of this invention is the ability to provide two or more of these functionalities in the coating system.
  • the functional additives that can be incorporated into these inventive constructs include, but are not limited to, carbon, metals, metal oxides (e.g., TiO2), fluoropolymers, acrylates, polyacrylic acid, heparin, permetherin, cerium oxide, benzophenone, nanoparticles, carbon nanotubes, quantum dots, cadmium selenium, lead selenium, dyes and pigments, antimony doped indium tin oxide.
  • Air permeable means that airflow is observed as determined by the Gurley test described below. It will be appreciated by one of skill in the art that an air permeable material will also be moisture vapor permeable.
  • Air-impermeable means that no airflow is observed for at least two minutes as determined by the Gurley test described below.
  • Hydrophilic material denotes a porous material whose pores become filled with liquid water when subjected to liquid water at a pressure of less than or equal to 1.0 psi.
  • “Microporous” term is used to denote a continuous layer of material comprised of interconnecting pores which create a passageway extending from one surface of the layer to the opposite surface of the layer.
  • Oleophobic means a material that has an oil rating of 1 or more, as measured by the Oil Repellency Test.
  • Coating refers to the presence of the material on at least a portion of a substrate.
  • Conformal coating refers to a coating which matches or follows the topography of the underlying substrate.
  • Gurley Densometer (ASTM) D726-58) manufactured by W. & L. E. Gurley & Sons. The results are reported in terms of Gurley Number, which is the time in seconds for 100 cubic centimeters of air to pass through 6.54 cm 2 of a test sample at a pressure drop of 1.215 kN/m 2 of water. A material is air-impermeable if no air passage is observed over a 120 second interval.
  • oil rating was measured using the AATCC Test Method 118-1983 when testing film composites.
  • the oil rating of a film composite is the lower of the two ratings obtained when testing the two sides of the composite. The higher the number, the better the oil repellency.
  • the test is modified as follows when testing laminates of the film composite with a textile. Three drops of the test oil are placed on the textile surface. A glass plate is placed directly on top of the oil drops. After 3 minutes, the reverse side of the laminate is inspected for a change in appearance indicating penetration or staining by the test oil.
  • the oil rating of the laminate corresponds to the highest number oil that does not wet through the laminate or cause visible staining from the reverse side of oil exposure. The higher the number, the better the oil repellency. A value of greater than 1 , preferably 2 or more, more preferably 4 or more, and most preferably, 6 or more, is preferred.
  • Spectral reflectance data is determined on the technical face of the sample (i.e., the camouflage printed side of the textile, laminate, or composite) and is obtained from 400 to 1100 nanometers (nm) at 20 nm intervals on a spectrophotometer (Data Color CS-5) (capable of measuring reflectance at wavelengths of 400-1100nm or greater) relative to a barium sulfate standard.
  • the spectral bandwidth is set at less than 26 nm at 860 nm. Reflectance measurements are made with the monochromatic mode of operation.
  • the samples were measured as a single layer, backed with six layers of the same fabric and shade. Measurements were taken on a minimum of two different areas and the data averaged. The measured areas were chosen to be at least 6-inches away from the selvage (edge). The specimen was viewed at an angle no greater than 10 degrees from the normal, with the specular component included.
  • Photometric accuracy of the spectrophotometer shall be within 1 percent and wavelength accuracy within 2 nm.
  • the standard aperture size used in the color measurement device shall be 1.0 to 1.25 inches in diameter for Woodland and Desert camouflage and 0.3725 inches in diameter for the Universal camouflage, MARPAT Woodland and MARPAT Desert. Any color having spectral reflectance values falling outside the limits at four or more of the wavelengths specified in MIL-DTL-31011A, MIL-DTL-31011 B, or MIL- PRF-32142 shall be considered a test failure.
  • Results are reported in terms of average reflectance for a particular wavelength range, unless otherwise specifically noted.
  • Example 1 was run to demonstrate that a low surface energy microporous substrate could be produced that was oleophobic, air permeable, and near infrared suppressive.
  • a microporous ePTFE membrane measuring 0.001 inch thick (0.2 ⁇ m nominal pore size, mass of 20 g/m 2 , obtained from W. L. Gore & Associates, Inc.) was coated with carbon black (Vulcan XC72, Cabot Corporation, Boston, MA) using a fluorocarbon polymer binder and wetting agents.
  • the binder system was formulated by mixing 2.6g of Witcolate ES2 (30% solution) (obtained from Witco Chemicals/Crompton Corporation,
  • this example gave an average reflection in the near infrared wavelength range of 720 nm to 1100 nm that was substantially reduced compared to the single functionality, control sample which was only oleophobic.
  • this example shows how a multi-functional coating system can be used to produce an air- permeable, microporous substrate having multiple functionalities.
  • Comparative A was produced similarly to Example 1 with the exception that no carbon was included in the fluorocarbon polymer binder and wetting agents. Average reflectance of the constructions was measured in the 720- 1100nm wavelength ranges. Results are reported as "Comparative A" in Table 1.
  • Example 2 To demonstrate the present invention is capable of providing both a different aesthetic color and oleophobicity (Example 2), the following composition was prepared (1.5 g of Witcolate ES-2 (Witco Chemical Co.), 0.6 g of 1-hexanol, 6.7 g of de-ionized water, 1.5 g of AG8025 (Asahi Glass Co. Ltd.), and 0.2 g of blue dye (Techtilon Blue). These ingredients were added in the order of: water, surfactant, and alcohol. To this aqueous system, the remaining functional additives were added. This aqueous system was mixed by shaking for approximately one minute at ambient conditions. This aqueous mixture was applied to one side of a 20 g/m 2 ePTFE membrane.
  • the aqueous mixture wet the ePTFE substrate within a second.
  • the coated membrane was cured in a lab oven at 19O 0 C for 2 min.
  • An air permeable blue colored oleophobic membrane resulted. Air permeability was confirmed by the coated membrane having a Gurley measurement of about 28 seconds.
  • the oil rating of the coated membrane was 8.
  • Example 3 To demonstrate that a pH indicating coating and pH switchable hydrophilicity could be imparted to a microporous substrate.
  • a mix of the following composition was prepared (1.3 g of Witcolate ES-2 (Witco Chemical Co.), 0.6g of 1-hexanol, 6.3g of de-ionized water, 2.Og of polyacrylic acid (Aldrich Chemical, 19203-1), and 0.3g of bromophenol blue. This mix immediately wet a 20 g/m 2 ePTFE membrane. The coated membrane was cured in a lab oven at 190 C for 2 min. An air permeable yellow colored membrane resulted. When exposed to a water droplet, this membrane remained yellow and did not wet even under light finger pressure.
  • This example provided the additional functional element of light blocking.
  • the uncoated membrane was placed on a page of writing under normal indoor lighting conditions, the writing was visible.
  • this multi-functional coated membrane was placed on the same page of writing under the same lighting conditions, the writing was not visible.

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  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Dispersion Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Inorganic Chemistry (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Paints Or Removers (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

A composition is described wherein a coating is provided on a microporous substrate, such as a low surface energy microporous substrate, which coating provides multiple functionalities to the underlying microporous material, while still maintaining porosity within at least a portion of the microporous substrate.

Description

TITLE OF THE INVENTION
MULTI-FUNCTIONAL COATINGS ON MICROPOROUS SUBSTRATES
FIELD OF THE INVENTION
The present invention relates to microporous substrates having a multifunctional coating thereon.
BACKGROUND OF THE INVENTION
Coated microporous substrates are used in many applications to take advantage of the properties of the microporous substrate while also taking advantage of the functionality of the coating material for a variety of applications.
Substrates of particular interest are polytetrafluoroethylene ("PTFE") and microporous polytetrafluoroethylene. Due to the inherent hydrophobicity of PTFE, membranes of these materials are of particular interest when in the form of repellant products such as rainwear. Expanded microporous, liquid waterproof polytetrafluoroethylene materials, such as those available from W. L. Gore and Associates, Inc., sold under the trademark GORE-TEX®, as well as expanded PTFE products available from other suppliers, are especially well suited for this purpose. The expanded PTFE materials are liquid waterproof, but allow water vapor, such as perspiration, to pass through. Polyurethanes and other polymers have been used for this purpose also.
U.S. Patent No. 4,194,041 describes the use of an additional coating on microporous polymers which is based on a thin, air-impermeable coating composed of a polyetherpolyurethane or polyperfluorosulfonic acid that transports water vapor molecules by diffusion. The thin coating completely fills at least a portion of the pores in the microporous structure. The thin coating is employed to reduce transmission of surface active agents and contaminating substances through the polymers. Owing to the chemical structure of the polymer, this monolithic coating on the microporous structure exhibits a high transport of water molecules, (high permeability to water vapor) through the polymeric material. Suitable coatings for microporous low surface energy materials are described in the art, many of which rely on solvents to wet the desired substrate. For example, EP 0581168 (Mitsubishi) describes the use of perfluoroalkyl methacrylates and perfluoroalkylethyl acrylates to coat porous polyethylene and polypropylene membranes where the coated substances are held in physical contact with the surface of the polyolefin porous membrane. To produce these coated porous membranes, the fluorinated monomer or fluorinated monomer and a crosslinking monomer together with a polymerization initiator are dissolved in a suitable solvent to produce a solution. For example, this solution typically may comprise about 15% wt. monomer and 85% wt. acetone. This solvent solution is coated onto the porous substrate. After coating, the solvent is vaporized off.
In a similar solvent-rich situation, a process for treating the surfaces of polymers with essentially pure solvent solutions containing low concentrations (e.g. less than 1.0% wt.) of amorphous fluoropolymers has also been reported (WO 92/10532).
In yet another similar manner, solutions of fluorine-containing polymers are also involved in a patent for coating ePTFE with an amorphous copolymer of tetrafluoroethylene (EP 0561875). In each of these cases, significant quantities of solvent are released during the coating coalescence process. These solvent emissions are both costly and environmentally undesirable.
U.S. Patent No. 6,228,477 teaches a means to coat a low surface energy, microporous PTFE substrate with an otherwise non-wetting, aqueous fluoropolymer dispersion through the use of significant percentages of isopropanol ("IPA").
U.S. Patent No. 5,460,872, to Wu et. al., teaches the use of fluorinated surfactants to lower the surface energy and contact angle with microporous PTFE as a means to produce a uniformly coated microporous PTFE substrate.
Other patents and publications (e.g., WO 91/01791 (Gelman Sciences Technology; EP 0561277 (Millipore)/U.S. Patent No. 5,217,802) propose treating a porous membrane with a fluorine-containing monomer and a crosslinker. The treatment is followed by polymerization.
Perfluoropolyethers in conjunction with ePTFE for use as water-repellent finish are mentioned in WO 92/21715. In addition, U. S. Patent No. 6,676,993 teaches a process that uses a mixture of isopropanol and water to wet microporous ePTFE substrates and when specific fluoroacrylates are dispersed in this solvent-laden solution, it can be used to coating to the ePTFE surfaces it wets.
While particles have conventionally been incorporated into ePTFE structures, they have not been incorporated in coatings which effectively bind the particles to the pore walls of the microporous structure. For example, U. S. Patent No. 5,279,742 teaches enmeshing carbon particles in the nodes and fibrils of ePTFE films for use as an extraction medium. European Patent No. EP 0528998B1 teaches the mechanical entrapment of therapeutic microspheres in an ePTFE matrix as a way to deliver drug therapy in a periodontal patch.
To date, microporous substrate coating technologies have focused on depositing a single homogenous material on the microstructure of the microporous substrate. Solvent wetting systems and aqueous wetting systems (e.g., such as described in U. S. Patent No. 6,228,477, etc.) have not been compatible with a range of additives or multiple additives. Typically, these wetting systems have been compatible with isolated, unique oleophobic monomer, polymers or emulsions. A need has existed for added flexibility in coating technology to provide two or more functionalities in a single conformal coating on a low surface energy microporous substrate without occluding the micropores of the substrate.
SUMMARY OF THE INVENTION
The present invention overcomes the limitation of the prior art by providing a single conformal coating on a microporous substrate, such as a low surface energy microporous substrate, which provides multiple functionalities to the underlying microporous material, while still maintaining porosity within at least a portion of the microporous substrate.
BRIEF DESCRIPTION OF THE FIGURES
Fig. 1 is a schematic sectional view of a coated microporous polymer layer.
Fig. 2 is a schematic angled cross-sectional view of a coated fibril of a coated, expanded polytetrafluoroethylene membrane. Fig. 3 is a schematic full cross-sectional view of a coated fibril of a coated, expanded polytetrafluoroethylene membrane.
DETAILED DESCRIPTION OF INVENTION
In the present invention, a microporous coated substrate is produced wherein the coating contains two or more functionalities. Specifically, the multifunctional coating includes at least two additives and each additive provides at least one functionality. In one embodiment, the first additive may form a film around, encompass or otherwise bind the second additive to the microporous structure. The first additive provides some functionality to the composite, such as hydrophobicity, hydrophilicity, etc., and the second additive provides some further functionality to the composite. In another aspect of this invention, the multi-functional coating combines a first functional additive such as but not limited to surface energy modifying (e.g., lowering, etc.) polymeric binders with additional functional additives wherein the resulting multi-functional coating exists on the pore surfaces of the microporous substrate. As used herein, the term "functional additive" is intended to refer to any additional material which renders further functionality to the coated microporous substrate than what otherwise exists in the absence of the functional additive, such as by changing the chemical, physical or mechanical properties of the microporous substrate. One class of polymeric binders of this invention are fluoropolymer binders since they can be used to alter the surface energy or wetting characteristics of the otherwise inherently hydrophobic expanded PTFE substrate. Surprisingly, additional functional additives can be included in the polymeric binder mix so that the resultant coated microporous substrate exhibits both a surface energy change due to the fluoropolymer binder but also a second functional change due to the additional functional additive. While surface energy altering polymeric binders are of particular interest in this invention, other embodiments encompass incorporating a non-polymeric binder. In such embodiments where a non-polymeric binder is used, the multi-functionality results from the incorporation of more than one functional additive onto the surfaces of the microporous substrate, where at least one of the functional additives also acts as a binder. As used herein, the term "binder" refers to a material which adheres or otherwise attaches to at least a portion of the underlying microporous structure and assists in retention of the second functional component.
The multi-functional coatings of this invention can be applied to the microporous substrate by any means which produces the desired coating uniformity on the surfaces of the microstructure and preferably does not occlude the pores of the microporous substrate. One aspect of this invention dissolves the functional polymeric binder in an organic solvent into which the additional functional additives, such as particles are added. The organic solvent selected must be capable of wetting the microporous substrate surface. This multi-functional-additive, solvent mix is then coated onto the microporous substrate and the solvent vaporized. The functional polymeric binder and the functional additive particles contained therein are deposited onto substrate surface in order to create a desired effect. Examples of functions that can be provided in such a multi-functional coating include, but are not limited to, color change in the case of a pigment, or hydrophilicity change in the case of pH sensitive materials, and infrared reflectivity changes in the case of infrared absorbing materials. Carbon particles are of particular interest in applications where a change in an electromagnetic spectral response or electric or thermal conductivity of the substrate is desired. A critical aspect of this invention is that the resultant microporous substrate must exhibit multiple functionalities such as that of the surface energy altering polymeric binder and a change in spectral, electromagnetic, or thermal response.
One important aspect of this invention is that the coating mix must be able to wet the substrate to which it is applied. In the case of microporous PTFE, the coating mix typically should have a surface tension around 30 dynes/cm or less.
In another embodiment of this invention, a multi-functional coating can be produced using an aqueous wetting system. In this embodiment, a polymeric binder and a second functional additive are stabilized in an aqueous wetting system which is then coated onto the desired microporous substrate. An aqueous wetting system containing a water insoluble alcohol (e.g., C5-C10 linear backbone) emulsified by a surfactant is one suitable system. The surfactant or surfactants can be selected to be compatible with the additives and any surfactants that may be used to stabilize the additives. The water is vaporized and the multi-functional coating is produced on the surfaces of the microporous substrate. Suitable functional additives include materials which have suitable stability to be delivered and which are either soluble in the wetting system (either the water or wetting agent) or dispersible in the wetting system. In one exemplary embodiment of the invention, if the substrate is a polymer layer that is not naturally oleophobic, it can be rendered oleophobic by incorporating within the aqueous delivery system a functional additive which is an oleophobic material. This unique feature of the invention provides significant advantages over conventional coated materials, in that the present invention can be tailored to readily facilitate coating at least a portion of the pore walls of the substrate. In one embodiment of this invention, suitable microporous materials can include fluoropolymers, e.g. polytetrafluoroethylene or polyvinylidene fluorides, polyolefins, e.g. polyethylene or polypropylene; polyamides; polyesters; polysulfone, poly(ethersulfone) and combinations thereof, polycarbonate, polyurethanes. In instances where retention of air permeability or high breathability is desired, the present invention should be designed to preserve the open microporous structure, as filling the micropores may destroy or severely lessen the water-vapor transmitting property of the microporous substrate. Thus, the walls defining the voids in the microporous polymer preferably have only a very thin coating in such an embodiment. Moreover, to maintain flexibility of the substrate, the coating of the functional material should be sufficiently thin to not impact the flexibility of the substrate when coated. Common oleophobic functional additive compositions suitable for this invention include oleophobic fluorocarbon compounds. For example, the fluorocarbon can be one that contains perfluoroalkyl groups CF3 ~(CF2)n — , where n is >0. The following compounds or classes of oleophobic materials, while not exhaustive, can be used:
■ Apolar perfluoropolyethers having CF3 side groups, such as Fomblin Y- Ausimont; Krytox-DuPont;
■ Mixtures of apolar perfluoroethers with polar monofunctional perfluoropolyethers PFPE (Fomblin and Galden MF grades available from
Ausimont);
■ Polar water-insoluble PFPE such as, for example, Galden MF with phosphate, silane, or amide, end groups;
■ Mixtures of apolar PFPE with fluorinated alkyl methacrylates and fluorinated alkyl acrylate as monomer or in polymer form. The above-mentioned compounds can also optionally be crosslinked by, for example, UV radiation in aqueous form solution or emulsion.
The following polymeric particle solutions, while again not exhaustive, can also be used: ■ Microemulsions based on PFPE (see EP 0615779, Fomblin Fe20 microemulsions);
■ Emulsions based on copolymers of siloxanes and perfluoroalkyl- substituted (meth)acrylates (Hoechst);
■ Emulsions based on perfluorinated or partially fluorinated co- or terpolymers, one component containing at least hexafluoropropene or perfluoroalkyl vinyl ether;
■ Emulsions based on perfluoroalkyl-substituted poly(meth)acrylates and copolymers (products of Asahi Glass, Hoechst, DuPont and others).
■ Microemulsions based on perfluoroalkyl-substituted poly(meth)acrylates and copolymers (WU, U.S. Pat. No. 5,539,072; U.S. Pat. No. 5,460,872);
The concentration of the functional material provided by this invention can vary greatly depending on the desired outcome. When an oleophobic fluoropolymer is used as the functional additive material, such as but not limited to, polymers having ~(CF2)n -CF3 pendant groups, functional materials of this type can impart very low surface energy values to the polymer and thus impart good oil and water resistance properties. Representative oleophobic polymers can be made from organic monomers having pendant perfluoroalkyl groups. These include fluoroalkyl acrylates and fluoroalkyl methacrylates having terminal perfluoroalkyl groups of the formula:
O Il
CF3(CF2)n- (CH2)m- O - C - C == CH2
I R
wherein n is a cardinal number of 1-21 , m is a cardinal number of 1-10, and R is H or CH3 ; fluoroalkyl aryl urethanes, fluoroalkyl allyl urethanes, fluoroalkyl urethane acrylates; fluoroalkyl acrylamides; fluoroalkyl sulfonamide acrylates and the like. When a low surface energy coating is desired, concentrations from about 1 % wt. up to about 30% wt. solids of oleophobic material based on total coating mix weight may be effective. When coating microporous substrates, the concentration of the oleophobic functional material preferably is between about 3% wt. up to about 12% wt. based on total coating mix weight. Alternate embodiments of this invention include other functional additive materials. The present invention can be used to deliver particulate functional materials to surfaces, provided that the particulate can be dispersed in the wetting system. In some instances, it may be advantageous to disperse the particulates in a dispersing agent which can subsequently be dispersed in the wetting system. In applications involving particulates, such as carbon, concentrations ranging from about 0.1% wt. up to about 5% wt. based on total mix weight are often appropriate to impart the desired functional effect of this additional functional additive.
The optional functional material of the present invention may also be materials that are either soluble in the inventive aqueous wetting system or dispersible in the inventive aqueous wetting system. The list of soluble materials that can be used in conjunction with the present invention include but are not limited to polyacrylic acid, polyacrylamide, melamine, polyvinyl alcohol, salts, and dyes. The list of dispersible materials that can be used in conjunction with the present invention include but are not limited to fluoroacrylates, polystyrene, pigments, carbon black, and aluminum oxide. One requirement for these dispersible materials is that the particle size be sufficiently small so that then can physically enter the pores of the microporous substrate to which they are being applied. When the microporous substrate is inherently hydrophobic, such a coating can change the surface characteristic from hydrophobic to hydrophilic.
In additional embodiments of this invention, a wide range of functionalities can be incorporated into the low surface energy microporous substrate. Some examples include but are not limited to functional additives that can be provided to change water absorption, hydrophobicity, oleophobicity, light shielding, color change, flame resistance and fire retardancy, antimicrobial, antistatic, elasticity, infrared and near infrared absorption, UV absorption, catalysts, photo catalysts, biocompatibility, and controlled release of therapeutic agents. One primary aspect of this invention is the ability to provide two or more of these functionalities in the coating system. In order to achieve some of the above embodiments, the functional additives that can be incorporated into these inventive constructs include, but are not limited to, carbon, metals, metal oxides (e.g., TiO2), fluoropolymers, acrylates, polyacrylic acid, heparin, permetherin, cerium oxide, benzophenone, nanoparticles, carbon nanotubes, quantum dots, cadmium selenium, lead selenium, dyes and pigments, antimony doped indium tin oxide.
Other useful permutations of this invention are also encompassed within the breadth of coated microporous substrates having a single coating with multiple functionalities provided to the substrate via the single coating. Additional advantages of this invention are that it can be used to provide both acidic and basic reactivities onto a single microporous substrate. In addition, because the addition of some particles may reduce the water entry pressure of a microporous substrate, this invention provides a way to maintain or even enhance the waterproofness of a microporous substrate while also providing the functionality of an additional functional additive or particulate. Additional functional additives of interest include but are not limited to metals, e.g. silver, metal carbonates, e.g. copper or zinc carbonates, metal oxides, e.g. cuprous oxide or molybdenum oxide, or organic materials such as triethylenediamine.
DEFINITIONS
For the purposes of this application the following terms shall be recognized to have the meaning set forth below unless otherwise indicated: "Air permeable" means that airflow is observed as determined by the Gurley test described below. It will be appreciated by one of skill in the art that an air permeable material will also be moisture vapor permeable.
"Air-impermeable" means that no airflow is observed for at least two minutes as determined by the Gurley test described below.
"Hydrophilic" material denotes a porous material whose pores become filled with liquid water when subjected to liquid water at a pressure of less than or equal to 1.0 psi.
"Microporous" term is used to denote a continuous layer of material comprised of interconnecting pores which create a passageway extending from one surface of the layer to the opposite surface of the layer.
"Oleophobic" means a material that has an oil rating of 1 or more, as measured by the Oil Repellency Test.
"Coating" refers to the presence of the material on at least a portion of a substrate. "Conformal coating" refers to a coating which matches or follows the topography of the underlying substrate.
TEST PROCEDURES
Air Permeability/Impermeability-Gurley Number Test
Gurley numbers were obtained as follows:
The resistance of samples to air flow was measured by a Gurley densometer (ASTM) D726-58) manufactured by W. & L. E. Gurley & Sons. The results are reported in terms of Gurley Number, which is the time in seconds for 100 cubic centimeters of air to pass through 6.54 cm2 of a test sample at a pressure drop of 1.215 kN/m2 of water. A material is air-impermeable if no air passage is observed over a 120 second interval.
Oil Repellency Test
In these tests, oil rating was measured using the AATCC Test Method 118-1983 when testing film composites. The oil rating of a film composite is the lower of the two ratings obtained when testing the two sides of the composite. The higher the number, the better the oil repellency. A value of greater than 1 , preferably 2 or more, more preferably 4 or more, is preferred.
The test is modified as follows when testing laminates of the film composite with a textile. Three drops of the test oil are placed on the textile surface. A glass plate is placed directly on top of the oil drops. After 3 minutes, the reverse side of the laminate is inspected for a change in appearance indicating penetration or staining by the test oil. The oil rating of the laminate corresponds to the highest number oil that does not wet through the laminate or cause visible staining from the reverse side of oil exposure. The higher the number, the better the oil repellency. A value of greater than 1 , preferably 2 or more, more preferably 4 or more, and most preferably, 6 or more, is preferred.
Average Reflectance Test for Visible and Near Infrared Spectra
Spectral reflectance data is determined on the technical face of the sample (i.e., the camouflage printed side of the textile, laminate, or composite) and is obtained from 400 to 1100 nanometers (nm) at 20 nm intervals on a spectrophotometer (Data Color CS-5) (capable of measuring reflectance at wavelengths of 400-1100nm or greater) relative to a barium sulfate standard. The spectral bandwidth is set at less than 26 nm at 860 nm. Reflectance measurements are made with the monochromatic mode of operation.
The samples were measured as a single layer, backed with six layers of the same fabric and shade. Measurements were taken on a minimum of two different areas and the data averaged. The measured areas were chosen to be at least 6-inches away from the selvage (edge). The specimen was viewed at an angle no greater than 10 degrees from the normal, with the specular component included.
Instrument: Photometric accuracy of the spectrophotometer shall be within 1 percent and wavelength accuracy within 2 nm. The standard aperture size used in the color measurement device shall be 1.0 to 1.25 inches in diameter for Woodland and Desert camouflage and 0.3725 inches in diameter for the Universal camouflage, MARPAT Woodland and MARPAT Desert. Any color having spectral reflectance values falling outside the limits at four or more of the wavelengths specified in MIL-DTL-31011A, MIL-DTL-31011 B, or MIL- PRF-32142 shall be considered a test failure.
Results are reported in terms of average reflectance for a particular wavelength range, unless otherwise specifically noted.
EXAMPLES
Example 1
Example 1 was run to demonstrate that a low surface energy microporous substrate could be produced that was oleophobic, air permeable, and near infrared suppressive. A microporous ePTFE membrane measuring 0.001 inch thick (0.2 μm nominal pore size, mass of 20 g/m2, obtained from W. L. Gore & Associates, Inc.) was coated with carbon black (Vulcan XC72, Cabot Corporation, Boston, MA) using a fluorocarbon polymer binder and wetting agents. The binder system was formulated by mixing 2.6g of Witcolate ES2 (30% solution) (obtained from Witco Chemicals/Crompton Corporation,
Middlebury, CT), 1.2g of 1-Hexanol (Sigma-Aldrich Chemical Corporation, St. Louis, MO), and 3.Og of fluoropolymer (AG8025, Asahi Glass, Japan) in 13.2g of deionized water. 0.015g of carbon black was added to the binder system. The mixture was sonicated for 1 minute. The membrane was hand coated with the mixture using a roller to a coating weight of approximately 3 g/m2. The coated membrane was cured at 1900C for 2.5 minutes. The resultant microporous expanded PTFE substrate had a Gurley number of about 29 seconds to about 49 seconds and a moisture vapor transmission rate of about 45,942 g/m2 (24 hours). The oil rating was 8. And this example gave an average reflection in the near infrared wavelength range of 720 nm to 1100 nm that was substantially reduced compared to the single functionality, control sample which was only oleophobic. Clearly, this example shows how a multi-functional coating system can be used to produce an air- permeable, microporous substrate having multiple functionalities.
Comparative A
Comparative A was produced similarly to Example 1 with the exception that no carbon was included in the fluorocarbon polymer binder and wetting agents. Average reflectance of the constructions was measured in the 720- 1100nm wavelength ranges. Results are reported as "Comparative A" in Table 1.
Table 1
Figure imgf000013_0001
Example 2 To demonstrate the present invention is capable of providing both a different aesthetic color and oleophobicity (Example 2), the following composition was prepared (1.5 g of Witcolate ES-2 (Witco Chemical Co.), 0.6 g of 1-hexanol, 6.7 g of de-ionized water, 1.5 g of AG8025 (Asahi Glass Co. Ltd.), and 0.2 g of blue dye (Techtilon Blue). These ingredients were added in the order of: water, surfactant, and alcohol. To this aqueous system, the remaining functional additives were added. This aqueous system was mixed by shaking for approximately one minute at ambient conditions. This aqueous mixture was applied to one side of a 20 g/m2 ePTFE membrane. The aqueous mixture wet the ePTFE substrate within a second. The coated membrane was cured in a lab oven at 19O0C for 2 min. An air permeable blue colored oleophobic membrane resulted. Air permeability was confirmed by the coated membrane having a Gurley measurement of about 28 seconds. The oil rating of the coated membrane was 8.
Example 3 To demonstrate that a pH indicating coating and pH switchable hydrophilicity could be imparted to a microporous substrate. A mix of the following composition was prepared (1.3 g of Witcolate ES-2 (Witco Chemical Co.), 0.6g of 1-hexanol, 6.3g of de-ionized water, 2.Og of polyacrylic acid (Aldrich Chemical, 19203-1), and 0.3g of bromophenol blue. This mix immediately wet a 20 g/m2 ePTFE membrane. The coated membrane was cured in a lab oven at 190 C for 2 min. An air permeable yellow colored membrane resulted. When exposed to a water droplet, this membrane remained yellow and did not wet even under light finger pressure. When exposed to a NaOH solution (~pH 10), the color of the membrane changed from yellow to blue and the membrane was penetrated by the dilute NaOH solution under light finger pressure. This membrane has hydrophilic properties towards basic solution and has a pH indicator to show the presence of a basic solution.
This example provided the additional functional element of light blocking. When the uncoated membrane was placed on a page of writing under normal indoor lighting conditions, the writing was visible. When this multi-functional coated membrane was placed on the same page of writing under the same lighting conditions, the writing was not visible.

Claims

CLAIMS:
1) A composite comprising: a microporous layer having pore walls and open porosity therein; and a multi-functional coating on at least a portion of the pore walls of the microporous layer, said multi-functional coating comprising a first functional additive and at least one additional functional additive, wherein the microporous layer retains at least some open porosity in the coated portion of the microporous structure.
2) The composite of claim 1 wherein said composite is microporous.
3) The composite of claim 1 wherein the microporous layer comprises expanded polytetrafluoroethylene.
4) The composite of claim 1 wherein the first functional additive is oleophobic.
5) The composite of claim 1 wherein the first functional additive comprises fluoroacrylate.
6) The composite of claim 1 wherein the at least one additional functional additive is a filler. 7) The composite of claim 6 wherein the filler is particulate.
8) The composite of claim 6 wherein the filler comprises carbon.
9) The composite of claim 6 wherein the filler comprises at least one material selected from the group consisting of a pigment, a metal, a metal oxide, and a mixed metal oxide. 10) The composite of claim 6 wherein the filler is present at less than or equal to 10% wt. based on total coating weight.
11) The composite of claim 6 wherein the filler is present at less than or equal to 5% wt. based on total coating weight.
12) The composite of claim 6 wherein the filler is present at less than or equal to 1 % wt. based on total coating weight.
13) The composite of claim 6 wherein the filler is present at less than or equal to 0.5% wt. based on total coating weight.
14) A composite comprising: a microporous polymer having pore walls and open porosity therein; and a multi-functional coating on at least a portion of the pore walls of the microporous polymer, said multi-functional coating comprising a first functional additive and at least one additional functional additive, wherein the microporous polymer retains at least some open porosity in the coated portion.
15) The composite of claim 14 wherein the first functional additive comprises a polymer, at least one surfactant in an amount of up to about 50% by weight of the coating based on total coating weight, and at least one water-insoluble alcohol having a C5-C10 linear backbone in an amount of up to about 30% by weight of the aqueous mixture used to coat the microporous polymer.
16) The composite of claim 14, wherein said composite further contains at least one additional coating.
17) The composite of claim 16, wherein said at least one further coating does not fill said pores of said microporous polymer. 18) The composite of claim 16, wherein said at least one further coating substantially fills at least a portion of said pores of said microporous polymer.
19) The composite of claim 14 wherein the microporous polymer comprises expanded polytetrafluoroethylene.
20) The composite of claim 14 wherein the first functional additive is oleophobic.
21) The composite of claim 14 wherein the first functional additive is a fluoropolymer.
22) The composite of claim 14 wherein the first functional additive comprises polyfluoroacrylate. 23) The composite of claim 14 wherein the first functional additive comprises styrene-butadiene copolymer.
24) The composite of claim 14 wherein the first functional additive is hydrophilic.
25) The composite of claim 14 wherein the first functional additive comprises polyacrylic acid.
26) The composite of claim 14 wherein the first functional additive is sodium polyacrylic acid.
27) The composite of claim 14 wherein the first functional additive is polyvinyl alcohol. 28) The composite of claim 14 wherein the first functional additive is polyethyleneimine.
29) The composite of claim 14 wherein the first functional additive comprises a copolymer of acrylic acid. 30) The composite of claim 14 wherein the first functional additive comprises a copolymer of acrylamide.
31) The composite of claim 14 wherein the first functional additive comprises a surfactant.
32) The composite of claim 14 wherein the first functional additive is a cross- linkable material.
33) The composite of claim 14 wherein the first functional additive is elastic.
34) The composite of claim 14 wherein the second functional additive is particulate.
35) The composite of claim 14 wherein the second functional additive is carbon.
36) The composite of claim 14 wherein the second functional additive is antimony oxide.
37) The composite of claim 14 wherein the second functional additive is present at less than or equal to 10%wt. based on total coating weight. 38) The composite of claim 14 wherein the second functional additive is present at less than or equal to 5%wt. based on total coating weight.
39) The composite of claim 14 wherein the second functional additive is present at less than or equal to 1 %wt. based on total coating weight.
40) The composite of claim 14 wherein the second functional additive is present at less than or equal to 0.5%wt. based on total coating weight.
41) A composite comprising: a microporous layer having a microporous structure having pore walls and open porosity therein; and a multi-functional coating on at least a portion of the pore walls of the microporous layer, said multi-functional coating comprising a first functional additive and at least one additional functional additive, wherein the microporous layer retains at least some open porosity in the coated portion, and wherein at least one of said first functional additive and said second functional additive binds said multi-functional coating to said microporous layer. 42) A method for forming a multi-functional coating on a microporous structure comprising: preparing an aqueous wetting mix; adding a first functional additive and a at least one additional functional additive to the wetting mix; coating said microporous structure with said aqueous wetting mix; and heating the coated microporous material and forming a coating thereon. 43) A method for forming a multi-functional coating on a microporous structure comprising: preparing a solvent wetting mix; adding a first functional additive and a at least one additional functional additive to the wetting mix; coating said microporous structure with said solvent wetting mix; and heating the coated microporous material and forming a coating thereon.
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JP2008542064A (en) 2008-11-27
CA2609519C (en) 2015-09-29
JP5307536B2 (en) 2013-10-02
RU2007148409A (en) 2009-06-27
CN104959041A (en) 2015-10-07
RU2435631C2 (en) 2011-12-10
PL1885476T3 (en) 2016-05-31
EP1885476B1 (en) 2015-07-08
EP1885476A2 (en) 2008-02-13
KR20080015022A (en) 2008-02-15
HK1108852A1 (en) 2008-05-23
NO341096B1 (en) 2017-08-21
NO20076525L (en) 2008-02-14
KR101393173B1 (en) 2014-05-21
CA2609519A1 (en) 2006-11-30
WO2006127946A3 (en) 2007-03-01
CN101218013A (en) 2008-07-09

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