Functionalized Textile Compositions and Products

Abstract

To provide textile materials that are resistant to various environmental conditions and offer significant performance enhancements, we offer a novel textile composition. [Solution] A functionalized textile material is provided. At least a portion of the textile surface includes a ceramic material such as a binderless porous structured ceramic, and optionally, one or more functional layers are applied to provide a textile material having one or more desirable functional properties such as hydrophilicity, hydrophobicity, flame retardancy, photocatalytic activity, antifouling, and / or deodorizing properties.

Description

[Technical Field]

[0001] Cross-reference of related applications This application claims priority to PCT application number PCT / US2019 / 065978 filed on 12 December 2019, and claims the benefit of U.S. Provisional Patent Applications No. 62 / 989,092, 62 / 989,150, 63 / 038,642, 63 / 038,693, and 63 / 039,965 filed on 13 March 2020, all of which are incorporated herein by reference in their entirety.

[0002] Technical field The present invention relates to textiles comprising a ceramic material, particularly a binderless ceramic such as a metal oxide and / or metal hydroxide ceramic, on the textile surface. The textile is modified to include one or more functionalities that provide enhanced properties in the intended use or environment. [Background technology]

[0003] Functionalizing textile surfaces provides desired benefits in terms of textile performance compared to non-functionalized textile layers. Novel textile compositions must be developed to supply textile materials that are resistant to various environmental conditions and offer significant performance enhancements. Desired operating characteristics can be provided through the functionalization of textile surfaces. [Overview of the project]

[0004] This specification provides compositions comprising a functionalized ceramic material on a porous substrate.

[0005] In one embodiment, a composition is provided comprising a binderless ceramic material on a porous substrate such as a textile or filter material. In one embodiment, the substrate contains pores having an average pore diameter of less than about 250 μm, and the ceramic material on the substrate does not substantially change the average pore diameter of the substrate. In another embodiment, the substrate contains pores having an average pore diameter of less than about 250 μm, and the ceramic material on the substrate partially or completely fills the pores of the substrate, thereby reducing the average pore diameter or eliminating the pores of the substrate, respectively. In some embodiments, the substrate has an air permeability of about 0.1 cubic feet per minute (CFM) to about 100 CFM according to ASTM D737 before the deposition of the ceramic material on the substrate.

[0006] In some embodiments, the ceramic material is primarily crystalline. In some embodiments, the ceramic material comprises a metal oxide, a hydrate of a metal oxide, a metal hydroxide, and / or a hydrate of a metal hydroxide. In some embodiments, the ceramic material comprises a metal hydroxide, and at least a portion of the metal hydroxide comprises a layered double hydroxide. In some embodiments, the ceramic material is a structured ceramic material, such as a nanostructured ceramic material.

[0007] In some embodiments, the ceramic material includes transition metals, Group II elements, rare earth elements, aluminum, tin, zinc, or lead. For example, the ceramic material may include one or more of zinc, aluminum, manganese, magnesium, cerium, copper, gadolinium, tungsten, tin, zinc, lead, and cobalt. A particular embodiment The ceramic material includes, for example, a mixture of zinc and aluminum oxides and / or hydroxides; a mixture of manganese and magnesium oxides and / or hydroxides; manganese oxides and / or hydroxides; aluminum oxides and / or hydroxides; mixed metallic manganese oxides and / or hydroxides; a mixture of magnesium and aluminum oxides and / or hydroxides; magnesium oxides and / or hydroxides; a mixture of magnesium, cerium, and aluminum oxides and / or hydroxides; a mixture of zinc, praseodymium, and aluminum oxides and / or hydroxides; a mixture of cobalt and aluminum oxides and / or hydroxides; a mixture of manganese and aluminum oxides and / or hydroxides; a mixture of cerium and aluminum oxides and / or hydroxides; a mixture of copper and aluminum oxides and / or hydroxides; a mixture of zinc and aluminum oxides and / or hydroxides; a mixture of Zn-aluminates; a mixture containing one or more phases including Zn, Al, and oxygen; zinc oxides and / or hydroxides; or a hydrate of any of the above compounds or a mixture thereof.

[0008] In some embodiments, the ceramic material includes a thickness of approximately 25 μm, such as a thickness of approximately 0.2 μm to approximately 25 μm.

[0009] In some embodiments, the ceramic material has a porosity of about 5% to about 80%, such as more than about 10% or about 30% to about 95%.

[0010] In some embodiments, the porous substrate includes or comprises woven material, knitted fabric, non-woven fabric or textile, or paper. The porous substrate may include or comprise, for example, polyamide, polyester, cotton, wool, polyethylene, polypropylene, cellulosic material, aramid, polyurethane, activated carbon, fiberglass, steel alloy, brass alloy, aluminum alloy, aluminum, or copper. In various embodiments, the porous substrate may be a textile material including or comprising natural fibers, synthetic fibers, metal mesh, or metal cloth, or a combination thereof. In some embodiments, the textile surface is oxidized, ashed, or activated, for example, before the deposition of ceramic material on the substrate. In one embodiment, the substrate is a metallized textile containing one or more metals on the textile surface, but not limited to, aluminum, iron, nickel, titanium, stainless steel alloys, or copper.

[0011] In some embodiments, the ceramic material and / or an optional topcoat (functional layer) material imparts one or more functional properties to the composition, including but not limited to hydrophilicity, hydrophobicity, flame retardancy, photocatalytic activity, antifouling, deodorizing properties, inhibition of microbial growth, ice or condensate management, anti-icing, anti-frosting, superhydrophobicity, superhydrophilicity, corrosion resistance, electromagnetic regulation, thermal modulation, permeability, dynamic wind resistance, and / or color. In certain embodiments, two or more such functional properties are imparted to a single layer of the composition (e.g., a single layer of textile, fabric, or filter material).

[0012] In some embodiments, the ceramic material is further modified by a functional layer. In some embodiments, the functional layer (e.g., top coat) material imparts one or more functional properties that are more advanced than the same functional properties imparted by the same top coat material deposited directly on the same textile surface that does not contain the ceramic material. For example, the ceramic material and the functional layer material can synergistically impart one or more functional properties that are more advanced than the same functional properties imparted by either the ceramic material or the functional layer material deposited independently on the same textile surface.

[0013] In some embodiments, the functional layer imparts hydrophobic properties. For example, the functional layer that imparts hydrophobic properties to the composition may include a fluoropolymer, an elastomer, a plastic, or a molecule having a head group and a tail group, where, for example, the head group includes a silane group, a phosphonate group, a phosphonic acid group, a carboxylic acid group, a vinyl group, an alcohol group, a hydroxide group, a thiolate group, and / or a thiol group, and the tail group includes a hydrocarbon group, a fluorocarbon group, a vinyl group, a phenyl group, an epoxide group, an acrylic group, an acrylate group, a hydroxyl group, a carboxylic acid group, a thiol group, and / or a quaternary ammonium group.

[0014] In some embodiments, the ceramic material on the substrate has a partially filled porous structure. For example, the pores may be partially filled with a second ceramic material or a molecule having a head group and a tail group.

[0015] In some embodiments, the composition exhibits a higher adhesion to low molecular weight substances than to components of sebum such as, but not limited to, triglycerides, wax esters, squalene, and / or free fatty acids.

[0016] In some embodiments, the composition has photocatalytic properties, and the material adhering to the surface is decomposed by the photocatalyst when exposed to light.

[0017] In some embodiments, the composition exhibits a higher adhesion to the durable water-repellent substance than the same substrate without the ceramic material.

[0018] In another aspect, there is provided a product comprising any of the compositions described herein (compositions comprising a functionalized ceramic material on a porous substrate). In certain non-limiting embodiments, the product includes filters, membranes, clothing items, outerwear, camping gear, pipe insulation, carpets, car seats, interior materials, floor coverings, building surfaces (e.g., wall materials, floor sheathing, or plywood), and window coverings.

[0019] In some embodiments, the composition or product as described herein can withstand a hydrostatic pressure of greater than about 1 kPa.

[0020] In some embodiments, the composition or product as described herein includes a water vapor transmission rate greater than about 80% of the vapor transmission rate of the same substrate not modified with the ceramic material (and in some embodiments, an optional functional layer).

[0021] In some embodiments, the composition or product as described herein includes a liquid water contact angle greater than about 150 degrees.

[0022] In some embodiments, the composition or product as described herein includes a manganese oxide ceramic and an alkylsilane or alkylphosphonate functional layer.

MODE FOR CARRYING OUT THE INVENTION

[0023] This specification provides compositions comprising a ceramic material, such as a binderless ceramic material, on a porous substrate, such as a textile. In some embodiments, the substrate contains pores having an average pore diameter of less than about 250 μm, and the ceramic does not substantially change the average pore diameter of the substrate. In other embodiments, the substrate contains pores having an average pore diameter of less than about 250 μm, and the ceramic partially or completely fills the pores, thereby reducing the average pore diameter or eliminating the pores in the substrate, respectively.

[0024] The present invention provides industrial textiles that include, but are not limited to, desirable functional properties such as hydrophilicity, hydrophobicity, flame retardancy, photocatalytic activity, antifouling, deodorizing properties, inhibition of microbial growth, ice or condensate management, anti-icing, anti-frosting, superhydrophobicity, superhydrophilicity, corrosion resistance, electromagnetic regulation, thermal modulation, breathability, dynamic wind resistance, and / or color, which are imparted to the textile surface by the composition described herein. In some embodiments, a single layer of the textile includes two or more of these functional properties, which are imparted to the textile surface by the composition (ceramic material) described herein.

[0025] A ceramic, for example, a porous ceramic (e.g., metal oxide and / or metal hydroxide) surface modification composition is deposited on the textile surface. In some embodiments, a ceramic, for example, a structured ceramic, is deposited on the substrate surface, and a functional layer (e.g., a topcoat) providing one or more functional properties is deposited or applied on the ceramic material.

[0026] The composition is provided on the surface of a substrate such as a textile as a binderless surface modifier, for example, a surface-immobilized ceramic material. In some embodiments, the ceramic material comprises a metal oxide and / or hydroxide ceramic, for example, a single metal or mixed metal oxide and / or hydroxide ceramic. In some embodiments, the ceramic material comprises a metal hydroxide and / or hydroxide ceramic, for example, a single metal or mixed metal oxide and / or hydroxide ceramic. In some embodiments, the ceramic material comprises a metal oxide and a metal hydroxide ceramic, where the metal oxide and metal hydroxide comprise the same or different single metal or mixed metal. In some embodiments, the ceramic material comprises a metal oxide and / or metal hydroxide ceramic, where the substrate is hydrated with water or other compounds, resulting in a change in surface energy and potentially in the ratio of the metal oxide to metal hydroxide composition of the ceramic. In some embodiments, the ceramic material contains a metal hydroxide, in which case at least a portion of the metal hydroxide is in the form of a layered double hydroxide, for example, at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% of the metal hydroxide is a layered double hydroxide.

[0027] In some embodiments of the compositions described herein, "metal oxide" or "metal hydroxide" may be in the form of a hydrate of a metal oxide or a metal hydroxide, respectively, or a portion of the metal oxide or metal hydroxide may be in the form of a hydrate of a metal oxide or a metal hydroxide, respectively.

[0028] Mixed metal oxides or mixed metal hydroxides may each contain, for example, more than one metal oxide or hydroxide, such as, but are not limited to, iron, cobalt, nickel, copper, manganese, chromium, titanium, vanadium, zirconium, molybdenum, tantalum, zinc, lead, tin, tungsten, cerium, praseodymium, samarium, gadolinium, lanthanum, magnesium, aluminum, or calcium.

[0029] The surface modifier described herein (e.g., a binderless porous ceramic material) is deposited onto a substrate without using a binder (e.g., by reaction with a metal on the substrate surface). In some embodiments, the surface modifier as described herein is immobilized on the substrate.

[0030] In some embodiments, the ceramic material is a structured ceramic material, such as one that is nanostructured.

[0031] Non-limiting examples of binderless ceramic surface modifiers are described herein by reference in their entirety. This is provided in the incorporated PCT application number PCT / US19 / 65978.

[0032] definition Numerical ranges provided herein include the numerical values ​​that define those ranges.

[0033] "A," "an," and "the" include plural references unless otherwise specified by the context.

[0034] When used herein and in the claims, the phrase "and / or" should be understood to mean "either or both" of the combined elements, that is, elements that exist sometimes conjugated and sometimes separately. Unless otherwise explicitly stated, other elements may exist at their discretion, whether related to or unrelated to the elements specifically identified by the "and / or" clause. Thus, as a non-restrictive example, when used in conjunction with unrestrictive language such as "includes," in one embodiment, A may refer to A without B (optionally including elements other than B); in another embodiment, B may refer to B without A (optionally including elements other than A); and in yet another embodiment, both A and B (optionally including other elements), and so on.

[0035] A "binder" or binder is any material or substance that holds or attracts other materials together to form a whole by mechanical, chemical, adhesive, or agglomeration.

[0036] "Binderless" refers to the absence of a binder, particularly in the case of organic binders or resins (e.g., polymers, adhesives, sealants, asphalt) or inorganic binders (e.g., lime, cement glass, plaster, etc.) that are specifically added to maintain the structural integrity of the material of interest.

[0037] A "capping agent" refers to a compound or active substance that slows crystal growth and allows for the modification of the morphology of nano-surfaces.

[0038] "Ceramics" refers to solid materials containing metals, nonmetals, or inorganic compounds with ionic and covalent bonds.

[0039] "Fabric" refers to a non-woven material that is constructed from fibers and may be bonded together by chemical, mechanical, thermal, and / or solvent treatments. Fabrics may include, for example, felt and other materials that are neither woven nor knitted.

[0040] "Fiber" refers to the threads or filaments from which textiles are formed.

[0041] "Hydrophilic" refers to a surface that has a high affinity for water. The contact angle may be very low and / or immeasurable.

[0042] "Layered double hydroxides" have a general sequence [AcB Z AcB] n This refers to a group of ionic solids characterized by a layered structure having, where c represents a layer of metal cations, A and B are layers of hydroxide anions, and Z is a layer of other anions and / or neutral molecules (such as water). Layered double hydroxides are also described in PCT application number PCT / US2017 / 052120, which is incorporated herein by reference.

[0043] In this specification, a "nanostructure" composition has at least one dimension of 100 nanometers. This refers to a composition that has the characteristic of being less than [amount missing].

[0044] In fluid dynamics, "permeability" is a measure of a porous material's ability to allow fluid to pass through. While the permeability of a medium is related to its porosity, it is also related to the shape of the pores in the medium and the level of their connectivity.

[0045] "Pore size distribution" refers to the relative abundance or range or pore diameter of each pore as measured by mercury intrusion porosimetry (MIP) and the Washburn equation.

[0046] Porosity is a measure of the amount of empty (i.e., "empty") space in a material, and is either a fraction of the volume of empty space relative to the total volume, between 0 and 1, or a percentage between 0% and 100%. Porosity can be measured by mercury intrusion porosimetry.

[0047] "Porous" refers to spaces, holes, or voids within a solid material.

[0048] "Superhydrophobic" refers to a surface that is extremely difficult to wet with water. In the case of superhydrophobic materials, the contact angle of a water droplet on a superhydrophobic surface is greater than 150°. A highly hydrophobic contact angle is greater than 120°.

[0049] "Surface area per square meter of projected substrate area" refers to the actual measured surface area (usually measured in square meters) obtained by dividing it by the surface area of ​​the substrate if it were atomically smooth (no surface roughness) (also typically in square meters).

[0050] "Synergistic" or "combined" refers to the interaction or cooperation between two or more substances, materials, or agents that result in a combined effect that is higher (positive synergy) or lower (negative synergy) than the sum of their individual separate effects.

[0051] "Textiles" refer to flexible materials consisting of networks of natural or synthetic fibers. For example, textile materials can be made by combining fibers or groups of fibers through knitting, weaving, felting, tufting, or bonding, in which case the fibers include both natural and synthetic forms of all lengths, including metallic fibers. Textiles also include ropes and cords.

[0052] "Thickness" refers to the distance between the surface of the substrate and the top layer of the surface-modified material (e.g., ceramic).

[0053] "Adjustable" refers to the ability to change or modify the function, characteristics, or quantity of a material.

[0054] "Vapor permeability" refers to the amount of vapor per unit time per unit area passing through a layer in a direction perpendicular to the layer's surface.

[0055] "Water column breakthrough pressure" refers to the relative height of a vertical water column at which the hydrostatic pressure acting on a layer at the bottom of the water column exceeds the capacity of the layer supporting the water column, resulting in water flow through the layer.

[0056] Base material Porous materials such as textile materials or fabrics serve as substrates for depositing ceramic materials as described herein. For example, the substrate is a woven material. The substrate may consist of knitted fabrics, non-woven fabrics or textiles, or paper. The substrate may include natural fibers, synthetic fibers, metal meshes, or metal cloths, or combinations thereof. In certain non-limiting embodiments, the substrate may include or consist of polymers (e.g., polyamides (e.g., nylon), polyesters, polyethylenes, polypropylenes, polyurethanes), cellulosic materials (e.g., rayon), cotton, wool, aramids, activated carbon, fiberglass, alloys (e.g., steel, brass, or aluminum alloys), or metals (e.g., aluminum, copper).

[0057] In some embodiments, the textile substrate is a metallized textile. The metallized textile contains one or more metals on the textile surface, including but not limited to aluminum, iron, nickel, titanium, or copper, or combinations thereof. In one embodiment, the metallized textile is metallized with aluminum. The thickness of the metal on the textile surface may be about 25 nm to about 2000 nm, about 25 nm to about 100 nm, about 50 nm to about 250 nm, about 100 nm to about 500 nm, about 500 nm to about 1000 nm, about 1000 nm to about 2000 nm, about 750 nm to about 1500 nm, about 100 nm to about 2000 nm, or about 500 nm to about 2000 nm.

[0058] In some embodiments, the substrate is oxidized, activated, or ashed before the deposition of the continuous ceramic material. In some embodiments, this oxidation step is performed by immersing the substrate in an oxidizing agent. In some embodiments, the oxidizing agent includes persulfates, permanganates, nitrates, or peroxides. In some embodiments, the oxidizing agent bath is heated. In some embodiments, the surface is oxidized using potassium persulfate, potassium permanganate, or hydrogen peroxide. In some embodiments, the substrate is oxidized, activated, or ashed using UV / ozone or plasma. In some embodiments, the surface is oxidized and / or activated using oxygen plasma.

[0059] In some embodiments, the air permeability of the substrate according to ASTM D737 is about 0.1 cubic feet per minute (CFM) to about 100 CFM. In other embodiments, the air permeability is about 0.5 CFM, about 1 CFM, about 2 CFM, about 5 CFM, about 10 CFM, about 20 CFM, about 30 CFM, about 40 CFM, about 50 CFM, about 60 CFM, about 70 CFM, about 80 CFM, about 90 CFM, or about 100 CFM. In other embodiments, the air permeability is about 1 CFM to about 5 CFM or about 1 CFM to about 20, about 0.1 CFM to about 0.5 CFM, about 20 CFM to about 50 CFM, or about 50 CFM to about 100 CFM. In some embodiments, the ceramic material or functionalized material does not vary the air permeability by more than about 20%.

[0060] Functionalization The porous substrate as described herein is a functionalized composition (e.g., industrial textile or filter material) containing one or more desirable functional properties. Such functional properties may include, but are not limited to, hydrophobicity, inhibition or resistance to microbial growth, flame retardancy, hydrophilicity, corrosion resistance, ice or condensate management, de-icing, frost protection, superhydrophobicity, superhydrophilicity, corrosion resistance, electromagnetic regulation, thermal modulation, permeability, dynamic wind resistance, and / or color, or a combination thereof.

[0061] In some embodiments, the functionalized substrate (e.g., textile) described herein does not contain fluorocarbon agents. In some embodiments, the functionalized substrate (e.g., textile) produced herein contains a plurality of desirable properties (functionality) in a single layer of the substrate. In some embodiments, the functionalized substrate (e.g., textile) produced herein contains a functionalized structured ceramic on a textile substrate containing natural or synthetic fibers.

[0062] In some embodiments, the ceramic deposited on the substrate can be designed with a desired porosity or open fraction that imparts functional characteristics and can even be used to prepare a bonding surface for the deposition of structured ceramic material.

[0063] In some embodiments, one or more functional layers, such as a topcoat material, are applied to the structured ceramic material to impart desired functional properties to the textile material. One or more functional properties can be imparted by the structured ceramic and / or the applied topcoat material. Non-limiting examples of functionalities imparted to textiles by the methods described herein include hydrophobicity, inhibition of microbial growth, flame retardancy, hydrophilicity, corrosion resistance, ice or condensate management, de-icing, frost protection, superhydrophobicity, superhydrophilicity, inhibition of microbial growth, corrosion resistance, electromagnetic regulation, thermal modulation, breathability, dynamic wind resistance, odor resistance or odor removal (e.g., deodorizing properties), and / or color, and combinations thereof. In some embodiments, multiple functionalities are imparted to a single layer of the textile material (i.e., a multifunctional single-layer textile).

[0064] In some embodiments, the functionality imparted by a topcoat material applied or deposited on a ceramic as described herein is enhanced compared to the functionality of the same material applied or deposited on the same substrate without the ceramic. In some embodiments, the ceramic material and the topcoat material synergistically impart one or more functional properties that are more advanced than the same functional properties imparted by either the ceramic material or the topcoat material independently deposited on the same substrate surface.

[0065] In some embodiments, hydrophobic functionality is provided by stearic acid or Scotchgard® (3M). In some embodiments, antimicrobial functionality is provided by SmartShield Antimicrobial Protective Spray (Sylvane). In some embodiments, flame retardancy is provided by No Burn 1005 Fabric Fire Protection (No-Burn, Inc.) or a halon-containing compound. In some embodiments, hydrophilic functionality is provided by polyvinylpyrrolidone (PVP), polyurethane, polyacrylic acid (PAA), polyethylene oxide (PEO), or a polysaccharide material.

[0066] In certain non-limiting embodiments, the topcoat may include paints, paint binders, hydrophobic materials, hydrophilic materials, metals or metal-containing compounds, or antimicrobial agents.

[0067] In some embodiments, the ceramic surface modifier is a partially filled porous structure. For example, the voids may be partially filled with a second ceramic material (e.g., a ceramic material different from the binderless porous ceramic material) or with head groups and tail groups, for example, the head groups may include silane groups, phosphonate groups, phosphonic acid groups, carboxylic acid groups, vinyl groups, alcohol groups, hydroxide groups, thiolate groups, thiol groups, and / or ammonium groups (e.g., quaternary ammonium groups), and the tail groups may include hydrocarbon groups, fluorocarbon groups, vinyl groups, phenyl groups, epoxide groups, acrylic groups, acrylate groups, hydroxyl groups, carboxylic acid groups, thiol groups, and / or quaternary ammonium groups.

[0068] In some embodiments, the topcoat is a surface that modifies the topcoat to reduce the viscous drag of external or internal fluids on the surface. In some embodiments, the coating is deposited on a surface containing a nanostructured coating composition and on a surface that modifies the topcoat to reduce the viscous drag of external or internal fluids, and further includes additional benefits such as corrosion resistance, fouling resistance, self-cleaning, heat transfer properties, and optical properties.

[0069] In some embodiments, the topcoat is or contains an antimicrobial agent. For example, the antimicrobial agent may be a charge-transfer compound or active substance that disrupts the movement of ions across the cell membrane, such as a quaternary amine. In some embodiments, the antimicrobial agent is a beta-lactam, aminoglycoside, tetracycline, chloramphenicol, macrolide, lincosamide, sulfonamide, quinolone, polyene, azole, or griseofulvin.

[0070] In some embodiments, the topcoat is or contains a paint binder. For example, the paint binder may be alkyd, acrylic, vinyl acrylic, vinyl acetate / ethylene (VAE), polyurethane, polyester, silicone, polyol, melamine resin, wax, epoxy, silane, or oil.

[0071] Ceramic material Deposit a ceramic material, such as a structured ceramic material as described herein, on at least a portion of the surface of the porous substrate. In some embodiments, the ceramic material is a nanostructured ceramic material. In some embodiments, the ceramic material is porous. In some embodiments, the ceramic material is a binderless ceramic material, such as a binderless nanostructured ceramic material. In some embodiments, the ceramic material is a binderless porous ceramic material, such as a binderless porous nanostructured ceramic material.

[0072] In some embodiments, the ceramic material has: a surface area of about 1.5 m 2 ~100 m 2 per square meter of projected substrate area, about 10 m 2 ~ about 1500 m 2 per square meter of projected substrate area, or about 70 m 2 ~ about 1000 m 2 per square meter of projected substrate area; a surface area of about 15 m 2 ~ about 1500 m 2 per gram of ceramic material, or about 50 m 2 ~ about 700 m 2 per gram of ceramic material; an average pore diameter of about 5 nm to about 200 nm, about 2 nm to about 20 nm, or about 4 nm to about 11 nm; a thickness of up to about 100 micrometers, up to about 50 micrometers, up to about 25 micrometers, up to about 20 micrometers, or about 0.2 micrometers to about 25 micrometers; a porosity of about 5% to about 95%, about 10% to about 90%, about 30% to about 70%, about 30% to about 95%, or greater than about 10%; a pore volume of about 100 mm 3 / g to about 7500 mm 3 / g determined by mercury intrusion porosimetry; including any combination thereof.

[0073] In some embodiments, the ceramic material (e.g., metal oxides, metal hydroxides, and / or hydrates thereof) includes one or more of zinc, aluminum, manganese, magnesium, cerium, copper, gadolinium, tungsten, tin, lead, and cobalt. In some embodiments, the ceramic material includes transition metals, Group II elements, rare earth elements (e.g., lanthanum, cerium, gadolinium, praseodymium, scandium, yttrium, samarium, or neodymium), aluminum, tin, zinc, or lead.

[0074] In some embodiments, the ceramic surface modifier includes thicknesses of about 0.5 or 1 to about 100 micrometers, or about 0.5 micrometers to about 20 micrometers, or up to about 50 micrometers, or up to about 25 micrometers. In some embodiments, the binderless porous ceramic material includes thicknesses of about 0.2 micrometers to about 25 micrometers. In some embodiments, the thickness is at least one of about 0.2, 0.5, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 micrometers. In some embodiments, the thickness is approximately 0.2 to 0.5, 0.5 to 1, 1 to 5, 3 to 7, 5 to 10, 7 to 15, 10 to 15, 12 to 18, 15 to 20, 18 to 25, 0.5 to 15, 2 to 10, and 1 to 10. These are either approximately 3 to 13, approximately 0.5 to 15, approximately 0.5 to 5, approximately 0.5 to 10, or approximately 5 to 15 micrometers.

[0075] In some embodiments, the ceramic surface modifier is present at a rate of approximately 1.1 m² per square meter of projected substrate area. 2 ~approximately 100m 2 This includes the surface area. In some embodiments, the binderless porous ceramic material has a surface area of ​​approximately 10 m² per square meter of projected substrate area. 2 ~about 1500m 2This includes the surface area. In some embodiments, the surface area is at least about 10, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, or 1500 m² per square meter of projected substrate area. 2 In some embodiments, the surface area is approximately 10 to 100, 50 to 250, 150 to 500, 250 to 750, 500 to 1000, 750 to 1200, 1000 to 1500, 70 to 1000, 150 to 800, 500 to 900, or 500 to 1000 m² per square meter of projected substrate area. 2 It is one of the following:

[0076] In some embodiments, the ceramic material is approximately 15 m³ per gram of ceramic material. 2 ~about 1500m 2 This includes the surface area. In some embodiments, the surface area is at least about 15, 50, 100, 150, 200, 250, 300, 350, 400, 450, 500, 550, 600, 650, 700, 750, 800, 850, 900, 950, 1000, 1050, 1100, 1150, 1200, 1250, 1300, 1350, 1400, 1450, or 1500 m² per gram of ceramic material. 2 In some embodiments, the surface area is approximately 15 to 100, 50 to 250, 150 to 500, 250 to 750, 500 to 1000, 750 to 1200, 1000 to 1500, 50 to 700, 75 to 600, 150 to 650, or 250 to 700 m² per gram of ceramic material. 2 It is one of the following:

[0077] In some embodiments, the ceramic surface modifier is porous and includes a mesoporous mean pore size in the range of about 2 nm to about 50 nm. In other embodiments, the mean pore size is in the range of about 50 nm to about 1000 nm. In some embodiments, the binderless porous ceramic material includes a mean pore diameter of about 2 nm to about 20 nm. In some embodiments, the mean pore diameter is at least one of about 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nm. In some embodiments, the mean pore diameter is one of about 2 to about 5, about 4 to about 9, about 5 to about 10, about 7 to about 12, about 9 to about 15, about 12 to about 18, about 15 to about 20, about 4 to about 11, about 5 to about 9, about 4 to about 8, or about 7 to about 11 nm.

[0078] In some embodiments, the ceramic surface modifier is porous and has a porosity of about 5% to about 95%. In some embodiments, the porosity may be at least about 5%, 10%, 15%, 20%, 25%, 30%, 35%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, or 95% or more. In some embodiments, the porosity is about 10% to about 90%, about 30% to about 90%, about 40% to about 80%, or about 50% to about 70%.

[0079] In some embodiments, the ceramic surface modifier is porous and has a transmittance of about 1 to 10,000 millidarcy. In some embodiments, the transmittance may be at least about 1, 10, 100, 500, 1000, 5000, or 10,000 millidarcy. In some embodiments, the transmittance may be about 1 to about 100, about 50 to about 250, about 100 to about 500, about 250 to about 750, about 500 to about 1000, about 750 to about 2000, about 1000 to about 2500, about 2000 to about 5000, about 3000 to about 7500, and about 50 The millidarcy ranges are approximately 0 to 10,000, approximately 1 to 1,000, approximately 1,000 to 5,000, or approximately 5,000 to 10,000.

[0080] In some embodiments, the ceramic material is porous, and when determined by mercury intrusion porosimetry, it has a density of approximately 100 mm. 3 / g ~ approx. 7500mm 3 The void volume includes a void volume of at least about 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1500, 2000, 2500, 3000, 3500, 4000, 4500, 5000, 5500, 6000, 6500, 7000, or 7500 mm². 3 The void volume is one of the following: / g. In some embodiments, the void volume is approximately 100-500, approximately 200-1000, approximately 400-800, approximately 500-1000, approximately 800-1500, approximately 1000-2000, approximately 1500-3000, approximately 2000-5000, approximately 3000-7500, approximately 250-5000, approximately 350-4000, approximately 400-3000, approximately 250-1000, approximately 250-2500, approximately 250-5000, or approximately 500-4000 mm 3 It is either / g or

[0081] The ceramic deposited layer can be designed to impart one or more functional features and to further prepare a bonding surface for functionalized layers such as topcoat materials.

[0082] Purpose of use The modified substrates (e.g., textiles) described herein include one or more functional properties that enhance performance in a system or application.

[0083] For example, a modified substrate may exhibit higher adhesion to low molecular weight molecules (e.g., low molecular weight organic compounds such as drugs or antibiotics (e.g., less than 900 Da and / or size 1 nm or less)) than to biomolecules or components of sebum (e.g., triglycerides, wax esters, squalene, and / or fatty acids). Such compositions can be provided, for example, in the form of a bandage (e.g., a cast liner) that is pre-coated with a drug or insecticide and does not accumulate odors from body oils (sebum).

[0084] In another embodiment, the substrate is functionalized to have photocatalytic properties, so that materials adhering to the surface are decomposed by the photocatalyst when exposed to light. For example, when exposed to light, odor-causing compounds such as sebum components can be decomposed.

[0085] In another embodiment, the composition exhibits greater adhesion to durable water-repellent substances than the same substrate that has not been modified with the ceramic material described herein. Several commercially available durable water-repellent formulations are fluoropolymer-based and, in contrast to the composition described herein, may require frequent reapplication to maintain performance. Other materials include perfluoroacids, per- and polyfluoroalkyl substances (PFAS), perfluorobutanesulfonic acid, perfluorooctanoic acid, Scotchgard, and Quarpel. Many of these materials have harmful health and environmental impacts.

[0086] Products comprising the compositions described herein are provided. Non-limiting examples of such products include filters, membranes, clothing, outerwear, camping gear (e.g., tents, sleeping bags), pipe insulation, carpets, interior materials, car seats (e.g., infant seats), floor coverings (e.g., water-resistant and breathable floor coverings such as bed sheets), building exterior materials, footwear, and window coverings.

[0087] In one embodiment, the composition is used as a membrane, such as in food packaging, but is not limited to this. For example, the membrane may serve as a barrier against certain compounds, while allowing oxygen and other materials to pass through, or it may serve to separate water from air. It can obtain (e.g., water repellency or water retention) or separate and retain solids from liquids (e.g., cheesecloth). In other embodiments, the film may allow the passage of water vapor but not liquid water.

[0088] The following examples are illustrative and not intended to limit the invention. [Examples]

[0089] Example 1 Ripstop nylon was used as a base material for producing water-resistant, breathable textile materials. Woven ripstop nylon was coated with aluminum by vapor deposition to produce aluminum-coated nylon with an aluminum thickness of 25 nm to 2000 nm, typically around 300 nm.

[0090] Next, the aluminum-coated samples were coated with a porous magnesium oxide-based ceramic deposited in a 25-75 mM aqueous solution of magnesium nitrate and an equivalent amount of hexamethylenetetramine at a temperature of approximately 60°C-80°C for approximately 5-90 minutes. The mesh was then calcined at a temperature of approximately 100°C-250°C for approximately 1 hour. The structure of the deposits was imaged to evaluate its uniformity.

[0091] The textiles were functionalized and given superhydrophobic properties by batch immersion in hexadecylphosphonic acid for 90 minutes, followed by drying at 105°C for 90 minutes. When the samples were tested against AATCC 127 and ASTM E96 standards, they were observed to have superior water resistance and water vapor permeability compared to existing waterproof and breathable products.

[0092] Example 2 A stainless steel mesh layer was pitted by acid etching and then coated with a binderless structured manganese oxide ceramic surface modifier deposited in a 25-75 mM aqueous solution of manganese nitrate and an equivalent amount of hexamethylenetetramine or urea at a temperature of approximately 60°C-80°C for approximately 60-240 minutes. The mesh was then calcined at a temperature of approximately 400°C-600°C for approximately 1 hour to impart hydrophilic properties to the surface. The water contact angle was measured to be less than 5 degrees by the droplet method. The mesh was placed in a cup containing approximately 1 cm of deionized water. After 2 minutes, the capillary rise was determined to be approximately 3 cm above the liquid surface. The capillary rise was determined as described in PCT application number PCT / US19 / 65978 (see, for example, Figures 1A-1C). The vapor transmission rate was 130 g / hour / m³. 2 It was determined that the layer could not support any measurable height of water column overpressure.

[0093] Example 3 A stainless steel mesh layer was coated with a ceramic material composed of manganese oxide using a method similar to that described in Example 2. The surface was then functionalized using a diluted solution (approximately 0.5%) of hexadecylphosphonic acid in isopropanol, thereby providing surface hydrophobic properties. The water contact angle was measured at 151 degrees by the droplet method. The layer was placed in a cup containing approximately 1 cm of deionized water. After 2 minutes, no significant water rise was observed above the liquid level. The vapor transmission rate was 145 g / hour / m². 2 It was determined that the water column break pressure was 25 cm in water head.

[0094] Example 4 A stainless steel mesh layer without any surface treatment was tested. The water contact angle was measured at 20 degrees by the droplet method. The layer was placed in a cup containing approximately 1 cm of deionized water. After several minutes, no significant rise of water was observed on the surface above the liquid level. The vapor transmission rate was 152 g / hour / m³. 2It was determined that the layer could not support any measurable height of water column overpressure.

[0095] Example 5 An aluminum mesh layer was coated with a ceramic material consisting of magnesium oxide deposited in a 25-75 mM aqueous solution of magnesium nitrate and an equivalent amount of hexamethylenetetramine at a temperature of approximately 60°C-80°C for approximately 30-90 minutes. The mesh was then calcined at a temperature of approximately 300°C-600°C for approximately 1 hour to impart hydrophilic properties to the surface. The water contact angle was measured to be less than 5 degrees by the droplet method. The layer was placed in a cup containing approximately 1 cm of deionized water. After 2 minutes, the capillary rise was determined to be approximately 5 cm above the liquid surface. The vapor transmission rate was approximately 150 g / hour / m³. 2 It was determined that the layer could not support any measurable height of water column overpressure.

[0096] Example 6 An aluminum mesh (Dutch twill) layer was coated with a ceramic material composed of magnesium oxide using the same procedure as described in Example 5. The surface was then functionalized using a diluted solution of hexadecylphosphonic acid in isopropanol, thereby providing surface hydrophobic properties. The water contact angle was measured at 160 degrees by the droplet method. The layer was placed in a cup containing approximately 1 cm of deionized water. After 2 minutes, no significant water rise was observed above the liquid level. The vapor transmission rate was 150 g / hour / m². 2 It was determined that the water column break pressure was 100 cm in water head.

[0097] Example 7 An aluminum mesh layer without any surface preparation was tested. The water contact angle was measured at 20 degrees by the droplet method. The layer was placed in a cup containing approximately 1 cm of deionized water. After 2 minutes, no significant rise of water was observed above the liquid level. The vapor transmission rate was 153 g / hour / m². 2It was determined that the layer could not support any measurable height of water column overpressure.

[0098] Example 8 Using a method similar to that described in Example 1, a 40d (40 denier) woven polyamide textile layer was coated with a ceramic material composed of magnesium oxide, thereby obtaining surface hydrophilic properties. The water contact angle was measured to be less than 5 degrees by the droplet method. The vapor transmission rate was 175 g / hour / m². 2 It was determined that the layer could not support any measurable height of water column overpressure.

[0099] Example 9 A 40d woven polyamide textile layer was coated with a ceramic material composed of magnesium oxide. The surface was then functionalized using a diluted solution of hexadecylphosphonic acid in isopropanol, thereby obtaining surface hydrophobic properties. The vapor transmission rate was 170 g / hour / m². 2 It is determined that the water column break pressure is 55 cm at the water head.

[0100] Example 10 A 40d woven polyamide textile layer without any surface treatment was tested. The vapor transmission rate was 170 g / hour / m². 2 It was determined that the layer could not support any measurable height of water column overpressure.

[0101] Example 11 Aluminum at approximately 250 nm was sputtered onto woven polyester textiles and woven nylon textiles. The textiles were cut into small pieces and coated with three different ceramic materials: a) magnesium oxide / hydroxide-based ceramic, b) manganese oxide / hydroxide-based ceramic, and c) zinc oxide / hydroxide-based ceramic. All three ceramics contained aluminum oxide / hydroxide. The ceramics were deposited in the same manner as described in Example 1 (using 2+ metal nitrates or metal sulfates for each individual cation found in the ceramic). When the samples were tested for contact angle, they showed a contact angle of less than 15 degrees. The ceramic-modified textiles were then immersion coated in a diluted bath (0.1%~1%) of hexadecylphosphonic acid in isopropanol or hexadecyltriethoxysilane in ethanol. In the case of silane, a small amount of acetic acid catalyst was sometimes used. The samples were then measured again for contact angle and showed a contact angle of approximately 150~160 degrees. Water vapor permeability was within the measurement margin of the unmodified fabric.

[0102] Example 12 Woven polyester textiles, polyamide textiles, and Tencel textiles were coated with zinc oxide-based ceramics by immersion in batches of approximately 200–500 mM zinc sulfate, approximately 50–150 mM potassium persulfate, and approximately 1.2–1.7 mol of ammonium hydroxide at room temperature for approximately 5–60 minutes. Nickel oxide deposits were also deposited on the polyester by using nickel sulfate instead of zinc sulfate. Manganese oxide deposits were also produced on the polyester by using manganese sulfate instead of zinc sulfate and permanganate instead of persulfate. These samples were then dried at a temperature of approximately 105°C–140°C for approximately 1–2 hours. When the samples were tested for contact angle, they showed a contact angle of less than 15 degrees. The ceramic-modified textiles were then coated by immersion in a diluted bath (0.1%–1%) of hexadecylphosphonic acid in isopropanol or hexadecyltriethoxysilane in ethanol. In the case of silane, a small amount of acetic acid catalyst was occasionally used. Subsequently, when the contact angle of the sample was measured again, it showed a contact angle of approximately 150-160 degrees.

[0103] Example 13 Woven polyamides and polyester textiles were activated by immersion in a bath of an oxidizing agent. A typical oxidation procedure involved immersing the textile in a water bath of potassium persulfate or potassium permanganate at a concentration of approximately 5 mM to approximately 200 mM and ammonium hydroxide at a concentration of approximately 10 mM to approximately 400 mM. A typical bath contained potassium permanganate or potassium persulfate and ammonium hydroxide in a molar ratio of approximately 1:2. The oxidation temperature ranged from approximately room temperature to approximately 80°C.

[0104] Example 14 Woven polyester and polyamide textiles were oxidized in UV / ozone and / or oxygen plasma to achieve better adhesion of the structured ceramic layer.

[0105] Example 15 Woven polyamides and polyester textiles were immersed in aqueous baths of approximately 5–200 mM potassium permanganate and approximately 10–400 mM ammonium hydroxide at temperatures ranging from approximately room temperature to approximately 80°C for approximately 5 minutes to approximately 1 hour. The typical ratio of permanganate to ammonium hydroxide was approximately 1–2. The substrates were then dried, and then a structured ceramic layer containing manganese oxide / hydroxide, zinc oxide / hydroxide, or magnesium oxide / hydroxide was deposited by immersing the substrates in 25–150 mM aqueous solutions of metal (Mn, Zn, or Mg) nitrates and similar amounts of hexamethylenetetramine at temperatures ranging from approximately 60°C to 80°C for approximately 5–90 minutes. The meshes were then dried at temperatures ranging from approximately 100°C to 250°C. The samples were dried for approximately one hour. The contact angles of these samples were measured and determined to be less than approximately 15 degrees. The ceramic-modified textiles were then coated by immersion in a diluted bath (0.1%–1%) of hexadecylphosphonic acid in isopropanol or hexadecyltriethoxysilane in ethanol. In the case of silane, a small amount of acetic acid catalyst was occasionally used. The samples were then measured again for contact angles, which showed contact angles of approximately 150–160 degrees.

[0106] Although the aforementioned invention has been described in some detail as examples and embodiments for the purpose of clarifying its understanding, it will be apparent to those skilled in the art that certain changes and modifications can be made without departing from the intent and scope of the invention as described in the attached claims. Therefore, these descriptions should not be interpreted as limiting the scope of the invention.

[0107] All publications, patents, and patent applications cited herein are incorporated herein by reference in whole for all purposes, to the same extent as any individual publication, patent, or patent application is specifically and individually incorporated herein by reference.

Claims

1. A composition comprising a binderless ceramic material on a porous substrate.

2. The composition according to claim 1, wherein the substrate contains pores having an average pore diameter of less than approximately 250 μm, and the ceramic material substantially does not change the average pore diameter.

3. The composition according to claim 1, wherein the substrate contains pores having an average pore diameter of less than approximately 250 μm, and the ceramic partially or completely fills the pores, thereby reducing the average pore diameter or removing the pores, respectively.

4. The composition according to any one of claims 1 to 3, wherein the substrate has an air permeability of about 0.1 cubic feet per minute (CFM) to about 100 CFM according to ASTM D737.

5. The composition according to any one of claims 1 to 3, wherein the ceramic material is mainly crystalline.

6. The composition according to any one of claims 1 to 3, wherein the ceramic material comprises a metal oxide, a hydrate of a metal oxide, a metal hydroxide, and / or a hydrate of a metal hydroxide.

7. The composition according to any one of claims 1 to 3, wherein the ceramic material comprises a metal hydroxide, and at least a portion of the metal hydroxide comprises a layered double hydroxide.

8. The composition according to any one of claims 1 to 3, wherein the ceramic material includes a nanostructured ceramic material.

9. The composition according to any one of claims 1 to 3, wherein the ceramic material comprises a transition metal, a group II element, a rare earth element, aluminum, tin, or lead.

10. The composition according to claim 9, wherein the ceramic material comprises one or more of zinc, aluminum, manganese, magnesium, cerium, copper, gadolinium, tungsten, tin, zinc, lead, and cobalt.

11. The composition according to claim 10, wherein the ceramic material comprises a mixture of zinc and aluminum oxides and / or hydroxides; a mixture of manganese and magnesium oxides and / or hydroxides; manganese oxides and / or hydroxides; aluminum oxides and / or hydroxides; mixed metallic manganese oxides and / or hydroxides; a mixture of magnesium and aluminum oxides and / or hydroxides; magnesium oxides and / or hydroxides; a mixture of magnesium, cerium, and aluminum oxides and / or hydroxides; a mixture of zinc, praseodymium, and aluminum oxides and / or hydroxides; a mixture of cobalt and aluminum oxides and / or hydroxides; a mixture of manganese and aluminum oxides and / or hydroxides; a mixture of cerium and aluminum oxides and / or hydroxides; a mixture of copper and aluminum oxides and / or hydroxides; a mixture of zinc and aluminum oxides and / or hydroxides; a mixture of Zn-aluminates; a mixture comprising one or more phases containing Zn, Al, and oxygen; zinc oxides and / or hydroxides; or a hydrate of any of the compounds or a mixture thereof.

12. The composition according to claim 11, wherein the ceramic material has a maximum thickness of about 25 μm.

13. The set according to claim 12, wherein the ceramic material has a thickness of about 0.2 μm to about 25 μm. Finished product.

14. The composition according to any one of claims 1 to 3, wherein the ceramic material has a porosity of about 5% to about 80%.

15. The composition according to claim 14, wherein the ceramic material contains a porosity of more than about 10%.

16. The composition according to claim 14, wherein the ceramic material has a porosity of about 30% to about 95%.

17. The composition according to any one of claims 1 to 3, wherein the porous substrate includes a woven material, a knitted fabric, a non-woven fabric or textile, or paper.

18. The composition according to claim 17, wherein the porous substrate comprises polyamide, polyester, cotton, wool, polyethylene, polypropylene, cellulosic material, aramid, polyurethane, activated carbon, fiberglass, steel alloy, brass alloy, aluminum alloy, aluminum, or copper.

19. The composition according to claim 17, wherein the porous substrate is a textile material comprising natural fibers, synthetic fibers, metal mesh, or metal cloth, or a combination thereof.

20. The composition according to claims 17 to 19, wherein the textile surface is oxidized, ashed, or activated.

21. The composition according to claim 17, wherein the base material is a metallized textile containing one or more metals on the surface of the textile.

22. The method according to claim 21, wherein the metal on the textile surface includes aluminum, iron, nickel, titanium, or copper.

23. The composition according to any one of claims 1 to 3, wherein the binderless ceramic imparts one or more functional properties to the composition.

24. The composition according to claim 23, wherein one or more of the functional properties include hydrophilicity, hydrophobicity, flame retardancy, photocatalytic activity, antifouling, deodorizing properties, inhibition of microbial growth, ice or condensate management, anti-icing, anti-frosting, superhydrophobicity, superhydrophilicity, corrosion resistance, electromagnetic regulation, thermal modulation, air permeability, dynamic wind resistance, and / or color.

25. The composition according to claim 23, wherein two or more of the above-mentioned functional characteristics are provided in a single layer of the composition.

26. The composition according to any one of claims 1 to 3, wherein the ceramic material is further modified by a functional layer.

27. The composition according to claim 26, wherein the functional layer imparts one or more functional properties that are superior to the same functional properties imparted by the same functional layer material directly deposited on the same textile surface that does not contain the ceramic material.

28. The ceramic material and the functional layer possess the same functional properties as those imparted by either the ceramic material or the functional layer material, which are independently deposited on the same textile surface. The composition according to claim 26, which synergistically imparts one or more functional properties that are also highly advanced.

29. The composition according to claim 26, wherein the functional layer imparts hydrophobic properties.

30. The composition according to claim 29, wherein the functional layer comprises a fluoropolymer, an elastomer, or a plastic.

31. The functional layer has head groups and tail groups, In this case, the head group includes a silane group, a phosphonate group, a phosphonic acid group, a carboxylic acid group, a vinyl group, an alcohol group, a hydroxide group, a thiolate group, a thiol group, and / or an ammonium group, The composition according to claim 29, wherein the tail group comprises a molecule containing a hydrocarbon group, a fluorocarbon group, a vinyl group, a phenyl group, an epoxide group, an acrylic group, an acrylate group, a hydroxyl group, a carboxylic acid group, a thiol group, and / or a quaternary ammonium group.

32. The composition according to any one of claims 1 to 3, wherein the ceramic material has a partially filled porous structure.

33. The composition according to claim 32, wherein the voids are partially filled with a second ceramic material or with molecules having head groups and tail groups.

34. The composition according to any one of claims 1 to 3, wherein the ceramic material exhibits higher adhesion to low molecular weight molecules than to biomolecules or components from sebum.

35. The composition according to claim 34, wherein the components derived from sebum include triglycerides, wax esters, squalene, and / or free fatty acids.

36. The composition according to any one of claims 1 to 3, wherein the ceramic material has photocatalytic properties, and the material adhering to the surface is decomposed by the photocatalyst when exposed to light.

37. The composition according to any one of claims 1 to 3, which exhibits higher adhesion to a durable water-repellent substance than the same substrate that does not contain the ceramic material.

38. A product comprising the composition according to any one of claims 1 to 37.

39. The product according to claim 38, selected from filters, membranes, clothing, outerwear, camping gear, pipe insulation, carpets, car seats, interior materials, floor coverings, footwear, building coverings, and window covers.

40. A composition or product according to any one of claims 1 to 39, which can withstand a hydrostatic pressure of more than approximately 1 kPa.

41. A composition or product according to any one of claims 1 to 39, comprising a water vapor transmission rate exceeding approximately 80% of the vapor transmission rate of the same substrate without the aforementioned ceramic material.

42. A composition or product according to any one of claims 1 to 39, comprising a droplet water contact angle greater than approximately 150 degrees.

43. It contains manganese oxide ceramic and an alkylsilane or alkylphosphonate functional layer. The composition or product according to any one of claims 1 to 39.