Antiviral preparation, antiviral filtration material, method for preparing the same, and antiviral face mask

Abstract

A first subject of the invention consists of an antiviral formulation comprising metallic copper particles in non-oxidized form with a median particle size of less than or equal to 200 nm, graphene oxide or reduced graphene oxide, and a binding matrix material. A second subject of the invention consists of an antiviral filtration material comprising a layer of fabric and at least one layer of an antiviral coating comprising metallic copper particles having a median particle size of less than or equal to 200 nm in non-oxidized form, graphene oxide or reduced graphene oxide, and a binding matrix to which both the metallic copper particles and the graphene oxide or reduced graphene oxide are fixed. The present invention also relates to methods for preparing antiviral formulations and antiviral filtration materials. Finally, the present invention consists of an antiviral face mask comprising a layer of fabric coated with an antiviral formulation.

Description

[Technical Field]

[0001] The present invention relates primarily to an antiviral formulation that can be used in several applications. In particular, the antiviral formulation can be used to coat a textile substrate in the preparation of an antiviral filter material. Therefore, the present invention also relates to an antiviral filter material prepared using the antiviral formulation. The present invention further relates to an antiviral face mask comprising the antiviral filter material. Finally, the present invention relates to a method for preparing an antiviral formulation and a method for preparing an antiviral filter material. [Background technology]

[0002] There is an urgent need for effective measures to prevent viruses in the air or on surfaces, such as SARS-CoV-2, from entering the human body.

[0003] Antimicrobial masks containing graphene oxide and copper-silver nanocomposites are known from publication CN108378440. Antimicrobial formulations are prepared from silver nitrate and copper nitrate.

[0004] However, silver is thought to have adverse effects on human health. Furthermore, copper salts have no known antiviral properties. Also, copper salts may be toxic. Finally, metal salts can be easily released, and the mask will lose its necessary antibacterial properties when it is first washed. [Prior art documents] [Patent Documents]

[0005] [Patent Document 1] Chinese Patent Application Publication No. 108378440 Specification [Overview of the project] [Problems that the invention aims to solve]

[0006] Therefore, the object of the present invention is to improve upon the shortcomings of the prior art by providing an antiviral and non-toxic formulation.

[0007] A further objective of the present invention is to provide an antiviral formulation that has stable antiviral activity while avoiding the leaching of the active ingredient.

[0008] Another objective of the present invention is to provide an antiviral filtration material having improved antiviral activity and good breathability.

[0009] A further object of the present invention is to provide an antiviral filtration material that avoids or at least limits the leaching of active ingredients after washing.

[0010] Finally, an object of the present invention is to provide a method for preparing the antiviral preparation and a method for preparing the antiviral filtration material, which is scalable and inexpensive.

[0011] Another object of the present invention is to provide an antiviral face mask. [Means for solving the problem]

[0012] For this purpose, the first subject of the present invention is an antiviral formulation comprising metallic copper particles having a median particle size of 200 nm or less in a non-oxidized form, graphene oxide or reduced graphene oxide, and a binding matrix material.

[0013] The antiviral formulations according to the present invention may also be considered individually or in combination with any of the following features: - Metallic copper particles are metallic copper nanoparticles; - Metallic copper particles are chemically bonded to graphene oxide or reduced graphene oxide; - The bonding matrix material contains an aqueous resin; - Water-based resins are polyurethane resins, acrylic resins, polyester resins, oligomers, or mixtures thereof; - The aqueous resin is a polyurethane resin or an acrylic resin, in which the ratio of graphene oxide or reduced graphene oxide to metallic copper particles is between 62:1 and 1:1, and the ratio of graphene oxide or reduced graphene oxide and copper suspension to the resin is between 1:1 and 600:1; - The formulation further contains functionalized nanosilica components; - Alternatively, the bonding matrix material may contain alkali hydrolyzed epoxysilane; - In this case, the copper particles are encapsulated in, for example, glycerin, polyvinyl acetate, or lignin. It may have.

[0014] A second subject of the present invention is an antiviral filtration material comprising a layer of fabric and at least one layer of an antiviral coating comprising metallic copper particles having a median particle size of 200 nm or less in a non-oxidized form, graphene oxide or reduced graphene oxide, and a binding matrix on which both the metallic copper particles and graphene oxide or reduced graphene oxide are fixed.

[0015] The antiviral filtration material according to the present invention may also be considered individually or in combination with any of the following features: - The binding matrix further contains functionalized nanosilica components; - The binding matrix contains an aqueous resin; - Water-based resins are polyurethane resins, acrylic resins, polyester resins, oligomers, or mixtures thereof; - The aqueous resin is a polyurethane resin or an acrylic resin, wherein the ratio of graphene oxide or reduced graphene oxide to metallic copper particles is between 62:1 and 1:1, and the ratio of graphene oxide or reduced graphene oxide and copper suspension to the resin is between 1:1 and 1500:1, preferably between 1:1 and 150:1; - Alternatively, the binding matrix may include a functionalized nanosilica network to which both graphene oxide and metallic copper particles are chemically bound; - Textiles include lignin fibers and / or natural fibers such as cotton, synthetic fibers, or mixtures thereof. may have.

[0016] The third subject of the present invention is a method for preparing an antiviral preparation, comprising at least the following steps: - preparing an aqueous dispersion of metallic copper particles, stabilized graphene oxide or stabilized reduced graphene oxide having a median particle size of 200 nm or less under alkaline conditions; - mixing the aqueous dispersion with a binding matrix material under alkaline conditions to obtain an antiviral preparation comprising non-oxidized metallic copper particles, graphene oxide or reduced graphene oxide and a binding matrix material. The method consists of.

[0017] The method for preparing the preparation according to the present invention may also have any of the following features, considered individually or in combination: - The preparation of the aqueous dispersion of metallic copper particles and graphene oxide or reduced graphene oxide comprises the following steps: · stabilizing graphene oxide or reduced graphene oxide by mixing a solvent, such as water, and a dispersion additive; · adding metallic copper particles to the solution and subjecting the resulting preparation to high-shear mixing; · centrifuging the resulting preparation; and · recovering the supernatant to obtain an aqueous dispersion of metallic copper particles and stabilized graphene oxide or stabilized reduced graphene oxide. These operations are all carried out under alkaline conditions, - The binding matrix material includes a polyurethane resin, an acrylic resin, a polyester resin, an oligomer or a mixture thereof, - The method may further comprise the additional step of adding an aqueous dispersion of functionalized nanosilica after mixing the aqueous dispersion with the binding matrix material. may have.

[0018] ​A fourth aspect of the present invention is a method for preparing an antiviral formulation according to a second embodiment, which involves at least the following steps to obtain an antiviral formulation comprising non-oxidized metallic copper particles, graphene oxide or reduced graphene oxide, and a binding matrix material: - A step of encapsulating metallic copper particles having a median particle size of 200 nm or less. - A step of adding epoxysilane to encapsulated metallic copper particles, - Step of hydrolyzing epoxysilane under sol-gel process conditions, - A step of adding graphene oxide or reduced graphene oxide under sol-gel process conditions, Includes, Here, all steps are carried out under alkaline conditions.

[0019] The method for preparing the formulation of the present invention according to this second embodiment also includes any of the following features, which may be considered individually or in combination: - The epoxysilane is 3-glycidoxypropyltrimethoxysilane, - Copper particle encapsulation is performed using glycerin, polyvinyl acetate, or lignin. - This method includes the further step of adding an aqueous resin after adding graphene oxide or reduced graphene oxide. It may have.

[0020] The fifth subject of the present invention is a method for preparing an antiviral filtration material, the method comprising at least the following steps: - The step of preparing the antiviral preparations listed above, - The steps of supplying a fabric, coating the fabric with the antiviral agent, and - A step of curing the coated fabric to obtain an antiviral filtration material, Includes.

[0021] The method for preparing the filter material according to the present invention also includes any of the following features, which may be considered individually or in combination: - The step of coating the fabric with an antiviral agent may be dipping, screen printing, spray coating, or roller coating. - The coated fabric is cured by operating it at a temperature between 70 and 230°C for 1 to 13 minutes. It may have.

[0022] Finally, the present invention comprises an antiviral face mask comprising a layer of fabric coated with an antiviral formulation comprising metallic copper particles having a median particle size of 200 nm or less in a non-oxidized form, and graphene oxide or reduced graphene oxide, as well as a binding matrix on which both the metallic copper particles and graphene oxide or reduced graphene oxide are immobilized.

[0023] Advantageously, the antiviral formulation further contains functionalized nanosilica components. [Modes for carrying out the invention]

[0024] Other features and advantages of the present invention will be described in more detail in the following description.

[0025] The median particle size, also known as D50, is the particle size value when the cumulative percentage reaches 50%. Similarly, D90 is the particle size value when the cumulative percentage reaches 90%. The particle size distribution can be measured, in particular, by SEM (scanning electron microscope), TEM (transmission electron microscope), laser diffraction according to ISO 13320:2020, and SAXS (small-angle X-ray scattering).

[0026] Nanoparticles are particles with a median particle size D50 of 100 nm or less.

[0027] <General presentation of the formulation> The present invention is based on the combined use of graphene oxide or reduced graphene oxide, metallic copper particles, and a binding matrix material. The present invention further relates to means of maintaining metallic copper in a non-oxidized form by operating under alkaline conditions and / or by encapsulating the copper.

[0028] In the antiviral formulation of the present invention, since both graphene oxide and reduced graphene are negatively charged, while viruses are positively charged, graphene oxide or reduced graphene acts as a means of capturing viruses. Therefore, graphene oxide and reduced graphene provide a barrier effect on fabrics coated with the antiviral formulation. Furthermore, graphene oxide or reduced graphene oxide adheres to stabilized copper particles and thus avoids leaching into the surroundings. In addition, graphene oxide or reduced graphene oxide plays a role in improving dispersion and therefore plays a role in improving the effectiveness of the copper particles.

[0029] Metallic copper is used as the antiviral active product in the antiviral formulation of the present invention. To impart an antiviral effect, the copper must be in a non-oxidized form. This is achieved by specific operating conditions for the preparation of the antiviral formulation, namely alkaline conditions and / or encapsulation of copper, as described below.

[0030] When applied to textiles or any other type of surface or substrate to be protected, copper and also graphene oxide or reduced graphene oxide must remain on the surface for as long as possible. The binding matrix forms a network to which copper particles are fixed for less leaching. In the case of epoxysilane, the binding matrix forms a 3D silica network to which copper is chemically bound.

[0031] The preparation of the antiviral filtration material is mainly carried out by coating a fabric with the antiviral formulation and then thermosetting the antiviral formulation.

[0032] <Non-oxidized form of metallic copper particles> The primary function of copper particles in antiviral formulations for filtration antiviral materials is to kill viruses. The antiviral properties of copper are already known. However, in order to exhibit effective antiviral properties, copper must be in a non-oxidized form. Therefore, oxidation of copper must be avoided during the preparation of the formulation so that it remains in a non-oxidized form when applied to the substrate. While we do not wish to be bound by any theory, graphene oxide and reduced graphene oxide are expected to improve the dispersibility of copper particles in the matrix and thus enhance the effectiveness of copper particles in damaging viruses.

[0033] As will be explained in more detail below, copper oxidation can be avoided by operating under alkaline conditions (pH 7 or higher) and / or by encapsulating copper during the preparation of antiviral formulations.

[0034] Furthermore, using copper particles avoids subsequent leaching, as opposed to copper salts such as copper nitrate. Copper particles also induce efficient antiviral activity, in contrast to the ionic form of copper. Therefore, the amount of copper in the formulation is directly related to its antiviral efficiency. Finally, copper does not have adverse effects on humans, as demonstrated in electrical appliances with copper-coated cookware.

[0035] As soon as copper is mixed with graphene oxide or reduced graphene oxide during the preparation of an antiviral formulation, the spontaneous covalent bonds that form between the copper and the graphene oxide or reduced graphene oxide enhance the stabilization of the copper in the formulation and in subsequent layers coated onto fabrics or any other substrates.

[0036] When epoxysilane is used as the bonding matrix material, particularly when alkali-hydrolyzed 3-glycidoxypropyltrimethoxysilane is used, copper is also chemically bonded to the hydroxyl groups resulting from the hydrolysis of the alkoxy groups of the epoxysilane during sol-gel processing. The hydroxyl groups from the silane adhere to the copper particles, enabling chemical bonding.

[0037] When an aqueous resin is used as the bonding matrix material, the copper is fixed within the resin network after thermal curing.

[0038] Such bonding and fixation configurations improve the stabilization of copper and its specific functionalization, and therefore prevent subsequent leaching.

[0039] The copper particles have a median particle size (D50) of 200 nm or less. Preferably, they have a particle size D90 of less than 200 nm. This particle size distribution contributes to the stability and efficiency of the antiviral formulation.

[0040] More preferably, the copper particles are nanoparticles. This further improves the efficiency of the formulation.

[0041] <Reduced Graphene Oxide - Graphene Oxide> Both graphene oxide and reduced graphene oxide are negatively charged due to their carboxyl groups. Consequently, the primary function of graphene oxide and reduced graphene oxide is to attract positively charged viruses. The carboxyl group is the only substance known to attract viruses.

[0042] Reduced graphene oxide has a lower bulk density and a higher surface area compared to graphene oxide. However, for cost reasons and thanks to a sufficient level of carboxyl groups, graphene oxide is preferred. More advantageously, the use of graphene oxide allows for improved dispersion and binding of copper particles in the matrix, and therefore enhances the effectiveness of the solution.

[0043] Both graphene oxide and reduced graphene oxide can be cost-effectively produced from quiche graphite.

[0044] According to the present invention, the stabilization and ultimately exfoliation of reduced graphene oxide and graphene oxide are carried out to stabilize the graphene layer and, where applicable, to reduce the number of stabilized layers to a maximum of 1-2, thereby increasing the specific surface area. For this purpose, reduced graphene oxide or graphene oxide is preferably subjected to a high-shear mixing operation using a dispersion additive, for example, using a Silverson mixer at about 8000 rpm, thereby forming stabilized single-layer graphene oxide or stabilized reduced graphene oxide.

[0045] The use of graphene oxide or reduced graphene oxide offers the following specific advantages: namely, it attracts viruses, improves copper dispersibility, and stabilizes copper through the previously described covalent bonds between copper and graphene oxide or reduced graphene oxide. Additionally, graphene oxide or reduced graphene oxide with a negatively charged surface has a greater attraction to positively charged fabrics, increasing the bonding of the antiviral coating.

[0046] The ratio of graphene oxide / reduced graphene oxide to copper must be optimized considering the need for both antiviral effect and air filtration efficiency. For this purpose, the ratio of graphene oxide / reduced graphene oxide to copper is between 62:1 and 1:1, more preferably between 18:1 and 1:1.

[0047] Finally, the resin or silane network resulting from the thermosetting of the antiviral agent fixes the graphene oxide or reduced graphene oxide, and then prevents subsequent leaching.

[0048] <Bonding matrix material: Water-based resin> According to a first embodiment of the present invention, the bonding matrix material is an aqueous resin. After thermal curing, both copper particles and graphene oxide or reduced graphene oxide are fixed in the resulting bonding matrix because crosslinking of the resin occurs during the drying and curing steps.

[0049] Furthermore, the thermal curing process also results in the bonding of the binding matrix with the substrate coated with the antiviral agent prior to thermal curing, which then ensures a firm adhesion between them. In summary, the network thus formed in the binding matrix after curing acts as a chemical binder to the fabric.

[0050] All types of water-based resins, such as polyurethane water-based resins, acrylic water-based resins, and polyester water-based resins, can be used for this purpose.

[0051] A preferred resin is, for example, a polyurethane resin sold according to commercial reference number Alberdingk 9000.

[0052] For acrylic water-based resins, commercial reference numbers such as Alberdingk AC2410 or Alberdingk AS2685, or mixtures thereof, can be used.

[0053] Advantageously, the acrylic aqueous resin contains amine groups, which are well-known biocides with active antiviral effects. Furthermore, the amine and acrylic groups preferentially attract the negatively charged spikes of the coronavirus.

[0054] Furthermore, combinations of these acrylic resins may be used. In particular, an acrylic dispersion containing Alberdingk® AC2410 and Alberdingk® AS2685 in a ratio between 20:1 and 1:20, more preferably between 5:1 and 1:1, can be used.

[0055] It is also possible to create a system of oligomers that form a 3D network containing amine groups by adding oligomers such as Dynasylan 2627 to a formulation.

[0056] Functionalized nanosilica components, such as aqueous dispersions of colloidal nanosilica, for example, those marketed under commercial reference number Levasil CC301, can be added to the formulation. Since the particles of Levasil CC301 are surface-modified with epoxysilane, the use of such dispersions results in the formation of a post-thermosetting network that allows for optimized air filtration and breathability.

[0057] <Binding matrix material: Epoxysilane precursor> According to a second embodiment of the present invention, the bonding matrix material is an epoxysilane. An epoxysilane is defined as a silane having the following general formula.

[0058] [ka] In the formula, R 1 , R 2 and R 3 R independently represents an alkyl group having 1 to 4 carbon atoms. For example, R 1 , R 2 and R 3 Q can independently represent methyl, ethyl, propyl, or butyl. Q represents a divalent organic linking group that does not contain interfering groups. Examples of Q include linear, cyclic, and / or branched alkylenes, arylenes, and combinations thereof, in which at least one carbon atom is substituted or unsubstituted with an N, S, or O atom, a sulfonyl group, a nitro group, a halogen, a carbonyl group, or a combination thereof. Epoxysilane compounds can be monomers, oligomers, or, in some cases, polymers, provided they have polymerizable epoxy groups and polymerizable trialkoxysilyl groups.

[0059] Typically, curable epoxysilane compounds are epoxy-terminated silane compounds having terminally polymerizable epoxy groups and terminally polymerizable silane groups.

[0060] Examples of useful epoxysilanes include glycidoxymethyltrimethoxysilane, glycidoxymethyltriethoxysilane, glycidoxymethyltrippropoxysilane, glycidoxymethyltributoxysilane, beta-glycidoxyethyltrimethoxysilane, beta-glycidoxyethyltriethoxysilane, beta-glycidoxyethyltrippropoxysilane, beta-glycidoxyethyltributoxysilane, beta-glycidoxyethyltrimethoxysilane, alpha-glycidoxyethyltriethoxysilane, alpha-glycidoxyethyl Repropoxysilane, alpha-glycidoxyethyltributoxysilane, gamma-glycidoxypropyltrimethoxysilane, gamma-glycidoxypropyltriethoxysilane, gamma-glycidoxypropyltripropoxysilane, gamma-glycidoxypropyltributoxysilane, beta-glycidoxypropyltrimethoxysilane, beta-glycidoxypropyltriethoxysilane, beta-glycidoxypropyltripropoxysilane, beta-glycidoxypropyltributoxysilane, alpha-glycidoxypropyltrimethoxy Sisilane, alpha-glycidoxypropyltriethoxysilane, alpha-glycidoxypropyltripropoxysilane, alpha-glycidoxypropyltributoxysilane, gamma-glycidoxybutyltrimethoxysilane, delta-glycidoxybutyltriethoxysilane, delta-glycidoxybutyltripropoxysilane, delta-glycidoxybutyltributoxysilane, delta-glycidoxybutyltrimethoxysilane, gamma-glycidoxybutyltriethoxysilane, gamma-glycidoxybutyltripropoxysilane, gamma- Propoxybutyltributoxysilane, delta-glycidoxybutyltrimethoxysilane, delta-glycidoxybutyltriethoxysilane, delta-glycidoxybutyltripropoxysilane, alpha-glycidoxybutyltrimethoxysilane, alpha-glycidoxybutyltriethoxysilane, alpha-glycidoxybutyltripropoxysilane, alpha-glycidoxybutyltributoxysilane, (3,4-epoxycyclohexyl)methyltrimethoxysilane, (3,4-epoxycyclohexyl)methyltriethoxysilane, (3,4-Epoxycyclohexyl)methyltripropoxysilane, (3,4-Epoxycyclohexyl)methyltributoxysilane, (3,4-Epoxycyclohexyl)ethyltrimethoxysilane, (3,4-Epoxycyclohexyl)ethyltriethoxysilane, (3,4-Epoxycyclohexyl)ethyltripropoxysilane, (3,4-Epoxycyclohexyl)ethyltributoxysilane, (3,4-Epoxycyclohexyl)propyltrimethoxysilane, (3,4-E Examples include (3,4-epoxycyclohexyl)propyltriethoxysilane, (3,4-epoxycyclohexyl)propyltripropoxysilane, (3,4-epoxycyclohexyl)propyltributoxysilane, (3,4-epoxycyclohexyl)butyltrimethoxysilane, (3,4-epoxycyclohexyl)butyltriethoxysilane, (3,4-epoxycyclohexyl)butyltripropoxysilane, and (3,4-epoxycyclohexyl)butyltributoxysilane.

[0061] For example, epoxysilane, also known as GPTMS, is gamma-glycidoxypropyltrimethoxysilane, which is a bifunctional organosilane having three methoxy groups on one side and an epoxy ring on the other.

[0062] According to the present invention, GPTMS is used as a silica precursor, and its functionalization is carried out under sol-gel treatment.

[0063] As will be further explained below in the description of the method for preparing the antiviral formulation, GPTMS is hydrolyzed under alkaline conditions during the preparation of the antiviral formulation, thus avoiding oxidation of copper and resulting in binding with copper particles by the hydroxyl groups thus formed.

[0064] The condensation of hydrolyzed GPTMS occurs during thermosetting, resulting in a very high-density 3D network bonded to the fabric by epoxy groups. Thus, the silica network adheres to both the fabric and the copper, as described above. The copper remains stabilized within the 3D silica network and is evenly distributed within it. As detailed below, the copper is protected from oxidation by encapsulation during the alkaline hydrolysis of GPTMS.

[0065] GPTMS can be used alone as a binding matrix material.

[0066] Further increases in the filtration efficiency of the resulting antiviral filter material can be achieved by adding a functionalized nanosilica aqueous dispersion (e.g., commercially available according to reference number Levasil CC301) to the epoxysilane. The amount of functionalized nanosilica aqueous dispersion added is preferably in the range of 1 to 8 volume%, more preferably 2 to 5 volume%, of the total solution to optimize filtration efficiency.

[0067] Further enhancement of the binding properties of antiviral agents to substrates can be achieved by adding oligomers such as Dynasylan2627 to create oligomer systems that form an extra 3D network.

[0068] Finally, aqueous resins (such as polyurethane, acrylic, polyester, and mixtures thereof) can also be added to the formulation to increase the binding between the active particles and the substrate.

[0069] <Base material-fabric> The antiviral formulation of the present invention can be used to coat textiles, more specifically, for the preparation of antiviral face masks. When coating textiles, the ratio of graphene oxide or reduced graphene oxide and copper suspension to the resin is preferably between 1:1 and 1500:1, more preferably between 1:1 and 150:1.

[0070] All types of textiles can be used in accordance with the present invention. Such textiles may be used for surgical gowns, clothing, and hotel textiles.

[0071] Preferably, nonwoven wood pulp PET fabric sold under commercial reference number Sontara® is used. Such fabrics contain approximately 50.4% wood pulp (lignin) and 49.6% polyethylene. When using Sontara® fabric, lignin cellulose can be incorporated into the antiviral formulation for crosslinking with the lignin of the substrate, which then produces a more stable chemical bond.

[0072] Alternatively, a combination of polyester, nylon, or polypropylene with PET (for example, GeoPunch® 100 sold by Geopannel) may be used as the base material.

[0073] Depending on the application, other fabrics containing polyester, cellulose, and cotton, either individually or in combination, can be used.

[0074] <Method for preparing an antiviral formulation using aqueous resin as a binding matrix material> To avoid oxidation of the metallic copper particles during the process, all steps are carried out under alkaline conditions.

[0075] An aqueous dispersion of metallic copper particles and graphene oxide or reduced graphene oxide is prepared by first high-shear mixing a solution of graphene oxide or reduced graphene oxide with a solvent (stabilizing the monolayer), then adding metallic copper particles to the solution to include dispersion additives, high-shear mixing of the resulting preparation, and collecting the supernatant after centrifugation.

[0076] Dispersion additives, such as Disperbyk-2010, Disperbyk 2012, or Disperbyk 2080, can be used to prepare both the graphene oxide or reduced graphene oxide solution and the copper particle solution before mixing them.

[0077] Next, the supernatant is mixed with the binding matrix material (aqueous resin) under still alkaline conditions.

[0078] A water-based dispersion of functionalized nanosilica (Levasil CC301) can be added after the water-based dispersion has been mixed with the binding matrix material.

[0079] The ratio of graphene oxide or reduced graphene oxide to metallic copper particles is between 62:1 and 1:1, more preferably between 18:1 and 1:1. The ratio of the mixture of graphene oxide (or reduced graphene oxide) and copper aqueous suspension to polyurethane or acrylic resin is between 1:1 and 600:1 when the resin is diluted, and between 1:1 and 3:2 when the resin is not diluted.

[0080] <Method for preparing an antiviral agent using epoxysilane as a binding matrix material> This formulation has the advantage of forming a 3D network that firmly fixes copper particles, particularly by forming chemical bonds between the silane network and the copper particles, thereby preventing the particles from leaching out.

[0081] This formulation involves the hydrolysis of epoxysilane under sol-gel process conditions and subsequent condensation during a thermosetting step. The problem with using such a formulation is that the most common method of hydrolyzing epoxysilane is under acidic conditions involving copper oxidation.

[0082] According to the present invention, a specific method has been developed that involves operating hydrolysis under alkaline conditions and double-protecting copper particles by encapsulating the copper in, for example, glycerin, polyvinyl acetate, or lignin. Thus, oxidation of copper is avoided during formulation preparation. Such a method, particularly under controlled alkaline conditions, also avoids oxidation of copper during use, for example, during textile washing, thanks to the formation of a high-density, nanometer-sized silica layer covering the copper particles.

[0083] In this method, 3-glycidoxypropyltrimethoxysilane (GPTMS) is used, but any of the epoxysilanes listed above that contain both epoxy and alkoxy groups may be used as alternatives.

[0084] The method for preparing the formulation according to this embodiment first includes the step of encapsulating metallic copper particles. This encapsulation is advantageously carried out using glycerin. For this purpose, glycerin is added to the mixture of copper and ethanol.

[0085] GPTMS is added to a pre-encapsulated copper solution and hydrolyzed with water under alkaline conditions. During this step, the reaction proceeds as a nucleophilic attack of the hydroxide on the silicon atom of 3-glycidoxypropyltrimethoxysilane, with the alkoxy group being released, and the copper bonding with the hydroxyl group of the hydrolyzed epoxysilane. The epoxy group remains unchanged.

[0086] In parallel, graphene oxide or reduced graphene oxide is subjected to a high-shear mixing operation, for example, using a Silverson mixer at approximately 8000 rpm, for the reasons described above. The stabilized graphene oxide or reduced graphene oxide is then added to the hydrolyzed GPTMS and encapsulated copper solution.

[0087] In all of these steps, the pH is controlled and / or adjusted, for example, with sodium hydroxide or ammonia, so that it is 8 or higher.

[0088] Advantageously, to enhance the bonding between the active particles and the fabric, the aqueous resin is added after the addition of graphene oxide or reduced graphene oxide. The aqueous resin may be a polyurethane resin, an acrylic aqueous resin, a polyester resin, or a mixture thereof.

[0089] To enhance the filtration efficacy of the antiviral filtration material, graphene oxide and, if applicable, an aqueous resin are added, followed by the addition of a functionalized nanosilica suspension to the formulation. The amount of nanosilica component depends on the porosity and properties of the fabric.

[0090] <Method for preparing antiviral filtration materials from antiviral agents> Both antiviral formulations (aqueous resin and epoxysilane) are stable and can be stored before the coating operation.

[0091] The fabric is impregnated with the formulation by dipping, screen printing, spray coating, or roller coating. One or more impregnations may be performed depending on the formulation's ability to form a thick layer and the desired filtration efficiency.

[0092] A thermosetting operation is applied after each impregnation. Typically, the coated fabric is cured by operating it for 1 to 13 minutes at a temperature between 70 and 230°C.

[0093] Alternative curing techniques, such as infrared curing and UV curing, may also be used in combination with thermal curing in some cases.

[0094] During curing and in both formulations (aqueous resin and epoxysilane as binding matrix materials), a network is formed to immobilize graphene oxide or reduced graphene oxide, copper particles, and any functionalized nanosilica. In both cases, the thus formed binding matrix adheres to the fabric. When 3-glycidoxypropyltrimethoxysilane is used, the 3D silica network is bound to the fabric via epoxy groups. [Examples]

[0095] [Example 1: Preparation of an aqueous dispersion of low-content metallic copper nanoparticles and reduced graphene oxide in a method for preparing an antiviral formulation using an aqueous resin as a binding matrix material]

[0096] During this preparation, the pH is adjusted at each step to maintain a pH between 7 and 8. 0.6 grams of solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK) is added to 1 liter of desalted H2O, which has been pre-adjusted to a pH between 7 and 8. 10 grams of reduced graphene oxide powder is added to the solution. This mixture is passed through a high-speed, high-shear mixer (Silverson®) at 8000 rpm for 80 minutes, and then placed in an ice bath.

[0097] In parallel, 0.1 grams of copper nanoparticles having a particle size distribution between 40 nm and 60 nm, with a median particle size D50 between 40 nm and 60 nm and a particle size D90 below 60 nm, are added to a mixture of 10 ml of ethanol and 3 drops of a solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK). This solution is treated ultrasonically for 10 minutes, added dropwise to a pre-prepared solution of reduced graphene oxide, and mixed in a high-speed, high-shear mixer (Silverson®) at 8000 rpm for 15 minutes. Finally, centrifugation is performed at 2000 rpm for 15 minutes. The resulting supernatant is separated to form an aqueous dispersion of low-content metallic copper nanoparticles and reduced graphene oxide.

[0098] [Example 2: Preparation of an aqueous dispersion of high-content metallic copper nanoparticles and reduced graphene oxide in a method for preparing an antiviral formulation using an aqueous resin as a binding matrix material]

[0099] This preparation is the same as in Example 1, except that the final centrifugation is performed at 1000 rpm for 10 minutes.

[0100] [Example 3: Preparation of an aqueous dispersion of metallic copper nanoparticles and graphene oxide in a method for preparing an antiviral formulation using an aqueous resin as a binding matrix material]

[0101] Similar to Examples 1 and 2, the pH is adjusted at each step to maintain it between 7 and 8.

[0102] Add 0.6 grams of solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK) to 1 liter of desalted H2O, which has been pre-adjusted to a pH between 7 and 8. Add 10 grams of graphene oxide powder to the solution. Mix the mixture in a high-speed, high-shear mixer (Silverson®) at 8000 rpm for 60 minutes, then place it in an ice bath.

[0103] In parallel, 0.1 grams of copper nanoparticles having a particle size distribution between 40 nm and 60 nm, with a median particle size D50 between 40 nm and 60 nm and a particle size D90 below 60 nm, are added to a mixture of 10 ml of ethanol and 3 drops of a solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK). This solution is treated with ultrasound for 10 minutes and added dropwise to a pre-prepared solution of graphene oxide, then mixed in a high-speed, high-shear mixer (Silverson®) at 5000 rpm for 20 minutes. Further centrifugation is not necessary for the stability of the graphene oxide. The supernatant is separated, and then an aqueous dispersion of metallic copper nanoparticles and graphene oxide is formed.

[0104] [Example 4: Preparation of an antiviral formulation using aqueous polyurethane resin as a binding matrix material]

[0105] The aqueous dispersion of Example 1, Example 2, or Example 3 is added to the polyurethane dispersion (Alberdingk® U9000) in a 1:1 ratio while stirring at 250 rpm in a magnetic stirrer. The pH of both dispersions is pre-controlled to be between 7 and 8, or adjusted with acetic acid or potassium hydroxide. Optionally, an aqueous dispersion of colloidal nanosilica (Levasil® CC301) is also added.

[0106] [Example 5: Preparation of an antiviral formulation using aqueous acrylic resin as a binding matrix material]

[0107] This preparation is the same as in Example 4, except that the resin used is an acrylic dispersion containing Alberdingk® AC2410 and Alberdingk® AS2685. The ratio between Alberdingk® AC2410 and Alberdingk® AS2685 is between 20:1 and 1:20.

[0108] [Example 6: Preparation of an antiviral formulation using epoxysilane as a binding matrix material according to the first embodiment]

[0109] Adjust the pH of a solution of 9 ml of H2O and 72 ml of ethanol to 8-9 with 1 M sodium hydroxide. Simultaneously, adjust the pH of 10 ml of glycerin to 8-9 with 1 M sodium hydroxide. Add 0.5 grams of copper nanoparticles, which have a particle size distribution between 40 nm and 60 nm, with a median particle size D50 between 40 nm and 60 nm and a particle size D90 below 60 nm, to the 10 ml of ethanol after sonication. Adjust the pH to 8-9. Mix this ethanol solution together with the glycerin and copper nanoparticle mixture.

[0110] 9 ml of GPTMS solution is added to the previous mixture of ethanol, glycerin, and copper nanoparticles under magnetic stirring, and the pH is adjusted to 8-9 with 1 M sodium hydroxide. This solution is then added to the previous prepared solution containing encapsulated nanoparticles. This mixture is operated for 6-8 hours to induce hydrolysis of the GPTMS. A small, dense silica network is obtained under alkaline hydrolysis.

[0111] In parallel, 0.6 grams of solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK) is added to 1 liter of desalted H2O adjusted to a pH between 7 and 8. 1.64 grams of graphene oxide powder is added to this solution. The mixture is passed through a high-speed, high-shear mixer (Silverson®) at 8000 rpm for 60 minutes, and then placed in an ice bath.

[0112] The pH of the graphene oxide solution is adjusted to 8-9, and this adjusted solution is added to the previously prepared mixture of hydrolyzed GPTMS and encapsulated nanoparticles. The pH is further adjusted between 8 and 9.

[0113] Finally, such a solution is added dropwise to an acrylic aqueous resin (Alberdingk® AC2410) to obtain an antiviral formulation having a GPTMS:graphene oxide:resin ratio of 11:48:32.

[0114] When using reduced graphene oxide instead of graphene oxide, the same preparation method is applied, except for the preparation of the reduced graphene oxide solution, which involves a high-shear mixing operation at 8000 rpm for 80 minutes.

[0115] [Example 7: Preparation of an antiviral formulation using epoxysilane as a binding matrix material according to the second embodiment]

[0116] This preparation is the same as in Example 6, except for the final step of adding the solution dropwise to the siloxane oligomer (Dynasylan® Hydrosyl 2627).

[0117] [Example 8: Antiviral activity of an antiviral filter material containing an antiviral formulation prepared from graphene oxide and polyurethane resin]

[0118] The antiviral formulation is prepared as follows: The aqueous dispersion of Example 3, using 2.5 g / L of graphene oxide and 0.2 g / L of copper nanoparticles, is added to a polyurethane dispersion (Alberdingk® U9000) while stirring at 250 rpm in a magnetic stirrer. The pH of both dispersions is pre-controlled or adjusted to between 7 and 8. An aqueous dispersion of colloidal nanosilica (Levasil® CC301) is also added.

[0119] The ratio of graphene oxide to copper is 12.5:1, and the ratio of graphene oxide + copper suspension to polyurethane is 3:2.

[0120] Test the following fabrics: - Sontara (registered trademark) is 55g / m² 2 It has an average density and contains 50.4% cellulose and 49.6% polyethylene. - Geopunch(registered trademark) 100 (Geopannel) is 100g / m 2 It has a density and contains 80% polypropylene and 20% polyethylene.

[0121] The coating and curing steps are performed as follows: - Coating: A two-step immersion coating process with a flow rate of 200 mm / min and a holding time of 10 seconds. - Curing: Two curing steps of 13 minutes at 90°C.

[0122] The TCID50 titration method is used to determine antiviral activity according to the ISO 18184-2019 standard. TCID50 (50% tissue culture infectious dose) is one of the methods used to verify viral titer. It refers to the concentration at which 50% of cells are infected when a diluted solution of the virus is incubated in a test tube or well plate in which cells are cultured. This is the preferred method in the ISO 18184 standard for determining antiviral activity in textiles.

[0123] Antiviral activity against murine norovirus is measured immediately after the coating and curing steps (t=0) and 24 hours later (t=24 hours). Antiviral measurements are also performed on each fabric tested, both with and without the coating.

[0124] The results regarding logarithmic decrease are shown in Table 1.

[0125] [Table 1]

[0126] A logarithmic decrease greater than 5.17 means the decrease is higher than the detection limit. Knowing that a logarithmic decrease of 3.71 corresponds to an antiviral efficiency of 99.9804%, the antiviral efficiency of the antiviral filtration material of the present invention is definitive.

[0127] At t=0, the Sontara® fabric exhibits a significant logarithmic decrease exceeding 5.17. The logarithmic decrease of the Geopunch® 100 fabric at t=0 is also very decisive.

[0128] At t=24, both coated fabrics exhibit a logarithmic decrease greater than 5.17.

[0129] However, while a reduction can be observed in uncoated fabrics after 24 hours, the time required to reach these reductions is too long. To obtain satisfactory results, a significant reduction must be achieved rapidly.

[0130] [Example 9 - Filtration efficiency and breathability of antiviral filtration material]

[0131] The filtration efficiency and breathability of the three antiviral filtration materials of the present invention are evaluated.

[0132] Referring to Table 2, the formulations tested were as follows: - Antiviral formulation 1: The antiviral formulation follows Example 4, except that the aqueous dispersion of Example 2 is used and the dispersion of colloidal nanosilica is not added to the formulation. The ratio of the polyurethane dispersion to the aqueous dispersion of copper nanoparticles and reduced graphene oxide is 1:1. - Antiviral formulation 2: The antiviral formulation follows Example 4, except that the aqueous dispersion of Example 2 is used. A dispersion of colloidal nanosilica (Levasil® CC301) is added to the formulation. The ratio of the polyurethane dispersion to the aqueous dispersion of copper nanoparticles and reduced graphene oxide is 1:1. - Formulation 3 is a pure polyurethane resin (Alberdingk® 9000) and is therefore outside the scope of the present invention.

[0133] The fabric used for each sample is Sontara® which has an average density of 55 g / m 2 and contains 50.4% cellulose and 49.6% polyethylene.

[0134] The coating of each sample is applied by two dipping coatings, each of which is carried out at a speed of 200 mm / min for a holding time of 10 seconds. The curing operation is carried out at 90 °C for 5 minutes after the first dipping coating and at 90 °C for 10 minutes after the second dipping coating.

[0135] The results regarding the visual aspect, adhesiveness, filtration efficiency and breathability are shown in Table 2.

[0136] [Table 2]

[0137] The filtration efficiency of the antiviral filtration material of the present invention is improved as compared to the polyurethane coating. The breathability, visual aspect and adhesion properties are also certified for each sample.

[0138] [Example 10: Filtration Efficiency and Pressure Drop of Antiviral Filtration Material]

[0139] The filtration efficiency of the filtration material is evaluated taking into account the pressure drop.

[0140] For each sample, the fabric is Sontara® which has an average density of 55 g / m 2 and contains 50.4% cellulose and 49.6% polyethylene.

[0141] Referring to Table 3, the tested filtration materials are as follows: - Material 1: Sontara® fabric without coating - Material 2: The Sontara® fabric is coated with the formulation according to Example 4, except that the aqueous dispersion of Example 2 is used. The dispersion of colloidal nanosilica (Levasil® CC301) is not added to the formulation. The ratio of the polyurethane dispersion to the aqueous dispersion of copper nanoparticles and reduced graphene oxide is 1:1. - Material 3: This is the same as Material 2, except that a dispersion of colloidal nanosilica (Levasil® CC301) is added to the formulation according to Example 4. - Material 4: Coat Sontara® fabric with polyurethane resin (Alberdingk® U9000). - Starting with material 5:11.5 g / L of graphene oxide and 0.5 g / L of copper nanoparticles, dilute the aqueous dispersion of Example 3 containing graphene oxide to a 1:1 ratio with water, and then coat the Sontara® fabric with the formulation according to Example 4, except that the aqueous dispersion of graphene oxide from Example 3 is used at a concentration of 5.5 g / L of graphene oxide and 0.2 g / L of copper nanoparticles. No dispersion of colloidal nanosilica (Levasil® CC301) is added to the formulation.

[0142] [Table 3]

[0143] These results, contrary to expectations, show that a higher pressure drop does not necessarily correlate with higher filtration efficiency. For material 4, the pressure drop is 178 mm for a 65% filtration efficiency, while for preferred material 2, the pressure drop is 110 mm for a 93% filtration efficiency.

[0144] [Implementation 11: Antiviral activity of antiviral materials, including antiviral formulations prepared from graphene oxide and polyurethane resin]

[0145] Refer to Table 4 and prepare the antiviral formulation as follows: Add the aqueous dispersion of Example 3, using 2.5 g / L of graphene oxide and 0.5 g / L of copper nanoparticles, to the polyurethane dispersion (Alberdingk® U9000) while stirring at 250 rpm in a magnetic stirrer. Pre-control or adjust the pH of both dispersions to between 7 and 8.

[0146] The ratio of graphene oxide to copper is 5:1, and the ratio of graphene oxide + copper suspension to polyurethane is 1.5:1 or 150:1, depending on the case.

[0147] The aforementioned Sontara® fabric will be used.

[0148] The coating and curing steps are performed as follows: - Coating: A single step of the immersion coating process with a flow rate of 200 mm / min and a holding time of 10 seconds. - Curing: One curing step of 13 minutes at 90°C.

[0149] The antiviral activity is determined according to the ISO 18184-2019 standard using the TCID50 titration method described above.

[0150] [Table 4]

[0151] At time t=0, coated Sontara® fabrics exhibit a remarkable 99.998% antiviral efficacy against murine norovirus when using a ratio of 1.5:1. When the ratio is increased to 150:1, the antiviral efficacy against the same type of virus is 99.718% after 2 hours.

[0152] [Example 12: Antiviral activity of antiviral materials including an antiviral formulation prepared from graphene oxide and polyurethane resin]

[0153] The antiviral formulation is prepared as follows: The aqueous dispersion of Example 3, using 1 g / L graphene oxide and 0.5 g / L copper nanoparticles, is added to the polyurethane dispersion (Alberdingk® U9000) while stirring at 250 rpm in a magnetic stirrer. The pH of both dispersions is pre-controlled or adjusted to between 7 and 8.

[0154] The ratio of graphene oxide to copper is 2:1, and the ratio of graphene oxide + copper suspension to polyurethane is 150:1.

[0155] The aforementioned Sontara® fabric will be used.

[0156] The coating and curing steps are performed as follows: - Coating: A single step of the immersion coating process with a flow rate of 200 mm / min and a holding time of 10 seconds. - Curing: One curing step of 13 minutes at 90°C.

[0157] The antiviral activity is determined according to the ISO 18184-2019 standard using the TCID50 titration method described above.

[0158] [Table 5]

[0159] At t=3 hours, Sontara® fabric exhibits remarkable antiviral efficacy of 99.992% against the 229E coronavirus when using a ratio of 150:1.

[0160] [Example 13: Antiviral activity of antiviral materials including an antiviral formulation prepared from graphene oxide and acrylic resin]

[0161] The antiviral formulation is prepared as follows: The aqueous dispersion of Example 3, using 1 g / L graphene oxide and 0.5 g / L copper nanoparticles, is added to an acrylic dispersion containing Alberdingk® AC2410 and Alberdingk® AS2685 while stirring at 250 rpm in a magnetic stirrer. The ratio of Alberdingk® AC2410 to Alberdingk® AS2685 is 3:1. The pH of both dispersions is pre-controlled or adjusted between 7 and 8.

[0162] The ratio of graphene oxide to copper is 2:1, and the ratio of graphene oxide + copper suspension to acrylic is 15:1.

[0163] The aforementioned Sontara® fabric will be used.

[0164] The coating and curing steps are performed as follows: - Coating: A single step of the immersion coating process with a flow rate of 200 mm / min and a holding time of 10 seconds. - Curing: One curing step of 13 minutes at 90°C.

[0165] The antiviral activity is determined according to the ISO 18184-2019 standard using the TCID50 titration method described above.

[0166] [Table 6]

[0167] At t=3 hours, Sontara® fabric exhibits a remarkable 99.766% antiviral efficacy against the 229E coronavirus when using a 15:1 ratio.

[0168] [Example 14: Preparation of an aqueous dispersion of metallic copper particles and graphene oxide in a method for preparing an antiviral formulation using an aqueous resin as a binding matrix material]

[0169] During this preparation, adjust the pH at each step to maintain it between 7 and 8.

[0170] Add 0.6 grams of solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK) to 1 liter of desalted H2O, which has been pre-adjusted to a pH between 7 and 8. Add 10 grams of graphene oxide powder to the solution. Mix the mixture in a high-speed, high-shear mixer (Silverson®) at 8000 rpm for 60 minutes, then place it in an ice bath.

[0171] In parallel, 0.1 grams of copper particles having a particle size distribution between 100 nm and 200 nm, with a median particle size D50 between 100 nm and 200 nm and a particle size D90 below 200 nm, are added to a mixture of 10 ml of ethanol and 3 drops of a solvent-free wetting and dispersing additive (DISPERBYK-2010, commercially available from BYK). This solution is treated with ultrasound for 10 minutes and added dropwise to a pre-prepared solution of graphene oxide, then mixed in a high-speed, high-shear mixer (Silverson®) at 5000 rpm for 20 minutes. Further centrifugation is not necessary for the stability of the graphene oxide. The supernatant is separated, and then an aqueous dispersion of metallic copper nanoparticles and graphene oxide is formed.

[0172] [Example 15: Antiviral activity of antiviral materials including an antiviral formulation prepared from graphene oxide and polyurethane resin]

[0173] The antiviral formulation is prepared as follows: The aqueous dispersion of Example 14, using 2.5 g / L of graphene oxide and 0.5 g / L of copper particles, is added to a polyurethane dispersion (Alberdingk® U9000) while stirring at 250 rpm in a magnetic stirrer. The pH of both dispersions is pre-controlled or adjusted to between 7 and 8.

[0174] The ratio of graphene oxide to copper is 5:1, and the ratio of graphene oxide + copper suspension to polyurethane is 50:1.

[0175] The aforementioned Sontara® fabric will be used.

[0176] The coating and curing steps are performed as follows: - Coating: Roller pressure 4 kg / cm 2 and one step of the padding process at a line speed of 15 m / min. - Curing: One curing step of 1 minute at 110°C.

[0177] The antiviral activity is determined according to the ISO 18184-2019 standard using the TCID50 titration method described above.

[0178] [Table 7]

[0179] Under typical industrial coating conditions, Sontara® fabrics exhibit 98.68% antiviral efficacy against murine norovirus after 2 hours and 99.00% antiviral efficacy against coronavirus 229E after 3 hours, when using a 50:1 ratio.

[0180] [Example 16: Antiviral activity of antiviral materials including an antiviral formulation prepared from graphene oxide and acrylic resin.]

[0181] The antiviral formulation is prepared as follows: The aqueous dispersion of Example 14, using 2.5 g / L of graphene oxide and 0.5 g / L of copper particles, is added to an acrylic dispersion containing Alberdingk® AC2410 and Alberdingk® AS2685 while stirring at 250 rpm in a magnetic stirrer. The ratio of Alberdingk® AC2410 to Alberdingk® AS2685 is 3:1. The pH of both dispersions is pre-controlled or adjusted between 7 and 8.

[0182] The ratio of graphene oxide to copper is 5:1, and the ratio of graphene oxide + copper suspension to acrylic is 18.75:1.

[0183] Test the following fabrics: - Density 30g / m 2 Polypropylene

[0184] The coating and curing steps are performed as follows: - Coating: 1 kg / cm 2 and one step of the padding process at a rolling speed of 2 rpm - Curing: One curing step of 5 minutes at 130°C.

[0185] The antiviral activity is determined according to the ISO 18184-2019 standard using the TCID50 titration method described above.

[0186] [Table 8]

[0187] At time t=0, polypropylene fabric exhibits 95.7% antiviral efficacy against murine norovirus when using a ratio of 18.75:1.

Claims

1. The invention comprises a layer of fabric and at least one layer of an antiviral coating comprising metallic copper particles having a median particle size of 200 nm or less in a non-oxidized form, graphene oxide or reduced graphene oxide, and a binding matrix material on which both the metallic copper particles and graphene oxide or reduced graphene oxide are fixed. The bonding matrix material further comprises a functionalized nanosilica component. Antiviral filtration material.

2. The antiviral filtration material according to claim 1, wherein the metallic copper particles and the graphene oxide or reduced graphene oxide are chemically bonded together.

3. The antiviral filtration material according to any one of claims 1 to 2, wherein the binding matrix material comprises an aqueous resin.

4. The antiviral filtration material according to claim 3, wherein the aqueous resin is a polyurethane resin, an acrylic resin, a polyester resin, or a mixture thereof.

5. The antiviral filtration material according to any one of claims 1 and 2, wherein the binding matrix material comprises an alkaline hydrolyzable epoxysilane.

6. The antiviral filtration material according to claim 1, wherein the bonding matrix material comprises a functionalized nanosilica network on which both graphene oxide and metallic copper particles are chemically bonded.

7. The antiviral filtration material according to any one of claims 1 to 6, wherein the fabric comprises natural fibers, synthetic fibers, or mixtures thereof.

8. At least the following steps, - A step of preparing an aqueous dispersion of metallic copper particles having a median particle size of 200 nm or less, and stabilized graphene oxide or stabilized reduced graphene oxide, under alkaline conditions. - To obtain an antiviral formulation comprising non-oxidized metallic copper particles, graphene oxide or reduced graphene oxide and a binding matrix material, the step is to mix the aqueous dispersion with the binding matrix material under alkaline conditions. A method for preparing an antiviral preparation containing [a specific substance].

9. The preparation of the aqueous dispersion of the aforementioned copper metal particles and graphene oxide or reduced graphene oxide is carried out in the following steps, namely: - A step of stabilizing graphene oxide or reduced graphene oxide by mixing it with a solvent and a dispersion additive. - Add metallic copper particles to the solution and mix the resulting preparation with high shear. - The step of centrifuging the obtained preparation, and - To obtain an aqueous dispersion of metallic copper particles and stabilized graphene oxide or stabilized reduced graphene oxide, the supernatant is collected. A method for preparing an antiviral preparation according to claim 8, comprising, wherein all of these operations are carried out under alkaline conditions.

10. A method for preparing an antiviral preparation according to any one of claims 8 to 9, wherein the binding matrix material comprises a polyurethane resin, an acrylic resin, a polyester resin, or a mixture thereof.

11. A method for preparing an antiviral formulation according to any one of claims 8 to 10, comprising the further step of adding an aqueous dispersion of functionalized nanosilica after mixing the binding matrix material with an aqueous dispersion.

12. At least the following steps, - A step of preparing an antiviral preparation by the method described in any one of claims 8 to 11, - A step of supplying a fabric and coating the fabric with the antiviral agent, - A step of curing the coated fabric to obtain an antiviral filtration material. A method for preparing an antiviral filtration material containing [specific material].

13. The method for preparing an antiviral filtration material according to claim 12, wherein the step of coating the fabric with the antiviral agent is immersion coating, screen printing, spray coating, or roller coating.

14. A method for preparing an antiviral filtration material according to any one of claims 12 to 13, wherein the curing of the coated fabric is performed at a temperature between 70 and 230°C for 1 to 13 minutes.

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