WO2021121509A2 - Textile non-tissé obtenu à partir de déchets de fruits et légumes recyclés - Google Patents

Textile non-tissé obtenu à partir de déchets de fruits et légumes recyclés Download PDF

Info

Publication number
WO2021121509A2
WO2021121509A2 PCT/DK2020/050369 DK2020050369W WO2021121509A2 WO 2021121509 A2 WO2021121509 A2 WO 2021121509A2 DK 2020050369 W DK2020050369 W DK 2020050369W WO 2021121509 A2 WO2021121509 A2 WO 2021121509A2
Authority
WO
WIPO (PCT)
Prior art keywords
woven textile
coating
pomace
hydrophobic
textile
Prior art date
Application number
PCT/DK2020/050369
Other languages
English (en)
Other versions
WO2021121509A3 (fr
Inventor
Xianrong SHAO
Thulasya RAMANATHAN
Hannah MICHAUD
Original Assignee
Beyond Leather Materials Aps
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beyond Leather Materials Aps filed Critical Beyond Leather Materials Aps
Priority to EP20828281.4A priority Critical patent/EP4077498A2/fr
Priority to CN202080087747.9A priority patent/CN114867771A/zh
Priority to CA3163928A priority patent/CA3163928A1/fr
Priority to US17/782,144 priority patent/US20230053954A1/en
Publication of WO2021121509A2 publication Critical patent/WO2021121509A2/fr
Publication of WO2021121509A3 publication Critical patent/WO2021121509A3/fr

Links

Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D06N3/0015—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using fibres of specified chemical or physical nature, e.g. natural silk
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4266—Natural fibres not provided for in group D04H1/425
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
    • D—TEXTILES; PAPER
    • D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/70—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres
    • D04H1/72—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged
    • D04H1/732—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres characterised by the method of forming fleeces or layers, e.g. reorientation of fibres the fibres being randomly arranged by fluid current, e.g. air-lay
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0002—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate
    • D06N3/0011—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the substrate using non-woven fabrics
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
    • D06N3/0061—Organic fillers or organic fibrous fillers, e.g. ground leather waste, wood bark, cork powder, vegetable flour; Other organic compounding ingredients; Post-treatment with organic compounds
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
    • D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/01—Waste products, e.g. sludge
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00—Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/02—Material of vegetable origin
    • D—TEXTILES; PAPER
    • D21—PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21H—PULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H27/00—Special paper not otherwise provided for, e.g. made by multi-step processes
    • D21H27/06—Vegetable or imitation parchment; Glassine paper
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2201/00—Chemical constitution of the fibres, threads or yarns
    • D06N2201/04—Vegetal fibres
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2209/00—Properties of the materials
    • D06N2209/14—Properties of the materials having chemical properties
    • D06N2209/142—Hydrophobic
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
    • D06N2211/00—Specially adapted uses
    • D06N2211/12—Decorative or sun protection articles
    • D06N2211/28—Artificial leather

Definitions

  • the present invention relates to a method of manufacturing non-woven textiles from cellulose-rich waste, such as fruit and vegetable pomace.
  • the present invention also describes a method of coating the non-woven textile to provide it with a hydrophobic surface.
  • the present invention relates to food waste upcycling by converting fruit and vegetable waste obtained as by-product in industrial production into high-value textiles. In this sense, the present invention can provide as a substitute material for conventional animal leather.
  • US20050147723A1 discloses a method for making a nutrient-rich supplement powder based on apple peel subjected to phytochemical preservation treatment.
  • the use of fruit and vegetable pomace must not be limited to low value applications. Instead, upcycling fruit and vegetable waste to textile represents an opportunity of adding substantial value to the otherwise wasted fruit and vegetable pomace. Additionally, the pomace-derived textile serves as a sustainable and environmentally friendly alternative to the conventional animal textiles, such as for example animal leather.
  • the fruit and vegetable pomace-based non-woven textile is environmentally favourable as it employs a sustainable manufacturing process using environmentally friendly ingredients.
  • the non-woven textile should retain features comparable to those of conventional textiles.
  • An alternative textile to the conventional animal leather should include comparable characteristics in terms of water resistance, tensile strength, and physical appeal.
  • US2009301347A1 discloses an apple textile composition made up of apple flour and 5 % polymer binder.
  • the manufacturing technique for obtaining the apple textile can only be used for dry powders.
  • US20130149512A1 discloses a natural non-woven material made from a multi-layered stack of discrete interconnected plant fibre layers bound by a biodegradable polymer.
  • the application relates to the use of plant-based fibres, in particular pineapple fibres, to manufacture a fused non-woven material.
  • W02015018711A1 discloses a method for making spinnable cellulose from citrus fruits discarded by citrus fruit plantations or wasted during industrial processing of citrus fruit derivatives.
  • the application discloses a method for chemical treatment used to extract cellulose from the citrus fruits.
  • the method disclosed is, however, limited to citrus fruits and involves polysaccharide separation processes.
  • an object of the present invention is to provide a non- woven textile from fruit and/or vegetable waste.
  • the resulting textile having physical properties comparable to those of conventional textiles, such as animal leather, concerning, for example, physical appeal, water resistance, and tensile strength of the textile.
  • the present disclosure seeks to address the problems of negative environmental impact of industrial production, damages to ecosystem integrity, and poor waste utilization, posed by conventional textile production and food processing.
  • a method for producing a hydrophobic non-woven textile comprising the steps of providing fruit or vegetable pomace comprising water in the range of 60 % to 95 % (w/w) and a plant fibre, comminuting, preferably by milling or refining, the pomace to provide a disrupted pomace having fibres of a fibre length of below or equal to 2.0 mm, such as in the range of from 0.3 mm to 2.0 mm, 0.3 mm to 1.5 mm, 0.3 mm to 1.0 mm, 0.5 mm to 1.5 mm, 0.5 mm to 1.0 mm or 0.3 mm to 0.8 mm, mixing the disrupted pomace with a first, e.g.
  • the non-woven textile is manufactured using an environmentally favourable production process.
  • the present invention can be produced in two forms: a sheet form, which is strong, flexible, stitchable, and durable, and in a vacuum-moulded 3D-form, which is strong, durable, and non-bendable.
  • the sheet form can be used in applications in which conventional animal leather is used, including, but not limited to, clothing, accessories, book bindings, sports equipment, footwear, bags, furnishings, interior decors, automobile furnishing, etc.
  • the vacuum-moulded 3D-form can be shaped into products with likeness to paper industry products, including, but not limited to, plates, bowls, packaging, wall panels, toys, etc.
  • the resulting textile material has an increased tensile strength, resulting in a versatile use of the textile material for several purposes.
  • lignocellulosic fibres as density-modifying agents has been proven to increase the tensile strength of the non-woven textile (Example 4, Table 7).
  • the addition of natural rubber milk has been found to increase durability of the textile.
  • the method of the invention furthermore provides a non-woven textile with improved tactile and optical characteristics as well as improved material flexibility. The process disclosed herein minimizes the economical strain associated with drying the fruit and vegetable waste, embraces the natural composition of the waste, and delivers a product that satisfies perceptive and tactility requirements of the consumer.
  • the disclosed process is particularly advantageous due to its robustness in incorporating pomace of different compositions and varieties, such as pomace derived from apple, pear, citrus fruits, ginger, rhubarb, cactus, mango, pineapple, carrot, cucumber, tomato and the like.
  • Fruit pomace generally includes a mixture of outer skin, fruit pulp, stems, and seeds, while vegetable pomace includes, outer skin, vegetable pulp, stalks, and roots.
  • the pomace employed in the disclosed process is apple pomace obtained from industrial juice and cider production.
  • the disclosed process employs comminuting fruit and vegetable pomace, preferably by milling or refining, as the first step in the manufacturing process.
  • the step of comminution is of particular relevance for the particle size and viscosity of the comminuted pomace and influence the texture of the final textile.
  • water is optionally added during comminution of the pomace.
  • the pomace is comminuted by milling, in which a toothed or stone colloidal mill is used, to reduce the particle size in the pomace from between 0.5 mm to 20 mm to a particle size of ⁇ 0.1 mm.
  • the milling step increases the water content of the pomace by 20 % to 80 %, thus reducing the density by 20 % to 80 %.
  • the mixing of the disrupted pomace with one or more density -modifying agents is at an amount of density -modifying agent in the range of 10 % (w/w) to 40 % (w/w) of the weight of the dry matter of the disrupted pomace.
  • the density-modifying agent is selected from the list comprising carbohydrates, plant fibres, proteins, polymer emulsions, gums, polyols, cationic polymers, siloxanes and fatty acids.
  • the density-modifying agent is selected from the list comprising carbohydrates, plant fibres, proteins, polymer emulsions, gums, polyols, and cationic polymers.
  • the density-modifying agent is selected from the list comprising siloxanes and fatty acids.
  • Non-limiting examples for suitable carbohydrates as density-modifying agents are starch, cellulose, microcrystalline cellulose, carrageenan, agar, sugar, and agaropectin.
  • suitable plant fibres as density-modifying agents are softwood pulp, paper pulp, hemp, jute, flax, cotton, nettle, ramie, corn, bamboo, and straw.
  • Non-limiting examples for suitable polymer emulsions as density-modifying agents are latex milk, natural latex milk, rubber milk, acrylonitrile-butadiene copolymer, acrylonitrile-butadiene copolymer, styrene-acrylic polymer emulsion, polyurethane, polylactic acid, acrylic, styrene, polyester, polyvinyl butyral (PVB), polyolefin copolymer and ethylene vinyl acetate copolymer.
  • PVB polyvinyl butyral
  • the inventors have surprisingly found that the addition of natural rubbers to the pomace can increase the durability of the non-woven textile product.
  • Non-limiting examples for suitable gums as density -modifying agents are guar gum, gum Arabic, gum ghatti, karaya gum, tara gum, dammar gum, and gum tragacanth.
  • the addition of gums was surprisingly found to increase flexibility of the non-woven textile product (example 4, Table 8).
  • Non-limiting examples for suitable polyols as density-modifying agents are glycerol (synonyms: glycerine, glycerin), glycol, pentaerythritol, and polyethylene glycol (PEG).
  • glycerol synthetic polyol
  • PEG polyethylene glycol
  • a non-limiting example for a suitable cationic polymer as density-modifying agent is polyacrylamide.
  • Non-limiting examples for suitable siloxanes as density-modifying agents are silicone glycols, silicone emulsion, cyclosiloxane, organosiloxane, carboxysiloxane, amino siloxane, polysiloxane, polysiloxane adduct, silicone elastomer, silicone gum, silicone rubber and epoxy modified siloxane.
  • Non-limiting examples for suitable fatty acids as density -modifying agents are palmitic acid, linolenic acid, tall oil fatty acid, fatty acid esters, stearic acid and oleic acid.
  • proteins are used as density-modifying agents
  • the proteins are preferably obtained from a plant source.
  • the plant source can be by-products from industrial processes.
  • proteins are soy protein, whey protein, chia protein, flax protein, black bean protein, and mycoprotein.
  • the protein can constitute up to 30 % (w/w) of the final composition of the textile.
  • the use of proteins has been found to be a suitable and efficient substrate for cross-linking reactions.
  • the density -modifying agent can act as a filler and has been found to enhance strength to the textile, to provide substrate for cross-linking reactions, or to aid in preserving moisture content in the textile.
  • natural latex milk has surprisingly been found to enhance the textile durability of the material significantly.
  • the density-modifying agent itself can act as a cross- linking agent.
  • One embodiment describes a non-woven textile fortified with at least one density -modifying agent.
  • Another embodiment describes a non-woven textile fortified with at least two, e.g. two different, density-modifying agent.
  • the density-modifying agent is included in the textile in concentrations between 10 % (w/w) to 85 % (w/w) of the dry weight of disrupted pomace.
  • water is added together with the density-modifying agent to the disrupted pomace.
  • a non-water-soluble complex carbohydrate or lignocellulosic fibre is preferred as density-modifying agent.
  • the non-water-soluble complex carbohydrate or lignocellulosic fibre comprises carbohydrates, such as starch, cellulose, microcrystalline cellulose, carrageenan, agar, and agaropectin; plant fibres, such as softwood pulp, paper pulp, hemp, jute, flax, cotton, nettle, ramie, corn, bamboo, and straw; proteins; polymer emulsions, such as latex milk, natural latex milk, rubber milk, acrylonitrile-butadiene copolymer, acrylonitrile-butadiene copolymer, styrene- acrylic polymer emulsion and ethylene vinyl acetate copolymer; gums, such as guar gum, gum Arabic, gum ghatti, karaya gum, tara gum, dammar gum, and gum tragacanth; and cationic polymers,
  • the textile can contain water-soluble carbohydrates.
  • water-soluble carbohydrates are sugars such as maltodextrin, glucose, sucrose, maltose, trehalose or combinations thereof; and polyols, such as pentaerythritol, glycerol, glycol and polyethylene glycol (PEG).
  • the soluble carbohydrate can constitute up to 20 % (w/w) of the final composition of the textile.
  • a step of odour and colour harmonization is included in the manufacturing process after the step of comminution of the pomace. In the fashion and design industries, it is important for a consumer product to have an appealing colour and smell. The optional step of odour and colour harmonization can, therefore, aid in obtaining a sensorial appealing textile.
  • Another embodiment employs sustainable bleaching using chlorine-free bleaching agents for odour and colour harmonization of the textile.
  • chlorine-free bleaching agents are hydrogen peroxide, sodium percarbonate, sodium perborate, benzoyl peroxide, potassium persulfate, sodium bicarbonate, sodium dithionite, sulfur dioxide, peracetic acid or ozone.
  • Bleaching is carried out in a closed vessel with 0.005 % (v/v) to 50 % (v/v) at 30°C to 90°C and pH 2 to 13, preferably pH 10, for 1 hours to 48 hours with continuous stirring.
  • the described embodiment is advantageous since it does not employ chlorine-containing agents.
  • Toxic organochlorine is formed when chlorine radicals are reacted with cellulosic material. This embodiment thereby limits the amount of toxic waste produced.
  • solvents can reduce the intensity of odour by solubilizing the molecules responsible for the odour.
  • the solvents used for treatment of the pomace can be isolated from the solvent-pomace slurry by, for example, different methods of distillation, including, but not limited to simple distillation, fractional distillation, steam distillation, vacuum distillation, and short path distillation. The distillation allows for the solvents to be reused. In the present embodiment, the solvents are economical and do not leave any residual odour or fragrance in the slurry.
  • Environmentally-friendly non-toxic solvents may include, but are not limited to, ethanol, butane, acetone, chlorine, 3 -m ethoxy-3 - methyl- 1 -butanol, ethylene glycol monobutyl ether, and supercritical carbon-dioxide, for example.
  • the solvents are acidified with weak organic acids, which may include, but are not limited to citric acid, acetic acid, formic acid, benzoic acid, phosphoric acid, oxalic acid, and lactic acid, for example.
  • the acidified solvent treatment is carried out in a closed vessel at between 25°C to 30°C and between pH 1 to 3, preferably pH 2, for 4 hours to 120 hours with continuous stirring.
  • cross-linking agents capable of cross-linking molecules of carbohydrates or molecules of proteins may be added during the manufacturing of the non-woven textile.
  • the cross-linking agent may be activated by a catalyst.
  • the addition of cross-linking agents in the manufacturing of the non-woven textile can help to increase the strength of the textile.
  • the cross-linking agent is selected from the list comprising bifunctional cross-linking agents, dialdehydes, acetals, polycarboxylic acids, phosphorus derivates, protein cross-linking agents, homo-bifunctional cross-linking agents, hetero-bifunctional cross-linking agents, enzymatic cross-linking agents, or combinations thereof.
  • the cross-linking agent is chosen for carbohydrates.
  • Non limiting examples for cross-linking agents are dialdehydes (such as glyoxal and glutaraldehyde), acetals (such as 1,1,4,4-tetramethoxybutane and 1, 1,5,5- tetramethoxybutane), polycarboxylic acids (such as acrylic, maleic, polymaleic, succinic polyitaconic, and citric acids), phosphorus derivatives (such as phosphoric acitriethyld and phosphate), silica derivatives (such as tetraethoxysilane), epichlorohydrin, polyepichlorohydrin, polyamidoamine epichlorohydrin (PAE), polyacrylamide, and glyloxilated polyacrylamide.
  • dialdehydes such as glyoxal and glutaraldehyde
  • acetals such as 1,1,4,4-tetramethoxybutane and 1, 1,5
  • the carbohydrate cross-linking agent may constitute 0.5 % (w/w) to 10 % (w/w) of the final composition of the textile.
  • the cross-linking agent chosen for proteins may be a chemical or enzymatic cross-linking agent.
  • Protein cross-linking agents are molecules that contain two or more reactive ends capable of chemically attaching to specific functional groups on proteins. Attachment between two groups on a single protein results in intramolecular cross-links, which stabilize the tertiary or quaternary structure of the protein. Attachment between groups of two different proteins results in intermolecular cross-links. The intermolecular cross-links stabilize protein-protein interaction.
  • Non-limiting examples for chemical cross-linking agents for proteins are homo-bifunctional agents, such as, glutaraldehyde, dithiobis (sulfosuccinimidylpropionate), dimethyl adipimidate (DMA), dimethyl suberimidate (DMS), and dimethyl pimelimidate (DMP), as well as hetero-bifunctional agents, such as, maleimides, pyridyl disulfides, bis[2-(4-azidosalicylamido)ethyl)] disulfide, succinimidyl 3-(2-pyridyldithio)propionate, and succinimidyl trans-4- (maleimidylmethyl)cyclohexane-l-carboxylate.
  • homo-bifunctional agents such as, glutaraldehyde, dithiobis (sulfosuccinimidylpropionate), dimethyl adipimidate (DMA), dimethyl suberimidate (DMS), and dimethyl
  • Non-limiting examples for enzymatic cross-linking agents are transglutaminases, sortases, lysyl oxidases, and oxidoreductases.
  • the protein cross-linking agent constitutes 0.1 % (w/w) to 10 % (w/w) of the final composition of the textile.
  • Non-limiting examples for catalysts for cross-linking agents are titanium dioxide, sodium dihydrogen phosphate, polyethylene glycol. Catalysts may constitute 0.2 % (w/w) to 1 % (w/w) of the final composition of the textile.
  • a surprising effect of the catalyst titanium dioxide in use together with the cross-linking agent citric acid on the tensile strength has been observed in one embodiment, namely in example 4 (Table 10).
  • the method for dehydrating the pomace to yield a water reduced pomace is selected from the list comprising heating, centrifugation, vacuum filtration, belt filtration, hot filtration, cold filtration, cloth filtration, mechanical press, hydraulic press or forging press.
  • the dehydrating step to reduce the water content of the disrupted pomace is achieved using the method of heating.
  • the temperature is in the range of 50°C to 80°C, and the pomace is maintained at the temperature for a given duration to reduce the water content in the pomace by 10 % (w/w) to 30% (w/w), preferably by 10% (w/w) to 20 % (w/w).
  • the density modifying agents and optionally the cross-linking agents may be added after the heating step in the manufacturing process. If, for example, the density -modifying agent or cross-linking agent has a low decomposition temperature, is volatile, is an enzyme, coagulates, or is toxic when heated, the agent is added after the heating step.
  • Heating the pomace allows homogeneous distribution and promotes carbohydrate/protein intra- or intermolecular interactions. Exemplary, the heating is carried out at 50°C to 80°C to reduce the water content of the pomace by 20 % to 25 %. Additionally or alternatively, the pomace mixture is continuously stirred during the heating to further improve the homogeneous distribution.
  • the second density-modifying agent added after heating of the disrupted pomace is the polymer emulsions, such as latex milk, natural latex milk, rubber milk, acrylonitrile-butadiene copolymer, acrylonitrile-butadiene copolymer, styrene-acrylic polymer emulsion and ethylene vinyl acetate copolymer, and gums such as guar gum, gum Arabic, gum ghatti, karaya gum, tara gum, dammar gum, and gum tragacanth.
  • a colorant and/or an antimicrobial agent is added to the pomace mixture after the dehydration step and before the forming and drying steps in the manufacturing process.
  • the inorganic colorants are metal oxide, such as titanium dioxide, iron oxide, and ultramarine blue, earth pigments, such as natural mineral powders and mica powders.
  • Non-limiting examples for the organic colorant are Indigofera tinctora , Haematoxylum campechianum , Rubia tinctorum , Maclura pomifera , Punica granatum , Schinopsis lorentzii , and Reseda luteola , phthalocyanine, diketopyrrolo-pyrrole, and quinacridone.
  • the colorant may constitute 0.1 % (w/w) to 50 % (w/w) of the final composition of the textile.
  • iron oxide colorant is used at a concentration of 0.5 % (w/w) with no binder to obtain a vibrant black-coloured sample.
  • colorant describes a substance, whether it being a pigment powder, pigment preparation or dye, that can inherently give the non-woven textile the wanted colour, shade or nuance.
  • colorant and dye are used interchangeably.
  • Colorants can be used in combination with binders.
  • binders are acetic acid, citric acid, alum, potassium bitartrate, ferrous sulphate, copper sulphate, and sodium carbonate, polyurethane, acrylic, styrene, polyester, polyvinyl butyral, polyolefin copolymer and vinyl chloride-vinyl acetate copolymer (VC/VAC copolymer).
  • the binder may constitute 0.1 % (w/w) to 10 % (w/w) of the final composition of the textile.
  • Non-limiting examples for antimicrobial agents are green preservatives, such as carvacol and lecithin mixtures, oligochitosan hydrochloride from mushrooms, green/ benzoates/sorbates from mushrooms, preservatives from Inula viscosa, tea tree oil, jojoba oil, and grapefruit extract, and antibiotic/antimicrobial agents non-toxic to humans.
  • antibiotic or antimicrobial agents which are non-toxic to humans are cephalosporins, penicillins, erythromycin, benzyl alcohol, dehydroacetic acid, salicylic acid, sorbic acid, and glycerin.
  • the antimicrobial agent may constitute 0.05 % (w/w) to 5 % (w/w) of the final composition of the textile. If the colorant or the antimicrobial agent is hydrophobic, they can be applied to the textile as a coating together with a binder after the drying step in the manufacturing process.
  • the disclosed method for manufacturing a hydrophobic non-woven textile includes a forming and drying step.
  • the water reduced pomace is distributed on a surface to have a thickness in the range of 0.2 mm to 20 mm, preferably in the range of from 1.0 mm to 10 mm, more preferably in the range of from 1.0 mm to 8 mm, and more preferably in the range of from 1.0 mm to 5 mm.
  • the water reduced pomace is distributed on a surface to have a thickness in the range of 0.5 mm to 2.0 mm. Prior to drying, the water reduced pomace is distributed in frames.
  • the forming frames are made up of materials, which may include, but are not limited to, glass, wood, stone, ceramic, unglazed ceramic, biodegradable polymer, and textiles.
  • the size and type of frame can be changed to fit the required application.
  • the frames aid in achieving a suitable shape, size, and texture of the non-woven textile.
  • the drying of the material into different shapes and thicknesses allows a very versatile use of the finished product, e.g. thin material for accessories and thick material for packaging.
  • the water reduced pomace can also be distributed on a conveying belt.
  • the conveying belt is made up of materials which may include, but are not limited to, urethane (polyurethane), polyolefin, silicone, PVC, mesh, nitrile, polyester, and polypropylene.
  • the belt convey the water reduced pomace through a gap consisting of conveyer belt and rollers, or scraper, or blades to define the width and thickness of the non-woven textile.
  • the disclosed drying step allows for reducing the water activity and water content of the pomace.
  • the reduced water activity and reduced water content of the pomace enable improved tensile strength, storage conditions, and avoid decay processes.
  • the pomace may be dried by any method known to a person skilled in the art. Exemplary, the pomace can be dried by air-drying, freeze-drying, roller-drying, spray-drying, vacuum-drying, microwave-drying, or combinations thereof.
  • the inventors have explored several drying techniques and were surprised to see that air drying had several advantages over the other drying techniques. Drying is carried out at between 20°C to 150°C, e.g. between 20°C to 90°C for 2 to 48 hours to reduce the water content of the pomace to 15 % to 30 %. It was observed that the moisture content for optimal flexibility and strength of the textile depends on the thickness of the samples, wherein thicker textile samples have higher moisture contents.
  • the step of distributing the water reduced pomace on a surface and drying the distributed water reduced pomace is carried out at a drying temperature in the range of 20°C to 90°C, preferably in the range of 40°C to 80°C, more preferably in the range of 45°C to 70°C, for a drying duration to reduce the water content to 10 % (w/w) to 30 % (w/w) of the water reduced pomace, preferably to 20 % (w/w) to 30 % (w/w), to provide a non-woven textile.
  • the drying step comprises drying of the pomace as a vacuum-moulded 3D-form.
  • Vacuum -moulding in a 3D-form allows the production of a non-woven textile which is strong, durable, and non-bendable.
  • the vacuum-moulded 3D-form can be shaped into products with likeness to paper industry products, including, but not limited to, plates, bowls, packaging, wall panels, toys, etc.
  • the coating comprises one or more of spray coating, wet spray coating, immersion dip coating, suspension plasma spraying, roller coating, direct coating, foamed foam coating, crushed foam coating, transfer coating, hotmelt extrusion coating, calendar coating, rotary screen coating, dry powder coating, curtain coating, slot-die coating, extrusion coating, mayer rod coating, kiss roll coating, gravure roll coating and reverse roll coating.
  • the non-woven textile is subjected to hydrophobic coating to achieve the hydrophobic non-woven textile.
  • the disclosed coating technique and coating formulations achieve good results in terms of coating uniformity, smoothness, adhesion, and water repellent properties.
  • the polymer solutions for coating are prepared at concentrations between 0.1 g per mL to 0.5 g per mL of solvent, together with conditioning agents at concentrations between 1 pL per ml to 10 pL per mL of solvent (if required), and held in stirred suspension at 25°C.
  • spray coatings a technique compatible with commercial wet-spray processes, which utilizes compressed air, has been developed in the disclosed method.
  • the polymer solutions are applied to the textile to form a coating film over the surface of the textile.
  • the solvent is evaporated at 25°C for 30 min before applying the next layer of coating.
  • suspension plasma spraying for coating the polymer is loaded into the feeder hopper and a combustion spray gun has been tested for trials.
  • the coating step comprises applying one or more coating layers, wherein each coating layer comprises one or more of an amphiphilic polymer, a hydrophobic polymer and a conditioning agent.
  • each coating layer comprises one or more of an amphiphilic polymer, a hydrophobic polymer and a conditioning agent.
  • a range of water resistant polymers may be used for coating the non-woven textile.
  • This includes a multi-layered coating comprising at least one hydrophobic polymer, optionally a layer comprising a binder, such as an amphiphilic polymer, and optionally a layer comprising a conditioning agent.
  • hydrophobic polymers are polyvinyl butyrate, poly dimethyl siloxane, sodium carbonate decahydrate, Colophonium, polylactic acid (PL A), poly-3 -hydroxybutyrate and carboxylated styrene-butadiene emulsion.
  • Non-limiting examples for amphiphilic polymers are polyacrylic acid, polyethyleneimine, polyvinylpyrrolidone, polyvinyl alcohol, polyvinyl acetate, carboxymethylcellulose, and hydroxyethyl cellulose.
  • Non limiting examples for conditioning agents are alkyl citrates, acetylated monoglycerides, epoxidized vegetable oils, methyl ricinoleate, dibutyl sebacate, dimethyl/dioctyl adipate, dibutyl/diisobutyl maleate, polyethylene glycol, polypropylene glycol, glycerol, potassium oleate, potassium cocoate, and potassium palm kemalate.
  • the coating layer comprising a hydrophobic polymer may additionally include a plasticizer.
  • Triethylene glycol bis(2-ehtylhexanoate) is a non-limiting example for a preferred plasticizer.
  • the plasticizer can be added to the coating layer of the non-woven textile to alter the physical properties of the material by increasing the plasticity or decreasing the viscosity of the textile material.
  • a hydrophobic non-woven textile is obtained by the method of producing a hydrophobic non-woven textile according to above described embodiments.
  • the disclosed method describes a process of upcycling fruit or vegetable pomace obtained as a by-product of industrial processes, such as those of juice and cider production, sugar extraction, and oil extraction, for example.
  • approximately 2 kg to 10 kg of fruit or vegetable pomace allow for the manufacturing of 1 square meter of the hydrophobic non-woven textile with a thickness of around 0.5 mm to 1.5 mm.
  • a non-woven hydrophobic textile which comprises water, a fruit or vegetable material comprising a plant fibre, a density -modifying agent, and a layer of hydrophobic coating, wherein the content of water is in the range of from 10 % (w/w) to 30 % (w/w), e.g. in the range of from 15 % (w/w) to 30 % (w/w), of the hydrophobic non-woven textile, the content of the density-modifying agent is in the range of from 4 % (w/w) to 70 % (w/w), e.g.
  • the hydrophobic non- woven textile in the range of from 4 % (w/w) to 40 % (w/w), of the hydrophobic non- woven textile, and plant fibre having a fibre length of below or equal to 2.0 mm, such as in the range of from 0.3 mm to 2.0 mm, 0.3 mm to 1.5 mm, 0.3 mm to 1.0 mm, 0.5 mm to 1.5 mm, 0.5 mm to 1.0 mm or 0.3 mm to 0.8 mm.
  • a non-woven hydrophobic textile which comprises a layer of a non-woven textile and a layer of hydrophobic coating, wherein the non-woven textile comprises water at a content in the range of from 10 % (w/w) to 30 % (w/w) of the hydrophobic non-woven textile, a fruit or vegetable material comprising a plant fibre having a fibre length of below or equal to 2.0 mm, and one or more density -modifying agents at a content in the range of from 4 % (w/w) to 70 % (w/w) of the hydrophobic non-woven textile, and the hydrophobic coating comprises a hydrophobic polymer.
  • the textile is water resistant, has a good tensile strength, and physical appeal. Furthermore, the disclosed non-woven textile is vegan and has a unique texture.
  • the pomace-based non-woven textile can be subjected to different colorants to achieve a coloured non-woven textile, to bleaching agents for odour and colour harmonization, and to multiple layers of coating for changing the physical properties of the non-woven textile.
  • the hydrophobic non-woven textile of the present invention comprises one or more density -modifying agents at a content in the range of from 4 % (w/w) to 40 % (w/w) of the hydrophobic non-woven textile.
  • the hydrophobic non-woven textile of the present invention has a thickness in the range of 0.2 mm to 20 mm, preferably in the range of from 1.0 mm to 10 mm, more preferably in the range of from 1.0 mm to 8 mm, more preferably in the range of from 1.0 mm to 5 mm.
  • the hydrophobic non-woven textile of the present invention has a thickness in the range of 0.5 mm to 2.0 mm. Providing the material in several thicknesses enables various applications of the material in different products. Also, the flexibility of the textile is to a large portion defined by the thickness of the textile. Thereby various degrees of material flexibility can be designed through pre-determined textile thickness.
  • the tensile strength of the textile is an important measure in the evaluation of the performance and durability of the textile.
  • the tensile strength is defined as a stress, which is measured as force per unit area. In the present invention, tensile strength is thus given in Newtons per squared millimetre (N/mm 2 ). Furthermore, in the present invention the tensile strength is determined according to standard ISO 3376-2011. It has surprisingly been found that the fibre particle length influences the tensile strength of the textile. Thereby the tensile strength can be designed through different ways of comminuting, achieving different fibre particle length depending on the intended use of the hydrophobic non-woven textile. Surprisingly, also cross-linking reactions and the type and amount of density modifying agent has been found to alter the tensile strength of the non-woven textile significantly.
  • the hydrophobic non-woven textile has a tensile strength in the range of from 5 N per mm 2 to 20 N per mm 2 , 5 N per mm 2 to 12 N per mm 2 , 6 N per mm 2 to 12 N per mm 2 , 6 N per mm 2 to 10 N per mm 2 , 6 N per mm 2 to 9 N per mm 2 or 8 N per mm 2 to 10 N per mm 2 .
  • the tensile strength of the textile is important when evaluating flexibility, strength, and durability of the product. A good tensile strength results in a textile with features suitable for the production of clothing, accessories, book bindings, sports equipment, footwear, bags, furnishings, interior decors, toys, and automobile furnishing, for example.
  • the non-woven textile comprises two different density-modifying agents.
  • the two different density-modifying agents are a first density -modifying agent at a content in the range of 4 % (w/w) to 40 % (w/w) of the hydrophobic non-woven textile and a second density -modifying, which is different from the first density -modifying agent, at a content in the range of 10 % (w/w) to 66 % (w/w) of the hydrophobic non-woven textile.
  • the two different density -modifying agents are a first density -modifying agent at a content in the range of 4 % (w/w) to 40 % (w/w) of the hydrophobic non-woven textile and a second density-modifying, which is different from the first density -modifying agent, at a content in the range of 10 % (w/w) to 40 % (w/w) of the hydrophobic non-woven textile.
  • the non-woven textile comprises two or more different density -modifying agents, such as three or four different density -modifying agents.
  • the hydrophobic non-woven textile comprises a density-modifying agent selected from the list consisting of carbohydrates, such as starch, cellulose, microcrystalline cellulose, carrageenan, agar, sugar, and agaropectin; plant fibres, such as softwood pulp, paper pulp, hemp, jute, flax, cotton, nettle, ramie, com, bamboo, and straw; proteins; polymer emulsions, such as latex milk, natural latex milk, rubber milk, acrylonitrile-butadiene copolymer, acrylonitrile-butadiene copolymer, styrene-acrylic polymer emulsion and ethylene vinyl acetate copolymer.; gums, such as guar gum, gum Arabic, gum ghatti, karaya gum, tara gum, dammar gum, and gum tragacanth; polyols, such as glycerol, glycol, pentaerythritol and polyethylene
  • the hydrophobic non-woven textile comprises at least 30% (w/w) of fruit or vegetable material. Additionally or alternatively, the non- woven textile comprises at least 40 % (w/w) fruit or vegetable material. Using a defined amount of fruit or vegetable material enables to control the overall amount of plant or vegetable fibres in the non-woven textile.
  • fruit or vegetable material from more than one type of fruit or vegetable are used for the production of the hydrophobic non-woven textile.
  • more than one type of fruit or vegetable useful characteristics of the fruit or vegetable compositions can be merged to produce non-woven textiles for various purposes.
  • the hydrophobic coating of the hydrophobic non- woven textile further comprises one or more of an amphiphilic polymer and a conditioning agent.
  • the listed polymers and agent can be coated as separated layers, such as one layer of the amphiphilic polymer, one layer of the hydrophobic polymer and one layer of the conditioning agent, or they can be coated as layers which partially mix with another.
  • the number of layers can be one, such as a single hydrophobic layer, two, such as a layer of a hydrophobic polymer and a layer of conditioning agent or such as a layer of a hydrophobic polymer and a layer of an amphiphilic polymer, or three, such as a first layer of amphiphilic polymer, a second layer of hydrophobic polymer and a third layer of conditioning agent.
  • the coating with different layers of polymers and/or agents provides a versatile platform to equip the textile with distinct hydrophobic properties for its use within e.g. clothing, accessories, sports equipment, footwear, bags, furnishings, and automobile furnishing, or other fields where hydrophobic properties are advantageous and/or desired by the customer.
  • a composite material which comprises the hydrophobic non-woven textile according to the present inventive concept, an adhesive layer and a backing.
  • the inventors have surprisingly found that the addition of a backing material to the hydrophobic non- woven textile of the present inventive concept enhances the overall performance of non-woven textile.
  • glue may be used as the adhesive layer between the non-woven textile and the backing.
  • the glue is selected from the list of dextrin, latex, modified latex, polyvinyl acetate, polyurethane, polyacrylic, polychloroprene, epoxy, cyanoacrylate, aliphatic resin, bone glue, hide glue and hotmelt including ethylene-vinyl acetate, polyolefins, polyamides and styrene block copolymers.
  • the glue is an ester acrylic copolymer. The glue used greatly influenced the final appearance of the composite material as well as the durability of the composite material.
  • the backing applied to the non-woven textile of the present invention via the adhesive layer may be selected from list of a textile backing, a glass fiber, a carbon fiber, a metal mesh and a latex sheeting.
  • the backing is a textile backing selected from the list consisting of non-woven textiles, woven textiles, polyester tulle textiles, cotton tulle textiles and knitted textiles.
  • woven textiles as textile backing are cotton plain woven textile, linen plain woven textil, pima cotton satin woven textile, cotton twill woven textile, polyester plain woven textile, chiffon, and regenerated cellulose twill woven textile.
  • weave patterns of the woven textile are plain weave, twill weave and satin weave.
  • Non-limiting examples for knitted textiles as textile backing are cotton knitted textile, cotton wrap knitted textile, wrap knitted textile of cotton/polyester-blend, polyester knitted textile, polyester wrap knitted textile and polypropene wrap knitted textile.
  • the performance of the composite material of the present invention may be evaluated by its tear strength.
  • the tear strength or tear resistance of the composite material is an important measure in the evaluation of how well a material can withstand the effects of tearing and thereby the durability of the composite material.
  • the tear strength is defined as the maximum force required to tear a material in a direction normal to (perpendicular to) the direction of the stress. In the present invention, the tear strength is thus given in Newtons (N). It has surprisingly been found that the textile backing influences the tear strength of the composite material significantly. Thereby the tear strength can be altered through variation in the textile backing depending on the intended use of the hydrophobic non-woven textile.
  • the composite material has a tear strength in the range of 2 N to 45 N, such as in the range of from 5 N to 40 N, 5 N to 35 N, 7 N to 40 N, 10 N to 35 N or 15 N to 35 N as tested and evaluated according to the standard ISO 3377-1-2016.
  • hydrophobic refers to the property of the non-woven textile to repel water at least on a portion of the surface of the non-woven textile.
  • a hydrophobic textile exhibits hydrophobicity and therefore may be termed hydrophobic.
  • the hydrophobic interaction is mostly an entropic effect originating from the disruption of the highly dynamic hydrogen bonds between molecules of liquid water by the nonpolar solute forming a clathrate-like structure around the non-polar molecules.
  • Hydrophobicity is the physical property of a hydrophobic molecule or material that is seemingly repelled from a mass of water, or vice versa, a mass of water which is seemingly repelled from a hydrophobic molecule or material, such as from a hydrophobic non-woven textile.
  • Hydrophobic molecules or materials tend to be nonpolar and, thus, prefer other neural molecules and solvents. Also, water on hydrophobic surfaces of hydrophobic materials or textiles will exhibit a low contact angle. Generally, if the water contact angle is smaller than 90°, the surface of the material or textile is considered hydrophobic, and if the water contact angle is larger than 90°, the surface of the material or textile is considered hydrophilic.
  • non-water-soluble refers to compounds that are mostly polymers, and is defined as non-water-soluble if ⁇ 10 % (w/w) of the compound does not dissolve completely in water at room temperature within 1 hour.
  • w/w refers to "weight for weight” or “weight by weight” and gives the proportion of a particular substance within a mixture, as measured by weight or mass.
  • v/v refers to the volume concentration of a solution and is expressed as % v/v, which stands for volume per volume of liquids in a solution.
  • the term “fruit or vegetable material” is the fruit and vegetable product comprising dry matter and water.
  • the fruit or vegetable material may be obtained from fruit and/or vegetable processing, such as from industrial production of for example juice and/or cider.
  • the term “one or more density modifying agents” is to be understood as at least one density-modifying agents being added, the density-modifying agent being selected from the list of different density modifying agents. When for example two, three or four density-modifying agents are used, then the two, three or four density-modifying agents are different density modifying agents.
  • the density modifying agent being added in the range of 10 % (w/w) to 85 % (w/w) of the weight of the dry matter of the disrupted pomace is to be understood as each individual density-modifying agent being added in the range of 10 % (w/w) to 85 % (w/w) of the weight of the dry matter of the disrupted pomace.
  • the term “carrageenan” describes a family of linear sulphated polysaccharides that are extracted from red edible seaweeds
  • the term “agar” (or “agar-agar”) describes a jelly-like substance obtained from red algae.
  • Agar is a mixture of two components: the linear polysaccharide agarose, and a heterogeneous mixture of smaller molecules called agaropectin.
  • hemp describes a strain of the Cannabis sativa plant species that is grown specifically for the industrial uses of its derived products, such as fibre products.
  • a synonym for hemp fibre is “bast”, which refers to the fibres which grow on the outside of the plant’s stalk.
  • jute describes a long, soft, shiny vegetable fibre which can be used for various textile application. Jute is produced primarily from plants in the genus Corchorus the term “flax” describes a bast fibre which is extracted from the plant of the linseed/flax plant ( Linum usitatissimu i).
  • the term “cotton” describes a soft, staple fibre that grows around the seeds of the cotton plants of the genus Gossypium in the mallow family Malvaceae
  • the term “nettle” describes a very strong fibre derived from the plant Urtica dioica
  • the term “ramie” describes any of several fibre-yielding plants of the genus Boehmeria , belonging to the nettle family ( Urticaceae ) and their fibre, one of the bast fibre group
  • the term “corn” or “corn fibre” describes any fibre derived from the corn plant Zea mays
  • the term “bamboo” or “bamboo fibres” describes a cellulosic fibre that is regenerated from bamboo plant, typically bamboo used for fibre preparation is 3 to 4 years old
  • the term “straw” describes fibre from straw as an agricultural by-product consisting of the dry stalks of cereal plants after the grain and chaff have been removed.
  • “hemp”, “jute”, “flax”, “cotton”, “nettle”, “ramie”, “com”, “bamboo”, and “straw” can exist in different forms, such as a newly harvested, or raw form, and in refined, or spun form, which influence the performance of the fibres.
  • softwood pulp describes a lignocellulosic fibrous material prepared by chemically or mechanically separating cellulose fibres from wood of softwood trees including spruce, pine, beech, aspen, fir, larch and hemlock
  • paper pulp describes a lignocellulosic fibrous material prepared by chemically or mechanically separating cellulose fibres from paper or waste paper.
  • guar gum also called guaran, describes a galactomannan polysaccharide extracted from guar beans with thickening and stabilizing properties
  • the term “gum Arabic”, also known as gum Sudani, acacia gum, Arabic gum, gum acacia, acacia, Senegal gum or India gum describes a natural gum consisting of the hardened sap of various species of the acacia tree
  • the term “gum ghatti”, also known as Indian gum describes a complex non-starch polysaccharide exuded from the bark of the tree Anogeissus latifolia of the family Combretaceae
  • the term “karaya gum”, also known as gum sterculia or Indian gum tragacanth describes an acid polysaccharide produced as an exudate by trees of the genus Sterculia
  • the term “tara gum”, also known as Tara spinosa describes a galactomannan polysaccharide
  • Fig. l is a flowchart for the production of the hydrophobic non-woven textile.
  • Fig. 2 discloses the effect of comminuting the apple pomace in relation to the fibre particle size in a sample of non-woven textile.
  • the present invention in a first aspect relates to a method for producing a hydrophobic non-woven textile from fruit or vegetable pomace.
  • the invention in a second aspect relates to a hydrophobic non-woven textile comprising a fruit or vegetable material, a density-modifying agent, and a layer of hydrophobic coating.
  • the invention in a third aspect, relates to a composite material comprising a hydrophobic non- woven textile comprising a fruit or vegetable material, a density-modifying agent and a layer of hydrophobic coating, an adhesive layer and a backing.
  • Figure 1 discloses the overall process of the disclosed method with the steps included in producing the hydrophobic non-woven textile.
  • the fruit/vegetable pomace is supplied as by-product from industrial production (A), such as from juice and cider production.
  • the pomace is comminuted (B), which yields a disrupted pomace.
  • the disrupted pomace is mixed with one or more density -modifying agent (C), following which the mixture is dehydrated (D) to obtain a water reduced pomace.
  • the water reduced pomace is formed (E) and dried (F) in suitable frames, depending on application, yielding a pomace-based non-woven textile.
  • the pomace-based non-woven textile is coated with one or more coating layers, of which at least one coating layer is a hydrophobic polymer to obtain the hydrophobic non-woven textile.
  • Figure 2 discloses the effect of pomace comminuting on fibre size and tensile strength in the product.
  • Fig. 2 A discloses a sample which was obtained without milling and has a tensile strength of 6.8 N/mm 2 .
  • Fig. 2 B discloses a sample which was obtained by milling performed in a toothed colloid mill and has a tensile strength of 9.33 N/mm 2 .
  • the described milling reduced the average fibre width to ⁇ 50 pm, and 70 % of the fibres had a fibre length of 0.2 - 0.5 mm.
  • the milling process significantly increased the tensile strength and influenced the texture of the textile.
  • the product obtained after milling has been found to be smooth, flexible, and strong.
  • Example 1 Composition of fruits
  • apple pomace is used as the starting material for the non-woven textile.
  • Apple pomace is obtained as a by-product of apple juice and/or cider production. 100 % (w/w) of the apple pomace can be used for production of the non-woven textile of the present invention.
  • the pomace of other fruits or vegetables can be used as a starting material in the present invention.
  • Tables 1-4 summarize the composition of regular biomass including apple pomace and banana peels. The percentages are given in % (w/w).
  • This example describes an odour and colour harmonization step as a part of the manufacturing process.
  • bleaching with oxidizing agents is described as a suitable method of odour and colour harmonization of the apple pomace.
  • Bleaching with hydrogen peroxide (H2O2) is carried out in a closed tank with 0.01 % (w/w) to 0.04 % (w/w) of 31 % H2O2 at 80°C and pH 10 for lh with continuous stirring.
  • the pH of the solution is preferably adjusted with a base, sodium hydroxide (NaOH) for example, to the desired pH.
  • NaOH sodium hydroxide
  • This example relates to the use of solvents for the odour and colour harmonization step during the manufacturing process of the non-woven textile.
  • Ethanol, acetone and chlorine treatment were carried out with 300 % (v/v) solvent in a closed vessel at 25°C for 120h with continuous stirring.
  • the pH of the solution is preferably adjusted to pH 3 with a weak organic acid, acetic acid for example.
  • Density -modifying agents are added in the manufacturing process of the non- woven textile.
  • at least one complex non-water-soluble carbohydrate or lignocellulosic fibre is added as density-modifying agent to the pomace.
  • the type of lignocellulosic fibre chosen can affect the tensile strength of the non-woven textile.
  • the type of lignocellulosic fibre is also evaluated based on its adhesion potential with apple pomace. The adhesion potential is important for the mixing during the manufacturing of the non-woven textile.
  • the textile may contain other insoluble carbohydrates, water-soluble carbohydrates, and proteins.
  • the soluble carbohydrate can constitute up to 20 % (w/w) of the final composition of the textile.
  • the protein can constitute up to 30 % (w/w) of the final composition of the textile.
  • Table 8 summarizes the influence of addition of different carbohydrates and proteins on tensile strength of the apple non-woven textile.
  • enzymatic cross-linking reaction can be performed.
  • the enzyme transglutaminase was used to crosslink soy protein.
  • the transglutaminase and soy protein were added to the sample containing apple pomace, 3 % soft wood fibres and 3 % sucrose at 35 °C. The sample then was mixed and dried at 35 °C for 6 h.
  • chemical cross-linking agents are added as density modifying agents.
  • Cross-linking agents have been found to alter the product strength.
  • a mixture of citric acid and TiCh was added to apple pomace together with 9 % soft wood fibres and 23 % sucrose, and thereafter heated at 80°C for lh. The sample then was dried at 70°C for 5 hours with or without curing at 165°C for 5 minutes. This treatment resulted in a tensile strength of 7.82 N/mm 2 for the final product.
  • polyamidoamine epichlorohydrin (PAE) was added as cross-linking agent.
  • PAE polyamidoamine epichlorohydrin
  • the hydrophobic non-woven textile may additionally or alternatively include a humectant as a density-modifying ingredient.
  • the humectant can constitute between 0.1 % (w/w) to 2 % (w/w) of the final composition of the textile and helps to preserve moisture content of the textile.
  • the use of glycerol as a humectant was tested. Glycerol at concentrations 0 % (w/w), 0.75 % (w/w) or 1.5 % (w/w) was added to the mixture containing milled apple pomace, 9 % soft wood fibres, and 23 %, 17.25% or 11.5% sucrose. The mixtures were heated at 70°C for 2h and dried at 70°C for 5h. As seen in Table 11, the treatment of the present embodiment adversely affected the tensile strength of the textile, however, improved the moisture retention in the apple pomace- based non-woven textile.
  • Example 6 Forming and drying The process disclosed in the present invention includes forming and drying as parts of manufacturing the non-woven pomace-based textile.
  • biodegradable cellulose acetate frames are used for forming the textile.
  • the sample is dried at 30°C under a free flow of air until the moisture content in the non- woven textile is reduced to 20 %.
  • the temperature setting for drying different samples can differ for each sample composition. Examples of drying temperature settings with regards to product composition are given in Table 12.
  • the non-woven pomace-based textile achieved by the process disclosed in the present inventive concept is coated with a hydrophobic polymer to increase water resistance and to control moisture transport.
  • a hydrophobic polymer to increase water resistance and to control moisture transport.
  • One embodiment exemplifies the use of the polymer-based coatings polyvinyl butyrate (PVB) and a polymer emulsion in the presence and absence of corona treatment to improve coating adhesiveness.
  • PVB polyvinyl butyrate
  • PVB polyvinyl butyrate
  • the aqueous liquid repellency test is carried out according to DS/ISO 23232:2009.
  • the non-woven pomace-based textile achieved by the process disclosed in the present inventive concept may be used to form a composite material by attaching a textile backing to the finished non-woven textile using a certain adhesive solution.
  • a textile backing As an example, at least one layer of textile is attached as a backing.
  • the types of woven textile backing can affect the tensile strength of the non-woven textile.
  • the type of textile backing is also evaluated based on the tear strength, measured in newtons (N) of the composite non-woven textile.
  • the tear strength is important for the durability of the final composite material.
  • the tear strength assessments are carried out and evaluated according to the standard ISO 3377-1-2016.
  • the adhesion used for the embodiments listed in Table 14-16 is ester acrylic copolymer.
  • the tear strength varies according to the types of backing textile used, e.g. when using linen plain woven textile the composite material has a high tear strength of 30.85 N (Table 14), whereas e.g. the use of cotton wrap knitted textile as backing for the composite non-woven textile results in a tear strength of 7.52 N (Table 15).
  • the textile is composed of a mixture of 54 % cotton and 46 % polyester.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Treatment Of Fiber Materials (AREA)

Abstract

La présente invention concerne un textile non tissé hydrophobe et son procédé de fabrication, le procédé de fabrication comprenant les étapes consistant : à se procurer un marc de fruit ou de légume, à pulvériser le marc, à mélanger le marc dissocié avec un agent de modification de densité, à déshydrater le marc dissocié, à répartir le marc à teneur en eau réduite sur une surface, à sécher le marc à teneur en eau réduite réparti et à recouvrir le textile non tissé avec un polymère hydrophobe pour obtenir le textile non tissé hydrophobe.
PCT/DK2020/050369 2019-12-16 2020-12-16 Textile non-tissé obtenu à partir de déchets de fruits et légumes recyclés WO2021121509A2 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP20828281.4A EP4077498A2 (fr) 2019-12-16 2020-12-16 Textile non-tissé obtenu à partir de déchets de fruits et légumes recyclés
CN202080087747.9A CN114867771A (zh) 2019-12-16 2020-12-16 来自升级利用的水果和蔬菜废弃物的非织造织物
CA3163928A CA3163928A1 (fr) 2019-12-16 2020-12-16 Textile non-tisse obtenu a partir de dechets de fruits et legumes recycles
US17/782,144 US20230053954A1 (en) 2019-12-16 2020-12-16 Non-woven textile from upcycled fruit and vegetable waste

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DKPA201970770A DK180600B1 (en) 2019-12-16 2019-12-16 Non-woven textile from upcycled fruit and vegetable waste
DKPA201970770 2019-12-16

Publications (2)

Publication Number Publication Date
WO2021121509A2 true WO2021121509A2 (fr) 2021-06-24
WO2021121509A3 WO2021121509A3 (fr) 2021-12-30

Family

ID=73855624

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/DK2020/050369 WO2021121509A2 (fr) 2019-12-16 2020-12-16 Textile non-tissé obtenu à partir de déchets de fruits et légumes recyclés

Country Status (6)

Country Link
US (1) US20230053954A1 (fr)
EP (1) EP4077498A2 (fr)
CN (1) CN114867771A (fr)
CA (1) CA3163928A1 (fr)
DK (1) DK180600B1 (fr)
WO (1) WO2021121509A2 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022218977A3 (fr) * 2021-04-12 2022-11-24 Nuvi Releaf Gmbh Nouveau composite stratifié destiné à être utilisé comme similicuir
WO2023136849A1 (fr) 2022-01-12 2023-07-20 Mink Shoes Inc. Matériau de type cuir à partir de déchets d'origine végétale, procédé de fabrication et utilisation dudit matériau de type cuir
WO2024042538A1 (fr) * 2022-08-20 2024-02-29 Mody Jinali Cuir végan à base de plante fabriqué à partir de déchets de culture de banane
WO2024076334A1 (fr) * 2022-10-08 2024-04-11 Relab Arge Teknoloji̇leri̇ Anoni̇m Şi̇rketi̇ Production de cuir végétalien (aegiaus) comportant des additifs polymères de silicone à partir de grignon et de déchets végétaux
WO2024078705A1 (fr) * 2021-10-19 2024-04-18 Persiskin, S.L. Matériau de type cuir d'origine végétale fabriqué à partir de purée de kaki

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20220167705A1 (en) * 2020-12-01 2022-06-02 Jennifer STUCKO Sustainable wearable item and method of manufacturing same

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100275214B1 (ko) 1998-05-26 2000-12-15 강민영 매실과육과 매실착즙박을 이용한 마쇄과육말랭이의 제조방법
US20050147723A1 (en) 2003-12-29 2005-07-07 Liu Rui H. Apple peel powder, methods of making, and uses thereof
US20090169694A1 (en) 2006-09-15 2009-07-02 Chocotech Gmbh Method and Apparatus for Producing Fruit Leather from a Fruit Mass
US20090301347A1 (en) 2006-07-28 2009-12-10 Alberto Volcan Composition based on products stemming from industrial residues in the processing of fruits, especially apples, use thereof, method for processing them and products thus obtained
US20130149512A1 (en) 2010-05-25 2013-06-13 Ananas Anam Limited Natural Nonwoven Materials
WO2015018711A1 (fr) 2013-08-08 2015-02-12 Santanocito Adriana Maria Production de textile à partir d'agrumes
CN106748544A (zh) 2017-02-13 2017-05-31 广西壮族自治区农业科学院蔬菜研究所 一种农村废弃物制作酵素有机肥的方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB191204332A (en) * 1912-02-21 1913-02-06 Harold Jackson Improvements in the Manufacture of Paper, Boards, Imitation Leather or Material for Packing, Insulating or other purposes.
US2023711A (en) * 1932-07-27 1935-12-10 Paterson Parchment Paper Compa Material containing parchmentized fiber and method of producing the same
US20210179867A1 (en) * 2017-12-07 2021-06-17 Tintex - Textiles, S.A Flexible material, its production method and uses
PL240444B1 (pl) * 2018-12-10 2022-04-04 Artur Bartkowiak Sposób wytwarzania sztucznej skóry
IT201900000073A1 (it) * 2019-02-04 2020-08-04 Vegea S R L Compound polimerici per la produzione di tessuti spalmati comprendenti biomasse derivate da Vitis quale ingrediente attivo e filler
CN110344276B (zh) * 2019-06-29 2021-08-06 华南理工大学 一种生物基高光泽度纯素皮革及其制造方法

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100275214B1 (ko) 1998-05-26 2000-12-15 강민영 매실과육과 매실착즙박을 이용한 마쇄과육말랭이의 제조방법
US20050147723A1 (en) 2003-12-29 2005-07-07 Liu Rui H. Apple peel powder, methods of making, and uses thereof
US20090301347A1 (en) 2006-07-28 2009-12-10 Alberto Volcan Composition based on products stemming from industrial residues in the processing of fruits, especially apples, use thereof, method for processing them and products thus obtained
US20090169694A1 (en) 2006-09-15 2009-07-02 Chocotech Gmbh Method and Apparatus for Producing Fruit Leather from a Fruit Mass
US20130149512A1 (en) 2010-05-25 2013-06-13 Ananas Anam Limited Natural Nonwoven Materials
WO2015018711A1 (fr) 2013-08-08 2015-02-12 Santanocito Adriana Maria Production de textile à partir d'agrumes
CN106748544A (zh) 2017-02-13 2017-05-31 广西壮族自治区农业科学院蔬菜研究所 一种农村废弃物制作酵素有机肥的方法

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022218977A3 (fr) * 2021-04-12 2022-11-24 Nuvi Releaf Gmbh Nouveau composite stratifié destiné à être utilisé comme similicuir
WO2024078705A1 (fr) * 2021-10-19 2024-04-18 Persiskin, S.L. Matériau de type cuir d'origine végétale fabriqué à partir de purée de kaki
WO2023136849A1 (fr) 2022-01-12 2023-07-20 Mink Shoes Inc. Matériau de type cuir à partir de déchets d'origine végétale, procédé de fabrication et utilisation dudit matériau de type cuir
WO2024042538A1 (fr) * 2022-08-20 2024-02-29 Mody Jinali Cuir végan à base de plante fabriqué à partir de déchets de culture de banane
WO2024076334A1 (fr) * 2022-10-08 2024-04-11 Relab Arge Teknoloji̇leri̇ Anoni̇m Şi̇rketi̇ Production de cuir végétalien (aegiaus) comportant des additifs polymères de silicone à partir de grignon et de déchets végétaux

Also Published As

Publication number Publication date
US20230053954A1 (en) 2023-02-23
DK180600B1 (en) 2021-10-14
CN114867771A (zh) 2022-08-05
WO2021121509A3 (fr) 2021-12-30
DK201970770A1 (en) 2021-08-03
CA3163928A1 (fr) 2021-06-24
EP4077498A2 (fr) 2022-10-26

Similar Documents

Publication Publication Date Title
US20230053954A1 (en) Non-woven textile from upcycled fruit and vegetable waste
Otoni et al. Recent advances on edible films based on fruits and vegetables—a review
KR102233086B1 (ko) 해조류계의 식품 포장 코팅
Merino et al. Avocado peels and seeds: processing strategies for the development of highly antioxidant bioplastic films
EP1833920A2 (fr) Ameliorations liees a des composites biodegradables
JP4117900B2 (ja) 植物由来の生分解性天然素材
Popović et al. Valorization of by-products from the production of pressed edible oils to produce biopolymer films
Tumwesigye et al. Integrated sustainable process design framework for cassava biobased packaging materials: critical review of current challenges, emerging trends and prospects
Aguilar et al. Evaluating how avocado residue addition affects the properties of cassava starch-based foam trays
US20220251390A1 (en) Biodegradable and edible bioplastic from renewable plant based polymer for packaging and the manufacturing method thereof
JP2022172609A (ja) 樹脂組成物、接着剤、樹脂成形品及び樹脂成形品の製造方法
Tapia-Blácido et al. Agroindustrial biomass: potential materials for production of biopolymeric films
Mirpoor et al. Cardoon seed oil cake proteins as substrate for microbial transglutaminase: Their application as matrix for bio-based packaging to extend the shelf-life of peanuts
Elkhateeb et al. Fungi-derived leather (mushroom leather)
KR20230105257A (ko) 맥주박을 이용한 생분해성 펄프컵 및 이의 제조방법
Hefft Developments and properties of plastic mimicking biopolymers for food packaging application
Shih Development and Characterization of Novel Muffin Products for Promoting Sustainability
Jayasinghe et al. Valorization of Banana Waste and Its Applications in Food Packaging
WO2021155889A1 (fr) Matériau à base de macroalgues
Acosta et al. Biodegradable-disposable containers made of Achiras leaves (Canna edulis) by thermoconforming
Lestari et al. Tropical Fruit Waste Management: Developing Pectin-based Biopolymer from Durian Rind (Durio zibethinus)
Raghunathan et al. Biodegradable Products from renewable sources: Impact on Replacing Single Use Plastic for Protecting the Environment
Zhang et al. Edible Packaging from Legume By-Products
Archana et al. Geophysical techniques for aquifer characteristic studies-a case study of Perumatty grama panchayath in Kerala
Fathima et al. Microclimatic characteristics of different types of protected structures

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 3163928

Country of ref document: CA

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2020828281

Country of ref document: EP

Effective date: 20220718

121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 20828281

Country of ref document: EP

Kind code of ref document: A2