WO2019158917A1 - Matériau composite - Google Patents

Matériau composite Download PDF

Info

Publication number
WO2019158917A1
WO2019158917A1 PCT/GB2019/050384 GB2019050384W WO2019158917A1 WO 2019158917 A1 WO2019158917 A1 WO 2019158917A1 GB 2019050384 W GB2019050384 W GB 2019050384W WO 2019158917 A1 WO2019158917 A1 WO 2019158917A1
Authority
WO
WIPO (PCT)
Prior art keywords
resin binder
binder composition
wood
sugar
composite material
Prior art date
Application number
PCT/GB2019/050384
Other languages
English (en)
Inventor
Andrew Peter Abbott
Robert Harris
Original Assignee
University Of Leicester
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 University Of Leicester filed Critical University Of Leicester
Publication of WO2019158917A1 publication Critical patent/WO2019158917A1/fr

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N3/00Manufacture of substantially flat articles, e.g. boards, from particles or fibres
    • B27N3/002Manufacture of substantially flat articles, e.g. boards, from particles or fibres characterised by the type of binder
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N1/00Pretreatment of moulding material
    • B27N1/006Pretreatment of moulding material for increasing resistance to swelling by humidity
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N1/00Pretreatment of moulding material
    • B27N1/02Mixing the material with binding agent
    • B27N1/0209Methods, e.g. characterised by the composition of the agent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N3/00Manufacture of substantially flat articles, e.g. boards, from particles or fibres
    • B27N3/02Manufacture of substantially flat articles, e.g. boards, from particles or fibres from particles
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27NMANUFACTURE BY DRY PROCESSES OF ARTICLES, WITH OR WITHOUT ORGANIC BINDING AGENTS, MADE FROM PARTICLES OR FIBRES CONSISTING OF WOOD OR OTHER LIGNOCELLULOSIC OR LIKE ORGANIC MATERIAL
    • B27N3/00Manufacture of substantially flat articles, e.g. boards, from particles or fibres
    • B27N3/04Manufacture of substantially flat articles, e.g. boards, from particles or fibres from fibres
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L97/00Compositions of lignin-containing materials
    • C08L97/02Lignocellulosic material, e.g. wood, straw or bagasse

Definitions

  • This invention relates to a composite material comprising a wood material comprising cellulose fibres, and a resin binder composition.
  • the resin binder composition is based upon a sugar and certain salts, and the composite material is substantially free of added inorganic acid ammonium salt.
  • the sugar and metal salt are present in the composite material in a combined amount of from about 2 to about 25 wt.%.
  • This invention also relates to the uses of such composite materials, articles comprising such composite materials and processes for preparing articles using these composite materials and a resin binder composition.
  • the resin binder composition has a particular application as a binder for fiberized materials, and in particular, for composite wood materials such as particle board, fibre board, HDF, MDF, chipboard and plywood.
  • cellulose-based composites are major materials for the worldwide construction industry. Most buildings contain cellulose-based composites as a significant component. An important advantage of cellulose-based composites is that they typically use waste products from the pulp and timber industries and so they are significantly less expensive than virgin timber. Typically, they are constructed of wood particles which are held together with a thermoset resin, wherein the amount of resin required is typically dependent on the size of the particles; composites such as particleboard are formed of larger particles and typically require 8 wt.% of thermoset resin and composites such as fibre board are formed of smaller particles requiring 10 wt.% of thermoset resin.
  • An innovative, alternative approach is to use a resin binder composition comprising sugar and environmentally friendly salts. It has surprisingly been found that the addition of environmentally friendly salts of group I or II metal halides, such as chlorides, and sulfates or acetates into binding compositions comprising sugar decreases the swelling of wood composite boards using such binders, allowing carcinogenic or more environmentally hazardous compounds in the binder to be significantly reduced or eliminated entirely. The use of these binder compositions also reduces the tendency of such boards to delaminate.
  • a composite material comprising:
  • a metal salt which is a halide, acetate or sulfate salt of a group I or II metal element; wherein the sugar and metal salt are present in the composite material in a combined amount of from about 2 to about 25 wt.% and wherein the resin binder composition is substantially free of added inorganic acid ammonium salt.
  • the composite material comprises wood material in an amount of from about 75 to about 98 wt.%, preferably from about 80 to about 95 wt.%, more preferably from about 85 to about 95 wt.%.
  • An advantage of the present invention is that the resin binder composition can be present in a much lower amount than resin binders used in current fibreboards, whilst maintaining or improving the properties of the fibreboards. This means that the fibreboards may have a much higher wood material content than currently used fibreboards, leading to a reduction in resin binder material use and an overall reduction in production costs.
  • the sugar and metal salt are present in the composite material in a combined amount of from about 5 to about 20 wt.%, more preferably in a combined amount of from about 5 to about 15 wt.%.
  • the composite material comprises wood material solids and resin solids in a weight ratio of from 75 to 98 : 2 to 25, such as 80 to 95 : 5 to 20, more preferably from 85 to 95 : 5 to 15.
  • solids refers to the materials within the invention in a dry form (i.e. in the absence of any solvent, such as water).
  • wood material solids refers to the cellulose fibres present in the invention on a dry matter basis
  • resin solids refers to the sugar and metal salt mix of the resin of the invention on a dry matter basis
  • sugar and metal salt mix of the resin of the invention refers to the sugar and metal salt mix of the resin of the invention on a dry matter basis
  • sugar solids the solids of the resin composition of the invention in a dry form (i.e., in the absence of any solvent, such as water).
  • the resin solids in the composite material comprise sugar solids : metal salt solids in a weight ratio of from 99: 1 to 34:66, for example from 98:2 to 50:50, preferably from 90: 10 to 60:40.
  • the resultant composite material comprises wood material solids : sugar solids : metal salt solids in a weight ratio of from 75 to 98 : 0.7 to 25 : 0.025 to 16.5, for example from 80 to 95 : 3 to 18 : 0.5 to 8, preferably from 85 to 95 : 3.5 to 12 : 1 to 4.5.
  • weight ratio refers to the ratio of the materials within the invention in a dry form (i.e. in the absence of any solvent, such as water). Indeed, when materials are present in a defined weight ratio this can be referred to as a dry weight ratio.
  • the cellulose fibres are selected from the group consisting of wood fibres, bagasse fibres, wood flour, wood particles and lignin fibres.
  • the cellulose fibres of the wood material may optionally be coated with a water-resistant material.
  • the composite material may further comprise an additive selected from flame retardants, waxes, fillers, stabilisers, anti-wear agents and blowing agents, and mixtures thereof.
  • the metal salt present in the resin binder composition is selected from the group consisting of sodium chloride, sodium sulfate, sodium acetate, potassium chloride, potassium sulfate, potassium acetate, magnesium chloride, magnesium sulfate, magnesium acetate, calcium chloride, calcium sulfate and calcium acetate, preferably wherein the metal salt is sodium chloride.
  • the metal salt present in the resin binder composition is a halide or acetate of a group I or group II metal element.
  • the metal salt present in the resin binder composition is a halide of a group I or group II metal element.
  • the metal salt in the resin binder composition may, for example, be selected from the group consisting of sodium chloride, sodium acetate, potassium chloride, potassium acetate, magnesium chloride, magnesium acetate, calcium chloride and calcium acetate, preferably the metal salt is sodium chloride.
  • the resin binder composition has no added inorganic acid ammonium salt.
  • the composite material has a water content of up to about 15 wt.%, such as up to about 15, 10, 5, 2 or 1 wt.% water, for example from about 1 to about 15 wt.%, preferably from about 1 to about 10 wt.%, more preferably from about 1 to about 8 wt.%.
  • the composite material may further comprise a conventional formaldehyde-based or formaldehyde-free resin binder as detailed above. When comprising such conventional binders, they are included in amounts lower than currently used in existing composite wood boards.
  • the composite article is a composite wood (also known as engineered wood, man made wood or manufactured board) which includes, but is not limited to HDF (high-density fibreboard) MDF (medium-density fibreboard), particle board, chipboard and plywood.
  • Composite wood is manufactured by binding or fixing the strands, particles, fibres, veneers or boards of wood, together using the resin binder composition described herein.
  • the composite article comprises wood material and resin solids in a weight ratio of from 75 to 98 : 2 to 25, such as 80 to 95 : 5 to 20, more preferably from 85 to 95 : 5 to 15.
  • the composite article comprises wood material solids : sugar solids : metal salt solids in a weight ratio of from 75 to 98 : 0.7 to 25 : 0.025 to 16.5, for example from 80 to 95 : 3 to 18 : 0.5 to 8, preferably from 85 to 95 : 3.5 to 12 : 1 to 4.5.
  • the composite article can be used for various applications, for example, building materials, furniture etc., in the same manner as a conventional wood-based material.
  • the composite wood may be coated with a water-resistant material optionally selected from the list consisting of polyvinylacetate, polyvinylalcohol or a wax selected from the group consisting of paraffin wax, beeswax, bayberry wax, candelilla wax, caranday wax, castor bean wax, shellac wax, spermaceti wax, sugar cane wax and wool wax (lanolin), and mixtures thereof.
  • a water-resistant material optionally selected from the list consisting of polyvinylacetate, polyvinylalcohol or a wax selected from the group consisting of paraffin wax, beeswax, bayberry wax, candelilla wax, caranday wax, castor bean wax, shellac wax, spermaceti wax, sugar cane wax and wool wax (lanolin), and mixtures thereof.
  • a metal salt which is a halide, acetate or sulfate salt of a group I or II metal element; and iii. no added inorganic acid ammonium salt;
  • the resin binder composition may comprise a solvent to modify viscosity and improve the process step of adding wood material to the resin binder composition.
  • the resin binder composition for use in the process has a dry solids to solvent ratio of from about 1 : 10 to about 5: 1 , such as from about 1 : 1 to about 4:1 , more preferably from about 2: 1 to 4: 1.
  • the solvent is preferably water.
  • the cellulose fibres are selected from the group consisting of wood fibres, bagasse fibres, wood flour, wood particles and lignin fibres.
  • the viscosity of the resin binder composition before addition of the wood material is from about 50 to about 500 cP, such as from about 100 to about 400 cP, for example from about 200 to about 300 cP. More preferably, the viscosity is less than, or equal to, 300 cP.
  • the composition after addition of the wood material i.e., in step (c) is pressed at a temperature of from about 50 to about 300°C, preferably from about 100 to about 250°C, more preferably from about 150 to about 230°C.
  • the composition after addition of the wood material is pressed at a pressure of from about 100 to about 10,000 kNrrr 2 , preferably from about 100 to about 5000 kNrrr 2 , more preferably from about 100 to about 2000 kNrrr 2 .
  • both heat and pressure When both heat and pressure are used to form the composite material according to the present invention, they may both be conveniently applied by way of a heated press.
  • the process may include a pre-press step, wherein the composite material is pressed at ambient temperature. Pre pressing the composite material aids in removing air pockets from the composite material.
  • the composite material in step (c) is pressed for a time of from 1 to about 30 minutes, preferably from about 1 to about 20 minutes, more preferably from about 2 to about 10 minutes.
  • the process comprises the step of flash drying the composite material before pressing.
  • the flash drying is carried out at a temperature of from about 50 to about 150°C, preferably from about 70 to about 130°C, more preferably from about 80 to about 100°C.
  • the flash drying is carried out for a period of from about 1 to about 300 seconds, preferably from about 1 to about 120 seconds, more preferably from about 1 to about 60 seconds.
  • the components of the resin binder composition i.e., sugar, and a metal salt which is a halide, acetate or sulfate salt of a group I or II metal element, may be added separately to the wood material. After addition, these components act as a resin binder in substantially the same manner as if they were added together.
  • the components of the resin binder composition may be added to the wood material in a sequential or simultaneous manner.
  • any of the embodiments outlined above with respect to the process where the components of the resin binder composition are pre-mixed before adding to the wood material may equally be applied to the process where the components of the resin binder composition are added separately to the wood material.
  • the composite articles, woods and materials prepared using the resin binder composition of the present invention may be provided with a coating (e.g., a hydrophobic coating) in order to improve their resistance to water.
  • a coating e.g., a hydrophobic coating
  • the wood fibres used in the invention may also be provided with a coating (e.g., a hydrophobic coating) in order to improve the resistance of the composite articles, woods and materials to water.
  • any of the water- resistant materials detailed above may be used for the coating.
  • Embodiments of this aspect of the invention includes composite articles, woods, materials and wood fibres wherein the coating of water-resistant material covers at least 50% (e.g., at least 60, 70, 80, 90, 95 or 99%, such as 100%) of the exposed surfaces of the composite article, wood, material or fibre.
  • exposed surfaces when used herein, includes references to surfaces of the composite article, wood, material or fibre that, at room temperatures and atmospheric pressure, are accessible to (externally-introduced) liquid water or water vapour.
  • water-resistant mafer/a/ includes references to materials that, at a temperature of 298 K, have a solubility in water of less than 50 ppm (or less than 50 mg/L, such as less than 25, 10, 5 or 1 mg/L).
  • water-resistant materials include waxes (e.g., waxes based upon molecules containing at least 20 C-atoms, such as from 20 to 30 C-atoms), hydrophobic polymers (e.g., polyvinylacetate) and polymers such as polyvinylalcohol.
  • waxes that may be mentioned in this respect include those selected from the group consisting of paraffin wax, beeswax, bayberry wax, candelilla wax, caranday wax, castor bean wax, shellac wax, spermaceti wax, sugar cane wax and wool wax (lanolin).
  • the resin binder composition of the composite material i.e. , the mixture of sugar and metal salt described herein can act as a resin and/or glue to bind the wood material of the composite.
  • the term‘resin’ to mean solid or semisolid viscous substances which principally act as varnishes and/or adhesives.
  • glue to mean an adhesive substance for sticking objects or materials together.
  • a resin binder composition comprising:
  • a metal salt which is a halide, acetate or sulfate salt of a group I or II metal element
  • sugar and metal salt are present in the composition in a weight ratio of 99:1 to 0.5: 1 and wherein the composition is substantially free of added inorganic acid ammonium salt.
  • the resin binder composition of the invention may be a resin binder composition as detailed above, particularly in respect of the composite material, composite article and the process for preparing the composite article.
  • any resin binder composition of the invention may be incorporated into a composite material or a composite article and/or may be used in a process for preparing a composite material or composite article of the invention.
  • resin binder composition is intended to refer to compositions which may, for example be applied as a dry composition or as a solution (i.e., a viscous or semi-viscous composition) and, after appropriate treatment, such as the application of pressure and/or temperature, can act as a glue or varnish.
  • compositions that comprise at most 5 wt.% e.g., at most 4, 3, 2, 1 , 0.5, 0.1 or 0.01 wt.% of added inorganic acid ammonium salt.
  • the resin binder has no added inorganic acid ammonium salt.
  • added when used herein in relation to inorganic acid ammonium salt, refers to inorganic acid ammonium salts purposefully added to the resin binder composition and is not envisaged to refer to any such salts already present in negligible quantities in the sugar starting material.
  • the resin binder composition comprises sugar in an amount of greater than or equal to about 41 wt.%, 42 wt.%, 43 wt.%, 44 wt.% or 45 wt.%, such as from about 41 to about 80 wt.%, for example from about 41 to about 70 wt.%, preferably from about 41 to about 56 wt.%, more preferably from 41 about to about 48 wt.%.
  • the sugar and metal salt are present in the composition in a relative weight ratio of from 99: 1 to 34:66, for example from 98:2 to 50:50, preferably from 90: 10 to 60:40.
  • the sugar of the inventive composition may be derived from sugar syrup.
  • sugar syrup refers to inter alia, processing/intermediate, final and storage syrups resulting from the processing of sugar raw materials such as sugar cane, sugar beet, sugar maple and Palmyra palm; syrups produced by dissolving solid sugars such as glucose powders, raw cane sugar (including high polarisation (HP) and very high polarisation (VHP)), refined sugars or recovery sugars; lactose syrups from whey processing; high fructose syrups, glucose syrups, glucose raffinate associated with glucose and high fructose syrup production from corn, wheat or other high starch raw materials; starch hydrolysates, directly from pure starch or from waste starch streams including wheat, corn, cassava, potato and carbohydrate hydrolysates or inulin; co-product or by-product syrups with high sugar content that result from the above processes, for example molasses, obtained when sugar is purified from sugar cane or sugar beet.
  • sugar raw materials such as sugar cane, sugar beet, sugar maple and Palmy
  • the sugar syrup is selected from the group consisting of process and storage syrups associated with the production of sucrose (from sugar cane, sugar beet and Palmyra palm molasses), caramel, sugar solutions produced by dissolving solid sugars, and juices of sugar containing raw materials (sugarcane, sugar beet, sugar maple, and Palmyra palm).
  • the sugar syrup is selected from the group consisting of process and storage syrups associated with the production of sucrose (from sugar cane, sugar beet and Palmyra palm), molasses or a sugar solution produced by dissolving solid sugars.
  • the sugar syrup is process and storage syrups associated with the production of sucrose (from sugar cane, sugar beet) and sugar syrup produced by dissolving solid sugars.
  • the sugars of the composition are predominantly mono- and/or disaccharides, such as greater than about 90 wt.% (e.g., greater than 91 , 92, 93, 94, 95, 96, 97, 98 or 99 wt.%) of the sugars are mono- and/or disaccharides. More preferably about 100 wt.% of the sugars are mono- and/or disaccharides.
  • monosaccharides include glucose, psicose, fructose, sorbose, tagatose, allose, altrose, mannose, gulose, idose, galactose, talose, fucose, fuculose and rhamnose.
  • trioses such as ketotriose and aldotriose
  • tetroses such as erythrulose, erthrose and threose
  • pentoses such as ribulose, xylulose, ribose, arabinose, xylose, lixose and deoxyribose.
  • disaccharides examples include sucrose, lactose, maltose, trehalose, turanose and cellobiose.
  • greater than about 90 wt.% e.g., greater than 91 , 92, 93, 94, 95, 96, 97, 98 or 99 wt.% of the sugars are a mixture of sucrose, glucose and fructose.
  • the metal salt in the binder composition is selected from the group consisting of sodium chloride, sodium sulfate, sodium acetate, potassium chloride, potassium sulfate, potassium acetate, magnesium chloride, magnesium sulfate, magnesium acetate, calcium chloride, calcium sulfate and calcium acetate
  • the metal salt in the binder composition is sodium chloride.
  • the metal salt present in the resin binder composition is a halide or acetate of a group I or group II metal element.
  • the metal salt present in the resin binder composition is a halide of a group I or group II metal element.
  • the metal salt present in the resin binder composition may, for example, be selected from the group consisting of sodium chloride, sodium acetate, potassium chloride, potassium acetate, magnesium chloride, magnesium acetate, calcium chloride and calcium acetate, preferably the metal salt is sodium chloride.
  • the resin binder composition comprises the metal salt in an amount of from about 0.5 to about 50 wt.%, preferably from about 5 to about 30 wt.%, more preferably from about 6 to about 28 wt. %.
  • the resin binder composition is preferably prepared in the form of a water-based solution. It will be obvious to those skilled in the art that different amounts of water may be added to the resin binder composition at different points in the supply chain. For example, sufficient water will need to be added to the sugar and/or metal salt to enable the solids to be dissolved and blended. If the resin is to be transported from a site of production to a site of use, then it is advantageous to minimise the amount of water transported by producing a resin with the highest possible solids content.
  • the resin will need to be transferred from storage to the point of use and subsequently added to the wood material. During this transferring and application process it may be preferable to reduce the viscosity of the resin binder composition by the addition of further water. As any water in the resin binder composition will subsequently be removed in the production process of the composite material of the composite article, the absolute water content of the resin binder composition is not a direct indicator of the ratio of wood material : resin in the final product.
  • the resin binder composition comprises water.
  • the resin binder composition is principally comprised of sugar, the metal salt and, optionally, water. That is to say, the resin binder composition comprises sugar, the metal salt and, optionally, water in a combined amount of equal to, or greater than, about 80 wt.%, such as equal to, or greater than, about 85, 90, or 95 wt.%.
  • the resin binder composition does not comprise any further component in an amount that is equal to, or greater than, the individual amounts of sugar, salt and, where present, water in the composition. That is to say, preferably the resin binder composition does not comprise any other component, except for wood material when it is incorporated into a composite material or article as defined above, in an amount that is greater than any one of these three components.
  • the resin binder composition may comprise water in an amount of from about 20 to about 50 wt.%, such as from about 25 to about 45 wt.%, for example from about 20 to about 40 wt.%, most preferably from about 30 to about 40 wt.%.
  • the resin binder composition is substantially free of yeast and/or yeast extract. That is to say, the resin binder composition comprises at most 5 wt.% (e.g., at most 4, 3, 2, 1 , 0.5, 0.1 or 0.01 wt.%) of yeast and/or yeast extract. Put differently, this includes references to compositions that comprise less than 5 wt.% (e.g., less than 4, 3, 2, 1 , 0.5, 0.1 or 0.01 wt.%) of yeast and/or yeast extract.
  • the resin binder composition is substantially free of plastics, such as polypropylene. That is to say, the resin binder composition comprises at most 5 wt.% (e.g., at most 4, 3, 2, 1 , 0.5, 0.1 or 0.01 wt.%) of plastics, such as polypropylene. Put differently, this includes references to compositions that comprise less than 5 wt.% (e.g., less than 4, 3, 2, 1 , 0.5, 0.1 or 0.01 wt.%) of plastics, such as polypropylene.
  • the water added to the composition of the invention is not particularly limited and includes distilled water, deionised water, pure water, tap water and industrial water.
  • the water source could already contain dissolved salts, including sea water, ion exchange resin regeneration effluent or washing solutions.
  • the resin binder composition comprises the sugar in an amount greater than about 40 wt.%, the metal salt in an amount of from about 0.5 to about 50 wt.% and water in an amount of from about 20 to about 50 wt.%.
  • the resin binder composition comprises the sugar in an amount of from about 41 to about 70 wt.%, the metal salt in an amount of from about 5 to about 30 wt.% and water in an amount of from about 25 to about 45 wt.%.
  • the resin binder composition comprises the sugar in an amount of from about 41 about to about 56 wt.%, the metal salt in an amount of from about 6 to about 28 wt. % and water in an amount of from about 30 to about 40 wt.%.
  • the viscosity of the resin binder composition is from about 50 to about 500 cP, such as from about 100 to about 400 cP, for example from about 200 to about 300 cP.
  • the viscosity of the resin binder composition in the composite material may be less than, or equal to, 300 cP.
  • FIGURES Figure 1 shows the effect of soaking the fabricated wood composite boards, having varying amounts of sodium chloride in the binder, in water at ambient temperature.
  • Figure 2 is an image of a 12mm composite wood article produced using a resin binder composition according to the invention.
  • aqueous binder composition 250 g was sprayed onto 1000 g of wood fibre.
  • the composite material was subsequently flash-dried at a temperature between 80 °C and 100 °C for approximately 30 seconds until reaching a moisture content of 4 to 10 wt.%.
  • Thick Juice was heated to 50°C and diluted with water in a ratio of 1 :0.33; to this solution crystalline NaCI was added in the ratio of 29.1 g per 133.0 g of diluted Thick Juice to produce a resin binder that consists of 7:3 sugar solids: salts solids ratio and a sugar content of 42%. This mixture was then stirred until the salt had fully dissolved and cooled to room temperature.
  • Thick Juice (British Sugar product number 72017) is an aqueous solution of sugars, salts and other beet sugar origin compounds. It is an intermediate product in the production of beet sugar and typically contains between 65% to 70% dissolved solids, of which typically 93%-96% will be sucrose.
  • the composite material was subsequently flash-dried at a temperature between 80 °C and 100 °C for approximately 30 seconds until reaching a moisture content of 4 to 10 wt.%.
  • the flash-dried composite material was evenly distributed within a press bed and the material was pre-pressed at ambient temperature to remove air pockets from the material and to ensure proper packing of the material.
  • the resulting fibre mat was then transferred to a hot-press and compressed to a thickness of 12 mm at 210 °C for 3 minutes.
  • the composite wood board was then removed and allowed to cool.
  • Thick Juice (British Sugar product number 72017) was heated to 50 °C and diluted with water in a ratio of 1 :0.28; to this solution NaCI was added in the ratio of 17.0 g per 128.0 g of diluted thick juice to produce a resin binder that consists of 8:2 sugar solids: salts solids ratio and a sugar content of 53%. This mixture was then stirred until the salt had fully dissolved and cooled to room temperature.
  • the composite material was subsequently flash-dried at a temperature between 80 °C and 100 °C for approximately 30 seconds until reaching a moisture content of 4 to 10 wt.%.
  • the flash-dried composite material was evenly distributed within a press bed and the material was pre-pressed at ambient temperature to remove air pockets from the material and to ensure proper packing of the material.
  • the resulting fibre mat was then transferred to a hot- press and compressed to a thickness of 12 mm at 210 °C for 3 minutes.
  • the composite wood board was then removed and allowed to cool.
  • Figure 1 also shows the effect of soaking the boards in water at ambient temperature for 30 minutes. It can be seen that in the absence of salt the boards swell significantly and delaminate, whereas the addition of salt, even at an amount of 1 wt.%, significantly decreases the swelling of the boards and decreases the level of delamination.
  • binder compositions have been found to be less expensive to produce, they maintain (or improve) the mechanical properties of fibreboards using such binder compositions and they do not require the inclusion of carcinogenic or environmentally unfriendly compounds.
  • a composite wood board having a thickness of 12 mm was prepared using a resin binder composition having a dry weight ratio of sugar solids to metal salt solids of 7 : 3, wherein the wood fibre solids to resin solids ratio is 90 : 10.
  • the image of this board in Figure 2 shows that a uniform board was prepared using this resin binder composition.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Manufacturing & Machinery (AREA)
  • Forests & Forestry (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Dry Formation Of Fiberboard And The Like (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne un matériau composite comprenant un matériau ligneux comprenant des fibres de cellulose et une composition de liant de résine comprenant (i) un sucre et (ii) un sel métallique qui est un halogénure, un acétate ou un sel de sulfate d'un élément métallique du groupe I ou II. Le sucre et le sel métallique sont présents dans le matériau composite en une proportion combinée d'environ 2 à environ 25 % en poids et la composition est sensiblement exempte de sel d'ammonium d'acide inorganique ajouté. La présente invention concerne également le liant de résine utilisé pour préparer le matériau composite, des utilisations de tels matériaux composites, des articles comprenant de tels matériaux composites et des procédés de préparation d'articles faisant appel à ces matériaux composites.
PCT/GB2019/050384 2018-02-14 2019-02-13 Matériau composite WO2019158917A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB1802423.2A GB201802423D0 (en) 2018-02-14 2018-02-14 Composite material
GB1802423.2 2018-02-14

Publications (1)

Publication Number Publication Date
WO2019158917A1 true WO2019158917A1 (fr) 2019-08-22

Family

ID=61731423

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2019/050384 WO2019158917A1 (fr) 2018-02-14 2019-02-13 Matériau composite

Country Status (2)

Country Link
GB (1) GB201802423D0 (fr)
WO (1) WO2019158917A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4144707A1 (fr) 2021-09-07 2023-03-08 Biolac GmbH & Co. KG Mélange destiné à la fabrication d'un corps moulé avec un liant amélioré

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015056367A1 (fr) * 2013-10-15 2015-04-23 パナソニックIpマネジメント株式会社 Composition liante et panneau
WO2017104134A1 (fr) * 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa Composition de collage aqueuse
WO2017169321A1 (fr) * 2016-03-28 2017-10-05 Henkel Ag & Co. Kgaa Composition de collage aqueuse

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015056367A1 (fr) * 2013-10-15 2015-04-23 パナソニックIpマネジメント株式会社 Composition liante et panneau
WO2017104134A1 (fr) * 2015-12-18 2017-06-22 Henkel Ag & Co. Kgaa Composition de collage aqueuse
WO2017169321A1 (fr) * 2016-03-28 2017-10-05 Henkel Ag & Co. Kgaa Composition de collage aqueuse

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP4144707A1 (fr) 2021-09-07 2023-03-08 Biolac GmbH & Co. KG Mélange destiné à la fabrication d'un corps moulé avec un liant amélioré

Also Published As

Publication number Publication date
GB201802423D0 (en) 2018-03-28

Similar Documents

Publication Publication Date Title
JP5879521B2 (ja) 接着用組成物
JP5472639B2 (ja) 加熱・加圧により硬化する組成物
US8323449B2 (en) Compositions and methods for resin-based wood glues
WO2015072437A1 (fr) Composition adhésive pour matériaux à base de bois
EP2032656B1 (fr) Système adhésif et procédé de fabrication d'un produit à base de bois
WO2013018707A1 (fr) Composition contenant un tannin condensé qui est durcie par application de chaleur et de pression
JP2022031549A (ja) ホルムアルデヒドを含まない木材バインダー
CN110366588B (zh) 用于热压成型的粘合剂、木质板及其制造方法
JP2015160366A (ja) 繊維板およびその製造方法
WO2019158917A1 (fr) Matériau composite
WO2020080046A1 (fr) Procédé de production de matériau moulé à base de biomasse, matériau moulé à base de biomasse, et procédé de production d'un article moulé à base de biomasse
JP2017140778A (ja) ボードの製造方法
JP7237076B2 (ja) セルロース含有材料のためのバインダー
JP2016006195A (ja) 接着用組成物
JP2016222843A (ja) 熱硬化性接着剤及びそれを用いた成形板
RU2803520C2 (ru) Связующее вещество для содержащих целлюлозу материалов
JP2014101489A (ja) 接着用組成物及び成形板

Legal Events

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

Ref document number: 19708881

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 19708881

Country of ref document: EP

Kind code of ref document: A1