WO1999043476A1 - Wood composite products - Google Patents

Wood composite products Download PDF

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Publication number
WO1999043476A1
WO1999043476A1 PCT/CA1999/000088 CA9900088W WO9943476A1 WO 1999043476 A1 WO1999043476 A1 WO 1999043476A1 CA 9900088 W CA9900088 W CA 9900088W WO 9943476 A1 WO9943476 A1 WO 9943476A1
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WO
WIPO (PCT)
Prior art keywords
zinc borate
producing
dispersion
wax
composite wood
Prior art date
Application number
PCT/CA1999/000088
Other languages
French (fr)
Inventor
David Fookes
Marek Jan Gnatowwski
Robert Leeson Pike
Derek Alexander Templeton
Original Assignee
Trus Joist Macmillan, A Limited Partnership
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 Trus Joist Macmillan, A Limited Partnership filed Critical Trus Joist Macmillan, A Limited Partnership
Priority to JP2000533260A priority Critical patent/JP2002504443A/en
Priority to NZ506281A priority patent/NZ506281A/en
Priority to AU24055/99A priority patent/AU741151B2/en
Priority to EP99903555A priority patent/EP1058607B1/en
Priority to CA002320297A priority patent/CA2320297C/en
Priority to DE69932322T priority patent/DE69932322T2/en
Publication of WO1999043476A1 publication Critical patent/WO1999043476A1/en

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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
    • B27N1/00Pretreatment of moulding material
    • 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

  • the present invention relates to consolidated composite wood products, more particularly, the present invention relates to a method of producing a consolidated wood product incorporating a biological degradation protection additive.
  • Composite wood products are generally formed from wood strands or the like bonded together by a suitable resin such as phenol formaldehyde (PF) or isocynate resins (MDI).
  • PF phenol formaldehyde
  • MDI isocynate resins
  • the strands may be random or parallel oriented relative to one another and in some cases, the composite product is made from layers with different orientation or strands in adjacent layers.
  • the present invention relates to a method of producing a composite wood product comprising forming a sprayable aqueous dispersion of zinc borate particles having a zinc borate content in the range of 20-75% by weight, applying said dispersion on surfaces of wood strands in the amount of between 5 and 25 grams of zinc borate per kg. of wood strands, also applying binder to said wood strands, forming a lay-up of said wood strands with said dispersion of zinc borate applied and said binder applied and then consolidating said lay-up of said wood strands under heat and pressure to form said composite product.
  • said zinc borate is present in said dispersion in the amount of between 30-70% by weight of said dispersion.
  • said dispersion is a wax, zinc borate dispersion containing wax and zinc borate in weight ratios of 1/1 to 1/2.
  • said zinc borate dispersion is mixed with a wax suspension to form said zinc borate dispersion containing wax dispersion.
  • said wax will be present in an amount of 5 parts wax solids to 5 to 10 parts zinc borate.
  • said wax comprises a slack wax.
  • said zinc particles have median particle sizes of 2 to 12 ⁇ m.
  • said zinc borate dispersion will contain an effective amount of thickener, defoamer disperser and surfactant.
  • said thickener will be present in the amount of less than 2% by weight.
  • said thickener will be present in the amount of less than 0.5% by weight.
  • said defoamer will be present in the amount of between 0.5 to 0.1 % by weight.
  • said disperser will be present in the amount of less than 5% by weight.
  • said disperser will be present in the amount of less than 1% by weight.
  • said surfactant will be present in the amount of less than 2% by weight. Preferably, said surfactant will be present in the amount of less than 0.5% by weight.
  • FIG. 1 is a flow diagram of the process of the present invention. Description of the Preferred Embodiments
  • wood strands which may be in the form of wafers, strips of wood, particles of wood, etc. as normally used in the manufacture of wood composites, such as strand board, wafer board, oriented strand board, medium density fiber board, or products such as those sold under the trademarks TimberStrand ® and
  • Parallam ® by Trus Joist MacMillan are delivered to the system as indicated at 10. These strands are then fed in the case of conventional strand or wafer board production to a blending operation indicated at 12 wherein the required amount of binder is applied to the strands and when practising the present invention the strands are coated with the desired amount of a dispersion containing zinc borate (such as those sold under the tradenames Firebrake, Borgard ZB or Composibor sold by US Borax). Sufficient zinc borate is applied to the strands to provide the desired degree of protection to the resultant composite product. The so coated strands are then formed into a mat as indicated at 14 and the mat is consolidated to form the composite wood product as indicated at 16.
  • a dispersion containing zinc borate such as those sold under the tradenames Firebrake, Borgard ZB or Composibor sold by US Borax.
  • a wax emulsion is also applied to the strands.
  • the wax preferably forms a significant part of the zinc borate dispersion as will be discussed below.
  • the emulsion is applied first particularly with
  • MDI type resins to limit the contact of the resin by water. Any suitable binder may be applied in 12.
  • the binders used to produce composite wood products and bind the strands or the like together are phenol formaldehyde (PF) type binders and isocynate (MDI) type resin binders and may also be useful with melamine and urea formaldehyde users.
  • PF phenol formaldehyde
  • MDI isocynate
  • the amounts of such binders applied need not be changed significantly relative to the amounts conventionally used when they are used in combination with the present invention wherein a zinc borate emulsion is also applied to the strands.
  • the process for making the composite wood product when practicing the present invention is essentially the same in all steps except in place of a powdered zinc borate being applied directly to the wood strands, Applicant forms a sprayable aqueous emulsion of the zinc borate and applies the zinc borate emulsion to the strands prior to consolidation preferable at the same time as the resin component of the composite is applied.
  • Wax is generally added as a separate step or with a binder.
  • the wax may be made part of the zinc borate emulsion and applied to the strands simultaneously with the zinc borate i.e. in the same emulsion.
  • the preferred embodiment incorporates wax in the zinc borate dispersion.
  • the zinc borate emulsion be reasonably stable over time at least until applied to the strands (with a reasonable margin of safety) particularly if the process requires premixing or premaking of the aqueous zinc emulsion well before its application in step 12.
  • the zinc borate emulsions of the present invention include water, thickeners, defoamers or anti-foaming agents, dispersers and surfactants.
  • the zinc borate dispersion are applied to provide between about 5 and 25 grams of zinc borate for each kilogram of wood.
  • thickeners such as suitable cellulose derivatives, water-swellable acrylics, clays, amorphous silica are used as thickeners in the zinc borate emulsion used with the present invention.
  • the cellulose type of thickeners such as hydroxy ethyl cellulose such as that sold by Union Carbide under the trademark CellosizeTM or under the trademark NatrosolTM by Aqualon are preferred.
  • these thickeners are present in the emulsions in the amounts of up to 2%. based on the weight of the emulsion and preferably less than 0.5% with the amount normally used being about 0.25% based on the weight of the emulsion.
  • Defoamers or anti-foaming agents are generally present in the range of up to about 1%) of the weight of suspension. Preferably, not less than 0.1%> with the normal usage being approximately 0.25% based on the weight of the dispersion.
  • Suitable anti- foaming agents used in the present invention include, antifoam HL-52 (Harcros Chemicals), BYK031 (BYK Chemie), Foamaster VL (Henkel), Dehydran 1293 (Henkel) and Nopko NXZ (Henkel).
  • Some polycarboxylic acid salts form dispersers suitable for use with the present invention. Generally, the disperser will be present in amounts up to 5%, preferably less than 1% and will normally be applied in a typical formulation at about 0.5% of the weight of the suspension.
  • Suitable commercially available dispersers compatible with other materials in the dispersion include Tamol 681 and Tamol 850, both available from Rohm & Haas.
  • Surfactant or wetting agents suitable for use with the present invention include suitable water soluble ethoxylated fluorol compounds (e.g. zonyl FSM by Dupont Inc.), ethoxylated alkyl phenols and alkylaryl polyethers.
  • the preferred surfactant or wetting agent found todate is a monylphenol ethoxylate sold under the tradename Igepal CO 630 by Stepan.
  • wetting agents are generally present in the amounts of up to 2%, preferably less than 0.5% with a typical suspension generally containing about 0.25% by weight of surfactant.
  • Suitable commercially available wetting agents include Igepal Co630 (Stepan), Polytergent B-300 (Harcros Chemical) and Triton X-100 (Union Carbide).
  • wax may be used as a significant element in the zinc borate dispersion.
  • wax is applied to the strands during the manufacture of composite wood products.
  • Suitable wax emulsion include Casco wax EW101 (Borden). When used, the wax will generally be present on a weight ratio of wax to zinc borate of about 1/1 to about 1/2.
  • the wax precipitates and encapsulates the zinc borate particles and helps to bind the zinc borate particles to the wood strands. It has been found that the combination of a zinc borate dispersion with a wax emulsion in the proper amounts, produces a surprisingly stable form of zinc borate dispersion.
  • a zinc borate dispersion which preferably contain wax emulsion
  • one first forms a zinc borate dispersion by mixing under high shear the water, thickener, disperser and deformer and then add further water followed by slow addition of zinc borate as indicated at 9 in Figure 1.
  • about half of the water is initially used in premixing and the other half is added at the time the zinc borate is added.
  • Zinc borate is added slowly to reduce the tendency of lumping and thickening.
  • a surfactant is added after the zinc borate dispersion has been made. It is very much preferred to use the zinc borate dispersion in combination with a wax emulsion.
  • the zinc borate and wax emulsion are mixed to generate the final zinc borate-wax dispersion as indicated at 9 for application to the strands as indicated at 12.
  • the dispersion and emulsion should be mixed slowly and gently to prevent breaking of the wax emulsion.
  • the amount of wax emulsion or wax solids basis in the final zinc borate dispersion should be sufficient to stabilize the zinc borate dispersion. This generally requires a significant amount of wax in the order of at least about 50% wax solids based on the zinc borate solids in the dispersion.
  • the total amount of wax suspension mixed with the zinc borate dispersion will vary depending on the composition of the actual wax being used. It has been found that a ratio 1 to 2 parts by weight of solid wax to 7 to 10 parts by weight of zinc borax was effective to significantly increase shelf life over the resultant zinc borax dispersion.
  • the pH of zinc borate or zinc borate- wax dispersion will not exceed a pH of 8.5.
  • a typical dispersion formulation containing wax is given in Table I.
  • Anti-foaming Agent (Antifoam HL-52) 0.025
  • zinc borate will have a fine particle size, i.e. a median particle size in the range of about 2 to 12 ⁇ m.
  • the maximum size of the particles is chosen to ensure that a significant number of the particles do not precipitate out of the emulsion and the minimum size is chosen to ensure that the viscosity of the emulsion is not unduly increased.
  • a borax having a median size of about 8 ⁇ m.
  • concentration of the zinc borate in the dispersion be sufficiently high so that too much water is not added to the composite product as excess water will interfere with the development of proper bonding during consolidation.
  • the zinc borate dispersion is preferably stable over time and it does not separate or thicken before application to the wood strands and should be capable of being sprayed, for example, using disk dispersing equipment conventionally used in the industry for application of resin and which has been found to effectively and with sufficient uniformity distribute the suspension over the strands.
  • the zinc borate suspension dispersion is suitable for application by such equipment but it generally is also suitable or may be made suitable for application by other equipment particularly spraying equipment, for example, airless sprayers).
  • dispersions of the present invention is of particular advantage in system wherein the blending stages are operated under negative pressure to prevent loss of materials.

Abstract

The resistance to biological degradation of composite wood products is improved by applying a suitable aqueous dispersion of zinc borate onto the fibers to uniformly distribute and to adhere the zinc borate to the strands of the wood composite, applying a suitable adhesive to the wood strands, forming a strand lay-up and consolidating a lay-up under heat and pressure to form a consolidated product with zinc borate uniformly distributed therethrough.

Description

PATENT APPLICATION wood composi te products
Field of Invention The present invention relates to consolidated composite wood products, more particularly, the present invention relates to a method of producing a consolidated wood product incorporating a biological degradation protection additive. Background of the Invention
Composite wood products are generally formed from wood strands or the like bonded together by a suitable resin such as phenol formaldehyde (PF) or isocynate resins (MDI). The strands may be random or parallel oriented relative to one another and in some cases, the composite product is made from layers with different orientation or strands in adjacent layers.
These composite products find a variety of different usages, many of which are enhanced by providing the product with improved biodurability.
It has been shown in U.S. patent 4,879,083 issued November 7, 1989 to Knudson et al. to apply anhydrous borax or zinc borate to the wood strand and bond the strands together into a composite product resistant to decay by insects and/or organisms using phenol formaldehyde as the binding agent. This teaching overcame a particular problem of the use of borax with phenol formaldehyde wherein the borax impeded the binding characteristics of the phenol formaldehyde.
It is also now known to add zinc borate to wood composites in conventional blending operations in processes using resins such as phenol formaldehyde as taught by Knudson et al. or other resins including isocynate resins for binding the strands for form the composite product resistant to biological degradation. Such addition of zinc borate in powdered form has been found to be difficult implement on a commercial scale as the powdered zinc borate and causes dusting and other problems regardless of the adhesive resin being used. For example, zinc borate sometimes absorbs liquid when MDI resin are used thereby reducing the internal bond of the product. Generally, the poor adhesion of the produced zinc borate causes waste and increase dust problem throughout the mill. Brief Description of the Present Invention
It is an object of the present invention to provide an improved system for applying zinc borate as a composite wood product.
Broadly, the present invention relates to a method of producing a composite wood product comprising forming a sprayable aqueous dispersion of zinc borate particles having a zinc borate content in the range of 20-75% by weight, applying said dispersion on surfaces of wood strands in the amount of between 5 and 25 grams of zinc borate per kg. of wood strands, also applying binder to said wood strands, forming a lay-up of said wood strands with said dispersion of zinc borate applied and said binder applied and then consolidating said lay-up of said wood strands under heat and pressure to form said composite product.
Preferably, said zinc borate is present in said dispersion in the amount of between 30-70% by weight of said dispersion.
Preferably, said dispersion is a wax, zinc borate dispersion containing wax and zinc borate in weight ratios of 1/1 to 1/2.
Preferably, said zinc borate dispersion is mixed with a wax suspension to form said zinc borate dispersion containing wax dispersion.
Preferably, said wax will be present in an amount of 5 parts wax solids to 5 to 10 parts zinc borate. Preferably, said wax comprises a slack wax.
Preferably, said zinc particles have median particle sizes of 2 to 12 μm.
Preferably, said zinc borate dispersion will contain an effective amount of thickener, defoamer disperser and surfactant.
Preferably, said thickener will be present in the amount of less than 2% by weight.
Preferably, said thickener will be present in the amount of less than 0.5% by weight.
Preferably, said defoamer will be present in the amount of between 0.5 to 0.1 % by weight. Preferably, said disperser will be present in the amount of less than 5% by weight. Preferably, said disperser will be present in the amount of less than 1% by weight.
Preferably, said surfactant will be present in the amount of less than 2% by weight. Preferably, said surfactant will be present in the amount of less than 0.5% by weight. Brief Description of the Drawings
Further features, objects and advantages will be evident from the following detailed description of the preferred embodiments of the present invention taken in conjunction with the accompanying drawings in which;
Figure 1 is a flow diagram of the process of the present invention. Description of the Preferred Embodiments
As shown in Figure 1, wood strands which may be in the form of wafers, strips of wood, particles of wood, etc. as normally used in the manufacture of wood composites, such as strand board, wafer board, oriented strand board, medium density fiber board, or products such as those sold under the trademarks TimberStrand® and
Parallam® by Trus Joist MacMillan are delivered to the system as indicated at 10. These strands are then fed in the case of conventional strand or wafer board production to a blending operation indicated at 12 wherein the required amount of binder is applied to the strands and when practising the present invention the strands are coated with the desired amount of a dispersion containing zinc borate (such as those sold under the tradenames Firebrake, Borgard ZB or Composibor sold by US Borax). Sufficient zinc borate is applied to the strands to provide the desired degree of protection to the resultant composite product. The so coated strands are then formed into a mat as indicated at 14 and the mat is consolidated to form the composite wood product as indicated at 16.
In most conventional operations, a wax emulsion is also applied to the strands. With the present invention, the wax preferably forms a significant part of the zinc borate dispersion as will be discussed below. In the blending operation, generally, the emulsion is applied first particularly with
MDI type resins to limit the contact of the resin by water. Any suitable binder may be applied in 12. Generally, the binders used to produce composite wood products and bind the strands or the like together are phenol formaldehyde (PF) type binders and isocynate (MDI) type resin binders and may also be useful with melamine and urea formaldehyde users. The amounts of such binders applied need not be changed significantly relative to the amounts conventionally used when they are used in combination with the present invention wherein a zinc borate emulsion is also applied to the strands. Thus, the process for making the composite wood product when practicing the present invention is essentially the same in all steps except in place of a powdered zinc borate being applied directly to the wood strands, Applicant forms a sprayable aqueous emulsion of the zinc borate and applies the zinc borate emulsion to the strands prior to consolidation preferable at the same time as the resin component of the composite is applied.
It is also common practice in manufacture of composite wood products to incorporate wax (generally a slack wax) in the product to improve water resistance. Wax is generally added as a separate step or with a binder.
It has been found that the wax may be made part of the zinc borate emulsion and applied to the strands simultaneously with the zinc borate i.e. in the same emulsion. The preferred embodiment incorporates wax in the zinc borate dispersion.
It is important that the zinc borate emulsion be reasonably stable over time at least until applied to the strands (with a reasonable margin of safety) particularly if the process requires premixing or premaking of the aqueous zinc emulsion well before its application in step 12.
The zinc borate emulsions of the present invention include water, thickeners, defoamers or anti-foaming agents, dispersers and surfactants. The zinc borate dispersion are applied to provide between about 5 and 25 grams of zinc borate for each kilogram of wood.
Generally, thickeners such as suitable cellulose derivatives, water-swellable acrylics, clays, amorphous silica are used as thickeners in the zinc borate emulsion used with the present invention. The cellulose type of thickeners such as hydroxy ethyl cellulose such as that sold by Union Carbide under the trademark Cellosize™ or under the trademark Natrosol™ by Aqualon are preferred. Generally, these thickeners are present in the emulsions in the amounts of up to 2%. based on the weight of the emulsion and preferably less than 0.5% with the amount normally used being about 0.25% based on the weight of the emulsion.
Defoamers or anti-foaming agents are generally present in the range of up to about 1%) of the weight of suspension. Preferably, not less than 0.1%> with the normal usage being approximately 0.25% based on the weight of the dispersion. Suitable anti- foaming agents used in the present invention include, antifoam HL-52 (Harcros Chemicals), BYK031 (BYK Chemie), Foamaster VL (Henkel), Dehydran 1293 (Henkel) and Nopko NXZ (Henkel). Some polycarboxylic acid salts form dispersers suitable for use with the present invention. Generally, the disperser will be present in amounts up to 5%, preferably less than 1% and will normally be applied in a typical formulation at about 0.5% of the weight of the suspension.
Suitable commercially available dispersers compatible with other materials in the dispersion include Tamol 681 and Tamol 850, both available from Rohm & Haas.
Surfactant or wetting agents suitable for use with the present invention include suitable water soluble ethoxylated fluorol compounds (e.g. zonyl FSM by Dupont Inc.), ethoxylated alkyl phenols and alkylaryl polyethers. The preferred surfactant or wetting agent found todate is a monylphenol ethoxylate sold under the tradename Igepal CO 630 by Stepan.
These wetting agents are generally present in the amounts of up to 2%, preferably less than 0.5% with a typical suspension generally containing about 0.25% by weight of surfactant.
Suitable commercially available wetting agents include Igepal Co630 (Stepan), Polytergent B-300 (Harcros Chemical) and Triton X-100 (Union Carbide).
Applicant has also found that wax may be used as a significant element in the zinc borate dispersion. In most commercial operations wax is applied to the strands during the manufacture of composite wood products. It is a distinct advantage to incorporate the wax into the zinc borate suspension or emulsion as both wax and the zinc borate may be combined into a single stable dispersion, thus be applied in a single step. Suitable wax emulsion include Casco wax EW101 (Borden). When used, the wax will generally be present on a weight ratio of wax to zinc borate of about 1/1 to about 1/2.
As above indicated, producing wax emulsions and applying them into the strands is well known. However, the making of a high concentration dispersion containing borate was found to be more difficult. When zinc borate is dispersed in pure water, it has a strong tendency to separate (sedimentation) if its concentration is too low - below approximately 65%. A dispersion with a high concentration of zinc borate (above about 75%) increases in viscosity significantly during storage thereby leading to rendering of the dispersion unusable for practical application. When the two (wax dispersion and zinc borate dispersion) are used separately, the wax dries to form a wax film while the zinc borate returns to powder form. By combining the two into a zinc borate/wax dispersion, the wax precipitates and encapsulates the zinc borate particles and helps to bind the zinc borate particles to the wood strands. It has been found that the combination of a zinc borate dispersion with a wax emulsion in the proper amounts, produces a surprisingly stable form of zinc borate dispersion.
To produce a zinc borate dispersion which preferably contain wax emulsion one first forms a zinc borate dispersion by mixing under high shear the water, thickener, disperser and deformer and then add further water followed by slow addition of zinc borate as indicated at 9 in Figure 1. Generally, about half of the water is initially used in premixing and the other half is added at the time the zinc borate is added. Zinc borate is added slowly to reduce the tendency of lumping and thickening. Preferably, a surfactant is added after the zinc borate dispersion has been made. It is very much preferred to use the zinc borate dispersion in combination with a wax emulsion. Thus, the zinc borate and wax emulsion are mixed to generate the final zinc borate-wax dispersion as indicated at 9 for application to the strands as indicated at 12. The dispersion and emulsion should be mixed slowly and gently to prevent breaking of the wax emulsion. Generally, the amount of wax emulsion or wax solids basis in the final zinc borate dispersion should be sufficient to stabilize the zinc borate dispersion. This generally requires a significant amount of wax in the order of at least about 50% wax solids based on the zinc borate solids in the dispersion. Obviously, the total amount of wax suspension mixed with the zinc borate dispersion will vary depending on the composition of the actual wax being used. It has been found that a ratio 1 to 2 parts by weight of solid wax to 7 to 10 parts by weight of zinc borax was effective to significantly increase shelf life over the resultant zinc borax dispersion.
Generally, the pH of zinc borate or zinc borate- wax dispersion will not exceed a pH of 8.5. A typical dispersion formulation containing wax is given in Table I.
Table I
Description %
Water 16.57
Thickener (Natrasol 250 HBR) 0.25
Disperser (Tamol 681) 0.5
Anti-foaming Agent (Antifoam HL-52) 0.025
Water 12.43
Zinc Borate (Firebrake) 49.72
Wetting Agent (Polytergent B-300) 0.25
Water 4.14
Figure imgf000009_0001
Wax (Casowax EW 403HS) 16.11
To produce the emulsion, zinc borate will have a fine particle size, i.e. a median particle size in the range of about 2 to 12 μm.
The maximum size of the particles is chosen to ensure that a significant number of the particles do not precipitate out of the emulsion and the minimum size is chosen to ensure that the viscosity of the emulsion is not unduly increased. Thus, it is preferred to use a borax having a median size of about 8 μm.
It is important that the concentration of the zinc borate in the dispersion be sufficiently high so that too much water is not added to the composite product as excess water will interfere with the development of proper bonding during consolidation.
The zinc borate dispersion, as above indicated, is preferably stable over time and it does not separate or thicken before application to the wood strands and should be capable of being sprayed, for example, using disk dispersing equipment conventionally used in the industry for application of resin and which has been found to effectively and with sufficient uniformity distribute the suspension over the strands. The zinc borate suspension dispersion is suitable for application by such equipment but it generally is also suitable or may be made suitable for application by other equipment particularly spraying equipment, for example, airless sprayers).
The following summarizes the weight percent for the various components of the dispersion.
Table π
Weight Percent t (100% Basis)
Broad Preferred
Water 5-80 15-45
Hydroxy ethyl Cellulose 0-2 0-0.5
Defoaming Agent 0-1.0 0-0.1
Dispersing Agent 0-5 0-1
Surfactant 0-2 0-0.5
Wax Emulsion 0-75 50 (50% solids)
Zinc Borate 20-75 30-70
Figure imgf000010_0001
100 100
The use of dispersions of the present invention is of particular advantage in system wherein the blending stages are operated under negative pressure to prevent loss of materials.
The use of the dispersion of the present invention with MDI type resins wherein the blender is under negative pressure has been found to be particularly effective over operations applying the zinc borate in powder form as it permits reduction of both zinc borate and resin use. It has been found that reductions as high as about 20% may be obtained with the same retention in the final product as when powdered zinc borate is used.
Having described the invention, modifications will be evident to those skilled in the art without departing from the scope of the invention as defined in the appended claims.

Claims

CLAIMSWe claim:
1. A method of producing a composite wood product comprising forming a sprayable aqueous dispersion of zinc borate particles having a zinc borate content in the range of 20-15% by weight, applying said dispersion on surfaces of wood strands in the amount of between 5 and 25 grams of zinc borate per kg. of wood strands, also applying binder to said wood strands, forming a lay-up of said wood strands with said dispersion of zinc borate and said binder applied and then consolidating said lay-up of said wood strands under heat and pressure to form said composite product.
2. A method of producing a composite wood product as defined in claim 1 wherein said zinc borate is present in said dispersion in the amount of between 30-70% by weight of said dispersion.
3. A method of producing a composite wood product as defined in claim 1 wherein said dispersion further includes wax in an amount to provide a wax to zinc borate weight ratio in said dispersion of between 1/1 and 1/2.
4. A method of producing a composite wood product as defined in claim 3 wherein said wax comprises a slack wax.
5. A method of producing a composite wood product as defined in claim 1 wherein said zinc particles have a median particle size in the range of 2 to 12 ╬╝m.
6. A method of producing a composite wood product as defined in claim 2 wherein said dispersion further includes wax.
7. A method of producing a composite wood product as defined in claim 6 wherein said wax comprises a slack wax, to provide a wax to zinc borate weight ratio in said dispersion of between 1/1 and 1/2.
8. A method of producing a composite wood product as defined in claim 2, 3 or 4 wherein said zinc particles have a median particle size in the range of 2 to 12 ╬╝m.
9. A method of producing a composite wood product as defined in claim 6 or 7 wherein said zinc particles have a median particle size in the range of 2 to 12 ╬╝m.
10. A method of producing a composite wood product as defined in claim 1 wherein said zinc borate suspension contains an effective amount of thickener, defoamer disperser and surfactant
11. A method of producing a composite wood product as defined in claim 10 wherein said thickener is present in the amount of less than 2% by weight.
12. A method of producing a composite wood product as defined in claim 11 wherein said thickener will be present in the amount of less than 1% by weight.
13. A method of producing a composite wood product as defined in claim 10, 11 or 12 wherein said defoamer will be present in the amount of between 1 to 0.1. by weight.
14. A method of producing a composite wood product as defined in claim 12 wherein said defoamer will be present in the amount of between 1 to 0.1. by weight.
15. A method of producing a composite wood product as defined in claim 10 wherein said disperser is present in the amount of less than 5% by weight.
16. A method of producing a composite wood product as defined in claim 10, 11, 12 or 15 wherein said disperser is present in the amount of less than 1% by weight.
17. A method of producing a composite wood product as defined in claim 10, 11, 12 or 15 wherein said surfactant is present in the amount of less than 2% by weight.
PCT/CA1999/000088 1998-02-26 1999-02-02 Wood composite products WO1999043476A1 (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
JP2000533260A JP2002504443A (en) 1998-02-26 1999-02-02 Wood composite products
NZ506281A NZ506281A (en) 1998-02-26 1999-02-02 Application of an aqueous dispersion of zinc borate in the preservation of wood composite products
AU24055/99A AU741151B2 (en) 1998-02-26 1999-02-02 Composite products
EP99903555A EP1058607B1 (en) 1998-02-26 1999-02-02 Wood composite products
CA002320297A CA2320297C (en) 1998-02-26 1999-02-02 Composite products
DE69932322T DE69932322T2 (en) 1998-02-26 1999-02-02 WOOD COMPOSITE MATERIALS

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/030,920 US5972266A (en) 1998-02-26 1998-02-26 Composite products
US09/030,920 1998-02-26

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357794A2 (en) * 2001-01-05 2003-11-05 Kop-Coat, Inc. Synergistici combination of fungicides to protect wood and wood-based products from fungal decay, mold and mildew damage
US7160606B2 (en) 2001-09-17 2007-01-09 Genics Inc. Method of treating building materials with boron and building materials
US7223415B1 (en) 2002-10-07 2007-05-29 Nisus Corporation Weather resistant granular bait with synergistic broad spectrum attractant system
US8597419B2 (en) 2007-01-17 2013-12-03 Genics Inc. Preservative compositions for wood and like materials

Families Citing this family (50)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19718771A1 (en) * 1997-05-03 1998-11-05 Dieffenbacher Gmbh Maschf Procedure for manufacture of derived timber product board, such as chip board and fibre board
US7585847B2 (en) * 2000-02-03 2009-09-08 Coley Pharmaceutical Group, Inc. Immunostimulatory nucleic acids for the treatment of asthma and allergy
US7163974B2 (en) * 2000-05-14 2007-01-16 U.S. Borax Inc. Lignocellulosic composites
US20010037035A1 (en) * 2000-05-24 2001-11-01 Kevin Kutcel Method for preparing polyborate compounds and uses for same
US7449130B2 (en) * 2000-07-17 2008-11-11 U.S. Borax Inc. Mixed solubility borate preservative
US20020182431A1 (en) * 2001-04-23 2002-12-05 Hatton Howard Wayne Calcium borate treated wood composite
US20030221775A1 (en) * 2002-05-31 2003-12-04 Martin Feng Method for producing wood composite products with phenolic resins and borate-treated wood materials
US7883651B1 (en) 2002-11-18 2011-02-08 Lords Additives LLC Lignoellulosic, borate filled, thermoplastic composites
US7056919B2 (en) * 2003-01-24 2006-06-06 Kopcoat, Inc. Synergistic combination of fungicides to protect wood and wood-based products and wood treated by such combination as well as methods of making the same
AU2004215420B2 (en) 2003-02-24 2010-04-08 Jeld-Wen, Inc Thin-layer lignocellulose composites having increased resistance to moisture and methods of making the same
US20060257578A1 (en) * 2003-04-09 2006-11-16 Jun Zhang Micronized wood preservative formulations comprising boron compounds
US20050249812A1 (en) * 2004-04-27 2005-11-10 Leach Robert M Micronized organic preservative formulations
US8637089B2 (en) 2003-04-09 2014-01-28 Osmose, Inc. Micronized wood preservative formulations
US8747908B2 (en) * 2003-04-09 2014-06-10 Osmose, Inc. Micronized wood preservative formulations
EP2345329B1 (en) 2003-04-09 2019-09-18 Koppers Performance Chemicals Inc. Micronized wood preservative formulations
US7943070B1 (en) 2003-05-05 2011-05-17 Jeld-Wen, Inc. Molded thin-layer lignocellulose composites having reduced thickness and methods of making same
JP4971790B2 (en) 2003-06-17 2012-07-11 オズモウズ,インコーポレーテッド Fine particle wood preservative and method for producing the same
US7258826B2 (en) * 2003-08-15 2007-08-21 Lord's Additives Llc Low dust preservative powders for lignocellulosic composites
US20050054807A1 (en) * 2003-09-05 2005-03-10 Weyerhaeuser Company Low-nitrogen content phenol-formaldehyde resin
US7141195B2 (en) * 2003-09-05 2006-11-28 Weyerhaeuser Co. Process for making engineered lignocellulosic-based panels
CN100420378C (en) * 2003-12-08 2008-09-24 奥斯缪斯公司 Composition and process for coloring and preserving wood
US20050147823A1 (en) * 2003-12-29 2005-07-07 Mark Oliver Treatment of porous filler materials for use with resins
US7740929B2 (en) 2004-01-27 2010-06-22 Lignor Limited Hard wood strand products
US20070131136A1 (en) * 2004-04-27 2007-06-14 Osmose, Inc. Composition And Process For Coloring Wood
WO2005114078A2 (en) 2004-05-13 2005-12-01 Osmose, Inc. Compositions and methods for treating cellulose-based materials with micronized additives
US20050252408A1 (en) 2004-05-17 2005-11-17 Richardson H W Particulate wood preservative and method for producing same
US7238654B2 (en) * 2004-05-17 2007-07-03 Phibro-Tech, Inc. Compatibilizing surfactant useful with slurries of copper particles
WO2006036713A2 (en) * 2004-09-22 2006-04-06 Commonwealth Scientific Industrial Research Organization (Csiro) Systems and methods for the production of steam-pressed long fiber reconsolidated wood products
US8075735B2 (en) * 2004-09-22 2011-12-13 Timtek, Llc System and method for the separation of bast fibers
AU2005291956A1 (en) 2004-09-30 2006-04-13 Jeld-Wen, Inc Treatment of wood for the production of building structures and other wood products
US20060112850A1 (en) 2004-10-14 2006-06-01 Jun Zhang Micronized wood preservative formulations in organic carriers
US20060086284A1 (en) * 2004-10-14 2006-04-27 Jun Zhang Non-alkaline micronized wood preservative formulations
US20060128886A1 (en) * 2004-12-14 2006-06-15 Winterowd Jack G Low-nitrogen content phenol-formaldehyde resin
US20060276468A1 (en) * 2005-05-12 2006-12-07 Blow Derek P Wood preservative formulations comprising Imazalil
US7655281B2 (en) * 2005-05-24 2010-02-02 Kop-Coat, Inc. Method of protecting wood through enhanced penetration of wood preservatives and related solution
US20070003747A1 (en) * 2005-06-30 2007-01-04 Gnatowski Marek J Composite wood product, methods for manufacturing the same and methods for determining organic biocide concentration in a composite wood product
US20070021385A1 (en) * 2005-07-21 2007-01-25 Jun Zhang Compositions and methods for wood preservation
CA2631424C (en) * 2005-11-29 2015-06-09 Timtek Australia Pty, Ltd. System and method for the preservative treatment of engineered wood products
DE102006003699B3 (en) * 2006-01-26 2007-10-11 Glunz Ag Wood fiber board with mold protection for roof and wall construction and method for its production
US8662121B2 (en) * 2006-03-30 2014-03-04 Weyerhaeuser Nr Company Method for reducing warp potential within lumber derived from a raw material
US7851021B2 (en) * 2006-08-30 2010-12-14 Louisiana-Pacific Corporation Treated wet process hardboard
US7632567B1 (en) 2006-08-31 2009-12-15 Osmose, Inc. Micronized wood preservative formulations comprising copper and zinc
US7678309B2 (en) * 2006-11-28 2010-03-16 Timtek, Llc System and method for the preservative treatment of engineered wood products
US7816343B2 (en) * 2007-03-08 2010-10-19 Hwd Acquisition, Inc. Wood preservative composition
US8058193B2 (en) 2008-12-11 2011-11-15 Jeld-Wen, Inc. Thin-layer lignocellulose composites and methods of making the same
US20090143334A1 (en) * 2009-02-05 2009-06-04 Ward Hans A Method of Protecting Wood Through Enhanced Penetration of Wood Preservatives and a Related Solution
US20110155315A1 (en) * 2009-12-24 2011-06-30 Ali'i Pacific LLC Preservative-treated i-joist and components thereof
US9125398B2 (en) 2011-04-05 2015-09-08 Kop-Coat, Inc. Method of employing enhanced penetration of wood preservatives to protect wood and a related solution
CN103406960B (en) * 2013-07-08 2016-04-20 中南林业科技大学 A kind of wooden bamboo wood highly effective flame-retardant processing method
US9931761B2 (en) 2013-07-25 2018-04-03 Timtek, Llc Steam pressing apparatuses, systems, and methods

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0264538A1 (en) * 1986-10-01 1988-04-27 Rütgerswerke Aktiengesellschaft Process for preparing boric acid suspensions
US4879083A (en) * 1988-06-17 1989-11-07 Macmillan Bloedel Limited Chemically treated wood particle board
US5246652A (en) * 1992-06-05 1993-09-21 Forintek Canada Corp. Method of making wood composites treated with soluble boron compounds

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4241133A (en) * 1979-04-02 1980-12-23 Board Of Control Of Michigan Technological University Structural members of composite wood material and process for making same
US4818779A (en) * 1987-11-25 1989-04-04 Dow Corning Corporation Poly(vinyl acetate) emulsion adhesives containing an alkoxysilane
US5763338A (en) * 1996-03-22 1998-06-09 Forintek Canada Corporation High level loading of borate into lignocellulosic-based composites

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0264538A1 (en) * 1986-10-01 1988-04-27 Rütgerswerke Aktiengesellschaft Process for preparing boric acid suspensions
US4879083A (en) * 1988-06-17 1989-11-07 Macmillan Bloedel Limited Chemically treated wood particle board
US5246652A (en) * 1992-06-05 1993-09-21 Forintek Canada Corp. Method of making wood composites treated with soluble boron compounds

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1357794A2 (en) * 2001-01-05 2003-11-05 Kop-Coat, Inc. Synergistici combination of fungicides to protect wood and wood-based products from fungal decay, mold and mildew damage
EP1357794A4 (en) * 2001-01-05 2004-02-11 Kop Coat Inc Synergistici combination of fungicides to protect wood and wood-based products from fungal decay, mold and mildew damage
US7160606B2 (en) 2001-09-17 2007-01-09 Genics Inc. Method of treating building materials with boron and building materials
US7223415B1 (en) 2002-10-07 2007-05-29 Nisus Corporation Weather resistant granular bait with synergistic broad spectrum attractant system
US7264827B1 (en) 2002-10-07 2007-09-04 Nisus Corporation Weather resistant granular bait with synergistic broad spectrum attractant, system
US8597419B2 (en) 2007-01-17 2013-12-03 Genics Inc. Preservative compositions for wood and like materials

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AU741151B2 (en) 2001-11-22
CA2320297C (en) 2007-04-17
EP1058607A1 (en) 2000-12-13
CN1291932A (en) 2001-04-18
EP1058607B1 (en) 2006-07-12
AU2405599A (en) 1999-09-15
CN1102880C (en) 2003-03-12
ATE332789T1 (en) 2006-08-15
CA2320297A1 (en) 1999-09-02
NZ506281A (en) 2002-12-20
US5972266A (en) 1999-10-26
DE69932322D1 (en) 2006-08-24
JP2002504443A (en) 2002-02-12
DE69932322T2 (en) 2007-07-19

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