WO2005018889A1 - Wood treatment - Google Patents

Wood treatment Download PDF

Info

Publication number
WO2005018889A1
WO2005018889A1 PCT/AU2004/001106 AU2004001106W WO2005018889A1 WO 2005018889 A1 WO2005018889 A1 WO 2005018889A1 AU 2004001106 W AU2004001106 W AU 2004001106W WO 2005018889 A1 WO2005018889 A1 WO 2005018889A1
Authority
WO
WIPO (PCT)
Prior art keywords
wood
smoke
liquid
methyl
wood smoke
Prior art date
Application number
PCT/AU2004/001106
Other languages
French (fr)
Inventor
Keith Ross Johnson
Narelle Louise Brown
Original Assignee
Mitchite Pty Ltd Acting For The Ca & Kr Johnson Family Trust
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
Priority claimed from AU2003904502A external-priority patent/AU2003904502A0/en
Application filed by Mitchite Pty Ltd Acting For The Ca & Kr Johnson Family Trust filed Critical Mitchite Pty Ltd Acting For The Ca & Kr Johnson Family Trust
Publication of WO2005018889A1 publication Critical patent/WO2005018889A1/en

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K5/00—Treating of wood not provided for in groups B27K1/00, B27K3/00
    • B27K5/001—Heating
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
    • B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34—Organic impregnating agents
    • B27K3/50—Mixtures of different organic impregnating agents

Definitions

  • This invention relates to methods for the treatment of wood to protect it against degradation as well as compositions suitable for providing such protection.
  • the fungi are minute thread-like organisms which use wood as a food source to grow and multiply. Typically they require reasonably warm temperatures and water as well as access to air to be able to grow.
  • the fungi produce enzymes which digest the wood and ultimately cause discoloration and/or decay of the wood.
  • sap stain The most common fungal damage is called "sap stain". As the name suggests, this is caused by fungi which affect the sapwood. Often, the discoloration caused by sap stain results in a blue stain on the wood. Fortunately, sap stain does not usually affect its strength but in some instances, its hardness or shock resistance may be affected.
  • Decay is a form of deterioration which is caused by decay fungi. Because the decay fungi can attack the entire log, apart from staining, it can also cause significant structural weakness of the wood. Thus, decay fungi represent a particularly undesirable cause of damage to wood although the structural damage they cause is generally likely to take longer than deterioration in the form of staining or discoloration.
  • Another type of fungi which causes discoloration is represented by molds. These can cause visible discoloration. However, the more serious aspect of structural damage is not of such concern as it is in the case of decay fungi.
  • Water spray systems are also commonly used, the water spray acting to prevent proliferation of fungi by restricting their access to air.
  • the cost of running water spray systems combined with the fact that the runoff from such systems can represent an environmental hazard again means that there are also restrictions on their use.
  • the invention provides in one aspect a method of protecting wood which comprises treating the wood with a fluid treatment agent chosen from at least one of liquid wood smoke, wood smoke vapour and a plurality of biologically active compounds comprised in the liquid wood smoke and wood smoke vapour.
  • a fluid treatment agent chosen from at least one of liquid wood smoke, wood smoke vapour and a plurality of biologically active compounds comprised in the liquid wood smoke and wood smoke vapour.
  • the biologically active compounds maybe active against at least one of fungi, stain and decay.
  • Liquid wood smoke is an aqueous condensate produced by absorbing in water the smoke vapour obtained from roasting or burning of wood. It may optionally be filtered to remove particulates.
  • wood smoke vapour may be produced from hard woods under controlled roasting conditions such as pyrolysis and it may be absorbed in water using a wet scrubber system.
  • Some of the biologically active compounds in liquid wood smoke and wood smoke vapour comprise syringol, guaiacol, eugenol, p-cresol, m-cresol, o-cresol, phenol, pyrocatechol, 2, 3 xylenol, 2, 4-xylenol, 2, 6-xylenol, 3,5-xylenol, formaldehyde, acetaldehyde, benzaldehyde, anisaldehyde, acetic acid, formic acid, butyric acid, valeric acid, fumaric acid, benzoic acid, salicyclic acid, methanol, ethanol and allyalcohol.
  • the concentration of the wood smoke used in relation to the invention is suitably determined by an acidity range.
  • the liquid wood smoke may have a concentration range of 2% to 16% acidity.
  • Example 1 shows how to test the level of acidity of liquid wood smoke.
  • Treatment of wood with liquid wood smoke or compounds comprised in liquid wood smoke may be applied by dipping the wood in the liquid wood smoke or liquid mixture containing active compounds comprised in wood smoke.
  • the wood may be treated with a spray shower or atomized treatment liquid applied to the timber surface.
  • the spray may typically be applied for a period of 20 to 60 seconds.
  • Application rates may typically be in excess of 0.25 litre/sqm more preferably 0.5 litre/sqm and even in excess of 1 litre/sqm.
  • the liquid wood smoke may be infused into the wood. It may be infused by allowing the wood to be submerged in the liquid or by creating pressure differential between the interior of the wood and outside air so as to cause liquid around the surface of the wood to be sucked into the wood as is known in the art.
  • hot wood smoke vapor may be applied directly to the wood.
  • the hot wood smoke may be generated by heating wood smoke liquid to produce hot wood smoke vapour. It may be applied for a period of 10 minutes to 60 minutes. It may be applied under conditions which cause the hot wood smoke vapour to be sucked into the wood.
  • the wood may be subjected to an evacuation procedure so as to create a sub atmospheric pressure within the wood prior to the treatment with hot wood smoke vapour or liquid treatment agent.
  • a feedstock wood may be roasted or pyrolysed to produce hot wood smoke which is then directly contacted with the surface wood being treated.
  • liquid treatment may also be used.
  • wood smoke vapour treatment may also be used.
  • the method of the invention may be used to protect wood against the deleterious effects of fungi.
  • it may be used to protect the wood against sap stain and decay.
  • sap stain fungi are Alteraria sp, Diplodia sp, Ophiostomum floccosum, Leptographium procerum.
  • decay fungi are Fibroporia vaillantii, Scizophyllum commune, Phlebiopsis gigantean.
  • the invention is particularly suitable for treatment of soft woods although there are instances where it is also applicable to hardwoods affected by fungi. Examples of woods to which the invention applies include radiate pine, white meranti, falcute and xylampayan.
  • the acidity of liquid wood smoke can be determined using standard titration techniques as outlined below:
  • Phenol level mg/ml 13.0 - 23.0
  • Debarked radiata pine surfaces were treated with liquid wood smoke having the composition specified in Example 2 by spraying for a period of 20 seconds.
  • Various strengths of liquid wood smoke namely 25%, 50% and 100% were applied.
  • the amount of liquid wood smoke applied per square metre of wood surface was about 0.85 litre/m 2 .
  • the liquid wood smoke was provided in the form of two commercially available brands of liquid wood smoke with the commercial names "Regen” and "Logon"
  • the results of treatments with different concentrations of liquid wood smoke over a period of 1 to 3 weeks as against a control are shown numerically in Tables 2 and 3 and graphically in Table 4.
  • Phenols Phenols (continued) Phenol 4-Methoxyphenol Dimethoxyphenol Methoxyethylphenol o-CresoI (2-methylphe ⁇ ol) 3,4 -Dimethoxyphenol Syringol (2,6-dimethoxyphcnol) m-Cresol (2-methylphenol) 4-Methylsyringol (2,6-dimethoxy-4- ethylphenol) p-Cresol (4-melhylphenol( 4-EthylsyringoI (2-dimethoxy-4- 2-Ethylphenol ethylphenol) 3-Ethylphenol 4-Ethylphenol 4-Propylsyringol (2,6-dimethoxy-4- 2-EthyI-5-methylphenol propylphenol) 3-Ethyl- -methylphenoI 2,3-Xylc ⁇ ol (2,3-dimethyIphenol) 4-Isopropylsyring
  • 2-Isopropylfuran Lactones 2-Propenylfuran ⁇ -Butyroiactone

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Forests & Forestry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

A method of protecting wood which comprises treating the wood with a fluid treatment agent chosen from at least one of, liquid wood smoke, wood smoke vapour and a plurality of biologically active compounds comprised in liquid wood smoke.

Description

WOOD TREATMENT
Field of the Invention
This invention relates to methods for the treatment of wood to protect it against degradation as well as compositions suitable for providing such protection.
Background of the Invention
Stored logs, lumber and milled timber can all suffer deterioration over time. Whilst such deterioration can arise from a number of causes, the most common forms of deterioration are caused by a number of different fungi types. As a result of this deterioration, the value of the wood can be substantially reduced. Add to this the fact that saw mills as part of their normal operating requirements often need to have large log inventories and it can be seen that the economic effect of deterioration of wood during storage can be quite significant.
There are three basic types of fungal damage from which wood may suffer in storage. The fungi are minute thread-like organisms which use wood as a food source to grow and multiply. Typically they require reasonably warm temperatures and water as well as access to air to be able to grow. The fungi produce enzymes which digest the wood and ultimately cause discoloration and/or decay of the wood.
The most common fungal damage is called "sap stain". As the name suggests, this is caused by fungi which affect the sapwood. Often, the discoloration caused by sap stain results in a blue stain on the wood. Fortunately, sap stain does not usually affect its strength but in some instances, its hardness or shock resistance may be affected.
Decay is a form of deterioration which is caused by decay fungi. Because the decay fungi can attack the entire log, apart from staining, it can also cause significant structural weakness of the wood. Thus, decay fungi represent a particularly undesirable cause of damage to wood although the structural damage they cause is generally likely to take longer than deterioration in the form of staining or discoloration.
Another type of fungi which causes discoloration is represented by molds. These can cause visible discoloration. However, the more serious aspect of structural damage is not of such concern as it is in the case of decay fungi.
Currently, various types of chemical sprays have been used to guard against deterioration by fungi. Examples of the chemicals used include pentachlorophenol, sodium pentachlorophenate and mixtures of sodium pentachlorophenate with borax.
Whilst such chemical treatments have a degree of effectiveness, the environmental hazards which they pose mean there must be restrictions on their use.
Water spray systems are also commonly used, the water spray acting to prevent proliferation of fungi by restricting their access to air. However, the cost of running water spray systems combined with the fact that the runoff from such systems can represent an environmental hazard again means that there are also restrictions on their use.
Thus, there is a need for development of an alternative approach which obviates or ameliorates one or more of the foregoing drawbacks of the prior art wood protection processes.
Disclosure of the Invention
The invention provides in one aspect a method of protecting wood which comprises treating the wood with a fluid treatment agent chosen from at least one of liquid wood smoke, wood smoke vapour and a plurality of biologically active compounds comprised in the liquid wood smoke and wood smoke vapour. The biologically active compounds maybe active against at least one of fungi, stain and decay. Liquid wood smoke is an aqueous condensate produced by absorbing in water the smoke vapour obtained from roasting or burning of wood. It may optionally be filtered to remove particulates.
Suitably, wood smoke vapour may be produced from hard woods under controlled roasting conditions such as pyrolysis and it may be absorbed in water using a wet scrubber system.
Some of the biologically active compounds in liquid wood smoke and wood smoke vapour comprise syringol, guaiacol, eugenol, p-cresol, m-cresol, o-cresol, phenol, pyrocatechol, 2, 3 xylenol, 2, 4-xylenol, 2, 6-xylenol, 3,5-xylenol, formaldehyde, acetaldehyde, benzaldehyde, anisaldehyde, acetic acid, formic acid, butyric acid, valeric acid, fumaric acid, benzoic acid, salicyclic acid, methanol, ethanol and allyalcohol.
The concentration of the wood smoke used in relation to the invention is suitably determined by an acidity range. Typically, the liquid wood smoke may have a concentration range of 2% to 16% acidity. Example 1 shows how to test the level of acidity of liquid wood smoke.
Some of the compounds which are comprised in the liquid wood smoke are listed in Table 1 attached hereto. It is to be appreciated that this is not a complete listing of the compounds. There may be other compounds in liquid wood smoke as well.
Treatment of wood with liquid wood smoke or compounds comprised in liquid wood smoke may be applied by dipping the wood in the liquid wood smoke or liquid mixture containing active compounds comprised in wood smoke.
Alternatively or additionally, the wood may be treated with a spray shower or atomized treatment liquid applied to the timber surface. The spray may typically be applied for a period of 20 to 60 seconds. Application rates may typically be in excess of 0.25 litre/sqm more preferably 0.5 litre/sqm and even in excess of 1 litre/sqm.
After treatment the wood should be allowed to dry before stacking.
In another application technique, the liquid wood smoke may be infused into the wood. It may be infused by allowing the wood to be submerged in the liquid or by creating pressure differential between the interior of the wood and outside air so as to cause liquid around the surface of the wood to be sucked into the wood as is known in the art.
In an alternative form of the invention, hot wood smoke vapor may be applied directly to the wood. The hot wood smoke may be generated by heating wood smoke liquid to produce hot wood smoke vapour. It may be applied for a period of 10 minutes to 60 minutes. It may be applied under conditions which cause the hot wood smoke vapour to be sucked into the wood. For this purpose, the wood may be subjected to an evacuation procedure so as to create a sub atmospheric pressure within the wood prior to the treatment with hot wood smoke vapour or liquid treatment agent. In a variation of this process, a feedstock wood may be roasted or pyrolysed to produce hot wood smoke which is then directly contacted with the surface wood being treated.
In another aspect of the invention, a combination of liquid treatment and wood smoke vapour treatment may also be used.
The method of the invention may be used to protect wood against the deleterious effects of fungi. In particular, it may be used to protect the wood against sap stain and decay. Examples of such sap stain fungi are Alteraria sp, Diplodia sp, Ophiostomum floccosum, Leptographium procerum. Examples of such decay fungi are Fibroporia vaillantii, Scizophyllum commune, Phlebiopsis gigantean. The invention is particularly suitable for treatment of soft woods although there are instances where it is also applicable to hardwoods affected by fungi. Examples of woods to which the invention applies include radiate pine, white meranti, falcute and xylampayan.
Preferred aspects of the invention will now be described with reference to the following example.
Example 1
The acidity of liquid wood smoke can be determined using standard titration techniques as outlined below:
Reagents required: Sodium Hydroxide (1.000 Normal) Distilled Water (200mls)
Materials required: 1 - 0-25ml burette 1 - pipettor (6mls) or (2 x 3 mis) 1 - pH meter and probe 1 - 400 ml beaker and stirrer
• Turn on pH Meter and Mixer (gentle stir) • Add 200 mis of Distilled Water to Beaker • Place Beaker onto Mixer plate • Place pH Meter Probe and Stirrer into Beaker • Fill the 0-25ml Burette with Sodium Hydroxide ++ to Level 0 • From the sample of Smoke Mix measure 6 mis into the pipettor and place in the Distilled Water • The reading on the pH Meter is the pH Result (To obtain an accurate pH result wait a couple of minutes and check against readings as per sample sheet from Store and MSDS) • For Acid Result - Pipette the Sodium Hydroxide slowly into the beaker until a pH reading of "5" to let the mixture catch up • Continue slowly pouring the Sodium Hydroxide until the pH meter reads "7" • The acidity is taken as the number of mis of Sodium Hydroxide required to give pH 7 eg. 10.6mls is equivalent to 10.6% acidity.
Example 2
The following table shows a typical specification showing the major components for an aqueous wood smoke condensate.
Acidity % 10.0 - 12.0
Staining index 68 -78
Carbonyl level g/lOOml 15.0 - 25.0
Phenol level mg/ml 13.0 - 23.0
Specific gravity 25 deg C 1.080 - 1.090
Density Lbs/gal 9.00 - 9.08
Benzopyrene Less than 1 part/billion pH level Ph 2.65
Colour Dark amber
Example 3
Debarked radiata pine surfaces were treated with liquid wood smoke having the composition specified in Example 2 by spraying for a period of 20 seconds. Various strengths of liquid wood smoke namely 25%, 50% and 100% were applied. The amount of liquid wood smoke applied per square metre of wood surface was about 0.85 litre/m2. The liquid wood smoke was provided in the form of two commercially available brands of liquid wood smoke with the commercial names "Regen" and "Logon" The results of treatments with different concentrations of liquid wood smoke over a period of 1 to 3 weeks as against a control are shown numerically in Tables 2 and 3 and graphically in Table 4.
It can be seen that treatment was most effective for prevention of decay. It was also effective to a lesser extent against stain and seemed to have little effect on mold.
Whilst the above description includes the preferred embodiments of the invention, it is to be understood that many variations, alterations, modifications and/or additions may be introduced into the constructions and arrangements of parts previously described without departing from the essential features or the spirit or ambit of the invention.
It will be also understood that where the word "comprise", and variations such as "comprises" and "comprising", are used in this specification, unless the context requires otherwise such use is intended to imply the inclusion of a stated feature or features but is not to be taken as excluding the presence of other feature or features.
The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that such prior art forms part of the common general knowledge in Australia.
Table 1. Compounds Identified in Wood Smoke
Acids Acids (continued) Formic (methanoic) Pelargoπic (nonanoic) Acetic (ethanoic) Capric (dccanoic) Laurie (dedecanoic) Myristic (tetradecaπoic) Glycolic (hydroxyethanoic) Peπtacecylic (peπtadecanoic) Propionic (propanoic) Palmitic (hexadecanoic) Stearic (octadecanoϊc) Isobutyric (2-methylpropaπoic) Oleic (9-octadecanoic) Arachidic (elcosanoic) Acrylic (propenoic) Behinic (docosanoic) ' Methacrylic (methylpropcnoic) Benzoic . Butyric (butanoic) Salicylic (O-hydroxybenzoic) 3-Methoxy-4-hydroxybenozic α-Mcthylbutyric Sorbic (2-4-hcxadieπoic) Isovϋleric (3-methylbutanoic) Vanillic (4-hydroxy-3-methoxyben- zoic) Crotonic (2-bulenoic) Abictiπic rra/ii--Crotonic (tra πj-2-buteπoic) Pimaric Lignoceric cf_--Crolonic (cw-2-butcnoic) 3-Butcnoic Alcohols Tiglic (2-mcthyl-2-butenoic) Methyl fmelhanol) Angelic ( j-2-methyl-2-butcnoic) Elhyl (elhanol) rrfl/2J-2-Mefhyl-2-butcπoic Propyl ( 1-propanol) Isopropyl (2-propanoI) Valeric (pcntanoic) Isobutyl (2-methyl-l-propanol) Allyl (2-propen-l -ol) α-Melhylvaleπc (2-rnethylpentanoic) Propan-2-on-l-ol Amyl (2-meihyl-2-butanoI) 3-Mcthylpenlanoic Isoamyl (3-methyI-2-butaπol) Isocaproic (4-mcthylpcrιtanoic) Butaπ-2-on-!-ol Butaπ-3-oπ-2-o! 4-MethyI-2-pcntcnoic 2-Buten-l -oI 2-Pentenoic Pcnlan-2-on-I -ol • 3-Peπtenoic Pcntan-3-on-2-ol Lcvuliπic (4-oxopcntanoιc) l-Penten-3-ol ' Caproic (hcxanoic) 1-Nonanol Phenylethylalcohol Enanthic (hcptanoϊc) Cyclohexanol Benzylalcohol 5-Hcptcnoic p-Hydroxybcnzylalcohol Caprylic (oclanoic) Fcπchyl (6-fcnchaπol) Dchydroxycaprylic Isofeπchyl (iso-6-fcπchanol) (continued) Table 1. (Continued)
Carbonyls (continued) Carbonyls (continued) Anisaldehydc (4-hydroxybcnzaIdehyde) 2-Ethyl-4-methyI-2-cyclopentcnone Dihydroxybenzaldehyde 2-Ethy!-5-mcthyl-2-cyclopentenone I 72-Dihydroxy-3-methylbenzaldehydc 3-Ethyl-2-mcthyl-2-cyclopentenone 2-Hydroxy-3-methoxybenzaldehydc 2,3-Dimelhyl-2-cyclopentenone 4-Hydroxy-2-methoxybcnzaIdehyde 2,4-Dimethyl-2-cyclopentenone 4-Hydroxy-3-methoxybenzaldehyde 2,5-Dimethyl-2-cyclopeπtenone (vanillin) 3,4 -DimethyI-2-cyclopentenone 3,5-Dimethyl-2-cyclopentenone 4-Hydroxy-3,5-dimethoxybenzaldehyde 2,3,4-TrimcthyI-2-cyclopentenone (syringaldehyde) 2,3,5-Trimethyl-2-cyclopentenone 3-/ι-Propyl-2-cycIopentenone 3,5-Dimethoxybenzaldehyde 3-Isopropyl-2-cyclopentenone Sinapaldehyde (3-(4'-hydroxy-3',5'- 3-Methyl-2-cyclopenten-2-ol-l -oπe dimethoxyphenyl)-2-propenaI) 3,4-DimethyI-2-cyclopenten-2-oI-l- Coniferaldyhyde (3- 4'-hydroxy-3'- one methoxyphcnyl)-2-propenaI) 3-Ethy!-2-cycloρenten-2-ol-l -one 3-(4'-Hydroxy-3'I5'-diπιethoxypheπyl)-l- propanal 2-Hydroxy-3-methylcyclopent-2-ene-I- 3-<4'Hydroxy-3'-methoxyphenyl)-l- one (cyclotene) propanal Cyclopeπtanone Cyclohexanone Methylcyciopentaπoπc 2,4,4 -Trimethylcyclohexanone Dimethylcyclopeπtanone 2-Cycloheχenone Tπmethylcyclopentanone 2,4-Dimethyl-4-cycIohexenone 3,3,5-Trimethylcyclopentanone 1 -Methyl-2-cyclohexen-5-one 1 ,2-Cyclopentanediol 5,5-Dimcthyl-l ,3-cyclohexaπedione 3-MethyI-l ,2,4-cyclopentanclrione Cyclohexanccarboxaldehyde 3-Methylcyclopenta-l ,2-dione Cyclohcxancpropioπaldehyde 3-Ethylcyclopenta-l ,2-dione 3,4-Dimethylcyclopenta-l ,2-dione Esters 2-Cyclopcntenonc Methyl formate Methyl acetate 2-Methyl-2-cyclopcntenone Methyl propionatc Methyl butyrate 4-Melhyl-2-cyclopentcnone Methyl isobutyrate 5-Methyl-2-cyclopcntenone Methyl crolonate 2-Ethyl-I-cyclopentcnone Methyl valeratc 3-Ethyl-2-cyclopentcnonc Methyl caproate 2-Ethyl-3-methyl-2-cyclopcntenone Methyl cnanthatc . Methyl myristate (continued) Table I. (Continued)
Phenols Phenols (continued) Phenol 4-Methoxyphenol Dimethoxyphenol Methoxyethylphenol o-CresoI (2-methylpheπol) 3,4 -Dimethoxyphenol Syringol (2,6-dimethoxyphcnol) m-Cresol (2-methylphenol) 4-Methylsyringol (2,6-dimethoxy-4- ethylphenol) p-Cresol (4-melhylphenol( 4-EthylsyringoI (2-dimethoxy-4- 2-Ethylphenol ethylphenol) 3-Ethylphenol 4-Ethylphenol 4-Propylsyringol (2,6-dimethoxy-4- 2-EthyI-5-methylphenol propylphenol) 3-Ethyl- -methylphenoI 2,3-Xylcπol (2,3-dimethyIphenol) 4-Isopropylsyringol (2,6-dimethoxy-4- isopropylphenolj 2,4-XyIenol (2,4-dimethylphenol) 4-Propeny!syringol (2,6-dimethoxy-4- propenylphenol) 2,5-Xylcnol (2,5-dimethyIphenol) . 4-fnι/7 -Propenylsyringol (2,6- dimcthoxy-4 -tran .r-propenylphenol) 2,6-Xylenol (2,6-dimethylpheπol) 4-c/j-Propenylsyringol (2,6-dimethoxy- 3,4-Xylcnol (3,4-dimcthylphenol) 4-ctf-ρropenylphenol) 3,5-Xylenol (3,5-dimethyIphenol) 4-Ally!syringol (2,6-dimethoxy-4- allylphenol) ' Dicthylphenol 2,3,5-TrimcthyIphenol 4-Vinylsyringol (2,6-dimethoxy-4- vinylphenol) 2,3,6-Trimcthylphcnol 4-Isobutylsyringol (2,6-dimcthoxy-4- 2,4,6-Trimclhylphcnol isobutylpheπol) 4-Propylphcπol 2,4-Dimcthoxy-4-allylphenol 4-lsoρropylphcnoI l ,2-Dihydroxy-4-mclhyIphcnol 2-Mcthyl-S-isoρropylphenol 2-Mcthoxy- -acetic acid phenol 4-Butylpheπol 3-Mclhoxy-4 -propan-2-onc phenol 2-lsobutylphcnol 2-Allylplιcnol Acctophcnol 3-AlIylphcnol 4-Isopropylacctophenol 4-Allylphenol 4-Hydroxy-3-mclhoxyacetophcnol 4-Vinylphcnol 3-Mcthoxyp cnol 3,4 -Dimcthoxyacclophcnone (continued) Table I. (Continued)
Esters (continued) Furans (continued) Methyl palmitate 2-Methyltetrahydrofuxan-3-one Methyl aery late 2,5-DimcthyItetrahydrofuran-3-one Ethyl myristate Ethyl benzoate 2-Acetyltetrahydrofuran-3-one Cresyl acetate 2-Furoic acid Hydroxy-2-butanone acetate 4-Methyl-2-furoic acid Hydroxy-2-propanone propionate Methyl-2-furoate . Salcylic acid methyl ester Furfuryl methyl ether 4-Methoxybenzoic acid methyl ester 2-Furfuryl methyl ketone 4-Hydroxy-4-melhoxybenzoic acid 3-Furfuryl methyl ketone methyl ester 2-Furfuryl propyl ketone 4-Hydroxy-315-dimethoxybenzoic acid 2-Furfuryl butyl ketone methyl ester 2-(5-Methyfuryl)-methyl ketone 3-Methoxy-4-hydroxyphenylacetic 2-Furfural acid methyl ester 3-Furfural
Furans 4-Methylfurfural Furfuryl alcohol 5-Methylfurfural 2-Furfuryl methyl alcohol Furan . 2-Methyl-3-furfural 2-Methylfuran 3-Methyl-2-furfural 2,5-Di ethylfuran 5-Hydroxymethyl-2 -furfural 2,4-Dimethylfuran 2-Ethylfuran 2,5-Difurfuryledine-l -cycIopenlanone 2-AcetyIfuran Propylfuran 2-Isopropylfuran Lactones 2-Propenylfuran γ-Butyroiactone 2-Acetyl-5-methylfuran J-Angelica lactone 2,5-Dimethyl-3-acetylfuran γ-Crotonolactone Amylfuran 7-Hydroxyvalerolactone 2,3,5-Trimethylfuran o^-Hydroxyvalerolactone 2-Viπylfuran α-Hydroxy-γ-hydroxyvalerolaclone 2-Viπyl-3-methylfuran Benzofuran 2-Butenolide 2-MethyIbenzofuran 2-Methyl-2-buteπoIide Dimethylbenzofuran 4-Methyl-2-butenolide Dibenzofuran . 2,3-Dimethyl-2-butenolide Bis-{furfuryl)-2-furan 2,4 -Dimethyl-2-buteπolidc 2,3-Dimcthyl-5-ethylfuran 3,4 -Dimethyl-2-butenolidc 3,4 -Dimethyl-5-ethylfuran 2,3,4-Trimethyl-2-buteno!ϊde 2-Ethyl-2,3-dihydro-5-methylfuran 4-EthyI-2-methyl-2-bulenolide 4-Ethylidiene-2-methyl-2-butenolide 2,5-Tctrahydrodimcthylfuran Methylvinyl-2-butenoIide Table 1. (Continued)
Phenols (continued) Phenols (continued) 2-Acetovanillone (4'-hydroxy-3'- 4 -Elhylpyrocatechol methoxyacetopheπone) 3-Methoxyρyrocatechol Rcsorcinol (1 ,3-dihydroxybcnzene) Guaiacol (2-methoxyphenol) 4 -Ethylresorcinal 4-Methylguaiacol (2-methoxy-4- Miscellaneous methylphenol) Methylamine Dimethylamine Trimethylamine 6-Methylguaiacol (2-methoxy-ό- Pyrazine methylphenol) Methylpyrazine 5-MethylguaiacoI (2-methoxy-5- 2,5-Dimethylpyr zine methylphenol) Pyrrole 3-Methylguaiacol (2-methoxy-3- 2-Acetyl pyrrole methylphenol) 2-Formylpyrrole 4-Ethylguaiacol (2-methoxy-4- α-Methyl pyrryl ketone ethylphenol) α-Ethyl pyrryl ketone Pyridine .. 4-PropylguaiacoI (2-methoxy-4- 4-Hydroxy-6-methyl-2,4-pyran-2- propylphenol) , one Maltol (3-hydroxy-2-methylpyrone) 4-Isopropylguaiacol (2-methoxy-4- isopropylphenol) 4-Vinylguaiacol (2-methoxy-4- Dimethoxymethane Yinylpheπol) Dimethoxyethane Methoxybenzene 5-Vϊnylguaiacol (2-methσxy-5- Thymol vinylphenol) Ethanediol 3,5-Dimethylguaiacol (2-mcthoxy-3,5- 1-Naphthol dimethylphenoi) Toluene Eugenol (2-methoxy-4-allylphenol) Styrene , Benzene Ethylbenzene rrαπj-Isoeu enol (2-methoxy-4- 5-Propyl-l,2,3-benzenetriol rππu-propenylphenol) 1 ,2-Dimethoxybenzenc (veratrol) 1 ,2-Dimethoxy-4-methylbenzene cjj-Isoeugenol (2-methoxy-4- (mcthylYeratrol) cύ-propenylphcnol) 1 ,2-Dimethoxy-4-ethyIbenzene (ethylveratrol) Pyrocatechol (1 ,2-benzencdiol) 1 ,4 -Dimethoxybenzene n-Pentadecane 3-Methylpyrocalechol 2,6,10,14-Tetramethylρentadecane 4-Methylρyrocatechol 5-Methylpyrocatechol 1-Indanonc Table 1. (Continued)
Carbonyls Carbonyls (continued) Methanal 2,4 -Dimelhylpentanone Ethanal Pentadiene Hydroxyethanal Methylpentadiene Phenylethanal 2,3-Pentanedione 2-Pyrroaldehyde 4-Pentanedienal Propanal 2,4 -Pentanedienal 2-Propanal (acrolein) Hexanal 2-MethyIpropanaI 2-Hexcnal 2,2-Dimethylpropanal 2-Hexanone 2-MethyIpropenal 3-Hexanone Acetone (2-propanone) 5-Methyl-2-hexanone 2-Methyl-3-hexanone Acetylacetone 3-Hexen-2-one 3-MethyIacetylacetone 5-Hexen-2-one I -Hydro ypropanone (acetol) 2,4-Hexadienal 2,4-Hexanedione 2-Hydroxypropanone 2,5-Hexanedione Acetoxypropanone . 3-Methyl-2,5-hexanedioπe l ,3'-Dimethoxy-4-phenyl-l-propanone 2-Heptanone ' 4-Heptanone l ,3'-Dimethoxy-4-phenyl-2-propanone 3,6-Octanedione Methyl ethyl ketone l ,5'-Dimethoxy-4-phenyl-2-propanone Methyl isopropyl ketone Methyl isopropenyl ketone α-Methyl-β-ethylpropenal Methyl butyl ketone Butanal Methyl vinyl ketone 2-Butenal Butyl methyl ketone 3-Methylbutanal Allyl methyl ketone 1 -Cyclohexyl methyl ketone 2-Methyl-2-butenal Cyclic ketone 2-Butanone Acetophenone (methyl phcnyl ketone) 3-Methyl-2-butanone 1 -Hydroxy-2-butanone m-Methylacetophenone 3-Hydroxy-2-butanone • p-Methylacetophenone 1 -Pheπyl-2-butanone Acetosyringone (4'-hydroxy-3',5'- 3,3-Dimethyl-2-butanone dimethoxyacetophenone) Diacetyl (2,3-butanedione) Propiosyringone (4'-hydroxy-3',5'- Pcntanal di ethoxypropioacetophenone) α-Methylpentanal 2-Methyl-2-pentenal 4'-Hydroxy-3'-methoxyacetophenone 2-Pentanone 3-Pentanone Benzaldehyde 4 -Hydroxy-2-pentanone Salicylaldehyde 4 -Hydro xy-4 -methyl-2-ρentanone (2-hydroxybenzaldehyde) 2-Methyl-3-pentanone Table 1. (Continued)
Miscellaneous (continued) Miscellaneous (continued) 2-Methyl-I-indanone ' 1 -Methylnaphthalene 3-M ethyl- 1 -indanone 2-MethyInaphthanlene 6-Methyl- 1 -indaπoπe 2-EthyInaphthaleπe Indene Trimethylnaphthalene 3-Methylindene Methylethylnaphthalene Trimethylindene Methylvinylnaphthalene 2,3-Dihydroindene Allylnaphthalene Dimethyliπdane 6-Methyl-1 ,2-dihydronaphthalene Naphthalene Methyldihydronaphthalene
Table 2
Decay Sapstain Mould Treatment MSC(%) 3 k MSC(%) 3 k MSC(%) 3wk
Logon (25%) 34.5 34.7 88
C cO Logon (50%) 0 1 88
CDO Logon (100%) 0 0 88
H H C H m Regen (25%) 6.2 71.3 88
CO m Regen (50%) 0 3 88 m Regen (100%) 0 1 88
73
C I- m r σ> Control 88 88 88
73 O
C NB: MSC = Microbial Surface Coverage
Table 3
Treatment Decay Stain Mould
Control 88 68 88
Regen (25%) 6.2 71.3 88
Logon (25%) 34.5 34.7 88
Regen (50%) 0 3 88
Logon (50%) 0 1 88
Regen (100%) 0 1 88
Logon (100%) 0 0 88
Table 4 Fungal coverage (MSC%) of test fungi on antisapstain treated radiata pine using Logon 100
Figure imgf000018_0001
Figure imgf000018_0002
Control Regen (25%) Logon (25%) Regen (50%) Logon (50%) Regen (100%) Logon (100%) Treatment

Claims

Claims
1. A method of protecting wood which comprises treating the wood with a fluid treatment agent chosen from at least one of, liquid wood smoke, wood smoke vapour and a plurality of biologically active compounds comprised in liquid wood smoke.
2. A method according to any one of the preceding claims wherein the wood is allowed to dry before stacking.
3. A method according to claim 1 or claim 2 wherein the wood is chosen from a wood species affected by sap stain.
4. A method according to claim 3 wherein the wood is chosen from radiata pine, white meranti, falcate and xylampayan.
5. A method according to any one of the claims 1 to 4 wherein the wood is contacted with liquid wood smoke.
6. A method according to claim 5 wherein the liquid wood smoke has an acidity greater than 2%.
7. A method according to claim 6 wherein the liquid wood smoke has an acidity in the range 2% to 16%.
8. A method according to claim 7 wherein the liquid wood smoke has an acidity in the range 10% to 12%.
9. A method according to any one of the preceding claims wherein the wood is treated with the fluid treatment agent by at least one of spraying, dipping, direct contact and infusion.
10. A method according to any one of the preceding claims wherein the liquid treatment agent is applied at the rate of 0.25 litre/sqm.
11. A method according to any one of the preceding claims wherein the liquid treatment agent contains effective levels of the biologically active compounds for treatment against sap stain.
12. A method according to claim 11 wherein the plurality of biologically active compounds are chosen from, syringol, guaiacol, eugenol, p-cresol, m-cresol, o-cresol, phenol, pyrocatechol, 2, 3 xylenol, 2, 4-xylenol, 2, 6-xylenol, 3,5-xylenol, formaldehyde, acetaldehyde, benzaldehyde, anisaldehyde, acetic acid, formic acid, butyric acid, valeric acid, fumaric acid, benzoic acid, salicyclic acid, methanol, ethanol and allyalcohol.
13. A method according to claim 12 wherein the liquid treatment agent comprises at least three different biologically active compounds.
14. A method according to claim 9 wherein the wood is treated by heating wood smoke to produce wood smoke vapour and contacting the wood with the wood smoke vapour.
15. A method according to claim 14 wherein the wood smoke vapour is contacted with the wood for a period of 10 to 60 minutes.
16. A method according to claim 14 or claim 15 wherein the wood smoke vapour is contacted with the wood after the wood has been subjected to evacuation.
17. A method according to claim 9 wherein a wood is pyrolysed to produce hot wood smoke vapour and the wood smoke vapour is directly contacted with the wood being treated.
18. A method according to claim 1 substantially as hereinbefore described.
19. Wood which has been treated in accordance with the method of any one of claims 1 to 18.
PCT/AU2004/001106 2003-08-22 2004-08-19 Wood treatment WO2005018889A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AU2003904502A AU2003904502A0 (en) 2003-08-22 Wood Treatment
AU2003904502 2003-08-22

Publications (1)

Publication Number Publication Date
WO2005018889A1 true WO2005018889A1 (en) 2005-03-03

Family

ID=34200698

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2004/001106 WO2005018889A1 (en) 2003-08-22 2004-08-19 Wood treatment

Country Status (1)

Country Link
WO (1) WO2005018889A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007147804A1 (en) * 2006-06-21 2007-12-27 Transfurans Chemicals Method for modifying wood and wood thereby obtained

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS581508A (en) * 1981-06-26 1983-01-06 農林水産省林業試験場長 Method of treating wood
JPH05269706A (en) * 1992-01-14 1993-10-19 Ebina Ringyo Kk Producing method and its device of rigid and modified lumber
JP2000094406A (en) * 1998-09-25 2000-04-04 Atsushi Kashima Mothproofing and rot proofing treatment method for wood for construction use, and wood for construction use

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS581508A (en) * 1981-06-26 1983-01-06 農林水産省林業試験場長 Method of treating wood
JPH05269706A (en) * 1992-01-14 1993-10-19 Ebina Ringyo Kk Producing method and its device of rigid and modified lumber
JP2000094406A (en) * 1998-09-25 2000-04-04 Atsushi Kashima Mothproofing and rot proofing treatment method for wood for construction use, and wood for construction use

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Week 198307, Derwent World Patents Index; Class C03, AN 1983-15880K *
DATABASE WPI Week 199346, Derwent World Patents Index; Class P14, AN 1993-364605 *
DATABASE WPI Week 200031, Derwent World Patents Index; Class C07, AN 2000-353402 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2007147804A1 (en) * 2006-06-21 2007-12-27 Transfurans Chemicals Method for modifying wood and wood thereby obtained
US8158206B2 (en) 2006-06-21 2012-04-17 Transfurans Chemicals Method for modifying wood and wood thereby obtained

Similar Documents

Publication Publication Date Title
CA2348945C (en) Bio-oil preservatives
Barnaba et al. Identification and quantification of 56 targeted phenols in wines, spirits, and vinegars by online solid-phase extraction–ultrahigh-performance liquid chromatography–quadrupole-orbitrap mass spectrometry
Adfa et al. Chemical components, antitermite and antifungal activities of Cinnamomum parthenoxylon wood vinegar
Oramahi et al. Antifungal and antitermitic activities of wood vinegar from oil palm trunk
De Simón et al. Effect of size, seasoning and toasting in the volatile compounds in toasted oak wood and in a red wine treated with them
AU757773B2 (en) Method for the treatment of wood with metallic treatment and wood treated by the method
Hart et al. Role of stilbenes in resistance of wood to decay
Vichi et al. Volatile and semi-volatile components of oak wood chips analysed by accelerated solvent extraction (ASE) coupled to gas chromatography–mass spectrometry (GC–MS)
Fernández-Costas et al. A sustainable treatment for wood preservation: enzymatic grafting of wood extractives
Toussaint-Dauvergne et al. Glycerol/glyoxal: a new boron fixation system for wood preservation and dimensional stabilization
Altgen et al. Wood degradation affected by process conditions during thermal modification of European beech in a high-pressure reactor system
Irbe et al. Characterisation of the initial degradation stage of Scots pine (Pinus sylvestris L.) sapwood after attack by brown-rot fungus Coniophora puteana
Füchtner et al. Hydrophobic and hydrophilic extractives in Norway spruce and Kurile larch and their role in brown-rot degradation
US6217939B1 (en) Wood treatment process
Pelit et al. Resistance of mechanically densified and thermally post-treated pine sapwood to wood decay fungi
Hsu et al. Effects of alkyl chain length of gallates on their antifungal property and potency as an environmentally benign preservative against wood-decay fungi
DE3874022T2 (en) GAS OR STEAM PHASE TREATMENT OF WOOD WITH BORON PRESERVATIVES.
WO2005018889A1 (en) Wood treatment
Suprianto et al. The antitermitic and antifungal activities and composition of vinegar from durian wood (Durio sp.)
WO1993008971A1 (en) Wood preservation method and wood preservative
Wang et al. Improvement on dimensional stability and mold resistance of wood modified by tannin acid and tung oil
Schoental Carcinogenicity of wood shavings
Oramahi et al. The composition and termicidal activity of vinegar from Medang Wood (Cinnamomum sp.) under different pyrolysis temperature
Wang et al. Evaluation of copper leaching in thermally modified southern yellow pine wood impregnated with ACQ-D
Barbero-López et al. Characterisation, recovery and activity of hydrophobic compounds in norway spruce log soaking pit water: could they be used in wood preservative formulations?

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
122 Ep: pct application non-entry in european phase