EP1377417A2 - Procede de traitement protecteur pour le bois et des materiaux a base de bois - Google Patents

Procede de traitement protecteur pour le bois et des materiaux a base de bois

Info

Publication number
EP1377417A2
EP1377417A2 EP02735172A EP02735172A EP1377417A2 EP 1377417 A2 EP1377417 A2 EP 1377417A2 EP 02735172 A EP02735172 A EP 02735172A EP 02735172 A EP02735172 A EP 02735172A EP 1377417 A2 EP1377417 A2 EP 1377417A2
Authority
EP
European Patent Office
Prior art keywords
wood
alkyl
amine
treatment
organic anion
Prior art date
Legal status (The legal status 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 status listed.)
Withdrawn
Application number
EP02735172A
Other languages
German (de)
English (en)
Inventor
Joachim Fritschi
Florian Lichtenberg
Hans-Norbert Marx
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Lonza AG
Original Assignee
Lonza AG
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 Lonza AG filed Critical Lonza AG
Priority to EP02735172A priority Critical patent/EP1377417A2/fr
Publication of EP1377417A2 publication Critical patent/EP1377417A2/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K5/00Treating of wood not provided for in groups B27K1/00, B27K3/00
    • B27K5/0085Thermal treatments, i.e. involving chemical modification of wood at temperatures well over 100°C
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34Organic impregnating agents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B27WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
    • B27KPROCESSES, 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
    • B27K3/00Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
    • B27K3/34Organic impregnating agents
    • B27K3/50Mixtures of different organic impregnating agents
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31971Of carbohydrate
    • Y10T428/31989Of wood

Definitions

  • the invention relates to a combined physical-chemical process for the treatment of wood, wood-based materials and wood-like substrates for protection against wood-destroying organisms.
  • Picea alba with low natural resistance in the different hazard classes without the use of chemical wood preservatives can only be realized to an insignificant extent. This also eliminates the possibility of using this technology to simplify the disposal of thermally treated wood compared to conventionally chemically protected ones.
  • the object of the present invention was therefore to provide a method for the protective treatment of wood and wood-based materials based on a heat treatment, but without the disadvantages described.
  • this object is achieved by the method according to claim 1 and the treated woods, wood materials and wood-like substrates obtainable thereby according to claim 5.
  • R 1 and R 4 is C ö _ 24 - alkyl
  • R 2 and R 3 are C 1 _ 24 -alkyl or - (CH 2 ) 3 -NH 2 ,
  • wood-based materials are to be understood in particular as plywood, plywood and glue, chipboard and fibreboard.
  • Wood-like substrates are vegetable products that have a similar composition to wood own, for example bamboo, reeds and materials available from them.
  • C x - y - alkyl here and in the following are to be understood as all linear or branched alkyl groups with x to v carbon atoms, that is to say under C 24 alkyl, for example methyl, ethyl, propyl, isopropyl, butyl, isobutyl, .sec-butyl, tert -Butyl, pentyl, isopentyl, tert-pentyl, neopentyl, hexyl, isohexyl, heptyl, octyl, decyl, dodecyl (lauryl), tetra-decyl (myristyl), hexadecyl (cetyl), octadecyl (stearyl), eicosyl (arachidyl), Docosyl (behenyl) or tetracosyl (lignoceryl).
  • Substituted phenyl is to be understood in particular to mean those phenyl groups which carry one or more identical or different substituents from the group consisting of halogens, Ci- ⁇ -alkyl groups and Ci- ⁇ -alkoxy groups.
  • Monovalent inorganic anions are to be understood in particular as halides such as fluoride, chloride, bromide or iodide, nitrate, hydrogen sulfate and dihydrogen phosphate.
  • Monovalent organic anions are to be understood in particular as the anions of low carboxylic acids such as formate, acetate, propionate or lactate or aliphatic or aromatic sulfonic acids such as methanesulfonate, benzenesulfonate or toluenesulfonate.
  • Polyvalent inorganic anions are understood to mean, for example, sulfate, monohydrogen phosphate or phosphate.
  • Polyvalent organic anions are understood to mean, for example, oxalate, malonate, tartrate, malate, maleinate, fumarate or phthalate.
  • Preferred amines (Ia) are in particular those in which R 1 is C 8 -C 8 alkyl and R 2 and R 3 are methyl or - (CH 2 ) 3 -NH 2 .
  • Preferred amine derivatives Ib are in particular those in which R is C 8 -C 8 -alkyl and R 5 and R 6 are methyl groups.
  • Preferred amine derivatives Ic are especially those in which R 7 is a C 8 _ 18 alkyl group or a benzyl group, R 8 is a C 8 _ ⁇ means 8 alkyl group and R 9 and R 10 are methyl groups or R 7 and R 8 are C 8 _ 8 alkyl groups, R 9 is a methyl group and R 10 is a group of the formula - [(CH 2 ) 2 -O] “H”.
  • the heat treatment can be carried out in a manner known per se, preferably at a temperature of 150 to 220 ° C.
  • the treatment time depends on the dimensions of the parts to be treated and the treatment temperature, it is usually 0.5 to 50 h, preferably 5 to 20 h.
  • the wood can be treated with the amines or amine derivatives by methods known per se, for example by using pressure differences, by diffusion impregnation or by surface treatment.
  • the treatment with amines and / or amine derivatives can follow the thermal treatment or, provided that the amines or amine derivatives in question have sufficient thermal stability and not too high volatility, also before this.
  • the thermal treatment is preferably carried out first.
  • the amine and / or amine derivative or the corresponding salt is preferably used in the form of a 0.1 to 20% solution in water or an organic solvent.
  • an inorganic or organic acid can optionally be added.
  • Suitable organic solvents are, for example, aliphatic or aromatic hydrocarbons such as mineral spirits, paraffin oils, toluene or xylenes or fatty oils, in particular drying oils such as linseed oil.
  • agents for the treatment with amines and / or amine derivatives in the process according to the invention can optionally contain additional active substances and / or auxiliary substances. These include in particular:
  • Insecticides such as, for example, imidacloprid to improve the resistance of the wood treated according to the invention to insects, in particular to termites.
  • Colorants for example dyes and / or pigments, for identifying or decorating the wood treated according to the invention
  • Penetration aids such as glycol derivatives to improve the penetration depth and the distribution of amines or amine derivatives in the wood treated according to the invention.
  • Water repellents such as wax dispersions, oils or silicone derivatives to improve the water-repellent properties of the wood treated according to the invention
  • UV stabilizers such as, for example, micronized titanium oxides, zinc oxides or silica sols or else organic UV protection agents to improve the light and weather resistance of the wood treated according to the invention
  • Binders such as plastic dispersions, drying oils, reactive resin solutions (eg melamine resin condensates) to improve the surface properties (hardness, smoothness, etc.) of the wood treated according to the invention
  • Supplementary biocides such as mold fungicides, molluscicides or other biocides to improve the durability of the wood treated according to the invention under particular stress, such as attack by Teredo navalis ("ship's boring worm") or Limnoria lignorum (drilling needle) in seawater.
  • Teredo navalis (“ship's boring worm") or Limnoria lignorum (drilling needle) in seawater.
  • Drinking solutions were prepared according to the following recipes:
  • Impregnation solution 7 (anhydrous)
  • Impregnation solution 9 (anhydrous)
  • antioxidant 10.0% o dipropylene glycol monomethyl ether
  • Impregnation solution 10 (anhydrous)
  • test specimens were exposed to a vacuum of approx. 1.3 mbar (approx. 1 Torr) for 2 h, in accordance with EN 113, then immersed in the impregnation solution and, after the vacuum was released, left submerged for a further 2 h.
  • the absorption of the soaking solution corresponded approximately to that of spruce wood samples without heat treatment.
  • the test specimens were conditioned (dried) for 4 weeks in accordance with EN 113 and then tested against the following basidiomycetes:
  • Gloeophyllum trabeum Poria placenta (Pp) Coniophora quina (Cp)
  • the test is considered passed (+) if the weight loss of the test specimen is less than 5% or failed (-) if this was 5%> or more.
  • the results are summarized in Table 1 below.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Forests & Forestry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)

Abstract

L'invention concerne un procédé pour le traitement protecteur du bois et de matériaux à base de bois, ainsi que de substrats semblables au bois, consistant en un traitement thermique à 60-250 °C et en un traitement complémentaire avec une amine et/ou un dérivé d'amine correspondant à la formule générale (Ia) ou (Ib), ou bien (Ic). Dans ces formules: R1 et R4 représentent, indépendamment l'un de l'autre, alkyle C¿6?-C24; R?2 et R3¿ représentent, indépendamment l'un de l'autre, alkyle C¿1?-C24 ou bien -(CH2)3-NH2; R?5, R6, R8 et R9¿ représentent, indépendamment l'un de l'autre, alkyle C¿1?-C24; R?7¿ représente alkyle C¿6?-C24 ou bien benzyle; R?10¿ représente alkyle C¿1?-C24 ou bien -[CH2)2-O]nR?11¿ où n = 1-20; R11 représente hydrogène ou phényle éventuellement substitué; et X représente un anion monovalent inorganique ou organique ou bien un équivalent d'un anion multivalent inorganique ou organique. Ledit traitement complémentaire peut être effectué avec un sel correspondant de ladite amine et/ou dudit dérivé d'amine. Les bois traités selon ce procédé présentent une bonne résistance également vis-à-vis des organismes nocifs qui ne peuvent pas être neuralisés de façon fiable avec seulement un traitement thermique. Ce procédé est mis en oeuvre sans composés contenant des métaux lourd et les bois ainsi traités ne créent aucune nuisance pour l'environnement, que ce soit pendant leur utilisation ou pendant leur élimination.
EP02735172A 2001-04-03 2002-03-25 Procede de traitement protecteur pour le bois et des materiaux a base de bois Withdrawn EP1377417A2 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP02735172A EP1377417A2 (fr) 2001-04-03 2002-03-25 Procede de traitement protecteur pour le bois et des materiaux a base de bois

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP01108389 2001-04-03
EP01108389 2001-04-03
PCT/EP2002/003308 WO2002081159A2 (fr) 2001-04-03 2002-03-25 Procede de traitement protecteur pour le bois et des materiaux a base de bois
EP02735172A EP1377417A2 (fr) 2001-04-03 2002-03-25 Procede de traitement protecteur pour le bois et des materiaux a base de bois

Publications (1)

Publication Number Publication Date
EP1377417A2 true EP1377417A2 (fr) 2004-01-07

Family

ID=8177037

Family Applications (1)

Application Number Title Priority Date Filing Date
EP02735172A Withdrawn EP1377417A2 (fr) 2001-04-03 2002-03-25 Procede de traitement protecteur pour le bois et des materiaux a base de bois

Country Status (4)

Country Link
US (1) US20040146733A1 (fr)
EP (1) EP1377417A2 (fr)
AU (1) AU2002310982A1 (fr)
WO (1) WO2002081159A2 (fr)

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FI118958B (fi) * 2003-07-25 2008-05-30 Stora Enso Oyj Lämpömodifioidun puun käsittely
DE202004009957U1 (de) * 2004-06-24 2005-11-03 F.W. Barth & Co. Gmbh Holzprodukt für den Außenbau
US20070167407A1 (en) * 2005-12-20 2007-07-19 Albemarle Corporation Quaternary ammonium borate compositions and substrate preservative solutions containing them
US20070148431A1 (en) * 2005-12-20 2007-06-28 Albemarle Corporation Quaternary ammonium compounds with novel mode of action for protection of wood structures
US20070155840A1 (en) * 2005-12-20 2007-07-05 Albemarle Corporation Use of quaternary ammonium compounds in the prevention of mold, mildew, and funguses in new and/or existing construction
US20080063723A1 (en) * 2006-09-08 2008-03-13 Sungmee Choi Isothiazolin-3-one-containing antimicrobial composition
CL2007003181A1 (es) * 2006-11-03 2008-05-23 Albemarle Corp Metodo de control de microorganismos que comprende aplicar un compuesto de amonio cuaternario a por lo menos un articulo de construccion.
CN102480934B (zh) * 2007-06-28 2014-04-16 巴斯夫公司 用经热处理的木料监测和控制白蚁的方法
WO2009158316A1 (fr) * 2008-06-27 2009-12-30 Whitmire Micro-Gen Research Laboratories, Inc. Bois traité thermiquement et procédé de traitement anti-insectes faisant appel audit bois
DE102010050788A1 (de) 2010-11-10 2012-05-10 FR. LÜRSSEN WERFT GmbH & Co.KG Verfahren zur Behandlung von Holz und Holzwerkstoffen sowie damit erhältliches Holz und Holzwerkstoffe
US10745587B1 (en) * 2017-03-29 2020-08-18 Psg-Functional Materials Llc Water-repellant wax compositions and applications thereof
CN110076868A (zh) * 2019-05-29 2019-08-02 南京林业大学 一种木材、竹材热处理-防霉协同改性方法

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US4357163A (en) * 1980-08-11 1982-11-02 Reichhold Chemicals, Inc. Water soluble pentachlorophenol and tetrachlorophenol wood treating systems containing fatty acid amine oxides
US4382105A (en) * 1981-08-28 1983-05-03 Reichhold Chemicals, Incorporated Water soluble pentachlorophenol and tetrachlorophenol wood treating systems containing fatty acid amine oxides
US4379810A (en) * 1981-08-28 1983-04-12 Reichhold Chemicals, Incorporated Water soluble pentachlorophenol and tetrachlorophenol wood treating systems containing fatty acid amine oxides
FR2626740B1 (fr) * 1988-02-08 1990-10-19 Xylochimie Concentres emulsionnables de matieres biocides, les microemulsions aqueuses obtenues et l'application de ces microemulsions au traitement du bois
DE3934935A1 (de) * 1989-10-20 1991-04-25 Wolman Gmbh Dr Polymere stickstoffverbindungen enthaltende holzschutzmittel
DE3937658A1 (de) * 1989-11-11 1991-05-16 Wolman Gmbh Dr Holzschutzmittel
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US5438034A (en) * 1993-06-09 1995-08-01 Lonza, Inc. Quaternary ammonium carbonate compositions and preparation thereof
US5641726A (en) * 1993-06-09 1997-06-24 Lonza, Inc. Quaternary ammonium carboxylate and borate compositions and preparation thereof
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WO1999039886A1 (fr) * 1998-02-06 1999-08-12 Lonza Ag Produit de preservation du bois
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US6348089B1 (en) * 1998-07-12 2002-02-19 Lonza Ag Compositions and process for the protective treatment of wood
MY130072A (en) * 1999-05-24 2007-05-31 Lonza Ag Amine oxide/iodine containing blends for wood preservation
PT1185401E (pt) * 1999-05-24 2006-08-31 Lonza Ag Conservantes de madeira de isotiazolona/oxido de amina

Non-Patent Citations (1)

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Also Published As

Publication number Publication date
AU2002310982A1 (en) 2002-10-21
WO2002081159A8 (fr) 2005-03-17
WO2002081159A2 (fr) 2002-10-17
WO2002081159A3 (fr) 2003-01-09
US20040146733A1 (en) 2004-07-29

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