JPH01182002A - Manufacture of modified timber - Google Patents
Manufacture of modified timberInfo
- Publication number
- JPH01182002A JPH01182002A JP659688A JP659688A JPH01182002A JP H01182002 A JPH01182002 A JP H01182002A JP 659688 A JP659688 A JP 659688A JP 659688 A JP659688 A JP 659688A JP H01182002 A JPH01182002 A JP H01182002A
- Authority
- JP
- Japan
- Prior art keywords
- wood
- water
- acid
- alcohol
- treatment liquid
- 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.)
- Pending
Links
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 9
- 238000011282 treatment Methods 0.000 claims abstract description 35
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000010438 heat treatment Methods 0.000 claims abstract description 10
- 239000002023 wood Substances 0.000 claims description 96
- 239000007788 liquid Substances 0.000 claims description 25
- 150000007519 polyprotic acids Polymers 0.000 claims description 19
- 229920001187 thermosetting polymer Polymers 0.000 claims description 12
- 150000005846 sugar alcohols Polymers 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 6
- 238000002156 mixing Methods 0.000 claims description 5
- 238000005470 impregnation Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 abstract description 18
- 239000000463 material Substances 0.000 abstract description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 abstract description 8
- 229920005610 lignin Polymers 0.000 abstract description 7
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract description 5
- 239000002253 acid Substances 0.000 abstract description 4
- 235000011187 glycerol Nutrition 0.000 abstract description 4
- 235000007173 Abies balsamea Nutrition 0.000 abstract description 2
- 241000218685 Tsuga Species 0.000 abstract description 2
- 238000005336 cracking Methods 0.000 abstract 1
- 238000013007 heat curing Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000008065 acid anhydrides Chemical class 0.000 description 12
- 239000002904 solvent Substances 0.000 description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 238000005886 esterification reaction Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000005299 abrasion Methods 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 4
- 239000002932 luster Substances 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000005056 compaction Methods 0.000 description 3
- 238000007596 consolidation process Methods 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000003825 pressing Methods 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- CYIDZMCFTVVTJO-UHFFFAOYSA-N pyromellitic acid Chemical compound OC(=O)C1=CC(C(O)=O)=C(C(O)=O)C=C1C(O)=O CYIDZMCFTVVTJO-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 238000003797 solvolysis reaction Methods 0.000 description 2
- 241000894007 species Species 0.000 description 2
- ARCGXLSVLAOJQL-UHFFFAOYSA-N trimellitic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C(C(O)=O)=C1 ARCGXLSVLAOJQL-UHFFFAOYSA-N 0.000 description 2
- MUTGBJKUEZFXGO-OLQVQODUSA-N (3as,7ar)-3a,4,5,6,7,7a-hexahydro-2-benzofuran-1,3-dione Chemical compound C1CCC[C@@H]2C(=O)OC(=O)[C@@H]21 MUTGBJKUEZFXGO-OLQVQODUSA-N 0.000 description 1
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- CCFAGRVEHSCROQ-UHFFFAOYSA-N 1-phenylpropane-1,2,3-triol Chemical compound OCC(O)C(O)C1=CC=CC=C1 CCFAGRVEHSCROQ-UHFFFAOYSA-N 0.000 description 1
- FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical compound ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 description 1
- MWSKJDNQKGCKPA-UHFFFAOYSA-N 6-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1CC(C)=CC2C(=O)OC(=O)C12 MWSKJDNQKGCKPA-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- 241001673272 Tsuga diversifolia Species 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
- 229940018557 citraconic acid Drugs 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- ANSXAPJVJOKRDJ-UHFFFAOYSA-N furo[3,4-f][2]benzofuran-1,3,5,7-tetrone Chemical compound C1=C2C(=O)OC(=O)C2=CC2=C1C(=O)OC2=O ANSXAPJVJOKRDJ-UHFFFAOYSA-N 0.000 description 1
- 238000007731 hot pressing Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野]
本発明は木材を化学的に改質すると同時に圧密化して木
材に新規に冨んだ化粧性を付与することのできる改質木
材の製造方法に関するものである。[Detailed Description of the Invention] [Industrial Application Field] The present invention provides a method for producing modified wood that can chemically modify wood and at the same time compact it to impart new rich cosmetic properties to the wood. It is related to.
従来から、木材の天然木目を緻密化する方法としては、
木材に水分を含浸させて木材全体を膨潤させたのち、加
圧すると共に乾燥、固化させる方法が採用されている。Traditionally, the methods for densifying the natural grain of wood are:
The method used is to impregnate wood with water to swell the entire wood, then pressurize it, dry it, and solidify it.
しかしながら、この方法によれば、水分により膨潤した
木材を単に物理的に圧縮変形させて固定するものである
から、水分を吸収すると復元することになり、形状の安
定化に劣ると共に木目を緻密化するだけであるから透明
感や光沢等に何らの変化がなく、化粧性に乏しいもので
あった。However, this method simply physically compresses and deforms the wood that has swollen due to moisture and fixes it, so it will return to its original shape once it absorbs moisture, resulting in poor shape stability and a dense wood grain. Since it is only a cosmetic, there is no change in transparency, gloss, etc., and the cosmetic properties are poor.
このため、本願出願人等は、特公昭62−47686号
公報に記載しているように、木材を化学的に処理する方
法を開発した。For this reason, the applicants of the present application have developed a method of chemically treating wood, as described in Japanese Patent Publication No. 62-47686.
この方法は、木材薄板を木材成分中の水酸基と反応し得
る反応体で処理して木材成分を非晶化したのち、加熱圧
締することにより、透明性、耐摩耗性、耐クラツク性に
富んだ木材薄板に変化させるものである。In this method, thin wood boards are treated with a reactant that can react with the hydroxyl groups in the wood components to amorphize the wood components, and then heat-pressed to improve transparency, abrasion resistance, and crack resistance. It is used to transform wood into thin boards.
[発明が解決しようとする課題]
しかしながらこの方法によれば、木材薄板をエステル化
剤やエーテル化剤などの木材成分中の水酸基と反応し得
る反応体によってセルロースを非晶化する段階と、この
ように化学的な処理を施した木材薄板を加熱加圧する段
階とを必要とし、特に、化学的処理に長時間を要して生
産性が悪いものであり、さらに、エステル化剤などの反
応体と木材成分との反応を促進させるためには硫酸、過
塩素酸等の触媒を必要として処理が煩雑化するばかりで
なく、エステル化剤として有機酸無水物を使用した場合
には、木材成分の水酸基等が反応すると副生物質が材中
に残存して洗滌、乾燥処理を要する等の生産上の問題点
があった。[Problems to be Solved by the Invention] However, according to this method, the steps of amorphizing the cellulose in the wood thin plate using a reactant capable of reacting with the hydroxyl groups in the wood components, such as an esterifying agent or an etherifying agent, and This process requires a step of heating and pressurizing the chemically treated thin wood board, which is particularly time-consuming and has poor productivity. In order to accelerate the reaction between wood and wood components, catalysts such as sulfuric acid and perchloric acid are required, which not only complicates the process, but also causes the reaction of wood components to occur when organic acid anhydrides are used as esterifying agents. When hydroxyl groups and the like react, by-products remain in the material, resulting in production problems such as the need for washing and drying treatments.
本発明は木材の化学修飾と圧密化処理を同時に行って木
材を容易に塑性変形させると共に透明性や光沢の付与、
及び耐摩耗性、耐クラツク性の向上を目的とした改質木
材の製造方法を提供するものである。The present invention simultaneously chemically modifies wood and consolidates it to easily plastically deform the wood, impart transparency and luster,
The present invention also provides a method for producing modified wood for the purpose of improving wear resistance and crack resistance.
上記目的を達成するために、本発明の改質木材の製造方
法においては、水又はアルコールに多塩基酸と多価アル
コールを混合してなる処理液を木材板状物に含浸させ、
この木材板状物を含浸処理液による湿潤状態のま\加熱
加圧して生成した熱硬化性物質を硬化させることを特徴
とするものである。In order to achieve the above object, in the method for producing modified wood of the present invention, a wood board is impregnated with a treatment liquid prepared by mixing a polybasic acid and a polyhydric alcohol with water or alcohol,
The method is characterized in that the wood board-like material is heated and pressurized while it is wet with an impregnating treatment solution to harden the thermosetting material produced.
処理液は水又はアルコール溶媒であるから、親水性であ
る木材との親和性に富んで木材中の微細空隙まで容易に
浸透し、木材成分中の水酸基等の活性基と接触する。Since the treatment liquid is a water or alcohol solvent, it has a high affinity with the hydrophilic wood, easily penetrating into the microscopic voids in the wood, and coming into contact with active groups such as hydroxyl groups in the wood components.
この状態で木材を加熱加圧すると、上記処理液中の多塩
基酸が酸無水物と水とに分解し、酸無水物が木材成分中
の活性基とエステル化反応し、可塑化すると共に多価ア
ルコールと架橋して木材内で熱硬化性物質を生成し、木
材が圧密化された状態で固定する。When the wood is heated and pressurized in this state, the polybasic acid in the treatment liquid decomposes into acid anhydride and water, and the acid anhydride undergoes an esterification reaction with the active groups in the wood components, resulting in plasticization and polybasic acid. It crosslinks with alcohol to create a thermosetting substance within the wood, which fixes the wood in a compacted state.
この際、多塩基酸の酸無水物が木材成分中の活性基とエ
ステル化反応する時に木材成分のリグニン等が酸性高温
下におけるソルボリシスにより低分子化して流動を生じ
る。その結果、木目が流れて摺曲したようになり、加熱
加圧前とは異なった新規な木目模様に変化すると共に木
材の空隙中に上記低分子化したリグニンと上記熱硬化性
物質とが浸入した状態で固化して透明感が増し、深みと
光沢を有する緻密な層が形成され、耐摩耗性、耐クラツ
ク性及び撥水性が向上するものである。At this time, when the acid anhydride of the polybasic acid undergoes an esterification reaction with the active group in the wood component, the lignin and the like in the wood component are reduced in molecular weight by solvolysis under acidic and high temperature conditions, resulting in fluidity. As a result, the wood grain appears to flow and curve, changing to a new wood grain pattern different from that before heating and pressing, and at the same time, the low-molecular lignin and the thermosetting substance infiltrate into the voids of the wood. When it solidifies, it becomes more transparent, forms a dense layer with depth and luster, and improves abrasion resistance, crack resistance, and water repellency.
本発明の実施例を詳述すると、水又はアルコールに多塩
基酸と多価アルコールを混合してなる処理液を木材板状
物に含浸させる工程と、この木材板状物を含浸処理液に
よる湿潤状態のま\加熱加圧して処理液の反応と同時に
木材板状物を圧密化する工程とからなるものであり、改
質される木材板状物としては挽板、単板などの薄板が適
するが比較的厚みを有する板状物、或いはブロック体で
あってもよい。To explain in detail the embodiments of the present invention, the process includes a step of impregnating a wood board with a treatment liquid made by mixing a polybasic acid and a polyhydric alcohol with water or alcohol, and moistening the wood board with the impregnation treatment liquid. It consists of the process of heating and pressurizing the wood board while it is in a state to react with the treatment liquid and simultaneously compacting the wood board. Thin boards such as sawn boards and veneers are suitable for the wood board to be modified. It may be a plate-like object or a block object having a relatively thick thickness.
又、処理液としての多塩基酸は、マレイン酸、フマル酸
、コハク酸、フタル酸、イソフタル酸、テレフタル酸、
トリメリット酸、ピロメリット酸、シトラコン酸、エチ
レン酸等が使用され、又、無水マレイン酸、無水コハク
酸、無水フタル酸、無水ピロメリット酸、テトラヒドロ
無水フタル酸、メチルテトラヒドロ無水フタル酸、メチ
ルへキサヒドロ無水フタル酸などの多塩基酸無水物に水
又はアルコールを反応させて多塩基酸としたものを使用
してもよい。In addition, the polybasic acids used as the treatment liquid include maleic acid, fumaric acid, succinic acid, phthalic acid, isophthalic acid, terephthalic acid,
Trimellitic acid, pyromellitic acid, citraconic acid, ethylene acid, etc. are used, and also maleic anhydride, succinic anhydride, phthalic anhydride, pyromellitic anhydride, tetrahydrophthalic anhydride, methyltetrahydrophthalic anhydride, methyl A polybasic acid obtained by reacting a polybasic acid anhydride such as hexahydrophthalic anhydride with water or alcohol may also be used.
多価アルコールとしては、プロピレングリコール、エチ
レングリコール、ブタンジオール、ジエチレングリコー
ル、ジプロピレングリコール、エチレンジオール、ペン
タジオール、トリメチレングリコール、グリセリン、ト
リメチロールプロパン、ペンタエリスリトール、フェニ
ルグリセリン等がある。Examples of polyhydric alcohols include propylene glycol, ethylene glycol, butanediol, diethylene glycol, dipropylene glycol, ethylenediol, pentadiol, trimethylene glycol, glycerin, trimethylolpropane, pentaerythritol, and phenylglycerin.
処理液の調製は、水又はアルコールに多塩基酸(多塩基
酸無水物の場合には水又はアルコールを反応させて多塩
基酸とする)と多価アルコールを混合することによって
行われるものであり、溶媒である水に溶解可能な組合わ
せを適宜選択して使用するのが好ましいが、水に溶けな
い場合にはアルコールを使用して溶解させる。The treatment liquid is prepared by mixing water or alcohol with a polybasic acid (in the case of polybasic acid anhydride, water or alcohol is reacted to form the polybasic acid) and polyhydric alcohol. It is preferable to appropriately select and use a combination that is soluble in water, which is a solvent, but if it is not soluble in water, alcohol is used to dissolve it.
水板外のアルコールを溶媒として使用することはコスト
面で不利であるが、水に不溶、難溶の多塩基酸であって
も、木材と又は木材中で充分に反応できる高濃度の反応
溶液を作成することができる利点がある。同様なことは
多価アルコールについてもいえることができ、水に不溶
のものでも溶媒にアルコールを使用すれば溶解するので
、木材板状物に容易に注入、含浸させることができる。Although it is disadvantageous in terms of cost to use alcohol other than water as a solvent, it is a highly concentrated reaction solution that can sufficiently react with or in wood, even with polybasic acids that are insoluble or poorly soluble in water. It has the advantage of being able to create The same can be said of polyhydric alcohols; even polyhydric alcohols that are insoluble in water can be dissolved by using alcohol as a solvent, so they can be easily injected and impregnated into wood planks.
木材板状物に対する処理液の注入方法としては木材の樹
種、板厚等によって、処理液を木材板状物に塗布する方
法、処理液中に木材板状物を浸漬する方法、或いは減圧
下、加圧下又は減圧加圧法を適宜採用すればよいが、木
材板状物の内部にまで処理液を充分含浸させなければ、
効果が低減するため、減圧・加圧法によって注入するこ
とが望ましい。The method of injecting the treatment liquid into the wood plate depends on the species of wood, the thickness of the wood, etc., and there are two methods: applying the treatment liquid to the wood plate, immersing the wood plate in the treatment liquid, or under reduced pressure. Pressurized or reduced pressure methods may be used as appropriate, but if the treatment solution is not sufficiently impregnated into the interior of the wood board,
Since the effect is reduced, it is preferable to inject by the pressure reduction/pressure method.
なお、減圧・加圧注入の場合には、溶解度や融点、溶媒
の沸点などの関係で注入が困難な場合が生じるので、溶
媒や溶質の組み合わせを適宜に考慮する必要がある。In the case of reduced pressure/pressure injection, injection may be difficult due to the solubility, melting point, boiling point of the solvent, etc., so it is necessary to appropriately consider the combination of solvents and solutes.
こうして内部にまで処理液を注入含浸した木材板状物は
、木材成分中の水酸基等の活性基と処理液とが接触した
湿潤状態のま\加熱加圧処理を行う。The wood plate material into which the treatment liquid has been injected and impregnated is subjected to heating and pressure treatment while in a wet state in which active groups such as hydroxyl groups in the wood components are in contact with the treatment liquid.
この時の加熱温度は100〜250°C1好ましくは1
40〜210°Cであり、圧力や処理時間は樹種や木材
板状物の厚みによって変更されるが、圧力は数10kg
/c+It以上、処理時間は数分〜数時間、好ましくは
5分〜120分に設定する。The heating temperature at this time is 100 to 250°C, preferably 1
The temperature is 40 to 210°C, and the pressure and processing time vary depending on the tree species and the thickness of the wood board, but the pressure is several tens of kg.
/c+It or more, the processing time is set to several minutes to several hours, preferably 5 minutes to 120 minutes.
このように処理液を含浸した木材板状物を加熱加圧処理
すると、処理液中の多塩基酸が酸無水物と水とに分解し
、酸無水物が木材成分中の活性基とエステル化反応し、
可塑化して変形し得る状態となる。When a wood board impregnated with the treatment liquid is treated under heat and pressure, the polybasic acid in the treatment liquid decomposes into acid anhydride and water, and the acid anhydride esterifies with the active groups in the wood components. react,
It becomes plasticized and becomes deformable.
この時、通常、多塩基酸は酸無水物と水に分解するには
常圧において高温下で反応させる必要があるが、木材内
において高圧状態で行われるため、分解反応温度以下の
加熱温度でも分解が可能である。At this time, polybasic acids usually need to be reacted at normal pressure and high temperature in order to decompose into acid anhydrides and water, but since the reaction is carried out under high pressure inside the wood, even heating temperatures below the decomposition reaction temperature can be used. Decomposition is possible.
多塩基酸の酸無水物が木材成分中の活性基とエステル化
反応する時に木材成分のリグニン等が酸性高温下におけ
るソルボリシスにより低分子化して流動を生じる。その
結果、木目が流れて摺曲したようになり、加熱加圧前と
は異なった新規な木自模様に変化した状態で前記熱硬化
性物質により固定される。この塑性変形は木材板状物の
圧密化の程度によって異なり、圧力を大きくすると、木
材の空隙中に侵入する熱硬化性物質が多くなり、透明性
が増大すると共に緻密化することができる。When the acid anhydride of a polybasic acid undergoes an esterification reaction with the active group in the wood component, the lignin, etc. in the wood component is reduced in molecular weight by solvolysis under acidic and high temperature conditions, resulting in fluidity. As a result, the wood grain appears to flow and curve, and the wood is fixed by the thermosetting substance in a state where it has changed into a new natural wood pattern different from that before heating and pressing. This plastic deformation varies depending on the degree of compaction of the wood board; the higher the pressure, the more thermosetting material will penetrate into the voids of the wood, which can increase transparency and densification.
その透明性を付与する上記生成熱硬化性樹脂分は溶媒で
ある水の配合割合を多くすると希薄となってリグニン等
の流動性が低下し、材色が淡色化する傾向を示すように
なる。The generated thermosetting resin component, which imparts transparency, becomes diluted when the proportion of water as a solvent is increased, resulting in a decrease in the fluidity of lignin, etc., and a tendency for the color of the material to become lighter.
例えば、厚みが1.5mmのベイツガ単板の場合にその
板厚の172程度にまで圧密化を行えば、摺曲した木目
模様が得られる。For example, if a hemlock veneer with a thickness of 1.5 mm is consolidated to about 172 mm thick, a curved wood grain pattern can be obtained.
なお、木材板状物に処理液を含浸させたのち、圧密処理
前に非圧締状態で数分〜数10分子備加熱を行っておけ
ば均一な圧密化が容易となるものである。又、熱圧によ
り水等の溶媒が抜ける際に、木質板状物に割れやピンホ
ール、反りを生じる場合は、熱圧と脱気を組合せたりク
ツション材を介することで防止する。In addition, after impregnating the wood plate with the treatment liquid, uniform compaction can be facilitated by preheating for several minutes to several tens of molecules in an uncompacted state before consolidation treatment. In addition, if cracks, pinholes, or warpage occur in the wooden plate when solvents such as water escape due to heat pressure, this can be prevented by combining heat pressure and deaeration or by using a cushioning material.
このように、処理液を含浸した木材板状物の圧密化を行
うと、上述したように、木材成分中の水酸基等の活性基
と多塩基酸の酸無水物とがエステル化反応すると同時に
多価アルコールと架橋して木材内で木材成分と化学結合
した熱硬化性樹脂が生成され、木材の空隙中にこの熱硬
化性物質が浸入した状態で固化して透明感が増した深み
と光沢を有する緻密な層が形成される。In this way, when a wood board impregnated with a treatment solution is compacted, as described above, active groups such as hydroxyl groups in the wood components and acid anhydrides of polybasic acids undergo an esterification reaction and, at the same time, polybasic acids. A thermosetting resin is produced that crosslinks with the alcohol and chemically bonds with the wood components within the wood, and this thermosetting resin solidifies while penetrating into the voids of the wood, giving it depth and luster with increased transparency. A dense layer is formed.
この処理において、圧力や温度を高くし、処理時間を多
くすると、上記木目の流動性や透明性が一層高められて
プラスチック状の外観を呈するようになり、木材の秋材
部分が濃く、春材部分が淡い特殊な外観が得られるもの
である。In this process, if the pressure and temperature are increased and the treatment time is increased, the fluidity and transparency of the wood grain will be further enhanced, resulting in a plastic-like appearance, and the autumn wood will become darker and the spring wood will become darker. It gives a special appearance with pale parts.
次に本発明の具体的な実施例を示す。Next, specific examples of the present invention will be shown.
実施例1
無水マレイン酸:グリセリン:水−2:1:2(重量比
)の割合で混合してなる処理液を1.5(厚さ)X10
0(幅)X100(長さ)のベイツガ単板に減圧・加圧
法によって注入した。Example 1 A treatment liquid prepared by mixing maleic anhydride: glycerin: water in a ratio of 2:1:2 (weight ratio) was 1.5 (thickness) x 10
It was injected into a Japanese hemlock veneer measuring 0 (width) x 100 (length) by the vacuum/pressure method.
この処理液注入単板を温度170°Cで非圧締状態下で
5分間、予備加熱したのち、上下熱器間に挿大して圧力
50kg/cIN、温度210°Cで100分間熱圧し
て1/2厚程度によって圧密化を行った。After preheating this treatment liquid-injected veneer for 5 minutes at a temperature of 170°C in an unpressed state, it was inserted between the upper and lower heaters and hot-pressed at a pressure of 50 kg/cIN and a temperature of 210°C for 100 minutes. Consolidation was performed with a thickness of about 2.
この結果、単板の木目が摺曲模様を呈すると共。As a result, the wood grain of the veneer exhibits a curved pattern.
に一部が透明化された意匠性に冨んだ硬質単板が得られ
た。A hard veneer with a rich design and partially transparent was obtained.
さらにこの硬質単板は、表面が緻密な平滑面を呈すると
共に耐摩耗性に富み、その上、水中に浸漬しても殆どス
プリングバックが生じない等の寸法安定性に優れたもの
であった。Furthermore, this hard veneer had a dense and smooth surface, was highly abrasion resistant, and had excellent dimensional stability with almost no springback even when immersed in water.
実施例2
上記実施例1と同じ処理によって得られた処理液注入単
板を温度210°Cで非圧締状態下で5〜10分間予備
加熱したのち、圧力300 kg / cf、温度21
0°Cで30分間熱圧して圧密化を行った。Example 2 A treatment liquid-injected veneer obtained by the same treatment as in Example 1 above was preheated at a temperature of 210°C for 5 to 10 minutes in an unpressed state, and then heated at a pressure of 300 kg/cf and a temperature of 21°C.
Consolidation was performed by hot pressing at 0°C for 30 minutes.
この結果、全体が透明性を有すると共に木目の流れ模様
を有する化粧性に冨んだシート状の硬化単板が得られた
。As a result, a sheet-like cured veneer was obtained which was entirely transparent and had a flow pattern of wood grain and was rich in cosmetic properties.
このように、処理圧を大きくすることによって透明性を
向上させることができるものである。In this way, transparency can be improved by increasing the processing pressure.
なお、上記処理液を注入したのち予備加熱処理を施した
だけの単板でも赤外線吸収スペクトル分析を行ったとこ
ろ、木材へのカルボキシル基の化学修飾が認められた。Furthermore, when infrared absorption spectroscopy was performed on a veneer that had only been preheated after being injected with the above-mentioned treatment solution, chemical modification of carboxyl groups to the wood was observed.
従って、処理液注入単板が加熱圧締していく段階では、
木材内部においてマレイン酸が無水マレイン酸と水とに
分解し、生じた無水マレイン酸が木材と容易にエステル
化反応を起こすと共にグリセリンとの架橋反応を起こし
ているものと思われる。Therefore, at the stage when the treatment liquid injected veneer is heated and pressed,
It is thought that maleic acid decomposes into maleic anhydride and water inside the wood, and the resulting maleic anhydride easily causes an esterification reaction with the wood and also causes a crosslinking reaction with glycerin.
(発明の効果]
以上のように本発明における改質木材の製造方法によれ
ば、使用する処理液は水又はアルコール溶媒であるから
、親水性である木材との親和性に冨んで木材中の微細空
隙まで容易に浸透し、木材成分中の水酸基等の活性基と
良好に接触させることができるものであり、この処理液
含浸木材板状物を加熱加圧すると、上記処理液中の多塩
基酸が酸無水物と水とに分解し、酸無水物が木材成分中
の活性基とエステル化反応して可塑化すると同時に多価
アルコールと架橋して木材内で木材成分と−11=
結合した熱硬化性物質を生成し、木材板状物を圧密化さ
れた状態で固定させることができる。(Effect of the invention) As described above, according to the method for producing modified wood according to the present invention, since the treatment liquid used is water or an alcohol solvent, it has a high affinity with the hydrophilic wood. It easily penetrates into microscopic voids and can be brought into good contact with active groups such as hydroxyl groups in wood components, and when a wood board impregnated with this treatment liquid is heated and pressurized, the polybasic acid in the treatment liquid is removed. The acid decomposes into acid anhydride and water, and the acid anhydride undergoes an esterification reaction with the active group in the wood component to plasticize it, and at the same time crosslinks with the polyhydric alcohol and bonds to the wood component within the wood. A thermosetting material can be produced to fix the wood slab in a compacted state.
さらに、この圧密化時に木材成分のリグニンが低分子化
して流動を生じ、その結果、木目が摺曲したように流れ
て加熱加圧前とは異なった新規な木目模様に変化させる
ことができると共に木材の空隙中に低分子化したリグニ
ンと上記熱硬化性物質が浸入した状態で固化して透明感
が増し、深みと光沢を有する緻密な層を形成することが
でき、耐摩耗性、耐クラツク性及び撥水性が向上した改
質された木材が得られるものである。Furthermore, during this compaction, the lignin, a wood component, becomes lower in molecular weight and flows, and as a result, the wood grain flows as if it were sliding, making it possible to change to a new wood grain pattern different from that before heating and pressing. Low-molecular lignin and the above thermosetting substances penetrate into the voids of the wood and solidify, increasing transparency and forming a dense layer with depth and luster, making it resistant to abrasion and cracks. Modified wood with improved properties and water repellency can be obtained.
又、上記熱硬化性物質は、木材成分と化学的に結合した
樹脂であるから、木材と強固に一体化しており、水等に
浸漬しても殆ど変形せず、優れた寸法安定性を発揮する
ものである。In addition, since the above thermosetting substance is a resin chemically bonded to wood components, it is strongly integrated with the wood, hardly deforming even when immersed in water, etc., and exhibits excellent dimensional stability. It is something to do.
Claims (1)
を混合してなる処理液を木材板状物に含浸させ、この木
材板状物を含浸処理液による湿潤状態のまゝ加熱加圧し
、生成する熱硬化性物質を硬化させることを特徴とする
改質木材の製造方法。(1) Impregnating a wood plate with a treatment liquid made by mixing polybasic acid and polyhydric alcohol with water or alcohol, heating and pressurizing the wood plate while moistened with the impregnation treatment liquid, A method for producing modified wood, characterized by curing a thermosetting substance produced.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP659688A JPH01182002A (en) | 1988-01-14 | 1988-01-14 | Manufacture of modified timber |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP659688A JPH01182002A (en) | 1988-01-14 | 1988-01-14 | Manufacture of modified timber |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01182002A true JPH01182002A (en) | 1989-07-19 |
Family
ID=11642710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP659688A Pending JPH01182002A (en) | 1988-01-14 | 1988-01-14 | Manufacture of modified timber |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01182002A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999065615A1 (en) * | 1998-06-17 | 1999-12-23 | Coating Development Group, Inc. | Method for pressure treating wood |
US6426118B2 (en) * | 1998-06-17 | 2002-07-30 | Coating Development Group, Inc. | Method for pressure treating wood |
JP2005533689A (en) * | 2002-07-26 | 2005-11-10 | ウッド ポリマー テクノロジーズ エーエスエー | Furan polymer impregnated wood |
JP2009298132A (en) * | 2008-06-12 | 2009-12-24 | Kono Shinsozai Kaihatsu Kk | Improved lumber and method of manufacturing the same |
JP2018051837A (en) * | 2016-09-27 | 2018-04-05 | パナソニックIpマネジメント株式会社 | Method for producing modified wood |
-
1988
- 1988-01-14 JP JP659688A patent/JPH01182002A/en active Pending
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1999065615A1 (en) * | 1998-06-17 | 1999-12-23 | Coating Development Group, Inc. | Method for pressure treating wood |
US6235346B1 (en) * | 1998-06-17 | 2001-05-22 | Coating Development Group, Inc. | Method for pressure treating wood |
US6426118B2 (en) * | 1998-06-17 | 2002-07-30 | Coating Development Group, Inc. | Method for pressure treating wood |
WO2002098578A1 (en) * | 2001-05-21 | 2002-12-12 | Coating Development Group, Inc. | Method for pressure treating wood |
JP2005533689A (en) * | 2002-07-26 | 2005-11-10 | ウッド ポリマー テクノロジーズ エーエスエー | Furan polymer impregnated wood |
JP2009298132A (en) * | 2008-06-12 | 2009-12-24 | Kono Shinsozai Kaihatsu Kk | Improved lumber and method of manufacturing the same |
JP2018051837A (en) * | 2016-09-27 | 2018-04-05 | パナソニックIpマネジメント株式会社 | Method for producing modified wood |
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