JPH01200903A - Method for modifying wood - Google Patents
Method for modifying woodInfo
- Publication number
- JPH01200903A JPH01200903A JP2550388A JP2550388A JPH01200903A JP H01200903 A JPH01200903 A JP H01200903A JP 2550388 A JP2550388 A JP 2550388A JP 2550388 A JP2550388 A JP 2550388A JP H01200903 A JPH01200903 A JP H01200903A
- Authority
- JP
- Japan
- Prior art keywords
- wood
- swelling
- etherification
- water
- amine
- 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.)
- Granted
Links
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)
本発明は木材の改質方法に関し、特に木材中の水酸基を
エーテル化剤によりエーテル化する木材の改質方法に関
する。DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for modifying wood, and more particularly to a method for modifying wood by etherifying hydroxyl groups in wood using an etherifying agent.
〈従来技術)
木材は、他の材料に比較して比強度が大であり弾性に冨
み良接着性である上易加工性でもあることから、各種建
築用材、家具用材等広範囲の用途に使用されている反面
、不均質性、腐朽性、吸湿性等があり、それらに伴う変
形等を避けることができないという致命的な欠点を有し
ている。このような木材の本質的な欠点を改善するため
に従来から種々の材質改良法について検討が行われて来
たが、中でも木材を種々のアルカリ性化合物で処理した
後エーテル化する方法は、木材の吸湿性に伴う変形を減
少せしめると同時に腐朽性の改善に寄与するという利点
を有することから、木材の材質改良方法として注目され
ている。(Prior art) Wood has a high specific strength compared to other materials, is highly elastic, has good adhesive properties, and is easy to process, so it is used in a wide range of applications such as various construction materials and furniture materials. On the other hand, it has the fatal disadvantage of being non-uniform, rotting, hygroscopic, etc., and the accompanying deformation cannot be avoided. Various methods for improving the quality of wood have been investigated in order to improve the inherent disadvantages of wood, but among them, the method of treating wood with various alkaline compounds and then etherifying it is a method that improves the quality of wood. It is attracting attention as a method for improving the quality of wood because it has the advantages of reducing deformation due to hygroscopicity and at the same time contributing to improving decay resistance.
この方法は、木材の吸湿が木材の構成物質中に存在する
親水性基、特に水酸基と水分子の結合に起因する点に注
目し、木材中の水酸基をエーテル化することにより木材
に筒効果(バルキング効果)を付与し、予め木材を膨潤
させるものであり、このことにより木材の吸脱湿性に伴
う変形を減少させ、もって寸法安定性を付与するという
ものである。特に、木材の吸湿性を減少させ寸法安定性
を高めるためには、木材中のOH基をエポキシ基で置換
するとともに、最大膨潤状態で木材を固定することによ
り、高湿度雰囲気下又は水中浸漬時等の木材膨潤雰囲気
下においてもそれ以上膨潤することを阻止するという必
要がある。This method focuses on the fact that moisture absorption in wood is caused by the bond between hydrophilic groups, especially hydroxyl groups, and water molecules present in the wood's constituent substances, and by etherifying the hydroxyl groups in wood, the wood has a tube effect. This method imparts a bulking effect (bulking effect) and swells the wood in advance, thereby reducing deformation due to moisture absorption and desorption of the wood, thereby imparting dimensional stability. In particular, in order to reduce the hygroscopicity of wood and increase its dimensional stability, it is necessary to replace the OH groups in the wood with epoxy groups and to fix the wood in the maximum swelling state. It is necessary to prevent further swelling even in wood swelling atmospheres such as wood swelling atmospheres.
この木材のエーテル化による材質改良法においては、各
種のアルカリ性化合物を触媒として使用する必要があり
、従来係る触媒としてトリエチルアミン、水酸化ナトリ
ウム等が使用されて来たが、これらのアルカリ性触媒は
木材の材質劣化を伴う上、改質後の木材の膨潤収縮量の
減少も不十分であるという欠点があった。In this material improvement method by etherification of wood, it is necessary to use various alkaline compounds as catalysts, and conventionally triethylamine, sodium hydroxide, etc. have been used as such catalysts, but these alkaline catalysts In addition to being accompanied by material deterioration, it also had the disadvantage that the amount of swelling and shrinkage of the wood after modification was insufficiently reduced.
本発明者等は従来の係る欠点等を解決すべく鋭意検討し
た結果、木材のエーテル化に際し、エーテル化反応を阻
害せず、且つ水よりも木材に対する膨潤係数の大きい物
質を共存せしめることにより、改質後の木材の膨潤収縮
量を大巾に改善することができることを見い出し本発明
に到達した。The inventors of the present invention have made intensive studies to solve the drawbacks of the conventional methods, and have found that, when etherifying wood, by coexisting a substance that does not inhibit the etherification reaction and has a larger swelling coefficient for wood than water, The present invention was achieved by discovering that the amount of swelling and shrinkage of wood after modification can be greatly improved.
(発明が解決しようとする課題)
従って本発明の第1の目的は、木材の材質劣化を伴うこ
とのない木材の改質方法を提供することにある。(Problems to be Solved by the Invention) Therefore, a first object of the present invention is to provide a method for modifying wood that does not involve deterioration of the quality of the wood.
本発明の第2の目的は、膨潤収縮量を十分に低減するこ
とのできる木材の改質方法を提供することにある。A second object of the present invention is to provide a method for modifying wood that can sufficiently reduce the amount of swelling and shrinkage.
く課題を解決するための手段)
本発明の上記の諸口的は、木材をエポキシ系エーテル化
剤と反応せしめるエーテル化方法において、該エーテル
化剤と共に水よりも木材に対する膨潤係数が大きいアミ
ン系又はアミド系化合物によって構成される群の中から
選択される少くとも1種の化合物を使用することを特徴
とする木材の改質方法によって達成された。The above-mentioned aspects of the present invention are characterized in that in an etherification method in which wood is reacted with an epoxy-based etherification agent, an amine-based or This was achieved by a wood modification method characterized by using at least one compound selected from the group consisting of amide compounds.
本発明で使用する木材には特に制限はなく、本発明の方
法は、すべての木材に対して通用することができる。The wood used in the present invention is not particularly limited, and the method of the present invention can be applied to all types of wood.
本発明において、木材をエーテル化するためのエーテル
化剤としては、通常水酸基とエーテル化反応する公知の
化合物の中から適宜選択して使用することができるが、
特に改質後の材質の観点からエポキシ系化合物を使用す
ることが好ましい。In the present invention, the etherifying agent for etherifying wood can be appropriately selected from known compounds that normally react with hydroxyl groups to etherify.
In particular, it is preferable to use an epoxy compound from the viewpoint of the quality of the material after modification.
このようなエポキシ系化合物としては、例えばエチレン
オキサイド、プロピレンオキサイド、ブチレンオキサイ
ド及びエピクロルヒドリン等を挙げることができる。Examples of such epoxy compounds include ethylene oxide, propylene oxide, butylene oxide, and epichlorohydrin.
上記の如き化合物を使用してエーテル化するに際しては
通常塩基性物質を触媒として使用する。When etherifying the above-mentioned compounds, a basic substance is usually used as a catalyst.
本発明においては、エーテル化に際して、木材に対する
膨潤係数が水よりも大きいアミン系又はアミド系化合物
の群から選択された少なくとも1種の化合物(以下アミ
ン等とする)を使用するが、これらの化合物は塩基性で
あるので、木材に対して膨潤剤として機能するのみなら
ず木材の水酸基とエポキシ化合物のエーテル化反応の触
媒としても機能するので、他に触媒を用いる必要はない
。In the present invention, at least one compound (hereinafter referred to as amine, etc.) selected from the group of amine-based or amide-based compounds whose swelling coefficient for wood is larger than that of water is used during etherification, but these compounds Since it is basic, it not only functions as a swelling agent for wood but also as a catalyst for the etherification reaction between the hydroxyl groups of wood and the epoxy compound, so there is no need to use any other catalyst.
しかしながら、必要に応じて他の触媒を併用しても良く
、又上記アミン系化合物とアミド系化合物を併用しても
良いことは当然である。However, it goes without saying that other catalysts may be used in combination as necessary, and the above amine compounds and amide compounds may also be used in combination.
本発明で使用することのできるアミン又はアミドとして
は、例えば、n−ブチルアミン、ピペリジン、ピリジン
、ジメチルホルムアミド等を挙げることができる。Examples of amines or amides that can be used in the present invention include n-butylamine, piperidine, pyridine, dimethylformamide, and the like.
(作用)
上記の如(、本発明で使用するアミン等は木材に対する
膨潤係数が水より大きいので、木材のエーテル化反応を
木材が水を吸収して膨潤した状態よりも更に膨潤した状
態で行わせることができる。(Function) As mentioned above, the amines used in the present invention have a larger swelling coefficient for wood than water, so the etherification reaction of wood is carried out in a state where the wood is more swollen than the state where the wood absorbs water and swells. can be set.
又、使用するアミン等はエーテル化反応の触媒としても
機能するから、木材の材質劣化を伴う従来の触媒を使用
する必要もない。Furthermore, since the amine used also functions as a catalyst for the etherification reaction, there is no need to use conventional catalysts that cause material deterioration of wood.
アミン等の使用量は、その膨潤機能を発揮することがで
きる程度に添加する。従って、通常エーテル化剤に対し
て少なくとも5重量%以上使用することが好ましい。ア
ミン等は高価であり、又改質後の木材が水を吸収しても
もはや殆ど膨潤しなくなれば、本発明の初期の目的は達
せられるので、水を吸収した時と同程度に膨潤せしめる
量のアミン等を使用すれば足りる。The amount of amine etc. to be used is such that it can exhibit its swelling function. Therefore, it is usually preferable to use at least 5% by weight of the etherifying agent. Amines and the like are expensive, and the initial objective of the present invention can be achieved if the wood after modification hardly swells even when it absorbs water, so it is necessary to use an amount that causes the wood to swell to the same extent as when it absorbs water. It is sufficient to use amines, etc.
本発明におけるエーテル化反応は公知の条件に従い、公
知の装置を使用して適宜行うことができる。The etherification reaction in the present invention can be suitably carried out under known conditions and using known equipment.
一般に、アミン等は生体に有害なものが多(、又高価で
もあるので、本発明においてはエーテル化反応終了後に
十分に水洗をして、アミンを水中に抽出し、回収するこ
とが好ましい。このように、アミンを回収しても木材は
既にエーテル化によって改質されているので収縮するこ
とがなく、又、水を吸収して膨潤することもない。In general, amines are often harmful to living organisms (and are also expensive), so in the present invention, it is preferable to thoroughly wash with water after the etherification reaction is completed, and extract the amines into water for recovery. Even if the amine is recovered, the wood will not shrink because it has already been modified by etherification, nor will it absorb water and swell.
(発明の効果)
本発明によれば木材が膨潤した状態でエーテル化される
ので、改質後の膨潤収縮量は従来のエーテル化による改
質の場合より大巾に改善される。(Effects of the Invention) According to the present invention, since the wood is etherified in a swollen state, the amount of swelling and shrinkage after modification is significantly improved compared to the conventional modification by etherification.
又、エーテル化に際して、木材の材質劣化を伴うアルカ
リ性触媒を使用する必要がないので改質後の木材の品質
は極めて良好である。Furthermore, since there is no need to use an alkaline catalyst that causes material deterioration of the wood during etherification, the quality of the wood after modification is extremely good.
(実施例)
次に、本発明を実施例によって更に詳述するが、本発明
はこれによって限定されるものではない。(Example) Next, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited thereto.
実施例1
アセトン抽出(80℃8Hrs、X2回)及び熱水抽出
(80℃8)(rs、X2回)処理を行ったアガチス四
方追補ブロック材(5X35X35mm)をプロピレン
オキサイド80部、ピペリジン20部からなる混合溶液
中に浸せきし、120℃、9.5Kg/cm2で60分
間エーテル化反応を行った。解圧後、残液を回収して試
験片を取り出し、送風乾燥機によって絶乾とし、体積増
加率6.5%、重量増加率28%のエーテル化処理ブロ
ック材を得た。これを20℃、93%RHの恒温恒湿雰
囲気中に放置し寸法変化率を測定したところ抗膨潤能(
ASE)は、T方向が83%、R方向が88%であり極
めて良好であった。Example 1 Agatis square supplement block material (5 x 35 x 35 mm) subjected to acetone extraction (80°C 8 hours, x 2 times) and hot water extraction (80°C 8 hours) (rs, x 2 times) was extracted from 80 parts of propylene oxide and 20 parts of piperidine. The etherification reaction was carried out at 120° C. and 9.5 kg/cm 2 for 60 minutes. After the pressure was released, the remaining liquid was collected, the test piece was taken out, and it was completely dried in a blow dryer to obtain an etherified block material with a volume increase rate of 6.5% and a weight increase rate of 28%. The anti-swelling ability (
ASE) was 83% in the T direction and 88% in the R direction, which was extremely good.
実施例2
プロピレンキサイド80部、ピペリジン20部からなる
混合溶液のかわりにプロピレンオキサイド80部、ジメ
チルホルムアミド20部からなる混合溶液を使用した他
は実施例1と同様に行い、体積増加率5.8%、重量増
加率27%のエーテル化処理ブロック材を得た。Example 2 The same procedure as in Example 1 was carried out except that a mixed solution of 80 parts of propylene oxide and 20 parts of dimethylformamide was used instead of the mixed solution of 80 parts of propylene oxide and 20 parts of piperidine, and the volume increase rate was 5. An etherified block material with a weight increase rate of 8% and a weight increase rate of 27% was obtained.
これを20℃、93%RHの 恒温恒湿雰囲気中に放置
し寸法変化率を測定したところ抗膨潤能(ASE)は、
T方向が78%、R方向が83%であった。When this was left in a constant temperature and humidity atmosphere of 20°C and 93% RH and the dimensional change rate was measured, the anti-swelling ability (ASE) was as follows.
It was 78% in the T direction and 83% in the R direction.
実施例3
実施例1で使用したプロピレンオキサイドとピペリジン
混合溶液の混合比率を97/3.9515.90/10
重量部とした他は実施例1と同様 −に行い抗膨潤能(
ASE)を測定したところ次表のような結果を得た。Example 3 The mixing ratio of the propylene oxide and piperidine mixed solution used in Example 1 was 97/3.9515.90/10
Anti-swelling ability (
ASE) was measured, and the results shown in the following table were obtained.
比較例1
実施例1において、ピペリジンに代えトリエタノールア
ミンを使用し、体積増加率4.8%、重量増加率28.
5%のブロック材を得た。これを恒温恒湿雰囲気中に放
置し寸法変化率を測定したところ抗膨潤能(ASE)は
、T方向58%、R方向62%と寸法変化の大きいもの
であった。Comparative Example 1 In Example 1, triethanolamine was used instead of piperidine, and the volume increase rate was 4.8% and the weight increase rate was 28%.
A 5% block material was obtained. When this was left in a constant temperature and humidity atmosphere and the dimensional change rate was measured, the anti-swelling ability (ASE) was 58% in the T direction and 62% in the R direction, which was a large dimensional change.
以上の実施例、比較例の結果から、水よりも膨潤係数の
大きいアミン等の存在下にエーテル化を行う本発明の有
効性が実証された。The results of the above Examples and Comparative Examples demonstrate the effectiveness of the present invention in which etherification is carried out in the presence of an amine or the like having a larger swelling coefficient than water.
Claims (1)
テル化方法において、該エーテル化剤と共に水よりも木
材に対する膨潤係数が大きいアミン系又はアミド系化合
物によって構成される群の中から選択される少くとも1
種の化合物を使用することを特徴とする木材の改質方法
。 2)アミン系又はアミド系化合物の添加量が、エーテル
化剤に対して少くとも5重量%以上である請求項1に記
載の木材の改質方法。[Scope of Claims] 1) In an etherification method in which wood is reacted with an epoxy-based etherification agent, a compound selected from among the group consisting of an amine-based or amide-based compound having a larger swelling coefficient for wood than water, together with the etherification agent. at least one selected from
A method for modifying wood characterized by using a seed compound. 2) The method for modifying wood according to claim 1, wherein the amount of the amine or amide compound added is at least 5% by weight based on the etherifying agent.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2550388A JPH01200903A (en) | 1988-02-05 | 1988-02-05 | Method for modifying wood |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2550388A JPH01200903A (en) | 1988-02-05 | 1988-02-05 | Method for modifying wood |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH01200903A true JPH01200903A (en) | 1989-08-14 |
| JPH0546284B2 JPH0546284B2 (en) | 1993-07-13 |
Family
ID=12167868
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2550388A Granted JPH01200903A (en) | 1988-02-05 | 1988-02-05 | Method for modifying wood |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH01200903A (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4877002A (en) * | 1972-01-18 | 1973-10-17 | ||
| JPS587309A (en) * | 1981-07-03 | 1983-01-17 | 大建工業株式会社 | Manufacture of decorative wood |
| JPS58148720A (en) * | 1982-02-27 | 1983-09-03 | 松下電工株式会社 | Method of decoloring woody material |
-
1988
- 1988-02-05 JP JP2550388A patent/JPH01200903A/en active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4877002A (en) * | 1972-01-18 | 1973-10-17 | ||
| JPS587309A (en) * | 1981-07-03 | 1983-01-17 | 大建工業株式会社 | Manufacture of decorative wood |
| JPS58148720A (en) * | 1982-02-27 | 1983-09-03 | 松下電工株式会社 | Method of decoloring woody material |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0546284B2 (en) | 1993-07-13 |
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