JPH0775843B2 - Modified wood and its manufacturing method - Google Patents
Modified wood and its manufacturing methodInfo
- Publication number
- JPH0775843B2 JPH0775843B2 JP27687491A JP27687491A JPH0775843B2 JP H0775843 B2 JPH0775843 B2 JP H0775843B2 JP 27687491 A JP27687491 A JP 27687491A JP 27687491 A JP27687491 A JP 27687491A JP H0775843 B2 JPH0775843 B2 JP H0775843B2
- Authority
- JP
- Japan
- Prior art keywords
- wood
- phenol
- caprolactam
- formaldehyde
- treating agent
- 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.)
- Expired - Fee Related
Links
- 239000002023 wood Substances 0.000 title claims description 38
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 35
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 28
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 11
- 238000011282 treatment Methods 0.000 claims description 10
- 239000000178 monomer Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- 238000009792 diffusion process Methods 0.000 claims description 3
- 238000010438 heat treatment Methods 0.000 claims description 2
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 229920005989 resin Polymers 0.000 description 8
- 239000011347 resin Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000002579 anti-swelling effect Effects 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000002845 discoloration Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 241000218645 Cedrus Species 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 1
- SLXKOJJOQWFEFD-UHFFFAOYSA-N 6-aminohexanoic acid Chemical compound NCCCCCC(O)=O SLXKOJJOQWFEFD-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229960002684 aminocaproic acid Drugs 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000005470 impregnation Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000005011 phenolic resin Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010875 treated wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Chemical And Physical Treatments For Wood And The Like (AREA)
Description
【発明の詳細な説明】Detailed Description of the Invention
【0001】[0001]
【産業上の利用分野】本発明は、木材あるいは木質材料
(以下、木材という。)の寸法安定化に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to dimensional stabilization of wood or wood materials (hereinafter referred to as wood).
【0002】[0002]
【従来の技術】従来より、木材の寸法安定性を改良する
ために、フェノ−ル−ホルムアルデヒド縮合樹脂を、減
圧加圧法や拡散法等により該木材の内部に含浸あるいは
注入し、然るのち乾燥あるいは硬化させる方法が知られ
ている。またε−カプロラクタムモノマ−を木材中に浸
漬させ、オ−トクレ−ブ等の圧力容器内で高温と高圧に
より木材中で樹脂化させる方法も試みられている。2. Description of the Related Art Conventionally, in order to improve the dimensional stability of wood, a phenol-formaldehyde condensation resin is impregnated or injected into the wood by a pressure reduction method or a diffusion method and then dried. Alternatively, a method of curing is known. There has also been attempted a method in which ε-caprolactam monomer is immersed in wood and resinified in wood by high temperature and high pressure in a pressure vessel such as an autoclave.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、フェノ
−ル−ホルムアルデヒド縮合樹脂を木材中に浸漬させて
処理する方法は該木材に変色を来し、またε−カプロラ
クタムモノマ−による方法は特殊な容器と高温高圧を要
し工業化するのは困難であった。However, the method of immersing the phenol-formaldehyde condensation resin in wood to treat it causes discoloration of the wood, and the method using ε-caprolactam monomer requires a special container. It was difficult to industrialize because it required high temperature and high pressure.
【0004】本発明は、寸法安定性に欠ける木材の性質
の改良に関し、上記のように変色を来さず、また高温高
圧を要せずに優れた寸法安定性を備えた改質木材の製法
を提供するものである。The present invention relates to improvement of properties of wood lacking dimensional stability, and relates to a method for producing a modified wood which does not cause discoloration as described above and has excellent dimensional stability without requiring high temperature and high pressure. Is provided.
【0005】[0005]
【課題を解決するための手段と作用】上記課題を解決す
るために、本発明は、圧力調整と蒸気放出可能な装置内
で、フェノ−ル、カプロラクタム、ホルムアルデヒドの
混合物ないしは化合物を主成分とする処理剤を、木材中
に減圧加圧法や拡散法等の含浸方法で浸漬し、次いで温
度100〜200℃の飽和蒸気を放出して加熱処理する
ことにより、該木材に優れた寸法安定性を付与するもの
である。In order to solve the above-mentioned problems, the present invention mainly comprises a mixture or compound of phenol, caprolactam and formaldehyde in a device capable of pressure adjustment and vapor discharge. The treating agent is immersed in wood by an impregnation method such as a depressurization method or a diffusion method, and then saturated steam at a temperature of 100 to 200 ° C. is released to perform heat treatment to impart excellent dimensional stability to the wood. To do.
【0006】本発明で用いる処理剤は、フェノ−ル、カ
プロラクタム、ホルムアルデヒドの混合物ないしは化合
物を主成分とし、その組成比はフェノ−ル1モルに対し
て、カプロラクタム0.5〜4モル、ホルムアルデヒド
1〜10モルであり、その他適宜アルコ−ル類、ケトン
類、芳香族炭化水素類等の溶媒が添加される。The treating agent used in the present invention contains a mixture or compound of phenol, caprolactam and formaldehyde as a main component, and the composition ratio thereof is 0.5 to 4 mol of caprolactam and 1 formaldehyde per mol of phenol. The amount is 10 to 10 mol, and other solvents such as alcohols, ketones and aromatic hydrocarbons are appropriately added.
【0007】木材への浸漬処理に際しては、反応装置中
で初期反応を行った上記組成の処理剤を用いてもよい
が、上記組成の各モノマ−の混合物からなる処理剤を用
いる方が該処理剤の木材中への浸漬効果が高く、また処
理剤の調製が容易となり好ましい。In the immersion treatment in wood, a treating agent having the above composition which has undergone an initial reaction in a reactor may be used, but the treating agent comprising a mixture of each monomer having the above composition is preferably used. This is preferable because the agent has a high dipping effect in wood and the treatment agent can be easily prepared.
【0008】該処理剤の木材に対する樹脂量は、30重
量%未満であると該木材に及ぼす寸法安定化の効果が顕
著でなく、100重量%以上では寸法安定性の指標であ
る抗膨潤能、抗防湿能ともほぼ平衡となり、効果、コス
トの面から好ましくない。従って、好ましい樹脂量は3
0〜100重量%、更に好ましくは50〜80重量%で
ある。ここで、樹脂量とは木材100に対する樹脂付着
量(重量%)であり、突板、単板、製材、チップなどの
木材製品に適用される。If the amount of resin of the treating agent with respect to wood is less than 30% by weight, the effect of dimensional stabilization on the wood is not remarkable, and if it is 100% by weight or more, the anti-swelling ability which is an index of dimensional stability, The anti-moisture-proof ability is almost in equilibrium, which is not preferable in terms of effect and cost. Therefore, the preferred amount of resin is 3
It is 0 to 100% by weight, more preferably 50 to 80% by weight. Here, the amount of resin is the amount of resin adhered (% by weight) to the wood 100, and is applied to wood products such as veneer, veneer, lumber, and chips.
【0009】該処理剤は木材中で過熱蒸気により加熱さ
れ、反応が促進され樹脂化することにより該木材の寸法
安定性を向上させるものであるが、カプロラクタム単体
による処理では、抗膨潤能は向上するものの、抗防湿能
は低下し、更にアミノカプロン酸とホルマリンによる処
理では両者の向上が見られず、むしろ低下することよ
り、上記処理剤はフェノ−ルとホルムアルデヒドによる
ノボラック型の反応、フェノ−ルとカプロラクタム、あ
るいはカプロラクタムとホルムアルデヒドとの付加ある
いは開環反応が該木材中で併行して進み、疏水化される
ものと考えられ、このような反応系であるため、木材を
変色させることもない。The treatment agent improves the dimensional stability of the wood by being heated by superheated steam in the wood to promote the reaction and resinification. However, the treatment with caprolactam alone improves the anti-swelling ability. However, the anti-moisture-proof ability is lowered, and further, both treatments with aminocaproic acid and formalin are not improved, but rather, the treatment agent is reduced, and therefore the above-mentioned treatment agent is a novolak-type reaction between phenol and formaldehyde, phenol. It is considered that the addition or ring-opening reaction of caprolactam or caprolactam or formaldehyde proceeds in parallel in the wood and is hydrophobized, and since it is such a reaction system, it does not discolor the wood.
【0010】また、過熱蒸気は該処理剤の反応を促進さ
せるばかりでなく、木材組織を膨潤させ、該処理材を該
木材の内部まで浸透させる作用もある。Further, the superheated steam not only accelerates the reaction of the treating agent, but also swells the wood structure to allow the treating material to penetrate into the wood.
【0011】[0011]
【実施例】実施例1,2,3 減圧加圧と蒸気放出の可能な容器内で、フェノ−ル1モ
ルに対して、カプロラクタム1モルおよびホルムアルデ
ヒドとして2モルのホルマリンを混合して得られた各モ
ノマ−からなる処理剤を、厚さ5mmの杉単板に減圧加圧
法により樹脂含有量45、55、75重量%となるよう
に浸漬したのち、温度150℃の過熱蒸気を60分間放
出して加熱し、実施例1,2,3の改質木材とした。Examples 1, 2, 3 Obtained by mixing 1 mol of caprolactam and 2 mol of formalin as formaldehyde with 1 mol of phenol in a container capable of pressurizing under reduced pressure and releasing steam. The treating agent consisting of each monomer was dipped in a cedar veneer having a thickness of 5 mm so as to have a resin content of 45, 55, and 75% by weight by a pressure reduction method, and then superheated steam at a temperature of 150 ° C. was released for 60 minutes. Then, the modified wood of Examples 1, 2 and 3 was heated.
【0012】実施例4 フェノ−ル1モルに対して、カプロラクタム1モルおよ
びホルムアルデヒドとして2モルのホルマリンを、還流
装置及び撹拌装置のついた反応装置に仕込み、pH1〜
2に調整したのち、温度90〜100℃で3時間反応さ
せ冷却して処理剤とした。次いでメチルエチルケトン、
キシレンの混合溶媒にて固形分を調整した処理剤を、減
圧加圧と蒸気放出の可能な容器内で、厚さ5mmの杉単板
に減圧加圧法により樹脂量55重量%となるように浸漬
したのち、温度150℃の過熱蒸気を60分間放出して
加熱し、実施例4の改質木材とした。Example 4 1 mol of phenol, 1 mol of caprolactam and 2 mol of formalin as formaldehyde were charged into a reactor equipped with a reflux device and a stirrer to adjust the pH to 1 to 1.
After adjusting to 2, the mixture was reacted at a temperature of 90 to 100 ° C. for 3 hours and cooled to obtain a treating agent. Then methyl ethyl ketone,
A treatment agent whose solid content was adjusted with a mixed solvent of xylene was immersed in a cedar veneer with a thickness of 5 mm in a container capable of pressurizing under reduced pressure and releasing steam so that the resin amount would be 55% by weight by a reduced pressure method. Then, the superheated steam having a temperature of 150 ° C. was discharged for 60 minutes to heat the steam, and the modified wood of Example 4 was obtained.
【0013】比較例1 フェノール1モルに対して、ホルムアルデヒドとして2
モルのホルマリンを環流し装置及び撹拌装置のついた反
応装置に仕込み、PH9〜10に調整したのち、温度8
0〜90℃で2時間反応して、冷却後、メチルアルコー
ルにて、固形分を調整して得た処理剤を、実施例4と同
様に処理して比較例1の改質木材とした。Comparative Example 1 2 mol of formaldehyde was added to 1 mol of phenol.
After adding mol of formalin to a reactor equipped with a reflux device and a stirring device and adjusting the pH to 9 to 10, the temperature was adjusted to 8
After reacting at 0 to 90 ° C. for 2 hours and cooling, the treating agent obtained by adjusting the solid content with methyl alcohol was treated in the same manner as in Example 4 to obtain modified wood of Comparative Example 1.
【0014】実施例1,2,3,4及び比較例1の各改
質木材を、40℃−30%RH、40℃−90%RHの
恒温恒湿槽に平衡になるまで静置し、抗吸湿能(Moistu
re Excluding Efficiency:MEE)及び抗膨潤能(Anti Sw
elling Efficiency:ASE)により寸法安定性を評価し、
表1に結果を示す。Each of the modified woods of Examples 1, 2, 3, 4 and Comparative Example 1 was allowed to stand until equilibrated in a constant temperature and humidity chamber at 40 ° C-30% RH and 40 ° C-90% RH. Moisture absorption (Moistu
re Excluding Efficiency (MEE) and anti-swelling ability (Anti Sw
elling Efficiency (ASE) to evaluate dimensional stability,
The results are shown in Table 1.
【0015】[0015]
【表1】 [Table 1]
【0016】[0016]
【発明の効果】本発明は、上記のように、合成反応させ
た処理剤を用いなくても、モノマ−の混合物を主体とす
る処理剤によっても木材に十分な寸法安定性を付与させ
ることができるため、処理剤の調製が容易で、しかも従
来のフェノ−ル樹脂による処理木材のように変色させる
ことがないため、木材の外観を損なうこともない。INDUSTRIAL APPLICABILITY As described above, the present invention makes it possible to impart sufficient dimensional stability to wood even by using a treating agent mainly composed of a mixture of monomers without using a treating agent which has undergone a synthetic reaction. Therefore, the preparation of the treating agent is easy, and since it does not cause discoloration unlike the treated wood with the conventional phenol resin, the appearance of the wood is not impaired.
【0017】また、カプロラクタム単体による処理法の
ように高温高圧を必要とせず、特殊な装置を用いる必要
もない。Further, unlike the treatment method using caprolactam alone, high temperature and high pressure are not required, and it is not necessary to use a special device.
Claims (3)
ルデヒドの混合物ないしは化合物を主成分とする処理剤
を、木材あるいは木質材料中に含有していることを特徴
とする改質木材。1. Modified wood containing a treating agent containing a mixture or compound of phenol, caprolactam and formaldehyde as a main component in wood or wood material.
ェノール、カプロラクタム、ホルムアルデヒドの混合物
ないしは化合物を主成分とする処理剤を、木材あるいは
木質材料中に、減圧加圧法や拡散法等の含浸方法で浸漬
し、次いで温度100〜200℃の飽和蒸気を放出して
加熱処理することを特徴とする改質木材の製法。2. A treatment agent containing a mixture or compound of phenol, caprolactam and formaldehyde as a main component is impregnated into a wood or wood material by a pressure reduction method or a diffusion method in a device capable of adjusting pressure and releasing steam. A method for producing modified wood, which is characterized in that it is soaked by the method, and then saturated steam at a temperature of 100 to 200 ° C. is released to perform heat treatment.
ロラクタム、ホルムアルデヒドの混合物のいずれもがモ
ノマーである請求項2記載の改質木材の製法。3. The method for producing modified wood according to claim 2, wherein all of the mixture of phenol, caprolactam and formaldehyde, which are the main components of the treating agent, are monomers.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27687491A JPH0775843B2 (en) | 1991-09-28 | 1991-09-28 | Modified wood and its manufacturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27687491A JPH0775843B2 (en) | 1991-09-28 | 1991-09-28 | Modified wood and its manufacturing method |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0584707A JPH0584707A (en) | 1993-04-06 |
| JPH0775843B2 true JPH0775843B2 (en) | 1995-08-16 |
Family
ID=17575612
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27687491A Expired - Fee Related JPH0775843B2 (en) | 1991-09-28 | 1991-09-28 | Modified wood and its manufacturing method |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0775843B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3356099B1 (en) * | 2015-09-29 | 2023-12-27 | Stora Enso Oyj | Modified wood product and a process for producing said product |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN117124417A (en) * | 2023-08-21 | 2023-11-28 | 南京林业大学 | Synergistic modifier of furfuryl alcohol and caprolactam and preparation method and application thereof |
-
1991
- 1991-09-28 JP JP27687491A patent/JPH0775843B2/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3356099B1 (en) * | 2015-09-29 | 2023-12-27 | Stora Enso Oyj | Modified wood product and a process for producing said product |
| US12220836B2 (en) | 2015-09-29 | 2025-02-11 | Stora Enso Oyj | Modified wood product and a process for producing said product |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0584707A (en) | 1993-04-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |