JPS59218806A - Method of improving woody material - Google Patents

Method of improving woody material

Info

Publication number
JPS59218806A
JPS59218806A JP9231783A JP9231783A JPS59218806A JP S59218806 A JPS59218806 A JP S59218806A JP 9231783 A JP9231783 A JP 9231783A JP 9231783 A JP9231783 A JP 9231783A JP S59218806 A JPS59218806 A JP S59218806A
Authority
JP
Japan
Prior art keywords
wood
reaction solution
reaction
essential
solution
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
Application number
JP9231783A
Other languages
Japanese (ja)
Other versions
JPH0311245B2 (en
Inventor
青木 英一
秀行 小林
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP9231783A priority Critical patent/JPS59218806A/en
Publication of JPS59218806A publication Critical patent/JPS59218806A/en
Publication of JPH0311245B2 publication Critical patent/JPH0311245B2/ja
Granted legal-status Critical Current

Links

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 本発明は、本質材を生産性よく、又強度低+4生ずるこ
となく改質できる本質材の改質方法に関づる一bのであ
る。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for modifying an essential material with good productivity and without causing the strength to deteriorate.

木材およびその加工側である木41甲板、木拐ブップ等
の本質材は、軽くて強く、独特の物性、月賀感をイ噛づ
−る441’31どして建築用材、家具用材は勿論のこ
と、その他広範囲な用途に利用されでいる。
Wood and its processed materials, such as Ki 41 Deck and Kikanbup, are light and strong, and have unique physical properties and a moonlit feel, making them ideal for building materials and furniture. It is used for a wide range of other purposes.

しかしながら、−)jでは、各種菌類の侵蝕や゛白!1
7I1等の虫害を受り°C’ l1i5(すし易く、昨
今のJ:うに気密性が高く、暖房装置の晋及が進んだ住
宅環境下にJ3いCは、このようなl出朽の発生はむし
ろ増加してきてd3す、本質材の耐久1!I低下の一因
として人さな問題となってきている。
However, in −)j, erosion by various fungi and ゛white! 1
Due to damage from insects such as 7I1 °C' l1i5 (easy to sip, J3C in recent years has a high degree of airtightness, and the development of heating systems has made it difficult for J3C to succumb to such problems.) In fact, it has been increasing and is becoming a serious problem as one of the causes of the decrease in the durability of essential materials.

J:lζ、木M’A +4 Lま湿気等の水分を周囲の
環境条件に応じて吸収し放散覆るという、所謂呼吸性を
右ザる反面、このような湿気等の吸収、/1文敗の繰返
しに伴って、反り、ねじれ、伸縮等の変形を生じるとい
う木質的な欠点を右している。
J:lζ, Wood M'A +4 LAlthough it absorbs moisture such as moisture according to the surrounding environmental conditions and dissipates it, it has good breathability, but on the other hand, it does not absorb such moisture, etc. This is due to the woody nature of deformations such as warping, twisting, expansion and contraction due to repeated use.

」−記烏朽に関づる問題の改善には、クレAソート曲等
、防腐防虫剤の本質材への含ン受処理が一般的/、c方
v1どして実施されているが、この方法では4iにアセ
デル化等の化学的処理を行・)て、その成分中の水酸基
を化学的に庇部すると効果のあること(よ知られている
。しかしながら、木質材は甲−成分から1.するーしの
でなく、MJ 711な成分構成と複711なMl織構
造を有り−るもの(・あるIこめに、木質材に1−配化
学的処理を行うのに用いられていた種々の方法は、反応
に4々めC長時間を要づるどともに、余剰の反応液や触
媒の除去が極めて困ツ11であり、また木質材の強瓜的
+J質が若しく低下づる宿より、工業生産的に行うこと
は困ff1ll−(”実用(11がないという問題を有
している。
” - Note To improve problems related to rotting, it is common to incorporate preservatives and insecticides into essential materials, such as CreA sort songs. In this method, it is well known that chemical treatment such as acedelization is applied to 4i to chemically protect the hydroxyl groups in the component. .It is not a single material, but has an MJ711 component composition and a complex M1 weave structure. This method requires a long time for the reaction, it is extremely difficult to remove the excess reaction solution and catalyst, and the quality of the wood material is slightly reduced. There is a problem that it is difficult to carry out industrial production.

本発明はかかる諸問題に鋸、みてなされたしのて゛、各
種菌類の侵蝕や白蟻等の虫害を受は難く、耐久性に優れ
て2.るとともに、反り、ねじれ、伸1+i等の変形を
生じデ11い改質された木1”[4Aを極めて生産性よ
く製造づ−ることがCさる木質材の改質方法を提供する
ものである。
The present invention has been developed in view of these problems, and has the following advantages:2. The present invention provides a method for modifying wood materials that can produce highly productively modified wood 1" [4A] which also causes deformations such as warping, twisting, elongation 1+i, etc. be.

寸なわら、本発明方法は、水″”11 JtAに酢酸塩
水溶液を含浸した後、乾燥しこの木質材にアセチル1ヒ
反応液を適宜方法にJ、り31人し、しかるのもこの改
質方法(゛ある。
However, in the method of the present invention, after impregnating 11 JtA of water with an acetate aqueous solution, drying the wood material and applying an acetyl reaction solution to the wood according to an appropriate method, this modification Quality method (゛There is.

以ド、本発明に係る方法につい゛(説明りる。The method according to the present invention will now be explained.

本発明に用いる木質材とは、水利、不利単板、木材デツ
プ°等のことで、先り”この木質材に触媒である酢酸塩
水溶液を念浸さUる。このにうな含浸は、例えば上記f
it酸塩水溶液中に木質材を浸漬りる等の方法で行うこ
ともぐきるか、含岸を迅速に行うために40°C〜80
’C程度に加温した酢酸塩水溶液を用いIζす、減バ加
圧釜内で酢M塩水溶31kを減汁注入、加圧注入、減L
1加圧注入にJ:リリウムt9であり、このような酢酸
に1は木質材を劣化さU゛ることがなく、また水洗にJ
、り除去が容易であり、しかも後述Jる反応を良好にか
つ迅速に行うことができるので好適なムのC−ある。
The wood materials used in the present invention include water-containing veneers, unfavorable veneers, wood depths, etc., and are first thoroughly immersed in an aqueous acetate solution as a catalyst. f
It is also possible to do this by immersing the wood in an aqueous solution of itate salts, or at 40°C to 80°C to speed up the process.
Using an acetate aqueous solution warmed to about
1 J for pressurized injection: Lilium T9, 1 for such acetic acid will not deteriorate wood materials, and J for water washing.
C- is preferred because it is easy to remove and the reaction described below can be carried out satisfactorily and quickly.

なお、V記酢酸塩水溶液の濃度は、特に限定するbので
は4iいが、通常、5〜30%程1良のa度のものを用
いればJ、い。
Note that the concentration of the acetate aqueous solution in V is not particularly limited to B, but it is usually J if a concentration of about 5 to 30% is used.

〒−行ってもにり、木質4Aの含水率が10%以下とな
るにうに行うのがその1受の反応を効率よく行−う上で
特に望ましい。
In order to carry out the first reaction efficiently, it is particularly desirable to carry out the reaction at such a time that the moisture content of the wood 4A is 10% or less.

乾燥された触媒○イj木質(Δは、続いてアしrデル化
反応液で処理して木質44成分の水酸基と反応さ°せる
。′ノ?セチル化反応液とし−C−は、3I!L水MY
 ITt又は無水酢酸と石(段溶媒との混合液を用いる
ことができ、後者の揚台、’hli笈溶に1に1−ル↓
ン、ギシレン、ベンビン等の芳百族炭化水素類やケ1−
ン21′Iを用いることができる。
The dried catalyst ○Ij wood (Δ) is then treated with an acylation reaction solution to react with the hydroxyl groups of the 44 components of wood. !L water MY
A mixture of ITt or acetic anhydride and a stone (step solvent) can be used;
Aromatic hydrocarbons such as
21'I can be used.

このような右楊i溶A1を゛)1!−水01酸に)[コ
入りることは高価な無水01酸の必装吊以上のbのを安
価な右l幾溶媒で置換゛りることがでさ、粁洛1!lに
優れてなるとともに、フハ(氷酢酸の強い刺)斂央をI
II減さ1士で作業環境をよくしたりあるい【J、無水
1’i+−酸による木質(Aの強度低−トをIIY減C
・きる簀の利点がある。
This kind of right Yang i melt A1 ゛)1! -Water (to acid) In addition to becoming good at glacial acetic acid, I also learned that Fuha (strong sting of glacial acetic acid)
Improve the working environment by reducing the strength of wood (A) by reducing the strength of wood (A) by reducing the strength of wood (A) by reducing the strength of
・It has the advantage of being a clear screen.

本発明方法では、木K14Aとiヒチル化反応液との反
応を次のJ、)にし“C行う。
In the method of the present invention, the reaction between wood K14A and the i-hytylation reaction solution is carried out in the following manner.

先ず、前記で19られた触媒含浸後乾燥した木質41に
上記反応液を注入りる。i1人は甲に反応液中に木5を
材を浸漬りることにまり行ってもJ、いか、(真空吸引
し脱気し′(木y゛目号空隙中の空気を除いておくのが
望ましい。
First, the above reaction solution is injected into the wood material 41 which has been dried after being impregnated with the catalyst. Even if one person gets stuck in immersing the wood 5 in the reaction solution, it is necessary to degas it by vacuum suction (to remove the air in the voids). is desirable.

)り(1こ反応液が注入されIこ木71444反In>
 ’/+に中に浸X’i L/で反応させる。このにう
イよ浸漬による反応【よ甲にン是)rシするだl−J 
t” !、1、反応nニア間が長<<2るのτ、通常1
00°C〜150°゛C稈疫の加湿し1.:反応液中で
行うのが好適ひあり、又このJ2うイ「反応を減圧加I
J釜内で加Jf下で行うこともできる。更には浸漬にJ
、る7’J rA J′J、外にも反応液のi・λ気温
中で行うノ’y rhム可能である。
) (1 reaction solution was injected and 71444 anti-In>
'/+ and react with X'i L/. This is the reaction caused by immersion.
t"!, 1, reaction n near is long << 2 τ, usually 1
Humidification of 00°C to 150°C 1. : It is preferable to carry out the reaction in the reaction solution.
It can also be carried out in a J pot under a JF. Furthermore, J
, 7'J rA J'J, it is also possible to perform the reaction at the i·λ temperature of the reaction solution.

このように反応液を木τ1月内に一〇注入処理しておさ
、引さjゾ、さ反応液中で反応させることは複雑な絹M
A 4m造を右1′る木V′口Aにあって、良好で迅速
なアセチル化反応を行わせる」−〇特に石川である。
In this way, the reaction solution was injected for 10 days within a month, and the reaction in the reaction solution was complicated.
A 4-meter building is located 1' to the right at the V' entrance A to perform a good and rapid acetylation reaction.''--Especially Ishikawa.

すなわち、−月注入処111!を行つ−Cおくことひ、
木質材内部から迅速]]つ11イ「実に反応が進み、反
応に伴って副生される酢酸はf31立((i斜にJ:つ
尤反応液中に浸出し代って木質4A内に無水ri1酸分
が浸入づ°るという現象が生じて均一な反応が11え、
1)0処ったものを用いてt)J、いのは勿論である。
That is, - month injection place 111! Do -C put,
Rapidly from inside the wood] 11 A: The reaction actually progresses, and the acetic acid produced as a by-product of the reaction leaches into the reaction solution and enters the wood 4A. A phenomenon occurs in which the acid anhydride infiltrates, resulting in a uniform reaction.
1) Using 0, t) J, Ino is of course.

尚、このような注入(こ用いる反応液及び反応液はい一
す゛れも繰返し使用できるしのであり、 !!返しにJ
、つてa1生されるfil’ n’s 、酢1やと61
酸塩との複塩、あるいは木質I申の抽出成分宿を若干含
んでいる。。
It should be noted that such injection (the reaction solution and the reaction solution used in this case can be used repeatedly).
, Tsute a1 born fil'n's, vinegar 1 and 61
Contains a double salt with an acid acid or a small amount of woody Ishin extract. .

従って、本発明方法にJ3いては、木質材に予めn1葭
塩が水溶液どしで含浸しているため、I’ll nり塩
が木質材中に均一かつ効率良くイ・1着し、しかも乾燥
により水分を除去−りるので、木Y′1祠内に浸入した
無水酢酸は良好に木質44成分と反応することが(・さ
る1゜ 1?1に、n1酸」)。1水tFf fi!4 ’6−
含浸1狡、 U1乾燥づることは木質4A内に浸入しに
ノ1(−水n1酸が、木質材中の水分と反応してl′l
i酸に転化覆るのを(Φ力少なく覆ることになり、従っ
て−[1乾燥覆−ることでこのような反応効率の顕:1
ζなII(−F ’a防ぐことができるも)豪1こより
IT rlQへの転化が抑制されるために、このJ、う
な本”i’i IJの強度低十をし軽減(さるものであ
おくことも考えられるが、酢酸塩が)ハ(水r41酸に
溶解しないことから反応液中の酢酸の除去に(J、効果
があるが、木質lの如く複利な相械構迄を右り−るI料
の場合には、酢酸塩の良好な触媒効果を期待することは
国力1である。
Therefore, in the J3 method of the present invention, since the wood material is impregnated with n1 salt in advance with an aqueous solution, the I'll n salt is uniformly and efficiently deposited in the wood material. Since water is removed by drying, the acetic anhydride that has penetrated into the wood Y'1 reacts well with the 44 wood components (. 1 water tFf fi! 4'6-
After impregnation, U1 drying penetrates into the wood 4A and the acid reacts with the water in the wood to form l'l.
The conversion to i acid will result in less overcoating (Φ), and therefore - [1 dry overlay - will reduce the efficiency of such a reaction: 1
ζ II (-F'a can be prevented) Since the conversion to IT rlQ is suppressed from Australia 1, this J, "i'i IJ's low strength is reduced (Sarumono de Although acetate is not soluble in water, it is effective in removing acetic acid from the reaction solution, but it does not require a compound interest mechanism like that of wood. - In the case of I materials, it is a national strength to expect a good catalytic effect of acetate.

さらに、触媒どしτ顔酸塩を用い−(いるので、汎用触
媒である硫酸や過塩素的の如く木質材の強度を茗しく低
下させることが1.さり、また余剰のnl酸塩は、木質
材を洗浄する口と(゛簡I41に除去でき″る。
In addition, the use of catalysts such as tau-face acid salts (1. A spout for cleaning wood materials (can be easily removed).

又、本発明方法では、水質(4(こ予め反応液を、触媒
含有木質材中に注入しlこのら加渇し1.:艮応;告中
で反応を行っているのC1従来の如く長い時間を要さず
短11iY間の内に1庁IJjよく木τ’t 4A l
、改7′(することができしかし木44成分の抽出を防
止でさる為に強度低下のない処理祠が111られるとい
う実用上多大な効果をも合U J5つものである。
In addition, in the method of the present invention, the water quality (4) is injected into the catalyst-containing wood material in advance, and then the reaction is carried out. It doesn't take much time to complete one office IJj well within a short 11iY interval.
However, in order to prevent the extraction of wood 44 components, it is possible to create a processing chamber that does not reduce strength, which is a great practical effect.

−実施例 − 3mm厚601unx 55 mmのでLゾ松111板
−10枚を5i−F 帛96 r’:= Jfi (1
) nl 酸−)−t−jJ ’/ ム水溶H’i 中
1w 浸漬L7、減I[加圧注入して単板内にl’il
酸す1〜リウム水溶液ら、メタ4:シレン:)1((水
nt酎−60: 40(7)IT!W1割合からイよる
反応if!?中にlノ11−シ減ル加汁して混合液を単
板内に注入けしめた。
-Example- 3mm thickness 601unx 55mm, so 10 pieces of L Zomatsu 111 board 5i-F 96r':= Jfi (1
) nl acid-)-t-jJ'/mu aqueous H'i medium 1w immersion L7, reduced I [pressure injected into the veneer
Aqueous solution of 1~lium acid, meta 4: silene:) 1 ((water nt chuu - 60: 40 (7) IT! Reaction based on the ratio of W1, if!? The mixed solution was injected into the veneer.

続いてこのン1人処J111711板を約125°(C
に加温された上記と同様のirシ合割合からなる反応液
中に>D、 irzし、加温状態を保ちつつ約20分間
反応さU反応終了後単板内に残存りる混合液を乾留によ
り除去し、温水洗浄後乾燥し゛C兄掛りのアビデル化率
が平均約25%のアセデル化甲板を得た。
Next, hold the board J111711 at about 125° (C
>D, irz into a reaction solution with the same ir mixture ratio as above, heated to 100 ml, and reacted for about 20 minutes while maintaining the heated state. After the reaction is completed, the mixed solution remaining in the veneer is It was removed by carbonization, washed with warm water, and dried to obtain an acedelized deck with an average avidelization rate of about 25%.

史にこのJ、)4f甲板のアセデル化を、反応液を繰返
し使用しながら同一条件T′C″10回行つl(がいり
゛れbゝ11均約20%以−1−のj7ヒFル化率を示
づアセデル1ヒq1板をt′:I/こ。このアセチル化
単板は割れ等がt4り良好なものでの−)た。
In this J,) acedelization of the 4f deck was carried out 10 times under the same conditions T'C'' while repeatedly using the reaction solution. The Acedel 1 Hq1 plate exhibiting a fluorinated rate was t':I/.This acetylated veneer was in good condition with no cracks or the like.

−比較例− 上記実施例ど同1コ1の10枚の触tI1.処理甲板を
約125’ Cの実施例ど同一の反応液中に浸iet 
L/加温払f111を保らつ゛つ、20分間反応し乾留
、洗浄、乾燥しlこがアしゾル化率は平均′18%であ
った。
-Comparative Example- 10 sheets of 1 piece tI1. The treatment deck was immersed in the same reaction solution as in the example at about 125'C.
The mixture was reacted for 20 minutes, carbonized, washed, and dried while maintaining a heating temperature of f111, and the sol conversion rate was 18% on average.

一方、同−条1′1に−C40分間・反応しlJものは
ア又、55回の繰返しの1東川により反応液は本質拐の
抽出成分にJこりNC7色に:l、染され、反応液を冷
却したら多へ1の複塩が析出しlこ。
On the other hand, the reaction solution was reacted with -C for 40 minutes in the same column 1'1, and the reaction solution was dyed with the extracted components of the essence by Higashikawa in 7 colors, and the reaction was carried out. When the liquid is cooled, a double salt of 1 is precipitated.

このJ、うに木願几明I、L ’j’レーfル化処J!
J! 11〜間を9.υ縮出来、′1−Jlr性を向上
出来ると共に、反応液の使用回故苓人1+に増加りるこ
とで二1ストの低減が可能どなり、又、処理04間の短
縮に伴い、木賀拐の成分抽出が防止され、木?°l(Δ
の強庶低下等が田止℃゛さるものである。
This J, Uniki Ganmei I, L 'j' rail conversion place J!
J! Between 11 and 9. In addition to improving the '1-Jlr property, it is also possible to reduce the number of strokes by increasing the usage cycle of the reaction solution to Reijin 1+. Is it possible to prevent component extraction of wood? °l(Δ
The decline in the strength of the system is a major cause of concern.

28−28-

Claims (2)

【特許請求の範囲】[Claims] (1)本質材に酢酸塩水溶液を含浸した後乾燥しこの本
質材にアセデル化反応液を適宜方法により注入し、しか
るのらこの反応液注入木質材を更に、加温されたアセデ
ル化反応液中に22 !L’i Llで反応さU、本質
材成分の水酸基をアレチル化することを特徴とづる本質
材の改71方法。
(1) After impregnating the essential material with an acetate aqueous solution and drying it, injecting the acetylation reaction solution into the essential material by an appropriate method, then further adding the reaction solution-injected wood material to the heated acetylation reaction solution. 22 inside! 71. A method for reforming essential materials, characterized by reacting with L'i Ll and aretylating the hydroxyl groups of the essential materials components.
(2)反応液が芳香族炭化小木等の有機溶媒と)1(を
氷酢酸どの混合液からなる特6′1請求の範囲第1項記
載の本質材の改Mツノ法。
(2) The modified M-horn method for producing essential materials according to claim 1, wherein the reaction solution is a mixture of an organic solvent such as aromatic carbonized small wood, etc., 1 (1) and glacial acetic acid.
JP9231783A 1983-05-27 1983-05-27 Method of improving woody material Granted JPS59218806A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9231783A JPS59218806A (en) 1983-05-27 1983-05-27 Method of improving woody material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9231783A JPS59218806A (en) 1983-05-27 1983-05-27 Method of improving woody material

Publications (2)

Publication Number Publication Date
JPS59218806A true JPS59218806A (en) 1984-12-10
JPH0311245B2 JPH0311245B2 (en) 1991-02-15

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP9231783A Granted JPS59218806A (en) 1983-05-27 1983-05-27 Method of improving woody material

Country Status (1)

Country Link
JP (1) JPS59218806A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012531332A (en) * 2009-06-25 2012-12-10 イーストマン ケミカル カンパニー Method for esterifying lignocellulosic materials

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58181604A (en) * 1982-04-16 1983-10-24 大建工業株式会社 Method of improving woody material

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58181604A (en) * 1982-04-16 1983-10-24 大建工業株式会社 Method of improving woody material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2012531332A (en) * 2009-06-25 2012-12-10 イーストマン ケミカル カンパニー Method for esterifying lignocellulosic materials

Also Published As

Publication number Publication date
JPH0311245B2 (en) 1991-02-15

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